Le Coz F, Funck-Brentano C, Poirier J M, Kibleur Y, Mazoit F X, Jaillon P
Clinical Pharmacology Unit, Saint-Antoine University Hospital, Paris, France.
Clin Pharmacol Ther. 1992 Oct;52(4):417-26. doi: 10.1038/clpt.1992.165.
The relationship between racemic sotalol plasma concentrations and QTc interval prolongation after both single-dose and repeated administration of three sotalol oral doses was studied in a randomized crossover protocol performed in 10 healthy volunteers. QTc interval increase was significant after the three single-dose sotalol administrations and was significantly related to the administered dose (p < 0.0001). In 21 of 30 analyses, QTc interval was linearly correlated with sotalol plasma concentrations. After the 320 mg dose, the linear model was a best fit for 90% of the cases, and no hysteresis was observed. After repeated sotalol administration, 69 of 87 QTc interval measurements at steady state could be predicted from the plasma concentration versus effect relationship established after single-dose 320 mg administration. Seventeen of 18 errors (94%) corresponded to QTc intervals that were significantly lower than predicted. These findings suggest that a short-term individual linear model determined after a 320 mg test dose of sotalol allows a good prediction of expected maximal increase in QTc duration in healthy subjects.
在一项对10名健康志愿者进行的随机交叉试验中,研究了单剂量和重复给予三种索他洛尔口服剂量后,消旋索他洛尔血浆浓度与QTc间期延长之间的关系。单次给予三种索他洛尔剂量后,QTc间期增加显著,且与给药剂量显著相关(p<0.0001)。在30次分析中的21次中,QTc间期与索他洛尔血浆浓度呈线性相关。给予320mg剂量后,线性模型在90%的病例中拟合最佳,且未观察到滞后现象。重复给予索他洛尔后,稳态下87次QTc间期测量中的69次可根据单剂量给予320mg后建立的血浆浓度与效应关系进行预测。18次误差中的17次(94%)对应的QTc间期显著低于预测值。这些发现表明,索他洛尔320mg试验剂量后确定的短期个体线性模型能够很好地预测健康受试者QTc间期预期的最大增加。