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迈向兽医临床细菌学中统一的实验室方法:一项欧洲调查的结果

Towards harmonized laboratory methodologies in veterinary clinical bacteriology: outcomes of a European survey.

作者信息

Koritnik Tom, Cvetkovikj Iskra, Zendri Flavia, Blum Shlomo Eduardo, Chaintoutis Serafeim Christos, Kopp Peter A, Hare Cassia, Štritof Zrinka, Kittl Sonja, Gonçalves José, Zdovc Irena, Paulshus Erik, Laconi Andrea, Singleton David, Allerton Fergus, Broens Els M, Damborg Peter, Timofte Dorina

机构信息

Department for Public Health Microbiology Ljubljana, Centre for Medical Microbiology, National Laboratory of Health, Environment and Food, Ljubljana, Slovenia.

Department of Microbiology and Immunology, Faculty of Veterinary medicine-Skopje, Ss Cyril and Methodius University in Skopje, Skopje, Republic of North Macedonia.

出版信息

Front Microbiol. 2024 Oct 10;15:1443755. doi: 10.3389/fmicb.2024.1443755. eCollection 2024.

Abstract

INTRODUCTION

Veterinary clinical microbiology laboratories play a key role in antimicrobial stewardship, surveillance of antimicrobial resistance and prevention of healthcare associated-infections. However, there is a shortage of international harmonized guidelines covering all steps of veterinary bacterial culture from sample receipt to reporting.

METHODS

In order to gain insights, the European Network for Optimization of Veterinary Antimicrobial Treatment (ENOVAT) designed an online survey focused on the practices and interpretive criteria used for bacterial culture and identification (C&ID), and antimicrobial susceptibility testing (AST) of animal bacterial pathogens.

RESULTS

A total of 241 microbiology laboratories in 34 European countries completed the survey, representing a mixture of academic (37.6%), governmental (27.4%), and private (26.5%) laboratories. The C&ID turnaround varied from 1 to 2 days (77.8%) to 3-5 days (20%), and 6- 8 days (1.6%), with similar timeframes for AST. Individual biochemical tests and analytical profile index (API) biochemical test kits or similar were the most frequent tools used for bacterial identification (77% and 56.2%, respectively), followed by PCR (46.6%) and MALDI-TOF MS (43.3%). For AST, Kirby-Bauer disk diffusion (DD) and minimum inhibitory concentration (MIC) determination were conducted by 43.8% and 32.6% of laboratories, respectively, with a combination of EUCAST and CLSI clinical breakpoints (CBPs) preferred for interpretation of the DD (41.2%) and MIC (47.6%) results. In the absence of specific CBPs, laboratories used human CBPs (53.3%) or veterinary CBPs representing another body site, organism or animal species (51.5%). Importantly, most laboratories (47.9%) only report the qualitative interpretation of the result (S, R, and I). As regards testing for AMR mechanisms, 48.5% and 46.7% of laboratories routinely screened isolates for methicillin resistance and ESBL production, respectively. Notably, selective reporting of AST results (i.e. excluding highest priority critically important antimicrobials from AST reports) was adopted by 39.5% of laboratories despite a similar proportion not taking any approach (37.6%) to guide clinicians towards narrower-spectrum or first-line antibiotics.

DISCUSSION

In conclusion, we identified a broad variety of methodologies and interpretative criteria used for C&ID and AST in European veterinary microbiological diagnostic laboratories. The observed gaps in veterinary microbiology practices emphasize a need to improve and harmonize professional training, innovation, bacterial culture methods and interpretation, AMR surveillance and reporting strategies.

摘要

引言

兽医临床微生物学实验室在抗菌药物管理、抗菌药物耐药性监测以及预防医疗保健相关感染方面发挥着关键作用。然而,目前缺乏涵盖从样本接收到报告的兽医细菌培养所有步骤的国际统一指南。

方法

为了深入了解情况,欧洲兽医抗菌治疗优化网络(ENOVAT)设计了一项在线调查,重点关注用于动物细菌病原体的细菌培养与鉴定(C&ID)以及抗菌药物敏感性测试(AST)的实践和解释标准。

结果

来自34个欧洲国家的总共241个微生物学实验室完成了该调查,这些实验室包括学术实验室(37.6%)、政府实验室(27.4%)和私人实验室(26.5%)的混合样本。C&ID的周转时间从1至2天(77.8%)到3至5天(20%)以及6至8天(1.6%)不等,AST的时间框架类似。单个生化试验和分析谱指数(API)生化试验试剂盒或类似产品是用于细菌鉴定最常用的工具(分别为77%和56.2%),其次是PCR(46.6%)和基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS,43.3%)。对于AST,43.8%的实验室进行了 Kirby-Bauer纸片扩散法(DD),32.6%的实验室进行了最低抑菌浓度(MIC)测定,在解释DD(41.2%)和MIC(47.6%)结果时,欧盟抗菌药物敏感性试验委员会(EUCAST)和美国临床和实验室标准协会(CLSI)临床断点(CBP)的组合更受青睐。在没有特定CBP的情况下,实验室使用人类CBP(53.3%)或代表其他身体部位、生物体或动物物种的兽医CBP(51.5%)。重要的是,大多数实验室(47.9%)仅报告结果的定性解释(敏感、耐药和中介)。关于AMR机制的检测,48.5%和46.7%的实验室分别常规筛查分离株的耐甲氧西林和超广谱β-内酰胺酶(ESBL)产生情况。值得注意的是,39.5%的实验室采用了选择性报告AST结果(即从AST报告中排除最高优先级的 critically important抗菌药物),尽管有相似比例(37.6%)的实验室未采取任何方法来指导临床医生使用窄谱或一线抗生素。

讨论

总之,我们确定了欧洲兽医微生物诊断实验室在C&ID和AST中使用的广泛多样的方法和解释标准。兽医微生物学实践中观察到的差距强调了改进和统一专业培训、创新、细菌培养方法和解释、AMR监测以及报告策略的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4533/11499178/9bdd1a176fe6/fmicb-15-1443755-g001.jpg

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