Wisplinghoff Laboratories, Horbeller Straße 18-20, 50858, Cologne, Germany.
Institute for Medical Microbiology, Immunology and Hygiene, University of Cologne, Goldenfelsstr, 19-21, 50935, Cologne, Germany.
Curr Microbiol. 2024 Jul 9;81(8):261. doi: 10.1007/s00284-024-03768-9.
A reliable and above all, rapid antimicrobial susceptibility test (AST) is required for the diganostics of blood stream infections (BSI). In this study, resistance testing using DxM MicroScan WalkAway (MicroScan) from a 4-h subculture is compared with the standard overnight culture (18-24 h). Randomly selected positive blood cultures (PBC, n = 102) with gram-negative bacteria were included in the study. PBC were sub-cultured onto appropriate agar plates and AST by MicroScan was performed after 4 h of incubation and repeated after incubation for 18-24 h as standard. In a total of 1909 drug-strain pairs, the 4-h subculture approach showed a very high essential agreement (EA) (98.6%) and categorical agreement (CA) (97.1%) compared with the standard. The incidence of minor error (mE), major error (ME), very major error (VME), and adjusted very major error (aVME) was 1.1%, 0.4%, 12.9%, and 5.3%, respectively. In summary, the use of 4-h subcultures for resistance testing with the MicroScan offers a very reliable and easy to realize time saving when testing positive blood cultures with gram-negative bacteria.
对于血流感染(BSI)的诊断,需要一种可靠的、尤其是快速的抗菌药物敏感性测试(AST)。在这项研究中,我们将使用 DxM MicroScan WalkAway(MicroScan)对 4 小时亚培养物进行耐药性测试,与标准过夜培养(18-24 小时)进行比较。本研究纳入了随机选择的革兰氏阴性菌阳性血培养物(PBC,n=102)。将 PBC 接种到适当的琼脂平板上,孵育 4 小时后进行 MicroScan AST,并在孵育 18-24 小时后重复标准测试。在总共 1909 对药敏株中,与标准相比,4 小时亚培养方法显示出非常高的基本一致率(EA)(98.6%)和分类一致率(CA)(97.1%)。小错误(mE)、大错误(ME)、非常大错误(VME)和调整非常大错误(aVME)的发生率分别为 1.1%、0.4%、12.9%和 5.3%。总之,使用 4 小时亚培养物进行 MicroScan 耐药性测试,在检测革兰氏阴性菌阳性血培养物时,提供了一种非常可靠且易于实现的节省时间的方法。