Department of Pharmacy Services, Brigham and Women's Hospital, Boston, MA, USA.
Clin Appl Thromb Hemost. 2023 Jan-Dec;29:10760296231172765. doi: 10.1177/10760296231172765.
Direct oral anticoagulants (DOACs) demonstrated similar efficacy and lower risk of intracranial hemorrhage than warfarin in patients with atrial fibrillation and venous thromboembolism. Given the lack of data identifying risk factors in patients who bled while on a DOAC, we sought to investigate these characteristics.
This retrospective chart review was approved by the Mass General Brigham Institutional Review Board and assessed patients who experienced bleeding events while on DOAC therapy from 6/1/2015 to 7/1/2020. Patient characteristics were evaluated, including age, sex, body mass index (BMI), renal function, concomitant therapies, and baseline comorbidities.
Eighty-seven patients were included for analysis, with a median age of 75.8 years. Most patients were female (51.7%) and 24 (27.6%) had a BMI >30. At time-of-event, 21 patients (24.1%) had acute kidney injury. Thirty-three patients (37.9%) were on concomitant antiplatelet therapy (APT), with 31 (35.6%) on single APT and 2 on dual APT. Pertinent comorbidities included hypertension (74.7%), ischemic cerebrovascular accident (28.7%), thyroid abnormality (23.0%), active cancer (14.9%), and anemia (13.8%). Eleven patients (12.6%) had a prior bleeding event. Most patients were on apixaban (69.0%) for the indication of stroke prevention in nonvalvular atrial fibrillation/flutter (72.4%). FDA-approved dosing was used in most patients (92.0%), and all deviations reflected underdosing. Most bleeding events were defined as major (95.4%), occurred at a critical organ site (72.4%), and developed spontaneously (58.6%).
These data provide insight into characteristics of patients who experience bleeding events while on DOAC therapy. Understanding these potential risk factors may optimize the safe use of these agents.
与华法林相比,直接口服抗凝剂(DOAC)在房颤和静脉血栓栓塞患者中显示出相似的疗效和较低的颅内出血风险。鉴于缺乏在 DOAC 治疗期间出血的患者的风险因素数据,我们试图对此进行调查。
这项回顾性图表审查得到了麻省总医院布列根和妇女医院机构审查委员会的批准,并评估了 2015 年 6 月 1 日至 2020 年 7 月 1 日期间在 DOAC 治疗期间发生出血事件的患者。评估了患者的特征,包括年龄、性别、体重指数(BMI)、肾功能、同时接受的治疗以及基线合并症。
共纳入 87 例患者进行分析,中位年龄为 75.8 岁。大多数患者为女性(51.7%),24 例(27.6%)BMI>30。在事件发生时,21 例(24.1%)患者出现急性肾损伤。33 例(37.9%)患者同时接受抗血小板治疗(APT),其中 31 例(35.6%)接受单一 APT,2 例接受双重 APT。相关合并症包括高血压(74.7%)、缺血性脑血管意外(28.7%)、甲状腺异常(23.0%)、活动性癌症(14.9%)和贫血(13.8%)。11 例(12.6%)患者有既往出血事件。大多数患者(69.0%)因非瓣膜性房颤/扑动的卒中预防而服用阿哌沙班(72.4%)。大多数患者(92.0%)使用了 FDA 批准的剂量,所有偏差均反映了剂量不足。大多数出血事件被定义为主要(95.4%),发生在关键器官部位(72.4%),自发性发生(58.6%)。
这些数据提供了在 DOAC 治疗期间发生出血事件的患者特征的深入了解。了解这些潜在的风险因素可能会优化这些药物的安全使用。