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Utility of polymerase chain reaction using two probes for rapid diagnosis of tubercular pleuritis in comparison to conventional methods

机译:与常规方法相比,使用两种探针进行聚合酶链反应以快速诊断结核性胸膜炎

摘要

We have used polymerase chain reaction (PCR) with IS6110 and a new set of primers from an insertion elementudlike repetitive sequence, (TRC4) to detect Mycobacterium tuberculosis in pleural effusion samples from 50udpatients having pleuritis. The results of PCR were compared with the results of conventional methods likeudsmear, culture and adenosine deaminase activity. Thirty six specimens were positive and 14 were negative byudPCR. Among the 36 samples, 33 were from patients with clinical evidence of tuberculosis including response toudanti-tuberculosis therapy. Only six samples were positive by the gold standard which is culture, and three wereudpositive by smear. The measurement of adenosine deaminase activity classified 19 samples as positives. Theudoverall sensitivity and specificity of PCR was 100 and 85 per cent respectively. PCR using IS6110 and TRC4udprimers is a sensitive test as compared to conventional tests for detection of M. tuberculosis from pleural fluidudsamples of patients with tubercular pleuritis.
机译:我们已使用IS6110的聚合酶链反应(PCR)和来自插入元件 udlike重复序列(TRC4)的一组新引物来检测50例患有胸膜炎患者的胸腔积液样品中的结核分枝杆菌。将PCR结果与常规方法的结果进行比较,如糊涂,培养和腺苷脱氨酶活性。通过 udPCR检测,有36份标本为阳性,而14份为阴性。在这36个样本中,有33个来自具有结核病临床证据的患者,包括对 udanti-结核病治疗的反应。通过培养的金标准,仅六个样品为阳性,而通过涂片,三个样品为阳性。腺苷脱氨酶活性的测量将19个样品分类为阳性。 PCR的总体敏感性和特异性分别为100%和85%。与常规检测相比,使用IS6110和TRC4 udprimers进行PCR是从结核性胸膜炎患者的胸水 udsamples中检测结核分枝杆菌的灵敏测试。

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