Problems with use of composite end points in cardiovascular trials: systematic review of randomised controlled trials
Top Cited Papers
- 2 April 2007
- Vol. 334 (7597) , 786-788A
- https://doi.org/10.1136/bmj.39136.682083.ae
Abstract
Objective To explore the extent to which components of composite end points in randomised controlled trials vary in importance to patients, the frequency of events in the more and less important components, and the extent of variability in the relative risk reductions across components. Design Systematic review of randomised controlled trials. Data sources Cardiovascular randomised controlled trials published in the Lancet, Annals of Internal Medicine, Circulation, European Heart Journal, JAMA, and New England Journal of Medicine, from 1 January 2002 to 30 June 2003. Component end points of composite end points were categorised according to importance to patients as fatal, critical, major, moderate, or minor. Results Of 114 identified randomised controlled trials that included a composite end point of importance to patients, 68% (n=77) reported complete component data for the primary composite end point; almost all (98%; n=112) primary composite end points included a fatal end point. Of 84 composite end points for which component data were available, 54% (n=45) showed large or moderate gradients in both importance to patients and magnitude of effect across components. When analysed by categories of importance to patients, the most important components were associated with lower event rates in the control group (medians of 3.3-3.7% for fatal, critical, and major outcomes; 12.3% for moderate outcomes; and 8.0% for minor outcomes). Components of greater importance to patients were associated with smaller treatment effects than less important ones (relative risk reduction of 8% for death and 33% for components of minor importance to patients). Conclusion The use of composite end points in cardiovascular trials is frequently complicated by large gradients in importance to patients and in magnitude of the effect of treatment across component end points. Higher event rates and larger treatment effects associated with less important components may result in misleading impressions of the impact of treatment.This publication has 12 references indexed in Scilit:
- Patients at the center: in our practice, and in our use of language.2004
- Measuring inconsistency in meta-analysesBMJ, 2003
- Composite Outcomes in Randomized TrialsJAMA, 2003
- Combined endpoints: can we use them?Statistics in Medicine, 2002
- Lessons Learned From Recent Cardiovascular Clinical Trials: Part ICirculation, 2002
- Intravascular Gamma Radiation for In-Stent Restenosis in Saphenous-Vein Bypass GraftsNew England Journal of Medicine, 2002
- Renoprotective Effect of the Angiotensin-Receptor Antagonist Irbesartan in Patients with Nephropathy Due to Type 2 DiabetesNew England Journal of Medicine, 2001
- One Thousand Health-Related Quality-of-Life EstimatesMedical Care, 2000
- An approach to evaluating thrombolytic therapy in acute myocardial infarction. The 'unsatisfactory outcome' end point.Circulation, 1992
- A method of assigning scores to the components of a composite outcome: An example from the MITI trialControlled Clinical Trials, 1992