Reduced-Dose Rivaroxaban Is Associated with Lower All-Cause Mortality in Older Patients with Nonvalvular Atrial Fibrillation

Author:

Chiou Wei-Ru12ORCID,Su Min-I12,Lee Ying-Hsiang234ORCID,Lin Po-Lin56,Liu Cheng-Wei78ORCID

Affiliation:

1. Division of Cardiology, Taitung MacKay Memorial Hospital, Taitung 95054, Taiwan

2. Department of Medicine, MacKay Medical College, New Taipei 25245, Taiwan

3. Cardiovascular Center, MacKay Memorial Hospital, Taipei 10449, Taiwan

4. Department of Artificial Intelligence and Medical Application, MacKay Junior College of Medicine, Nursing, and Management, Taipei 11260, Taiwan

5. Department of Nursing, MacKay Junior College of Medicine, Nursing, and Management, Taipei 11260, Taiwan

6. Division of Cardiology, Hsinchu MacKay Memorial Hospital, Hsinchu 30046, Taiwan

7. Division of Cardiology, Department of Medicine, Kuang Tien General Hospital, Taichung 43302, Taiwan

8. Department of Nutrition, Hungkuang University, Taichung 433304, Taiwan

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 (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.

Publisher

MDPI AG

Subject

General Medicine

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