Institute for Medical Microbiology, Immunology and Hygiene, University of Cologne, Cologne, Germany.
Clinical Microbiology, Royal University Hospital, Saskatchewan Health Authority and the University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
J Glob Antimicrob Resist. 2022 Dec;31:82-89. doi: 10.1016/j.jgar.2022.08.002. Epub 2022 Aug 7.
This study presents 2016-2018 in vitro antimicrobial activity data and rates of resistant phenotypes for clinical isolates of Acinetobacter baumannii from Africa/Middle East, Asia/South Pacific, Europe, Latin America, and North America.
A total of 4320 A. baumannii isolates were collected across all regions between 2016 and 2018. The in vitro antimicrobial activities of amikacin, colistin, levofloxacin, meropenem, and tigecycline were determined using the broth microdilution methodology of the Clinical and Laboratory Standards Institute. MICs were interpreted using the European Committee on Antimicrobial Susceptibility Testing (EUCAST) breakpoints (version 11.0). Rates of subsets that were resistant to amikacin, colistin, levofloxacin, and meropenem, according to EUCAST breakpoints, are also presented.
In each region, tigecycline and colistin were active against isolates of A. baumannii (MIC values, 1 or 2 mg/L) and the lowest rate of resistance was to colistin (1.2%-7.3%). The rates of resistance to the panel of agents were generally lower among A. baumannii from North America (1.3%-42.7%), compared with the other regions. Fewer than 11% of meropenem-resistant A. baumannii were also resistant to colistin. The rates of amikacin-, levofloxacin- and meropenem-resistant A. baumannii were lowest in North America and mostly higher in Africa/Middle East and Latin America.
In each geographical region, tigecycline and colistin maintained good in vitro antimicrobial activity against isolates of A. baumannii, including antimicrobial-resistant subsets. The higher rates of meropenem-resistant isolates, particularly in Africa/Middle East and Latin America, require continued monitoring because of the scarcity of effective treatment options.
本研究介绍了 2016 年至 2018 年来自非洲/中东、亚洲/南太平洋、欧洲、拉丁美洲和北美的鲍曼不动杆菌临床分离株的体外抗菌活性数据和耐药表型率。
在 2016 年至 2018 年期间,在所有地区共收集了 4320 株鲍曼不动杆菌分离株。采用临床和实验室标准协会的肉汤微量稀释法测定阿米卡星、黏菌素、左氧氟沙星、美罗培南和替加环素的体外抗菌活性。使用欧洲抗菌药物敏感性试验委员会(EUCAST)折点(第 11.0 版)解释 MIC 值。还根据 EUCAST 折点报告了对阿米卡星、黏菌素、左氧氟沙星和美罗培南耐药的亚组的耐药率。
在每个地区,替加环素和黏菌素对鲍曼不动杆菌分离株均具有活性(MIC 值为 1 或 2mg/L),且黏菌素的耐药率最低(1.2%-7.3%)。与其他地区相比,来自北美的鲍曼不动杆菌对该药物组的耐药率普遍较低(1.3%-42.7%)。少于 11%的美罗培南耐药鲍曼不动杆菌也对黏菌素耐药。在北美,阿米卡星、左氧氟沙星和美罗培南耐药鲍曼不动杆菌的耐药率最低,而在非洲/中东和拉丁美洲,耐药率则较高。
在每个地理区域,替加环素和黏菌素对鲍曼不动杆菌分离株均保持良好的体外抗菌活性,包括对耐药亚组的抗菌活性。由于缺乏有效的治疗选择,美罗培南耐药分离株的比率较高,特别是在非洲/中东和拉丁美洲,需要持续监测。