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首页> 外文期刊>International journal of clinical practice >Emerging clinical role of pivmecillinam in the treatment of urinary tract infections caused by Extended Spectrum βeta‐lactamase βeta‐lactamase (ESBL) producing Enterobacteriaceae Enterobacteriaceae
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Emerging clinical role of pivmecillinam in the treatment of urinary tract infections caused by Extended Spectrum βeta‐lactamase βeta‐lactamase (ESBL) producing Enterobacteriaceae Enterobacteriaceae

机译:Pivmecillinam在延长光谱βeta-乳酰胺β-乳酰胺酶(ESBL)产生的尿路感染治疗中的临床作用,生产肠杆菌纤维酰胺肠杆菌酸癌

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Abstract Background Extended Spectrum βeta‐lactamase (ESBL)‐producing Enterobacteriaceae causing urinary tract infections (UTIs) appear resistant to many common oral agents. There is a growing need to discover new antibiotics to combat with emerging antibiotic resistance problem. Until the discovery of new antimicrobials, we can bring back forgotten antibiotics to our clinical formulary. Pivmecillinam (prodrug of mecillinam), an oral antimicrobial agent is effective against ESBL producing organisms. We analysed the sensitivity rates of ESBL‐producing Enterobacteriaceae from urine samples to mecillinam and to document if pivmecillinam is a suitable alternative option in the treatment of UTI. Materials/methods This retrospective study was conducted from September 2015 to September 2017. Data were collected from the pathology information system. Antimicrobial sensitivity testing on ESBL‐producing Enterobacteriaceae isolates was carried out by disc diffusion method in accordance with The European Committee on Antimicrobial Susceptibility Testing. Results A total of 986 ESBL‐producing Enterobacteriaceae were tested for mecillinam during the study period. Of 986 organisms, Escherichia coli was the most common organism (889); followed by Klebsiella species (71) and others Enterobacteriaceae (26). Mecillinam sensitivity was found in 96% Escherichia coli (855/889 isolates), 83% Klebsiella species (59/71 isolates) and 88% other Enterobacteriaceae (23/26 isolates). Overall 95% (935/986 isolates) of ESBL‐producing urinary isolates were sensitive to mecillinam. Conclusions Pivmecillinam appears to be suitable option to treat ESBL‐producing Enterobacteriaceae causing uncomplicated UTI. Our results showed low resistance rate to mecillinam. We recommend the use of pivmecillinam in uncomplicated UTIs because of ESBL‐producing Enterobacteriaceae . More studies on in vitro activity of mecillinam against ESBL producing organism and its use and clinical outcome should be tried in future.
机译:摘要背景扩展光谱βeta-乳酰胺酶(ESBL) - 产生导致泌尿道感染(UTI)的肠杆菌痤疮(UTI)对许多常见口服剂进行抗性。越来越需要发现新的抗生素与新出现的抗生素抗性问题进行打击。直到发现新的抗菌药物,我们可以将被遗忘的抗生素带回我们的临床美制。 Pivmecillinam(麦考蛋白的前药),口服抗微生物剂对ESBL产生生物有效。我们分析了ESBL产生的ESBL生成肠杆菌的敏感性率从尿液样本到梅西肽,如果PIVMECILLINAM是治疗UTI的合适替代选择。材料/方法本回顾性研究于2015年9月至2017年9月进行。从病理信息系统中收集数据。通过欧洲抗菌易感检测委员会通过盘扩散法进行ESBL生成的肠杆菌的抗微生物敏感性试验。结果在研究期间,在麦考蛋白测试了总共986个产生的Esbl胚胎菌。 986个生物体,大肠杆菌是最常见的生物(889);其次是Klebsiella物种(71)和其他肠杆菌(26)。在96%的大肠杆菌(855/889分离物)中发现了梅西肽敏感性,83%的Klebsiella(59/71分离物)和88%的其他肠杆菌(23/26分离物)。总共95%(935/986分离物)的ESBL制剂尿液分离物对梅西肽敏感。 Conclusions Pivmecillinam appears to be suitable option to treat ESBL‐producing Enterobacteriaceae causing uncomplicated UTI.我们的结果表明对麦考蛋白的耐抵抗率低。我们建议使用PIVMECILLINAM在简单的UTIS中,因为ESBL-产生的肠易氧杀菌膜。将来应该努力在将来审判麦考肽对Esbl产生生物体的体外活性的研究及其使用和临床结果。

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