Tsai Chuan-Tsai, Liao Jo-Nan, Chan Yi-Hsin, Kuo Ling, Liu Chih-Min, Lip Gregory Y H, Chao Tze-Fan
Division of Cardiology, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
Institute of Clinical Medicine, and Cardiovascular Research Center, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Int J Cardiol Heart Vasc. 2023 Dec 25;50:101333. doi: 10.1016/j.ijcha.2023.101333. eCollection 2024 Feb.
Reduced-dose (Low-dose [LD]) apixaban is recommended in patients with atrial fibrillation (AF) who fulfill 2 of 3 criteria: age ≥ 80 years, body weight ≤ 60 kg, and a serum creatinine (sCr) ≥ 1.5 mg/dl. However, the suitable (appropriate) dose for Asian patients who have a sCr < 1.5 mg/dl but an estimated glomerular filtration rate (eGFR) < 50 mL/min is unknown.
This is a retrospective study using the Chang Gung Memorial hospital medical database in Taiwan. A total of 13,508 AF patients receiving oral anticoagulants (OACs) from 2012 to 2018 were reviewed and 1595 patients with a sCr < 1.5 mg/dL and an eGFR < 50 mL/min who met 1 criterion of dose reduction of apixaban other than sCr (that is, age ≥ 80 years or body weight < 60 kg) were identified. Clinical outcomes were compared between LD and SD apixaban versus warfarin.
Their OACs use was as follows: 343 receiving apixaban (128 patients on standard dose [SD] and 215 on LD), 174 receiving warfarin, and 1078 on other NOACs. Patients with an eGFR < 50 mL/min had higher risk of mortality (adjusted hazard ratio [aHR], 1.264; 95 % confidence interval [CI], 1.086-1.472) and composite endpoint of 'ischemic stroke/systemic embolism (IS/SE) or major bleeding or mortality (aHR, 1.202; 95 % CI, 1.056-1.370) compared to those with an eGFR ≥ 50 mL/min whereas the risk of IS/SE and major bleeding were similar. LD apixaban was associated with lower risk of composite endpoint of IS/SE or major bleeding (aHR, 0.567; 95 % CI, 0.331 - 0.972), mortality (aHR, 0.336; 95 % CI, 0.138 - 0.815), and 'IS/SE or major bleeding or mortality (aHR, 0.551; 95 % CI, 0343 - 0.886) compared to warfarin while the risk was comparable between SD apixaban and warfarin (aHR, 0.745; 95 % CI, 0.402 - 1.378; aHR, 0.407; 95 % CI, 0.145 - 1.143; aHR, 0.619; 95 % CI, 0.354 - 1.084, respectively).
In patients with sCr < 1.5 mg/dL and eGFR < 50 mL/min, SD and LD apixaban were comparable in the prevention of IS/SE, but LD apixaban was superior in reducing the composite endpoint of 'IS/SE or major bleeding or mortality'. Therefore, LD apixaban might be a preferred dose for this population.
对于符合以下三项标准中两项的心房颤动(AF)患者,推荐使用低剂量阿哌沙班:年龄≥80岁、体重≤60kg、血清肌酐(sCr)≥1.5mg/dl。然而,对于sCr<1.5mg/dl但估计肾小球滤过率(eGFR)<50ml/min的亚洲患者,合适的剂量尚不清楚。
这是一项利用台湾长庚纪念医院医疗数据库进行的回顾性研究。回顾了2012年至2018年期间共13508例接受口服抗凝剂(OACs)治疗的AF患者,确定了1595例sCr<1.5mg/dL且eGFR<50ml/min、符合阿哌沙班除sCr外的一项剂量降低标准(即年龄≥80岁或体重<60kg)的患者。比较了低剂量和标准剂量阿哌沙班与华法林的临床结局。
他们使用OACs的情况如下:343例接受阿哌沙班治疗(128例使用标准剂量[SD],215例使用低剂量[LD]),174例接受华法林治疗,1078例使用其他新型口服抗凝药。与eGFR≥50ml/min的患者相比,eGFR<50ml/min的患者死亡风险更高(调整后风险比[aHR],1.264;95%置信区间[CI],1.086 - 1.472),“缺血性卒中/全身性栓塞(IS/SE)或大出血或死亡”的复合终点风险也更高(aHR,1.202;95%CI,1.056 - 1.370),而IS/SE和大出血的风险相似。与华法林相比,低剂量阿哌沙班与IS/SE或大出血的复合终点风险较低(aHR,0.567;95%CI,0.331 - 0.972)、死亡风险较低(aHR,0.336;95%CI,0.138 - 0.815)以及“IS/SE或大出血或死亡”风险较低(aHR,0.551;95%CI,0.343 - 0.886),而标准剂量阿哌沙班与华法林的风险相当(分别为aHR,0.745;95%CI,0.402 - 1.378;aHR,0.407;95%CI,0.145 - 1.143;aHR,0.619;95%CI,0.354 - 1.084)。
在sCr<1.5mg/dL且eGFR<50ml/min的患者中,标准剂量和低剂量阿哌沙班在预防IS/SE方面相当,但低剂量阿哌沙班在降低“IS/SE或大出血或死亡”的复合终点方面更具优势。因此,低剂量阿哌沙班可能是该人群的首选剂量。