Omar Almaadawy , Rahma AbdElfattah Ibrahim , Obaid Haque , Mohamed Elnady , Yakubu Bene-Alhasan , Ahmad Elashery
{"title":"5 -羟色胺能抗抑郁药增加左心室辅助装置心力衰竭患者出血风险:系统回顾和荟萃分析","authors":"Omar Almaadawy , Rahma AbdElfattah Ibrahim , Obaid Haque , Mohamed Elnady , Yakubu Bene-Alhasan , Ahmad Elashery","doi":"10.1016/j.cardfail.2024.10.057","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><div>Serotonergic antidepressants (SAs) are the primary pharmacological treatment for depressive symptoms in patients with heart failure (HF). However, concerns have been raised about the potential for bleeding events in patients with left ventricular assist devices (LVADs).</div></div><div><h3>Hypothesis</h3><div>This systematic review and meta-analysis aim to quantify the bleeding risk in patients with heart failure with LVADs who are taking serotonergic antidepressants.</div></div><div><h3>Methods</h3><div>A systematic review and meta-analysis were conducted on clinical trials retrieved from Scopus, Cochrane, PubMed, and Web of Science databases from their inception until March 2024. Studies reporting on the association of bleeding events with the use of SSRI/SNRI therapy were included. The primary outcome was the occurrence of any bleeding events. Data from the studies were pooled using RevMan V5.4, and odds ratios (OR) and confidence intervals (CI) were calculated for the outcome.</div></div><div><h3>Results</h3><div>The meta-analysis included four studies, mainly observational retrospective studies, as the search yielded no randomized controlled trials, with a total of 1006 participants. Among them, 183 of the 408 (44.8%) patients taking SSRIs/SNRIs experienced bleeding, compared to 207 of the 598 (34.6%) patients not taking SSRIs/SNRIs. The increased risk of bleeding was statistically significant (P=0.005), with an odds ratio of 1.45 [95% CI: 1.12, 1.89], favoring the control group (not taking SSRIs/SNRIs). The limitation of this study is the non-availability of randomized data. Also, the bleeding outcome differs across the studies, with two studies reporting the occurrence of any bleeding, two studies reporting gastrointestinal bleeding, and one study reporting hospitalization for any bleeding.</div></div><div><h3>Conclusion</h3><div>The findings suggest that the rate of bleeding is higher in patients with heart failure with LVADs who are treated with serotonergic antidepressants compared to those who are not treated with serotonergic antidepressants. This underscores the need for careful monitoring when prescribing these medications. However, further research is needed to confirm the findings and identify the optimal serotonergic antidepressant associated with less or no bleeding.</div></div>","PeriodicalId":15204,"journal":{"name":"Journal of Cardiac Failure","volume":"31 1","pages":"Page 202"},"PeriodicalIF":9.9000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Serotonergic Antidepressants Increase Bleeding Risk In Heart Failure Patients With Left Ventricular Assist Device: A Systematic Review And Meta-analysis\",\"authors\":\"Omar Almaadawy , Rahma AbdElfattah Ibrahim , Obaid Haque , Mohamed Elnady , Yakubu Bene-Alhasan , Ahmad Elashery\",\"doi\":\"10.1016/j.cardfail.2024.10.057\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Introduction</h3><div>Serotonergic antidepressants (SAs) are the primary pharmacological treatment for depressive symptoms in patients with heart failure (HF). However, concerns have been raised about the potential for bleeding events in patients with left ventricular assist devices (LVADs).</div></div><div><h3>Hypothesis</h3><div>This systematic review and meta-analysis aim to quantify the bleeding risk in patients with heart failure with LVADs who are taking serotonergic antidepressants.</div></div><div><h3>Methods</h3><div>A systematic review and meta-analysis were conducted on clinical trials retrieved from Scopus, Cochrane, PubMed, and Web of Science databases from their inception until March 2024. Studies reporting on the association of bleeding events with the use of SSRI/SNRI therapy were included. The primary outcome was the occurrence of any bleeding events. Data from the studies were pooled using RevMan V5.4, and odds ratios (OR) and confidence intervals (CI) were calculated for the outcome.</div></div><div><h3>Results</h3><div>The meta-analysis included four studies, mainly observational retrospective studies, as the search yielded no randomized controlled trials, with a total of 1006 participants. Among them, 183 of the 408 (44.8%) patients taking SSRIs/SNRIs experienced bleeding, compared to 207 of the 598 (34.6%) patients not taking SSRIs/SNRIs. The increased risk of bleeding was statistically significant (P=0.005), with an odds ratio of 1.45 [95% CI: 1.12, 1.89], favoring the control group (not taking SSRIs/SNRIs). The limitation of this study is the non-availability of randomized data. Also, the bleeding outcome differs across the studies, with two studies reporting the occurrence of any bleeding, two studies reporting gastrointestinal bleeding, and one study reporting hospitalization for any bleeding.</div></div><div><h3>Conclusion</h3><div>The findings suggest that the rate of bleeding is higher in patients with heart failure with LVADs who are treated with serotonergic antidepressants compared to those who are not treated with serotonergic antidepressants. This underscores the need for careful monitoring when prescribing these medications. However, further research is needed to confirm the findings and identify the optimal serotonergic antidepressant associated with less or no bleeding.</div></div>\",\"PeriodicalId\":15204,\"journal\":{\"name\":\"Journal of Cardiac Failure\",\"volume\":\"31 1\",\"pages\":\"Page 202\"},\"PeriodicalIF\":9.9000,\"publicationDate\":\"2025-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Cardiac Failure\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1071916424004792\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/14 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"CARDIAC & CARDIOVASCULAR SYSTEMS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Cardiac Failure","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1071916424004792","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/14 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CARDIAC & CARDIOVASCULAR SYSTEMS","Score":null,"Total":0}
引用次数: 0
摘要
5 -羟色胺能抗抑郁药(SAs)是治疗心力衰竭(HF)患者抑郁症状的主要药物。然而,人们对左心室辅助装置(lvad)患者出血事件的可能性表示担忧。假设:本系统综述和荟萃分析旨在量化lvad心力衰竭患者服用血清素能抗抑郁药的出血风险。方法对检索自Scopus、Cochrane、PubMed和Web of Science数据库至2024年3月的临床试验进行系统评价和meta分析。研究报告了出血事件与使用SSRI/SNRI治疗的关联。主要结局是出血事件的发生。使用RevMan V5.4对研究数据进行汇总,并计算结果的优势比(OR)和置信区间(CI)。结果meta分析包括4项研究,主要是观察性回顾性研究,因为搜索没有随机对照试验,共有1006名参与者。其中,408例服用SSRIs/SNRIs的患者中有183例(44.8%)出现出血,598例未服用SSRIs/SNRIs的患者中有207例(34.6%)出现出血。出血风险增加有统计学意义(P=0.005),优势比为1.45 [95% CI: 1.12, 1.89],有利于对照组(不服用SSRIs/SNRIs)。本研究的局限性是缺乏随机数据。此外,各研究的出血结局也不同,有两项研究报告了出血的发生,两项研究报告了胃肠道出血,一项研究报告了因出血而住院的情况。结论经血清素能抗抑郁药治疗的lvad心力衰竭患者出血率高于未经血清素能抗抑郁药治疗的患者。这强调了在开这些药物处方时仔细监测的必要性。然而,需要进一步的研究来证实这些发现,并确定与出血较少或无出血相关的最佳血清素能抗抑郁药。
Serotonergic Antidepressants Increase Bleeding Risk In Heart Failure Patients With Left Ventricular Assist Device: A Systematic Review And Meta-analysis
Introduction
Serotonergic antidepressants (SAs) are the primary pharmacological treatment for depressive symptoms in patients with heart failure (HF). However, concerns have been raised about the potential for bleeding events in patients with left ventricular assist devices (LVADs).
Hypothesis
This systematic review and meta-analysis aim to quantify the bleeding risk in patients with heart failure with LVADs who are taking serotonergic antidepressants.
Methods
A systematic review and meta-analysis were conducted on clinical trials retrieved from Scopus, Cochrane, PubMed, and Web of Science databases from their inception until March 2024. Studies reporting on the association of bleeding events with the use of SSRI/SNRI therapy were included. The primary outcome was the occurrence of any bleeding events. Data from the studies were pooled using RevMan V5.4, and odds ratios (OR) and confidence intervals (CI) were calculated for the outcome.
Results
The meta-analysis included four studies, mainly observational retrospective studies, as the search yielded no randomized controlled trials, with a total of 1006 participants. Among them, 183 of the 408 (44.8%) patients taking SSRIs/SNRIs experienced bleeding, compared to 207 of the 598 (34.6%) patients not taking SSRIs/SNRIs. The increased risk of bleeding was statistically significant (P=0.005), with an odds ratio of 1.45 [95% CI: 1.12, 1.89], favoring the control group (not taking SSRIs/SNRIs). The limitation of this study is the non-availability of randomized data. Also, the bleeding outcome differs across the studies, with two studies reporting the occurrence of any bleeding, two studies reporting gastrointestinal bleeding, and one study reporting hospitalization for any bleeding.
Conclusion
The findings suggest that the rate of bleeding is higher in patients with heart failure with LVADs who are treated with serotonergic antidepressants compared to those who are not treated with serotonergic antidepressants. This underscores the need for careful monitoring when prescribing these medications. However, further research is needed to confirm the findings and identify the optimal serotonergic antidepressant associated with less or no bleeding.
期刊介绍:
Journal of Cardiac Failure publishes original, peer-reviewed communications of scientific excellence and review articles on clinical research, basic human studies, animal studies, and bench research with potential clinical applications to heart failure - pathogenesis, etiology, epidemiology, pathophysiological mechanisms, assessment, prevention, and treatment.