Pollak P T, Sharma A D, Carruthers S G
Department of Medicine, Victoria General Hospital, Dalhousie University, Halifax, Nova Scotia, Canada.
Am J Cardiol. 1989 Nov 15;64(18):1138-43. doi: 10.1016/0002-9149(89)90866-7.
Pharmacokinetic-dynamic relations for amiodarone have been difficult to define. Few studies have successfully correlated serum amiodarone concentration with either dose or pharmacodynamic effects. Reduction in heart rate, prolongation of corrected QT interval and accumulation of corneal microdeposits are 3 clinical effects well suited for making kinetic-dynamic comparisons because they occur in virtually all patients receiving amiodarone. Data on heart rate, corrected QT interval, corneal microdeposits, cumulative dose and serum concentrations of amiodarone and desethylamiodarone (DEA) were collected over the course of 1 year after initiation of therapy in 27 patients (mean age 55.4 +/- 2.35 years). Mean elimination half-lives in this study population were 56 days for amiodarone and 129 days for DEA, as estimated from cumulation kinetics without drug withdrawal. The extremely long half-lives of amiodarone and DEA make demonstration of steady-state concentration-response relations difficult. A new approach using analysis of sequential data before steady-state reveals general relations between dose, DEA concentration and 3 clinically observable effects of amiodarone. A linear relation was evident between DEA concentration and log mean cumulative amiodarone dose (mg/kg) for the population. The steep segments of the concentration-response curves for heart rate, microdeposits and corrected QT interval occurred at low, medium and high serum amiodarone and DEA concentrations, respectively. Patients not developing a decrease in heart rate or corneal microdeposits likely have very low serum drug concentrations and may not be adequately treated. The monitoring of heart rate, corrected QT interval and corneal microdeposits as an aid to assessing adequacy of amiodarone therapy requires further study.
胺碘酮的药代动力学-药效学关系一直难以确定。很少有研究成功地将血清胺碘酮浓度与剂量或药效学效应联系起来。心率降低、校正QT间期延长和角膜微沉积物积累是3种很适合进行药代动力学-药效学比较的临床效应,因为几乎所有接受胺碘酮治疗的患者都会出现这些效应。在27例患者(平均年龄55.4±2.35岁)开始治疗后的1年时间里,收集了有关心率、校正QT间期、角膜微沉积物、胺碘酮和去乙基胺碘酮(DEA)的累积剂量及血清浓度的数据。根据未停药情况下的累积动力学估算,该研究人群中胺碘酮的平均消除半衰期为56天,DEA为129天。胺碘酮和DEA极长的半衰期使得证明稳态浓度-反应关系变得困难。一种利用稳态前序贯数据分析的新方法揭示了剂量、DEA浓度与胺碘酮3种临床可观察效应之间的一般关系。该人群中DEA浓度与对数平均胺碘酮累积剂量(mg/kg)之间存在明显的线性关系。心率、微沉积物和校正QT间期浓度-反应曲线的陡峭部分分别出现在低、中和高血清胺碘酮及DEA浓度时。未出现心率降低或角膜微沉积物的患者可能血清药物浓度非常低,可能未得到充分治疗。将心率、校正QT间期和角膜微沉积物监测作为评估胺碘酮治疗充分性的辅助手段需要进一步研究。