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Safety and efficacy of oral anticoagulants in extreme weights.
Chin-Hon, J; Davenport, L; Huang, J; Akerman, M; Hindenburg, A.
Afiliación
  • Chin-Hon J; NYU Langone Hospital - Long Island, Department of Pharmacy, United States of America; NYU Long Island School of Medicine, United States of America. Electronic address: jamie.chin@nyulangone.org.
  • Davenport L; NYU Langone Hospital - Long Island, Department of Pharmacy, United States of America.
  • Huang J; Perlmutter Cancer Center at NYU Langone Hematology Oncology Associates - Mineola, United States of America.
  • Akerman M; NYU Long Island School of Medicine, United States of America.
  • Hindenburg A; NYU Long Island School of Medicine, United States of America; Perlmutter Cancer Center at NYU Langone Hematology Oncology Associates - Mineola, United States of America.
Thromb Res ; 231: 1-6, 2023 11.
Article en En | MEDLINE | ID: mdl-37738772
ABSTRACT

BACKGROUND:

The 2021 International Society on Thrombosis and Haemostasis' (ISTH) recommends standard doses of apixaban and rivaroxaban regardless of high body mass index (BMI) and weight, but had not compare DOACs head-to-head in obesity or address underweight patients.

METHODS:

Our aim is to evaluate the safety and efficacy of DOACs in underweight and obese patients compared to warfarin. The primary endpoints include incidence of thromboembolic and bleeding events. Descriptive statistics was used for continuous variables. The Kruskal-Wallis test was used to compare the four-groups for continuous measures and the chi-square test or Fisher's exact test was used to analyze categorical data. The chi-square test or Fisher's exact test, was used for categorical variables, and the Mann-Whitney test (the non-parametric counterpart to the two-sample t-test) for continuous data.

RESULTS:

Of 2940 patients receiving anticoagulation for venous thromboembolism (VTE) treatment or atrial fibrillation (AF), 492 met eligibility criteria. Within each group, 248 patients received warfarin, 101 received apixaban, 100 received rivaroxaban and 43 received dabigatran. Patients were characterized in 4 body mass index (BMI) categories, in which 80 were underweight and 412 were obese.

CONCLUSIONS:

When each DOAC was compared to warfarin in rates of VTE, apixaban showed statistically significant lower rate of VTE (p = 0.0149). However, no statistical significance was identified in the rate of VTE between DOACs combined vs. warfarin (p = 0.1529). When each DOAC was compared to warfarin, apixaban showed the lowest rate of overall bleeding (p = 0.0194). However, no statistical difference in the rate of bleeding was observed between DOACs combined vs. warfarin (p = 0.3284). Patients with extreme body weights requiring anticoagulation for VTE and AF may safety benefit from DOAC therapy. This evaluation showed apixaban with the lowest rate of VTE and bleeding compared to warfarin, rivaroxaban, and dabigatran. These results provide experience for the clinician to use DOACs, particularly apixaban, in underweight and obese populations.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fibrilación Atrial / Tromboembolia Venosa Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Thromb Res Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fibrilación Atrial / Tromboembolia Venosa Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Thromb Res Año: 2023 Tipo del documento: Article