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Aliskiren for heart failure: a systematic review and meta-analysis of randomized controlled trials
OBJECTIVE: To systematically review and synthesize the currently available evidence of aliskiren for the treatment of heart failure. MATERIALS AND METHODS: We systematically searched the Cochrane, Embase and PubMed databases to identify the randomized controlled trials (RCT) on the effects of aliski...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5675703/ https://www.ncbi.nlm.nih.gov/pubmed/29152151 http://dx.doi.org/10.18632/oncotarget.21112 |
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author | Liu, Hongzhi Luo, Hongxing Wang, Suqin Zhang, Cong Hao, Jialiang Gao, Chuanyu |
author_facet | Liu, Hongzhi Luo, Hongxing Wang, Suqin Zhang, Cong Hao, Jialiang Gao, Chuanyu |
author_sort | Liu, Hongzhi |
collection | PubMed |
description | OBJECTIVE: To systematically review and synthesize the currently available evidence of aliskiren for the treatment of heart failure. MATERIALS AND METHODS: We systematically searched the Cochrane, Embase and PubMed databases to identify the randomized controlled trials (RCT) on the effects of aliskiren on heart failure. Data were synthesized with random effects model and presented in forest plot. Publication bias was evaluated with funnel plot. Heterogeneity was evaluated with Begg's test and Egger's test. RESULTS: Of 124 studies, 6 RCT of 9845 heart failure patients were included for meta-analysis, including 3727 patients receiving aliskiren. Compared with the controls, aliskiren did not significantly reduce the all-cause mortality (1.02 [0.91–1.14], I(2) = 0%) or cardiovascular mortality (1.02 [0.88–1.17], I(2) = 7.3%) of heart failure patients. Total adverse events, renal dysfunction, hypotension and hyperkalaemia were not significantly different between the aliskiren group and control group. Begg's test and Egger's test indicated low heterogeneity. Funnel plots indicated low publication bias. CONCLUSIONS: Aliskiren, either used alone or combined with standard medical therapy, does not significantly reduce the all-cause mortality or cardiovascular mortality of heart failure patients. Although aliskiren does not cause statistically higher adverse events, its adverse events may not be neglected. |
format | Online Article Text |
id | pubmed-5675703 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-56757032017-11-18 Aliskiren for heart failure: a systematic review and meta-analysis of randomized controlled trials Liu, Hongzhi Luo, Hongxing Wang, Suqin Zhang, Cong Hao, Jialiang Gao, Chuanyu Oncotarget Meta-Analysis OBJECTIVE: To systematically review and synthesize the currently available evidence of aliskiren for the treatment of heart failure. MATERIALS AND METHODS: We systematically searched the Cochrane, Embase and PubMed databases to identify the randomized controlled trials (RCT) on the effects of aliskiren on heart failure. Data were synthesized with random effects model and presented in forest plot. Publication bias was evaluated with funnel plot. Heterogeneity was evaluated with Begg's test and Egger's test. RESULTS: Of 124 studies, 6 RCT of 9845 heart failure patients were included for meta-analysis, including 3727 patients receiving aliskiren. Compared with the controls, aliskiren did not significantly reduce the all-cause mortality (1.02 [0.91–1.14], I(2) = 0%) or cardiovascular mortality (1.02 [0.88–1.17], I(2) = 7.3%) of heart failure patients. Total adverse events, renal dysfunction, hypotension and hyperkalaemia were not significantly different between the aliskiren group and control group. Begg's test and Egger's test indicated low heterogeneity. Funnel plots indicated low publication bias. CONCLUSIONS: Aliskiren, either used alone or combined with standard medical therapy, does not significantly reduce the all-cause mortality or cardiovascular mortality of heart failure patients. Although aliskiren does not cause statistically higher adverse events, its adverse events may not be neglected. Impact Journals LLC 2017-09-21 /pmc/articles/PMC5675703/ /pubmed/29152151 http://dx.doi.org/10.18632/oncotarget.21112 Text en Copyright: © 2017 Liu et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Meta-Analysis Liu, Hongzhi Luo, Hongxing Wang, Suqin Zhang, Cong Hao, Jialiang Gao, Chuanyu Aliskiren for heart failure: a systematic review and meta-analysis of randomized controlled trials |
title | Aliskiren for heart failure: a systematic review and meta-analysis of randomized controlled trials |
title_full | Aliskiren for heart failure: a systematic review and meta-analysis of randomized controlled trials |
title_fullStr | Aliskiren for heart failure: a systematic review and meta-analysis of randomized controlled trials |
title_full_unstemmed | Aliskiren for heart failure: a systematic review and meta-analysis of randomized controlled trials |
title_short | Aliskiren for heart failure: a systematic review and meta-analysis of randomized controlled trials |
title_sort | aliskiren for heart failure: a systematic review and meta-analysis of randomized controlled trials |
topic | Meta-Analysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5675703/ https://www.ncbi.nlm.nih.gov/pubmed/29152151 http://dx.doi.org/10.18632/oncotarget.21112 |
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