Population Health Research Institute, McMaster University, 237 Barton St. East, Hamilton, Ontario, Canada.
J Am Coll Cardiol. 2013 Sep 3;62(10):900-8. doi: 10.1016/j.jacc.2013.05.042. Epub 2013 Jun 13.
This study sought to compare the net clinical benefit of dabigatran 110 mg bid and 150 mg bid with that of warfarin in patients with atrial fibrillation (AF).
In patients with AF, dabigatran 110 mg bid and 150 mg bid are associated with similar rates of death. However, the higher dose reduces ischemic stroke and increases bleeding compared with the lower dose. Therefore, there is uncertainty about how to evaluate the overall benefit of the 2 doses.
In 18,113 AF patients in the RE-LY (Randomized Evaluation of Long Term Anticoagulant Therapy) trial, we used a previously developed method for integrating ischemic and bleeding events as "ischemic stroke equivalents" in order to compare a weighted benefit of 2 doses of dabigatran with each other, and with that of warfarin.
Compared with warfarin, there was a significant decrease in ischemic stroke equivalents with both dabigatran doses: -0.92 per 100 patient years (95% confidence interval [CI]: -1.74 to -0.21, p = 0.02) with dabigatran 110 mg bid and -1.08 (95% CI: -1.86 to -0.34, p = 0.01) with dabigatran 150 mg bid. There was no significant difference in ischemic stroke equivalents between the 2 doses: -0.16 (95% CI: -0.80 to 0.43) comparing dabigatran 150 mg bid with 110 bid. When including death in the weighted benefit calculations, the results were similar.
On a group level both doses of dabigatran as compared with warfarin have similar benefits when considering a weighted estimate including both efficacy and safety. The similar overall benefits of the 2 doses of dabigatran versus warfarin support individualizing the dose based on patient characteristics and physician and patient preferences. (Randomized Evaluation of Long Term Anticoagulant Therapy [RE-LY] With Dabigatran Etexilate; NCT00262600).
本研究旨在比较达比加群 110mg,bid 和 150mg,bid 与华法林在房颤(AF)患者中的净临床获益。
在 AF 患者中,达比加群 110mg,bid 和 150mg,bid 的死亡率相似。然而,高剂量与低剂量相比,可降低缺血性卒中和增加出血。因此,对于如何评估这两种剂量的整体获益存在不确定性。
在 RE-LY(长期抗凝治疗随机评估)试验的 18113 例 AF 患者中,我们使用了一种先前开发的方法,将缺血性和出血性事件整合为“缺血性卒中等效事件”,以便比较两种达比加群剂量之间的相互加权获益,以及与华法林的比较。
与华法林相比,两种达比加群剂量均显著降低缺血性卒中等效事件:达比加群 110mg,bid 组为 -0.92/100 患者年(95%置信区间 [CI]:-1.74 至-0.21,p=0.02),达比加群 150mg,bid 组为 -1.08/100 患者年(95% CI:-1.86 至-0.34,p=0.01)。两种剂量之间的缺血性卒中等效事件无显著差异:达比加群 150mg,bid 组与 110mg,bid 组比较为-0.16(95% CI:-0.80 至 0.43)。当将死亡纳入加权获益计算时,结果相似。
在群体水平上,与华法林相比,两种达比加群剂量在考虑包括疗效和安全性的加权估计时具有相似的获益。达比加群两种剂量与华法林的总体获益相似,支持根据患者特征和医生及患者的偏好个体化剂量。(RE-LY(达比加群酯的长期抗凝治疗随机评估)试验;NCT00262600)。