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抗血小板治疗 - 替格瑞洛。

Antiplatelet therapy - ticagrelor.

机构信息

Department of Internal Medicine III, Cardiology, University Hospital Heidelberg, Germany.

出版信息

Hamostaseologie. 2012;32(3):177-85. doi: 10.5482/HAMO-12-05-0003. Epub 2012 Jun 28.

Abstract

UNLABELLED

Ticagrelor, a cyclopentyltriazolopyrimidine (CPTP), is the representative of a new chemical class of P2Y(12) receptor inhibitors that differ from thienopyridines (ticlopidin, clopidogrel, prasugrel) as ticagrelor is not a prodrug requiring active biotransformation by cytochromes in the liver and thus is characterized by a more rapid, more effective and more consistent platelet inhibition than ticlopidin or clopidogrel. An extensive study program for dose finding and safety for AZD6140 (DISPERSE studies) and a large-scaled phase III trial (PLATO) were undertaken on more than 18,000 patients for validation of efficacy and safety. In the PLATO trial, patients presenting with the broad spectrum of ACS, i.e. unstable angina, non-STEMI or STEMI, were randomized to ticagrelor (Brilique, Brilinta) or clopidogrel within 24 hours after onset of symptoms, regardless whether they were allocated to a planned invasive or conservative treatment. Compared to clopidogrel, ticagrelor reduced rates of the primary endpoint consisting of cardiovascular death, non-fatal MI, or stroke, without an excess of the primary safety endpoint that was PLATO-defined major bleedings. Results from the pre-specified confirmatory subgroup of patients undergoing planned invasive treatment was consistent with PLATO main trial. In addition, the primary endpoint, as well as CV death and all cause death were consistently reduced with ticagrelor in numerous exploratory subgroups including STEMI patients, those planned for non-invasive treatment, patients undergoing CABG, patients with renal failure, and those with diabetes mellitus, although patients were pretreated before coronary angiography and patients with clopidogrel pretreatment were not excluded.

CONCLUSIONS

The pharmacological properties and convincing study results of the PLATO trial have stimulated a paradigm change for dual antiplatelet therapy. The new ESC guidelines on the management of ACS without ST segment elevation recommend the use of clopidogrel only when a new antiplatelet drug, e.g. ticagrelor or prasugrel is not available or contraindicated.

摘要

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替格瑞洛是一种环戊基三唑嘧啶(CPTP),是新一代 P2Y(12)受体抑制剂的代表,与噻吩吡啶(噻氯匹定、氯吡格雷、普拉格雷)不同,替格瑞洛不是需要在肝脏中经细胞色素进行主动生物转化的前体药物,因此其具有更快、更有效和更一致的血小板抑制作用,优于噻氯匹定或氯吡格雷。AZD6140(DISPERSE 研究)的剂量发现和安全性进行了广泛的研究计划,并在超过 18000 名患者中进行了大规模的 III 期试验(PLATO),以验证疗效和安全性。在 PLATO 试验中,患有广泛 ACS 的患者,即不稳定型心绞痛、非 ST 段抬高型心肌梗死或 ST 段抬高型心肌梗死,在症状发作后 24 小时内随机接受替格瑞洛(Brilique、Brilinta)或氯吡格雷治疗,无论他们是否被分配到计划的侵入性或保守性治疗。与氯吡格雷相比,替格瑞洛降低了由心血管死亡、非致死性心肌梗死或中风组成的主要终点的发生率,且未增加 PLATO 定义的主要安全性终点即大出血。计划进行侵入性治疗的患者预先指定的确认亚组的结果与 PLATO 主要试验一致。此外,在包括 STEMI 患者、计划进行非侵入性治疗的患者、接受 CABG 的患者、肾衰竭患者和糖尿病患者在内的众多探索性亚组中,替格瑞洛也一致降低了主要终点以及心血管死亡和全因死亡。尽管在冠状动脉造影前对患者进行了预处理,且未排除氯吡格雷预处理的患者。

结论

PLATO 试验的药理学特性和令人信服的研究结果激发了双重抗血小板治疗的范式转变。新的 ESC 关于非 ST 段抬高型急性冠脉综合征管理指南建议,仅在无法获得或禁忌使用新的抗血小板药物(如替格瑞洛或普拉格雷)时才使用氯吡格雷。

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