Evidence map›Paper›PMID 36227390›Full record

ArticleEcoHealth2022

Aetiology and Potential Animal Exposure in Central Nervous System Infections in Vietnam.

Hannah E Brindle, Behzad Nadjm, Marc Choisy, Rob Christley, Michael Griffiths, Stephen Baker, Juliet E Bryant, James I Campbell, Van Vinh Chau Nguyen, Thi Ngoc Diep Nguyen and 19 more

Erratum issuedOpen access · hybridAbstract readMulticenter Study
In one paragraph

Article in EcoHealth, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
0.2field-weighted citation impact, top 47% of its field
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 synthesis or guideline pooled it, 3 citations in OpenAlex.

  1. Pooled it
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

29 authors at 14 institutions in 7 countries.

Hannah E BrindleOxford University Clinical Research Unit, Hanoi, Vietnam. hbrindle@liverpool.ac.uk.ORCID 0000-0003-1684-5801
Behzad NadjmOxford University Clinical Research Unit, Hanoi, Vietnam.
Marc ChoisyOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam. mchoisy@oucru.org.
Rob ChristleyInstitute of Infection and Global Health and National Institute, University of Liverpool, Liverpool, UK.
Michael GriffithsInstitute of Infection and Global Health and National Institute, University of Liverpool, Liverpool, UK.
Stephen BakerOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Juliet E BryantOxford University Clinical Research Unit, Hanoi, Vietnam.
James I CampbellOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Van Vinh Chau NguyenHospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
Thi Ngoc Diep NguyenOxford University Clinical Research Unit, Hanoi, Vietnam.
Ty Thi Hang VuOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Van Hung NguyenDak Lak General Hospital, Buon Ma Thuot City, Vietnam.
Bao Long HoangOxford University Clinical Research Unit, Hanoi, Vietnam.
Xuan Luat LeNational Hospital for Tropical Diseases, Hanoi, Vietnam.
Ha My PhamOxford University Clinical Research Unit, Hanoi, Vietnam.
Thi Dieu Ngan TaNational Hospital for Tropical Diseases, Hanoi, Vietnam.
Dang Trung Nghia HoHospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
Thua Nguyen TranHue Central Hospital, Hue City, Vietnam.
Thi Han Ny NguyenOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
My Phuc TranOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Thi Hong Phuong PhamDong Thap General Hospital, Cao Lanh, Vietnam.
Van Tan LeOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Dac Thuan NguyenKhanh Hoa General Hospital, Nha Trang, Vietnam.
Thi Thu Trang HauOxford University Clinical Research Unit, Hanoi, Vietnam.
Ngoc Vinh NguyenBa Vi District Hospital, Hanoi, Vietnam.
Heiman F L WertheimOxford University Clinical Research Unit, Hanoi, Vietnam.
Guy E ThwaitesOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
H Rogier van DoornOxford University Clinical Research Unit, Hanoi, Vietnam.
VIZIONS Consortium
Oxford University Clinical Research Unit · VNHospital for Tropical Diseases · VNUniversity of Liverpool · GBUniversity of Oxford · GBAngkor Hospital for Children · KHDong Thap Hospital · VNGlobal Fund to Fight AIDS, Tuberculosis and Malaria · CHHanoi Medical University · VNHue Central Hospital · VNMRC Unit the Gambia · GMNational Institute of Infectious Diseases · JPRadboud University Nijmegen · NLUniversity of Cambridge · GBWellcome Sanger Institute · GB

Funding

Medical Research Council MC_UU_00031/7Wellcome Trust 093724Wellcome Trust 102465Wellcome Trust 204904/Z/16/Z
6 · The paper itself

Abstract

An estimated 73% of emerging infections are zoonotic in origin, with animal contact and encroachment on their habitats increasing the risk of spill-over events. In Vietnam, close exposure to a wide range of animals and animal products can lead to acquisition of zoonotic pathogens, a number of which cause central nervous system (CNS) infections. However, studies show the aetiology of CNS infections remains unknown in around half of cases. We used samples and data from hospitalised patients with CNS infections, enrolled into the Vietnam Initiative on Zoonotic Infections multicentre study, to determine the association between aetiology and animal contact including those in whom the cause was unknown. Among 933 patients, a pathogen or an antibody response to it was identified in 291 (31.2%, 95% CI 28.3-34.3%). The most common pathogens were Streptococcus suis (n = 91 (9.8%, 8.0-11.9%)) and Japanese encephalitis virus (JEV) (n = 72 (7.7%, 6.1-9.7%)). Commonly reported animal contact included keeping, raising or handling (n = 364 (39.0%, 35.9-42.2%)) and handling, cooking or consuming raw meat, blood or viscera in the 2 weeks prior to symptom onset (n = 371 (39.8%, 36.6-43.0%)), with the latter most commonly from pigs (n = 343 (36.9%, 33.8-40.1%). There was no association between an unknown aetiology and exposure to animals in a multivariate logistic regression. Further testing for unknown or undetected pathogens may increase diagnostic yield, however, given the high proportion of zoonotic pathogens and the presence of risk factors, increasing public awareness about zoonoses and preventive measures can be considered.

Indexed as

Central Nervous System InfectionsSwine DiseasesAnimalsRisk FactorsSwineVietnamZoonosesCentral nervous system infectionsDisease of unknown aetiologyEmerging infectionsVietnamZoonosis

Identifiers

PMID36227390
PMCPMC9558024
OpenAlexW4304891928

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.