Key result
Reduced-dose rivaroxaban linked to ~60% lower all-cause mortality vs full-dose in NVAF patients ≥85 years.
Why the study?
It remained unclear whether treatment with reduced-dose versus full-dose rivaroxaban is associated with all-cause mortality in older patients with nonvalvular atrial fibrillation.
Does reduced-dose rivaroxaban reduce all-cause mortality in older patients (≥85 years) with nonvalvular atrial fibrillation compared to full-dose rivaroxaban?
Cohort (n=2,386)
Does reduced-dose rivaroxaban reduce all-cause mortality in older patients (≥85 years) with nonvalvular atrial fibrillation compared to full-dose rivaroxaban?
Reduced-dose rivaroxaban (10 mg) is associated with lower all-cause mortality and heart failure hospitalization in patients ≥85 years with nonvalvular atrial fibrillation compared to full-dose rivaroxaban.
Answers are grounded in this paper and cite their sources.
May warrant caution with full-dose rivaroxaban in ≥85 y AF; hypothesis-generating and leaves open need for RCTs.
Background: Reduced-dose rivaroxaban (10 mg) was used in the J-ROCKET AF trial, demonstrating safety in the Asian population. It remains unclear whether treatment with reduced-dose versus full-dose rivaroxaban (20 mg/15 mg) is associated with all-cause mortality in older patients with nonvalvular atrial fibrillation. Proposed: To evaluate the effects of reduced-dose rivaroxaban on all-cause mortality in patients over 85. Methods: We retrospectively enrolled medical records representing the period from October 2012 to November 2016. The 2 × 2 factorial design incorporated age (≥85 vs. <85) and rivaroxaban use (reduced vs. full dose). The primary study outcomes were all-cause and cardiac-related mortality. Results: The study enrolled 2386 patients with a mean age of 76.6 ± 10.4 years; 51.8% were male. In the ≥85 group (n = 593), the reduced-dose subgroup had lower all-cause (5.3% vs. 10.6%, p = 0.02) and cardiac-related mortality (1.9% vs. 5.1%, p = 0.04), whereas the younger patients receiving reduced-dose rivaroxaban had higher all-cause mortality (3.7% vs. 1.8%, p = 0.01) but no difference in cardiac-related mortality (1.2% vs. 0.7%, p = 0.33). The rate of hospitalization for heart failure was significantly lower in the elderly group with reduced-dose rivaroxaban (7.2% vs. 15.7%, p < 0.01) but not in the younger group. After adjusting for confounders in the older group, treatment with reduced-dose rivaroxaban was associated with lower risk of all-cause mortality (adjusted HR (aHR): 0.40, 95% CI: 0.21–0.74, p < 0.01) and hospitalization for heart failure (aHR: 0.54, 95% CI: 0.29–0.99, p = 0.05). No associations were found between rivaroxaban dose and cardiac-related mortality in either group, nor between younger age and any outcome. Conclusions: Reduced-dose rivaroxaban was associated with lower risks of all-cause mortality and hospitalization for heart failure in older patients with nonvalvular atrial fibrillation. Future studies can investigate the effect of reduced-dose rivaroxaban on prognoses in elderly individuals ≥85 years in the west.
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Chiou et al. (2023) conducted a cohort in Nonvalvular atrial fibrillation (n=2,386). Rivaroxaban vs. Full-dose rivaroxaban (20 mg/15 mg) was evaluated on All-cause mortality (aHR 0.40, 95% CI 0.21-0.74, p=<0.01). Reduced-dose rivaroxaban was associated with lower all-cause mortality compared to full-dose therapy in patients ≥85 years with nonvalvular atrial fibrillation (aHR 0.40; 95% CI 0.21-0.74; p<0.01).
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