Department of General Medicine and Primary Care, Kumamoto University Hospital, 1-1-1 Honjyo Chuo-ku, Kumamoto, 860-8556, Japan.
Department of Cardiovascular Medicine, National Cerebral and Cardiovascular Center, Suita, Japan.
Sci Rep. 2024 Jun 22;14(1):14423. doi: 10.1038/s41598-024-65237-4.
The number of patients with atrial fibrillation is increasing, and frailty prevalence increases with age, posing challenges for physicians in prescribing anticoagulants to such patients because of possible harm. The effects of frailty on anticoagulant therapy in older Japanese patients with nonvalvular atrial fibrillation (NVAF) are unclear. Herein, we prescribed rivaroxaban to Japanese patients with NVAF and monitored for a mean of 2.0 years. The primary endpoint was stroke or systemic embolism. The secondary endpoints were all-cause or cardiovascular death, composite endpoint, and major or non-major bleeding. Frailty was assessed using the Japanese long-term care insurance system. A multiple imputation technique was used for missing data. The propensity score (PS) was obtained to estimate the treatment effect of frailty and was used to create two PS-matched groups. Overall, 5717 older patients had NVAF (mean age: 73.9 years), 485 (8.5%) were classified as frail. After PS matching, background characteristics were well-balanced between the groups. Rivaroxaban dosages were 10 and 15 mg/day for approximately 80% and the remaining patients, respectively. Frailty was not associated with the primary endpoint or secondary endpoints. In conclusion, frailty does not affect the effectiveness or safety of rivaroxaban anticoagulant therapy in older Japanese patients with NVAF.Trial registration: UMIN000019135, NCT02633982.
房颤患者人数不断增加,衰弱的患病率随年龄增长而增加,这给医生开具抗凝药物带来了挑战,因为可能会造成伤害。衰弱对日本老年非瓣膜性房颤(NVAF)患者抗凝治疗的影响尚不清楚。在此,我们为日本 NVAF 患者开瑞伐沙班,并进行了平均 2.0 年的监测。主要终点为卒中或全身性栓塞。次要终点为全因或心血管死亡、复合终点和大出血或非大出血。衰弱采用日本长期护理保险系统进行评估。采用多重插补技术处理缺失数据。获得倾向评分(PS)以估计衰弱的治疗效果,并用于创建两组 PS 匹配的组。总体而言,5717 名老年患者患有 NVAF(平均年龄:73.9 岁),485 名(8.5%)被归类为衰弱。经过 PS 匹配后,两组之间的背景特征得到了很好的平衡。瑞伐沙班的剂量分别为 10 和 15 mg/天,约占 80%和其余患者。衰弱与主要终点或次要终点无关。结论:衰弱不影响瑞伐沙班抗凝治疗在日本老年 NVAF 患者中的有效性和安全性。试验注册:UMIN000019135,NCT02633982。