Kurniawan Ricky Gusanto, Song Yunsun, Kwon Boseong, Ahn Yura, Suh Dae Chul
Neurovascular division National Brain Center, Prof. DR. dr. Mahar Mardjono Hospital, Jakarta, Indonesia.
Faculty of Medicine, University of Airlangga, Surabaya, Indonesia.
Neuroradiology. 2020 Dec;62(12):1709-1715. doi: 10.1007/s00234-020-02496-8. Epub 2020 Jul 13.
In patients requiring stent procedures, resistance or hyperresponsiveness to antiplatelet medications is often observed. This study aims to evaluate the efficacy and safety of tailoring medications in these patients.
This retrospective study included 223 patients who underwent endovascular treatment for intracranial aneurysm between October 2018 and October 2019. Patients were categorized as hyporesponsive, hyperresponsive, and normoresponsive groups according to the initial PRU response. For the hypo- or hyperresponders, we tailored medication by modifying the dose or changing the drug. PRUs before and after tailoring were compared in each group. PRU reponses in patients who underwent Cytochrome P450 2C19 (CYP2C19) genotyping were also determined.
Of the 73 clopidogrel-resistant patients, the mean PRU values after tailoring showed a greater decrease in the group that switched to prasugrel (n = 56), from 223 to 131, than in the clopidogrel reloading group (n = 17), from 238 to 209. In 31 hyperresponders, PRU increased from 49 to 94 after the dose adjustment. CYP2C19 genotyping showed that PRU tended to increase as the number of mutated alleles increased. There were five (2.3%) ischemic events (three transient ischemic attacks and two minor strokes) in a mean follow-up of 8 months, but no hemorrhage.
The stent-assisted coiling was successfully performed with acceptable range of ischemic events and without hemorrhage in all patients, including those who applied tailored medication. Low-dose prasugrel was effective for obtaining appropriate PRU values for initial medication as well as for clopidogrel-resistant patients. The genetic test did not provide reliable results in determining clopidogrel resistance.
在需要进行支架手术的患者中,经常观察到对抗血小板药物的抵抗或高反应性。本研究旨在评估为这些患者量身定制药物的疗效和安全性。
这项回顾性研究纳入了2018年10月至2019年10月期间接受颅内动脉瘤血管内治疗的223例患者。根据初始血小板反应单位(PRU)反应,将患者分为低反应性、高反应性和正常反应性组。对于低反应者或高反应者,我们通过调整剂量或更换药物来量身定制药物。比较每组患者调整药物前后的PRU。还测定了接受细胞色素P450 2C19(CYP2C19)基因分型患者的PRU反应。
在73例对氯吡格雷耐药的患者中,改用普拉格雷的组(n = 56)调整药物后PRU平均值下降幅度更大,从223降至131,而氯吡格雷再负荷组(n = 17)从238降至209。在31例高反应者中,调整剂量后PRU从49增至94。CYP2C19基因分型显示,随着突变等位基因数量的增加,PRU有升高趋势。平均随访8个月期间发生了5例(2.3%)缺血性事件(3例短暂性脑缺血发作和2例轻度中风),但无出血事件。
包括应用量身定制药物的患者在内,所有患者均成功进行了支架辅助弹簧圈栓塞术,缺血性事件在可接受范围内,且无出血。低剂量普拉格雷对于获得初始用药及氯吡格雷耐药患者的合适PRU值有效。基因检测在确定氯吡格雷耐药性方面未提供可靠结果。