INOVATION IN THE ANTICOAGULANT THERAPY

Detalhes bibliográficos
Autor(a) principal: Ramos, Sofia
Data de Publicação: 2013
Outros Autores: Oliveira Martins, Sofia
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://doi.org/10.25756/rpf.v5i3.45
Resumo: Introdution: Atherothrombosis and venous thromboembolism are the leading causes of morbidity and mortality. Anticoagulant therapy is crucial to decrease these factors by preventing the clotting of blood.Objective: Describe some of the new anticoagulant drugs, introduced in an attempt to overcome the limitations of traditional anticoagulant drugs (heparins, warfarin and acenocumarol).Method: Narrative literature review of relevant scientific articles published between 2006 and 2012.Results: A new strategy for the design of new antithrombotic drugs is based on selective inhibition of a specific coagulation factor, with potential to be more effective, safe and easy to use. These include direct thrombin inhibitors (dabigatran, bivalirudin, desirudin, lepirudin and argatroban) and factor Xa inhibitors (otamixaban, rivaroxaban, o apixaban, edoxaban and fondaparinux). Also, a new vitamin K antagonist has been developed, tecarfarin. This does not present the same limitations as the other, which is due essencially to the fact that is not metabolized by CYP450 enzymes.Conclusion: Anticoagulant therapy has been the target of an intense review so that its use in the clinical practice becomes indeed innovative and revolutionary. Currently, in Portugal, only fondaparinux, the dabigatran etexilate and rivaroxaban have been approved and commercialized.
id RCAP_fc26018733abd0ca449748922c01c1ab
oai_identifier_str oai:ojs.farmacoterapia.pt:article/45
network_acronym_str RCAP
network_name_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository_id_str 7160
spelling INOVATION IN THE ANTICOAGULANT THERAPYINOVAÇÃO NA TERAPÊUTICA ANTICOAGULANTEIntrodution: Atherothrombosis and venous thromboembolism are the leading causes of morbidity and mortality. Anticoagulant therapy is crucial to decrease these factors by preventing the clotting of blood.Objective: Describe some of the new anticoagulant drugs, introduced in an attempt to overcome the limitations of traditional anticoagulant drugs (heparins, warfarin and acenocumarol).Method: Narrative literature review of relevant scientific articles published between 2006 and 2012.Results: A new strategy for the design of new antithrombotic drugs is based on selective inhibition of a specific coagulation factor, with potential to be more effective, safe and easy to use. These include direct thrombin inhibitors (dabigatran, bivalirudin, desirudin, lepirudin and argatroban) and factor Xa inhibitors (otamixaban, rivaroxaban, o apixaban, edoxaban and fondaparinux). Also, a new vitamin K antagonist has been developed, tecarfarin. This does not present the same limitations as the other, which is due essencially to the fact that is not metabolized by CYP450 enzymes.Conclusion: Anticoagulant therapy has been the target of an intense review so that its use in the clinical practice becomes indeed innovative and revolutionary. Currently, in Portugal, only fondaparinux, the dabigatran etexilate and rivaroxaban have been approved and commercialized.Introdução: A trombose arterial e a trombose venosa são ainda a principal causa de morbilidade e mortalidade.A terapêutica anticoagulante é fundamental para diminuir esta morbimortalidade, permitindo a não ocorrência ou o aumento de trombos.Objetivo: Descrever alguns dos novos fármacos anticoagulantes que surgem na tentativa de colmatar as limitações da atual terapêutica (heparinas, varfarina e acenocumarol).Métodos: Revisão narrativa de artigos científicos relevantes publicados entre os anos de 2006 e 2012.Resultados: A estratégia destes novos fármacos antitrombóticos baseia-se na inibição seletiva de um fatorde coagulação específico, obtendo assim inibidores seletivos com potencial para serem mais eficazes, seguros e fáceis de usar. Esta nova classe tem como principais alvos a trombina (bivalirudina, desirudina, lepirudina, argatrobana e dabigatrano) e o FXa (fondaparinux, rivaroxabano, o apixabano, edoxabano), verificando-se, no entanto, também o desenvolvimento de um novo antagonista da vitamina K, a tecarfarina, sem as limitações dos que estão atualmente comercializados, o que se deve essencialmente ao metabolismo não ocorrer via citocromo P450.Conclusões: A terapêutica anticoagulante está a ser alvo de uma intensa investigação, de modo a que a sua utilização na prática clínica seja de facto inovadora e revolucionária. Atualmente, em Portugal, ainda só estão aprovados e comercializáveis o fondaparinux sódico, o dabigatrano etexilato e o rivaroxabano.Formifarma2013-09-23info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://doi.org/10.25756/rpf.v5i3.45https://doi.org/10.25756/rpf.v5i3.45Revista Portuguesa de Farmacoterapia / Portuguese Journal of Pharmacotherapy; Vol 5 No 3 (2013): Julho; 30-43Revista Portuguesa de Farmacoterapia; v. 5 n. 3 (2013): Julho; 30-432183-73411647-354Xreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPporhttp://revista.farmacoterapia.pt/index.php/rpf/article/view/45http://revista.farmacoterapia.pt/index.php/rpf/article/view/45/34Direitos de Autor (c) 2017 Revista Portuguesa de Farmacoterapiahttp://creativecommons.org/licenses/by-nc-nd/4.0info:eu-repo/semantics/openAccessRamos, SofiaOliveira Martins, Sofia2023-09-01T04:33:04Zoai:ojs.farmacoterapia.pt:article/45Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T15:11:31.298285Repositório 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 INOVATION IN THE ANTICOAGULANT THERAPY
INOVAÇÃO NA TERAPÊUTICA ANTICOAGULANTE
title INOVATION IN THE ANTICOAGULANT THERAPY
spellingShingle INOVATION IN THE ANTICOAGULANT THERAPY
Ramos, Sofia
title_short INOVATION IN THE ANTICOAGULANT THERAPY
title_full INOVATION IN THE ANTICOAGULANT THERAPY
title_fullStr INOVATION IN THE ANTICOAGULANT THERAPY
title_full_unstemmed INOVATION IN THE ANTICOAGULANT THERAPY
title_sort INOVATION IN THE ANTICOAGULANT THERAPY
author Ramos, Sofia
author_facet Ramos, Sofia
Oliveira Martins, Sofia
author_role author
author2 Oliveira Martins, Sofia
author2_role author
dc.contributor.author.fl_str_mv Ramos, Sofia
Oliveira Martins, Sofia
description Introdution: Atherothrombosis and venous thromboembolism are the leading causes of morbidity and mortality. Anticoagulant therapy is crucial to decrease these factors by preventing the clotting of blood.Objective: Describe some of the new anticoagulant drugs, introduced in an attempt to overcome the limitations of traditional anticoagulant drugs (heparins, warfarin and acenocumarol).Method: Narrative literature review of relevant scientific articles published between 2006 and 2012.Results: A new strategy for the design of new antithrombotic drugs is based on selective inhibition of a specific coagulation factor, with potential to be more effective, safe and easy to use. These include direct thrombin inhibitors (dabigatran, bivalirudin, desirudin, lepirudin and argatroban) and factor Xa inhibitors (otamixaban, rivaroxaban, o apixaban, edoxaban and fondaparinux). Also, a new vitamin K antagonist has been developed, tecarfarin. This does not present the same limitations as the other, which is due essencially to the fact that is not metabolized by CYP450 enzymes.Conclusion: Anticoagulant therapy has been the target of an intense review so that its use in the clinical practice becomes indeed innovative and revolutionary. Currently, in Portugal, only fondaparinux, the dabigatran etexilate and rivaroxaban have been approved and commercialized.
publishDate 2013
dc.date.none.fl_str_mv 2013-09-23
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/10.25756/rpf.v5i3.45
https://doi.org/10.25756/rpf.v5i3.45
url https://doi.org/10.25756/rpf.v5i3.45
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv http://revista.farmacoterapia.pt/index.php/rpf/article/view/45
http://revista.farmacoterapia.pt/index.php/rpf/article/view/45/34
dc.rights.driver.fl_str_mv Direitos de Autor (c) 2017 Revista Portuguesa de Farmacoterapia
http://creativecommons.org/licenses/by-nc-nd/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Direitos de Autor (c) 2017 Revista Portuguesa de Farmacoterapia
http://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 Formifarma
publisher.none.fl_str_mv Formifarma
dc.source.none.fl_str_mv Revista Portuguesa de Farmacoterapia / Portuguese Journal of Pharmacotherapy; Vol 5 No 3 (2013): Julho; 30-43
Revista Portuguesa de Farmacoterapia; v. 5 n. 3 (2013): Julho; 30-43
2183-7341
1647-354X
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_ 1799129985473052672