PARADIGM‐HF Trial: Secondary Analyses Address Unanswered Questions

医学 缬沙坦 沙库比林、缬沙坦 沙库比林 依那普利 耐受性 心力衰竭 临床终点 临床试验 重症监护医学 人口 内科学 射血分数 心脏病学 不利影响 血压 血管紧张素转换酶 环境卫生
作者
Kristin R. Smith,Chia‐Chi Hsu,Theodore J. Berei,Ahmed Aldemerdash,Ian B. Hollis,Orly Vardeny,Jo E. Rodgers
出处
期刊:Pharmacotherapy [Wiley]
卷期号:38 (2): 284-298 被引量:11
标识
DOI:10.1002/phar.2075
摘要

Our aim was to summarize published secondary analyses of the PARADIGM ‐ HF trial. In the original trial, published in September 2014, sacubitril/valsartan significantly reduced the primary composite outcome of cardiovascular death or heart failure hospitalization compared to enalapril. This summary provides a resource for clinicians to review subsequent analyses of the landmark trial evaluating the benefit of sacubitril/valsartan in various subgroups and providing information regarding optimal use of this new therapy in the broader heart failure population. A full list of publications of the existing PARDADIGM ‐ HF post hoc analyses was obtained and summarized, grouped by focus (e.g., severity of illness, tolerability). Twenty‐six publications and one abstract analyzing the PARADIGM ‐ HF trial were reviewed, summarizing the most important results that compared the benefits of sacubitril/valsartan to enalapril, including pertinent subgroup information from each analysis. Key publications evaluated the treatment effect of sacubitril/valsartan based on heart failure severity (i.e., ejection fraction or heart failure risk scores), impact on alternate outcomes, influence of additional therapies, tolerability in patients with comorbidities (i.e., diabetes), long‐term benefits, and cost‐effectiveness. In addition, nine ongoing phase III and phase IV clinical trials with sacubitril/valsartan were briefly summarized to address potential future uses in more extensive heart failure settings. The benefit of sacubitril/valsartan over enalapril for the primary endpoint in the PARADIGM ‐ HF trial is maintained throughout numerous secondary analyses. Though the subgroups analyzed are based on participants from a single clinical trial, clinicians can more confidently incorporate this novel therapy into practice with expanded knowledge of these existing analyses as well as ongoing prospective trials.

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