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首页> 外文期刊>Journal of Clinical Microbiology >Multicenter Clinical Evaluation of ETEST Plazomicin (PLZ) for Susceptibility Testing of Enterobacterales
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Multicenter Clinical Evaluation of ETEST Plazomicin (PLZ) for Susceptibility Testing of Enterobacterales

机译:Eleest Plazomicin(PLZ)的多中心临床评价,用于肠杆菌的易感性测试

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ABSTRACT Plazomicin (PLZ), brand name ZEMDRI (Cipla Therapeutics), is a novel aminoglycoside antibiotic approved by the U.S. Food and Drug Administration (FDA) for treatment of complicated urinary tract infections including pyelonephritis. ETEST? is a gradient diffusion method that represents an alternative to the more laborious broth micro-dilution (BMD) method for performing antimicrobial susceptibility testing (AST). A multi-center evaluation of the performance of the new ETEST PLZ (bioMérieux) was conducted in comparison with BMD following FDA and International Standards Organization (ISO) recommendations using FDA-defined breakpoints. Clinical isolates of Enterobacterales ( n ?=?598) were included. Fifty-three isolates were resistant to PLZ according to BMD. Overall, the ETEST PLZ demonstrated 99.0% essential agreement (EA), 92.8% category agreement (CA), 1.9% very major errors (VME), 0% major errors (ME), and 7.0% minor errors (mE) with both clinical and challenge isolates of Enterobacterales. The VME was found for a single Serratia marcescens strain. Individual species demonstrated EA rates?≥?90%. In conclusion, we report that ETEST PLZ represents an accurate tool for performing PLZ AST of Enterobacterales.
机译:摘要Plazomicin(PLZ),品牌Zemdri(Cipla Therapeutics),是由美国食品和药物管理局(FDA)批准的一种新型氨基糖苷类抗生素,用于治疗包括肾盂肾炎,包括肾盂肾炎的复杂尿路感染。好吗?是一种梯度扩散方法,其代表更富有少量少量的肉汤微量稀释(BMD)方法的替代方法,用于进行抗微生物易感性测试(AST)。与使用FDA定义的断点的FDA和国际标准组织(ISO)建议进行比较,对新ETEST PLZ(BioMérieux)进行了多中心评估(BioMérieux)进行了比较。包括肠杆菌的临床分离物(n?=α598)。根据BMD,五十三个分离株对PLZ具有抗性。总体而言,Etest PLZ展示了99.0%的必要协议(EA),92.8%类别协议(CA),1.9%非常严重的错误(VME),0%主要错误(ME)和7.0%的小错误(ME),临床并挑战肠杆菌的分离物。发现VME用于单一的乳房菌株。个体种类证明了EA率?≥?90%。总之,我们报告说,ETEST PLZ代表了用于执行肠杆菌的PLZ AST的准确工具。

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