Ferrarotto Hospital and University of Catania, Catania, Italy; ETNA Foundation, Catania, Italy.
Int J Cardiol. 2013 Aug 20;167(4):1237-41. doi: 10.1016/j.ijcard.2012.03.148. Epub 2012 Apr 10.
Warfarin, despite its known limitations, is the reference standard treatment for patients with AF and risk factors for stroke. We performed a meta-analysis of phase III trials that compare novel oral anticoagulants (NOACs) with warfarin to determine whether they improve clinical outcomes of patients with non-valvular atrial fibrillation (AF).
Three randomized trials that compared NOACs with warfarin in AF were selected. The primary efficacy endpoint was the incidence of stroke or systemic embolism. The primary safety endpoint was the incidence of major bleeding.
A total of 50578 patients were included. NOACs significantly decreased stroke or systemic embolism (2.8% vs 3.5%, odds ratio [OR] 0.82, 95% confidence interval [CI] 0.74-0.91, P<0.001), death (6.0% vs 6.3%, OR 0.88, 95% CI 0.82-0.95, P=0.001) and stroke (2.4% vs 3.0%, OR 0.79, 95% CI 0.71-0.88, P<0.001). The reduction in stroke was mainly driven by fewer hemorrhagic strokes (0.3% vs 0.8%, OR 0.79, 95% CI 0.71-0.88, P<0.001). Major bleeding occurred in 5.0% and 5.6% of patients in the NOACs and warfarin groups (OR 0.85, 95% CI 0.69-1.05, P=0.14 in the random-effects model). NOACs were associated with lower rates of intracranial bleeding (0.6% vs 1.3%, P<0.001) and higher rates of gastrointestinal bleeding (2.3% vs 1.3%, P=0.036).
In patients with non-valvular AF, NOACs decrease stroke or systemic embolism, hemorrhagic stroke and mortality, with similar risk of major bleeding compared to warfarin.
尽管华法林存在已知的局限性,但它仍是伴有房颤和卒中风险因素患者的标准治疗药物。我们对比较新型口服抗凝剂(NOACs)与华法林的 III 期临床试验进行了荟萃分析,以确定它们是否能改善非瓣膜性房颤(AF)患者的临床结局。
选择了 3 项比较 NOACs 与华法林在 AF 中的应用的随机试验。主要疗效终点是卒中或全身性栓塞的发生率。主要安全性终点是大出血的发生率。
共纳入 50578 例患者。NOACs 可显著降低卒中或全身性栓塞(2.8% vs 3.5%,比值比[OR]0.82,95%置信区间[CI]0.74-0.91,P<0.001)、死亡(6.0% vs 6.3%,OR 0.88,95% CI 0.82-0.95,P=0.001)和卒中(2.4% vs 3.0%,OR 0.79,95% CI 0.71-0.88,P<0.001)的发生率。卒中发生率的降低主要归因于出血性卒中发生率的降低(0.3% vs 0.8%,OR 0.79,95% CI 0.71-0.88,P<0.001)。NOACs 组和华法林组的大出血发生率分别为 5.0%和 5.6%(OR 0.85,95% CI 0.69-1.05,P=0.14 在随机效应模型中)。NOACs 与较低的颅内出血发生率(0.6% vs 1.3%,P<0.001)和较高的胃肠道出血发生率(2.3% vs 1.3%,P=0.036)相关。
在非瓣膜性房颤患者中,与华法林相比,NOACs 可降低卒中或全身性栓塞、出血性卒中和死亡率,且大出血风险相似。