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Cited 7 time in webofscience Cited 12 time in scopus
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The effect of selective serotonin reuptake inhibitors on major adverse cardiovascular events: a meta-analysis of randomized-controlled studies in depression

Authors
Kim, YongHwanLee, Young SookKim, Myeong GyuSong, Yun-KyoungKim, YoungwonJang, HayoungKim, Jae HyunHan, NayoungJi, EunheeKim, In-WhaOh, Jung Mi
Issue Date
Jan-2019
Publisher
LIPPINCOTT WILLIAMS & WILKINS
Keywords
evidence based practice; major adverse cardiovascular event; meta-analysis; selective serotonin reuptake inhibitors
Citation
INTERNATIONAL CLINICAL PSYCHOPHARMACOLOGY, v.34, no.1, pp.9 - 17
Journal Title
INTERNATIONAL CLINICAL PSYCHOPHARMACOLOGY
Volume
34
Number
1
Start Page
9
End Page
17
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/2001
DOI
10.1097/YIC.0000000000000238
ISSN
0268-1315
Abstract
It has been reported that selective serotonin reuptake inhibitors (SSRIs) might induce major adverse cardiovascular events (MACE), but the association between the use of SSRIs and MACE has not been elucidated as yet. Therefore, the aim of this study was to evaluate the association between the use of SSRIs and MACE in depressed patients with previous cardiovascular events. Two researchers independently selected randomizedcontrolled studies (RCTs) according to the predefined inclusion criteria and evaluated the quality of articles. A quantitative analysis was carried out to estimate pooled risk ratios (RRs) for the association between the use of SSRIs and MACE. Ten RCTs were selected in the final analysis. The use of SSRIs in depressed patients with previous cardiovascular events significantly decreased the risk of MACE [RR: 0.74; 95% confidence interval (CI): 0.55-0.99]. The risk of myocardial infarction was also reduced significantly (RR: 0.59, 95% CI: 0.37-0.93), associations with stroke and all-cause-death (cardiac or other causes): risk of stroke (RR: 0.88, 95% CI: 0.35-2.25) or all-cause death (RR: 0.83; 95% CI: 0.66-1.05). This metaanalysis suggests that the use of SSRIs decreased the risk of MACE by significantly reducing the risk of myocardial infraction in patients with depression and previous cardiovascular events. Int Clin Psychopharmacol 34: 91-7 Copyright (c) 2018 Wolters Kluwer Health, Inc. All rights reserved.
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