Shepherd A N, Bouchier I A
Eur J Clin Pharmacol. 1985;28(5):581-3. doi: 10.1007/BF00544070.
The pharmacokinetics of piretanide, a new loop diuretic, were studied in seven patients with severe liver disease before and after resolution of ascites. The time to maximum concentration was significantly prolonged by the presence of ascites. Tmax after relief of ascites was similar to that seen for normal volunteers. Area under the curves, bioavailability, volumes of distribution and elimination half-lives did not change after resolution of the ascites: two patients in whom diuretic resistant ascites occurred showed similar pharmacokinetics to that of the diuretic responders. Reduced responsiveness to piretanide therapy in patients with gross ascites does not appear to be the result of decreased bioavailability.
在七名严重肝病患者腹水消退前后,对新型袢利尿剂吡咯他尼的药代动力学进行了研究。腹水的存在显著延长了达峰时间。腹水消退后的达峰时间与正常志愿者相似。腹水消退后,曲线下面积、生物利用度、分布容积和消除半衰期均未改变:两名出现利尿剂抵抗性腹水的患者表现出与利尿剂反应者相似的药代动力学。大量腹水患者对吡咯他尼治疗反应性降低似乎并非生物利用度降低所致。