Suppr超能文献

在接受或未接受氯吡格雷长期治疗的冠心病患者中给予600毫克氯吡格雷负荷剂量。

Loading with 600 mg clopidogrel in patients with coronary artery disease with and without chronic clopidogrel therapy.

作者信息

Kastrati Adnan, von Beckerath Nicolas, Joost Alexander, Pogatsa-Murray Gisela, Gorchakova Olga, Schömig Albert

机构信息

Deutsches Herzzentrum and 1 Medizinische Klinik rechts der Isar; Technische Universität, Munich, Germany.

出版信息

Circulation. 2004 Oct 5;110(14):1916-9. doi: 10.1161/01.CIR.0000137972.74120.12. Epub 2004 Jul 19.

Abstract

BACKGROUND

It is not known whether further suppression of platelet function can be achieved with clopidogrel beyond that provided by currently recommended loading and maintenance doses. We performed a comparative assessment of the antiplatelet effects of a 600-mg loading dose of clopidogrel given to patients with and without chronic clopidogrel therapy.

METHODS AND RESULTS

Those eligible for this prospective study were aspirin-treated patients with suspected or documented coronary artery disease admitted to hospital for coronary angiography. Two series of 20 consecutive patients each were assessed in this study. The first series included patients who had never received clopidogrel (first-use group); the second series included patients on chronic therapy with a daily dose of 75 mg clopidogrel for > or =1 month (chronic therapy group). Blood samples were drawn before and 6 hours after oral administration of 600 mg clopidogrel for aggregometry and flow cytometry studies. In the first-use group, loading with 600 mg clopidogrel inhibited ADP 5 micromol/L-induced platelet aggregation from 90+/-9% to 51+/-19% (P<0.001). In the chronic therapy group, loading with 600 mg clopidogrel yielded further inhibition of ADP 5 micromol/L-induced platelet aggregation in addition to that achieved by the maintenance dose of 75 mg/d, from 52+/-14% to 33+/-12% (P<0.001). In both groups, 600 mg clopidogrel loading significantly inhibited ADP-induced expression of glycoprotein IIb/IIIa and P-selectin receptors.

CONCLUSIONS

Further platelet inhibition can be achieved with clopidogrel in addition to that provided by currently recommended loading and maintenance doses. Higher doses may be warranted after assessment of their clinical efficacy and safety.

摘要

背景

目前尚不清楚氯吡格雷在超出当前推荐的负荷剂量和维持剂量之外,是否还能进一步抑制血小板功能。我们对给予或未给予氯吡格雷长期治疗的患者使用600mg负荷剂量氯吡格雷的抗血小板作用进行了比较评估。

方法与结果

本前瞻性研究的入选对象为因冠状动脉造影而入院的、接受阿司匹林治疗的疑似或确诊冠心病患者。本研究评估了两个系列,每个系列各20例连续患者。第一个系列包括从未接受过氯吡格雷治疗的患者(首次使用组);第二个系列包括每日服用75mg氯吡格雷≥1个月的长期治疗患者(长期治疗组)。在口服600mg氯吡格雷前及服药后6小时采集血样,用于血小板聚集试验和流式细胞术研究。在首次使用组,600mg氯吡格雷负荷剂量使5μmol/L ADP诱导的血小板聚集率从90±9%降至51±19%(P<0.001)。在长期治疗组,600mg氯吡格雷负荷剂量除了能产生75mg/d维持剂量所带来的抑制作用外,还能进一步抑制5μmol/L ADP诱导的血小板聚集,使其从52±14%降至33±12%(P<0.001)。在两组中,600mg氯吡格雷负荷剂量均显著抑制ADP诱导的糖蛋白IIb/IIIa和P选择素受体的表达。

结论

除了目前推荐的负荷剂量和维持剂量外,氯吡格雷还能进一步抑制血小板功能。在评估其临床疗效和安全性后,可能需要更高的剂量。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验