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Rivaroxaban for treatment of suspected or confirmed heparin-induced thrombocytopenia study.
Linkins, L A; Warkentin, T E; Pai, M; Shivakumar, S; Manji, R A; Wells, P S; Wu, C; Nazi, I; Crowther, M A.
Afiliação
  • Linkins LA; Department of Medicine, McMaster University, TAARI, Hamilton, ON, Canada.
  • Warkentin TE; Department of Medicine, McMaster University, TAARI, Hamilton, ON, Canada.
  • Pai M; Department of Pathology and Molecular Medicine, McMaster University, Hamilton, ON, Canada.
  • Shivakumar S; Department of Medicine, McMaster University, TAARI, Hamilton, ON, Canada.
  • Manji RA; Department of Pathology and Molecular Medicine, McMaster University, Hamilton, ON, Canada.
  • Wells PS; Department of Medicine, Dalhousie University, Halifax, NS, Canada.
  • Wu C; Department of Surgery and Cardiac Sciences Program, University of Manitoba, Winnipeg, MB, Canada.
  • Nazi I; Department of Medicine, University of Ottawa, Ottawa Hospital Research Institute, Ottawa, Canada.
  • Crowther MA; Department of Medicine, University of Alberta, Edmonton, AB, Canada.
J Thromb Haemost ; 14(6): 1206-10, 2016 06.
Article em En | MEDLINE | ID: mdl-27061271
ABSTRACT
UNLABELLED Essentials Heparin-induced thrombocytopenia (HIT) is a thrombogenic condition that is difficult to treat. We evaluated rivaroxaban as a treatment option in patients with suspected or confirmed HIT. One patient had recurrent thrombosis and 9/10 patients with thrombocytopenia had platelet recovery. Rivaroxaban may be an effective and safe treatment option for HIT.

SUMMARY:

Background Rivaroxaban is a direct oral anti-Xa inhibitor that has the potential to greatly simplify treatment of heparin-induced thrombocytopenia (HIT). Objectives To evaluate the efficacy and safety of rivaroxaban in this patient population, we conducted a multicenter, single-arm, prospective cohort study of patients with suspected or confirmed HIT. Patients/Methods Twenty-two consecutive adults with suspected or confirmed HIT received rivaroxaban 15 mg bid until a local HIT assay result was available. Participants with a positive local assay result continued rivaroxaban 15 mg bid until platelet recovery (or until day 21 if they had acute thrombosis at study entry), then stepped down to rivaroxaban 20 mg daily until day 30. Results and Conclusions The primary outcome measure, incidence of new symptomatic, objectively-confirmed venous and arterial thromboembolism at 30 days, occurred in one HIT-positive participant (4.5%; 95% confidence interval [CI], 0-23.5%) and one HIT-positive participant required limb amputation despite platelet recovery. Platelet recovery was achieved in nine out of 10 HIT-positive patients with thrombocytopenia. Rivaroxaban appears to be effective for treating patients with confirmed HIT, although the small number of patients enrolled limits precision.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Trombocitopenia / Heparina / Inibidores do Fator Xa / Rivaroxabana Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País/Região como assunto: America do norte Idioma: En Revista: J Thromb Haemost Assunto da revista: HEMATOLOGIA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Trombocitopenia / Heparina / Inibidores do Fator Xa / Rivaroxabana Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País/Região como assunto: America do norte Idioma: En Revista: J Thromb Haemost Assunto da revista: HEMATOLOGIA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Canadá