首页> 外文期刊>Clinical Pharmacology: Advances and Applications >Simultaneous administration of high-dose atorvastatin and clopidogrel does not interfere with platelet inhibition during percutaneous coronary intervention
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Simultaneous administration of high-dose atorvastatin and clopidogrel does not interfere with platelet inhibition during percutaneous coronary intervention

机译:大剂量阿托伐他汀和氯吡格雷同时给药不会干扰经皮冠状动脉介入治疗期间的血小板抑制

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Background: Reloading with high-dose atorvastatin shortly before percutaneous coronary interventions (PCIs) has been proposed as a strategy to reduce periprocedural myonecrosis. There has been a concern that statins that are metabolized by cytochrome P450 3A4 may interfere with clopidogrel metabolism at high doses. The impact of simultaneous administration of high doses of atorvastatin and clopidogrel on the efficacy of platelet inhibition has not been established. Methods: Subjects (n=60) were randomized to receive atorvastatin 80 mg together with clopidogrel 600 mg loading dose (n=28) versus clopidogrel 600 mg alone (n=32) at the time of PCI. Platelet aggregation was measured at baseline, 4 hours after clopidogrel loading dose, and 16–24 hours after clopidogrel loading dose by light transmittance aggregometry using adenosine diphosphate as agonist. Results: Platelet aggregation was similar at baseline in both the atorvastatin and the control groups (adenosine diphosphate 10 μM: 57%±19% vs 61%±21%; P =0.52). There was no significant difference in platelet aggregation between the atorvastatin and the control groups at 4 hours (37%±18% vs 39%±21%; P =0.72) and 16–24 hours post-clopidogrel loading dose (35%±17% vs 37%±18%; P =0.75). No significant difference in incidence of periprocedural myonecrosis was observed between the atorvastatin and control groups (odds ratio: 1.02; 95% confidence interval 0.37–2.8). Conclusion: High-dose atorvastatin given simultaneously with clopidogrel loading dose at the time of PCI does not significantly alter platelet inhibition by clopidogrel. Statin reloading with high doses of atorvastatin at the time of PCI appears to be safe without adverse effects on platelet inhibition by clopidogrel (ClinicalTrials.gov: NCT00979940).
机译:背景:已提出在经皮冠状动脉介入治疗(PCIs)之前不久使用大剂量阿托伐他汀作为减少围手术期肌坏死的策略。人们担心,被细胞色素P450 3A4代谢的他汀类药物可能会在高剂量下干扰氯吡格雷的代谢。同时给药大剂量的阿托伐他汀和氯吡格雷对血小板抑制功效的影响尚未确定。方法:受试者(n = 60)在PCI时被随机分配接受阿托伐他汀80 mg和氯吡格雷600 mg负荷剂量(n = 28),而单独接受氯吡格雷600 mg(n = 32)。使用二磷酸腺苷作为激动剂,在基线,氯吡格雷负荷量后4小时和氯吡格雷负荷量后16-24小时通过血小板凝集测定血小板聚集。结果:阿托伐他汀和对照组的血小板聚集在基线时相似(二磷酸腺苷10μM:57%±19%对61%±21%; P = 0.52)。阿托伐他汀与对照组之间在第4小时(37%±18%vs 39%±21%; P = 0.72)和氯吡格雷负荷剂量后16-24小时(35%±17)之间的血小板聚集没有显着差异。 %对37%±18%; P = 0.75)。阿托伐他汀与对照组之间的围手术期肌坏死发生率没有显着差异(优势比:1.02; 95%置信区间0.37–2.8)。结论:PCI时同时给予大剂量阿托伐他汀和氯吡格雷负荷剂量不能显着改变氯吡格雷对血小板的抑制作用。在PCI时用大剂量的阿托伐他汀重载他汀似乎是安全的,并且不会对氯吡格雷抑制血小板产生不利影响(ClinicalTrials.gov:NCT00979940)。

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