首页> 外文OA文献 >A multicenter prospective trial to asses a new real-time polymerase chain reaction for detection of Treponema pallidum, herpes simplex-1/2 and Haemophilus ducreyi in genital, anal and oropharyngeal ulcers
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A multicenter prospective trial to asses a new real-time polymerase chain reaction for detection of Treponema pallidum, herpes simplex-1/2 and Haemophilus ducreyi in genital, anal and oropharyngeal ulcers

机译:一项评估新的实时聚合酶链反应的多中心前瞻性试验,用于检测生殖器,肛门和口咽溃疡中的梅毒螺旋体,单纯疱疹1/2和杜克嗜血杆菌

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摘要

Treponema pallidum, herpes simplex virus types 1 or 2 (HSV-1/2) and Haemophilus ducreyi are sexually transmitted pathogens that can cause genital, anal and oropharyngeal ulcers. Laboratory evaluation of these pathogens in ulcers requires different types of specimens and tests, increasing the risk of improper specimen handling and time lapse until analysis. We sought to develop a new real-time PCR (TP-HD-HSV1/2 PCR) to facilitate the detection of T. pallidum, HSV-1/2 and H. ducreyi in ulcers. The TP-HD-HSV1/2 PCR was tested (i) in a retrospective study on 193 specimens of various clinical origin and (ii) in a prospective study on 36 patients with genital, anal or oropharyngeal ulcers (ClinicalTrials.gov # NCT01688258). The results of the TP-HD-HSV1/2 PCR were compared with standard diagnostic methods (T. pallidum: serology, dark field microscopy; HSV-1/2: PCR; H. ducreyi: cultivation). Sensitivity and specificity of the TP-HD-HSV1/2 PCR for T. pallidum were both 100%, for HSV-1 100% and 98%, and for HSV-2 100% and 98%, respectively. T. pallidum and HSV-1/2 were detected in 53% and 22% of patients in the prospective study; H. ducreyi was not detected. In the prospective study, 5/19 (26%) specimens were true positive for T. pallidum in the TP-HD-HSV1/2 PCR but non-reactive in the VDRL. The TP-HD-HSV1/2 PCR is sensitive and specific for the detection of T. pallidum and HSV-1/2 in routine clinical practice and it appears superior to serology in early T. pallidum infections.
机译:梅毒螺旋体,1型或2型单纯疱疹病毒(HSV-1 / 2)和杜克嗜血杆菌是性传播病原体,可引起生殖器,肛门和口咽溃疡。对溃疡中这些病原体的实验室评估需要不同类型的标本和测试,从而增加了标本处理不当的风险以及分析之前所花费的时间。我们试图开发一种新的实时PCR(TP-HD-HSV1 / 2 PCR)以促进溃疡中T.pallidum,HSV-1 / 2和H.ducreyi的检测。 TP-HD-HSV1 / 2 PCR进行了测试(i)对193种不同临床来源的标本进行回顾性研究,并且(ii)对36例生殖器,肛门或口咽溃疡患者进行了前瞻性研究(ClinicalTrials.gov#NCT01688258) 。将TP-HD-HSV1 / 2 PCR的结果与标准诊断方法进行比较(苍白锥虫:血清学,暗视野显微镜; HSV-1 / 2:PCR; H.ducreyi:培养)。 TP-HD-HSV1 / 2 PCR对梅毒螺旋体的敏感性和特异性分别为100%,HSV-1 100%和98%,HSV-2 100%和98%。前瞻性研究中分别有53%和22%的患者检出了T.pallidum和HSV-1 / 2;未检测到H.ducreyi。在前瞻性研究中,TP-HD-HSV1 / 2 PCR中5/19(26%)的标本为T.pallidum阳性,但在VDRL中无反应。 TP-HD-HSV1 / 2 PCR对常规临床实践中检出T.pallidum和HSV-1 / 2敏感且特异,在早期T.pallidum感染中似乎优于血清学。

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