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The factor VIII:C/VWF:Ag ratio as a useful tool to predict relapse in patients with acquired haemophilia A: A retrospective cohort study.
Trossaert, Marc; Graveleau, Julie; Thiercelin-Legrand, Marie-Françoise; Sigaud, Marianne; Guerrero, Felipe; Neel, Antoine; Fouassier, Marc; Sailler, Laurent; Chauveau, Dominique; Ternisien, Catherine; Huart, Antoine; Gillet, Benjamin; Hamidou, Mohamed; Bene, Marie C; Voisin, Sophie.
Afiliação
  • Trossaert M; Laboratoire d'hémostase, Service d'Hématologie Biologique, CHU de Nantes, France.
  • Graveleau J; Service de Médecine Interne, CHU de Nantes, France.
  • Thiercelin-Legrand MF; Service de Médecine Interne, CHU de Toulouse, France.
  • Sigaud M; Laboratoire d'hémostase, Service d'Hématologie Biologique, CHU de Nantes, France.
  • Guerrero F; Laboratoire d'Hématologie, CHU de Toulouse, France.
  • Neel A; Service de Médecine Interne, CHU de Nantes, France.
  • Fouassier M; Laboratoire d'hémostase, Service d'Hématologie Biologique, CHU de Nantes, France.
  • Sailler L; Laboratoire d'Hématologie, CHU de Toulouse, France.
  • Chauveau D; Département de Néphrologie et Transplantation d'Organes, CHU Rangueil et Université Paul Sabatier, Toulouse, France.
  • Ternisien C; Laboratoire d'hémostase, Service d'Hématologie Biologique, CHU de Nantes, France.
  • Huart A; Service de Médecine Interne, CHU de Toulouse, France.
  • Gillet B; Laboratoire d'hémostase, Service d'Hématologie Biologique, CHU de Nantes, France.
  • Hamidou M; Service de Médecine Interne, CHU de Nantes, France.
  • Bene MC; Laboratoire d'hémostase, Service d'Hématologie Biologique, CHU de Nantes, France.
  • Voisin S; Laboratoire d'Hématologie, CHU de Toulouse, France.
Haemophilia ; 25(3): 527-534, 2019 May.
Article em En | MEDLINE | ID: mdl-31050100
ABSTRACT

INTRODUCTION:

Acquired haemophilia A (AHA) is a rare autoimmune bleeding disorder caused by the presence of autoantibodies against coagulation factor VIII (FVIII). The mortality rate remains high. International recommendations define complete remission as undetectable inhibitor (<0.6 Bethesda Units [BU]) and normal FVIII activity (FVIIIC) that persists after immunosuppressive therapy stopped. For patients achieving remission, the risk of relapse reaches 20%. The risk factors for this relapse are not well known.

AIM:

In this study, we examined the accuracy of the FVIII/W ratio (FVIIIC/von Willebrand Factor Antigen (VWFAg) ratio) to predict relapse in 64 consecutive patients with AHA.

RESULTS:

In this cohort, all patients had a very low FVIII/W ratio at the time of diagnosis, and this value progressively increased in the first weeks of immunosuppressive treatment. In our study, 9/55 (14%) did not achieve complete remission. Twenty-seven patients were followed long enough (more than a year) to show that in the 22 patients who did not relapse, the FVIII/W ratio remained durably normalized. By contrast, in the five patients who relapsed during follow-up, we noted either no normalization of the FVIII/W ratio, or a secondary decrease to an abnormal value of <0.7 after initial normalization. In all patients who relapsed, the ratio was the first abnormal biological result to be observed, always preceding changes in the activated partial thromboplastin time (aPTT), FVIIIC and anti-FVIII reappearance.

CONCLUSION:

These data suggest that the FVIII/W ratio could be considered a sensitive biological marker to predict recovery and/or relapse in AHA.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fator VIII / Fator de von Willebrand / Hemofilia A Tipo de estudo: Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Haemophilia Assunto da revista: HEMATOLOGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fator VIII / Fator de von Willebrand / Hemofilia A Tipo de estudo: Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Haemophilia Assunto da revista: HEMATOLOGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: França
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