Ahn J E, Cloyd J C, Brundage R C, Marino S E, Conway J M, Ramsay R E, White J R, Musib L C, Rarick J O, Birnbaum A K, Leppik I E
Department of Experimental and Clinical Pharmacology, University of Minnesota, Minneapolis, MN 55455, USA.
Neurology. 2008 Jul 1;71(1):38-43. doi: 10.1212/01.wnl.0000316392.55784.57.
Phenytoin (PHT) is widely used to treat epilepsy in elderly patients, but information on its pharmacokinetics in this population is limited.
The purpose of this study was to investigate the effects of age and sex on PHT pharmacokinetics using stable-labeled (SL) isotopes of PHT or fosphenytoin (FOS) administered IV or IM while patients remained on their oral maintenance regimen.
Subjects were patients 18 years or older with epilepsy, but otherwise healthy, on a maintenance regimen of PHT who were not taking interacting medications. Subjects were given a single injection of a 100 mg dose of SL-PHT or SL-FOS followed by their usual morning PHT dose less 100 mg. Serial blood samples were collected up to 196 hours after the SL dose. Plasma PHT and SL-PHT concentrations were measured by a gas chromatographic-mass spectrometric assay. PHT pharmacokinetics were characterized using a population-based, nonlinear, mixed-effects model.
Sixty-three subjects completed the study, 45 of whom were 65 years or older. There was no difference between adult and elderly or men and women in PHT clearance, distribution volume, and elimination half-life. The mean elimination half-life was 40 hours.
Healthy elderly adults appear to have the same phenytoin (PHT) pharmacokinetics as younger adults. Reduced PHT dosage requirements may be due to age-related changes in patients' sensitivity to the therapeutic and toxic effects of the drug. The prolonged elimination half-life suggests that most patients can take PHT once daily and the time to reach steady-state may extend to 2-3 weeks.
苯妥英(PHT)广泛用于治疗老年癫痫患者,但其在该人群中的药代动力学信息有限。
本研究旨在通过静脉或肌肉注射稳定同位素标记(SL)的苯妥英或磷苯妥英(FOS),同时患者维持口服维持治疗方案,研究年龄和性别对苯妥英药代动力学的影响。
研究对象为18岁及以上癫痫患者,身体健康,正在接受苯妥英维持治疗且未服用相互作用药物。研究对象单次注射100mg剂量的SL-苯妥英或SL-磷苯妥英,然后给予其常规早晨苯妥英剂量减去100mg。在注射SL剂量后长达196小时内采集系列血样。采用气相色谱-质谱分析法测定血浆苯妥英和SL-苯妥英浓度。使用基于群体的非线性混合效应模型对苯妥英药代动力学进行表征。
63名受试者完成了研究,其中45名年龄在65岁及以上。在苯妥英清除率、分布容积和消除半衰期方面,成年人与老年人或男性与女性之间没有差异。平均消除半衰期为40小时。
健康老年人的苯妥英药代动力学似乎与年轻人相同。苯妥英剂量需求降低可能是由于患者对药物治疗和毒性作用的敏感性随年龄变化所致。消除半衰期延长表明大多数患者可以每日服用一次苯妥英,达到稳态的时间可能延长至2-3周。