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首页> 外文期刊>Journal of Clinical Microbiology >Usefulness of PCR and Antigen Latex Agglutination Test with Samples Obtained by Transthoracic Needle Aspiration for Diagnosis of Pneumococcal Pneumonia
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Usefulness of PCR and Antigen Latex Agglutination Test with Samples Obtained by Transthoracic Needle Aspiration for Diagnosis of Pneumococcal Pneumonia

机译:经胸针抽吸获得的样本PCR和抗原胶乳凝集试验对肺炎球菌肺炎的诊断价值

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In a large number of cases, the etiology of community-acquired pneumonia (CAP) is not established. Some cases are probably caused byStreptococcus pneumoniae. Transthoracic needle aspiration (TNA) culture has a limited sensitivity which might be improved by antigen detection or gene amplification techniques. We evaluated the capacity of a PCR assay and a latex agglutination test to detectS. pneumoniae in samples obtained by TNA from 95 patients with moderate-to-severe CAP. Latex agglutination and PCR had sensitivities of 52.2 and 91.3%, specificities of 88.7 and 83.3%, positive predictive values of 62.3 and 65.6%, and negative predictive values of 83.3 and 96.5%, respectively, when culture techniques were used as the “gold standard.” When we considered expanded criteria for the diagnosis of pneumococcal pneumonia as a standard for our calculations, latex agglutination and PCR had sensitivities of 53.6 and 89.7%, specificities of 93.0 and 90.0%, positive predictive values of 78.9 and 81.3%, and negative predictive values of 80.3 and 94.7%, respectively. The additional diagnosis provided by the PCR assay compared to latex agglutination was 12.2% (95% confidence interval of the difference from 0.4 to 20.1%). PCR was more sensitive than TNA culture, particularly in patients who had received prior antibiotic therapy (83.3 versus 33.3%). Although PCR is a very sensitive and specific technique, it has not proved to be cost-effective in clinical practice. Conversely, latex agglutination is a fast and simple method whose results might have significant implications for initial antibiotic therapy.
机译:在许多情况下,尚未建立社区获得性肺炎的病因。某些情况可能是由肺炎链球菌引起的。经胸针穿刺术(TNA)培养的灵敏度有限,可通过抗原检测或基因扩增技术加以改善。我们评估了PCR检测和乳胶凝集测试检测em的能力。 TNA从95例中重度CAP患者中获得的肺炎。当将培养技术用作“金标准”时,乳胶凝集和PCR的敏感性分别为52.2和91.3%,特异性为88.7和83.3%,阳性预测值为62.3和65.6%,阴性预测值为83.3和96.5%。 。”当我们以诊断肺炎球菌性肺炎的扩展标准作为计算标准时,乳胶凝集和PCR的敏感性为53.6和89.7%,特异性为93.0和90.0%,阳性预测值为78.9和81.3%,阴性预测值为分别为80.3和94.7%。与乳胶凝集相比,PCR分析提供的其他诊断为12.2%(95%的置信区间从0.4到20.1%的差异)。 PCR比TNA培养更为敏感,特别是在接受过抗生素治疗的患者中(83.3%对33.3%)。尽管PCR是一种非常敏感和特异的技术,但尚未证明在临床实践中具有成本效益。相反,乳胶凝集是一种快速而简单的方法,其结果可能对最初的抗生素治疗产生重大影响。

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