Wilson J T, Höjer B, Rane A
Clin Pharmacol Ther. 1976 Jul;20(1):48-58. doi: 10.1002/cpt197620148.
Epileptic children were given phenytoin (DPH) in loading (four doses of 4.4 to 6.3 mg/kg/dose given 8-hourly and then 6 mg/kg/day) or conventional (5 to 9 mg/kg/day) doses. Plasma levels of DPH and its main metabolite (p-OH-DPH) were measured by a mass fragmentographic technique. Plasma DPH levels of more than 10 mug/ml were achieved within 16 to 38 hr in the children given loading doses and within 5 days in the conventionally dosed children. No immediate side effects were noted, but within 8 to 10 days 9 of 13 children developed a generalized skin rash. Plasma p-OH-DPH (free or conjugated) paralleled DPH during the accumulation phase but not during DPH elimination. The ratio of metabolite to DPH in plasma showed both an interindividual variation and an inverse relation to the level of DPH. Identical twins in the study had a similar ratio and plasma level-time course profile. It is concluded that the loading dose regiment achieves an appropriate plasma level of DPH rapidly, that saturation kinetics are operative for p-OH-DPH formation, that the ratio of metabolite to DPH in plasma is an individual characteristic in children, and that further studies on the delayed toxicity are needed before the loading dose regimen can be recommended.
癫痫患儿接受了苯妥英(DPH)的负荷剂量(每8小时给予4剂,每剂4.4至6.3毫克/千克,然后每天6毫克/千克)或常规剂量(每天5至9毫克/千克)治疗。采用质量碎片图谱技术测定血浆中DPH及其主要代谢产物(对羟基苯妥英,p-OH-DPH)的水平。接受负荷剂量治疗的患儿在16至38小时内血浆DPH水平达到10微克/毫升以上,接受常规剂量治疗的患儿则在5天内达到该水平。未观察到即时副作用,但在8至10天内,13名患儿中有9名出现全身性皮疹。在DPH蓄积阶段,血浆中游离或结合的p-OH-DPH与DPH平行,但在DPH消除阶段则不然。血浆中代谢产物与DPH的比值显示出个体差异,且与DPH水平呈反比关系。该研究中的同卵双胞胎具有相似的比值和血浆水平-时间过程曲线。结论是,负荷剂量方案能迅速达到适当的血浆DPH水平,对羟基苯妥英的形成存在饱和动力学,血浆中代谢产物与DPH的比值是儿童的个体特征,在推荐负荷剂量方案之前,需要对延迟毒性进行进一步研究。