Differences in children and adolescents with SARS-CoV-2 infection: a cohort study in a Brazilian tertiary referral hospital
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , , , , , , , , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Clinics |
Texto Completo: | https://www.revistas.usp.br/clinics/article/view/212877 |
Resumo: | OBJECTIVES: To compare demographic/clinical/laboratory/treatments and outcomes among children and adolescents with laboratory-confirmed coronavirus disease 2019 (COVID-19). METHODS: This was a cross-sectional study that included patients diagnosed with pediatric COVID-19 (aged <18 years) between April 11, 2020 and April 22, 2021. During this period, 102/5,951 (1.7%) of all admissions occurred in neonates, children, and adolescents. Furthermore, 3,962 severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) detection samples were processed in patients aged <18 years, and laboratory-confirmed COVID-19 occurred in 155 (4%) inpatients and outpatients. Six/155 pediatric patients were excluded from the study. Therefore, the final group included 149 children and adolescents (n=97 inpatients and 52 outpatients) with positive SARS-CoV-2 results. RESULTS: The frequencies of sore throat, anosmia, dysgeusia, headache, myalgia, nausea, lymphopenia, pre-existing chronic conditions, immunosuppressive conditions, and autoimmune diseases were significantly reduced in children and adolescents (p<0.05). Likewise, the frequencies of enoxaparin use (p=0.037), current immunosuppressant use (p=0.008), vasoactive agents (p=0.045), arterial hypotension (p<0.001), and shock (p=0.024) were significantly lower in children than in adolescents. Logistic regression analysis showed that adolescents with laboratory-confirmed COVID-19 had increased odds ratios (ORs) for sore throat (OR 13.054; 95% confidence interval [CI] 2.750-61.977; p=0.001), nausea (OR 8.875; 95% CI 1.660-47.446; p=0.011), and lymphopenia (OR 3.575; 95% CI 1.355-9.430; p=0.010), but also had less hospitalizations (OR 0.355; 95% CI 0.138-0.916; p=0.032). The additional logistic regression analysis on patients with preexisting chronic conditions (n=108) showed that death as an outcome was significantly associated with pediatric severe acute respiratory syndrome (SARS) (OR 22.300; 95% CI 2.341-212.421; p=0.007) and multisystem inflammatory syndrome in children (MIS-C) (OR 11.261; 95% CI 1.189-106. 581; p=0.035). CONCLUSIONS: Half of the laboratory-confirmed COVID-19 cases occurred in adolescents. Individuals belonging to this age group had an acute systemic involvement of SARS-CoV-2 infection. Pediatric SARS and MIS-C were the most important factors associated with the mortality rate in pediatric chronic conditions with COVID-19. |
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oai:revistas.usp.br:article/212877 |
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Clinics |
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Differences in children and adolescents with SARS-CoV-2 infection: a cohort study in a Brazilian tertiary referral hospitalCOVID-19ChildrenAdolescentOutcomeChronic DiseaseMultisystem Inflammatory SyndromeOBJECTIVES: To compare demographic/clinical/laboratory/treatments and outcomes among children and adolescents with laboratory-confirmed coronavirus disease 2019 (COVID-19). METHODS: This was a cross-sectional study that included patients diagnosed with pediatric COVID-19 (aged <18 years) between April 11, 2020 and April 22, 2021. During this period, 102/5,951 (1.7%) of all admissions occurred in neonates, children, and adolescents. Furthermore, 3,962 severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) detection samples were processed in patients aged <18 years, and laboratory-confirmed COVID-19 occurred in 155 (4%) inpatients and outpatients. Six/155 pediatric patients were excluded from the study. Therefore, the final group included 149 children and adolescents (n=97 inpatients and 52 outpatients) with positive SARS-CoV-2 results. RESULTS: The frequencies of sore throat, anosmia, dysgeusia, headache, myalgia, nausea, lymphopenia, pre-existing chronic conditions, immunosuppressive conditions, and autoimmune diseases were significantly reduced in children and adolescents (p<0.05). Likewise, the frequencies of enoxaparin use (p=0.037), current immunosuppressant use (p=0.008), vasoactive agents (p=0.045), arterial hypotension (p<0.001), and shock (p=0.024) were significantly lower in children than in adolescents. Logistic regression analysis showed that adolescents with laboratory-confirmed COVID-19 had increased odds ratios (ORs) for sore throat (OR 13.054; 95% confidence interval [CI] 2.750-61.977; p=0.001), nausea (OR 8.875; 95% CI 1.660-47.446; p=0.011), and lymphopenia (OR 3.575; 95% CI 1.355-9.430; p=0.010), but also had less hospitalizations (OR 0.355; 95% CI 0.138-0.916; p=0.032). The additional logistic regression analysis on patients with preexisting chronic conditions (n=108) showed that death as an outcome was significantly associated with pediatric severe acute respiratory syndrome (SARS) (OR 22.300; 95% CI 2.341-212.421; p=0.007) and multisystem inflammatory syndrome in children (MIS-C) (OR 11.261; 95% CI 1.189-106. 581; p=0.035). CONCLUSIONS: Half of the laboratory-confirmed COVID-19 cases occurred in adolescents. Individuals belonging to this age group had an acute systemic involvement of SARS-CoV-2 infection. Pediatric SARS and MIS-C were the most important factors associated with the mortality rate in pediatric chronic conditions with COVID-19.Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2021-11-26info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/21287710.6061/clinics/2021/e3488Clinics; Vol. 76 (2021); e3488Clinics; v. 76 (2021); e3488Clinics; Vol. 76 (2021); e34881980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/212877/194899Copyright (c) 2023 Clinicsinfo:eu-repo/semantics/openAccessMarques, Heloisa Helena de SousaPereira, Maria Fernanda BadueSantos, Angélica Carreira dosFink, Thais ToledoPaula, Camila Sanson Yoshino deLitvinov, NadiaSchvartsman, ClaudioDelgado, Artur FigueiredoGibelli, Maria Augusta Bento CicaroniCarvalho, Werther Brunow deVicente Filho, OdoneTannuri, UenisCarneiro-Sampaio, MagdaGrisi, SandraDuarte, Alberto José da SilvaAntonangelo, LeilaFrancisco, Rossana Pucineli VieiraOkay, Thelma SuelyBatisttella, Linamara RizzoCarvalho, Carlos Roberto Ribeiro deBrentani, Alexandra Valéria MariaSilva, Clovis ArturHC-FMUSP Pediatric COVID Study Group2023-07-06T13:04:05Zoai:revistas.usp.br:article/212877Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2023-07-06T13:04:05Clinics - Universidade de São Paulo (USP)false |
dc.title.none.fl_str_mv |
Differences in children and adolescents with SARS-CoV-2 infection: a cohort study in a Brazilian tertiary referral hospital |
title |
Differences in children and adolescents with SARS-CoV-2 infection: a cohort study in a Brazilian tertiary referral hospital |
spellingShingle |
Differences in children and adolescents with SARS-CoV-2 infection: a cohort study in a Brazilian tertiary referral hospital Marques, Heloisa Helena de Sousa COVID-19 Children Adolescent Outcome Chronic Disease Multisystem Inflammatory Syndrome |
title_short |
Differences in children and adolescents with SARS-CoV-2 infection: a cohort study in a Brazilian tertiary referral hospital |
title_full |
Differences in children and adolescents with SARS-CoV-2 infection: a cohort study in a Brazilian tertiary referral hospital |
title_fullStr |
Differences in children and adolescents with SARS-CoV-2 infection: a cohort study in a Brazilian tertiary referral hospital |
title_full_unstemmed |
Differences in children and adolescents with SARS-CoV-2 infection: a cohort study in a Brazilian tertiary referral hospital |
title_sort |
Differences in children and adolescents with SARS-CoV-2 infection: a cohort study in a Brazilian tertiary referral hospital |
author |
Marques, Heloisa Helena de Sousa |
author_facet |
Marques, Heloisa Helena de Sousa Pereira, Maria Fernanda Badue Santos, Angélica Carreira dos Fink, Thais Toledo Paula, Camila Sanson Yoshino de Litvinov, Nadia Schvartsman, Claudio Delgado, Artur Figueiredo Gibelli, Maria Augusta Bento Cicaroni Carvalho, Werther Brunow de Vicente Filho, Odone Tannuri, Uenis Carneiro-Sampaio, Magda Grisi, Sandra Duarte, Alberto José da Silva Antonangelo, Leila Francisco, Rossana Pucineli Vieira Okay, Thelma Suely Batisttella, Linamara Rizzo Carvalho, Carlos Roberto Ribeiro de Brentani, Alexandra Valéria Maria Silva, Clovis Artur HC-FMUSP Pediatric COVID Study Group |
author_role |
author |
author2 |
Pereira, Maria Fernanda Badue Santos, Angélica Carreira dos Fink, Thais Toledo Paula, Camila Sanson Yoshino de Litvinov, Nadia Schvartsman, Claudio Delgado, Artur Figueiredo Gibelli, Maria Augusta Bento Cicaroni Carvalho, Werther Brunow de Vicente Filho, Odone Tannuri, Uenis Carneiro-Sampaio, Magda Grisi, Sandra Duarte, Alberto José da Silva Antonangelo, Leila Francisco, Rossana Pucineli Vieira Okay, Thelma Suely Batisttella, Linamara Rizzo Carvalho, Carlos Roberto Ribeiro de Brentani, Alexandra Valéria Maria Silva, Clovis Artur HC-FMUSP Pediatric COVID Study Group |
author2_role |
author author author author author author author author author author author author author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Marques, Heloisa Helena de Sousa Pereira, Maria Fernanda Badue Santos, Angélica Carreira dos Fink, Thais Toledo Paula, Camila Sanson Yoshino de Litvinov, Nadia Schvartsman, Claudio Delgado, Artur Figueiredo Gibelli, Maria Augusta Bento Cicaroni Carvalho, Werther Brunow de Vicente Filho, Odone Tannuri, Uenis Carneiro-Sampaio, Magda Grisi, Sandra Duarte, Alberto José da Silva Antonangelo, Leila Francisco, Rossana Pucineli Vieira Okay, Thelma Suely Batisttella, Linamara Rizzo Carvalho, Carlos Roberto Ribeiro de Brentani, Alexandra Valéria Maria Silva, Clovis Artur HC-FMUSP Pediatric COVID Study Group |
dc.subject.por.fl_str_mv |
COVID-19 Children Adolescent Outcome Chronic Disease Multisystem Inflammatory Syndrome |
topic |
COVID-19 Children Adolescent Outcome Chronic Disease Multisystem Inflammatory Syndrome |
description |
OBJECTIVES: To compare demographic/clinical/laboratory/treatments and outcomes among children and adolescents with laboratory-confirmed coronavirus disease 2019 (COVID-19). METHODS: This was a cross-sectional study that included patients diagnosed with pediatric COVID-19 (aged <18 years) between April 11, 2020 and April 22, 2021. During this period, 102/5,951 (1.7%) of all admissions occurred in neonates, children, and adolescents. Furthermore, 3,962 severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) detection samples were processed in patients aged <18 years, and laboratory-confirmed COVID-19 occurred in 155 (4%) inpatients and outpatients. Six/155 pediatric patients were excluded from the study. Therefore, the final group included 149 children and adolescents (n=97 inpatients and 52 outpatients) with positive SARS-CoV-2 results. RESULTS: The frequencies of sore throat, anosmia, dysgeusia, headache, myalgia, nausea, lymphopenia, pre-existing chronic conditions, immunosuppressive conditions, and autoimmune diseases were significantly reduced in children and adolescents (p<0.05). Likewise, the frequencies of enoxaparin use (p=0.037), current immunosuppressant use (p=0.008), vasoactive agents (p=0.045), arterial hypotension (p<0.001), and shock (p=0.024) were significantly lower in children than in adolescents. Logistic regression analysis showed that adolescents with laboratory-confirmed COVID-19 had increased odds ratios (ORs) for sore throat (OR 13.054; 95% confidence interval [CI] 2.750-61.977; p=0.001), nausea (OR 8.875; 95% CI 1.660-47.446; p=0.011), and lymphopenia (OR 3.575; 95% CI 1.355-9.430; p=0.010), but also had less hospitalizations (OR 0.355; 95% CI 0.138-0.916; p=0.032). The additional logistic regression analysis on patients with preexisting chronic conditions (n=108) showed that death as an outcome was significantly associated with pediatric severe acute respiratory syndrome (SARS) (OR 22.300; 95% CI 2.341-212.421; p=0.007) and multisystem inflammatory syndrome in children (MIS-C) (OR 11.261; 95% CI 1.189-106. 581; p=0.035). CONCLUSIONS: Half of the laboratory-confirmed COVID-19 cases occurred in adolescents. Individuals belonging to this age group had an acute systemic involvement of SARS-CoV-2 infection. Pediatric SARS and MIS-C were the most important factors associated with the mortality rate in pediatric chronic conditions with COVID-19. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-11-26 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://www.revistas.usp.br/clinics/article/view/212877 10.6061/clinics/2021/e3488 |
url |
https://www.revistas.usp.br/clinics/article/view/212877 |
identifier_str_mv |
10.6061/clinics/2021/e3488 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://www.revistas.usp.br/clinics/article/view/212877/194899 |
dc.rights.driver.fl_str_mv |
Copyright (c) 2023 Clinics info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Copyright (c) 2023 Clinics |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo |
publisher.none.fl_str_mv |
Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo |
dc.source.none.fl_str_mv |
Clinics; Vol. 76 (2021); e3488 Clinics; v. 76 (2021); e3488 Clinics; Vol. 76 (2021); e3488 1980-5322 1807-5932 reponame:Clinics instname:Universidade de São Paulo (USP) instacron:USP |
instname_str |
Universidade de São Paulo (USP) |
instacron_str |
USP |
institution |
USP |
reponame_str |
Clinics |
collection |
Clinics |
repository.name.fl_str_mv |
Clinics - Universidade de São Paulo (USP) |
repository.mail.fl_str_mv |
||clinics@hc.fm.usp.br |
_version_ |
1800222766111129600 |