Immune neonatal thrombocytopenia - review
Main Author: | |
---|---|
Publication Date: | 2020 |
Other Authors: | , , , |
Format: | Article |
Language: | eng |
Source: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
Download full: | https://doi.org/10.25753/BirthGrowthMJ.v29.i1.17587 |
Summary: | Introduction: Thrombocytopenia is the most frequent hematological change in the neonatal period, with immune thrombocytopenia as the main cause of moderate-to-severe thrombocytopenia in apparently healthy newborns. Immune thrombocytopenia in the fetus or newborn may result from platelet alloantibodies against paternal antigens inherited by the fetus (alloimmune thrombocytopenia) or platelet autoantibodies due to maternal autoimmune disease (autoimmune thrombocytopenia). Objetives: To review published literature about immune thrombocytopenia in newborns, including the latest advances in pathogenesis, diagnosis, treatment, and prevention. Results: Neonatal alloimmune thrombocytopenia is the most common cause of severe thrombocytopenia and intracranial hemorrhage in term neonates. Clinical presentation varies from mild thrombocytopenia to life-threatening bleeding and death. As maternal screening is not routinely performed, most cases are diagnosed in the first child. Despite intensive research, a consensus strategy for prevention and treatment of the condition is lacking. Diagnosis of neonatal autoimmune thrombocytopenia is usually apparent from maternal medical history and thrombocytopenia. Although maternal immune thrombocytopenic purpura does not carry a high risk of perinatal hemorrhage, it may lead to thrombocytopenia in the newborn, mostly mild-to-moderate. Clinical presentation varies from no symptoms to mucocutaneous signs of thrombocytopenia and may persist for weeks to months requiring long-term monitoring. Conclusions: Fetal and Neonatal alloimmune thrombocytopenia can cause severe disease in the affected fetus or newborn. Facing the lack of routine antenatal screening, the strategies currently proposed for pregnancies at risk. We also discussed the latest research and therapies in development, aiming at potential improvements in diagnosis, treatment, and prevention of this disease. Neonatal autoimmune thrombocytopenia may cause long-lasting low platelet count, that need regular checking. |
id |
RCAP_6f9d8fae95c1c81b8f9a57cf5351bddf |
---|---|
oai_identifier_str |
oai:ojs.revistas.rcaap.pt:article/17587 |
network_acronym_str |
RCAP |
network_name_str |
Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
repository_id_str |
https://opendoar.ac.uk/repository/7160 |
spelling |
Immune neonatal thrombocytopenia - reviewTrombocitopenia neonatal imune - revisãoReview ArticlesIntroduction: Thrombocytopenia is the most frequent hematological change in the neonatal period, with immune thrombocytopenia as the main cause of moderate-to-severe thrombocytopenia in apparently healthy newborns. Immune thrombocytopenia in the fetus or newborn may result from platelet alloantibodies against paternal antigens inherited by the fetus (alloimmune thrombocytopenia) or platelet autoantibodies due to maternal autoimmune disease (autoimmune thrombocytopenia). Objetives: To review published literature about immune thrombocytopenia in newborns, including the latest advances in pathogenesis, diagnosis, treatment, and prevention. Results: Neonatal alloimmune thrombocytopenia is the most common cause of severe thrombocytopenia and intracranial hemorrhage in term neonates. Clinical presentation varies from mild thrombocytopenia to life-threatening bleeding and death. As maternal screening is not routinely performed, most cases are diagnosed in the first child. Despite intensive research, a consensus strategy for prevention and treatment of the condition is lacking. Diagnosis of neonatal autoimmune thrombocytopenia is usually apparent from maternal medical history and thrombocytopenia. Although maternal immune thrombocytopenic purpura does not carry a high risk of perinatal hemorrhage, it may lead to thrombocytopenia in the newborn, mostly mild-to-moderate. Clinical presentation varies from no symptoms to mucocutaneous signs of thrombocytopenia and may persist for weeks to months requiring long-term monitoring. Conclusions: Fetal and Neonatal alloimmune thrombocytopenia can cause severe disease in the affected fetus or newborn. Facing the lack of routine antenatal screening, the strategies currently proposed for pregnancies at risk. We also discussed the latest research and therapies in development, aiming at potential improvements in diagnosis, treatment, and prevention of this disease. Neonatal autoimmune thrombocytopenia may cause long-lasting low platelet count, that need regular checking.Introdução: Trombocitopenia é a alteração hematológica mais frequente no período neonatal, sendo trombocitopenia imune a principal causa de trombocitopenia moderada a grave em recém-nascidos aparentemente saudáveis. O desenvolvimento de trombocitopenia imune no feto ou no recém-nascido pode dever-se à passagem transplacentária de anticorpos plaquetários maternos, nomeadamente aloanticorpos dirigidos a antigénios paternos herdados pelo feto (aloimune) ou autoanticorpos sintetizados por patologia autoimune materna (autoimune). Objetivos: Rever a literatura pulicada até à data sobre o tema, incluindo os últimos avanços sobre patogénese, diagnóstico, tratamento e prevenção de trombocitopenia imune em recém-nascidos. Resultados: Trombocitopenia neonatal aloimune é a causa mais comum de trombocitopenia grave e hemorragia intracraniana em recém-nascidos de termo. A apresentação clínica varia entre trombocitopenia ligeira isolada e hemorragia intracraniana letal. Dado que o rastreio pré-natal não é efetuado por rotina, a maioria dos casos são diagnosticados no primeiro filho. Apesar de intensa investigação, não existe atualmente uma estratégia consensual de prevenção e tratamento da condição. Deve existir suspeita de trombocitopenia neonatal autoimune em presença de história materna sugestiva ou trombocitopenia materna. Púrpura trombocitopénica imune materna não comporta um risco elevado de hemorragia perinatal, embora possa originar trombocitopenia –na maioria dos casos, ligeira a moderada − no recém-nascido. A apresentação clínica varia entre ausência de sintomas a presença de sinais mucocutâneos de trombocitopenia e pode persistir durante semanas a meses, requerendo monitorização a longo prazo. Conclusões: A trombocitopenia aloimune fetal e neonatal é causa de doença grave no feto ou no recém-nascido afetado. Dada a inexistência de rastreio pré-natal de rotina, é efectuada a revisão das estratégias propostas atualmente para as gestações de risco, assim como a discussão da investigação mais recente e das terapias em desenvolvimento, cujo objectivo é melhorar o diagnóstico, tratamento e prevenção dessa doença. A trombocitopenia neonatal autoimune pode levar a baixa contagem de plaquetas persistente, sendo necessário um controlo regular.Unidade Local de Saúde de Santo António2020-03-24info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://doi.org/10.25753/BirthGrowthMJ.v29.i1.17587eng2183-9417Sequeira, Ana Isabel RibeiroRocha, DalilaDias, Carla JoãoCarreira, LuisaCleto, Esmeraldainfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-05-07T09:44:53Zoai:ojs.revistas.rcaap.pt:article/17587Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T14:39:41.015685Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse |
dc.title.none.fl_str_mv |
Immune neonatal thrombocytopenia - review Trombocitopenia neonatal imune - revisão |
title |
Immune neonatal thrombocytopenia - review |
spellingShingle |
Immune neonatal thrombocytopenia - review Sequeira, Ana Isabel Ribeiro Review Articles |
title_short |
Immune neonatal thrombocytopenia - review |
title_full |
Immune neonatal thrombocytopenia - review |
title_fullStr |
Immune neonatal thrombocytopenia - review |
title_full_unstemmed |
Immune neonatal thrombocytopenia - review |
title_sort |
Immune neonatal thrombocytopenia - review |
author |
Sequeira, Ana Isabel Ribeiro |
author_facet |
Sequeira, Ana Isabel Ribeiro Rocha, Dalila Dias, Carla João Carreira, Luisa Cleto, Esmeralda |
author_role |
author |
author2 |
Rocha, Dalila Dias, Carla João Carreira, Luisa Cleto, Esmeralda |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Sequeira, Ana Isabel Ribeiro Rocha, Dalila Dias, Carla João Carreira, Luisa Cleto, Esmeralda |
dc.subject.por.fl_str_mv |
Review Articles |
topic |
Review Articles |
description |
Introduction: Thrombocytopenia is the most frequent hematological change in the neonatal period, with immune thrombocytopenia as the main cause of moderate-to-severe thrombocytopenia in apparently healthy newborns. Immune thrombocytopenia in the fetus or newborn may result from platelet alloantibodies against paternal antigens inherited by the fetus (alloimmune thrombocytopenia) or platelet autoantibodies due to maternal autoimmune disease (autoimmune thrombocytopenia). Objetives: To review published literature about immune thrombocytopenia in newborns, including the latest advances in pathogenesis, diagnosis, treatment, and prevention. Results: Neonatal alloimmune thrombocytopenia is the most common cause of severe thrombocytopenia and intracranial hemorrhage in term neonates. Clinical presentation varies from mild thrombocytopenia to life-threatening bleeding and death. As maternal screening is not routinely performed, most cases are diagnosed in the first child. Despite intensive research, a consensus strategy for prevention and treatment of the condition is lacking. Diagnosis of neonatal autoimmune thrombocytopenia is usually apparent from maternal medical history and thrombocytopenia. Although maternal immune thrombocytopenic purpura does not carry a high risk of perinatal hemorrhage, it may lead to thrombocytopenia in the newborn, mostly mild-to-moderate. Clinical presentation varies from no symptoms to mucocutaneous signs of thrombocytopenia and may persist for weeks to months requiring long-term monitoring. Conclusions: Fetal and Neonatal alloimmune thrombocytopenia can cause severe disease in the affected fetus or newborn. Facing the lack of routine antenatal screening, the strategies currently proposed for pregnancies at risk. We also discussed the latest research and therapies in development, aiming at potential improvements in diagnosis, treatment, and prevention of this disease. Neonatal autoimmune thrombocytopenia may cause long-lasting low platelet count, that need regular checking. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-03-24 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://doi.org/10.25753/BirthGrowthMJ.v29.i1.17587 |
url |
https://doi.org/10.25753/BirthGrowthMJ.v29.i1.17587 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
2183-9417 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.publisher.none.fl_str_mv |
Unidade Local de Saúde de Santo António |
publisher.none.fl_str_mv |
Unidade Local de Saúde de Santo António |
dc.source.none.fl_str_mv |
reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia instacron:RCAAP |
instname_str |
FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
collection |
Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
repository.name.fl_str_mv |
Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia |
repository.mail.fl_str_mv |
info@rcaap.pt |
_version_ |
1833594797396328448 |