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On estimating a constrained bivariate random effects model for meta-analysis of test accuracy studies
Tailored meta-analysis uses setting-specific knowledge for the test positive rate and disease prevalence to constrain the possible values for a test's sensitivity and specificity. The constrained region is used to select those studies relevant to the setting for meta-analysis using an unconstra...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8829734/ https://www.ncbi.nlm.nih.gov/pubmed/34994667 http://dx.doi.org/10.1177/09622802211065157 |
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author | Baragilly, Mohammed Willis, Brian Harvey |
author_facet | Baragilly, Mohammed Willis, Brian Harvey |
author_sort | Baragilly, Mohammed |
collection | PubMed |
description | Tailored meta-analysis uses setting-specific knowledge for the test positive rate and disease prevalence to constrain the possible values for a test's sensitivity and specificity. The constrained region is used to select those studies relevant to the setting for meta-analysis using an unconstrained bivariate random effects model (BRM). However, sometimes there may be no studies to aggregate, or the summary estimate may lie outside the plausible or “applicable” region. Potentially these shortcomings may be overcome by incorporating the constraints in the BRM to produce a constrained model. Using a penalised likelihood approach we developed an optimisation algorithm based on co-ordinate ascent and Newton-Raphson iteration to fit a constrained bivariate random effects model (CBRM) for meta-analysis. Using numerical examples based on simulation studies and real datasets we compared its performance with the BRM in terms of bias, mean squared error and coverage probability. We also determined the ‘closeness’ of the estimates to their true values using the Euclidian and Mahalanobis distances. The CBRM produced estimates which in the majority of cases had lower absolute mean bias and greater coverage probability than the BRM. The estimated sensitivities and specificity for the CBRM were, in general, closer to the true values than the BRM. For the two real datasets, the CBRM produced estimates which were in the applicable region in contrast to the BRM. When combining setting-specific data with test accuracy meta-analysis, a constrained model is more likely to yield a plausible estimate for the sensitivity and specificity in the practice setting than an unconstrained model. |
format | Online Article Text |
id | pubmed-8829734 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-88297342022-02-11 On estimating a constrained bivariate random effects model for meta-analysis of test accuracy studies Baragilly, Mohammed Willis, Brian Harvey Stat Methods Med Res Original Research Articles Tailored meta-analysis uses setting-specific knowledge for the test positive rate and disease prevalence to constrain the possible values for a test's sensitivity and specificity. The constrained region is used to select those studies relevant to the setting for meta-analysis using an unconstrained bivariate random effects model (BRM). However, sometimes there may be no studies to aggregate, or the summary estimate may lie outside the plausible or “applicable” region. Potentially these shortcomings may be overcome by incorporating the constraints in the BRM to produce a constrained model. Using a penalised likelihood approach we developed an optimisation algorithm based on co-ordinate ascent and Newton-Raphson iteration to fit a constrained bivariate random effects model (CBRM) for meta-analysis. Using numerical examples based on simulation studies and real datasets we compared its performance with the BRM in terms of bias, mean squared error and coverage probability. We also determined the ‘closeness’ of the estimates to their true values using the Euclidian and Mahalanobis distances. The CBRM produced estimates which in the majority of cases had lower absolute mean bias and greater coverage probability than the BRM. The estimated sensitivities and specificity for the CBRM were, in general, closer to the true values than the BRM. For the two real datasets, the CBRM produced estimates which were in the applicable region in contrast to the BRM. When combining setting-specific data with test accuracy meta-analysis, a constrained model is more likely to yield a plausible estimate for the sensitivity and specificity in the practice setting than an unconstrained model. SAGE Publications 2022-01-07 2022-02 /pmc/articles/PMC8829734/ /pubmed/34994667 http://dx.doi.org/10.1177/09622802211065157 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Articles Baragilly, Mohammed Willis, Brian Harvey On estimating a constrained bivariate random effects model for meta-analysis of test accuracy studies |
title | On estimating a constrained bivariate random effects model for meta-analysis of test accuracy studies |
title_full | On estimating a constrained bivariate random effects model for meta-analysis of test accuracy studies |
title_fullStr | On estimating a constrained bivariate random effects model for meta-analysis of test accuracy studies |
title_full_unstemmed | On estimating a constrained bivariate random effects model for meta-analysis of test accuracy studies |
title_short | On estimating a constrained bivariate random effects model for meta-analysis of test accuracy studies |
title_sort | on estimating a constrained bivariate random effects model for meta-analysis of test accuracy studies |
topic | Original Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8829734/ https://www.ncbi.nlm.nih.gov/pubmed/34994667 http://dx.doi.org/10.1177/09622802211065157 |
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