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首页> 外文期刊>Journal of Clinical Microbiology >Direct detection of group B streptococci from vaginal specimens compared with quantitative culture.
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Direct detection of group B streptococci from vaginal specimens compared with quantitative culture.

机译:与定量培养相比,直接从阴道标本中直接检测出B组链球菌。

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Determination of prenatal vaginal carriage of group B streptococci (GBS) is important in the management of newborns. A pronase extraction-latex particle agglutination method (Streptex; Wellcome Diagnostics, Dartford, England) was used to rapidly detect GBS species-specific antigen directly from vaginal specimens. It was compared with quantitative and broth enrichment cultures. A total of 434 vaginal swab specimens were obtained before delivery. GBS cultures were positive for 14.7% of the specimens (64 of 434). Colony counts ranged from 2 to greater than 10(6) CFU per swab. The sensitivities of the direct antigen analysis were 19% (12 of 64) for all cultures and 63% (12 of 19) for specimens heavily colonized with GBS (greater than 10(4) CFU per swab). The specificity of the antigen test was 99.7%, with only one false-positive. There were three false-negative tests with colony counts of greater than 10(6) CFU per swab. The predictive values were 92% for a positive antigen test and 88% for a negative antigen test. The direct immunochemical detection of GBS antigen can be useful in a population of heavily colonized women. Direct latex particle agglutination does not appear to be salutary for a lightly colonized population and does not appear to be able to replace either culture or antigen detection after growth amplification at this time.
机译:B组链球菌(GBS)的产前阴道运输的确定对新生儿的治疗很重要。链酶提取乳胶颗粒凝集法(Streptex; Wellcome Diagnostics,达特福德,英格兰)用于直接从阴道标本中快速检测GBS物种特异性抗原。将其与定量和肉汤富集培养进行了比较。分娩前共采集了434个阴道拭子标本。 GBS培养阳性的样本占14.7%(434个中的64个)。每个拭子的菌落计数范围从2到大于10(6)CFU。对于所有培养物,直接抗原分析的灵敏度分别为19%(64中的12)和63%(19中的12),对于大量定居于GBS的标本(每支拭子大于10(4)CFU)。抗原测试的特异性为99.7%,只有一个假阳性。有3个假阴性测试,每个拭子的菌落计数大于10(6)CFU。阳性抗原测试的预测值为92%,阴性抗原测试的预测值为88%。 GBS抗原的直接免疫化学检测可用于大量定植的女性人群。对于轻度定居的种群,直接乳胶颗粒凝集似乎并不有益,并且在此时生长扩增后似乎无法取代培养物或抗原检测。

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