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
  • [11] A Commentary on Clinical Trials in Chronic Heart Failure
    Poole-Wilson, Philip A.
    Lyon, Alexander R.
    Jacques, Adam M.
    SEMINARS IN CARDIOTHORACIC AND VASCULAR ANESTHESIA, 2006, 10 (03) : 242 - 245
  • [12] The Current Focus of Heart Failure Clinical Trials
    Pothineni, Naga Venkata
    Kattoor, Ajoe John
    Kovelamudi, Swathi
    Kenchaiah, Satish
    JOURNAL OF CARDIAC FAILURE, 2018, 24 (05) : 321 - 329
  • [13] Selection of endpoints for heart failure clinical trials
    Zanolla, L
    Zardini, P
    EUROPEAN JOURNAL OF HEART FAILURE, 2003, 5 (06) : 717 - 723
  • [14] Clinical Trials in Heart Failure: Where Are We?
    Pothineni, Naga Venkata K.
    Kattoor, Ajoe J.
    Kovelamudi, Swathi
    Kenchaiah, Satish
    CIRCULATION, 2016, 134
  • [15] Women in Heart Failure Clinical Trials, a Must!
    Raparelli, Valeria
    Wali, Muhammad Ahmer
    Pilote, Louise
    JACC-HEART FAILURE, 2019, 7 (08) : 732 - 733
  • [16] Carvedilol for heart failure: Clinical trials in progress
    McGowan J.
    Murphy R.
    Cleland J.G.F.
    Heart Failure Reviews, 1999, 4 (1) : 89 - 96
  • [17] Clinical Trials of Heart Failure: Is There a Question of Sex?
    Sohani, Zahra N.
    Alyass, Akram
    Pilote, Louise
    CANADIAN JOURNAL OF CARDIOLOGY, 2021, 37 (09) : 1303 - 1309
  • [18] Heart failure treatment — clinical trials versus clinical practice
    Jay N. Cohn
    Nature Reviews Cardiology, 2016, 13 : 316 - 318
  • [19] Ageism in heart failure clinical trials and clinical practice.
    Binns, KG
    Morkane, CM
    O'Mahony, MS
    JOURNAL OF THE AMERICAN GERIATRICS SOCIETY, 2006, 54 (04) : S105 - S105
  • [20] Heart failure treatment - clinical trials versus clinical practice
    Cohn, Jay N.
    NATURE REVIEWS CARDIOLOGY, 2016, 13 (06) : 316 - 317