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头孢洛扎-他唑巴坦对2015 - 2018年美国重症监护病房肺炎患者铜绿假单胞菌临床分离株的活性

Ceftolozane-tazobactam activity against clinical isolates of Pseudomonas aeruginosa from ICU patients with pneumonia: United States, 2015-2018.

作者信息

Pfaller Michael A, Shortridge Dee, Harris Kelly A, Garrison Mark W, DeRyke C Andrew, DePestel Daryl D, Moise Pamela A, Sader Helio S

机构信息

JMI Laboratories, North Liberty, IA, USA; University of Iowa College of Medicine, Iowa City, IA, USA.

JMI Laboratories, North Liberty, IA, USA.

出版信息

Int J Infect Dis. 2021 Nov;112:321-326. doi: 10.1016/j.ijid.2021.09.064. Epub 2021 Sep 29.

Abstract

OBJECTIVES

To report on the activity of ceftolozane-tazobactam and comparators against Pseudomonas aeruginosa isolates collected from hospitalized patients with pneumonia in US intensive care units (ICUs) between 2015 and 2018. Activity against all P. aeruginosa and common resistant phenotypes are described to better inform decision-making and support antimicrobial stewardship efforts.

METHODS

In total, 781 P. aeruginosa isolates were collected from 28 US hospitals. These isolates were tested for susceptibility to ceftolozane-tazobactam and comparators by Clinical and Laboratory Standards Institute (CLSI) broth microdilution methodology using CLSI (2020) breakpoints. Phenotypes analysed included piperacillin-tazobactam-non-susceptible (NS), cefepime-NS, ceftazidime-NS, meropenem-NS and difficult-to-treat resistance (DTR).

RESULTS

Ceftolozane-tazobactam was the most potent agent tested (minimum inhibitory concentration to inhibit 50% and 90% of isolates of 0.5 and 2 mg/L, respectively, inhibiting 97.2% at the susceptible breakpoint of ≤4 mg/L). Traditional first-line antipseudomonal β-lactam antibiotics (piperacillin-tazobactam, cefepime and ceftazidime) demonstrated <33% susceptibility when P. aeruginosa was NS to one or more agent. Although escalation of therapy to meropenem is commonly employed clinically, meropenem susceptibility ranged from 33.6% to 44.9% if P. aeruginosa was NS to any traditional first-line antipseudomonal β-lactam agent. Conversely, ceftolozane-tazobactam remained active against isolates that were NS to other agents, inhibiting 88.4% of isolates NS to piperacillin-tazobactam, 85.0% of isolates NS to cefepime and ceftazidime, and 90.3% of isolates NS to meropenem. Ceftolozane-tazobactam also maintained activity against 73.0% of DTR isolates.

CONCLUSIONS

Ceftolozane-tazobactam maintained high activity against P. aeruginosa isolated from hospitalized patients with pneumonia in US ICUs, and had the greatest activity against isolates NS to one or more antipseudomonal β-lactams and DTR isolates.

摘要

目的

报告头孢洛扎/他唑巴坦及对照药物对2015年至2018年在美国重症监护病房(ICU)住院肺炎患者中分离出的铜绿假单胞菌的活性。描述其对所有铜绿假单胞菌及常见耐药表型的活性,以更好地为决策提供信息并支持抗菌药物管理工作。

方法

共从28家美国医院收集了781株铜绿假单胞菌分离株。采用临床和实验室标准协会(CLSI)肉汤微量稀释法,依据CLSI(2020)标准对这些分离株进行头孢洛扎/他唑巴坦及对照药物的敏感性测试。分析的表型包括哌拉西林/他唑巴坦不敏感(NS)、头孢吡肟不敏感、头孢他啶不敏感、美罗培南不敏感及难治性耐药(DTR)。

结果

头孢洛扎/他唑巴坦是所测试药物中活性最强的(抑制50%和90%分离株的最低抑菌浓度分别为0.5和2 mg/L,在≤4 mg/L的敏感断点时抑制率为97.2%)。当铜绿假单胞菌对一种或多种药物不敏感时,传统一线抗假单胞菌β-内酰胺类抗生素(哌拉西林/他唑巴坦、头孢吡肟和头孢他啶)的敏感性<33%。尽管临床上通常会升级治疗至美罗培南,但如果铜绿假单胞菌对任何传统一线抗假单胞菌β-内酰胺类药物不敏感,美罗培南的敏感性范围为33.6%至44.9%。相反,头孢洛扎/他唑巴坦对其他药物不敏感的分离株仍有活性,对哌拉西林/他唑巴坦不敏感的分离株抑制率为88.4%,对头孢吡肟和头孢他啶不敏感的分离株抑制率为85.0%,对美罗培南不敏感的分离株抑制率为90.3%。头孢洛扎/他唑巴坦对73.0%的DTR分离株也保持活性。

结论

头孢洛扎/他唑巴坦对从美国ICU住院肺炎患者中分离出的铜绿假单胞菌保持高活性,对一种或多种抗假单胞菌β-内酰胺类药物不敏感的分离株及DTR分离株活性最强。

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