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Comparison of LightCycler PCR Rapid Antigen Immunoassay and Culture for Detection of Group A Streptococci from Throat Swabs

机译:比较LightCycler PCR快速抗原免疫测定和培养物以检测咽拭子中A组链球菌的方法

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摘要

We compared the performance characteristics of a real-time PCR method, the LightCycler Strep-A assay (Roche Applied Science, Indianapolis, Ind.), to those of a rapid antigen immunoassay, the Directigen 1-2-3 Group A Strep Test kit (BD Diagnostic Systems, Sparks, Md.), and a standard culture method for detection of group A streptococci (GAS) from 384 throat swabs. The LightCycler PCR produced more positive results (n = 58) than either culture (n = 55) or the Directigen immunoassay (n = 31). The results of the LightCycler PCR and the Directigen method were independently compared to the results of the accepted “gold standard,” bacterial culture. The sensitivities, specificities, and positive and negative predictive values for this comparison were as follows: for the Directigen method, 55, 99, 97, and 93%, respectively; for the LightCycler PCR, 93, 98, 88, and 99%, respectively. In no case was a throat swab positive by both the LightCycler PCR and the Directigen method but negative by culture. The medical histories of patients whose throat swabs were negative by culture but positive by either the LightCycler PCR (n = 7) or the Directigen method (n = 1) were reviewed. All of these patients had signs or symptoms compatible with GAS disease, and therefore, all of these discordant positive results (along with positive results by either the Directigen method or the LightCycler PCR that agreed with the culture results) were counted as true positives for statistical analysis. For this analysis, the LightCycler PCR detected more true-positive results than the culture method (58 versus 55 swabs); however, this difference was not statistically significant (P = 0.5465). In contrast, statistically significantly more true-positive results occurred by culture than by the Directigen method (55 versus 31 swabs; P < 0.0001) and by the LightCycler PCR than by the Directigen method (58 versus 31 swabs; P < 0.0001). The LightCycler PCR is a suitable stand-alone method for the detection of GAS from throat swabs. Additionally, this method requires less than half the personnel time and the procedure can be completed in considerably less time (∼1 h) than our standard approach (up to 2 days) for detection of GAS in throat swabs (i.e., testing by the Directigen method with negative results verified by culture).
机译:我们将实时PCR方法LightCycler Strep-A测定(罗氏应用科学公司,印第安纳州印第安纳州)与快速抗原免疫测定Directigen 1-2-3 A组Strep检测试剂盒的性能特征进行了比较(BD Diagnostic Systems,Sparks,MD)和一种标准培养方法来检测384个咽拭子中的A组链球菌(GAS)。与培养物(n = 55)或Directigen免疫测定法(n = 31)相比,LightCycler PCR产生的阳性结果(n = 58)更多。将LightCycler PCR和Directigen方法的结果分别与公认的“金标准”细菌培养的结果进行比较。该比较的敏感性,特异性以及阳性和阴性预测值如下:对于Directigen方法,分别为55%,99%,97%和93%。对于LightCycler PCR,分别为93%,98%,88和99%。在任何情况下,LightCycler PCR和Directigen方法均未检测到咽拭子阳性,而培养结果则为阴性。回顾了经文化阴性但通过LightCycler PCR(n = 7)或Directigen方法(n = 1)阳性的咽拭子患者的病史。所有这些患者均具有与GAS疾病相适应的体征或症状,因此,所有这些不一致的阳性结果(以及与培养结果一致的Directigen方法或LightCycler PCR的阳性结果)均被视为统计学上的阳性。分析。对于此分析,与培养方法相比,LightCycler PCR检测到的真阳性结果更多(58个拭子对55个拭子)。但是,这种差异在统计学上不显着(P = 0.5465)。相反,与Directigen方法(55个棉签,31个拭子; P <0.0001)和LightCycler PCR相比,培养产生的真阳性结果在统计学上显着多于Directigen方法(58个棉签,对31个棉签; P <0.0001)。 LightCycler PCR是用于检测咽拭子中GAS的合适独立方法。此外,这种方法所需的人员时间不到一半,而且与检测咽拭子中GAS的标准方法(即Directigen进行的检测)相比,该过程可在比标准方法(最多2天)短得多的时间(约1小时)内完成。培养结果为阴性的方法)。

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