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Imputation of missing covariate in randomized controlled trials with a continuous outcome: Scoping review and new results

In this article, we first review the literature on dealing with missing values on a covariate in randomized studies and summarize what has been done and what is lacking to date. We then investigate the situation with a continuous outcome and a missing binary covariate in more details through simulat...

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Autores principales: Kayembe, Mutamba T., Jolani, Shahab, Tan, Frans E. S., van Breukelen, Gerard J. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7687108/
https://www.ncbi.nlm.nih.gov/pubmed/32510791
http://dx.doi.org/10.1002/pst.2041
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author Kayembe, Mutamba T.
Jolani, Shahab
Tan, Frans E. S.
van Breukelen, Gerard J. P.
author_facet Kayembe, Mutamba T.
Jolani, Shahab
Tan, Frans E. S.
van Breukelen, Gerard J. P.
author_sort Kayembe, Mutamba T.
collection PubMed
description In this article, we first review the literature on dealing with missing values on a covariate in randomized studies and summarize what has been done and what is lacking to date. We then investigate the situation with a continuous outcome and a missing binary covariate in more details through simulations, comparing the performance of multiple imputation (MI) with various simple alternative methods. This is finally extended to the case of time‐to‐event outcome. The simulations consider five different missingness scenarios: missing completely at random (MCAR), at random (MAR) with missingness depending only on the treatment, and missing not at random (MNAR) with missingness depending on the covariate itself (MNAR1), missingness depending on both the treatment and covariate (MNAR2), and missingness depending on the treatment, covariate and their interaction (MNAR3). Here, we distinguish two different cases: (1) when the covariate is measured before randomization (best practice), where only MCAR and MNAR1 are plausible, and (2) when it is measured after randomization but before treatment (which sometimes occurs in nonpharmaceutical research), where the other three missingness mechanisms can also occur. The proposed methods are compared based on the treatment effect estimate and its standard error. The simulation results suggest that the patterns of results are very similar for all missingness scenarios in case (1) and also in case (2) except for MNAR3. Furthermore, in each scenario for continuous outcome, there is at least one simple method that performs at least as well as MI, while for time‐to‐event outcome MI is best.
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spelling pubmed-76871082020-12-03 Imputation of missing covariate in randomized controlled trials with a continuous outcome: Scoping review and new results Kayembe, Mutamba T. Jolani, Shahab Tan, Frans E. S. van Breukelen, Gerard J. P. Pharm Stat Main Papers In this article, we first review the literature on dealing with missing values on a covariate in randomized studies and summarize what has been done and what is lacking to date. We then investigate the situation with a continuous outcome and a missing binary covariate in more details through simulations, comparing the performance of multiple imputation (MI) with various simple alternative methods. This is finally extended to the case of time‐to‐event outcome. The simulations consider five different missingness scenarios: missing completely at random (MCAR), at random (MAR) with missingness depending only on the treatment, and missing not at random (MNAR) with missingness depending on the covariate itself (MNAR1), missingness depending on both the treatment and covariate (MNAR2), and missingness depending on the treatment, covariate and their interaction (MNAR3). Here, we distinguish two different cases: (1) when the covariate is measured before randomization (best practice), where only MCAR and MNAR1 are plausible, and (2) when it is measured after randomization but before treatment (which sometimes occurs in nonpharmaceutical research), where the other three missingness mechanisms can also occur. The proposed methods are compared based on the treatment effect estimate and its standard error. The simulation results suggest that the patterns of results are very similar for all missingness scenarios in case (1) and also in case (2) except for MNAR3. Furthermore, in each scenario for continuous outcome, there is at least one simple method that performs at least as well as MI, while for time‐to‐event outcome MI is best. John Wiley & Sons, Inc. 2020-06-08 2020 /pmc/articles/PMC7687108/ /pubmed/32510791 http://dx.doi.org/10.1002/pst.2041 Text en © 2020 The Authors. Pharmaceutical Statistics published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Main Papers
Kayembe, Mutamba T.
Jolani, Shahab
Tan, Frans E. S.
van Breukelen, Gerard J. P.
Imputation of missing covariate in randomized controlled trials with a continuous outcome: Scoping review and new results
title Imputation of missing covariate in randomized controlled trials with a continuous outcome: Scoping review and new results
title_full Imputation of missing covariate in randomized controlled trials with a continuous outcome: Scoping review and new results
title_fullStr Imputation of missing covariate in randomized controlled trials with a continuous outcome: Scoping review and new results
title_full_unstemmed Imputation of missing covariate in randomized controlled trials with a continuous outcome: Scoping review and new results
title_short Imputation of missing covariate in randomized controlled trials with a continuous outcome: Scoping review and new results
title_sort imputation of missing covariate in randomized controlled trials with a continuous outcome: scoping review and new results
topic Main Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7687108/
https://www.ncbi.nlm.nih.gov/pubmed/32510791
http://dx.doi.org/10.1002/pst.2041
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