综合卒中中心颅内出血患者抗凝治疗的安全性

Sarah Boyko, O. Morgan, Kruti A. Shah, K. Chester
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引用次数: 0

摘要

背景:大约10%到15%的颅内出血(ICHs)患者接受抗凝治疗。此外,脑出血后患者可能出现抗凝指征。在脑出血后开始抗凝治疗的指导很少,大多数证据已经评估了维生素K拮抗剂(VKA)。目的:本研究的目的是评估非创伤性脑出血后抗凝处方与VKA、低分子肝素(LMWH)或直接口服抗凝剂(DOACs)的安全性。方法:回顾性分析2015年2月至2018年6月在某城市三级综合脑卒中中心收治的非外伤性脑出血并有抗凝指征的患者。主要目的是评估这些患者开抗凝处方的安全性。对两组患者进行回顾以评估主要结局:脑出血后开始抗凝治疗的患者(抗凝组)和未开始抗凝治疗的比较组(对照组)。主要终点是通过复发性脑出血、大出血事件和血栓栓塞事件的综合发生率来衡量。结果:23例有抗凝指征的患者在2个月内开始抗凝治疗。35例患者进行抗凝治疗。两组间的综合主要终点无差异(P = 0.29)。开始抗凝治疗的中位时间为21天(IQR 7 ~ 28天)。结论:本研究表明,在我们的队列患者中,近期脑出血患者开始抗凝治疗是安全的,并强调需要更有力的证据来指导临床决策。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Safety of Anticoagulation in Patients With an Intracranial Hemorrhage at a Comprehensive Stroke Center
Background: Approximately 10% to 15% of patients who suffer intracranial hemorrhages (ICHs) are on therapeutic anticoagulation. Additionally, patients may develop an indication for anticoagulation after ICH. There is minimal guidance with starting anticoagulation after an ICH, and most evidence has evaluated vitamin K antagonists (VKA). Objective: The aim of this study was to evaluate the safety of anticoagulation prescribing following a nontraumatic ICH with VKA, low molecular weight heparin (LMWH), or direct oral anticoagulants (DOACs). Methods: A retrospective chart review was conducted of patients admitted with a nontraumatic ICH and an indication for anticoagulation between February 2015 to June 2018 at an urban tertiary comprehensive stroke center. The primary objective was to evaluate the safety of prescribing anticoagulation in these patients. Two groups were reviewed to evaluate the primary outcome: patients who were started on anticoagulation after ICH (anticoagulation group) and a comparator group not started on anticoagulation (control group). The primary endpoint was measured by a composite incidence of recurrent ICH, major bleeding events, and thromboembolic events. Results: Anticoagulation was started within 2 months in 23 patients with an indication for anticoagulation. Anticoagulation was held in 35 patients. There was no difference in the composite primary endpoint between the 2 groups (P = .29). The median time to starting anticoagulation was 21 days (IQR 7-28 days). Conclusions: This study shows the safety of starting anticoagulation in patients with recent ICH in our cohort of patients and highlights the need for more robust evidence to guide clinical decision making.
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