Research inefficiencies in external validation studies of the Framingham Wilson coronary heart disease risk rule: A systematic review

Background: External validation studies create evidence about a clinical prediction rule’s (CPR’s) generalizability by evaluating and updating the CPR in populations different from those used in the derivation, and also by contributing to estimating its overall performance when meta-analysed in a sy...

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Main Authors: Ban, J, Abel, L, Stevens, R, Perera, R
Format: Journal article
Language:English
Published: Public Library of Science 2024
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author Ban, J
Abel, L
Stevens, R
Perera, R
author_facet Ban, J
Abel, L
Stevens, R
Perera, R
author_sort Ban, J
collection OXFORD
description Background: External validation studies create evidence about a clinical prediction rule’s (CPR’s) generalizability by evaluating and updating the CPR in populations different from those used in the derivation, and also by contributing to estimating its overall performance when meta-analysed in a systematic review. While most cardiovascular CPRs do not have any external validation, some CPRs have been externally validated repeatedly. Hence, we examined whether external validation studies of the Framingham Wilson coronary heart disease (CHD) risk rule contributed to generating evidence to their full potential. Methods: A forward citation search of the Framingham Wilson CHD risk rule’s derivation study was conducted to identify studies that evaluated the Framingham Wilson CHD risk rule in different populations. For external validation studies of the Framingham Wilson CHD risk rule, we examined whether authors updated the Framingham Wilson CHD risk rule when it performed poorly. We also assessed the contribution of external validation studies to understanding the Predicted/Observed (P/O) event ratio and c statistic of the Framingham Wilson CHD risk rule. Results: We identified 98 studies that evaluated the Framingham Wilson CHD risk rule; 40 of which were external validation studies. Of these 40 studies, 27 (67.5%) concluded the Framingham Wilson CHD risk rule performed poorly but did not update it. Of 23 external validation studies conducted with data that could be included in meta-analyses, 13 (56.5%) could not fully contribute to the meta-analyses of P/O ratio and/or c statistic because these performance measures were neither reported nor could be calculated from provided data. Discussion: Most external validation studies failed to generate evidence about the Framingham Wilson CHD risk rule’s generalizability to their full potential. Researchers might increase the value of external validation studies by presenting all relevant performance measures and by updating the CPR when it performs poorly.
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spelling oxford-uuid:d26a9c0c-21c4-4d72-b14c-5b671c091cad2024-09-13T20:07:09ZResearch inefficiencies in external validation studies of the Framingham Wilson coronary heart disease risk rule: A systematic reviewJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:d26a9c0c-21c4-4d72-b14c-5b671c091cadEnglishJisc Publications RouterPublic Library of Science2024Ban, JAbel, LStevens, RPerera, RBackground: External validation studies create evidence about a clinical prediction rule’s (CPR’s) generalizability by evaluating and updating the CPR in populations different from those used in the derivation, and also by contributing to estimating its overall performance when meta-analysed in a systematic review. While most cardiovascular CPRs do not have any external validation, some CPRs have been externally validated repeatedly. Hence, we examined whether external validation studies of the Framingham Wilson coronary heart disease (CHD) risk rule contributed to generating evidence to their full potential. Methods: A forward citation search of the Framingham Wilson CHD risk rule’s derivation study was conducted to identify studies that evaluated the Framingham Wilson CHD risk rule in different populations. For external validation studies of the Framingham Wilson CHD risk rule, we examined whether authors updated the Framingham Wilson CHD risk rule when it performed poorly. We also assessed the contribution of external validation studies to understanding the Predicted/Observed (P/O) event ratio and c statistic of the Framingham Wilson CHD risk rule. Results: We identified 98 studies that evaluated the Framingham Wilson CHD risk rule; 40 of which were external validation studies. Of these 40 studies, 27 (67.5%) concluded the Framingham Wilson CHD risk rule performed poorly but did not update it. Of 23 external validation studies conducted with data that could be included in meta-analyses, 13 (56.5%) could not fully contribute to the meta-analyses of P/O ratio and/or c statistic because these performance measures were neither reported nor could be calculated from provided data. Discussion: Most external validation studies failed to generate evidence about the Framingham Wilson CHD risk rule’s generalizability to their full potential. Researchers might increase the value of external validation studies by presenting all relevant performance measures and by updating the CPR when it performs poorly.
spellingShingle Ban, J
Abel, L
Stevens, R
Perera, R
Research inefficiencies in external validation studies of the Framingham Wilson coronary heart disease risk rule: A systematic review
title Research inefficiencies in external validation studies of the Framingham Wilson coronary heart disease risk rule: A systematic review
title_full Research inefficiencies in external validation studies of the Framingham Wilson coronary heart disease risk rule: A systematic review
title_fullStr Research inefficiencies in external validation studies of the Framingham Wilson coronary heart disease risk rule: A systematic review
title_full_unstemmed Research inefficiencies in external validation studies of the Framingham Wilson coronary heart disease risk rule: A systematic review
title_short Research inefficiencies in external validation studies of the Framingham Wilson coronary heart disease risk rule: A systematic review
title_sort research inefficiencies in external validation studies of the framingham wilson coronary heart disease risk rule a systematic review
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