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商业肉汤微量稀释法检测囊性纤维化患者铜绿假单胞菌分离株两种读出方法的重复性。

Reproducibility between two readout methods of a commercial broth microdilution assay for Pseudomonas aeruginosa isolates from patients with Cystic Fibrosis.

机构信息

a Department of Medical Microbiology , University Medical Centre Utrecht , Utrecht , The Netherlands.

出版信息

Infect Dis (Lond). 2019 Jan;51(1):50-55. doi: 10.1080/23744235.2018.1500705. Epub 2019 Jan 17.

DOI:10.1080/23744235.2018.1500705
PMID:30654670
Abstract

BACKGROUND

Pseudomonas aeruginosa isolates from Cystic fibrosis (CF) patients are growing slowly, and frequently rendering automated susceptibility testing unsuitable. Colistin is an important antibiotic for treatment of P. aeruginosa infections. Broth microdilution is the only EUCAST endorsed antimicrobial susceptibility test for colistin. The VIZION™ device aids in reading broth microdilution plates and allows safe data transfer to laboratory information systems. In this study, reproducibility between visual MIC readout and readout, employing the VIZION™ device was assessed in susceptibility testing of colistin and beta-lactam antibiotics in P. aeruginosa isolates from CF patients.

METHODS

Fifty-six unique P. aeruginosa isolates were derived from respiratory secretions of CF patients. Susceptibility testing was performed using commercially available microdilution plates. MIC readout by VIZION™ was compared to visual readout aided by a mirror (reference test).

RESULTS

Pseudomonas aeruginosa isolates displayed significantly slower growth rates compared to quality control isolates. Colistin exact MIC agreement between VIZION™ and visual readout after 24 and 48 h incubation, respectively, was 82% and 95%, essential MIC agreement was 98% and 100%, categorical agreement was 98% and 98% and reliability (weighted kappa) was 0.95 (95% CI = 0.91-0.99) and 0.99 (95% CI = 0.97-1.00). For all five antibiotics, the total number of errors (using VIZION™, in comparison with visual readout) decreased from 15 (5%) to 10 (4%) after 24 and 48 h incubation, respectively.

CONCLUSIONS

VIZION™ readout reproducibly determines MIC values in comparison with visual readout after 24 h of incubation. Reproducibility between the VIZION™ and visual readout increases after prolonged incubation of 48 h.

摘要

背景

来自囊性纤维化 (CF) 患者的铜绿假单胞菌分离株生长缓慢,经常导致自动化药敏试验不合适。多粘菌素是治疗铜绿假单胞菌感染的重要抗生素。微量肉汤稀释法是唯一被 EUCAST 认可的多粘菌素药敏检测方法。VIZION™设备有助于读取肉汤微量稀释板,并允许安全地将数据传输到实验室信息系统。在这项研究中,评估了 VIZION™设备在 CF 患者分离的铜绿假单胞菌对多粘菌素和β-内酰胺类抗生素药敏检测中的目视 MIC 读数与读数之间的重现性。

方法

从 CF 患者的呼吸道分泌物中分离出 56 株独特的铜绿假单胞菌。使用市售的微量稀释板进行药敏试验。VIZION™的 MIC 读数与借助镜子(参考试验)进行的目视读数进行比较。

结果

与质控分离株相比,铜绿假单胞菌分离株的生长速度明显较慢。在分别孵育 24 和 48 小时后,VIZION™和目视读数的多粘菌素精确 MIC 一致性分别为 82%和 95%,基本 MIC 一致性分别为 98%和 100%,分类一致性分别为 98%和 98%,可靠性(加权kappa)分别为 0.95(95%CI=0.91-0.99)和 0.99(95%CI=0.97-1.00)。对于所有五种抗生素,与视觉读数相比,使用 VIZION™的总错误数(错误率)分别从孵育 24 小时和 48 小时后减少了 15(5%)至 10(4%)。

结论

VIZION™读数在孵育 24 小时后与目视读数相比可重现地确定 MIC 值。在孵育 48 小时后,VIZION™与目视读数之间的重现性增加。

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