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Colchicine in cardiac disease: a systematic review and meta-analysis of randomized controlled trials

BACKGROUND: Colchicine has unique anti-inflammatory properties that may be beneficial in various cardiovascular conditions. This systematic review and meta-analysis of randomized controlled trials (RCTs) examines this issue. METHODS: We searched MEDLINE, EMBASE, and the Cochrane Database from incept...

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Autores principales: Verma, Subodh, Eikelboom, John W., Nidorf, Stefan M., Al-Omran, Mohammed, Gupta, Nandini, Teoh, Hwee, Friedrich, Jan O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4553011/
https://www.ncbi.nlm.nih.gov/pubmed/26318871
http://dx.doi.org/10.1186/s12872-015-0068-3
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author Verma, Subodh
Eikelboom, John W.
Nidorf, Stefan M.
Al-Omran, Mohammed
Gupta, Nandini
Teoh, Hwee
Friedrich, Jan O.
author_facet Verma, Subodh
Eikelboom, John W.
Nidorf, Stefan M.
Al-Omran, Mohammed
Gupta, Nandini
Teoh, Hwee
Friedrich, Jan O.
author_sort Verma, Subodh
collection PubMed
description BACKGROUND: Colchicine has unique anti-inflammatory properties that may be beneficial in various cardiovascular conditions. This systematic review and meta-analysis of randomized controlled trials (RCTs) examines this issue. METHODS: We searched MEDLINE, EMBASE, and the Cochrane Database from inception to June 2014 for RCTs using colchicine in adult patients with cardiac diseases. Results were pooled using random effects. RESULTS: 15 RCTs (n = 3431 patients, median treatment 3 and follow-up 15 months) were included. All but 2 used colchicine 1 mg/day. In 5 trials, n = 1301) at risk for cardiovascular disease (coronary artery disease, acute coronary syndrome or stroke, post-angioplasty [2 RCTs], or congestive heart failure), colchicine reduced composite cardiovascular outcomes by ~60 % (risk ratio [RR] 0.44, 95 % confidence interval [CI] 0.28-0.69, p = 0.0004; I(2) = 0 %) and showed a trend towards lower all-cause mortality (RR 0.50, 95 % CI 0.23-1.08, p = 0.08; I(2) = 0 %). In pericarditis or post-cardiotomy, colchicine decreased recurrent pericarditis or post-pericardiotomy syndrome (RR 0.50, 95 % CI 0.41-0.60, p < 0.0001; I(2) = 0 %; 8 RCTs, n = 1635), and post-pericardiotomy or ablation induced atrial fibrillation (RR 0.65, 95 % CI 0.51-0.82, p = 0.0003; I(2) = 31 %; 4 RCTs, n = 1118). The most common adverse event was diarrhea. Treatment discontinuation overall and due to adverse events (RR 4.34, 95 % CI 1.70-11.07, p = 0.002; I(2) = 29 %; 7 RCTs, 83/790 [10.5 %] vs. 11/697 [1.6 %]) was higher in colchicine-assigned patients. CONCLUSIONS: Current RCT data suggests that colchicine may reduce the composite rate of cardiovascular adverse outcomes in a range of patients with established cardiovascular disease. Furthermore, colchicine reduces rates of recurrent pericarditis, post-pericardiotomy syndrome, and peri-procedural atrial fibrillation following cardiac surgery. Further RCTs evaluating the potential of colchicine for secondary prevention of cardiovascular events would be of interest.
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spelling pubmed-45530112015-08-30 Colchicine in cardiac disease: a systematic review and meta-analysis of randomized controlled trials Verma, Subodh Eikelboom, John W. Nidorf, Stefan M. Al-Omran, Mohammed Gupta, Nandini Teoh, Hwee Friedrich, Jan O. BMC Cardiovasc Disord Research Article BACKGROUND: Colchicine has unique anti-inflammatory properties that may be beneficial in various cardiovascular conditions. This systematic review and meta-analysis of randomized controlled trials (RCTs) examines this issue. METHODS: We searched MEDLINE, EMBASE, and the Cochrane Database from inception to June 2014 for RCTs using colchicine in adult patients with cardiac diseases. Results were pooled using random effects. RESULTS: 15 RCTs (n = 3431 patients, median treatment 3 and follow-up 15 months) were included. All but 2 used colchicine 1 mg/day. In 5 trials, n = 1301) at risk for cardiovascular disease (coronary artery disease, acute coronary syndrome or stroke, post-angioplasty [2 RCTs], or congestive heart failure), colchicine reduced composite cardiovascular outcomes by ~60 % (risk ratio [RR] 0.44, 95 % confidence interval [CI] 0.28-0.69, p = 0.0004; I(2) = 0 %) and showed a trend towards lower all-cause mortality (RR 0.50, 95 % CI 0.23-1.08, p = 0.08; I(2) = 0 %). In pericarditis or post-cardiotomy, colchicine decreased recurrent pericarditis or post-pericardiotomy syndrome (RR 0.50, 95 % CI 0.41-0.60, p < 0.0001; I(2) = 0 %; 8 RCTs, n = 1635), and post-pericardiotomy or ablation induced atrial fibrillation (RR 0.65, 95 % CI 0.51-0.82, p = 0.0003; I(2) = 31 %; 4 RCTs, n = 1118). The most common adverse event was diarrhea. Treatment discontinuation overall and due to adverse events (RR 4.34, 95 % CI 1.70-11.07, p = 0.002; I(2) = 29 %; 7 RCTs, 83/790 [10.5 %] vs. 11/697 [1.6 %]) was higher in colchicine-assigned patients. CONCLUSIONS: Current RCT data suggests that colchicine may reduce the composite rate of cardiovascular adverse outcomes in a range of patients with established cardiovascular disease. Furthermore, colchicine reduces rates of recurrent pericarditis, post-pericardiotomy syndrome, and peri-procedural atrial fibrillation following cardiac surgery. Further RCTs evaluating the potential of colchicine for secondary prevention of cardiovascular events would be of interest. BioMed Central 2015-08-29 /pmc/articles/PMC4553011/ /pubmed/26318871 http://dx.doi.org/10.1186/s12872-015-0068-3 Text en © Verma et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0 (http://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Verma, Subodh
Eikelboom, John W.
Nidorf, Stefan M.
Al-Omran, Mohammed
Gupta, Nandini
Teoh, Hwee
Friedrich, Jan O.
Colchicine in cardiac disease: a systematic review and meta-analysis of randomized controlled trials
title Colchicine in cardiac disease: a systematic review and meta-analysis of randomized controlled trials
title_full Colchicine in cardiac disease: a systematic review and meta-analysis of randomized controlled trials
title_fullStr Colchicine in cardiac disease: a systematic review and meta-analysis of randomized controlled trials
title_full_unstemmed Colchicine in cardiac disease: a systematic review and meta-analysis of randomized controlled trials
title_short Colchicine in cardiac disease: a systematic review and meta-analysis of randomized controlled trials
title_sort colchicine in cardiac disease: a systematic review and meta-analysis of randomized controlled trials
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4553011/
https://www.ncbi.nlm.nih.gov/pubmed/26318871
http://dx.doi.org/10.1186/s12872-015-0068-3
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