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万古霉素肾毒性的危险因素及万古霉素治疗期间肾功能的时间进程。

Risk factors for vancomycin nephrotoxicity and time course of renal function during vancomycin treatment.

机构信息

Department of Pharmacy, Tokyo Women's Medical University Medical Center East, 2-1-10, Nishiogu, Arakawa-ku, Tokyo, 116-0011, Japan.

Department of Pharmacometrics and Pharmacokinetics, Meiji Pharmaceutical University, 2-522-1 Noshio, Kiyose, Tokyo, 204-8588, Japan.

出版信息

Eur J Clin Pharmacol. 2019 Jun;75(6):859-866. doi: 10.1007/s00228-019-02648-7. Epub 2019 Feb 15.

Abstract

PURPOSE

Vancomycin (VCM) is used for the treatment of methicillin-resistant Staphylococcus aureus. Although the risk factors for VCM nephrotoxicity have been evaluated, the time course of renal function during VCM treatment is unknown. We assessed risk factors for VCM nephrotoxicity and how renal function varied over time.

METHODS

We conducted a retrospective analysis of patients receiving intravenous VCM treatment between June 2015 and August 2017 at Tokyo Women's Medical University, Medical Center East. VCM nephrotoxicity was defined as an increase in serum creatinine levels > 50%. We performed multivariate logistic regression analysis to assess risk factors for VCM nephrotoxicity. The time course of renal function with VCM nephrotoxicity was compared and stratified by risk factors for VCM nephrotoxicity. Clinical course of VCM nephrotoxicity and VCM trough concentration were assessed.

RESULTS

In total, 42 (17.3%) of 243 patients developed VCM nephrotoxicity. Risk factors for VCM nephrotoxicity were VCM trough concentration > 20 μg/mL and concomitant use of renal hypoperfusion medications (angiotensin-converting enzyme inhibitor/angiotensin receptor blocker, loop/thiazide diuretics, and non-steroidal anti-inflammatory drugs). Although time course of renal function stratified by renal hypoperfusion medications was comparable, the time course of renal function significantly deteriorated in patients with loop/thiazide diuretics. Focusing on patients continuing VCM treatment, VCM nephrotoxicity recovered in 40% of the patients and VCM trough concentration improved to 10-20 μg/mL in 75% of the patients.

CONCLUSIONS

VCM trough concentration > 20 μg/mL and concomitant use of renal hypoperfusion medications are associated with VCM nephrotoxicity. Recovery of VCM nephrotoxicity was poor compared to the improvement of VCM trough concentration.

摘要

目的

万古霉素(VCM)用于治疗耐甲氧西林金黄色葡萄球菌。尽管已经评估了 VCM 肾毒性的危险因素,但在 VCM 治疗期间肾功能的时间过程尚不清楚。我们评估了 VCM 肾毒性的危险因素以及肾功能随时间的变化。

方法

我们对 2015 年 6 月至 2017 年 8 月在东京女子医科大学医疗中心东接受静脉 VCM 治疗的患者进行了回顾性分析。VCM 肾毒性定义为血清肌酐水平升高>50%。我们进行了多变量逻辑回归分析,以评估 VCM 肾毒性的危险因素。比较 VCM 肾毒性的肾功能时间过程,并按 VCM 肾毒性的危险因素进行分层。评估了 VCM 肾毒性的临床过程和 VCM 谷浓度。

结果

总共 243 例患者中有 42 例(17.3%)发生了 VCM 肾毒性。VCM 肾毒性的危险因素是 VCM 谷浓度>20μg/mL 和同时使用肾低灌注药物(血管紧张素转换酶抑制剂/血管紧张素受体阻滞剂、环利尿剂/噻嗪类利尿剂和非甾体抗炎药)。尽管根据肾低灌注药物分层的肾功能时间过程相似,但在使用环利尿剂/噻嗪类利尿剂的患者中,肾功能明显恶化。关注继续接受 VCM 治疗的患者,40%的患者 VCM 肾毒性恢复,75%的患者 VCM 谷浓度改善至 10-20μg/mL。

结论

VCM 谷浓度>20μg/mL 和同时使用肾低灌注药物与 VCM 肾毒性相关。与 VCM 谷浓度的改善相比,VCM 肾毒性的恢复较差。

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