Chiou Wei-Ru, Su Min-I, Lee Ying-Hsiang, Lin Po-Lin, Liu Cheng-Wei
Division of Cardiology, Taitung MacKay Memorial Hospital, Taitung 95054, Taiwan.
Department of Medicine, MacKay Medical College, New Taipei 25245, Taiwan.
J Clin Med. 2023 Oct 23;12(20):6686. doi: 10.3390/jcm12206686.
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.
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.
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.
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.
在J-ROCKET AF试验中使用了低剂量利伐沙班(10毫克),证明了其在亚洲人群中的安全性。对于老年非瓣膜性心房颤动患者,低剂量与全剂量利伐沙班(20毫克/15毫克)治疗与全因死亡率之间的关系仍不清楚。提议:评估低剂量利伐沙班对85岁以上患者全因死亡率的影响。
我们回顾性纳入了代表2012年10月至2016年11月期间的医疗记录。2×2析因设计纳入了年龄(≥85岁与<85岁)和利伐沙班使用情况(低剂量与全剂量)。主要研究结局为全因死亡率和心脏相关死亡率。
该研究纳入了2386例患者,平均年龄为76.6±10.4岁;51.8%为男性。在≥85岁组(n = 593)中,低剂量亚组的全因死亡率(5.3%对10.6%,P = 0.02)和心脏相关死亡率(1.9%对5.1%,P = 0.04)较低,而接受低剂量利伐沙班的年轻患者全因死亡率较高(3.7%对1.8%,P = 0.01),但心脏相关死亡率无差异(1.2%对0.7%,P = 0.33)。低剂量利伐沙班的老年组心力衰竭住院率显著较低(7.2%对15.7%,P<0.01),但年轻组无此差异。在老年组调整混杂因素后,低剂量利伐沙班治疗与较低的全因死亡率风险(调整后HR(aHR):0.40,95%CI:0.21 - 0.74,P<0.01)和心力衰竭住院风险(aHR:0.54,95%CI:0.29 - 0.99,P = 0.05)相关。在两组中,利伐沙班剂量与心脏相关死亡率之间均未发现关联,年轻年龄与任何结局之间也未发现关联。
低剂量利伐沙班与老年非瓣膜性心房颤动患者较低的全因死亡率和心力衰竭住院风险相关。未来的研究可以调查低剂量利伐沙班对西方≥85岁老年人预后的影响。