Evidence map›Paper›PMID 40750843›Full record

ArticleBMC medical research methodology2025

Correcting for case-mix shift when developing clinical prediction models.

Haya Elayan, Matthew Sperrin, Glen P Martin, Niels Peek, Frieder Braunschweig, Jonas Faxén, Joakim Alfredsson, David A Jenkins

Abstract read
In one paragraph

Article in BMC medical research methodology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Haya ElayanDivision of Informatics, Imaging and Data Science, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK. haya.elayan@postgrad.manchester.ac.uk.
Matthew SperrinDivision of Informatics, Imaging and Data Science, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.
Glen P MartinDivision of Informatics, Imaging and Data Science, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.
Niels PeekDivision of Informatics, Imaging and Data Science, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.
Frieder BraunschweigDepartment of Cardiology, Karolinska University Hospital, Stockholm, Sweden.
Jonas FaxénDepartment of Physiology and Pharmacology, Karolinska Institute, Stockholm, Sweden.
Joakim AlfredssonDepartment of Health, Medicine and Caring Sciences, Linköping University, Linköping, Sweden.
David A JenkinsDivision of Informatics, Imaging and Data Science, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.

Funding

NIHR Manchester Biomedical Research Centre NIHR203308
6 · The paper itself

Abstract

backgroundWhen developing a clinical prediction model (CPM), a case-mix shift could occur in the development dataset where the distribution of individual predictors changes, potentially affecting model performance. This study exploits the case-mix shift that is already observed in the development dataset to address the case-mix shift between the development and deployment phase of a CPM.

methodsWe propose a Membership-based method to correct for case-mix shift in the development phase of CPMs. This method uses a probabilistic similarity metric to re-weight data samples in the source set (before the case-mix shift) to more closely match the target set (after the case-mix shift), assuming the target set reflects the target population. We apply the proposed method in a real-world dataset of myocardial infarction patients with out-of-hospital cardiac arrest within 90 days as the outcome. We design nine scenarios (including case-mix shift and no case-mix shift with a range of target/source sets sample sizes) to explore the impact on predictive performance of CPM developed with the proposed method in comparison to CPMs developed by either using all data samples but ignore the shift, or only using the most recent data. We report calibration and discrimination on development and 200 bootstrap samples. RESULTS AND

conclusionsThe proposed method shows promise in accounting for case-mix shift when developing a CPM, particularly when the target set sample size is insufficient. In a partial case-mix shift scenario with an insufficient target sample size, the Membership-based model achieved an optimism-adjusted calibration slope (c-slope) of 0.98, outperforming other models. Conversely, when the target set sample size is sufficient, the Unweighted model on target data only had an optimism-adjusted c-slope of 0.95, compared to 0.92 for the Membership-based model. In complete case-mix shift cases, the Membership-based and Unweighted on target data only models performed similarly. Both achieved an optimism-adjusted c-slope of 0.77 with insufficient target sample size, and optimism-adjusted c-slope of 0.94 with a sufficient target sample size. Further investigation and testing are needed, as well as accounting for other types of data distribution shift to improve model fit for the latest distribution shift in the development dataset.

Indexed as

Diagnosis-Related GroupsModels, StatisticalMyocardial InfarctionOut-of-Hospital Cardiac ArrestAlgorithmsHumansCase-Mix ShiftClinical Prediction ModelsMembership Propensity ScoreWeighted Logistic Regression

Identifiers

PMID40750843
PMCPMC12317593

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.