Evidence map›Paper›PMID 38428358›Full record

ArticleEpidemics2024

Age-time-specific transmission of hand-foot-and-mouth disease enterovirus serotypes in Vietnam: A catalytic model with maternal immunity.

Yining Chen, Lam Anh Nguyet, Le Nguyen Thanh Nhan, Phan Tu Qui, Le Nguyen Truc Nhu, Nguyen Thi Thu Hong, Nguyen Thi Han Ny, Nguyen To Anh, Le Kim Thanh, Huynh Thi Phuong and 10 more

Abstract read
In one paragraph

Article in Epidemics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
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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

20 authors.

Yining ChenSaw Swee Hock School of Public Health, National University of Singapore and National University Health System, Singapore. Electronic address: yining.chen@u.nus.edu.
Lam Anh NguyetOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
Le Nguyen Thanh NhanChildren's Hospital 1, Ho Chi Minh City, Viet Nam.
Phan Tu QuiHospital for Tropical Diseases, Ho Chi Minh City, Viet Nam.
Le Nguyen Truc NhuOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
Nguyen Thi Thu HongOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
Nguyen Thi Han NyOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
Nguyen To AnhOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
Le Kim ThanhOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
Huynh Thi PhuongOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
Nguyen Ha Thao VyOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
Nguyen Thi Le ThanhOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
Truong Huu KhanhChildren's Hospital 1, Ho Chi Minh City, Viet Nam.
Nguyen Thanh HungChildren's Hospital 1, Ho Chi Minh City, Viet Nam.
Do Chau VietChildren's Hospital 2, Ho Chi Minh City, Viet Nam.
Nguyen Tran NamCity Children's Hospital, Ho Chi Minh City, Viet Nam.
Nguyen Van Vinh ChauOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam; Hospital for Tropical Diseases, Ho Chi Minh City, Viet Nam.
H Rogier van DoornOxford University Clinical Research Unit, Hanoi, Viet Nam; Centre for Tropical Medicine and Global Health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom.
Le Van TanOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam; Centre for Tropical Medicine and Global Health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom.
Hannah ClaphamSaw Swee Hock School of Public Health, National University of Singapore and National University Health System, Singapore.

Funding

Wellcome Trust
6 · The paper itself

Abstract

Hand, foot and mouth disease (HFMD) is highly prevalent in the Asia Pacific region, particularly in Vietnam. To develop effective interventions and efficient vaccination programs, we inferred the age-time-specific transmission patterns of HFMD serotypes enterovirus A71 (EV-A71), coxsackievirus A6 (CV-A6), coxsackievirus A10 (CV-A10), coxsackievirus A16 (CV-A16) in Ho Chi Minh City, Vietnam from a case data collected during 2013-2018 and a serological survey data collected in 2015 and 2017. We proposed a catalytic model framework with good adaptability to incorporate maternal immunity using various mathematical functions. Our results indicate the high-level transmission of CV-A6 and CV-A10 which is not obvious in the case data, due to the variation of disease severity across serotypes. Our results provide statistical evidence supporting the strong association between severe illness and CV-A6 and EV-A71 infections. The HFMD dynamic pattern presents a cyclical pattern with large outbreaks followed by a decline in subsequent years. Additionally, we identify the age group with highest risk of infection as 1-2 years and emphasise the risk of future outbreaks as over 50% of children aged 6-7 years were estimated to be susceptible to CV-A16 and EV-A71. Our study highlights the importance of multivalent vaccines and active surveillance for different serotypes, supports early vaccination prior to 1 year old, and points out the potential utility for vaccinating children older than 5 years old in Vietnam.

Indexed as

BenzeneacetamidesEnterovirusFoot-and-Mouth DiseaseHand, Foot and Mouth DiseasePiperidonesAnimalsChildChild, PreschoolChinaHumansInfantSerogroupVietnamantineoplaston A10BenzeneacetamidesPiperidonesCatalytic modelForce of infectionHand, foot and mouth diseaseSerological data

Identifiers

PMID38428358
PMCPMC10945305

What OpenQuestion holds

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LicenceCC BY
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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.