ArticleStatistics in medicine2025
Multiple Imputation of Missing Covariates When Using the Fine-Gray Model.
Article in Statistics in medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
2 citing papers in PubMed.
- Impact of maternal and neonatal factors on mortality in the first six weeks of life: A comprehensive cohort study in Kinshasa, DR Congo.PLOS global public health · 2026Article
- Multiple Imputation of Missing Covariates When Using the Fine-Gray Model.Statistics in medicine · 2025Article
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Authors and funding
8 authors.
Funding
Abstract
The Fine-Gray model for the subdistribution hazard is commonly used for estimating associations between covariates and competing risks outcomes. When there are missing values in the covariates included in a given model, researchers may wish to multiply impute them. Assuming interest lies in estimating the risk of only one of the competing events, this paper develops a substantive-model-compatible multiple imputation approach that exploits the parallels between the Fine-Gray model and the standard (single-event) Cox model. In the presence of right-censoring, this involves first imputing the potential censoring times for those failing from competing events, and thereafter imputing the missing covariates by leveraging methodology previously developed for the Cox model in the setting without competing risks. In a simulation study, we compared the proposed approach to alternative methods, such as imputing compatibly with cause-specific Cox models. The proposed method performed well (in terms of estimation of both subdistribution log hazard ratios and cumulative incidences) when data were generated assuming proportional subdistribution hazards, and performed satisfactorily when this assumption was not satisfied. The gain in efficiency compared to a complete-case analysis was demonstrated in both the simulation study and in an applied data example on competing outcomes following an allogeneic stem cell transplantation. For individual-specific cumulative incidence estimation, assuming proportionality on the correct scale at the analysis phase appears to be more important than correctly specifying the imputation procedure used to impute the missing covariates.
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Registered trials
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