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在两家西班牙三级医院中,亚胺培南/雷巴他定对革兰氏阴性临床分离株的体外活性。

In vitro activity of imipenem/relebactam against Gram-negative clinical isolates in two Spanish tertiary hospitals.

机构信息

Francisco Javier Candel González. Clinical Microbiology and Infectious Diseases. IdISCC and IML Health Research Institutes. Hospital Clinic San Carlos. Madrid, Spain.

出版信息

Rev Esp Quimioter. 2021 Dec;34(6):668-671. doi: 10.37201/req/102.2021. Epub 2021 Oct 13.

Abstract

OBJECTIVE

The aim of this study was to analyze the activity of the imipenem-relebactam combination (IMI/REL) against a collection of multidrug-resist Enterobacterales, Pseudomonas aeruginosa and Acinetobacter baumannii clinical isolates.

METHODS

The study was conducted in two tertiary hospitals in Spain and included 192 clinical isolates of these 3 genera (139 resistant and 53 susceptible to IMI). The MICs for IMI with and without REL (at a fixed concentration of 4 mg/L) were determined by a standard broth microdilution method according to international recommendations.

RESULTS

All IMI-susceptible E. coli strains were also susceptible to IMI/REL. Enterobacterales resistant to IMI due to the production of carbapenemases, the MIC50 and MIC90 decreased from 64/256 with IMI to 8/64 mg/L with IMI/REL. This high activity was principally detected among isolates with KPC enzymes. Enterobacterales with class B carbapenemases, P. aeruginosa carrying VIM carbapenemase and A. baumannii strains showed no changes on IMI MIC50 or MIC90 after adding REL. Among P. aeruginosa strains without carbapenemase the MIC for IMI/REL was reduced between 1 to 5 dilutions.

CONCLUSIONS

IMI/REL showed high activity against the strains that carry Klebsiella pneumoniae carbapenemase (KPC) and against carbapenem-resistant P. aeruginosa unrelated to the VIM enzyme, mainly AmpC beta lactamase associated with impermeability. Against strains carrying oxacillinase 48 (OXA-48) associated with extended-spectrum beta-lactamase (ESBL), IMI/REL presented activity only slightly better than IMI and had no beneficial effect superior to IMI against A. baumannii.

摘要

目的

本研究旨在分析亚胺培南-雷巴他定组合(IMI/REL)对多药耐药肠杆菌科、铜绿假单胞菌和鲍曼不动杆菌临床分离株的活性。

方法

该研究在西班牙的两家三级医院进行,包括这 3 个属的 192 株临床分离株(139 株对 IMI 耐药,53 株对 IMI 敏感)。根据国际建议,采用标准肉汤微量稀释法测定含和不含 REL(固定浓度为 4mg/L)的 IMI 的 MIC。

结果

所有对 IMI 敏感的大肠杆菌菌株也对 IMI/REL 敏感。由于产生碳青霉烯酶而对 IMI 耐药的肠杆菌科,其 MIC50 和 MIC90 从 IMI 的 64/256 降至 IMI/REL 的 8/64mg/L。这种高活性主要在携带 KPC 酶的分离株中检测到。携带 B 类碳青霉烯酶的肠杆菌科、携带 VIM 碳青霉烯酶的铜绿假单胞菌和鲍曼不动杆菌分离株在添加 REL 后,其 IMI MIC50 或 MIC90 没有变化。在没有碳青霉烯酶的铜绿假单胞菌菌株中,IMI/REL 的 MIC 降低了 1 至 5 个稀释度。

结论

IMI/REL 对携带肺炎克雷伯菌碳青霉烯酶(KPC)的菌株和与 VIM 酶无关的耐碳青霉烯铜绿假单胞菌具有高活性,主要与通透性相关的 AmpC 内酰胺酶有关。对携带与超广谱β-内酰胺酶(ESBL)相关的 48 型氧西林酶(OXA-48)的菌株,IMI/REL 的活性仅略优于 IMI,对鲍曼不动杆菌没有优于 IMI 的有益作用。

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