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抗血小板治疗指征也适用于同时服用直接口服抗凝剂的患者。

Antiplatelet therapy indication in patients also prescribed direct oral anticoagulants.

机构信息

Department of Pharmacotherapy, University of Utah College of Pharmacy, Salt Lake City, UT, 84132, USA.

University of Utah Health Thrombosis Service, Murray, UT, 84107, USA.

出版信息

J Thromb Thrombolysis. 2023 Jan;55(1):185-188. doi: 10.1007/s11239-021-02602-4. Epub 2022 Apr 20.

Abstract

Direct oral anticoagulants (DOACs) are standard of care for venous thromboembolism (VTE) treatment and stroke prevention in atrial fibrillation (AF). Adding antiplatelet therapy (APT) to an oral anticoagulant (OAC) causes a 2-fold increase in major bleeding. As such, recent guidelines recommend limiting the duration and indication of combined therapy in patients already on an OAC. Despite these recommendations, approximately one-third of anticoagulated patients are prescribed concomitant APT. University of Utah Health patients receiving DOAC + APT between August 1, 2019 and November 30, 2019 were included. These were categorized into four groups by APT indication: primary atherosclerotic cardiovascular disease (ASCVD) prevention, ASCVD-no percutaneous coronary intervention (PCI), ASCVD-PCI ≤ 12 months prior, ASCVD-PCI > 12 months prior. The primary outcome was the proportion of DOAC patients receiving concomitant APT for each indication. During the study period, 347 patients received DOAC + APT, primarily for AF (59.1%) or VTE (33.1%), and the most common DOAC was apixaban (76.7%).The most common indication for APT was ASCVD-no PCI (47.3%), followed by ASCVD-PCI > 12 months prior (30.8%), primary ASCVD prevention (18.7%), and ASCVD-PCI ≤ 12 months prior (1.7%). Five patients (1.4%) were on APT with unclear indication. Based on recent guidelines limiting indications and duration of APT added to anticoagulation, over 95% of patients in this single-center study warranted re-assessment of APT indication, with stable ASCVD and primary prevention being prime targets for APT de-prescribing. This study highlights the tremendous potential to improve patient safety and reduce bleeding harm.

摘要

直接口服抗凝剂(DOAC)是静脉血栓栓塞症(VTE)治疗和心房颤动(AF)卒中预防的标准治疗方法。将抗血小板治疗(APT)与口服抗凝剂(OAC)联合使用会使大出血的风险增加两倍。因此,最近的指南建议限制已经接受 OAC 治疗的患者联合治疗的持续时间和适应证。尽管有这些建议,大约三分之一的接受抗凝治疗的患者仍被开具同时使用 APT 的处方。

本研究纳入了 2019 年 8 月 1 日至 2019 年 11 月 30 日期间在犹他大学健康中心接受 DOAC+APT 治疗的患者。根据 APT 的适应证,将这些患者分为四组:主要动脉粥样硬化性心血管疾病(ASCVD)预防、ASCVD 无经皮冠状动脉介入治疗(PCI)、ASCVD-PCI<12 个月前、ASCVD-PCI>12 个月前。主要结局是每个适应证下接受 DOAC 联合 APT 治疗的 DOAC 患者比例。

在研究期间,347 名患者接受了 DOAC+APT 治疗,主要用于 AF(59.1%)或 VTE(33.1%),最常用的 DOAC 是阿哌沙班(76.7%)。APT 的最常见适应证是 ASCVD 无 PCI(47.3%),其次是 ASCVD-PCI>12 个月前(30.8%)、主要 ASCVD 预防(18.7%)和 ASCVD-PCI≤12 个月前(1.7%)。有 5 名患者(1.4%)接受 APT 的适应证不明确。

根据最近限制抗凝治疗中添加 APT 的适应证和持续时间的指南,这项单中心研究中超过 95%的患者需要重新评估 APT 的适应证,稳定的 ASCVD 和一级预防是 APT 停药的主要目标。这项研究强调了提高患者安全性和减少出血危害的巨大潜力。

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