Literature DB >> 31724442

Use of Direct Oral Anticoagulants in Patients with Sickle Cell Disease and Venous Thromboembolism: A Prospective Cohort Study of 12 Patients.

Jacques-Robert Christen1, Julien Bertolino1, Estelle Jean1, Laurence Camoin2, Mikael Ebbo1, Jean-Robert Harlé1, Nicolas Schleinitz1, Gabrielle Sarlon3, Emmanuelle Bernit1.   

Abstract

Patients with sickle cell disease have an increased risk of venous thromboembolism (VTE) and with a mortality 2-fold higher. The anticoagulation of VTE in a young population is an important question. Indeed, hemorrhagic complications of anticoagulation may occur more frequently than in the general population. The use of a direct oral anticoagulant (DOAC) is not recommended for VTE in patients with sickle cell disease because those patients were not included in the clinical studies. We aimed to study the safety of using DOACs in a prospective cohort of patients with sickle cell disease and VTE. We prospectively followed the cohort of all sickle cell disease patients undergoing recent DOAC treatment for VTE at a sickle cell disease reference center. Twelve patients received rivaroxaban for VTE (eight women and four men). The median age was 27 years (20-45). The sickle cell disease variants included homozygous Hb SS (HBB: c.20A>T) in eight patients, Hb S-β+-thalassemia (Hb S-β+-thal) in two, Hb S-β0-thal in one and Hb S-Hb C (HBB: c.19G>A) in one. The cumulative duration of follow-up was 3134 days under rivaroxaban treatment. There were two thrombotic events, including a patient with a double positivity of antiphospholipid antibodies. No major bleeding was observed, and 6/12 patients presented minor bleeding (epistaxis: n = 4; anal fissure bleeding: n = 1; menorrhagia n = 4). Of these, 3/6 required their treatment to be switched to apixaban, which stopped the bleeding. Direct oral anticoagulants may be an alternative treatment for VTE in patients with sickle cell disease, except for an associated antiphospholipid syndrome.

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Keywords:  Apixaban; Rivaroxaban; direct oral anticoagulants (DOACs); sickle cell disease; venous thromboembolism (VTE)

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Year:  2019        PMID: 31724442     DOI: 10.1080/03630269.2019.1689997

Source DB:  PubMed          Journal:  Hemoglobin        ISSN: 0363-0269            Impact factor:   0.849


  3 in total

Review 1.  Abnormal uterine bleeding in users of rivaroxaban and apixaban.

Authors:  Amanda E Jacobson-Kelly; Bethany T Samuelson Bannow
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2020-12-04

2.  Anticoagulation strategies and recurrence of venous thromboembolic events in patients with sickle cell disease: a systematic review and meta-analysis.

Authors:  Nadirah El-Amin; Audra Iness; John W Cyrus; India Sisler; Oliver Karam
Journal:  Ann Hematol       Date:  2022-07-27       Impact factor: 4.030

3.  Thrombin activation of PAR-1 contributes to microvascular stasis in mouse models of sickle cell disease.

Authors:  Erica M Sparkenbaugh; Chunsheng Chen; Tomasz Brzoska; Julia Nguyen; Shaobin Wang; Gregory M Vercellotti; Nigel S Key; Prithu Sundd; John D Belcher; Rafal Pawlinski
Journal:  Blood       Date:  2020-05-14       Impact factor: 25.476

  3 in total

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