Suppr超能文献

头孢他啶/阿维巴坦的治疗药物监测:为何一条腿不够用。

Therapeutic drug monitoring of ceftazidime/avibactam: why one leg is not enough to run.

机构信息

Department of Medical and Surgical Sciences, Alma Mater Studiorum, University of Bologna, Bologna, Italy.

Clinical Pharmacology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Via Massarenti 9, Bologna 40138, Italy.

出版信息

J Antimicrob Chemother. 2024 Jan 3;79(1):195-199. doi: 10.1093/jac/dkad367.

Abstract

BACKGROUND

Therapeutic drug monitoring (TDM) is becoming an increasingly recommended approach for assessing optimal pharmacokinetic/pharmacodynamic (PK/PD) target attainment of ceftazidime/avibactam. Some authors hypothesized that the PK/PD target attainment of ceftazidime/avibactam could be assessed by means of the TDM of solely ceftazidime, since avibactam concentrations might be extrapolated based on the fixed 4:1 ceftazidime-to-avibactam ratio present in the vial. The reliability of this hypothesis could be called into question if a wide interindividual variability in the ceftazidime-to-avibactam ratio would exist among patients. This study aimed to assess the distribution of the individual ceftazidime-to-avibactam ratios in relation to renal function in a cohort of adult patients who were treated with continuous infusion ceftazidime/avibactam and underwent TDM of both ceftazidime and avibactam.

METHODS

Individual ceftazidime-to-avibactam ratio was calculated at each TDM assessment. Receiving operating characteristics (ROC) curve analysis was performed for testing the potential impact of renal function on ceftazidime-to-avibactam ratio variability.

RESULTS

A total of 188 TDM assessments were collected from 107 patients. The ceftazidime-to-avibactam ratios ranged from 1.29:1 to 13.46:1. Seventy-seven out of 188 ceftazidime-to-avibactam ratios (41.0%) were >5:1, and 36 (19.1%) were >6:1. Patients without renal dysfunction had significantly higher proportions of ceftazidime-to-avibactam ratio >5:1 (59.3% versus 23.8%; P < 0.001) and >6:1 (32.1% versus 6.3%; P < 0.001) compared with those with mild-to-severe renal dysfunction.

CONCLUSIONS

The findings may strengthen the contention that for properly assessing the PK/PD target attainment of ceftazidime/avibactam, both ceftazidime and avibactam concentrations should be measured, given the unpredictability of the ceftazidime-to-avibactam ratio occurring among patients.

摘要

背景

治疗药物监测(TDM)正成为评估头孢他啶/阿维巴坦最佳药代动力学/药效学(PK/PD)目标的一种越来越受推荐的方法。一些作者假设,通过仅测定头孢他啶的 TDM,即可评估头孢他啶/阿维巴坦的 PK/PD 目标,因为基于小瓶中存在的固定 4:1 头孢他啶-阿维巴坦比例,可推断出阿维巴坦的浓度。如果患者之间的头孢他啶-阿维巴坦比例存在广泛的个体间变异性,那么这一假设的可靠性可能会受到质疑。本研究旨在评估在接受连续输注头孢他啶/阿维巴坦治疗并同时进行头孢他啶和阿维巴坦 TDM 的成人患者队列中,个体头孢他啶-阿维巴坦比例与肾功能之间的关系。

方法

在每次 TDM 评估时计算个体头孢他啶-阿维巴坦比值。进行接收者操作特征(ROC)曲线分析,以检验肾功能对头孢他啶-阿维巴坦比值变异性的潜在影响。

结果

从 107 例患者中收集了 188 次 TDM 评估。头孢他啶-阿维巴坦比值范围为 1.29:1 至 13.46:1。188 个头孢他啶-阿维巴坦比值中有 77 个(41.0%)大于 5:1,36 个(19.1%)大于 6:1。无肾功能障碍的患者头孢他啶-阿维巴坦比值大于 5:1(59.3%比 23.8%;P < 0.001)和大于 6:1(32.1%比 6.3%;P < 0.001)的比例明显高于轻度至重度肾功能障碍患者。

结论

这些发现可能会加强以下观点,即由于患者之间头孢他啶-阿维巴坦比例的不可预测性,为了正确评估头孢他啶/阿维巴坦的 PK/PD 目标,应同时测定头孢他啶和阿维巴坦的浓度。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验