Verpooten G A, Verbist L, Buntinx A P, Entwistle L A, Jones K H, De Broe M E
Br J Clin Pharmacol. 1984 Aug;18(2):183-93. doi: 10.1111/j.1365-2125.1984.tb02451.x.
The antibiotic imipenum (thienamycin-formamidine) is partially hydrolyzed during excretion by a renal brush border dehydropeptidase. The co-administration of imipenum with the renal dehydropeptidase inhibitor cilastatin results in an increase of the urinary recovery of the antibiotic, both in animals and humans. To study the pharmacokinetics of imipenem and cilastatin, subjects with normal renal function and patients with different degrees of renal insufficiency received intravenously 250 mg imipenum alone and 250 mg imipenem with 250 mg cilastatin. The mean plasma half-life of imipenem varied from 52 min in subjects with normal renal function to 173 min in subjects with end-stage renal failure studied while off-dialysis. The plasma half-life of imipenem was not affected by the co-administration of cilastatin. The mean plasma half-life of cilastatin varied from 54 min in normals to 798 min in patients with end-stage renal failure. The co-administration of cilastatin resulted in an increase of the urinary concentration and in the urinary recovery of imipenem, the effect being more pronounced in the subjects with normal or only mildly impaired renal function. The plasma clearance of imipenem was decreased when cilastatin was co-administered, possibly due to inhibition of tubular secretion of imipenem. Elimination studies performed during haemodialysis indicated efficient removal of both imipenem and cilastatin during a 4 h session. In view of the important increase in half-life of cilastatin as a function of increasing renal failure, a dosage reduction is proposed in patients with severe renal failure. It is recommended that the maximum dose of imipenem/cilastatin would be limited to either 1000/1000 mg twice daily or 500/500 mg four times daily in patients with a creatinine clearance of less than 15 ml/min. Also, a supplementary dose of imipenem and cilastatin after dialysis is recommended.
抗生素亚胺培南(硫霉素-甲脒)在经肾刷状缘脱氢肽酶排泄过程中会部分水解。亚胺培南与肾脱氢肽酶抑制剂西司他丁合用,在动物和人体中均可使该抗生素的尿回收率增加。为研究亚胺培南与西司他丁的药代动力学,肾功能正常的受试者和不同程度肾功能不全的患者分别静脉注射250mg亚胺培南以及250mg亚胺培南与250mg西司他丁的混合物。亚胺培南的平均血浆半衰期在肾功能正常的受试者中为52分钟,而在接受非透析治疗的终末期肾衰竭受试者中为173分钟。西司他丁的合用对亚胺培南的血浆半衰期无影响。西司他丁的平均血浆半衰期在正常人中为54分钟,在终末期肾衰竭患者中为798分钟。西司他丁的合用可使亚胺培南的尿浓度和尿回收率增加,在肾功能正常或仅轻度受损的受试者中这种作用更为明显。合用西司他丁时,亚胺培南的血浆清除率降低,这可能是由于其肾小管分泌受到抑制。血液透析期间进行的清除研究表明,在4小时的透析过程中亚胺培南和西司他丁均可有效清除。鉴于西司他丁的半衰期会随着肾衰竭程度的加重而显著延长,建议严重肾衰竭患者减少剂量。对于肌酐清除率低于15ml/min的患者,建议亚胺培南/西司他丁的最大剂量限制为每日两次1000/1000mg或每日四次500/500mg。此外,建议在透析后补充一剂亚胺培南和西司他丁。