Mohammed M J, Tenover F C
Hospital Infections Program, Centers for Disease Control and Prevention, Atlanta, Georgia 30333, USA.
J Clin Microbiol. 2000 May;38(5):1713-6. doi: 10.1128/JCM.38.5.1713-1716.2000.
Antimicrobial resistance continues to increase worldwide among isolates of Streptococcus pneumoniae and other species of streptococci. Increasing rates of penicillin resistance, particularly in viridans group streptococci, and resistance to multiple classes of antimicrobial agents, including beta-lactams, macrolides, and fluoroquinolones, in pneumococci have increased the importance of having accurate antimicrobial susceptibility testing results for guiding therapy. One commercial method of assessing resistance in streptococci is the PASCO Strep Plus panel. This broth microdilution-based method has recently been expanded to include a variety of newer antimicrobial agents. Therefore, we compared the results of the new PASCO Strep Plus panels for 26 antimicrobial agents against the results generated using the National Committee for Clinical Laboratory Standards (NCCLS) broth microdilution reference method for 75 pneumococci and 68 other streptococcal isolates. Only 4 (0.2%) very major errors (all with pneumococci and each with a different antimicrobial agent) were observed. There were 5 (0.3%) major errors observed with pneumococci (each with a different antimicrobial agent), but only 1 major error with nonpneumococcal streptococci. All of the very major and major errors resolved on retesting. Of the 65 (3.9%) and 17 (1.6%) minor errors observed with pneumococci and other streptococci, respectively, all were within 1 dilution of the broth microdilution reference MIC result. Thus, the PASCO Strep Plus panel has comparable accuracy to the NCCLS broth microdilution reference method.
在全球范围内,肺炎链球菌及其他链球菌分离株的抗菌药物耐药性持续上升。青霉素耐药率不断增加,尤其是在草绿色链球菌中,而肺炎球菌对包括β-内酰胺类、大环内酯类和氟喹诺酮类在内的多类抗菌药物的耐药性,使得获得准确的抗菌药物敏感性检测结果以指导治疗变得愈发重要。评估链球菌耐药性的一种商业方法是PASCO Strep Plus检测板。这种基于肉汤微量稀释法的检测方法最近已扩展到包括多种更新的抗菌药物。因此,我们比较了新型PASCO Strep Plus检测板针对26种抗菌药物的检测结果与使用美国国家临床实验室标准委员会(NCCLS)肉汤微量稀释参考方法对75株肺炎球菌和68株其他链球菌分离株所产生的结果。仅观察到4例(0.2%)非常重大错误(均为肺炎球菌,且每种错误对应一种不同的抗菌药物)。观察到5例(0.3%)肺炎球菌重大错误(每种错误对应一种不同的抗菌药物),但非肺炎链球菌仅出现1例重大错误。所有非常重大错误和重大错误在重新检测时均得到解决。在肺炎球菌和其他链球菌中分别观察到65例(3.9%)和17例(1.6%)小错误,所有这些小错误与肉汤微量稀释参考MIC结果的差异均在1个稀释度以内。因此,PASCO Strep Plus检测板的准确性与NCCLS肉汤微量稀释参考方法相当。