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Management of acquired hemophilia A: results from the Spanish registry.


ABSTRACT: The Spanish Acquired Hemophilia A (AHA) Registry is intended to update the status of AHA in Spain. One hundred and fifty-four patients were included and retrospectively followed for a median of 12 months. Patients were predominantly male (56.3%), with median age at diagnosis of 74 years. AHA was more frequently idiopathic (44.1%) and autoimmune disorder-associated (31.7%). Thirty-four percent of patients were on antithrombotic therapy at diagnosis. Hemostatic treatment was used in 70% of patients. Recombinant activated factor VII was more frequently infused (60.3% vs 20.6% activated prothrombin complex concentrate). Only 1 patient did not achieve control of hemorrhage. Complete remission (CR) was achieved by 84.2% of cases after immunosuppressive therapy. Steroids alone were less efficient than the other strategies (68.2% vs 87.2%, P = .049), whereas no differences existed among these (steroids/cyclophosphamide, 88.5%, vs steroids/calcineurin inhibitors, 81.2%, vs rituximab-based regimens, 87.5%). Female sex and high inhibitor levels influenced CR negatively. Thirty-six deaths (23.8%) were reported. Main causes of death were infection (15 patients, 9.9%) and hemorrhage (5 patients, 3.3%). All hemorrhage-related and half the infection-related deaths occurred within 2 months of diagnosis. Prior antithrombotic therapy was inversely associated with survival, irrespective of age. Median age of nonsurvivors was significantly higher (79 vs 73 years in survivors). Patients dying of infection were older than the other nonsurvivors (85 vs 78 years). In summary, fatal infection in the first months is common in our series. Antithrombotic therapy is associated with mortality. Particular care should be taken to avoid misdiagnosis.

SUBMITTER: Mingot-Castellano ME 

PROVIDER: S-EPMC8679668 | biostudies-literature | 2021 Oct

REPOSITORIES: biostudies-literature

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Management of acquired hemophilia A: results from the Spanish registry.

Mingot-Castellano María-Eva ME   Pardos-Gea Josep J   Haya Saturnino S   Bastida-Bermejo José-María JM   Tàssies Dolors D   Marco-Rico Ana A   Núñez Ramiro R   García-Candel Faustino F   de Mora María-Carmen Fernández-Sanchez MF   Soto Inmaculada I   Álvarez-Román María-Teresa MT   Asenjo Susana S   Carrasco Marina M   Lluch-García Rafael R   Martín-Antorán José-Manuel JM   Rodríguez-Alén Agustín A   Roselló Elena E   Torres-Miñana Laura L   Marcellini-Antonio Shally S   Moretó-Quinana Ana A   Rodríguez-García José-Antonio JA   Aguinaco-Culebras Reyes R   Alonso-Escobar Nieves N   Cervero-Santiago Carlos C   Fernández-Mosteirín Núria N   Martínez-Badás María-Paz MP   Pérez-Sánchez Montserrat M   Pérez-Montes Rocío R   Rodríguez-González Ramón R   Uribe-Barrientos Marisol M   Caparrós-Miranda Isabel Socorro IS   Iglesias-Fernández Miriam M   Baena Ángela Á   Rodríguez-López Manuel M   Sebrango-Sandia Ana A   Vázquez-Fernández Irene I   Marco Pascual P  

Blood advances 20211001 19


The Spanish Acquired Hemophilia A (AHA) Registry is intended to update the status of AHA in Spain. One hundred and fifty-four patients were included and retrospectively followed for a median of 12 months. Patients were predominantly male (56.3%), with median age at diagnosis of 74 years. AHA was more frequently idiopathic (44.1%) and autoimmune disorder-associated (31.7%). Thirty-four percent of patients were on antithrombotic therapy at diagnosis. Hemostatic treatment was used in 70% of patient  ...[more]

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