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首页> 外文期刊>Annals of Clinical Microbiology and Antimicrobials >Performance evaluation of a rapid whole-blood immunoassay for the detection of IgG antibodies against Helicobacter pylori in daily clinical practice
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Performance evaluation of a rapid whole-blood immunoassay for the detection of IgG antibodies against Helicobacter pylori in daily clinical practice

机译:在日常临床实践中快速全血免疫测定法检测幽门螺杆菌IgG抗体的性能评估

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Background A growing number of rapid Helicobacter pylori antibody tests are commercially available now, however, some of these tests are often used without sufficient evaluation. The aim of this study was to evaluate the performance of a commercially available rapid whole-blood immunoassay (gabControl? H. pylori ; gabmed GmbH, K?ln, Germany), for the qualitative detection of IgG antibodies against H. pylori with the 13C-urea breath test (13C-UBT) serving as a reference method. Methods A total of 108 consecutive outpatients, who were referred for 13C-UBT by general practitioners and specialists, were also tested for H. pylori infection by the gabControl? H. pylori immunoassay. The clinical performance of this rapid whole-blood test was evaluated by determining the sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) compared to the 13C-UBT. The agreement between the two tests was calculated using Cohen’s Kappa (κ) with 95?% confidence intervals (CI). Results The agreement between the gabControl? H. pylori assay and the 13C-UBT was 0.62 [95?% confidence intervals (CIs) 0.47–0.76; P?13C-UBT serving as the non-invasive gold standard method of H. pylori diagnosis, the gabControl? H. pylori assay demonstrated a sensitivity and specificity of 91.4 and 76.7?%, respectively, with a PPV of 65.3?% and a NPV of 94.9?%. Seventeen (15.7?%) individuals with a positive H. pylori anamnesis showed a negative 13C-UBT and were typed positive by the gabControl? H. pylori assay. Of these, 13 (76.5?%) and 3 individuals (17.6?%) had completed one and two eradication therapies, respectively. Conclusions The gabControl? H. pylori immunoassay is a rapid and easy to use first line screening tool for H. pylori IgG antibody detection in daily clinical practice. However, this assay should not be used for confirmation of the successful H. pylori eradication after antibiotic treatment.
机译:背景技术现在有越来越多的快速幽门螺杆菌抗体检测方法可商购,但是,其中一些检测方法经常在没有充分评估的情况下使用。这项研究的目的是评估用于定量检测IgG抗体的市售快速全血免疫测定法(gabControl ? H. pylori; gabmed GmbH,K?ln,Germany)的性能。以 13 C-尿素呼气试验( 13 C-UBT)针对幽门螺杆菌。方法由gabControl ? H对总共108名由全科医生和专科医生转诊 13 C-UBT的门诊患者进行了幽门螺杆菌感染的检测。幽门螺杆菌免疫测定。通过确定与 13 C-UBT相比的敏感性,特异性,阳性预测值(PPV)和阴性预测值(NPV)来评估该快速全血试验的临床表现。两次测试之间的一致性是使用Cohen的Kappa(κ)和95%的置信区间(CI)计算的。结果gabControl ?幽门螺杆菌测定与 13 C-UBT之间的一致性为0.62 [95%置信区间(CI)0.47-0.76; P?13 C-UBT作为幽门螺杆菌诊断的非侵入性金标准方法,gabControl ?幽门螺杆菌检测的敏感性和特异性分别为91.4和76.7%。 PPV为65.3%,NPV为94.9%。幽门螺杆菌阳性的17名(15.7%)个体显示 13 C-UBT阴性,并通过gabControl ?幽门螺杆菌检测呈阳性。其中,分别有13(76.5%)和3(17.6%)个人完成了一种和两种根除疗法。结论gabControl ?幽门螺杆菌免疫测定法是在日常临床实践中用于幽门螺杆菌IgG抗体检测的快速且易于使用的一线筛选工具。但是,该方法不应用于确认抗生素治疗后成功根除幽门螺杆菌。

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