Department of Hematology and Clinical Oncology, Hospital General Universitario Morales Meseguer, Instituto Murciano de Investigación Biosanitaria (IMIB-Arrixaca), CIBER-CV, Murcia, Spain.
Department of Cardiology, Hospital Clínico Universitario Virgen de la Arrixaca, Instituto Murciano de Investigación Biosanitaria (IMIB-Arrixaca), CIBER-CV, Murcia, Spain.
Mayo Clin Proc. 2018 Aug;93(8):1065-1073. doi: 10.1016/j.mayocp.2018.01.028. Epub 2018 May 2.
To investigate the incidence and risk of adverse clinical outcomes in a "real-world" cohort of patients with atrial fibrillation (AF) anticoagulated with vitamin K antagonists (VKAs) from the Murcia AF Project in comparison with the warfarin arm of the randomized clinical trial (RCT) AMADEUS (Evaluating the Use of SR34006 Compared to Warfarin or Acenocoumarol in Patients With Atrial Fibrillation).
We included 1361 patients with AF from the Murcia AF Project (recruitment from May 1, 2007, to December 1, 2007) and 2293 from the AMADEUS trial (started in September 2003 and primary completed in March 2006), all taking VKA treatment. After propensity score matching (PSM), we investigated differences in rates and risks of several events, including major bleeding, ischemic stroke, and all-cause mortality at 365 (interquartile range, 275-428) days of follow-up.
After PSM there were 1324 patients for the comparative analysis, whereby annual event rates for most adverse events were significantly higher in the "real-world" population. Cox regression analyses demonstrated that the risk of primary outcomes was also increased in the "real-world" (vs RCT: hazard ratio [HR], 6.32; 95% CI, 2.84-14.03 for major bleeding; HR, 3.56, 95% CI, 1.22-10.42 for ischemic stroke; HR, 5.13, 95% CI, 3.02-8.69 for all-cause mortality). The risk of all other adverse events was higher in the real-world cohort, except for cardiovascular mortality.
This study comparing the Murcia AF Project and the AMADEUS trial demonstrates that there is a great heterogeneity in both populations, which is translated into a higher risk of several adverse outcomes in the real-world cohort, including major bleeding, ischemic stroke, and mortality.
通过与随机临床试验(RCT)AMADEUS(评估在房颤患者中 SR34006 与华法林或 acenocoumarol 的使用比较)的华法林组相比,调查“真实世界”队列中接受维生素 K 拮抗剂(VKA)抗凝治疗的房颤(AF)患者不良临床结局的发生率和风险。
我们纳入了来自 Murcia AF 项目的 1361 例 AF 患者(招募时间为 2007 年 5 月 1 日至 2007 年 12 月 1 日)和来自 AMADEUS 试验的 2293 例患者(于 2003 年 9 月开始,主要在 2006 年 3 月完成),所有患者均接受 VKA 治疗。在进行倾向评分匹配(PSM)后,我们研究了在 365(275-428)天随访期间,几种事件(包括大出血、缺血性卒中和全因死亡率)的发生率和风险差异。
在 PSM 后,我们对 1324 例患者进行了比较分析,发现“真实世界”人群中大多数不良事件的年发生率明显较高。Cox 回归分析表明,“真实世界”中的主要结局风险也增加(与 RCT 相比:大出血的危险比 [HR],6.32;95%可信区间 [CI],2.84-14.03;缺血性卒中的 HR,3.56;95% CI,1.22-10.42;全因死亡率的 HR,5.13;95% CI,3.02-8.69)。除了心血管死亡率,“真实世界”队列中其他不良事件的风险也更高。
本研究对比了 Murcia AF 项目和 AMADEUS 试验,表明这两个人群存在很大的异质性,这转化为“真实世界”队列中几种不良结局(包括大出血、缺血性卒中和死亡率)的风险更高。