Thomas Michele, DiPaula Bethany A, Grimm Beverley
(Corresponding author) Assistant Director of Pharmacy, Springfield Hospital Center, University of Maryland School of Pharmacy Baltimore, Sykesville, Maryland,
Associate Professor, University of Maryland School of Pharmacy Baltimore, Baltimore, Maryland; Director of Pharmacy, Springfield Hospital Center, Sykesville, Maryland.
Ment Health Clin. 2018 Jun 29;8(4):195-197. doi: 10.9740/mhc.2018.07.195. eCollection 2018 Jul.
To describe a patient case in which a drug interaction involving quetiapine and phenytoin resulted in an absence of clinical response and serum quetiapine levels below the point of detection.
This patient was on concurrent phenytoin, valproic acid, and quetiapine therapy for 10 months. Prior to discontinuing phenytoin, a serum quetiapine level was found to be less than 10 ng/mL. It took approximately 1 month after phenytoin's discontinuation for quetiapine levels to attain measurable concentrations. The patient's clinical response to quetiapine improved significantly after this interaction resolved.
Phenytoin is an inducer of cytochrome P450 3A4, and quetiapine is a substrate of this enzyme. Patients on concurrent phenytoin and quetiapine therapy may require monitoring of quetiapine concentrations, which is often not routine practice, as this drug interaction can result in a clinically significant reduction in quetiapine levels contributing to a lack of efficacy.
描述一例涉及喹硫平和苯妥英钠的药物相互作用导致临床无反应且血清喹硫平水平低于检测限的患者病例。
该患者同时服用苯妥英钠、丙戊酸和喹硫平治疗10个月。在停用苯妥英钠之前,发现血清喹硫平水平低于10 ng/mL。停用苯妥英钠后大约1个月,喹硫平水平才达到可测量的浓度。这种相互作用解决后,患者对喹硫平的临床反应显著改善。
苯妥英钠是细胞色素P450 3A4的诱导剂,喹硫平是该酶的底物。同时接受苯妥英钠和喹硫平治疗的患者可能需要监测喹硫平浓度,而这在常规做法中往往并不常见,因为这种药物相互作用可导致喹硫平水平在临床上显著降低,进而导致疗效不佳。