Revisão sistemática sobre o papel do caplacizumab no tratamento da púrpura trombocitopénica trombótica
Autor(a) principal: | |
---|---|
Data de Publicação: | 2021 |
Tipo de documento: | Dissertação |
Idioma: | por |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | https://hdl.handle.net/10216/139720 |
Resumo: | Background: Acquired thrombotic thrombocytopenic purpura is a rare disorder in which clots form in small blood vessels, and may even block blood flow to downstream organs. Caplacizumab is a humanised bivalent nanobody that prevents the ultralarge von Willebrand factor-mediated platelet adhesion. The goal of this review is to analyze the effect of the inclusion of caplacizumab in the treatment of acquired thrombotic thrombocytopenic purpura. Methods: The systematic review of the literature was carried out in several databases with the keywords "caplacizumab" and "thrombotic thrombocytopenic purpura". We considered different study designs, in which was reported the clinical follow-up of individuals diagnosed with thrombotic thrombocytopenic purpura and whose therapeutic scheme included caplacizumab. All steps outlined by the PRISMA guidelines were completed and described. Results: We included 8 articles that met the eligibility criteria, published between 2016 and 2020, only 2 of which consisted of original clinical trials and all the others used these as a model for comparison. Discussion: The efficacy and safety of caplacizumab in adults experiencing an episode of aTTP were established in 2 randomised, controlled studies. The therapeutic scheme defined by the phase III study "HERCULES" was replicated in most of the other reported clinical cases, including in the pediatric stratum, except for those that excluded plasmapheresis. Conclusion: There are benefits to including caplacizumab in the therapeutic regimen of acquired thrombotic thrombocytopenic purpura, but further studies are needed to better understand its effects. Keywords: ADAMTS13 Protein (MeSH); Plasma Exchange (MeSH); Purpura, Thrombotic Thrombocytopenic (MeSH); von Willebrand Factor (MeSH). |
id |
RCAP_9df4635ccf7a3076a29e9ad56179b303 |
---|---|
oai_identifier_str |
oai:repositorio-aberto.up.pt:10216/139720 |
network_acronym_str |
RCAP |
network_name_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository_id_str |
7160 |
spelling |
Revisão sistemática sobre o papel do caplacizumab no tratamento da púrpura trombocitopénica trombóticaMedicina clínicaClinical medicineBackground: Acquired thrombotic thrombocytopenic purpura is a rare disorder in which clots form in small blood vessels, and may even block blood flow to downstream organs. Caplacizumab is a humanised bivalent nanobody that prevents the ultralarge von Willebrand factor-mediated platelet adhesion. The goal of this review is to analyze the effect of the inclusion of caplacizumab in the treatment of acquired thrombotic thrombocytopenic purpura. Methods: The systematic review of the literature was carried out in several databases with the keywords "caplacizumab" and "thrombotic thrombocytopenic purpura". We considered different study designs, in which was reported the clinical follow-up of individuals diagnosed with thrombotic thrombocytopenic purpura and whose therapeutic scheme included caplacizumab. All steps outlined by the PRISMA guidelines were completed and described. Results: We included 8 articles that met the eligibility criteria, published between 2016 and 2020, only 2 of which consisted of original clinical trials and all the others used these as a model for comparison. Discussion: The efficacy and safety of caplacizumab in adults experiencing an episode of aTTP were established in 2 randomised, controlled studies. The therapeutic scheme defined by the phase III study "HERCULES" was replicated in most of the other reported clinical cases, including in the pediatric stratum, except for those that excluded plasmapheresis. Conclusion: There are benefits to including caplacizumab in the therapeutic regimen of acquired thrombotic thrombocytopenic purpura, but further studies are needed to better understand its effects. Keywords: ADAMTS13 Protein (MeSH); Plasma Exchange (MeSH); Purpura, Thrombotic Thrombocytopenic (MeSH); von Willebrand Factor (MeSH).2021-09-142021-09-14T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfhttps://hdl.handle.net/10216/139720TID:203176227porAna Catarina Almeida Pinheiroinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-11-29T14:37:48Zoai:repositorio-aberto.up.pt:10216/139720Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T00:05:29.744934Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Revisão sistemática sobre o papel do caplacizumab no tratamento da púrpura trombocitopénica trombótica |
title |
Revisão sistemática sobre o papel do caplacizumab no tratamento da púrpura trombocitopénica trombótica |
spellingShingle |
Revisão sistemática sobre o papel do caplacizumab no tratamento da púrpura trombocitopénica trombótica Ana Catarina Almeida Pinheiro Medicina clínica Clinical medicine |
title_short |
Revisão sistemática sobre o papel do caplacizumab no tratamento da púrpura trombocitopénica trombótica |
title_full |
Revisão sistemática sobre o papel do caplacizumab no tratamento da púrpura trombocitopénica trombótica |
title_fullStr |
Revisão sistemática sobre o papel do caplacizumab no tratamento da púrpura trombocitopénica trombótica |
title_full_unstemmed |
Revisão sistemática sobre o papel do caplacizumab no tratamento da púrpura trombocitopénica trombótica |
title_sort |
Revisão sistemática sobre o papel do caplacizumab no tratamento da púrpura trombocitopénica trombótica |
author |
Ana Catarina Almeida Pinheiro |
author_facet |
Ana Catarina Almeida Pinheiro |
author_role |
author |
dc.contributor.author.fl_str_mv |
Ana Catarina Almeida Pinheiro |
dc.subject.por.fl_str_mv |
Medicina clínica Clinical medicine |
topic |
Medicina clínica Clinical medicine |
description |
Background: Acquired thrombotic thrombocytopenic purpura is a rare disorder in which clots form in small blood vessels, and may even block blood flow to downstream organs. Caplacizumab is a humanised bivalent nanobody that prevents the ultralarge von Willebrand factor-mediated platelet adhesion. The goal of this review is to analyze the effect of the inclusion of caplacizumab in the treatment of acquired thrombotic thrombocytopenic purpura. Methods: The systematic review of the literature was carried out in several databases with the keywords "caplacizumab" and "thrombotic thrombocytopenic purpura". We considered different study designs, in which was reported the clinical follow-up of individuals diagnosed with thrombotic thrombocytopenic purpura and whose therapeutic scheme included caplacizumab. All steps outlined by the PRISMA guidelines were completed and described. Results: We included 8 articles that met the eligibility criteria, published between 2016 and 2020, only 2 of which consisted of original clinical trials and all the others used these as a model for comparison. Discussion: The efficacy and safety of caplacizumab in adults experiencing an episode of aTTP were established in 2 randomised, controlled studies. The therapeutic scheme defined by the phase III study "HERCULES" was replicated in most of the other reported clinical cases, including in the pediatric stratum, except for those that excluded plasmapheresis. Conclusion: There are benefits to including caplacizumab in the therapeutic regimen of acquired thrombotic thrombocytopenic purpura, but further studies are needed to better understand its effects. Keywords: ADAMTS13 Protein (MeSH); Plasma Exchange (MeSH); Purpura, Thrombotic Thrombocytopenic (MeSH); von Willebrand Factor (MeSH). |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-09-14 2021-09-14T00:00:00Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/masterThesis |
format |
masterThesis |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://hdl.handle.net/10216/139720 TID:203176227 |
url |
https://hdl.handle.net/10216/139720 |
identifier_str_mv |
TID:203176227 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
repository.mail.fl_str_mv |
|
_version_ |
1799135978750738432 |