Diagnostic Prediction Model for Tuberculous Meningitis: An Individual Participant Data Meta-Analysis

Anna M. Stadelman-Behar, Nicki Tiffin, Jayne Ellis, Fiona V. Creswell, Kenneth Ssebambulidde, Edwin Nuwagira, Lauren Richards, Vittoria Lutje, Adriana Hristea, Raluca Elena Jipa, José E. Vidal, Renata G.S. Azevedo, Sérgio Monteiro de Almeida, Gislene Botao Kussen, Keite Nogueira, Felipe Augusto Souza Gualberto, Tatiana Metcalf, Anna Dorothee Heemskerk, Tarek Dendane, Abidi KhalidAmine Ali Zeggwagh, Kathleen Bateman, Uwe Siebert, Ursula Rochau, Arjan van Laarhoven, Reinout van Crevel, Ahmad Rizal Ganiem, Sofiati Dian, Joseph Jarvis, Joseph Donovan, Thuong Nguyen Thuy Thuong, Guy E. Thwaites, Nathan C. Bahr, David B Meya, David R. Boulware, Tom H. Boyles

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

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.

Original languageEnglish (US)
Pages (from-to)546-553
Number of pages8
JournalAmerican Journal of Tropical Medicine and Hygiene
Volume111
Issue number3
DOIs
StatePublished - Sep 2024

Bibliographical note

Publisher Copyright:
© 2024 American Society of Tropical Medicine and Hygiene.

PubMed: MeSH publication types

  • Journal Article
  • Meta-Analysis
  • Systematic Review

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