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头孢洛扎/他唑巴坦对澳大利亚血流感染分离的铜绿假单胞菌的活性。

Activity of ceftolozane/tazobactam against a collection of Pseudomonas aeruginosa isolates from bloodstream infections in Australia.

机构信息

UQ Centre for Clinical Research, The University of Queensland, Brisbane, Qld, Australia; Infection Management Services, Princess Alexandra Hospital, Brisbane, Qld, Australia.

UQ Centre for Clinical Research, The University of Queensland, Brisbane, Qld, Australia.

出版信息

Pathology. 2018 Dec;50(7):748-752. doi: 10.1016/j.pathol.2018.08.009. Epub 2018 Nov 2.

Abstract

Pseudomonas aeruginosa is a common pathogen causing nosocomial infection. In particular, bloodstream infection (BSI) is associated with a high rate of morbidity and mortality. Ceftolozane/tazobactam is a new β-lactam/β-lactamase antimicrobial with activity against P. aeruginosa as well as multidrug resistant (MDR) Gram negative Enterobacteriaceae. Ceftolozane/tazobactam has frequently been used in salvage therapy for MDR P. aeruginosa infections. The aim of this study was to determine the activity of ceftolozane/tazobactam against P. aeruginosa isolates from BSIs collected from three clinical microbiology laboratories in Queensland, Australia, with a high proportion of isolates demonstrating β-lactam resistance. Antimicrobial susceptibility testing was performed by broth microdilution using custom made sensititre plates sourced from ThermoFisher Scientific. In addition to ceftolozane/tazobactam, we also tested piperacillin/tazobactam, ceftazidime, cefepime, meropenem, doripenem, imipenem, aztreonam, ciprofloxacin, levofloxacin, gentamicin, amikacin, tobramycin and colistin. Overall, ceftolozane/tazobactam was the most active agent tested [(MIC = 1/2 μg/mL, 96% susceptible (S)]. Against 44 isolates with resistance to at least one other β-lactam agent, 40 were susceptible to ceftolozane/tazobactam. Three ceftolozane/tazobactam resistant isolates were susceptible to colistin, with one of those isolates also susceptible to levofloxacin but not to any other antimicrobials tested. One ceftolozane/tazobactam resistant isolate was susceptible only to meropenem and doripenem but was non-susceptible to imipenem. An association was found between fluoroquinolone resistance and aminoglycoside resistance but not with β-lactam resistance. In summary, ceftolozane/tazobactam was active against most strains tested, including those resistant to other β-lactams. Laboratories should consider testing P. aeruginosa against ceftolozane/tazobactam in suspected MDR or extensively drug resistant (XDR) infections.

摘要

铜绿假单胞菌是一种常见的病原体,可引起医院获得性感染。特别是血流感染(BSI),其发病率和死亡率都很高。头孢洛扎/他唑巴坦是一种新的β-内酰胺/β-内酰胺酶抗菌药物,对铜绿假单胞菌以及多药耐药(MDR)革兰氏阴性肠杆菌科具有活性。头孢洛扎/他唑巴坦经常被用于治疗 MDR 铜绿假单胞菌感染的挽救治疗。本研究的目的是确定头孢洛扎/他唑巴坦对来自澳大利亚昆士兰州三个临床微生物学实验室的 BSI 分离株的活性,这些分离株中有很大一部分显示出β-内酰胺耐药性。药敏试验采用来自 ThermoFisher Scientific 的定制 sensiitre 板进行肉汤微量稀释法。除头孢洛扎/他唑巴坦外,我们还测试了哌拉西林/他唑巴坦、头孢他啶、头孢吡肟、美罗培南、多尼培南、亚胺培南、氨曲南、环丙沙星、左氧氟沙星、庆大霉素、阿米卡星、妥布霉素和粘菌素。总的来说,头孢洛扎/他唑巴坦是测试中最有效的药物 [(MIC = 1/2 μg/mL,96%敏感(S)]。对于至少对一种其他β-内酰胺药物耐药的 44 株分离株,有 40 株对头孢洛扎/他唑巴坦敏感。3 株头孢洛扎/他唑巴坦耐药分离株对粘菌素敏感,其中 1 株对左氧氟沙星敏感,但对其他测试的抗菌药物均不敏感。1 株头孢洛扎/他唑巴坦耐药分离株仅对美罗培南和多尼培南敏感,但对亚胺培南不敏感。氟喹诺酮类耐药与氨基糖苷类耐药之间存在相关性,但与β-内酰胺类耐药无关。总之,头孢洛扎/他唑巴坦对大多数测试菌株有效,包括对其他β-内酰胺类耐药的菌株。实验室应考虑在疑似多药耐药(MDR)或广泛耐药(XDR)感染时对铜绿假单胞菌进行头孢洛扎/他唑巴坦测试。

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