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Updated: Mar 7, 2026

Establishing a Competing Risk Regression Nomogram Model for Survival Data
Published on: October 23, 2020
Statistical Methods for Cohort Studies of CKD: Survival Analysis in the Setting of Competing Risks
Jesse Yenchih Hsu1,2, Jason A Roy1,2, Dawei Xie1,2
1Department of Biostatistics and Epidemiology and.
Insights
Survival analysis in chronic kidney disease (CKD) must account for competing risks, where events like death can censor outcomes such as end-stage renal disease (ESRD). This study reviews methods to handle dependent censoring in CKD research.
Area of Science:
- Nephrology
- Biostatistics
- Clinical Epidemiology
Background:
- Survival analysis is crucial for evaluating outcomes like end-stage renal disease (ESRD) and mortality in chronic kidney disease (CKD) populations.
- Traditional methods assume independent censoring, which is often violated in clinical settings due to competing risks such as death.
- Dependent censoring, where a competing event influences the time to the event of interest, is common in CKD research.
Purpose of the Study:
- To describe clinical scenarios in renal research involving competing risks.
- To review statistical approaches for analyzing survival data with competing risks.
- To compare cause-specific hazards models and the Fine and Gray approach for competing risks analysis.
Main Methods:
- Review of statistical methodologies for handling competing risks in survival analysis.
- Comparison of cause-specific hazards models and subdistribution hazards models (Fine and Gray approach).
- Application of these methods using data from the Chronic Renal Insufficiency Cohort Study, examining fibroblast growth factor 23 and risks of mortality and ESRD.
Main Results:
- Dependent censoring due to competing risks is prevalent in CKD populations.
- Cause-specific hazards models and Fine and Gray models offer different perspectives on risk estimation.
- The choice of method impacts the interpretation of survival data in the presence of competing risks.
Conclusions:
- Accurate survival analysis in CKD requires explicit consideration of competing risks.
- Understanding the assumptions and interpretations of different competing risks models is essential for clinical research.
- Practical recommendations are provided for analyzing and interpreting survival data incorporating competing risks in CKD studies.
Abstract:
Survival analysis is commonly used to evaluate factors associated with time to an event of interest (e.g., ESRD, cardiovascular disease, and mortality) among CKD populations. Time to the event of interest is typically observed only for some participants. Other participants have their event time censored because of the end of the study, death, withdrawal from the study, or some other competing event. Classic survival analysis methods, such as Cox proportional hazards regression, rely on the assumption that any censoring is independent of the event of interest. However, in most clinical settings, such as in CKD populations, this assumption is unlikely to be true. For example, participants whose follow-up time is censored because of health-related death likely would have had a shorter time to ESRD, had they not died. These types of competing events that cause dependent censoring are referred to as competing risks. Here, we first describe common circumstances in clinical renal research where competing risks operate and then review statistical approaches for dealing with competing risks. We compare two of the most popular analytical methods used in settings of competing risks: cause-specific hazards models and the Fine and Gray approach (subdistribution hazards models). We also discuss practical recommendations for analysis and interpretation of survival data that incorporate competing risks. To demonstrate each of the analytical tools, we use a study of fibroblast growth factor 23 and risks of mortality and ESRD in participants with CKD from the Chronic Renal Insufficiency Cohort Study.
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