Key result
Underweight status is linked to a ~5-fold greater likelihood of exceeding peak apixaban concentrations vs normal weight.
Why the study?
DOACs are generally preferred over warfarin, but their efficacy and safety in patients with extremely low body weight are uncertain.
Does low body weight (≤50 kg) increase the risk of exceeding expected peak anti-factor Xa levels in patients taking apixaban compared to normal body weight?
Does low body weight (≤50 kg) increase the risk of exceeding expected peak anti-factor Xa levels in patients taking apixaban compared to normal body weight?
Patients with low body weight (≤50 kg) taking apixaban are significantly more likely to exceed expected peak anti-factor Xa levels, suggesting a potential need for dose adjustment or closer monitoring in this population.
Low body weight was associated with exceeding apixaban Cpeak range; leaves open whether monitoring or adjustment improves outcomes.
Background: Direct oral anticoagulants (DOACs) are generally preferred over warfarin for preventing arterial and venous thromboembolism. However, the efficacy and safety of DOACs in patients with extremely low body weight (BW) are uncertain. This study investigates anti-factor Xa (anti-FXa) activity of apixaban and compares it between patients with normal BW (>50 kg) and underweight (≤50 kg). Methods: We enrolled 150 patients on branded generic apixaban (ApixanTM) for atrial fibrillation (AF), venous thromboembolism, and intracardiac thrombus. Anti-FXa activity of apixaban was measured at peak concentration (Cpeak) and trough concentration (Ctrough) after at least one week of therapy. Results: Mean age was 64.0 ± 12.7 years, with 53.3% being male. Mean BW was 61.3 ± 15.3 kg. Of the 150 patients, 132 (88%) had AF, and 43 (28.7%) had low BW. Overall, 87.3% and 84.7% of patients had Ctrough and Cpeak within the expected range. Underweight patients had significantly higher mean Ctrough and Cpeak than normal BW patients. A higher proportion of low-BW patients exceeded the expected Cpeak range compared to normal-BW patients (25.6% vs. 3.7%, p < 0.001). Low BW was the only independent predictor of exceeding Cpeak specified range (adjusted OR 4.87, 95% CI 1.31–18.15, p = 0.018). Conclusions: Most patients maintained apixaban levels within expected ranges, but those with low BW were more likely to exceed the specified range of Cpeak.
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Wongcharoen et al. (2025) studied this question. Underweight patients on apixaban were 4.87 times more likely to exceed the specified peak concentration range compared to normal weight patients (p < 0.001).
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