Department of Cardiovascular Medicine, Chonnam National University Hospital, Gwangju, Korea.
Department of Internal Medicine, Chonnam National University Medical School, Gwangju, Korea.
Clin Appl Thromb Hemost. 2023 Jan-Dec;29:10760296231171081. doi: 10.1177/10760296231171081.
Anticoagulation with warfarin in Asian patients with atrial fibrillation (AF) often has been decreased as an international normalized ratio (INR) of prothrombin time 1.6-2.6 due to fear of bleeding, although universal criteria recommend an INR of 2.0-3.0. In this randomized, open-label trial, low-intensity anticoagulation (INR 1.6-2.6) was compared with standard-intensity anticoagulation (INR 2.0-3.0) with warfarin. A total 616 patients with AF and at least 1 risk factor for stroke were randomized to low-intensity anticoagulation (n = 308) and standard-intensity anticoagulation (n = 308) groups. The intention-to-treat analysis was performed to determine differences. The baseline characteristics of the two groups were comparable. New-onset stroke occurred in 2 patients (0.44% per year) in the low-intensity group and 5 patients (1.05% per year) in the standard-intensity group (HR 0.42, 95% CI 0.08-2.15). Major bleeding occurred in 4 patients (0.89% per year) in the low-intensity group and 5 patients (1.06% per year) in the standard-intensity group (HR 0.84, 95% CI 0.22-3.11). The rate of the net clinical outcome (composite of stroke, systemic embolism, major bleeding, and death) was 1.33% per year in the low-intensity group compared with 2.12% per year in the standard-intensity group (HR 0.63, 95% CI 0.23-1.72). In Asian patients with AF, clinical outcomes were not different between low-intensity and standard-intensity anticoagulation with warfarin.
在亚洲房颤(AF)患者中,华法林抗凝治疗通常将国际标准化比值(INR)设定为 1.6-2.6,以防止出血,尽管通用标准建议 INR 范围为 2.0-3.0。在这项随机、开放标签试验中,低强度抗凝(INR 1.6-2.6)与华法林标准强度抗凝(INR 2.0-3.0)进行了比较。共有 616 名 AF 且至少有 1 个中风危险因素的患者被随机分配到低强度抗凝组(n=308)和标准强度抗凝组(n=308)。进行意向治疗分析以确定差异。两组的基线特征相当。低强度组有 2 例(0.44%/年)新发卒中,标准强度组有 5 例(1.05%/年)新发卒中(HR 0.42,95%CI 0.08-2.15)。低强度组有 4 例(0.89%/年)发生大出血,标准强度组有 5 例(1.06%/年)发生大出血(HR 0.84,95%CI 0.22-3.11)。低强度组净临床结局(卒中、全身性栓塞、大出血和死亡的复合结局)发生率为 1.33%/年,标准强度组为 2.12%/年(HR 0.63,95%CI 0.23-1.72)。在亚洲 AF 患者中,华法林低强度和标准强度抗凝的临床结局无差异。