Yadav Kajal S, Pawar Satyajeet, Yadav Suvarna A, Patil Satish
Microbiology, Krishna Institute of Medical Science, Krishna Vishwa Vidyapeeth, Karad, IND.
Cureus. 2024 Dec 30;16(12):e76646. doi: 10.7759/cureus.76646. eCollection 2024 Dec.
Background Colistin, a last-resort antibiotic, has witnessed a surge in resistance, posing a significant threat to public health. Accurate and timely detection of colistin resistance is crucial for effective clinical management. This study aims to compare two commonly used methods, the VITEK® 2 Compact (bioMerieux, Marcy-l'Étoile, France) system and broth microdilution (BMD), for identifying colistin resistance in clinical isolates. Materials and methods The study was carried out in the Microbiology Department at Krishna Institute of Medical Sciences, Karad. The laboratory processed the specimens for identification, followed by antimicrobial susceptibility testing using the automated VITEK® 2 Compact system and the gold-standard BMD method. Results A total of 92 isolates were examined using automation (VITEK® 2 Compact) and the BMD methods, and the findings were analyzed. A gender-based analysis of the study population showed that 67% were males and 33% were females. Among the various specimens received, the highest number of colistin-resistant isolates was found in urine (38 isolates, 41.30%), then pus (25 isolates, 25.17%), endotracheal tube (13 isolates, 14.13%), sterile fluid (7 isolates, 7.60%), blood (3 isolates, 3.26%), sputum (3 isolates, 3.26%), vaginal swab (2 isolates, 2.17%), and catheter (1 isolate, 1.08%). Of the 92 isolates, 59 (64.1%) were resistant to colistin by the BMD, while 41 (44.56%) were resistant by the VITEK® 2 Compact. Conclusion Colistin is increasingly used for multidrug-resistant Gram-negative infections. In this study, some isolates showed differing results between VITEK® 2 Compact and BMD. The statistical analysis showed moderate kappa agreement, confirming the consistent reliability of the VITEK® 2 Compact system for testing colistin minimum inhibitory concentrations. Consequently, we can employ the VITEK® 2 Compact automated system as an alternative.
背景
黏菌素作为一种最后的抗菌药物,耐药性呈激增态势,对公众健康构成重大威胁。准确及时地检测黏菌素耐药性对于有效的临床管理至关重要。本研究旨在比较两种常用方法,即VITEK® 2 Compact(法国生物梅里埃公司,马西 - 埃图瓦勒)系统和肉汤微量稀释法(BMD),用于鉴定临床分离株中的黏菌素耐药性。
材料与方法
该研究在卡拉德克里希纳医学科学研究所微生物学系开展。实验室对标本进行鉴定处理,随后使用自动化的VITEK® 2 Compact系统和金标准BMD方法进行抗菌药物敏感性测试。
结果
共使用自动化方法(VITEK® 2 Compact)和BMD方法检测了92株分离株,并对结果进行分析。基于性别的研究人群分析显示,67%为男性,33%为女性。在收到的各类标本中,尿液中黏菌素耐药分离株数量最多(38株,41.30%),其次是脓液(25株,25.17%)、气管内导管(13株,14.13%)、无菌液体(7株,7.60%)、血液(3株,3.26%)、痰液(3株,3.26%)、阴道拭子(2株,2.17%)和导管(1株,1.08%)。在92株分离株中,BMD法检测显示59株(64.1%)对黏菌素耐药,而VITEK® 2 Compact法检测显示41株(44.56%)耐药。
结论
黏菌素越来越多地用于治疗多重耐药革兰氏阴性菌感染。在本研究中,一些分离株在VITEK® 2 Compact和BMD方法之间显示出不同结果。统计分析显示kappa一致性中等,证实了VITEK® 2 Compact系统在检测黏菌素最低抑菌浓度方面的持续可靠性。因此,我们可以采用VITEK® 2 Compact自动化系统作为替代方法。