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

Author:

Silva Alessandra Rodrigues1ORCID,Martini Alexandre Goes12,Canto Graziela De Luca3,Guerra Eliete Neves da Silva4,Neves Francisco de Assis Rocha1

Affiliation:

1. Laboratory of Molecular Pharmacology, Faculty of Health Sciences, University of Brasília, Brazil

2. Department of Internal Medicine, Erasmus Medical Center, Rotterdam, the Netherlands

3. Center for Evidence-Based Health Research, Department of Dentistry, Federal University of Santa Catarina, Brazil

4. Laboratory of Oral Histopathology, Faculty of Health Sciences, University of Brasília, Brazil

Abstract

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.

Publisher

Hindawi Limited

Subject

Endocrinology,Internal Medicine

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