Sylvester R K, Lewis F B, Caldwell K C, Lobell M, Perri R, Sawchuk R A
Ther Drug Monit. 1984;6(3):302-5. doi: 10.1097/00007691-198409000-00008.
A 24-year-old woman experienced grand mal seizures temporally related to cisplatin, vinblastine, and bleomycin (CVB) administration. A second episode of seizures occurred when the patient's phenytoin level was estimated to be in the range of 15 micrograms/ml. Her plasma phenytoin level at the time had dropped to 2 microgram/ml despite a recent dosage increase. To evaluate the cause of the subtherapeutic phenytoin levels, daily plasma phenytoin levels and 24-h urine collections were obtained during her next CVB cycle. Data revealed a mean phenytoin absorption of 32% (normal greater than 80%), establishing that phenytoin malabsorption occurred. The disruption of phenytoin absorption at a cellular level by CVB therapy is the proposed mechanism. Frequent monitoring of plasma phenytoin levels is recommended for patients receiving CVB.
一名24岁女性在接受顺铂、长春碱和博来霉素(CVB)治疗期间出现了与用药时间相关的癫痫大发作。当估计患者苯妥英水平在15微克/毫升范围内时,发生了第二次癫痫发作。尽管最近增加了剂量,但当时她的血浆苯妥英水平已降至2微克/毫升。为了评估苯妥英水平低于治疗剂量的原因,在她的下一个CVB治疗周期中,每天检测血浆苯妥英水平并收集24小时尿液。数据显示苯妥英的平均吸收率为32%(正常大于80%),证实发生了苯妥英吸收不良。推测CVB治疗在细胞水平上破坏苯妥英吸收是其机制。建议对接受CVB治疗的患者频繁监测血浆苯妥英水平。