Treatment of high-risk bleeding with susoctocog alfa in a patient with acquired haemophilia A and a nosocomial severe acute respiratory syndrome coronavirus 2 infection

UDC.coleccionInvestigaciónes_ES
UDC.endPage179es_ES
UDC.grupoInvFarmacia hospitalaria (INIBIC)es_ES
UDC.institutoCentroINIBIC - Instituto de Investigacións Biomédicas de A Coruñaes_ES
UDC.issue3es_ES
UDC.journalTitleEuropean Journal of Hospital Pharmacyes_ES
UDC.startPage177es_ES
UDC.volume30es_ES
dc.contributor.authorFernández-Oliveira, Carla
dc.contributor.authorRotea-Salvo, Sandra
dc.contributor.authorFernández-Docampo, Marta
dc.contributor.authorGonzález-Piñeiro, Sara
dc.contributor.authorMartín-Herranz, Isabel
dc.date.accessioned2025-02-19T08:25:40Z
dc.date.available2025-02-19T08:25:40Z
dc.date.issued2023-04-21
dc.descriptionCase reportes_ES
dc.description.abstract[Abstract] We report the case of a man in his early 70s with idiopathic acquired haemophilia A and persistent high-titre type II inhibitors on immunosuppressive treatment to eradicate the inhibitor. As complications, he had a nosocomial severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, which caused severe pneumonia and an explosive inflammatory reaction that required tocilizumab and remdesivir treatment, and a high-risk retroperitoneal haematoma. Recombinant porcine factor VIII, susoctocog alfa, was requested from the Pharmacy Service in view of the extreme risk of thromboembolism resulting from the concomitant inflammatory storm caused by SARS-CoV-2. Improvement in the SARS-CoV-2 infection made it possible to complete the immunosuppressive treatment with rituximab. The patient was discharged with mycophenolate mofetil as immunosuppressive treatment after 89 days in hospital and 22 days of treatment with susoctocog alfa. His SARS-CoV-2 infection resolved and the haematoma evolved favourably.es_ES
dc.identifier.citationFernández-Oliveira C, Rotea-Salvo S, Fernández-Docampo M, González-Piñeiro S, Martín-Herranz I. Treatment of high-risk bleeding with susoctocog alfa in a patient with acquired haemophilia A and a nosocomial severe acute respiratory syndrome coronavirus 2 infection. Eur J Hosp Pharm. 2023 May;30(3):177-179.es_ES
dc.identifier.doi10.1136/ejhpharm-2021-002805
dc.identifier.issn2047-9956
dc.identifier.urihttp://hdl.handle.net/2183/41206
dc.language.isoenges_ES
dc.publisherBMJes_ES
dc.relation.urihttps://doi.org/10.1136/ejhpharm-2021-002805es_ES
dc.rights.accessRightsopen accesses_ES
dc.subjectCOVID-19es_ES
dc.subjectClinical laboratory techniqueses_ES
dc.subjectDrug monitoringes_ES
dc.subjectDrug-related side effects and adverse reactionses_ES
dc.subjectHematologyes_ES
dc.subjectPharmaceutical preparationses_ES
dc.titleTreatment of high-risk bleeding with susoctocog alfa in a patient with acquired haemophilia A and a nosocomial severe acute respiratory syndrome coronavirus 2 infectiones_ES
dc.typejournal articlees_ES
dspace.entity.typePublication

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