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Meta-analysis and meta-modelling for diagnostic problems

BACKGROUND: A proportional hazards measure is suggested in the context of analyzing SROC curves that arise in the meta–analysis of diagnostic studies. The measure can be motivated as a special model: the Lehmann model for ROC curves. The Lehmann model involves study–specific sensitivities and specif...

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Autores principales: Charoensawat, Suphada, Böhning, Walailuck, Böhning, Dankmar, Holling, Heinz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4007022/
https://www.ncbi.nlm.nih.gov/pubmed/24758534
http://dx.doi.org/10.1186/1471-2288-14-56
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author Charoensawat, Suphada
Böhning, Walailuck
Böhning, Dankmar
Holling, Heinz
author_facet Charoensawat, Suphada
Böhning, Walailuck
Böhning, Dankmar
Holling, Heinz
author_sort Charoensawat, Suphada
collection PubMed
description BACKGROUND: A proportional hazards measure is suggested in the context of analyzing SROC curves that arise in the meta–analysis of diagnostic studies. The measure can be motivated as a special model: the Lehmann model for ROC curves. The Lehmann model involves study–specific sensitivities and specificities and a diagnostic accuracy parameter which connects the two. METHODS: A study–specific model is estimated for each study, and the resulting study-specific estimate of diagnostic accuracy is taken as an outcome measure for a mixed model with a random study effect and other study-level covariates as fixed effects. The variance component model becomes estimable by deriving within-study variances, depending on the outcome measure of choice. In contrast to existing approaches – usually of bivariate nature for the outcome measures – the suggested approach is univariate and, hence, allows easily the application of conventional mixed modelling. RESULTS: Some simple modifications in the SAS procedure proc mixed allow the fitting of mixed models for meta-analytic data from diagnostic studies. The methodology is illustrated with several meta–analytic diagnostic data sets, including a meta–analysis of the Mini–Mental State Examination as a diagnostic device for dementia and mild cognitive impairment. CONCLUSIONS: The proposed methodology allows us to embed the meta-analysis of diagnostic studies into the well–developed area of mixed modelling. Different outcome measures, specifically from the perspective of whether a local or a global measure of diagnostic accuracy should be applied, are discussed as well. In particular, variation in cut-off value is discussed together with recommendations on choosing the best cut-off value. We also show how this problem can be addressed with the proposed methodology.
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spelling pubmed-40070222014-05-19 Meta-analysis and meta-modelling for diagnostic problems Charoensawat, Suphada Böhning, Walailuck Böhning, Dankmar Holling, Heinz BMC Med Res Methodol Research Article BACKGROUND: A proportional hazards measure is suggested in the context of analyzing SROC curves that arise in the meta–analysis of diagnostic studies. The measure can be motivated as a special model: the Lehmann model for ROC curves. The Lehmann model involves study–specific sensitivities and specificities and a diagnostic accuracy parameter which connects the two. METHODS: A study–specific model is estimated for each study, and the resulting study-specific estimate of diagnostic accuracy is taken as an outcome measure for a mixed model with a random study effect and other study-level covariates as fixed effects. The variance component model becomes estimable by deriving within-study variances, depending on the outcome measure of choice. In contrast to existing approaches – usually of bivariate nature for the outcome measures – the suggested approach is univariate and, hence, allows easily the application of conventional mixed modelling. RESULTS: Some simple modifications in the SAS procedure proc mixed allow the fitting of mixed models for meta-analytic data from diagnostic studies. The methodology is illustrated with several meta–analytic diagnostic data sets, including a meta–analysis of the Mini–Mental State Examination as a diagnostic device for dementia and mild cognitive impairment. CONCLUSIONS: The proposed methodology allows us to embed the meta-analysis of diagnostic studies into the well–developed area of mixed modelling. Different outcome measures, specifically from the perspective of whether a local or a global measure of diagnostic accuracy should be applied, are discussed as well. In particular, variation in cut-off value is discussed together with recommendations on choosing the best cut-off value. We also show how this problem can be addressed with the proposed methodology. BioMed Central 2014-04-24 /pmc/articles/PMC4007022/ /pubmed/24758534 http://dx.doi.org/10.1186/1471-2288-14-56 Text en Copyright © 2014 Charoensawat et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Charoensawat, Suphada
Böhning, Walailuck
Böhning, Dankmar
Holling, Heinz
Meta-analysis and meta-modelling for diagnostic problems
title Meta-analysis and meta-modelling for diagnostic problems
title_full Meta-analysis and meta-modelling for diagnostic problems
title_fullStr Meta-analysis and meta-modelling for diagnostic problems
title_full_unstemmed Meta-analysis and meta-modelling for diagnostic problems
title_short Meta-analysis and meta-modelling for diagnostic problems
title_sort meta-analysis and meta-modelling for diagnostic problems
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4007022/
https://www.ncbi.nlm.nih.gov/pubmed/24758534
http://dx.doi.org/10.1186/1471-2288-14-56
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