Francisco Javier Candel González. Clinical Microbiology and Infectious Diseases. IdISCC and IML Health Research Institutes. Hospital Clinic San Carlos. Madrid, Spain.
Rev Esp Quimioter. 2021 Dec;34(6):668-671. doi: 10.37201/req/102.2021. Epub 2021 Oct 13.
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.
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.
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.
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.
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。
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。
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。
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。