Developing prediction models to estimate the risk of two survival outcomes both occurring: A comparison of techniques

Author:

Pate Alexander1ORCID,Sperrin Matthew1ORCID,Riley Richard D.2ORCID,Sergeant Jamie C.34ORCID,Van Staa Tjeerd1ORCID,Peek Niels1ORCID,Mamas Mamas A.5ORCID,Lip Gregory Y. H.67,O'Flaherty Martin8ORCID,Buchan Iain8ORCID,Martin Glen P.1ORCID

Affiliation:

1. Division of Informatics, Imaging and Data Science, Faculty of Biology, Medicine and Health University of Manchester, Manchester Academic Health Science Centre Manchester UK

2. Institute of Applied Health Research University of Birmingham Birmingham UK

3. Centre for Epidemiology Versus Arthritis, Centre for Musculoskeletal Research, Manchester Academic Health Science Centre University of Manchester Manchester UK

4. Centre for Biostatistics, Manchester Academic Health Science Centre University of Manchester Manchester UK

5. Keele Cardiovascular Research Group Keele University Stoke‐on‐Trent UK

6. Liverpool Centre for Cardiovascular Science at University of Liverpool Liverpool John Moores University and Liverpool Heart & Chest Hospital Liverpool UK

7. Department of Clinical Medicine Aalborg University Aalborg Denmark

8. Institute of Population Health, Faculty of Health and Life Sciences University of Liverpool Liverpool UK

Abstract

IntroductionThis study considers the prediction of the time until two survival outcomes have both occurred. We compared a variety of analytical methods motivated by a typical clinical problem of multimorbidity prognosis.MethodsWe considered five methods: product (multiply marginal risks), dual‐outcome (directly model the time until both events occur), multistate models (msm), and a range of copula and frailty models. We assessed calibration and discrimination under a variety of simulated data scenarios, varying outcome prevalence, and the amount of residual correlation. The simulation focused on model misspecification and statistical power. Using data from the Clinical Practice Research Datalink, we compared model performance when predicting the risk of cardiovascular disease and type 2 diabetes both occurring.ResultsDiscrimination was similar for all methods. The product method was poorly calibrated in the presence of residual correlation. The msm and dual‐outcome models were the most robust to model misspecification but suffered a drop in performance at small sample sizes due to overfitting, which the copula and frailty model were less susceptible to. The copula and frailty model's performance were highly dependent on the underlying data structure. In the clinical example, the product method was poorly calibrated when adjusting for 8 major cardiovascular risk factors.DiscussionWe recommend the dual‐outcome method for predicting the risk of two survival outcomes both occurring. It was the most robust to model misspecification, although was also the most prone to overfitting. The clinical example motivates the use of the methods considered in this study.

Funder

Medical Research Council Canada

Publisher

Wiley

Subject

Statistics and Probability,Epidemiology

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