Introduction to the Analysis of Survival Data in the Presence of Competing Risks

Competing risks occur frequently in the analysis of survival data. A competing risk is an event whose occurrence precludes the occurrence of the primary event of interest. In a study examining time to death attributable to cardiovascular causes, death attributable to noncardiovascular causes is a co...

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Published inCirculation (New York, N.Y.) Vol. 133; no. 6; pp. 601 - 609
Main Authors Austin, Peter C., Lee, Douglas S., Fine, Jason P.
Format Journal Article
LanguageEnglish
Published United States by the American College of Cardiology Foundation and the American Heart Association, Inc 09.02.2016
Lippincott Williams & Wilkins
Subjects
Online AccessGet full text
ISSN0009-7322
1524-4539
1524-4539
DOI10.1161/CIRCULATIONAHA.115.017719

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Abstract Competing risks occur frequently in the analysis of survival data. A competing risk is an event whose occurrence precludes the occurrence of the primary event of interest. In a study examining time to death attributable to cardiovascular causes, death attributable to noncardiovascular causes is a competing risk. When estimating the crude incidence of outcomes, analysts should use the cumulative incidence function, rather than the complement of the Kaplan-Meier survival function. The use of the Kaplan-Meier survival function results in estimates of incidence that are biased upward, regardless of whether the competing events are independent of one another. When fitting regression models in the presence of competing risks, researchers can choose from 2 different families of modelsmodeling the effect of covariates on the cause-specific hazard of the outcome or modeling the effect of covariates on the cumulative incidence function. The former allows one to estimate the effect of the covariates on the rate of occurrence of the outcome in those subjects who are currently event free. The latter allows one to estimate the effect of covariates on the absolute risk of the outcome over time. The former family of models may be better suited for addressing etiologic questions, whereas the latter model may be better suited for estimating a patient’s clinical prognosis. We illustrate the application of these methods by examining cause-specific mortality in patients hospitalized with heart failure. Statistical software code in both R and SAS is provided.
AbstractList Competing risks occur frequently in the analysis of survival data. A competing risk is an event whose occurrence precludes the occurrence of the primary event of interest. In a study examining time to death attributable to cardiovascular causes, death attributable to noncardiovascular causes is a competing risk. When estimating the crude incidence of outcomes, analysts should use the cumulative incidence function, rather than the complement of the Kaplan-Meier survival function. The use of the Kaplan-Meier survival function results in estimates of incidence that are biased upward, regardless of whether the competing events are independent of one another. When fitting regression models in the presence of competing risks, researchers can choose from 2 different families of models: modeling the effect of covariates on the cause-specific hazard of the outcome or modeling the effect of covariates on the cumulative incidence function. The former allows one to estimate the effect of the covariates on the rate of occurrence of the outcome in those subjects who are currently event free. The latter allows one to estimate the effect of covariates on the absolute risk of the outcome over time. The former family of models may be better suited for addressing etiologic questions, whereas the latter model may be better suited for estimating a patient’s clinical prognosis. We illustrate the application of these methods by examining cause-specific mortality in patients hospitalized with heart failure. Statistical software code in both R and SAS is provided.
Supplemental Digital Content is available in the text. Competing risks occur frequently in the analysis of survival data. A competing risk is an event whose occurrence precludes the occurrence of the primary event of interest. In a study examining time to death attributable to cardiovascular causes, death attributable to noncardiovascular causes is a competing risk. When estimating the crude incidence of outcomes, analysts should use the cumulative incidence function, rather than the complement of the Kaplan-Meier survival function. The use of the Kaplan-Meier survival function results in estimates of incidence that are biased upward, regardless of whether the competing events are independent of one another. When fitting regression models in the presence of competing risks, researchers can choose from 2 different families of models: modeling the effect of covariates on the cause-specific hazard of the outcome or modeling the effect of covariates on the cumulative incidence function. The former allows one to estimate the effect of the covariates on the rate of occurrence of the outcome in those subjects who are currently event free. The latter allows one to estimate the effect of covariates on the absolute risk of the outcome over time. The former family of models may be better suited for addressing etiologic questions, whereas the latter model may be better suited for estimating a patient’s clinical prognosis. We illustrate the application of these methods by examining cause-specific mortality in patients hospitalized with heart failure. Statistical software code in both R and SAS is provided.
Competing risks occur frequently in the analysis of survival data. A competing risk is an event whose occurrence precludes the occurrence of the primary event of interest. In a study examining time to death attributable to cardiovascular causes, death attributable to noncardiovascular causes is a competing risk. When estimating the crude incidence of outcomes, analysts should use the cumulative incidence function, rather than the complement of the Kaplan-Meier survival function. The use of the Kaplan-Meier survival function results in estimates of incidence that are biased upward, regardless of whether the competing events are independent of one another. When fitting regression models in the presence of competing risks, researchers can choose from 2 different families of modelsmodeling the effect of covariates on the cause-specific hazard of the outcome or modeling the effect of covariates on the cumulative incidence function. The former allows one to estimate the effect of the covariates on the rate of occurrence of the outcome in those subjects who are currently event free. The latter allows one to estimate the effect of covariates on the absolute risk of the outcome over time. The former family of models may be better suited for addressing etiologic questions, whereas the latter model may be better suited for estimating a patient’s clinical prognosis. We illustrate the application of these methods by examining cause-specific mortality in patients hospitalized with heart failure. Statistical software code in both R and SAS is provided.
Competing risks occur frequently in the analysis of survival data. A competing risk is an event whose occurrence precludes the occurrence of the primary event of interest. In a study examining time to death attributable to cardiovascular causes, death attributable to noncardiovascular causes is a competing risk. When estimating the crude incidence of outcomes, analysts should use the cumulative incidence function, rather than the complement of the Kaplan-Meier survival function. The use of the Kaplan-Meier survival function results in estimates of incidence that are biased upward, regardless of whether the competing events are independent of one another. When fitting regression models in the presence of competing risks, researchers can choose from 2 different families of models: modeling the effect of covariates on the cause-specific hazard of the outcome or modeling the effect of covariates on the cumulative incidence function. The former allows one to estimate the effect of the covariates on the rate of occurrence of the outcome in those subjects who are currently event free. The latter allows one to estimate the effect of covariates on the absolute risk of the outcome over time. The former family of models may be better suited for addressing etiologic questions, whereas the latter model may be better suited for estimating a patient's clinical prognosis. We illustrate the application of these methods by examining cause-specific mortality in patients hospitalized with heart failure. Statistical software code in both R and SAS is provided.Competing risks occur frequently in the analysis of survival data. A competing risk is an event whose occurrence precludes the occurrence of the primary event of interest. In a study examining time to death attributable to cardiovascular causes, death attributable to noncardiovascular causes is a competing risk. When estimating the crude incidence of outcomes, analysts should use the cumulative incidence function, rather than the complement of the Kaplan-Meier survival function. The use of the Kaplan-Meier survival function results in estimates of incidence that are biased upward, regardless of whether the competing events are independent of one another. When fitting regression models in the presence of competing risks, researchers can choose from 2 different families of models: modeling the effect of covariates on the cause-specific hazard of the outcome or modeling the effect of covariates on the cumulative incidence function. The former allows one to estimate the effect of the covariates on the rate of occurrence of the outcome in those subjects who are currently event free. The latter allows one to estimate the effect of covariates on the absolute risk of the outcome over time. The former family of models may be better suited for addressing etiologic questions, whereas the latter model may be better suited for estimating a patient's clinical prognosis. We illustrate the application of these methods by examining cause-specific mortality in patients hospitalized with heart failure. Statistical software code in both R and SAS is provided.
Author Austin, Peter C.
Fine, Jason P.
Lee, Douglas S.
AuthorAffiliation From Institute for Clinical Evaluative Sciences, Toronto, Ontario, Canada (P.C.A., D.S.L.); Institute of Health Management, Policy and Evaluation, University of Toronto, Ontario, Canada (P.C.A., D.S.L.); Schulich Heart Research Program, Sunnybrook Research Institute, Toronto, Ontario, Canada (P.C.A.); Department of Medicine, University of Toronto, Ontario, Canada (D.S.L.); Peter Munk Cardiac Center, Department of Medicine, and the Joint Department of Medical Imaging, University Health Network, Toronto, Ontario, Canada (D.S.L.); Department of Biostatistics, University of North Carolina, Chapel Hill, NC (J.P.F.); and Department of Statistics & Operations Research, University of North Carolina, Chapel Hill (J.P.F.)
AuthorAffiliation_xml – name: From Institute for Clinical Evaluative Sciences, Toronto, Ontario, Canada (P.C.A., D.S.L.); Institute of Health Management, Policy and Evaluation, University of Toronto, Ontario, Canada (P.C.A., D.S.L.); Schulich Heart Research Program, Sunnybrook Research Institute, Toronto, Ontario, Canada (P.C.A.); Department of Medicine, University of Toronto, Ontario, Canada (D.S.L.); Peter Munk Cardiac Center, Department of Medicine, and the Joint Department of Medical Imaging, University Health Network, Toronto, Ontario, Canada (D.S.L.); Department of Biostatistics, University of North Carolina, Chapel Hill, NC (J.P.F.); and Department of Statistics & Operations Research, University of North Carolina, Chapel Hill (J.P.F.)
Author_xml – sequence: 1
  givenname: Peter
  surname: Austin
  middlename: C.
  fullname: Austin, Peter C.
  organization: From Institute for Clinical Evaluative Sciences, Toronto, Ontario, Canada (P.C.A., D.S.L.); Institute of Health Management, Policy and Evaluation, University of Toronto, Ontario, Canada (P.C.A., D.S.L.); Schulich Heart Research Program, Sunnybrook Research Institute, Toronto, Ontario, Canada (P.C.A.); Department of Medicine, University of Toronto, Ontario, Canada (D.S.L.); Peter Munk Cardiac Center, Department of Medicine, and the Joint Department of Medical Imaging, University Health Network, Toronto, Ontario, Canada (D.S.L.); Department of Biostatistics, University of North Carolina, Chapel Hill, NC (J.P.F.); and Department of Statistics & Operations Research, University of North Carolina, Chapel Hill (J.P.F.)
– sequence: 2
  givenname: Douglas
  surname: Lee
  middlename: S.
  fullname: Lee, Douglas S.
– sequence: 3
  givenname: Jason
  surname: Fine
  middlename: P.
  fullname: Fine, Jason P.
BackLink https://www.ncbi.nlm.nih.gov/pubmed/26858290$$D View this record in MEDLINE/PubMed
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Issue 6
Keywords risk assessment
cumulative incidence function
models, statistical
survival analysis
data interpretation, statistical
incidence
proportional hazards models
Language English
License 2016 The Authors.
Circulation is published on behalf of the American Heart Association, Inc., by Wolters Kluwer. This is an open access article under the terms of the Creative Commons Attribution Non-Commercial-NoDervis License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited, the use is noncommercial, and no modifications or adaptations are made.
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Snippet Competing risks occur frequently in the analysis of survival data. A competing risk is an event whose occurrence precludes the occurrence of the primary event...
Supplemental Digital Content is available in the text. Competing risks occur frequently in the analysis of survival data. A competing risk is an event whose...
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StartPage 601
SubjectTerms Aged
Aged, 80 and over
Cardiovascular Diseases - diagnosis
Cardiovascular Diseases - mortality
Databases, Factual - statistics & numerical data
Databases, Factual - trends
Female
Humans
Kaplan-Meier Estimate
Male
Models, Statistical
Risk Factors
Statistical Primer for Cardiovascular Research
Statistics as Topic - methods
Survival Analysis
Title Introduction to the Analysis of Survival Data in the Presence of Competing Risks
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https://www.proquest.com/docview/1764337913
https://pubmed.ncbi.nlm.nih.gov/PMC4741409
http://doi.org/10.1161/CIRCULATIONAHA.115.017719
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