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持续非卧床腹膜透析患者替考拉宁的药代动力学

Pharmacokinetics of teicoplanin in patients on continuous ambulatory peritoneal dialysis.

作者信息

Traina G L, Gentile M G, Fellin G, Rosina R, Cavenaghi L, Buniva G, Bonati M

出版信息

Eur J Clin Pharmacol. 1986;31(4):501-4. doi: 10.1007/BF00613532.

Abstract

We have studied the pharmacokinetics of teicoplanin, a new glycopeptide antibiotic active against Gram-positive aerobic and anaerobic bacteria, in five patients with end-stage renal disease on continuous ambulatory peritoneal dialysis (CAPD). Although teicoplanin was eliminated in the peritoneal fluid, relatively little was recovered (6.8 +/- 1.2% of the given dose). The following values were obtained: elimination half-time 102-347 h; total body clearance 4.16-7.38 ml X h-1 X kg-1, peritoneal clearance 0.31-0.37 ml X h-1 X kg-1. Because the elimination of teicoplanin is about four times less in patients undergoing CAPD compared with subjects with normal renal function, the dose of teicoplanin should be reduced appropriately in such cases.

摘要

我们研究了替考拉宁(一种对革兰氏阳性需氧菌和厌氧菌有效的新型糖肽类抗生素)在5例终末期肾病且持续非卧床腹膜透析(CAPD)患者中的药代动力学。尽管替考拉宁可经腹膜清除,但回收量相对较少(占给药剂量的6.8±1.2%)。得到以下数值:消除半衰期为102 - 347小时;全身清除率为4.16 - 7.38毫升·小时⁻¹·千克⁻¹,腹膜清除率为0.31 - 0.37毫升·小时⁻¹·千克⁻¹。由于与肾功能正常的受试者相比,接受CAPD治疗的患者中替考拉宁的清除率约低四倍,因此在此类情况下应适当降低替考拉宁的剂量。

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