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持续非卧床腹膜透析中腹透液中万古霉素的清除及腹腔内万古霉素的平衡

Clearance from dialysate and equilibration of intraperitoneal vancomycin in continuous ambulatory peritoneal dialysis.

作者信息

Neal D, Bailie G R

机构信息

University of Manchester Department of Pharmacy, England.

出版信息

Clin Pharmacokinet. 1990 Jun;18(6):485-90. doi: 10.2165/00003088-199018060-00005.

Abstract

This article reports on a study of the disposition of loading doses (1g and 15 mg/kg) of vancomycin given intraperitoneally to 6 patients on continuous ambulatory peritoneal dialysis with Gram-positive peritonitis. Dialysate samples were collected every 30 minutes during the first dwell, and serum samples were collected after the first 5 exchanges and after 7 or 14 days. The dialysate concentration/time data were fitted to a monoexponential curve for 4 patients and to a biexponential curve for 2 others. Dialysis clearance was 0.73 +/- 0.04 L/h (1g dose) and 0.70 +/- 0.23 L/h (15 mg/kg dose). Total body clearance was 0.51 +/- 0.36 L/h. Serum concentrations reached 14 to 18 mg/L (15 mg/kg dose) and 6.75 to 24 mg/L (1g dose) at the end of the first dwell. The half-life of equilibration of vancomycin across the peritoneal membrane was 2.5 +/- 2.3 hours. Intraperitoneal loading doses of vancomycin produce concomitant serum concentrations in excess of the minimum inhibitory concentrations for susceptible organisms. Administration on a milligram per kilogram basis produces more consistent serum concentrations than using a standard loading dose which is not based on bodyweight.

摘要

本文报道了一项针对6例持续性非卧床腹膜透析合并革兰氏阳性腹膜炎患者腹腔注射负荷剂量万古霉素(1g和15mg/kg)的处置研究。在首次留腹期间,每30分钟采集一次透析液样本,在最初5次交换后以及7天或14天后采集血清样本。4例患者的透析液浓度/时间数据拟合为单指数曲线,另外2例拟合为双指数曲线。透析清除率为0.73±0.04L/h(1g剂量)和0.70±0.23L/h(15mg/kg剂量)。总体清除率为0.51±0.36L/h。首次留腹结束时,血清浓度达到14至18mg/L(15mg/kg剂量)和6.75至24mg/L(1g剂量)。万古霉素透过腹膜平衡的半衰期为2.5±2.3小时。腹腔内注射万古霉素负荷剂量可使血清浓度同时超过敏感菌的最低抑菌浓度。按每千克体重给药比使用不基于体重的标准负荷剂量产生的血清浓度更稳定。

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