University of Missouri-Columbia, Five Hospital Drive, CE306, Columbia, MO 65212, USA.
Stroke. 2012 Dec;43(12):3291-7. doi: 10.1161/STROKEAHA.112.664144. Epub 2012 Oct 2.
Apixaban reduces stroke with comparable bleeding risks when compared with aspirin in patients with atrial fibrillation who are unsuitable for vitamin k antagonist therapy. This analysis explores patterns of bleeding and defines bleeding risks based on stroke risk with apixaban and aspirin.
The Apixaban versus Acetylsalicylic Acid to Prevent Stroke in Atrial Fibrillation Patients Who Have Failed or Are Unsuitable for Vitamin k Antagonist Treatment (AVERROES) trial randomized 5599 patients with atrial fibrillation and risk factors to receive either apixaban or aspirin. Bleeding events were defined as the first occurrence of either major bleeding or clinically relevant nonmajor bleeding.
The rate of a bleeding event was 3.8%/year with aspirin and 4.5%/year with apixaban (hazard ratio with apixaban, 1.18; 95% CI, 0.92-1.51; P=0.19). The anatomic site of bleeding did not differ between therapies. Risk factors for bleeding common to apixaban and aspirin were use of nonstudy aspirin>50% of the time and a history of daily/occasional nosebleeds. The rates of both stroke and bleeding increased with higher CHADS2 scores but apixaban compared with aspirin was associated with a similar relative risk of bleeding (P interaction 0.21) and a reduced relative risk of stroke (P interaction 0.37) irrespective of CHADS2 category.
Anatomic sites and predictors of bleeding are similar for apixaban and aspirin in these patients. Higher CHADS2 scores are associated with increasing rates of bleeding and stroke, but the balance between risks and benefits of apixaban compared with aspirin is favorable irrespective of baseline stroke risk. Clinical Trial Registration Information- www.clinicaltrials.gov. Unique identifier: NCT 00496769.
在不适合华法林治疗的房颤患者中,与阿司匹林相比,阿哌沙班在降低卒中风险的同时出血风险相当。本分析旨在探讨出血模式,并根据阿哌沙班和阿司匹林的卒中风险定义出血风险。
房颤患者应用阿哌沙班或阿司匹林预防卒中和血栓栓塞的临床试验(AVERROES)中,5599 名伴有房颤和危险因素的患者被随机分配接受阿哌沙班或阿司匹林治疗。出血事件定义为首次发生大出血或临床相关非大出血。
阿司匹林组出血事件的年发生率为 3.8%,阿哌沙班组为 4.5%(阿哌沙班组的危险比为 1.18,95%可信区间为 0.92-1.51;P=0.19)。两种治疗方法的出血部位无差异。阿哌沙班和阿司匹林共有的出血危险因素包括非研究用阿司匹林使用率>50%和经常/偶尔鼻出血史。随着 CHADS2 评分的升高,卒中及出血风险均增加,但与阿司匹林相比,阿哌沙班出血的相对风险相似(P 交互作用 0.21),卒中的相对风险降低(P 交互作用 0.37),与 CHADS2 类别无关。
在这些患者中,阿哌沙班和阿司匹林的出血部位和预测因素相似。CHADS2 评分越高,出血和卒中的发生率越高,但与阿司匹林相比,阿哌沙班的风险获益比在整个基线卒中风险范围内均有利。临床试验注册信息- www.clinicaltrials.gov。注册号:NCT 00496769。