The use of concomitant medications on nephrotoxicity associated with teicoplanin: A retrospective observational study.

IF 1.9 4区 医学 Q3 INFECTIOUS DISEASES Journal of Infection and Chemotherapy Pub Date : 2024-09-03 DOI:10.1016/j.jiac.2024.08.026
Yuki Shimizu, Kazuhiko Hanada, Takeaki Watanabe, Yuka Sasaki, Tomoka Yamazaki, Emi Komasaka, Keiko Kadota
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Abstract

Background: Teicoplanin (TEIC) is a nephrotoxic agent. However, little is known about the effects of concomitant medications on nephrotoxicity. In this study, we investigated the effects of concomitant drugs on nephrotoxicity.

Methods: A retrospective observational case-control study was conducted on patients (≥18 years) who started TEIC at the Tokyo Dental College, Ichikawa General Hospital, between January 2013 and April 2023. The primary outcome was nephrotoxicity, defined as an increase in serum creatinine levels of ≥50 % or ≥0.5 mg/dL from baseline. Logistic regression analysis was used to determine the risk factors for nephrotoxicity associated with TEIC. In addition, we investigated the relationship between nephrotoxicity and predicted free TEIC concentrations.

Results: Of 305 patients, 43 (14.1 %) developed nephrotoxicity. The multivariate logistic regression analysis identified that serum albumin (odds ratio [OR] = 0.50, 95 % confidence interval [CI] 0.27-0.89, p = 0.02), concomitant use of loop diuretics (OR = 2.22, 95 % CI 1.10-4.59, p = 0.03), antivirals (OR = 3.24, 95 % CI 1.32-7.62, p < 0.01), and vasopressors (OR = 2.57, 95 % CI 1.10-5.78, p = 0.03) were the associated risk factors for nephrotoxicity in patients administered with TEIC. In 216 patients, predicted TEIC concentrations were 3.6 [interquartile range (IQR), 2.6-4.9] μg/mL in the nephrotoxicity group versus 3.6 [IQR, 2.5-4.7] μg/mL in the non-nephrotoxicity group, with no significant difference (p = 0.69).

Conclusion: Our results indicate the importance of modifying the concomitant use of loop diuretics, antivirals, and vasopressors.

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使用伴随药物对替考拉宁相关肾毒性的影响:一项回顾性观察研究。
背景:替考拉宁(TEIC)是一种肾毒性药物。然而,人们对伴随药物对肾毒性的影响知之甚少。本研究调查了伴随药物对肾毒性的影响:方法:我们对 2013 年 1 月至 2023 年 4 月期间在东京牙科大学市川综合医院开始接受 TEIC 治疗的患者(≥18 岁)进行了一项回顾性病例对照观察研究。主要结果是肾毒性,定义为血清肌酐水平比基线增加≥50%或≥0.5 mg/dL。我们采用逻辑回归分析来确定与 TEIC 相关的肾毒性风险因素。此外,我们还研究了肾毒性与预测游离 TEIC 浓度之间的关系:在 305 名患者中,43 人(14.1%)出现了肾毒性。多变量逻辑回归分析发现,血清白蛋白(几率比[OR] = 0.50,95% 置信区间[CI] 0.27-0.89,P=0.02)、同时使用襻利尿剂(OR = 2.22,95% CI 1.10-4.59,P=0.03)、抗病毒药物(OR = 3.24,95% CI 1.32-7.62,P 结论:我们的研究结果表明,调整肾毒性与预测游离 TEIC 浓度之间的关系非常重要:我们的研究结果表明,改变同时使用襻利尿剂、抗病毒药物和血管加压药的做法非常重要。
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来源期刊
Journal of Infection and Chemotherapy
Journal of Infection and Chemotherapy INFECTIOUS DISEASES-PHARMACOLOGY & PHARMACY
CiteScore
4.10
自引率
4.50%
发文量
303
审稿时长
47 days
期刊介绍: The Journal of Infection and Chemotherapy (JIC) — official journal of the Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases — welcomes original papers, laboratory or clinical, as well as case reports, notes, committee reports, surveillance and guidelines from all parts of the world on all aspects of chemotherapy, covering the pathogenesis, diagnosis, treatment, and control of infection, including treatment with anticancer drugs. Experimental studies on animal models and pharmacokinetics, and reports on epidemiology and clinical trials are particularly welcome.
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