AI Article Synopsis

  • The J-ROCKET AF trial found that reduced-dose rivaroxaban (10 mg) is safe for the Asian population, but its impact on all-cause mortality in patients over 85 remained unclear.
  • A study reviewed medical records from 2012 to 2016, comparing the effects of reduced-dose versus full-dose rivaroxaban on mortality and hospitalization rates in patients aged 85 and older versus younger patients.
  • Results showed that older patients on reduced-dose rivaroxaban had significantly lower all-cause and cardiac-related mortality and fewer hospitalizations for heart failure, while younger patients experienced higher all-cause mortality with reduced doses.

Article Abstract

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 ( = 593), the reduced-dose subgroup had lower all-cause (5.3% vs. 10.6%, = 0.02) and cardiac-related mortality (1.9% vs. 5.1%, = 0.04), whereas the younger patients receiving reduced-dose rivaroxaban had higher all-cause mortality (3.7% vs. 1.8%, = 0.01) but no difference in cardiac-related mortality (1.2% vs. 0.7%, = 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%, < 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, < 0.01) and hospitalization for heart failure (aHR: 0.54, 95% CI: 0.29-0.99, = 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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10607242PMC
http://dx.doi.org/10.3390/jcm12206686DOI Listing

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