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Equivalent thrombotic risk with Warfarin, Dabigatran, or Enoxaparin after failure of initial direct oral anticoagulation (DOAC) therapy.
Shyu, Margaret; Liu, Angela; Srikureja, Anya; Gregorian, Alison; Srisuwananukorn, Andrew; Tremblay, Douglas; Naymagon, Leonard.
Affiliation
  • Shyu M; Icahn School of Medicine at Mount Sinai, New York, NY, USA. mshyu@stanford.edu.
  • Liu A; Division of Oncology, Stanford University School of Medicine, 300 Pasteur Drive MC 5151, Stanford, CA, USA. mshyu@stanford.edu.
  • Srikureja A; Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, United States of America.
  • Gregorian A; Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Srisuwananukorn A; Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, United States of America.
  • Tremblay D; Division of Hematology, The Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.
  • Naymagon L; Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, United States of America.
J Thromb Thrombolysis ; 57(5): 871-876, 2024 Jun.
Article de En | MEDLINE | ID: mdl-38643437
ABSTRACT

BACKGROUND:

The direct oral anticoagulants (DOACs) are now commonly regarded as first line anticoagulants in most cases of venous thromboembolism (VTE). However, the optimal choice of subsequent anticoagulant in instances of first line DOAC failure is unclear.

OBJECTIVES:

To describe and compare outcomes with second line anticoagulants used after DOAC failure.

METHODS:

Patients seen at an urban hospital system for an episode of acute VTE initially treated with either apixaban or rivaroxaban who experienced a subsequent recurrent thrombosis while on anticoagulation (1st recurrent thrombosis) were included.

RESULTS:

In total, 166 patients after apixaban or rivaroxaban failure were included. Following DOAC failure (1st recurrent thrombosis), the subsequent anticoagulant was warfarin in 60 patients (36%), dabigatran in 42 patients (25%), and enoxaparin in 64 patients (39%). Enoxaparin was preferentially prescribed in patients with a malignancy-associated etiology for 1st recurrent thrombosis (p < 0.01). The median follow-up time in our cohort was 16 months. There was no difference in 2nd recurrent thrombosis-free survival (p = 0.72) or risk for major bleeding event (p = 0.30) among patients treated with dabigatran, warfarin, or enoxaparin.

CONCLUSIONS:

In this retrospective analysis of patients failing first line DOAC therapy, rates of 2nd recurrent thrombosis and bleeding did not differ among subsequently chosen anticoagulants. Our study provides evidence that the optimal 2nd anticoagulant is not clear, and the choice of 2nd anticoagulant should continue to balance patient preference, cost, and provider experience.
Sujet(s)
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Warfarine / Énoxaparine / Thromboembolisme veineux / Dabigatran / Anticoagulants Limites: Aged / Female / Humans / Male / Middle aged Langue: En Journal: J Thromb Thrombolysis Sujet du journal: ANGIOLOGIA Année: 2024 Type de document: Article Pays d'affiliation: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Warfarine / Énoxaparine / Thromboembolisme veineux / Dabigatran / Anticoagulants Limites: Aged / Female / Humans / Male / Middle aged Langue: En Journal: J Thromb Thrombolysis Sujet du journal: ANGIOLOGIA Année: 2024 Type de document: Article Pays d'affiliation: États-Unis d'Amérique