IHMA, 2122 Palmer Drive, Schaumburg, IL 60173, USA; Department of Medical Microbiology and Infectious Diseases, Max Rady College of Medicine, University of Manitoba, Room 543-745 Bannatyne Avenue, Winnipeg, Manitoba, R3E 0J9, Canada.
IHMA, 2122 Palmer Drive, Schaumburg, IL 60173, USA.
Int J Antimicrob Agents. 2022 Mar;59(3):106535. doi: 10.1016/j.ijantimicag.2022.106535. Epub 2022 Jan 26.
This study aimed to determine the prevalence of extended-spectrum β-lactamase (ESBL) non-carbapenem-resistant Enterobacterales (non-CRE) phenotype among clinical Escherichia coli and Klebsiella pneumoniae isolates collected in 2018-2019 for the SMART global surveillance programme and review trends in prevalence over 5 years (2015-2019). MICs were determined by CLSI reference broth microdilution. ESBL non-CRE phenotypes were defined as non-susceptible to ceftriaxone (MIC ≥ 2 μg/mL) and susceptible to ertapenem (MIC ≤ 0.5 μg/mL). In 2018-2019, ESBL non-CRE phenotypes among E. coli were more common in respiratory tract infection isolates than other infection sources across all global regions; for K. pneumoniae there was wide variation by geographic region in the specimen source most frequently associated with this phenotype. In most regions, ESBL non-CRE phenotype isolates were found more frequently in samples from ICU patients than non-ICU patients and from patients with hospital length of stay at time of specimen collection ≥48 h versus <48 h. ESBL non-CRE phenotypes exceeded 50% of isolates for E. coli from India, Thailand, Vietnam, China, Russia, Mexico, Kenya and Kuwait and for K. pneumoniae from Lithuania and Kuwait. ESBL non-CRE phenotype E. coli increased significantly (P < 0.05) in Asia (excluding China), Australia/New Zealand and Latin America from 2015-2019, while ESBL non-CRE phenotype K. pneumoniae increased significantly in Latin America, USA and Canada. There was marked variability in ESBL rates across countries, over time, and by sample source and ward type. Trending data from 2015-2019 showed ESBL rates are increasing in many regions worldwide.
本研究旨在确定 2018-2019 年 SMART 全球监测计划中收集的临床大肠埃希菌和肺炎克雷伯菌分离株中,非碳青霉烯类耐药肠杆菌科(non-CRE)产超广谱β-内酰胺酶(ESBL)表型的流行率,并回顾 5 年来(2015-2019 年)流行率的趋势。采用 CLSI 参考肉汤微量稀释法测定 MIC。ESBL 非 CRE 表型定义为对头孢曲松(MIC≥2μg/mL)不敏感且对厄他培南(MIC≤0.5μg/mL)敏感。2018-2019 年,在所有全球区域中,呼吸道感染分离株的大肠埃希菌 ESBL 非 CRE 表型比其他感染源更为常见;而肺炎克雷伯菌的这一表型与地理区域的标本来源存在广泛差异。在大多数区域,与 ICU 患者相比,ESBL 非 CRE 表型分离株在 ICU 患者和住院时间≥48 小时的标本采集时更常见;与非 ICU 患者和住院时间<48 小时的标本采集时相比,ESBL 非 CRE 表型分离株更常见。印度、泰国、越南、中国、俄罗斯、墨西哥、肯尼亚和科威特的大肠埃希菌和立陶宛和科威特的肺炎克雷伯菌的 ESBL 非 CRE 表型分离株超过 50%。2015-2019 年,亚洲(中国除外)、澳大利亚/新西兰和拉丁美洲的 ESBL 非 CRE 表型大肠埃希菌显著增加(P<0.05),而拉丁美洲、美国和加拿大的 ESBL 非 CRE 表型肺炎克雷伯菌显著增加。各国之间、随时间推移以及样本来源和病房类型的 ESBL 率存在显著差异。2015-2019 年的趋势数据显示,全球许多地区的 ESBL 率正在上升。