Evidence map›Paper›PMID 42764339›Full record

Observational studyNature communications2026

Improving early prediction for adverse dengue outcomes using data from the IDAMS prospective multicentre study.

Lam Phung Khanh, Kerstin Daniela Rosenberger, Tam Dong Thi Hoai, Kieu Nguyen Tan Thanh, Ngoc Tran Van, Nam Nguyen Tran, Viet Do Chau, Kinh Nguyen Van, Sophie Yacoub, Ngoun Chanpheaktra and 25 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

35 authors.

Lam Phung KhanhOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam. phungkhanhlam@gmail.com.ORCID http://orcid.org/0000-0001-7968-473X
Kerstin Daniela RosenbergerSection Clinical Tropical Medicine, Department of Infectious Diseases, Heidelberg University Hospital, Heidelberg, Germany.ORCID http://orcid.org/0000-0003-3459-3812
Tam Dong Thi HoaiOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
Kieu Nguyen Tan ThanhOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
Ngoc Tran VanHospital for Tropical Diseases, Ho Chi Minh City, Viet Nam.
Nam Nguyen TranChildren's Hospital Number 2, Ho Chi Minh City, Viet Nam.
Viet Do ChauChildren's Hospital Number 2, Ho Chi Minh City, Viet Nam.
Kinh Nguyen VanNational Hospital for Tropical Diseases, Hanoi, Viet Nam.
Sophie YacoubOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
Ngoun ChanpheaktraAngkor Hospital for Children, Siem Reap, Cambodia.
Varun KumarAngkor Hospital for Children, Siem Reap, Cambodia.
Lucy Lum Chai SeeFaculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.ORCID http://orcid.org/0000-0002-7452-4208
Jameela SatharAmpang Hospital, Kuala Lumpur, Malaysia.
Ernesto Pleités SandovalHospital Nacional de Niños Benjamin Bloom, San Salvador, El Salvador.
Gabriela Maria MarónHospital Nacional de Niños Benjamin Bloom, San Salvador, El Salvador.
Ida Safitri LaksanawatiCenter for Tropical Medicine, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Yogyakarta, Indonesia.
Yodi MahendradhataCenter for Tropical Medicine, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Yogyakarta, Indonesia.
Md Zabir HassanBRAC James P Grant School of Public Health, BRAC University, Dhaka, Bangladesh.
Firoz AhmedInternational Centre for Diarrhoeal Disease Research, Dhaka, Bangladesh.
Andrea CapraraUniversidade Estadual Do Ceará, Fortaleza, Brazil.
Bruno Souza BenevidesUniversidade Estadual Do Ceará, Fortaleza, Brazil.
Ernesto T A MarquesInstituto Aggeu Magalhães, Fundação Oswaldo Cruz, Recife, Pernambuco, Brazil.ORCID http://orcid.org/0000-0003-3826-9358
Tereza MagalhaesInstituto Aggeu Magalhães, Fundação Oswaldo Cruz, Recife, Pernambuco, Brazil.
Patricia BrasilInstituto Nacional de Infectologia Evandro Chagas, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil.ORCID http://orcid.org/0000-0001-9555-7976
Marco NettoSecretaria Municipal de Saúde de Resende, Rio de Janeiro, Brazil.
Adriana TamiFacultad de Ciencias de la Salud, Universidad de Carabobo, Valencia, Venezuela.ORCID http://orcid.org/0000-0002-1918-9144
Sarah E BethencourtFacultad de Ciencias de la Salud, Universidad de Carabobo, Valencia, Venezuela.
Maria G GuzmanInstitute of Tropical Medicine Pedro Kouri, PAHO/WHO Collaborating Center for Dengue and its Control, Havana, Cuba.ORCID http://orcid.org/0000-0003-3927-0844
Cameron SimmonsOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
Quyen Nguyen Than HaOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.ORCID http://orcid.org/0000-0001-5417-2738
Marcel WolbersOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
Ronald B GeskusOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.ORCID http://orcid.org/0000-0002-2740-3155
Thomas JaenischSection Clinical Tropical Medicine, Department of Infectious Diseases, Heidelberg University Hospital, Heidelberg, Germany.
Bridget WillsOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam. bwills@oucru.org.ORCID http://orcid.org/0000-0001-9086-8804
International Research Consortium on Dengue Risk Assessment, Management, and Surveillance Clinical Investigators Group

Funding

EC | EC Seventh Framework Programm | FP7 Ideas: European Research Council (FP7-IDEAS-ERC - Specific Programme: "Ideas" Implementing the Seventh Framework Programme of the European Community for Research, Technological Development and Demonstration Activities (2007 to 2013)) 281803Wellcome TrustWellcome Trust (Wellcome) 106680/Z/14/Z
6 · The paper itself

Abstract

Early identification of individuals at risk of complications is important to improve dengue case-management and promote appropriate use of limited resources in high burden settings. In this prospective observational cohort, 7428 febrile outpatients were enrolled across 8 countries in Asia and Latin America and followed daily; 2230 individuals with confirmed dengue were included in the analysis, among whom 304 (14%) progressed to moderate/severe dengue and 38 (2%) to severe dengue during follow-up. We demonstrate evolving relationships between common clinical features, WHO clinical warning signs, and simple haematological parameters, with progression. Key predictors of moderate/severe dengue include low lymphocyte percentage, low total white blood cell count, low platelet count, and persistent vomiting and significant abdominal pain/tenderness. Multivariable models incorporating these variables predict the risk of moderate/severe dengue, initially with modest performance (AUC ~ 0.68), but improving subsequently as new daily data is included into the predictions (AUC ~ 0.73-0.85). We also demonstrate that using these models in combination with clinical decision-making pathways could facilitate earlier admission of high-risk patients without markedly increasing admissions of uncomplicated cases. These results should prove instrumental for updating guidelines on dengue triage and management, potentially providing major public health benefits in resource poor settings.

Indexed as

DengueSevere DengueAdolescentAdultAsiaDisease ProgressionFemaleHumansLatin AmericaMaleMiddle AgedProspective StudiesYoung Adult

Identifiers

PMID42764339
PMCPMC13590484

What OpenQuestion holds

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Registered trials

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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.