Gray V S
Department of Pharmacy Practice, McWhorter School of Pharmacy, Samford University, Birmingham, AL 35229, USA.
Ann Pharmacother. 1998 Jun;32(6):648-51. doi: 10.1345/aph.17288.
To report a case of QT prolongation and syncopal episodes resulting from concomitant use of cisapride and agents known to inhibit its metabolism.
A 53-year-old white woman was involved in two motor vehicle accidents on the same day after experiencing syncopal episodes. Cardiac and neurologic evaluations were negative; the syncopal episodes were attributed to QT prolongation associated with the concomitant use of cisapride and agents known to inhibit its metabolism.
This is the first case published in the English-language literature describing QT prolongation resulting from the concomitant use of cisapride and agents known to inhibit its metabolism. Clarithromycin inhibits CYP3A4, the isoenzyme responsible for the metabolism of cisapride. Concomitant administration of cisapride with agents known to inhibit CYP3A4 (i.e., azole antifungals, erythromycin, clarithromycin) may result in elevated cisapride concentrations. Elevated cisapride concentrations have been associated with QT prolongation, syncopal episodes, and cardiac dysrhythmias.
Acquired QT prolongation is a well-recognized adverse effect of several drugs. Recognition of newer drugs and drug combinations that place patients at risk for this potentially fatal adverse event is imperative for appropriate monitoring and prevention.
报告一例因同时使用西沙必利和已知可抑制其代谢的药物而导致QT间期延长和晕厥发作的病例。
一名53岁白人女性在经历晕厥发作后于同一天发生了两起机动车事故。心脏和神经系统评估均为阴性;晕厥发作归因于同时使用西沙必利和已知可抑制其代谢的药物所导致的QT间期延长。
这是英文文献中发表的首例描述因同时使用西沙必利和已知可抑制其代谢的药物而导致QT间期延长的病例。克拉霉素可抑制CYP3A4,这是负责西沙必利代谢的同工酶。西沙必利与已知可抑制CYP3A4的药物(即唑类抗真菌药、红霉素、克拉霉素)同时给药可能会导致西沙必利浓度升高。西沙必利浓度升高与QT间期延长、晕厥发作和心律失常有关。
获得性QT间期延长是几种药物公认的不良反应。认识到使患者面临这种潜在致命不良事件风险的新药和药物组合对于进行适当监测和预防至关重要。