Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.
Division of Clinical Microbiology, Linköping University Hospital, Linköping, Sweden.
J Antimicrob Chemother. 2023 Oct 3;78(10):2563-2571. doi: 10.1093/jac/dkad272.
Rapidly instituted antimicrobial therapy is important in severe infections, and reduced time to the antimicrobial susceptibility testing (AST) report is thus of importance. Disc diffusion (DD) is a cheap, rapidly adaptable, flexible and comprehensive method for phenotypic AST. Previous studies have shown that early reading of inhibition zones for non-fastidious species is possible.
To evaluate zone reading after short incubation of DD in Haemophilus influenzae (n = 73) and Streptococcus pneumoniae (n = 112).
The readability was evaluated and susceptibility interpretation (SIR) was performed, using the EUCAST 18 ± 2 h incubation breakpoint table (version 12.0), after 6 and 8 h of incubation. Categorical agreement (CA) and error rates were calculated using standard DD and broth microdilution as reference.
The proportion of readable zones in H. influenzae was 19% (6 h) and 89% (8 h). The CA was 98% after 8 h. The corresponding readability in S. pneumoniae was 63%/98% and CA was 95%/97% after 6 and 8 h, respectively. Early reading of the screening discs (benzylpenicillin 1 unit in H. influenzae and oxacillin 1 µg in S. pneumoniae) correctly identified 18/22 of the H. influenzae isolates and all the readable S. pneumoniae isolates with reduced β-lactam susceptibility. For non-β-lactam agents, very major errors were most common for quinolones in S. pneumoniae. Introduction of areas of technical uncertainty (ATUs) reduced the error rate to ≤1.1%.
We conclude that shortened incubation is feasible for H. influenzae and S. pneumoniae. To reduce the risk of false categorization a buffer zone (i.e. ATU) near the breakpoints must be used.
在严重感染中,及时进行抗菌治疗至关重要,因此,缩短获得抗菌药物敏感性检测(AST)报告的时间非常重要。纸片扩散法(DD)是一种廉价、快速适应、灵活且全面的表型 AST 方法。先前的研究表明,对于非苛养菌,可以进行早期读取抑菌圈。
评估流感嗜血杆菌(n=73)和肺炎链球菌(n=112)的 DD 短孵育后进行的抑菌圈读取。
使用 EUCAST 18±2 h 孵育折点表(版本 12.0),在 6 和 8 h 孵育后评估可读取性,并进行药敏判断(SIR)。使用标准 DD 和肉汤微量稀释法作为参考,计算分类一致性(CA)和错误率。
在流感嗜血杆菌中,可读抑菌圈的比例分别为 19%(6 h)和 89%(8 h)。8 h 后 CA 为 98%。在肺炎链球菌中,相应的可读率为 63%/98%,CA 分别为 6 h/95%和 8 h/97%。早期读取筛选药敏纸片(流感嗜血杆菌中苯唑西林 1 单位和肺炎链球菌中苯唑西林 1 µg)正确识别了 18/22 株流感嗜血杆菌分离株和所有具有降低β-内酰胺类药物敏感性的可读肺炎链球菌分离株。对于非β-内酰胺类药物,肺炎链球菌中喹诺酮类药物的主要错误率最高。引入技术不确定区(ATU)可将错误率降低至≤1.1%。
我们得出结论,缩短孵育时间对于流感嗜血杆菌和肺炎链球菌是可行的。为了降低错误分类的风险,必须在折点附近使用缓冲区(即 ATU)。