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Published in: BMC Medical Research Methodology 1/2013

Open Access 01-12-2013 | Research article

Adjusting for multiple prognostic factors in the analysis of randomised trials

Authors: Brennan C Kahan, Tim P Morris

Published in: BMC Medical Research Methodology | Issue 1/2013

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Abstract

Background

When multiple prognostic factors are adjusted for in the analysis of a randomised trial, it is unclear (1) whether it is necessary to account for each of the strata, formed by all combinations of the prognostic factors (stratified analysis), when randomisation has been balanced within each stratum (stratified randomisation), or whether adjusting for the main effects alone will suffice, and (2) the best method of adjustment in terms of type I error rate and power, irrespective of the randomisation method.

Methods

We used simulation to (1) determine if a stratified analysis is necessary after stratified randomisation, and (2) to compare different methods of adjustment in terms of power and type I error rate. We considered the following methods of analysis: adjusting for covariates in a regression model, adjusting for each stratum using either fixed or random effects, and Mantel-Haenszel or a stratified Cox model depending on outcome.

Results

Stratified analysis is required after stratified randomisation to maintain correct type I error rates when (a) there are strong interactions between prognostic factors, and (b) there are approximately equal number of patients in each stratum. However, simulations based on real trial data found that type I error rates were unaffected by the method of analysis (stratified vs unstratified), indicating these conditions were not met in real datasets. Comparison of different analysis methods found that with small sample sizes and a binary or time-to-event outcome, most analysis methods lead to either inflated type I error rates or a reduction in power; the lone exception was a stratified analysis using random effects for strata, which gave nominal type I error rates and adequate power.

Conclusions

It is unlikely that a stratified analysis is necessary after stratified randomisation except in extreme scenarios. Therefore, the method of analysis (accounting for the strata, or adjusting only for the covariates) will not generally need to depend on the method of randomisation used. Most methods of analysis work well with large sample sizes, however treating strata as random effects should be the analysis method of choice with binary or time-to-event outcomes and a small sample size.
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Literature
1.
go back to reference Hernandez AV, Steyerberg EW, Habbema JD: Covariate adjustment in randomized controlled trials with dichotomous outcomes increases statistical power and reduces sample size requirements. J Clin Epidemiol. 2004, 57 (5): 454-460. 10.1016/j.jclinepi.2003.09.014.CrossRefPubMed Hernandez AV, Steyerberg EW, Habbema JD: Covariate adjustment in randomized controlled trials with dichotomous outcomes increases statistical power and reduces sample size requirements. J Clin Epidemiol. 2004, 57 (5): 454-460. 10.1016/j.jclinepi.2003.09.014.CrossRefPubMed
2.
go back to reference Turner EL, Perel P, Clayton T, Edwards P, Hernandez AV, Roberts I, Shakur H, Steyerberg EW: Covariate adjustment increased power in randomized controlled trials: an example in traumatic brain injury. J Clin Epidemiol. 2012, 65 (5): 474-481. 10.1016/j.jclinepi.2011.08.012.CrossRefPubMed Turner EL, Perel P, Clayton T, Edwards P, Hernandez AV, Roberts I, Shakur H, Steyerberg EW: Covariate adjustment increased power in randomized controlled trials: an example in traumatic brain injury. J Clin Epidemiol. 2012, 65 (5): 474-481. 10.1016/j.jclinepi.2011.08.012.CrossRefPubMed
3.
4.
go back to reference Hernandez AV, Eijkemans MJ, Steyerberg EW: Randomized controlled trials with time-to-event outcomes: how much does prespecified covariate adjustment increase power?. Ann Epidemiol. 2006, 16 (1): 41-48. 10.1016/j.annepidem.2005.09.007.CrossRefPubMed Hernandez AV, Eijkemans MJ, Steyerberg EW: Randomized controlled trials with time-to-event outcomes: how much does prespecified covariate adjustment increase power?. Ann Epidemiol. 2006, 16 (1): 41-48. 10.1016/j.annepidem.2005.09.007.CrossRefPubMed
5.
go back to reference Hernandez AV, Steyerberg EW, Butcher I, Mushkudiani N, Taylor GS, Murray GD, Marmarou A, Choi SC, Lu J, Habbema JD, et al: Adjustment for strong predictors of outcome in traumatic brain injury trials: 25% reduction in sample size requirements in the IMPACT study. J Neurotrauma. 2006, 23 (9): 1295-1303. 10.1089/neu.2006.23.1295.CrossRefPubMed Hernandez AV, Steyerberg EW, Butcher I, Mushkudiani N, Taylor GS, Murray GD, Marmarou A, Choi SC, Lu J, Habbema JD, et al: Adjustment for strong predictors of outcome in traumatic brain injury trials: 25% reduction in sample size requirements in the IMPACT study. J Neurotrauma. 2006, 23 (9): 1295-1303. 10.1089/neu.2006.23.1295.CrossRefPubMed
6.
go back to reference McHugh GS, Butcher I, Steyerberg EW, Marmarou A, Lu J, Lingsma HF, Weir J, Maas AI, Murray GD: A simulation study evaluating approaches to the analysis of ordinal outcome data in randomized controlled trials in traumatic brain injury: results from the IMPACT project. Clin Trials. 2010, 7 (1): 44-57. 10.1177/1740774509356580.CrossRefPubMed McHugh GS, Butcher I, Steyerberg EW, Marmarou A, Lu J, Lingsma HF, Weir J, Maas AI, Murray GD: A simulation study evaluating approaches to the analysis of ordinal outcome data in randomized controlled trials in traumatic brain injury: results from the IMPACT project. Clin Trials. 2010, 7 (1): 44-57. 10.1177/1740774509356580.CrossRefPubMed
7.
go back to reference Negassa A, Hanley JA: The effect of omitted covariates on confidence interval and study power in binary outcome analysis: a simulation study. Contemp Clin Trials. 2007, 28 (3): 242-248. 10.1016/j.cct.2006.08.007.CrossRefPubMed Negassa A, Hanley JA: The effect of omitted covariates on confidence interval and study power in binary outcome analysis: a simulation study. Contemp Clin Trials. 2007, 28 (3): 242-248. 10.1016/j.cct.2006.08.007.CrossRefPubMed
8.
go back to reference Yu LM, Chan AW, Hopewell S, Deeks JJ, Altman DG: Reporting on covariate adjustment in randomised controlled trials before and after revision of the 2001 CONSORT statement: a literature review. Trials. 2010, 11: 59-10.1186/1745-6215-11-59.CrossRefPubMedPubMedCentral Yu LM, Chan AW, Hopewell S, Deeks JJ, Altman DG: Reporting on covariate adjustment in randomised controlled trials before and after revision of the 2001 CONSORT statement: a literature review. Trials. 2010, 11: 59-10.1186/1745-6215-11-59.CrossRefPubMedPubMedCentral
9.
go back to reference Kahan BC, Morris TP: Improper analysis of trials randomised using stratified blocks or minimisation. Stat Med. 2012, 31 (4): 328-340. 10.1002/sim.4431.CrossRefPubMed Kahan BC, Morris TP: Improper analysis of trials randomised using stratified blocks or minimisation. Stat Med. 2012, 31 (4): 328-340. 10.1002/sim.4431.CrossRefPubMed
10.
go back to reference Kahan BC, Morris TP: Reporting and analysis of trials using stratified randomisation in leading medical journals: review and reanalysis. BMJ. 2012, 345: e5840-10.1136/bmj.e5840.CrossRefPubMedPubMedCentral Kahan BC, Morris TP: Reporting and analysis of trials using stratified randomisation in leading medical journals: review and reanalysis. BMJ. 2012, 345: e5840-10.1136/bmj.e5840.CrossRefPubMedPubMedCentral
11.
go back to reference Parzen M, Lipsitz SR, Dear KBG: Does clustering affect the usual test statistics of no treatment effect in a randomized clinical trial?. Biom J. 1998, 40: 385-402. 10.1002/(SICI)1521-4036(199808)40:4<385::AID-BIMJ385>3.0.CO;2-#.CrossRef Parzen M, Lipsitz SR, Dear KBG: Does clustering affect the usual test statistics of no treatment effect in a randomized clinical trial?. Biom J. 1998, 40: 385-402. 10.1002/(SICI)1521-4036(199808)40:4<385::AID-BIMJ385>3.0.CO;2-#.CrossRef
12.
go back to reference Kahan BC, Morris TP: Assessing potential sources of clustering in individually randomised trials. BMC Med Res Methodol. 2013, 13 (1): 58-10.1186/1471-2288-13-58.CrossRefPubMedPubMedCentral Kahan BC, Morris TP: Assessing potential sources of clustering in individually randomised trials. BMC Med Res Methodol. 2013, 13 (1): 58-10.1186/1471-2288-13-58.CrossRefPubMedPubMedCentral
13.
go back to reference Weir CJ, Lees KR: Comparison of stratification and adaptive methods for treatment allocation in an acute stroke clinical trial. Stat Med. 2003, 22 (5): 705-726. 10.1002/sim.1366.CrossRefPubMed Weir CJ, Lees KR: Comparison of stratification and adaptive methods for treatment allocation in an acute stroke clinical trial. Stat Med. 2003, 22 (5): 705-726. 10.1002/sim.1366.CrossRefPubMed
14.
go back to reference Kahan BC, Morris TP: Analysis of multicentre trials with continuous outcomes: when and how should we account for centre effects?. Stat Med. 2013, 32 (7): 1136-1149. 10.1002/sim.5667.CrossRefPubMed Kahan BC, Morris TP: Analysis of multicentre trials with continuous outcomes: when and how should we account for centre effects?. Stat Med. 2013, 32 (7): 1136-1149. 10.1002/sim.5667.CrossRefPubMed
15.
go back to reference Rosenberger WF, Lachin JM: Randomization in clinical trials: theory and practice. 2002, New York: John Wiley & Sons, Inc.CrossRef Rosenberger WF, Lachin JM: Randomization in clinical trials: theory and practice. 2002, New York: John Wiley & Sons, Inc.CrossRef
16.
go back to reference Kahan BC: Rank minimization with a two-step analysis should not replace randomization in clinical trials. J Clin Epidemiol. 2012, 65 (7): 808-809.CrossRefPubMed Kahan BC: Rank minimization with a two-step analysis should not replace randomization in clinical trials. J Clin Epidemiol. 2012, 65 (7): 808-809.CrossRefPubMed
17.
go back to reference Agresti A, Hartzel J: Strategies for comparing treatments on a binary response with multi-centre data. Stat Med. 2000, 19 (8): 1115-1139. 10.1002/(SICI)1097-0258(20000430)19:8<1115::AID-SIM408>3.0.CO;2-X.CrossRefPubMed Agresti A, Hartzel J: Strategies for comparing treatments on a binary response with multi-centre data. Stat Med. 2000, 19 (8): 1115-1139. 10.1002/(SICI)1097-0258(20000430)19:8<1115::AID-SIM408>3.0.CO;2-X.CrossRefPubMed
18.
go back to reference Pickering RM, Weatherall M: The analysis of continuous outcomes in multi-centre trials with small centre sizes. Stat Med. 2007, 26 (30): 5445-5456. 10.1002/sim.3068.CrossRefPubMed Pickering RM, Weatherall M: The analysis of continuous outcomes in multi-centre trials with small centre sizes. Stat Med. 2007, 26 (30): 5445-5456. 10.1002/sim.3068.CrossRefPubMed
19.
go back to reference Chu R, Thabane L, Ma J, Holbrook A, Pullenayegum E, Devereaux PJ: Comparing methods to estimate treatment effects on a continuous outcome in multicentre randomized controlled trials: a simulation study. BMC Med Res Methodol. 2011, 11: 21-10.1186/1471-2288-11-21.CrossRefPubMedPubMedCentral Chu R, Thabane L, Ma J, Holbrook A, Pullenayegum E, Devereaux PJ: Comparing methods to estimate treatment effects on a continuous outcome in multicentre randomized controlled trials: a simulation study. BMC Med Res Methodol. 2011, 11: 21-10.1186/1471-2288-11-21.CrossRefPubMedPubMedCentral
20.
go back to reference Localio AR, Berlin JA, Ten Have TR, Kimmel SE: Adjustments for center in multicenter studies: an overview. Ann Intern Med. 2001, 135 (2): 112-123. 10.7326/0003-4819-135-2-200107170-00012.CrossRefPubMed Localio AR, Berlin JA, Ten Have TR, Kimmel SE: Adjustments for center in multicenter studies: an overview. Ann Intern Med. 2001, 135 (2): 112-123. 10.7326/0003-4819-135-2-200107170-00012.CrossRefPubMed
21.
go back to reference Glidden DV, Vittinghoff E: Modelling clustered survival data from multicentre clinical trials. Stat Med. 2004, 23 (3): 369-388. 10.1002/sim.1599.CrossRefPubMed Glidden DV, Vittinghoff E: Modelling clustered survival data from multicentre clinical trials. Stat Med. 2004, 23 (3): 369-388. 10.1002/sim.1599.CrossRefPubMed
22.
go back to reference Neuhaus JM, McCulloch CE, Boylan R: Estimation of covariate effects in generalized linear mixed models with a misspecified distribution of random intercepts and slopes. Stat Med. 2013, 32 (14): 2419-2429. 10.1002/sim.5682.CrossRefPubMed Neuhaus JM, McCulloch CE, Boylan R: Estimation of covariate effects in generalized linear mixed models with a misspecified distribution of random intercepts and slopes. Stat Med. 2013, 32 (14): 2419-2429. 10.1002/sim.5682.CrossRefPubMed
23.
go back to reference Hauck WW, Anderson S, Marcus SM: Should we adjust for covariates in nonlinear regression analyses of randomized trials?. Control Clin Trials. 1998, 19 (3): 249-256. 10.1016/S0197-2456(97)00147-5.CrossRefPubMed Hauck WW, Anderson S, Marcus SM: Should we adjust for covariates in nonlinear regression analyses of randomized trials?. Control Clin Trials. 1998, 19 (3): 249-256. 10.1016/S0197-2456(97)00147-5.CrossRefPubMed
24.
go back to reference Robinson LD, Jewell NP: Some surprising results about covariate adjustment in logistic regression models. Int Stat Rev. 1991, 58: 227-240.CrossRef Robinson LD, Jewell NP: Some surprising results about covariate adjustment in logistic regression models. Int Stat Rev. 1991, 58: 227-240.CrossRef
25.
go back to reference Rahman NM, Maskell NA, West A, Teoh R, Arnold A, Mackinlay C, Peckham D, Davies CW, Ali N, Kinnear W, et al: Intrapleural use of tissue plasminogen activator and DNase in pleural infection. N Engl J Med. 2011, 365 (6): 518-526. 10.1056/NEJMoa1012740.CrossRefPubMed Rahman NM, Maskell NA, West A, Teoh R, Arnold A, Mackinlay C, Peckham D, Davies CW, Ali N, Kinnear W, et al: Intrapleural use of tissue plasminogen activator and DNase in pleural infection. N Engl J Med. 2011, 365 (6): 518-526. 10.1056/NEJMoa1012740.CrossRefPubMed
26.
go back to reference Kahan BC: Bias in randomised factorial trials. Stat Med. 2013, 10.1002/sim.5869. Kahan BC: Bias in randomised factorial trials. Stat Med. 2013, 10.1002/sim.5869.
27.
go back to reference Jairath V, Kahan BC, Logan RF, Hearnshaw SA, Dore CJ, Travis SP, Murphy MF, Palmer KR: Outcomes following acute nonvariceal upper gastrointestinal bleeding in relation to time to endoscopy: results from a nationwide study. Endoscopy. 2012, 44 (8): 723-730.CrossRefPubMed Jairath V, Kahan BC, Logan RF, Hearnshaw SA, Dore CJ, Travis SP, Murphy MF, Palmer KR: Outcomes following acute nonvariceal upper gastrointestinal bleeding in relation to time to endoscopy: results from a nationwide study. Endoscopy. 2012, 44 (8): 723-730.CrossRefPubMed
28.
go back to reference Jairath V, Kahan BC, Logan RF, Hearnshaw SA, Dore CJ, Travis SP, Murphy MF, Palmer KR: National audit of the use of surgery and radiological embolization after failed endoscopic haemostasis for non-variceal upper gastrointestinal bleeding. Br J Surg. 2012, 99 (12): 1672-1680. 10.1002/bjs.8932.CrossRefPubMed Jairath V, Kahan BC, Logan RF, Hearnshaw SA, Dore CJ, Travis SP, Murphy MF, Palmer KR: National audit of the use of surgery and radiological embolization after failed endoscopic haemostasis for non-variceal upper gastrointestinal bleeding. Br J Surg. 2012, 99 (12): 1672-1680. 10.1002/bjs.8932.CrossRefPubMed
29.
go back to reference Jairath V, Kahan BC, Logan RF, Hearnshaw SA, Travis SP, Murphy MF, Palmer KR: Mortality from acute upper gastrointestinal bleeding in the United Kingdom: does it display a “weekend effect”?. Am J Gastroenterol. 2011, 106 (9): 1621-1628. 10.1038/ajg.2011.172.CrossRefPubMed Jairath V, Kahan BC, Logan RF, Hearnshaw SA, Travis SP, Murphy MF, Palmer KR: Mortality from acute upper gastrointestinal bleeding in the United Kingdom: does it display a “weekend effect”?. Am J Gastroenterol. 2011, 106 (9): 1621-1628. 10.1038/ajg.2011.172.CrossRefPubMed
30.
go back to reference Jairath V, Kahan BC, Stanworth SJ, Logan RF, Hearnshaw SA, Travis SP, Palmer KR, Murphy MF: Prevalence, management, and outcomes of patients with coagulopathy after acute nonvariceal upper gastrointestinal bleeding in the United Kingdom. Transfusion. 2012, 53 (5): 1069-1076.CrossRefPubMed Jairath V, Kahan BC, Stanworth SJ, Logan RF, Hearnshaw SA, Travis SP, Palmer KR, Murphy MF: Prevalence, management, and outcomes of patients with coagulopathy after acute nonvariceal upper gastrointestinal bleeding in the United Kingdom. Transfusion. 2012, 53 (5): 1069-1076.CrossRefPubMed
31.
go back to reference Christensen E, Neuberger J, Crowe J, Altman DG, Popper H, Portmann B, Doniach D, Ranek L, Tygstrup N, Williams R: Beneficial effect of azathioprine and prediction of prognosis in primary biliary cirrhosis. Final results of an international trial. Gastroenterology. 1985, 89 (5): 1084-1091.CrossRefPubMed Christensen E, Neuberger J, Crowe J, Altman DG, Popper H, Portmann B, Doniach D, Ranek L, Tygstrup N, Williams R: Beneficial effect of azathioprine and prediction of prognosis in primary biliary cirrhosis. Final results of an international trial. Gastroenterology. 1985, 89 (5): 1084-1091.CrossRefPubMed
32.
go back to reference Bender R, Augustin T, Blettner M: Generating survival times to simulate Cox proportional hazards models. Stat Med. 2005, 24 (11): 1713-1723. 10.1002/sim.2059.CrossRefPubMed Bender R, Augustin T, Blettner M: Generating survival times to simulate Cox proportional hazards models. Stat Med. 2005, 24 (11): 1713-1723. 10.1002/sim.2059.CrossRefPubMed
Metadata
Title
Adjusting for multiple prognostic factors in the analysis of randomised trials
Authors
Brennan C Kahan
Tim P Morris
Publication date
01-12-2013
Publisher
BioMed Central
Published in
BMC Medical Research Methodology / Issue 1/2013
Electronic ISSN: 1471-2288
DOI
https://doi.org/10.1186/1471-2288-13-99

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