How robust are clinical trials in heart failure?

被引:63
|
作者
Docherty, Kieran F. [1 ]
Campbell, Ross T. [2 ]
Jhund, Pardeep S. [2 ]
Petrie, Mark C. [1 ]
McMurray, John J. V. [2 ]
机构
[1] Golden Jubilee Natl Hosp, Glasgow G81 4DY, Lanark, Scotland
[2] Univ Glasgow, BHF Cardiovasc Res Ctr, Inst Cardiovasc & Med Sci, Glasgow G12 8TA, Lanark, Scotland
关键词
Heart failure; Clinical trials; CARDIAC-RESYNCHRONIZATION THERAPY; LEFT-VENTRICULAR DYSFUNCTION; CONVERTING-ENZYME INHIBITORS; RANDOMIZED CONTROLLED-TRIAL; ARTERY-BYPASS SURGERY; STATISTICAL SIGNIFICANCE; SYSTOLIC FUNCTION; DOUBLE-BLIND; MORTALITY; MORBIDITY;
D O I
10.1093/eurheartj/ehw427
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims Guidelines for the management of chronic heart failure (CHF) cite the results of randomized controlled trials (RCTs) to support treatment recommendations. The significance of an observed treatment-effect relies on the use of a boundary P-value, most commonly P<0.05. There is concern about relying on arbitrary threshold P-values to report results as `statistically significant'. The `fragility index' (FI) has been proposed as an additional measure of the robustness of trial findings. FI is the minimum number of events needing to change from a non-event to an event in order to render a significant result non-significant. We calculated the FI to examine the robustness of statistically significant RCTs in CHF. Methods and results Two reviewers extracted data from RCTs supporting treatment recommendations in CHF guidelines. Twenty-five eligible trials were identified with a median sample size of 2331 patients (range 129-8399) and a median number of primary endpoints of 688.5 (range 88-2031). For the primary endpoint (analysed for 20 trials), the median FI was 26 (range 0-118). The FI was <= 10 in 7 (35%) of these 20 trials, and in 4 (20%) trials the number of patients lost to follow-up in the treatment group exceeded the FI. Conclusion The results of some large RCTs in CHF hinge on a small number of events. The FI offers an additional, easy to understand metric, which augments the standard reporting of boundary P-values for statistical significance. The FI helps in the interpretation of the robustness of the results of RCTs.
引用
收藏
页码:338 / +
页数:10
相关论文
共 50 条
  • [1] HEART FAILURE Heart failure clinical trials: how do we define success?
    Ziaeian, Boback
    Fonarow, Gregg C.
    NATURE REVIEWS CARDIOLOGY, 2013, 10 (09) : 492 - 494
  • [2] Clinical trials in heart failure
    Hobbs, R
    ADVANCES IN HEART FAILURE, 2002, : 351 - 356
  • [3] Clinical trials on heart failure
    Aguilar, JC
    Martínez, AH
    REVISTA ESPANOLA DE CARDIOLOGIA, 2001, 54 : 22 - 31
  • [4] Heart failure clinical trials: how do we define success?
    Boback Ziaeian
    Gregg C. Fonarow
    Nature Reviews Cardiology, 2013, 10 : 492 - 494
  • [5] Conduct of Clinical Trials in Acute Heart Failure: Regional Differences in Heart Failure Clinical Trials
    Fiuzat, Mona
    Califf, Robert M.
    HEART FAILURE CLINICS, 2011, 7 (04) : 539 - +
  • [6] Rethinking heart failure clinical trials: the heart failure collaboratory
    Alkalbani, Mutaz
    Psotka, Mitchell A.
    FRONTIERS IN CARDIOVASCULAR MEDICINE, 2024, 11
  • [7] Clinical trials in diastolic heart failure
    Massie, BM
    Fabi, MR
    PROGRESS IN CARDIOVASCULAR DISEASES, 2005, 47 (06) : 389 - 395
  • [8] Clinical trials of carvedilol in heart failure
    Tang W.H.W.
    Fowler M.B.
    Heart Failure Reviews, 1999, 4 (1) : 79 - 88
  • [9] Novel Endpoints for Heart Failure Clinical Trials
    Hamo C.E.
    Gheorghiade M.
    Butler J.
    Current Heart Failure Reports, 2017, 14 (4) : 210 - 216
  • [10] Update in recent clinical trials in heart failure
    Parikh, Vishal
    Bhardwaj, Anju
    Nair, Ajith
    Bozkurt, Biykem
    CURRENT OPINION IN CARDIOLOGY, 2019, 34 (04) : 307 - 314