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Practical recommendations for reporting Fine‐Gray model analyses for competing risk data
In survival analysis, a competing risk is an event whose occurrence precludes the occurrence of the primary event of interest. Outcomes in medical research are frequently subject to competing risks. In survival analysis, there are 2 key questions that can be addressed using competing risk regression...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698744/ https://www.ncbi.nlm.nih.gov/pubmed/28913837 http://dx.doi.org/10.1002/sim.7501 |
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author | Austin, Peter C. Fine, Jason P. |
author_facet | Austin, Peter C. Fine, Jason P. |
author_sort | Austin, Peter C. |
collection | PubMed |
description | In survival analysis, a competing risk is an event whose occurrence precludes the occurrence of the primary event of interest. Outcomes in medical research are frequently subject to competing risks. In survival analysis, there are 2 key questions that can be addressed using competing risk regression models: first, which covariates affect the rate at which events occur, and second, which covariates affect the probability of an event occurring over time. The cause‐specific hazard model estimates the effect of covariates on the rate at which events occur in subjects who are currently event‐free. Subdistribution hazard ratios obtained from the Fine‐Gray model describe the relative effect of covariates on the subdistribution hazard function. Hence, the covariates in this model can also be interpreted as having an effect on the cumulative incidence function or on the probability of events occurring over time. We conducted a review of the use and interpretation of the Fine‐Gray subdistribution hazard model in articles published in the medical literature in 2015. We found that many authors provided an unclear or incorrect interpretation of the regression coefficients associated with this model. An incorrect and inconsistent interpretation of regression coefficients may lead to confusion when comparing results across different studies. Furthermore, an incorrect interpretation of estimated regression coefficients can result in an incorrect understanding about the magnitude of the association between exposure and the incidence of the outcome. The objective of this article is to clarify how these regression coefficients should be reported and to propose suggestions for interpreting these coefficients. |
format | Online Article Text |
id | pubmed-5698744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56987442017-11-30 Practical recommendations for reporting Fine‐Gray model analyses for competing risk data Austin, Peter C. Fine, Jason P. Stat Med Research Articles In survival analysis, a competing risk is an event whose occurrence precludes the occurrence of the primary event of interest. Outcomes in medical research are frequently subject to competing risks. In survival analysis, there are 2 key questions that can be addressed using competing risk regression models: first, which covariates affect the rate at which events occur, and second, which covariates affect the probability of an event occurring over time. The cause‐specific hazard model estimates the effect of covariates on the rate at which events occur in subjects who are currently event‐free. Subdistribution hazard ratios obtained from the Fine‐Gray model describe the relative effect of covariates on the subdistribution hazard function. Hence, the covariates in this model can also be interpreted as having an effect on the cumulative incidence function or on the probability of events occurring over time. We conducted a review of the use and interpretation of the Fine‐Gray subdistribution hazard model in articles published in the medical literature in 2015. We found that many authors provided an unclear or incorrect interpretation of the regression coefficients associated with this model. An incorrect and inconsistent interpretation of regression coefficients may lead to confusion when comparing results across different studies. Furthermore, an incorrect interpretation of estimated regression coefficients can result in an incorrect understanding about the magnitude of the association between exposure and the incidence of the outcome. The objective of this article is to clarify how these regression coefficients should be reported and to propose suggestions for interpreting these coefficients. John Wiley and Sons Inc. 2017-09-15 2017-11-30 /pmc/articles/PMC5698744/ /pubmed/28913837 http://dx.doi.org/10.1002/sim.7501 Text en © 2017 The Authors. Statistics in Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (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. |
spellingShingle | Research Articles Austin, Peter C. Fine, Jason P. Practical recommendations for reporting Fine‐Gray model analyses for competing risk data |
title | Practical recommendations for reporting Fine‐Gray model analyses for competing risk data |
title_full | Practical recommendations for reporting Fine‐Gray model analyses for competing risk data |
title_fullStr | Practical recommendations for reporting Fine‐Gray model analyses for competing risk data |
title_full_unstemmed | Practical recommendations for reporting Fine‐Gray model analyses for competing risk data |
title_short | Practical recommendations for reporting Fine‐Gray model analyses for competing risk data |
title_sort | practical recommendations for reporting fine‐gray model analyses for competing risk data |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698744/ https://www.ncbi.nlm.nih.gov/pubmed/28913837 http://dx.doi.org/10.1002/sim.7501 |
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