Pharmacokinetic parameters of thiamazole in hyperthyroid patients responding rapidly and slowly to the treatment.

A Syrenicz, B Gawrońska-Szklarz, J Wójcicki, S Czekalski
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Abstract

Pharmacokinetic parameters of thiamazole were compared in two groups of patients with hyperthyroidism due to Graves-Basedow disease, differing in the period required to achieve clinical euthyrosis (less than 28 days, group R, n = 23, and not less than 35 days, group D, n = 18) after treatment with the "full" dose of the drug. The drug absorption from the GI tract in both groups was similar, but the serum concentrations of the drug (Cmax and AUC) were higher, and distribution volume and total clearance lower in the R than in D group. No evidence was found for the importance of initial plasma levels of thyroxine or triiodothyronine on pharmacokinetic parameters of thiamazole.

甲状腺机能亢进患者对噻马唑药代动力学参数的快速反应和缓慢反应。
比较两组Graves-Basedow病所致甲状腺功能亢进患者的药代动力学参数,两组患者在使用“全”剂量的药物治疗后达到临床甲状腺功能正常所需的时间不同(少于28天,R组,n = 23,不少于35天,D组,n = 18)。两组药物在胃肠道的吸收相似,但药物的血清浓度(Cmax和AUC)高于D组,分布体积和总清除率低于R组。没有证据表明初始血浆甲状腺素或三碘甲状腺原氨酸水平对噻马唑药代动力学参数的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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