Clinical epidemiology of COVID-19 among hospitalized children in rural western Kenya.


Journal

PLOS global public health
ISSN: 2767-3375
Titre abrégé: PLOS Glob Public Health
Pays: United States
ID NLM: 9918283779606676

Informations de publication

Date de publication:
2023
Historique:
received: 28 02 2023
accepted: 12 05 2023
medline: 14 6 2023
pubmed: 14 6 2023
entrez: 14 6 2023
Statut: epublish

Résumé

The epidemiology of pediatric COVID-19 in sub-Saharan Africa and the role of fecal-oral transmission in SARS-CoV-2 are poorly understood. Among children and adolescents in Kenya, we identify correlates of COVID-19 infection, document the clinical outcomes of infection, and evaluate the prevalence and viability of SARS-CoV-2 in stool. We recruited a prospective cohort of hospitalized children aged two months to 15 years in western Kenya between March 1 and June 30 2021. Children with SARS-CoV-2 were followed monthly for 180-days after hospital discharge. Bivariable logistic regression analysis was used to identify the clinical and sociodemographics correlates of SARS-CoV-2 infection. We also calculated the prevalence of SARS-CoV-2 detection in stool of confirmed cases. Of 355 systematically tested children, 55 (15.5%) were positive and were included in the cohort. The commonest clinical features among COVID-19 cases were fever (42/55, 76%), cough (19/55, 35%), nausea and vomiting (19/55, 35%), and lethargy (19/55, 35%). There were no statistically significant difference in baseline sociodemographic and clinical characteristics between SARS-CoV-2 positive and negative participants. Among positive participants, 8/55 (14.5%, 95%CI: 5.3%-23.9%) died; seven during the inpatient period. Forty-nine children with COVID-19 had stool samples or rectal swabs available at baseline, 9 (17%) had PCR-positive stool or rectal swabs, but none had SARS-CoV-2 detected by culture. Syndromic identification of COVID-19 is particularly challenging among children as the presenting symptoms and signs mirror other common pediatric diseases. Mortality among children hospitalized with COVID-19 was high in this cohort but was comparable to mortality seen with other common illnesses in this setting. Among this small set of children with COVID-19 we detected SARS-CoV-2 DNA, but were not able to culture viable SARs-CoV-2 virus, in stool. This suggests that fecal transmission may not be a substantial risk in children recently diagnosed and hospitalized with COVID-19 infection.

Identifiants

pubmed: 37315023
doi: 10.1371/journal.pgph.0002011
pii: PGPH-D-23-00293
pmc: PMC10266603
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e0002011

Subventions

Organisme : Bill & Melinda Gates Foundation
ID : INV-016894
Pays : United States

Informations de copyright

Copyright: This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Adino Tesfahun Tsegaye (AT)

Department of Epidemiology, University of Washington, Seattle, Washington, United States of America.

Christina Sherry (C)

Departments of Global Health, University of Washington, Seattle, Washington, United States of America.

Chrisantus Oduol (C)

Center for Clinical Research, Kenya Medical Research Institute, Nairobi, Kenya.

Joyce Otieno (J)

Center for Clinical Research, Kenya Medical Research Institute, Nairobi, Kenya.

Doreen Rwigi (D)

Center for Clinical Research, Kenya Medical Research Institute, Nairobi, Kenya.

Mary Masheti (M)

Center for Clinical Research, Kenya Medical Research Institute, Nairobi, Kenya.

Irene Machura (I)

Kisii Teaching and Referral Hospital, Kisii, Kenya.

Meshack Liru (M)

Homa Bay County Referral Hospital, Homa Bay, Kenya.

Joyce Akuka (J)

Migori County Referral Hospital, Migori, Kenya.

Deborah Omedo (D)

Kisii Teaching and Referral Hospital, Kisii, Kenya.

Samwel Symekher (S)

Center for Virus Research, Kenya Medical Research Institute, Nairobi, Kenya.

Samoel A Khamadi (SA)

Center for Virus Research, Kenya Medical Research Institute, Nairobi, Kenya.

Lynda Isaaka (L)

KEMRI/Wellcome Trust Research Programme, Nairobi, Kenya.

Morris Ogero (M)

KEMRI/Wellcome Trust Research Programme, Nairobi, Kenya.

Livingstone Mumelo (L)

KEMRI/Wellcome Trust Research Programme, Nairobi, Kenya.

James A Berkley (JA)

KEMRI/Wellcome Trust Research Programme, Nairobi, Kenya.
The Childhood Acute Illness and Nutrition Network (CHAIN), Nairobi, Kenya.
Centre for Tropical Medicine & Global Health Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
Department of Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, United Kingdom.

Ambrose Agweyu (A)

KEMRI/Wellcome Trust Research Programme, Nairobi, Kenya.
Department of Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, United Kingdom.

Judd L Walson (JL)

The Childhood Acute Illness and Nutrition Network (CHAIN), Nairobi, Kenya.
Departments of Global Health, Medicine (Infectious Disease), Pediatrics and Epidemiology, University of Washington, Seattle, Washington, United States of America.

Benson O Singa (BO)

Center for Clinical Research, Kenya Medical Research Institute, Nairobi, Kenya.

Kirkby D Tickell (KD)

Departments of Global Health, University of Washington, Seattle, Washington, United States of America.
The Childhood Acute Illness and Nutrition Network (CHAIN), Nairobi, Kenya.

Classifications MeSH