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多药耐药肠杆菌科和铜绿假单胞菌临床分离株中磷霉素药敏试验的药敏纸片扩散法和肉汤微量稀释法的性能。

Performance of disk diffusion and broth microdilution for fosfomycin susceptibility testing of multidrug-resistant clinical isolates of Enterobacterales and Pseudomonas aeruginosa.

机构信息

Grupo de Investigación en Resistencia Antimicrobiana y Epidemiologia Hospitalaria, Universidad El Bosque, Bogotá, Colombia; Division of Infectious Diseases and HIV Medicine, Case Western Reserve University, 10900 Euclid Av Cleveland, OH 44106, United States.

Grupo de Investigación en Resistencia Antimicrobiana y Epidemiologia Hospitalaria, Universidad El Bosque, Bogotá, Colombia.

出版信息

J Glob Antimicrob Resist. 2020 Jun;21:391-395. doi: 10.1016/j.jgar.2020.01.003. Epub 2020 Jan 28.

Abstract

OBJECTIVES

This study aimed to evaluate the susceptibility of clinical isolates of Enterobacterales and Pseudomonas aeruginosa to fosfomycin and to determine the concordance of disk diffusion (DD) and broth microdilution (BMD) with agar dilution (AD) for fosfomycin susceptibility testing.

METHODS

The activity of fosfomycin against 225 clinical isolates of Escherichia coli (n = 64), Klebsiella pneumoniae (n = 68), Enterobacter spp. (n = 28) and P. aeruginosa (n = 65) was tested by AD, DD and BMD. For DD, results were recorded considering and not considering colonies growing within the inhibition halo as recommended by the CLSI and EUCAST, respectively. Escherichia coli breakpoints were used for all Enterobacterales. Results were reported as categorical agreement (CA), major error (ME; false-resistant), very major error (VME; false-susceptible) and minor error (any other discrepancies).

RESULTS

Fosfomycin susceptibility of all tested species was >90% by AD. Following CLSI guidelines, DD was the only method reaching ≥90% CA with AD for E. coli and K. pneumoniae, albeit yielding 6% ME. Neither DD nor BMD achieved acceptable CA percentages for Enterobacter spp. Following EUCAST guidelines, none of the methods had CA ≥ 90%. For Enterobacterales, the best performance of DD is achieved when read as indicated by EUCAST but interpreted according the CLSI breakpoints (>97% CA; 0% VME; ≤2% ME). For P. aeruginosa, BMD yielded the best results (89% CA; 0% VME; 11% ME).

CONCLUSION

Neither DD or BMD provide accurate results owing to unacceptable ME and VME percentages even when performed as intended by the guidelines.

摘要

目的

本研究旨在评估临床分离的肠杆菌科和铜绿假单胞菌对磷霉素的敏感性,并确定纸片扩散法(DD)和肉汤微量稀释法(BMD)与琼脂稀释法(AD)在磷霉素药敏试验中的一致性。

方法

通过 AD、DD 和 BMD 检测 225 株临床分离的大肠埃希菌(n=64)、肺炎克雷伯菌(n=68)、肠杆菌属(n=28)和铜绿假单胞菌(n=65)对磷霉素的活性。对于 DD,分别按照 CLSI 和 EUCAST 的建议,记录考虑和不考虑抑制晕圈内生长的菌落的结果。所有肠杆菌科均采用大肠埃希菌的折点。结果报告为分类一致性(CA)、主要误差(ME;假耐药)、非常大的主要误差(VME;假敏感)和次要误差(任何其他差异)。

结果

所有测试的种属的磷霉素药敏性均通过 AD >90%。根据 CLSI 指南,仅 DD 法在大肠埃希菌和肺炎克雷伯菌的情况下,当按照 EUCAST 的建议读取但按照 CLSI 折点解释时,可达到≥90%的 CA,尽管存在 6%的 ME。DD 和 BMD 对肠杆菌属均未达到可接受的 CA%。根据 EUCAST 指南,没有一种方法的 CA≥90%。对于肠杆菌科,当按照 EUCAST 建议读取但按照 CLSI 折点解释时,DD 法的表现最佳(CA>97%;VME 为 0%;ME 为≤2%)。对于铜绿假单胞菌,BMD 产生的结果最佳(CA 为 89%;VME 为 0%;ME 为 11%)。

结论

即使按照指南的意图进行操作,DD 和 BMD 也不能提供准确的结果,因为 ME 和 VME 的百分比不可接受。

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