Department of Infectious Diseases, Unit for Mycotic and Parasitic Agents and Mycobacteria, Robert Koch Institute, Seestrasse 10, 13353, Berlin, Germany.
European Programme for Public Health Microbiology (EUPHEM), European Centre for Disease Prevention and Control (ECDC), Stockholm, Sweden.
BMC Infect Dis. 2020 Jul 16;20(1):514. doi: 10.1186/s12879-020-05234-w.
Worldwide, an increase in antimicrobial resistance (AMR) of Neisseria gonorrhoeae has been observed. Until now, no protocol for an external quality assessment (EQA) has been available for Germany. The German gonococcal resistance network (GORENET) performed an EQA of primary laboratories in Germany in order to assess quality of antibiotic susceptibility testing, to gain information about laboratory procedures and to assess the impact of these procedures on test results.
Laboratories assessed drug susceptibility to cefixime, ceftriaxone, azithromycin, penicillin and ciprofloxacin for five N. gonorrhoeae strains, using their standard laboratory protocols. Minimal inhibitory concentrations (MICs) were compared to World Health Organisation (WHO) consensus results (or, if not available, reference laboratory results), while deviation by +/- one doubling dilution was accepted. Data on laboratory procedures were collected via a standardised questionnaire. Generalized linear models and conditional inference trees (CTREE) were used to assess relationships between laboratory procedures and testing outcomes.
Twenty-one primary laboratories participated in the EQA in June 2018. 96% of ciprofloxacin MICs were reported within accepted deviations, as well as 88% for cefixime, 85% for ceftriaxone, 79% for penicillin and 70% for azithromycin. The use of interpretation standards and general laboratory procedures like agar base, incubation settings or the use of control strains strongly differed between laboratories. In statistical analysis, incubation time of cultures < 24 h was associated with correct measurements. Additionally, a 5% CO concentration was associated with correct results regarding azithromycin compared to 3%. CTREE analysis showed that incubation time, humidity and CO concentration had the greatest influence on the average deviation from consensus results.
In conclusion, we report the development of a protocol for N. gonorrhoeae antimicrobial susceptibility testing in Germany. While testing results were in accordance with the expected consensus results in 70-96%, depending on the antibiotic agent, laboratory methodology was heterogeneous and may significantly affect the testing quality. We therefore recommend the development of a standard operating procedure (SOP) for N. gonorrhoeae susceptibility testing in Germany.
全球范围内,淋病奈瑟菌的抗微生物药物耐药性(AMR)有所增加。迄今为止,德国还没有可供使用的外部质量评估(EQA)方案。德国淋球菌耐药网络(GORENET)对德国的主要实验室进行了 EQA,以评估抗生素药敏试验的质量,了解实验室程序,并评估这些程序对试验结果的影响。
实验室使用其标准实验室方案评估五种淋病奈瑟菌菌株对头孢克肟、头孢曲松、阿奇霉素、青霉素和环丙沙星的药物敏感性。最小抑菌浓度(MIC)与世界卫生组织(WHO)共识结果进行比较(如果没有共识结果,则与参考实验室结果进行比较),同时接受 +/- 一个稀释度的偏差。通过标准化问卷收集有关实验室程序的数据。使用广义线性模型和条件推断树(CTREE)评估实验室程序与测试结果之间的关系。
2018 年 6 月,21 家主要实验室参加了 EQA。96%的环丙沙星 MIC 值在可接受的偏差范围内报告,头孢克肟为 88%,头孢曲松为 85%,青霉素为 79%,阿奇霉素为 70%。各实验室对解释标准和琼脂基础、孵育条件或使用对照菌株等一般实验室程序的使用存在较大差异。在统计分析中,培养物 <24 小时的孵育时间与正确的测量结果相关。此外,与 3%相比,5%的 CO 浓度与阿奇霉素的正确结果相关。CTREE 分析表明,孵育时间、湿度和 CO 浓度对抗微生物药物药敏试验的平均偏差影响最大。
总之,我们报告了德国开发淋病奈瑟菌抗微生物药物敏感性检测方案的情况。虽然测试结果在 70-96%的情况下与预期的共识结果一致,这取决于抗生素,但实验室方法学存在异质性,可能会显著影响测试质量。因此,我们建议德国制定淋病奈瑟菌药敏试验的标准操作程序(SOP)。