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首页> 外文期刊>Diagnostic microbiology and infectious disease >Community-acquired pneumonia in children due to Mycoplasma pneumoniae: diagnostic performance of a seminested 16S rDNA-PCR.
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Community-acquired pneumonia in children due to Mycoplasma pneumoniae: diagnostic performance of a seminested 16S rDNA-PCR.

机译:儿童肺炎支原体引起的社区获得性肺炎:半巢式16S rDNA-PCR的诊断性能。

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摘要

A 16S rDNA-PCR assay for Mycoplasma pneumoniae applied to nasopharyngeal secretion (NPS) or pharyngeal swab (PS) from children with community-acquired pneumonia (CAP) was prospectively compared to serological tests including complement fixation (CF) test, a mu-capture enzyme immuno assay (EIA) for the detection of specific IgM, and an EIA for the detection of specific IgG. During a 24-months-period diagnosis of active M. pneumoniae infection was established in 32 (12.6%) of 253 patients for whom paired sera were available. In the acute phase, the sensitivities of PCR from NPS and PS, CF test, IgM EIA, and IgG EIA were 90.0%, 79.3%, 46.9%, 78.1%, and 59.4%, respectively. The corresponding specificities were 98.1%, 98.6%, 97.6%, 87.1%, and 72.4%, respectively. Thus, the 16S rDNA-PCR assay provides a highly sensitive and accurate tool for the rapid diagnosis of M. pneumoniae infection in children with CAP.
机译:将16S rDNA-PCR检测的肺炎支原体应用于社区获得性肺炎(CAP)儿童的鼻咽分泌物(NPS)或咽拭子(PS),将其与包括补体固定法(CF),mu-capture在内的血清学检查进行比较酶免疫法(EIA)用于检测特异性IgM,EIA用于检测特异性IgG。在24个月的诊断中,在253例可配对血清的患者中,有32例(12.6%)确诊了活动性肺炎支原体感染。在急性期,来自NPS和PS,CF测试,IgM EIA和IgG EIA的PCR敏感性分别为90.0%,79.3%,46.9%,78.1%和59.4%。相应的特异性分别为98.1%,98.6%,97.6%,87.1%和72.4%。因此,16S rDNA-PCR测定法为快速诊断CAP儿童肺炎支原体感染提供了一种高度灵敏和准确的工具。

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