Calibration plots for multistate risk prediction models

Author:

Pate Alexander1ORCID,Sperrin Matthew12ORCID,Riley Richard D.3,Peek Niels12,Van Staa Tjeerd1,Sergeant Jamie C.45,Mamas Mamas A.6,Lip Gregory Y. H.78,O'Flaherty Martin910,Barrowman Michael9,Buchan Iain1011,Martin Glen P.1ORCID

Affiliation:

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

2. NIHR Manchester Biomedical Research Centre University of Manchester Manchester UK

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

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

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

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

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

8. Department of Clinical Medicine Aalborg University Aalborg Denmark

9. NIHR Applied Research Collaboration NW Coast University of Liverpool Liverpool UK

10. Independent Researcher Manchester UK

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

Abstract

IntroductionThere is currently no guidance on how to assess the calibration of multistate models used for risk prediction. We introduce several techniques that can be used to produce calibration plots for the transition probabilities of a multistate model, before assessing their performance in the presence of random and independent censoring through a simulation.MethodsWe studied pseudo‐values based on the Aalen‐Johansen estimator, binary logistic regression with inverse probability of censoring weights (BLR‐IPCW), and multinomial logistic regression with inverse probability of censoring weights (MLR‐IPCW). The MLR‐IPCW approach results in a calibration scatter plot, providing extra insight about the calibration. We simulated data with varying levels of censoring and evaluated the ability of each method to estimate the calibration curve for a set of predicted transition probabilities. We also developed and evaluated the calibration of a model predicting the incidence of cardiovascular disease, type 2 diabetes and chronic kidney disease among a cohort of patients derived from linked primary and secondary healthcare records.ResultsThe pseudo‐value, BLR‐IPCW, and MLR‐IPCW approaches give unbiased estimates of the calibration curves under random censoring. These methods remained predominately unbiased in the presence of independent censoring, even if the censoring mechanism was strongly associated with the outcome, with bias concentrated in low‐density regions of predicted transition probabilities.ConclusionsWe recommend implementing either the pseudo‐value or BLR‐IPCW approaches to produce a calibration curve, combined with the MLR‐IPCW approach to produce a calibration scatter plot. The methods have been incorporated into the “calibmsm” R package available on CRAN.

Funder

Medical Research Council

Publisher

Wiley

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