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Kim Zhipei Wang

Publications and source records attributed to Kim Zhipei Wang.

2 recordsLinked to original sources

Population-Level Decision Curve Analysis May Mislead the Evaluation of Prediction Model Usefulness under Subgroup Utility Heterogeneity

Background Decision curve analysis (DCA) evaluates prediction model usefulness using net benefit (NB). Population-level NB is often interpreted as a proxy for population-level expected utility, but this assumes comparability of utility across subgroups. We aimed to characterize when subgroup utility heterogeneity may invalidate population-level DCA conclusions. Methods We compared prediction-driven treatment with default strategies in populations containing subgroups with different utility values. We derived an inconsistency region: combinations of subgroup-specific ΔNB values for which population-level NB and utility favor different strategies. We also developed a practical robustness framework. Results Opposite signs of subgroup-specific ΔNB provide a warning signal for possible inconsistency. The inconsistency region is larger when subgroup sizes are more similar and subgroup-specific \(a-c\) values are more different, where \(a-c\) is the incremental utility of a true positive relative to a false negative. When \(a-c\) differs across subgroups, population-level NB combines quantities on different implicit utility scales and may conflict with population utility. A real-world case study illustrates the problem. Conclusions Using population-level NB as a proxy for population utility implicitly assumes homogeneous \(a-c\) across subgroups. Subgroup DCA and our framework can identify and assess when utility heterogeneity may invalidate population-level conclusions.

stat.ME↗

Value-of-Information Analysis for External Validation of Risk Prediction Models in Multicenter Studies and Systematic Reviews

External validation studies have finite sample sizes, creating uncertainty about whether a prediction model's Net Benefit (NB) exceeds default strategies' NB. The expected value of perfect information (EVPI) quantifies consequences of uncertainty. Current EVPI methods focus on single studies, ignoring between-center heterogeneity. We extend EVPI and expected value of partial perfect information (EVPPI) to account for between-cluster heterogeneity in multicenter studies and meta-analyses. We distinguish between the global and local optimal strategy and between observed and unobserved clusters. We define EVPIglobal, EVPIcluster_j, EVPIcluster, and EVPPIcluster,prevalence, implemented in the MetaNB R package, and illustrate them using a systematic review across 36 centers of the ADNEX model for ovarian cancer diagnosis. Assuming one global decision regarding ADNEX adoption, there is no need for further data to confirm ADNEX is superior overall (EVPIglobal 0). Meta-analysis borrows information across observed clusters, resulting in consistent local superiority of ADNEX and nonzero but typically lower EVPIcluster_j than when considering local data alone. There is 0.03 probability default strategies are superior in unobserved centers. Eliminating uncertainty on performance and prevalence in each (EVPIcluster) would gain 1134 net avoided false positives (FP) per year, assuming 350000 tumors annually with 20% malignancies. Determining only local prevalence with certainty (EVPPIcluster, prevalence) would gain net 158 avoided FP per year. EVPI extensions disentangle sources of uncertainty and quantify the need for further validation to determine the global or locally optimal strategy. Considering uncertainty and heterogeneity in clinical utility across clusters is essential to decide whether additional validation studies are warranted.

stat.AP↗