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长期口服给药期间维拉帕米清除率降低。

Reduced verapamil clearance during long-term oral administration.

作者信息

Shand D G, Hammill S C, Aanonsen L, Pritchett E L

出版信息

Clin Pharmacol Ther. 1981 Nov;30(5):701-6. doi: 10.1038/clpt.1981.223.

Abstract

Plasma concentrations of verapamil and its metabolite, norverapamil, were measured in six patients with supraventricular tachycardia after the first and seventh dose of a regimen consisting of 120 mg every 8 hr by month. Steady state was reached by the seventh dose and the area under the concentration-time curve (AUC) at steady state (1999 +/- 435[SD] ng/ml . hr) was greater than that after the first dose (788 +/- 224, P less than 0.001). This unexpected cumulation was associated with prolongation of verapamil half-life (t1/2) from 2.75 +/- 1.14 to 4.52 +/- 1.10 hr. Norverapamil AUC also rose from 1225 +/- 405 to 2312 +/- 963 ng/ml/hr during the attainment of steady state. We conclude that verapamil cumulates to a greater extent than predicted from its t1/2, due to reduction in hepatic clearance.

摘要

对6例室上性心动过速患者,每月每8小时服用120毫克维拉帕米,在首剂和第七剂给药后测定血浆中维拉帕米及其代谢产物去甲维拉帕米的浓度。第七剂时达到稳态,稳态时浓度-时间曲线下面积(AUC)(1999±435[标准差]纳克/毫升·小时)大于首剂后(788±224,P<0.001)。这种意外的蓄积与维拉帕米半衰期(t1/2)从2.75±1.14小时延长至4.52±1.10小时有关。在达到稳态过程中,去甲维拉帕米AUC也从1225±405上升至2312±963纳克/毫升/小时。我们得出结论,由于肝清除率降低,维拉帕米的蓄积程度比根据其t1/2预测的更大。

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