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      Fine‐Gray subdistribution hazard models to simultaneously estimate the absolute risk of different event types: Cumulative total failure probability may exceed 1

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          Abstract

          The Fine‐Gray subdistribution hazard model has become the default method to estimate the incidence of outcomes over time in the presence of competing risks. This model is attractive because it directly relates covariates to the cumulative incidence function (CIF) of the event of interest. An alternative is to combine the different cause‐specific hazard functions to obtain the different CIFs. A limitation of the subdistribution hazard approach is that the sum of the cause‐specific CIFs can exceed 1 (100%) for some covariate patterns. Using data on 9479 patients hospitalized with acute myocardial infarction, we estimated the cumulative incidence of both cardiovascular death and non‐cardiovascular death for each patient. We found that when using subdistribution hazard models, approximately 5% of subjects had an estimated risk of 5‐year all‐cause death (obtained by combining the two cause‐specific CIFs obtained from subdistribution hazard models) that exceeded 1. This phenomenon was avoided by using the two cause‐specific hazard models. We provide a proof that the sum of predictions exceeds 1 is a fundamental problem with the Fine‐Gray subdistribution hazard model. We further explored this issue using simulations based on two different types of data‐generating process, one based on subdistribution hazard models and other based on cause‐specific hazard models. We conclude that care should be taken when using the Fine‐Gray subdistribution hazard model in situations with wide risk distributions or a high cumulative incidence, and if one is interested in the risk of failure from each of the different event types.

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          A Proportional Hazards Model for the Subdistribution of a Competing Risk

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            Balance diagnostics for comparing the distribution of baseline covariates between treatment groups in propensity-score matched samples

            The propensity score is a subject's probability of treatment, conditional on observed baseline covariates. Conditional on the true propensity score, treated and untreated subjects have similar distributions of observed baseline covariates. Propensity-score matching is a popular method of using the propensity score in the medical literature. Using this approach, matched sets of treated and untreated subjects with similar values of the propensity score are formed. Inferences about treatment effect made using propensity-score matching are valid only if, in the matched sample, treated and untreated subjects have similar distributions of measured baseline covariates. In this paper we discuss the following methods for assessing whether the propensity score model has been correctly specified: comparing means and prevalences of baseline characteristics using standardized differences; ratios comparing the variance of continuous covariates between treated and untreated subjects; comparison of higher order moments and interactions; five-number summaries; and graphical methods such as quantile–quantile plots, side-by-side boxplots, and non-parametric density plots for comparing the distribution of baseline covariates between treatment groups. We describe methods to determine the sampling distribution of the standardized difference when the true standardized difference is equal to zero, thereby allowing one to determine the range of standardized differences that are plausible with the propensity score model having been correctly specified. We highlight the limitations of some previously used methods for assessing the adequacy of the specification of the propensity-score model. In particular, methods based on comparing the distribution of the estimated propensity score between treated and untreated subjects are uninformative. Copyright © 2009 John Wiley & Sons, Ltd.
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              Introduction to the Analysis of Survival Data in the Presence of Competing Risks

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                Author and article information

                Contributors
                peter.austin@ices.on.ca
                Journal
                Stat Med
                Stat Med
                10.1002/(ISSN)1097-0258
                SIM
                Statistics in Medicine
                John Wiley & Sons, Inc. (Hoboken, USA )
                0277-6715
                1097-0258
                09 May 2021
                30 August 2021
                : 40
                : 19 ( doiID: 10.1002/sim.v40.19 )
                : 4200-4212
                Affiliations
                [ 1 ] ICES Toronto Ontario Canada
                [ 2 ] Institute of Health Management, Policy and Evaluation University of Toronto Toronto Ontario Canada
                [ 3 ] Sunnybrook Research Institute Toronto Ontario Canada
                [ 4 ] Department of Public Health Erasmus MC Rotterdam The Netherlands
                [ 5 ] Department of Biomedical Data Sciences Leiden University Medical Centre Leiden The Netherlands
                Author notes
                [*] [* ] Correspondence

                Peter C. Austin, ICES, G106, 2075 Bayview Avenue, Toronto, ON M4N 3M5, Canada.

                Email: peter.austin@ 123456ices.on.ca

                Author information
                https://orcid.org/0000-0003-3337-233X
                https://orcid.org/0000-0002-7787-0122
                https://orcid.org/0000-0001-5395-1422
                Article
                SIM9023
                10.1002/sim.9023
                8360146
                33969508
                a9219b6d-7337-433e-bdfc-2c5481952344
                © 2021 The Authors. Statistics in Medicine published by John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 20 April 2021
                : 15 January 2021
                : 21 April 2021
                Page count
                Figures: 4, Tables: 1, Pages: 13, Words: 6067
                Funding
                Funded by: Canadian Institutes of Health Research , doi 10.13039/501100000024;
                Award ID: PJT 166161
                Funded by: Heart and Stroke Foundation of Canada , doi 10.13039/100004411;
                Award ID: Mid‐Career Investigator Award
                Funded by: Ontario Ministry of Health and Long‐Term Care , doi 10.13039/501100000226;
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                30 August 2021
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.0.5 mode:remove_FC converted:12.08.2021

                Biostatistics
                cause‐specific hazard function,competing risks,cumulative incidence function,subdistribution hazard,survival analysis

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