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Multisystem inflammatory syndrome drug treatment in countries with different income profiles: a scoping review

Objective: The purpose of this study was to map and describe the studies that have investigated therapeutic alternatives for the management of paediatric multisystem inflammatory syndrome in children (MIS-C) associated with COVID-19. Considering the origin of the studies performed (low-, middle- and...

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Autores principales: Nagem Lopes, Luis Phillipe, da Cunha, Lidiane Gomes, Silva, Alice Ramos Oliveira, Land, Marcelo Gerardin Poirot, Fonseca, Adriana Rodrigues, Lopes, Luciane Cruz, Lima, Elisangela Costa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10481533/
https://www.ncbi.nlm.nih.gov/pubmed/37680713
http://dx.doi.org/10.3389/fphar.2023.1228986
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author Nagem Lopes, Luis Phillipe
da Cunha, Lidiane Gomes
Silva, Alice Ramos Oliveira
Land, Marcelo Gerardin Poirot
Fonseca, Adriana Rodrigues
Lopes, Luciane Cruz
Lima, Elisangela Costa
author_facet Nagem Lopes, Luis Phillipe
da Cunha, Lidiane Gomes
Silva, Alice Ramos Oliveira
Land, Marcelo Gerardin Poirot
Fonseca, Adriana Rodrigues
Lopes, Luciane Cruz
Lima, Elisangela Costa
author_sort Nagem Lopes, Luis Phillipe
collection PubMed
description Objective: The purpose of this study was to map and describe the studies that have investigated therapeutic alternatives for the management of paediatric multisystem inflammatory syndrome in children (MIS-C) associated with COVID-19. Considering the origin of the studies performed (low-, middle- and high-income countries), a systematic scoping review was conducted with primary studies that reported the use of medications for the treatment of patients with MIS-C. Sources: The searches were performed in MEDLINE, Embase, Lilacs, Epistemonikos, CINAHL, and CENTRAL, in the grey literature (theses and dissertations from CAPES, ProQuest, and PROSPERO) and in clinical trial databases until May 2022. The selection and extraction of studies were performed independently by two reviewers. Summary of the findings: A total of 173 studies were included, most of which were published as case reports or series. No randomized controlled clinical trials (RCTs) were identified. The investigated drugs were immunoglobulins, glucocorticoids, monoclonal antibodies, anticoagulants, and antiplatelet agents. Conclusion: The dosages, when reported, were heterogeneous among the studies. The ethnicity and comorbidity of the participants were poorly reported. Monoclonal antibodies, drugs with higher costs, were mostly described in studies of high-income countries.
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spelling pubmed-104815332023-09-07 Multisystem inflammatory syndrome drug treatment in countries with different income profiles: a scoping review Nagem Lopes, Luis Phillipe da Cunha, Lidiane Gomes Silva, Alice Ramos Oliveira Land, Marcelo Gerardin Poirot Fonseca, Adriana Rodrigues Lopes, Luciane Cruz Lima, Elisangela Costa Front Pharmacol Pharmacology Objective: The purpose of this study was to map and describe the studies that have investigated therapeutic alternatives for the management of paediatric multisystem inflammatory syndrome in children (MIS-C) associated with COVID-19. Considering the origin of the studies performed (low-, middle- and high-income countries), a systematic scoping review was conducted with primary studies that reported the use of medications for the treatment of patients with MIS-C. Sources: The searches were performed in MEDLINE, Embase, Lilacs, Epistemonikos, CINAHL, and CENTRAL, in the grey literature (theses and dissertations from CAPES, ProQuest, and PROSPERO) and in clinical trial databases until May 2022. The selection and extraction of studies were performed independently by two reviewers. Summary of the findings: A total of 173 studies were included, most of which were published as case reports or series. No randomized controlled clinical trials (RCTs) were identified. The investigated drugs were immunoglobulins, glucocorticoids, monoclonal antibodies, anticoagulants, and antiplatelet agents. Conclusion: The dosages, when reported, were heterogeneous among the studies. The ethnicity and comorbidity of the participants were poorly reported. Monoclonal antibodies, drugs with higher costs, were mostly described in studies of high-income countries. Frontiers Media S.A. 2023-08-23 /pmc/articles/PMC10481533/ /pubmed/37680713 http://dx.doi.org/10.3389/fphar.2023.1228986 Text en Copyright © 2023 Nagem Lopes, da Cunha, Silva, Land, Fonseca, Lopes and Lima. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Nagem Lopes, Luis Phillipe
da Cunha, Lidiane Gomes
Silva, Alice Ramos Oliveira
Land, Marcelo Gerardin Poirot
Fonseca, Adriana Rodrigues
Lopes, Luciane Cruz
Lima, Elisangela Costa
Multisystem inflammatory syndrome drug treatment in countries with different income profiles: a scoping review
title Multisystem inflammatory syndrome drug treatment in countries with different income profiles: a scoping review
title_full Multisystem inflammatory syndrome drug treatment in countries with different income profiles: a scoping review
title_fullStr Multisystem inflammatory syndrome drug treatment in countries with different income profiles: a scoping review
title_full_unstemmed Multisystem inflammatory syndrome drug treatment in countries with different income profiles: a scoping review
title_short Multisystem inflammatory syndrome drug treatment in countries with different income profiles: a scoping review
title_sort multisystem inflammatory syndrome drug treatment in countries with different income profiles: a scoping review
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10481533/
https://www.ncbi.nlm.nih.gov/pubmed/37680713
http://dx.doi.org/10.3389/fphar.2023.1228986
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