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
[21]   Decompressive surgery for the treatment of malignant infarction of the middle cerebral artery (DESTINY) [J].
Juttler, Eric ;
Schwab, Stefan ;
Schmiedek, Peter ;
Unterberg, Andreas ;
Hennerici, Michael ;
Woitzik, Johannes ;
Witte, Steffen ;
Jenetzky, Ekkehart ;
Hacke, Werner .
STROKE, 2007, 38 (09) :2518-2525
[22]   Minocycline treatment in acute stroke - An open-label, evaluator-blinded study [J].
Lampl, Y. ;
Boaz, M. ;
Gilad, R. ;
Lorberboym, M. ;
Dabby, R. ;
Rapoport, A. ;
Anca-Hershkowitz, M. ;
Sadeh, M. .
NEUROLOGY, 2007, 69 (14) :1404-1410
[23]   NXY-059 for acute ischemic stroke [J].
Lees, KR ;
Zivin, JA ;
Ashwood, T ;
Davalos, A ;
Davis, SM ;
Diener, H ;
Grotta, J ;
Lyden, P ;
Shuaib, A ;
Hårdemark, H ;
Wasiewski, WW .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (06) :588-600
[24]   CAN SIMPLE QUESTIONS ASSESS OUTCOME AFTER STROKE [J].
LINDLEY, RI ;
WADDELL, F ;
LIVINGSTONE, M ;
SANDERCOCK, P ;
DENNIS, MS ;
SLATTERY, J ;
SMITH, B ;
WARLOW, C .
CEREBROVASCULAR DISEASES, 1994, 4 (04) :314-324
[25]   TISSUE-PLASMINOGEN ACTIVATOR FOR ACUTE ISCHEMIC STROKE [J].
MARLER, JR ;
BROTT, T ;
BRODERICK, J ;
KOTHARI, R ;
ODONOGHUE, M ;
BARSAN, W ;
TOMSICK, T ;
SPILKER, J ;
MILLER, R ;
SAUERBECK, L ;
JARRELL, J ;
KELLY, J ;
PERKINS, T ;
MCDONALD, T ;
RORICK, M ;
HICKEY, C ;
ARMITAGE, J ;
PERRY, C ;
THALINGER, K ;
RHUDE, R ;
SCHILL, J ;
BECKER, PS ;
HEATH, RS ;
ADAMS, D ;
REED, R ;
KLEI, M ;
HUGHES, S ;
ANTHONY, J ;
BAUDENDISTEL, D ;
ZADICOFF, C ;
RYMER, M ;
BETTINGER, I ;
LAUBINGER, P ;
SCHMERLER, M ;
MEIROSE, G ;
LYDEN, P ;
RAPP, K ;
BABCOCK, T ;
DAUM, P ;
PERSONA, D ;
BRODY, M ;
JACKSON, C ;
LEWIS, S ;
LISS, J ;
MAHDAVI, Z ;
ROTHROCK, J ;
TOM, T ;
ZWEIFLER, R ;
DUNFORD, J ;
ZIVIN, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (24) :1581-1587
[26]   Calculation of sample size for stroke trials assessing functional outcome: comparison of binary and ordinal approaches [J].
Bath P. .
INTERNATIONAL JOURNAL OF STROKE, 2008, 3 (02) :78-84
[27]  
Peters Gary R., 1996, Stroke, V27, P195
[28]   Subgroup analysis, covariate adjustment and baseline comparisons in clinical trial reporting: current practice and problems [J].
Pocock, SJ ;
Assmann, SE ;
Enos, LE ;
Kasten, LE .
STATISTICS IN MEDICINE, 2002, 21 (19) :2917-2930
[29]   How to select covariates to include in the analysis of a clinical trial [J].
Raab, GM ;
Day, S ;
Sales, J .
CONTROLLED CLINICAL TRIALS, 2000, 21 (04) :330-342
[30]  
Sandercock P, 1997, LANCET, V349, P1569