Adverse events in low versus normal body weight patients prescribed apixaban for atrial fibrillation.


Journal

Journal of thrombosis and thrombolysis
ISSN: 1573-742X
Titre abrégé: J Thromb Thrombolysis
Pays: Netherlands
ID NLM: 9502018

Informations de publication

Date de publication:
May 2023
Historique:
accepted: 15 01 2023
medline: 1 5 2023
pubmed: 31 1 2023
entrez: 30 1 2023
Statut: ppublish

Résumé

Safety and efficacy of direct oral anticoagulants (DOAC) in low weight patients with atrial fibrillation (AF) is unclear due to few low body weight patients enrolled in clinical trials. To assess bleeding and thrombotic event rates for patients with AF that are prescribed apixaban and have a low versus normal body weight. We analyzed patients with AF prescribed apixaban from 2017 to 2020 with at least 12 months of follow-up. Patients were divided into low [< 60 kg (kg)] and normal (60-100 kg) weight cohorts. Bleeding and thrombotic event rates were compared. Poisson regression and Cox proportional hazard models were used to estimate adjusted adverse event rates. A total of 545 patients met inclusion criteria. In the unadjusted analysis, there was an increase in non-major bleeding events requiring an Emergency Department visit more often in the low versus normal weight cohort (10.8 versus 7.4 per 100 patient-years, p = 0.15). Thrombotic event rates also occurred more often in the lower versus normal weight cohort (2.4 versus 0.9 per 100 patient-years, p = 0.09). However, adjusted analysis found no statistically significant difference in bleeding or thrombotic events between low and normal weight cohorts. The adjusted hazard ratio for bleeding was similar between the two weight cohorts. The use of apixaban in low body weight patients was not associated with higher rates of bleeding or thrombotic events, compared to those with normal body weight, after adjusting for potential confounding covariates. Larger studies may offer further insight into the overall safety and efficacy of DOAC therapy in these patients.

Identifiants

pubmed: 36715882
doi: 10.1007/s11239-023-02777-y
pii: 10.1007/s11239-023-02777-y
doi:

Substances chimiques

Warfarin 5Q7ZVV76EI
apixaban 3Z9Y7UWC1J
Anticoagulants 0
Rivaroxaban 9NDF7JZ4M3
Pyridones 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

680-684

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Références

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doi: 10.1111/jth.13139 pubmed: 26356595
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doi: 10.1093/ajhp/zxaa059 pubmed: 32426845
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Auteurs

Deborah DeCamillo (D)

Division of Cardiovascular Medicine, Department of Internal Medicine, Frankel Cardiovascular Center, University of Michigan, Ann Arbor, MI, USA. debdecam@med.umich.edu.
Division of Vascular and Cardiovascular Medicine, University of Michigan, Arbor Lakes, Building 3, Floor 3 (MCORRP) 4251 Plymouth Road, Ann Arbor, MI, 48105, USA. debdecam@med.umich.edu.

Brian Haymart (B)

Division of Vascular and Cardiovascular Medicine, University of Michigan, Arbor Lakes, Building 3, Floor 3 (MCORRP) 4251 Plymouth Road, Ann Arbor, MI, 48105, USA.

Xiaowen Kong (X)

Division of Cardiovascular Medicine, Department of Internal Medicine, Frankel Cardiovascular Center, University of Michigan, Ann Arbor, MI, USA.

Scott Kaatz (S)

Division of Hospital Medicine, Henry Ford Health, Detroit, MI, USA.

Mona A Ali (MA)

Department of Heart and Vascular Services, Corewell Health William Beaumont University Hospital, Royal Oak, MI, USA.

Geoffrey D Barnes (GD)

Division of Cardiovascular Medicine, Department of Internal Medicine, Frankel Cardiovascular Center, University of Michigan, Ann Arbor, MI, USA.

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