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Assessing discriminative ability of risk models in clustered data

BACKGROUND: The discriminative ability of a risk model is often measured by Harrell’s concordance-index (c-index). The c-index estimates for two randomly chosen subjects the probability that the model predicts a higher risk for the subject with poorer outcome (concordance probability). When data are...

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Autores principales: van Klaveren, David, Steyerberg, Ewout W, Perel, Pablo, Vergouwe, Yvonne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3897966/
https://www.ncbi.nlm.nih.gov/pubmed/24423445
http://dx.doi.org/10.1186/1471-2288-14-5
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author van Klaveren, David
Steyerberg, Ewout W
Perel, Pablo
Vergouwe, Yvonne
author_facet van Klaveren, David
Steyerberg, Ewout W
Perel, Pablo
Vergouwe, Yvonne
author_sort van Klaveren, David
collection PubMed
description BACKGROUND: The discriminative ability of a risk model is often measured by Harrell’s concordance-index (c-index). The c-index estimates for two randomly chosen subjects the probability that the model predicts a higher risk for the subject with poorer outcome (concordance probability). When data are clustered, as in multicenter data, two types of concordance are distinguished: concordance in subjects from the same cluster (within-cluster concordance probability) and concordance in subjects from different clusters (between-cluster concordance probability). We argue that the within-cluster concordance probability is most relevant when a risk model supports decisions within clusters (e.g. who should be treated in a particular center). We aimed to explore different approaches to estimate the within-cluster concordance probability in clustered data. METHODS: We used data of the CRASH trial (2,081 patients clustered in 35 centers) to develop a risk model for mortality after traumatic brain injury. To assess the discriminative ability of the risk model within centers we first calculated cluster-specific c-indexes. We then pooled the cluster-specific c-indexes into a summary estimate with different meta-analytical techniques. We considered fixed effect meta-analysis with different weights (equal; inverse variance; number of subjects, events or pairs) and random effects meta-analysis. We reflected on pooling the estimates on the log-odds scale rather than the probability scale. RESULTS: The cluster-specific c-index varied substantially across centers (IQR = 0.70-0.81; I( 2 ) = 0.76 with 95% confidence interval 0.66 to 0.82). Summary estimates resulting from fixed effect meta-analysis ranged from 0.75 (equal weights) to 0.84 (inverse variance weights). With random effects meta-analysis – accounting for the observed heterogeneity in c-indexes across clusters – we estimated a mean of 0.77, a between-cluster variance of 0.0072 and a 95% prediction interval of 0.60 to 0.95. The normality assumptions for derivation of a prediction interval were better met on the probability than on the log-odds scale. CONCLUSION: When assessing the discriminative ability of risk models used to support decisions at cluster level we recommend meta-analysis of cluster-specific c-indexes. Particularly, random effects meta-analysis should be considered.
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spelling pubmed-38979662014-02-05 Assessing discriminative ability of risk models in clustered data van Klaveren, David Steyerberg, Ewout W Perel, Pablo Vergouwe, Yvonne BMC Med Res Methodol Research Article BACKGROUND: The discriminative ability of a risk model is often measured by Harrell’s concordance-index (c-index). The c-index estimates for two randomly chosen subjects the probability that the model predicts a higher risk for the subject with poorer outcome (concordance probability). When data are clustered, as in multicenter data, two types of concordance are distinguished: concordance in subjects from the same cluster (within-cluster concordance probability) and concordance in subjects from different clusters (between-cluster concordance probability). We argue that the within-cluster concordance probability is most relevant when a risk model supports decisions within clusters (e.g. who should be treated in a particular center). We aimed to explore different approaches to estimate the within-cluster concordance probability in clustered data. METHODS: We used data of the CRASH trial (2,081 patients clustered in 35 centers) to develop a risk model for mortality after traumatic brain injury. To assess the discriminative ability of the risk model within centers we first calculated cluster-specific c-indexes. We then pooled the cluster-specific c-indexes into a summary estimate with different meta-analytical techniques. We considered fixed effect meta-analysis with different weights (equal; inverse variance; number of subjects, events or pairs) and random effects meta-analysis. We reflected on pooling the estimates on the log-odds scale rather than the probability scale. RESULTS: The cluster-specific c-index varied substantially across centers (IQR = 0.70-0.81; I( 2 ) = 0.76 with 95% confidence interval 0.66 to 0.82). Summary estimates resulting from fixed effect meta-analysis ranged from 0.75 (equal weights) to 0.84 (inverse variance weights). With random effects meta-analysis – accounting for the observed heterogeneity in c-indexes across clusters – we estimated a mean of 0.77, a between-cluster variance of 0.0072 and a 95% prediction interval of 0.60 to 0.95. The normality assumptions for derivation of a prediction interval were better met on the probability than on the log-odds scale. CONCLUSION: When assessing the discriminative ability of risk models used to support decisions at cluster level we recommend meta-analysis of cluster-specific c-indexes. Particularly, random effects meta-analysis should be considered. BioMed Central 2014-01-15 /pmc/articles/PMC3897966/ /pubmed/24423445 http://dx.doi.org/10.1186/1471-2288-14-5 Text en Copyright © 2014 van Klaveren 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 cited. 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
van Klaveren, David
Steyerberg, Ewout W
Perel, Pablo
Vergouwe, Yvonne
Assessing discriminative ability of risk models in clustered data
title Assessing discriminative ability of risk models in clustered data
title_full Assessing discriminative ability of risk models in clustered data
title_fullStr Assessing discriminative ability of risk models in clustered data
title_full_unstemmed Assessing discriminative ability of risk models in clustered data
title_short Assessing discriminative ability of risk models in clustered data
title_sort assessing discriminative ability of risk models in clustered data
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3897966/
https://www.ncbi.nlm.nih.gov/pubmed/24423445
http://dx.doi.org/10.1186/1471-2288-14-5
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