The clinical profile and the therapeutic management of the HELLP syndrome: integrative review
Autor(a) principal: | |
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Data de Publicação: | 2021 |
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/22194 |
Resumo: | This study has as objective to describe the clinical profile and therapeutic management of HELLP syndrome. The study has used as method an integrative literature review, developed through a search in the Pubmed database using the crossings of the descriptors in English “HELLP syndrome”, “complications”. To evaluate the research problem and its stratification, the PVO strategy was used. The strategy previously mentioned allowed us to formulate the following guiding question: What are the clinical manifestations of HELLP syndrome, and how does therapeutic management work? The pathophysiology of the disease is not known yet. However, it is believed to be caused by placental insufficiency and generalized endothelial dysfunction. Vague presentation is common; hypertension and proteinuria that characterize preeclampsia are usually absent when HELLP syndrome presents. It can present with nonspecific signs and symptoms, none of which are diagnostic and in most cases asymptomatic, but with symptoms such as persistent hyperreflexia, headache, confusion, abdominal pain, nausea and vomiting. Misdiagnosis and late recognition of HELLP syndrome are common due to its vague and variable presentation. When HELLP syndrome is identified, childbirth is necessary to avoid catastrophic maternal and neonatal outcomes. The identification of baseline parameters predictive of disease progression is, therefore, of great importance to define which obstetric approach should be prioritized. |
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The clinical profile and the therapeutic management of the HELLP syndrome: integrative reviewPerfil clínico y manejo terapéutico del síndrome de HELLP: revisión integrativaO perfil clínico e o manejo terapêutico da síndrome HELLP: revisão integrativaHELLP SyndromeManagemenComplications.GestiónSíndrome de HELLPComplicaciones.ManejoSíndrome HELLPComplicações.This study has as objective to describe the clinical profile and therapeutic management of HELLP syndrome. The study has used as method an integrative literature review, developed through a search in the Pubmed database using the crossings of the descriptors in English “HELLP syndrome”, “complications”. To evaluate the research problem and its stratification, the PVO strategy was used. The strategy previously mentioned allowed us to formulate the following guiding question: What are the clinical manifestations of HELLP syndrome, and how does therapeutic management work? The pathophysiology of the disease is not known yet. However, it is believed to be caused by placental insufficiency and generalized endothelial dysfunction. Vague presentation is common; hypertension and proteinuria that characterize preeclampsia are usually absent when HELLP syndrome presents. It can present with nonspecific signs and symptoms, none of which are diagnostic and in most cases asymptomatic, but with symptoms such as persistent hyperreflexia, headache, confusion, abdominal pain, nausea and vomiting. Misdiagnosis and late recognition of HELLP syndrome are common due to its vague and variable presentation. When HELLP syndrome is identified, childbirth is necessary to avoid catastrophic maternal and neonatal outcomes. The identification of baseline parameters predictive of disease progression is, therefore, of great importance to define which obstetric approach should be prioritized.Este estudio tiene como objetivo describir el perfil clínico y el manejo terapéutico del síndrome HELLP. El estudio utilizó como método la revisión integrativa de la literatura, realizada a través de una búsqueda en la base de datos Pubmed utilizando los cruces de los descriptores en inglés “HELLP syndrome”, “complicaciones”. Para evaluar el problema de investigación y su estratificación se utilizó la estrategia PVO. La estrategia antes mencionada nos permitió formular la siguiente pregunta orientadora: ¿Cuáles son las manifestaciones clínicas del síndrome HELLP y cómo funciona el manjo terapéutico? Aún no se conoce la fisiopatología de la enfermedad. Sin embargo, se cree que es causado por insuficiencia placentaria y disfunción endotelial generalizada. La presentación vaga es común; la hipertensión y la proteinuria que caracterizan la preeclampsia suelen estar ausentes cuando se presenta el síndrome HELLP. Puede presentarse con signos y síntomas inespecíficos, ninguno de los cuales es diagnóstico y en la mayoría de los casos asintomáticos, pero con síntomas como hiperreflexia persistente, cefalea, confusión, dolor abdominal, náuseas y vómitos. El diagnóstico erróneo y el reconocimiento tardío del síndrome HELLP son comunes debido a su presentación vaga y variable. Cuando se identifica el síndrome HELLP, el parto es necesario para evitar resultados maternos y neonatales catastróficos. La identificación de los parámetros basales que predicen la progresión de la enfermedad es, por tanto, de gran importancia para definir qué abordaje obstétrico debe priorizarse.O presente estudo tem como objetivo descrever o perfil clínico e o manejo terapêutico da síndrome HELLP. O estudo utilizou como método a revisão integrativa da literatura, realizado por meio de uma busca na base de dados Pubmed usando os cruzamentos os descritores em inglês “HELLP syndrome”, “complications”. Para a avaliação do problema de pesquisa e sua estratificação foi utilizada a estratégia PVO. A estratégia supracitada permitiu formular a seguinte questão norteadora: Quais são as manifestações clínicas da síndrome HELLP e como funciona o manejo terapêutico? A fisiopatologia da doença ainda não é conhecida. No entanto, acredita-se que seja causada por insuficiência placentária e disfunção endotelial generalizada. A apresentação vaga é comum; hipertensão e proteinúria que caracterizam a pré-eclâmpsia geralmente estão ausentes quando a síndrome HELLP se apresenta. Pode-se apresentar com sinais e sintomas inespecíficos, nenhum dos quais são diagnósticos e sendo na maioria dos casos assintomáticos, mas tendo como sintomas a hiperreflexia persistente, dor de cabeça, confusão, dor abdominal, náuseas e vômitos. O diagnóstico incorreto e o reconhecimento tardio da síndrome HELLP são comuns devido à apresentação vaga e variável. Quando a síndrome HELLP é identificada, o parto é necessário para evitar desfechos maternos e neonatais catastróficos. A identificação dos parâmetros basais preditivos da evolução da doença é, portanto, de grande importância para definir qual abordagem obstétrica deve ser priorizada.Research, Society and Development2021-11-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/2219410.33448/rsd-v10i14.22194Research, Society and Development; Vol. 10 No. 14; e450101422194Research, Society and Development; Vol. 10 Núm. 14; e450101422194Research, Society and Development; v. 10 n. 14; e4501014221942525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIporhttps://rsdjournal.org/index.php/rsd/article/view/22194/19774Copyright (c) 2021 Ana Klara Rodrigues Alves; Barbara Beatriz Lira da Silva; Francisco Robson de Oliveira Alves; Larissa dos Santos Silva; Lívia Filomena Castelo Branco Machado; Alvaro Martins Pinho; Fábio Landel Alysson Araújo Franklin; Maria de Lourdes Pereira Ibiapina; Francisco Matheus Carvalho Noronha; Lia Moreira de Vasconcelos Almeida; Savir Igor de Oliveira Gonçalves ; Amanda Milhomem Medeiros; Noé Araujo Fortes Neto; Luiza Emiliana Queiroz Bucar; Iluska Guimarães Rodrigues https://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessAlves, Ana Klara Rodrigues Silva, Barbara Beatriz Lira da Alves, Francisco Robson de Oliveira Silva, Larissa dos Santos Machado, Lívia Filomena Castelo Branco Pinho, Alvaro Martins Franklin, Fábio Landel Alysson Araújo Ibiapina, Maria de Lourdes Pereira Noronha, Francisco Matheus Carvalho Almeida, Lia Moreira de Vasconcelos Gonçalves , Savir Igor de Oliveira Medeiros, Amanda Milhomem Fortes Neto, Noé Araujo Bucar, Luiza Emiliana Queiroz Rodrigues , Iluska Guimarães 2021-12-04T11:48:39Zoai:ojs.pkp.sfu.ca:article/22194Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-01-17T09:41:25.436764Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false |
dc.title.none.fl_str_mv |
The clinical profile and the therapeutic management of the HELLP syndrome: integrative review Perfil clínico y manejo terapéutico del síndrome de HELLP: revisión integrativa O perfil clínico e o manejo terapêutico da síndrome HELLP: revisão integrativa |
title |
The clinical profile and the therapeutic management of the HELLP syndrome: integrative review |
spellingShingle |
The clinical profile and the therapeutic management of the HELLP syndrome: integrative review Alves, Ana Klara Rodrigues HELLP Syndrome Managemen Complications. Gestión Síndrome de HELLP Complicaciones. Manejo Síndrome HELLP Complicações. |
title_short |
The clinical profile and the therapeutic management of the HELLP syndrome: integrative review |
title_full |
The clinical profile and the therapeutic management of the HELLP syndrome: integrative review |
title_fullStr |
The clinical profile and the therapeutic management of the HELLP syndrome: integrative review |
title_full_unstemmed |
The clinical profile and the therapeutic management of the HELLP syndrome: integrative review |
title_sort |
The clinical profile and the therapeutic management of the HELLP syndrome: integrative review |
author |
Alves, Ana Klara Rodrigues |
author_facet |
Alves, Ana Klara Rodrigues Silva, Barbara Beatriz Lira da Alves, Francisco Robson de Oliveira Silva, Larissa dos Santos Machado, Lívia Filomena Castelo Branco Pinho, Alvaro Martins Franklin, Fábio Landel Alysson Araújo Ibiapina, Maria de Lourdes Pereira Noronha, Francisco Matheus Carvalho Almeida, Lia Moreira de Vasconcelos Gonçalves , Savir Igor de Oliveira Medeiros, Amanda Milhomem Fortes Neto, Noé Araujo Bucar, Luiza Emiliana Queiroz Rodrigues , Iluska Guimarães |
author_role |
author |
author2 |
Silva, Barbara Beatriz Lira da Alves, Francisco Robson de Oliveira Silva, Larissa dos Santos Machado, Lívia Filomena Castelo Branco Pinho, Alvaro Martins Franklin, Fábio Landel Alysson Araújo Ibiapina, Maria de Lourdes Pereira Noronha, Francisco Matheus Carvalho Almeida, Lia Moreira de Vasconcelos Gonçalves , Savir Igor de Oliveira Medeiros, Amanda Milhomem Fortes Neto, Noé Araujo Bucar, Luiza Emiliana Queiroz Rodrigues , Iluska Guimarães |
author2_role |
author author author author author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Alves, Ana Klara Rodrigues Silva, Barbara Beatriz Lira da Alves, Francisco Robson de Oliveira Silva, Larissa dos Santos Machado, Lívia Filomena Castelo Branco Pinho, Alvaro Martins Franklin, Fábio Landel Alysson Araújo Ibiapina, Maria de Lourdes Pereira Noronha, Francisco Matheus Carvalho Almeida, Lia Moreira de Vasconcelos Gonçalves , Savir Igor de Oliveira Medeiros, Amanda Milhomem Fortes Neto, Noé Araujo Bucar, Luiza Emiliana Queiroz Rodrigues , Iluska Guimarães |
dc.subject.por.fl_str_mv |
HELLP Syndrome Managemen Complications. Gestión Síndrome de HELLP Complicaciones. Manejo Síndrome HELLP Complicações. |
topic |
HELLP Syndrome Managemen Complications. Gestión Síndrome de HELLP Complicaciones. Manejo Síndrome HELLP Complicações. |
description |
This study has as objective to describe the clinical profile and therapeutic management of HELLP syndrome. The study has used as method an integrative literature review, developed through a search in the Pubmed database using the crossings of the descriptors in English “HELLP syndrome”, “complications”. To evaluate the research problem and its stratification, the PVO strategy was used. The strategy previously mentioned allowed us to formulate the following guiding question: What are the clinical manifestations of HELLP syndrome, and how does therapeutic management work? The pathophysiology of the disease is not known yet. However, it is believed to be caused by placental insufficiency and generalized endothelial dysfunction. Vague presentation is common; hypertension and proteinuria that characterize preeclampsia are usually absent when HELLP syndrome presents. It can present with nonspecific signs and symptoms, none of which are diagnostic and in most cases asymptomatic, but with symptoms such as persistent hyperreflexia, headache, confusion, abdominal pain, nausea and vomiting. Misdiagnosis and late recognition of HELLP syndrome are common due to its vague and variable presentation. When HELLP syndrome is identified, childbirth is necessary to avoid catastrophic maternal and neonatal outcomes. The identification of baseline parameters predictive of disease progression is, therefore, of great importance to define which obstetric approach should be prioritized. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-11-09 |
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/22194 10.33448/rsd-v10i14.22194 |
url |
https://rsdjournal.org/index.php/rsd/article/view/22194 |
identifier_str_mv |
10.33448/rsd-v10i14.22194 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
https://rsdjournal.org/index.php/rsd/article/view/22194/19774 |
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. 10 No. 14; e450101422194 Research, Society and Development; Vol. 10 Núm. 14; e450101422194 Research, Society and Development; v. 10 n. 14; e450101422194 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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1797052758035005440 |