Cardiology Department-Ferrarotto Hospital, University of Catania, Italy.
Thromb Haemost. 2011 Dec;106(6):1149-57. doi: 10.1160/TH11-05-0346. Epub 2011 Oct 20.
Studies specifically designed to assess clopidogrel response in the elderly as well as treatment alternatives to improve platelet inhibition in this high-risk population are lacking. This study aimed to define pharmacodynamic (PD) profiles, including high platelet reactivity (HPR) rates, among elderly patients on maintenance clopidogrel therapy and to assess the PD effects of prasugrel 5 mg/day in elderly with HPR. This was a prospective observational PD study enrolling consecutive ≥ 75-year-old patients on maintenance clopidogrel therapy (75 mg/day) who were tested for clopidogrel response by the VerifyNow P2Y12 assay and light transmittance aggregometry (LTA). HPR rates were estimated using multiple definitions. HPR patients identified by the VerifyNow P2Y12 assay [P2Y12 reaction unit (PRU) ≥ 230] were switched to prasugrel 5 mg/day, and platelet function testing was performed after 15 days of treatment. PD testing was completed in 100 patients. The HPR prevalence varied between 25% and 32%, depending on the definition used. A PRU ≥ 230 was observed in 25 patients; of these, 20 switched to prasugrel 5 mg/day. This resulted in significant reduction in PRU mean values (279.8 ± 45.1 vs. 171.7 ± 65.2, p=0.0002) with an absolute between-treatment difference of 108.1 (95% confidence intervals 75.2-140.9). Accordingly, switching to prasugrel 5 mg/day overcame HPR in most (80%) patients. Consistently, all LTA measures were significantly lower after prasugrel compared with clopidogrel. In conclusion, a considerable proportion of elderly patients exhibit HPR while on standard clopidogrel therapy. Switching to 5 mg/day prasugrel in elderly patients with HPR is associated with enhanced platelet inhibition and overcomes HPR in the majority of these patients.
专门评估老年人氯吡格雷反应的研究以及改善该高危人群血小板抑制的治疗选择的研究还很缺乏。本研究旨在确定接受维持性氯吡格雷治疗的老年患者的药效学(PD)特征,包括高血小板反应性(HPR)的发生率,并评估普拉格雷 5mg/日在 HPR 老年患者中的 PD 效应。这是一项前瞻性观察性 PD 研究,纳入了连续的≥75 岁接受维持性氯吡格雷治疗(75mg/日)的患者,他们通过 VerifyNow P2Y12 测定和光透射聚集测定(LTA)检测氯吡格雷的反应。使用多种定义来估计 HPR 发生率。通过 VerifyNow P2Y12 测定[P2Y12 反应单位(PRU)≥230]确定的 HPR 患者转换为普拉格雷 5mg/日,并在治疗 15 天后进行血小板功能检测。完成了 100 例患者的 PD 检测。HPR 的流行率因定义不同而在 25%至 32%之间变化。在 25 例患者中观察到 PRU≥230,其中 20 例转换为普拉格雷 5mg/日。这导致 PRU 平均值显著降低(279.8±45.1 vs. 171.7±65.2,p=0.0002),治疗间绝对差异为 108.1(95%置信区间 75.2-140.9)。因此,大多数(80%)患者转换为普拉格雷 5mg/日可克服 HPR。同样,与氯吡格雷相比,普拉格雷治疗后所有 LTA 测量值均显著降低。总之,相当一部分老年患者在接受标准氯吡格雷治疗时表现出 HPR。在 HPR 老年患者中转换为普拉格雷 5mg/日与增强的血小板抑制相关,并在大多数这些患者中克服了 HPR。