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氨苄西林和舒巴坦在持续性非卧床腹膜透析(CAPD)中的药代动力学和药效学

Ampicillin and sulbactam pharmacokinetics and pharmacodynamics in continuous ambulatory peritoneal dialysis (CAPD).

作者信息

Blackwell B G, Leggett J E, Johnson C A, Zimmerman S W, Craig W A

机构信息

Department of Pharmacy, Lutheran General Hospital, Park Ridge, Illinois.

出版信息

Perit Dial Int. 1990;10(3):221-6.

PMID:2099158
Abstract

The fixed combination antibiotic ampicillin/sulbactam may provide a new, safe, and effective method of treating dialysis-related bacterial peritonitis. The pharmacokinetics of this antibiotic combination were determined in patients receiving continuous ambulatory peritoneal dialysis (CAPD). The pharmacodynamic activity of this drug was also determined by use of mean bactericidal titers against selected bacterial strains. Six noninfected CAPD patients in a randomized two-way crossover study were given a fixed dose of ampicillin (2 gm) and sulbactam (1 gm) either intravenously or intraperitoneally. The mean peak ampicillin and sulbactam serum concentrations following intravenous dosing were 170.3 and 87.5 micrograms/mL, respectively. The mean peak serum concentrations of ampicillin and sulbactam following intraperitoneal dosing were 48.0 and 27.8 micrograms/mL, respectively. Absolute bioavailabilities of the intraperitoneal ampicillin and sulbactam doses were 60% and 68%. Both drugs exhibited similar distribution and elimination characteristics. Renal failure markedly reduced drug elimination. Intraperitoneal administration of ampicillin/sulbactam provided satisfactory inhibitory and bactericidal antibiotic titers for most organisms in dialysate at 6 h but not 24 h. Ampicillin/sulbactam (2 gm/1 gm) should be administered every 12 h to patients with peritoneal dialysis-related peritonitis.

摘要

固定复方抗生素氨苄西林/舒巴坦可能为治疗透析相关细菌性腹膜炎提供一种新的、安全有效的方法。在接受持续性非卧床腹膜透析(CAPD)的患者中测定了这种抗生素组合的药代动力学。还通过对选定细菌菌株的平均杀菌效价来确定该药物的药效学活性。在一项随机双向交叉研究中,6名未感染的CAPD患者静脉内或腹腔内给予固定剂量的氨苄西林(2克)和舒巴坦(1克)。静脉给药后氨苄西林和舒巴坦的平均血清峰值浓度分别为170.3和87.5微克/毫升。腹腔给药后氨苄西林和舒巴坦的平均血清峰值浓度分别为48.0和27.8微克/毫升。腹腔内氨苄西林和舒巴坦剂量的绝对生物利用度分别为60%和68%。两种药物表现出相似的分布和消除特征。肾衰竭显著降低了药物消除。腹腔内给予氨苄西林/舒巴坦在6小时而非24小时时为透析液中的大多数微生物提供了令人满意的抑菌和杀菌抗生素效价。对于患有腹膜透析相关腹膜炎的患者,应每12小时给予氨苄西林/舒巴坦(2克/1克)。

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