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首页> 外文期刊>Acta Cytologica: The Journal of Clinical Cytology and Cytopathology >Detection of Chlamydia trachomatis in pregnant women by the Papanicolaou technique, enzyme immunoassay and polymerase chain reaction.
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Detection of Chlamydia trachomatis in pregnant women by the Papanicolaou technique, enzyme immunoassay and polymerase chain reaction.

机译:通过帕潘尼古拉技术,酶免疫法和聚合酶链反应检测孕妇沙眼衣原体。

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摘要

OBJECTIVE: To compare Papanicolaou staining, enzyme immunoassay (EIA) and the polymerase chain reaction (PCR) techniques for detecting Chlamydia trachomatis in pregnant women. STUDY DESIGN: Endocervical specimens were taken randomly from 125 pregnant women with or without symptoms. These women attended their first medical consultation at the Regional General Ignacio Zaragoza Hospital. Samples were analyzed for detection of C trachomatis. When results differed between tests, specimens were evaluated by direct immunofluorescence staining. RESULTS: The prevalence of chlamydial infection was 2.4%. The characteristics of patients positive for Chlamydia were: average age, 24 years; first sexual encounter at age 21 years, one partner and six to nine months of gestation. The sensitivity, specificity, accuracy, positive predictive values and negative predictive values were 100%, 99.18%, 99.20%, 75% and 100%, respectively, for Papanicolaou staining; 100%, 92.62%, 92%, 25% and 100% for EIA; and 100%, 100%, 100% and 100% for PCR. CONCLUSION: Both Papanicolaou staining and PCR were adequate for diagnosis of C trachomatis infection. EIA was not reliable and therefore is not recommended for use as a diagnostic technique in a pregnant population with low risk and low prevalence.
机译:目的:比较帕潘尼古拉染色法,酶联免疫法(EIA)和聚合酶链反应(PCR)技术检测孕妇沙眼衣原体的能力。研究设计:随机抽取125例有症状或无症状的孕妇的宫颈标本。这些妇女在伊格纳西奥萨拉戈萨地区总医院参加了第一次医疗会诊。分析样品以检测沙眼衣原体。当测试之间的结果不同时,通过直接免疫荧光染色评估标本。结果:衣原体感染的发生率为2.4%。衣原体阳性患者的特征是:平均年龄24岁;第一次性交年龄为21岁,一个伴侣,并且怀孕六到九个月。巴氏染色的敏感性,特异性,准确性,阳性预测值和阴性预测值分别为100%,99.18%,99.20%,75%和100%。 EIA为100%,92.62%,92%,25%和100%; PCR分别为100%,100%,100%和100%。结论:Papanicolaou染色和PCR都足以诊断沙眼衣原体感染。 EIA不可靠,因此不建议将其用于低风险和低患病率的孕妇人群中作为诊断技术。

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