Uthman B M, Wilder B J, Ramsay R E
Neurology Service, Department of Veterans Affairs Medical Center, Gainesville, FL 32608, USA.
Neurology. 1996 Jun;46(6 Suppl 1):S24-8. doi: 10.1212/wnl.46.6_suppl_1.24s.
Phenobarbital, diazepam, lorazepam, and phenytoin are all currently used for the treatment of acute seizures, including status epilepticus. None of these drugs is considered ideal. Fosphenytoin is a new phenytoin prodrug that fulfills many of the properties of an ideal anticonvulsant drug. The safety, tolerance, and pharmacokinetics of intramuscularly administered fosphenytoin have been evaluated in three clinical trials involving patients requiring loading or maintenance doses of phenytoin. These investigations demonstrated that fosphenytoin is rapidly and completely absorbed after injection into muscle and is quickly converted to produce therapeutic phenytoin plasma concentrations within 30 min of administration. Plasma concentrations of phenytoin achieved with i.m. fosphenytoin exceeded those associated with an equimolar dose of oral phenytoin. i.m. fosphenytoin was well tolerated both locally and systemically. Only mild and transient reactions occurred at the injection site. The most common systemic adverse events reported--somnolence, nystagmus, dizziness, and ataxia--are side effects commonly seen with phenytoin and tended to be mild. Preexisting seizure disorders remained stable. Combination treatment with i.v. diazepam or lorazepam to attain rapid seizure control and i.m. fosphenytoin to maintain the anticonvulsant effect theoretically offers many advantages for control of acute seizures and should be studied.
苯巴比妥、地西泮、劳拉西泮和苯妥英目前均用于治疗急性惊厥,包括癫痫持续状态。这些药物均非理想药物。磷苯妥英是一种新型苯妥英前体药物,具备理想抗惊厥药物的许多特性。三项涉及需要苯妥英负荷剂量或维持剂量的患者的临床试验评估了肌肉注射磷苯妥英的安全性、耐受性和药代动力学。这些研究表明,磷苯妥英注射入肌肉后能迅速且完全吸收,并在给药后30分钟内迅速转化以产生治疗性苯妥英血浆浓度。肌肉注射磷苯妥英所达到的苯妥英血浆浓度超过了等摩尔剂量口服苯妥英所对应的浓度。肌肉注射磷苯妥英在局部和全身耐受性良好。注射部位仅出现轻微和短暂的反应。所报告的最常见全身不良事件——嗜睡、眼球震颤、头晕和共济失调——是苯妥英常见的副作用,且往往较为轻微。既往存在的癫痫疾病保持稳定。理论上,静脉注射地西泮或劳拉西泮以实现快速控制惊厥,以及肌肉注射磷苯妥英以维持抗惊厥效果的联合治疗在控制急性惊厥方面具有诸多优势,值得研究。