平衡风险完整性指数(BRII):竞争风险与删失下评估临床预测警报的分层指标
Balanced Risk Integrity Index: a stratum-level metric for evaluating clinical prediction alerts under competing risks and censoring
研究提出分层指标平衡风险完整性指数(BRII),定义为被标记高风险层中目标事件占目标事件、竞争死亡与早期删失观察的比例,并与阳性预测值(PPV)代数相关。
Abstract
Background: Conventional discrimination metrics, such as the area under the receiver operating characteristic curve (AUROC), do not characterize the composition of outcomes among patients flagged as high risk by clinical prediction models. This limitation is particularly relevant in critical care, where competing deaths and incomplete follow-up can complicate the interpretation of prediction alerts. We developed the Balanced Risk Integrity Index (BRII), a stratum-level metric defined as the proportion of target events among target events, competing deaths, and early-censored observations in a flagged high-risk stratum. BRII is algebraically related to positive predictive value (PPV) and is reported alongside its component decomposition to characterize the outcome composition of flagged patients. Methods: We evaluated BRII using seven acute kidney injury (AKI) prediction models developed in MIMIC-IV and externally validated in MIMIC-III and eICU-CRD (116,010 patients in total). Additional simulations examined the effects of competing deaths and early censoring on BRII and conventional model performance metrics. Results: For 48-hour AKI prediction in the top 10% risk stratum, BRII ranged from 0.90 to 0.96 in MIMIC-III, compared with less than 0.26 across all models in eICU-CRD, where 61.5% of evaluated patients were censored before the prediction horizon. In the eICU-CRD top 10% strata for the same target, 37.0% to 50.2% of patients were censored early, 12.2% to 15.5% had AKI, and 3.4% to 8.1% died before AKI. BRII and PPV ordered at least one model pair differently in 34 of 48 cohort-outcome-top-k groups. Under simulated random censoring for 48-hour AKI prediction, BRII declined by up to 0.80 while binary-label AUROC changed by less than 0.02. Conclusions: BRII provided complementary information on high-risk stratum composition, yielding different model rankings from PPV and revealing substantial differences across external validation cohorts. Interpreted alongside PPV and its component decomposition, BRII offers a standardized approach to evaluating clinical prediction alerts across models and observation environments.
Competing Interest Statement
The authors have declared no competing interest.
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Data Availability
MIMIC-IV, MIMIC-III, and eICU-CRD are publicly available through PhysioNet (https://physionet.org). Source data for all figures and tables are provided with this paper.
Funder Information Declared
Institute of Information & Communications Technology Planning & Evaluation, IITP-2026-RS-2022-00156439
National Research Foundation of Korea, RS-2026-25477844
来源:medRxiv · 临床预印本 · medrxiv.org