Jensen P, Lehne G, Fauchald P, Simonsen S
Department of Dermatology, Rikshospitalet, University of Oslo, Norway.
Acta Derm Venereol. 1996 Jul;76(4):280-1. doi: 10.2340/0001555576280281.
Eleven patients with either kidney, heart or lung transplants, immunosuppressed with cyclosporin A, and with culture-proven dermatophyte toe nail infection, were given 250 mg terbinafine orally daily for 12 weeks. No changes in cyclosporin A dosage were made. A statistically significant decrease in mean specific cyclosporin A blood trough levels was found at 4, 8 and 12 weeks. No other statistically significant changes in the pharmacokinetic profile of cyclosporin A were seen. Terbinafine possibly induces a cyclosporin A metabolic degradation, which, however, is of little clinical significance. Terbinafine treatment is a safe therapeutical option in cyclosporin A-treated patients with dermatophyte nail infection. Cyclosporin A levels should be controlled during treatment.
11例接受环孢素A免疫抑制治疗的肾、心或肺移植患者,经培养证实患有皮肤癣菌趾甲感染,每天口服250mg特比萘芬,持续12周。未改变环孢素A的剂量。在第4、8和12周时,平均环孢素A血药谷浓度有统计学意义的显著下降。环孢素A的药代动力学特征未见其他有统计学意义的变化。特比萘芬可能诱导环孢素A的代谢降解,然而,这在临床上意义不大。特比萘芬治疗是环孢素A治疗的皮肤癣菌甲感染患者的一种安全治疗选择。治疗期间应监测环孢素A的水平。