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头孢他啶/阿维巴坦、头孢洛扎/他唑巴坦、亚胺培南/雷巴坦、美罗培南/沃巴坦和对照药物对皮肤软组织感染患者分离的铜绿假单胞菌的抗菌活性。

Antimicrobial activities of ceftazidime/avibactam, ceftolozane/tazobactam, imipenem/relebactam, meropenem/vaborbactam, and comparators against Pseudomonas aeruginosa from patients with skin and soft tissue infections.

机构信息

JMI Laboratories, North Liberty, Iowa, USA.

JMI Laboratories, North Liberty, Iowa, USA.

出版信息

Int J Infect Dis. 2021 Dec;113:279-281. doi: 10.1016/j.ijid.2021.10.022. Epub 2021 Oct 17.

Abstract

BACKGROUND

The limited armamentarium against multidrug-resistant Gram-negative bacilli led to the development of a new generation of β-lactam/β-lactamase inhibitor combinations (BL/BLI).

OBJECTIVES

To evaluate the in vitro activity of ceftazidime/avibactam, ceftolozane/tazobactam, meropenem/vaborbactam, and imipenem/relebactam against Pseudomonas aeruginosa isolates recovered from patients hospitalized with skin and soft tissue infections (SSTIs) in several countries around the world.

METHODS

A total of 360 P. aeruginosa isolates were consecutively collected from 47 medical centers located in Western Europe, Eastern Europe, the Asia-Pacific region, and Latin America. Susceptibility testing was performed by broth microdilution method at a monitoring laboratory. EUCAST breakpoints were applied.

RESULTS

Ceftazidime/avibactam (98.3% susceptible), ceftolozane/tazobactam (98.6% susceptible), and imipenem/relebactam (98.3% susceptible) were the most active compounds after colistin (100.0% susceptible) and retained activity against isolates nonsusceptible to piperacillin/tazobactam, meropenem, imipenem, and/or ceftazidime. Meropenem-vaborbactam was active against 94.2% of isolates. Ceftazidime/avibactam was the most active BL/BLI against meropenem-nonsusceptible (92.6% susceptible) and imipenem-resistant (93.8% susceptible) isolates, whereas ceftolozane/tazobactam was the most active BL/BLI against piperacillin/tazobactam-resistant (91.1% susceptible) and ceftazidime-resistant (91.7% susceptible) isolates.

CONCLUSIONS

The recently approved BL/BLIs demonstrated potent activity and broad coverage against contemporary P. aeruginosa isolates from patients with SSTIs.

摘要

背景

针对多药耐药革兰氏阴性杆菌的有限武器库导致了新一代β-内酰胺/β-内酰胺酶抑制剂组合(BL/BLI)的发展。

目的

评估头孢他啶/阿维巴坦、头孢洛扎/他唑巴坦、美罗培南/沃巴坦和亚胺培南/雷利巴坦对来自世界各地多个国家住院治疗皮肤和软组织感染(SSTIs)患者的铜绿假单胞菌分离株的体外活性。

方法

共从西欧、东欧、亚太地区和拉丁美洲的 47 家医疗中心连续收集了 360 株铜绿假单胞菌分离株。在监测实验室通过肉汤微量稀释法进行药敏试验。应用 EUCAST 折点。

结果

头孢他啶/阿维巴坦(98.3%敏感)、头孢洛扎/他唑巴坦(98.6%敏感)和亚胺培南/雷利巴坦(98.3%敏感)在粘菌素(100.0%敏感)之后是最有效的化合物,并保留了对哌拉西林/他唑巴坦、美罗培南、亚胺培南和/或头孢他啶不敏感的分离株的活性。美罗培南-沃巴坦对 94.2%的分离株有效。头孢他啶/阿维巴坦是对美罗培南不敏感(92.6%敏感)和亚胺培南耐药(93.8%敏感)分离株最有效的 BL/BLI,而头孢洛扎/他唑巴坦是对哌拉西林/他唑巴坦耐药(91.1%敏感)和头孢他啶耐药(91.7%敏感)分离株最有效的 BL/BLI。

结论

最近批准的 BL/BLI 对 SSTIs 患者的铜绿假单胞菌分离株表现出强大的活性和广泛的覆盖范围。

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