Evaluation of performance measures in predictive artificial intelligence models to support medical decisions: overview and guidance

机器学习 人工智能 计算机科学 度量(数据仓库) 接收机工作特性 预测建模 校准 预测值 期限(时间) 数据挖掘 决策支持系统 二进制数 决策树 二元分类 统计模型 钥匙(锁) 预测效度 领域(数学分析) 统计 领域知识 统计假设检验
作者
Ben VAN CALSTER,Professor Gary S. Collins,Andrew Julian Vickers,Laure Wynants,Kathleen F. Kerr,Lasai Barreñada,Gael P. Varoquaux,Karandeep Singh,Karel G.M. Moons,Tina Hernandez‐Boussard,Dirk Timmerman,David J. McLernon,Maarten van Smeden,Ewout Willem Steyerberg
出处
期刊:The Lancet Digital Health [Elsevier BV]
卷期号:7 (12): 100916-100916 被引量:201
标识
DOI:10.1016/j.landig.2025.100916
摘要

Numerous measures have been proposed to illustrate the performance of predictive artificial intelligence (AI) models. Selecting appropriate performance measures is essential for predictive AI models intended for use in medical practice. Poorly performing models are misleading and may lead to wrong clinical decisions that can be detrimental to patients and increase financial costs. In this Viewpoint, we assess the merits of classic and contemporary performance measures when validating predictive AI models for medical practice, focusing on models that estimate probabilities for a binary outcome. We discuss 32 performance measures covering five performance domains (discrimination, calibration, overall performance, classification, and clinical utility) along with corresponding graphical assessments. The first four domains address statistical performance, whereas the fifth domain covers decision-analytical performance. We discuss two key characteristics when selecting a performance measure and explain why these characteristics are important: (1) whether the measure's expected value is optimised when calculated using the correct probabilities (ie, whether it is a proper measure) and (2) whether the measure solely reflects statistical performance or decision-analytical performance by properly accounting for misclassification costs. 17 measures showed both characteristics, 14 showed one, and one (F1 score) showed neither. All classification measures were improper for clinically relevant decision thresholds other than when the threshold was 0·5 or equal to the true prevalence. We illustrate these measures and characteristics using the ADNEX model which predicts the probability of malignancy in women with an ovarian tumour. We recommend the following measures and plots as essential to report: area under the receiver operating characteristic curve, calibration plot, a clinical utility measure such as net benefit with decision curve analysis, and a plot showing probability distributions by outcome category.
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