Department of Medical Microbiology, Vestre Viken Hospital Trust, Bærum, Norway.
Department of Microbiology and Infection Control, Reference Centre for Detection of Antimicrobial Resistance, University Hospital of North Norway, Tromsø, Norway, and Department of Medical Biology, Research Group for Host-Microbe Interactions, Faculty of Health Sciences, University of Tromsø, Tromsø, Norway.
PLoS One. 2014 Jan 15;9(1):e85889. doi: 10.1371/journal.pone.0085889. eCollection 2014.
A population-based study was performed to investigate the efficacy of mecillinam treatment of community-acquired urinary tract infections (CA-UTI) caused by extended-spectrum β-lactamase (ESBL) producing Escherichia coli. The study was conducted in South-Eastern Norway. Data from patients with CA-UTI caused by ESBL-producing and non-producing (random controls) E. coli were collected through interviews, questionnaires, medical records and the Norwegian Prescription Database. Treatment failure was defined as a new antibiotic prescription appropriate for UTI prescribed within two weeks after the initial antimicrobial therapy. Multivariable logistic regression analysis was performed to identify treatment agents and patient- or bacterial traits associated with treatment failure. A total of 343 patients (mean age 59) were included, of which 158 (46%) were treated with mecillinam. Eighty-one patients (24%, mean age 54) had infections caused by ESBL producing E. coli, and 41 of these patients (51%) received mecillinam as the primary treatment. Mecillinam treatment failure was observed in 18 (44%) of patients infected by ESBL-producing strains and in 16 (14%) of patients with a CA-UTI caused by ESBL non-producing strains. Multivariable analysis showed that ESBL status (odds ratio (OR) 3.2, 95% confidence interval (CI) 1.3-7.8, p = 0.009) and increased MIC of mecillinam (OR 2.0 for each doubling value of MIC, CI 1.4-3.0, p<0.001) were independently associated with mecillinam treatment failure. This study showed a high rate of mecillinam treatment failure in CA-UTIs caused by ESBL producing E. coli. The high failure rate could not be explained by the increased MIC of mecillinam alone. Further studies addressing the use of mecillinam against ESBL-producing E. coli, with emphasis on optimal dosing and combination therapy with β-lactamase inhibitors, are warranted.
一项基于人群的研究旨在调查美西林治疗产超广谱β-内酰胺酶(ESBL)大肠埃希菌引起的社区获得性尿路感染(CA-UTI)的疗效。该研究在挪威东南部进行。通过访谈、问卷调查、病历和挪威处方数据库收集了由产 ESBL 和非产 ESBL(随机对照)大肠埃希菌引起的 CA-UTI 患者的数据。治疗失败定义为在初始抗菌治疗后两周内开具新的适合尿路感染的抗生素处方。采用多变量逻辑回归分析确定与治疗失败相关的治疗药物和患者或细菌特征。共纳入 343 例患者(平均年龄 59 岁),其中 158 例(46%)接受美西林治疗。81 例(24%,平均年龄 54 岁)患者感染产 ESBL 的大肠埃希菌,其中 41 例(51%)患者接受美西林作为初始治疗。产 ESBL 菌株感染患者中 18 例(44%)和产 ESBL 非产菌株 CA-UTI 患者中 16 例(14%)观察到美西林治疗失败。多变量分析显示,ESBL 状态(比值比(OR)3.2,95%置信区间(CI)1.3-7.8,p = 0.009)和美西林 MIC 值升高(MIC 每增加一倍,OR 2.0,95%CI 1.4-3.0,p<0.001)与美西林治疗失败独立相关。本研究显示产 ESBL 大肠埃希菌引起的 CA-UTI 中美西林治疗失败率较高。MIC 值升高不能单独解释美西林治疗失败率高的原因。需要进一步研究美西林治疗产 ESBL 大肠埃希菌的应用,重点关注最佳剂量和与β-内酰胺酶抑制剂的联合治疗。