Department of Cardiology, National Hospital Organization Kyoto Medical Center, 1-1 Fukakusa Mukaihata-cho, Fushimi-ku, Kyoto, Kyoto, 612-8555, Japan.
Department of Cardiovascular Medicine, The Cardiovascular Institute, Tokyo, Japan.
Heart Vessels. 2021 Jul;36(7):1035-1046. doi: 10.1007/s00380-021-01777-3. Epub 2021 Jan 24.
Dose reduction of apixaban is applied in atrial fibrillation (AF) patients fulfilling ≥ 2 of the following criteria: (1) age ≥ 80 years, (2) body weight ≤ 60 kg and (3) serum creatinine ≥ 1.5 mg/dL. However, the clinical significance of each criterion remains unclear. The J-ELD AF Registry is a prospective observational study of elderly (≥ 75 years) Japanese AF patients receiving on-label dose of apixaban. In patients receiving the standard dose (5 mg bid, n = 1243), the incidence rates (% per patient-year) of stroke or systemic embolism in those fulfilling none [n = 516] or one of the above criteria (1) [n = 328], (2) [n = 378] and (3) [n = 21] were 1.24, 2.32, 1.41 and 4.93 (log-rank P = 0.422), respectively, and those of bleeding requiring hospitalization were 1.03, 0.99, 1.98 and 4.93 (P = 0.318), respectively. In patients receiving a reduced dose (2.5 mg bid, n = 1,515), the incidences of stroke or systemic embolism in those fulfilling (1)/(2) [n = 1,331], (1)/(3) [n = 65], (2)/(3) [n = 23] and all three criteria [n = 96] were 1.38, 1.64, 4.67 and 3.51 (P = 0.295), respectively, and those of bleeding requiring hospitalization were 2.04, 1.64, 0.00 and 4.71 (P = 0.318), respectively. Univariate analysis demonstrated that the types or combinations of each criterion was not significantly associated with the incidence of thromboembolic or bleeding events. The types or combinations of the three apixaban dose reduction criteria did not have significant impact on effectiveness and safety in Japanese elderly AF patients receiving on-label dose of apixaban, although the impact of the creatinine criterion remains uncertain due to the few number of the patients.
阿哌沙班剂量减少适用于满足以下≥2 项标准的房颤(AF)患者:(1)年龄≥80 岁,(2)体重≤60kg 和(3)血清肌酐≥1.5mg/dL。然而,每个标准的临床意义仍不清楚。J-ELD AF 登记研究是一项针对接受阿哌沙班标准剂量(5mg bid,n=1243)的老年(≥75 岁)日本 AF 患者的前瞻性观察性研究。在接受标准剂量的患者中(n=1243),无任何一项标准(n=516)或满足上述标准之一(1)(n=328)、(2)(n=378)和(3)(n=21)的患者发生卒中或全身性栓塞的发生率(每患者-年%)分别为 1.24%、2.32%、1.41%和 4.93%(对数秩检验 P=0.422),需要住院治疗的出血发生率分别为 1.03%、0.99%、1.98%和 4.93%(P=0.318)。在接受减少剂量(n=1515,2.5mg bid)的患者中,满足(1)/(2)(n=1331)、(1)/(3)(n=65)、(2)/(3)(n=23)和所有三个标准(n=96)的患者发生卒中或全身性栓塞的发生率分别为 1.38%、1.64%、4.67%和 3.51%(P=0.295),需要住院治疗的出血发生率分别为 2.04%、1.64%、0.00%和 4.71%(P=0.318)。单变量分析表明,每个标准的类型或组合与血栓栓塞或出血事件的发生率无显著相关性。在接受阿哌沙班标准剂量的日本老年 AF 患者中,三种阿哌沙班剂量减少标准的类型或组合对有效性和安全性没有显著影响,尽管由于患者人数较少,肌酐标准的影响仍不确定。