Trichomonas vaginalis and BTUB FRET PCR, using s'/> Comparison between the Gen-Probe Transcription-Mediated Amplification Trichomonas vaginalis Research Assay and Real-Time PCR for Trichomonas vaginalis Detection Using a Roche LightCycler Instrument with Female Self-Obtained Vaginal Swab Samples and Male Urine Samples
首页> 外文期刊>Journal of Clinical Microbiology >Comparison between the Gen-Probe Transcription-Mediated Amplification Trichomonas vaginalis Research Assay and Real-Time PCR for Trichomonas vaginalis Detection Using a Roche LightCycler Instrument with Female Self-Obtained Vaginal Swab Samples and Male Urine Samples
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Comparison between the Gen-Probe Transcription-Mediated Amplification Trichomonas vaginalis Research Assay and Real-Time PCR for Trichomonas vaginalis Detection Using a Roche LightCycler Instrument with Female Self-Obtained Vaginal Swab Samples and Male Urine Samples

机译:Gen-Probe转录介导的阴道毛滴虫研究测定与实时PCR的比较(使用罗氏LightCycler仪器与女性自测阴道拭子样品和男性尿液样品进行检测)的比较

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摘要

This study compared two assays for Trichomonas vaginalis detection, Gen-Probe's transcription-mediated amplification (TMA) assay for Trichomonas vaginalis and BTUB FRET PCR, using self-obtained clinical samples from 611 patients. Infection status was defined as two positive results by two different tests. The initial TMA assay sensitivity was 96.7%; specificity was 97.5%. The TMA assay was comparable to BTUB FRET PCR.
机译:这项研究比较了两种自发获得的临床样品,用于检测阴道毛滴虫的两种检测方法,用于阴道毛滴虫的Gen-Probe转录介导扩增(TMA)检测和BTUB FRET PCR的检测方法。 611名患者。通过两个不同的测试,感染状态定义为两个阳性结果。 TMA分析的初始灵敏度为96.7%;特异性为97.5%。 TMA分析与BTUB FRET PCR相当。

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