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Effects of dual blockade in heart failure and renal dysfunction: Systematic review and meta-analysis

OBJECTIVE: The effect of dual renin–angiotensin system (RAS) inhibition in heart failure (HF) is still controversial. Systematic reviews have shown that dual RAS blockade may reduce mortality and hospitalizations, yet it has been associated with the increased risk of renal dysfunction (RD). Surprisi...

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Autores principales: Silva, Alessandra Rodrigues, Martini, Alexandre Goes, Canto, Graziela De Luca, Guerra, Eliete Neves da Silva, Neves, Francisco de Assis Rocha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906583/
https://www.ncbi.nlm.nih.gov/pubmed/31814505
http://dx.doi.org/10.1177/1470320319882656
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author Silva, Alessandra Rodrigues
Martini, Alexandre Goes
Canto, Graziela De Luca
Guerra, Eliete Neves da Silva
Neves, Francisco de Assis Rocha
author_facet Silva, Alessandra Rodrigues
Martini, Alexandre Goes
Canto, Graziela De Luca
Guerra, Eliete Neves da Silva
Neves, Francisco de Assis Rocha
author_sort Silva, Alessandra Rodrigues
collection PubMed
description OBJECTIVE: The effect of dual renin–angiotensin system (RAS) inhibition in heart failure (HF) is still controversial. Systematic reviews have shown that dual RAS blockade may reduce mortality and hospitalizations, yet it has been associated with the increased risk of renal dysfunction (RD). Surprisingly, although RD in patients with HF is frequent, the effect of combining RAS inhibitors in HF patients with RD has never been studied in a meta-analysis. METHODS: A systematic review and meta-analysis of randomized clinical trials involving HF patients with RD who received dual blockade analyzing death, cardiovascular (CV) death or HF hospitalization, and adverse events. RESULTS: Out of 2258 screened articles, 12 studies were included (34,131 patients). Compared with monotherapy, dual RAS inhibition reduced hazard ratio of death to 0.94 (p=0.07) and significantly reduced CV death or HF hospitalization to 0.89 (p=0.0006) in all individuals, and to 0.86 (p=0.005) in patients with RD and to 0.91 (p=0.04) without RD. Nevertheless, dual RAS blockade significantly increased the risk of renal impairment (40%), hyperkalemia (44%), and hypotension (42%), although discontinuation of treatment occurs only in 3.68% versus 2.19% (p=0.00001). CONCLUSIONS: Dual RAS inhibition therapy reduces the risk of CV death or HF hospitalization. However, cautions monitoring for specific adverse events may be warranted.
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spelling pubmed-69065832019-12-18 Effects of dual blockade in heart failure and renal dysfunction: Systematic review and meta-analysis Silva, Alessandra Rodrigues Martini, Alexandre Goes Canto, Graziela De Luca Guerra, Eliete Neves da Silva Neves, Francisco de Assis Rocha J Renin Angiotensin Aldosterone Syst Original Article OBJECTIVE: The effect of dual renin–angiotensin system (RAS) inhibition in heart failure (HF) is still controversial. Systematic reviews have shown that dual RAS blockade may reduce mortality and hospitalizations, yet it has been associated with the increased risk of renal dysfunction (RD). Surprisingly, although RD in patients with HF is frequent, the effect of combining RAS inhibitors in HF patients with RD has never been studied in a meta-analysis. METHODS: A systematic review and meta-analysis of randomized clinical trials involving HF patients with RD who received dual blockade analyzing death, cardiovascular (CV) death or HF hospitalization, and adverse events. RESULTS: Out of 2258 screened articles, 12 studies were included (34,131 patients). Compared with monotherapy, dual RAS inhibition reduced hazard ratio of death to 0.94 (p=0.07) and significantly reduced CV death or HF hospitalization to 0.89 (p=0.0006) in all individuals, and to 0.86 (p=0.005) in patients with RD and to 0.91 (p=0.04) without RD. Nevertheless, dual RAS blockade significantly increased the risk of renal impairment (40%), hyperkalemia (44%), and hypotension (42%), although discontinuation of treatment occurs only in 3.68% versus 2.19% (p=0.00001). CONCLUSIONS: Dual RAS inhibition therapy reduces the risk of CV death or HF hospitalization. However, cautions monitoring for specific adverse events may be warranted. SAGE Publications 2019-12-09 /pmc/articles/PMC6906583/ /pubmed/31814505 http://dx.doi.org/10.1177/1470320319882656 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Article
Silva, Alessandra Rodrigues
Martini, Alexandre Goes
Canto, Graziela De Luca
Guerra, Eliete Neves da Silva
Neves, Francisco de Assis Rocha
Effects of dual blockade in heart failure and renal dysfunction: Systematic review and meta-analysis
title Effects of dual blockade in heart failure and renal dysfunction: Systematic review and meta-analysis
title_full Effects of dual blockade in heart failure and renal dysfunction: Systematic review and meta-analysis
title_fullStr Effects of dual blockade in heart failure and renal dysfunction: Systematic review and meta-analysis
title_full_unstemmed Effects of dual blockade in heart failure and renal dysfunction: Systematic review and meta-analysis
title_short Effects of dual blockade in heart failure and renal dysfunction: Systematic review and meta-analysis
title_sort effects of dual blockade in heart failure and renal dysfunction: systematic review and meta-analysis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906583/
https://www.ncbi.nlm.nih.gov/pubmed/31814505
http://dx.doi.org/10.1177/1470320319882656
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