Department of Cardiology, Faculty of Medicine, Ondokuz Mayıs University; Samsun-Turkey.
Department of Cardiology, Faculty of Medicine, Trakya University; Edirne-Turkey.
Anatol J Cardiol. 2021 Mar;25(3):196-204. doi: 10.5152/AnatolJCardiol.2021.57635.
This study aimed to evaluate the safety of direct oral anticoagulants (DOACs) in patients with non-valvular atrial fibrillation (NVAF) during daily clinical practice.
This was a prospective study conducted between January 01, 2016, and April 01, 2017, in patients aged ≥18 years with a diagnosis of NVAF. We performed the study in 9 clinical centers from different regions of Turkey, and the mean follow-up period was 12+2 months. We investigated major and minor bleeding events of DOAC.
A total of 1807 patients with NVAF were enrolled. The mean age of the patients was 73.6±10.2 years, CHA2DS2-VASc score was 3.6±1.4, and HAS-BLED score was 2±1.2. The most frequently prescribed DOAC was dabigatran 110 mg bid in 409 (22.6%) patients. The patients on apixaban 2.5 mg bid were older (p<0.001). Patients on rivaroxaban 15 mg od also had a higher prevalence of chronic renal failure, 46 (16.7%) patients. A total of 205 (11.4%) bleeding events were observed; among these, 34 (1.9%) patients had major bleeding and 171 (9.4%) patients had minor bleeding. The major and minor bleeding events were 2/273 (0.7%) and 30/273 (10.9%) in patients receiving dabigatran 150 mg bid, 13/409 (3%) and 44/409 (10.7%) in patients receiving dabigatran 110 mg bid, 4/385 (1%) and 42/385 (10.9%) in patients receiving rivaroxaban 20 mg od, 8/276 (2.9%) and 27/276 (9.7%) in patients receiving rivaroxaban 15 mg od, 3/308 (0.9%) and 14/308 (4.5%) in patients receiving apixaban 5 mg bid, 4/156 (2.5%) and 14/156 (9%) in patients receiving apixaban 2.5 mg bid, respectively. The total bleeding events were 17 (5.6%) in patients receiving apixaban 5 mg, less than those receiving other DOACs. On multivariate analyses, rivaroxaban 20 mg od (p=0.002), ATRIA and HAS-BLED scores, and peripheral artery disease were independent indicators of bleeding. The most frequent location of major bleeding was the gastrointestinal system (GIS) [17 (0.9%) patients], and the most frequent location of minor bleeding was the gingiva [45 (2.5%) patients].
This study showed that similar results as the previous real-life study; however, we had some different results, such as the GIS tract bleeding was more frequent in patients receiving dabigatran 110 mg bid. The major and intracranial bleeding events were similar for different DOACs; and among DOACs, only rivaroxaban 20 mg od was associated with a high risk of bleeding.
本研究旨在评估非瓣膜性心房颤动(NVAF)患者在日常临床实践中使用直接口服抗凝剂(DOAC)的安全性。
这是一项在 2016 年 1 月 1 日至 2017 年 4 月 1 日期间进行的前瞻性研究,纳入年龄≥18 岁且诊断为 NVAF 的患者。我们在土耳其不同地区的 9 个临床中心进行了这项研究,平均随访时间为 12+2 个月。我们调查了 DOAC 的主要和次要出血事件。
共纳入 1807 例 NVAF 患者。患者的平均年龄为 73.6±10.2 岁,CHA2DS2-VASc 评分为 3.6±1.4,HAS-BLED 评分为 2±1.2。最常开的 DOAC 是 110mg 每日两次的达比加群[409(22.6%)例]。服用阿哌沙班 2.5mg 每日两次的患者年龄更大(p<0.001)。服用利伐沙班 15mg 每日一次的患者也更常见慢性肾功能衰竭,46(16.7%)例。共观察到 205(11.4%)例出血事件;其中,34(1.9%)例患者有主要出血,171(9.4%)例患者有轻微出血。达比加群 150mg 每日两次组的主要和轻微出血事件分别为 2/273(0.7%)和 30/273(10.9%),达比加群 110mg 每日两次组为 13/409(3%)和 44/409(10.7%),利伐沙班 20mg 每日一次组为 4/385(1%)和 42/385(10.9%),利伐沙班 15mg 每日一次组为 8/276(2.9%)和 27/276(9.7%),阿哌沙班 5mg 每日两次组为 3/308(0.9%)和 14/308(4.5%),阿哌沙班 2.5mg 每日两次组为 4/156(2.5%)和 14/156(9%)。接受阿哌沙班 5mg 的患者总出血事件为 17(5.6%),少于其他 DOAC 组。多变量分析显示,利伐沙班 20mg 每日一次(p=0.002)、ATRIA 和 HAS-BLED 评分以及外周动脉疾病是出血的独立指标。主要出血的最常见部位是胃肠道系统(GIS)[17(0.9%)例],轻微出血的最常见部位是牙龈[45(2.5%)例]。
本研究显示与之前的真实世界研究结果相似;然而,我们也有一些不同的结果,例如接受达比加群 110mg 每日两次治疗的患者 GIS 出血更常见。不同 DOAC 的主要和颅内出血事件相似;在 DOAC 中,只有利伐沙班 20mg 每日一次与高出血风险相关。