Cargando…

Investigating Health Disparities Associated With Multisystem Inflammatory Syndrome in Children After SARS-CoV-2 Infection

Multisystem inflammatory syndrome in children (MIS-C) is a postinfectious severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)–related complication that has disproportionately affected racial/ethnic minority children. We conducted a pilot study to investigate risk factors for MIS-C aiming to...

Descripción completa

Detalles Bibliográficos
Autores principales: Zambrano, Laura D., Ly, Kathleen N., Link-Gelles, Ruth, Newhams, Margaret M., Akande, Manzilat, Wu, Michael J., Feldstein, Leora R., Tarquinio, Keiko M., Sahni, Leila C., Riggs, Becky J., Singh, Aalok R., Fitzgerald, Julie C., Schuster, Jennifer E., Giuliano, John S., Englund, Janet A., Hume, Janet R., Hall, Mark W., Osborne, Christina M., Doymaz, Sule, Rowan, Courtney M., Babbitt, Christopher J., Clouser, Katharine N., Horwitz, Steven M., Chou, Janet, Patel, Manish M., Hobbs, Charlotte, Randolph, Adrienne G., Campbell, Angela P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9555608/
https://www.ncbi.nlm.nih.gov/pubmed/36102740
http://dx.doi.org/10.1097/INF.0000000000003689
_version_ 1784806897200660480
author Zambrano, Laura D.
Ly, Kathleen N.
Link-Gelles, Ruth
Newhams, Margaret M.
Akande, Manzilat
Wu, Michael J.
Feldstein, Leora R.
Tarquinio, Keiko M.
Sahni, Leila C.
Riggs, Becky J.
Singh, Aalok R.
Fitzgerald, Julie C.
Schuster, Jennifer E.
Giuliano, John S.
Englund, Janet A.
Hume, Janet R.
Hall, Mark W.
Osborne, Christina M.
Doymaz, Sule
Rowan, Courtney M.
Babbitt, Christopher J.
Clouser, Katharine N.
Horwitz, Steven M.
Chou, Janet
Patel, Manish M.
Hobbs, Charlotte
Randolph, Adrienne G.
Campbell, Angela P.
author_facet Zambrano, Laura D.
Ly, Kathleen N.
Link-Gelles, Ruth
Newhams, Margaret M.
Akande, Manzilat
Wu, Michael J.
Feldstein, Leora R.
Tarquinio, Keiko M.
Sahni, Leila C.
Riggs, Becky J.
Singh, Aalok R.
Fitzgerald, Julie C.
Schuster, Jennifer E.
Giuliano, John S.
Englund, Janet A.
Hume, Janet R.
Hall, Mark W.
Osborne, Christina M.
Doymaz, Sule
Rowan, Courtney M.
Babbitt, Christopher J.
Clouser, Katharine N.
Horwitz, Steven M.
Chou, Janet
Patel, Manish M.
Hobbs, Charlotte
Randolph, Adrienne G.
Campbell, Angela P.
author_sort Zambrano, Laura D.
collection PubMed
description Multisystem inflammatory syndrome in children (MIS-C) is a postinfectious severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)–related complication that has disproportionately affected racial/ethnic minority children. We conducted a pilot study to investigate risk factors for MIS-C aiming to understand MIS-C disparities. METHODS: This case-control study included MIS-C cases and SARS-CoV-2-positive outpatient controls less than 18 years old frequency-matched 4:1 to cases by age group and site. Patients hospitalized with MIS-C were admitted between March 16 and October 2, 2020, across 17 pediatric hospitals. We evaluated race, ethnicity, social vulnerability index (SVI), insurance status, weight-for-age and underlying medical conditions as risk factors using mixed effects multivariable logistic regression. RESULTS: We compared 241 MIS-C cases with 817 outpatient SARS-CoV-2-positive at-risk controls. Cases and controls had similar sex, age and U.S. census region distribution. MIS-C patients were more frequently previously healthy, non-Hispanic Black, residing in higher SVI areas, and in the 95th percentile or higher for weight-for-age. In the multivariable analysis, the likelihood of MIS-C was higher among non-Hispanic Black children [adjusted odds ratio (aOR): 2.07; 95% CI: 1.23–3.48]. Additionally, SVI in the 2nd and 3rd tertiles (aOR: 1.88; 95% CI: 1.18–2.97 and aOR: 2.03; 95% CI: 1.19–3.47, respectively) were independent factors along with being previously healthy (aOR: 1.64; 95% CI: 1.18–2.28). CONCLUSIONS: In this study, non-Hispanic Black children were more likely to develop MIS-C after adjustment for sociodemographic factors, underlying medical conditions, and weight-for-age. Investigation of the potential contribution of immunologic, environmental, and other factors is warranted.
format Online
Article
Text
id pubmed-9555608
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Lippincott Williams & Wilkins
record_format MEDLINE/PubMed
spelling pubmed-95556082022-10-14 Investigating Health Disparities Associated With Multisystem Inflammatory Syndrome in Children After SARS-CoV-2 Infection Zambrano, Laura D. Ly, Kathleen N. Link-Gelles, Ruth Newhams, Margaret M. Akande, Manzilat Wu, Michael J. Feldstein, Leora R. Tarquinio, Keiko M. Sahni, Leila C. Riggs, Becky J. Singh, Aalok R. Fitzgerald, Julie C. Schuster, Jennifer E. Giuliano, John S. Englund, Janet A. Hume, Janet R. Hall, Mark W. Osborne, Christina M. Doymaz, Sule Rowan, Courtney M. Babbitt, Christopher J. Clouser, Katharine N. Horwitz, Steven M. Chou, Janet Patel, Manish M. Hobbs, Charlotte Randolph, Adrienne G. Campbell, Angela P. Pediatr Infect Dis J COVID Reports Multisystem inflammatory syndrome in children (MIS-C) is a postinfectious severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)–related complication that has disproportionately affected racial/ethnic minority children. We conducted a pilot study to investigate risk factors for MIS-C aiming to understand MIS-C disparities. METHODS: This case-control study included MIS-C cases and SARS-CoV-2-positive outpatient controls less than 18 years old frequency-matched 4:1 to cases by age group and site. Patients hospitalized with MIS-C were admitted between March 16 and October 2, 2020, across 17 pediatric hospitals. We evaluated race, ethnicity, social vulnerability index (SVI), insurance status, weight-for-age and underlying medical conditions as risk factors using mixed effects multivariable logistic regression. RESULTS: We compared 241 MIS-C cases with 817 outpatient SARS-CoV-2-positive at-risk controls. Cases and controls had similar sex, age and U.S. census region distribution. MIS-C patients were more frequently previously healthy, non-Hispanic Black, residing in higher SVI areas, and in the 95th percentile or higher for weight-for-age. In the multivariable analysis, the likelihood of MIS-C was higher among non-Hispanic Black children [adjusted odds ratio (aOR): 2.07; 95% CI: 1.23–3.48]. Additionally, SVI in the 2nd and 3rd tertiles (aOR: 1.88; 95% CI: 1.18–2.97 and aOR: 2.03; 95% CI: 1.19–3.47, respectively) were independent factors along with being previously healthy (aOR: 1.64; 95% CI: 1.18–2.28). CONCLUSIONS: In this study, non-Hispanic Black children were more likely to develop MIS-C after adjustment for sociodemographic factors, underlying medical conditions, and weight-for-age. Investigation of the potential contribution of immunologic, environmental, and other factors is warranted. Lippincott Williams & Wilkins 2022-09-07 2022-11 /pmc/articles/PMC9555608/ /pubmed/36102740 http://dx.doi.org/10.1097/INF.0000000000003689 Text en Copyright © 2022 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle COVID Reports
Zambrano, Laura D.
Ly, Kathleen N.
Link-Gelles, Ruth
Newhams, Margaret M.
Akande, Manzilat
Wu, Michael J.
Feldstein, Leora R.
Tarquinio, Keiko M.
Sahni, Leila C.
Riggs, Becky J.
Singh, Aalok R.
Fitzgerald, Julie C.
Schuster, Jennifer E.
Giuliano, John S.
Englund, Janet A.
Hume, Janet R.
Hall, Mark W.
Osborne, Christina M.
Doymaz, Sule
Rowan, Courtney M.
Babbitt, Christopher J.
Clouser, Katharine N.
Horwitz, Steven M.
Chou, Janet
Patel, Manish M.
Hobbs, Charlotte
Randolph, Adrienne G.
Campbell, Angela P.
Investigating Health Disparities Associated With Multisystem Inflammatory Syndrome in Children After SARS-CoV-2 Infection
title Investigating Health Disparities Associated With Multisystem Inflammatory Syndrome in Children After SARS-CoV-2 Infection
title_full Investigating Health Disparities Associated With Multisystem Inflammatory Syndrome in Children After SARS-CoV-2 Infection
title_fullStr Investigating Health Disparities Associated With Multisystem Inflammatory Syndrome in Children After SARS-CoV-2 Infection
title_full_unstemmed Investigating Health Disparities Associated With Multisystem Inflammatory Syndrome in Children After SARS-CoV-2 Infection
title_short Investigating Health Disparities Associated With Multisystem Inflammatory Syndrome in Children After SARS-CoV-2 Infection
title_sort investigating health disparities associated with multisystem inflammatory syndrome in children after sars-cov-2 infection
topic COVID Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9555608/
https://www.ncbi.nlm.nih.gov/pubmed/36102740
http://dx.doi.org/10.1097/INF.0000000000003689
work_keys_str_mv AT zambranolaurad investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection
AT lykathleenn investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection
AT linkgellesruth investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection
AT newhamsmargaretm investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection
AT akandemanzilat investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection
AT wumichaelj investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection
AT feldsteinleorar investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection
AT tarquiniokeikom investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection
AT sahnileilac investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection
AT riggsbeckyj investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection
AT singhaalokr investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection
AT fitzgeraldjuliec investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection
AT schusterjennifere investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection
AT giulianojohns investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection
AT englundjaneta investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection
AT humejanetr investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection
AT hallmarkw investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection
AT osbornechristinam investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection
AT doymazsule investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection
AT rowancourtneym investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection
AT babbittchristopherj investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection
AT clouserkatharinen investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection
AT horwitzstevenm investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection
AT choujanet investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection
AT patelmanishm investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection
AT hobbscharlotte investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection
AT randolphadrienneg investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection
AT campbellangelap investigatinghealthdisparitiesassociatedwithmultisysteminflammatorysyndromeinchildrenaftersarscov2infection