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头孢他啶/阿维巴坦治疗碳青霉烯类耐药革兰氏阴性菌引起的中枢神经系统感染的药代动力学/药效学:一项前瞻性研究。

The pharmacokinetics/pharmacodynamics of ceftazidime/avibactam for central nervous system infections caused by carbapenem-resistant Gram-negatives: a prospective study.

机构信息

Intensive Care Unit, Drum Tower Hospital Affiliated to Nanjing University School of Medicine, Nanjing 210008, Jiangsu, China.

Department of Pharmacy, Drum Tower Hospital Affiliated to Nanjing University School of Medicine, Nanjing 210008, China.

出版信息

J Antimicrob Chemother. 2024 Apr 2;79(4):820-825. doi: 10.1093/jac/dkae035.

DOI:10.1093/jac/dkae035
PMID:38366379
Abstract

OBJECTIVES

To describe the pharmacokinetics/pharmacodynamics (PK/PD) of ceftazidime/avibactam in critically ill patients with CNS infections.

METHODS

A prospective study of critically ill patients with CNS infections who were treated with ceftazidime/avibactam and the steady-state concentration (Css) of ceftazidime/avibactam in serum and/or CSF was conducted between August 2020 and May 2023. The relationship between PK/PD goal achievement, microbial eradication and the clinical efficacy of ceftazidime/avibactam was evaluated.

RESULTS

Seven patients were finally included. The ceftazidime/avibactam target attainment in plasma was optimal for three, quasi-optimal for one and suboptimal for three. In three patients with CSF drug concentrations measured, ceftazidime/avibactam target attainment in CSF was 100% (3/3), which was optimal. The AUCCSF/serum values were 0.59, 0.44 and 0.35 for ceftazidime and 0.57, 0.53 and 0.51 for avibactam. Of the seven patients, 100% (7/7) were treated effectively, 71.4% (5/7) achieved microbiological eradication, 85.7% (6/7) survived and 14.3% (1/7) did not survive.

CONCLUSIONS

The limited clinical data suggest that ceftazidime/avibactam is effective in the treatment of CNS infections caused by MDR Gram-negative bacilli (MDR-GNB), can achieve the ideal drug concentration of CSF, and has good blood-brain barrier penetration.

摘要

目的

描述中枢神经系统(CNS)感染的危重症患者中头孢他啶/阿维巴坦的药代动力学/药效学(PK/PD)。

方法

在 2020 年 8 月至 2023 年 5 月期间,进行了一项前瞻性研究,纳入了接受头孢他啶/阿维巴坦治疗且血清和/或脑脊液中头孢他啶/阿维巴坦稳态浓度(Css)可测量的 CNS 感染危重症患者。评估了 PK/PD 目标达成情况、微生物清除率和头孢他啶/阿维巴坦的临床疗效之间的关系。

结果

最终纳入 7 例患者。头孢他啶/阿维巴坦在血浆中的目标达成情况对 3 例患者是最佳的,对 1 例患者是接近最佳的,对 3 例患者是次最佳的。在 3 例可测量脑脊液药物浓度的患者中,头孢他啶/阿维巴坦在脑脊液中的目标达成率为 100%(3/3),为最佳。头孢他啶的 AUCCSF/血清值分别为 0.59、0.44 和 0.35,阿维巴坦的 AUCCSF/血清值分别为 0.57、0.53 和 0.51。7 例患者中,100%(7/7)治疗有效,71.4%(5/7)微生物清除率,85.7%(6/7)存活,14.3%(1/7)未存活。

结论

有限的临床数据表明,头孢他啶/阿维巴坦对治疗耐多药革兰阴性杆菌(MDR-GNB)引起的 CNS 感染有效,可达到理想的脑脊液药物浓度,且具有良好的血脑屏障穿透性。

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