Department of Neurology, Wayne State University School of Medicine, Detroit, Michigan, USA.
Department of Medicine, Wayne State University School of Medicine, Detroit, Michigan, USA.
J Neurointerv Surg. 2019 Apr;11(4):362-366. doi: 10.1136/neurintsurg-2018-014082. Epub 2018 Sep 10.
Pipeline embolization devices (PEDs) are increasingly used in the treatment of cerebral aneurysms. Yet, major ischemic or hemorrhagic complications after PED treatment associated with antiplatelet regimens are not well-established.
To investigate the risk of ischemic and hemorrhagic complications associated with common antiplatelet regimens following PED treatment, and to examine whether platelet function testing (PFT) is associated with a lower risk of these complications.
We searched Medline, Embase, and Cochrane from 2009 to 2017. Twenty-nine studies were included that had reported a uniform antiplatelet regimen protocol and had provided data on major ischemic and hemorrhagic complications following PED treatment. Random-effect meta-analysis was used to pool overall ischemic and hemorrhagic event rates across studies. The rate of these complications with respect to the antithrombotic regimen and PFT was assessed by χ proportional tests.
Overall, 2002 patients (age 55.9 years, 76% female) were included. A low-dose acetylsalicylic acid (ASA) regimen before and after PED treatment was associated with a higher rate of late ischemic complications than with high-dose ASA therapy (2.62 (95% CI 1.46 to 4.69) and 2.56 (1.41 to 4.64), respectively). Duration of post-procedure clopidogrel therapy <6 months was associated with greater rates of ischemic complications (1.56, 95% CI 1.11 to 2.20) than a clopidogrel regimen of ≥6 months. Performing PFT before PED treatment was not associated with the risk of ischemic complications (1.27, 95% CI 0.77 to 2.10).
High-dose ASA therapy and clopidogrel treatment for at least 6 months were associated with a reduced incidence of ischemic events, without affecting the risk of hemorrhagic events.
Pipeline 栓塞装置(PED)在治疗脑动脉瘤中的应用越来越广泛。然而,与抗血小板方案相关的 PED 治疗后发生的主要缺血或出血并发症尚未得到充分证实。
研究常见抗血小板方案与 PED 治疗后缺血和出血并发症的关系,并探讨血小板功能检测(PFT)是否与降低这些并发症的风险相关。
我们检索了 2009 年至 2017 年的 Medline、Embase 和 Cochrane。共纳入 29 项研究,这些研究报告了统一的抗血小板方案,并提供了 PED 治疗后主要缺血和出血并发症的数据。采用随机效应荟萃分析对研究间总体缺血和出血事件发生率进行汇总。采用 χ2 比例检验评估抗血栓形成方案和 PFT 与这些并发症发生率的关系。
共纳入 2002 例患者(年龄 55.9 岁,76%为女性)。PED 治疗前后低剂量乙酰水杨酸(ASA)方案与高剂量 ASA 治疗相比,晚期缺血性并发症发生率更高(分别为 2.62(95%CI 1.46 至 4.69)和 2.56(1.41 至 4.64))。PED 治疗后 6 个月内氯吡格雷治疗时间<6 个月与缺血性并发症发生率增加相关(1.56,95%CI 1.11 至 2.20),而氯吡格雷治疗时间≥6 个月则无相关性。PED 治疗前进行 PFT 与缺血性并发症风险无关(1.27,95%CI 0.77 至 2.10)。
高剂量 ASA 治疗和至少 6 个月的氯吡格雷治疗可降低缺血性事件的发生率,而不影响出血事件的风险。