首页> 外文期刊>The American Journal of Tropical Medicine and Hygiene >Short report: A prospective evaluation of real-time PCR assays for the detection of Orientia tsutsugamushi and Rickettsia spp. for early diagnosis of rickettsial infections during the acute phase of undifferentiated febrile illness
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Short report: A prospective evaluation of real-time PCR assays for the detection of Orientia tsutsugamushi and Rickettsia spp. for early diagnosis of rickettsial infections during the acute phase of undifferentiated febrile illness

机译:简短报告:前瞻性评估实时荧光定量PCR检测东方虫和立克次体的方法。在未分化的高热疾病急性期早期诊断infection病感染

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摘要

One hundred and eighty febrile patients were analyzed in a prospective evaluation of Orientia tsutsugamushi and Rickettsia spp. real-time polymerase chain reaction (PCR) assays for early diagnosis of rickettsial infections. By paired serology, 3.9% (7 of 180) and 6.1% (11 of 180) of patients were confirmed to have acute scrub or murine typhus, respectively. The PCR assays for the detection of O. tsutsugamushi and Rickettsia spp. had high specificity (99.4% [95% confidence interval (CI): 96.8-100] and 100%[95%CI: 97.8-100], respectively). The PCR results were also compared with immunoglobulinM(IgM) immunofluorescence assay (IFA) on acute sera. For O. tsutsugamushi, PCR sensitivity was twice that of acute specimen IgM IFA (28.6% versus 14.3%; McNemar's P = 0.3). For Rickettsia spp., PCR was four times as sensitive as acute specimen IgM IFA (36.4% versus 9.1%; P = 0.08), although this was not statistically significant. Whole blood and buffy coat, but not serum, were acceptable specimens for these PCRs. Further evaluation of these assays in a larger prospective study is warranted.
机译:在对Or虫东方虫和立克次体属的前瞻性评估中分析了180位发热患者。实时聚合酶链反应(PCR)测定法可用于diagnosis病的早期诊断。通过配对血清学,分别确认有3.9%(180名中的7名)和6.1%(180名中的11名)患者患有急性灌木或鼠伤寒。用于检测虫和立克次体的PCR方法。具有高特异性(分别为99.4%[95%置信区间(CI):96.8-100]和100%[95%CI:97.8-100])。 PCR结果也与免疫球蛋白M(IgM)免疫荧光测定(IFA)在急性血清中进行了比较。对于O虫曲霉,PCR敏感性是急性标本IgM IFA的两倍(28.6%对14.3%; McNemar's P = 0.3)。对于立克次体来说,PCR的敏感性是急性标本IgM IFA的四倍(36.4%对9.1%; P = 0.08),尽管这在统计学上不显着。这些PCR可以接受全血和血沉棕黄层,但不能接受血清。有必要在较大的前瞻性研究中进一步评估这些测定。

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