Should Stroke Trials Adjust Functional Outcome for Baseline Prognostic Factors?

被引:54
作者
Bath, Philip [1 ,2 ]
Gray, Laura J.
Collier, Timothy
机构
[1] Univ Nottingham, Div Stroke Med, Queens Med Ctr, Stroke Trials Unit, Nottingham NG7 2UH, England
[2] London Sch Hyg & Trop Med, Med Stat Unit, London WC1, England
基金
英国医学研究理事会;
关键词
clinical trials; statistical analysis; stroke; ACUTE ISCHEMIC-STROKE; RANDOMIZED CONTROLLED-TRIALS; MIDDLE CEREBRAL-ARTERY; COVARIATE ADJUSTMENT; DECOMPRESSIVE SURGERY; MALIGNANT INFARCTION; EFFICACY TRIAL; CITICOLINE; PREDICTORS;
D O I
10.1161/STROKEAHA.108.519207
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose-Many stroke trials have provided neutral results. Suboptimal statistical analyses may be failing to detect effective interventions. Adjusting outcomes for baseline prognostic factors in the analysis may improve the efficiency of analysis of outcomes. Methods-Data from 23 stroke trials (25 674 patients) assessing functional outcome were included. The prognostic variables considered were age, sex, and baseline severity. Unadjusted and adjusted ordinal logistic regression models were compared using simulated data from each trial (10 000 simulations per trial). Three levels of treatment effect were assessed with ORs of 0.95, 0.74, and 0.57. The reduction in sample size gained from using the adjusted models, as compared with an unadjusted model, was then calculated as a reflection of the increase in statistical power. Results-Adjusting outcome for baseline factors led to a reduction in sample size, which was similar across all 3 treatment effects (median percentage reduction, interquartile range): OR = 0.95: 35.3% (21.0 to 42.1); OR = 0.74: 38.4% (29.4 to 42.7); and OR = 0.57: 38.4% (27.4 to 42.2). As the treatment effect increased, the proportion of simulations in which the treatment effect for the adjusted model was greater than for the unadjusted model also increased. Conclusion-Adjusting for prognostic factors in stroke trials can reduce sample size by at least 20% to 30% (the lower interquartile range) for a given power. Conversely, trialists may want to power for an unadjusted analysis and then increase statistical power by adjusting for prognostic factors. (Stroke. 2009; 40: 888-894.)
引用
收藏
页码:888 / 894
页数:7
相关论文
共 46 条
[1]   Emergency administration of abciximab for treatment of patients with acute ischemic stroke -: Results of a randomized phase 2 trial [J].
Adams, HP ;
Hacke, W ;
Oemar, B ;
Dávalos, A ;
Cook, RA ;
Trouillas, P ;
Fazekas, F ;
Bogousslavsky, J ;
Hilburn, J ;
Torner, J ;
Leclerc, J ;
Shuaib, A ;
Reid, P .
STROKE, 2005, 36 (04) :880-890
[2]  
Agresti A., 1984, ANAL ORDINAL CATEGOR, V1st
[3]   The virtual international stroke trials archive [J].
Ali, Myzoon ;
Bath, Philip M. W. ;
Curram, John ;
Davis, Stephen M. ;
Diener, Hans-Christoph ;
Donnan, Geoffrey A. ;
Fisher, Marc ;
Gregson, Barbara A. ;
Grotta, James ;
Hacke, Werner ;
Hennerici, Michael G. ;
Hommel, Marc ;
Kaste, Markku ;
Marler, John R. ;
Sacco, Ralph L. ;
Teal, Philip ;
Wahlgren, Nils-Gunnar ;
Warach, Steven ;
Weir, Christopher J. ;
Lees, Kennedy R. .
STROKE, 2007, 38 (06) :1905-1910
[4]   Can we improve the statistical analysis of stroke trials? Statistical reanalysis of functional outcomes in stroke trials [J].
Bath, Philip M. W. .
STROKE, 2007, 38 (06) :1911-1915
[5]   Statin treatment withdrawal in ischemic stroke -: A controlled randomized study [J].
Blanco, M. ;
Nombela, F. ;
Castellanos, M. ;
Rodriguez-Yanez, M. ;
Garcia-Gil, M. ;
Leira, R. ;
Lizasoain, I. ;
Serena, J. ;
Vivancos, J. ;
Moro, M. A. ;
Davalos, A. ;
Castillo, J. .
NEUROLOGY, 2007, 69 (09) :904-910
[6]  
CANDELISE L, 1995, LANCET, V346, P1509
[7]   Indications for early aspirin use in acute ischemic stroke - A combined analysis of 40 000 randomized patients from the Chinese Acute Stroke Trial and the International Stroke Trial [J].
Chen, ZM ;
Sandercock, P ;
Pan, HC ;
Counsell, C ;
Collins, R ;
Liu, LS ;
Xie, JX ;
Warlow, C ;
Peto, R .
STROKE, 2000, 31 (06) :1240-1249
[8]   A randomized efficacy trial of citicoline in patients with acute ischemic stroke [J].
Clark, WM ;
Williams, BJ ;
Selzer, KA ;
Zweifler, RM ;
Sabounjian, LA ;
Gammans, RE .
STROKE, 1999, 30 (12) :2592-2597
[9]   A randomized dose-response trial of citicoline in acute ischemic stroke patients [J].
Clark, WM ;
Warach, SJ ;
Pettigrew, LC ;
Gammans, RE ;
Sabounjian, LA .
NEUROLOGY, 1997, 49 (03) :671-678
[10]   A phase III randomized efficacy trial of 2000 mg citicoline in acute ischemic stroke patients [J].
Clark, WM ;
Wechsler, LR ;
Sabounjian, LA ;
Schwiderski, UE .
NEUROLOGY, 2001, 57 (09) :1595-1602