Neonatal screening for severe combined immunodeficiency syndrome
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Research, Society and Development |
Texto Completo: | https://rsdjournal.org/index.php/rsd/article/view/33572 |
Resumo: | Severe combined immunodeficiency (SCID), also known as “bubble boy disease” is a serious defect in cellular and humoral immunity that makes children susceptible to infections. Its diagnosis is made through Neonatal Screening, and in Brazil it is done by the foot test. The treatment is based on the Hematopoietic Stem Cell Treatment (HSCT). Late diagnosis or lack of treatment can cause sequelae or death. Therefore, it is important to implement newborn screening to detect cases of SCID early to avoid irreversible damage. Therefore, the objective of this review is to evaluate neonatal screening for severe combined immunodeficiency and its contribution to carriers. This is a systematic literature review approved by the PROSPERO platform under number CDR42020206341, carried out in MEDLINE, LILACS, in English, Portuguese and Spanish, to be reviewed by two independent authors. Randomized and non-randomized clinical trials, case-control trials, cohort studies and cross-sectional studies in the last five years will be included. After the combined search and application of the inclusion and exclusion criteria, 12 articles were selected to compose the final sample. Neonatal screening is performed by different methods around the world, however, regardless of how it is done, it is possible to note its importance within the health of neonates. The ease of collection contributes to quality care, and the information offered during prenatal care ensures that parents are aware of the need to perform the exam to identify early pathologies that can cause sequelae and even deaths. |
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Neonatal screening for severe combined immunodeficiency syndromeCribado neonatal del síndrome de inmunodeficiencia combinada graveTriagem neonatal para síndrome da imunodeficiência combinada graveSevere Combined ImmunodeficiencyNeonatal ScreeningChild HealthChild health.Immunodeficiencia Combinada GraveTamizaje NeonatalSalud infantil.Imunodeficiência Combinada SeveraTriagem NeonatalSaúde da criança.Severe combined immunodeficiency (SCID), also known as “bubble boy disease” is a serious defect in cellular and humoral immunity that makes children susceptible to infections. Its diagnosis is made through Neonatal Screening, and in Brazil it is done by the foot test. The treatment is based on the Hematopoietic Stem Cell Treatment (HSCT). Late diagnosis or lack of treatment can cause sequelae or death. Therefore, it is important to implement newborn screening to detect cases of SCID early to avoid irreversible damage. Therefore, the objective of this review is to evaluate neonatal screening for severe combined immunodeficiency and its contribution to carriers. This is a systematic literature review approved by the PROSPERO platform under number CDR42020206341, carried out in MEDLINE, LILACS, in English, Portuguese and Spanish, to be reviewed by two independent authors. Randomized and non-randomized clinical trials, case-control trials, cohort studies and cross-sectional studies in the last five years will be included. After the combined search and application of the inclusion and exclusion criteria, 12 articles were selected to compose the final sample. Neonatal screening is performed by different methods around the world, however, regardless of how it is done, it is possible to note its importance within the health of neonates. The ease of collection contributes to quality care, and the information offered during prenatal care ensures that parents are aware of the need to perform the exam to identify early pathologies that can cause sequelae and even deaths.La inmunodeficiencia combinada severa (SCID), también conocida como “enfermedad del niño burbuja”, es un defecto grave en la inmunidad celular y humoral que hace que los niños sean susceptibles a las infecciones. Su diagnóstico se realiza a través del Tamizaje Neonatal, y en Brasil se realiza por la prueba del pie. El tratamiento se basa en el Tratamiento de Células Madre Hematopoyéticas (TPH). El diagnóstico tardío o la falta de tratamiento pueden causar secuelas o la muerte. Por lo tanto, es importante implementar el tamizaje neonatal para detectar casos de SCID de manera temprana para evitar daños irreversibles. Por lo tanto, el objetivo de esta revisión es evaluar el tamizaje neonatal para inmunodeficiencia combinada severa y su contribución a los portadores. Esta es una revisión sistemática de la literatura aprobada por la plataforma PROSPERO con el número CDR42020206341, realizada en MEDLINE, LILACS, en inglés, portugués y español, para ser revisada por dos autores independientes. Se incluirán ensayos clínicos aleatorizados y no aleatorizados, ensayos de casos y controles, estudios de cohortes y estudios transversales en los últimos cinco años. Después de la búsqueda combinada y la aplicación de los criterios de inclusión y exclusión, se seleccionaron 12 artículos para componer la muestra final. El tamizaje neonatal se realiza por diferentes métodos alrededor del mundo, sin embargo, independientemente de cómo se realice, es posible notar su importancia dentro de la salud de los recién nacidos. La facilidad de recolección contribuye a la calidad de la atención, y la información ofrecida durante el prenatal asegura que los padres sean conscientes de la necesidad de realizar el examen para identificar tempranamente patologías que pueden causar secuelas e incluso la muerte.A imunodeficiência combinada grave (SCID), também conhecida como “doença do menino da bolha” é um defeito grave na imunidade celular e humoral que torna as crianças suscetíveis à infecções. Seu diagnóstico se dá através da Triagem Neonatal, e no Brasil é feita pelo teste do pezinho. O tratamento é feito a partir do Tratamento de Células-Tronco Hematopoiéticas (TCTH). O diagnóstico tardio ou a ausência de tratamento podem ocasionar sequelas ou óbitos. Portanto, é importante implementar a triagem neonatal para detectar os casos de SCID precocemente para evitar danos irreversíveis. Por isso, o objetivo desta revisão é avaliar a triagem neonatal para imunodeficiência combinada grave e sua contribuição para os portadores. Trata-se de uma revisão sistemática de literatura aprovada pela plataforma PROSPERO sob nº CDR42020206341, realizada nas bases MEDLINE, LILACS, nos idiomas inglês, português e espanhol, a ser revisados por dois autores independentes. Serão incluídos ensaios clínicos randomizados e não randomizados, ensaios de caso controle, estudos de coorte e estudos transversais, nos últimos cinco anos. Após a busca combinada e aplicação dos críterios de inclusão e exclusão foram selecionados 12 artigos para compor a amostra final. A triagem neonatal é realizada por diferentes métodos ao redor do mundo, no entanto, independente de como seja feita, é possível notar a sua importância dentro da saúde de neonatos. A facilidade na coleta contribui para uma assistência de qualidade, e as informações oferecidas durante o pré-natal garantem que os genitores estejam cientes da necessidade em realizar o exame para identificar de forma precoce patologias que podem ocasionar sequelas e até óbitos.Research, Society and Development2022-08-16info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/3357210.33448/rsd-v11i11.33572Research, Society and Development; Vol. 11 No. 11; e104111133572Research, Society and Development; Vol. 11 Núm. 11; e104111133572Research, Society and Development; v. 11 n. 11; e1041111335722525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIporhttps://rsdjournal.org/index.php/rsd/article/view/33572/28247Copyright (c) 2022 Vitoria Vilas Boas da Silva Bomfim; Paulo da Costa Araújo; Lisiane Madalena Treptow; Emanuel Osvaldo de Sousa; Célio Pereira de Sousa Júnior; Débora Fernandes Barros Cabral; Bruna Raquel Luna Pedroso Santos; Carolina Marques Ribeiro Pessoa; Deborah Regina Cavalcante da Silva; Guilherme de Andrade Ruelahttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessBomfim, Vitoria Vilas Boas da Silva Araújo, Paulo da Costa Treptow, Lisiane Madalena Sousa, Emanuel Osvaldo de Sousa Júnior, Célio Pereira de Cabral, Débora Fernandes Barros Santos, Bruna Raquel Luna Pedroso Pessoa, Carolina Marques Ribeiro Silva, Deborah Regina Cavalcante da Ruela, Guilherme de Andrade 2022-09-05T13:24:46Zoai:ojs.pkp.sfu.ca:article/33572Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-01-17T09:49:10.898425Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false |
dc.title.none.fl_str_mv |
Neonatal screening for severe combined immunodeficiency syndrome Cribado neonatal del síndrome de inmunodeficiencia combinada grave Triagem neonatal para síndrome da imunodeficiência combinada grave |
title |
Neonatal screening for severe combined immunodeficiency syndrome |
spellingShingle |
Neonatal screening for severe combined immunodeficiency syndrome Bomfim, Vitoria Vilas Boas da Silva Severe Combined Immunodeficiency Neonatal Screening Child Health Child health. Immunodeficiencia Combinada Grave Tamizaje Neonatal Salud infantil. Imunodeficiência Combinada Severa Triagem Neonatal Saúde da criança. |
title_short |
Neonatal screening for severe combined immunodeficiency syndrome |
title_full |
Neonatal screening for severe combined immunodeficiency syndrome |
title_fullStr |
Neonatal screening for severe combined immunodeficiency syndrome |
title_full_unstemmed |
Neonatal screening for severe combined immunodeficiency syndrome |
title_sort |
Neonatal screening for severe combined immunodeficiency syndrome |
author |
Bomfim, Vitoria Vilas Boas da Silva |
author_facet |
Bomfim, Vitoria Vilas Boas da Silva Araújo, Paulo da Costa Treptow, Lisiane Madalena Sousa, Emanuel Osvaldo de Sousa Júnior, Célio Pereira de Cabral, Débora Fernandes Barros Santos, Bruna Raquel Luna Pedroso Pessoa, Carolina Marques Ribeiro Silva, Deborah Regina Cavalcante da Ruela, Guilherme de Andrade |
author_role |
author |
author2 |
Araújo, Paulo da Costa Treptow, Lisiane Madalena Sousa, Emanuel Osvaldo de Sousa Júnior, Célio Pereira de Cabral, Débora Fernandes Barros Santos, Bruna Raquel Luna Pedroso Pessoa, Carolina Marques Ribeiro Silva, Deborah Regina Cavalcante da Ruela, Guilherme de Andrade |
author2_role |
author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Bomfim, Vitoria Vilas Boas da Silva Araújo, Paulo da Costa Treptow, Lisiane Madalena Sousa, Emanuel Osvaldo de Sousa Júnior, Célio Pereira de Cabral, Débora Fernandes Barros Santos, Bruna Raquel Luna Pedroso Pessoa, Carolina Marques Ribeiro Silva, Deborah Regina Cavalcante da Ruela, Guilherme de Andrade |
dc.subject.por.fl_str_mv |
Severe Combined Immunodeficiency Neonatal Screening Child Health Child health. Immunodeficiencia Combinada Grave Tamizaje Neonatal Salud infantil. Imunodeficiência Combinada Severa Triagem Neonatal Saúde da criança. |
topic |
Severe Combined Immunodeficiency Neonatal Screening Child Health Child health. Immunodeficiencia Combinada Grave Tamizaje Neonatal Salud infantil. Imunodeficiência Combinada Severa Triagem Neonatal Saúde da criança. |
description |
Severe combined immunodeficiency (SCID), also known as “bubble boy disease” is a serious defect in cellular and humoral immunity that makes children susceptible to infections. Its diagnosis is made through Neonatal Screening, and in Brazil it is done by the foot test. The treatment is based on the Hematopoietic Stem Cell Treatment (HSCT). Late diagnosis or lack of treatment can cause sequelae or death. Therefore, it is important to implement newborn screening to detect cases of SCID early to avoid irreversible damage. Therefore, the objective of this review is to evaluate neonatal screening for severe combined immunodeficiency and its contribution to carriers. This is a systematic literature review approved by the PROSPERO platform under number CDR42020206341, carried out in MEDLINE, LILACS, in English, Portuguese and Spanish, to be reviewed by two independent authors. Randomized and non-randomized clinical trials, case-control trials, cohort studies and cross-sectional studies in the last five years will be included. After the combined search and application of the inclusion and exclusion criteria, 12 articles were selected to compose the final sample. Neonatal screening is performed by different methods around the world, however, regardless of how it is done, it is possible to note its importance within the health of neonates. The ease of collection contributes to quality care, and the information offered during prenatal care ensures that parents are aware of the need to perform the exam to identify early pathologies that can cause sequelae and even deaths. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-08-16 |
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://rsdjournal.org/index.php/rsd/article/view/33572 10.33448/rsd-v11i11.33572 |
url |
https://rsdjournal.org/index.php/rsd/article/view/33572 |
identifier_str_mv |
10.33448/rsd-v11i11.33572 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
https://rsdjournal.org/index.php/rsd/article/view/33572/28247 |
dc.rights.driver.fl_str_mv |
https://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by/4.0 |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Research, Society and Development |
publisher.none.fl_str_mv |
Research, Society and Development |
dc.source.none.fl_str_mv |
Research, Society and Development; Vol. 11 No. 11; e104111133572 Research, Society and Development; Vol. 11 Núm. 11; e104111133572 Research, Society and Development; v. 11 n. 11; e104111133572 2525-3409 reponame:Research, Society and Development instname:Universidade Federal de Itajubá (UNIFEI) instacron:UNIFEI |
instname_str |
Universidade Federal de Itajubá (UNIFEI) |
instacron_str |
UNIFEI |
institution |
UNIFEI |
reponame_str |
Research, Society and Development |
collection |
Research, Society and Development |
repository.name.fl_str_mv |
Research, Society and Development - Universidade Federal de Itajubá (UNIFEI) |
repository.mail.fl_str_mv |
rsd.articles@gmail.com |
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1797052770663006208 |