Department of Pharmacy, Affiliated Jinhua Hospital, Zhejiang University School of Medicine, Jinhua, 321000, People's Republic of China.
Department of Cardiology, Affiliated Jinhua Hospital, Zhejiang University School of Medicine, Jinhua, 321000, People's Republic of China.
Drug Des Devel Ther. 2024 May 13;18:1573-1582. doi: 10.2147/DDDT.S459658. eCollection 2024.
Atrial fibrillation (AF) is the most common abnormal heart rhythm in elderly patients. Rivaroxaban has been widely used for stroke prevention. The anticoagulant response to rivaroxaban increases with age, which may make elderly patients susceptible to adverse outcomes resulting from small differences in bioavailability between generic and brand products.
We designed a cohort study of ≥65-year-old inpatients with AF. Sociodemographic and laboratory measures of qualified patients who received brand or generic rivaroxaban for at least 72 hours at the study hospital from January 2021 to June 2023 were collected retrospectively. The primary outcome was the incidence of bleeding.
A total of 1008 qualifying patients were included for analysis, with 626 (62.1%) receiving brand rivaroxaban and 382 (37.9%) receiving generic rivaroxaban. After propensity score matching and weighting to account for confounders, the odds ratios comparing brand vs generic rivaroxaban (95% confidence intervals) for the bleeding was 1.15 (0.72-1.82). Results from subgroup analyses of patients with age ≥85, HAS-BLED score ≥ 3, containment of antiplatelet drugs, and female patients were consistent with the primary analysis.
It provides evidence regarding the clinical safety outcome of generic rivaroxaban in the elderly AF population that may be particularly susceptible to adverse outcomes resulting from small allowable differences in pharmacokinetics.
心房颤动(AF)是老年患者中最常见的异常心律。利伐沙班已广泛用于预防中风。利伐沙班的抗凝反应随年龄增长而增加,这可能使老年患者易受到生物利用度在仿制药和品牌产品之间的微小差异导致的不良结果的影响。
我们设计了一项≥65 岁的 AF 住院患者的队列研究。回顾性收集了 2021 年 1 月至 2023 年 6 月在研究医院至少接受了 72 小时品牌或仿制药利伐沙班治疗的合格患者的社会人口统计学和实验室指标。主要结局是出血的发生率。
共有 1008 名符合条件的患者被纳入分析,其中 626 名(62.1%)接受了品牌利伐沙班,382 名(37.9%)接受了仿制药利伐沙班。在进行倾向评分匹配和加权以考虑混杂因素后,与品牌利伐沙班相比,仿制药利伐沙班的出血比值比(95%置信区间)为 1.15(0.72-1.82)。对年龄≥85 岁、HAS-BLED 评分≥3、抗血小板药物控制和女性患者的亚组分析结果与主要分析一致。
该研究为老年 AF 人群中仿制药利伐沙班的临床安全性结局提供了证据,这些患者可能特别容易受到因药代动力学允许的微小差异而导致的不良结果的影响。