Value-of-Information Analysis for External Validation of Risk Prediction Models

被引:1
|
作者
Sadatsafavi, Mohsen [1 ]
Lee, Tae Yoon [1 ]
Wynants, Laure [2 ,3 ]
Vickers, Andrew J. [4 ]
Gustafson, Paul [5 ]
机构
[1] Univ British Columbia, Fac Pharmaceut Sci, Resp Evaluat Sci Program, Room 4110,2405 Wesbrook Mall, Vancouver V6T 1Z3, BC, Canada
[2] Maastricht Univ, CAPHRI Care & Publ Hlth Res Inst, Dept Epidemiol, Maastricht, Netherlands
[3] Katholieke Univ Leuven, Dept Dev & Regenerat, Leuven, Belgium
[4] Mem Sloan Kettering Canc Ctr, Dept Epidemiol & Biostat, New York, NY USA
[5] Univ British Columbia, Dept Stat, Vancouver, BC, Canada
基金
美国国家卫生研究院; 加拿大健康研究院;
关键词
predictive analytics; precision medicine; decision theory; value of information; bayesian statistics;
D O I
10.1177/0272989X231178317
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background A previously developed risk prediction model needs to be validated before being used in a new population. The finite size of the validation sample entails that there is uncertainty around model performance. We apply value-of-information (VoI) methodology to quantify the consequence of uncertainty in terms of net benefit (NB). Methods We define the expected value of perfect information (EVPI) for model validation as the expected loss in NB due to not confidently knowing which of the alternative decisions confers the highest NB. We propose bootstrap-based and asymptotic methods for EVPI computations and conduct simulation studies to compare their performance. In a case study, we use the non-US subsets of a clinical trial as the development sample for predicting mortality after myocardial infarction and calculate the validation EVPI for the US subsample. Results The computation methods generated similar EVPI values in simulation studies. EVPI generally declined with larger samples. In the case study, at the prespecified threshold of 0.02, the best decision with current information would be to use the model, with an incremental NB of 0.0020 over treating all. At this threshold, the EVPI was 0.0005 (relative EVPI = 25%). When scaled to the annual number of heart attacks in the US, the expected NB loss due to uncertainty was equal to 400 true positives or 19,600 false positives, indicating the value of further model validation. Conclusion VoI methods can be applied to the NB calculated during external validation of clinical prediction models. While uncertainty does not directly affect the clinical implications of NB findings, validation EVPI provides an objective perspective to the need for further validation and can be reported alongside NB in external validation studies.
引用
收藏
页码:564 / 575
页数:12
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