The American journal of tropical medicine and hygiene · 2024
Diagnostic Prediction Model for Tuberculous Meningitis: An Individual Participant Data Meta-Analysis.
СтатьяМетаанализСистематический обзорНазвание и аннотация: Перевод пока не подготовлен
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Stadelman-Behar Anna M, Tiffin Nicki, Ellis Jayne, Creswell Fiona V, Ssebambulidde Kenneth, Nuwagira Edwin, Richards Lauren, Lutje Vittoria, Hristea Adriana, Jipa Raluca Elena, Vidal José E, Azevedo Renata G S, Monteiro de Almeida Sérgio, Kussen Gislene Botão, Nogueira Keite, Gualberto Felipe Augusto Souza, Metcalf Tatiana, Heemskerk Anna Dorothee, Dendane Tarek, Khalid Abidi, Ali Zeggwagh Amine, Bateman Kathleen, Siebert Uwe, Rochau Ursula, van Laarhoven Arjan, van Crevel Reinout, Ganiem Ahmad Rizal, Dian Sofiati, Jarvis Joseph, Donovan Joseph, Nguyen Thuy Thuong Thuong, Thwaites Guy E, Bahr Nathan C, Meya David B, Boulware David R, Boyles Tom H
Аннотация
No accurate and rapid diagnostic test exists for tuberculous meningitis (TBM), leading to delayed diagnosis. We leveraged data from multiple studies to improve the predictive performance of diagnostic models across different populations, settings, and subgroups to develop a new predictive tool for TBM diagnosis. We conducted a systematic review to analyze eligible datasets with individual-level participant data (IPD). We imputed missing data and explored three approaches: stepwise logistic regression, classification and regression tree (CART), and random forest regression. We evaluated performance using calibration plots and C-statistics via internal-external cross-validation. We included 3,761 individual participants from 14 studies and nine countries. A total of 1,240 (33%) participants had "definite" (30%) or "probable" (3%) TBM by case definition. Important predictive variables included cerebrospinal fluid (CSF) glucose, blood glucose, CSF white cell count, CSF differential, cryptococcal antigen, HIV status, and fever presence. Internal validation showed that performance varied considerably between IPD datasets with C-statistic values between 0.60 and 0.89. In external validation, CART performed the worst (C = 0.82), and logistic regression and random forest had the same accuracy (C = 0.91). We developed a mobile app for TBM clinical prediction that accounted for heterogeneity and improved diagnostic performance (https://tbmcalc.github.io/tbmcalc). Further external validation is needed.