Multisystem inflammatory syndrome associated with COVID-19 in pediatric patients

Detalhes bibliográficos
Autor(a) principal: Fernández, Gerardo
Data de Publicação: 2022
Outros Autores: Acosta, Josué
Tipo de documento: Artigo
Idioma: spa
Título da fonte: Sapienza (Curitiba)
Texto Completo: https://journals.sapienzaeditorial.com/index.php/SIJIS/article/view/306
Resumo: Pediatric Multisystem Inflammatory Syndrome (P-MIS) linked to SARS-CoV-2 is a generalized inflammatory reaction that develops approximately 4-6 weeks after COVID-19 illness. The aim of the article was to analyze the immunopathogenesis, diagnosis and treatment of P-MIS. A systematic literature review was performed using databases such as Embase, Redalyc, LILACS, SciELO, Springer, Elsevier, EBSCO and Google Scholar and the keywords: Coronavirus disease, Kawasaki disease, child, intravenous immunoglobulins. Inclusion criteria were: full articles, published between the years 2019-2022, in English and Spanish. Of the 273 articles found, 243 articles were rejected for not meeting the established criteria, with 30 articles selected as eligible. According to the results, SIM-P is characterized by fever, myocardial injury, shock and development of coronary artery aneurysms; laboratory tests show: elevation of markers of inflammation, changes in coagulation tests, especially significant elevation of D-dimer and fibrinogen and elevation of markers of myocardial injury, troponin and natriuretic peptide. Phase 1 treatment occurs with the administration of intravenous immunoglobulin G (IVIG), corticosteroids, low molecular weight heparin in a prophylactic dose; in phase 2, treatment consists of administration of a second dose of IVIG, progressive reduction of prednisone and use of biological therapy; and, in phase 3, infliximab or tocilizumab is used. In conclusion, SIM-P has elevated inflammatory markers and multi-organ involvement, with no associated bacterial diagnosis, with evidence of infection or recent exposure to SARS-CoV-2.
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spelling Multisystem inflammatory syndrome associated with COVID-19 in pediatric patientsSíndrome inflamatorio multisistémico asociado a COVID-19 en pacientes pediátricosSíndrome inflamatória multissistêmica associada à COVID-19 em pacientes pediátricosDoença de coronavírus 2019-nCoV; Doença de Kawasaki; crianças; imunoglobulinas intravenosasCoronavirus disease 2019-nCoV; Kawasaki disease; little boy; intravenous immunoglobulinsenfermedad por Coronavirus 2019-nCoV; enfermedad de Kawasaki; niño; inmunoglobulinas intravenosasPediatric Multisystem Inflammatory Syndrome (P-MIS) linked to SARS-CoV-2 is a generalized inflammatory reaction that develops approximately 4-6 weeks after COVID-19 illness. The aim of the article was to analyze the immunopathogenesis, diagnosis and treatment of P-MIS. A systematic literature review was performed using databases such as Embase, Redalyc, LILACS, SciELO, Springer, Elsevier, EBSCO and Google Scholar and the keywords: Coronavirus disease, Kawasaki disease, child, intravenous immunoglobulins. Inclusion criteria were: full articles, published between the years 2019-2022, in English and Spanish. Of the 273 articles found, 243 articles were rejected for not meeting the established criteria, with 30 articles selected as eligible. According to the results, SIM-P is characterized by fever, myocardial injury, shock and development of coronary artery aneurysms; laboratory tests show: elevation of markers of inflammation, changes in coagulation tests, especially significant elevation of D-dimer and fibrinogen and elevation of markers of myocardial injury, troponin and natriuretic peptide. Phase 1 treatment occurs with the administration of intravenous immunoglobulin G (IVIG), corticosteroids, low molecular weight heparin in a prophylactic dose; in phase 2, treatment consists of administration of a second dose of IVIG, progressive reduction of prednisone and use of biological therapy; and, in phase 3, infliximab or tocilizumab is used. In conclusion, SIM-P has elevated inflammatory markers and multi-organ involvement, with no associated bacterial diagnosis, with evidence of infection or recent exposure to SARS-CoV-2.El Síndrome inflamatorio multisistémico pediátrico (SIM-P) vinculado a SARS-CoV-2 es una reacción inflamatoria generalizada desarrollada aproximadamente 4-6 semanas después de haber presentado la enfermedad COVID-19.  El objetivo del artículo fue analizar la inmunopatogénesis,  diagnóstico y tratamiento del SIM-P. Se aplicó un diseño documental, con revisión de bibliografías en bases de datos como Embase, Redalyc, LILACS, SciELO, Springer, Elsevier, EBSCO y Google Académico, utilizando los descriptores: enfermedad por Coronavirus, enfermedad de Kawasaki, niño, inmunoglobulinas intravenosas. Los criterios de inclusión fueron: artículos completos, publicados entre los años 2019-2022, en idiomas inglés y español. Se incluyó la revisión de 273 artículos en total rechazando 243 artículos por no contener la información a razón de búsqueda, seleccionados 30 artículos al cumplir con los criterios de elegibilidad. En los resultados SIM-P se caracteriza por fiebre, lesión miocárdica, shock y desarrollo de aneurismas de las arterias coronarias, en las pruebas de laboratorios: elevación de los marcadores de inflamación, alteraciones en las pruebas de coagulación, especialmente elevación significativa del dímero D y fibrinógeno, ascenso de los marcadores de lesión miocárdica de troponina y péptido natriurético. El tratamiento en la fase1 con la administración de inmunoglobulina G intravenosa (IGIV), corticoides, heparina de bajo peso molecular en dosis profiláctica, fase 2 una segunda dosis de IGIV y un descenso progresivo de prednisona y fase 3 utilización de terapia biológica con infliximab o tocilizumab. En las conclusiones SIM-P presenta elevación de marcadores inflamatorios, compromiso de múltiples órganos sin diagnósticos bacterianos asociados, con evidencia de infección o exposición reciente a SARS-CoV-2. A Síndrome Inflamatória Multissistêmica Pediátrica (P-MIS) ligada ao SARS-CoV-2 é uma reação inflamatória generalizada que se desenvolve em, aproximadamente, 4-6 semanas após a doença COVID-19. O objetivo do artigo foi analisar a imunopatogenia, o diagnóstico e tratamento do SIM-P. Uma revisão sistemática da literatura foi realizada, utilizando-se bases de dados como Embase, Redalyc, LILACS, SciELO, Springer, Elsevier, EBSCO e Google Scholar e os descritores: Coronavirus disease, Kawasaki disease, child, intravenous immunoglobulins. Os critérios de inclusão foram: artigos completos, publicados entre os anos de 2019-2022, em inglês e espanhol. Do montante de 273 artigos encontrados, 243 artigos foram rejeitados por não se enquadrarem nos critérios estabelecidos, sendo 30 artigos selecionados como elegíveis. De acordo com os resultados, a SIM-P caracteriza-se por febre, lesão miocárdica, choque e desenvolvimento de aneurismas de artéria coronária; em exames laboratoriais, observam-se: elevação dos marcadores de inflamação, alterações nos testes de coagulação, especialmente elevação significativa do dímero D e fibrinogênio e elevação dos marcadores da lesão miocárdica, troponina e peptídeo natriurético. O tratamento na fase 1 ocorre com a administração de imunoglobulina G intravenosa (IGIV), corticosteróides, heparina de baixo peso molecular em dose profilática; na fase 2, o tratamento consiste na administração de uma segunda dose de IGIV, diminuição progressiva da prednisona e uso de terapia biológica; e, na fase 3, utiliza-se infliximabe ou tocilizumabe. Em conclusão, a SIM-P apresenta marcadores inflamatórios elevados e envolvimento de múltiplos órgãos, sem diagnóstico bacteriano associado, com evidência de infecção ou exposição recente ao SARS-CoV-2.Sapienza Grupo Editorial2022-04-30info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://journals.sapienzaeditorial.com/index.php/SIJIS/article/view/30610.51798/sijis.v3i2.306Sapienza: International Journal of Interdisciplinary Studies; Vol. 3 No. 2 (2022): Multidisciplinary Contributions; 38-56Sapienza: International Journal of Interdisciplinary Studies; Vol. 3 Núm. 2 (2022): Aportes Multidisciplinarios; 38-56Sapienza: International Journal of Interdisciplinary Studies; v. 3 n. 2 (2022): Contribuições Multidisciplinares; 38-562675-978010.51798/sijis.v3i2reponame:Sapienza (Curitiba)instname:Sapienza Grupo Editorialinstacron:SAPIENZAspahttps://journals.sapienzaeditorial.com/index.php/SIJIS/article/view/306/181Copyright (c) 2022 Gerardo Fernández, Josué Acostahttps://creativecommons.org/licenses/by-nc-nd/4.0info:eu-repo/semantics/openAccessFernández, Gerardo Acosta, Josué2022-12-26T21:19:06Zoai:ojs2.journals.sapienzaeditorial.com:article/306Revistahttps://journals.sapienzaeditorial.com/index.php/SIJISPRIhttps://journals.sapienzaeditorial.com/index.php/SIJIS/oaieditor@sapienzaeditorial.com2675-97802675-9780opendoar:2023-01-12T16:42:55.330909Sapienza (Curitiba) - Sapienza Grupo Editorialfalse
dc.title.none.fl_str_mv Multisystem inflammatory syndrome associated with COVID-19 in pediatric patients
Síndrome inflamatorio multisistémico asociado a COVID-19 en pacientes pediátricos
Síndrome inflamatória multissistêmica associada à COVID-19 em pacientes pediátricos
title Multisystem inflammatory syndrome associated with COVID-19 in pediatric patients
spellingShingle Multisystem inflammatory syndrome associated with COVID-19 in pediatric patients
Fernández, Gerardo
Doença de coronavírus 2019-nCoV; Doença de Kawasaki; crianças; imunoglobulinas intravenosas
Coronavirus disease 2019-nCoV; Kawasaki disease; little boy; intravenous immunoglobulins
enfermedad por Coronavirus 2019-nCoV; enfermedad de Kawasaki; niño; inmunoglobulinas intravenosas
title_short Multisystem inflammatory syndrome associated with COVID-19 in pediatric patients
title_full Multisystem inflammatory syndrome associated with COVID-19 in pediatric patients
title_fullStr Multisystem inflammatory syndrome associated with COVID-19 in pediatric patients
title_full_unstemmed Multisystem inflammatory syndrome associated with COVID-19 in pediatric patients
title_sort Multisystem inflammatory syndrome associated with COVID-19 in pediatric patients
author Fernández, Gerardo
author_facet Fernández, Gerardo
Acosta, Josué
author_role author
author2 Acosta, Josué
author2_role author
dc.contributor.author.fl_str_mv Fernández, Gerardo
Acosta, Josué
dc.subject.por.fl_str_mv Doença de coronavírus 2019-nCoV; Doença de Kawasaki; crianças; imunoglobulinas intravenosas
Coronavirus disease 2019-nCoV; Kawasaki disease; little boy; intravenous immunoglobulins
enfermedad por Coronavirus 2019-nCoV; enfermedad de Kawasaki; niño; inmunoglobulinas intravenosas
topic Doença de coronavírus 2019-nCoV; Doença de Kawasaki; crianças; imunoglobulinas intravenosas
Coronavirus disease 2019-nCoV; Kawasaki disease; little boy; intravenous immunoglobulins
enfermedad por Coronavirus 2019-nCoV; enfermedad de Kawasaki; niño; inmunoglobulinas intravenosas
description Pediatric Multisystem Inflammatory Syndrome (P-MIS) linked to SARS-CoV-2 is a generalized inflammatory reaction that develops approximately 4-6 weeks after COVID-19 illness. The aim of the article was to analyze the immunopathogenesis, diagnosis and treatment of P-MIS. A systematic literature review was performed using databases such as Embase, Redalyc, LILACS, SciELO, Springer, Elsevier, EBSCO and Google Scholar and the keywords: Coronavirus disease, Kawasaki disease, child, intravenous immunoglobulins. Inclusion criteria were: full articles, published between the years 2019-2022, in English and Spanish. Of the 273 articles found, 243 articles were rejected for not meeting the established criteria, with 30 articles selected as eligible. According to the results, SIM-P is characterized by fever, myocardial injury, shock and development of coronary artery aneurysms; laboratory tests show: elevation of markers of inflammation, changes in coagulation tests, especially significant elevation of D-dimer and fibrinogen and elevation of markers of myocardial injury, troponin and natriuretic peptide. Phase 1 treatment occurs with the administration of intravenous immunoglobulin G (IVIG), corticosteroids, low molecular weight heparin in a prophylactic dose; in phase 2, treatment consists of administration of a second dose of IVIG, progressive reduction of prednisone and use of biological therapy; and, in phase 3, infliximab or tocilizumab is used. In conclusion, SIM-P has elevated inflammatory markers and multi-organ involvement, with no associated bacterial diagnosis, with evidence of infection or recent exposure to SARS-CoV-2.
publishDate 2022
dc.date.none.fl_str_mv 2022-04-30
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv https://journals.sapienzaeditorial.com/index.php/SIJIS/article/view/306
10.51798/sijis.v3i2.306
url https://journals.sapienzaeditorial.com/index.php/SIJIS/article/view/306
identifier_str_mv 10.51798/sijis.v3i2.306
dc.language.iso.fl_str_mv spa
language spa
dc.relation.none.fl_str_mv https://journals.sapienzaeditorial.com/index.php/SIJIS/article/view/306/181
dc.rights.driver.fl_str_mv Copyright (c) 2022 Gerardo Fernández, Josué Acosta
https://creativecommons.org/licenses/by-nc-nd/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2022 Gerardo Fernández, Josué Acosta
https://creativecommons.org/licenses/by-nc-nd/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Sapienza Grupo Editorial
publisher.none.fl_str_mv Sapienza Grupo Editorial
dc.source.none.fl_str_mv Sapienza: International Journal of Interdisciplinary Studies; Vol. 3 No. 2 (2022): Multidisciplinary Contributions; 38-56
Sapienza: International Journal of Interdisciplinary Studies; Vol. 3 Núm. 2 (2022): Aportes Multidisciplinarios; 38-56
Sapienza: International Journal of Interdisciplinary Studies; v. 3 n. 2 (2022): Contribuições Multidisciplinares; 38-56
2675-9780
10.51798/sijis.v3i2
reponame:Sapienza (Curitiba)
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instname_str Sapienza Grupo Editorial
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reponame_str Sapienza (Curitiba)
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repository.mail.fl_str_mv editor@sapienzaeditorial.com
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