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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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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. |
format | Online Article Text |
id | pubmed-3897966 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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