Emergency Medicine, Department of Emergency and Critical Care Medicine, Wan Fang Hospital, Taipei Medical University, Taipei, Taiwan; Department of Emergency, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Royal Perth Hospital, Perth, WA, Australia.
Int J Antimicrob Agents. 2016 Apr;47(4):328-34. doi: 10.1016/j.ijantimicag.2016.01.008. Epub 2016 Feb 17.
A total of 9599 isolates of Gram-negative bacteria (GNB) causing urinary tract infections (UTIs) were collected from 60 centres in 13 countries in the Asia-Pacific region from 2010-2013. These isolates comprised Enterobacteriaceae species (mainly Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis, Klebsiella oxytoca, Enterobacter cloacae and Morganella morganii) and non-fermentative GNB species (predominantly Pseudomonas aeruginosa and Acinetobacter baumannii). In vitro susceptibilities were determined by the agar dilution method and susceptibility profiles were determined using the minimum inhibitory concentration (MIC) interpretive breakpoints recommended by the Clinical and Laboratory Standards Institute in 2015. Production of extended-spectrum β-lactamases (ESBLs) amongst E. coli, K. pneumoniae, P. mirabilis and K. oxytoca isolates was determined by the double-disk synergy test. China, Vietnam, India, Thailand and the Philippines had the highest rates of GNB species producing ESBLs and the highest rates of cephalosporin resistance. ESBL production and hospital-acquired infection (isolates obtained ≥48 h after admission) significantly compromised the susceptibility of isolates of E. coli and K. pneumoniae to ciprofloxacin, levofloxacin and most β-lactams, with the exception of imipenem and ertapenem. However, >87% of ESBL-producing E. coli strains were susceptible to amikacin and piperacillin/tazobactam, indicating that these antibiotics might be appropriate alternatives for treating UTIs due to ESBL-producing E. coli. Fluoroquinolones were shown to be inappropriate as empirical therapy for UTIs. Antibiotic resistance is a serious problem in the Asia-Pacific region. Therefore, continuous monitoring of evolutionary trends in the susceptibility profiles of GNB causing UTIs in Asia is crucial.
共从亚太地区 13 个国家的 60 个中心收集了 2010-2013 年期间引起尿路感染(UTI)的 9599 株革兰氏阴性菌(GNB)分离株。这些分离株包括肠杆菌科物种(主要是大肠埃希菌、肺炎克雷伯菌、奇异变形杆菌、产酸克雷伯菌、阴沟肠杆菌和摩氏摩根菌)和非发酵性 GNB 物种(主要是铜绿假单胞菌和鲍曼不动杆菌)。通过琼脂稀释法测定体外药敏性,根据 2015 年临床和实验室标准协会推荐的最小抑菌浓度(MIC)解释折点确定药敏谱。通过双碟协同试验确定大肠埃希菌、肺炎克雷伯菌、奇异变形杆菌和产酸克雷伯菌分离株中产超广谱β-内酰胺酶(ESBLs)的情况。中国、越南、印度、泰国和菲律宾的 GNB 物种产 ESBLs 率和头孢菌素耐药率最高。ESBL 产生和医院获得性感染(入院后≥48 小时获得的分离株)显著降低了大肠埃希菌和肺炎克雷伯菌分离株对环丙沙星、左氧氟沙星和大多数β-内酰胺类药物(除亚胺培南和厄他培南外)的敏感性。然而,>87%的产 ESBL 大肠埃希菌对阿米卡星和哌拉西林/他唑巴坦敏感,表明这些抗生素可能是治疗产 ESBL 大肠埃希菌引起的 UTI 的合适替代药物。氟喹诺酮类药物不适合作为 UTI 的经验性治疗。抗生素耐药性是亚太地区的一个严重问题。因此,持续监测引起 UTI 的 GNB 敏感性谱的进化趋势对亚洲至关重要。