Key result
Among patients with high factor Xa levels, age ≥80 linked to ~547% higher major bleeding risk.
Why the study?
Differences in the exposure-response relationship for factor Xa inhibitors between patients aged ≥ 80 and < 80 years were not well characterized.
Does age ≥ 80 years modify the association between high factor Xa inhibitor concentrations and major bleeding risk in patients with atrial fibrillation?
Cohort (n=1,037)
Does age ≥ 80 years modify the association between high factor Xa inhibitor concentrations and major bleeding risk in patients with atrial fibrillation?
Effect estimate: aHR 6.47 (95% CI 2.07-20.28)
In patients with atrial fibrillation, those aged ≥ 80 years are particularly vulnerable to major bleeding when exposed to high factor Xa inhibitor concentrations compared to younger patients.
Suggests greater bleeding vulnerability to high FXaI levels in elderly AF patients; leaves open whether monitoring or dose adjustment improves outcomes.
This study aimed to analyze differences in the exposure-response relationship for factor Xa inhibitors (FXaI) between patients aged ≥ 80 and < 80 years. Patients with atrial fibrillation (AF) taking rivaroxaban, apixaban, or edoxaban were enrolled, and a single steady-state trough concentration was measured. FXaI concentrations were compared with the expected range reported in clinical trials to define high or low drug levels. The primary outcome was major bleeding, and the secondary outcome was ischemic stroke or transient ischemic attack (IS/TIA). From 2016 to 2023, 1,037 patients aged from 30 to 105 years were enrolled (average, 75.4 ± 10.0 years; 33.8% were aged ≥ 80 years). During a median follow-up of 2.35 years, 48 major bleeding events and 32 IS/TIA events were observed. Although drug concentrations were similar between the two age groups, those aged ≥ 80 years with high FXaI levels experienced a greater increase in major bleeding risk compared to those aged < 80 years with high levels (aHR 6.47 [2.07, 20.28] vs. 3.45 [1.15, 10.30]). Additionally, patients aged ≥ 80 years without elevated FXaI levels also had a higher risk of major bleeding compared to those aged < 80 years without elevated levels (aHR 2.39 [1.20, 4.76]). While low FXaI concentrations were associated with IS/TIA, the risk was not significantly different across age groups. In conclusion, despite similar FXaI concentrations, patients aged ≥ 80 years have a higher baseline risk of major bleeding and experience a greater increase in bleeding risk at high drug levels compared to those aged < 80 years.
No takes yet. Share an insight, caveat, or question.
Lin et al. (2025) conducted a cohort in Atrial fibrillation (n=1,037). Factor Xa inhibitors (rivaroxaban, apixaban, edoxaban) vs. Patients aged < 80 years was evaluated on Major bleeding (aHR 6.47, 95% CI 2.07-20.28). Patients aged ≥80 years with high factor Xa inhibitor levels experienced a greater increase in major bleeding risk (aHR 6.47; 95% CI 2.07-20.28) compared to those aged <80 years with high levels.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: