Assessing discriminative ability of risk models in clustered data
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Published on: September 16, 2022
David van Klaveren1, Ewout W Steyerberg, Pablo Perel
1Department of Public Health, Erasmus MC, Dr, Molewaterplein 50, Rotterdam 3015 GE, The Netherlands. d.vanklaveren.1@erasmusmc.nl.
Insights
This study explores methods for estimating within-cluster concordance probability in clustered data, crucial for risk models supporting decisions within specific centers. Random effects meta-analysis of cluster-specific concordance indexes is recommended for accurate assessment.
Area of Science:
- Biostatistics
- Epidemiology
- Health Services Research
Background:
- Risk models are vital for clinical decision-making, with Harrell's concordance-index (c-index) measuring discriminative ability.
- In clustered data (e.g., multicenter studies), within-cluster and between-cluster concordance are distinguished.
- Within-cluster concordance is most relevant for risk models guiding decisions at the local (cluster) level.
Purpose of the Study:
- To explore and compare different approaches for estimating the within-cluster concordance probability in clustered data.
- To identify the most suitable meta-analytical techniques for pooling cluster-specific concordance indexes.
Main Methods:
- Utilized data from the CRASH trial (2,081 patients, 35 centers) to develop a risk model for mortality after traumatic brain injury.
- Calculated cluster-specific c-indexes to assess model discrimination within each center.
- Applied various meta-analytical techniques, including fixed and random effects models, to pool cluster-specific c-indexes.
Main Results:
- Cluster-specific c-indexes showed substantial variation across centers (IQR: 0.70-0.81).
- Fixed effect meta-analysis yielded summary estimates ranging from 0.75 to 0.84.
- Random effects meta-analysis estimated a mean c-index of 0.77 with a 95% prediction interval of 0.60 to 0.95, accounting for heterogeneity.
Conclusions:
- Meta-analysis of cluster-specific c-indexes is recommended for evaluating risk models that support cluster-level decisions.
- Random effects meta-analysis is particularly advised due to observed heterogeneity in discriminative ability across clusters.
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; I2 = 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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