Department of Pharmacy Services, Medical University of South Carolina, 150 Ashley Avenue, MSC 584, Charleston, SC, 29425, USA.
Am J Cardiovasc Drugs. 2021 Sep;21(5):545-551. doi: 10.1007/s40256-021-00470-0. Epub 2021 Mar 30.
Direct oral anticoagulants (DOACs) have become favorable choices for anticoagulation due to their fixed-dose schedule, limited need for monitoring, and non-inferiority or superiority to warfarin. DOACs are currently not recommended in patients with a body weight ≥ 120 kg or body mass index ≥ 40 kg/m due to limited data regarding safety and efficacy.
The aim of this study was to compare the safety and efficacy of DOACs in patients with nonvalvular atrial fibrillation (NVAF) and weighing ≥ 120 kg with those weighing < 120 kg.
A single-center, retrospective study was conducted in patients weighing ≥ 120 kg who received either apixaban, dabigatran, or rivaroxaban for stroke risk reduction in NVAF, and matched to patients who weighed < 120 kg. The primary outcome was the incidence of stroke, deep vein thrombosis, pulmonary embolism, or myocardial infarction, while the safety outcome was the incidence of major or clinically relevant non-major bleeding based on the International Society on Thrombosis and Haemostasis (ISTH) definitions.
A total of 318 patients weighing ≥ 120 kg with NVAF and meeting the inclusion criteria were evaluated and matched with 318 patients weighing < 120 kg. The primary outcome occurred in 2.5% of patients in the ≥ 120 kg group and in 3.1% of patients in the < 120 kg group (p = 0.632). The safety outcome occurred in 5.3% and 6.6% of patients in these respective groups (p = 0.503).
Apixaban, dabigatran, or rivaroxaban may be well-tolerated and effective anticoagulant options in patients with NVAF weighing ≥ 120 kg.
由于固定剂量方案、监测需求有限以及与华法林相比非劣效或更优效,直接口服抗凝剂(DOACs)已成为抗凝治疗的首选。由于关于安全性和疗效的数据有限,DOACs 目前不推荐用于体重≥120kg 或体重指数≥40kg/m2的患者。
本研究旨在比较体重≥120kg 的非瓣膜性心房颤动(NVAF)患者与体重<120kg 的患者使用 DOACs 的安全性和疗效。
对体重≥120kg 且接受阿哌沙班、达比加群或利伐沙班用于 NVAF 卒中风险降低的患者进行了一项单中心、回顾性研究,并与体重<120kg 的患者进行了匹配。主要结局是卒中、深静脉血栓形成、肺栓塞或心肌梗死的发生率,而安全性结局是根据国际血栓和止血学会(ISTH)定义的主要或临床相关非主要出血的发生率。
共评估了 318 例符合纳入标准的体重≥120kg 的 NVAF 患者,并与 318 例体重<120kg 的患者进行了匹配。≥120kg 组中有 2.5%的患者发生主要结局,<120kg 组中有 3.1%的患者发生主要结局(p=0.632)。两组分别有 5.3%和 6.6%的患者发生安全性结局(p=0.503)。
阿哌沙班、达比加群或利伐沙班可能是体重≥120kg 的 NVAF 患者耐受良好且有效的抗凝选择。