Evidence map›Paper›PMID 41662365›Full record

ArticlePLOS digital health2026

Early individualized risk prediction using clinical data for children during the febrile phase of dengue in outpatient settings in Vietnam and Thailand.

Sorawat Sangkaew, Bethan Cracknell Daniels, Damien K Ming, Bernard Hernandez, Pau Herrero, Piyarat Suntarattiwong, Siripen Kalayanarooj, Anon Srikiatkhachorn, Alan L Rothman, Darunee Buddhari and 9 more

Abstract read
In one paragraph

Article in PLOS digital health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors.

Sorawat SangkaewDepartment of Social Medicine, Hatyai Hospital, Songkhla, Thailand.ORCID https://orcid.org/0000-0002-1862-0879
Bethan Cracknell DanielsMRC Centre for Global Infectious Disease Analysis, Department of Infectious Disease Epidemiology, School of Public Health, Imperial College London, London, United Kingdom.ORCID https://orcid.org/0000-0002-3707-5706
Damien K MingCentre for Antimicrobial Optimisation, Imperial College London, London, United Kingdom.
Bernard HernandezDepartment of Electrical and Electronic Engineering, Imperial College London, London, United Kingdom.
Pau HerreroDepartment of Electrical and Electronic Engineering, Imperial College London, London, United Kingdom.
Piyarat SuntarattiwongDepartment of Pediatrics, Queen Sirikit National Institute of Child Health, Bangkok, Thailand.
Siripen KalayanaroojDepartment of Pediatrics, Queen Sirikit National Institute of Child Health, Bangkok, Thailand.
Anon SrikiatkhachornFaculty of Medicine, King Mongkut's Institute of Technology Ladkrabang, Bangkok, Thailand.ORCID https://orcid.org/0000-0002-2423-8545
Alan L RothmanInstitute for Immunology and Informatics and Department of Cell and Molecular Biology, University of Rhode Island, Providence, Rhode Island, United States of America.
Darunee BuddhariDepartment of Virology, WRAIR-AFRIMS, Bangkok, Thailand.
Nguyen Lam VuongOxford University Clinical Research Unit, Wellcome Trust Asia Programme, Ho Chi Minh City, Vietnam.ORCID https://orcid.org/0000-0003-2684-3041
Phung Khanh LamOxford University Clinical Research Unit, Wellcome Trust Asia Programme, Ho Chi Minh City, Vietnam.
Minh Tuan NguyenChildren's Hospital No. 1, Ho Chi Minh City, Vietnam.
Bridget WillsOxford University Clinical Research Unit, Wellcome Trust Asia Programme, Ho Chi Minh City, Vietnam.
Cameron SimmonsDepartment of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, University of Melbourne, Parkville, Melbourne, Australia.
Christl A DonnellyMRC Centre for Global Infectious Disease Analysis, Department of Infectious Disease Epidemiology, School of Public Health, Imperial College London, London, United Kingdom.
Sophie YacoubOxford University Clinical Research Unit, Wellcome Trust Asia Programme, Ho Chi Minh City, Vietnam.
Alison HolmesCentre for Antimicrobial Optimisation, Imperial College London, London, United Kingdom.
Ilaria DorigattiMRC Centre for Global Infectious Disease Analysis, Department of Infectious Disease Epidemiology, School of Public Health, Imperial College London, London, United Kingdom.ORCID https://orcid.org/0000-0001-9959-0706

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dengue severity prediction models are usually developed using hospitalized patient data, but triage and hospital admission are mainly evaluated in outpatient settings. This study developed models using clinical and laboratory data from patients in outpatient settings during the febrile phase. Data from two cohort studies in Vietnam and Thailand were used to develop and validate six models: logistic regression with warning signs, Lasso-selected logistic regression, random forest, extreme gradient boosted classification, support vector machine, and artificial neural network. Models predicted dengue shock syndrome (DSS) as the primary endpoint and moderate plasma leakage and/or DSS as the secondary endpoint. We assessed model performance, discrimination, and calibration, using sensitivity, specificity, accuracy, Brier score, AUROC, CITL, calibration slope, calibration plots, and decision curve analysis. The optimal model was the Lasso-selected logistic regression for predicting DSS and the combined endpoint of moderate plasma leakage and/or DSS (Brier score: 0.044 [95% CI 0.043, 0.044] and 0.104 [95% CI 0.104, 0.105]; AUROC: 0.789 [95% CI 0.787, 0.791] and 0.741 [95% CI 0.740, 0.742]). We identified hematocrit, platelet count, lymphocyte count, and aspartate aminotransferase as predictors for DSS, and abdominal pain or tenderness, vomiting, mucosal bleeding, white blood cell count, lymphocyte count, platelet count, aspartate aminotransferase, and serum albumin as predictors for the secondary endpoint. Logistic regression and machine learning models using clinical and laboratory data during the febrile phase can support early prediction of severe disease in outpatient settings. Integrating risk prediction models into a decision support system could improve triage and optimize healthcare and resource allocation in endemic and resource-limited areas.

Identifiers

PMID41662365
PMCPMC12885294

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.