Severity detection tool for patients with infectious disease.

ANSD level HFMD autonomic nervous system dysfunction cardiology classifying ANSD levels difficult problem diseases electrocardiogram electrocardiography enormous healthcare resources feature extraction frequency domains health care high mortality rate infectious disease learning (artificial intelligence) low-cost wearable sensors medical computing medical signal processing middle-income countries neurophysiology patient care patient diagnosis patient treatment photoplethysmogram waveforms physiological patient data proof-of-principle resource-demanding serious infectious diseases severity detection tool standard heart rate variability analysis support vector machine support vector machines tetanus patients young children

Journal

Healthcare technology letters
ISSN: 2053-3713
Titre abrégé: Healthc Technol Lett
Pays: England
ID NLM: 101646459

Informations de publication

Date de publication:
Apr 2020
Historique:
received: 13 05 2019
revised: 12 11 2019
accepted: 16 01 2020
entrez: 21 5 2020
pubmed: 21 5 2020
medline: 21 5 2020
Statut: epublish

Résumé

Hand foot and mouth disease (HFMD) and tetanus are serious infectious diseases in low- and middle-income countries. Tetanus, in particular, has a high mortality rate and its treatment is resource-demanding. Furthermore, HFMD often affects a large number of infants and young children. As a result, its treatment consumes enormous healthcare resources, especially when outbreaks occur. Autonomic nervous system dysfunction (ANSD) is the main cause of death for both HFMD and tetanus patients. However, early detection of ANSD is a difficult and challenging problem. The authors aim to provide a proof-of-principle to detect the ANSD level automatically by applying machine learning techniques to physiological patient data, such as electrocardiogram waveforms, which can be collected using low-cost wearable sensors. Efficient features are extracted that encode variations in the waveforms in the time and frequency domains. The proposed approach is validated on multiple datasets of HFMD and tetanus patients in Vietnam. Results show that encouraging performance is achieved. Moreover, the proposed features are simple, more generalisable and outperformed the standard heart rate variability analysis. The proposed approach would facilitate both the diagnosis and treatment of infectious diseases in low- and middle-income countries, and thereby improve patient care.

Identifiants

pubmed: 32431851
doi: 10.1049/htl.2019.0030
pii: HTL.2019.0030
pmc: PMC7199289
doi:

Types de publication

Journal Article

Langues

eng

Pagination

45-50

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 204904/Z/16/Z
Pays : United Kingdom

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Auteurs

Girmaw Abebe Tadesse (GA)

Institute of Biomedical Engineering, University of Oxford, Oxford, UK.
IBM Research | Africa, Nairobi, Kenya.

Tingting Zhu (T)

Institute of Biomedical Engineering, University of Oxford, Oxford, UK.

Nhan Le Nguyen Thanh (N)

Children's Hospital Number 1, Ho Chi Minh City, Vietnam.

Nguyen Thanh Hung (NT)

Children's Hospital Number 1, Ho Chi Minh City, Vietnam.

Ha Thi Hai Duong (HTH)

Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.

Truong Huu Khanh (TH)

Children's Hospital Number 1, Ho Chi Minh City, Vietnam.

Pham Van Quang (PV)

Children's Hospital Number 1, Ho Chi Minh City, Vietnam.

Duc Duong Tran (DD)

Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.

Lam Minh Yen (LM)

Oxford Clinical Research Unit, Ho Chi Minh City, Vietnam.

Rogier Van Doorn (RV)

Oxford University Clinical Research Unit, Hanoi, Vietnam.
Centre for Tropical Medicine and Global Health, Oxford University, UK.

Nguyen Van Hao (NV)

Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.

John Prince (J)

Institute of Biomedical Engineering, University of Oxford, Oxford, UK.

Hamza Javed (H)

Institute of Biomedical Engineering, University of Oxford, Oxford, UK.

Dani Kiyasseh (D)

Institute of Biomedical Engineering, University of Oxford, Oxford, UK.

Le Van Tan (LV)

Oxford Clinical Research Unit, Ho Chi Minh City, Vietnam.

Louise Thwaites (L)

Oxford Clinical Research Unit, Ho Chi Minh City, Vietnam.
Centre for Tropical Medicine and Global Health, Oxford University, UK.

David A Clifton (DA)

Institute of Biomedical Engineering, University of Oxford, Oxford, UK.

Classifications MeSH