Delgado Almandoz Josser E, Kadkhodayan Yasha, Crandall Benjamin M, Scholz Jill M, Fease Jennifer L, Tubman David E
Division of Interventional Neuroradiology, Neuroscience Institute, Abbott Northwestern Hospital, Minneapolis, Minnesota, USA.
J Neurointerv Surg. 2014 Dec;6(10):767-73. doi: 10.1136/neurintsurg-2013-010976. Epub 2013 Dec 18.
Variability in response to clopidogrel therapy is increasingly being recognized as an important factor in thromboembolic and hemorrhagic complications encountered after neurointerventional procedures. This study aims to determine the variability in response to clopidogrel therapy and associated complications in patients undergoing endovascular treatment of unruptured cerebral aneurysms.
We recorded baseline patient characteristics, co-administered medications, P2Y12 reaction units (PRU) values with VerifyNow, clopidogrel dosing, and thromboembolic and hemorrhagic complications in patients undergoing endovascular treatment of unruptured cerebral aneurysms at our institution during a 19 month period.
100 patients were included in the study, 76 women and 24 men, mean age 57.3 years. 15 patients exhibited an initial clopidogrel hypo-response (PRU >240) and 21 patients an initial clopidogrel hyper-response (PRU <60). 36 patients had a follow-up VerifyNow test performed without changes to the standard 75 mg daily clopidogrel dose, which demonstrated that 59% of patients who had initially been within the target 60-240 PRU range exhibited a delayed conversion to clopidogrel hyper-response. In our cohort, a clopidogrel hypo-response was associated with a significantly increased risk of thromboembolic complications in patients undergoing cerebral aneurysm treatment with stent assistance or the pipeline embolization device (60%, p=0.003), while a clopidogrel hyper-response was associated with a significantly increased risk of major hemorrhagic complications in all patients undergoing endovascular treatment of cerebral aneurysms (11%, p=0.016).
We found wide and dynamic variability in response to clopidogrel therapy in patients undergoing endovascular treatment of unruptured cerebral aneurysms, which was significantly associated with thromboembolic and major hemorrhagic complications in our cohort.
氯吡格雷治疗反应的变异性日益被视为神经介入手术后血栓栓塞和出血并发症的一个重要因素。本研究旨在确定未破裂脑动脉瘤血管内治疗患者对氯吡格雷治疗的反应变异性及相关并发症。
我们记录了在19个月期间,于本机构接受未破裂脑动脉瘤血管内治疗患者的基线特征、联合使用的药物、使用VerifyNow检测的P2Y12反应单位(PRU)值、氯吡格雷剂量以及血栓栓塞和出血并发症情况。
100例患者纳入研究,其中女性76例,男性24例,平均年龄57.3岁。15例患者初始表现为氯吡格雷低反应(PRU>240),21例患者初始表现为氯吡格雷高反应(PRU<60)。36例患者在氯吡格雷每日标准剂量75mg未改变的情况下接受了VerifyNow随访检测,结果显示,最初处于目标PRU范围60 - 240内的患者中有59%出现延迟转变为氯吡格雷高反应。在我们的队列中,对于接受支架辅助或Pipeline栓塞装置治疗脑动脉瘤的患者,氯吡格雷低反应与血栓栓塞并发症风险显著增加相关(60%,p = 0.003),而对于所有接受脑动脉瘤血管内治疗的患者,氯吡格雷高反应与严重出血并发症风险显著增加相关(11%,p = 0.016)。
我们发现未破裂脑动脉瘤血管内治疗患者对氯吡格雷治疗的反应存在广泛且动态的变异性,这与我们队列中的血栓栓塞和严重出血并发症显著相关。