4.5 Article

Off-label underdosed apixaban use in Asian patients with non-valvular atrial fibrillation

Journal

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/ehjcvp/pvab004

Keywords

Atrial fibrillation; Anticoagulation; Direct oral anticoagulant; Stroke; Off-label underdose

Funding

  1. Korea government (Ministry of Science and ICT) [202013B14]
  2. Korea government (Ministry of Trade, Industry and Energy) [202013B14]
  3. Korea government (Ministry of Health & Welfare, Republic of Korea) [202013B14]
  4. Korea government (Ministry of Food and Drug Safety) [202013B14]
  5. Korea National Research Foundation - Ministry of Education, Science and Technology [2020R1F1A106740]

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In Asian patients with atrial fibrillation, off-label underdosed apixaban use without meeting dose reduction criteria was associated with higher risks of ischemic stroke and all-cause death compared to on-label standard dose apixaban use.
Aims To compare the effectiveness and safety of off-label underdosed apixaban with on-label standard dose apixaban in Asian patients with atrial fibrillation (AF). Methods and results Using the Korean nationwide claims database, we identified patients who were prescribed apixaban and did not fulfil the dose reduction criteria for apixaban between January 2015 and December 2017. A multivariable Cox hazard regression model was performed, and hazard ratios (HRs) for ischaemic stroke, major bleeding (MB), all-cause death, and composite outcome were analysed. Compared to patients prescribed on-label standard dose apixaban (n=4194), patients prescribed off-label underdosed apixaban (n=2890) showed a higher risk of ischaemic stroke [adjusted HR (aHR) 1.38, 95% confidence interval (CI) 1.06-1.81], all-cause death (aHR 1.19, 95% CI 1.01-1.39), and the composite outcome (aHR 1.17, 95% CI 1.03-1.34), but with no significant differences in MB between the two groups. Among the patients who did not meet any dose reduction criteria, off-label underdosed apixaban use was associated with a significantly higher risk of ischaemic stroke than on-label standard dose apixaban use (aHR 1.85, 95% CI 1.25-2.73). Among the patients who met a single dose reduction criterion, off-label underdosed apixaban use was associated with a higher risk of all-cause death than on-label standard dose apixaban (aHR 1.32, 95% CI 1.07-1.64). Conclusion The off-label underdosed apixaban group showed higher risks of ischaemic stroke, all-cause death, and composite clinical outcomes than the on-label standard dose apixaban group, but both showed comparable risks of MB. Label adherence to apixaban dosing should be emphasized to achieve the best clinical outcomes for Asian patients with AF.

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