Is cardiorespiratory disease associated with increased susceptibility of SARS-CoV-2 in children?


Journal

Pediatric pulmonology
ISSN: 1099-0496
Titre abrégé: Pediatr Pulmonol
Pays: United States
ID NLM: 8510590

Informations de publication

Date de publication:
12 2021
Historique:
revised: 29 07 2021
received: 05 04 2021
accepted: 19 08 2021
pubmed: 3 9 2021
medline: 15 12 2021
entrez: 2 9 2021
Statut: ppublish

Résumé

There are limited data in pediatric populations evaluating whether chronic cardiorespiratory conditions are associated with increased risk of coronavirus disease 2019 (COVID-19). We aimed to compare the rates of chronic cardiac and respiratory disease in children testing positive severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2[+]) compared with those testing negative (SARS-CoV-2[-]) at our institution. Prospective cohort with nested case-control study of all children tested by polymerase chain reaction (PCR) for SARS-CoV-2 by nasopharyngeal/oropharyngeal sampling between March and October 2020. Children were identified prospectively via laboratory notification with age and sex-matching of SARS-CoV-2[+] to SARS-CoV-2[-] (1:2). Clinical data were extracted from the electronic medical record. In total, 179 SARS-CoV-2[+] children (44% females, median age 3.5 years, range: 0.1-19.0 years) were matched to 391 SARS-CoV-2[-] children (42% female, median age 3.7 years, range: 0.1-18.3 years). The commonest comorbidities showed similar frequencies in the SARS-CoV-2[+] and [-] groups: asthma (n = 9, 5% vs. n = 17, 4.4%, p = 0.71), congenital heart disease (n = 6, 3.4% vs. n = 7, 1.8%, p = 0.25) and obstructive sleep apnoea (n = 4, 2.2% vs. n = 10, 2.3%, p = 0.82). In the SARS-CoV-2[+] group, the prevalence of symptomatic disease was similar among children with and without cardiorespiratory comorbidities (n = 12, 75% vs. n = 103, 57%, p = 0.35). A high proportion of children hospitalized with SARS-CoV-2 infection had cardiac comorbidities (23.8%). In this single site data set, rates of pre-existing cardiorespiratory disease were similar in SARS-CoV-2[+] and SARS-CoV-2[-] children. Rates of symptomatic infection were similar between children with and without cardiorespiratory comorbidity. High rates of comorbid cardiac disease were observed among hospitalized children with COVID-19 warranting further research to inform vaccine prioritization.

Sections du résumé

BACKGROUND
There are limited data in pediatric populations evaluating whether chronic cardiorespiratory conditions are associated with increased risk of coronavirus disease 2019 (COVID-19). We aimed to compare the rates of chronic cardiac and respiratory disease in children testing positive severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2[+]) compared with those testing negative (SARS-CoV-2[-]) at our institution.
METHOD
Prospective cohort with nested case-control study of all children tested by polymerase chain reaction (PCR) for SARS-CoV-2 by nasopharyngeal/oropharyngeal sampling between March and October 2020. Children were identified prospectively via laboratory notification with age and sex-matching of SARS-CoV-2[+] to SARS-CoV-2[-] (1:2). Clinical data were extracted from the electronic medical record.
RESULTS
In total, 179 SARS-CoV-2[+] children (44% females, median age 3.5 years, range: 0.1-19.0 years) were matched to 391 SARS-CoV-2[-] children (42% female, median age 3.7 years, range: 0.1-18.3 years). The commonest comorbidities showed similar frequencies in the SARS-CoV-2[+] and [-] groups: asthma (n = 9, 5% vs. n = 17, 4.4%, p = 0.71), congenital heart disease (n = 6, 3.4% vs. n = 7, 1.8%, p = 0.25) and obstructive sleep apnoea (n = 4, 2.2% vs. n = 10, 2.3%, p = 0.82). In the SARS-CoV-2[+] group, the prevalence of symptomatic disease was similar among children with and without cardiorespiratory comorbidities (n = 12, 75% vs. n = 103, 57%, p = 0.35). A high proportion of children hospitalized with SARS-CoV-2 infection had cardiac comorbidities (23.8%).
CONCLUSIONS
In this single site data set, rates of pre-existing cardiorespiratory disease were similar in SARS-CoV-2[+] and SARS-CoV-2[-] children. Rates of symptomatic infection were similar between children with and without cardiorespiratory comorbidity. High rates of comorbid cardiac disease were observed among hospitalized children with COVID-19 warranting further research to inform vaccine prioritization.

Identifiants

pubmed: 34473903
doi: 10.1002/ppul.25642
pmc: PMC8661609
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3664-3668

Subventions

Organisme : The Influenza Complications Alert Network Surveillance System
Organisme : Centers of Excellence in Influenza Research and Surveillance - Cross-Center Southern Hemisphere Project
Organisme : Paediatric Active Enhanced Disease Surveillance and Sentinel Travelers and Research Preparedness Platform for Emerging Infectious Disease
Organisme : Murdoch Children's Research Institute

Informations de copyright

© 2021 Wiley Periodicals LLC.

Références

Pediatr Pulmonol. 2021 Dec;56(12):3664-3668
pubmed: 34473903
EClinicalMedicine. 2020 Dec;29:100630
pubmed: 33200120
Clin Infect Dis. 2020 Dec 3;71(9):2469-2479
pubmed: 32392337
J Cyst Fibros. 2020 Nov;19(6):868-871
pubmed: 33183965
ERJ Open Res. 2020 Oct 26;6(4):
pubmed: 33263054
N Engl J Med. 2020 Apr 23;382(17):1663-1665
pubmed: 32187458
JAMA Netw Open. 2021 Jun 1;4(6):e2111182
pubmed: 34097050
Eur J Pediatr. 2021 Mar;180(3):689-697
pubmed: 32914200
Am J Otolaryngol. 2020 Sep - Oct;41(5):102573
pubmed: 32531620
Lancet Child Adolesc Health. 2020 Sep;4(9):653-661
pubmed: 32593339
JAMA Pediatr. 2020 Sep 1;174(9):882-889
pubmed: 32320004
Acta Paediatr. 2020 Jun;109(6):1088-1095
pubmed: 32202343
J Pediatr. 2020 Aug;223:14-19.e2
pubmed: 32407719
Eur Respir J. 2021 Mar 4;57(3):
pubmed: 32978309
Eur J Pediatr. 2020 Jul;179(7):1079-1087
pubmed: 32474800
Lancet Respir Med. 2020 May;8(5):e35-e36
pubmed: 32304639
J Allergy Clin Immunol Pract. 2021 Feb;9(2):684-692.e1
pubmed: 33242628

Auteurs

Cassidy Du Berry (C)

Division of Infection and Immunity, Murdoch Children's Research Institute, Melbourne, Australia.
The Royal Children's Hospital Melbourne, Melbourne, Australia.
Department of Paediatrics, The University of Melbourne, Melbourne, Australia.

Thomas Saunders (T)

Division of Infection and Immunity, Murdoch Children's Research Institute, Melbourne, Australia.
The Royal Children's Hospital Melbourne, Melbourne, Australia.
Department of Paediatrics, The University of Melbourne, Melbourne, Australia.

Alissa McMinn (A)

Division of Infection and Immunity, Murdoch Children's Research Institute, Melbourne, Australia.
The Royal Children's Hospital Melbourne, Melbourne, Australia.

Shidan Tosif (S)

Division of Infection and Immunity, Murdoch Children's Research Institute, Melbourne, Australia.
The Royal Children's Hospital Melbourne, Melbourne, Australia.
Department of Paediatrics, The University of Melbourne, Melbourne, Australia.

Shivanthan Shanthikumar (S)

Division of Infection and Immunity, Murdoch Children's Research Institute, Melbourne, Australia.
The Royal Children's Hospital Melbourne, Melbourne, Australia.
Department of Paediatrics, The University of Melbourne, Melbourne, Australia.

Moya Vandeleur (M)

Division of Infection and Immunity, Murdoch Children's Research Institute, Melbourne, Australia.
The Royal Children's Hospital Melbourne, Melbourne, Australia.
Department of Paediatrics, The University of Melbourne, Melbourne, Australia.

Joanne Harrison (J)

Division of Infection and Immunity, Murdoch Children's Research Institute, Melbourne, Australia.
The Royal Children's Hospital Melbourne, Melbourne, Australia.
Department of Paediatrics, The University of Melbourne, Melbourne, Australia.

David Burgner (D)

Division of Infection and Immunity, Murdoch Children's Research Institute, Melbourne, Australia.
The Royal Children's Hospital Melbourne, Melbourne, Australia.
Department of Paediatrics, The University of Melbourne, Melbourne, Australia.

Sarath Ranganathan (S)

Division of Infection and Immunity, Murdoch Children's Research Institute, Melbourne, Australia.
The Royal Children's Hospital Melbourne, Melbourne, Australia.
Department of Paediatrics, The University of Melbourne, Melbourne, Australia.

Nigel Crawford (N)

Division of Infection and Immunity, Murdoch Children's Research Institute, Melbourne, Australia.
The Royal Children's Hospital Melbourne, Melbourne, Australia.
Department of Paediatrics, The University of Melbourne, Melbourne, Australia.

Danielle Wurzel (D)

Division of Infection and Immunity, Murdoch Children's Research Institute, Melbourne, Australia.
The Royal Children's Hospital Melbourne, Melbourne, Australia.
Department of Paediatrics, The University of Melbourne, Melbourne, Australia.
Allergy and Lung Health Unit, School of Population and Global Health, The University of Melbourne, Melbourne, Victoria, Australia.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH