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Antidepressant treatment in patients following acute coronary syndromes: a systematic review and Bayesian meta‐analysis

AIMS: The aim of this study is to investigate the effect of antidepressant therapy on mortality and cardiovascular outcomes in patients with acute coronary syndrome (ACS). METHODS AND RESULTS: We systematically searched PubMed, Embase, and the Cochrane Central Register of Controlled Trials and perfo...

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Autores principales: Sweda, Romy, Siontis, George C.M., Nikolakopoulou, Adriani, Windecker, Stephan, Pilgrim, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754966/
https://www.ncbi.nlm.nih.gov/pubmed/32935927
http://dx.doi.org/10.1002/ehf2.12861
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author Sweda, Romy
Siontis, George C.M.
Nikolakopoulou, Adriani
Windecker, Stephan
Pilgrim, Thomas
author_facet Sweda, Romy
Siontis, George C.M.
Nikolakopoulou, Adriani
Windecker, Stephan
Pilgrim, Thomas
author_sort Sweda, Romy
collection PubMed
description AIMS: The aim of this study is to investigate the effect of antidepressant therapy on mortality and cardiovascular outcomes in patients with acute coronary syndrome (ACS). METHODS AND RESULTS: We systematically searched PubMed, Embase, and the Cochrane Central Register of Controlled Trials and performed a Bayesian random‐effects meta‐analysis of randomized controlled trials that investigated antidepressant pharmacotherapy in patients following ACS. The primary outcome was all‐cause mortality. Secondary outcomes were repeat hospitalizations and recurrent myocardial infarctions (MIs). Ten randomized controlled trials with a total of 1935 patients qualified for inclusion. Selective serotonin reuptake inhibitors were investigated in six, bupropion in three, and mirtazapine in one trial. Placebo was used as control in eight trials. There was no difference in all‐cause mortality [odds ratio (OR) 0.97, 95% credible interval (CrI) 0.66–1.42] and recurrent MI (OR 0.64, 95% CrI 0.40–1.02) between patients receiving antidepressants compared with controls, whereas antidepressant therapy was associated with less repeat hospitalizations (OR 0.62, 95% CrI 0.40–0.94). In patients with ACS and concomitant depression, antidepressants reduced the odds of recurrent MI compared with usual care/placebo (OR 0.45, 95% CrI 0.25–0.81). Extended funnel plots suggest robustness of the observations. CONCLUSIONS: Antidepressants in patients following ACS have no effect on mortality but reduce repeat hospitalizations; in patients with depression, there is a reduced risk of recurrent MI with antidepressant therapy.
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spelling pubmed-77549662020-12-23 Antidepressant treatment in patients following acute coronary syndromes: a systematic review and Bayesian meta‐analysis Sweda, Romy Siontis, George C.M. Nikolakopoulou, Adriani Windecker, Stephan Pilgrim, Thomas ESC Heart Fail Original Research Articles AIMS: The aim of this study is to investigate the effect of antidepressant therapy on mortality and cardiovascular outcomes in patients with acute coronary syndrome (ACS). METHODS AND RESULTS: We systematically searched PubMed, Embase, and the Cochrane Central Register of Controlled Trials and performed a Bayesian random‐effects meta‐analysis of randomized controlled trials that investigated antidepressant pharmacotherapy in patients following ACS. The primary outcome was all‐cause mortality. Secondary outcomes were repeat hospitalizations and recurrent myocardial infarctions (MIs). Ten randomized controlled trials with a total of 1935 patients qualified for inclusion. Selective serotonin reuptake inhibitors were investigated in six, bupropion in three, and mirtazapine in one trial. Placebo was used as control in eight trials. There was no difference in all‐cause mortality [odds ratio (OR) 0.97, 95% credible interval (CrI) 0.66–1.42] and recurrent MI (OR 0.64, 95% CrI 0.40–1.02) between patients receiving antidepressants compared with controls, whereas antidepressant therapy was associated with less repeat hospitalizations (OR 0.62, 95% CrI 0.40–0.94). In patients with ACS and concomitant depression, antidepressants reduced the odds of recurrent MI compared with usual care/placebo (OR 0.45, 95% CrI 0.25–0.81). Extended funnel plots suggest robustness of the observations. CONCLUSIONS: Antidepressants in patients following ACS have no effect on mortality but reduce repeat hospitalizations; in patients with depression, there is a reduced risk of recurrent MI with antidepressant therapy. John Wiley and Sons Inc. 2020-09-16 /pmc/articles/PMC7754966/ /pubmed/32935927 http://dx.doi.org/10.1002/ehf2.12861 Text en © 2020 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of the European Society of Cardiology This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Research Articles
Sweda, Romy
Siontis, George C.M.
Nikolakopoulou, Adriani
Windecker, Stephan
Pilgrim, Thomas
Antidepressant treatment in patients following acute coronary syndromes: a systematic review and Bayesian meta‐analysis
title Antidepressant treatment in patients following acute coronary syndromes: a systematic review and Bayesian meta‐analysis
title_full Antidepressant treatment in patients following acute coronary syndromes: a systematic review and Bayesian meta‐analysis
title_fullStr Antidepressant treatment in patients following acute coronary syndromes: a systematic review and Bayesian meta‐analysis
title_full_unstemmed Antidepressant treatment in patients following acute coronary syndromes: a systematic review and Bayesian meta‐analysis
title_short Antidepressant treatment in patients following acute coronary syndromes: a systematic review and Bayesian meta‐analysis
title_sort antidepressant treatment in patients following acute coronary syndromes: a systematic review and bayesian meta‐analysis
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754966/
https://www.ncbi.nlm.nih.gov/pubmed/32935927
http://dx.doi.org/10.1002/ehf2.12861
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