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评价高剂量万古霉素致日本患者肾毒性的相关危险因素。

Evaluation of risk factors for nephrotoxicity associated with high-dose vancomycin in Japanese patients.

机构信息

Department of Pharmacy, University of Fukui Hospital, Fukui;, Email:

Department of Pharmacy, University of Fukui Hospital, Fukui; Infection Control and Prevention, University of Fukui Hospital, Fukui.

出版信息

Pharmazie. 2021 Feb 25;76(2):114-118. doi: 10.1691/ph.2021.0138.

Abstract

Considering the physique of the Japanese population, the standard daily vancomycin dose of 2 g/day and doses ≥ 3 g/day are high in terms of dose per body weight. Studies have reported that administering high-dose vancomycin to achieve a high target trough concentration has been associated with nephrotoxicity. The risk of high-dose vancomycin-associated nephrotoxicity is believed to be exceptionally high for Japanese patients because of their relatively low body weights, but data on the population is lacking. In this retrospective study, we aimed to evaluate risk factors associated with nephrotoxicity in Japanese patients treated with vancomycin. We examined the medical records of 107 Japanese patients who received vancomycin (3 to 4 g/day). They were divided into two groups based on the presence or absence of nephrotoxicity, and their demographics and clinical characteristics were compared. : The incidence of nephrotoxicity in patients receiving high-dose vancomycin was 13%. Age (≥ 60 years) and concurrent use of piperacillin/tazobactam were independent risk factors for vancomycin-associated nephrotoxicity (P = 0.027 and 0.017, respectively). : We conclude that the nephrotoxicity risk of high-dose vancomycin in Japanese patients is not excessively high when administered within the confines of a therapeutic drug-monitoring program. However, special care must be taken with patients who are older or on concurrent piperacillin/tazobactam therapy.

摘要

考虑到日本人的体格,每天 2 克的万古霉素标准剂量和剂量≥3 克/天在体重剂量方面都很高。研究报告称,给予高剂量万古霉素以达到高目标谷浓度与肾毒性有关。由于日本患者的体重相对较低,高剂量万古霉素相关肾毒性的风险被认为特别高,但缺乏针对该人群的数据。在这项回顾性研究中,我们旨在评估接受万古霉素治疗的日本患者发生肾毒性的相关危险因素。我们检查了 107 名接受万古霉素(3 至 4 克/天)治疗的日本患者的病历。根据是否存在肾毒性将他们分为两组,并比较了他们的人口统计学和临床特征。结果:接受高剂量万古霉素治疗的患者中,肾毒性的发生率为 13%。年龄(≥60 岁)和同时使用哌拉西林/他唑巴坦是万古霉素相关性肾毒性的独立危险因素(P=0.027 和 0.017)。结论:我们得出结论,在治疗药物监测方案的限制内,日本患者高剂量万古霉素的肾毒性风险并不高。然而,对于年龄较大或同时接受哌拉西林/他唑巴坦治疗的患者,必须特别注意。

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