Geographical validation of the Smart Triage Model by age group.


Journal

PLOS digital health
ISSN: 2767-3170
Titre abrégé: PLOS Digit Health
Pays: United States
ID NLM: 9918335064206676

Informations de publication

Date de publication:
Jul 2024
Historique:
received: 27 06 2023
accepted: 25 05 2024
medline: 1 7 2024
pubmed: 1 7 2024
entrez: 1 7 2024
Statut: epublish

Résumé

Infectious diseases in neonates account for half of the under-five mortality in low- and middle-income countries. Data-driven algorithms such as clinical prediction models can be used to efficiently detect critically ill children in order to optimize care and reduce mortality. Thus far, only a handful of prediction models have been externally validated and are limited to neonatal in-hospital mortality. The aim of this study is to externally validate a previously derived clinical prediction model (Smart Triage) using a combined prospective baseline cohort from Uganda and Kenya with a composite endpoint of hospital admission, mortality, and readmission. We evaluated model discrimination using area under the receiver-operator curve (AUROC) and visualized calibration plots with age subsets (< 30 days, ≤ 2 months, ≤ 6 months, and < 5 years). Due to reduced performance in neonates (< 1 month), we re-estimated the intercept and coefficients and selected new thresholds to maximize sensitivity and specificity. 11595 participants under the age of five (under-5) were included in the analysis. The proportion with an endpoint ranged from 8.9% in all children under-5 (including neonates) to 26% in the neonatal subset alone. The model achieved good discrimination for children under-5 with AUROC of 0.81 (95% CI: 0.79-0.82) but poor discrimination for neonates with AUROC of 0.62 (95% CI: 0.55-0.70). Sensitivity at the low-risk thresholds (CI) were 85% (83%-87%) and 68% (58%-76%) for children under-5 and neonates, respectively. After model revision for neonates, we achieved an AUROC of 0.83 (95% CI: 0.79-0.87) with 13% and 41% as the low- and high-risk thresholds, respectively. The updated Smart Triage performs well in its predictive ability across different age groups and can be incorporated into current triage guidelines at local healthcare facilities. Additional validation of the model is indicated, especially for the neonatal model.

Identifiants

pubmed: 38949998
doi: 10.1371/journal.pdig.0000311
pii: PDIG-D-23-00249
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e0000311

Informations de copyright

Copyright: © 2024 Zhang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

John Mark Ansermino serves as a section editor for PLOS Digital Health.

Auteurs

Cherri Zhang (C)

Institute for Global Health, BC Children's and Women's Hospitals, Vancouver, British Columbia, Canada.

Matthew O Wiens (MO)

Institute for Global Health, BC Children's and Women's Hospitals, Vancouver, British Columbia, Canada.
Department of Anaesthesiology, Pharmacology & Therapeutics, University of British Columbia, Vancouver, British Columbia, Canada.
BC Children's Hospital Research Institute, Vancouver, British Columbia, Canada.

Dustin Dunsmuir (D)

Institute for Global Health, BC Children's and Women's Hospitals, Vancouver, British Columbia, Canada.
BC Children's Hospital Research Institute, Vancouver, British Columbia, Canada.

Yashodani Pillay (Y)

Institute for Global Health, BC Children's and Women's Hospitals, Vancouver, British Columbia, Canada.

Charly Huxford (C)

Institute for Global Health, BC Children's and Women's Hospitals, Vancouver, British Columbia, Canada.

David Kimutai (D)

Mbagathi County Hospital, Nairobi, Kenya.

Emmanuel Tenywa (E)

Jinja Regional Referral Hospital, Jinja, Uganda.

Mary Ouma (M)

Mbagathi County Hospital, Nairobi, Kenya.

Joyce Kigo (J)

Health Services Unit, KEMRI-Wellcome Trust Research Program, Nairobi, Kenya.

Stephen Kamau (S)

Health Services Unit, KEMRI-Wellcome Trust Research Program, Nairobi, Kenya.

Mary Chege (M)

Department of Pediatrics, Kiambu County Referral Hospital, Kiambu, Kenya.

Nathan Kenya-Mugisha (N)

World Alliance for Lung and Intensive Care Medicine in Uganda, Kampala, Uganda.

Savio Mwaka (S)

World Alliance for Lung and Intensive Care Medicine in Uganda, Kampala, Uganda.

Guy A Dumont (GA)

Department of Anaesthesiology, Pharmacology & Therapeutics, University of British Columbia, Vancouver, British Columbia, Canada.
BC Children's Hospital Research Institute, Vancouver, British Columbia, Canada.
Department of Electrical and Computer Engineering, University of British Columbia, Vancouver, British Columbia, Canada.

Niranjan Kissoon (N)

BC Children's Hospital Research Institute, Vancouver, British Columbia, Canada.
Department of Pediatrics, University of British Columbia, Vancouver, British Columbia, Canada.

Samuel Akech (S)

Health Services Unit, KEMRI-Wellcome Trust Research Program, Nairobi, Kenya.

J Mark Ansermino (JM)

Institute for Global Health, BC Children's and Women's Hospitals, Vancouver, British Columbia, Canada.
Department of Anaesthesiology, Pharmacology & Therapeutics, University of British Columbia, Vancouver, British Columbia, Canada.
BC Children's Hospital Research Institute, Vancouver, British Columbia, Canada.

Classifications MeSH