End Points for Clinical Trials in Acute Heart Failure Syndromes

被引:84
作者
Allen, Larry A. [1 ]
Hernandez, Adrian F. [2 ,3 ]
O'Connor, Christopher M. [2 ,3 ]
Felker, G. Michael [2 ,3 ]
机构
[1] Univ Colorado Denver, Dept Med, Div Cardiol, Aurora, CO USA
[2] Duke Univ, Med Ctr, Dept Med, Duke Clin Res Inst, Durham, NC 27710 USA
[3] Duke Univ, Med Ctr, Dept Med, Div Cardiol, Durham, NC 27710 USA
关键词
acute heart failure syndromes/acute decompensated heart failure; end points; randomized controlled trial design; RANDOMIZED-TRIALS; OUTCOMES; DYSPNEA; RISK; TOLVAPTAN; REGISTRY; DEATH; HOSPITALIZATION; ANTAGONIST; MANAGEMENT;
D O I
10.1016/j.jacc.2008.12.079
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Acute heart failure syndromes (AHFS) remain a major cause of morbidity and mortality, in part because the development of new therapies for these disorders has been marked by frequent failure and little success. The heterogeneity of current approaches to AHFS drug development, particularly with regard to end points, remains a major potential barrier to progress in the field. End points involving hemodynamic status, biomarkers, symptoms, hospital stay, end organ function, and mortality have all been employed either alone or in combination in recent randomized clinical trials in AHFS. In this review, we will discuss the various end point domains from both a clinical and a statistical perspective, summarize the wide variety of end points used in completed and ongoing AHFS studies, and suggest steps for greater standardization of end points across AHFS trials. (J Am Coll Cardiol 2009; 53: 2248-58) (C) 2009 by the American College of Cardiology Foundation
引用
收藏
页码:2248 / 2258
页数:11
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