October 2025
Biofeedback support in stress urinary incontinence the effect of pelvic floor muscle training on muscle activity potential
Büşra İnce 1, Devrim Tarakçı 2, Aykut Başer 3
1 Departmen of Physiotherapy and Rehabilitation, Graduated School of Health Sciences, Istanbul Medipol University, Istanbul, 2 Departmen of Physiotherapy and Rehabilitation, Faculty of Health Sciences, Istanbul Medipol University, Istanbul, 3 Department of Urology, Faculty of Medical, Bandirma Onyedi Eylul University, Balıkesir, Turkiye
DOI: 10.4328/ACAM.22379 Received: 2024-08-21 Accepted: 2024-10-21 Published Online: 05-03-2025 Printed: 2025-10-01 Ann Clin Anal Med 2025;16(10):683-687
Corresponding Author: Büşra İnce, Departmen of Physiotherapy and Rehabilitation, Graduated School of Health Sciences, Istanbul Medipol University, Istanbul, Turkiye. E-mail: fztbusrakalli@gmail.com P: +90 542 479 71 50 Corresponding Author ORCID ID: https://orcid.org/0000-0002-7954-6289
Other Authors ORCID ID: Devrim Tarakçı, https://orcid.org/0000-0001-9804-368X . Aykut Başer, https://orcid.org/0000-0003-0457-512X
This study was approved by the Ethics Committee of Istanbul Medipol University (Date: 2023-05-13, No: E-10840098-772.02-3157)
Aim: The study aims to investigate the effect of biofeedback (BF) assisted pelvic floor muscle training (PFMT) on muscle activity potential in stress urinary incontinence (SUI).
Materials and Methods: The study included 42 women diagnosed with SUI between the ages of 45-65. Individuals were divided into three groups: PFMT with BF, PFMT alone, and control group. All groups were given medical treatment. The treatment was carried out for 6 weeks and 3 days a week. In the PFMT program, 360-degree diaphragmatic breathing training, dynamic neuromuscular stabilization exercises, and pelvic floor muscle exercises were applied. Electromyography (EMG) evaluation was applied to the participants at the beginning of the program and at the end of the 6th week.
Results: No difference was observed between the pre-treatment demographic characteristics and EMG values of the groups. While EMG parameters showed improvement in all groups after treatment. The highest increase in the work average value was in the PFMT + BF group. Peak and maximum voluntary contraction (%) value increases were found to be higher in the training groups compared to the control group, and there was no difference between the training groups.
Discussion: It was found that the PFMT + BF combined treatment method was beneficial in terms of its effect on muscle activity potential in SUI patients.
Keywords: stress urinary incontinence, biofeedback, pelvic floor muscle training, dynamic neuromuscular stabilization, diaphragmatic breathing
Introduction
Stress urinary incontinence is not a fatal or life-threatening condition, but it is a growing public health problem because it generally has a negative impact on the quality of life and causes physical, social, and emotional problems in the individual [1]. There are surgical and conservative methods for the treatment of SUI. Conservative treatment methods include PFMT, BF, electrical stimulation, vaginal cones, bladder training, and dynamic neuromuscular stabilization (DNS). The International Continence Society reports that PFMT should be the first recommended treatment for conservative treatment of SUI. The success rate of PFMT in the treatment of SUI has been found to be 56% to 75% [2, 3]. These exercises prevent pelvic floor insufficiencies by increasing anal sphincter muscle strength, urethral closure pressure and resistance. The patient’s complaints decrease in the 6th-8th weeks. The exercise program should be continued for at least 8-12 weeks, and when the continence level is reached, it should be combined with daily activities and become a lifelong lifestyle. For this, it is important to do the exercise regularly and correctly [4].
Studies have shown that more than 30% of women with SUI who were given PFMT were unable to contract their muscles correctly. In one study, approximately half of the women were unable to perform an effective contraction when verbally commanded, and one-fourth adopted a technique that could potentially worsen symptoms [5]. The BF method, which is frequently used to facilitate this situation, provides information about the activity of striated muscles by giving visual and auditory stimuli to teach and control the correct contraction of the muscles.
The BF method is generally applied as an auxiliary method with PFMT rather than being used alone. With BF, the person increases the strength of this group of muscles by contracting only the PFM without contracting the abdominal muscles. Thus, the patient learns to selectively contract and relax the PFM by recognizing it. Superficial and internal electrodes, mobile applications, and EMG games are used for BF treatment [6].
There is no evidence that PFMT together with BF for the treatment of SUI in women provides superior therapeutic benefits compared to other types of applications (such as no application or PFMT alone) or that adding BF to other applications is more effective than applications alone [7]. When the studies are examined, pelvic floor rehabilitation studies are found to investigate outcome measures such as urinary symptom severity, quality of life, and muscle strength [8, 9]. There are few studies that investigate the effect of PFMT activity potentials with the EMG method [10]. In this respect, the results of our study are very important for the literature.
The aim of our study was to investigate the effect of BF-supported PFMT on muscle activity potential in SUI. It was aimed to provide a new perspective on the treatment protocol and to contribute to the literature by developing a more accessible exercise program that women diagnosed with SUI would enjoy and willingly participate in.
Materials and Methods
Procedure
This study was conducted in the Urology Department between May 2023 and July 2024. All individuals participating in the study were given detailed information about the purpose and method of the study and their permissions were obtained by signing the informed consent form.
Participants
In the study, 60 female volunteers were evaluated for eligibility and 18 were excluded from the study. The study was conducted on 42 female volunteers between the ages of 40-65 who participated in the study voluntarily. Individuals were randomized into three groups: EMG – BF + PFMT group (n = 14), PFMT group (n = 14), and control group (n = 14) according to the envelope method. Medical treatment was also applied to all groups. Exclusion criteria from the study were; being pregnant, having an active urinary tract infection or a history of pelvic organ prolapse, and having undergone vaginal and pelvic surgery within the last 6 months. A demographic assessment form including age, height, weight, obstetric and gynecological characteristics, incontinence characteristics, and consumption habits was filled out for each participant. The treatment was carried out for 6 weeks and 3 days a week. Participants underwent EMG evaluation at the beginning of the treatment and at the end of week 6. All evaluations were performed by the same physiotherapist.
Measurements
Electromyography (EMG)
The electrical activity of a muscle is an indicator of muscle function. A single-channel NeuroTrac brand Myoplus 2 (Verity Medical Ltd, UK) EMG measuring device integrated with computer software was used to measure PTC activation in order to obtain electromyographic signals, digital analysis, and reports. Two active and one passive surface electrode were used in valid and reliable noninvasive surface EMG measurements. Active surface electrodes were placed on the right and left of the perineal body at 2 and 7 o’clock. The passive surface electrode was placed on the right thigh. The supine position with the PFM extremely relaxed was preferred during the measurement. In this position, the patient’s knees were flexed at 140 degrees, the soles of the feet were in full contact with the bed, and the thighs and feet were 30 cm apart. Only tonic PFM was evaluated during the measurement. The contraction and rest periods were set to five seconds on the device, and a total of 5 contractions and 5 resting EMG activities were measured for 50 seconds. The device gave a voice command of “work” to obtain a contraction response and “rest” to obtain a relaxation response. The average values of the EMG activity in the working and resting states in 50 seconds were recorded. At the end of the measurement, muscle activation was recorded in microvolts (μV).
Treatment Program
PFMT treatment
All cases were first taught how the correct function of the PFMT (correct contraction, relaxation, etc.) is. In the PFMT session, thoracic diaphragm activation, dynamic neuromuscular stabilization exercises (in supine, prone, and crawling positions), and endurance exercises were performed to retrain the ability to lengthen and extend the PFM. In thoracic diaphragm activation, 360° diaphragm breathing was taught with the hips and knees in 90° flexion. For DNS exercises, 3 and 6-month supine positions, 3, 6 and 7-month prone positions, 9-month crawling positions, and 3 and 4-month supine positions with a pilates ball were selected. Each development position was accepted as an exercise position. After correct positioning, the number of exercises was determined as the number of breaths. 3 sets, 10 repetitions, and 10 seconds of 360° expansive diaphragm breathing were performed in each position. A 2-minute rest period was given between sets and positions. An endurance exercise program was prepared that included cycles followed by a rest period twice as long as the contraction period in the retraining of the ability to shorten and lengthen the PFM. During this phase of training, one group performed exercises with BF support, while the other group performed exercises without BF. Slow contraction exercises were continued as 10 seconds of muscle holding and 20 seconds of relaxation, and fast contraction exercises were continued as 1-second contraction and 2 seconds of relaxation. An exercise program of 5 sets of 10 repetitions was created for each type of contraction. A 2-minute rest period was given between sets.
EMG-BF treatment
Animated EMG-BF treatment was performed with the NeuroTrac brand Myoplus 2 device and was performed in the same position (supine) as in the evaluation. Appropriate games (rabbit game, airplane game) were determined for animated EMG-BF treatment. Before starting the treatment, training was applied to show how to control the PFM and external urethral sphincter. Games were determined for animated EMG-BF treatment. There is a game protocol that includes 10 s contraction and 20 s relaxation cycles. Fast contraction exercises were continued as 1 s contraction and 2 s relaxation. There was an exercise program consisting of 5 sets of 10 repetitions for the type of contraction. A 2-minute rest period was given between sets. During the contraction (working phase), the patient was asked to count out loud so that the glottis would not close. In addition, the physiotherapist placed his hands on the abdominal and adductor muscles to prevent associated muscle contractions and observed the gluteal muscles.
Statistical Analysis
In the descriptive statistics of the data, mean, standard deviation, median lowest, highest, frequency, and ratio values were used. Kolmogorov Smirnov in the status of variables was measured with the Shapiro-Wilk test. Kruskal-Wallis test was recorded in the analysis of beautiful independent data with non-normal distribution. Wilcoxon test record in the analysis of dependent quantitative data. SPSS 28.0 program was used in the analyses.
Ethical Approval
This study was approved by the Ethics Committee of the Non-Interventional Clinical Research Ethics Committee of Istanbul Medipol University (Date: 2023-05-13, No: E-10840098-772.02-3157).
Results
In our study investigating the effects of BF-supported PFMT on muscle activity potential in SUI, no significant difference was found between the groups in terms of demographic characteristics (p > 0.05) (Table 1).
There was no significant difference between the pre-treatment groups in terms of all EMG values. The analysis of the participants’ EMG parameters is shown in the table (Table 2).
When the changes before and after treatment were compared, the study work average value showed a significant increase in all groups (p < 0.05). The pre-treatment/post-treatment value increase was found to be significantly higher in the PFMT + BF group than in the PFMT and control groups, and in the PFMT group than in the control group (p < 0.05).
When the changes before and after treatment were compared, the peak value showed a significant increase in all groups (p < 0.05). While the pre-treatment/post-treatment value increase was found to be significantly higher in the PFMT + BF and PFMT groups than in the control group (p < 0.05), no significant difference was found between the PFMT + BF and PFMT groups (p > 0.05).
When the changes before and after treatment were compared, the MVC (%) value showed a significant increase in all groups (p < 0.05). While the pre-treatment/post-treatment value increase was found to be significantly higher in the PFMT + BF and PFMT groups than in the control group (p < 005), no significant difference was found between the PFMT + BF and PFMT groups (p > 0.05) (Table 3).
Discussion
Surface electromyography (sEMG) is considered a tool for assessing PFM function by real-time assessment of PFM contractions and identification of motor unit action potentials. Electrical signals from muscles are generated by the activation of motor units during contraction. The bioelectrical activity of a muscle is monitored as a representation of muscle function [11]. Dannecker et al., Bertotto A et al., Aukee et al. used sEMG to assess treatment progress, and increases in muscle activity were expressed in μV of amplitude. In these studies, it was reported that PFM resulted in a significantly greater increase in sEMG amplitude when the group receiving BF combined with PFMT was compared to the group receiving PFMT alone [12-14]. In the study by Bertotto et al., improvements in muscle strength and EMG activity were observed in the PFMT + BF group, with the most significant gains reported in precontraction, endurance, and MVCs. The addition of BF to the treatment of muscle dysfunctions aims to improve voluntary motor activity by inducing neuroplasticity or functional neural regeneration mechanisms of the central nervous system. This neuroplasticity helps patients control and monitor future muscle activities and movements. sEMG-assisted BF was associated with a significant increase in the sEMG amplitude recorded during the tests [13]. Aukee et al. reported greater improvement in patients who received sEMG-assisted BF training compared to those who received PFMT alone. The authors reported increased PFMT activity (μV) and fewer leakage episodes [14]. Dannecker et al. attempted to determine the effect of 12 weeks of sEMG-BF-assisted training on PFMT in a study of 390 women diagnosed with SUI (80%) and MUI (20%). They observed that the sEMG electrical potential of the PFMTs increased from an average of 11.3 to 22 μV, thus confirming the high efficacy of PFMT [12]. Rett et al., in their study of 26 women with SUI, found that all contractions (tonic and phasic) had significantly better PFM strength and sEMG amplitudes (μV) after 12 BF sessions [15]. Yoo et al. reported that there was a significant change in the mean amplitude of tonic contraction measured by vaginal sEMG activity after the 8th session and that BF-assisted PFMT was successful in 57% of women with urinary incontinence [16]. In 2017, Ptaszkowski et al. aimed to objectively evaluate the resting and functional bioelectrical activity of PFMT in women during menopause and compare it in three different positions of the pelvis (anterior pelvic tilt – position 1 (P1), posterior pelvic tilt – position 2 (P2), and neutral pelvic tilt – position 3 (P3)). The highest mean resting activity of sEMG PFMT (μV) was observed at P2, and this value was 11.6 μV (SD = 5.5 μV). The P1 value was found to be 9.8 μV (SD = 4.8 μV) and the P3 value was found to be 9.0 μV (SD = 4.2 μV). The results revealed a significant statistical difference. As a result, the posterior pelvic tilt position determines the higher resting and functional bioelectrical activity of the PFM [17]. In our study, the posterior pelvic tilt position was preferred during the treatments. The EMG measurement results we made to determine the muscle activation values before and after the application support the literature. Finally, a study conducted in 2024 evaluated the effectiveness of DNS compared to traditional Kegel exercises and its effect on pelvic floor strength and core muscle activation in women diagnosed with SUI. The DNS group showed a greater increase in PFM strength compared to the Kegel exercise group. In other words, statistically, it was observed that DNS exercises provided more significant improvements in EMG measurements (average, peak, and MVC) compared to traditional Kegel exercises [3]. In our study, the respiratory and stabilization approaches of the DNS method were used within the scope of pelvic floor training in individuals diagnosed with SUI. As a result, a significant improvement was observed in EMG parameters in the treatment groups with DNS exercises compared to the control group.
Limitations
As a limitation of our study, the short-term effects of the treatment were investigated. Long-term effects could also have been examined to obtain information about the permanence of the observed improvements.
Conclusion
It was found that the combined treatment method of PFMT + BF was beneficial in terms of its effect on muscle activity potential in SUI patients.
Scientific Responsibility Statement
The authors declare that they are responsible for the article’s scientific content including study design, data collection, analysis and interpretation, writing, some of the main line, or all of the preparation and scientific review of the contents and approval of the final version of the article.
Animal and Human Rights Statement
All procedures performed in this study were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.
Funding: None
Conflict of Interest
The authors declare that there is no conflict of interest.
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Download attachments: 10.4328.ACAM.22379
Büşra İnce, Devrim Tarakçı, Aykut Başer. Biofeedback support in stress urinary incontinence the effect of pelvic floor muscle training on muscle activity potential. Ann Clin Anal Med 2025;16(10):683-687
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Long-term evaluation of the ocular surface after reconstructive surgery in malignant periocular tumors
Neşe Arslan 1, Ahmet Alp Bilgiç 2, Naciye Kabataş 3, Mutlu Acar 4
1 Department of Ophthalmology, Diskapi Yıldırım Beyazıt Research and Education Hospital, 2 Department of Opthalmology, Ulucanlar Research and Education Eye Hospital, 3 Department of Opthalmology, Venividi Private Eye Hospiatal Groups, 4 Department of Ophthalmology, Liv Private Hospital, Ankara, Turkey
DOI: 10.4328/ACAM.22420 Received: 2024-09-27 Accepted: 2025-03-10 Published Online: 2025-03-15 Printed: 2025-10-01 Ann Clin Anal Med 2025;16(10):688-692
Corresponding Author: Neşe Arslan, Department of Ophthalmology, Diskapi Yıldırım Beyazıt Research and Education Hospital, Ankara, Turkey. E-mail: arslannese75@gmail.com P: +90 537 347 74 61 Corresponding Author ORCID ID: https://orcid.org/0000-0001-6352-9786
Other Authors ORCID ID: Ahmet Alp Bilgiç, https://orcid.org/0000-0001-8033-7970 . Naciye Kabataş, https://orcid.org/0000-0001-7434-4576 . Mutlu Acar, https://orcid.org/0000-0002-0300-7350
This study was approved by the Ethics Committee of University of Health Sciences, Diskapi Yildirim Beyazit Training and Research Hospital (Date: 2020-04-20, No: 85/05)
Aim: Our aim in this study was to evaluate postoperative complications and dry eye parameters after reconstructive surgery for primary periocular malignant lesions.
Materials and Methods: Patients who underwent reconstructive surgery after malignant eyelid and periocular tumor excision were evaluated in two groups: those with defects involving the lid margin and those with defects sparing the lid margin. Demographics, histopathology, lesion location, horizontal eyelid defect size, surgical procedure, postoperative complications, and dry eye test results were compared between the groups.
Results: The study included 68 patients: 35 with lesions involving the lid margin and 33 with lesions sparing the lid margin. The mean age was 69.9±14.95 years. Histopathology confirmed basal cell carcinoma in 86.8% of the cases, and 54.4% of the tumors were on the lower lid. Cases involving the lid margin had more postoperative complications, as well as a higher rate of postoperative dry eye disease (DED) (p<0,05).
Discussion: Our results indicate that reconstructive surgeries for tumors involving the lid margin are more prone to postoperative complications and may also cause the onset or exacerbate preexisting DED.
Keywords: eyelid neoplasm, dry eye syndrome, reconstructive, basal cell carcinoma, squamous cell carcinoma
Introduction
Eyelid tumors are the most frequent neoplasms encountered in clinical ophthalmology practice [1,2]. Malignant eyelid tumors constitute approximately 5-10% of all skin cancers and represent the main reason for eyelid reconstruction in oculoplastic surgery [3-5 3-4]. A successful reconstruction of the eyelid and periocular region requires good knowledge of its complex structure. The choice of surgical procedure depends on the size, location, and depth of the lesion. Anterior lamellar defects not involving the eyelid margin are repaired by primary closure, rotational flaps, or free skin grafts according to the size of the defect. For full-thickness defects that involve the eyelid margin, repair by primary closure with or without cantholysis is recommended for those less than 30% of the horizontal lid width, whereas larger defects covering more than 30% require tarsoconjunctival flaps, rotational flaps, or myocutaneous semicircular flaps, free grafts, or a combination of these procedures [5]. The Tenzel technique (myocutaneous semicircular flap) is a one-stage procedure used in full-thickness defects affecting 30% to 50% of the horizontal length of the lid [6]. The Hughes procedure (tarsoconjunctival flap) is a reliable two-stage eyelid-sharing technique for the reconstruction of full-thickness defects that span more than 50% of the lid [7]. Each of these procedures has its advantages and disadvantages.
Dry eye disease (DED) is an ocular surface disorder frequently encountered after eyelid surgery [8, 9]. The TFOS DEWS II revised the definition of dry eye as “a multifactorial disease of the ocular surface characterized by a loss of homeostasis of the tear film and accompanied by ocular symptoms, in which tear film instability and hyperosmolarity, ocular surface inflammation and damage, and neurosensory abnormalities play etiological roles” [10]. As some reconstructive surgeries involve a full-thickness lid defect, DED is inevitable [11]. For this reason, a good understanding of the anatomy and physiology of the eyelid and ocular surface is necessary to manage dry eye after eyelid surgery.
The importance of the ocular surface and possible dry eye complications may be overlooked while focusing on the excision and complete treatment of malignant tumors. Therefore, we aimed in this study to retrospectively analyze the surgical outcomes of reconstructive procedures performed in patients with periocular malignant lesions and evaluate their effects on the ocular surface and tear film.
Materials and Methods
Data were collected from the clinical notes and electronic records of patients who underwent reconstructive surgery after malignant eyelid and periocular tumor excision in the ophthalmology department of Diskapi Yıldırım Beyazıt Training and Research Hospital between 2014 and 2023. The patients were divided into two groups, those with lesions involving the lid margin and those with lesions sparing the lid margin. In addition to lid margin involvement, we evaluated the patient’s demographic characteristics, the histologic type, and the location of the lesion according to Spinelli and Jelks [12], horizontal defect size in lesions involving the lid margin, the surgical procedure performed, postoperative complications, and dry eye test results. Patients with at least 6 months of postoperative follow-up were included in the study to allow evaluation of long-term complications.
In both margin-involving and margin-sparing cases, surgical procedures were selected according to lesion location and defect size after excision, as follows:
1. Lesions involving the lid margin:
a. Primary closure for full-thickness defects < 30% of the lid width (Figure 1).
b. Tenzel’s lateral advancement flap for defects 30%-50% of lid width.
c. Hughe’s tarsoconjunctival flap with skin graft for defects > 50% of lid width.
2. Lesions sparing the lid margin:
a. Primary closure for elliptical defects ≤ 2 cm × 1 cm.
b. Secondary closure with a rotational flap or free graft for irregular defects > 1 cm × 1 cm (Figure 2).
The surgical excision was performed either by leaving 3-4 mm of intact tissue around the tumor border and frozen section examination at the same intervention or excisional biopsy of the suspicious lesion in a prior surgery. If malignant tumor cells were detected in the surgical margin, further excision was performed until a clear margin was obtained.
Based on the TFOS DEWS II report, the dry eye assessment included Ocular Surface Disease Index (OSDI), noninvasive tear break-up time (NIBUT), and ocular surface staining [10]. Dry eye assessment was compared between groups preoperatively and postoperatively with intervals of 6 months, 1 year, and 3 years.
Ocular Surface Disease Index
The patients completed the OSDI questionnaire before the examination to ensure their responses would not be influenced by the clinical procedures. The 12 items on the OSDI questionnaire were rated from 0 to 4, with 0 indicating the stated symptom occurred “none of the time”; 1, “some of the time”; 2, “half of the time”; 3, “most of the time”; or 4, “all of the time”. The total OSDI value was then calculated with the following formula: OSDI = (sum of the scores for all questions answered × 100) / (total number of questions answered × 4) [13,14]. The previously validated Turkish version of the OSDI questionnaire was used [13]. An OSDI value between 0 and 12 was considered normal, and values of 13 or more were considered pathologic.
Noninvasive Tear Break-up Time
The NIBUT of the participants was measured using a Sirius multifunctional topography device according to the manufacturer’s instructions. Before starting the measurement, the image was centered and sharpened. The patient was instructed to blink twice to spread the tear film across the ocular surface, then keep their eyes open as long as possible. The device automatically measures after the patient blinks twice. The device evaluates time-dependent changes in the integrity of the tear film spread over the anterior corneal surface. The test is performed through videokeratoscopy, a video recording of the Placido disk ring projection on the patient’s precorneal tear film. A homogeneously distributed tear film on the ocular surface causes a regular appearance in the rings and any deformation or disruption in the tear film results in deformation in one or more rings. The device records the time from the patient’s double blink to distortion or interruption in the Placido disk pattern as the NIBUT. The mean duration of all break-up intervals occurring in the precorneal tear film after blinking is recorded by the device as the average NIBUT. A NIBUT ≥10 s was considered normal [10].
Ocular Surface Fluorescein Staining
After NIBUT measurement, the ocular surface was stained with fluorescein and examined using a cobalt blue filter [15,16]. Pathologic fluorescein staining was evaluated according to the TFOS DWES II report and defined as: > 5 corneal spots, > 9 conjunctival spots, or lid margin staining (≥ 2 mm length and ≥ 25% width).
Statistical Analysis
Statistical analysis was performed using IBM SPSS Statistics for Windows version 21.0 (IBM Corp., Armonk, NY, USA). Descriptive statistics are presented as mean ± SD. The chi-square test was used for categorical variables. Parametric variables were compared between groups via analysis of variance and t-test. Nonparametric data were compared using the Kruskal-Wallis and Mann-Whitney U tests, as appropriate. The level of statistical significance was set at p < 0.05.
Ethical Approval
This study was approved by the ethics committee of the University of Health Sciences, Diskapi Yildirim Beyazit Training and Research Hospital in Ankara, Turkey (Date: 2020-04-20, No: 85/05).
Results
A total of 68 patients who underwent eyelid and periocular reconstructive surgery were identified for inclusion in the study. The mean age was 69.9 ± 14.95 years (range: 32-93 years; 68.6 ± 14.4 years in patients with lid involvement, 71.3 ± 15.6 years in those without lid involvement) (p=0,46). There was a male preponderance, with 72% (n=49) of the patients being men. Sex distribution was statistically similar in groups (p=0,17). Histopathology confirmed that 86.8% (n=59) of the eyelid and periocular malignancies were basal cell carcinoma (BCC) (Figure 1,2). The most common location was the lower eyelid (54.4%, n=37). The patients’ lesion locations, horizontal defect sizes, and surgical procedures are summarized in Table 1. Postoperative complications among patients with eyelid margin involvement included ectropion in two patients after Hughe’s procedure and mild entropion without trichiasis in 1 patient after Tenzel’s procedure for lid reconstruction. Four patients exhibited acceptably mild lid margin notching after Tenzel’s procedure in three patients and pentagon excision with primary closure in one patient (Figure 1b). Among the lid-sparing cases, only one patient with a lesion near the medial canthus developed mild ectropion that was treated 6 months later with a lazy-T procedure. The other two cases of ectropion developed after Hughe’s procedure were treated after approximately 5 months with lateral tarsal strip fixation. The patients with entropion and eyelid notching were satisfied with their results and no further surgery was performed.
Preoperatively only the mean OSDI score was significantly higher in the lid margin involved group. In the postoperative period assessments, the OSDI score was higher in the lid margin spared group in the first year of control. The NIBUT and corneal staining was more common among patients with lid margin involvement in the 6-month and 1st year of control, but the differences did not reach statistical significance in the 3rd year of control. Detailed patients’ dry eye test results are summarized in Table 2.
Discussion
A stable precorneal tear film and healthy ocular surface are essential for comfort and clear vision. Periocular tumors, especially those involving the lid margin, can alter tear film composition and homeostasis by affecting the meibomian glands, which leads to changes in tear volume and turnover and results in ocular surface dysfunction and discomfort. Surgical excision of these lesions can also result in postoperative complications such as lagophthalmos and DED by causing iatrogenic meibomian gland loss, irregular lid margin contour, and lid retractor and orbicularis oculi muscle loss or dysfunction [10,11]. Management of such complications is as important as removing the malignant tumor for quality of life after tumor excision. Therefore, we aimed in this study to emphasize the importance of maintaining a healthy ocular surface and a stable tear film after preocular malignant tumor excision.
Hyperemic and/or hypertrophic eyelid margins, ectropion, entropion, ocular irritation, and persistent mucoid discharge are reported complications after eyelid reconstructions [7]. Our study revealed that complications were statistically more frequent in cases involving the lid margin. Two cases of ectropion, one case of entropion, and four cases of lid margin notching were reported after surgical treatment among those with lid margin involvement, whereas only one case of ectropion was reported among those with excisional defects sparing the lid margin. Ectropion required correction in a secondary surgery 5 to 6 months after the first operation. Luu et al. [17] reported hypertrophic changes in the lower eyelid margin after Hughe’s procedure. Aggarwal et al. [18] reported one patient with a small pyogenic granuloma and another with mild ectropion after Hughe’s procedure. They also stated that using an amniotic membrane in the second stage of Hughe’s procedure prevented the hypertrophic changes in the lid margin. In our study, only one case of ectropion was reported after Hughe’s procedure.
According to TFOS DEWS II, the lid margin and meibomian glands are recognized as key components in the etiology of DED, and eyelid surgeries are listed as an iatrogenic cause of DED onset or worsening of preoperative dry eye [19]. The management of DED should start with a preoperative evaluation and continue postoperatively, especially in patients with preexisting DED [9].
In this study, the results of dry eye assessments showed no significant difference between groups except for the OSDI score (OSDI score p=0,0001; NIBUT p=0,94; corneal staining p=0,97). This could be explained as a result of the affected lid and lid margin as we mentioned above. Whereases, in the postoperative assessments the lid margin involved group showed a significantly lower NIBUT and a higher prevalence of fluorescein corneal staining in the 6th month (p=0,008; p=0,001respectively) and 1st year of control (p=0,017; p=0,049 respectively). As patients in our study had a high mean age (69.9 ± 15.0 years), which is considered another risk factor for DED, these patients were followed up in our clinic with dry eye treatment postoperatively. Therefore; results of dry eye assessments in the 3rd year of control were comparable in both groups showing better results with no significant difference (OSDI score p=0,54; NIBUT p=0,085; corneal staining p=0,96).
To the best of our knowledge, this is the first study to evaluate ocular surface findings and dry eye tests; according to the TFOS DEWS II 2017 report [19]; in patients with malignant eyelid and periocular tumors after surgical treatment, with comparison according to lid margin involvement for three years. Klein-Theyer et al. [20] conducted a study evaluating the ocular surface and tear film function in 18 patients following the modified Hughe’s procedure and observed a lower fluorescein tear break-up time (TBUT) (p=0.03), higher OSDI, and increased corneal staining in operated eyes compared to non-operated eyes. Similarly, Zaky et al. [21] reported lower TBUT in operated eyes than in non-operated eyes after the modified Hughe’s procedure. Wang et al. [22] also reported that McMonnies dry eye score was significantly higher and NIBUT was lower in operated eyes after the modified Hughe’s procedure when compared to contralateral eyes (p<0.05). In the abovementioned studies, dry eye tests were compared between operated and contralateral non-operated eyes, especially after modified Hughe’s procedure. In contrast, Gonnermann et al. [23] compared 17 patients who underwent full-thickness eyelid reconstruction with a control group and observed no significant difference in TBUT and Schirmer test results.
DED after periocular tumor excision is a multifactorial disease. The mechanism of DED in these cases is mainly attributed to one or more of the following factors: meibomian gland loss, changes in the eyelid anatomy that affect normal eyelid closure and its relation with the cornea, and loss of the orbicularis oculi in some cases, which might lead to decreased blink rate and lagophthalmos. In patients with lid margin involvement, loss of meibomian glands in both the upper and lower eyelids after Hughe’s procedure and the lower eyelid in Tenzel’s procedure causes decreased lipid secretion and hence an unstable tear film. Also, changes in the eyelid anatomy and its position relative to the ocular surface increase the risk of DED or exacerbate the pre-existing condition.
Limitations
There are several limitations of this study, including the relatively small number of patients per group and our evaluation of only operated eyes in both groups. In addition, our evaluation did not include inflammatory markers or osmolarity. Therefore, we believe that further studies should be conducted with a larger number of subjects and a more comprehensive analysis including pre- and postoperative inflammatory cytokines and osmolarity to more clearly understand the effects of eyelid reconstructive surgery on DED.
Conclusion
In conclusion, tumor size and location are the best factors in selecting a surgical procedure for eyelid repair and reconstruction. Very good results are achievable depending on proper surgical planning, surgical experience, and postoperative care. Our results indicate that surgical procedures for tumors involving the lid margin are more prone to postoperative complications and might induce DED or exacerbate pre-existing DED. Therefore, for the best functional and esthetic results, we believe that the reconstruction of large defects after malignant tumor excision should be performed by experienced surgeons. Furthermore, preoperative and postoperative DED management should not be neglected in all patients with periocular tumors.
Scientific Responsibility Statement
The authors declare that they are responsible for the article’s scientific content including study design, data collection, analysis and interpretation, writing, some of the main line, or all of the preparation and scientific review of the contents and approval of the final version of the article.
Animal and Human Rights Statement
All procedures performed in this study were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.
Funding: None
Conflict of Interest
The authors declare that there is no conflict of interest.
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2. Deprez M, Uffer S. Clinicopathological features of eyelid skin tumors. A retrospective study of 5504 cases and review of the literature. Am J Dermatopathol. 2009;31(3):256–62.
3. Eren MA, Gündüz. Demographic features and histopathological diagnosis in primary eyelid tumors: results over 19 years from a tertiary center in Ankara, Turkey. Int J Ophthalmol. 2020;13(8): 1287–93.
4. Burgic M, Iljazovic E, Vodencarevic AN, et al. Clinical Characteristics and Outcome of Malignant Eyelid Tumors: A Five-Year Retrospective Study. Med Arch. 2019;73(3): 209–12.
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6. Cha JA, Lee KA. Reconstruction of periorbital defects using a modified Tenzel flap. Arch Craniofac Surg. 2020; 21(1): 35–40.
7. Hishmi AH, Koch KR, Matthaei M, Bölke E, Cursiefen C, Heindl LM. Modified Hughes procedure for reconstruction of large full-thickness lower eyelid defects following tumor resection. Eur J Med Res. 2016;21(1):27.
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Neşe Arslan, Ahmet Alp Bilgiç, Naciye Kabataş, Mutlu Acar.vLong-term evaluation of the ocular surface after reconstructive surgery in malignant periocular tumors.Ann Clin Anal Med 2025;16(10):688-692
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In vitro assessment of wear in peripheral nerve block needles for re-use
Eyup Aydogan 1, Betül Kozanhan 2, Yasin Tire 2, Munise Yıldız 2
1 Department of Anesthesiology and Reanimation, Alanya Training and Research Hospital, Alanya, 2 Department of Anesthesiology and Reanimation, Konya Training and Research Hospital, Konya, Turkiye
DOI: 10.4328/ACAM.22491 Received: 2025-01-15 Accepted: 2025-03-03 Published Online: 2025-03-13 Printed: 2025-10-01 Ann Clin Anal Med 2025;16(10):693-698
Corresponding Author: Eyup Aydogan, Department of Anesthesiology and Reanimation, Alanya Training and Research Hospital, Alanya, Turkiye. E-mail: eypaydogan@hotmail.com P: +90 242 513 48 41 Corresponding Author ORCID ID: https://orcid.org/0000-0003-3432-4946
Other Authors ORCID ID: Betül Kozanhan, https://orcid.org/0000-0002-5097-9291 . Yasin Tire, https://orcid.org/0000-0002-9905-8856 . Munise Yıldız, https://orcid.org/0000-0003-2644-7540
This study was approved by the Ethics Committee of the Institutional Review Board of Alanya Alaaddin Keykubat University (Date: 2022-05-13, No: 10354421)
Aim: This study aims to assess the safety and effectiveness of reusing peripheral nerve block needles, focusing on electrical resistance and immersion forces. Peripheral nerve block needles are typically single-use, but reusing them could reduce costs associated with needle disposal and purchase. While safety concerns exist, especially regarding infection and needle blunting, these issues need to be thoroughly evaluated.
Materials and Methods: We measured immersion loads and electrical resistances of 20 unused peripheral nerve block needles. Four anesthetists applied loads to a model tissue with these needles. Nine needles were selected for reuse, assigned to anesthetists, and immersed in model tissue at 2.5 cm depth. After rinsing with isotonic solution, the needles underwent sterilization, and this cycle was repeated 20 times.
Results: The mean load and electrical resistance of the initial 20 needles were 443.6 ± 74.39 and 1.855 ± 0.27, respectively. No significant differences in electrical resistance or load measurements were noted among anesthetists with varying experience levels (p-values ≥ 0.150). Likewise, no statistical difference existed between the initial and reused needles (p=0.265).
Discussion: The study indicates no significant difference in forces applied by male and female practitioners or across experience levels, suggesting that the reuse of peripheral nerve block needles is viable. The needles can safely undergo at least 20 cycles of reuse using the employed sterilization technique without compromising electrical conduction or immersion efficacy.
Keywords: medical, device, peripheral nerve, block, re-use
Introduction
Medical products, including peripheral nerve block needles, are mainly manufactured for single use. Although peripheral nerve block needles are cheaper, they are used in much more numbers. Reusing peripheral nerve block needles was considered a severe saving tool [1-3]. Both the needle price and the need to dispose of used needles as medical waste increases the cost. (Needle unit price is about 12 $-Invoiced to the institution, Sterilization costs 0.2 $ per needle (The Institutional conditions)). Also, this approach is compatible with producing less waste (less CO2 emission) [4]. The needles have been reported to be effectively sterilized by current techniques [2, 3]. The sterilization cost is meager compared to the needle unit price.
For this reason, the objective evaluation of the wear problem caused by reuse is essential. If they are reused, the reuse procedure should be proofed that it’s safe, and there must be an identified(and also written) reuse procedure. It is envisaged that physical wear of the peripheral block needles will result in breakage of the needles, loss of transmitting cables, and reduced transmission of electricity. The peripheral nerve block needles work with the principle of getting a contraction response from the relevant muscle tissue by giving low-voltage electrical current to the nerves. Healthy electrical conduction means the robust operation of a nerve stimulator.
On the other hand, our study includes proven sterilization methods for peripheral nerve block needles, and our results are thought to improve reuse standards. The cycle determined by our study can be used alone as a standard of reuse. The study is planned on these principles.
According to our hypothesis, each time the needle is used (every time it is immersed in the artificial tissue), it should be a little blunter, it should be pushed into the tissue with a bit more force the next time, and also the electrical resistance should increase with wear. If these increases do not occur, it will be seen that the functionality of the needles does not decrease in reuse. In addition, it has been aimed to determine whether chemicals, temperature, and other unpredictable factors used for sterilization have a corrosive effect on the needle and whether these effects affect the needle’s operability. This entire cycle will be expressed with numerical data and analyzed by statistical methods. It has been investigated whether there is a significant difference between the interventions in applied load and resistance to electric current.
Materials and Methods
Firstly, to numerically express the electrical resistance of the peripheral nerve block needles and the immersion forces in the model tissue, the immersion loads and average electrical resistances of the 20 unused needles were measured.
The male participant, who had 5 years or more experience, was chosen as the practitioner in the random selection between the 4 participants anesthetists to apply the load of the first 20 needles to the model tissue. In our study, the Pajunk® Sonoplex Stim cannula model 22 gauge 50 mm peripheral nerve block needle was used. As model tissue, Genesis® brand, Spinal Injection Smilation (model code 800.866.3342) has been used. Model artificial working tissue was placed on sensitive scales (Swan® Digital Precision (2018 China) scales (with an accuracy of ± 0.1 g)) and the block needle was immersed to a depth of 2,5 cm, the highest values (force in-grams applied to the needle) recorded with the measuring instrument were recorded and the average values were calculated. In the next stage, the electrical resistance of each needle (T-Technic A830L (2017 China) digital multimeter) was measured with a multimeter (recorded in ohms). The calculation of these values has been determined as a reference of the mean for the electrical resistance and force required for immersion of an average needle. That data would able to be used for determining and comparison with the increase/decrease in the force requirement and electrical resistance changes in successive interventions with a single needle in subsequent measurements.
In the second stage, 9 of the needles were randomly selected and divided into five groups. Two needles were given to each anesthetist. One needle was reserved as a reference for comparison of visible physical wear.
The needles were immersed in the model working tissue, at a depth of 2.5 cm, perpendicular to the ground (the force applied to the needle was detected by tare), and after the measurements were taken, the needles were rinsed with an isotonic solution. They were then sent to the sterilization unit. The needles packaged in the sterilization unit were sterilized in a CASP brand CASP-120 model sterilization device with 55-60 % hydrogen peroxide at 45 ± 5 °C in 53 minutes and a cycle was completed. This described cycle was repeated 20 times and data was recorded. The force applied to the needle was recorded in grams (gr) and the measured electrical resistance was in ohms (Ω). Thus, 20 cycles of use, mechanical fatigue, and chemical contact cycles were simulated. The metal alloy of the needle used was worn fairly by exposure to mechanical trauma and chemicals. This whole cycle will be expressed with numerical data and analyzed by statistical methods, it is investigated whether there is a significant difference in terms of the power applied between the enterprises. The measuring device is shown in Figures 1, 2, and 3. The study was carried out at an ambient temperature of 18-22 °C to avoid temperature effects. The cycle described above was performed by a total of 4 anesthetists. Visible signs of wear (bending, twisting, disintegration, etc.) occurring in the needles were also added to the data, if any, were noted.
Statistical Analysis
When histogram plot analysis was performed, the distribution of measurements was parametric. When the Skewness and Kurtosis normality analysis and confidence interval values were examined, Repeated Measures ANOVA tests for proportions were used to assess the correct identification of each of the four anesthesiologists. The 0.05 level of significance was used to reject the null hypothesis. Power analysis showed that a sample of 20 times of use will yield 80 % power to detect a difference in the proportion of correct identifications of each four anesthesiologists. Statistical analyses were performed using IBM SPSS Statistics version 22 (IBM) and Rex version 3.5.3 (RexSoft Inc).
Ethical Approval
This study was approved by the Ethics Committee of the Institutional Review Board of Alanya Alaaddin Keykubat University Medicine Faculty (Date: 2022-05-13, No:10354421).
Results
The mean load and electrical resistance measurements of the first 20 block needles are 443.6 ± 74.39 and 1.855 ± 0.27 with their standard deviations(Table 1). A total of four anesthetists were included in the study (n = 4). When histogram plot analysis was performed, the distribution of measurements was non-parametric. When the Skewness and Kutosis normality analysis and confidence interval values were examined, no statistical significance was found in the measurements. In this sense, p-value was found to be 0.163 and 0.308, respectively, in load measurements, those with 5 years or more and less than 5 years (Coinfidence Interval = -0.719 / -0.064). For electrical resistance measurements, p values were found to be 0.150 and 0.361 for those with 5 years and more experience and less than 5 years (Confidence Interval = 0.540 / 1.110). In the analyses made with the Repeatedy ANOVA test, no statistically significant difference was observed in the load and electrical resistance measurement values in those with 5 years and more experience and less than 5 years (p-value = 0.587 and 0.250 respectively) (Table 2). The mean load measurements (505.31 ± 63.87) in participants with less than 5 years of experience were less than those with 5 years or more (514 ± 39.95). In addition, whether the experience is an effective factor was evaluated with the Logistic Regression test. Accordingly, there was not a sufficient statistical difference between the groups (Adjusted R square = – 0.004, p <0.498). The average of electrical resistance measurements (1.68 ± 0.30) in the participants with less than 5 years of experience was higher than those with 5 years of experience (1.65 ± 0.37). In addition, whether the experience is an effective factor was evaluated with the Logistic Regression test. Accordingly, there was not a sufficient statistical difference between the groups (Adjusted R square = – 0.005, p <0.597). There was no statistical difference between the mean load the first 20 block needle and the mean loads of participants. (p=0,265) Also, there was no statistical difference between the mean electrical resistance of the first 20 block needle and the mean loads of participants. (p=0.117)(Table 3).
Discussion
The medical equipment reuse debate has been ongoing for a long time. There are discussions on many issues, such as principles to be followed, procedures to be applied, and the selection of sterilization/disinfection methods. The reason for the reuse of medical equipment may be economical [1], environmental [2], or different reasons related to access to medical equipment. It has been reported that they can be used safely by adhering to the principles regarding reuse [2, 3]. However, written procedures based on clinical studies should be applied, a person responsible for daily operations (reuse manager) should be determined, use should be found on the patient’s knowledge, and criteria should be developed to determine how much time a device/material can be used before wearing away. Also, ‘wearing’ should be described for each medical device/equipment [1]. The things to be done for the first three criteria are clear, but for the fourth criterion, it is necessary to work separately for each device/material as stated.
The debate regarding the reuse of medical equipment is multi-faceted, enveloping a wide range of issues such as the principles to be adhered to, applicable procedures, and the selection of suitable sterilization or disinfection methods. The rationale for reusing medical equipment is multi-dimensional, involving economic incentives, environmental considerations, and access-related challenges. While economic motivations signify cost reductions [1], environmental concerns underline the need for sustainable practices [3-5], and access issues highlight the necessity to make medical equipment available in resource-limited settings.
Historically, the reuse of medical devices has been met with skepticism due to concerns about safety and efficacy. However, numerous studies suggest that these devices can be safely reused if stringent protocols are followed. Key to this process is the implementation of standardized procedures grounded in clinical research, designating a responsible individual or ‘reuse manager’ to oversee daily operations. Furthermore, patients should be informed about potential reuse, and specific criteria must be established to assess the lifespan and wear of each device or material. The concept of ‘wear’ must be clearly defined for each piece of medical equipment to ensure patient safety [3, 4, 6].
In our comprehensive study, we explored the reuse potential of nerve block needles utilized in regional anesthesia. These needles were subjected to a rigorous sterilization process, proven for their efficacy, and reused up to 20 times. Our findings demonstrated that the needles retained sufficient strength and sharpness, with no notable change in the force required to pierce tissue. Moreover, the sterilization process did not alter the electrical resistance of the needles, ensuring their ability to safely conduct electrical stimulation even after multiple uses. This aspect is crucial, as it assures that the needles maintain their functionality and reliability throughout their reuse cycle.
The reuse of medical equipment extends beyond nerve block needles. For instance, the reuse of PPMs has shown significant economic advantages, providing life-saving devices to patients who lack the financial means to afford new units [1]. Although nerve block needles are less costly compared to PPMs, the frequency of their use suggests that the financial gains from reuse could be substantial. In the clinical setting, the cost per nerve block needle is approximately $12, whereas the cost for sterilization and packaging for reuse is a mere $0.20. Consequently, this presents a potential savings of more than $8.50 per needle. Additionally, the disposal costs for used block needles as medical waste are reduced, further contributing to economic savings.
From an environmental standpoint, the reduction of medical waste through the reuse of equipment is a critical factor. Decreasing the volume of medical waste not only cuts down disposal costs but also aids in reducing carbon dioxide emissions, thus contributing to environmental sustainability [3, 7]. The commitment to reducing the carbon footprint aligns with broader global initiatives aimed at combating climate change and promoting eco-friendly practices in healthcare.
Given the environmental benefits, healthcare facilities are increasingly considering the implementation of reuse policies. However, this requires careful planning and adherence to safety protocols to mitigate the risk of infection and ensure patient safety. The effectiveness of these protocols is pivotal, as it determines the feasibility and acceptance of medical device reuse on a wider scale.
Ultrasound (US) probes provide a compelling example of how reusable medical equipment can be integrated into clinical practice. In US-guided procedures, these probes can act as vectors for pathogen transmission, necessitating stringent disinfection protocols. The importance of US probe disinfection parallels that of other medical materials used in invasive procedures guided by ultrasound [5, 6, 8]. While there have been few reported cases of infections linked to US probe disinfection techniques [7-9], these instances underline the necessity for effective sterilization methods that ensure patient safety without compromising the functionality of the devices.
In regional anesthesia practices that utilize ultrasound guidance, various disinfection methods are employed, each validated for their efficacy in different studies [10, 11]. The success of these methods indicates that with the proper protocols in place, medical devices such as US probes can be reused safely and effectively—a conclusion that can be extended to other medical devices under appropriate conditions.
In clinics that permit equipment reuse, institutions must adopt a comprehensive framework of principles to ensure safe reuse practices. This includes a detailed examination of potential problems associated with each specific type of reused device. Our study specifically investigated peripheral nerve block needles and found no evidence of needle tip blunting or compromised electrical conduction following multiple use cycles. Importantly, no visible damage was observed on these needle tips even when examined under 10x magnification (Figure 3). This finding is crucial, as it demonstrates the structural integrity and operational safety of the needles upon reuse.
Furthermore, variations in the electrical conduction of block needles present a potential concern in reuse practices. However, our study has provided a foundation for understanding these variations, contributing valuable insights to the literature where such assessments have been limited. The consistency in electrical conduction observed in our research underscores the notion that proper sterilization and handling can maintain the functional integrity of these devices.
Each medical device intended for reuse must have a defined “final number of use cycles” based on empirical evidence. For nerve block needles, our research suggests that up to 20 reuse cycles are both safe and cost-effective. This level of reuse can reduce expenditures for each needle by more than 80%, highlighting significant cost efficiencies without sacrificing safety or performance.
Despite the apparent benefits, the reuse of medical devices is not without challenges. One primary concern is the potential for infection or cross-contamination if sterilization is not meticulously performed. This underscores the necessity for rigorous training and adherence to established protocols by medical personnel tasked with sterilizing and reusing equipment. Institutions must remain vigilant in monitoring compliance with these standards to safeguard against potential risks.
Moreover, patient perceptions and acceptance of reused medical devices can vary, influencing the broader adoption of reuse practices. Transparent communication with patients about the safety measures in place and the quality assurance processes followed is essential. Education about the environmental and economic benefits of device reuse can also foster greater acceptance and support for these practices within the patient community.
Future research should continue to evaluate the long-term effects of reusing various medical devices, diversifying the types of equipment studied, and extending the generalizability of findings to different clinical settings. Innovations in sterilization technology and new materials for medical devices might further enhance the feasibility and safety of reuse, advancing this cost-saving and eco-friendly practice.
Limitations
Limitations of the study include: the sample size, involving only 20 needles and four anesthetists, which may not broadly represent clinical diversity. Additionally, the study is confined to testing 20 reuse cycles, leaving the effects of further cycles unexplored. Examination of wear was primarily based on visible signs and electrical resistance, without delving deeply into potential microscopic damage or long-term effects of reuse in real clinical environments. Furthermore, the study did not evaluate direct patient outcomes or address how the reuse might be perceived by medical professionals and patients. To enhance reliability and applicability, future research could expand on these aspects, incorporating a larger and more varied sample, alternative sterilization techniques, and considerations of patient safety and acceptance.
Conclusion
The reuse of medical equipment, exemplified by our study on nerve block needles, offers significant economic and environmental benefits while maintaining high standards of patient safety. As healthcare systems worldwide strive to balance cost management with quality care, the development and implementation of effective reuse practices present a viable pathway to achieving these goals.
As more healthcare facilities consider adopting reuse strategies, the insights from empirical studies such as ours provide the groundwork necessary for informed decision-making. By fostering a culture of sustainability and safety, the medical community can leverage the reuse of equipment as a means of enhancing access to healthcare resources, reducing environmental impact, and ensuring patient safety remains paramount.
Overall, establishing comprehensive protocols and investing in education and training for healthcare providers are critical steps to enabling the successful integration of medical equipment reuse into modern medical practice. As we continue to explore the potential and challenges of this practice, collaboration between healthcare institutions, regulatory bodies, and academic researchers will be vital in optimizing reuse practices for future applications.
Scientific Responsibility Statement
The authors declare that they are responsible for the article’s scientific content including study design, data collection, analysis and interpretation, writing, some of the main line, or all of the preparation and scientific review of the contents and approval of the final version of the article.
Animal and Human Rights Statement
All procedures performed in this study were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or compareable ethical standards.
Funding: None
Conflict of Interest
The authors declare that there is no conflict of interest.
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Download attachments: 10.4328.ACAM.22491
Eyup Aydogan, Betül Kozanhan, Yasin Tire, Munise Yıldız. In vitro assessment of wear in peripheral nerve block needles for re-use. Ann Clin Anal Med 2025;16(10):693-698
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Clinical and histological outcomes of entecavir and lamivudine in chronic hepatitis B therapy
Neslihan Mandacı Şanlı 1, Mevlüt Başkol 2
1 Department of Hematology and Bone Marrow Transplant Center, 2 Department of Internal Medicine, Faculty of Medicine, Erciyes University, Kayseri, Türkiye
DOI: 10.4328/ACAM.22567 Received: 2025-01-16 Accepted: 2025-03-19 Published Online: 2025-03-28 Printed: 2025-10-01 Ann Clin Anal Med 2025;16(10):699-704
Corresponding Author: Neslihan Mandacı Şanlı, Department of Hematology and Bone Marrow Transplant Center, Faculty of Medicine, Erciyes University, Kayseri, Türkiye. E-mail: drneslihansanli@gmail.com P: +90 505 700 7392 Corresponding Author ORCID ID: https://orcid.org/0000-0002-6298-9884
Other Authors ORCID ID: Mevlüt Başkol, https://orcid.org/0000-0003-0358-2619
This study was approved by the Ethics Committee of Erciyes University (Date: 2010-12-08, No: 2011/339)
Aim: Chronic hepatitis B (CHB) is one of the major health concerns on the globe with an estimated 350 to 400 million cases and complications, including liver cirrhosis and hepatocellular carcinoma (HCC). The objective of this study is to assess the impact of entecavir and lamivudine treatment in the long-term viability of CHB patients, such as biochemical, serological, and histological outcomes.
Materials and Methods: Data from a total of 75 patients diagnosed with chronic hepatitis B were taken. All the patients had received oral antiviral medications, including lamivudine or entecavir, for more than two years. The initial step included evaluation of clinical and lab parameters, which included serum levels of HBV DNA, ALT, HBeAg seroconversion, HBsAg histology, HAI score, and fibrosis score. The marks chosen for the study were 24,36, and 48 months. In-depth statistical analysis was then derived to study the effective treatment and compare the two moulds of treatment of CHB.
Results: Entecavir demonstrated superior virological suppression, with 96.2%, 92.1%, and 100% of patients achieving HBV DNA levels <20 IU/mL at 24, 36, and 48 months, respectively, compared to 73.9%, 92.1%, and 90% in the lamivudine group. ALT normalization was observed in 90.5% of patients by the 48th month, with no significant difference between the two treatments. Both of the groups reported significant HAI lowering scores, i.e, a reduction of at least 2 throughout 36 moths with a composite improvement of at least 61.3 %. In comparison to this result, patients witnessing a reduction in fibrosis of a minimum of 1 point showed a minor decrease, which was not significant. All patients treated reported no signs of HBsAg clearance, while some were able to convert to anti-HBs.
Discussion: Entecavir has better virological effectiveness and similar biochemical and histological advantages in comparison to lamivudine on a long-term basis for converting patients with CHB. However, both regimens show only minimal reversal of fibrosis and are serologically unresponsive. This justifies the development of new treatment approaches such as combination therapies and immune modulators to facilitate performance improvements and fulfill unmet needs in the care of CHB.
Keywords: chronic hepatitis B, entecavir, lamivudine, antiviral therapy, virological suppression
Introduction
Chronic Hepatitis B infection (HBV) is prevalent in 350-400 million people around the globe and continues to be a major contributing factor in liver diseases and death. 20-40% of individuals suffering from chronic HBV infection are additionally diagnosed with decompensated liver failure, cirrhosis, or hepatocellular carcinoma (HCC) [1, 2]. In consideration of these complications, the levels of viral replication are also significant. Patients that have an HBV DNA level less than (<300 copies/ml) are less likely to develop cirrhosis (4.5%) and HCC (1.3%). But in the cases for patients with high HBV DNA levels (≥10⁶ copies/ml), the possibility for them to develop cirrhosis increases to 36.2% while the possibility for HCC is at 15% [3, 4].
The liver is one of the few organs in the body that is capable of regeneration to a remarkable extent; however, when this regenerative capacity is exceeded due to continuous injury to the liver, it results in the development of fibrosis that, over some time, leads to cirrhosis. It would be worthwhile pointing out that several recent studies have established that hepatofibrosis is reversible after the relevant cause for liver damage is removed. This treatment process is also dependent on antiviral therapy, which goes a long way in not only controlling the replication of the virus but also in ameliorating the histology of the liver, helping to slow down the development of fibrosis and associated long-term complications [1, 5].
The therapeutic approaches currently employed in the management of HBV infections are classified into two principles, immune modulatory agents (for example, Peg-IFN-alpha) and orally active nucleos(t)ide analogs such as lamivudine, entecavir, and tenofovir. Nucleoside analogs are exceptionally successful in deterring the replication of viral DNA, normalizing aminotransferase (AT) levels, and averting complications [2,6].
On the other hand, entecavir has greater resistance rates, which makes it a suitable option when managing patients long term. Data suggests that the patients start developing resistance to entecavir in under 1% after the 4-year mark and are nucleoside ignorant, in stark contrast with mono-resistant lamivudine patients who have a 40% resistance rate [1,3]. Studies conducted after following certain steps conclude that as far as having renal failure involved, entecavir is much more suitable as compared to TDF [4,7].
The main purpose of this research is to compare entecavir and lamivudine long-term therapy in chronic hepatitis B (CHB) patients. The study pays careful attention to the impact of both therapeutic schemes upon virological, ALT normalization, histological (changes in HAI and fibrosis scores), and serological (HBsAg clearance and anti-HBs seroconversion) responses. It intends to assess the clinical efficacy of these alternatives to treatment and their input to the long-term management of patients. This research attempts to fill these clinical gaps by presenting evidence on the safety and efficacy of entecavir and lamivudine therapies.
This study focuses on the long-term effectiveness of entecavir and lamivudine about virological, biochemical, histological, and serological outcomes. The restricted gains achieved in current therapies are outlined by the limited serological responses like HBsAg clearance and anti-HBs seroconversion. The research was conducted in Turkey, which is an intermediate HBV endemic region, so the results help inform health policies as well as clinical practice at a more localized level using advanced strategies to treat CHB.
Materials and Methods
This retrospective study was conducted between 2000 and 2011 at the Gastroenterology Outpatient Clinic of Erciyes University Faculty of Medicine. The medical records of 150 patients diagnosed with chronic hepatitis B (CHB) were analyzed, excluding 47 patients due to insufficient follow-up data and 28 patients who had received antiviral treatments other than entecavir or lamivudine.
Inclusion criteria: HBsAg positivity for at least six months, compensated liver disease (total bilirubin ≤2.5 mg/dL, INR ≤1.5, albumin ≥3.0 g/dL, and no history of variceal bleeding, hepatic encephalopathy, or ascites), baseline HBV DNA ≥10⁴ copies/mL, ALT levels between 1.3–10 times the upper limit of normal (ULN), and a minimum of two years of treatment with entecavir or lamivudine.
Exclusion criteria
Coinfection with HCV, HDV, or HIV, interferon therapy for more than 12 weeks, use of herbal treatments, or treatment with other oral antivirals.
Data collection
Demographic information, baseline and follow-up laboratory results (ALT, HBV DNA, HBsAg, HBeAg, anti-HBs, anti-HBe), and liver biopsy findings (fibrosis and histological activity index [HAI]) were analyzed over a minimum two-year period.
Evaluation criteria
HBV DNA suppression (<20 IU/mL), ALT normalization (<40 IU/mL), HBsAg loss, anti-HBs seroconversion, HBeAg seroconversion, and histological improvement (≥2-point reduction in HAI score, ≥1-point reduction in fibrosis score, or stabilization of fibrosis). Liver biopsies were assessed using the modified Knodell HAI and fibrosis scoring systems.
Statistical Analysis
All statistical analyses were conducted using SPSS version 20 for Windows XP. Results were expressed as mean ± standard deviation (SD) or median (25th–75th percentile). Comparisons of paired data were performed using the Wilcoxon signed-rank test, while categorical variables were analyzed using the Chi-square test and McNemar test. A p-value <0.05 was considered statistically significant.
Ethical Approval
This study was approved by the Ethics Committee of Erciyes University (Date: 2010-12-08, No: 2011/339).
Results
A total of 75 patients who received entecavir or lamivudine treatment for at least two years were included in the study. The mean age of the patients was 49±10.9 years, with 69.3% receiving entecavir and 30.7% receiving lamivudine. All patients were HBsAg-positive and anti-HBs-negative. At baseline, 14.7% of patients were HBeAg-positive, while 85.3% were anti-HBe-positive. Laboratory findings showed a median HBV DNA level of 2.62 × 10⁶ IU/ml (1 × 10⁴ – 5.62 × 10⁷), an ALT level of 85 IU/ml (61-149), a histological activity index (HAI) of 5 (4-6), and a median fibrosis score of 2 (1-3).
A significant decrease in HBV DNA levels was observed during the treatment period. At the 24th month, 89.3% of patients achieved HBV DNA levels below 20 IU/ml, with this rate remaining at 88.9% at the 36th month and increasing to 95.2% at the 48th month. Similarly, ALT levels showed marked improvement, with 68% of patients achieving ALT levels below 40 IU/ml at the 24th month, rising to 77.8% at the 36th month, and 90.5% at the 48th month (p<0.05). Regarding serological parameters, 88% of patients were HBeAg-negative and anti-HBe-positive at the 24th month, increasing to 96.1% at the 36th month and 100% at the 48th month. However, no changes were observed in HBsAg or anti-HBs status, as all patients remained HBsAg-positive and anti-HBs-negative throughout the treatment period. A marked reduction in HBV DNA levels was noted, with 89.3% of patients achieving HBV DNA <20 IU/ml at the 24th month, 88.9% at the 36th month, and 95.2% at the 48th month (p<0.05). ALT levels also showed significant improvement, with 68% of patients achieving ALT levels <40 IU/ml at the 24th month, 77.8% at the 36th month, and 90.5% at the 48th month (p<0.05).
The division of patients into two subgroups based on the use of entecavir or lamivudine revealed the results of liver biopsies performed at 24, 36, and 48 months of treatment, as detailed in Table 1.
When compared to pre-treatment levels, statistically significant biochemical improvements were observed across all treatment groups at 24, 36, and 48 months (p-values: 0.00, 0.00, and 0.00, respectively) (Table 1).
In terms of HBeAg seroconversion, only 18% (n=2) of the 11 HBeAg-positive patients at baseline achieved HBeAg seroconversion at the 24th month, with no seroconversion observed at the 36th and 48th months (p>0.05) (Table 2).
Histological activity index (HAI) improvements of ≥2 points were observed in 40% of patients at the 24th month, 61.3% at the 36th month, and 36.8% at the 48th month. These improvements were statistically significant, with p-values of 0.008, 0.000, and 0.045, respectively. Improvements in fibrosis scores of ≥1 point were observed in 24% of patients at the 24th month, 41.9% at the 36th month, and 31.6% at the 48th month. However, these changes were not statistically significant at any time point (p>0.05). (Table 2)
Among patients who continued treatment for 24 months, 96.2% of those receiving entecavir and 73.9% of those receiving lamivudine achieved HBV DNA negativity (<20 IU/ml). At the 36th month, this rate remained at 92.1% for both groups, while at the 48th month, 100% of entecavir-treated patients and 90% of lamivudine-treated patients achieved HBV DNA negativity (Table 3).
Similar improvements were observed in ALT levels. At the 24th month, ALT levels fell below 40 IU/ml in 73.1% of entecavir-treated patients and 56.5% of lamivudine-treated patients. At the 36th month, these rates were 78% and 75%, respectively. By the 48th month, ALT levels were within normal limits (<40 IU/ml) in 90.9% of entecavir-treated patients and 90% of lamivudine-treated patients. These improvements in ALT levels were statistically significant in both groups (p<0.05).
In histological evaluation, the rate of ≥2-point improvement in HAI scores was 38.9% in the entecavir group and 42.9% in the lamivudine group at the 24th month. At the 36th month, these rates increased to 64% and 50%, respectively. At the 48th month, 44.4% of entecavir-treated patients and 30% of lamivudine-treated patients achieved ≥2-point improvements in HAI scores. At the 36th month, this rate increased to 52% in the entecavir group and remained at 16.7% in the lamivudine group. At the 48th month, ≥1-point improvement in fibrosis scores was observed in 33.3% of entecavir-treated patients and 30% of lamivudine-treated patients. However, these changes were not statistically significant in either group (p>0.05) (Table 3).
Discussion
The present study provides a comprehensive analysis of the long-term virological, biochemical, and histological outcomes of entecavir and lamivudine treatments in chronic hepatitis B (CHB) patients, contributing valuable insights into their comparative efficacy.
In both therapy groups, our data demonstrated noteworthy virological suppression, with 95.2% of patients achieving HBV DNA levels below 20 IU/ml at 48 months. Entecavir showed the best results in terms of virological efficacy, mainly at the earlier stages, with 96.2% patients from the entecavir group being HBV DNA negative at 24 months compared to 73.9% in the lamivudine group instead. This coincides with the results of Huang et al. [9] and Aljumah et al. [10], who noted the strong entecavir virological response in both the clinical trials and real life. Despite this, patients on lamivudine therapy had a higher frequency of virologic breakthroughs, consistent with Litwin et al. [2], who pointed out that the development of lamivudine resistance is a major drawback when used for a prolonged period.
Across all treatment groups, biochemical efficiency increased, particularly with normalising ALT levels. It was found that 90.6% of patients managed to keep their ALT levels below 40 IU/ml by the 48th month. These results are similar to those previously reported by Ozdemir et al. [11], who reported adequate control of ALT levels in subjects who were receiving long-term ALT therapy. Patients on entecavir did seem to have a slightly greater rate of ALT normalization than those on lamivudine in the early phases of treatment, although this study aligns with Gui et al. [1], who stated that entecavir-based regimens are more effective biochemically. By the 48th month of the study, the graphs presented are comparable, indicating the effectiveness of both techniques in the reduction of hepatic inflammation over time.
Data concerning histological outcomes showed improvement in the histological activity index (HAI) scores of the participants of the study, whereby there was a reduction of ≥2-point in 40%, 61.3%, and 36.8% of patients over 24, 36, and 48 months, respectively. These findings are indicative of histological improvements achieved through the use of antiviral therapies relevant to the research conducted by Gui et al. [1], which noted an improvement in histological features in patients receiving entecavir with combination therapy. On the other hand, the level of fibrosis reversal (≥1-point improvement and even lower was comparatively less and has not been found statistically significant) was found to be more moderate, which is in agreement with studies conducted by Çerçioğlu et al. [12] and Li et al. [6] regarding reversal of advanced fibrosis. Lamivudine was suggested by Hu et al. [13] to have greater histological reversibility if used in pediatric patients in comparison to adult patients. Primary etiology – advanced fibrotic noncirrhotic renovation (and decomposition) – warrants additional exploration.
Our study highlights the limited serological responses to antiviral therapy, particularly the lack of significant HBsAg and anti-HBs seroconversion. This aligns with findings by van Campenhout et al. [14] and Sarıkaya et al. [7], who emphasized that modern antiviral treatments do not fully eliminate CHB or prevent liver disease progression. In contrast, Li et al. [8] suggested that adjunctive therapies, such as immunomodulators or novel treatment approaches, may improve outcomes.
Concerns about antiviral toxicity remain relevant, especially in patients with coexisting HIV and CHB. While some studies, including Kara et al. [15] and Sarıkaya et al. [7], raised concerns about tenofovir-containing regimens, our findings suggest that entecavir remains a well-tolerated option. However, differences in monitoring and safety profiles across treatment regimens require further investigation.
Overall, our results support entecavir as a first-line therapy due to its superior virological and biochemical efficacy. However, the modest histological improvements and limited serological responses underscore the challenges in fully addressing CHB pathogenesis. These findings highlight the need for personalized treatment approaches, considering factors such as disease stage, patient age, and comorbidities, to optimize long-term outcomes.
Future steps in research should take a clinical perspective instead of focusing on particular medical strategies by evaluating combinational therapy methods and adjunctive medical strategies that bolster the overall outcome. In particular, these studies: Tatar et al. [16], Gui et al.[1] imply that the combination of antiviral therapy with immune modulators or antifibrotic agents would result in a more profound method of treating CHB. But still, the lack of effective therapeutics for HBsAg clearance is a serious unresolved concern in combating CHB.
This study confirms the role of entecavir as a primary strategy while addressing CHB disease, especially during virological and biochemical optimization. Modification of therapeutic techniques would be facilitated by targeting wider therapeutic improvement since both histological change and surgical response proved to be minimal. There is a growing agreement in the literature and, in this sense, our results are consistent with that CHB can be more effectively combat for if it is in the patients’ best interests to customize the optimal approach to treatment; that the applications are continuously controlled and that combined therapies are also used.
Limitations
This study is limited by its retrospective design and the data collected within a specific period, which may affect the generalizability of the findings.
Conclusion
This study highlights the long-term efficacy of entecavir and lamivudine in virological suppression and biochemical improvement in chronic hepatitis B. Entecavir showed superior early virological response, reinforcing its role as a first-line therapy. Both treatments reduced ALT levels and hepatic inflammation, but fibrosis regression was limited, and HBsAg clearance remained unmet. These findings support individualized treatment strategies for long-term efficacy and safety. While entecavir remains a strong option, future research should explore combination therapies and immune modulators to improve histological and serological outcomes, aiming for better clinical results and functional cure rates.
Scientific Responsibility Statement
The authors declare that they are responsible for the article’s scientific content including study design, data collection, analysis and interpretation, writing, some of the main line, or all of the preparation and scientific review of the contents and approval of the final version of the article.
Animal and Human Rights Statement
All procedures performed in this study were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.
Funding: None
Conflict of Interest
The authors declare that there is no conflict of interest.
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Neslihan Mandacı Şanlı, Mevlüt Başkol. Clinical and histological outcomes of entecavir and lamivudine in chronic hepatitis b therapy. Ann Clin Anal Med 2025;16(10):699-704
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The relatieonship between multi-inflammatory index and nondipping circadian pattern in patients with a new-diagnosis of essential hypertension
Erdoğan Sökmen, Muhammet Salih Ateş
Department of Cardiology, Kırsehir Ahi Evran Education and Research Hospital, Kırsehir, Turkiye
DOI: 10.4328/ACAM.22594 Received: 2025-02-04 Accepted: 2025-03-10 Published Online: 2025-03-17 Printed: 2025-10-01 Ann Clin Anal Med 2025;16(10):705-709
Corresponding Author: Erdoğan Sökmen, Department of Cardiology, Kırsehir Ahi Evran Education and Research Hospital, Kırsehir, Turkiye. E-mail: erdoganmen@gmail.com P: +90 551 553 99 14 Corresponding Author ORCID ID: https://orcid.org/0000-0002-8170-5912
Other Authors ORCID ID: Muhammet Salih Ateş, https://orcid.org/0000-0003-4099-0064
This study was approved by the Ethics Committee of Kırşehir Ahi Evran University (Date: 2024-10-22, No: 2024-17/149)
Aim: Previous studies showed that essential hypertension (EHT) had been related to chronic inflammation. A non-dipping circadian blood pressure (BP) pattern confers a greater cardiovascular morbidity and mortality. The multi-inflammatory index (MII) is a novel systemic inflammatory parameter. We aimed to assess the association between MII and the non-dipping BP pattern.
Materials and Methods: A total of 158 EHT patients were stratified into nondipper (n=78) and dipper groups (n=80) on the basis of 24h-ambulatory BP monitoring (24h-ABPM). 176 healthy subjects were recruited as control group. Data regarding 24h-ABPM, clinical and laboratory findings were collected from the hospital records. MII was calculated as: Neutrophil count × C-reactive protein/Lymphocyte count.
Results: MII was greater in the non-dippers as compared with the dippers and the controls [5.9(1.21-10.1), 3.32(1.34-8.87), and 1.79(0-4.1), respectively, p=0.003]. MII was found to show correlation with age (0.200, p=0.011), 24h-systolic BP 0.234, p=0.003), daytime systolic BP (0.192, p=0.016), nighttime systolic BP (0.277, p<0.001), and LVMI (-0.195, p=0.021). In the multivariate logistic regression model, daytime systolic BP [Odd ratio: 1.171(1.077-1.272, p<0.001] and MII [Odd ratio: 1.150(1.029-1.284), p=0.013] were found to be significantly associated with the non-dipping BP pattern. ROC curve analysis revealed a cut-off value of 2.01 with 71.1% sensitivity and 50.4% specificity for MII to predict the nondippers among the EHT patients.
Discussion: MII is significantly associated with nondipping circadian BP pattern. MII could be a simple and useful marker to predict the nondippers among the EHT patients.
Keywords: multi-inflammatory index, nondipper hypertension, essential hypertension, inflammation
Introduction
Hypertension continues to be a global issue, contributing significantly to morbidity and mortality. Although repeated blood pressure (BP) measurements in clinical settings have traditionally been the cornerstone for diagnosing essential hypertension (EHT), 24-hour ambulatory blood pressure monitoring (24-h ABPM) is now also used not only for diagnostic purposes but to reveal circadian patterns in hypertension. Normally, both systolic and diastolic blood pressures are expected to decrease by at least 10% during nighttime, a phenomenon known as the dipping blood pressure pattern. In contrast, when there is no such reduction of at least 10% of daytime BP readings during sleep, this is referred to as the non-dipping blood pressure pattern [1]. Previous studies have demonstrated that a non-dipping BP pattern has been linked with a higher cardiac risk and increased all-cause mortality compared to the dipping BP pattern [2-5].
The multi-inflammatory index (MII) is a novel index encompassing C-reactive protein (CRP) and hematological parameters such as neutrophil and lymphocyte counts. Although initially proposed as a prognostic indicator in colorectal cancer, recent studies have also shown a significant relationship between MII and several cardiovascular diseases, such as atrial fibrillation, cerebrovascular events, and pulmonary embolism [6-9]. However, its association with the circadian pattern of hypertension has yet to be elucidated.
The purpose of the present study is to determine the potential relationship between the novel MII and the dipping and non-dipping BP patterns in subjects with a new diagnosis of EHT.
Materials and Methods
This is a retrospective and cross-sectional study. The hospital’s digital database regarding the patients with a new diagnosis of EHT between October 2022 and May 2024 was interrogated. Records of 312 patients with a new diagnosis of hypertension were examined. 154 patients were excluded from the study based on our exclusion criteria, and finally, a total of 158 subjects with newly diagnosed EHT were enrolled. On the other hand, 176 age- and sex-matched normotensive healthy subjects were also recruited in our study to comprise the control group. Relevant demographic and clinical data of the subjects with a new diagnosis of EHT and the controls were obtained from digital hospital records. Exclusion criteria were set as: diabetes mellitus, known coronary artery disease, kidney failure, secondary hypertension, atrial fibrillation, active infection, malignancy, chronic rheumatic or inflammatory diseases, history of cerebrovascular events, and the use of steroids or anti-inflammatory medications. The patient group was then stratified into those with a dipping circadian BP pattern (the DG, n=78) and those with a non-dipping pattern (NDG, n=80) based on ambulatory blood pressure monitoring (ABPM) readings. The study was conducted by the standards set forth by the Helsinki Declaration.
At the office, a regular sphygmomanometer was used in each participant to measure the BP in the arm. Subjects were seated at least 10 minutes before the BP measurement, and 3 consecutive BP measurements were made at 5-minute intervals. Subjects with a mean office BP greater than 140/90 mm Hg (systolic or diastolic or both) were followed for twenty-four hours with ABPM (Mobil-O-Graph, Aachen, Germany). In daytime (07:00-23:00), the device performed BP measurements at 15-minute intervals, while in nighttime (23:00-07:00) at 30-minute intervals. After ruling out the secondary causes of hypertension, the diagnosis of EHT was made based on a 24-hour systolic BP mean >130 mm Hg/diastolic BP mean >80 mm Hg, a daytime mean systolic BP >135/diastolic BP >85 mm Hg, or a nighttime systolic BP mean >120 mm Hg/diastolic BP >70 mm Hg [13]. A ≥10% reduction in daytime BP during the night was considered a dipping BP pattern. Patients without this 10% decrease were classified as non-dippers.
Echocardiographic assessment was conducted using the PowerVision 6000 (Toshiba, Tokyo, Japan). Simpson’s rule was utilized in the determination of the left ventricular ejection fraction (LVEF) [10]. In each patient, LV mass index (LVMI) was calculated, and left ventricular hypertrophy was defined as LVMI >95 g/m² for females and >115 g/m² for males [10].
Blood samples were analyzed using an automatic CBC analysis device (Beckman Coulter Inc., CA, US). MII was calculated using the formula: Neutrophil count × C-reactive protein / Lymphocyte count [6].
Statistical Analysis
Statistical analysis was conducted using SPSS (Version 29.0 for Windows, IBM Corp., Armonk, NY, USA). Assessment of the distribution of quantitative data was made using the Kolmogorov-Smirnov test. Continuous data were expressed either as mean ± standard deviation or as median (25th and 75th interquartile range). On the other hand, categorical variables were expressed as counts (percentages). χ² test, one-way ANOVA, and the Kruskal-Wallis H test were utilized based on data type. Multinominal logistic regression analysis was implemented to evaluate the associations of the variables with NDG. An analysis of the receiver operating characteristic (ROC) curve was implemented to delineate the cutoff of MII for NDG, if any. Any p-value <0.05 was accepted to be significant.
Ethical Approval
This study was approved by the Ethics Committee of Kırşehir Ahi Evran University Medical Faculty (Date: 2024-10-22, No: 2024-17/149).
Results
The groups were similar regarding gender, age, body-mass index, and baseline biochemistry parameters. The DG and NDG were similar in terms of smoking habits (p<0.05); however, smoking was more common in the control group compared to the EHT patients (p<0.001). The demographic and clinical variable of the subgroups were depicted in Table 1. MII was higher in the NDG compared with both the DG and controls [5.9 (1.21-10.1), 3.32 (1.34-8.87), and 1.79 (0-4.1), respectively, p=0.003]. Neutrophil counts and hs-CRP levels were higher in the NDG than in both of the DG and control groups [for neutrophils 5610 (4200-6700), 4175 (2967-5577), and 4170 (3500-5300), respectively, p=0.037; for hs-CRP 3 (1-6), 2.1 (1-3.4), and 1.75 (1-3), respectively, p=0.006], while lymphocyte counts were higher in the DG and control group compared with the NDG [2155±544, 2331±918, and 2556±844, respectively, p=0.008].
LVMI was similar between the NDG and DG, but lower in the controls compared to the EHT patients [88.5 (78.4-105.6), 88.7 (79.7-106.4), and 84.2 (72.2-102.1), respectively, p=0.013] (Table 1). Office systolic and diastolic BPs were similar between the dipper and non-dipper groups but lower in the controls compared to the EHT patients (p<0.001). Ambulatory daytime and nighttime systolic and diastolic BPs were highest in the NDG and lowest in the controls (p<0.001). While 24-hour systolic and diastolic BPs were similar between the DG and NDG, they were lower in the controls compared to the EHT patients (p<0.001) (Table 1).
Table 2 depicted the significant correlation of MII with LVMI (-0.195, p=0.021), age (0.200, p=0.011), 24-hour systolic BP (0.234, p=0.003), daytime systolic BP (0.192, p=0.016), and nighttime systolic BP (0.277, p<0.001). Multinominal logistic regression identified daytime systolic BP [Odd ratio: 1.171 (1.077-1.272), p<0.001] and MII [Odd ratio: 1.150 (1.029-1.284), p=0.013] as significant predictors of the non-dipping BP pattern (Table 3). ROC curve analysis revealed a cutoff value of 2.01 with 71.1% sensitivity and 50.4% specificity for MII in predicting NDG among EHT patients (Figure 1).
Discussion
The key findings of our study may be summarized as follows: 1) compared with DG, MII is higher in NDG; 2) regression analysis revealed a significant association between MII and the non-dipping circadian BP pattern; and 3) ROC curve analysis demonstrated a cutoff value of 2.01 for MII in predicting non-dippers. The current study is the first to evaluate the relationship between MII and the non-dipping EHT, to the best of our knowledge.
Inflammation and the development of EHT are closely intertwined, leading to arterial wall inflammation and remodeling [11, 12]. For instance, depletion of B and T cells using mycophenolate mofetil has been shown to protect against hypertension and renal disease in animal models [11]. Innate immune cells and endothelial cells express NLR-family pyrin domain-containing proteins NLRP1 and NLRP3, which activate inflammatory responses in the vessel wall through the release of interleukin (IL)-1β, high mobility group box 1 protein, and IL-18 [13]. Moreover, elevated levels of angiotensin II and endothelin 1 contribute to increased BP and vascular endothelial damage, leading to oxidative stress. This increased oxidative stress further triggers the T lymphocyte activation and the release of pro-inflammatory cytokines such as interferon-γ, Tumor necrosis factor-α, IL-17, and IL-6, hence creating a vicious cycle of inflammation [13-15]. Kim et al. [16] found that alterations in circulating cytokine levels contributed to variations in BP. In a Japanese cohort, neutrophil counts were significantly associated with EHT risk in both sexes after adjusting for demographic factors [17]. Similarly, we found that neutrophil counts were higher in NDG as compared with the DG and the control group.
The cardiovascular risk (CV) conferred by the non-dipping BP pattern has been greater compared to the dipping pattern due to more widespread end-organ damage, increased endothelial dysfunction, impaired diastolic left ventricular function, and chronic sympathetic nervous system activation [1]. Coleman et al. [18] demonstrated significantly elevated central systolic BP and worsened central hemodynamics in non-dipper EHT patients, which may contribute to increased CV mortality. Akyüz et al. [19] reported higher neutrophil counts, neutrophil-to-lymphocyte ratios, and systemic inflammation-immune indices in non-dipper EHT patients compared to the DG. Sökmen et al. [1] found elevated levels of growth differentiation factor-15, an inflammatory cytokine, in patients with non-dipper EHT compared to those with a dipping BP pattern. Elçik et al. [20] observed faster coronary artery atherosclerotic deterioration in subjects with coronary artery disease who were in NDG.
In our study, MII was higher in non-dipper EHT patients, which is consistent with previous findings. Goztas et al. [21] demonstrated that MII could serve as a simple and useful mortality predictor in severe COVID-19 patients. Demirel et al. [8] reported that MII could indicate poor prognosis in ischemic stroke. Yüksel et al. [7] suggested that MII could predict new-onset atrial fibrillation in patients undergoing coronary bypass surgery. Doğanay et al. [22] found an association between higher MII, acute stent thrombosis, and early mortality in patients with acute coronary syndrome. Likewise, we found that MII was significantly associated with the non-dipping pressure rhythm, with a cutoff value of 2.01 as a simple and useful marker for predicting non-dippers among EHT patients.
Limitations
The relatively small sample size is a limitation of this study. Additionally, we did not assess the prognostic value of MII in non-dipper EHT patients. Lastly, the study was conducted at a single center, representing a relatively narrow patient population. Future studies with larger, multicenter cohorts are required to validate the results of our study.
Conclusion
This investigation demonstrated that MII was correlated with daytime, nighttime, and 24-hour systolic BP. Furthermore, MII was significantly associated with the non-dipping circadian pressure rhythm. MII could prove to be a simple and useful marker in the prediction of non-dipper EHT patients.
Scientific Responsibility Statement
The authors declare that they are responsible for the article’s scientific content including study design, data collection, analysis and interpretation, writing, some of the main line, or all of the preparation and scientific review of the contents and approval of the final version of the article.
Animal and Human Rights Statement
All procedures performed in this study were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.
Funding: None
Conflict of Interest
The authors declare that there is no conflict of interest.
References
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2. Brotman DJ, Davidson MB, Boumitri M, Vidt DG. Impaired diurnal blood pressure variation and all-cause mortality. Am J Hypertens. 2008;21(1):92-7.
3. Giles TD. Circadian rhythm of blood pressure and the relation to cardiovascular events. J Hypertens. 2006;24(Suppl.2):S11-6.
4. Mohammed AAS, Lin X, Yangyang Y, et al. The association of morning surge and night-time dipping blood pressure with significant and complex coronary artery lesions. High Blood Press Cardiovasc Prev. 2021;28(5):467-74.
5. Kalaycı B, Erten YT, Akgün T, Karabag T, Kokturk F. The relationship of age-adjusted Charlson comorbidity ındex and diurnal variation of blood pressure. Clin Exp Hypertens. 2019;41(2):113-7.
6. Agircan D, Bal M, Demir TG, Ethemoglu O. Multi-inflammatory index as a new predictive and prognostic marker of acute symptomatic seizures in patients with cerebral venous sinus thrombosis. J Stroke Cerebrovasc Dis. 2023;32(12):107453.
7. Yuksel A, Velioglu Y, Atasoy MS, et al. Multi-inflammatory index as a novel predictor of new-onset atrial fibrillation after off-pump coronary artery bypass grafting. Kardiol Pol. 2024;82(7-8):733-40.
8. Demirel ME, Akunal Türel C. The role of the multi-inflammatory index as a novel predictor of hospital mortality in acute ischemic stroke. Cureus. 2023;15(8):e43258.
9. Boyuk F. The role of the multi-inflammatory index as a novel inflammation-related index in the differential diagnosis of massive and non-massive pulmonary embolism. Int J Clin Pract. 2021;75(12):e14966.
10. Lang RM, Badano LP, Mor-Avi V, et al. Recommendations for cardiac chamber quantification by echocardiography in adults: an update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging. J Am Soc Echocardiogr. 2015;28(1):1-39.e14.
11. Idris-Khodja N, Mian MO, Paradis P, Schiffrin EL. Dual opposing roles of adaptive immunity in hypertension. Eur Heart J. 2014;35(19):1238-44.
12. Agita A, Alsagaff MT. Inflammation, immunity, and hypertension. Acta Med Indones. 2017;49(2):158-65.
13. Aboukhater D, Morad B, Nasrallah N, et al. Inflammation and hypertension: Underlying mechanisms and emerging understandings. J Cell Physiol. 2023;238(6):1148-59.
14. Guzik TJ, Touyz RM. Oxidative stress, inflammation, and vascular aging in hypertension. Hypertension. 2017;70(4):660-7.
15. Sylvester MA, Brooks HL. Sex-specific mechanisms in inflammation and hypertension. Curr Hypertens Rep. 2019;21(7):53.
16. Kim KI, Lee JH, Chang HJ, et al. Association between blood pressure variability and inflammatory marker in hypertensive patients. Circ J. 2008;72(2):293-8.
17. Tomoyuki K, Maki M, Harumi U, Takako S. Neutrophil cl count is related to hypertension in workers: A cross-sectional study. Vascular Disease Prevention (Discontinued). 2007;4(3):225-8.
18. Coleman CT, Stowasser M, Jenkins C, Marwick TH, Sharman JE. Central hemodynamics and cardiovascular risk in nondippers. J Clin Hypertens (Greenwich). 2011;13(8):557-62.
19. Akyüz A, Işık F. Systemic immune-inflammation index: A novel predictor for non-dipper hypertension. Cureus. 2022;14(8):e28176.
20. Elçik D, Duran M, Keleşoğlu Ş, et al. Effect of nondipper hypertension on coronary artery disease progression in patients with chronic coronary syndrome. Turk J Med Sci. 2021;51(3):1273-80.
21. Gozdas HT, Kayis SA, Damarsoy T, et al. Multi-inflammatory index as a novel mortality predictor in critically Ill COVID-19 patients. J Intensive Care Med. 2022;37(11):1480-5.
22. Doğanay B, Ozcan Celebi O. A novel inflammation indicator of acute stent thrombosis and in-hospital mortality in acute coronary syndrome: Multiple inflammation index. Journal of Medicine and Palliative Care. 2023;4(2):168-75.
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Valentino’s syndrome with two different clinical phenotypes in adolescents and adults; a case series
Betul Keskinkılıç Yağız 1, Sertaç Hancıoğlu 2
1 Department of General Surgery, Gazi State Hospital, 2 Department of Pediatric Surgery, School of Medicine, Ondokuz Mayıs University, Samsun, Turkey
DOI: 10.4328/ACAM.22638 Received: 2025-03-08 Accepted: 2025-04-15 Published Online: 2025-05-29 Printed: 2025-10-01 Ann Clin Anal Med 2025;16(10):710-714
Corresponding Author: Sertaç Hancıoğlu, Department of Pediatric Surgery, School of Medicine, Ondokuz Mayıs University, Samsun, Turkey. E-mail: dr_sertach@hotmail.com Corresponding Author ORCID ID: https://orcid.org/0000-0003-0534-1931
Other Authors ORCID ID: Betul Keskinkılıç Yağız, https://orcid.org/0000-0003-2271-2116
This study was approved by the Ethics Committee of Ondokuz Mayıs University (Date: 2024-04-24, No: 2024-211)
Aim: Valentino’s Syndrome is a very rare condition and basically can be described as duodenal ulcer perforation mimicking the clinical findings of acute appendicitis. It is named after the actor Rudolph Valentino, who had undergone surgery for assumed acute appendicitis and turned out to have a perforated ulcer. The actor died in 1926 days after the surgery. We present a case series of adult and adolescent patients with Valentino’s Syndrome with two different clinical presentations.
Materials and Methods: Medical records of 6 patients who had Valentino’s Syndrome were retrospectively evaluated.
Results: All of the patients were males with a median age of 16,65 years (range: 13-27 years). Clinical and radiological findings suggested acute appendicitis in all of them. On surgical exploration, all had duodenal perforation with a grossly normal appearing appendix. Duodenal wall was intact in 3 (50%), suggesting recovered perforation, and all underwent appendectomy without an attempt for duodenal repair. The other 3 received duodenal repair for obvious perforation.
Discussion: Although Valentino’s is regarded as a myth by many, we present the most satisfactory and well-documented series. Differential diagnosis of patients with acute abdomen has become more prominent recently as the popularity of nonoperative management of acute appendicitis is increasing. Although rare, Valentino’s should be kept in mind in patients with unexpected operative findings or in patients with inconsistent clinical findings.
Keywords: duodenal ulcer perforation, laparoscopy, acute appendicitis, right lower quadrant
Introduction
Acute appendicitis is one of the most common abdominal surgical emergencies in children and adults. Although it is assumed to be as old as human existence, its etiology remains contentious, and management has not become available until the last centuries due to a lack of anesthesia, a crucial ingredient for the existence of surgery [1,2]. As the art of medicine evolves, the successful management of acute appendicitis has improved significantly such that studies advocating nonoperative management increased dramatically during the last 2 decades (3). However, the accurate diagnosis of acute appendicitis remains challenging, and many attempts have been made to create scoring systems to increase the accuracy of the diagnosis of acute appendicitis (Alvarado, Pediatric Appendicitis Score, AIRS, etc). Another issue is the lack of consensus about the definitive diagnosis of acute appendicitis. Although consensus dictates surgical exploration and histological evaluation, we think there is a shortage of data in the literature about the definitive diagnosis of acute appendicitis. Similarly, although the term ‘negative appendectomy’ is commonly used, there is no clear or agreed definition of the term. In uncomplicated cases, definitive diagnosis may remain unclear as the appendix is already a lymphoid tissue that accommodates inflammatory cells without the presence of acute appendicitis, and apparently, such specimens are diagnosed as lymphoid hyperplasia.
Valentino’s Syndrome is a very rare condition that describes the clinical condition characterized by duodenal ulcer perforation mimicking the clinical findings of acute appendicitis. It is named after the American actor Rudolph Valentino, who underwent surgery for assumed acute appendicitis but was found to have a perforated duodenal ulcer and deceased during the process after surgery. The proposed mechanism for Valentino’s Syndrome is that the leaked duodenal content travels through the right paracolic gutter, reaching to right lower quadrant and pelvis, causing the clinical picture mimicking acute appendicitis.
Despite the advanced medical technology and widespread availability of medical services, the definitive diagnosis of acute appendicitis is still challenging, and Valentino’s Syndrome stands as a rare, mysterious condition that needs to be considered in the differential diagnosis while dealing with patients with abdominal pain for possible acute appendicitis.
In this study, our aim is to present our case series of Valentino’s Syndrome in children and adults and describe a different clinical entity in adolescents, which we believe has not been reported before.
Materials and Methods
The patients who underwent surgery for suspected acute appendicitis but concluded to have Valentino’s syndrome between 2020 and 2024 are enrolled in the study. The cause of admittance, preoperative radiological and clinical findings, intraoperative surgical findings, and postoperative results were retrospectively evaluated. The patients without sufficient data are excluded from the study, and a total of 6 patients are enrolled.
Ethical Approval
This study was approved by the Ethics Committee of Ondokuz Mayıs University (Date: 2024-04-24, No: 2024-211).
Results
A total of 6 patients are enrolled in the study. All patients were males and the median age of the patients was 16,65 years (range: 13-27 years ). All patients were admitted with abdominal pain lasting for no more than 4 days. Clinically, physical examination findings suggested acute appendicitis (tenderness/guarding/rebound at the right lower quadrant) in all of the patients, and all underwent abdominal exploration for suspected acute appendicitis but were finally concluded as Valentino’s Syndrome. In 1 patient with free air on plain x-ray examination (Figure 1), Valentino’s Syndrome was suspected before the operation and confirmed with laparoscopic exploration (Patient no:5). The duodenal perforation was possibly healed as no leak was observed after freeing the para-duodenal adhesions and air leak test was performed through the nasogastric tube. All patients had turbulent fluid in the pelvis and right paracolic gutter, but appendix vermiformis appeared as ‘innocent’ and was not perforated or inflamed enough to be the cause of turbulent fluid (Figure 2a-2d). Therefore, the attending surgeon urged to find the primary cause in all patients. Exploration of the whole abdomen was possible in 5 patients who underwent laparoscopic exploration but not in 1 patient who underwent open surgery. Periduodenal inflammation and omental adhesions were noticed in these patients (Figure 3a, 3b, 3c). When these adhesions were bluntly dissected, obvious duodenal perforation was visible in 2 patients (Figure 3d). The procedure was converted to open in these patients to repair the duodenal ulcer perforation. However, the adhesions on the duodenal wall were dense and dissection was challenging and regarded as hazardous in 3 patients, suggesting a chronic process and a possible healed perforation (Figure 3a and 3b). In the first case of these 3 patients, a simultaneous gastroscopy was performed during the operation, which demonstrated multiple duodenal ulcers, and integrity of the duodenal wall was confirmed (by air leak test and endoscopic vision). In the other 2 patients, a leak test was performed under laparoscopic vision by applying air through the NG tube. Appendectomy was performed in all these 3 patients due to the mystic nature of the condition, and the appendiceal lumen was found intact on histological examinations. No further action was performed, but all received medical treatment for duodenal ulcer until they had an elective gastroscopy. In 2 of these patients, intraperitoneal fluid was sampled intraoperatively for amylase and lipase levels with concomitant blood samples to compare with serum levels, and was found significantly higher. Intraperitoneal/serum amylase levels were 596/88 u/L and 150/59 U/L, lipase levels were 1551/29 U/L and 91/20 U/L. These findings are regarded as evidence of the duodenal origin of the intraperitoneal fluid. These 3 patients were subgroupped as Type B (occult, recovered, or healed duodenal perforation), and others were subgrouped as Type A (non-patent, disrupted duodenal wall).
Another patient (patient no=3) was consulted intraoperatively, who underwent a laparotomy through a right transverse lower quadrant incision for suspected appendicitis. An unexpected turbulent fluid in the right lower quadrant was found, which was not correlated with the gross appearance of the appendix vermiformis, exploration of the whole intestine was performed, but no cause was observed. For possible upper gastrointestinal perforation, methylene blue dye was given through the nasogastric tube and seen to spread into the peritoneal cavity. Another separate midline incision was performed, and a duodenal perforation was found and repaired.
All patients, except 2, denied any previous history of dyspeptic symptoms. All patients underwent plain X-ray examination in an erect position and ultrasonographic examination, but only 2 underwent computerized tomography (CT) with IV contrast before the operation. Suggestive findings of acute appendicitis on US examination were double wall thickness > 6mm (n = 4), increased mesenteric echogenicity at the right lower quadrant (n = 5), and right paracolic and/or pelvic fluid (n = 6). Suggestive findings of acute appendicitis on CT were double wall thickness > 6 mm (n = 1) and right paracolic and pelvic fluid (n = 1). In 1 patient (patient 5), free air under the diaphragm was noted in plain x-ray in the erect position (Figure 1), but no obvious open perforation was found when periduodenal inflamed tissues were dissected and regarded as Type b (Figure 3a and 3b). No free air was demonstrated in any of the plain X-rays or CT images except for this patient. All patients had physical examination findings suggestive of acute appendicitis (tenderness, guarding, and/or rebound localized to the right lower quadrant), and inflammatory markers were elevated in all (white blood cell count and C-reactive protein). Laparoscopic approach was performed in 5 patients but converted to open surgery in 2, at the discretion of the attending surgeon. One patient underwent open surgery but needed an additional separate open incision for repair of an open duodenal perforation. Intraoperative gastroscopy was performed in 1 patient to confirm the patency of the duodenal wall (patient 2). All patients underwent gastroscopy after the recovery period of the operation, and findings of bulbar duodenitis were present in all. Helicobacter pylori was confirmed histologically in 4 patients.
The patency of the other intraperitoneal organs (the whole intestine, gallbladder..) was confirmed in all patients during the surgery to exclude and avoid overlooking any other co-existing.
Discussion
Although acute appendicitis is one of the most renowned and oldest surgical conditions of humans, it still remains a clinical challenge for both accurate diagnosis and differential diagnosis in adults and children [3,4]. Actually, acute appendicitis is a final diagnosis that necessitates surgery and histological evaluation for confirmation of the diagnosis [5]. Nevertheless, patients admitted with abdominal pain are individually challenging closed books in terms of differential diagnosis. There are many common conditions for differential diagnosis in patients with acute abdomen.
Historically, surgical correction of acute appendicitis was as challenging as diagnosis of the disease [1]. With improvements in anesthesia and medical technology, surgery became a simple step in the management of acute appendicitis. Although diagnostic accuracy has also been improved in parallel with technological advancements, it still remains a significant challenge and prominent issue when dealing with patients with acute abdominal pain. Contemporarily, management principles evolved from conventional surgery to laparoscopic, endoscopic, and nonoperative management [6,7]. Especially nonoperative management became prominent for the management of uncomplicated appendicitis during the last 2 decades [3].
The incidence of peptic ulcer disease appears to be increasing in children in recent years. Although not uncommon in adults, complications of peptic ulcer disease (bleeding and mainly perforation) are significantly rare in children [8,9]. Commonly, peptic ulcer disease is classified among the causes of upper abdominal pain [8]. Less commonly, patients may be admitted with chest or back pain. However, patients may be admitted with atypical clinical presentation with symptoms and clinical findings located in the right lower quadrant, which is not commonly mentioned in the textbooks.
Valentino’s Syndrome appears as a medical myth describing perforated peptic ulcer disease mimicking acute appendicitis due to gastric/duodenal content that travels through the right paracolic gutter and is usually diagnosed during the operation intended for acute appendicitis removal or even after the operation secondary to missing the condition [10-12]. A PubMed search returned 17 publications containing around 30 cases of Valentino’s Syndrome. Interestingly, all were published after the year 2005, and there is not much information about who named the syndrome or who published it first. This scarce data deepens the mystery of Valentino’s Syndrome. It was reported in children, in the elderly, and even in pregnant patients [10,11,13]. Most of the patients were males and rarely recognised before the operation [14-16].
Classically, a perforated ulcer can easily be identified on surgical exploration, and free air in radiological studies may be encountered in some cases [9]. However, there was no intraperitoneal free air in 5 of our 6 cases, and no obvious/visible perforation was identified in 3 of our patients (Type B). In these 3 cases with no obvious perforation on surgical exploration, Valentino’s syndrome was concluded due to periduodenal inflammatory changes/adhesions, turbulent fluid in the right lower quadrant and pelvis with a normal appearing appendix, and/or increased levels of amylase and lipase in this turbulent fluid (Table 1). All 3 had undergone laparoscopic exploration for assumed acute appendicitis, enabling exploration of the whole intraperitoneal space. However, care should be taken that evaluation of the intraperitoneal space may not be enough, as some cases were also reported with retroperitoneal perforation without any intraperitoneal fluid accumulation, which constitutes a diagnostic pitfall and warrants caution [12,17,18].
Surgical confirmation of healed Valentino’s (Type B, as we called it) was not reported before and contradicts the common belief that spontaneous healing of a perforated peptic ulcer would hardly be possible. However, there are many studies indicating peptic ulcer perforations heal without surgery, even in the era before antibiotics and anti-secretory agents [17,19,20]. The most likely mechanism is that the adhesive behavior of the periduodenal structures or omentum would enable the spontaneous healing of the perforated ulcer after the intraperitoneal spilling of the chymus. Additionally, widespread prescription of antibiotics and gastric secretion inhibitors (omeprazole, etc) may change the usual course of the peptic ulcer disease process, and spontaneous healing may be accelerated.
In the modern era of nonoperative management of acute appendicitis, many questions and potential drawbacks emerge. Despite stunning developments in medical technology in the last century, proper diagnosis of acute appendicitis remains challenging. Although data about the definitive diagnosis of acute appendicitis is vague, the most common agreement is that it can be best achieved by surgical exploration and histological evaluation of the removed appendix, and the decision to operate or not remains challenging[6]. Accordingly, this new trend of nonoperative management constitutes a new challenge for surgeons to properly diagnose patients who are admitted with abdominal pain without performing surgery and obtaining a specimen for histological evaluation. Accurate clinical and radiological diagnosis is challenging in females, children, and elderly people [21,22]. Also, as physicians commonly focus on obtaining a diagnosis, the possibility of false positive results of diagnostic tools appears to be underestimated and stands as a significant pitfall [23]. These factors lead to unexpected scenarios during nonoperative or operative management of patients with acute abdomen. Therefore, in cases of inconsistent radiological and/or clinical findings, unexpected findings during surgery, and unsatisfactory improvement during the clinical follow-up when nonoperative management is preferred, other rare causes of acute abdomen should be considered, and patients should be re-evaluated. Laparoscopy is a reliable ally and tool for surgeons for evaluation of the whole peritoneal space, unless the surgeon notices something is ‘not right’ and has an extended list of ‘other causes’ of acute abdomen in mind.
Limitations
Limitations of our study are a small number of cases and a retrospective design. However, due to the rare nature of the condition, current literature has limited data with a limited number of case reports, and our study is the largest and most well-documented study.
Conclusion
Although stunning advances in medicine and medical technology provided improved diagnostic accuracy, many pitfalls remain during the evaluation of patients with ‘acute abdomen’. Acute appendicitis is a diagnosis mostly confirmed after surgery and histological evaluation; therefore, it is advised to identify the patients as ‘acute abdomen’ before the surgery to keep the clinician alert. Although significantly rare, Valentino’s syndrome (with obvious or occult perforation) is rare but should be considered amongst the differential diagnosis of patients with acute abdomen, and an intact duodenal or bulbar wall does not necessarily exclude it.
Scientific Responsibility Statement
The authors declare that they are responsible for the article’s scientific content including study design, data collection, analysis and interpretation, writing, some of the main line, or all of the preparation and scientific review of the contents and approval of the final version of the article.
Animal and Human Rights Statement
All procedures performed in this study were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.
Funding: None
Conflict of Interest
The authors declare that there is no conflict of interest.
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Betul Keskinkılıç Yağız, Sertaç Hancıoğlu. Valentino’s Syndrome with two different clinical phenotypes in adolescents and adults; a case series. Ann Clin Anal Med 2025;16(10):710-714
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Diagnostic and prognostic value of laboratory parameters in pediatric COVID 19 patients referred to intensive care unit by age groups
Bensu Bulut 1, Murat Genç 2, Medine Akkan Öz 1, Mustafa Önder Gönen 3, Ramiz Yazıcı 4, Dilek Atik 5, Hüseyin Mutlu 6, Zekeriya Uykan 7
1 Department of Emergency Medicine, Health Science University, Ankara Gulhane Training and Research Hospital, Ankara, Turkey, 2 Department of Emergency Medicine, Ankara Training and Research Hospital, Ankara, Turkey, 3 Department of Emergency Medicine, Meram State Hospital, Konya, Turkey, 4 Department of Emergency Medicine, Health Science University, Istanbul Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, Turkey, 5 Department of Emergency Medicine, Karamanoglu Mehmetbey University, Karaman Training and Research Hospital, Karaman, Turkey, 6 Department of Emergency Medicine, Aksaray University, Aksaray Training and Research Hospital, Aksaray, Turkey, 7 College of Engineering and Technology, American University of the Middle East, Egaila, Kuwait
DOI: 10.4328/ACAM.22675 Received: 2025-03-25 Accepted: 2025-05-12 Published Online: 2025-08-10 Printed: 2025-10-01 Ann Clin Anal Med 2025;16(10):715-719
Corresponding Author: Bensu Bulut, Department of Emergency Medicine, Health Science University, Ankara Gulhane Training and Research Hospital, Ankara, Turkey. E-mail: bensu.bulut@gmail.com P: +90 553 181 93 62 Corresponding Author ORCID ID: https://orcid.org/0000-0002-5629-3143
Other Authors ORCID ID: Murat Genç, https://orcid.org/0000-0003-3407-1942 . Medine Akkan, https://orcid.org/0000-0002-6320-9667 . Mustafa Önder Gönen, https://orcid.org/0000-0002-6059-4387 . Ramiz Yazıcı, https://orcid.org/0000-0001-9210-914X . Dilek Atik, https://orcid.org/0000-0002-3270-8711 . Hüseyin Mutlu, https://orcid.org/0000-0002-1930-3293 . Zekeriya Uykan, https://orcid.org/0000-0002-9526-9218
This study was approved by the Ethics Committee of Dr. Abdurrahman Yurtaslan Ankara Oncology Training And Research Hospital (Date: 2020-07-08, No: 2020/07.702)
Aim: The aim of this study was to investigate the diagnostic and prognostic value of laboratory parameters according to age groups in paediatric COVID-19 patients referred to the intensive care unit.
Materials and Method: The study was conducted in Ankara Yenimahalle Training and Research Hospital Emergency Department COVID-19 Outpatient Clinic between 30 March 2020 – 1 June 2020. A total of 65 patients under the age of 18 years who were diagnosed with COVID-19 by RT-PCR test and later referred to the intensive care unit were evaluated. The patients were divided into four different groups according to age: 0-2 years (n=22), 3-6 years (n=9), 7-11 years (n=13) and 12-18 years (n=21). Demographic data, laboratory parameters, and clinical outcomes were analyzed retrospectively.
Results: There were significant differences in clinical outcomes between age groups (p<0.05). According to the ROC analysis results, CRP had the highest predictive value for clinical outcomes (AUC: 0.845, 95% CI: 0.730-0.961). When the cut-off value for CRP was set at 35.5 mg/L, clinical outcome could be predicted with 85.7% sensitivity and 78.2% specificity. WBC (cut-off value: 10.67×10^9/L) also had a significant predictive value (AUC: 0.811).
Discussion: It was found that laboratory parameters in paediatric COVID-19 patients referred to intensive care differed according to age groups, and these parameters have an important role in the diagnosis and prognostic evaluation of the disease. In particular, CRP, WBC, lymphocyte, NLR and MLR levels stand out as markers that can be used to predict the clinical course.
Keywords: COVID-19, pediatric patients, intensive care, laboratory parameters, prognosis
Introduction
SARS-CoV-2 (severe acute respiratory syndrome coronavirus-2), which spread rapidly around the world and caused severe pneumonia, was declared a pandemic by the World Health Organization on 11 March 2000 [1, 3]. Initially, it was seen more commonly in the adult population, but a significant increase in pediatric cases was observed in the later stages of the pandemic [3]. Although COVID-19 infection in childhood is usually asymptomatic or mildly symptomatic, it can lead to more severe disease, particularly in children with underlying chronic diseases or in specific age groups [2,4].
The clinical and laboratory features of pediatric COVID-19 patients differ from those of adult patients [3, 4]. Reasons for the milder course of COVID-19 in children include developmental characteristics of the immune system, differences in angiotensin-converting enzyme 2 (ACE2) receptor expression levels, and fewer comorbidities [3,5]. However, there are also significant differences in clinical and laboratory findings between different pediatric age groups.
Laboratory parameters play an important role in the diagnosis, severity assessment, and prognosis determination of COVID-19 infections. Although the laboratory findings associated with COVID-19 in adult patients are well-defined, there is limited data on the diagnostic and prognostic value of these parameters in the pediatric population especially in different age groups [4,5]. Parameters such as white blood cell (WBC) count, lymphocyte count, neutrophil-to-lymphocyte ratio (NLR), platelet count, C-reactive protein (CRP), lactate dehydrogenase (LDH), ferritin and D-dimer are associated with disease severity in patients with COVID-19 [5,9].
Paediatric COVID-19 patients requiring intensive care may present with a more severe clinical picture and abnormal laboratory parameters. In order to develop appropriate treatment strategies and reduce mortality these patients, early diagnosis and identification of risk factors is very important [5, 8]. Especially in cases where PCR testing cannot be performed, or until the test results are available, evaluation of laboratory parameters can guide the clinician in the diagnosis and especially in the treatment approach [8,10].
The aim of this study was to investigate the diagnostic and prognostic value of laboratory parameters according to age groups in paediatric COVID-19 patients referred to the intensive care unit. It is our hope that the data obtained here will help clinicians in the management of paediatric COVID-19 patients and inform future studies.
Materials and Methods
Study Design and Participants
This study was conducted at Ankara Yenimahalle Training and Research Hospital Emergency Department Covid-19 Outpatient Clinic between 30 March 2020 and 01 June 2020. It consisted of patients under the age of 18 who came to Ankara Yenimahalle Training and Research Hospital Emergency Department Covid-19 Outpatient Clinic, were diagnosed with COVID-19 by reverse transcriptase polymerase chain reaction (RT-PCR) test and were later referred to intensive care unit (ICU) due to the need for a higher level of care. Case demographics, chronic diseases, emergency admission patterns, laboratory parameters, and patient outcomes were analyzed separately and collected retrospectively. In our hospital, patients presenting to the COVID-19 emergency department undergo a routine physical examination, and a haemogram and biochemical parameters are requested from each patient. Routine laboratory parameters, including haemogram results, were obtained from the first blood sample taken after the patients were admitted to the ED. PLR (platelet-to-lymphocyte ratio) was calculated as platelet count divided by lymphocyte count, MLR (monocyte-to-lymphocyte ratio) as monocyte count divided by lymphocyte count, and NLR (neutrophil-to-lymphocyte ratio) as neutrophil count divided by lymphocyte count. Patients under 18 years of age presenting to the COVID-19 emergency department undergo routine assessment and are referred to intensive care if they have a severe illness, including fever, dyspnoea, and/or chest imaging consistent with SARS-CoV-2 pneumonia, or new or increased need for supplemental oxygen and/or ventilation support; or critical illness, including respiratory failure requiring mechanical ventilation, acute respiratory distress syndrome, shock or systemic inflammatory response syndrome and/or multi-organ failure. Patients were divided into four groups according to age: 0-2 years (infancy), 3-6 years (primary childhood), 7-11 years (secondary childhood) and 12-18 years (adolescence). Those under 18 years of age, diagnosed with COVID-19 by RT-PCR, referred to intensive care unit, and with complete data were included in the study. Cases over 18 years of age, diagnosed with COVID-19 by RT-PCR and not requiring intensive care, not diagnosed by RT-PCR, and missing any of the parameters studied were excluded from the study. The study was conducted by the tenets of the Declaration of Helsinki. Informed consent was not required due to the retrospective nature of the study.
Statistical Analysis
All statistical analyses were performed using SPSS version 20.0 for Windows. Descriptive statistics were used for the demographic analysis of patients. Chi-squared and Fisher exact tests were used to compare rates of categorical variables. Numerical values in the study data were expressed as mean ± standard deviation and minimum-maximum values. Kruskal-Wallis H test and Mann-Whitney U test were used in statistical evaluations according to the categorical (nominal or ordinal) and numerical independent group status of the statistically nonparametric variables. Based on the prognosis of adult and geriatric COVID-19 patients referred to the intensive care unit, laboratory parameters were evaluated with the receiver operating characteristics curve (ROC curve). When evaluating the ROC analysis, parameters with AUC<0.6 and not statistically significant (P>0.05) were excluded. Results were evaluated at a significance level of p<0.05.
Ethical Approval
This study was approved by the Ethics Committee of Dr. Abdurrahman Yurtaslan Ankara Oncology Training And Research Hospital (Date: 2020-07-08, No: 2020/07.702).
Results
Out of 3470 patients under 18 years of age who presented to the COVID-19 emergency department, 65 patients who fulfilled the criteria were included in the study (Figure 1). The mean age of the patient groups was 0.8± 0.8 for Group 1 (n=22), 5± 0.8 for Group 2 (n=9), 8.11± 2.3 for Group 3 (n=13), 14.7± 2.1 for Group 4 (n=21) and 54.5% (n=36) of all patients were male. Patient demographics, length of ICU stay, clinical outcome, and use of mechanical ventilation are shown in Table 1. When evaluating the clinical outcome of the patients, there was a significant difference between groups (p<0.05). Rates for discharge from ICU were high in the 0-2 age group, decreased significantly in the 3-11 age group, and increased in the 12-18 age group. Although the rate of ventilation was similar between age groups, death was only observed in the 12-18 age group. Significant differences (p<0.05) were found between the groups in WBC, lymphocyte, platelet, platelet-lymphocyte ratio (PLR), NLR, MLR ratios, RDW, and CRP values (Table-2). According to the results of ROC analysis performed on the parameters that were significant in terms of clinical prognosis in pediatric COVID-19 patients, the parameter with the highest predictive value for clinical outcome was found to be CRP (AUC: 0.845, 95% CI: 0.730-0.961). When the cut-off for CRP was set at 35.5, it was predictive with 85.7% sensitivity and 78.2% specificity. WBC (cut-off: 10.67) also had a significant predictive value (AUC: 0.811). NLR and MLR had a lower predictive value (AUC: 0.713 and 0.689 respectively) (Table 3) (Figure 2).
Discussion
The diagnostic value of laboratory parameters in pediatric patients played an important role in early diagnosis and prognosis during the COVID-19 pandemic [2,5]. In our study, there were significant differences in WBC, lymphocyte, platelet, PLR, NLR, MLR, RDW and CRP levels between different age groups in pediatric COVID-19 patients admitted to the Intensive Care Unit (ICU). Our results suggest that CRP, WBC, NLR, and MLR are strong markers of clinical outcomes in pediatric COVID-19 patients.
Similar to our study, Perk et al. found that lymphopenia, anemia, and CRP elevation were observed in approximately 50% of pediatric COVID-19 patients [12]. In addition, lymphopenia was observed in 65.4%, anemia in 48.1%, and thrombocytopenia in 27.2% of patients in their study. In a study by Demir et al, leukocyte and lymphocyte levels were found to be statistically significantly lower in healthy children than in pediatric patients diagnosed with COVID-19 (p=0.01, p<0.001) [5]. In our study, upon examination of lymphocyte values according to age groups in pediatric COVID-19 patients, they were 6.4±4.2×109/L in the 0-2 age group, 3.1±1.1×109/L in the 3-6 age group, 3.1±1.1×109/L in the 7-11 age group, and 1.4±0.6×109/L in the 12-18 age group, and there was a significant difference between age groups (p<0.05).
One of the important findings of our study was that WBC values showed a significant difference between age groups. WBC values were 16.6±12.7×109/L in the 0-2 age group, 8.6±3.6×109/L in the 3-6 age group, 5.8±2.4×109/L in the 7-11 age group and 9±6.1×109/L in the 12-18 age group (p=0.001). This is similar to the results of the study performed by Gumus et al. where they evaluated the clinical characteristics of pediatric COVID-19 infections [13]. The aforementioned study found that leukocyte levels may be low, especially in the early stages of infection, and may come back to normal parameters in the later stages of the disease. Similar results were found in other studies that followed patients in pediatric intensive care units during the pandemic. Furthermore, investigating the role of laboratory parameters in the diagnosis of pediatric COVID-19 in the absence of PCR, Solmaz et al. found that WBC, neutrophil, platelet, and lymphocyte levels were significantly lower in patients than in the control group, and logistic regression analysis indicated that the best model was the one that included these parameters [11].
Platelet count and hematological parameters are important markers that can be used to predict the severity and prognosis of COVID-19 infections. In our study, the platelet count showed a significant difference between age groups (p<0.05) and was found to be 481±278×109/L in the 0-2 age group and 242±123×109/L in the 12-18 age group. Demir et al. found no significant change in platelet count in pediatric patients with COVID-19 [5], whereas Solmaz et al. reported that platelet count was significantly lower in the patient group than in the control group [11]. These different results suggest that COVID-19 infection shows a heterogeneous clinical manifestation in the pediatric age group and that laboratory parameters may vary depending on the age group.
In terms of inflammatory markers, CRP and procalcitonin levels were of particular note in our study. In the pediatric age group, CRP levels ranged from 13.6±55 to 17.8±14 mg/dL and a significant difference was found between the groups (p=0.005). A study performed by Xia et al. in pediatric COVID-19 patients reported that CRP levels were elevated in 45% of their patients [5]. In addition, many studies have reported that CRP is elevated in pediatric COVID-19 patients [3, 6-11, 13]. In our study, elevated CRP was an important laboratory finding in pediatric patients diagnosed with COVID-19. The predictive value of CRP was determined to be 35.5 mg/L by ROC analysis, and it was found to be a significant marker in terms of clinical course with a sensitivity of 85.7% and specificity of 78.2%. This suggests that CRP is an important marker of clinical severity and prognosis in pediatric COVID-19 patients.
Another notable finding in our study was that NLR (neutrophil/lymphocyte ratio) and MLR (monocyte/lymphocyte ratio) values differed significantly between age groups. NLR values were 1.6±2 in the 0-2 age group and 2.5±2.2 in the 12-18 age group (p=0.04). MLR values were 0.16±0.14 in the 0-2 age group and 0.40±0.29 in the 12-18 age group (p=0.001). Liu et al. reported that NLR was an important predictor of disease severity in COVID-19 patients and that high NLR values were associated with poor prognosis [15]. Seyit et al. also found that NLR, MLR, and PLR could be used to predict the severity of COVID-19 infections [16]. Similar to these studies, we also found that NLR and MLR had a high predictive value for clinical outcomes in paediatric COVID-19 patients (AUC: 0.713 and 0.689, respectively).
D-dimer elevation is considered an indicator of coagulopathy and thromboembolic complications in COVID-19 infections. In our study, D-dimer levels were 1304±267 ng/mL in the 0-2 age group, 255±311 ng/mL in the 3-6 age group, 92±137 ng/mL in the 7-11 age group and 509±907 ng/mL in the 12-18 age group. Although no statistically significant difference was found between the groups (p=0.260), it is noteworthy that D-dimer levels were particularly high in the 0-2 age group. Wang et al. reported that D-dimer elevation was observed in 51.5% of pediatric COVID-19 patients [17]. Similarly, D-dimer elevation was found in a significant proportion of patients in the study by Perk et al [12]. These findings suggest that the coagulation system may be affected in pediatric COVID-19 patients and that this may be related to the severity of the disease.
Limitations
Our study has several limitations. First, the study was conducted with single-centre data and the results may not be generalised to the whole population; second, some clinical data may not have been fully evaluated due to the retrospective design of our study. Finally, data from pediatric COVID-19 patients and healthy pediatric patients were not compared.
Conclusion
It was found that laboratory parameters in pediatric COVID-19 patients admitted to the ICU differed depending on the age group and that these parameters play an important role in the diagnosis and prognostic assessment of the disease, in particular CRP, WBC, lymphocyte, NLR, and MLR levels stand out as markers that can be used to predict the clinical outcome. Interpreting these parameters alongside clinical assessment is thought to help determine disease severity and prognosis. It will be useful to confirm these findings in future prospective multicentre studies with large patient populations.
Scientific Responsibility Statement
The authors declare that they are responsible for the article’s scientific content including study design, data collection, analysis and interpretation, writing, some of the main line, or all of the preparation and scientific review of the contents and approval of the final version of the article.
Animal and Human Rights Statement
All procedures performed in this study were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.
Funding: None
Conflict of Interest
The authors declare that there is no conflict of interest.
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Download attachments: 10.4328.ACAM.22675
Bensu Bulut, Murat Genç, Medine Akkan Öz, Mustafa Önder Gönen, Ramiz Yazıcı, Dilek Atik, Hüseyin Mutlu, Zekeriya Uykan. Diagnostic and prognostic value of laboratory parameters in pediatric COVID 19 patients referred to intensive care unit by age groups. Ann Clin Anal Med 2025;16(10):715-719
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The relationship between depression, anxiety, and alexithymia in Huntington’s disease
Dilek İşcan 1, Huriye Ünlüel 2, Hilal Özgüner 3, Şengül Şenel 4
1 Department of Neurology, Faculty of Medicine, Nigde Ömer Halisdemir University, Nigde, 2 Department of Neurology, Faculty of Medicine, Yozgat Bozok University, Yozgat, 3 Department of Neurology, Nigde Training and Research Hospital, Nigde, 4 Department of Gerontology, Nigde Training and Research Hospital, Nigde, Turkey
DOI: 10.4328/ACAM.22794 Received: 2025-07-02 Accepted: 2025-08-04 Published Online: 2025-08-18 Printed: 2025-10-01 Ann Clin Anal Med 2025;16(10):720-724
Corresponding Author: Dilek İşcan, Department of Neurology, Faculty of Medicine, Nigde Omer Halisdemir University, Nigde, Turkey. E-mail: dilekiscann@gmail.com P: +90 536 562 26 63 Corresponding Author ORCID ID: https://orcid.org/0000-0002-0773-7780
Other Authors ORCID ID: Huriye Ünlüel, https://orcid.org/0000-0002-6188-8328 . Hilal Özgüner, https://orcid.org/0000-0002-7117-9090 . Şengül Şenel, https://orcid.org/0009-0005-4599-0997
This study was approved by the Ethics Committee of Nigde Ömer Halisdemir University (Date: 2024-10-24, No:2024/90).
Aim: Numerous studies have been conducted on psychiatric complaints such as depression, anxiety, and apathy in HD; however, due to the scarcity of studies examining alexithymia and their conflicting results, this study was deemed necessary. It was aimed to demonstrate alexithymia and the presence of difficulties in recognising and expressing emotions and extroverted thinking, which are subgroups of alexithymia, in patients with HD.
Materials and Methods: Sixteen HD patients and sixteen healthy controls were assessed using the Beck Depression Inventory (BDI), Beck Anxiety Inventory (BAI), and the Toronto Alexithymia Scale-20 (TAS-20). Both groups were compared, including the TAS-20 subscales: TAS-A for difficulty identifying emotions, TAS-B for difficulty describing emotions, and TAS-C for externally-oriented thinking.
Results: BDI, BAI, and TAS-20 scores were significantly higher in the patient group (P<0.02). Similarly, TAS-A, TAS-B, and TAS-C scores were also significantly higher in the patient group (P<0.02). While there were 2 possible alexithymics in the healthy group, there were 6 possible alexithymics and 6 definite alexithymics in the patient group.
Discussion: It has been shown that in HD, which has a high psychiatric burden, alexithymia and its subscales, difficulty in recognizing, expressing emotions, and externally-oriented thinking, increase.
Keywords: Huntington’s disease, alexithymia, depression, anxiety, TAS-20
Introduction
Huntington’s Disease (HD) is a progressive neurodegenerative disorder resulting from abnormal expansions of cytosine-adenine-guanine (CAG) repeats in the huntingtin gene (HTT) on chromosome 4p16, presenting with cognitive, motor, and neuropsychiatric symptoms [1]. The neuropathological hallmark of HD includes the selective vulnerability of medium spiny neurons in the striatum, which make up over 90% of the cells, and the presence of intracellular aggregates known as inclusion bodies of mutant huntingtin protein (mHTT) [2,3]. According to a meta-analysis of 33 studies published between 2010 and 2022, the incidence of HD was 0.48 per 100,000 cases [4]. Although there is a juvenile form of the disease, it typically manifests in middle age, with an average onset age between 35 and 50 [3]. Motor symptoms seen in HD include choreiform movements, dysarthria, balance disorders, and parkinsonism. In HD, effects on the limbic system alongside the frontostriatal networks have been shown to cause cognitive changes [5]. Emotions, sleep modulation, motivational behavior, memory, and social cognition, which are controlled by the amygdala, hippocampus, hypothalamus, and thalamus that constitute the limbic system, are also affected in HD [6]. In HD, one can observe apathy, depression, generalized anxiety disorder, panic attacks, impulse control disorders, and psychosis [7]. While motor symptoms are the most noticeable, psychiatric symptoms often cause more distress to patients and their relatives [8].
Alexithymia is a multidimensional personality structure that includes difficulty in recognising and defining emotions, difficulty in distinguishing emotions from somatic symptoms, extroverted thinking, and limitations in imagination [9,10]. Individuals with high levels of alexithymia have difficulty perceiving emotions, identifying their emotions, and expressing their emotions to others. Along with the decrease in emotional attention, it leads to a decrease in memory and executive functioning. In individuals with high levels of alexithymia, a decrease in problem solving, tracking the information that needs to be carried out to solve the problem, synthesizing old and new information (updating), shifting between different mental tasks, and inhibiting dominant and automatic functions when necessary has been observed. All of these emphasize the importance of detecting the presence of alexithymia in the follow-up of HD patients [11]. While alexithymia has been studied in many diseases, it has rarely been addressed in HD, which has such an intense psychiatric burden. Due to the different results in the few studies in the literature [12,13] and the lack of studies examining alexithymia in terms of difficulties in recognizing, expressing emotions, and externally-oriented thinking, this study was deemed necessary.
Materials and Methods
This study was conducted at the Neurology Outpatient Clinic Niğde Training and Research Hospital. Before the study, all participants were thoroughly informed about the study and provided written consent. The study was approved by the Non-Invasive Clinical Research Ethics Committee of Niğde Ömer Halisdemir University with protocol number 2024/90 on October 24, 2024. All procedures conformed to institutional or national ethical standards and the 1964 Declaration of Helsinki. Compliance with the ‘Regulation on Pharmaceutical Research’ (Official Gazette no. 27089, 23 December 2008).
Sixteen genetically diagnosed HD patients were included in the study. Sixteen healthy individuals, matched for age and sex, without psychiatric complaints, chronic neurological diseases, a family history of neurodegenerative diseases in first-degree relatives, or medication use, who came to the hospital as companions to patients, were selected as the control group.
Patients with dementia, known psychiatric diagnoses, or those using antidepressants, antipsychotics, or anxiolytics were excluded from the study.
For both HD patients and the healthy control group, depression was assessed with the Beck Depression Inventory (BDI), anxiety with the Beck Anxiety Inventory (BAI), and alexithymia with the Toronto Alexithymia Scale-20 (TAS-20).
Beck Depression Inventory (BDI): This scale is used to assess the severity of depression. The reliability and validity of the Turkish version were carried out by Hisli Şahin in 1998 [14]. It consists of 21 items, each scored from 0 to 3; scores range from 0-9 for normal, 10-16 for mild depression, 17-29 for moderate depression, and 30-63 for severe depression.
Beck Anxiety Inventory (BAI): Used to measure anxiety severity, the validity and reliability study of the Turkish version was conducted by Ulusoy at al [15]. It consists of 21 items, each scored from 0 to 3; 0-7 points indicate normal, 8-15 points indicate mild anxiety symptoms, 16-25 points indicate moderate anxiety symptoms, and 26-63 points indicate severe anxiety symptoms.
Toronto Alexithymia Scale-20 (TAS-20): This 20-item scale, developed by Bagby and colleagues, assesses alexithymia [16]. The Turkish version’s validity and reliability were studied by Güleç at al [17]. Questions 4, 5, 10, 18, and 19 are reverse-scored. A TAS score ≤51 indicates no alexithymia, 52-60 suggests possible alexithymia, and ≥61 indicates definite alexithymia. TAS-A, composed of questions 1, 3, 6, 7, 9, 13, and 14, measures difficulty in identifying emotions; TAS-B, composed of questions 2, 4 (reverse), 11, 12, and 17, measures difficulty in describing emotions; TAS-C, composed of questions 5, 8, 10, 15, 16, 18, 19, and 20, provides insight into externally-oriented thinking.
Statistical Analysis
For statistical analysis, SPSS 26.0 (IBM SPSS Statistics 26 software; Armonk, NY: IBM Corp.) was used. The normality distribution of the data was evaluated using the Shapiro-Wilks test and histograms. Numerical variables were presented as mean ± standard deviation, and categorical variables as number (n) and percentage (%). The Chi-Square test was used to compare categorical variables between groups, with the Likelihood Ratio test preferred when expected cell frequencies were low. The Independent Samples t-test was used to compare age, depression, total alexithymia, TAS-B, and TAS-C scores between the HD patient and control groups, while the Mann -Whitney U test was used for anxiety and TAS-A scores. Spearman correlation analysis was applied to examine the relationship between the age and disease duration of HD patients with depression, anxiety, and alexithymia. Correlation coefficients were interpreted as follows: 0.00-0.25 = very weak, 0.26-0.49 = weak, 0.50-0.69 = moderate, 0.70-0.89 = high, and 0.90-1.00 = very high. The significance level was accepted as p<0.05.
Ethical Approval
This study was approved by the Ethics Committee of Nigde Ömer Halisdemir University (Date: 2024-10-24, No:2024/90).
Results
The study included 16 HD patients (7 women, 9 men) and 16 controls with similar demographic characteristics (9 women, 7 men). The mean age of HD patients was 58.62 ± 13.00 (minimum 26, maximum 77), while that of the control group was 51.50 ± 10.35 (minimum 26, maximum 70) (p=0.097). The disease duration was 10.50 ± 8.77 years. Depression, anxiety, and alexithymia levels of the patient and control groups were compared, as shown in Table 1, where BDI, BAI, and TAS-20 scores were significantly higher in the patient group. According to BDI, mild depression was observed in 6, moderate depression in 3, and severe depression in 6 of the HD patients, and mild depression was observed in 7, and moderate depression was observed in 2 of the healthy control group. Based on BAI, 6 of the patients with HD had mild, 6 had moderate, and 3 had severe anxiety, whereas 5 of the healthy control group had mild, 6 had moderate, and 3 had severe anxiety. In the healthy control group, only 2 individuals had possible alexithymia according to TAS-20, while in HD, there were 6 patients with possible alexithymia and 6 with definite alexithymia. TAS-A, TAS-B, and TAS-C scores were higher in HD patients (p<0.02). As shown in Table 2, there was a positive correlation between disease duration and TAS-20 and TAS-A. There was a positive correlation between BDI and BAI with TAS-B.
Discussion
Depression, anxiety, and alexithymia were shown to be higher in HD patients compared to healthy individuals. Additionally, in the patient group, difficulties in identifying emotions, expressing emotions, and externally-oriented thinking, as assessed by TAS-20, were also higher. There was a positive correlation between depression, anxiety, and difficulty in expressing emotions.
In a study by Trinkler et al. involving 13 HD patients, no difference was found in TAS-20 scores between the patient and control groups, nor between emotions like anger, disgust, fear, happiness, surprise, and sadness. According to Trinckler et al., since emotion recognition and processing are similarly impaired in Parkinson’s disease and vascular lesions of the striatum, emotion recognition and processing may be similarly impaired in HD, which also progresses with striatal degeneration. In this study, the researchers thought that the scales may have been misleading even if alexithymia was present in patients with HD [18]. In another study by Trinkler et al., involving 26 HD patients, alexithymia was not found to be increased [12]. In our study, TAS-20 was significantly higher. Alt-hough neither study by Trinkler et al. showed an increase in alexithymia in HD compared to controls, a reduction in EEG activation during voluntary production of emotional facial expressions in patients with mild HD was demonstrated [12,18].
In Eddy et al.’s study using a 26-item TAS, scores of 62 or above were considered possible alexithymia, and 74 or above were considered definite alexithymia. Among 25 HD patients, 23 scored over 62, and 14 scored even higher. As in our study, the TAS score was higher in HD patients compared to the control group [13]. Also, the TAS score was higher in manifest patients than in the pre-manifest group, which could support the increase in TAS-20 with disease duration observed in our study.
A meta-analysis including sixteen studies indicated that the recognition of angry facial expressions was impaired in HD, and there was a tendency for the recognition of all negative emotions in both facial expressions and voice to be impaired [19]. In Dupoux et al.’s study, HD patients had difficulty expressing emotions through both voice and language compared to healthy controls [20]. Consistent with these studies, our study showed that HD patients have difficulty in recognizing and expressing emotions. The emotional recognition deficit in HD is partly explained by the general decline in cognitive and motor functions associated with the disease and partly by social-emotional deficits reflected in reduced eye tracking [21]. Although there are few studies on the prevalence of alexithymia in HD in the literature, it was stated in the review published by Cataine et al. that the frequency of depression and apathy correlated with emotional recognition deficit in Parkinson’s disease and HD. With disease progression, a decrease in emotional recognition and expression was observed. It has been observed that emotional recognition deficit, deterioration in interpersonal relationships, and social behavior problems [22]. This was consistent with the positive correlation between disease duration and TAS-20 in our study.
In the study conducted by Tabrizi et al., the only cognitive impairment observed in presymptomatic individuals with HD genetic was found to be emotional recognition deficit. In the pre-HD period, the first complaint was observed as loss of empathy [23].
Limitations
The limitations of the study include the fact that it was conducted in a single centre, the small number of patients, the fact that the relationships between emotion recognition and facial expression recognition, and alexithymia were not examined, and that genetically diagnosed but presymptomatic individuals were not included in the study.
Conclusion
HD is a neurodegenerative disease with movement disorders, cognitive changes, and psychiatric symptoms. We aimed to highlight psychiatric symptoms, which might affect quality of life as much as motor symptoms, and to emphasize that these patients experience difficulties in recognizing, expressing, and externalizing emotions even before dementia develops.
Scientific Responsibility Statement
The authors declare that they are responsible for the article’s scientific content including study design, data collection, analysis and interpretation, writing, some of the main line, or all of the preparation and scientific review of the contents and approval of the final version of the article.
Animal and Human Rights Statement
All procedures performed in this study were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.
Funding: None
Conflict of Interest
The authors declare that there is no conflict of interest.
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Dilek İşcan, Huriye Ünlüel, Hilal Özgüner, Şengül Şenel. The relationship between depression, anxiety, and alexithymia in Huntington’s disease. Ann Clin Anal Med 2025;16(10):720-724
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Comparison of the analgesic efficacy of transversus abdominis plane block and quadratus lumborum block after caesarean section under general anaesthesia: A randomised controlled trial
Melih Bestel 1, Elif Ucar 1, Abdulhakim Şengel 2, Nesrin Burcu Kaya 3, Güven Arslan 4, Erkan Şimşek 5
1 Department of Midewifery, Faculty of Health Sciences, Istanbul Esenyurt University, Istanbul, 2 Department of Anesthesiology and Reanimation, Faculty of Medicine, Harran University, Sanliurfa, 3 Department of Anesthesiology and Reanimation, Siverek Government Hospital, Sanliurfa, 4 Department of Gynecology and Obstetrics, Kahramanmaras Necip Fazıl City Hospital, Kahramanmaras, 5 Department of Gynecologic Oncology, Gaziantep City Hospital, Gaziantep, Turkey
DOI: 10.4328/ACAM.22795 Received: 2025-07-02 Accepted: 2025-09-08 Published Online: 2025-09-16 Printed: 2025-10-01 Ann Clin Anal Med 2025;16(10):725-729
Corresponding Author: Elif Ucar, Department of Obstetrics and Gynecology, Private Esencan Hospital, Istanbul, Turkey. E-mail: eliflyyhotmail.com Corresponding Author ORCID ID: https://orcid.org/0000-0001-5302-4688
Other Authors ORCID ID: Melih Bestel, https://orcid.org/0000-0001-6677-2087 . Abdulhakim Şengel, https://orcid.org/0000-0003-0905-1018 . Nesrin Burcu Kaya, https://orcid.org/0009-0000-3750-9554 . Güven Arslan, https://orcid.org/0000-0001-9013-1191 . Erkan Şimşek, https://orcid.org/0000-0002-6723-1773
This study was approved by the Ethics Committee of Esenyurt University (Date: 2025-05-14, No: 2025/04-52)
Aim: Postoperative pain following caesarean section is a significant clinical issue affecting maternal comfort, mobilisation, and recovery. This study aimed to compare the analgesic efficacy of ultrasound-guided Transversus Abdominis Plane (TAP) block and Quadratus Lumborum Block (QLB) in patients undergoing caesarean section under general anaesthesia.
Materials and Methods: Fifty pregnant women scheduled for elective caesarean section between 2020 and 2021 were enrolled in this randomised controlled trial. Participants were randomly assigned into two groups: Group 1 received TAP block (n=25), and Group 2 received QLB (n=25). Postoperative pain was assessed using the Visual Analogue Scale (VAS) at the 1st, 3rd, 12th, and 24th hours. Additional parameters such as time to first analgesic requirement, total analgesic use within 24 hours, haemodynamic data, and complications were also recorded.
Results: VAS scores were significantly lower in the QLB group at all measured time points (p<0.05). Moreover, analgesia was required later, and total analgesic consumption was lower in the QLB group compared to the TAP group. Although nausea and vomiting were more frequent in the TAP group, the difference was not statistically significant. Haemodynamic parameters remained stable in both groups.
Discussion: Both TAP and QLB blocks are safe and effective for postoperative pain control after caesarean delivery. However, QLB offers superior analgesic outcomes, including lower pain scores, delayed analgesic need, reduced analgesic consumption, and potentially greater patient comfort. QLB may therefore be a preferred technique in enhancing postoperative recovery in caesarean section patients.
Keywords: cesarean section, postoperative analgesia, transversus abdominis plane block, quadratus lumborum block, regional anesthesia, VAS score
Introduction
Caesarean section is an invasive surgical procedure that is frequently preferred in high-risk situations for maternal and fetal health. This operation decreases patient comfort and may adversely affect the healing process due to incisional pain, which is frequently observed in the postoperative period. Uncontrolled postoperative pain may lead to cardiac complications as well as impaired respiratory function, inability to cough, atelectasis, and pulmonary complications [1]. When appropriate analgesia is provided, the risk of these complications decreases and patient satisfaction and mobilisation process are positively affected. In recent years, regional block techniques have an important place in postoperative pain management. Transversus Abdominis Plane (TAP) block, one of these techniques, is widely used in abdominal surgeries and provides effective analgesia by blocking somatic nerves in the anterolateral abdominal wall [2]. In this technique, local anaesthetic agents are injected into the fascial space between the internal oblique muscle and the transversus abdominis muscle, and nerve conduction is blocked [3]. Direct visualisation of anatomical structures is possible with ultrasonography guidance, thus increasing both the accuracy and safety of block application [4]. TAP block is widely preferred in the management of analgesia after caesarean section because it reduces the need for opioids and increases patient comfort [3,5,6]. Alternatively, Quadratus Lumborum Block (QLB) is applied by injection into the interfascial space more posterior to the transversus abdominis muscle and is thought to provide a more comprehensive analgesia by targeting both somatic and visceral pain [7]. In the literature, it has been reported that QLB not only provides longer-lasting analgesia, but also reduces opioid use and contributes to early postoperative mobilisation [8]. Compared with TAP, QLB has been suggested to be superior, especially in terms of duration of analgesia and efficacy on visceral pain [9]. However, a definite superiority between these two techniques in terms of analgesic efficacy, opioid requirement, and patient satisfaction has not been determined. Although there are studies in the literature comparing both blocks in different surgical fields, comparative studies in caesarean section are limited. In this context, this study aimed to compare the effects of TAP and QLB blocks on postoperative pain management, analgesic requirement, and patient comfort in women undergoing caesarean section.
Materials and Methods
Fifty patients who gave birth by caesarean section in a secondary care hospital between 2020-2021 were included in the study. Women who underwent caesarean section under general anaesthesia were included in the study. Women who underwent caesarean section under spinal anaesthesia, women with pain problems such as chronic fibromyalgia, women with unexplained and unexplained pain problems, or women receiving treatment were not included in the study.The pregnant women included in the study underwent caesarean section under general anaesthesia by the same physician, and the patients were divided into 2 groups by coin flip technique. Group 1 patients (n=25) received Transversus Abdominis Plane (TAP) block, while Group 2 patients (n=25) received Quadratus Lumborum Block (QLB). Pulse rate, blood pressure, pain intensity, the number of hours, and the number of times analgesia was needed postoperatively and complications were recorded.
Statistical Analysis
Statistical analyses of the data obtained in this study were performed using SPSS (Statistical Package for Social Sciences) software. Firstly, the suitability of continuous variables for normal distribution was evaluated by using kurtosis and skewness values, and the range of -3 to +3 was accepted as the critical value. In the comparison of two independent groups in terms of continuous variables, Independent Groups T test was applied when the data were suitable for normal distribution, and Mann-Whitney U test was applied when the data did not show normal distribution. The Chi-Square test was used to compare categorical variables between groups and to evaluate their relationships. Repeated Measures ANOVA test was used for time-dependent repeated measurements (Mean Arterial Pressure, Pulse, and VAS (Visual Analog Scale) scores) during and after the operation, and time-dependent changes were evaluated separately within the groups.
Ethical Approval
This study was approved by the Ethics Committee of Esenyurt University (Date: 2025-05-14, No: 2025/04-52) and designed in accordance with the Declaration of Helsinki.
Results
Demographic data of 50 patients included in the study are given in Table 1. Comparisons of complications and vital signs between the groups are given in Table 2. Information on the analgesia needs of the patients and the distribution of the pain felt by the patients according to the hours are shown in Table 3. When the complications were analysed, nausea was observed with a rate of 16% in the TAP block group and 8.0% in the QLB group, and no significant relationship was found between the groups. Similarly, while the frequency of vomiting was 4% in the TAP block group, no case of vomiting was detected in the QLB group, and no significant relationship was found between the groups. Urinary retention was not observed in any patient in both groups. While 96% of the patients in the TAP block group were in the ASA 2 anaesthesia group, all of the patients in the QLB group were in the ASA 2 anaesthesia group.
Discussion
This study aims to compare the effectiveness of Transversus Abdominis Plane (TAP) block and Quadratus Lumborum Block (QLB) on postoperative analgesia during caesarean section operations. The study findings show that both subjective pain scores (VAS) and analgesic requirements were significantly lower and patient satisfaction was higher in patients who underwent QLB. In addition, patient satisfaction scores were significantly higher in the QLB group, suggesting that this block method provides advantages not only in pain control but also in patient comfort and quality of the surgical experience. The Enhanced Recovery After Surgery (ERAS) protocol is currently used in most surgical fields to reduce morbidity, length of hospital stay, and promote postoperative recovery [10]. However, postoperative pain is one of the undesirable outcomes that decreases postoperative quality of life for patients [11]. Pain after abdominal surgery is largely related to somatic pain signals in the abdomen [12]. To reduce this pain and increase patient comfort, local anaesthetics can be injected into the space between the internal oblique and transversus abdominis muscles to block the T6-L1 nerves, usually under ultrasonographic guidance [13]. The literature has also shown that the dose of local anaesthesia in the TAP block is of great importance in the pain felt by the patient in the postoperative period. Some studies have argued that this block should be performed preoperatively to interrupt early pain impulses and reduce the need for opioids [14].
Alsharari et al. reported that TAP block was used as an effective strategy for pain management in laparoscopic colectomy patients, and the application of this procedure in addition to general anaesthesia reduced opioid consumption and accelerated the recovery time of patients [15].
Some studies have found that there was no reduction in the need for opioids in the first 12 hours in patients who underwent TAP block [5]. Erol et al. compared the VAS scores of the TAP blog combined with different types of anaesthesia and found that the 12th hour VAS scores were significantly higher in the groups in which only general anaesthesia, TAP with general anaesthesia, TAP with spinal anaesthesia and TAP with epidural anaesthesia were performed compared to the groups in which TAP was not performed [6]. In a study conducted in Canada, it was found that the duration of analgesia requirement after TAP was prolonged up to 24 hours [16]. These results have been shown to have favourable effects on patient satisfaction [2]. Baaj et al. also found that there was better analgesia and patient satisfaction and less opioid requirement in the group in which TAP blog was applied compared to the group in which placebo was applied [17]. In studies, it has been observed that QLB provides effective analgesia and decreases the mean VAS score [18]. In addition, it has been reported that the side effects of QLB application are minimal and patients provide rapid mobilisation after general anaesthesia [19]. In some studies comparing the analgesic superiority of both blogs, it has been claimed that the TAP blog has superior analgesic effects compared to QLB [20]. There are studies showing that these blocks have similar effects. However, in this study, it was also reported that the TAP block was easier to administer and a lower level of expertise was required. It is also said to have less risk of nausea and vomiting [21]. In our study, no significant difference was found in the incidence of nausea between the two block types. Although there is no consensus in the literature about the superiority of these two blocks, the QLB block comes to the fore. Roy et al. found a 25% decrease in fentanyl consumption with the QLB block compared to the TAP block up to 24 hours after the block, and also found that the duration of the need for additional analgesia was significantly longer [9]. Dam et al. found that TAP block decreased opioid consumption during the operation in patients with percutaneous nephrolithotomy, but QLB was more effective in opioid consumption and analgesia [22]. In a study comparing TAP block and QLB in patients undergoing total abdominal hysterectomy, it was observed that the duration of postoperative analgesia was higher in the QLB group than in the TAP group, and opioid requirement was significantly reduced in the QLB group [23]. In their study, Blanco et al. observed that QLB block was better than TAP block for pain relief after caesarean section with longer-acting analgesia exceeding 24 hours and less additional opioid consumption [8]. Verma et al. found that QLB block reduced the number of analgesic dose consumption and prolonged the duration of analgesia for 72 hours after caesarean section compared to patients receiving TAP block [20]. Various studies have also shown that QLB block has less opioid requirement and analgesic effect persists for a longer period of time compared to TAP block despite the use of different analgesic agents [24]. However, some recent studies have shown that QLB block failed to reduce morphine consumption in the first 12 hours [25]. In parallel with this result, there are studies claiming that TAP block leads to better analgesia in the early short postoperative period, whereas QLB block provides more prolonged analgesia [9]. In this study, VAS scores were found to be lower in all time periods in the QLB group. This difference was statistically significant, especially at the 1st, 3rd, 12th, and 24th hours (p<0.05). This strongly supports that QLB is more effective in pain control than TAP block. In addition, it was observed that patients in the QLB group needed analgesia later, consumed less analgesics in 24 hours, and had higher satisfaction levels. These findings suggest that QLB block is superior to TAP block in terms of postoperative comfort and analgesia. However, it was also observed that the techniques had similar effects on haemodynamic stability. These findings are in agreement with the literature that QLB provides a more generalised analgesia that covers both visceral and somatic pain. While TAP block blocks only the somatic nerves of the anterolateral abdominal wall, QLB can provide deeper and longer-lasting analgesia by affecting both somatic and visceral afferent fibres thanks to the spread of local anaesthetics to the paravertebral area [8]. This difference is manifested by lower VAS scores and less opioid requirement in the QLB group, especially in the first 24 hours. In addition, later analgesic requirement in the QLB group suggests that this method may increase early mobilisation and maternal comfort in the postoperative period. Similarly, Vaghela et al. reported that QLB provided more effective analgesia than TAP block in abdominal surgeries such as appendectomy and inguinal hernia repair, which supports the results of our study [7]. Thus, QLB can be considered as an effective alternative to increase maternal safety and patient satisfaction, especially in obstetric surgeries.
Limitations
This study has some limitations. First of all, the study was conducted in a single centre with a limited number of patients (n=50), and the generalisability of the results is limited. In addition, the use of coin toss technique as a randomisation method cannot completely eliminate the potential selection bias. Considering that the efficacy of the applied blocks may depend on the experience of the operator, the single practitioner may pose other limitations in terms of external validity. In addition, the subjective measure of VAS score was used for analgesia assessment, which may influence the results due to individual differences in patients’ pain threshold and perception. Finally, the follow-up period was limited to 24 hours, and late pain and complications were not evaluated. Therefore, studies with larger samples, multicentre and long-term follow-up are needed.
Conclusion
This study comparatively evaluated the efficacy of QLB and TAP blocks in postoperative pain management after caesarean section. Results showed that QLB provided a superior analgesic effect compared to TAP block with lower VAS scores, later analgesic requirement, less analgesic consumption, and higher patient satisfaction, especially in the first 24 hours. Both blocks were found to be safe and had similar effects on haemodynamic stability. These results increase the preferability of QLB in the management of analgesia after obstetric surgery and guide clinical practice to provide more effective patient comfort. However, the validity of the proposed approach will be further strengthened by supporting the findings with larger sample sizes and multicentre studies.
Scientific Responsibility Statement
The authors declare that they are responsible for the article’s scientific content including study design, data collection, analysis and interpretation, writing, some of the main line, or all of the preparation and scientific review of the contents and approval of the final version of the article.
Animal and Human Rights Statement
All procedures performed in this study were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.
Funding: None
Conflict of Interest
The authors declare that there is no conflict of interest.
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Laboratory biomarkers associated with suicidal ideation in major depressive disorder: A retrospective study in the emergency department
Melih Çamcı 1,2, Nur Efşan Akıncı 2,3, Gülsüm Akdeniz 2,3
1 Department of Emergency Medicine, Ankara Yıldırım Beyazıt University, Ankara Bilkent City Hospital, 2 Department of Neuroscience, Institute of Health Science, Ankara Yıldırım Beyazıt University, 3 Department of Biophysics, Faculty of Medicine, Ankara Yıldırım Beyazıt University, Ankara, Turkiye
DOI: 10.4328/ACAM.22823 Received: 2025-07-23 Accepted: 2025-09-22 Published Online: 2025-09-30 Printed: 2025-10-01 Ann Clin Anal Med 2025;16(9):730-735
Corresponding Author: Melih Çamcı, Department of Emergency Medicine, Ankara Bilkent City Hospital, Ankara Yıldırım Beyazıt University, Ankara, Turkiye. E-mail: drmelih112@gmail.com P: +90 505 883 91 81 Corresponding Author ORCID ID: https://orcid.org/0000-0003-4797-0816
Other Authors ORCID ID: Nur Efşan Akıncı, https://orcid.org/0000-0001-8490-1663 . Gülsüm Akdeniz, https://orcid.org/0000-0002-9411-3318
Aim: Major Depressive Disorder (MDD) is a prevalent psychiatric condition that significantly contributes to global disease burden. Suicidal ideation (SI), a common manifestation of MDD, represents a critical point along the suicide risk continuum. Recent research has indicated that MDD may be associated not only with psychological symptoms but also with systemic physiological alterations detectable through laboratory biomarkers. This study aims to investigate the association between routinely collected laboratory parameters and SI in patients with MDD presenting to the emergency department (ED), with the goal of identifying potential biological indicators of acute suicide risk.
Materials and Methods: This retrospective observational study utilized data from the MIMIC-IV database (v2.2). A total of 123 adult patients (≥18 years) diagnosed with MDD (ICD-9: 296.20; ICD-10: F32.9) and presenting to the ED with SI as the chief complaint were included. Laboratory data from the first 24 hours of admission were analyzed. Statistical analyses included t-tests, Mann–Whitney U tests, chi-square tests, and subgroup analyses.
Results: Among the 123 patients (54.5% male), 45.5% had a history of multiple suicide attempts, 48.0% had psychiatric comorbidities, and 31.7% had substance use disorders. Abnormal white blood cell counts (80.5%), neutrophils (64.2%), hemoglobin (36.6%), and creatinine (29.9%) were prevalent. Male patients exhibited significantly higher rates of abnormal ALT, creatinine, hemoglobin, and hematocrit values. Patients with multiple suicide attempts had higher rates of antidepressant use, smoking, alcohol consumption, and chronic medical conditions.
Discussion: This study underscores the complex interplay between psychiatric, behavioral, and physiological factors in MDD patients with SI. Routine laboratory parameters may serve as accessible adjunctive markers in acute suicide risk stratification. Integrating biological data with psychiatric assessment in ED settings may enhance early identification and intervention for high-risk individuals.
Keywords: major depressive disorder, suicidal ideation, emergency department, biomarkers, MIMIC-IV database
Introduction
Major Depressive Disorder (MDD) is one of the leading causes of neuropsychiatric impairment worldwide and represents a substantial contributor to overall disease burden. MDD has been estimated to account for approximately 49.4 million disability-adjusted life years globally in 2020, highlighting its significant impact on population health [1]. MDD is a prevalent psychiatric condition involving depressive episodes of at least two weeks with mood changes, reduced interest, cognitive impairments, and physiological disturbances [2]. Emerging evidence suggests that MDD is associated not only with psychological symptoms but also with measurable alterations in systemic biomarkers. Increased concentrations of inflammatory markers such as C-reactive protein [3], interleukin-6 [4], and various other pro-inflammatory cytokines [5] have been consistently identified in individuals with MDD, indicating the presence of a persistent low-grade inflammatory state. Higher serum albumin levels have been inversely associated with depressive symptoms, as shown by Zhang et al. [6], and were also significantly linked to lower odds of depression in another study [7]. Additionally, abnormalities in serum sodium, creatinine, white blood cell counts, and liver enzymes have been noted in some cohorts, potentially reflecting the somatic burden or comorbid conditions frequently co-occurring with MDD [3]. Suicidal ideation (SI), defined as thoughts of engaging in behavior intended to end one’s life, represents a critical early marker in the continuum of suicidal behavior, which may progress to suicide planning, attempts, and completed suicide if unaddressed [8]. SI is strongly associated with psychological factors such as hopelessness, feelings of worthlessness, and impaired problem-solving, as well as neurobiological alterations including serotonergic dysfunction and hypothalamic-pituitary-adrenal (HPA) axis dysregulation [9, 10]. The biological disturbances in individuals with MDD are not only markers of disease severity but may also contribute to the heightened mortality in this population. Individuals diagnosed with MDD face an overall mortality rate that is 1.8 times higher than that of the general population [11]. This elevated disease burden is partly attributed to the increased likelihood of SI and suicidal behaviors, including suicide attempts and completed suicides [11]. Emergency departments (EDs) frequently represent the first point of contact for individuals in suicidal crisis, serving as critical gateways for mental health triage, stabilization, and referral [12]. Presentations to the ED for suicidal thoughts or behaviors, whether ideation, planning, or recent attempts, are considered psychiatric emergencies that demand immediate and comprehensive evaluation to assess risk and initiate appropriate intervention strategies [13]. In these acute care settings, routine laboratory testing is commonly employed as part of medical clearance protocols prior to psychiatric admission or transfer. While primarily aimed at identifying underlying medical conditions or substance intoxication, these tests can also yield physiological data relevant to psychiatric evaluation [14].
The Medical Information Mart for Intensive Care IV (MIMIC-IV) is a large, publicly available electronic health database developed through a collaboration between the Massachusetts Institute of Technology and Beth Israel Deaconess Medical Center, comprising comprehensive, de-identified clinical data from over 60,000 patients between 2008 and 2019 [15]. This dataset integrates a wide range of information, including ED encounters, vital signs, laboratory results, medications, diagnoses, procedures, and demographic characteristics. Given its granularity and longitudinal structure, MIMIC-IV enables researchers to investigate complex relationships between psychiatric presentations and associated physiological markers across diverse clinical settings. The objective of this study is to investigate the association between laboratory biomarkers and SI among patients diagnosed with MDD who present to the ED. By analyzing routinely collected laboratory data during initial ED evaluation, the study aims to determine whether certain physiological markers indicate acute psychiatric risk. Ultimately, this approach may contribute to the identification of biological indicators that could assist clinicians in the early detection of SI in high-risk patients and to explore whether specific laboratory parameters may serve as biological markers of suicidality in individuals with MDD.
Materials and Methods
Participants and Study Design
This retrospective observational study utilized data from the MIMIC-IV database (version 2.2). In accordance with institutional and data access regulations, the required approvals to access the MIMIC-IV database were obtained, including certification through the Collaborative Institutional Training Initiative (Record ID: 68301129). Compliance with data use protocols and the performance of all data extraction procedures for the present study were ensured. We identified adults (≥18 years) diagnosed with MDD who presented to the ED for SI. This was determined using the following International Classification of Diseases codes: ICD-9 code 296.20 and ICD-10 code F32.9. Patients were included if they had at least one ED admission recorded in the MIMIC-IV database. This initial selection yielded a cohort of 1,635 unique patients. To ensure the clinical relevance and specificity of the sample, further inclusion and exclusion criteria were applied. Patients were retained in the final sample only if SI was explicitly documented as the chief complaint during the ED visit. Individuals were excluded if they had comorbid acute medical conditions, additional psychiatric diagnoses listed as the primary reason for admission, or multiple ED visits, with only the first admission per patient included in the analysis. After these criteria were applied, a total of 123 patients remained eligible for analysis. Laboratory values from the first 24 hours were averaged if multiple results were present. Abnormalities were defined according to the reference ranges embedded in the MIMIC-IV database. The use of the de-identified, publicly available MIMIC-IV database was approved by the MIT Institutional Review Board, with informed consent waived due to the anonymized nature of the data.
Data Collection
Demographic information included age, sex, ethnicity, smoking status and multiple suicide attempts. Relevant comorbidities were identified, including substance use disorder, alcohol use disorder, psychiatric disorders and chronic diseases including diabetes, hypertension, and asthma. Information regarding psychotropic medications at the time of admission such as antidepressants, were also obtained. Laboratory data were collected exclusively from the first 24 hours following admission and included serum sodium, serum creatinine, bicarbonate, albumin, aspartate aminotransferase (AST), alanine aminotransferase (ALT), white blood cell (WBC), hemoglobin, hematocrit, lymphocytes, neutrophils, eosinophils, monocytes, and alkaline phosphatase.
Statistical Analysis
All statistical analyses were performed using IBM SPSS Statistics (version 27). Continuous variables were assessed for normality using the Kolmogorov–Smirnov test and were presented as median (IQR) according to data distribution, whereas categorical variables were expressed as proportions. The t-test and Mann–Whitney U test were used to analyze continuous variables. The chi-square test was applied for the analysis of categorical variables. Subgroup analyses were conducted to compare patients with SI, as well as those with and without substance use disorders or other psychiatric comorbidities, in terms of the prevalence and distribution of abnormal laboratory values. In cases involving multiple comparisons, Bonferroni correction was applied to adjust for the inflated risk of Type I error. A p-value < 0.05 was considered statistically significant.
Ethical Approval
This study did not require ethical approval as it utilized the publicly available and fully de-identified MIMIC-IV database. According to the data usage policy of MIMIC-IV, all data are de-identified in compliance with the Health Insurance Portability and Accountability Act (HIPAA) standards, and no individual consent or institutional review board approval is necessary for analysis. The use of the database was approved through completion of the required training (CITI Program Record ID: 68301129). All procedures were conducted in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.
Results
A total of 123 adult patients (male: 54.5%) aged between 18 and 39 years (59.3%) and diagnosed with MDD who presented to the ED were included in the analysis. A notable proportion had chronic medical conditions (43.9%) and a history of multiple suicide attempts (45.5%). Antidepressant use was reported by 71.5% of participants, and 48.0% had at least one comorbid psychiatric disorder, most commonly bipolar disorder and schizophrenia spectrum disorders. Additionally, 31.7% of the samples had a diagnosed substance use disorder, with cocaine and polysubstance use being the most frequent. Detailed demographic and clinical characteristics are presented in Table 1. Among the laboratory parameters, abnormal white blood cell count was observed in 80.5% of patients, followed by neutrophils (64.2%), hematocrit (38.2%), lymphocytes (38.2%), hemoglobin (36.6%), and monocytes (35.8%) (Table 2). Table 3 presents the comparison of clinical and behavioral characteristics between patients with and without multiple suicide attempts. Patients with multiple suicide attempts had a significantly higher prevalence of substance use disorder (p = 0.0087), psychiatric comorbidities (p < 0.0001), and alcohol use disorder (p < 0.0001), compared to those with no history of multiple attempts. Similarly, the rate of antidepressant use was notably elevated among patients with multiple suicide attempts (94.6% vs. 52.2%, p < 0.0001). Smoking was also more frequent in this group (26.8% vs. 10.4%, p = 0.0341). Additionally, the presence of chronic medical conditions was significantly higher in the multiple attempt group (p < 0.0001). Figure 1 illustrates the strength and direction of monotonic relationships between continuous laboratory parameters using Spearman’s rank correlation. The strongest positive associations were found between ALT and AST (r = 0.79, p < 0.001) and hemoglobin and hematocrit (r = 0.74, p < 0.001), reflecting expected clinical parallels. In contrast, a moderate negative correlation was identified between creatinine and bicarbonate (r = –0.23, p = 0.011), potentially indicating metabolic compensation. Additional weak but significant correlations included ALT and alkaline phosphatase (ALP) (r = 0.30) and sodium and monocytes (r = –0.24). Statistically significant gender differences were found in the frequency of abnormal hemoglobin (male: 46.3%, female: 25.0%), hematocrit (male: 50.8%, female: 23.2%), alanine aminotransferase (male: 25.8%, female: 7.6%), and creatine (male: 29.9%, female: 12.7%) values. Abnormal hemoglobin, hematocrit, alanine aminotransferase, and creatinine levels were more frequent in males than in females. Figure 2 illustrates the gender-based distribution of abnormal laboratory values for hemoglobin, hematocrit, creatinine, and ALT. The total number of abnormal laboratory parameters was significantly higher in male patients compared to females (p < 0.0001), and in those taking antidepressants compared to non-users (p = 0.0139). No significant difference was observed between patients with and without chronic disease (p = 0.1313).
Discussion
This study analyzes patients with MDD and SI in the ED, integrating demographic, clinical, and laboratory data. In addition to examining the behavioral and diagnostic characteristics of individuals with multiple suicide attempts, we also assessed physiological changes using routine lab data collected acutely. Our results reveal that patients with repeated suicidal behavior exhibit a higher burden of psychiatric comorbidity, substance and alcohol use, and chronic medical illness, alongside distinct physiological alterations, including abnormal laboratory parameters. Together, these findings suggest that suicidality in MDD may reflect not only psychological distress but also underlying biological dysregulation, offering a more comprehensive view of acute suicide risk in emergency contexts.
A study by Bachmann [16] conducted a narrative review examining the global epidemiology of suicide, highlighting psychiatric comorbidity, substance use, and gender differences as key risk factors. Bachmann emphasized the heightened suicide risk shortly after psychiatric discharge, particularly in males and individuals with prior suicide attempts. Combinations of mood and substance-related disorders were noted to significantly amplify this risk. Another study by Reneses et al. [17] proposed a clinical staging model of depressive disorders, emphasizing that treatment resistance and persistent residual symptoms are markers of more advanced stages of illness, often associated with greater functional impairment and increased suicide risk. Consistent with these findings, our study revealed that 45.5% of participants had a history of multiple suicide attempts and over half were male. Additionally, 48.0% had comorbid psychiatric disorders, mainly bipolar and schizophrenia spectrum, and 31.7% had substance use disorders, particularly involving cocaine and polysubstance use. This convergence of psychological and physiological burden suggests that these individuals may represent a clinically complex, treatment-resistant subtype of MDD. The high rate of antidepressant use (71.5%) further supports this interpretation, underscoring the importance of sustained, multidisciplinary suicide prevention strategies. Our results support the conceptualization of suicidality not as an isolated symptom but as a dynamic, multifactorial process, reinforcing the need for integrated risk assessment strategies in emergency settings, aimed at delivering targeted psychiatric and medical interventions. The clustering of these risk factors highlights the necessity for enhanced screening and longitudinal follow-up beyond the immediate crisis.Another key finding of this study was the high prevalence of abnormal laboratory parameters among patients with MDD presenting with SI, particularly in those with repeated suicide attempts and among male patients. A study by Ceresa et al. [18] investigated gender-based differences in clinical and biochemical profiles among 234 patients hospitalized for unipolar depression. They found that male patients hospitalized for unipolar depression had elevated liver enzymes, creatinine, and hemoglobin levels, indicating gender-specific biochemical profiles. Similarly, Jiang et al. [19] investigated gender-specific differences in clinical and biochemical profiles among first-episode, drug- naïve MDD patients with suicide attempts. They reported that female MDD patients with suicide attempts showed elevated lipid and thyroid profiles, whereas males had lower BMI and free triiodothyronine, suggesting sex-specific metabolic vulnerabilities. In line with these findings, our results revealed significantly higher rates of abnormal ALT, creatinine, hemoglobin, and hematocrit in males, as well as elevated inflammatory markers such as white blood cell and neutrophil counts across the entire sample. Patients with a history of multiple suicide attempts exhibited significantly higher rates of chronic medical conditions, alcohol use disorder, and smoking compared to those without such a history. This supports the notion that suicidality in MDD often emerges within a broader context of physical health deterioration and behavioral risk patterns. Prior studies have linked medical comorbidities such as cardiovascular disease and chronic pain to elevated suicide risk in mood disorders [20, 21], likely due to reduced quality of life and cumulative psychological burden. Additionally, alcohol misuse is a well-established proximal risk factor, contributing to disinhibition and affective dysregulation [22]. Hughes, highlighted that chronic nicotine use modulates mesolimbic dopaminergic pathways involved in reward processing and increasing impulsivity and mood instability [23]. In line with these, our finding of significantly higher smoking rates among patients with multiple suicide attempts supports the hypothesis that smoking may serve as a behavioral marker of shared neurobiological vulnerabilities in reward and impulse regulation. Collectively, these results emphasize the need for comprehensive suicide prevention approaches that extend beyond psychiatric diagnosis to include physical health, substance use, and lifestyle behaviors, especially in emergency settings where acute presentations may obscure chronic risk accumulation.
Limitations
One limitation of this study is the absence of a control group including either MDD patients without suicidality or healthy individuals, which constrains the ability to assess whether the observed clinical and laboratory patterns are specific to SI. Due to the retrospective and observational nature of this study, it is not possible to determine causal relationships between SI and the observed laboratory parameters. Additionally, the acute stress factors inherent in ED presentations could influence laboratory values, confounding the interpretation of results. The MIMIC-IV database lacks details on severity, duration, stressors, and psychiatric assessments. These limitations highlight the need for future prospective, multi-center studies incorporating richer clinical data to validate and expand upon the current findings.
Conclusion
This study presents a multifaceted examination of patients with MDD presenting to the ED with SI, highlighting the interplay between psychiatric comorbidities, behavioral risks, and systemic physiological disturbances. Our findings underscore the heightened vulnerability of individuals with a history of multiple suicide attempts, particularly in males, who are associated not only with elevated rates of psychiatric comorbidity and substance use, but also with systemic physiological alterations observable through routine laboratory assessments. Integrating lab data—especially inflammatory, metabolic, and hematologic—may improve risk assessment and clinical decision-making. By incorporating these biomarkers into risk stratification protocols, clinicians may enhance the early identification of patients at heightened risk for self-harm. Taken together, these observations support the implementation of a multidimensional suicide prevention model that integrates neurocognitive screening, biological monitoring, and continuity of psychiatric care, emphasizing the importance of early identification, multidisciplinary follow-up, and long-term support beyond the point of crisis stabilization in the ED.
Scientific Responsibility Statement
The authors declare that they are responsible for the article’s scientific content including study design, data collection, analysis and interpretation, writing, some of the main line, or all of the preparation and scientific review of the contents and approval of the final version of the article.
Animal and Human Rights Statement
All procedures performed in this study were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.
Funding: None
Conflict of Interest
The authors declare that there is no conflict of interest.
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Melih Çamcı, Nur Efşan Akıncı, Gülsüm Akdeniz. Laboratory biomarkers associated with suicidal ideation in major depressive disorder: A retrospective study in the emergency department. Ann Clin Anal Med 2025;16(9):730-735
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Clinical efficacy of digital flexible ureteroscopy for renal stone management and postoperative quality of life for the treatment of lower pole stones: A single-center, non-randomized study
Nguyen Huu Thanh 1,2, Nguyen Minh Tuan 2, Hoang Long 1, Dinh Anh Duc 3, Dong Ngoc Minh 4, Ngo Xuan Cuong 2, Nguyen Truong Giang 2, Tran Quoc Khanh 2, Nguyen Tuan Anh 1,6, Nguyen Thanh Vinh 5
1 Department of Surgery, Faculty of Medicine, Hanoi Medical University, 2 Department of Urological Surgery, Bach Mai Hospital, 3 Department of Surgery, Viet Nam National Children’s Hospital, 4 Department of Surgery, Viet Duc Hospital, 5 Department of Surgery, Ha Dong General Hospital, 6 Department of Forensic Medicine, Faculty of Medicine, Hanoi Medical University, Hanoi, Vietnam
DOI: 10.4328/ACAM.22843 Received: 2025-08-04 Accepted: 2025-09-05 Published Online: 2025-09-19 Printed: 2025-10-01 Ann Clin Anal Med 2025;16(10):736-740
Corresponding Author: Nguyen Huu Thanh, Department of Surgery, Faculty of Medicine, Hanoi Medical University, Hanoi, Vietnam. E-mail: drthanh121982@gmail.com P: +84 963 221 283 Corresponding Author ORCID ID: https://orcid.org/0009-0005-6682-1172
Other Authors ORCID ID: Nguyen Minh Tuan, https://orcid.org/0009-0009-6258-8237 . Hoang Long, https://orcid.org/0000-0002-1714-8074 . Dinh Anh Duc, https://orcid.org/0009-0003-7038-4847 . Dong Ngoc Minh, https://orcid.org/0009-0004-3695-7354 . Ngo Xuan Cuong, https://orcid.org/0009-0002-6625-3070 . Nguyen Truong Giang, https://orcid.org/0009-0009-3845-4925 . Tran Quoc Khanh, https://orcid.org/0009-0008-4135-4709 . Nguyen Tuan Anh, https://orcid.org/0009-0002-3303-1930 . Nguyen Thanh Vinh https://orcid.org/0009-0000-7257-3594
This study was approved by the Ethics Committee of Institutional Review Board of Hanoi Medical University (Date: 2023-07-13, No: 876/GCN-HĐĐĐNCYSH-ĐHYHN)
Aim: This study aimed to evaluate the safety and efficacy of digital flexible ureteroscopy in the management of lower pole stones and to assess patients’ postoperative quality of life.
Materials and Methods: A longitudinal, single-center, nonrandomized cohort study was conducted on patients with renal calculi eligible for flexible ureteroscopy. The study population comprised 44 patients diagnosed with treatment of lower pole stones who underwent treatment at Bach Mai Hospital between January 2023 and October 2024. Surgical outcomes, including surgery duration, stone-free rate, duration of hospitalization, surgical complications, and quality of life, were evaluated and monitored during the follow-up period.
Results: The mean age of the patients was 51.4 years, and the mean stone size was 13.7 mm. Immediately postoperative stone-free rates were 79.5 %, 77.3 % at 1-month, and 68.2 % at 3-month. The mean operative time was 73.4 minutes, the lithotripsy duration was 55.7 minutes, and the average hospital stay was 5.7 days. Only 1 minor complication (2.3%) was recorded. The quality-of-life scores significantly improved over time (p < 0.001), with most patients reporting no disruption to daily activities after 1 month.
Discussion: Single-use digital flexible ureteroscopy is a safe and effective modality for managing lower-pole renal stones, offering high stone-free rates, low complication rates, and significant improvements in patient quality of life. Further large-scale, controlled studies are needed to confirm these findings and evaluate long-term outcomes.
Keywords: digital flexible ureteroscopy, renal stones, stone-free rate, lower pole stones, quality of life
Introduction
Renal calculi represent one of the most prevalent urological conditions. Globally, the prevalence is notably high, with reported rates ranging from 7 to 13% in North America, 5–9% in Europe, and approximately 1–5% in Asia [1]. The prevalence of urinary stones in Vietnam ranges from 2% to 12%, and approximately 40% of cases are renal calculi [2]. This elevated incidence is potentially associated with dehydration due to high ambient temperatures during the summer months, resulting in reduced urine output [3]. With the ongoing rise in global temperatures attributable to climate change, projections suggest that the number of individuals affected by urinary stones could increase from 1.6 to 2.2 million by the year 2050 [4]. If renal calculi are not appropriately managed, the patient may experience severe complications, including pyelonephritis, interstitial nephritis, hydronephrosis, pyonephrosis, anuria, oliguria, and both acute and chronic renal failure [5].
Currently, a variety of treatment modalities for upper urinary tract stones are being implemented in Vietnam and all over the globe. The adoption of flexible endoscopes has gained momentum because of their demonstrated efficacy and safety profiles [6]. In recent decades, there have been substantial advancements in both the technology and clinical application of minimally invasive procedures within the field of urology. Flexible ureteroscopy has evolved to become a widely used diagnostic and therapeutic tool for many upper urinary tract pathologies. The most common indication for ureteroscopy is treatment of upper urinary tract stones with the aid of holmium, mainly Yttrium Aluminum Garnet (YAG) laser lithotripsy. This technique is recognized for its high efficacy and favorable safety profile, with relatively few complications. However, the effectiveness of lithotripsy for lower pole stones remains suboptimal due to the anatomical constraints of the lower calyx. Several studies have indicated that the infundibulopelvic angle (IPA) plays a critical role in determining the success of flexible ureteroscopy (FURS) combined with holmium laser lithotripsy [7]. A systematic review of the literature reported that an acute IPA (<30°) is significantly associated with lower success rates, particularly when accompanied by prolonged operative time or larger stone size. In contrast, factors such as the use of a ureteral access sheath, infundibular width (IW), and infundibular length (IL) were not found to significantly impact treatment outcomes [8]. Ongoing innovations in flexible ureteroscopic technology have further expanded its clinical utility, positioning it as a first-line treatment option in the management of urolithiasis [9]. In addition, the use of flexible endoscopes may alleviate hand fatigue experienced by surgeons during prolonged procedures, as it eliminates the need for continuous manual deflection control, which is beneficial when managing calculi located in the lower pole calyx [11]. To address these limitations, flexible endoscopes have been developed as an alternative to conventional reusable models. Numerous studies have demonstrated their high efficacy in the treatment of urolithiasis [10,12,13].
In many regions, including Vietnam, the management of renal calculi remains suboptimal due to limited access to advanced endourological techniques, delayed diagnosis, and inconsistent follow-up. However, to date, there has been no comprehensive and systematic investigation specifically addressing the use of digital flexible ureteroscopy for the treatment of urinary stones, particularly lower pole stones, and post-treatment patient monitoring. Accordingly, the present study aims to evaluate the safety and efficacy of digital flexible ureteroscopy in the management of renal calculi with lower pole stones and to assess patients’ postoperative quality of life.
Materials and Methods
Study participants
This study was designed as a single-center, non-randomized study. The study population comprised 44 patients diagnosed with lower pole renal calculi who underwent treatment at Bach Mai Hospital between January 2023 and October 2024.
We defined patients with lower pole renal calculi as those with stones located in calyces arising from the lower third of the renal collecting system, as determined by preoperative imaging (non-contrast CT or ultrasound). The exclusion criteria were urinary tract obstructions (e.g., urethral or ureteral strictures, ureteropelvic junction obstruction, Grade 4 hydronephrosis), non-functioning kidneys, pregnancy, age under 16, congenital renal anomalies (e.g., duplex or horseshoe kidney), and significant spinal deformities.
A total of 240 patients underwent endoscopic treatment for urolithiasis at the Nephrology Department of Bach Mai Hospital between 2023 and 2024; we excluded 23 subjects who declined to participate in the study. We also excluded 43 patients who were lost in the follow-up period, and 30 patients were removed because their stones were not located in the lower pole of the kidney. Data for 44 subjects were analyzed in this study (Figure 1).
Clinical characteristics
The following clinical variables were recorded at the time of patient evaluation: age, sex, body mass index (BMI), prior history of treatment on the affected kidney, and reason for hospital admission. Comorbid conditions, including hypertension, diabetes mellitus, or other endocrine disorders, were also documented. BMI is calculated as weight in kilograms divided by the square of the height in meters (kg/m²) and is categorized into four groups according to the Asian-Pacific cutoff points [14].
Ultrasound assessment
All patients underwent renal ultrasonography to assess stone size, location, and the degree of hydronephrosis. Stone size was measured by maximum length, and the location was classified as upper, middle, or lower calyx.
Technical procedure
All procedures were performed under general anesthesia with the patient in the lithotomy position, consistent with conventional retrograde ureteroscopy. A C-arm fluoroscopy unit was positioned to allow for continuous imaging from the bladder to the renal pelvis. A 6 Fr JJ stent (Marflow, Switzerland) was placed 7–14 days before facilitating passive ureteral dilation. In the absence of prior stenting, ureteral dilation was achieved intraoperatively using a semi-rigid ureteroscope, followed by JJ stent placement.
A cystoscope was introduced to retrieve the distal end of the JJ stent, and a guidewire was advanced through the stent into the renal pelvis under C-arm guidance. For cases involving ureteral, renal pelvic, or upper calyceal stones, a semi-rigid ureteroscope was advanced along the guidewire for initial lithotripsy; subsequently, it was withdrawn, leaving the guidewire in place. A 12–14 Fr ureteral access sheath (Navigator HD™, Boston Scientific, USA) was then introduced over the guidewire into the renal pelvis under C-arm control. Afterwards, the guidewire and obturator were removed. A single-use digital flexible ureteroscope (Uscope UE3022™, Pusen Medical Technology Co., Zhuhai, China) was inserted through the sheath to access the collecting system, guided by both direct vision and fluoroscopy, with continuous irrigation using normal saline. The ureteroscope had an outer shaft diameter of 9.2 Fr, a lens tip diameter of 9.5 Fr (ø2.8 mm), a 3.6 Fr working channel, 270° dual deflection, and a working length of 650 mm.
This single-use flexible ureteroscope was inserted through the sheath to access the collecting system, guided by both direct vision and fluoroscopy, with continuous irrigation using normal saline. When the ureter was adequately dilated, the flexible ureteroscope could be introduced directly over the guidewire. Stones were identified, measured, and repositioned if necessary—particularly from the lower to the upper calyx or renal pelvis—to minimize scope deflection. Lithotripsy was performed using a 230 µm holmium, for which a YAG laser fiber was introduced through the ureteroscope’s working channel via a protective sheath. Stone clearance was assessed intraoperatively using both direct endoscopic visualization and fluoroscopy. Patients were considered stone-free if no residual fragments >4 mm were detected. Small residual fragments (≤4 mm) were measured based on their largest diameter and included in postoperative stone size calculations, which explains the occasional median values slightly above 4 mm despite meeting stone-free criteria. A JJ stent was placed at the end of the procedure to ensure adequate drainage.
Treatment outcomes
-Postoperative assessment and follow-up
The procedure was considered successful when only fine gravel or stone fragments measuring ≤4 mm remained in situ or when no residual stones were visualized on intraoperative C-arm fluoroscopy [15]. Stone-free status was assessed at 1 month and 3 months postoperatively using either plain abdominal radiography or renal ultrasonography. Patients were considered stone-free if no radiopaque shadows were detected at the site of the preoperative renal stone (in cases of radiopaque stones) or if any residual stone fragment or cluster had a maximal diameter of ≤4 mm.
-Complication assessment
Complications were recorded throughout the perioperative and follow-up periods. All were classified according to the Clavien–Dindo classification system, a standardized surgical complication grading system revised in 2004 by Dindo and Clavien based on their earlier 1994 proposal [16].
-Quality of life assessment
The EQ-5D-5L instrument was used to assess quality of life at admission, immediately after surgery, and postoperatively (1-month and 3-month follow-up). The EQ-5D-5L instrument comprises a descriptive system and a visual analog scale [17].
Statistical Analysis
The basic characteristics of the participants are shown according total number of patients. Continuous variables were reported as means ± standard deviation (SD), and comparisons of mean values were made using Student’s t-test. Categorical variables were expressed as numbers (percentages, %), and comparisons of proportions were made using the chi-square test. A paired t-test was used to compare the mean values, and McNemar’s test was used to compare proportions and calculate the p-values with variables that had 2-time follow-ups. Repeated measurement analysis was used to compare the mean and calculated p-values with variables from 3-time follow-ups. Statistical analyses were performed using SPSS (IBM Corporation, US) version 29.0 for Mac. All statistical tests were based on two-sided probabilities, and a p-value <0.05 is considered significant.
Ethical Approval
This study was approved by the Ethics Committee of the Institutional Review Board of Hanoi Medical University (Date: 2023-07-13, No: 876/GCN-HĐĐĐNCYSH-ĐHYHN).
Results
Patient characteristics
The characteristics of the study population are presented in Table 1. The mean age of the participants was 51.4 years. The overall mean body mass index (BMI) was 22.4 kg/m². The median stone size was 13.7 mm. The number of stones detected did not differ significantly between the sexes. Preoperative hematuria was reported in four patients (9.1%). A history of hypertension and diabetes was recorded in seven and five patients, respectively.
Surgical and follow-up outcomes
The surgical outcomes are presented in Table 2. The mean operative time was 73.4 minutes. The average lithotripsy time was 55.7 minutes. The mean postoperative hospital duration was 6.2 days. The overall stone-free rate immediately after surgery was 79.5%. There was one recorded intraoperative complication (2.3%).
The median size of the largest stone decreased over time, being 4.5 ± 0.7 mm immediately after surgery, 2.2 ± 0.6 mm at the 1-month follow-up mark, and 1.1 ± 0.4 mm at the 3-month follow-up mark (p < 0.001). The stone-free rate improved from 77.3% at 1 month to 68.2 % at 3 months (p = 0.289). Additionally, the mean post-operative quality of life score increased significantly over the follow-up period (p < 0.001), with most patients reporting no disruption to daily activities after 1 month.
Discussion
The findings of this study demonstrate that single-use flexible ureteroscopy is a highly effective modality for the management of lower-pole stones. This minimally invasive approach not only achieves a high rate of stone clearance but also contributes to significant improvements in patients’ postoperative quality of life. These results support the growing role of flexible ureteroscopy as a safe and efficient method in the treatment of lower-pole stones.
The average lithotripsy time was 55.6 ± 27.4 minutes. The lithotripsy time in our study was similar to that reported in some other studies [13]. A study by José A. Salvadó et al. (2018) reported an average lithotripsy time of 56.6 ± 38.0 minutes [18]. Another study, conducted by Qiang Jing et al. (2024), reported an average lithotripsy time of 51.27 ± 13.8 minutes [19]. Qinghua He et al. (2024) recorded a longer lithotripsy time, averaging about 72.4 ± 14.4 minutes [20]. These differences in lithotripsy time may be due to the complexity of the stones or the difficulty of performing the procedure in each study.
In our study, the average hospital stay was 5.7 days (Table 2). This is comparable to findings from other studies utilizing minimally invasive techniques. Huayu Gao et al. (2019) reported a mean hospital stay of 4.33 ± 1.55 days following digital endoscopic lithotripsy, while Qinghua He et al. (2024) observed a duration of approximately 3.9 ± 1.2 days. When comparing different minimally invasive approaches, both Gao and He noted that the hospital stay after digital endoscopic stone removal was shorter than that observed after percutaneous nephrolithotomy (PCNL) [20,21]. Although flexible ureteroscopy is associated with short hospital stays in many international settings, the mean postoperative hospitalization duration in our study was influenced by local clinical protocols, which favor extended inpatient observation even in the absence of complications. This practice may differ from global trends prioritizing early discharge.
In the present study, the overall postoperative stone-free rate (SFR) was 79.2% (Table 2). These findings are consistent with those reported in the international literature. El-Nahas et al. reported an SFR of 86.5% following flexible ureteroscopy (f-URS) for the treatment of 10–20 mm lower pole stones [22]. Similarly, Gao et al. (2019) reported a postoperative SFR of 78.2% at three days in a cohort of 100 patients treated with digital endoscopic lithotripsy [20]. The overall postoperative stone-free rate (SFR) was 70.5% after 3 months of follow-up. He et al. (2024) also recorded a 3-month stone-free rate of 71.5% [21].
In our study, only one minor complication (surgical fever) was recorded during the follow-up period, further supporting the idea of the procedure being minimally invasive in nature. In comparison, other studies have reported slightly higher complication rates. For example, José A. Salva et al. (2018) noted two complications following f-URS: surgical fever and hematuria [18]. In a study by Huayu Gao et al. (2019), complications included fever in 23.6% of cases, abdominal pain in 7.3% of cases, and urinary tract infection in 3.6% of cases [21]. Additionally, in their study, Fankhauser et al. (2021) reported that Clavien–Dindo Grade 2 complications occurred in approximately 5% of patients undergoing ureteroscopy [23]. These differences may reflect differences in patient populations, surgical techniques, or perioperative management protocols. Complications were minimal in this study, further supporting the favorable safety profile of digital flexible ureteroscopy.
To our knowledge, there are relatively few studies that comprehensively assess patients’ quality of life following laparoscopic lithotripsy. One such study reported significantly greater improvements in quality-of-life scores with digital flexible ureteroscopy compared to minimally invasive percutaneous nephrolithotomy [23]. In the present study, we assessed the patient-reported quality of life four times: preoperatively, immediately postoperatively, and at 1 and 3 months postoperatively. The results revealed a consistent improvement in quality-of-life scores over time, with most patients reporting minimal disruption to daily activities by the 1-month follow-up.
Limitations
Several limitations should be acknowledged. The non-randomized, single-center study design limits the ability to establish causality or control for confounding factors. Additionally, the relatively small sample size may reduce the generalizability of the findings. Finally, the analysis did not fully address risk factors associated with postoperative complications, indicating the need for further investigation to improve clinical outcomes and guide patient selection. Future studies should consider employing randomized controlled trial designs and involving multiple centers to enhance the external validity and robustness of findings.
Conclusion
The findings of this study indicate that flexible ureteroscopy is a promising and effective modality for the management of lower-pole renal stones, demonstrating a high stone-free rate and notable improvements in patient-reported quality of life. Future studies should include larger sample sizes, comparative evidence-based study designs, and longer follow-up periods to generate more robust and generalizable conclusions that could inform clinical practice.
Scientific Responsibility Statement
The authors declare that they are responsible for the article’s scientific content including study design, data collection, analysis and interpretation, writing, some of the main line, or all of the preparation and scientific review of the contents and approval of the final version of the article.
Animal and Human Rights Statement
All procedures performed in this study were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.
Funding: None
Conflict of Interest
The authors declare that there is no conflict of interest.
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Nguyen Huu Thanh, Nguyen Minh Tuan, Hoang Long, Dinh Anh Duc, Dong Ngoc Minh, Ngo Xuan Cuong, Nguyen Truong Giang, Tran Quoc Khanh, Nguyen Tuan Anh, Nguyen Thanh Vinh. Clinical efficacy of digital flexible ureteroscopy for renal stone management and postoperative quality of life for the treatment of lower pole stones: A single-center, non-randomized study. Ann Clin Anal Med 2025;16(10):736-740
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Metabolic syndrome’s echo on the obese heart: A closer look at diastolic function and myocardial performance index
Murat Özmen 1, Faik Özel 2, Ramazan Aslan 3, Erhan Arıkan 4, İsa Ardahanlı 5
1 Department of Cardiology, Erzurum City Hospital, Erzurum, 2 Department of Internal Medicine, School of Medicine, Seyh Edebali University, Bilecik, 3 Department of Cardiology, Bilecik Training and Research Hospital, Bilecik, 4 Department of Emergency Medicine, School of Medicine, Seyh Edebali University, Bilecik, 5 Department of Cardiology, School of Medicine, Bilecik Seyh Edebali University, Bilecik, Türkiye
DOI: 10.4328/ACAM.22846 Received: 2025-08-06 Accepted: 2025-09-29 Published Online: 2025-09-30 Printed: 2025-10-01 Ann Clin Anal Med 2025;16(10):741-746
Corresponding Author: Murat Özmen, Department of Cardiology, Erzurum City Hospital, Erzurum, Türkiye. E-mail: drmuratt1987@gmail.com P: +90 554 176 72 20 Corresponding Author ORCID ID: https://orcid.org/0000-0002-6237-1398
Other Authors ORCID ID: Faik Özel, https://orcid.org/0000-0002-2429-5355 . Ramazan Aslan, https://orcid.org/0000-0002-1255-7880 . Erhan Arıkan, https://orcid.org/0000-0002-4800-3206 . İsa Ardahanlı, https://orcid.org/0000-0002-9309-803X
This study was approved by the Ethics Committee of Bilecik Şeyh Edebali University, Faculty of Medicine (Date: 2024-10-02, No: 4)
Aim: This study investigated the effect of the presence or absence of metabolic syndrome (MetS) on cardiac structure and function in obese individuals.
Materials and Methods: A retrospective, cross-sectional, and observational study design was used. 125 patients diagnosed with obesity were included in the study and divided into two groups according to the presence of MetS. Demographic, clinical, and echocardiographic data of the patients were analyzed.
Results: No significant difference was found in diastolic functions and myocardial performance index (MPI) between obese individuals with and without MetS. However, a trend was observed in these parameters compared to the normal population in both groups. Systolic blood pressure, triglyceride, LDL-cholesterol, and total cholesterol levels were significantly higher in the MetS group than in the non-MetS group.
Discussion: Obesity may have adverse effects on cardiac structure and function, regardless of the presence of MetS. Therefore, echocardiography is an important tool for the assessment and management of cardiovascular risks in obese individuals, even if they do not develop MetS. Targeted strategies such as lifestyle changes, pharmacological treatments, and regular cardiac monitoring should be developed to protect and improve the cardiovascular health of patients with obesity and MetS.
Keywords: obesity, metabolic syndrome, diastolic dysfunction, myocardial performance index
Introduction
Obesity and metabolic syndrome (MetS) are two of the most significant public health challenges, with increasing global prevalence and well-documented associations with cardiovascular (CV) diseases [1]. Obesity is a multifactorial condition characterized by excessive body weight, systemic inflammation, oxidative stress, and metabolic disturbances, whereas MetS represents a cluster of CV risk factors, including central obesity, insulin resistance, dyslipidemia, and hypertension [2]. The combined effects of these conditions promote adverse structural and functional changes in the myocardium, leading to a markedly increased risk of CV morbidity and mortality [3]. Given this burden, early and accurate assessment of myocardial function is essential for effective prevention and management strategies. While numerous studies have shown that both obesity and MetS impair myocardial function [4], direct comparisons between individuals with obesity alone and those with both obesity and MetS remain scarce, particularly regarding early markers of dysfunction.
Echocardiography is a non-invasive and widely available modality for assessing myocardial performance. The myocardial performance index (MPI) is a simple, reproducible echocardiographic parameter that integrates systolic and diastolic function [5] and has proven valuable in identifying subclinical myocardial impairment [6]. This study aims to compare MPI values between obese patients with and without MetS, providing deeper insight into the additive effects of MetS on myocardial function and reinforcing the utility of MPI in CV risk stratification and management in this high-risk group.
Materials and Methods
This retrospective, cross-sectional, single-center observational cohort study aims to quantitatively evaluate the synergistic effects of obesity and metabolic MetS comorbidity on left ventricular diastolic dysfunction (LVDD) and myocardial performance MPI. The STROBE (Strengthening the Reporting of Observational Studies in Epidemiology) guidelines design the study protocol, and data collection and analysis processes were conducted per the principles of Good Clinical Practice [7].
The study population consisted of adults aged 18-75 years who were followed up at the Cardiology and Endocrinology Clinic of Bilecik Education and Research Hospital between 01.01.2022-31.12.2024, diagnosed with obesity with a BMI ≥30 kg/m² according to the TEMD (Turkish Society of Endocrinology and Metabolism) criteria [8] and underwent echocardiographic examination. The patients’ demographic, medical history, anthropometric, and laboratory data were extracted from the hospital data system by a double-blind method (2 independent researchers). Inclusion criteria included a complete echocardiographic data set (LVEF, E/A ratio, MPI), lipid profile, fasting glucose measurement in the last 3 months, and the recording of anthropometric measurements by WHO standards. Patients will be divided into two groups according to the presence of metabolic syndrome according to NCEP-ATP III criteria: (1) Obese Patients with Metabolic Syndrome and (2) Obese Patients Without Metabolic Syndrome. Metabolic syndrome will be diagnosed by the presence of at least three of the following NCEP-ATP III criteria [9].
Metabolic syndrome criteria:
• Abdominal Obesity (Waist circumference); Male ≥94 cm, female ≥80 cm
• Hypertriglyceridemia ≥150 mg/dL
• HDL-Cholesterol Male <40 mg/dL, female <50 mg/dL
• Blood Pressure Systolic ≥130 mmHg or diastolic ≥85 mmHg
• Fasting Glucose ≥100 mg/dL
Exclusion criteria:
• Known cardiovascular disease history (Angiographically confirmed CAD (≥50% stenosis), NYHA Class II-IV heart failure
• Moderate-severe valvular heart disease
• Renal Dysfunction (eGFR <60 mL/min/1.73m² according to CKD-EPI formula)
• Liver Disease (Child-Pugh Score ≥B8 or ALT >3xULN)
• Active infection or inflammatory disease
• During pregnancy or lactation
• Thyroid dysfunction
Echocardiographic protocol
All examinations were performed using the Philips EPIQ CVx device and the X5-1 matrix probe in accordance with the ASE (American Society of Echocardiography) guidelines [10].
E and A waves will be measured from mitral inflow using pulsed-wave Doppler, and the E/A ratio will be calculated to evaluate left ventricular diastolic function. In addition, E’ wave velocities measured from septal and lateral regions of the mitral annulus using tissue Doppler imaging (TDI) and E/e’ ratio were evaluated. Myocardial performance index (MPI) measurement was calculated according to the IVCT+IVRT/ET formula using isovolumetric contraction time (IVCT), isovolumetric relaxation time (IVRT), and ejection time (ET). (Figure 1). Each parameter was measured in 3 consecutive cardiac cycles, and their averages were taken. Images were archived in DICOM format and analyzed unthinkingly by two cardiologists with expert-level echocardiography certificates. In echocardiographic measurements, interobserver ICC was 0.92 (95% CI 0.88-0.95). Data extraction error rate was <0.5% (6 sigma quality control).
Statistical Analysis
To determine the statistical significance of quantitative differences between experimental groups, a two-tailed unpaired t-test and one-way ANOVA with Tukey’s multiple comparison test (95% confidence level) were conducted using GraphPad 8.1 software (GraphPad Software, San Diego, California). On the other hand, parts of whole analyses were used to illuminate the relationships between categorical variables in qualitative data. Descriptive and fraction of total statistics were applied to reveal the basic characteristics of the obtained data (mean, standard deviation, median, percentage, etc.). The significance level was always set at a 95% confidence interval, denoted as * p≤0.05, ** p≤0.01, *** p≤0.001, **** p≤0.0001. Non-significant p-values are presented without any asterisks. The results are presented as mean ± standard deviation (SD).
Ethical Approval
This study was approved by the Bilecik Şeyh Edebali University, Faculty of Medicine Ethics Committee (Date: 2024-10-02, No: 4).
Results
Participant demographics and clinical features
The study included 125 obese patients (74 females, 51 males): 73 (58.4%) had MetS and 52 (41.6%) did not. Mean age was similar between groups (MetS: 56.7 ± 9.2 vs. non-MetS: 54.9 ± 9.8 years, p=0.288). The female prevalence was higher in the MetS group (p < 0.05). Anthropometric measures showed no significant differences: BMI (31.5 ± 1.4 vs. 31.7 ± 2.5 kg/m², p = 0.566) and waist circumference (102.8 ± 14.2 vs. 104.0 ± 16.1 cm, p = 0.664). Cardiometabolic parameters revealed higher systolic BP (137.5 ± 62.1 vs. 125.9 ± 32.6 mmHg, p=0.005) and triglycerides (185.1 ± 64.0 vs. 135.3 ± 26.2 mg/dL, p<0.001) in the MetS group. Diastolic BP was borderline significant (84.5 ± 10.3 vs. 80.7 ± 11.7 mmHg, p=0.055). LDL (137.5 ± 62.1 vs. 111.0 ± 48.8 mg/dL, p = 0.012) and total cholesterol (218.4 ± 58.3 vs. 183.5 ± 49.0 mg/dL, p = 0.001) levels were significantly higher in patients with MetS. Fasting glucose (132.5 ± 26.7 vs. 125.9 ± 32.6 mg/dL, p=0.219) and HDL (43.9 ± 8.7 vs. 45.2 ± 4.8 mg/dL, p=0.315) showed no significant difference.
Echocardiographic findings
Diastolic function parameters showed no statistically significant differences between the groups. Mitral E velocity was slightly lower in the MetS group compared to the non-MetS group (64.4 ± 12.8 vs. 67.5 ± 10.4 cm/s, p=0.156), while mitral A velocity was similar (74.5 ± 18.5 vs. 73.7 ± 9.5 cm/s, p=0.792). Lateral mitral annulus early diastolic velocity (Em) measured by tissue Doppler imaging was lower in the MetS group (13.2 ± 2.5 vs. 14.2 ± 2.1 cm/s), though this difference did not reach significance (p=0.254). Diastolic indices, such as the E/A ratio (0.89 ± 0.21 vs. 0.92 ± 0.15, p = 0.459) and E/Em ratio (5.11 ± 1.68 vs. 4.90 ± 1.24, p = 0.454), were comparable between groups. Systolic time intervals, including isovolumetric contraction time (IVCT: 60.5 ± 12.9 vs. 62.2 ± 12.8 ms, p=0.476), isovolumetric relaxation time (IVRT: 99.0 ± 19.3 vs. 97.2 ± 16.5 ms, p=0.589), and ejection time (ET: 279.4 ± 40.2 vs. 281.4 ± 31.0 ms, p=0.758), also showed no significant differences. Both groups had similar MPI values (0.58 ± 0.11 vs. 0.57 ± 0.10, p=0.694). Full details of group-wise echocardiographic parameters are summarized in Table 1.
Correlation analysis revealed a positive association of MPI with systolic blood pressure (r=0.28, p=0.006), triglycerides (r=0.33, p<0.001), and fasting glucose (r=0.21, p=0.022). HDL levels positively correlated with E/A ratio (r=0.25, p=0.008), while no other significant correlations were found (Table 2). A gender-based analysis revealed a higher BMI in obese women with MetS compared to women without MetS (32.23 ± 2.83 vs. 31.54 ± 1.67 kg/m², p = 0.022). Total cholesterol (p=0.007) and triglycerides (p<0.001) were significantly elevated in both men and women with MetS versus controls. In women, systolic BP (138.2 ± 10.2 vs. 127.0 ± 14.6 mmHg, p=0.004) and fasting glucose (133.4 ± 27.5 vs. 115.1 ± 29.5 mg/dL, p=0.031) were significantly higher in the MetS group, while no such differences were observed in men. No significant differences were found between genders in echocardiographic parameters, inflammatory markers, or diastolic indices (p>0.05). Full gender-based distributions are presented in Table 3. Figure 2 and Figure 3 show the comparison of demographic, anthropometric, and echocardiographic measurements between the groups.
Discussion
The main finding of this study is that obesity is associated with early cardiac dysfunction, independent of the presence of metabolic syndrome (MetS). Our findings demonstrate that obesity itself contributes to adverse structural and functional cardiac changes, supporting its recognition as an independent cardiovascular (CV) risk marker. These results emphasize the importance of evaluating obesity’s direct effects on cardiac morbidity, apart from metabolic comorbidities. Even in obese individuals without MetS, a trend toward impaired diastolic function, reflected by reduced E/A ratio, decreased E/Em, and elevated myocardial performance index (MPI), was observed. These findings align with emerging evidence that “metabolically healthy obesity” is not truly benign, as subclinical myocardial changes may occur early in disease progression. A large-scale cohort study by Rozenbaum et al. (2019) similarly reported increased diastolic dysfunction risk in metabolically healthy obese individuals compared to normal-weight controls [11].
The lack of statistically significant differences in diastolic parameters between obese groups with and without MetS in our study suggests that obesity-related myocardial alterations may develop independently of the synergistic burden of MetS. One explanation is that visceral adipose tissue (VAT) promotes systemic inflammation and lipotoxicity, leading to diastolic dysfunction [12]. Proinflammatory cytokines such as IL-6 and TNF-α, as well as adipokines like leptin, are known to impair endothelial function, promote fibrosis, and induce myocyte hypertrophy [13]. A recent study demonstrated a direct, MetS-independent association between VAT volume and left ventricular diastolic dysfunction [14]. Additionally, free fatty acids (FFA), key mediators of myocardial lipotoxicity, contribute to oxidative stress and impaired calcium ATPase pump activity, delaying calcium reuptake and diastolic relaxation [15]. These mechanisms are consistent with the prolonged isovolumetric relaxation time (IVRT) and reduced diastolic filling observed in both obese groups in this study.
The strong correlations between MPI and factors such as systolic blood pressure (SBP), triglycerides, and fasting glucose further underscore the interplay between hemodynamic and metabolic stress in myocardial remodeling. Increased left ventricular ejection fraction (LVEF), often observed in obesity, may initially reflect compensatory adaptation but is associated with elevated wall stress and fibrosis, as reported in earlier studies linking increased LVEF to higher MPI [16]. Hypertriglyceridemia, another hallmark of obesity, has been shown to disrupt myocardial energy metabolism through VLDL accumulation, resulting in lipotoxic damage and diastolic dysfunction [17]. Our results support these findings, showing a strong association between triglyceride levels and MPI.
Gender-specific analysis in this study revealed that obese women with MetS exhibited more pronounced increases in BMI, SBP, and fasting glucose compared to men, reflecting gender-related pathophysiological differences. Estrogen decline in postmenopausal women exacerbates visceral fat deposition, insulin resistance, and myocardial fibrosis [18]. Moreover, leptin resistance, more common in women, may heighten sympathetic nervous system activation, increasing hypertension risk and myocardial ischemia [19,20]. These results emphasize the need for sex-specific approaches to CV risk stratification and treatment [21].
Overall, our findings highlight the clinical relevance of echocardiographic screening in obese patients, regardless of MetS status. Subclinical changes in MPI and diastolic function parameters can serve as early warning signs of cardiac dysfunction and may help guide preventive interventions [22]. Identifying early myocardial impairment in obesity could lead to timely lifestyle modification, medical management, and closer follow-up, potentially mitigating long-term cardiovascular complications.
Limitations
The limitations of this study include its retrospective, single-center design and the lack of measurements such as epicardial adipose tissue (EAT) thickness. Although causality cannot be established, the findings remain clinically relevant. A recent study identified EAT thickness ≥7 mm as an independent predictor of diastolic dysfunction [23], highlighting the value of incorporating this parameter in future research. Additionally, the homogeneity and regional selection of the study population limit generalizability, but also guide future work. Prospective studies and multi-omics approaches may better define the causal pathways linking obesity to cardiac dysfunction.
Conclusion
In conclusion, this study shows that obesity has a central role in cardiovascular risk assessment and may trigger myocardial dysfunction independently of MS. Early detection of subclinical findings has the potential to reduce cardiac morbidity through lifestyle interventions (diet, exercise) and targeted pharmacological treatments. Clinicians should consider routine echocardiographic evaluation in obese individuals and develop personalized treatment strategies. Furthermore, recognizing obesity as a disease and managing it with multidisciplinary approaches may improve cardiovascular survival.
Scientific Responsibility Statement
The authors declare that they are responsible for the article’s scientific content including study design, data collection, analysis and interpretation, writing, some of the main line, or all of the preparation and scientific review of the contents and approval of the final version of the article.
Animal and Human Rights Statement
All procedures performed in this study were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.
Funding: None
Conflict of Interest
The authors declare that there is no conflict of interest.
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Murat Özmen, Faik Özel, Ramazan Aslan, Erhan Arıkan, İsa Ardahanlı. Metabolic syndrome’s echo on the obese heart: A closer look at diastolic function and myocardial performance index. Ann Clin Anal Med 2025;16(10):741-746
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Can Dyslipidemia be a significant factor in myofascial pain syndrome?
Nilüfer Aygün Bilecik 1, Serpil Demir 2, Yunus Çoşkun 3, Sıdıka Büyükvural Şen 1, Meryem Kösehasanoğulları 1
1 Department of Physical Therapy and Rehabilitation, Faculty of Medicine, Adana City Hospital, Adana, 2 Department of Physical Therapy and Rehabilitation, Faculty of Medicine, Akdeniz University, Antalya, 3 Department of Internal Medicine, Faculty of Medicine, Adana City Hospital, Adana,Turkey
DOI: 10.4328/ACAM.22857 Received: 2025-08-19 Accepted: 2025-09-22 Published Online: 2025-09-30 Printed: 2025-10-01 Ann Clin Anal Med 2025;16(10):747-751
Corresponding Author: Nilüfer Aygün Bilecik, Department of Physical Therapy and Rehabilitation, Faculty of Medicine, Adana City Hospital, Adana, Turkey. E-mail: drnilaygun@gmail.com P: +90 505 740 27 52 Corresponding Author ORCID ID: https://orcid.org/0000-0002-5113-2287
Other Authors ORCID ID: Serpil Demir, https://orcid.org/0000-0001-8717-1141 . Yunus Çoşkun, https://orcid.org/0000-0002-4580-2678 . Sıdıka Büyükvural Şen, https://orcid.org/0000-0003-1084-4226 . Meryem Kösehasanoğulları, https://orcid.org/0000-0001-5893-0823
This study was approved by the Ethics Committee of Adana City Training and Research Hospital (Date: 2024-10-10, No: 173)
Aim: To investigate the presence of myofascial pain syndrome (MPS) in patients whose lipid profiles were assessed and to examine the relationship of lipid levels with pain and muscle spasm.
Materials and Methods: In this study, 197 patients whose lipid profiles were evaluated were assessed for the presence of characteristic trigger points in the neck, back, and shoulder muscles, referred pain in a reference zone, and the state of muscle spasm.
Results: The groups were classified as dyslipidemic and healthy based on their lipid levels. The prevalence of MPS in the dyslipidemic group was found to be significantly higher compared to the group with normal lipid levels.
Discussion: A strong association was identified between dyslipidemia and MPS, and individuals with dyslipidemia were found to have a higher likelihood of developing MPS.
Keywords: myofascial pain syndrome, pain, dyslipidemia, lipid
Introduction
Myofascial pain syndrome (MPS) is a disorder characterized by the presence of palpable, tender, and active myofascial trigger points in the skeletal muscles [1]. The etiology of the disease is not fully understood; however, factors such as trauma, excessive muscle strain, fatigue, stress, and structural and genetic abnormalities have been implicated [2]. These trigger points are characteristically painful upon pressure and cause referred pain [3]. Taut bands on palpation, local twitch responses, localized tingling sensations, jump signs, and referred pain are the most commonly observed findings in MPS [4]. The prevalence of MPS in individuals aged 30–60 years has been reported as 37% in men and 65% in women [5].
In recent years, it has been proposed that the pathophysiology of MPS may not be limited to the musculoskeletal system alone and that systemic factors may also play a role. Furthermore, local biochemical microscopic analyses conducted on active myofascial trigger points have shown elevated levels of inflammatory mediators, neuropeptides, catecholamines, and pro-inflammatory cytokines compared to asymptomatic muscle tissue [6]. In this context, there is growing research into the effects of lipid levels on MPS [7]. Dyslipidemia is a clinical condition characterized by one or more abnormalities (either elevations or reductions) in total cholesterol, low-density lipoprotein (LDL), high-density lipoprotein (HDL), or triglyceride (TG) levels. It may have both genetic and environmental origins [8]. According to the guidelines for the diagnosis and treatment of dyslipidemia, screening should include total cholesterol, TG, HDL cholesterol (HDL-c), LDL cholesterol (LDL-c), and non-HDL cholesterol. The Turkish Endocrinology and Metabolism Society defines the following as optimal values: TG < 150 mg/dL, total cholesterol < 200 mg/dL, LDL < 70 mg/dl, and HDL > 60 mg/dL [9].
In the literature, some studies have reported a potential association between musculoskeletal symptoms and hyperlipidemia [10-12]. These studies have emphasized that elevated lipoprotein and lipid levels in symptoms such as oligoarthritis, Achilles tendinitis, arthralgia in various joints, migratory polyarthritis, and myalgia may be related to a disorder in lipid metabolism [10,11]. This relationship has also been noted in fibromyalgia syndrome (FMS), similarly to MPS [13]. It has been highlighted that hyperlipidemia and other related cardiovascular comorbidities observed in patients with FMS may often be due to the strong association between FMS and obesity [14].
Although the effects of elevated lipid levels on MPS have not yet been fully elucidated, inflammation, oxidative stress, and neurological mechanisms are being implicated. High lipid levels may trigger inflammatory responses. Specifically, high-sensitivity C-reactive protein and phospholipase A2 levels have been reported to be higher in patients with MPS compared to healthy individuals [15]. Lipid peroxidation is a marker of oxidative stress and may play a role in the pathophysiology of MPS. Recent studies have brought attention to the possibility that MPS may not be solely a local mechanical issue but may also be associated with systemic metabolic changes, particularly disorders in lipid metabolism [16]. However, to the best of our knowledge, there is a significant lack of studies in the literature that directly investigate the relationship between dyslipidemia and MPS, as well as the impact of lipid levels on pain and other symptoms.
In this study, we aimed to investigate the prevalence of MPS in individuals with dyslipidemia and to examine the relationship between lipid levels and MPS symptoms.
Materials and Methods
This study included patients who presented to the Department of Internal Medicine and Physical Medicine and Rehabilitation of Adana City Training and Research Hospital and underwent lipid profile assessment. Medical records of 197 patients (132 females and 65 males) without inflammatory disease and with normal blood inflammatory markers [erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP)] were retrospectively reviewed.
Exclusion criteria were defined as the presence of inflammatory rheumatic diseases, inflammatory bowel diseases, a history of acute trauma or recent surgery, and myocardial infarction within the previous month. The diagnosis of myofascial pain syndrome (MPS) was established according to the diagnostic criteria described by Travell and Simons.
Data extracted from patient files included demographic characteristics (sex, age, weight, height, body mass index [BMI]), comorbidities, regular exercise habits, and Visual Analog Scale (VAS) scores. The severity of palpable muscle spasm was assessed using the four-point Pressure Pain Threshold Scale (PPTS), and only patients who underwent this evaluation were included in the study. Biochemical parameters, including serum triglycerides (TG), total cholesterol, high-density lipoprotein cholesterol (HDL-c), and low-density lipoprotein cholesterol (LDL-c) levels, were also recorded.
VAS and PPTS assessments, as well as lipid profile evaluations, were performed by the same physician to ensure consistency. All data were collected and verified through a comprehensive review of the patients’ medical records.
All participants were called to the laboratory after an average fasting period of 12 hours, and 5 mL of blood was drawn from the antecubital vein. The blood samples were transferred into plain tubes and allowed to clot. The samples were centrifuged at 4,000 rpm for 5 minutes at 4°C to separate the serum. Total cholesterol, TG, HDL-c, and LDL-c levels were measured in the separated serum. A Beckman Coulter AU5800 clinical chemistry autoanalyzer was used to measure the plasma lipid levels of individuals in the case and control groups. Measurements were performed using enzymatic colorimetric methods. The results were obtained in mg/dL.
Statistical methods
Statistical analyses were performed using the SPSS v. 21 program. The demographic and clinical characteristics of the participants were summarized using means, standard deviations, medians, and minimum and maximum values. For group comparisons, the normality assumption was assessed using the Shapiro-Wilk and Kolmogorov-Smirnov tests. Differences between two independent groups were examined using the independent-sample t-test for normally distributed data and the Mann-Whitney U test for non-normally distributed data.
Logistic regression analysis was performed to predict dyslipidemia and MPS. In this analysis, the following predictors were used: dyslipidemia, MPS, age, sex, BMI, diabetes mellitus (DM), hypertension, and thyroid disease. The statistical adequacy of the model was determined by calculating the events per variable (EVP). This analysis included the events of the dyslipidemia group (175 cases). The independent variables in the logistic regression model were age, sex, BMI, DM, hypertension, thyroid disease, and MPS. The EVP was computed as follows:
EVP = total number of events (175) / number of independent variables (8) = 21.8
In the logistic regression analysis conducted to predict MPS, dyslipidemia, age, sex, BMI, DM, hypertension, and thyroid disease were identified as predictors (EPV = 19.3).
Ethical Approval
This study was approved by the Ethics Committee of Adana City Training and Research Hospital (Date: 2024-10-10, No: 173).
Results
A total of 197 participants were evaluated for inclusion in this study. Among the 197 participants, 132 were female and 65 were male, with a mean age of 51.3 years (standard deviation: 11.48). Table 1 summarizes the demographic and clinical characteristics of the participants.
SD: standard deviation, BMI: body mass index, VAS: Visual Analog Scale, DM: diabetes mellitus, MPS: myofascial pain syndrome, CAD: coronary artery disease, PPTS: Pressure Pain Threshold Scale, LDL: low-density lipoprotein, HDL: high-density lipoprotein, TG: triglyceride
The frequency of MPS and BMI was significantly higher in the dyslipidemia group than in the healthy control group (p < 0.01 for all) (Table 2).
When the participants were grouped according to their lipid levels (normal, borderline high, and high) and their clinical features were compared, the frequency of MPS was found to be higher in the borderline high group than in the healthy group. While VAS values were higher in the borderline high group than in the controls, PPTS scores differed across all three lipid groups (p < 0.05 for all) (Table 3).
In the logistic regression analysis conducted for dyslipidemia prediction, sex and MPS were found to be significant (p < 0.01 for both, odds ratio: 13.781 and 8.618, respectively). The model was statistically significant (χ²(8) = 31.546, p < 0.001), explaining 29.4% of the variance (R²CS = 0.148, R²N = 0.294, -2LL = 106.356).
Discussion
This study aimed to investigate the prevalence of MPS in dyslipidemia and the relationship between lipid levels and MPS symptoms. The results demonstrated that the frequency and severity of MPS increased in patients with dyslipidemia and that MPS could serve as a predictive factor for dyslipidemia.
In this study, the prevalence of MPS in the dyslipidemic group was found to be significantly higher than in the group with normal lipid levels. This suggests a strong association between dyslipidemia and MPS and indicates a higher likelihood of developing MPS among individuals with dyslipidemia.
Lipids are biomolecules involved not only in energy metabolism but also in membrane stability, signal transduction, and inflammatory processes. It has been proposed that elevated serum lipid levels may trigger myofascial pain by inducing oxidative stress and inflammation in tissue [15].
In a study, the serum lipid profiles between patients with MPS and healthy individuals, no significant differences were found in total cholesterol, TG, HDL, LDL, or very low-density lipoprotein levels [7]. However, another study published in the Abant Medical Journal reported that lipid levels in patients with MPS were higher than in healthy controls and that these levels were positively correlated with pain intensity and muscle spasm [16]. Similarly, Ozgocmen and Ardicoglu showed that even borderline high lipid levels were associated with increased MPS and pain severity. They identified a significant relationship between total cholesterol and LDL levels and tissue compliance at trigger points, suggesting that MPS symptoms might undergo substantial changes even in the early stages of dyslipidemia [13]. The findings of our study are consistent with the literature, indicating that the frequency and severity of MPS increase in dyslipidemia and that the presence of MPS may act as a predictor for dyslipidemia. These results support the hypothesis of a relationship between dyslipidemia and MPS and reinforce the notion that individuals with dyslipidemia are more likely to experience MPS. These findings suggest that dyslipidemia may influence musculoskeletal health and general pain experiences, which emphasizes the importance of considering pain in dyslipidemia management and underlines the need for a multidisciplinary approach.
This study also examined the relationship between dyslipidemia and MPS, as well as other demographic and clinical features, and showed that both the prevalence of MPS and BMI values were significantly higher in the dyslipidemia group compared to the healthy group, which is consistent with the literature [17]. Nijs et al. provided evidence that chronic pain and inflammation might affect lipid metabolism, or conversely, that dyslipidemia might increase susceptibility to muscle pain through systemic inflammation and microvascular changes [18]. Our findings not only suggest that dyslipidemia may contribute to the development of MPS but also reveal that the median PPTS score in the dyslipidemic group was higher than in the healthy group, indicating that pain and other MPS symptoms are more severe in individuals with dyslipidemia. These results underscore the importance of considering dyslipidemia in patients with MPS in clinical practice and highlight the relevance of lipid-lowering interventions in the management of pain.
In our study, the median BMI value in the dyslipidemic group was significantly higher than in the healthy group with normal lipid levels. This finding supports the strong association between dyslipidemia and overweight or obesity. The literature has emphasized that high BMI is a significant risk factor for dyslipidemia [19].
Although there is compelling evidence in the literature indicating a relationship between MPS and lipid levels, heterogeneity exists among study results. Variability may stem from differences in patient populations, sample sizes, and insufficient control of comorbid conditions affecting dyslipidemia (e.g., DM and obesity). Moreover, discrepancies in laboratory methods and diagnostic criteria used across studies contribute to this variability. Existing data suggest that abnormalities in lipid metabolism may play a role in the pathogenesis of MPS. However, it remains unclear whether this relationship is causal. Therefore, there is a need for prospective longitudinal studies and randomized controlled trials that assess the effects of lipid-lowering treatments on MPS symptoms.
Limitations
Among the strengths of our study is its comprehensive statistical examination of the relationship between MPS and dyslipidemia. Nonetheless, there are also limitations. As this is a cross-sectional study, causality cannot be established. Future prospective studies will be valuable in clarifying the direction of this relationship and elucidating underlying mechanisms. Moreover, including a larger sample size and incorporating diverse ethnic groups would enhance the generalizability of the findings. Lastly, stratification of dyslipidemia subtypes and the inclusion of inflammatory markers could provide deeper insight into the pathophysiology of this relationship.
Conclusion
This study demonstrated an association between dyslipidemia and both the prevalence and severity of MPS symptoms and further suggested that MPS could serve as a predictive factor for dyslipidemia. These results highlight the importance of considering MPS in the management of dyslipidemia and recognizing the presence of dyslipidemia in the evaluation and treatment of MPS and pain in clinical practice.
Scientific Responsibility Statement
The authors declare that they are responsible for the article’s scientific content including study design, data collection, analysis and interpretation, writing, some of the main line, or all of the preparation and scientific review of the contents and approval of the final version of the article.
Animal and Human Rights Statement
All procedures performed in this study were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.
Funding: None
Conflict of Interest
The authors declare that there is no conflict of interest.
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Download attachments: 10.4328.ACAM.22857
Nilüfer Aygün Bilecik, Serpil Demir, Yunus Çoşkun, Sıdıka Büyükvural Şen, Meryem Kösehasanoğulları. Can Dyslipidemia be a significant factor in myofascial pain syndrome? Ann Clin Anal Med 2025;16(10):747-751
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Prognostic significance of APRI index and neutrophil/lymphocyte ratio in hepatocellular carcinoma patients undergoing liver transplantation
İmam Bakır Batı 1, Umut Tüysüz 2
1 Department of Liver Transplant Surgery, Faculty of Medicine, Acıbadem University, 2 Department of General Surgery, Şişli Etfal Hamidiye Training and Research Hospital, Istanbul, Turkey
DOI: 10.4328/ACAM.22861 Received: 2025-08-22 Accepted: 2025-09-22 Published Online: 2025-09-30 Printed: 2025-10-01 Ann Clin Anal Med 2025;16(10):752-758
Corresponding Author: Umut Tüysüz, Department of General Surgery, Şişli Etfal Hamidiye Training and Research Hospital, Istanbul, Turkey. E-mail: umutuysuz@gmail.com P: +90 505 476 18 26 Corresponding Author ORCID ID: https://orcid.org/0000-0002-8948-4050
Other Authors ORCID ID: İmam Bakır Batı, https://orcid.org/0000-0002-0066-1170
This study was approved by the Ethics Committee of Acıbadem University (Date: 2025-06-26, No:10/380)
Aim: Hepatocellular carcinoma (HCC) is one of the most common cancers worldwide. Liver transplantation (LT) is the only curative treatment that eliminates both the cirrhotic liver and the cancer. Our study aimed to demonstrate the ability of systemic and local inflammatory factors to predict prognosis and long-term survival outcomes for LT.
Materials and Methods: We analyzed 220 patients undergoing LT for HCC in two separate transplant centers between January 2012 and December 2024. The primary objectives were overall survival (OS), recurrence-free survival (RFS), and recurrence risk.
Results: The optimal cutoff values for neutrophil to lymphocyte ratio (NLR) and aspartate aminotransferase/platelet count ratio index (APRI) for OS and RFS were 0.451 and 0.68, respectively. We showed that the APRI > 0.68 (high) group had significantly better overall survival outcomes for RFS and OS. Borderline significance was observed in OS for the NLR > 4.51 group. In particular, tumor size and tumor number were found to be significant factors negatively affecting survival.
Discussion: We determined that a high systemic NLR level was useful for predicting OS, but this was not significant for recurrence or RFS. It is not a useful systemic inflammatory index for screening patients undergoing LT at high risk of recurrence. In our study, a high APRI score was associated with an increased mortality rate. Conversely, a high APRI score was associated with a better RFS. We found that a high APRI value was associated with a better OS.
Keywords: hepatocellular carcinoma, liver transplantation, survival, inflammatory markers
Introduction
HCC is the sixth most common cancer worldwide. As the third most common cause of death, it continues to be an increasingly important health problem [1]. Treatment options include LT, surgical resection, and locoregional treatment modalities. LT is one of the most effective treatment modalities for patients with early-stage HCC. LT eliminates both cancer and liver disease, such as cirrhosis. Thus, important risk factors for new tumor formation are eliminated [2]. Although HCC patients who undergo LT are selected according to strict selection criteria, the recurrence rate after LT is approximately 10–20% [3]. Since this directly affects long-term outcomes, selecting patients with the best probability of survival after LT in transplantation management is extremely important for the efficient use of scarce liver donor resources. Systemic markers associated with fibrosis and inflammation must be taken into consideration in the preoperative evaluation. The importance of changes in systemic inflammation in preoperatively predicting surgical and oncological outcomes in liver cancers, including HCC, has been shown in many studies [4]. A number of inflammation-based biomarkers and biomarkers related to the degree of liver fibrosis were developed to predict prognosis [5]. One of the most frequently used tools to assess patient outcomes is NLR. High NLR levels were reported to be associated with poor prognosis in patients with HCC who underwent liver resection [6]. The influence of tumor-associated neutrophils (TANs) on tumor growth, invasion, and metastasis has been revealed [7]. In parallel, there have been significant advances in the relationship between HCC progression and the tumor microenvironment (TME). As a result, NLR has begun to be used as a useful inflammatory marker to predict HCC recurrence [8]. Furthermore, several models have been developed that predict liver fibrosis status and HCC-related outcomes, including APRI.
To our knowledge, inflammatory markers associated with HCC recurrence can guide clinicians in identifying patients with poor prognosis preoperatively and postoperatively in patients undergoing LT. Numerous prognostic models for HCC have been proposed. Most of these generally incorporate clinicopathological features of the patient and tumor [9]. These models often fail to reveal the specific inflammatory factors that influence long-term outcomes. Recent studies evaluating the role of inflammatory biomarkers and markers related to liver fibrosis grade in HCC patients in the context of LT have yielded inconsistent results and remained uncertain regarding their ability to predict survival [10]. Our study aimed to demonstrate the ability of systemic and local inflammatory factors to predict prognosis and long-term survival outcomes.
Materials and Methods
For this study, patients undergoing living and deceased donor liver transplantation were recruited consecutively at two separate transplant centers between January 2012 and December 2024. During this period, a total of 1,530 patients underwent LT for any reason. Of these, 220 patients underwent LT for HCC. Inclusion criteria were those who had not received pre-LT radiotherapy or chemotherapy. The exclusion criteria were: 1) patients with concurrent tumors from other organs or metastatic liver tumors, 2) patients with other organ transplantation but missing clinical or follow-up information, and 3) patients with mixed tumors (HCC and cholangiocarcinoma) and recurrent HCC. Ultimately, 200 patients met the inclusion criteria. The primary objectives were OS, RFS, and recurrence risk ratio. The secondary aim was to investigate the relationship between high and low APRI and NLR and demographic and tumor characteristics. Inflammatory markers NLR and APRI were analyzed using cutoff values determined based on the Receiver Operating Characteristic (ROC) curve analysis. Preoperative serum samples were collected one week before liver transplantation in patients with HCC. NLR, a marker of inflammation with demonstrated prognostic value in liver resection for HCC, and APRI, as a non-invasive liver fibrosis marker, were used: APRI = (AST / AST upper limit of normal) / platelet count × 100. Post-LT follow-up was performed every three months using contrast-enhanced computed tomography (CT), AFP. OS was defined as the time from surgery to death or loss of follow-up. RFS was defined as the time from surgery to the detection of recurrence. Post-LT immunosuppressive protocol was performed as previously determined [11].
Statistical Analysis
Data were calculated as means, medians, frequencies, and percentages. The Mann–Whitney U test and the Kruskal–Wallis test were used to compare continuous variables. The area under the ROC curve (AUC) was used to determine the optimal cutoff value for RFS and OS analyses. ROC curve analysis was employed to determine optimal cut-off values for APRİ and NLR indices with respect to OS and RFS. Survival probabilities were estimated using the Kaplan–Meier method, and differences between groups were evaluated using the log-rank test. The Youden index was used to select thresholds that provided the best balance between sensitivity and specificity. All statistical analyses were performed using SPSS version 27.0.
Ethical Approval
This study was approved by the Ethics Committee of Acıbadem University (Date: 2025-06-26, No:10/380).
Results
There were no differences in clinic-demographic features (Table 1). We evaluated the relationship between post-LT results and preoperative inflammatory indices (Figure 1). The optimal cutoff values for NLR and APRI for predicting postoperative OS and RFS were 0.451 and 0.68, respectively (Figure 2 a,b). Borderline significance was observed in OS for the NLR > 4.51 group (Figure2 c). We analyzed also RFS for NLR(Figure2 d). Considering the relationship between APRI and tumor characteristics well-known to be associated with disease progression, alpha-fetoprotein (AFP) levels were significantly higher in the high APRI. When prognostic indicators were analyzed, the mortality rate was significantly higher in the low APRI group (36.8% vs. 19.9%)(Figure2 e). Interestingly, RFS was longer in the high APRI group (median: 55 months vs. 35 months)(Figure 2 f). Follow-up was significantly longer in the high APRI group (median: 64 months vs. 36 months). Kaplan-Meier analysis produced on the entire cohort showed that the high APRI group had significantly better overall survival outcomes for RFS and OS (Figure 2 e,f). In univariate Cox regression analysis, some clinical features and tumor variables were found to be significantly associated with OS. In particular, tumor size and tumor number were found to be significant factors negatively affecting survival. MVI was also associated with a significantly increased risk of mortality. An APRI ≤ 0.68 was found to be a significant prognostic factor increasing the risk of death by approximately 2.2-fold. In the analysis for NLR, although survival was better in patients with NLR ≤ 4.51, the difference was not significant (Table 2).
According to multivariate Cox regression analysis, only APRI ≤ 0.68 remained a significant independent factor affecting overall survival (p = 0.023, HR = 2.40, 95% CI: 1.130–5.081). Tumor size and tumor number, although close to the significance threshold, were not statistically significant in multivariate analysis. Similarly, MVI also lost significance in the multivariate model. Other variables were not found to be independent factors affecting OS (Table 2). The lowest p value was found for early-stage tumor differentiation, which trended toward a reduced risk of recurrence (p = 0.060, HR = 0.235, 95% CI: 0.052–1.062), but did not reach statistical significance (Table 2). When patient and tumor variables were compared with high and low NLR, no difference was observed in terms of gender, age, and disease etiology, while AFP and CP B and C ratios were found to be higher in high NLR. Similarly, RFS was significantly longer in high NLR. The APRI score, an indicator of fibrosis level, was significantly higher in the group with NLR >4.51. This suggests that high NLR may be associated with advanced liver disease (Table 3). When disease and tumor characteristics were examined with high and low APRI, a significant association was observed between high AFP and APRI > 0.68. While the mortality rate was found to be lower with high APRI, RFS and recurrence-free follow-up time were observed to be significantly longer (Table3). AUC were 0.55 and 0.51 for APRİ and NLR. respectively. For OS with APRI≤0.68, sensitivity was 30.4%, specificity was 84.3%, positive predictive value (PPV) was 36.8%, negative predictive value (NPV) was 80.1%, and accuracy was 71.9%. For OS with NLR≤4.51, sensitivity was 67.4%, specificity was 19.6%, PPV was 20.1%, NPV was 66.7%, and accuracy was 30.7%. In the analysis for RFS, for APRI≤0.68, sensitivity was 18.8%, specificity was 80.8%, PPV was 15.8%, NPV was 83.9% and accuracy rate was 70.9%; for NLR≤4.51, sensitivity was 78.1%, specificity was 22.8%, PPV was 16.2%, NPV was 84.4% and accuracy rate was 31.7%.
Discussion
We also aimed to explore the association of APRI and NLR with OS and RFS in the patients with HCC after LT. We determined that a high systemic NLR level was useful for predicting OS, but this was not significant for recurrence or RFS. It is not a useful systemic inflammatory index for screening patients undergoing LT at high risk of recurrence. In our study, a low APRI score was associated with an increased mortality rate. Conversely, a high APRI score was associated with a better RFS. The time to recurrence was not different between high and low scores. We found that a high APRI value was associated with a better OS. This is inconsistent with other studies showing an association between high APRI and shorter OS [12]. However, the results of the analysis for sensitivity, specificity, PPV, and NPV showed that APRI provided high specificity and acceptable accuracy in predicting mortality, but had limited screening power due to its low sensitivity. Based on these results, we demonstrated that while NLR has high sensitivity for mortality, its discriminatory power is limited due to very low specificity and low accuracy. Analysis of tumor recurrence revealed that although APRI has relatively higher specificity, its sensitivity remained low, while NLR, despite its high sensitivity, has low specificity and accuracy. Overall, we can suggest that while APRI and NLR provide some contribution to the prediction of mortality and overall survival, their clinical utility in predicting tumor recurrence is limited due to their low PPV values. While studies showed that an increased APRI score predicts the risk of developing HCC in patients with chronic hepatitis B [13], the findings of studies investigating the relationship between a high APRI and HCC prognosis are inconsistent. Most of these were single-center studies and were limited to specific populations, such as hepatitis B-associated HCC or those following hepatectomy. We also eliminated liver fibrosis and cirrhosis, which are important risk factors for the development of HCC. We reflect the true outcome of the scoring system based on these factors. Our study is also consistent with the conclusion that a low fibrosis index after LT is a poor prognostic factor for HCC, as demonstrated in our previous study [14]. APRI, a marker associated with liver fibrosis, were found to be prognostic factors for OS in HCC patients, but were not statistically significant for RFS. Markers related to inflammation and nutrition are known to be prognostic factors in HCC patients undergoing hepatic resection. Of these, high NLR is associated with poor outcomes [15], but whether it is a predictor of poor survival in HCC patients undergoing LT is unclear. We found that high NLR was a poor prognostic marker for OS. These results may be attributable to tumor pathogenesis, study population size, and the varying cutoff values used in previous studies. In our study, we demonstrated for the first time that APRI is an independent prognostic factor in HCC patients undergoing LT. Contrary to other studies, we analyzed whether high APRI levels are definitive predictors of poor survival. Our results showed that NLR and APRI were associated with high CP B and C, liver disease, including advanced cirrhosis, and high AFP reflecting aggressive tumors. Our multivariate results demonstrated that NLR and APRI scores, when combined with established prognostic factors such as MVI, tumor number and size, and AFP, can predict poor OS and RFS before LT in patients with HCC. Tumor aggressiveness is closely related to surgical outcomes. Furthermore, NLR and APRI, both reflecting liver functional capacity and degree of fibrosis, have been shown to be important predictors of poor prognosis in patients undergoing surgery. Our study is a two-center study that included cirrhotic patients from diverse etiologies, encompassing a diverse population. In addition to the group of patients who did not receive preoperative systemic therapy, it also did not include factors that could affect long-term outcomes after surgery, such as ablation, vascular interventional therapy, or molecular-targeting therapy. Systemic lymphocyte count indicates the recipient’s cytotoxic immune response in HCC [16]. One of the main reasons for post-LT extrahepatic recurrences is that tumor cells escape immune surveillance with immunosuppressive therapy, which facilitates extrahepatic organ metastasis [17]. Serum albumin level is one of the factors that plays a role in the immune response to tumor in addition to nutritional status [18]. NLR may affect surgery-related inflammation and the immune response in the transplanted graft in patients undergoing LT [19]. In parallel, a high NLR increases the risk of early complications, including tumor recurrence. This is associated with decreased survival and poor prognosis in the post-LT period [20].
According to these results, LT in patients with HCC should be individualized based on the clinical and pathological characteristics of the tumor, organ suitability, and the comparison of donor risk and recipient benefit expectations. Numerous HCC prognostic factors and models were identified in the past decades. Most of these were based on clinic-pathological, donor, and recipient factors [9,21]. NLR is one of the inflammation-related risk factors, reflecting both the antitumoral effect of the immune system and the systemic inflammatory state. Systemic inflammatory markers can be used to predict recurrence in high-risk patients. Neutrophils are classified according to their functional phenotypes in different inflammatory states. Although there are studies based on whether it promotes tumor progression or inhibits it due to the
complex diversity [22]. However, NLR and APRI-based results should be interpreted with caution because these biomarkers are influenced by several factors. Neoplasms such as HCC can influence the inflammatory and immune responses of patients [23]. Identifying a high-risk population by analyzing NLR and APRI in LT for HCC also constitutes a precise advantage in reducing failure-to-rescue.
Inflammatory parameters are reproducible, easy to perform, and cost-effective because they have very low variability even in complete blood counts that include different leukocyte types [24]. Complete blood count results and associated inflammatory markers could have been affected by acute rejection, immunosuppressive or systemic chemotherapy, and infections. However, HCC patients did not receive systemic therapy before LT, and surgery was not performed until the infection was controlled. Therefore, our results were not affected by these factors.
Limitations
To assess cutoff values for poor long-term survival, curve analysis of NLR and APRI may not be fully representative as this may not provide accurate long-term predictive value for LT outcomes. However, large-scale, multicenter studies would be beneficial to investigate better prognostic models for reducing postoperative recurrence and developing targeted therapies.
Conclusion
Our study demonstrated the prognostic importance of inflammatory and fibrosis markers in patients with HCC undergoing LT. We demonstrated that low APRI and high NLR are associated with poor long-term outcomes in LT for HCC. The APRI score is an independent prognostic factor in HCC patients undergoing LT. NLR and APRI scores may be clinically helpful in making treatment decisions and predicting post-LT oncological outcomes in HCC patients. One of the limitation of this work is the retrospective nature of the data. They may affect the accuracy of the recorded biochemical and clinical parameters. According to these considerations, LT for HCC patients should be based on clinic-pathological characteristics, organ availability and the cost-benefit ratio of LT. Further research is needed to confirm the effectiveness of the markers as prognostic factor in HCC patients who underwent LT and to identify any interactions with other risk factors and outcome predictors.
Scientific Responsibility Statement
The authors declare that they are responsible for the article’s scientific content including study design, data collection, analysis and interpretation, writing, some of the main line, or all of the preparation and scientific review of the contents and approval of the final version of the article.
Animal and Human Rights Statement
All procedures performed in this study were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.
Funding: None
Conflict of Interest
The authors declare that there is no conflict of interest.
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İmam Bakır Batı, Umut Tüysüz. Prognostic significance of APRI index and neutrophil/lymphocyte ratio in hepatocellular carcinoma patients undergoing liver transplantation. Ann Clin Anal Med 2025;16(10):752-758
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Incidental pathological findings in cholecystectomy: A single-center retrospective analysis
Osman Gökhan Gökdere, Bahadır Öndeş
Department of General Surgery, Faculty of Medicine, Malatya Turgut Özal University, Malatya, Türkiye
DOI: 10.4328/ACAM.22871 Received: 2025-08-30 Accepted: 2025-09-29 Published Online: 2025-09-30 Printed: 2025-10-01 Ann Clin Anal Med 2025;16(10):759-762
Corresponding Author: Osman Gökhan Gökdere, Department of General Surgery, Faculty of Medicine, Malatya Turgut Özal University, Malatya, Türkiye. E-mail: osman.gokdere@ozal.edu.tr P: +90 532 669 85 56 Corresponding Author ORCID ID: https://orcid.org/0000-0003-0161-6600
Other Authors ORCID ID: Bahadır Öndeş, https://orcid.org/0000-0002-8080-9664
This study was approved by the Ethics Committee of Malatya Turgut Özal University (Date: 2025-06-03, No: E-30785963-020-307299)
Aim: Chronic cholecystitis and cholelithiasis are the most frequently encountered pathologies in cholecystectomy specimens; however, additional histopathological findings that are not clinically suspected may incidentally be detected. This study aimed to evaluate the frequency and distribution of incidental pathological findings in patients who underwent cholecystectomy at a single center.
Materials and Methods: The data of 3,084 patients who underwent cholecystectomy at our institution between January 2021 and December 2024, and for whom pathology reports were available, were retrospectively analyzed. Histopathological diagnoses other than chronic cholecystitis, acute cholecystitis, and cholelithiasis were considered incidental findings. These findings were classified according to their types, and their proportions were calculated.
Results: Incidental pathological findings were detected in 390 of 3,084 cases (12.65%). The most frequent incidental lesions were metaplasia (n=182, 46.6%), adenomyomatous hyperplasia (n=79, 20.3%), and cholesterol polyps (n=77, 19.7%). Less common findings included xanthogranulomatous cholecystitis (n = 23, 5.9%), dysplasia (n = 18, 4.6%), and adenocarcinoma (n = 11, 2.8%). Among the adenocarcinoma cases, 81.8% occurred in women, with a mean age of 67.2 years.
Discussion: Incidental pathological findings are observed at a noteworthy frequency in cholecystectomy specimens. The presence of clinically significant lesions such as metaplasia, dysplasia, and adenocarcinoma underscores the importance of routine histopathological examination of all gallbladder specimens.
Keywords: cholecystectomy, incidental pathology, adenocarcinoma, metaplasia, adenomyomatous hyperplasia
Introduction
Gallbladder diseases, particularly cholelithiasis and chronic cholecystitis, are among the most common gastrointestinal surgical indications worldwide [1]. The prevalence of cholelithiasis varies geographically, being reported in approximately 10–15% of the adult population in Western countries, while higher rates have been documented in certain regions such as Turkey [2]. Chronic inflammation related to gallstones can drive mucosal changes that may ultimately progress to carcinoma [3].
Cholecystectomy is currently regarded as the gold-standard surgical treatment for symptomatic cholelithiasis and its complications [4]. Postoperative histopathological examination not only confirms the diagnosis but also allows the detection of incidental pathologies that may remain clinically silent and undetectable on imaging studies [5]. These incidental findings can be categorized into benign alterations (adenomyomatosis, cholesterol polyps), preneoplastic lesions (metaplasia, dysplasia), and malignant tumors (adenocarcinoma) [6].
Gallbladder carcinoma is thought to arise mainly through chronic inflammation associated with gallstones, along with precursor lesions such as biliary intraepithelial neoplasia (BilIN), intracholecystic papillary neoplasm (ICPN), and pyloric gland adenoma (PGA), which are considered sequential steps in the metaplasia–dysplasia–carcinoma pathway [7]. These lesions provide important insights into tumor biology and may offer opportunities for earlier detection.
Within this pathological spectrum, the clinical significance of incidental findings becomes particularly evident when preneoplastic or malignant lesions are identified. Gallbladder adenocarcinoma is most often diagnosed at an advanced stage and is associated with a poor prognosis; however, when incidentally detected at an early stage, surgical resection can achieve curative outcomes [8]. In the literature, the reported incidence of incidentally identified adenocarcinoma ranges between 0.2% and 2.0%, emphasizing the indispensable role of routine histopathological evaluation of cholecystectomy specimens [9].
In this study, the pathology reports of patients who underwent cholecystectomy at our institution were retrospectively reviewed to determine the frequency and distribution of incidental pathological findings. Furthermore, the clinical significance of these findings was assessed in the context of current literature.
Materials and Methods
This retrospective study included all patients who underwent cholecystectomy at our institution between January 2021 and December 2024 and for whom pathology reports were available. Inclusion criteria consisted of cases with complete pathology reports and those who underwent cholecystectomy for gallbladder pathology. Exclusion criteria were incomplete pathology reports and cases in which no additional histopathological finding other than chronic or acute cholecystitis and cholelithiasis was identified.
In this study, incidental pathological findings were defined as additional histopathological diagnoses other than chronic cholecystitis, acute cholecystitis, and cholelithiasis. The detected findings were classified as adenocarcinoma, adenomyomatous hyperplasia, cholesterol polyps, metaplasia, dysplasia, xanthogranulomatous cholecystitis, and other rare lesions.
Data analysis was performed using SPSS Statistics v.26.0 (IBM Corp., Armonk, NY, USA). Continuous variables (e.g., age) were assessed for normality using the Kolmogorov–Smirnov test. Normally distributed data were expressed as mean ± standard deviation (SD), while non-normally distributed data were presented as median (minimum–maximum).
Categorical variables (sex, presence of incidental findings, and types of findings) were presented as counts and percentages. Comparisons between categorical variables were performed using the chi-square test or Fisher’s exact test when the expected cell counts were small. For continuous variables, the independent samples t-test was used for normally distributed data, while the Mann–Whitney U test was applied for non-normally distributed data.
Additionally, the relationship between types of incidental findings and demographic variables such as age and sex was specifically examined. A p-value of <0.05 was considered statistically significant in all analyses.
Ethical Approval
This study was approved by the Ethics Committee of Malatya Turgut Özal University (Date: 2025-06-03, No: E-30785963-020-307299). This study was conducted in accordance with the principles of the Declaration of Helsinki. Owing to the retrospective nature of the study, the requirement for informed consent was waived.
Results
Among the 3,084 cholecystectomy cases included in the study, incidental pathological findings were identified in 390 patients (12.65%). The most frequent lesion was metaplasia, detected in 182 cases (46.6%), followed by adenomyomatous hyperplasia (n=79, 20.3%) and cholesterol polyps (n=77, 19.7%). Less common findings included xanthogranulomatous cholecystitis (n = 23, 5.9%), dysplasia (n = 18, 4.6%), and adenocarcinoma (n = 11, 2.8%) (Table 1). Adenocarcinoma cases were analyzed separately. This tumor was detected in 11 patients (0.36%). Of these, nine were women (81.8%) and two were men (18.2%), with a mean age of 67.2 ± 13 years (range: 43–95 years). Although none of the patients had a preoperative suspicion of malignancy, most of the cases with available staging data were classified as pT2–pT3 (Table 2). In total, incidental pathological findings were identified in 390 patients (12.65%). In multivariable logistic regression analysis including age and sex, increasing age was found to be independently associated with incidental findings (OR = 1.02 per year; 95% CI: 1.01–1.03; p = 0.004). Female sex, on the other hand, was not significantly associated with the presence of incidental lesions (OR = 1.12; 95% CI: 0.89–1.41; p = 0.32).
Discussion
In the present study, the rate of incidental pathological findings in cholecystectomy specimens was determined to be 12.65%. This rate is clinically relevant, particularly considering the presence of preneoplastic and malignant lesions. The most frequently encountered incidental finding in our series was metaplasia, which has been reported in the literature to arise in the setting of chronic inflammation and to represent an important step in the pathogenesis of gallbladder adenocarcinoma [10]. Dysplasia, on the other hand, is directly associated with carcinogenesis, and its detection warrants close clinical surveillance and, when necessary, additional surgical evaluation [11]. Incidental dysplasia is generally managed with simple cholecystectomy if margins are negative, though close follow-up may be advisable in elderly patients [12]. For incidental adenocarcinoma, management depends on tumor stage: pT1a is cured with cholecystectomy alone, whereas pT1b or higher requires extended resection with lymphadenectomy [13].
Furthermore, multivariate analysis revealed that advancing age was independently associated with incidental findings, whereas sex showed no significant effect. This suggests that elderly patients represent a higher-risk group for preneoplastic and malignant changes, underscoring the value of routine histopathological evaluation in this population[14].
Another important aspect in the prevention and early detection of gallbladder carcinoma is the management of gallbladder polyps. Frequently detected incidentally, these lesions are clinically relevant because of their premalignant potential. Current guidelines recommend that polyps ≤ 5–6 mm without risk factors do not require follow-up, whereas 6–9 mm polyps with additional risk factors should be monitored by ultrasound at 6, 12, and 24 months. Polyps ≥ 10 mm are generally regarded as an indication for cholecystectomy [15]. Incorporating these recommendations into clinical practice is particularly important in settings such as ours, where incidental pathological findings were not uncommon, as it may help reduce unnecessary surgical procedures while ensuring timely treatment of high-risk patients.
In our study, the incidence of adenocarcinoma was 0.36%, which is consistent with the 0.2–2.0% range reported in the literature [16]. The majority of cases occurred in elderly female patients, and none had preoperative suspicion of malignancy. This finding clearly highlights the diagnostic value and clinical importance of routine histopathological examination of cholecystectomy specimens.
Gallbladder adenocarcinoma is a malignancy that can be completely cured with surgical resection when detected at an early stage; however, due to its frequent diagnosis at advanced stages, the prognosis remains poor [17]. Preoperative radiological examinations are often insufficient in terms of sensitivity, particularly in the presence of small lesions, and as a result, malignant cases can be easily overlooked [18]. In this context, routine histopathological examination not only facilitates the identification of malignant tumors but also allows for the recognition of preneoplastic lesions, thereby contributing to the implementation of appropriate surgical or medical strategies before progression to advanced disease [19].
In some centers, it has been suggested that routine histopathological examination may be omitted for gallbladder specimens that appear macroscopically normal, primarily due to cost constraints or workload considerations [20]. However, both our study and similar reports have demonstrated incidental cases of adenocarcinoma and dysplasia, clearly indicating that such an approach carries significant clinical risks [21]. In countries with a high prevalence of cholelithiasis, foregoing histopathological evaluation may result in a substantial number of missed diagnoses and late-stage detections.
Although routine histopathological examination of all cholecystectomy specimens may raise concerns regarding cost and workload, its value in detecting clinically silent premalignant and malignant lesions outweighs the economic burden, especially in regions with high gallstone disease prevalence. From a health policy perspective, modeling studies show that in a cohort of 10,000 patients, routine histology can yield an additional 12 life years at an incremental cost of approximately €76,500 per life year gained compared with macroscopic selective approaches[22]. In low incidence settings, however, selective histology may offer a more cost-effective balance between diagnostic yield and resource use.
Therefore, international guidelines and numerous studies recommend the routine histopathological assessment of all cholecystectomy specimens as the gold-standard approach [23].
Limitations
The main limitations of this study are its retrospective and single-center design. In addition, radiological–pathological correlations were not systematically evaluated, which may have provided further insight into the preoperative detectability of incidental lesions. Nevertheless, the large sample size and the systematic histopathological evaluation of all specimens represent the major strengths of our study.
Conclusion
In this study, the rate of incidental pathological findings in cholecystectomy specimens was determined to be 12.65%, with clinically significant lesions such as metaplasia, dysplasia, and adenocarcinoma among the findings. Notably, the detection of adenocarcinoma in 0.36% of cases underscores the presence of malignant lesions that may remain undiagnosed in the preoperative period.
Routine histopathological examination facilitates not only the identification of malignancies but also the recognition of preneoplastic alterations, thereby contributing to the planning of appropriate surgical and follow-up strategies. Therefore, the histopathological evaluation of all gallbladder specimens remains indispensable, both for individual patient management and from a broader public health perspective.
Scientific Responsibility Statement
The authors declare that they are responsible for the article’s scientific content including study design, data collection, analysis and interpretation, writing, some of the main line, or all of the preparation and scientific review of the contents and approval of the final version of the article.
Animal and Human Rights Statement
All procedures performed in this study were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.
Funding: None
Conflict of Interest
The authors declare that there is no conflict of interest.
References
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Osman Gökhan Gökdere, Bahadır Öndeş. Incidental pathological findings in cholecystectomy: A single-center retrospective analysis. Ann Clin Anal Med 2025;16(10):759-762
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