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纸片扩散法对临床分离菌的评价。

Evaluation of the Disk Diffusion Test for Group Clinical Isolates.

机构信息

Department of Laboratory Medicine, Hanyang University College of Medicine, Seoul, Korea.

Department of Laboratory Medicine, Research Institute of Bacterial Resistance, Yonsei University College of Medicine, Seoul, Korea.

出版信息

Ann Lab Med. 2025 Jan 1;45(1):70-76. doi: 10.3343/alm.2024.0159. Epub 2024 Sep 30.

Abstract

BACKGROUND

group (BFG) isolates are the most frequently isolated gram-negative anaerobic bacteria and exhibit higher levels of antimicrobial resistance than other anaerobic bacteria. Reliable susceptibility testing is needed because of reports of resistance to the most active antibiotics. Recently, the European Committee on Antimicrobial Susceptibility Testing (EUCAST) introduced disk zone diameter breakpoints. We evaluated the disk diffusion test (DDT) for susceptibility testing of BFG isolates compared with the agar dilution method.

METHODS

In total, 150 BFG isolates were collected from three institutes in Korea. The agar dilution method was conducted according to the CLSI guidelines. DDT was performed following the EUCAST guideline. Fastidious anaerobe agar supplemented with 5% defibrinated horse blood was used as the culture medium. Nine antimicrobials were evaluated: penicillin, cefoxitin, cefotetan, imipenem, meropenem, piperacillin-tazobactam, clindamycin, moxifloxacin, and metronidazole.

RESULTS

The categorical agreement (CA) between the two methods was >90.0% for imipenem, meropenem, clindamycin, and metronidazole. However, the CA for piperacillintazobactam was low, at 83.2%. Major errors were found: 5.4% for imipenem, 7.4% for meropenem, and 12.8% for piperacillin-tazobactam. All minor errors were <10%. We propose using the area of technical uncertainty (ATU) zone-overlapping area for susceptible and resistant strains to reduce errors in the DDT. Outside the ATU, the CAs of cefoxitin, cefotetan, and piperacillin-tazobactam were >90.0%, whereas that of moxifloxacin was increased to 88.5%.

CONCLUSIONS

The DDT can be a useful alternative antimicrobial susceptibility test for BFG isolates when using the ATU zone to reduce errors.

摘要

背景

BFG 分离株是最常分离的革兰氏阴性厌氧菌,其对抗菌药物的耐药率高于其他厌氧菌。由于有报道称某些最有效的抗生素也存在耐药性,因此需要进行可靠的药敏试验。最近,欧洲抗菌药物敏感性试验委员会(EUCAST)引入了纸片扩散试验(DDT)的抑菌环直径折点。我们评估了 DDT 与琼脂稀释法(agar dilution method)相比,对 BFG 分离株进行药敏试验的效果。

方法

共收集了韩国三家机构的 150 株 BFG 分离株。琼脂稀释法按照 CLSI 指南进行。DDT 按照 EUCAST 指南进行。使用添加 5%去纤维马血的选择性厌氧菌琼脂作为培养基。评估了 9 种抗菌药物:青霉素、头孢西丁、头孢替坦、亚胺培南、美罗培南、哌拉西林-他唑巴坦、克林霉素、莫西沙星和甲硝唑。

结果

两种方法的分类符合率(CA)对于亚胺培南、美罗培南、克林霉素和甲硝唑均>90.0%。然而,哌拉西林-他唑巴坦的 CA 较低,为 83.2%。发现主要错误:亚胺培南为 5.4%,美罗培南为 7.4%,哌拉西林-他唑巴坦为 12.8%。所有次要错误均<10%。我们建议使用技术不确定区(ATU)重叠区来减少 DDT 的误差,从而用于敏感和耐药菌株。在 ATU 之外,头孢西丁、头孢替坦和哌拉西林-他唑巴坦的 CA 均>90.0%,而莫西沙星的 CA 增加到 88.5%。

结论

当使用 ATU 区来减少误差时,DDT 可作为 BFG 分离株的有用替代抗菌药物敏感性试验方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a83f/11609709/19d099370ad0/alm-45-1-70-f1a.jpg

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