Breitenstein Alexander, Gay Alain, Vogtländer Kai, Fox Keith A A, Steffel Jan
Department of Cardiology, University Hospital Zurich, 8091 Zurich, Switzerland.
University of Zurich, 8006 Zurich, Switzerland.
J Clin Med. 2024 Mar 28;13(7):1956. doi: 10.3390/jcm13071956.
: In the COMPASS trial, the combination of acetylsalicylic acid (ASA) plus 2.5 mg rivaroxaban twice daily (dual-pathway inhibition, DPI) has been shown to be superior to ASA monotherapy for the reduction in ischemic major adverse cardiovascular events (MACEs, i.e., cardiovascular death, stroke, or myocardial infarction). : The international XATOA registry (Xarelto plus Acetylsalicylic acid: Treatment patterns and Outcomes in patients with Atherosclerosis) is a prospective post-approval registry that investigates the cardiovascular outcomes of patients taking ASA plus 2.5 mg rivaroxaban. The aim of this pre-specified analysis was to determine the net clinical outcome (NCO), i.e., a combination of MACEs and bleeding events, of DPI in patients from daily clinical practice. : Among the 5615 patients, the presence of multiple risk factors resulted in an increase in the total risk of experiencing an NCO event, e.g., from 1.27% (one risk factor) to 2.18% (two risk factors) and 4.07% (three or more risk factors), respectively, with ischemic MACE representing the primary driver of bleeding complications. : In the real-world XATOA registry, the annual rate of NCO events was low and numerically similar to those seen in the treatment group in the randomized COMPASS trial.
在COMPASS试验中,已证明乙酰水杨酸(ASA)联合每日两次2.5毫克利伐沙班(双途径抑制,DPI)在降低缺血性主要不良心血管事件(MACE,即心血管死亡、中风或心肌梗死)方面优于ASA单药治疗。国际XATOA注册研究(利伐沙班加乙酰水杨酸:动脉粥样硬化患者的治疗模式和结局)是一项批准后前瞻性注册研究,旨在调查服用ASA加2.5毫克利伐沙班患者的心血管结局。这项预先设定分析的目的是确定日常临床实践中患者DPI的净临床结局(NCO),即MACE和出血事件的综合情况。在5615例患者中,多种危险因素的存在导致发生NCO事件的总风险增加,例如分别从1.27%(一个危险因素)增至2.18%(两个危险因素)和4.07%(三个或更多危险因素),缺血性MACE是出血并发症的主要驱动因素。在真实世界的XATOA注册研究中,NCO事件的年发生率较低,且在数值上与随机COMPASS试验治疗组中观察到的发生率相似。