July 2024
Maternal and fetal outcomes of COVID-19 infection: A retrospective study from Istanbul, Turkey
Narin Ece Çakmak 1, Burak Çakmak 1, Gül Özel Doğan 1, Alev Atış Aydın 2
1 Department of Obstetrics and Gynecology, 2 Department of Perinatology, Şişli Hamidiye Etfal Research and Training Hospital, İstanbul, Turkey
DOI: 10.4328/ACAM.22103 Received: 2024-01-10 Accepted: 2024-03-05 Published Online: 2024-04-29 Printed: 2024-07-01 Ann Clin Anal Med 2024;15(7):449-452
Corresponding Author: Narin Ece Çakmak, Department of Obstetrics and Gynecology, Şişli Hamidiye Etfal Research and Training Hospital, 34470, İstanbul, Turkey. E-mail: rol.narinece@gmail.com P: +90 533 380 35 47 Corresponding Author ORCID ID: https://orcid.org/0000-0001-5497-4490
Other Authors ORCID ID: Burak Çakmak, https://orcid.org/0000-0001-8371-6183 . Gül Özel Doğan, https://orcid.org/0000-0001-9555-1128 . Alev Atış Aydın, https://orcid.org/0000-0002-8504-5755
This study was approved by the Ethics Committee of Health Science University Sisli Hamidiye Etfal Research and Training Hospital (Date: 2022-10-07, No:3676)
Aim: The COVID-19 pandemic, caused by the SARS-CoV-2 virus, poses unique challenges for pregnant women due to physiological changes that make them more susceptible to infections. This retrospective study investigated the impact of COVID-19 on 632 pregnant women, including 267 with confirmed COVID-19 and 365 without, from January 2020 to August 2022. The pandemic’s potential effects on maternal and fetal health raised concerns, given the unique immune alterations during pregnancy. Previous coronaviruses, SARS-CoV and MERS-CoV, share genetic similarities with SARS-CoV-2.
Material and Methods: Data from electronic medical records were collected for demographics, medical history, and outcomes. Statistical analyses compared COVID-19-positive and -negative groups using SPSS 15.0.
Results: Pregnant women with COVID-19 were older but had similar delivery modes and neonatal outcomes, including birth weight, height, Apgar scores, and mortality. Neonates born to mothers with COVID-19 in the second trimester had decreased birth height.
Discussion: While no significant differences were found in cesarean delivery rates and neonatal outcomes between groups, the study acknowledges limitations, including its retrospective nature and small sample size from a single center. Despite these limitations, the study emphasizes the importance of ongoing monitoring, vaccination, and protective measures for pregnant women during the pandemic.
In conclusion, pregnant women should be vigilant in following preventive measures, and further research is needed to comprehensively understand the impact of COVID-19 on maternal and fetal health. Healthcare providers should continue close monitoring and support for pregnant patients with COVID-19.
Keywords: Maternal, Fetal, Covid-19, Pregnancy
Introduction
The COVID-19 pandemic caused by the SARS-CoV-2 virus has affected millions of people worldwide, including pregnant women starting on 2020 January 9 [1]. Pregnancy is a unique physiological state that alters the immune system and makes women more susceptible to infections. This has raised concerns about the potential impact of COVID-19 on maternal and fetal health [2].
Coronaviruses are enveloped, non-segmented, single-stranded ribonucleic acid (RNA) viruses causing diseases from common colds to severe fetal disorders. The two best-known fetal viruses are SARS-CoV, which causes severe acute respiratory syndrome (SARS), and MERS-CoV, which causes Middle East respiratory syndrome (MERS). The genome of SARS-CoV-2 shares about 80% and 50% similarity with SARS-CoV and MERS-CoV, respectively [3].
COVID-19 infection has a broad impact, from death to being asymptomatic. Several studies have investigated the maternal and fetal outcomes of COVID-19 in pregnancy [4]. The evidence suggests pregnant women with COVID-19 are more likely to require hospitalization and intensive care unit admission than non-pregnant women with COVID-19. Additionally, pregnant women with COVID-19 may have an increased risk of preterm birth, cesarean delivery, and stillbirth compared to those without COVID-19.
Overall, short-term outcomes of infants born to mothers who developed COVID-19 during pregnancy seem favorable. Rates of transmission of SARS-CoV-2 are estimated at 1.9 per 100 pregnancies. Postnatal transmission of SARS-CoV-2 accounts for the majority of infections reported in neonates. Adverse neonatal outcomes of infants of mothers with COVID-19 disorder, such as death, have been mainly attributed to prematurity or comorbidities [5].
Material and Methods
Two hundred sixty-seven pregnant patients who had COVID-19 infection during their pregnancy from January 2020 to August 2022, with confirmed positive PCR test results, were included in our study as a patient group. Three hundred sixty-five pregnant patients who did not have COVID-19 infection during pregnancy were included.
Study Design and Population
This retrospective study included 632 pregnant women who gave birth between January 2020 and December 2022 at a single tertiary care center. Of these, 267 women were confirmed to be COVID-19 positive during pregnancy, and 365 were COVID-19 negative.
Data Collection
Data were collected from electronic medical records, including maternal demographics, medical history, pregnancy outcomes, maternal COVID-19 infection time (week of pregnancy), and neonatal outcomes. All data were collected by trained research personnel and reviewed by a senior obstetrician/gynecologist for accuracy.
Maternal and Fetal Outcomes
Maternal outcomes included hospitalization, admission to the intensive care unit, the indication of labor, type of labor, and maternal mortality. Neonatal outcomes included birth weight, birth height, Apgar scores at 1 and 5 minutes, neonatal intensive care unit admission, and neonatal mortality.
Statistical Analysis
SPSS 15.0 for Windows program was used for statistical analysis. Descriptive statistics: numbers and percentages for categorical variables, mean, standard deviation, minimum, maximum, and median for numerical variables. The rates in the groups were compared with the Chi-Square Test. Comparisons of the numerical variable between two independent groups were made using the Mann-Whitney U test since the normal distribution condition was not met. The alpha significance level was accepted as p˂0.05.
Limitations
This study has several limitations, including its retrospective design, the possibility of selection bias, and the relatively small sample size. Additionally, the study was conducted at a single tertiary care center, which may limit the generalizability of the findings to other settings. Furthermore, COVID-19 PCR tests may give false negative results, leading to an error during the grouping of patients.
Ethical Approval
This study was approved by the Ethics Committee of Health Science University Sisli Hamidiye Etfal Research and Training Hospital (Date: 2022-10-07, No:3676).
Results
A total of 632 pregnant women were included in this retrospective study, of whom 267 were COVID-19 positive and 365 were COVID-19 negative. The mean age of the study population was 29.2 years (SD = 5.6 years), and the mean gestational age at delivery was 38.5 weeks (SD = 1.9 weeks).
Maternal outcomes
Pregnant women who had COVID-19 infection during any time of their pregnancy period were at an older age (29.9 vs. 28.7, p<0.003). The mean delivery week was 38.6 in the COVID-19 positive group and 38.4 in the COVID-19 negative group (p<0.72).
Regarding delivery mode, pregnant women with COVID-19 infection had a similar rate of cesarean section delivery (51% vs. 44.5%, p < 0.112) compared to the control group (Table 1).
Among 267 COVID-19-positive patients, 42 women (17%) had COVID-19 infection in the first trimester, 113 women (45.7%) had COVID-19 disease in the second trimester, and 92 women (37.2%) had COVID-19 infection in the third trimester.
Neonatal outcomes
Birth weight and birth height were similar between the two groups, with a mean birth weight of 3,277 grams (SD = 466 grams) in the COVID-19 positive group and 3,255 grams (SD = 533 grams) in the COVID-19 negative group(Table 2) and mean birth height of 49.9 cm (SD = 2.4 cm) in COVID-19 positive group and 49.8 cm (SD = 3.0 cm) in COVID-19 negative group (Table 3).
Additionally, Apgar scores at 1. minute and 5. minutes (1’ 7.67 and 5’ 9.19 vs. 1’ 7.65 and 5’ 9.17 p < 0.88) were also similar between the two groups. There was no neonatal mortality observed. Neonates’ hospitalization duration was close, with 0.23 days vs. 0.64 days (p<0.518).
There is a statistically meaningful difference between birth heights when we analyze pregnant women who had COVID-19 infection according to trimesters. Neonates who had been born to women who had COVID-19 infection during 2. Trimester had a mean birth height of 49.5 cm (SD=2.4) vs. 50.4 cm (SD=2.3) who had an infection during 3. Trimester (p<0.049). There was no statistically significant difference between birth weights.
Overall, these results suggest that women who had COVID-19 infection during pregnancy had no increased risk of low birth weight and height, preterm birth, cesarean section delivery, and low APGAR scores compared to women who had not been diagnosed with COVID-19 disease during their pregnancy period. In contrast, results also showed that neonates born to women with COVID-19 infection during the second trimester are at more risk of decreased birth height.
Discussion
The COVID-19 pandemic has affected millions of people worldwide, including pregnant women, raising concerns about the potential impact of COVID-19 on maternal and fetal health. The evidence suggests that pregnant women with COVID-19 are more likely to require hospitalization, intensive care unit admission, preterm birth, cesarean delivery, and stillbirth than pregnant women without COVID-19. Adverse neonatal outcomes of infants of mothers with COVID-19 infection have been mainly attributed to prematurity or comorbidities.
This study included 267 pregnant women with COVID-19 infection during pregnancy and 365 pregnant women who did not have COVID-19 disease during pregnancy, with a mean age of 29.2 years and a mean gestational age at delivery of 38.5 weeks. The study found that pregnant women who had COVID-19 infection during any time of their pregnancy period were older than the control group.
There are plenty of studies that show that COVID-19 infection during pregnancy may cause preterm birth. [6, 7, 9, 13, 14, 17, 18]. An important cohort study compared the outcomes of pregnant women, who underwent childbirth with versus without COVID-19 infection. It was found that pregnant women with COVID-19, compared with those without COVID-19, were more likely to have a preterm delivery. [16] In another cohort study done by the Spanish Obstetric Emergency Group, it is stated that more preterm births are observed among COVID + women but that was mainly because of the increase in iatrogenic preterm births. [12] In our study, the are no significant differences in gestational age between the two groups. Similar to our study, another cohort study took place in a large tertiary maternity unit in North West England and stated that there was no significant change in the risk of preterm delivery between COVID-19 + and COVID-19 – mothers [10].
Another conclusion in our study is that the pregnant women with COVID-19 infection during pregnancy had a similar rate of cesarean section delivery compared to the control group. Contrary to our findings, some researchers published that cesarean rates are higher in COVID-19 + patients[6, 10, 11, 12, 13, 18, 19] According to the meta-analysis of Marchand, G. et al. (2022) [7], A high rate of cesarean delivery (53.2%) was observed among pregnant women with COVID-19. In a systematic review of 104 cases, cesarean delivery was more common than normal spontaneous vaginal delivery [8].
Neonatal outcomes such as birth weight, birth height, Apgar scores, and neonatal mortality were identical between the two groups. Parallel to this study, there are several studies indicating that the birth weights of the neonates’ of the two groups have no significant difference [13, 14, 17].
Conclusion
In conclusion, the COVID-19 pandemic has affected millions of people worldwide, including pregnant women.
This retrospective study included 267 pregnant patients with COVID-19 infection during pregnancy and 365 pregnant patients who did not have COVID-19 disease during pregnancy. The study found that pregnant women with COVID-19 infection during pregnancy had a similar rate of cesarean section delivery compared to the control group. The study also found no significant differences in neonatal outcomes, including birth weight, birth height, Apgar scores at 1 and 5 minutes, neonatal intensive care unit admission, and neonatal mortality, between the two groups.
Still, this research is limited because is a retrospective study, had only a small group of participants and potentially has selection biases. The study was conducted at a single tertiary care center, which may limit the generalizability of the findings to other settings. Additionally, COVID-19 PCR tests may give false negative results, leading to an error during the grouping of patients. Despite these limitations, this study provides valuable information about the outcomes of pregnant women with COVID-19 infection and their neonates.
Further research is needed to fully understand the impact of COVID-19 on maternal and fetal health during pregnancy. But still, pregnant women should be vaccinated against COVID-19 when possible, wear masks, practice social distancing, and wash their hands frequently. Healthcare providers should also continue to monitor pregnant patients with COVID-19 closely to provide appropriate care and support.
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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Narin Ece Çakmak, Burak Çakmak, Gül Özel Doğan, Alev Atış Aydın. Maternal and fetal outcomes of COVID-19 infection: A retrospective study from Istanbul, Turkey. Ann Clin Anal Med 2024;15(7):449-452
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Right ventricular dysfunction as a predictor of mortality in patients with sepsis or septic shock in the emergency department
Peter Maher William Beshara 1, Tamer Abdallah Helmy 2, Sherif Wagdy Ayad 3, Khaled Salah Mustafa 1
1 Department of Emergency Medicine, 2 Department of Critical Care Medicine, 3 Department of Cardiology, Faculty of Medicine, Alexandria University, Alexandria, Egypt
DOI: 10.4328/ACAM.22104 Received: 2024-01-11 Accepted: 2024-03-19 Published Online: 2024-06-05 Printed: 2024-07-01 Ann Clin Anal Med 2024;15(7):453-457
Corresponding Author: Peter Maher William Beshara, Department of Emergency Medicine, Faculty of Medicine, Alexandria University, Alexandria, Egypt. E-mail: p_william15@alexmed.edu.eg P: +90 127 548 87 35 Corresponding Author ORCID ID: https://orcid.org/0000-0003-0596-0345
Other Authors ORCID ID: Tamer Abdallah Helmy, https://orcid.org/0009-0006-3275-7755 . Sherif Wagdy Ayad, https://orcid.org/0000-0002-1737-0142 . Khaled Salah Mustafa, https://orcid.org/0009-0003-3305-6916
This study was approved by the Ethics Committee of the Alexandria University (Date: 2021-10-20, No: 0201570)
Aim: Sepsis and septic shock present a significant challenge in the emergency department (ED) owing to their high mortality rates. The presence of right ventricle (RV) dysfunction during sepsis could potentially exacerbate unfavorable outcomes. However, the precise relationship between RV dysfunction and mortality in septic patients remains poorly understood. Therefore, this study aims to investigate the prognostic value of RV dysfunction as a predictor of mortality in patients presenting with sepsis or septic shock in the ED of Alexandria main university hospital.
Material and Methods: A prospective observational study was performed on 75 patients who presented to the ED with sepsis or septic shock. Echocardiographic parameters, including the tricuspid annulus systolic plane excursion (TAPSE) and the fractional area change, were measured within 24 hours after admission for assessment of RV dysfunction; then, patients were evaluated according to sequential organ failure score (SOFA) and acute physiologic and chronic health assessment (APACHE). Using multivariate regression, the current study assessed the relationship between 28-day mortality and the presence of RV dysfunction, SOFA, and APACHE.
Results: There were 75 patients in the study. 22 patients (29%) had RV dysfunction. When compared to patients without RV dysfunction, those with RV dysfunction had a greater mortality rate (68% vs. 34%, p<0.001). RV dysfunction was shown to be associated with mortality in univariate regression analysis (OR:4.16, CI:1.44-12, P<0.008), and multivariable regression analysis revealed a high correlation between RV dysfunction and mortality (OR:3.98, CI:1.3-11.9, P<0.013). With a statistically significant area under the curve, sensitivity, specificity, positive predictive value, and negative predictive value of 0.64, 45.5, 83.8, 68.2, and 66%, respectively, the receiver operator curve (ROC) indicated that RV dysfunction was linked to a considerable mortality rate.
Discussion: RV dysfunction was found in nearly one-third of the studied patients with sepsis and is associated with fourfold higher 28-day mortality.
Keywords: Right Ventricular Dysfunction, Sepsis, Septic Shock, Sepsis-Induced Cardiomyopathy, Mortality, Echocardiography
Introduction
Sepsis is defined as “life-threatening organ dysfunction caused by a dysregulated host response to infection” [1]. The emergence of cardiac failure is one of the most significant events that occur during sepsis, as it directly relates to morbidity and mortality, it is also known as Sepsis-induced cardiomyopathy (SICM) [2]. SICM is common and poses a significant load on the healthcare system where studies show that 40% to 50% of sepsis patients have myocardial damage [3].
There is no single definition that is universally accepted for SICM, despite the fact that many studies have shown evidence of circulatory dysfunction in septic patients [4]. However, the primary feature of SICM is contractile dysfunction [5]. It presents with: dilatation of both ventricles, Left ventricular (LV) systolic and/or diastolic dysfunction, and/or right ventricular (RV) impairment [6].
The majority of studies have been almost exclusively concerned with LV function. On the other hand, the RV is neglected in research, given its smaller muscle mass and single organ function. Nevertheless, the RV is a vital part in circulation as it is the second-largest pump in the circulatory system and is connected in series with the LV. Additionally, RV plays an important role in SICM.
During sepsis, the RV suffers from diminished filling, reduced contractility, and increased afterload. This will lead to a failure of the RV output to match the increased LV afterload as a result, CO will decline due to decreased LV preload [7]. Ventricular interdependence results from the RV and the LV being connected not only in series but also by a common septum [8].
Transthoracic echocardiography (TTE) is a minimally invasive, bedside method that may provide repeatable estimations of RV size and contractility [9]. Compared to the LV, imaging the RV is more challenging. As a result, there continues to be a divergence of opinions regarding the selection of echocardiographic parameters to define RV dysfunction.
The results of recent studies evaluating RV dysfunction were variable; whereas some showed no difference between survivors and non-survivors [10], others discovered a significant incidence of RV dysfunction that was linked to short and long-term mortality [11, 12].
Due to the fluctuating nature of these findings, there remains a necessity for a more dependable characterization of RV dysfunction in sepsis and septic shock, applicable for both research and clinical purposes.
The hypothesis of this study posits that the presence and severity of RV dysfunction upon presentation to the ED will be positively correlated with mortality in patients with sepsis or septic shock.
Material and Methods
This prospective observational study was performed on a registry of 75 patients who presented to the ED of Alexandria main university hospital (AMUH) with sepsis or septic shock. The aim of this study was to investigate the prognostic value of RV dysfunction as a predictor of mortality in patients presenting with sepsis or septic shock in the ED of AMUH.
Sample Size
Using the Power Analysis and Sample Size (PASS 2020) software (NCSS, LIC, Kaysville, Utah, USA, ness.com/software/pass), the Department of Medical Statistics, Medical Research Institute, Alexandria University, calculated the sample size while accounting for the 5% level of significance and the 5% precision using the Z-test [13].
Inclusion criteria
Adult patients over the age of eighteen and admitted to the emergency department (ED) with sepsis or septic shock, using the operational definitions provided by the surviving sepsis campaign (2021) [1].
Exclusion criteria
Poor echo window, moderate or severe mitral and/or aortic valve disease, regional wall motion abnormalities suggesting regional ischemia or prior infarction, pulmonary hypertension or cor-pulmonale, and pregnant females.
Informed Consent was obtained from each patient participating in the study or from their family, after providing detailed explanations about the research’s objectives and procedures. Throughout the study, strict confidentiality measures were upheld to safeguard the privacy of all individuals involved.
Complete history taking, a thorough physical examination upon admission that included the Glasgow Coma Scale (GCS) [14], vital signs, oxygen saturation, central venous pressure, and urine output were all performed for each patient. Upon admission, an electrocardiogram (ECG) and arterial blood gases were done, and the hypoxemia index (PaO2/Fio2) was calculated.
On the first day of hospitalization, scores for the quick sequential organ failure assessment (qSOFA) [15], the sequential organ failure assessment (SOFA), and the acute physiologic and chronic health evaluation (APACHE II) scores were calculated [16].
The criteria for the Surviving Sepsis Campaign in 2021 were followed during the treatment of the patients [1].
All hemodynamic, respiratory/ventilatory, vasoactive therapy, and fluid balance were recorded.
Using a 2.8–4 MHz phased array probe and a Vivid e machine (General Electric, Boston, USA), all patients were investigated by TTE performed by an emergency physician during the first 24 hours of diagnosis.
RV assessment
RV fractional area change (FAC) and tricuspid annular plane systolic excursion (TAPSE), assessed by M-mode, are used to evaluate the RV function from the apical four-chamber 2D perspective. RV dysfunction is characterized by a TAPSE of less than 1.6 cm or a FAC of less than 35% [17].
LV assessment
In the apical four and two chamber view, the modified biplane Simpson equation was used to calculate the left ventricular ejection fraction (LVEF). From the apical four-chamber view, the peak mitral inflow E and A velocity waves on the pulsed wave Doppler, the E/A ratio, and the E wave deceleration time (EDT) were measured. Using pulsed wave tissue Doppler imaging at the lateral mitral annulus on the four-chamber apical view, the diastolic e’ peak velocity was determined, and E/e’ was computed. LV systolic dysfunction was defined as LVEF <45%. E/e’ < 13 was the definition of LV diastolic dysfunction[18]. Systolic or diastolic dysfunction is referred to as LV dysfunction [19].
Statistical analysis of the data
The computer was given data, and IBM SPSS software package version 20.0 was used for analysis. (IBM Corp., Armonk, NY) Numbers and percentages were used to describe the qualitative data. To confirm that the distribution was normal, the Shapiro-Wilk test was performed. The terms range (minimum and maximum), mean, standard deviation, median, and interquartile range (IQR) were used to characterize quantitative data. At the 5% level, the results’ significance was assessed.
Ethical approval
This study was approved by the Ethics Committee of the Alexandria University (Date: 2021-10-20, No: 0201570).
Results
128 patients were assessed in this study, 53 patients were excluded while 75 patients were enrolled; 23 patients had sepsis (31%), whereas 52 patients had septic shock (69%), 75% of whom were mechanically ventilated, and 64% of whom received vasopressors. Overall mortality in the study was 44%. The mean length of the ICU stay was 10 days.
A statistically significant difference between survivors (44 ±8 %) and non-survivors (40 ±9 %) regarding FAC was observed, with a mean value of 42±9%. In addition, there was a statistically significant difference between survivors (21.2 ±3.9 mm) and non-survivors (15.7±4.5 mm) regarding TAPSE, with a mean of 18.8 (±5) mm for all cases. (Table 1).
RV dysfunction was present in 22 patients (29%). Similarly, LV systolic dysfunction was found in 27 patients (36%), and LV diastolic dysfunction was found in 37 patients (49.3%). LV dysfunction (systolic & diastolic) was found in 55 patients (77%). Only nine patients (19%) had isolated RV dysfunction, despite the significant overlap we found between LV and RV dysfunction (Table 1).
Patients with RV failure had lower ventilator-free days (2 vs. 7.8, p < 0.001) and increased mortality compared to patients without RV dysfunction (68% vs. 34%, p < 0.001).
Mortality and RV dysfunction were correlated (OR: 4.16, CI: 1.44-12, P < 0.008), but not with LV diastolic dysfunction (OR: 1.16, CI: 0.46-2.9, P < 0.73) or LV systolic dysfunction (OR: 0.5, CI: 0.18-1.3, P < 0.16), according to univariate regression analysis.
RV dysfunction and mortality had a high correlation according to the multivariate regression analysis (OR: 3.98, CI: 1.3-11.9, P < 0.013) (Table 2). Regarding the dysfunction of the RV, where an area under the curve, sensitivity, specificity, positive predictive value, and negative predictive value were 0.64, 45.5, 83.8, 68.2, and 66%, respectively, that was statistically significant, the receiver operator curve (ROC) indicated that it was related to substantial mortality. A similar outcome was obtained with TAPSE and FAC, with an APACHE II score of > 18 and an initial sofa score of > 9 (Figure 1).
Discussion
The study enrolled 75 patients who were admitted to the ICU with sepsis or septic shock. To assess RV dysfunction, different cut-offs derived from echocardiography and pulmonary artery catheterization were used in previous studies. In the current study, thresholds were chosen following published guidelines where, TAPSE < 16 mm or FAC < 35% were used to define RV dysfunction [17]. Those parameters were selected because they are widely used in clinical practice and are simple to measure. The same definition was used by Lasnpa et al.[19], a similar definition was used by Innocenti et al., [20] who defined RV dysfunction as TAPSE < 16 mm.
The current study involved 22 patients; 29.3% of patients were suffering from RV dysfunction, either isolated or combined with LV dysfunction. Other studies have agreed with the current study that RV dysfunction is common in sepsis, Innocenti et al. [20], found RV dysfunction in 34% of patients, and Kim et al., [21] reported that 40.7 % of patients had RV dysfunction.
The risk of mortality was four times greater in patients with RV dysfunction. It was discovered that RV dysfunction contributed independently to mortality. Our findings support and add to existing recent research on RV in sepsis. In a meta-analysis of observational studies, Vallabhajosyula et al.[22], discovered a correlation between RV dysfunction and higher mortality over the long term (OR 2.26, 95% CI 1.29-3.95, P = 0.004) as well as the short term (OR 2.42, 95% CI 1.52-3.85, P = 0.002).
This correlation can be explained by the increased cardiomyocyte cellular dysfunction within the dysregulated humoral metabolic context of sepsis, which is thought to be the pathophysiology of the observed RV dysfunction in septic patients in the present study and others. However, some other postulated mechanisms deserve discussion.
First, RV dysfunction may be an indirect measure of the severity of lung disease, which is the direct cause of death in those patients, since RV is impacted by the afterload exerted by the pulmonary circulation.
Second, the administration of catecholamines may have directly contributed to the mortality by causing RV dysfunction; in other words, RV dysfunction may have been a bystander to the increased mortality rather than the cause.
Consequently, rather than being a result of an underlying cardiac issue, RV dysfunction in sepsis may simply be a side effect of the overuse of vasopressors and fluid administration during the sepsis process.
In the current study, there was no significant difference between patients with RV dysfunction and patients without RV dysfunction regarding the need for mechanical ventilation (MV), PaO2/ FiO2, or the need for vasopressors. There was a significant difference regarding the vasopressor dose [5].
The current observational research did not standardize the time of fluid delivery, or TTE. Nevertheless, we were unable to find any meaningful difference in the cumulative balance between individuals who had RV dysfunction and those who did not. This demonstrates that different methods of administering fluids are not the main reason behind RV dysfunction.
Previous research has demonstrated that RV dysfunction has a separate effect on short-term mortality. In patients with and without RV dysfunction, the rates of acute respiratory distress syndrome (ARDS) were similar in the meta-analysis conducted by Vallabhajosyula et al.[22], although the rates of invasive MV were lower.
According to a different study by Vallabhajosyula et al. [23] patients with and without PHTN experienced similar levels of illness severity, including the need for MVs and ARDS.
Although the current study revealed a strong correlation between high short-term mortality and RV dysfunction, whether it occurred alone or in conjunction with LV systolic or diastolic dysfunction, mortality was not linked to LV systolic or diastolic dysfunction by itself.
In line with this finding, Lanspa et al.[19] discovered no correlation between mortality and LV diastolic or systolic dysfunction. They stated that both LV diastolic dysfunction (OR 0.94, CI 0.54-1.61, P = 0.81) and LV systolic dysfunction (OR 0.92, CI 0.57-1.5, P = 0.73) did not correlate with death, according to their univariate regression analysis.
Additionally, Kim et al.[21], produced similar findings, concluding that LV dysfunction (systolic and diastolic) was prevalent. Nevertheless, the only condition linked to mortality was RV dysfunction.
The inconsistent connection between RV and LV (either systolic or diastolic) and mortality in this study raises concerns because previous research has shown increased mortality.
The criteria of EF < 45% employed to identify LV dysfunction are probably very sensitive and may detect even minor cases of LV dysfunction, despite adhering to established standards; employing a lower threshold might have yielded different associations.
On the other hand, the thresholds for RV dysfunction (FAC < 35% and TAPSE < 16 mm) may exclusively flag severe cases of illness and could potentially target a subset of patients who are more critically ill.
Furthermore, even though LV diastolic dysfunction has been linked to mortality in septic patients, a correlation in this group of patients was not found. This could be because of the study’s strong signal for RV dysfunction, the low prevalence of isolated diastolic dysfunction, or the link between diastolic parameters and fluid intake. Lastly, the TTE, or fluid reception time, of our study may be different from that of other studies.
Study strength
This study focused on the RV’s echo parameters, and the association between RV dysfunction and mortality. The scarcity of research focusing on the right ventricle makes it a point of strength in this study.
Limitation
Several limitations have been encountered during the process of conducting our study. Since this is a single-center study, patient selection and treatment may have been impacted by regional management practices. The study was limited by its observational nature, which hinders any causal claim about the link between RV dysfunction and survival in sepsis patients.
We did not have enough pre-sepsis information on our patients to evaluate whether the RV dysfunction was caused by sepsis or if the patients had underlying RV dysfunction, even when individuals with clear chronic heart disease were eliminated.
Patients with RV dysfunction in this research tended to be older, to have more severe illnesses, and to have more concomitant conditions. These variables could distort the correlation between RV dysfunction and mortality.
TTE was performed on the first day of admission. However, the circumstances differed as the same patient had already received fluids, a vasopressor infusion, or mechanical ventilation. All of which may have affected the RV function. We think that serial TTE would yield stronger evidence.
Conclusion
RV dysfunction was found in nearly one-third of the studied septic patients and is associated with over fourfold higher 28-day mortality.
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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Sexual satisfaction and beliefs in sexual myths in patients with obsessive compulsive disorder: A cross-sectional study
Feyza Yılmaz 1, Ömer Böke 2, Pelin Göksel 2, Ahmet Rifat Şahin 2, Hatice Özyıldız 2, Gökhan Sarısoy 2, Aytül Karabekiroğlu 2, Selçuk Özdin 2
1 Department of Psychiatry, Amasya Şerafettin Sabuncuoğlu Education Research Hospital, Amasya, 2 Department of Psychiatry, Faculty of Medicine, Ondokuz Mayis University, Samsun, Türkiye
DOI: 10.4328/ACAM.22140 Received: 2024-02-09 Accepted: 2024-04-02 Published Online: 2024-05-05 Printed: 2024-07-01 Ann Clin Anal Med 2024;15(7):458-462
Corresponding Author: Feyza Yilmaz, Department of Psychiatry, Amasya Şerafettin Sabuncuoğlu Education Research Hospital, Amasya, Türkiye. E-mail: dr.feyzayilmaz93@gmail.com P: +90 538 695 96 43 Corresponding Author ORCID ID: https://orcid.org/0000-0002-4900-9685
Other Authors ORCID ID: Ömer Böke, https://orcid.org/0000-0003-1556-5226 . Pelin Göksel, https://orcid.org/0000-0002-6328-2557 . Ahmet Rifat Şahin, https://orcid.org/0000-0002-6897-3891 . Hatice Özyildiz, https://orcid.org/0000-0002-3883-6845 . Gökhan Sarisoy, https://orcid.org/0000-0003-0050-8157 . Aytül Karabekiroğlu, https://orcid.org/0000-0001-5048-7951 . Selçuk Özdin, https://orcid.org/0000-0003-1127-1132
This study was approved by the Ethics Committee of Ondokuz Mayıs University (Date: 2021-05-05, No: 2021/202)
Aim: Our study aimed to evaluate the sexual satisfaction levels and beliefs in sexual myths of Obsessive Compulsive Disorder (OCD) patients and control groups.
Material and Methods: Our study involved 40 OCD patients, 40 Anxiety Disorder (AD) patients currently in remission, and 40 healthy controls (HC). Dimensional Obsessive Compulsive Scale (DOCS), Golombok-Rust Inventory of Sexual Satisfaction (GRISS), Sexual Myths Scale (SMS), Hamilton Anxiety Rating Scale (HARS) were used as measurement tools.
Results: Our study showed that OCD patients had lower sexual satisfaction and stronger beliefs in sexual myths than controls. Female OCD patients reported dissatisfaction in satisfaction, touch, avoidance, and anorgasmia, while male OCD patients struggled with frequency, avoidance, and touch. Female patients had significant relationships between sexual myths and satisfaction, communication, and avoidance. Male patients only showed a relationship with avoidance. Disease duration was the main predictor of satisfaction, while age and education influenced sexual myths.
Discussion: These findings emphasize the need for targeted psychotherapeutic approaches for OCD patients’ sexual behaviors and beliefs.
Keywords: Obsessive Compulsive Disorder, Sexual Satisfaction, Sexual Myths, Anxiety Disorder
Introduction
Obsessive-compulsive disorder is a mental illness characterized by intrusive obsessions that cause distress and recurring behaviors or mental acts that the individual cannot control [1]. OCD is considered one of the primary causes of problems in family and social relationships and a decrease in quality of life among all mental disorders [2].
Sexual satisfaction is an emotional response based on an individual’s subjective evaluation and includes positive and negative experiences related to their sexual relationship [3]. Sexual myths are among the factors that might lead to sexual dysfunction and decrease sexual satisfaction. These myths usually involve exaggerated, erroneous, and irrational beliefs about sexual life that the person accepts as reality. Sexual myths may cause regret and guilt, unfounded expectations, and worries about sexual life. Sexual dysfunctions might begin and persist as a result of these causes. Studies on the relationship between OCD and sexual life have shown that OCD has a significant negative impact on sexual health by decreasing the level of sexual functions and sexual satisfaction [4].
The effect of sexual myths on the level of sexual satisfaction in OCD has not been extensively researched. This study aimed to evaluate the sexual satisfaction levels and beliefs of sexual myths of patients with OCD.
Material and Methods
Participants
Patients who applied to Hospital of Ondokuz Mayıs University psychiatry outpatient clinic and inpatients in the psychiatry service were included in this study. The patient group consisted of 40 OCD patients, and the control groups consisted of 40 AD patients currently in remission and 40 HC. The anxiety in remission group was established to match OCD in terms of drug use and exclude drug effects. Participants were selected based on specific inclusion and exclusion criteria. For the OCD group, individuals between the ages of 18 and 65 who met the diagnostic criteria for OCD according to DSM-5 were included. Similarly, for the AD group, individuals meeting the diagnostic criteria for anxiety disorder and in remission were included. HC group consisted of individuals willing to participate in the study and engage in assessments and interviews. Exclusion criteria included various psychiatric and medical conditions, as well as cognitive impairments.
Data Collection Tools
Dimensional Obsessive Compulsive Scale
The scale developed by Abramowitz [5] measures symptom clusters and symptom severity in patients with Obsessive Compulsive Disorder. Cronbach’s alpha value is 0.874 for the entire scale. It has been determined that the Turkish version of the scale is valid and reliable in Turkish society and supports the four-factor structure of the DOCS [6].
Golombok-Rust Inventory of Sexual Satisfaction
The scale used to determine the quality of sexual intercourse, sexual dysfunctions and the severity of sexual problems was developed by Rust and Golombok [7]. The reliability coefficient was found to be 0.94 in women and 0.87 in men. Turkish validity and reliability study was conducted by Tugrul et al. [8].
Sexual Myths Scale
The scale is used to determine individuals’ levels of belief in sexual myths. It was developed by Gölbaşı et al. and its validity and reliability studies were conducted [9]. The Cronbach Alpha coefficient of the scale was found to be 0.91, and in the repeated reliability test study, the coefficient was found to be 0.814.
Hamilton Anxiety Rating Sace
The scale was developed by Hamilton [10]. This scale was prepared to determine the anxiety level and symptom distribution in individuals and to measure the change in severity. Turkish validity and reliability study was conducted by Yazıcı et al. [11].
Statistical Analysis
The research data were analyzed using SPSS for Windows 22.0 (SPSS Inc, Chicago, IL). Descriptive statistics, including mean, standard deviation, median, frequency distribution, and percentage, were used to summarize the data. The normality of variables was assessed through visual (histogram and probability graphs) and analytical methods (Kolmogorov-Smirnov/Shapiro-Wilk Tests). Non-parametric tests such as Mann-Whitney U Test, Kruskal-Wallis, and Chi-square tests were employed for group comparisons, while the one-way ANOVA test was used for normally distributed variables. The relationship between variables was examined using the Spearman Correlation Test. Univariate and multivariate linear regression analyses were conducted, with a retrospective elimination model employed for multivariate analyses. The statistical significance level was set at p<0.05.
Ethical Approval
This study was approved by the Ethics Committee of Ondokuz Mayıs University (Date: 2021-05-05, No: 2021/202).
Results
It was observed that there was no statistically significant difference between the groups in terms of age, gender, educational status, marital status, socioeconomic status, and having children. All patients in the OCD and AD were receiving psychiatric treatment. When the clinical data of the groups were compared, it was determined that there was no statistically significant difference in terms of medications used, inpatient treatment and sexual problems. It was observed that the control group received significantly higher sexual education than the OCD and AD groups (χ²:6,771 0,034).
In the post-hoc test, it was observed that the SMS mean score of the OCD group was statistically significantly higher than the AD and HC groups (F:8,436, p:0,001). It was observed that the total scores of the GRISS did not follow a normal distribution in the groups. When the total score was compared between the groups, it was observed that there was a significant difference between the groups, and in the post-hoc analysis, the total score of the OCD group was observed to be higher than the AD and HC groups (KW: 20,356 p:0,001).
The comparisons of the SMS and GRISS total scores mean for each group revealed a significant difference between the groups. The post-hoc tests showed that the mean SMS and GRISS scores of the OCD group were significantly higher than the AD and HC groups. A comparison of SMS and GRISS total scores between groups is shown in Table 1.
The results of the correlation between SMS and GRISS in people with OCD showed a significant positive correlation between sexual myths and total score, communication, and avoidance in females and a significant positive correlation between sexual myths and avoidance in males. The correlation between SMS and GRISS in the OCD group is shown in Table 2. Univariate analyses were carried out first in the analysis used to predict sexual satisfaction and sexual myths using sociodemographic and clinical characteristics defined in the OCD group. Univariate analyses revealed that age, the duration of the illness, having completed high school or a higher education level, and having received sexual education all significantly affected sexual satisfaction. The best model was obtained at the 6th step of the analysis (F:9,114, p:0.005) performed with all variables by the backward elimination method. Only the disease duration variable remained in this model. Age, disease duration, marital status, education level, number of children, and sexual education significantly affected sexual myths, as demonstrated by univariate analyses. The best model was obtained at the 5th step of the analysis (F:23.447, p:0.001) performed with all variables by the backward elimination method. The education level and age variables remained in the model. The results of the regression analysis are shown in Table 3.
Discussion
Based on the results of our study, we comprehended that OCD group patients exhibited a significantly higher belief in sexual myths compared to both groups. According to a study, people with a higher sensation of responsibility and higher levels of perfectionism are more likely to believe in sexual myths [12]. Furthermore, many studies have shown that OCD patients have a high sense of responsibility and perfectionism [13]. OCD patients, known for their perfectionism, may be more prone to endorsing sexual myths.
Our study also revealed that OCD patients received less sexual education compared to HC. Previous research in the literature has consistently highlighted the role of sexual education in the formation of sexual myths, emphasizing that limited knowledge or misinformation plays a crucial role [14, 15]. Hence, the significant increase in belief in sexual myths among our OCD group may be associated with their limited access to sexual education, resulting in a higher belief in sexual myths.
Existing literature demonstrates a clear relationship between OCD and poorer sexual performance, increased sexual dysfunction, and limited sexual satisfaction [16]. Numerous research studies have consistently shown the negative impact of OCD on sexual functions and sexual satisfaction [17- 19]. Our study also found that the OCD group exhibited lower levels of sexual satisfaction when compared to the control groups.
The use of drugs in OCD patients has been identified as a potential contributor to sexual dysfunction and decreased sexual satisfaction [20]. However, some studies have stated that OCD patients who use drugs show worse sexual function independent of the drug effect [18]. In our study, the observation that the OCD group had lower sexual satisfaction than both the anxiety group and the remission control group is significant as it suggests that impaired sexual satisfaction can be attributed to OCD itself, independent of the drug’s influence. Nevertheless, it should be noted that a portion of the decline in sexual satisfaction may be associated with sexual dysfunctions resulting from potential side effects of the medication. Another important consideration is the presence of comorbid depression, anxiety, or other physical illnesses, which can adversely affect sexual functions [4]. Although these conditions were excluded from our study, impaired sexual satisfaction may arise from unidentified illnesses.
Upon reviewing the literature, no previous studies investigating the relationship between sexual myths and sexual satisfaction specifically in OCD patients were found. However, in our study, we observed a significant relationship between sexual myths and the total score of the GRISS, as well as its communication and avoidance sub-dimensions in female OCD patients. Among male OCD patients, a relationship was identified between the avoidance sub-dimension and sexual myths. In a study conducted with healthy individuals, it was revealed that higher sexual myth scores were linked to increased avoidance of sexual intercourse [21]. Another study examining anxiety, sexual myths, and sexual satisfaction demonstrated that as sexual myths increased, total sexual satisfaction scores, as well as scores in sub-dimensions such as avoidance, communication, touch, satisfaction, impotence, premature ejaculation, and vaginismus, also increased [22]. Our study’s findings are valuable as they highlight a higher belief in sexual myths in OCD patients compared to control groups and their detrimental impact on sexual satisfaction.
We showed a relationship between avoidance and sexual myths in both male and female OCD patients. In a study, it was revealed that OCD patients avoid sexuality [17]. Studies on sexual life in OCD patients show that mental contamination negatively affects sexual life [23]. It is known that OCD patients have a disgust sensitivity and it triggers avoidance of sexual life [19]. It is known that an increase in belief in sexual myths can lead to patterns in sexual life, contribute to sexual dysfunctions, and restrict individuals’ expectations regarding sexual experiences. Therefore, it can be inferred that sexual myths are associated with the avoidance of sexual activities.
Correlation analysis results from our study align with findings from previous research conducted in healthy populations and patients with anxiety disorders, highlighting the link between sexual myths and sexual satisfaction [21, 22]. However, this relationship could not be observed in male OCD patient groups. In these groups, factors such as medication use, disease burden, and relationship problems may have had a greater impact on sexual satisfaction, overshadowing the influence of sexual myths. Nevertheless, this relationship was consistently demonstrated in all female patient groups and remains consistent with existing studies.
Our analysis revealed that the duration of the disease has a significant impact on sexual satisfaction. In OCD patients, it has been observed that sexual satisfaction tends to decrease as the duration of the disease increases. When considering other sociodemographic and clinical factors, the duration of the disease remains a significant predictor of sexual satisfaction. Longer disease duration is often associated with more severe symptom content in OCD patients [24]. Additionally, a study found that as the duration of the disease increased, patients’ relationship with their environment deteriorated [14]. These findings suggest that a longer disease duration may lead to increased medication use and a greater decline in sexual functioning.
Our analysis results indicated that age and education level have a significant influence on sexual myths, with an increase in age corresponding to a higher belief in sexual myths. This finding aligns with previous studies that have also shown a positive correlation between age and belief in sexual myths [22]. It is recognized that sexual myths can vary with age [15], and older individuals may have been exposed to more traditional and conservative attitudes toward sexuality during their upbringing. Hence, it is likely that older individuals exhibit a more conservative attitude toward sexual experiences.
Furthermore, our study revealed higher belief levels of sexual myths among individuals with lower levels of education. Other studies have similarly found a positive association between lower educational attainment and belief in sexual myths, particularly among individuals with primary and high school education [15, 25]. It could be suggested that higher education levels promote critical thinking, analytical skills, and access to accurate information, leading to a decreased belief in sexual myths.
The study has several limitations. It heavily relies on self-reported evaluations, potentially affecting the accuracy of participants’ responses about their sexual lives due to existing taboos and defensive attitudes. Only patients from an outpatient clinic were included, which might not fully represent the entire population. The inclusion of drug-using patients complicates the analysis due to variations in drug types and doses. The study lacked a standardized method for assessing sexual education and only considered education from families or schools. Moreover, the sexual satisfaction scale used was limited to evaluating heterosexual individuals with partners, excluding non-partnered and non-heterosexual patients from the analysis.
Conclusion
Based on our study findings, we observed that individuals with OCD had lower levels of sexual satisfaction and a higher prevalence of sexual myths compared to those in AD and HC groups. We also identified a negative association between belief in sexual myths and sexual satisfaction in OCD patients. Specifically, certain sub-dimensions of sexual satisfaction were negatively impacted, and sexual myths played a role in this relationship. Given these results, clinicians need to be aware that OCD patients may experience lower levels of sexual satisfaction and that there is a connection between sexual satisfaction and sexual myths.
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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Feyza Yılmaz, Ömer Böke, Pelin Göksel, Ahmet Rifat Şahin, Hatice Özyıldız, Gökhan Sarısoy, Aytül Karabekiroğlu, Selçuk Özdin. Sexual satisfaction and beliefs in sexual myths in patients with obsessive compulsive disorder: A cross-sectional study. Ann Clin Anal Med 2024;15(7):458-462
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Relationship of smartphone use time with cervical range of motion, shoulder-girdle muscle strength, posture, and neck pain in university students
Aysenur Yılmaz 1, Nilufer Cetıslı Korkmaz 2, Esra Dogru Huzmelı 3
1 Department of Physiotherapy and Rehabilitation, Faculty of Health Sciences, Hitit University, Çorum, 2 Department of Physiotherapy and Rehabilitation, Pamukkale University, Denizli, 3 Department of Physiotherapy and Rehabilitation, Faculty of Health Sciences, Hatay Mustafa Kemal University, Hatay, Türkiye
DOI: 10.4328/ACAM.22141 Received: 2024-02-09 Accepted: 2024-04-19 Published Online: 2024-06-04 Printed: 2024-07-01 Ann Clin Anal Med 2024;15(7):463-467
Corresponding Author: Aysenur Yılmaz, Department of Physiotherapy and Rehabilitation, Faculty of Health Sciences, Hitit University, Çorum, Türkiye. E-mail: fzt.aysenurgungor@gmail.com P: +90 543 283 38 19 Corresponding Author ORCID ID: https://orcid.org/0000-0002-2357-0351
Other Authors ORCID ID: Nilufer Cetıslı Korkmaz, https://orcid.org/0000-0003-3471-8240 . Esra Dogru Huzmelı, https://orcid.org/0000-0002-7025-8192
This study was approved by the Ethics Committee of Hatay Mustafa Kemal University Non-Interventional Clinical Research Ethics Committee (Date: 2014-12-23, No:241)
Aim: This study aimed to examine the relationship between smartphone (SP) use time and cervical range of motion, shoulder-girdle muscle strength, posture, and neck pain in university students.
Material and Methods: 100 volunteers were divided into 4 groups according to their duration of use. Postural analysis, goniometric measurements, and manual muscle tests were performed.
Results: When the difference between the groups in terms of neck pain was examined with the VAS-activity results, it was found that the difference was significant (p<0.05). The presence of scoliosis, passive and active neck extension, and neck range of motion (ROM) of passive rotation were found to be significantly different between the groups (p<0.05).
Discussion: Long-term use of SP by young people could trigger neck pain, limit ROM, and cause postural impairments. Therefore, it is important to increase the awareness of individuals to minimize damage to the musculoskeletal system and maintain correct use and posture during SP usage.
Keywords: Smartphone, Pain, Posture, Cervical Range Of Motion, Muscle Strength
Introduction
Technology is developing rapidly to make life easier and meet the needs of the growing global population. It is indisputable that one of the most groundbreaking sectors of technology is mobile telephones. Previously, phones only allowed us to hear another person’s voice, but now they can be used as a computer, music and video player, camera, navigator, and for fast internet access [1]. For these reasons, these smartphones (SP), which meet many needs and are small, are actively and continuously used by many people and have become a basic everyday item that is always with them. The age of SP start-up usage is declining, and the incidence of SP usage reached more than 5.19 billion users worldwide in 2020, with an increase of approximately 124 million (2.4%) each year compared with the previous year ((available at: https://datareportal.com/reports/digital-2020-global-digital-overview). Consequently, this widespread use lays the groundwork for some health problems. Excessive SP use causes various musculoskeletal and physical health problems, such as blurred vision and pain in the wrists and neck [2, 3]. A previous study reported that impaired hand function caused pain in the thumb and decreased finger grip strength [4]. Prolonged and continuous SP usage causes postural changes in the cervical and lumbar vertebrae, and proprioception deficiencies in the cervical region [5]. Upper crossed syndrome develops in individuals who work continuously in a head forward posture, and after the posture begins to deteriorate, an imbalance between the muscles causes pain. The young onset of SP usage also lays the groundwork for the development of upper crossed syndrome [6].
While the person is looking at an SP, the head is in a sustained flexion position for a long period and a spasm develops in the neck muscles. Therefore, if no precautions are taken, current conditions can lead to muscular and bone deformities. If populations are not warned about this, staying in a poor sustained posture becomes a habit, and the pathological disorders of cumulative neck pain negatively affect the activities of daily living (ADL) and reduce the quality of life (QoL) [5, 6].
According to previous research, various etiological, psychosocial, and personal factors play a role in neck pain. Unfortunately, it is another fact that in some cases, the cause cannot be determined. Tasks performed by repeatedly raising the upper limbs and bending the neck forward have been associated with neck pain [7]. Because of neck pain, QoL deteriorates and work efficiency decreases. Considering that increasing numbers of patients create a burden on the healthcare system, neck pain causes both personal and governmental economic burdens. Moreover, neck pain almost seriously affects the psychology of the individual negatively [8]. Among people using an SP, the neck is constantly flexed; however, the elbows are not supported. This can cause an excessive static load on the neck and shoulder areas. In addition, SPs are often held with one hand and controlled with one finger. These repetitive movements cause microtraumas in the musculoskeletal system, resulting in chronic pain, paresthesia, and weakness in the neck and upper extremities over time [9]. In a study conducted with students, SP use and the relationship between the musculoskeletal system were examined, and almost half of the participants reported shoulder pain [10].
In this respect, recent studies of SP usage have examined psychological well-being and the social and psychosocial dimensions of the individual, such as the level of loneliness. However, although there are very few scientific studies in the literature that examine the relationship between SP usage time and the musculoskeletal system, there are no studies addressing shoulder-girdle muscle strength in university students [11]. Therefore, this study aimed to examine the relationship between SP usage time and normal range of motion, shoulder-girdle muscle strength, posture, and neck pain in university students.
Material and Methods
Participants
The study included 100 university students between the ages of 18 and 26 years, who were using SP. To determine the relationship between SP usage and neck pain, subjects with any neck pathology were excluded. All participants gave written informed consent before participation after receiving information about the study protocol, which conformed to the standards for human experiments set by the Declaration of Helsinki.
Measurements
To determine the use time of SP in a day, and the duration and severity of neck pain at the end of the day, face-to-face interviews and assessments were performed. Demographic information was recorded for each subject.
The study participants were separated into four groups according to SP use time. The visual analog scale (VAS), manual muscle test, postural analysis, and ROM assessments were performed in a sequence. VAS was used to determine the severity of pain during rest, activities, and SP usage [12]. The muscles in the neck and shoulder girdle were evaluated manually [13]. Posture analysis was performed using a plump line and observation from the anterior, lateral, and posterior sides to determine the postural changes, especially in the spine, head, shoulders, and chest region [14]. To evaluate ROM, flexion-extension, right-left lateral flexion, and rotation movements of the cervical region were measured using a universal goniometer [15].
Statistical analysis
The statistical package SPSS 21.00 for Windows (SPSS Inc., Chicago, IL, USA) was used for statistical analysis. Descriptive statistics were used to describe the characteristics of the participants. All continuous variables were evaluated for normality using the Kolmogorov–Smirnov test. To determine the differences between the 4 groups, an ANOVA test was used. Correlation analysis was performed using the Spearman Correlation Analysis method. The level of correlation was classified as very weak (rho = 0–0.19), weak (rho = 0.2– 0.39), moderate (rho = 0.40–0.59), strong (rho = 0.6– 0.79), and very strong (rho = 0.8–1). In the analyses, p<0.05 was accepted as statistically significant.
Ethical Approval
This study was approved by the Ethics Committee of Hatay Mustafa Kemal University Non-Interventional Clinical Research Ethics Committee (Date: 2014-12-23, No:241).
Results
The demographic characteristics of the groups were also similar (p>0.05, Table 1). It was seen that VAS scores in activity were higher than those in rest. Interestingly, VAS scores were higher in the 61-90 min SP users’ group, both in rest (1.62±1.96) and activity (4.19±1.83), than the other groups. While there was a statistically significant difference between the groups for the neck pain severity in activities, because of the higher scores in the 61-90 min SP users’ group (p<0.05), the neck pain at rest was so low and not different between the groups (p>0.05, Table 2). When the groups were compared with respect to posture, muscle strength, and ROM, statistically significant differences were determined in the more than 90 min SP users’ group with respect to the presence of scoliosis (p<0.05), passive and active ROM of neck extension (p≤0.001), and passive ROM of neck rotation (p<0.05) (Tables 2 and 3).
Discussion
This study examined the relationship between SP use duration and cervical ROM, shoulder-girdle muscle strength, posture, and neck pain in university students. As a result of our study, it was determined that as the duration of SP use increased, the severity of neck pain in activity, presence of scoliosis in posture, neck passive and active extension, and passive rotation ROM were found to be significantly different between the groups, especially in the more than 90 min SP users’ groups. SPs are used in all areas of life and have become a basic need. Although there are undeniable benefits of mobile phones, long-term usage can cause several health problems. SP overuse can lead to problems such as pain in the neck and shoulders, reduced proprioception, postural problems, reduced normal joint movement, increased musculoskeletal system problems, anxiety and depression, and headache [2, 3, 5].
Xie et al. (2015) compared the use of one or both hands when messaging on a telephone and observed high muscle activity in the upper trapezius and cervical erector spinae muscles in young subjects with neck and shoulder pain [16]. In a study, 292 subjects were examined with respect to the duration of SP use, screen size, pain, purpose, and position of use. It was reported that pain developed most in the neck, eyes, and shoulders, and also as screen size increased complaints in the lower back and legs increased, complaints were higher when the telephone was used in a sitting or supine position, used for internet searches and chatting, whereas <2 hours users had the fewest complaints [17]. In the current study, when the subjects were questioned about neck pain during activity, a significant difference was determined between the groups with respect to the VAS at activity scores. It can be considered that pain increased because of muscle fatigue formed by staying in the same position for a long time. It is well-known that muscle fatigue and increased activity of some muscles are a reason for pain in the neck and shoulders. In general, the cervical flexion angle during SP use causes muscle fatigue in the upper trapezius muscle and pain [18].
Factors that increase the presence of scoliosis include prolonged sitting, incorrect posture, working at a desk, pelvis asymmetry, and lower extremity inequality [10]. In this study, while the neck muscle strength results were similar between the groups, it was found that the presence of scoliosis was different, in favor of 61-90 min SP users’ group (18.8%). People generally do not pay attention to their posture while using the SPs. Postural impairments should be prevented from an early ages. In a previous study, changes in cervical spine posture were compared in two groups of young adults with and without mild neck pain when using an SP. In a study by Kim et al. (2015), it was stated that the flexion angle of the cervical spine was significantly higher in the group with mild neck pain during SP use than in the group with no pain [11].
There is no general concept of posture for SP users; different postures could be seen, with the head held in front, and incorrect postures such as rounded shoulders or oblique posture are the most frequently seen postures [10]. It is very difficult to maintain a proper posture while looking at the SP screen for a long time. Continuous and static repetitive movements in the same position reduce blood circulation and prevent nutrients from being delivered to the muscles. Ultimately, it causes fatigue, pain, and musculoskeletal disorders [17]. Neck pain causes postural deformity around the cervical vertebra, and most people with neck pain experience biomechanical changes in the cervical vertebrae due to abnormal posture. Head-forward posture is a common condition in society that occurs when sitting at a desk for a long time. The head-anterior posture causes excessive extension of the cervical spine, which is defined as upper cervical extension and lower cervical flexion [19]. The head-anterior posture causes the sternocleidomastoid, levator scapula, upper trapezius, and posterior cervical extension muscles to be shortened with the weakening of the anterior cervical vertebra muscles [20]. Research has reported that more than 90% of university students adopt a neck flexion posture with protracted shoulders and non-neutral wrist postures on the side where they use pocket devices [21]. Our study was conducted on young adults, in whom these problems are not normally observed. While the presence of head anterior tilt (39.3%) was higher in the more than 90 min SP daily users’ group, the difference was not interestingly significant between the groups. The fact that there is no muscle weakness problem for now, the accumulated stress could damage the musculoskeletal system and then could affect muscle strength in the future. It can be thought that postural defects not formed yet, as the study sample was composed of young university students, who were highly active with dynamic and good muscle strength. However, the manifestation of scoliosis indicates the onset of postural problems that could be huge problems in the future. In order to take precautions, it is important to reduce the time of SP daily use from younger ages and to gain the correct posture. As the anterior tilt of the head increases, the load on the cervical region also increases. In the neutral position of the head, the amount of load carried in the cervical area is an average of 4.5-5.5 kg of the head’s own weight. It is estimated that this load reaches 13.61 kg at 30 degrees. Children, in particular, are at greater risk because their head weight is higher than their body [22].
In a study by Samir et al. (2019), it was reported that there was a significant difference between volunteers using SP for less than 4 h/day and those using SP for more than 4 h/day with respect to neck extension, lateral flexion, and rotation movements [23]. In our study, it was recorded that there was a significant difference between the groups with respect to the ROM of neck rotation and extension. We thought that this could be due to keeping the neck in flexion and rotation to one side in long-term use of the SP, limiting extension and rotation to the other side. It was stated that the students using SP performed an anterior head tilt of 30 degrees on average, whereas it was at most 20 degrees when the students were not using the phone and engaged in other activities [20]. This could be the main cause of limited ROM during extension and rotation. Starting to use mobile telephones at a young age often lays the ground for upper crossed syndrome. Previous studies have shown that the flexion angle of the neck is increased in a normal stance [6, 19]. For this reason, governmental and public health issues should be addressed as soon as possible in order to increase awareness of the proper position and daily usage time of SP.
This study was conducted before the COVID-19 pandemic lockdowns, during which all education methods were applied using distance and online teaching approaches. As a result, most students had to use SP for extremely long periods. Future studies are needed that focus on the musculoskeletal, pain, and postural problems associated with the increased daily use of SP following the COVID-19 pandemic. In addition, it is important to prevent problems that will arise with prolonged and long-term use by regulating the duration of use.
Limitation
Our study sample number was higher than the samples in the literature; however, it has limitations in grouping the same number of participants in groups and including the participants with higher daily use duration. In future studies, different body regions and more bio-psycho-social parameters could be handled with longer daily use durations and long-term follow-ups.
Conclusions
In conclusion, prolonged daily SP use by young people can trigger neck pain, and cause postural impairments and limitation in normal range of movements. Using SP for longer durations causes restricted movement in the neck over time, which could lead to muscle strength imbalance in the future and make these individuals vulnerable to neck and musculoskeletal pathologies. Although the users are young and healthy, awareness of the negative effects of SP usage with longer durations and incorrect postures as well as preventive methods should be increased with governmental, public health, and community-based rehabilitation approaches.
Acknowledgment
The authors would like to thank all the university students who participated in this study. Special thanks to the physiotherapists Ayse CELIK and Merve ERKASKA for their kind assistance in collecting the data of the university students.
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: A bursary for Ayse CELIK and Merve ERKASKA was received from TÜBİTAK-BIDEB – 1919B011501881.
Conflict of Interest
The authors declare that there is no conflict of interest.
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Aysenur Yılmaz, Nilufer Cetıslı Korkmaz, Esra Dogru Huzmelı. Relationship of smartphone use time with cervical range of motion, shoulder-girdle muscle strength, posture, and neck pain in university students. Ann Clin Anal Med 2024;15(7):463-467
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The correlation between mentalization, internalized stigma and functioning in bipolar disorder patients
Neşe Burcu Bal 1, Ali Çayköylü 2
1 Department of Psychiatry, Abdurrahman Yurtaslan Ankara Training and Research Hospital, 2 Department of Psychiatry, Faculty of Medicine, Yıldırım Beyazıt University, Ankara, Türkiye
DOI: 10.4328/ACAM.22153 Received: 2024-02-18 Accepted: 2024-04-02 Published Online: 2024-05-09 Printed: 2024-07-01 Ann Clin Anal Med 2024;15(7):468-472
Corresponding Author: Neşe Burcu Bal, Department of Psychiatry, Abdurrahman Yurtaslan Ankara Training and Research Hospital, Ankara, Türkiye. E-mail: neseburcutepe@gmail.com P: +90 507 375 25 11 Corresponding Author ORCID ID: https://orcid.org/0000-0002-6445-9393
Other Author ORCID ID: Ali Çayköylü, https://orcid.org/0000-0003-1586-9334
This study was approved by the Ethics Committee of SBÜ Dr. Abdurrahman Yurtaslan Ankara Oncology SUAM Non-Interventional Clinical Research (Date: 2022-02-10, No: 2022/-01/39)
Aim: This study aims to investigate the effects of mentalizing disorder and internalized stigma on patients’ functioning in patients with bipolar disorder (BD).
Material and Methods: Our study was conducted on a total of 75 patients in remission diagnosed with BD Type 1 according to DSM-5 diagnostic criteria who applied to Ankara Oncology Hospital Bipolar Disorders outpatient clinic in 2023. Sociodemographic data form, Hamilton Depression Rating Scale (HDRS), The Young Mania Rating Scale (YMRS), The Reading the Mind in the Eyes Test (RMET), Functional Assessment Short Test (FAST), and Internalized Stigma of Mental Illness Scale (ISMI) were administered to the participants.
Results: In the study, no correlation was found between ISMI and RMET scores and functioning. A significant correlation was found between the HDRS scores and the total scores of the FAST (r=0.266 p<0.05). In addition, those who used alcohol or drugs were significantly higher than those who did not, those who did not have a regular job were significantly higher than those who did, and those who had a lifetime history of suicide attempts were significantly higher than those who did not (p<0.05).
Discussion: Internalized stigma and mentalization levels do not affect functionality in patients with BD during remission. However, subthreshold depression symptoms, alcohol and substance abuse, and suicide attempts in the past may negatively affect the functioning of these patients even in the remission period, so it is important to evaluate these conditions carefully.
Keywords: Bipolar Disorder, Mentalization, Internalized Stigma, Functioning
Introduction
Bipolar disorder is recognised as a psychiatric disorder characterised by emotional fluctuations and mood swings [1, 2]. Patients diagnosed with bipolar disorder alternate between episodes of mania and depression, which requires them to cope with a wide range of psychosocial challenges at different periods of their lives. However, they struggle not only with these challenges but also with bipolar disorder itself [3].
In recent years, it has been observed that bipolar disorder patients’ mentalizing deficits further complicate this situation. Mentalizing involves the ability to understand other people’s thoughts, feelings and intentions and is important in social interactions. It has been reported that bipolar disorder patients may also have mentalizing deficits especially during mood episodes, and even during remission periods, this situation causes impairment in functionality [4] Bodnar and Rybakowski [5] reported that deficits in mentalizing among Bipolar I patients were significantly associated with cognitive impairments, predominantly during depressive episodes. Inanc et al. [6] revealed the existence of a relationship between mentalization and stigma perception. Pal et al. [7] reported that high levels of internalized stigma have negative effects such as social withdrawal, poor functioning and poor quality of life. Cerit et al. [8] stated that internalized stigma has a fundamental role in predicting functionality. Different studies conducted in patients with bipolar disorder consistently confirm the effects of mentalizing deficits and internalized stigma on functioning. These studies indicate the existence of a complex relationship between these three entities in bipolar disorder patients.
This study investigates the effects of mentalizing deficits and internalized stigma in patients with bipolar disorder on patients’ functioning. Internalized stigma means judging one’s own condition or symptoms in a negative way and identifying these negative judgements with one’s own identity, [9] while functioning includes the ability to perform tasks and activities related to different life domains [10]. Due to mentalization disorders, bipolar disorder may cause patients to stigmatise themselves and may cause patients to experience problems in the areas of work, education, social relationships and personal life. As a result of this situation, patients’ compliance and response to treatment may be prolonged. Our research aims to provide new perspectives on clinical practice and treatment strategies in this field and to help patients with bipolar disorder achieve a better quality of life.
Material and Methods
Participants
In our study, a total of 75 patients who applied to the Bipolar Disorders Branch outpatient clinic of Ankara Oncology Hospital in 2023 and were diagnosed with Bipolar Disorder Type 1 in accordance with the Diagnostic and Statistical Manual (DSM-5) diagnostic criteria were included in the study. These patients were selected from those with Young Mania Rating Scale (YMRS) scores below 7 and Hamilton Depression Rating Scale (HDRS) scores below 7. Participants were given detailed information about the study and written informed consent was obtained from the patients who agreed to participate. Patients were selected among individuals who met the inclusion criteria. Inclusion criteria included being between the ages of 18 and 65, meeting the diagnosis of Bipolar Disorder 1 according to DSM-5 diagnostic criteria, having the mental and physical abilities to adapt to the research protocol, giving written consent, and having at least 8 years of basic education. Those who were diagnosed with mental retardation or severe cognitive impairment, pervasive developmental disorder, social phobia or personality disorder, those who had a history of neurological or medical disease causing significant sequelae, those who could not perform the tests due to hearing or visual problems, and those who did not have at least 8 years of basic education were excluded from the study.
Data Collection
Socio-demographic Data Form
The questionnaire developed by the researcher was used to determine the disease characteristics and demographic information of the participants.
The Functioning Assessment Short Test (FAST)
The Functioning Assessment Short Test (FAST) is a scale developed by Rosa et al. [11] to assess functioning difficulties. It consists of 24 items and is administered and graded by interviewers using a four-point Likert-type scale. The FAST was adapted into Turkish by Aydemir and Uykur [12] and reliability analyses showed high internal consistency (Cronbach’s alpha = 0.960) and test-retest reliability (0.945). Validity analysis revealed five factors related to social activities, occupational functioning, autonomy, cognitive functioning, and financial issues. Confirmatory factor analysis indicated good fit (comparative fit index = 0.912, RMSEA = 0.085). Convergent validity was assessed by correlating the FAST with the related subscales of the BCI, showing a weak to moderate correlation. The FAST was also able to differentiate between symptomatic patients, recovered patients, and healthy controls, with an area under the ROC curve of 0.824. Overall, the FAST is a reliable and valid tool for assessing functioning difficulties.
The Internalised Stigma of Mental Illness Scale (ISIS)
The Internalised Stigma of Mental Illness Scale (ISIS) is a self-report scale developed by Ritsher et al. [13] in 2003 to assess internalised stigmatisation related to mental illness. The scale consists of 29 items and has been adapted into Turkish by Ersoy and Varan in 2007 [14]. The reliability of the scale was assessed using Cronbach’s alpha coefficients, which ranged from .63 to .87 for the subscales and .93 for the whole scale. In terms of convergent validity, the total score of the RHIDÖ scale was found to be significantly correlated with scores from various measures, including the Beck Depression Inventory, Rosenberg Self-Esteem Scale, Sociotropy-Autonomy Scale, Brief Symptom Inventory, Multidimensional Perceived Social Support Scale, Clinical Global Impression Scale, and General Assessment of Functioning Scale, in the expected direction.
Reading the Mind in the Eyes Test (RMET)
A Turkish adaptation study was conducted by Yildirim et al. [15] the 34-question Turkish adaptation was applied to 117 healthy volunteers, and 70 of the volunteers were retested two weeks later. Test-test repeat reliability was analysed by the Bland and Altman method. When items 19 and 21 with low reliability coefficients were excluded, the mean correct responses were 23.64 (SD=3.38) and 23.40 (SD=4.32), respectively. It was concluded that the 32-question test can be used to assess the theory of mind and emotion recognition skills in adults.
The Hamilton Depression Rating Scale (HDRS)
The Hamilton Depression Rating Scale (HDRS or Ham-D) is a widely used tool for assessing depression, consisting of 17 items (HDRS17) focused on symptoms from the past week. Originally intended for hospitalized patients, it emphasizes melancholic and physical manifestations. A 21-item version (HDRS21) adds items for subtyping depression, occasionally misused for severity assessment. While widely employed, HDRS has limitations, excluding atypical symptoms like hypersomnia and hyperphagia [16].
The Young Mania Rating Scale (YMRS)
The Young Mania Rating Scale (YMRS) is a brief and widely accepted tool for evaluating manic symptoms. Comprising 11 items, it assesses a patient’s condition over the last 48 hours, incorporating clinical observations. Items, aligned with mania core symptoms, are rated on severity (four items: 0-8, seven items: 0-4). In severe cases, the former items carry more weight to account for lack of cooperation. Descriptive anchors define each severity level, permitting full or half point ratings. YMRS baseline scores may vary based on patient characteristics. Noteworthy for its brevity and ease of use, the scale is widely embraced in clinical settings [17].
Statistics
Descriptive statistics for continuous data were used to analyse the distribution of the data. These statistics include mean, standard deviation, median, minimum and maximum values that show the centre and spread of the data distribution. For discrete data, percentage values were presented. Shapiro-Wilk test was used to evaluate the suitability of the data for normal distribution. Mann Whitney U test for independent variables with two groups and Kruskal Wallis Analysis of Variance for independent variables with more than two groups were used to evaluate the relationship between scale scores and independent variables. The Spearman Correlation Coefficient was used to determine the relationship between the scale scores. Multivariate linear regression model was used to determine the effective variables to explain the FAST scale scores. All analyses were performed using IBM SPSS for Windows 20.0 (SPSS Inc. Chicago, IL) and p<0.05 was accepted as a statistical significance level.
Ethical Approval
This study was approved by SBÜ Dr. Abdurrahman Yurtaslan Ankara Oncology SUAM Non-Interventional Clinical Research Ethics Committee (Date: 2022-02-10, No: 2022/-01/39).
Results
There was no correlation discovered between age, disease characteristics, and FAST Total scores (p>0.05). However, a positive correlation was noted between HDRS scores and FAST Total scores (r=0.266 p<0.05). The investigation found no connection between ISIS Total and ISIS sub-dimension scores, and FAST Total scores (p>0.05). Similarly, no correlation was detected between RMET scores and FAST Total scores (p>0.05) (Table 1).
Table 1. Correlations Between Age, Disease Characteristics, Scale Scores and FAST Total Scores of Patients
FAST scores did not differ significantly according to gender, educational level, marital status or living area groups (p>0.05). However, a significant difference in FAST scores was observed between employment status groups; patients who worked regularly had significantly lower scores than those who did not work (p=0.013). In addition, FAST scores differed significantly between patients who used alcohol or drugs and those who did not, with the former having higher scores (p<0.05), but there was no significant difference in FAST scores between patients with and without comorbidities (p>0.05). There is a significant difference between patients with and without a history of lifetime suicide attempts (p<0.05). The mean FAST score of patients with a history of lifetime suicide attempt was 19.11 ± 9.88, while this score was 13.42 ± 9.41 in patients without a history of lifetime suicide attempts. This suggests that patients with a history of lifetime suicide attempts have lower functioning and higher FAST scores (Table 2). The variables included in the model for the total score of the FAST were not found to be significant (R² =0.100, F=1.919, p=0.117) (Table 3).
Discussion
In our study, we examined the effect of mentalizing and internalized stigma levels on the functioning of patients with bipolar disorder in remission. Our findings show that these two factors do not significantly affect functioning. A striking point in our study is that the majority of our sample consisted of individuals with at least 8 years of education. As it is known, increasing education level will contribute to the development of mentalizing skills. This may explain why the functionality of this sample is high. In addition, regular follow-up of these patients in the outpatient clinic and psycho-education and family support may positively affect functionality. Therefore, we think that their level of internalized stigma may be low.
Another important finding of our study indicates that subthreshold depression symptoms and even suicide attempts may negatively affect functioning even in remission. This is an important finding not only for patients with bipolar disorder but also for the design and orientation of services in the field of mental health in general.
In the study conducted by Can and Tanrıverdi [18] a significant negative relationship was found between patients’ internalized stigma levels and their social functioning. Yanos et al. [19] reported that change in self-stigmatization was significantly negatively associated with change in social functioning and control of negative symptoms. Picco et al. [20] reported that there was no significant socio-demographic or clinical correlation with internalized stigma. The results of independent studies in the literature indicate that internalized stigma may be an effective factor in individuals’ social functioning, but this effect may vary depending on various factors. Gustemps et al. [21] also revealed in their study that adults with Obsessive-Compulsive Disorder (OCD) exhibit different functional impairment profiles depending on their age. According to the results of this study, younger patients experience more functional impairment in the field of autonomy, while older patients face more difficulties in interpersonal relationships. In Rosa et al. [22] study, bipolar patients exhibited worse functioning in all domains of the FAST. Four variables were found to be associated with poorer functioning: advancing age, depressive symptoms, number of previous mixed episodes and number of previous hospitalisations. Icick et al. [23] reported that among patients diagnosed with BD, those with the comorbidity of alcohol use disorder (AUD) exhibited a more severe clinical profile than those without AUD. In our study, we observed a similar relationship in participants with subthreshold depressive symptoms. Although there was no diagnosis of AUD in our sample, we observed that the level of functioning was significantly lower in individuals with alcohol use. These results, together with other factors mentioned in the literature, are important in terms of showing the complexity of various variables affecting functioning in individuals with bipolar disorder.
Another important finding in our study was the FAST scores between patients with and without suicide attempts. FAST scores were found to be higher in patients who attempted suicide. Literature It has been reported that suicide is an important source of illness burden in bipolar disorder [24,25]. Suicide attempts often negatively affect the functionality of individuals. Physical and emotional health may be severely damaged after such attempts, which may lead to an increase in FAST scores. Furthermore, suicide attempts are often associated with challenging life events or intense emotional stress, which may reduce functioning.
Conclusion
This study analyzed factors influencing the functionality of bipolar disorder patients. Sociodemographic factors like age, disease characteristics, education, marital status, living areas, psychiatric diagnoses, psychotic features, movement disorders, and side effects showed no direct impact. However, employment status, alcohol/substance use, and suicide attempts significantly affected functioning, underlining the disorder’s complexity. Suicide risk and substance use emerged as crucial determinants. These findings underscore the necessity for more research, tailored treatment strategies, and individualized approaches for bipolar disorder 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 compareable ethical standards.
Funding: None
Conflict of Interest
The authors declare that there is no conflict of interest.
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Neşe Burcu Bal,Ali Çayköylü. The correlation between mentalization, internalized stigma and functioning in bipolar disorder patients. Ann Clin Anal Med 2024;15(7):468-472
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Association of first trimester maternal serum ferritin, vitamin D, folic acid, vitamin B12 levels and pregnancy losses
Berkay Soyupak, Gül Özel Doğan, Alev Atış Aydın
Department of Gynecology and Obstetrics, University of Health Sciences, Sisli Hamidiye Etfal Education and Research Hospital, Istanbul, Türkiye
DOI: 10.4328/ACAM.22155 Received: 2024-02-23 Accepted: 2024-04-19 Published Online: 2024-05-05 Printed: 2024-07-01 Ann Clin Anal Med 2024;15(7):473-478
Corresponding Author: Gül Özel Doğan, Department of Gynecology and Obstetrics, University of Health Sciences, Sisli Hamidiye Etfal Education and Research Hospital, 34371, Istanbul, Türkiye. E-mail: dr.gulozel@hotmail.com P: +90 530 142 88 76 Corresponding Author ORCID ID: https://orcid.org/0000-0001-9555-1128
Other Authors ORCID ID: Berkay Soyupak, https://orcid.org/0000-0003-0907-8608 . Alev Atış Aydın, https://orcid.org/0000-0002-8504-5755
This study was approved by the Ethics Committee of the University of Health Sciences, Sisli Hamidiye Etfal Training and Research Hospital (Date: 2023-02-21, No: 2243)
Aim: Supplementing women with vitamins in early pregnancy is reported to prevent miscarriage, as micronutrient deficiencies have been linked to an increased risk of fetal loss. The objectives of this study were to determine the effectiveness and protective features of serum ferritin, Vitamin D, folic acid, and Vitamin B12 levels on miscarriage to provide a basis for clinically targeted therapy.
Material and Methods: The results of 88 pregnant women between 5-14 gestational weeks and 88 healthy pregnant women at the same gestational weeks were compared. The demographic and pregnancy characteristics of all pregnant women were recorded. Ferritin, Vitamin B12, folic acid, and Vitamin D levels were measured in serum samples obtained from the patient and control groups at similar weeks.
Results: Vitamin B12, folic acid, and ferritin serum levels were significantly lower in women with miscarriage than the control group (p=0.019, p<0.001, p<0.001, retrospectively). Vitamin D levels did not show a statistical difference among both groups (p>0.05). Logistic regression analysis showed that Vitamin B12 and ferritin levels within normal limits were found to be protective factors against miscarriage (p=0.043, OR=0.451; p=0.020, OR=0.395); however, folic acid and Vitamin D levels were not protective factors. Ferritin levels of women with missed abortions were detected significantly lower than women with spontaneous abortion (p=0.017).
Discussion: Our results indicated that the first trimester levels of maternal vitamin B12, folic acid, and ferritin were linked to fetal loss; however, there was insufficient evidence to support a link between maternal vitamin D levels and fetal loss.
Keywords: Pregnancy, Abortion, Vitamin Deficiency, Ferritin, Dietary Supplements
Introduction
The first trimester of pregnancy marks a crucial period characterized by rapid fetal development and physiological changes within the maternal body. Central to this developmental journey are essential vitamins and minerals such as Vitamin D, iron, folic acid, and Vitamin B12, each playing pivotal roles in supporting maternal health and fetal growth. Deficiencies in these micronutrients during early pregnancy have been closely linked to an increased risk of miscarriages. Understanding the intricate interplay between these micronutrients is paramount in elucidating potential preventive strategies to safeguard maternal and fetal well-being [1].
A Cochrane meta-analysis on vitamin supplementation for preventing miscarriage research suggests that there is insufficient evidence to examine the effects of different combinations of vitamins on miscarriage and miscarriage-related outcomes [2]. However, it is reported that unfavorable pregnancy issues such as preterm birth, intrauterine growth restriction, and early miscarriages are all directly related to changes in the mother’s nutritional condition during her pregnancy [3].
Low serum ferritin levels are related to severe reproductive disturbances in women with recurrent pregnancy loss [4]. Because of fetal growth and the expansion of the mother’s blood volume to satisfy the increased oxygen requirements of both the mother and the fetus, there is a higher requirement for iron during pregnancy [5]. In addition to iron, folate and vitamin B12 are extremely essential as they play a crucial role in the biosynthesis of DNA, RNA and proteins, which is critical to the fetus’ development [6]. The requirement of folate increases during pregnancy substantially. Nelen et al. reported that a low serum level of folate might be responsible for recurrent pregnancy losses [7]. Vitamin D deficiency was first linked to bone metabolism, but it has since been linked to anemia and impaired fetal development, among other health issues [1, 8]. These findings suggest that there may be an interaction between micronutrients such as iron, folic acid, Vitamin D and B12 metabolism which may underlie miscarriages and spontaneous abortus. For this reason, vitamin supplementation has been recommended as a miscarriage prevention strategy based on information from observational studies.
A strong link between pregnancy complications and decreased antioxidant defence has been identified in certain research, but some have not found a significant correlation [9, 10]. In our study, considering the possible role of micronutrients in the pathophysiology of fetal loss, we aimed to measure the serum ferritin, vitamin d, folic acid, and vitamin B12 levels in women with miscarriage during the 1st trimester, to compare it with a healthy pregnant control group as this might lead to a better understanding of the association.
Material and Methods
Consecutive patients with pregnancy who were admitted to the gynocology clinic for 3 months from 01.04.2023 to 01.07.2023 were enrolled in this prospective, cross-sectional study.
Participants
Eighty-eight pregnant women with miscariage between 5-14 gestational weeks over 18 years of age and 88 healthy pregnant individuals who were compatible with this group in terms of age, gestational week, and parity were included. All participants, who had a singleton pregnancy, did not receive any prophylactic nutrition supplement at their admission. Patients’ data were recorded in a database that included the clinical and demographical characteristics, hemogram, International Normalized Ratio (INR), serum levels of vitamin B12, Vitamin D, folic acid, and ferritin tests. Both groups were questioned in terms of age, smoking, alcohol consumption, consanguineous marriage and chronic diseases.
The participants did not have any genetic, anatomic abnormalities and endocrine disorders, inflammatory diseases, and maternal-fetal blood group incompatibility. Pregnant women under the age of 18 and over the age of 40, women with autoimmune diseases and chronic diseases related to blood pressure, patients with multiple pregnancies and women with pregnancy loss outside of 5-14 gestational weeks or with a positive fetal heartbeat were excluded.
The gestational week of these patients was calculated according to their last menstrual date. Those included in the study group were divided into two groups as spontaneous abortion (sudden abortion) and missed abortion. The spontaneous abortion group consisted of patients who presented with bleeding and were diagnosed with complete or incomplete abortion. The missed abortion group consisted of anembryonic pregnancies in which the gestational sac was larger than 25 mm and no fetal image was observed and/or patients with a fetal image larger than 7 mm and no fetal heart activity. Ultrasonographic examination was performed by the same physician on all patients.
Collection of Samples
After 8 hours of fasting, morning venous blood samples were collected into vacuum gel tubes to investigate hemogram and INR. Vitamin B12 levels in the samples were measured by chemiluminescence emission technique. The reference range was 197-771 ng/L. 25(OH)D levels were measured by chemiluminescence emission technique. The reference range was taken as <12ug/L vitamin D deficiency, 12-20ug/L vitamin D insufficiency, >20 ug/L adequate/normal. Folic acid levels were measured by chemiluminescence emission technique. The reference range was taken as 3.89-26.8 ug/L. Ferritin levels were measured by chemiluminescence emission technique. The reference range was taken as 13-150 ug/L.
Statistical Analysis
For statistical analysis, the Windows application SPSS 15.0 was utilized. Descriptive statistics were given as numbers and percentages for categorical variables and mean, standard deviation, minimum, maximum, and median for numerical variables. In two independent groups, numerical variables were analyzed by Mann-Whitney U Test. Proportions in the groups were compared with the Chi-Square test. Protective effects were analyzed by Logistic Regression Analysis. The statistical alpha significance level was accepted as p<0.05.
Ethical Approval
This study was approved by the ethics committee of the University of Health Sciences, Sisli Hamidiye Etfal Training and Research Hospital (Date: 2023-02-21, No: 2243) and was performed in accordance with the Declaration of Helsinki. Written informed consent was obtained from all participants.
Results
The ages of the participants ranged between 18 and 40 years, the mean age of women with miscarriage was 31.9 ± 6.4 years and the mean age of healthy pregnant women was 31.5 ± 5.7 years, (p>0.05). The mean gravida, parity and miscarriage frequencies of the study group were significantly higher in the women with miscarriage group; however, the mean gestational week according to the last menstrual period were significantly lower (p=0.005, p=0.017, p=0.014, p<0.001, retrospectively). The two groups did not differ significantly in terms of smoking, consanguineous marriage, or Rh incompatibility (p>0.05). None of the participants had alcohol use and chronic diseases. Table 1 illustrates the demographic and clinical characteristics of patients. Vitamin B12, folic acid, and ferritin seum levels were found to be significantly lower in women with miscarriage group than in the control group (p=0.019, p<0.001, p<0.001, retrospectively). Hemoglobin, folic acid, and INR levels were not significantly different between both groups (p>0.05). However, 25(OH) vitamin D level, 25(OH) vitamin D <12ug/L deficiency ratio, 25(OH) vitamin D 12-20 ug/L insufficiency ratio, and 25(OH) vitamin D >20 ug/L adequate/normal ratio did not show a statistically difference among both groups (Table 2). Logistic regression analysis showed that Vitamin B12 and ferritin levels within normal limits were found to be protective factors (p=0.043, OR=0.451; p=0.020, OR=0.395); however, folic acid and 25(OH) vitamin D levels were not found to be protective factors (p>0.05), (Table 3). The women with miscarriage group was divided into two subgroups: 1- patients with missed abortion, 2- patients with spontaneous abortion. We did not find any statistically meaningful differences in terms of age, gravida, parity, history of abortion, gestational week according to last menstrual period, smoking, consanguineous marriage, and RH incompatibility in subgroups (p>0.05). Vitamin B12, folic acid, and vitamin D levels were not significantly different; however, ferritin levels of women with missed abortion were detected significantly lower than women with spontaneous abortion (p=0.017).
Discussion
The purpose of this study was to assess serum ferritin, vitamin D, folic acid, and vitamin B12 levels in women with miscarriage during the first trimester, to compare it with women with healthy pregnancies. Moreover, we evaluated the levels of these micronutrients and ferritin to detect their association between spontaneous abortion and missed abortion. In this study, which examined miscarriage women and healthy pregnant women with similar demographic and clinical characteristics, serum vitamin B12, folic acid and ferritin levels were found to be significantly lower in women with miscarriage than in healthy controls. Advanced statistical studies showed that ferritin may be a protective factor for pregnancy loss. Additionally, the blood analysis of patients with missed abortion and spontaneous abortion showed that ferritin was significantly lower in the women with the missed abortion subgroup.
Folate is essential for the developing fetus, as it is directly involved in the biosynthesis of DNA, RNA and proteins. In addition to folate deficiency, defective folate metabolism, such as hyperhomocysteinemia and vitamin B12 deficiency, is known to increase the risk of neural tube defects, congenital abnormalities, placental abruption and heart defects [1, 11]. Our results showed that serum Vitamin B12 and folic acid levels of pregnant women diagnosed with miscarriage were significantly lower than healthy pregnants and linear regression studies that conducted in this study found that Vitamin B12 acts as a protective factor from miscarriages. In a study from our country, it was reported that iron and vitamin B12 deficiencies were relatively common in the pregnant population [12]. Research to date has shown a relationship between maternal serum folic acid and Vitamin B12 status and the presence of miscarriage [11, 13]. Zhang et al. reported that folic acid supplements were identified as protective factors for the prevention of missed abortions [14]. A recently published Cochrane review suggests the use of folic acid supplements for pregnant women in low- and middle-income countries [11]. Our results support that vitamin B12 supplementation in addition to folate could be considered for the wellbeing of the fetus where the dietary patterns of women are generally based on vegetables.
Although traditionally associated with maternal and neonatal bone disease, vitamin D deficiency is more common in women who develop major reproductive and obstetric complications such as pre-eclampsia, gestational diabetes, and preterm delivery [1]. The prevalence of hypovitaminosis D among pregnant women in their first trimester was up to 70% [15]. The placenta is a key tissue for Vitamin D accumulation, having important effects on trophoblast invasion, remodeling of placental arteries. These processes are impaired in case of abortion [16, 17]. Vitamin D prevents the occurrence of antiphospholipid syndrome by reducing the expression levels of anti-β2 glycoprotein and tissue factor in cases of recurrent pregnancy loss [18]. There is also an inverse relationship between vitamin D and thyroid peroxidase antibody levels in patients with recurrent pregnancy loss and autoimmune thyroid disease [19]. Research on vitamin D-related diseases in pregnancy has attracted extensive and active research interest because of its complexity in the process of pregnancy. Hou et al. investigated low 25(OH)D vitamin levels in early pregnancy losses [20]. A total of 120 women were included in their study, and their results showed an association between pregnancy loss and low Vitamin D levels. The fact that this study was conducted in China with a different population and average age may have led to different results from our study. Our findings revealed that both women with miscarriage and healthy pregnant groups had low serum Vitamin D levels; however, there was no significant difference in mean serum levels of Vitamin D among both groups. It has been reported that Vitamin D deficiency is common in pregnant women and their neonates even in spring time in Türkiye, generally due to their lifestyle and dietary patterns of the mothers [21]. These issues may explain the reason for low Vitamin D levels in all participants’ results of this study. Ji et al. compared 215 women with recurrent pregnancy loss with 77 women with one or more healthy deliveries. Vitamin D) level was found lower in the group with recurrent pregnancy loss [22]. In this study conducted in China, although the control group remained below the insufficiency limit, the lower level in the group with recurrent pregnancy losses made the result significant. In addition to the research methods that are different from ours, the difference in populations between our study and others may have also affected the results, as the control group in our study also had insufficiency and deficiency of Vitamin D.
Anemia has been associated with many complications, including maternal mortality, stillbirth, preterm birth, low birth weight, small-for-gestational-age birth and other pregnancy complications [1]. Ferritin is a protein whose job is to store iron and serum ferritin concentration reflects body iron stores. It is also an acute-phase reactant and iron-independent synthesis of inflammatory cytokines and oxidative stress increased. Iron is essential for placental and fetal development. Severe iron deficiency can lead to adverse pregnancy outcomes such as increased risk of preterm delivery and fetal loss. In addition to placental and fetal growth, it is required for the expansion of the maternal red blood cell compartment [23]. Georgsen et al. reported that serum ferritin levels are related to pregnancy losses in women with recurrent pregnancy loss [9]. Their results showed that women with repetitive fetal loss had lower serum ferritin compared with women without fertility problems, and reported an inverse association between serum ferritin levels and pregnancy losses, supporting our results. Furthermore, we found that ferritin was important as it was a protective factor against miscarriage. Xu et al. investigated the relationship between pre-pregnancy hemoglobin concentration and the risk of spontaneous abortion in a cohort study conducted on more than 3.9 million women in rural China [24]. Severe anemia and low hemoglobin concentrations before pregnancy were associated with an increased risk of spontaneous abortion. The sample size of this study is a strength; however, serum values obtained 6 months before pregnancy were used, and the use of iron supplements was not noted, which is a weakness. In our study, we excluded individuals taking iron supplements, potentially yielding more realistic results as we observed both hemoglobin and ferritin values during pregnancy. While our study revealed no significant difference in serum hemoglobin values, there was a significant difference in serum ferritin values. It is a known-fact that women with repetitive fetal loss have a greater prevalence of iron deficiency [25]. Our results encourage the evaluation of maternal serum hemoglobin, ferritin and iron levels in the first trimester of pregnancies.
Limitation
Our study has a few limitations. First, it is a hospital based, tertiary clinic study. Second, these women were not followed during pregnancy and further micronutritional status could not be evaluated. The strength of the present study lies in its inclusion of a relatively high number of participants who were not under supplement intake and shared a similar demographic and clinical background. In addition, this study pointed out that there are several problems which need to be clarified and evaluated in further studies regarding micronutritional supplementation during pregnancy in our country.
Conclusion
These results indicated that maternal Vitamin B12, folic acid and ferritin levels in the first trimester were associated with fetal loss; however, we found limited evidence for the association of maternal Vitamin D levels in contrary to up-to-date research data. This suggested that sufficient maternal Vitamin B12, folic acid, and iron level was an important factor in improving fetal growth and development. The possibility of interaction among vitamin D levels during pregnancy warrants further research to explore the risk of adverse pregnancy outcomes.
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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A novel predictor behind conventional risk factors of new-onset atrial fibrillation after off-pump coronary artery bypass graft surgery: The triglyceride-glucose index
Ilke Erbay 1, Can Ozkan 2
1 Department of Cardiology, Faculty of Medicine, Karabuk University, Karabuk, 2 Department of Cardiology, University of Health Sciences, Bursa City Hospital, Bursa, Turkey
DOI: 10.4328/ACAM.22156 Received: 2024-02-23 Accepted: 2024-04-02 Published Online: 2024-04-25 Printed: 2024-07-01 Ann Clin Anal Med 2024;15(7):479-484
Corresponding Author: Ilke Erbay, Department of Cardiology, Faculty of Medicine, Karabuk University, Karabuk, Turkey. E-mail: ilkeerbay@gmail.com P: +90 535 385 59 91
Corresponding Author ORCID ID: https://orcid.org/0000-0002-6817-4686
Other Authors ORCID ID: Can Ozkan, https://orcid.org/0000-0001-6255-711X
This study was approved by the Ethics Committee of Karabuk University (Date: 2022-12-19, No: 2022/1171)
Aim: Atrial fibrillation (AF), which frequently occurs after coronary artery bypass graft surgery (CABG), raises the risk of adverse events such as stroke and heart failure. Insulin resistance (IR) is a major risk factor for developing postoperative AF (POAF), and the triglyceride-glucose (TyG) index offers a more precise and reliable assessment of IR compared to the homeostasis model. This study investigated the correlation between preoperative TyG index levels and POAF in patients undergoing off-pump CABG.
Material and Methods: Four hundred sixteen patients undergoing isolated off-pump CABG were included in the study. The preoperative TyG index and the presence of POAF were evaluated in all patients. Significant variables (P<0.05) from univariate analysis were included in multivariate logistic regression to identify potential POAF risk factors. The TyG index’s predictive efficacy for POAF was assessed in two models: one with conventional risk factors and the other adding the TyG index.
Results: POAF was detected in 106 patients (25.5%), with significantly higher TyG index levels observed in POAF patients compared to those without POAF [9.8 (8.0-11.7) vs. 9.0 (7.7-11.1), P<0.001]. The TyG index was found to be an independent predictor of POAF (P<0.001) with moderate predictive power (AUC=0.767). Adding the TyG index to the model, which included age and left atrial diameter, significantly improved its predictive capacity for POAF (P=0.038).
Discussion: In our retrospective study, we identified the TyG index as an independent predictor of POAF in patients undergoing off-pump CABG.
Keywords: Triglyceride-Glucose Index, Atrial Fibrillation, Off-Pump, Coronary Artery Bypass Grafting, Insulin Resistance
Introduction
Atrial fibrillation (AF) is the prevailing arrhythmia that manifests after coronary artery bypass graft surgery (CABG), and is present in approximately 33% of cases, typically within the first few days after the procedure. Noteworthy risk factors, including advanced age, impaired ventricular function, hypertension, and left atrial dilatation, are closely linked to the development of postoperative AF (POAF) [1, 2]. However, it may be crucial to identify high-risk patients for POAF before CABG, as it enables preoperative preventive measures and evaluation of modifiable risk factors.
Insulin resistance is associated with inflammation and oxidative stress, which have been identified as contributing factors in the remodeling of the left atrium. Studies have shown IR is a recognized risk factor for developing POAF following CABG [3, 4]. However, there remains a gap in a practical and accessible clinical tool that can predict the AF after CABG and provide insights into IR.
The hyperglycemic-hyperinsulinemic clamp test is the reference method for evaluating IR in clinical settings. Although this test provides a comprehensive examination of IR by accurately measuring the insulin sensitivity of peripheral tissues, given the difficulties in conducting the hyperglycemic-hyperinsulinemic clamp test, the homeostasis model is often employed as a convenient option for evaluating IR in clinical practice [5]. However, this test has limitations because of the need to measure fasting blood insulin [5], which is not routinely conducted. In the context of evaluating IR, the triglyceride-glucose (TyG) index, which can be conveniently emanated from triglyceride and glucose measurements, may offer a more accurate and reliable assessment compared to the traditional homeostasis model [6, 7]. The primary focus of this study was to investigate the association between preoperative TyG index levels and the development of POAF in patients undergoing off-pump CABG.
Material and Methods
Study Population
This retrospective cross-sectional study enrolled 515 patients who received off-pump CABG at the Department of Cardiovascular Surgery, from January 2015 to November 2022 and had no previous history of AF. The inclusion criteria included being 18 years or older, undergoing their first off-pump CABG procedure after acute coronary syndrome or elective coronary angiography, and having normal sinus rhythm. The decision to focus specifically on the off-pump CABG technique was made to minimize confounding factors related to different surgical approaches based on the higher prevalence of its use in our clinic. Exclusion criteria included a history of high-degree heart block or permanent pacemaker placement, cardiogenic shock, left atrial diameter ≥55mm, severe valve pathologies (stenosis or regurgitation), previous paroxysmal AF attacks, prior amiodarone treatment, autoimmune diseases, malignancy, pregnancy, hyperthyroidism, chronic kidney failure patients receiving hemodialysis or peritoneal dialysis, advanced stage liver disease, and the need for additional procedures such as valvular surgery or left ventricular aneurysmectomy. As a primary outcome, we evaluated the occurrence of POAF during the hospitalization period.
Surgical technique and procedural strategies
For all patients, the surgical technique chosen was off-pump CABG. All patients underwent off-pump CABG surgery through midline sternotomy using standard surgical techniques. Saphenous vein grafts were harvested for conduit, and internal mammary artery grafts were utilized in most patients (93.5%).
Potassium levels were closely monitored and maintained within the 4.0-4.5 mEq/L range. As part of our clinic’s standard postoperative protocol, all patients received oral metoprolol succinate tablets ranging from 25 to 200 mg to maintain heart rates below 80 bpm.
Laboratory assessments
The demographic and clinical characteristics and the preoperative triglyceride and glucose values were meticulously obtained by thoroughly reviewing the patients’ medical charts. Before the operation morning, all patients underwent standard laboratory tests following a minimum 8-hour period of fasting. Fasting serum triglyceride and glucose levels were measured using an automated analyzer, specifically the Roche Cobas 8000 (Roche Diagnostics, Mannheim, Germany), and the TyG index calculated as ln [fasting TG (mg/dL) × fasting plasma glucose (mg/dL)/2].
Cardiac rhythm evaluation
Cardiac rhythm assessment was performed using bedside monitors and twelve-lead electrocardiograms (ECGs) immediately after the surgery and daily until patients were discharged. All ECGs recordings obtained from patient files and clinical observation records were used. Postoperative atrial fibrillation was described as AF lasting at least 5 minutes or requiring cardioversion with electrical or antiarrhythmic drugs.
Echocardiographic measurements
All patients underwent transthoracic echocardiography using a Philips EPIQ 7C ultrasound machine with a S5-1 transthoracic probe. The echocardiographic evaluation included measurements of left atrial anteroposterior diameter, ejection fraction, and assessment of valve pathologies.
Statistical Analysis
The Kolmogorov-Smirnov test evaluated the distribution of the data’s normality, and variables were shown as percentages (%), means with standard deviations (±), and medians with minimum and maximum values (min-max). Group comparisons of continuous variables were conducted using independent sample t-tests or Mann-Whitney U tests, as appropriate. Categorical variables were evaluated under the chi-square test. The threshold for the TyG index in predicting POAF was determined using Receiver Operating Characteristic (ROC) analysis. To identify potential risk factors for POAF, significant variables from the univariate analysis (P-value <0.05) were included in the multivariate logistic regression models. The backward method was employed for all regression analyses. The predictive performance of the TyG index for POAF was compared between two models: one included conventional risk factors reported in the literature, while the other conventional risk factors plus the TyG index. A value of P<0.05 was used to determine statistical significance, and IBM SPSS Statistics version 26 software (IBM Corp., Armonk, NY) was used for all statistical analyses.
Ethical Approval
This study was approved by the Ethics Committee of Karabuk University (Date: 2022-12-19, No: 2022/1171).
Results
Of the 515 patients at baseline, 56 were excluded because of missing pre-CABG triglyceride values, 23 did not meet the diagnostic criteria for AF episodes, and 20 did not meet the other criteria, leaving 416 patients in the analysis (Figure 1). The study patients’ demographic characteristics, echocardiographic findings, and laboratory results are presented in Table 1. The study included predominantly male participants (78.1%) with a median age of 64 years (40-86). Following the surgery, POAF was identified in 106 patients (25.5%). The POAF group had higher TyG index figures in comparison to those without POAF [9.8 (8.0-11.7) vs. 9.0 (7.7-11.1), P<0.001].
Patients with POAF had a higher body mass index [29.4 (19.7-51.0) vs. 27.8 (17.0-44.1) kg/m2, P=0.010], and a higher prevalence of hyperlipidemia (P=0.029), hypertension (P<0.001), and diabetes (P=0.002) compared to those without POAF.
Patients with POAF had greater left atrial anteroposterior diameter (41.6 ± 4.2 vs. 37.4 ± 3.5 mm, P<0.001) and lowered ejection fraction (EF) values (49.7 ± 9.7 vs. 53.3 ± 8.9 %, P=0.001). However, no notable correlations were encountered between POAF and the presence of mild or moderate mitral regurgitation (P=0.057). Compared to patients without POAF, those with POAF experienced prolonged durations of mechanical ventilation [9.0 (2.0–39.0) vs. 7.0 (3.5–46.0) hours, P<0.001] and postoperative periods in the intensive care unit [4 (1–29) vs. 3 (1–12) day, P<0.001] (Table 1).
The relationship between the TyG index and AF in individuals with and without diabetes has yielded varied findings in previous studies [8-10]. In light of this, we conducted an analysis focusing on the TyG index and its association with AF, considering the patients’ diabetic status. For non-diabetic patients, significantly elevated TyG index values were observed who developed POAF compared to those without POAF [9.5 (8.0-10.4) vs. 8.8 (7.7-9.9), P<0.001]. Additionally, a similar difference in TyG index was observed among diabetic patients who developed POAF compared to those without POAF [10.4 (8.2-11.7) vs. 9.3 (8.3-11.1), P=0.003].
The results of the univariate analysis demonstrated significant associations between POAF and various preoperative variables, including age, hyperlipidemia, diabetes mellitus, hypertension, LVEF, left atrial diameter, mechanical ventilation time, BMI, and TyG index. However, male sex and mild or moderate mitral regurgitation did not show correlations with POAF. The multivariate analysis revealed that age (odds ratio [OR]: 1.047, P=0.025), left atrial diameter (OR: 1.373, P<0.001), and TyG index (OR: 6.824, P<0.001) independently contributed to the risk of POAF, as indicated in Table 2.
The TyG index showed promise as a predictor for POAF, as evidenced by its performance in the receiver operating characteristic (ROC) curve analysis. The TyG index cutoff value of 9.38 demonstrated a sensitivity of 69.8% and a specificity of 30% in identifying patients at risk of POAF. The area under the ROC curve for the TyG index was 0.767 (95% CI: 0.709–0.826, P<0.001), indicating moderate predictive power. Notably, the inclusion of the TyG index in the model, which consisted of age and left atrial diameter, significantly enhanced its predictive capacity for POAF in patients undergoing off-pump CABG (area under the ROC curve: 0.709 (0.663–0.752) vs. 0.774 (0.731–0.813), P=0.038) (Figure 2).
Discussion
To the best of our knowledge, this study is the first to establish the TyG index as a predictor for POAF in patients undergoing isolated off-pump CABG procedures. Our findings, along with the ROC curve analysis, present notable evidence endorsing the TyG index as a reliable predictive tool to identify individuals susceptible to POAF. Moreover, including the TyG index with standard risk factors significantly enhanced our predictive ability for POAF after surgery.
The prevalence of POAF in our study was 25.5%, which closely resembles the reported rate of 24.9% in patients following CABG based on the most up-to-date data [11]. After surgical revascularization, patients who experience POAF tend to have higher postoperative morbidity and mortality rates and extended stays in the intensive care unit and hospitalization [12, 13]. According to our findings, it was revealed that patients with POAF had prolonged mechanical ventilation times and hospitalization. Hence, it may be important to identify patients at high risk for POAF in patients undergoing CABG.
In the study reported by Garg et al. [14], it was stated that either fasting or post-glucose insulin levels as indicators of IR could not predict the risk of AF. Therefore, in indices such as the homeostasis model, which requires fasting insulin levels, the TyG index emerges as an IR indicator that can provide more valuable information regarding cardiovascular events, such as AF [15-17].
The precise mechanism connecting the TyG index to POAF has not been definitively established. However, the TyG index, as an IR marker, holds significant potential in elucidating the underlying factors contributing to the development of POAF. The TyG index formula indicates that a higher TyG index can be attributed to elevated levels of triglycerides or glucose, which in turn is indicative of impaired glucose uptake and utilization, a hallmark characteristic of IR. An animal experiment showed that IR caused changes in atrial structure in rats. It has also been shown that it increases the sensitivity of cells to AF by disrupting the calcium balance within cells because of hyperglycemia [18]. Studies have indicated that irregular handling of calcium ions (Ca2+) is associated with abnormal electrical activity that triggers AF [18, 19]. Given the detrimental effects of hyperglycemia on calcium Ca2+ regulation, it can exert a considerable impact on atrial electrical and structural remodeling, hence contributing to the initiation of AF [20, 21].
Consistent with prior studies, our research demonstrates a robust association between IR and AF [3, 4]. Chen et al. [8] supported the meaningful role of the TyG index as a predictor of AF, serving as a marker for IR. They utilized the TyG index, presented compelling evidence indicating a meaningful correlation between IR and AF, and observed a higher prevalence of AF among hospitalized patients with elevated TyG index values. Notably, the TyG index maintained its independent association with AF, even after adjusting for other predisposing factors [8].
Our study revealed an association between increased TyG index levels and POAF in diabetic and non-diabetic patients. Although this connection has been established in previous research for non-diabetic patients [8, 9], the significant link between the TyG index and AF in diabetic patients remains less extensively explored. Shi et al. [22] conducted a study involving 3244 diabetic patients and found a strong linear correlation between the TyG index and AF prevalence in diabetic patients. Their findings indicated the TyG index’s potential to enhance AF detection among individuals with diabetes. The primary driver of oxidative stress in diabetes is hyperglycemia, which triggers the generation of reactive oxygen species This oxidative stress is implicated in initiating cellular changes within atrial tissue, leading to disturbances in electrical activity—a pivotal factor contributing to the development of POAF [23]. In our study, the TyG index’s predictive efficacy for POAF among diabetic patients might be attributed to its incorporation of high blood glucose levels, a TyG index component, and its association with heightened oxidative stress. This suggests a potential mechanistic pathway through which the TyG index could serve as a valuable prognostic marker for identifying individuals at risk of developing POAF in the context of diabetes.
In patients undergoing cardiac surgery, advanced age has been widely recognized as a primary risk factor for the development of POAF. Additionally, left atrial enlargement has shown a strong correlation with the predictive value for POAF [1, 24]. Therefore, we included age and left atrial diameter as conventional risk factors in our predictive model to assess the TyG index’s ability to predict POAF. Similarly, a study conducted by Wei et al. [25] on patients who underwent septal myectomy found that the TyG index independently predicted the occurrence of POAF. However, unlike their findings, the inclusion of the TyG index in our model significantly enhanced the accuracy of our predictive model, enabling the identification of patients at risk of developing POAF.
Limitation
Our study has certain limitations that should be acknowledged. Firstly, the retrospective design restricted our ability to capture all potential factors that could influence the occurrence of POAF. Additionally, the fasting plasma triglyceride and glucose levels assessment was limited to a single measurement before surgery, preventing us from evaluating the impact of changes in the TyG index on POAF. Lastly, the generalizability of our findings to other cardiac surgical procedures, such as on-pump CABG, may be limited as our study exclusively focused on off-pump CABG patients.
Conclusion
In the patients undergoing off-pump CABG, the TyG index was a notable independent predictor for POAF, regardless of their diabetic status. However, more large-scale multicenter and prospective studies are needed to confirm its efficacy before it can be used 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 compareable ethical standards.
Funding: None
Conflict of Interest
The authors declare that there is no conflict of interest.
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Ilke Erbay, Can Ozkan. A novel predictor behind conventional risk factors of new-onset atrial fibrillation after off-pump coronary artery bypass graft surgery: The triglyceride-glucose index. Ann Clin Anal Med 2024;15(7):479-484
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Damage control surgery and packing in patients with blunt abdominal trauma
Huseyin Kilavuz 1, Feyyaz Gungor 1, Ertugrul Altug 2, Ali Bekraki 1, Sibel Yaman 1, Murat Demir 1, Birkan Bozkurt 1, Idris Kurtulus 1
1 Department of General Surgery, 2 Department of Emergency Medicine, Health Sciences University, Basaksehir Cam and Sakura City Hospital, Istanbul, Turkey
DOI: 10.4328/ACAM.22167 Received: 2024-03-06 Accepted: 2024-05-06 Published Online: 2024-05-23 Printed: 2024-07-01 Ann Clin Anal Med 2024;15(7):485-490
Corresponding Author: Huseyin Kilavuz, Department of General Surgery, Health Sciences University, Basaksehir Cam and Sakura City Hospital, Istanbul, Turkey. E-mail: drhuseyinkilavuz@gmail.com P: +90 212 909 60 00 Corresponding Author ORCID ID: https://orcid.org/0000-0001-8860-0630
Other Authors ORCID ID: Feyyaz Gungor, https://orcid.org/0000-0002-4066-6072 . Ertugrul Altug, https://orcid.org/0000-0001-6807-643X . Ali Bekraki, https://orcid.org/0000-0002-9396-6124 . Sibel Yaman, https://orcid.org/0000-0002-4783-7225 . Murat Demir, https://orcid.org/0000-0003-3097-1441 . Birkan Bozkurt, https://orcid.org/0000-0001-6550-358X . Idris Kurtulus, https://orcid.org/0000-0001-9101-6363
This study was approved by the Ethics Committee of Basaksehir Cam and Sakura City Hospital (Date: 2023-09-04, No:547)
Aim: Blunt abdominal traumas (BAT), which account for a large proportion of traumatic injuries, form a significant proportion of patients in emergency departments and are the leading cause of death in people under 45 years of age. In this study, we aimed to present the results of our patients who were admitted to our emergency department with BAT and underwent packing procedures during damage control laparotomy.
Material and Methods: The patients aged ≥18 years who underwent emergency laparotomy for BAT and underwent packing with damage control surgery between 01.01.2021 and 31.12.2023 in our tertiary care hospital, a level 1 trauma center, were retrospectively analyzed in this study.
Results: Of the15 patients included in the study, 11 (73.3 %) were male. The mean age of the patients was 36.13 ± 1 4.16 years. Traffic accidents and occupational injuries were the most common causes of blunt trauma. The median duration of hospitalization was 14 (1-124) days, and mortality was observed in 3 patients (20%). In 13 patients (87.7%), both ultrasonography and computed tomography imaging were performed. Shock index, Glasgow Coma Scale (GCS), Injury Severity Score (ISS), Revised Trauma Score (RTS), and Trauma and Injury Severity Score (TRISS) values were calculated. The mean ISS was found to be 37.2 ± 9.4.
Discussion: Damage control surgery, which is an essential approach for reducing mortality and morbidity rates in blunt abdominal trauma, remains crucial. The formation of multidisciplinary trauma teams with well-equipped trauma centers is necessary to achieve successful treatment outcomes in trauma patients.
Keywords: Blunt Abdominal Trauma, Damage Control Surgery, Liver Trauma, Trauma Surgery
Introduction
Traumas are the seventh most common cause of death in the general population and among the most common causes of death in the group under 45 years of age. As the third most common anatomical region affected by trauma, abdominal traumas constitute a significant proportion of patients in emergency departments. Abdominal traumas are classified as penetrating and blunt according to their etiology, and blunt abdominal traumas (BAT) constitute the majority with a rate of 85% [1].
The spleen and liver are the two most common organs injured in blunt abdominal trauma. Intestines, mesentery, pancreas, and retroperitoneal region are other structures that can be injured [2]. Abdominal injuries account for 15-20% of all trauma-related deaths. Mortality rates can be reduced with early intervention in abdominal traumas compared to head and chest traumas, which are more fatal [3]. The approach to trauma should be systematic and prioritized. Damage control surgery (DCS), which includes laparotomy, packing, and rapid wound closure to prevent bleeding and septic foci in order to restore physiological stability in trauma patients with hypothermia, acidosis, and coagulopathy, called the “death triad”, was defined in 1993 [4].
In this study, we aimed to present our perioperative results of packing procedures during damage control laparotomies in a group of patients who were admitted to our emergency department with BAT and were not eligible for nonoperative treatment conditions.
Material and Methods
This retrospective cross-sectional study was conducted in a level one trauma center of a tertiary care training and research hospital. The study included patients aged 18 years and older who were diagnosed with blunt abdominal trauma in the emergency department between 01.01.2021 and 31.12.2023 and underwent packing with damage control surgery. Patients who were followed up without surgery for blunt abdominal trauma, patients who underwent surgery for trauma other than blunt abdominal trauma, patients who underwent packing in an operation other than trauma surgery, and patients who underwent surgery for blunt abdominal trauma but did not receive packing were excluded from the study.
Demographic characteristics, vital parameters, cause of trauma, presence of additional injuries, laboratory and radiologic imaging, intraoperative findings, surgical intervention, duration of surgery, number of hospitalization days, mortality, and complications were retrospectively scanned through the hospital information management system and recorded on data forms. Shock Index (SI), Injury Severity Score (ISS), Revised Trauma Score (RTS), Trauma and Injury Severity Score (TRISS), and Glasgow Coma Scale (GCS) scores were calculated according to the data obtained from vital signs, radiological examinations, and consultation notes of other trauma branches [5]. The extent of liver and spleen injury was reported using the “Injury Scoring Scale” recommended by the American Association of Trauma Surgery (AAST) [6].
All patients were resuscitated according to advanced trauma life support guidelines from the time of admission to the emergency department. Sonographic evaluation in the emergency department – Focused abdominal sonography for trauma (FAST) – was performed by experienced emergency medicine specialists. All operations were performed by trauma surgery teams in the general surgery clinic. In cases with major liver injury, surgeons with experience in hepatobiliary surgery were also invited to the case. Post-discharge follow-up of patients without mortality was carried out in the outpatient clinics of the emergency surgery unit.
Surgical Technique
Informed consent forms for surgical procedures were signed by the patients and/or their relatives before surgery. Necessary safe surgical procedures were followed. Patients who underwent emergency laparotomy for blunt abdominal trauma were studied through a midline incision above and below the umbilicus. After rapid exploration, the procedure was started with four-quadrant packing, then the area with intense bleeding was identified, and interventions were performed for the injured organ. Although repairs or resections were performed in luminal organ injuries, anastomosis was not carried out in the first session. Splenectomy was performed if there was a high-grade injury to the spleen. Primary suturing, hemostatic agent, and/or packing were applied according to the extent of the injury in the liver. Interventions were managed according to the patient’s stability, depending on the status of injuries to other organs. After packing, the patients continued to be treated in the intensive care unit, and their general condition was expected to stabilize for depacking surgery within 24 to 48 hours.
Statistical Analysis
All data analyses were performed using the Statistical Package for the Social Sciences (SPSS, International Business Machines, New York, USA ) version 25. Since the sample size of the study was smaller than 30 (n<30), the conformity of the data to normal distribution was examined by the Shapiro-Wilk test. Normally distributed data were expressed as mean and standard deviation (±SD). Data that did not show normal distribution characteristics were summarized with median, 1st quartile (25% value, Q1), 3rd quartile (75% value, Q3), and minimum and maximum (min-max) values. Nonparametric data were expressed as numbers (n) and percentages (%).
Ethical Approval
This study was approved by the Clinical Research Ethics Committee of Basaksehir Cam and Sakura City Hospital (Date: 2023-09-04, No:547).
Results
In our study, the data of a total of 15 patients, including 11 (73.3 %) males and 4 (26.7 %) females, were analyzed. The mean age of the patients was 36.13 ± 1 4.16 years. Although traffic accidents were the most common cause of blunt trauma in the mechanism of blunt trauma, blunt traumas in the form of impact and crushing due to occupational accidents ranked first with a rate of 33.3% in terms of subtypes (Table 1). Complete blood count, aspartate aminotransferase (AST), alanine aminotransferase (ALT) and other laboratory test results of the patients measured at the time of admission to the emergency department are given in Table 2 (Table 2). Median days of hospitalization was 14 (1-124) days. Mortality was observed in a total of 3 patients (20%). All patients were evaluated with FAST, and 13 patients (87.7%), excluding 2 patients, were imaged with both FAST and computed tomography.
Shock index, ISS, RTS, TRISS, and GCS values of the patients and the organs with injuries are presented in Table 3 (Table 3).
Splenorrhaphy was successful in 4 patients (26.6%) with grade 2 lacerations, and splenectomy was performed in the other three patients with grade 4 injuries. One of the 14 patients (93.3%) with liver injury underwent non-anatomical right hepatectomy during depacking. In this patient and another patient with a large hematoma in segment 5, cholecystectomy was performed during depacking, and a catheter was placed in the cystic duct and removed from the abdomen. One of the two patients with renal injury was followed up. In the other, total nephrectomy was performed in the first session. The findings of the exitus patients are given in Table 4 (Table 4). Two patients with intracranial hemorrhage also had a mortal outcome. Sphincterotomy and stenting were performed by endoscopic retrograde cholangiopancreatography (ERCP) in a patient with a pancreatic fistula and in a patient who underwent liver repair and had a bile fistula through the drain.
Discussion
Our study includes the results of our practices in a three-year period in our hospital, a regional trauma center. In addition to being the largest trauma center in the region, our health facility is in a location with dense industrial facilities and a high population rate.
In a study involving patients presenting with abdominal trauma, the majority of whom were BAT (70.8%), the mean age was 36 years, and the proportion of males was 79%. [7]. The majority of the patients in our study were also male, and the mean age (36 ± 14) was below 45 years, consistent with the literature. Traffic accidents rank first in the etiology of blunt abdominal injuries, followed by falls and battery cases, respectively [8]. The most common cause of BAT in our study was traffic accidents, followed by occupational accidents and falls from height, respectively.
Radiographic imaging is an important part of the clinical examination in BAT. Focused abdominal sonography (FAST) for trauma is preferred as the first screening method after the primary evaluation in trauma algorithms for thoracoabdominal injuries [9]. However, due to various limitations caused by ultrasonography, computed tomography (CT) is considered the gold standard in trauma imaging evaluation. CT should only be performed under the supervision of the trauma team in patients who are hemodynamically stable or respond to fluid resuscitation [10]. All patients in our study underwent bedside FAST assessment at the time of presentation to the emergency department. Two patients with unstable general conditions and diffuse intra-abdominal hemorrhagic fluid detected by FAST underwent emergency surgery without a CT scan.
Since the most commonly injured organs in blunt abdominal trauma are the spleen and liver, it is crucial to perform complete blood count and liver function tests in laboratory tests. AST is initially higher than ALT due to rhabdomyolysis caused by blunt trauma. Newton et al. reported that ALT may be preferred as a screening tool for hepatic trauma [11]. Bilgic et al. suggested that patients with thresholds of ALT ≤76 U/L, AST <130 U/L had a low-grade liver injury and that these patients could be treated without surgery [12]. Similarly, high mean AST and ALT were associated with liver injury in our study.
With the establishment of trauma centers in many large healthcare facilities in recent years, patients with hemodynamically stable or treatment-stabilized trauma can be managed with nonoperative management (NOM) [13]. In patients with abdominal trauma, systolic blood pressure (SBP) less than 90 mmHg at the first examination in the emergency department is an important finding indicating the severity of injury and hemodynamic instability. Harvin et al. found SBP <90 mmHg in 23% of 1,706 patients who underwent emergency laparotomy in their study of 74,048 patients in 12 trauma centers over a two-year period. In the same study, the rate of damage control laparotomy was reported as 38% [14].
The Shock Index (SI), which is heart rate divided by SBP, may be a simple tool to identify patients with hemorrhagic shock. Four groups were defined as SI <0.6 (no shock), SI ≥0.6 to <1.0 (mild shock), SI ≥1.0 to <1.4 (moderate shock), and SI ≥1.4 (severe shock) [15]. In our study, the mean SBP of the patients was below 90 mmHg, the pulse rate was above 100/min, and the mean SI was 1.3, which was in the moderate shock category.
As reported in various studies in the literature, the liver is one of the most common organ injuries secondary to trauma. Therefore, the treatment strategies to be applied in trauma-related liver injury should be thoroughly familiarized. According to the World Society of Emergency Surgery (WSES) liver trauma management guidelines, in laparotomy, in the absence of major bleeding, compression alone, electrocautery, bipolar devices, topical hemostatic agents, or simple suturing of the liver parenchyma may be sufficient to stop bleeding [10]. However, in case of rapid deterioration of hemodynamics and high blood loss during surgery, perihepatic tamponade (packing) should be performed. Hemostasis is aimed to be achieved by compression between the tampons placed above and below the bleeding parenchyma [16]. It is recommended to avoid hepatic resections in the treatment of unstable patients and during damage control procedures. Despite this, hepatic resection may be required in 2-4% of cases of major liver trauma [10]. In the liver injuries in our study, mainly bipolar cauterization, primary suturing, and packing using hemostatic agents were performed, and hepatic resection during DCS was not used in any patient. During the depacking procedure, one patient underwent a right hepatectomy due to completely circulatory compromised liver segments.
Trauma scoring systems are a common means to facilitate the assessment of injury severity and comparison of treatment outcomes. The most commonly used scoring systems include the Glasgow Coma Scale (GCS), Injury Severity Score (ISS), Revised Trauma Score (RTS), and Trauma and Injury Severity Score (TRISS). The ISS score is the most common anatomical scoring system utilized for patients with multiple injuries. Duration of hospitalization is associated with morbidity and mortality [5]. Bolorunduro et al. divided ISS into four groups as mild (<9), moderate (9-15), severe (16-25), and profound (>25) [17]. The mean ISS we calculated was 37.2 ± 9.4, and all patients were in the riskiest group. The most common injury accompanying abdominal trauma was thorax trauma with a rate of 53%.
Due to its low sensitivity and specificity, ISS cannot distinguish between survivors and non-survivors. Instead, it has been suggested that RTS and TRISS can be used to predict the survival rates of trauma patients [18]. In our study, the ISS was above 40 points in all three patients with mortality, while both RTS and TRISS values were significantly lower in two of them compared to the surviving patients.
The timing of emergency laparotomy is one of the most important prognostic factors in patients with major trauma and hemodynamic instability. Although there is no strict time limit for emergency laparotomy, the American College of Surgeons Committee on Trauma (ACS-COT) recommends intervention within 120 minutes [19]. Although DCS contributes to decreased mortality, it also carries complications such as sepsis, abscesses, biliary fistulas, abdominal compartment syndrome, gastrointestinal fistulas, and abdominal hernias [20, 21]. Minor bile duct injuries often heal spontaneously within 14 days and do not require any intervention, but major bile duct injury or persistent bile leaks can be treated with ERCP and biliary stent drainage. Biliary complications rarely require surgical treatment except in cases of failure of conservative treatment or uncontrolled sepsis [22]. In our study, we performed cholecystectomy and transcystic catheter placement through the cystic duct in a depacking procedure in two patients. Furthermore, one patient who underwent only liver repair needed stenting with ERCP due to a biliary fistula in the postoperative period. Similarly, a patient with pancreatic fistula required ERCP. As we applied packing to all patients in our study, no fascia closure was performed as a temporary abdominal closure method, and only skin closure was performed. No signs of abdominal compartment syndrome were observed in any of our patients.
Although NOM has become a frequently used method in trauma centers in recent years, mortality is also observed in these patients. Even in high-volume trauma centers, the overall mortality rate in the treatment of trauma patients was reported to be 10% [23]. It was reported that in-hospital mortality was 10.9% in primary surgical treatment patients and 3.6% in NOM patients, while the mortality rate in primary surgery cases was 23.8% in patients with combined hepato-spleen injury [24]. In our study, no combined liver-spleen injury was observed in the patients with mortality. However, the presence of retroperitoneal bleeding or intracranial bleeding was noted in these patients. Talih et al. reported that ISS level, hypotension, and hemorrhagic shock on admission were significant risk factors for mortality in their study in which the mortality rate was found to be 47% [25]. Although DCS in trauma aims to reduce mortality, studies indicating that high complications were observed in survivors were also reported. Roberts et al. reported that there were significant differences between the indications for DCS in different trauma centers and that there were unnecessary referrals to this procedure. There is a growing number of studies examining admissions to DCS due to its high complicative consequences [20]. Lack of information about the causes of trauma and the patient can negatively impact surgical decision-making, leading to less effective clinical choices. Therefore, it is important to determine which patient should be treated with which treatment protocol. For this reason, the concept of teamwork emerges.
In addition to being a major trauma center, the structure and dynamics of emergency trauma teams are determined by an in-house protocol. In fact, a division of labor within the team has been determined for emergencies that may cause a large number of trauma patients to apply, such as earthquakes, mass traffic accidents, and explosions. Having a trauma team contributes greatly to making joint treatment decisions for patients and taking the best decision.
Limitation
Our study had several limitations due to its retrospective and single-center design. Since we retrospectively scanned through the “packing” code in the surgical record system, we were able to screen only patients who underwent damage control surgery and packing. Therefore, we could not screen patients who were followed nonoperatively or underwent damage control surgery without packing. This led to the lack of a control group in our study. Although the number of patients in the study seems to be limited, we think that it is significant in terms of reflecting our packing results in our hospital, which has a level 1 trauma center.
Conclusion
Despite all the advances in the nonoperative management of patients with blunt abdominal trauma, damage-control laparotomies remain an effective procedure in the management of severe trauma in a group of patients with massive bleeding and coagulopathy. It is possible to achieve acceptable mortality and morbidity rates with trauma surgery teams experienced in damage control surgery. Furthermore, establishing well-equipped trauma centers and managing the process with a multidisciplinary approach are among the most crucial factors in increasing the success rates of trauma surgeries.
Acknowledgment
We would like to thank Zeynep Kucukakcali from Malatya İnönü University, Department of Biostatistics and Medical Informatics, for her participation in the statistical analyses.
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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Premature mortality rates and affecting risk factors: A three-year experience
Sevim Çakar 1, Füsun Atlıhan 2
1 Department of Pediatrics, Faculty of Medicine, Dokuz Eylül University, 2 Department of Pediatrics, Dr. Behçet Uz Children’s Hospital, Izmir, Türkiye
DOI: 10.4328/ACAM.22169 Received: 2024-03-06 Accepted: 2024-05-06 Published Online: 2024-06-02 Printed: 2024-07-01 Ann Clin Anal Med 2024;15(7):491-494
Corresponding Author: Sevim Çakar, Department of Pediatrics, Faculty of Medicine, Dokuz Eylül University, Izmir, Türkiye. E-mail: drsevimgokgoz@gmail.com P: +90 505 824 23 40 Corresponding Author ORCID ID: https://orcid.org/0000-0001-5129-0923
Other Author ORCID ID: Füsun Atlıhan, https://orcid.org/0000-0001-5689-8153
This study was approved by the Ethics Committee of Dr. Behçet Uz Children’s Hospital (Date: 2008-09-10, No: 25)
Aim: Preterm infants are immature and have a high risk for mortality. This study aims to draw attention to the high mortality rate and the problems of premature newborns affecting the mortality rate.
Material and Methods: In this retrospective study, preterm newborns hospitalized in a tertiary hospital for three years having the study admission criteria, were enrolled.
Results: 870 preterm infants (48.4% were girls) were included in the three-year study period. In the three years, 28.7% of the cases resulted in death, and a significant decrease was observed in premature baby mortality rates over the years (p<0.001). The most common causes of death were found to be respiratory distress syndrome, sepsis, and pneumothorax. As the gestational age and birth weight decreased, mortality was found to be significantly higher (p<0.001 and p<0.001). A significantly higher mortality rate was found in those born via normal vaginal delivery than in those born via cesarean section (p=0.010). Mortality was also higher in babies requiring oxygen immediately after birth (p<0.001).
Discussion: As a result, the decrease in mortality rates in our center from 45.7% to 26.9% and then to 16.7% over the years is encouraging, but it is much higher than the data of developed countries. The role of these data is to determine the main problems and to create solutions for preventing premature mortality.
Keywords: Mortality, Prematurity, Risk Factors
Introduction
According to the World Health Organization (WHO) reports, there are 4 million newborn deaths annually. The mortality rate of under-five children in a country is considered the most important indicator in assessing the health situation. It is known that the infant mortality rate is a good indicator of the level of socioeconomic development in a country. Although neonatal mortality is decreasing all over the world due to developing technology, newly developed drugs and increasing knowledge, it still maintains its importance [1]. Although newborn infant mortality rates are not known due to insufficient records in our country, according to WHO data, it has been determined that the rate is mostly related to infections at 32% and problems related to prematurity at 24% [2].
To prevent perinatal and neonatal mortality, it is becoming increasingly important to know the causes and to determine strategies to prevent infant deaths.
Material and Methods
Mortality rates, causes of mortality, and antenatal, natal and postnatal factors affecting the risk of mortality of a total of 870 preterm babies who were monitored as inpatients in the Premature Intensive Care Unit of a tertiary care children’s hospital between 2005 and 2007 were examined in our study. Since some patients were diagnosed with more than one disease, the single most important cause of death was determined. The babies born before the 38th week of gestation, whose gestational age was calculated in the first 24 hours according to the new Ballard method, were included in the study. Data were collected retrospectively by reviewing patient files.
Statistical analysis of the data was performed with SPSS 11.0 Microsoft for Windows program. In determining the factors that increase the mortality risk, one-way analysis was used; the difference in numerical variables between the groups was investigated by the student-t test and ANOVA analysis. The relationship of the groups with other groups was investigated by chi-square and Fisher’s exact test when possible.
Ethical Approval
This study was approved by the Ethics Committee of Dr Behçet Uz Children’s Hospital (Date: 2008-09-10, No: 25).
Results
Descriptive data
48.4% of the 870 cases included in the study were female. The rate of those born through spontaneous pregnancy was 93.4%, and assisted reproductive techniques were used in 6.6%. While 2.3% of babies were born at home, 51.4% were transported from an external center under appropriate conditions.
80.8% of the cases were found to be appropriate for gestational age (AGA), 16.9% were small for gestational age (SGA), and 2.3% were large for gestational age (LGA). While prenatal risk factors (infection, medication, smoking, trauma, hypertension and diabetes) were present in 37.6% of pregnancy follow-ups, a significant decrease in prenatal risk factors was detected over the years (p = 0.011). There were natal risk factors (need for resuscitation at birth, premature rupture of membranes, placenta anomaly) in 20.9% of pregnancies, and the presence of these factors decreased significantly over the years (p<0.001). Antenatal steroids were applied in only 2.5% of the cases, and a significant increase in the application was observed over the years (p<0.05).
42.3% of the patients had a normal vaginal delivery, and no significant increase in cesarean deliveries was detected over the years (p>0.05). Surfactant therapy was applied in 18.0% of the cases, and an increase in this application was observed over the years (p<0.05). 66.2% of the patients received oxygen support and respiratory support, and 41.0% of the patients received mechanical ventilator support for a period.
In a total three-year period, 28.7% of the cases resulted in death, and a significant decrease was observed in premature infant mortality rates over the years respectively 45.7%, 26.9%, and 16.9% (p<0.001).
The detailed distribution of the causes of mortality by years is given in Table 1.
Mortality relationship with antenatal and perinatal factors
It was determined that maternal age, number of pregnancies, parental consanguinity, and use of assisted reproductive techniques did not affect mortality (p>0.05). There was no difference in the mortality rates in preterm with maternal risk factors (infection, drug or cigarette use, history of trauma, hypertension, diabetes history) and antenatal steroid administration (p>0.05).
A significantly higher mortality rate was found in those born via normal vaginal delivery (than in those born via cesarean section 33.4% versus 25.3% (p=0.010). Mortality was also higher in babies who needed oxygen immediately after birth with 41.3% versus 4.1% (p<0.001).
Relationship between fetal factors and mortality
A mortality rate of 25.4% in girls was significantly higher than the rate of 31.8% in boys (p = 0.043). In our data, the average birth weight of the deceased cases was 1306 g, while the living ones were 1595 g (p<0.001). While the mean gestational age was 29.8 weeks in the deceased cases, it was 32.1 weeks in the surviving cases (p<0.001). As the week of gestation and birth weight decreased, mortality was found to be significantly higher (p<0.001 and p<0.001) (Tables 2 and 3).
Mortality rates were similar in SGA, LGA and AGA (p=0.495).
There was a mortality rate of 48.2% in babies diagnosed with respiratory distress syndrome (RDS), and RDS was observed at a rate of 33.3% in all babies. Cardiopulmonary resuscitation, premature rupture of membranes, presence of placental anomalies and surfactant administration were found to increase mortality (p<0.001). It was also shown that the diagnoses of Patent Ductus Arteriosus and sepsis increased mortality (p=0.043, p=0.001). Pneumothorax was detected in 4% of the cases and 48.6% of these resulted in death.
Discussion
Prematurity remains one of the most important causes of mortality in the perinatal, neonatal and post-neonatal periods. While the mortality rate of premature babies in neonatal intensive care units has decreased over time, the frequency of complications accompanying this condition has increased.
If we look at our country’s data, according to the study conducted at Hacettepe University, the mortality rate was found to be 57% in those born younger than the 31st week [3]. In another study conducted at Dr. Sami Ulus Children’s Hospital, the preterm mortality rate was found to be 20% [4]. When the data abroad are evaluated, the mortality rates are 12.1, and 23.2% in very low-weight babies in Japan and Portugal, respectively, and 8.4% in France for patients born before 32 weeks, which is much lower than our data with 28.7% [5-7]. However, although it is encouraging that the mortality rates in our center have decreased over the years from 45.7% to 26.9% and then to 16.7%, it is still much higher than the data of developed countries. It was thought that these high rates may be caused by the lack of delivery room and obstetrics department within our hospital, delays due to transportation difficulties, errors in the transportation system and the low socioeconomic conditions of the patients admitted to the hospital.
In studies, neonatal mortality rates are 8-10 times higher in adolescent and advanced maternal-age pregnancies, and in our study, the effect of maternal age on mortality was not found to be significant [8]. Mortality rates in multiple pregnancies were found to be significantly higher, consistent with the literature [9]. Other significant risk factors that supported the literature data were cardiopulmonary resuscitation, premature rupture of membranes, and placenta anomaly [8].
The lack of a decrease in the mortality rate with steroid application did not coincide with the data in the literature, but it was thought that the factor in this may be the use of steroids in a small number of patients [10]. WHO recommends that the cesarean birth rate be kept under 12%, but in our study, this rate was 57.7% and the mortality rates were found to be significantly lower in those born this way. This data supports studies showing that mortality is reduced by cesarean section in very low-weight babies [11]. Some studies have determined that vaginal birth has a positive effect on survival. In our study, the mortality rate of male preterm babies was found to be higher, which supports the literature [12].
It has been shown that the most important factors determining the chances of survival of preterms are birth weight and gestational age [13]. In the study conducted by the Turkish Neonatology Association in 2007, in which 31 centers participated, the mortality rates were 92% in babies with birth weights under 500 g, 67% in those with birth weights of 500-749 g, 40% in -999 g, 18% in 1000-1249 g, and 14% in1250-1499 g, 12% in 1500-1999 g, 6% in 1500-1999 g, and 4% in 2000-2499 g.
The mean gestational age was smaller in the deceased cases, which was consistent with the literature [13]. Although gestational age and birth weight are the most important determinants of mortality and morbidity, gestational age may not reflect reality if good prenatal follow-up and necessary ultrasound are not performed [14]. For this reason, it is thought to be more practical to use since birth weight can be determined more easily and is objective [15].
In the literature, in a multi-center study conducted in our country in 2007, the mortality data in preterms diagnosed with RDS was 21.9% with lower rate to our data, and these rates vary between 0-54.5% in other countries [16].
The second most common cause of death is sepsis, which occurs in 34.2% of our cases, and the mortality rate in these patients is 36.2%, which is similar to the 15-50% data in the literature [17]. Our third most common diagnosis of death is pneumothorax, which is detected in 4% of cases, and is similar to the rates of 3.2-9.2% in literature data [18].
The fact that our study is retrospective and includes only three years can be considered among its limitations, but it is thought to contribute to Turkey’s data.
Conclusion
As a result, the decrease in mortality rates in our center over the years, from 45.7% to 26.9% and then to 16.7%, is encouraging, but it is much higher than the data of developed countries. The most important reasons for the improvement in mortality rates in our country and in our center over the years were associated with improvements in technical equipment, more effective use of mechanical ventilation, regular training of service staff, and the introduction of surfactant and other supportive treatments in premature babies. Factors that determine the baby’s chance of survival start before the baby’s birth. The most important element is to provide antenatal care that will eliminate preventable causes of premature birth. A good pregnancy follow-up and delivery under appropriate conditions with a sufficiently equipped team will significantly affect mortality.
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.
References
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Comparison of serum neuropeptide-FF and catestatin levels in hypertensive pregnant women
Hamdin Günsel 1, Semra Oruç 2, Fatma Taneli 2, Mulaim Sizer 1, Kenan Kırteke 2, Nebahat Sunar 1, Erhan Okuyan 1, Adem Yoldaş 1
1 Department of Obstetrics and Gynecology, Batman Training and Research Hospital, Batman, 2 Department of Obstetrics and Gynecology, Faculty of Medicine, Celal Bayar University, Manisa, Turkey
DOI: 10.4328/ACAM.22174 Received: 2024-03-08 Accepted: 2024-05-06 Published Online: 2024-06-28 Printed: 2024-07-01 Ann Clin Anal Med 2024;15(7):495-499
Corresponding Author: Mulaim Sizer, Department of Obstetrics and Gynecology, Batman Training and Research Hospital, Batman, Turkey. E-mail: mulayimsizer@hotmail.com P: +90 506 856 42 85 Corresponding Author ORCID ID: https://orcid.org/0000-0003-4864-7287
Other Authors ORCID ID: Hamdin Günsel, https://orcid.org/0000-0001-5963-1147 . Semra Oruç, https://orcid.org/0000-0003-0138-1186 . Fatma Taneli, https://orcid.org/0000-0002-5194-0460 . Kenan Kırteke, https://orcid.org/0000-0002-2153-7646 . Nebahat Sunar, https://orcid.org/0000-0002-5404-1241 . Erhan Okuyan, https://orcid.org/0000-0001-9636-9539 . Adem Yoldas, https://orcid.org/0000-0002-8315-9759
This study was approved by the Ethics Committee of the local University Faculty of Medicine Non-Invasive Clinical Research (Date: 2019-10-14, No: 153)
Aim: We aimed to compare the levels of Neuropeptide-FF and Catestatin in the sera of hypertensive and normotensive pregnant women, to determine the possible changes in hypertensive diseases of pregnancy and to examine the possible place of pregnancy in hypertensive diseases.
Material and Methods: We used the quantitative analysis method to test the hypotheses of the research and examine the relationship between variables. Neuropeptide FF and Catestatin levels were analyzed by Enzyme Linked Immunoassay (ELISA) method. Neuropeptide-FF and Catestatin values of patient and control groups were analyzed with Mann-Whitney and Chi-square tests.
Results: A higher Catestatin value was determined in the patient group compared to the control group, and this difference was statistically significant(p = 0.000). Catestatin value in the patient group was 31.61 ± 12.54, and value in the control group was 48.46 ± 22.45 and the relation was statistically found significant (p <0.05). The neuropeptide-FF was not statistically significant in the patient and control group compared to the control group (p = 0.916). Therefore, the Neuropeptide-FF value in the patient group was 134.30 ± 93.72; this value was found as 139.49 ± 96.41 in the control group, but the relation statistically was not found significant (p> 0.05). According to the analysis results of our study, a statistically significant difference was found for Catestatin at the 5% significance level between the patient group and the control group.
Discussion: Decreased NPFF expression in the hypothalamus of hypertensive patients may lead to impaired interaction with other neurochemical systems and therefore may play a role in the pathogenesis of hypertensive disease.
Keywords: Preeclampsia, Neuropeptide-FF, Catestatin, Hypertensive Diseases
Introduction
Hypertensive diseases during pregnancy are one of the leading causes of maternal and fetal morbidity and mortality [1]. This condition is reported to affect approximately 3% to 5% of all pregnant women [2]. It is also estimated that preeclampsia and other hypertensive diseases in pregnancy are responsible for approximately 100,000 maternal deaths each year. Although some researchers have suggested that preeclampsia is caused by multiple factors including vasospasm, endothelial dysfunction, inflammation, angiogenesis defect and oxidative stress, its pathogenesis is still poorly understood [1].
Neuropeptide FF (Phe-Leu-Phe-Gln-Pro-Gln-Arg-2), found in the human central nervous system and peripheral tissues, is an important member of the RFamide peptide family that was first identified. Although it was first described to cause hyperalgesia by inhibiting the antinociceptive effects of opiates, it has important functions in the central structuring of visceral autonomic signals related to food intake, central cardiovascular responses, stress and neuroendocrine regulation [3].
Catestatin functions as a vasodilator and the finding that plasma catestatin levels are decreased in human hereditary (essential) hypertension suggests that early defects in this peptide may predispose to the development of hypertension in the future. Because new data put forward by many scientists in the literature have revealed that natural variants in human catestatin alter autonomic functions and blood pressure [4].
Although there are many studies on pregnancy, neuropeptides and hypertension in the literature, the pathophysiology of hypertensive diseases in pregnancy is not fully understood. In addition, data on the possible association between neuropeptide-FF, catestatin levels in serum and hypertensive diseases and scientific studies examining these data are also insufficient. Therefore, in this study, we aimed to compare the levels of Neuropeptide-FF and Catestatin in the serum of hypertensive and normotensive pregnant women to determine the possible changes in hypertensive diseases of pregnancy and to examine the possible role of pregnancy in hypertensive diseases.
Material and Methods
The study was conducted on pregnant women between the ages of 19 and 42 years at Celal Bayar University Gynecology and Obstetrics Clinic after obtaining hospital and ethics committee permissions. 39 healthy pregnant women and 39 pregnant women complicated with hypertension totaling 78 pregnant women were included in the study. One tube of blood was collected from each pregnant woman who agreed to participate in the study. Gestational age was calculated according to the date of the last menstrual period and this data was confirmed by ultrasonographic records. Pregnant women who applied to our clinic were offered to participate in the study. A signed consent form was obtained from the consenting pregnant women. Pregnant volunteer women in the Gynecology and Obstetrics Clinic were included in the hypertensive group if their blood pressure was above 140/90 mmHg and in the healthy group if their blood pressure was below 140/90 mmHg.
Blood pressure (BP) measurements were based on the guidelines published by the European Society of Hypertension (ESH) and the European Society of Cardiology (ESC) in 2013. BP of each pregnant woman was measured by a standardized measurement technique and recorded in the patient files. BP was measured from the brachial artery in a sitting position, after 5 minutes of rest, with the cuff at the level of the heart. Measurements were performed by trained healthcare personnel using a sphygmomanometer with a cuff size suitable for the patient. Pregnant women with blood pressure values above 140/90 mmHg in blood pressure measurements performed at half-hour intervals during rest and calm were included in the hypertensive group; pregnant women with blood pressure values below 140/90 mmHg were included in the healthy group. 43 healthy pregnant women and 40 pregnant women complicated with hypertension were included in the study. In the control group, 4 patients were excluded because they did not meet the criteria. In the patient group, 1 patient was excluded because she did not meet the criteria. In total, 78 patients were studied. Gestational age was calculated according to the date of the last menstrual period and confirmed by ultrasonographic records.
Criteria for the patient group
-Blood pressure values above 140/90 mmHg in blood pressure measurements performed at half-hour intervals while the pregnant woman is resting and calm
-Between 19-42 years old
-Must be at least 20 weeks pregnant.
Exclusion Criteria of the patient group
-Pregnant women with multiple pregnancies
-Pregnant women with an intrauterine dead fetus
-Pregnant women with diabetes mellitus
-Pregnant women with identified fetal or placental abnormalities
-Women who are younger than 19 years or older than 42 years,
-Pregnant women with less than 20 weeks gestation were excluded
Inclusion Criteria for the control group
-Blood pressure values below 140/90 mmHg in blood pressure measurements performed at half-hour intervals while the pregnant woman is resting and calm
-Between 19-42 years old
-Must be at least 20 weeks pregnant
Exclusion Criteria of the control group
-Pregnant women with multiple pregnancies
-Pregnant women with an intrauterine dead fetus
-Pregnant women with diabetes mellitus
-Pregnant women with identified fetal or placental abnormalities
-Pregnant women younger than 19 years or older than 42 years
-Blood pressure measured above 140/90
-Pregnant women with less than 20 weeks gestation were not included in the control group
Biochemical analysis
Venous blood samples were collected from the patients in the morning on an empty stomach from the forearm into anticoagulant-free tubes. Blood samples were centrifuged at 3000 rpm at +40C for 15 minutes and serum was separated and stored at -800C until analysis and analyzed in a single run. Neuropeptide FF and Catestatin levels in serum samples were analyzed by Enzyme Linked Immunoassay (ELISA) method. Analyses were performed in the laboratories of Manisa Celal Bayar University Faculty of Medicine, Department of Medical Biochemistry. During the analysis, ELISA washing was performed with an automatic washing device (BioTek ELx50 BioTek Instruments Inc. Highland Park, Winooski, VT, USA) and absorbance readings were performed on an ELISA reader (BioTekEpoch, BioTek Instruments Inc. Highland Park, Winooski, VT, USA).
Neuropeptide FF levels in serum samples were determined with a commercial kit (BT LAB Human Neuropeptide FF Elisa Kit Cat.No E6978Hu, Zhejiang, China) and Catestatin levels (Mybiosource Human Catestatin (CST) Elisa Kit Cat. No: MBS3800529, Southern California, San Diego, USA) commercial kits.
The reading range of the Neuropeptide FF kit was 7-1500ng/L, the limit of detection was 3.32ng/L and the intra-assay precision values of the kit had a correlation coefficient (CV) <8% and inter-assay precision CV <10%.
Catestatin kit has a reading range of 50-800pg/ml, detection limit of 1pg/ml, intra-assay CV <8% and inter-assay CV <10%.
Statistical Analysis
The data obtained from the patients sampled in the study were subjected to statistical analysis with the help of SPSS (21.0) program. After testing the frequency analysis, a normal distribution test was performed for all variables. Since the data were not normally distributed, analysis was performed with nonparametric tests. For this purpose, Neuropeptide-FF and Catestatin values of the patient and control groups were compared with Mann-Whitney test. Hypertension was designed as dependent variable and Neuropeptide-FF and Catestatin as independent variables. In addition, Chi-square test was performed to find the power of change in age and gestational week in the control and patient groups. Cronbach’s Alpha value was calculated for the reliability of the data. Variables were expressed as mean ± standard error of the mean, categorical variables as number or %. In all statistical comparisons, p≤0.05 values were considered statistically significant.
Ethical Approval
This study was approved by the Ethics Committee of the local University Faculty of Medicine Non-Invasive Clinical Research (Date: 2019-10-14, No: 153).
Results
The distribution and percentages of the participants according to age groups are given in Table 1. Chi-Square test was applied to determine whether there was a significant difference between the patient and control groups according to age.
The aim of this study was to evaluate the Neuropeptide-FF and Catestatin levels of pregnant patients complicated with TA comparatively. For this purpose, Neuropeptide-FF and Catestatin levels of the patient and control groups were compared. The values obtained are shown in Table 3.
According to the results in Table 3, there is a statistically significant difference between the patient group and the control group for Catestatin at 5% significance level. A lower Catestatin value was determined in the patient group compared to the control group and this difference was statistically significant (p=0.000). However, there was no statistically significant difference between the experimental and control groups for Neuropeptide-FF (p=0,916). Although a lower Neuropeptide-FF value was found in the patient group compared to the control group, this difference was not statistically significant.
Discussion
In our study, we found a statistically significant difference between the mean catestatin levels in both control and patient pregnant women (p<0.05). In other words, this result indicates that there is a significant difference in catestatin levels between hypertensive and normotensive groups. Thus, lower catestatin predicts enhanced pressor responses, suggesting that decreased catestatin may be a powerful mechanism for the increased risk of subsequent development of hypertension. In our study, we did not find a statistically significant difference between the means of Neuropeptide-FF (p>0.05). This shows that there is no significant difference in NPFF levels between hypertensive and normotensive groups. Catestatin is a new endogenous peptide that regulates cardiac function and blood pressure [5]. It has been suggested that neuropeptides, which are defined as polypeptides synthesized and secreted in neuronal cells and regulate the endocrine system, cardiovascular system and nervous system, may contribute to the pathogenesis of hypertension [6].
There are many studies in the literature that address these two variables, Neuropeptide-FF and Catestatin, separately. However, most of these studies were conducted especially on animal subjects such as cattle and rats. Because human, bovine and rat catestatins have similar effects [7].
In addition, there are studies in the literature that have examined the relationship of Neuropeptide-FF and Catestatin separately with blood pressure and hypertension. Decreased NPFF expression in the hypothalamus of hypertensive patients may be a reason for impaired interaction with other neurochemical systems and therefore may play a role in the pathogenesis of the disease. In addition, it is also thought that GABAergic input may play a role in the formation of NPFF disinhibition of parvocellular PVN neurons [6]. Because intracerebroventricular injections of NPFF cause increases in arterial blood pressure [8].
Jhamandas et al. [11] found in an animal study that NPFF, a peptide belonging to the RF amide peptide family, significantly increased γ- aminobutyric acid (GABA)-mediated synaptic activity in magnocellular neurosecretory cells (MNCs) of the hypothalamic paraventricular nucleus (PVN). They also showed that NPFF increased the frequency of mIPSCs without affecting the amplitude or decay time constant of miniature inhibitory postsynaptic currents (mIPSCs). This suggests that the peptide has a presynaptic locus for its actions. NPFF and NPVF also decreased the frequency of GABAergic mIPSCs without affecting the amplitude or decay time constant of mIPSCs, suggesting that these peptides also have a presynaptic locus for their actions [9]. In conclusion, these investigators demonstrated in their laboratory studies that NPFF injections cause a rapid dose-dependent hypertensive effect.
Ma et al. [12] reported that PrRP binds the NPFF2 receptor when it increases, inhibits the receptor by competitive inhibition of the NPFF receptor and consequently causes an increase in blood pressure. On the other hand, Laguzzi et al. [10] suggested that focal injection of NPFF into the nucleus solitarius caused a decrease in blood pressure and heart rate. Goncharuk et al. [6] found decreased expression of Neuropeptide FF in the hypothalamus of hypertensive individuals and reported that this may contribute to the pathogenesis of hypertension by disrupting the interaction of other neurochemical systems. These studies on NPFF contradict the results of our study. Because we did not find a significant relationship between NPFF and hypertension in our study (p>0.05).
In contrast to the studies we have cited above, Asico et al. [13] found that NPFFs did not have a statistically significant association with hypertension, supporting our study.
This study on NPFFs overlaps with the results of our study. Because in our study, we did not find a statistically significant difference between the mean levels of Neuropeptide-FF in control and patient pregnant women (p>0.05). This shows that there is no significant difference in NPFF levels between hypertensive and normotensive groups.
Mahapatra et al. [6] suggested that catestatin, an endogenous peptide, is a novel regulator of cardiac function and blood pressure. Rao et al. [14] concluded that catestatin induces major changes in human autonomic activity in both the parasympathetic and sympathetic systems and specifically reduces the risk of developing hypertension. Kiranmayi et al. [15] also found that catestatin altered systemic blood pressure and the risk of hypertension in humans.
In another study, they found that catestatin, a bioactive peptide, was reduced in subjects with a familial predisposition for hypertension [16]. They reported that decreased catestatin levels may increase the risk of hypertension. Fung et al. [17] showed in their study that catestatin dilates human blood vessels in vivo, especially in women. They also suggested that catestatin may influence the complex predisposition to hypertension, especially in women, and that local infusion of exogenous catestatin in vivo caused vasodilation in healthy subjects [17]. They reported that their observation that catestatin is deficient in hypertension was based on direct evidence of vasodilation and the effects of endogenous genetic variation of catestatin (specifically Gly364Ser) on autonomic physiology and BP10 [14]. Furthermore, O’Connor et al. [16] concluded that catestatin is reduced very early in the development of hypertension, even in normotensives with the disease. There are also studies concluding that catestatin levels are significantly reduced in hypertensive patients and also in normotensive individuals with a familial history of hypertension, moreover, high catecholamine levels are observed in hypertensive individuals, therefore catestatin shows a strong correlation between catecholamine and hypertension [16].
Decreased catestatin is observed not only in hypertensive individuals but also in early normotensive children of hypertensive patients. This suggests that early catestatin deficiency may play a pathogenic role in the subsequent development of the disease [16]. In addition, as mentioned before, there are also studies indicating that catestatin causes major changes in human autonomic activity in both the parasympathetic and sympathetic systems and reduces the risk of developing hypertension [14]. These studies also support the results related to catestatin, which is a variable of our study. In other words, this result shows that there is a significant difference between hypertensive and normotensive groups in catestatin levels. Thus, lower catestatin predicts enhanced pressor responses, suggesting that decreased catestatin may be a powerful mechanism for the increased risk of later development of hypertension.
In conclusion, we think that such different results in the literature may be due to the fact that patients with preeclampsia or eclampsia have not been studied with sufficient samples in terms of parameters that may affect blood pressure levels. We believe that a more detailed study of these parameters with different samples may be useful to better understand the possible mechanism. Therefore, decreased NPFF expression in the hypothalamus of hypertensive patients may lead to impaired interaction with other neurochemical systems and therefore may play a role in the pathogenesis of hypertensive disease.
In future studies, it may be investigated whether Catestatin and Neuropeptide-FF levels are associated with blood pressure and whether Catestatin and Neuropeptide-FF levels of pregnant women who develop preeclampsia are different from those who do not.
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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2. Cunningham F, Leveno K, Bloom S, Spong CY, Dashe J. Williams Obstetrics. 24th ed. New York: McGraw-Hill; 2014.
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4. Biswas N, Gayen J, Mahata M, Su Y, Mahata SK, O’Connor DT. Novel peptide isomer strategy for stable inhibition of catecholamine release: Application to hypertension. Hypertension. 2012;60(6):1552-9.
5. Mahapatra NR. Catestatin is a novel endogenous peptide that regulates cardiac function and blood pressure. Cardiovasc Res. 2008;80(3):330-8.
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7. Cortez V, Santana M, Marques AP, Mota A, Rosmaninho-Salgado J, Cavadas C. Regulation of catecholamine release in human adrenal chromaffin cells by β-adrenoceptors. Neurochem Int. 2012;60(4):387-93.
8. Jhamandas JH, MacTavish D. Central administration of neuropeptide FF causes activation of oxytocin paraventricular hypothalamic neurones that project to the brainstem. J Neuroendocrinol. 2003;15(1):24-32.
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10. Laguzzi R, Nosjean A, Mazarguil H, Allard M. Cardiovascular effects induced by the stimulation of neuropeptide FF receptors in the dorsal vagal complex: An autoradiographic and pharmacological study in the rat. Brain Res. 1996;711(1-2):193-202.
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Download attachments: 10.4328.ACAM.22174
Hamdin Günsel, Semra Oruç, Fatma Taneli, Mulaim Sizer, Kenan Kırteke, Nebahat Sunar, Erhan Okuyan, Adem Yoldaş. Comparison of serum neuropeptide-FF and catestatin levels in hypertensive pregnant women. Ann Clin Anal Med 2024;15(7):495-499
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Does the experience affect the knowledge about auxiliary portals in shoulder arthroscopy? A questionnaire study and review of the auxiliary portals
Gokhan Ilyas, Oguzhan Gokalp
Department of Orthopaedics and Traumatology, Faculty of Medicine, Usak University, Usak, Turkey
DOI: 10.4328/ACAM.22176 Received: 2024-03-11 Accepted: 2024-05-06 Published Online: 2024-05-31 Printed: 2024-07-01 Ann Clin Anal Med 2024;15(7):500-504
Corresponding Author: Oguzhan Gokalp, Department of Orthopaedics and Traumatology, Faculty of Medicine, Usak University, Usak, Turkey. E-mail: oguzhangokalp@gmail.com P: +90 505 950 32 31 Corresponding Author ORCID ID: https://orcid.org/0000-0003-4062-8559
Other Author ORCID ID: Gokhan Ilyas, https://orcid.org/0000-0002-5750-1346
This study was approved by the Ethics Committee of Usak University Clinical Researches (Date: 2022-04-06, No: 62-62-06)
Aim: This questionnaire study investigated the usability of need-driven portals from the safe zone instead of seconder-specific portals.
Material and Methods: A face-to-face questionnaire concerning the anatomic localization of auxiliary specific secondary portals and in which pathology treatment they were used was conducted with 24 orthopedic surgeons. Seven specific seconder portals were included and four portals out of the safe zone were excluded from the study. Observers were divided into two groups according to their shoulder arthroscopy experiences and comparative evaluations were carried out.
Results: SPSS 24. Ver Fisher-Exact test was used for statistical analysis and p<0.05 was accepted as significant. The existence of poor and medium results more often than good results in the study indicated that need-driven portals from the safe zone are more convenient. Additionally, the surgical experience was observed to have a more positive effect on the results. When the groups were statistically evaluated with the Fisher Exact Test in terms of anatomical localization and which pathology treatment they are used for, no significant difference was obtained (p=0.059-0.444), except for the Wilmington portal used in pathological treatment (p=0.018).
Discussion: It has been observed that recalling and applying specific secondary portals in daily surgical practice is challenging. Instead, many surgeons find it appropriate to open a portal from a suitable area within the safe zone, with an inside-out or outside-to-inside technique, depending on the location and type of pathology.
Keywords: Portal, Auxiliary Portals, Shoulder Arthroscopy, Experience, Questionnaire, Arthroscopic Surgery
Introduction
The anatomic spots to be identified before going into the joint in shoulder arthroscopy are acromion anterior-lateral-posterior borders, clavicula anterior and posterior, scapular spine anterior and posterior, acromioclavicular joint, and coracoid process. The basic portals used are the posterior, anterior, and lateral portals [1]. In addition to the basic ones, there are several specific seconder portals defined for the treatment of various pathologies. Among those, there exists an anterosuperior portal, anteroinferior portal, superior lateral portal, anterolateral portal, Wilmington portal, posterolateral portal, and posteroinferior (7 o’clock) portal, 5 o’clock portal, Neviaser portal, G portal, and transpectoral portal (Figure 1) [2]. Awareness of seconder-specific portals is noteworthy in various pathology treatments; yet, recalling and administering those properly can be challenging during operations.
On the condition that it remains in the posterior portal and coracoid process lateral, the area up to 5 cm distal of acromion lateral is defined as a safe zone for portal entrances in shoulder arthroscopy (Figure 2) [3].
The purpose of this study is to research the usability of portals that are opened from the safe zone from the inside to the outside or from the outside to the inside, depending on the surgeon’s decision, instead of the auxiliary specific secondary portals used in shoulder arthroscopy applications. No research has been done on this subject before. It was hypothesized that the localization of the seconder-specific portals and the awareness of which pathology treatment they are using would give positive results depending on the surgical experience.
Material and Methods
A face-to-face questionnaire designed by researchers was conducted with 24 orthopedic surgeons who perform shoulder arthroscopy operations. The 5 o’clock portal, the Neviaser portal, the G portal, and the transpectoral portal were excluded from the study as they were not located within the safe zone. The other identified seven auxiliary-specific seconder portals were included in our study.
The observers who have been surgeons for at least three years (n=24) were divided into two groups those who regularly perform arthroscopic shoulder operations and those who do not. In the first group, there were 13 orthopedic surgeons who irregularly perform arthroscopic shoulder operations and 11 orthopedic surgeons who regularly perform arthroscopic shoulder operations (>50 operations/year) in the second group.
In the questionnaire study, the names of the auxiliary specific secondary portals were given, and the anatomical localization and the options for the treatment of each pathology were mutually given. Moreover, the observers were asked to choose the correct option and the use of the specific secondary portal in the surgical practice was questioned. Which portals were used in the correct pathology treatment with the correct anatomical definition, and whether need-driven portals opened from the safe zone were used during the operation instead of specific secondary portals were investigated. The correct answer was marked as 1, and the wrong answer as 0. The correct answer rates were evaluated; 75%< was determined as a good result, 50-74% as a moderate, and 49%> as a poor result. SPSS 24 version for Windows was used for statistical analysis. Categorical data between groups were analyzed by Fisher-Exact Test. P<0.05 was accepted as a significant value.
Ethical Approval
This study was approved by the Ethics Committee of Usak University Clinical Researches (Date: 2022-04-06, No: 62-62-06).
Results
The average age of the participant surgeons in the study (n=24) was 40.35±4.83 (32-51), and the average duration of the surgical experience was 11.04±4.72 (3-21) years.
When examined in terms of anatomical localization, one portal had good (antero-inferior=75%) and the other six portals had moderate results (antero-superior=63%, supero-lateral=71%, postero-lateral=67%, 7 o’clock=71%, Wilmington=54%, antero-lateral=58%). When the groups were evaluated separately, five portals were moderate (antero-superior=54%, supero-lateral=62%, antero-inferior=69%, postero-lateral=62%, 7 o’clock=54%) and two portals were poor (Wilmington=38%, antero-lateral=46%) in the first group; 3 portals were good (supero-lateral=82%, antero-inferior=82%, 7 o’clock=91%), and four portals were moderate (antero-superior=73%, postero-lateral=73%, Wilmington=73%, antero-lateral=73%) in the second group (Figure 3). When evaluated in terms of which pathology treatment they are used for, two portals had moderate (supero-lateral=54%, antero-inferior=54%) and five portals had poor results (antero-superior=46%, postero-lateral=46%, 7 o’clock=42%, Wilmington=29%, antero-lateral=42%). When the groups were evaluated separately, while all seven portals had poor results (antero-superior=38%, supero-lateral=46%, antero-inferior=38%, postero-lateral=31%, 7 o’clock=31%, Wilmington=8%, antero-lateral=31%) in the first group, seven portals in the second group had moderate results (antero-superior=55%, supero-lateral=64%, antero-inferior=73%, postero-lateral=64%, 7 o’clock=55%, Wilmington=55%, antero-lateral=55%) (Figure 3). When the groups were statistically evaluated with the Fisher Exact Test in terms of anatomical localization and which pathology treatment they are used for, no significant difference was obtained (p=0.059-0.444), except for the Wilmington portal used in pathological treatment (p=0.018) (Table 1,2). It was determined that four (17%) of the 24 participant surgeons utilized specific secondary portals as standard in their surgical practices whereas the other 20 (83%) surgeons generally used the safe zone after determining the appropriate portal localization. Of the four surgeons using specific secondary portals as standard, one was from the less experienced group and the other three were from the second group.
Discussion
There exist secondary specific portals defined to help the treatment of various pathologies in addition to primary portals in shoulder arthroscopy applications. The anatomical localization of these portals and which pathology treatment they are used for are barely recalled by many surgeons during the operation [4]. The literal approach is to quickly review these portals during preoperative planning and determine the most appropriate ones for the patient’s pathology [5].
Anteroinferior portal is located just lateral to the coracoid. The anterosuperior and anteroinferior portals provide the finest visibility for treatments affecting the anterior capsule, and their usage allows for surgical triangulation in the anterior glenohumeral joint. It provides good visibility of the glenoid neck and inferior; it is used in anterior labral and IGHL repairs and it opens with the inside out technique. The cephalic vein and the axillary nerve are the structures at risk. Placement of anchors via the trans-subscapularis portal has been shown to provide a safe alternative method with better positioning of the lowest anchor compared to traditional AI [6].
The anterosuperior portal is located right off the acromion’s anterolateral border. Starting at the midpoint of the coracoid and the acromion, an outside-in technique is used to form the anterosuperior portal [2]. It remains medial to the superolateral portal, and it is used in cuff repair, SLAP repair, and subacromial decompression. During superior labral anterior-posterior (SLAP) repair, the anterosuperior portal also provides a suitable angle for anchor placement on the anterosuperior glenoid. It opens with an outside-to-inside technique. Though the risk is less than the anteroinferior portal, the cephalic vein and axillary nerve are the structures at risk.
On a line traced from the acromion to the coracoid, the superolateral portal is located just lateral to the acromion. It provides direct visualization of the anterior glenoid and it is especially used in cuff repair as well as helping labral stabilization. It opens with an outside-to-inside technique [7].
The anterolateral portal incision is performed 2 to 3 cm distal to the lateral margin, aligned with the anterior acromion. SLAP is used in the treatment of subacromial impingement and acromioclavicular joint pathology. The axillary nerve is at risk if it remains inferior. Recently, Aouad et al. They concluded that a single anterolateral working portal may be sufficient for rotator cuff repair, acromioplasty, distal clavicle excision, and long head biceps tenodesis [8].
The portal of Wilmington is located 1 cm anterior and 1 cm lateral to the posterolateral corner of the acromion. It is effective in SLAP and also in posterior Bankart treatment by providing anchor placement at a 45-degree angle to the posterosuperior glenoid [9].
The posterolateral portal is located 2-3 cm below the posterolateral corner of the acromion. It is used in subacromial decompression and acromioplasty; additionally, it helps in cuff repair and posterior labral repairs. It opens with an outside-to-inside technique. The axillary nerve is the structure at risk. This portal can also be used for viewing in acromioplasty and rotator cuff repairs [10].
The 7 o’clock (posteroinferior portal) portal is located 2-3 cm inferior to the posterior portal. Davidson has shown that it can be opened inside-out or outside-to-inside [11]. It helps in loose body removal and posteroinferior labral fixation. The suprascapular nerve and artery, axillary nerve, and posterior circumflex artery are neurovascular structures at risk.
The portal of Neviaser is in the sulcus between the posterior of the acromioclavicular joint and the scapular spine. It is used for arthroscopic clavicle distal end resection and anterior supraspinatus repair. A recent study has shown that this portal is also a valid option for antegrade nailing of humeral fractures [12]. A cadaveric study has shown that the minimum distance between the suprascapular nerve and an instrument directed towards the acromioclavicular joint through this portal is 18.5 mm [13].
The 5 o’clock portal is 1 cm inferior to the anteroinferior portal and is accessed via the subscapularis tendon. It is used in low anchor placement in anterior shoulder instability. It is opened with the inside-out technique. Some authors do not recommend its use due to its proximity to neurovascular structures and its risk of cartilage [7]. Although a more medial variation of this portal is not superior to the standard approach, the standard approach has also been recommended for HAGL repair [14].
The G (suprascapular nerve portal) portal is located 2 cm medial to the Neviaser portal, between the clavicle and the scapular spine. It was defined by Lafosse5. It is used in suprascapular nerve decompression by cutting the superior transverse scapular ligament. It is opened with an outside-to-inside technique. The suprascapular nerve and artery are the structures at risk.
The transpectoral portal was defined by Dunn for use in graft and screw placement in arthroscopic Latarjet operation. It is opened with an outside-to-inside technique. It is located medial to the coracoid [15].
Instead, auxiliary portals that open from the inside to the outside or from the outside to the inside from the area determined as the safe zone are frequently preferred. The results of our questionnaire indicated that the poor and moderate results were more in number than the good results, which showed that specific secondary portals are less useful in daily life.
Need-driven portals opened from the safe zone are utilized by many surgeons in daily practice. When auxiliary portals opened from the safe zone were retrospectively examined, they were observed to show similarities with specific secondary portals.
Defined specific secondary portals have been in successful use in shoulder arthroscopy operations for a long time. However, where the anatomical localization of each portal is during the operation and which pathological repair it is used for has been an ongoing concern. For this reason, portals that are opened from the inside to the outside or from the outside to the area that the surgeon needs during the operation are practical and useful.
The seven portals included in the study are located in the safe zone. These portals, which are mostly found to be sufficient in arthroscopic shoulder operations, have a low risk of neurovascular injury. The 5 o’clock portal, the Neviaser portal, and the G portals, which are excluded from the study because of being outside the safe zone, are used less frequently and the risk of neurovascular injury is higher.
The localization of specific secondary portals is determined by a certain distance from anatomical landmarks. These distances can differ between a thin and short patient and a fat and tall patient. As a result of the prolongation of the operation length, the determination of these anatomical landmarks is even more difficult although the appropriate drawings are preoperatively made. Determining the most suitable region by using a spinal needle during the operation and opening the portal prevents this situation in the treatment of pathology. When considering that their clinical training is within a certain standard framework, the main limitation of the study is that not all surgeons are from separate clinics.
Limitation
Due to the design of the study, surgeons were asked to show portal localizations in writing, and although some surgeons did not know the exact definition, they could better show the correct localization on the model or the patient. The absence of a similar study in the literature eliminated the possibility of comparing the results of our study with literature information.
Conclusion
It has been observed that recalling and applying specific secondary portals in daily surgical practice is challenging. Instead, many surgeons find it appropriate to open a portal from a suitable area within the safe zone, with an inside-out or outside-to-inside technique, depending on the location and type of pathology.
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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Gokhan Ilyas, Oguzhan Gokalp. Does the experience affect the knowledge about auxiliary portals in shoulder arthroscopy? a questionnaire study and review of the auxiliary portals. Ann Clin Anal Med 2024;15(7):500-504
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Effect of fusion and disc prosthesis methods on cervical lordosis and adjacent segment degeneration
Atakan Besnek 1, Muhammed Erkan Emrahoğlu 2
1 Departmant of Neurosurgery, Şanlıurfa Training and Research Hospital, Şanlıurfa, 2 Departmant of Neurosurgery, University of Health Sciences, Ankara Etlik City Hospital, Ankara, Turkey
DOI: 10.4328/ACAM.22193 Received: 2024-03-22 Accepted: 2024-05-06 Published Online: 2024-05-16 Printed: 2024-07-01 Ann Clin Anal Med 2024;15(7):505-509
Corresponding Author: Atakan Besnek, Departmant of Neurosurgery, Şanlıurfa Training and Research Hospital, Şanlıurfa, Turkey. E-mail: atakanbesnek80@gmail.com P: +90 506 304 63 69 Corresponding Author ORCID ID: https://orcid.org/0000-0001-6579-6976
Other Author ORCID ID: Muhammed Erkan Emrahoğlu, https://orcid.org/0000-0002-0939-3117
This study was approved by the Ethics Committee of Harran University (Date: 2023-12-25, No: HRÜ/23.24.30)
Aim: Anterior cervical discectomy and fusion (ACDF) and cervical disc prosthesis (CDP) methods, which are applied after anterior cervical discectomy, aim to preserve disc space height and cervical alignment. The aim of this study was to investigate the effect of both methods on cervical lordosis and adjacent segment degeneration.
Material and Methods: Forty-four patients who underwent anterior cervical discectomy between 2019 and 2020 were included in the study. Patients operated on for reasons other than disc herniation or cervical spinal canal narrowing, patients operated on at more than one level, and patients without access to necessary radiological imaging data were not included in the study. Preoperative-postoperative changes in cervical lordosis angle and adjacent segment degenerations were examined.
Results: The preoperative-postoperative change in cervical lordosis angle was −4.1 degrees in the ACDF group and −0.1 degrees in the CDP group (p < 0.001). It was found that preoperative-postoperative upper segment degeneration grades increased in 61.9% of patients in the ACDF group and 8.7% of patients in the CDP group (p < 0.001). It was found that preoperative and postoperative lower segment degeneration grades increased in 47.6% of patients in the ACDF group and 8.7% of patients in the CDP group (p < 0.004).
Discussion: The results obtained in the present study showed that the CDP method was superior to the ACDF method in terms of cervical lordosis angle change and adjacent segment degeneration.
Keywords: Disc Prosthesis, Fusion, Cervical Degeneration
Introduction
Anterior cervical discectomy is a surgical method aimed at reducing nerve compression, preserving disc space height, and maintaining cervical alignment. The Anterior cervical discectomy and fusion (ACDF) method, first introduced by Smith and Robinson in 1958, has been widely acknowledged as the gold standard for degenerative cervical disc disease [1]. Studies and patient follow-ups over time have shown that the ACDF method increases the range of motion in adjacent segments by restricting motion in the operated segment [2, 3]. Although it is not clear whether the adjacent segment disease seen after cervical discectomy is a natural process or is related to changes in range of motion, the cervical disc prosthesis (CDP) method has been employed with this consideration in mind. The method, initially described by Fernström, aims to maintain mobility by employing a disc replacement that allows movement in multiple directions and aims to fulfill the role of the disc [4].
In addition to adjacent segment degeneration and disease, the effect of the two methods on cervical sagittal alignment is also being questioned. In spinal surgery, there has been a significant focus on sagittal balance in recent years. It is well-known that pathologies occurring in areas with significant mobility, particularly in the lumbar and cervical regions, can influence each other [5]. Decreased cervical lordosis is associated with neck pain severity and aggravates the course of myelopathy [6]. Studies comparing ACDF and CDP methods have investigated a cervical range of motion and lordosis angles, yielding varying results. In this study, we aimed to retrospectively examine patients who underwent ACDF and CDP methods, evaluating the effects of the methods on cervical lordosis and adjacent segment degeneration over a three-year follow-up period.
Material and Methods
The study was designed as a retrospective cohort study. Forty-four patients over the age of 18 who underwent anterior cervical discectomy between 2019 and 2020 in the Neurosurgery Clinics of Health Sciences University Dışkapı Yıldırım Beyazıt Training and Research Hospital and Şanlıurfa Training and Research Hospital were included in the study. Of the 44 patients included in the study, 32 were female and 12 were male. The mean age of the patients was 45.4 years. The mean age of patients who underwent CDP was 44, and the mean age of ACDF patients was 47. The exclusion criteria included patients who underwent anterior cervical discectomy operations for reasons other than disc herniation or cervical spinal canal narrowing and had anterior cervical discectomy operations at more than one level. The preoperative and postoperative 3rd year imaging results of the patients were reviewed through the hospital database and patients whose preoperative and postoperative status could not be examined with appropriate imaging methods were not included in the study. The same surgical technique was utilized in both clinics, and following anterior cervical discectomy, two methods were used to complete the surgeries: blade cage or cervical disc prosthesis. The dimensions of the material to be used were decided by examining preoperative cervical two-way radiographs. The blade peek cages used are standard peek cages that do not allow movement, with a locking knife mechanism, a toothed surface and X-ray visible markers. (Figure 1) All disc prostheses used are made of titanium alloy and allow ±8° flexion/extension, ±8° lateral bending and ±5° rotation (Figure 2).
The cervical lordosis angle of the patients was measured by the Cobb method as the angle between the lines passing through the C2 lower end and C7 upper end plate. For the adjacent segment angle, the angle between the lines passing through the upper vertebral lower end and lower vertebral upper end plate adjacent to the discectomized vertebrae was measured. For these measurements, lateral radiographs in which the upper and lower end plates of the C1-7 vertebrae could be observed were used in all patients.
The grading system of Suzuki et al. was used to classify adjacent segment degeneration (Table 1). In this grading system, magnetic resonance imaging (MRI) was used as the basis and grading was based on disc height, nucleus density and structure, nucleus-annulus separation, and presence or absence of disc herniation/bulging. Using preoperative and postoperative 3rd year MRI examinations of the patients, the degree of degeneration was documented and the changes between these periods were recorded.
Ethical Approval
The study was approved by the medical research ethics committee of Harran University (Date: 2023-12-25, No: HRÜ/23.24.30). Due to the retrospective design of the study, informed consent was not required.
Results
A total of 44 patients were included in the study. Of the patients, 21 (47.7%) underwent the ACDF method and 23 (52.3%) underwent the CDP method. Of the patients operated with the ACDF method, 13 (61.9%) were female and 8 (38.1%) were male, while 19 (82.6%) of the patients operated with the CDP method were female and 4 (17.4%) were male. The mean age was 47 years in the ACDF group and 44 years in the CDP group. In the ACDF group, 57.1% of the patients (n=12) were operated at the C6-7 level, while 52.2% of the patients (n = 12) were operated at the C5-6 level in the CDP group.
The preoperative-postoperative change in cervical lordosis angle was −4.1 degrees in the ACDF group and −0.1 degrees in the CDP group (p < 0.001). In preoperative-postoperative measurements of adjacent segments, the difference was −1.6 ± 2.1 degrees in the ACDF group and −1.0 ± 1.2 degrees in the CDP group (p 0.213) (Table 2). When ACDF and CDP groups were evaluated within themselves, cervical lordosis angles in the ACDF group were measured as 14.9 (12.1–17.6) degrees preoperatively and 10.1 (6.1–12.6) degrees postoperatively (p < 0.001). In the CDP group, adjacent segment angles were measured as 7.4 ± 3.4 degrees preoperatively and 6.4 ± 3.3 degrees postoperatively (p = 0.001) (Table 2).
In the ACDF group, among six patients with preoperative Grade 1 degeneration at the upper level, the degeneration level remained unchanged in one patient, Grade 2 degeneration was observed in three patients (50.0%), and Grade 3 degeneration was observed in two patients (33.3%). In 61.5% (n = 8) of patients who initially had Grade 2 degeneration (n = 13), Grade 3 degeneration was observed. Among 10 patients with preoperative Grade 1 degeneration at the lower level, degeneration progressed to Grade 2 in seven patients, while no progression was detected in three patients. Among 9 patients with Grade 2 degeneration at the lower level, degeneration progressed to Grade 3 in three patients (p = 0.007).
In the CDP group, only two of the 13 patients with Grade 1 degeneration at the upper level progressed to Grade 2 degeneration and no progression to Grade 3 was observed in patients with Grade 2 degeneration (p = 0.500). Two of the four patients with Grade 1 degeneration at the lower level progressed to Grade 2 degeneration, while no changes were detected in patients with Grade 2 and Grade 3 degeneration (p = 0.157).
When the two groups were compared, upper segment preoperative-postoperative degeneration grades increased in 61.9% of patients in the ACDF group and 8.7% in the CDP group (p < 0.001). Lower segment preoperative-postoperative degeneration grades increased in 47.6% of patients in the ACDF group and 8.7% in the CDP group (p < 0.004) (Table 3).
Statistical analyses were performed using SPSS 29.0 program. P < 0.05 was accepted as statistically significant in all analyses. Chi-square and Fisher’s exact tests were used to compare independent categorical variables, and the variables were presented in numbers and percentages. The conformity of independent continuous variables to normal distribution was evaluated by the Shapiro-Wilk test. Student’s t-test was used to compare normally distributed continuous variables between groups and the values were presented as mean and standard deviation. Mann-Whitney U test was used to compare non-normally distributed continuous variables between the groups and the values were presented as median and 25 and 75 percentile values. In the dependent analyses, McNemar’s test was used for categorical variables, and either the Wilcoxon signed-rank test or the dependent samples t-test was used for continuous variables according to the normality of distribution.
Discussion
For over 60 years, the ACDF method has been safely applied in patients with cervical disc herniation. However, increased range of motion in adjacent segments, increased intradiscal pressure, and consequently, the development of degeneration and adjacent segment disease have brought the CDP method into prominence, which has been increasingly used in the last decade [7]. The fundamental idea of the CDP method is to provide mobility in the operated segment [8]. In the present study, 23 patients operated with the CDP method and 21 patients operated with the ACDF method were analyzed. In the ACDF group, 57.1% of the patients (n = 12) were operated at the C6-7 level, while in the CDP group, 52.2% of the patients (n = 12) were operated at the C5-6 level. In studies focusing on ranges of motion, significant differences in sagittal balance and range of motion were not observed in surgeries performed at the C5-6 and C6-7 levels. It was reported that for a difference to occur, a significantly larger number of patients would be required [9, 10]. In the present study, we focused on three parameters during postoperative follow-ups: changes in cervical lordosis angle, changes in adjacent segment angles, and changes in the degree of degeneration in adjacent segments.
Studies on the ACDF method have shown that this technique, when applied to a specific segment, terminates mobility in that segment, consequently increasing the range of motion in adjacent segments. In studies focusing on lordosis, short-term follow-ups have shown lordosis loss compared to the CDP method, while limited studies with long-term follow-up reported contradictory results. Donki et al. conducted a study on the sagittal alignment following anterior cervical discectomy, where they observed differences in cervical alignment in the early stages after CDP or ACDF methods. However, their one-year follow-up did not reveal any significant differences [11].Anakwenze et al. found that there was no significant difference in total cervical lordosis angle between CDP and ACDF methods at one-year follow-up [12]. Pandey et al. found the preoperative lordosis angles to be 15.55 ± 2.48 and 15.30 ± 2.14 degrees in the CDP and ACDF groups, respectively, and 16.1 ± 2.3 and 14.98 ± 1.74 degrees in the TDR and ACDF groups, respectively, at 12 months postoperative follow-up. They found a significant difference between the two groups in terms of lordosis angle during the follow-up period (p > 0.05).[7] Eliseev et al. measured cervical lordosis angles preoperatively and at 12 months postoperatively, and reported the angles as 6.9 [−12.2; 2.1] and −14.4 [−17.3; −12.2] in the ACDF method and 5.4 [−3.78; 10.6] and −8.7 [−9.5; 4.9] in the CDP method, respectively (p < 0.001).[9] In the present study, the preoperative-postoperative change in cervical lordosis angles was −4.1 degrees in the ACDF group and −0.1 degrees in the CDP group (p < 0.001). When ACDF and CDP groups were evaluated within themselves, preoperative and postoperative cervical lordosis angles were 15.1 (12.1–17.6) and 10.1 (6.1–12.6) degrees in ACDF group and 11.6 (7.9–14.8) and 11.4 (6.8–15.6) degrees in CDP group (p < 0.001). Even though different results were observed in one-year follow-ups, our study demonstrated that after a three-year follow-up, there was greater cervical lordosis loss in the ACDF method.
Studies conducted on adjacent segments have shown that there is more loss of lordosis and range of motion in the CDP method compared to the ACDF method [9, 10, 12]. Since the present study was conducted retrospectively, we did not focus on range of motion in order to maintain the sample size. Instead, we statistically examined the change in adjacent segment lordosis angle, considering its potential contribution to the literature. In the present study, preoperative and postoperative adjacent segment lordosis angles were measured as 8.8 ± 2.6 and 7.2 ± 2.1 degrees in the ACDF group (p = 0.002) and 7.4 ± 3.4 and 6.4 ± 3.3 degrees in the CDP group (p = 0.001), respectively. The change in the CDP group was statistically significant.
The CDP method preserves motion at the operated segment and reduces stress on adjacent segments, theoretically resulting in a lower incidence of adjacent segment degeneration and disease. The opposite is true with the ACDF method. While this is theoretically the case, many studies have attempted to determine whether this is true in practice. Yan et al. showed that adjacent segment degeneration was less common in the CDP method compared to the ACDF method.[13] Dong et al. and Luo et al. conducted meta-analyses that showed substantially lower adjacent segment degeneration in the CDP method compared to the ACDF method.[14, 15] In the present study, we used the cervical disc degeneration grading system described by Suzuki et al. and examined MRI findings. In addition, changes in degeneration grades in the upper and lower segments in the ACDF and CDP groups were also examined separately. When the two groups were compared, it was found that upper segment preoperative-postoperative degeneration grades increased in 61.9% of patients in the ACDF group and in 8.7% of patients in the CDP group (p < 0.001). It was found that preoperative-postoperative lower segment degeneration grades increased in 47.6% of patients in the ACDF group and 8.7% of patients in the CDP group (p < 0.004). This may be attributed to the fact that the operations were mostly performed at the C5-6 and C6-7 levels and the lower range of motion at the lower levels.
The results obtained in the present study are important as both cervical lordosis and adjacent segment degeneration were examined over a 3-year follow-up period. However, the retrospective study design, the fact that not all patients could be reached in this respect that follow-up imaging could not be performed in all patients, and that imaging studies could not be performed in the same time interval constitute the limitations of this study.
Conclusion
Two commonly used methods were compared in the present study and the changes in adjacent segment and cervical lordosis angles were examined over a long-term follow-up period. The results showed that the CDP method was superior to the ACDF method in terms of cervical lordosis and adjacent segment degeneration. These results can contribute to the literature considering the long follow-up period and the variables analyzed. However, further prospective studies with long-term follow-up are needed.
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.
References
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2. Dahl MC, Rouleau JP, Papadopoulos S, Nuckley DJ, Ching RP. Dynamic characteristics of the intact, fused, and prosthetic-replaced cervical disk. J Biomech Eng. 2006;128(6):809-14.
3. Fuller DA, Kirkpatrick JS, Emery SE, Wilber RG, Davy DT. A kinematic study of the cervical spine before and after segmental arthrodesis. Spine (Phila Pa 1976). 1998;23(15):1649-56.
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5. Morishita Y, Buser Z, D’Oro A, Shiba K, Wang JC. Clinical relationship of degenerative changes between the cervical and lumbar spine. Asian Spine J. 2018;12(2):343-8.
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7. Pandey PK, Pawar I, Gupta J, Verma RR. Comparison of outcomes of single-level anterior cervical discectomy with fusion and single-level artificial cervical disc replacement for single-level cervical degenerative disc disease. Spine (Phila Pa 1976). 2017;42(1):E41-e9.
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9. Eliseev AS, Bokov AE, Mlyavykh SG. Sagittal balance parameters after anterior cervical discectomy with spondylodesis and arthroplasty using endocarbon endoprosthesis: Results of randomized study. Sovrem Tekhnologii Med. 2022;14(4):50-7.
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Atakan Besnek, Muhammed Erkan Emrahoğlu. Effect of fusion and disc prosthesis methods on cervical lordosis and adjacent segment degeneration. Ann Clin Anal Med 2024;15(7):505-509
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Relationship between eosinophil count and mortality in emergency hemodialysis patients
Ramiz Yazıcı, Efe Demir Bala, Ayşe Fethiye Basa Kalafat, İsmail Enver Obuz, Abdullah Aksu, Utku Murat Kalafat, Serkan Doğan
Department of Emergency Medicine, University of Health Sciences, Istanbul Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, Turkey
DOI: 10.4328/ACAM.22200 Received: 2024-03-27 Accepted: 2024-05-13 Published Online: 2024-06-25 Printed: 2024-07-01 Ann Clin Anal Med 2024;15(7):510-513
Corresponding Author: Utku Murat Kalafat, Department of Emergency Medicine, University of Health Sciences, Istanbul Kanuni Sultan Suleyman Training and Research Hospital, 34303 Istanbul, Turkey. E-mail: utkumuratk@yahoo.com P: +90 507 262 74 04 Corresponding Author ORCID ID: https://orcid.org/0000-0003-1749-8098
Other Authors ORCID ID: Ramiz Yazıcı, https://orcid.org/0000-0001-9210-914X . Efe Demir Bala, https://orcid.org/0009-0008-6289-355X . Ayşe Fethiye Basa Kalafat, https://orcid.org/0000-0002-2139-2061 . İsmail Enver Obuz, https://orcid.org/0009-0006-7830-7717 . Abdullah Aksu, https://orcid.org/0009-0003-1631-2770 . Serkan Doğan, https://orcid.org/0000-0001-8923-2489
This study was approved by the Ethics Committee of İstanbul Kanuni Sultan Süleyman Training and Research Hospital (Date: 2022-05-11, No: KAEK/2022.05.98)
Aim: Chronic kidney disease and acute kidney injury are global healthcare problems. Renal replacement treatments, such as hemodialysis, are performed regularly in an emergency setting to treat these conditions. Predicting the outcomes of these patients can help physicians shape their treatment plan. Eosinophils have been shown to play an important role in the inflammatory response. Recent studies also show that they may play a role in endothelial function. Previous studies have shown that using the peripheral eosinophil count (EOC) could be effective in tracking the prognosis of patients receiving hemodialysis. In our study, our aim was to provide an outlook on the correlation of mortality and EOC alongside other laboratory parameters.
Material and Methods: We analyzed the data of 823 selected patients who received emergency hemodialysis treatment in our dialysis unit between the dates 01/01/2020 and 01/04/2022. Data analysis was performed using the IBM SPSS 27.0 statistical package program.
Results: We have found increased serum levels of lactate and potassium in addition to increased white blood cell count and neutrophil count in the mortality group. We have also found decreased levels of EOC and lymphocyte count along with decreased serum creatinine and sodium levels in the mortality group.
Discussion: Chronic Kidney Disease and acute kidney injury are significant causes of morbidity and mortality. While EOC can provide a limited outlook on their short-term mortality rate, more large-scale studies are needed to establish this connection.
Keywords: Eosinophil, Emergency Hemodialysis, Renal Failure, Mortality
Introduction
Eosinophils are blood cells that play a role in innate mucosal immunity and allergic response in human biology. These cells comprise about %1-5 of all circulating leukocytes [1]. Under nominal conditions, the number of peripheral eosinophils is tightly regulated by various mechanisms [2]. However, it is suggested that various diseases and conditions are correlated with peripheral eosinophil count (EOC). Although the roles of eosinophils are well established in hypersensitivity reactions, allergic reactions, and asthma [3], there are also studies that report their involvement in chronic diseases such as diabetes, cardiovascular diseases, and chronic kidney disease [4, 5].
Chronic kidney disease (CKD) is a significant global healthcare challenge with 843 million people affected globally [6]. As a result of the large number of patients and the progressive nature of the disease, CKD has emerged as one of the leading causes of mortality and morbidity, as mentioned by the Global Burden of Disease study [7]. Therefore, it is important for healthcare providers to make good use of any possible biomarkers that can potentially predict disease progression or mortality.
There are several studies that report the correlation between CKD and EOC [8-10]. Furthermore, in some studies, patients receiving renal replacement therapies such as hemodialysis, peritoneal dialysis, or renal transplantation are suggested to be more prone to eosinophilia [10, 11]. In addition to CKD, there are also studies that mention correlations between EOC and another common kidney disease worldwide, acute kidney injury [12].
Acute kidney injury (AKI) is a common condition seen in %5,0-%7,5 of hospitalized patients and %50-60 of critically ill patients [13]. Although its pathophysiology can vary depending on the actual cause of the damage done to the kidney, the result can progress to similar results to CKD. AKI patients may also need renal replacement therapies as an emergency but temporary solution before recovery.
In our study, our objective was to provide an outlook on the correlation between mortality in patients requiring emergency hemodialysis and hemogram parameters, focusing primarily on EOC.
Material and Methods
Study design and settings
This study was designed as a retrospective observational cohort study, conducted between 01/01/2020 and 01/04/2022 in a training and research hospital in the western part of Istanbul. The patients were retrospectively enrolled in the dialysis center registrations.
All authors and researchers followed the rules and guidelines presented by the Declaration of Helsinki while preparing the study protocol. As a retrospective study, we were unable to obtain the approval forms for the participating patients.
Study size
A total of 919 patients were found to have been treated with hemodialysis in our hospital unit according to the records. As this was a retrospective study, no additional form of approval was presented to the individual patients. We excluded patients under 18 years of age from the study. To eliminate possible confounders such as toxidromes, liver encephalopathy, and hypercalcemia, we have excluded 16 patients who were treated with hemodialysis but were not diagnosed with AKI or CKD. After data collection and evaluation, we failed to collect mortality data for 24 patients, so we excluded these patients from the study.56 Patients were excluded from the study as their laboratory results were not complete or faulted.
After all data collection, evaluations, and exclusions were completed, a total of 823 patients were found to be eligible to participate in this study.
Potential sources of bias
As this was a retrospective study, the physician evaluating the patient was unaware of the study. This helped to blind the primary physician, but also limited our ability to fully evaluate the patient by ourselves. We used our hospital records to minimize bias in this regard. This study was carried out in a single center; therefore, the results could be affected by the local population and conditions.
Statistical Analysis
Data analysis was performed using the IBM SPSS 27.0 statistical package program (Armonk, NY: IBM Corp.). In the study, patients were divided into two groups: those with or without mortality. Categorical data are shown as numbers and percentages, and the Pearson chi-square test was used in their analysis. In the analysis of continuous variables; The suitability of the data for normal distribution was analyzed with Kolmogorov–Smirnov and Shapiro Wilk tests and skewness and kurtosis values. The Independent Samples t test was used for comparisons of normally distributed continuous variables, and the Mann Whitney U test was used for data that did not fit. The statistical significance level was accepted as p<0.05.
Ethical Approval
This study was approved by the Ethics Committee of İstanbul Kanuni Sultan Süleyman Training and Research Hospital (Date: 2022-05-11, No: KAEK/2022.05.98).
Results
We have included a total of 823 patients in our study. 475 (%57,7) of these patients were male, while 348 of these patients were female. We detected that 640 (%77,8) of our patients had a preestablished diagnosis of CKD, while the remaining 183 (%22,2) had an AKI that required emergency hemodialysis. Our data also revealed that 458 of our patients have already been treated with routine renal replacement therapy, and all of this group receives hemodialysis regularly. Follow-up data has shown that out of all 823 patients that we have treated with emergency hemodialysis, 429 (%52,1) of the cases resulted in mortality during the duration of our study. We did not detect any correlation between mortality during the duration of our study and receiving emergency hemodialysis with the diagnosis of CKD or AKI. The correlation between mortality and causes of emergency hemodialysis is shown in Table 1. We have detected that serum potassium levels, white blood cell count, neutrophil count, and serum lactate levels were statistically significantly elevated in the mortality group (p=0.003, 0.005, <0.001, <0.001 and <0.001, respectively). Data also showed that lymphocyte, eosinophil, creatinine, and sodium levels were statistically significantly decreased in the mortality group compared to the nonmortality group. (p<0.001, 0.001, <0.001 and 0.009, respectively). Our study did not find any other statistically significant correlation between other parameters and mortality (Table 2).
Discussion
In our study, we have analyzed hemogram parameters and more specifically eosinophil counts in patients who have received emergency hemodialysis. We aimed to find whether there was any correlation between mortality in hemodialysis patients and peripheral eosinophil count and hemogram parameters.
Our study had some limitations. As a retrospective study, we did not have the possibility to evaluate patients in real time. We had to use data records from our hemodialysis unit. This study was conducted in a single center, which also limits the potential scope of the patients.
We have found a mortality rate of %52,1 in patients we treated with emergency hemodialysis, during our study. This high rate of mortality can be explained by the frailty of patients in need of emergency hemodialysis. In a study conducted by Garcia-Canton et al., short-term mortality rates of frail patients were detected as %58,5. The same study also mentioned that chronic kidney disease is a great contributor to frailty [14].
Our findings suggest that the EOC decreased statistically significantly in the mortality group. This result was also in line with the study by Kang et al., which also reported that a slightly increased and decreased EOC was associated with mortality in hemodialysis patients [15]. The mechanisms behind the increase and decrease in eosinophils in hemodialysis patients with mortality are still not well defined. However, in addition to their role in immunologic and allergic reactions, there are studies reporting eosinophils as markers of endothelial damage in the progression of vascular disease. This may be one of the reasons behind the change in EOC in patients on hemodialysis with mortality [16]. Eosinophils also have pro-inflammatory and pro-oxidation properties and these can also cause damage to hemodialysis patients [15].
Our study also found an increase in white blood cells and neutrophils along with a decrease in lymphocytes in hemodialysis patients within the mortality group. The parallel increase in white blood cells and neutrophils along with a decrease in lymphocytes suggests neutrophilic dominance in hemodialysis patients with mortality. This result can be attributed to the reduced antibacterial properties of neutrophils in hemodialysis patients. In a study by Anding et al., a decreased neutrophil killing capacity in patients was reported to be caused by hyperuremia that results in functional impairment in neutrophils from hemodialysis [17]. They did not report a decrease in radical oxygen species (ROS) production, despite phagocyte ability. Another recent study conducted by Talal et al. reports that neutrophils of patients receiving hemodialysis have shown a dramatic reduction in ROS production and severely impaired extracellular trap formation during an oxidative burst [18]. However, both studies support that neutrophils have a decreased functionality in terms of killing power in hemodialysis patients.
Our data suggest that potassium levels were increased in patients in the mortality group. As mentioned by a study conducted by Sun et al., hyperkalemia is a major concern in hemodialysis patients, as it can cause arrhythmias and sudden death. Thus, most patients receiving regular hemodialysis have their dietary potassium intake checked according to current clinical practice [19]. However, another study conducted by Yamaguchi et al. reports that the variability of serum potassium level has an impact on mortality in hemodialysis patients rather than the mean serum potassium level alone [20].
We have detected a decrease in creatinine in patients in the mortality group. This result could be explained by decreased body mass and sarcopenia in critically ill patients. In a study conducted by Mae et al., it was reported that creatinine generation rate can detect sarcopenia in hemodialysis patients [21]. Therefore, our findings supported the study by Harada et al. that reported that sharp decreases in creatinine over time increase the all-cause risk of mortality in hemodialysis patients [22].
Our data reports a decrease in serum sodium levels in patients in the mortality group. This outcome could be supported by the fact that decreased kidney functions and malnutrition in patients who receive hemodialysis can lead to hyponatremia [23]. In a study conducted by Rhee et al., hyponatremia in hemodialysis patients was reported to be associated with an increased risk of mortality [24].
We have found an increase in the serum lactate level in patients in the mortality group. Serum lactate levels could be increased by sepsis and hypoperfusion; however, lactate is metabolized to a lesser extent in kidneys, compared to the liver. Therefore, decreased kidney function could also lead to increased lactate. Although the relationship between lactate and end-stage renal disease remains unclear as mentioned by Puskarich et al., our result could be attributed to impaired perfusion and decreased lactate clearance [25].
Conclusion
Chronic kidney disease and acute kidney injury can cause significant morbidity and mortality. Predicting the short-term outcome of these patients is important in their evaluation in emergency departments. Peripheral eosinophil count has been reported as a possible biomarker for this task in multiple studies, as well as ours; however, there are more large-scale studies needed to establish this connection.
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.
References
1. Klion AD, Ackerman SJ, Bochner BS. Contributions of eosinophils to human health and disease. Annu Rev Pathol. 2020;15:179-209.
2. Rothenberg ME. Eosinophilia. N Engl J Med. 1998;338(22):1592-1600.
3. Akuthota P, Wang HB, Spencer LA, Weller PF. Immunoregulatory roles of eosinophils: A new look at a familiar cell. Clin Exp Allergy. 2008;38(8):1254-63.
4. Syeda MZ, Hong T, Zhang C, Ying S, Shen H. Eosinophils: A friend or foe in human health and diseases. Kidney Dis (Basel). 2022;9(1):26-38.
5. Jackson DJ, Akuthota P, Roufosse F. Eosinophils and eosinophilic immune dysfunction in health and disease. Eur Respir Rev. 2022;31(163):210150.
6. Jager KJ, Kovesdy C, Langham R, Rosenberg M, Jha V, Zoccali C. A single number for advocacy and communication-worldwide more than 850 million individuals have kidney diseases. Nephrol Dial Transplant. 2019;34(11):1803-1805.
7. GBD 2013 Mortality and Causes of Death Collaborators. Global, regional, and national age-sex specific all-cause and cause-specific mortality for 240 causes of death, 1990-2013: A systematic analysis for the Global Burden of Disease Study 2013. Lancet. 2015;385(9963):117-171.
8. Hattori K, Sakaguchi Y, Oka T, Asahina Y, Kawaoka T, Yamamoto R, et al. Interstitial eosinophilic aggregates and kidney outcome in patients with CKD. Clin J Am Soc Nephrol. 2023;18(12):1563-1572.
9. Kielar D, Jones AM, Wang X, Stirnadel-Farrant H, Katial RK, Bansal A, et al. Association between elevated blood eosinophils and chronic kidney disease progression: Analyses of a large United States electronic health records database. Int J Nephrol Renovasc Dis. 2023;16:269-280.
10. Pongdee T, Manemann SM, Decker PA, Larson NB, Moon S, Killian JM, et al. Rethinking blood eosinophil counts: Epidemiology, associated chronic diseases, and increased risks of cardiovascular disease. J Allergy Clin Immunol Glob. 2022;1(4):233-240.
11. Yang J, Fan J, Fan L, Yi C, Lin J, Mao H, et al. Higher eosinophils predict death-censored technique failure in peritoneal dialysis patients. Int Arch Allergy Immunol. 2020;181(10):765-773.
12. Gauckler P, Shin JI, Mayer G, Kronbichler A. Eosinophilia and kidney disease: More than just an incidental finding?. J Clin Med. 2018;7(12):529.
13. Yoon SY, Kim JS, Jeong KH, Kim SK. Acute kidney injury: Biomarker-guided diagnosis and management. Medicina (Kaunas). 2022;58(3):340.
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15. Kang DH, Lee Y, Kleine CE, Lee YK, Park C, Hsiung JT, et al. Eosinophil count and mortality risk in incident hemodialysis patients. Nephrol Dial Transplant. 2020;35(6):1032-1042.
16. Diskin CJ, Stokes TJ, Dansby LM, Radcliff L, Carter TB. The prevalence and meaning of eosinophilia in renal diseases on a nephrology consultation service. Nephrol Dial Transplant. 2011;26(8):2549-2558.
17. Anding K, Gross P, Rost JM, Allgaier D, Jacobs E. The influence of uraemia and haemodialysis on neutrophil phagocytosis and antimicrobial killing. Nephrol Dial Transplant. 2003;18(10):2067-2073.
18. Talal S, Mona K, Karem A, Yaniv L, Reut HM, Ariel S, et al. Neutrophil degranulation and severely impaired extracellular trap formation at the basis of susceptibility to infections of hemodialysis patients. BMC Med. 2022;20(1):364.
19. Sun Z, Jiao J, Lu G, Liu R, Li Z, Sun Y, et al. Overview of research progress on the association of dietary potassium intake with serum potassium and survival in hemodialysis patients, does dietary potassium restriction really benefit hemodialysis patients?. Front Endocrinol (Lausanne). 2023;14:1285929.
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Download attachments: 10.4328.ACAM.22200
Ramiz Yazıcı, Efe Demir Bala, Ayşe Fethiye Basa Kalafat, İsmail Enver Obuz, Abdullah Aksu, Utku Murat Kalafat, Serkan Doğan. Relationship between eosinophil count and mortality in emergency hemodialysis patients. Ann Clin Anal Med 2024;15(7):510-513
Citations in Google Scholar: Google Scholar
This work is licensed under a Creative Commons Attribution 4.0 International License. To view a copy of the license, visit https://creativecommons.org/licenses/by-nc/4.0/
The association between systemic inflammatory indices and prognosis in acute coronary syndrome
Azmi Eyiol 1, Birsen Ertekin 2, Tarık Acar 2
1 Department of Cardiology, University of Health Sciences, Beyhekim Training and Research Hospital, 2 Department of Emergency, University of Health Sciences, Beyhekim Training and Research Hospital, Konya, Turkey
DOI: 10.4328/ACAM.22216 Received: 2024-04-03 Accepted: 2024-05-20 Published Online: 2024-06-05 Printed: 2024-07-01 Ann Clin Anal Med 2024;15(7):514-518
Corresponding Author: Azmi Eyiol, Department of Cardiology, University of Health Sciences, Beyhekim Training and Research Hospital, Konya, Turkey. E-mail: azmieyiol@yahoo.com P: +90 535 479 24 63 Corresponding Author ORCID ID: https://orcid.org/0000-0003-2740-1966
Other Authors ORCID ID: Birsen Ertekin, https://orcid.org/0000-0002-0630-8634 . Tarık Acar, https://orcid.org/0000-0002-1131-4027
This study was approved by the Ethics Committee of Necmettin Erbakan University, Faculty of Medicine (Date: 2024-04-05, No: 2024(4883)(ID:18697)
Aim: This study investigated the prognosis in patients with acute coronary syndrome (ACS) and the relationship with systemic inflammatory indices such as neutrophil-lymphocyte ratio (NLR), platelet-lymphocyte ratio (PLR), systemic immune inflammation index (SII), systemic inflammatory response index (SIRI), prognostic nutritional index (PNI).
Material and Methods: A total of 215 patients diagnosed with ACS between 01.09.2023 and 01.03.2024 were evaluated retrospectively. Patients were divided into two groups as survivors and non-survivors. NLR, PLR, SII, SIRI and PNI levels were statistically compared between these two groups. Variables that may be associated with mortality were subjected to receiver operating characteristic (ROC) analysis.
Results: NLR, PLR, SII and SIRI were significantly higher, whereas PNI was lower in the non-surviving group (p<0.05 for all). According to ROC analysis, SII had the highest and PLR the lowest predictive power of the inflammation indices (Area Under Curve [AUC] : 0.919 and 0.827, respectively).
Discussion: NLR, PLR, SII, SIRI and PNI levels may predict risk stratification and prognosis in patients with ACS.
Keywords: Acute Coronary Syndrome, Neutrophil-lymphocyte Ratio, Platelet-lymphocyte Ratio, Systemic Immune Inflammation Index, Systemic Inflammation Response Index, Prognostic Nutritional Index, Prognosis
Introduction
Acute coronary syndrome (ACS), classified as unstable angina (UAP), non-ST-elevation myocardial infarction (NSTEMI) and ST-elevation myocardial infarction (STEMI), is a leading cause of death worldwide. Modern antithrombotic therapy, secondary prevention and percutaneous coronary intervention (PCI) have reduced mortality from cardiac causes; however, these patients require continuous follow-up to assess and improve their prognosis [1]. In recent years, the use of early risk classification methods and biomarkers to predict the prognosis of patients with ACS has been recommended [2].
Patient assessment using diagnostic tools such as history, physical examination, electrocardiogram (ECG) and cardiac biomarkers are the traditional methods used to differentiate low-risk from high-risk patients; however, none of these methods can reliably exclude ACS. Therefore, several clinical risk scores (e.g. HEART [history, ECG, age, risk factors and troponin], Thrombolysis in Myocardial Infarction [TIMI], The Global Registry of Acute Coronary Events [GRACE], etc.) have been developed to evaluate suspected patients [2]. In addition, although new biomarkers measured from peripheral blood can be used for this purpose, there is still a need for a cheap and easily accessible ideal indicator that can predict clinical outcomes [3].
Atherosclerosis is defined as a continuous, dynamic and inflammatory process in blood vessels. Inflammation and thrombosis have been recognised as an important part of the ischaemia-reperfusion injury in patients with ACS [4]. Indices related to prothrombotic status and inflammation, such as the platelet-to-lymphocyte ratio (PLR) and neutrophil-to-lymphocyte ratio (NLR), which are complete blood count (CBC) markers, may indicate the severity and prognosis of patients with ACS [5]. In recent years, it has been reported that the systemic immune inflammation index (SII) and the systemic inflammation response index (SIRI), which consist of three routine blood markers, can be used for risk classification and prediction of adverse events in cardiovascular disease [6]. Previous studies have shown that low serum albumin levels are associated with poor outcomes and prognosis in ACS. Therefore, it has been highlighted that albumin may be a better acute phase reactant than CBC parameters because it reflects both nutritional status and inflammatory response [7]. The prognostic nutritional index (PNI) calculated from albumin and total lymphocytes was found to be independently associated with all-cause mortality in critically ill patients with ACS [1]. Therefore, in our study, we investigated the relationship between these indices and prognosis in patients with ACS.
Material and Methods
Study design and patient population
Between 01.09.2023 and 01.03.2024, patients who presented to the emergency department (ED) of a training and research hospital, who were diagnosed with ACS based on complaints, history, ECG, and laboratory investigations and underwent coronary angiography (CAG) were evaluated retrospectively, respectively. Patients older than 18 years of age, male or female, whose all clinical and laboratory information could be accessed from the hospital registration system and whose diagnosis of ACS was confirmed according to current guidelines were included in the study [8].
To determine lesion severity, TIMI and HEART scores of patients with UAP/NSTEMI at the time of presentation to the ED and SYNTAX risk scores of all patients after CAG were calculated [9, 10, 11]. Age, gender, history, routine blood tests,type of ACS [STEMI, NSTEMI, UAP], need for vasopressor support and/or mechanical ventilation (MV) in the intensive care unit (ICU), length of ICU stay (LOICUS), length of hospital stay (LOHS) and outcomes (discharge/mortality) were obtained through the hospital registry system and patient epicrises. Mortality evaluation was based on in-hospital mortality.
Patients under 18 years of age, patients receiving acute thrombolytic therapy, pregnant women, patients with a history of acute/chronic haematological diseases, cancers, presence of active infection, immunosuppressive patients and patients whose information could not be accessed from the electronic registry system were excluded from the study. NLR: neutrophil/lymphocyte count, PLR: platelet/lymphocyte count, SII: neutrophil × platelet/lymphocyte count, SIRI: neutrophil × monocyte/lymphocyte count and PNI: 10 × serum albumin (g/dl) + 0.005 × total lymphocyte count (mm3) [1, 5, 12]. Patients were divided into two groups as survivors and non-survivors. All parameters including NLR, PLR, SII, SIRI and PNI levels were statistically compared between these two groups. Variables that may be associated with mortality were subjected to receiver operating characteristic (ROC) analysis. The correlation of inflammatory indices with TIMI, HEART and SYNTAX risk scores was also evaluated.
Haematological and biochemical analysis
Neutrophil, monocyte, lymphocyte, platelet, albumin and Troponin I values were measured in blood samples taken at the time of admission to the ED. CBC markers were determined using Mindray auto haematology analyzer BC-6800 (Shenzhen, China). Mindray chemistry analyzer BS-2000M device was used for biochemical parameters (Shenzhen, China).
Statistical Analysis
Numerical parameters were expressed as median (min-max) or mean±SD, and categorical variables were expressed as frequency and percentage (%). Kolmogrov-Smirnov test, histogram analyses and skewness/kurtosis data were used to evaluate the conformity of the numerical variables to normal distribution. Levene’s test was used to analyse the intergroup homogeneity of the numerical parameters. For the comparison of two independent groups, independent t-test was used for the parameters showing normal distribution characteristics and Mann-Witney U test was used for parameters that did not show normal distribution characteristics. Variables that may be associated with mortality were detailed by ROC analysis and diagnostic/predictive data have been revealed. Correlation relationships were analysed by Spearman’s two-way correlation analysis. In our study, type-I error (alpha) was taken as 0.05 (5%), p<0.05 was accepted as significant and SPSS 21.0 (IBM Inc, Chicago, IL, USA) programme was used.
Ethical Approval
This study was approved by The Necmettin Erbakan University Faculty of Medicine Local Ethics Committee (Date: 2024-04-05, No: 2024(4883)(ID:18697).
Results
A comparison of demographic, clinical and laboratory findings between the surviving and non-surviving patient groups is shown in Table 1. Out of a total of 215 patients, 191 patients survived and 24 patients died. When the surviving and non-surviving patients were compared in terms of gender, platelets, SYNTAX score, LOHS and LOICUS, no significant difference was detected (p>0.05 for all). Age, neutrophils, monocytes, troponin, NLR, PLR, SII, SIRI, TIMI score, HEART score, the proportion of patients requiring MV support and vasopressors were significantly higher in the non-surviving group (p<0.05 for all). In addition, lymphocyte, albumin, PNI, STEMI, NSTEMI, USAP rates and EF values were significantly lower in the non-survival group (p<0.05 for all). ROC analyses of blood parameters, inflammatory indices and risk scores in predicting mortality are shown in Table 2. Among all parameters, platelets and SYNTAX scores were not statistically significant (p>0.05 for all). Among the blood parameters, neutrophils had the highest and monocytes had the lowest predictive value (AUC: 0.950, 0.719, respectively). Among risk scores, TIMI and HEART had the highest and lowest AUC values (AUC: 0.813, 0.719, respectively). Among the inflammation indices, SII and PLR had the highest and lowest predictive power, respectively (AUC: 0.919, 0.827, respectively). The correlation analysis of the inflammatory indices with the risk scores is shown in Table 3. According to this analysis, NLR, PLR, SII and SIRI had a weak positive correlation and PNI a weak negative correlation with the TIMI risk score. Only PNI had a slightly significant negative correlation with the HEART score. Only SIRI had a slightly significant positive correlation with the SYNTAX score. In addition, SIRI had a positive and slightly significant correlation with LOICUS (p<0.05 for all).
Discussion
Coronary artery disease (CAD) is a complex disease involving multiple pathways including inflammation, oxidative stress, myocardial injury, apoptosis, neurohormonal activation and haemodynamic stress. Biomarkers reflecting these pathways may aid in the diagnosis, management and prognosis of CAD and its complications [13]. Different components of the CBC are currently being investigated to determine the severity and prognosis of CAD. Neutrophils, platelets and monocytes have been associated with inflammation, atherosclerosis and the incidence of adverse cardiac events [5]. Lymphocyte-based indices of inflammation are readily available in clinical practice [6]. Indices such as NLR and PLR may have high values in predicting the prognosis of various cardiovascular diseases. Karaca G. et al., associated high NLR values with a higher risk of adverse outcomes in hospitalised STEMI patients [13]. The NLR ratio has been shown to reflect the systemic inflammatory response process that often accompanies myocardial ischaemia and irreversible cardiac damage [14]. In another study, NLR and PLR were significantly correlated with SYNTAX score and GENSINI score. In logistic regression analyses, only NLR was an independent predictor of CAD [15]. Li Q et al suggested that PLR has limited prognostic value in ACS patients and should be used together with other indices to predict cardiovascular outcomes [6]. In our study, NLR and PLR were found to be significantly higher in the non-surviving patient group. However, NLR had a higher predictive power than PLR in predicting mortality (AUC: 0.913, 0.827, respectively). Therefore, NLR may have a stronger ability to predict systemic inflammatory response and mortality than PLR when assessing high-risk patients.
SII and SIRI, which can simultaneously reflect the body’s inflammatory and immune status, are novel prognostic markers that have recently been investigated for cardiovascular mortality. It is thought that SII and SIRI may have a higher predictive power for cardiovascular disease outcomes than NLR and PLR due to their interactions between three different blood cells [16]. In a study of 5602 patients with CAD, higher SII levels were found in the ACS group compared to the non-ACS group, which is thought to reflect the severity of inflammation [3]. In another study of STEMI patients, NLR and SII were found to be useful in predicting the risk of non-reflow after primary PCI [11]. Li et al. found that compared with other markers of systemic inflammation (NLR, PLR, MLR and SII), SIRI was more predictive of future major adverse cardiovascular events (MACE) in patients with CAD [6]. Chen Y et al. also showed that both SII and SIRI were associated with the risk of all-cause mortality in elderly patients with ACS [12]. In our study, both SII and SIRI showed high AUC values for predicting mortality, which is consistent with the literature. In addition, SIRI appears to be a useful index for predicting poor outcomes due to its significant correlation with TIMI, SYNTAX risk scores and LOICUS.
Malnutrition is common in ACS patients and is strongly associated with cardiovascular events [7]. Albumin levels, which have been used for many years to monitor the nutritional status of patients, are an indicator of increased morbidity and mortality in many diseases [17]. In recent years, PNI, another marker that can indicate inflammation and nutritional status, may also be used as a prognostic marker in patients with ACS [7]. Huang Y et al. found that ACS patients with low PNI had longer LOICUS and higher risk of in-hospital mortality compared to patients with high PNI levels [1]. Koçaş BB et al also reported that PNI was an independent predictor of MACE and all-cause mortality in patients with ACS. In addition, it has been highlighted that PNI has the ability to discriminate patients at risk better than other inflammatory indices [7]. In our study, PNI was significantly lower in non-survivors than in survivors. PNI was significantly correlated with both TIMI and HEART risk scores and predicted mortality better than these two risk scores. Therefore, PNI alone may be a useful marker for risk stratification of these patients.
Limitation
The study has several limitations. It is a retrospective and single-center study with a relatively small sample size and therefore cannot be generalized. Second, unmeasured confounders and short follow-up of patients may have affected the results. Therefore, larger prospective studies with longer follow-up periods are needed to confirm the findings. Third, the inflammatory indices investigated in our study were calculated only from CBC parameters at admission and their changes at different times may provide additional prognostic information.
Conclusion
NLR, PLR, SII, SIRI and PNI levels are inflammatory markers that prognosis in patients with ACS. Additionally, NLR, PLR, SII and SIRI had a positive correlation and PNI a negative correlation with the TIMI risk score. For this reason, these markers can early predict risk stratification and assist physicians in the management of ACS.
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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Our mid-and long-term results of endovenous radiofrequency ablation in great saphenous vein insufficiency
Sonay Oğuz
Department of Cardiovascular Surgery, Faculty of Medicine, Canakkale Onsekiz Mart University, Canakkale, Turkey
DOI: 10.4328/ACAM.22217 Received: 2024-04-11 Accepted: 2024-05-20 Published Online: 2024-06-04 Printed: 2024-07-01 Ann Clin Anal Med 2024;15(7):519-522
Corresponding Author: Sonay Oğuz, Department of Cardiovascular Surgery, Faculty of Medicine, Canakkale Onsekiz Mart University, 17100, Canakkale, Turkey. E-mail: soguz@comu.edu.tr P: +90 543 473 39 28 Corresponding Author ORCID ID: https://orcid.org/0000-0002-4274-3828
This study was approved by the Ethics Committee of Çanakkale Onsekiz Mart Univesity (Date: 2023-09-20, No: 2023/12-12)
Aim: Venous insufficiency may occur due to problems in the return of blood to the heart and reverse flows. Endovascular procedures have emerged as an alternative to classical open surgery in treatment. In this study, we aimed to examine the mid- and long-term results of our radiofrequency ablation (RF) applications, which is an endovascular method.
Material and Method: In our study, we included 193 patients who underwent RF in our clinic between June 2017 and March 2022. All patients underwent ablation with an RF catheter by entering the great saphenous vein (GSV) at the appropriate level under local tumescent anesthesia and under Dopplerultrasound guidance. Postoperative follow-up of the patients and Dopplerultrasound controls at the 1st, 6th, 12th and 24th months were performed, and GSV patency and reflux conditions were recorded.
Results: 133 patients were female (68.9%) and 60 patients were male (31.1%). The age range was 22-82 (mean: 52). It was determined that GSV recanalisation and reflux developed in 6 patients (3.1%) at the 1-month follow-up, in 9 patients (4.6%) at the 6th month, and in 11 patients (5.6%) at the 12th and 24th months.
Discussion: RF method is a feasible method with low complications, high patient comfort and success in suitable patients. However, recanalization and recurrence still occur. To achieve higher success rates, the reasons underlying recanalization and recurrence should be examined.
Keywords: Venous Insufficiency, Varicose Vein, Radiofrequency Ablation, Endovenous, Deep Vein Thrombosis
Introduction
The condition in which superficial veins gain elongation and tortuosity is defined as varicose veins [1]. In the pathogenesis of venous disease, venous insufficiency occurs especially with the formation of reflux flows. Deterioration of the valves, which allow flow in one direction, is held responsible for this situation. The vessel that loses its function creates venous hypertension in the distal part, threatening other vessels and increasing the symptoms of the disease at the tissue level. These may impair the quality of life with leg pain, swelling, restlessness, night cramps, and skin changes that may lead to ulceration [2].
It is known that telectasias (C1), known as capillary varicose veins, are seen in 80% of the population, varicose veins (C2) in 20-64%, venous insufficiency (C3-6) in 5% and ulcers (C5-6) in 1-2% [3]. As the disease progresses, it reduces the person’s quality of life and work capacity with increasing symptoms and loss of function and creates an additional burden on the country’s economy with treatment costs [4]. Therefore, it is of particular importance to treat the disease early, before it reaches advanced stages.
The radiofrequency ablation method, which is one of the methods popularly known as closed surgery performed without surgical incisions, stitches, or general anesthesia. It is a method that is easy to apply, has fewer side effects, faster recovery and even allows you to continue working on the same day. Thanks to these advantages, it can be a method that is easily accepted and preferred by patients.
Another important part of the treatment is educating patients and informing them about the things they must follow throughout their life regarding the disease. The main point in this regard is focused on reducing venous pressure. These are a combination of lifestyle, appropriate elastic compression, physical activity regulation, weight regulation and venotonic agents. However, the most important point of the entire treatment is the early correction of the basic damaged vascular pathology. In this regard, the importance of a method that is acceptable to the patient becomes evident.
In this study, we aimed to evaluate the mid- and long-term results of the radiofrequency ablation method we applied in great saphenous vein insufficiency.
Material and Methods
We included 193 patients who underwent RF with the diagnosis of venous insufficiency in our clinic between June 2017 and March 2022. In our study, 133 patients were female (68.9%) and 60 patients were male (31.1%). While the age range was 22-82, the average age was 52±30 (Table 1). All of our patients were diagnosed with Dopplerultrasonography (USG), which was the indication for surgery. In USG, the procedure was performed on patients with GSV reflux lasting more than 2 seconds and BSV diameter over 5.5 mm in the knee area. The average diameter of the BSV in all cases was 6.9 mm (5.5-15 mm). The procedure was performed on both legs of 13 patients, but in separate sessions.
Since the procedure would be performed under local anesthesia, patients did not need preoperative anesthesia evaluation. Before the procedure, the GSV course, diameter, sapheno-femoral junction relationship, aneurysm status, location of the anterior accessory branch, diameter, distal feeding power, and collateral vessels were examined with ultrasound while the patient was standing. Other accompanying venous pathologies (perforating reflux, small safenous vein diameter and course) and most importantly the packages contained in the venous system were marked by determining what should be intervened and what should be removed. No patient required spinal or general anesthesia or sedation. After the patient was monitored, betadine was applied to the leg and sterile conditions were provided with a surgical drape. The USG vascular probe was taken to the operating table through the camera cover. Under USG guidance, a sheath (7F) is placed in the GSV at an appropriate level, mostly below the knee, using the Seldinger technique. Radiofrequency catheter (Veineo®, Fcare system NV, Belgium) was placed through the sheath under USG control, approximately 1 cm distal to the saphenofemoral junction, leaving the epigastric superior vein open. Then, tumescent anesthesia (2 pieces of 8.4% sodium bicarbonate, 20 mL 2% prilocaine, 0.5 mg adrenaline in 500 mL isotonic at +4°C) was infiltrated around the great saphenous vein under USG guidance. RF was applied by reaching 120°C for 4 seconds in each 1 cm segment. After the procedure, USG control showed that GSV was closed. Additional pouch excision and perforating ligation were performed on patients when necessary. After all procedures were completed, the leg was put under elastic compression and the patient was taken to the service for lower extremity elevation. The patient was mobilized postoperatively and was discharged. After the elastic bandage was done for 24 hours, the patient was allowed to wear medium pressure (20-30 mmHg) compression stockings. Additionally, calcium dobesilate 2 x 500mg was added to the patients’ treatment. The first 10th day and 1st, 6th, 12th and 24th month follow-ups were performed, and any developing complications, DopplerUSG and GSV clearances, and reflux status were recorded.
Ethical Approval
This study was approved by the Ethics Committee of Çanakkale Onsekiz Mart Univesity (Date: 2023-09-20, No: 2023/12-12).
Results
According to the preoperative CEAP calcification of the patients, 130 patients (67%) were determined as C2, 155 patients (80%) were determined as C3, and 49 patients (25%) were determined as C4. In preoperative DopplerUSG, the diameter of the GSV in the knee region was found to be an average of 6.7 mm in men, 7.1 mm in women, and 6.9 mm in all cases. All procedures were completed within 20 – 60 minutes. The procedure was performed on one leg of the patients, and 13 patients needed the procedure on the other leg and another session was performed. While the procedure was performed on the left leg in 105 (54.4%) patients, the procedure was performed on the right leg in 88 (45.6%) patients. All patients were mobilized and discharged on the same day (Table 1).
On the 10th postoperative day, there was tenderness along the GSV line in 17 patients (8.8%), erythema in 15 patients (7.7%), phlebitis in 9 patients (4.6%), ecchymosis in 6 patients (3.2%), and cellulite in 2 patients (2.1%). Skin-epidermal abrasion due to elastic bandage was detected in 2 patients (1%). All complaints resolved with local treatment.
At the 1-month follow-up, hardness along the GSV trace and hyperpigmentation at the same level occurred in 24 patients (12.4%). In the 1st month DopplerUSG controls, it was determined that the GSV was open and reflux occurred in 6 (3.1%) patients.
At the 1-year follow-up, DopplerUSG revealed that 11 (5.6%) patients developed open recanalization and reflux in the GSV. The same patency rate was observed at the 2-year follow-up (Table 2).
Discussion
Venous insufficiency and varicose veins continue to be a common disease today. Although stripping and other additional procedures performed with open surgery, which is a traditional method, are still applied, they have disadvantages such as postoperative pain, bleeding, ecchymosis, nerve damage, cosmetic problems and the need for general or spinal anesthesia [5]. It is aimed to reduce these undesirable situations that occur in open surgery with the new endovenous developing methods. Radiofrequency ablation method is one of these systems. The aim is to close the vein by ablation method by sending radiofrequency energy from outside to the catheter placed in the malfunction of the vein segment through percutaneous access.
The lower complication rate and better recovery time of RF compared to open surgery have led to the increasing popularity of minimally invasive interventions in the treatment of venous diseases [6, 7]. The number of thermal ablation methods, including RF, for the treatment of venous disease has surpassed the number of open surgeries in many countries in recent years [8, 9]. Some scientific and medical authorities have begun to recommend RF ablation as the first step in varicose veins and venous insufficiency [10, 11].
In the EVOLVeS study, it was shown that patients who underwent RF ablation with open surgery were able to return to their daily routines and business lives earlier and provided less pain and better cosmetic results [12].
As with open surgery, deep vein thrombosis (DVT) may develop after endovenous interventions. Akça et al. reported in their study that they observed DVT at a rate of 0.7% after RF [13], and in 2 of our patients, DVT developed in the early post-procedure period. One of these patients had Down syndrome, and hematological disorders can also be seen in these syndromic cases. In the subsequent genetic examination of the patient, Factor XIII and MTHFR (A1298C) heterozygous mutations were detected, which may predispose to thrombus. This is a condition that may be related to developed thrombus. The presence of additional accessory saphenous veins in both patients and their wide base connection with the saphenous femoral junction (SFJ) may have triggered the formation of stasis currents and the development of thrombus. However, studies with a larger patient group are needed to support this.
Avacedo et al. In their study, they found the recanalization rate in GSV to be 8.7% in the 3rd year after RF. Current meta-analysis studies found RF ablation rates less than 5 years to be 11.6% and more than 5 years to be 12.9% [14]. In our study, we found the 2-year rate to be 5.6%. Although the advantages and short-term results of RF ablation are widely known, Whiteley et al. [15] also demonstrated its long-term benefit by reporting a 15-year RF ablation success rate of 88% with a good result. Studies have found the surgical stripping recurrence rates to be 17.9% before 5 years and 32.8% after 5 years [14]. This rate shows that the recurrence rate in classical surgical practices is significantly higher over time. This situation once again shows the importance of prioritizing endovascular applications.
Conclusion
Endovenous applications are the generally preferred and prioritized methods. RF method is also an option that should be considered in suitable cases with low complications, high patient comfort and success. However, recanalization and recurrence still occur. To achieve higher success rates, the reasons underlying recanalization and recurrence should be examined.
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.22217
Sonay Oğuz. Our mid-and long-term results of endovenous radiofrequency ablation in great saphenous vein insufficiency. Ann Clin Anal Med 2024;15(7):519-522
Citations in Google Scholar: Google Scholar
This work is licensed under a Creative Commons Attribution 4.0 International License. To view a copy of the license, visit https://creativecommons.org/licenses/by-nc/4.0/