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耐多药嗜麦芽窄食单胞菌的联合药敏试验来自囊性纤维化患者。

Combination antimicrobial susceptibility testing of multidrug-resistant Stenotrophomonas maltophilia from cystic fibrosis patients.

机构信息

Microbiology Department, Aberdeen Royal Infirmary, Foresterhill, Aberdeen, United Kingdom.

出版信息

Antimicrob Agents Chemother. 2012 Aug;56(8):4071-7. doi: 10.1128/AAC.00072-12. Epub 2012 May 14.

Abstract

Stenotrophomonas maltophilia is increasingly being isolated from the respiratory tract of individuals with cystic fibrosis, and, because of its multidrug-resistant nature, the selection of suitable treatment regimens can be problematical. Etest methodology was used to facilitate MIC and antimicrobial combination testing on 80 isolates of S. maltophilia cultured from the respiratory tract of Scottish individuals with cystic fibrosis between 2001 and 2010. The overall rate of susceptibility for the 1,410 MIC tests was 23.1%, and resistance was 68.9%. The most active antimicrobials were minocycline, co-trimoxazole, and doxycycline, with 92.4%, 87.3%, and 58.8% of isolates being susceptible, respectively. Of the 517 combinations, 13.2% were synergistic, with the most synergistic being ticarcillin/clavulanate plus aztreonam (91.7% synergistic), ticarcillin/clavulanate plus colistin (40%), and ticarcillin/clavulanate plus levofloxacin (19.4%). Colistin plus tobramycin was the only antagonistic combination (0.2%). By the median susceptible breakpoint index, the most active combinations were minocycline plus co-trimoxazole (median index, 20), minocycline plus piperacillin-tazobactam (median, 20), and co-trimoxazole plus ceftazidime (median, 16.5). The increasing problem of multidrug resistance in organisms recovered from the respiratory tracts of individuals with cystic fibrosis is not going to go away. Current susceptibility testing methods do not address the slow-growing organisms associated with chronic infection, and interpretive standards are based on achievable blood levels of antimicrobials. Addressing these issues specifically for organisms recovered from the respiratory tracts of individuals with cystic fibrosis should lead to better therapeutic outcomes and improved wellbeing of individuals with cystic fibrosis.

摘要

嗜麦芽窄食单胞菌日益从囊性纤维化患者的呼吸道中分离出来,由于其具有多种耐药性,因此选择合适的治疗方案可能会成为一个问题。采用 Etest 方法对 2001 年至 2010 年间从苏格兰囊性纤维化患者呼吸道中培养的 80 株嗜麦芽窄食单胞菌进行 MIC 和抗菌药物联合试验。1410 次 MIC 试验的总敏感性率为 23.1%,耐药率为 68.9%。最有效的抗菌药物分别为米诺环素、复方磺胺甲噁唑和多西环素,分别有 92.4%、87.3%和 58.8%的分离株敏感。在 517 种组合中,有 13.2%具有协同作用,最具协同作用的是替卡西林/克拉维酸加氨曲南(91.7%协同)、替卡西林/克拉维酸加黏菌素(40%)和替卡西林/克拉维酸加左氧氟沙星(19.4%)。唯一的拮抗组合是黏菌素加妥布霉素(0.2%)。根据敏感中位数切点指数,最有效的组合是米诺环素加复方磺胺甲噁唑(中位数指数 20)、米诺环素加哌拉西林/他唑巴坦(中位数,20)和复方磺胺甲噁唑加头孢他啶(中位数,16.5)。从囊性纤维化患者呼吸道中分离出的生物体日益面临多种药物耐药的问题,而且这种情况不会消失。目前的药敏试验方法不能解决与慢性感染相关的生长缓慢的生物体问题,而且解释标准基于可达到的抗菌药物血液水平。针对从囊性纤维化患者呼吸道中分离出的生物体具体解决这些问题,应该可以改善治疗效果,提高囊性纤维化患者的生活质量。

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