Cholecystectomy in a man with hemophilia A and inhibitor on emicizumab prophylaxis: a case report

Detalhes bibliográficos
Autor(a) principal: Paula Cella Giacometto
Data de Publicação: 2021
Outros Autores: Marcello Tortelli Bavaresco, Juliana Alvares Teodoro, Ricardo Mesquita Camelo
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Institucional da UFMG
Texto Completo: https://doi.org/10.1016/j.htct.2022.10.003
http://hdl.handle.net/1843/56591
https://orcid.org/0000-0002-4023-275X
https://orcid.org/0000-0003-3685-1555
https://orcid.org/0000-0002-0210-0721
https://orcid.org/0000-0001-9025-0289
Resumo: Inherited hemophilia A is a rare bleeding disorder due to absent/reduced activity of the clotting factor VIII (FVIII).1 Therefore, its treatment is based on regular FVIII infusions to prevent (i.e., prophylaxis) or treat (i.e., on demand) bleedings.1 The most impacting complication of this treatment is the development of anti-FVIII antibodies (i.e., inhibitors).1 Inhibitors reduce/abolish the clotting activity of FVIII, rendering the patients with the previous or worse bleeding phenotype, which ultimately leads to increased morbimortality.1 Although bypassing agents (recombinant activated factor VII [rFVIIa] and partially activated prothrombin complex [aPCC]) can be prescribed for both prophylactic and on-demand treatments, the current recommended prophylactic drug in such cases is the humanized bispecific antibody emicizumab.1,2 Emicizumab mimics the clotting effect of FVIII and, since its structure is not similar to the FVIII structure, anti-FVIII inhibitors have no effect on its clotting activity.1,2 There are few reports about the hemostatic effectiveness and safety of this biopharmaceutical on major non-orthopedic surgeries.3, 4, 5 In addition, since the introduction of emicizumab in the armamentarium for hemophilia treatment in Brazil, in 2018, no major surgical procedures have been reported in Brazilian patients on emicizumab prophylaxis. Herein we described a man with severe hemophilia A and high-responding inhibitor under emicizumab prophylaxis who was submitted to open cholecystectomy due to acute-on-chronic calculous cholecystitis. This report was approved by the local Committee on Ethics on Research (May/29/2019). The patient signed the Consent Form before his data was reviewed on the hospital medical files.
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spelling 2023-07-18T16:50:29Z2023-07-18T16:50:29Z20214314https://doi.org/10.1016/j.htct.2022.10.0032531-1379http://hdl.handle.net/1843/56591https://orcid.org/0000-0002-4023-275Xhttps://orcid.org/0000-0003-3685-1555https://orcid.org/0000-0002-0210-0721https://orcid.org/0000-0001-9025-0289Inherited hemophilia A is a rare bleeding disorder due to absent/reduced activity of the clotting factor VIII (FVIII).1 Therefore, its treatment is based on regular FVIII infusions to prevent (i.e., prophylaxis) or treat (i.e., on demand) bleedings.1 The most impacting complication of this treatment is the development of anti-FVIII antibodies (i.e., inhibitors).1 Inhibitors reduce/abolish the clotting activity of FVIII, rendering the patients with the previous or worse bleeding phenotype, which ultimately leads to increased morbimortality.1 Although bypassing agents (recombinant activated factor VII [rFVIIa] and partially activated prothrombin complex [aPCC]) can be prescribed for both prophylactic and on-demand treatments, the current recommended prophylactic drug in such cases is the humanized bispecific antibody emicizumab.1,2 Emicizumab mimics the clotting effect of FVIII and, since its structure is not similar to the FVIII structure, anti-FVIII inhibitors have no effect on its clotting activity.1,2 There are few reports about the hemostatic effectiveness and safety of this biopharmaceutical on major non-orthopedic surgeries.3, 4, 5 In addition, since the introduction of emicizumab in the armamentarium for hemophilia treatment in Brazil, in 2018, no major surgical procedures have been reported in Brazilian patients on emicizumab prophylaxis. Herein we described a man with severe hemophilia A and high-responding inhibitor under emicizumab prophylaxis who was submitted to open cholecystectomy due to acute-on-chronic calculous cholecystitis. This report was approved by the local Committee on Ethics on Research (May/29/2019). The patient signed the Consent Form before his data was reviewed on the hospital medical files.porUniversidade Federal de Minas GeraisUFMGBrasilFAR - DEPARTAMENTO DE FARMÁCIA SOCIALHematology, Transfusion and Cell TherapyHemofiliaInibidoresColecistectomiaHemophilia AInhibitorEmicizumabSurgeryCholecystectomyCholecystectomy in a man with hemophilia A and inhibitor on emicizumab prophylaxis: a case reportinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://www.sciencedirect.com/science/article/pii/S2531137922014584?via%3DihubPaula Cella GiacomettoMarcello Tortelli BavarescoJuliana Alvares TeodoroRicardo Mesquita Cameloinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFMGinstname:Universidade Federal de Minas Gerais (UFMG)instacron:UFMGLICENSELicense.txtLicense.txttext/plain; charset=utf-82042https://repositorio.ufmg.br/bitstream/1843/56591/1/License.txtfa505098d172de0bc8864fc1287ffe22MD51ORIGINALCholecystectomyinamanwithhemophiliaAand inhibitoronemicizumabprophylaxis Acasereport.pdfCholecystectomyinamanwithhemophiliaAand inhibitoronemicizumabprophylaxis Acasereport.pdfapplication/pdf466255https://repositorio.ufmg.br/bitstream/1843/56591/2/CholecystectomyinamanwithhemophiliaAand%20inhibitoronemicizumabprophylaxis%20Acasereport.pdfe642fa762df68bd4ed4c68e28c228086MD521843/565912023-07-18 13:50:29.534oai:repositorio.ufmg.br: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Repositório de PublicaçõesPUBhttps://repositorio.ufmg.br/oaiopendoar:2023-07-18T16:50:29Repositório Institucional da UFMG - Universidade Federal de Minas Gerais (UFMG)false
dc.title.pt_BR.fl_str_mv Cholecystectomy in a man with hemophilia A and inhibitor on emicizumab prophylaxis: a case report
title Cholecystectomy in a man with hemophilia A and inhibitor on emicizumab prophylaxis: a case report
spellingShingle Cholecystectomy in a man with hemophilia A and inhibitor on emicizumab prophylaxis: a case report
Paula Cella Giacometto
Hemophilia A
Inhibitor
Emicizumab
Surgery
Cholecystectomy
Hemofilia
Inibidores
Colecistectomia
title_short Cholecystectomy in a man with hemophilia A and inhibitor on emicizumab prophylaxis: a case report
title_full Cholecystectomy in a man with hemophilia A and inhibitor on emicizumab prophylaxis: a case report
title_fullStr Cholecystectomy in a man with hemophilia A and inhibitor on emicizumab prophylaxis: a case report
title_full_unstemmed Cholecystectomy in a man with hemophilia A and inhibitor on emicizumab prophylaxis: a case report
title_sort Cholecystectomy in a man with hemophilia A and inhibitor on emicizumab prophylaxis: a case report
author Paula Cella Giacometto
author_facet Paula Cella Giacometto
Marcello Tortelli Bavaresco
Juliana Alvares Teodoro
Ricardo Mesquita Camelo
author_role author
author2 Marcello Tortelli Bavaresco
Juliana Alvares Teodoro
Ricardo Mesquita Camelo
author2_role author
author
author
dc.contributor.author.fl_str_mv Paula Cella Giacometto
Marcello Tortelli Bavaresco
Juliana Alvares Teodoro
Ricardo Mesquita Camelo
dc.subject.por.fl_str_mv Hemophilia A
Inhibitor
Emicizumab
Surgery
Cholecystectomy
topic Hemophilia A
Inhibitor
Emicizumab
Surgery
Cholecystectomy
Hemofilia
Inibidores
Colecistectomia
dc.subject.other.pt_BR.fl_str_mv Hemofilia
Inibidores
Colecistectomia
description Inherited hemophilia A is a rare bleeding disorder due to absent/reduced activity of the clotting factor VIII (FVIII).1 Therefore, its treatment is based on regular FVIII infusions to prevent (i.e., prophylaxis) or treat (i.e., on demand) bleedings.1 The most impacting complication of this treatment is the development of anti-FVIII antibodies (i.e., inhibitors).1 Inhibitors reduce/abolish the clotting activity of FVIII, rendering the patients with the previous or worse bleeding phenotype, which ultimately leads to increased morbimortality.1 Although bypassing agents (recombinant activated factor VII [rFVIIa] and partially activated prothrombin complex [aPCC]) can be prescribed for both prophylactic and on-demand treatments, the current recommended prophylactic drug in such cases is the humanized bispecific antibody emicizumab.1,2 Emicizumab mimics the clotting effect of FVIII and, since its structure is not similar to the FVIII structure, anti-FVIII inhibitors have no effect on its clotting activity.1,2 There are few reports about the hemostatic effectiveness and safety of this biopharmaceutical on major non-orthopedic surgeries.3, 4, 5 In addition, since the introduction of emicizumab in the armamentarium for hemophilia treatment in Brazil, in 2018, no major surgical procedures have been reported in Brazilian patients on emicizumab prophylaxis. Herein we described a man with severe hemophilia A and high-responding inhibitor under emicizumab prophylaxis who was submitted to open cholecystectomy due to acute-on-chronic calculous cholecystitis. This report was approved by the local Committee on Ethics on Research (May/29/2019). The patient signed the Consent Form before his data was reviewed on the hospital medical files.
publishDate 2021
dc.date.issued.fl_str_mv 2021
dc.date.accessioned.fl_str_mv 2023-07-18T16:50:29Z
dc.date.available.fl_str_mv 2023-07-18T16:50:29Z
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 http://hdl.handle.net/1843/56591
dc.identifier.doi.pt_BR.fl_str_mv https://doi.org/10.1016/j.htct.2022.10.003
dc.identifier.issn.pt_BR.fl_str_mv 2531-1379
dc.identifier.orcid.pt_BR.fl_str_mv https://orcid.org/0000-0002-4023-275X
https://orcid.org/0000-0003-3685-1555
https://orcid.org/0000-0002-0210-0721
https://orcid.org/0000-0001-9025-0289
url https://doi.org/10.1016/j.htct.2022.10.003
http://hdl.handle.net/1843/56591
https://orcid.org/0000-0002-4023-275X
https://orcid.org/0000-0003-3685-1555
https://orcid.org/0000-0002-0210-0721
https://orcid.org/0000-0001-9025-0289
identifier_str_mv 2531-1379
dc.language.iso.fl_str_mv por
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dc.relation.ispartof.pt_BR.fl_str_mv Hematology, Transfusion and Cell Therapy
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv Universidade Federal de Minas Gerais
dc.publisher.initials.fl_str_mv UFMG
dc.publisher.country.fl_str_mv Brasil
dc.publisher.department.fl_str_mv FAR - DEPARTAMENTO DE FARMÁCIA SOCIAL
publisher.none.fl_str_mv Universidade Federal de Minas Gerais
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFMG
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