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Clinical Value of Treponema pallidum Real-Time PCR for Diagnosis of Syphilis

机译:梅毒螺旋体实时荧光定量PCR在梅毒诊断中的临床价值

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摘要

The diagnosis of syphilis can be complicated when it is based on diverse clinical manifestations, dark-field microscopy, and serology. In the present study, therefore, we examined the additional clinical value of a Treponema pallidum real-time TaqMan PCR for the detection of primary and secondary syphilis. The additional value of the T. pallidum real-time PCR for the diagnosis of primary syphilis was evaluated by the use of three different algorithms: (i) a head-to-head comparison of the dark-field microscopy result and the T. pallidum real-time PCR result, (ii) comparison of the clinical diagnosis made in a sexually transmitted infection clinic (STI) (including by dark-field microscopy) and the T. pallidum real-time PCR result, and (iii) comparison of the clinical diagnosis made in a general practitioner's office (without dark-field microscopy) and the T. pallidum real-time PCR result. A fourth algorithm was used to determine the performance of the T. pallidum real-time PCR regarding the detection of secondary syphilis. From December 2006 to April 2008, 716 patients with suspected cases of primary syphilis and 133 patients with suspected cases of secondary syphilis were included in the study. A kappa value of 0.601 was found for the agreement between dark-field microscopy and the T. pallidum real-time PCR. Good agreement was found between the T. pallidum real-time PCR and both the diagnosis of the general practitioner (kappa = 0.745) and the diagnosis of the STI clinic (kappa = 0.769). The sensitivity with respect to the STI clinic diagnosis was 72.8%, the specificity was 95.5%, the positive predictive value was 89.2%, and the negative predictive value was 95.0%. The T. pallidum real-time PCR is a fast, efficient, and reliable test for the diagnosis of primary syphilis in an STI outpatient clinic and a general practitioner setting, but it has no added diagnostic value for the diagnosis of secondary syphilis.
机译:基于多种临床表现,暗视野显微镜检查和血清学检查,梅毒的诊断可能会很复杂。因此,在本研究中,我们检查了梅毒螺旋体实时TaqMan PCR在检测原发性和继发性梅毒中的附加临床价值。使用三种不同的算法评估了梅毒螺旋体实时PCR在诊断原发性梅毒中的附加价值:(i)暗视野显微镜检查结果与梅毒螺旋体的头对头比较实时PCR结果,(ii)比较性传播感染诊所(STI)的临床诊断(包括通过暗视野显微镜检查)和苍白锥虫实时PCR结果,以及(iii)比较在全科医生办公室进行临床诊断(无暗场显微镜检查)和梅毒螺旋体实时PCR结果。第四种算法用于确定关于梅毒继发性梅毒的梅毒螺旋体实时PCR的性能。从2006年12月至2008年4月,该研究包括716例疑似原发性梅毒患者和133例疑似继发性梅毒患者。对于暗视野显微镜和苍白锥虫实时PCR之间的一致性,发现κ值为0.601。苍白锥虫实时荧光定量PCR与全科医生的诊断(kappa = 0.745)和STI诊所的诊断(kappa = 0.769)之间发现了很好的一致性。对STI临床诊断的敏感性为72.8%,特异性为95.5%,阳性预测值为89.2%,阴性预测值为95.0%。梅毒螺旋体实时PCR是在STI门诊和全科医生中诊断梅毒的快速,有效和可靠的测试方法,但是对于继发梅毒的诊断没有附加的诊断价值。

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