Evidence map›Paper›PMID 40680024›Full record

ArticlePLOS digital health2025

An artificial intelligence-based approach to identify volume status in patients with severe dengue using wearable PPG data.

Ngan Nguyen Lyle, Ho Quang Chanh, Hao Nguyen Van, James Anibal, Stefan Karolcik, Damien Ming, Giang Nguyen Thi, Huyen Vu Ngo Thanh, Huy Nguyen Quang, Hai Ho Bich and 11 more

Abstract read
In one paragraph

Article in PLOS digital health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Dengue virus infection.Nature reviews. Disease primers · 2026
    Review
  2. 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

21 authors.

Ngan Nguyen LyleOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.ORCID https://orcid.org/0000-0002-7162-9127
Ho Quang ChanhOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Hao Nguyen VanUniversity of Medicine and Pharmacy, Ho Chi Minh City, Vietnam.
James AnibalDepartment of Engineering Science, University of Oxford, Oxford, United Kingdom.
Stefan KarolcikCentre for Bio-Inspired Technology, Imperial College London, London, United Kingdom.
Damien MingCentre for Antimicrobial Optimisation, Imperial College London, London, United Kingdom.
Giang Nguyen ThiOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Huyen Vu Ngo ThanhOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Huy Nguyen QuangOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Hai Ho BichOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Khoa Le Dinh VanOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Van Hoang Minh TuOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.ORCID https://orcid.org/0000-0001-6551-6356
Khanh Phan Nguyen QuocOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Huynh Trung TrieuHospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
Qui Tu PhanHospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
Tho Phan VinhHospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
Tai Luong Thi HueHospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
Pantelis GeorgiouCentre for Bio-Inspired Technology, Imperial College London, London, United Kingdom.
Louise ThwaitesOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Sophie YacoubOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Vietnam ICU Translational Applications Laboratory (VITAL) investigators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dengue shock syndrome (DSS) is a serious complication of dengue infection which occurs when critical plasma leakage results in haemodynamic shock. Treatment is challenging as fluid therapy must balance the risk of hypoperfusion with volume overload. In this study, we investigate the potential utility of wearable photoplethysmography (PPG) to determine volume status in DSS. In this prospective observational study, we enrolled 250 adults and children with a clinical diagnosis of dengue admitted to the Hospital for Tropical Diseases, Ho Chi Minh City. PPG monitoring using a wearable device was applied for a 24-hour period. Clinical events were then matched to the PPG data by date and time. We predefined two clinical states for comparison: (1) the 2-hour period before a shock event was an "empty" volume state and (2) the 2-hour period between 1 and 3 hours after a fluid initiation event was a "full" volume state. PPG data were sampled from these states for analysis. Variability and waveform morphology features were extracted and analyzed using principal components analysis and random forest. Waveform images were used to develop a computer vision model. Of the 250 patients enrolled, 90 patients experienced the predefined outcomes, and had sufficient data for the analysis. Principal components analysis identified four principal components (PCs), from the 23 pulse wave features. Logistic regression using these PCs showed that the empty state is associated with PCs 1 (p = 0.016) and 4 (p = 0.036) with both PCs denoting increased sympathetic activity. Random forest showed that heart rate and the LF-HF ratio are the most important features. A computer vision model had a sensitivity of 0.81 and a specificity of 0.70 for the empty state. These results provide proof of concept that an artificial intelligence-based approach using continuous PPG monitoring can provide information on volume states in DSS.

Identifiers

PMID40680024
PMCPMC12273927

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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.