Sakai M, Ohkawa S, Kaku T, Kuboki K, Chida K, Imai T
Division of Cardiology, Tokyo Metropolitan Geriatric Hospital, Japan.
Eur J Clin Pharmacol. 1993;44(4):387-9. doi: 10.1007/BF00316479.
We have investigated the pharmacokinetics of the direct vasodilator flosequinan in elderly patients with congestive heart failure. Eight patients received a single dose of 50 mg, and 8 patients received once-daily treatment with 25 mg for two weeks. In the single dose study, the tmax of flosequinan was 2.5 h, Cmax was 1.17 microgram.ml-1 and t1/2 was 5.63 h. The tmax of the metabolite BTS 53554 was 20.3 h, Cmax was 1.44 microgram.ml-1 and t1/2 was 62.0 h. BTS 53554 accumulated gradually in the 14-day repeated dose study and steady-state was reached after approximately 2 weeks. Flosequinan was not found to accumulate. Adverse reactions were not observed in either the single or repeated dose study. It is advisable to consider renal function and body weight when flosequinan is to be administered to elderly patients with congestive heart failure. The initial dose should be 25 mg.
我们研究了直接血管扩张剂氟司喹南在老年充血性心力衰竭患者中的药代动力学。8名患者接受了50mg的单次剂量,8名患者接受了每日一次25mg的治疗,持续两周。在单次剂量研究中,氟司喹南的tmax为2.5小时,Cmax为1.17微克·毫升-1,t1/2为5.63小时。代谢物BTS 53554的tmax为20.3小时,Cmax为1.44微克·毫升-1,t1/2为62.0小时。在为期14天的重复剂量研究中,BTS 53554逐渐蓄积,约2周后达到稳态。未发现氟司喹南蓄积。在单次或重复剂量研究中均未观察到不良反应。当给老年充血性心力衰竭患者使用氟司喹南时,建议考虑肾功能和体重。初始剂量应为25mg。