Use of re-randomized data in meta-analysis

<p>Abstract</p> <p>Background</p> <p>Outcomes collected in randomized clinical trials are observations of random variables that should be independent and identically distributed. However, in some trials, the patients are randomized more than once thus violating both of...

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Main Authors: Clark Otavio, Djulbegovic Benjamin, Hozo Iztok, Lyman Gary H
Format: Article
Language:English
Published: BMC 2005-05-01
Series:BMC Medical Research Methodology
Online Access:http://www.biomedcentral.com/1471-2288/5/17
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spelling doaj-1ff0c4cfb3b845e286de685642bfc03b2020-11-25T00:20:34ZengBMCBMC Medical Research Methodology1471-22882005-05-01511710.1186/1471-2288-5-17Use of re-randomized data in meta-analysisClark OtavioDjulbegovic BenjaminHozo IztokLyman Gary H<p>Abstract</p> <p>Background</p> <p>Outcomes collected in randomized clinical trials are observations of random variables that should be independent and identically distributed. However, in some trials, the patients are randomized more than once thus violating both of these assumptions. The probability of an event is not always the same when a patient is re-randomized; there is probably a non-zero covariance coming from observations on the same patient. This is of particular importance to the meta-analysts.</p> <p>Methods</p> <p>We developed a method to estimate the relative error in the risk differences with and without re-randomization of the patients. The relative error can be estimated by an expression depending on the percentage of the patients who were re-randomized, multipliers (how many times more likely it is to repeat an event) for the probability of reoccurrences, and the ratio of the total events reported and the initial number of patients entering the trial.</p> <p>Results</p> <p>We illustrate our methods using two randomized trials testing growth factors in febrile neutropenia. We showed that under some circumstances the relative error of taking into account re-randomized patients was sufficiently small to allow using the results in the meta-analysis. Our findings indicate that if the study in question is of similar size to other studies included in the meta-analysis, the error introduced by re-randomization will only minimally affect meta-analytic summary point estimate.</p> <p>We also show that in our model the risk ratio remains constant during the re-randomization, and therefore, if a meta-analyst is concerned about the effect of re-randomization on the meta-analysis, one way to sidestep the issue and still obtain reliable results is to use risk ratio as the measure of interest.</p> <p>Conclusion</p> <p>Our method should be helpful in the understanding of the results of clinical trials and particularly helpful to the meta-analysts to assess if re-randomized patient data can be used in their analyses.</p> http://www.biomedcentral.com/1471-2288/5/17
collection DOAJ
language English
format Article
sources DOAJ
author Clark Otavio
Djulbegovic Benjamin
Hozo Iztok
Lyman Gary H
spellingShingle Clark Otavio
Djulbegovic Benjamin
Hozo Iztok
Lyman Gary H
Use of re-randomized data in meta-analysis
BMC Medical Research Methodology
author_facet Clark Otavio
Djulbegovic Benjamin
Hozo Iztok
Lyman Gary H
author_sort Clark Otavio
title Use of re-randomized data in meta-analysis
title_short Use of re-randomized data in meta-analysis
title_full Use of re-randomized data in meta-analysis
title_fullStr Use of re-randomized data in meta-analysis
title_full_unstemmed Use of re-randomized data in meta-analysis
title_sort use of re-randomized data in meta-analysis
publisher BMC
series BMC Medical Research Methodology
issn 1471-2288
publishDate 2005-05-01
description <p>Abstract</p> <p>Background</p> <p>Outcomes collected in randomized clinical trials are observations of random variables that should be independent and identically distributed. However, in some trials, the patients are randomized more than once thus violating both of these assumptions. The probability of an event is not always the same when a patient is re-randomized; there is probably a non-zero covariance coming from observations on the same patient. This is of particular importance to the meta-analysts.</p> <p>Methods</p> <p>We developed a method to estimate the relative error in the risk differences with and without re-randomization of the patients. The relative error can be estimated by an expression depending on the percentage of the patients who were re-randomized, multipliers (how many times more likely it is to repeat an event) for the probability of reoccurrences, and the ratio of the total events reported and the initial number of patients entering the trial.</p> <p>Results</p> <p>We illustrate our methods using two randomized trials testing growth factors in febrile neutropenia. We showed that under some circumstances the relative error of taking into account re-randomized patients was sufficiently small to allow using the results in the meta-analysis. Our findings indicate that if the study in question is of similar size to other studies included in the meta-analysis, the error introduced by re-randomization will only minimally affect meta-analytic summary point estimate.</p> <p>We also show that in our model the risk ratio remains constant during the re-randomization, and therefore, if a meta-analyst is concerned about the effect of re-randomization on the meta-analysis, one way to sidestep the issue and still obtain reliable results is to use risk ratio as the measure of interest.</p> <p>Conclusion</p> <p>Our method should be helpful in the understanding of the results of clinical trials and particularly helpful to the meta-analysts to assess if re-randomized patient data can be used in their analyses.</p>
url http://www.biomedcentral.com/1471-2288/5/17
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