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Comparison of two different stool antigen tests for the primary diagnosis of Helicobacter pylori infection in Turkish patients with dyspepsia

机译:比较两种不同粪便抗原测试对土耳其消化不良患者幽门螺杆菌感染的初步诊断

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Aim. To assess the reliability of two different enzyme immunoassays in detecting the Helicobacter pylori status in stool specimens of Turkish patients with dyspepsia.Materials and methods. One hundred and fifty-one patients [74 with nonulcer dyspepsia (NUD), 64 with duodenal ulcer (DU) and 13 with gastric cancer] who were admitted to the endoscopy unit of Istanbul University, Cerrahpasa Medical Faculty for upper gastrointestinal endoscopy because of dyspepsia were enrolled in the study. Helicobacter pylori infection was confirmed in all patients by histology, rapid urease test and culture. A patient was classified as being H. pylori-positive if the culture alone or both the histology and the rapid urease test were positive and as negative only if all of these tests remained negative. Stool samples were obtained from patients to assess the reliability of a monoclonal (FemtoLab H. pylori) and a polyclonal (Premier Platinum HpSA) stool antigen test and to compare the diagnostic accuracies of these two tests. A chi(2) test was used for statistical comparisons.Results. Using cut-off values of 0.19 for FemtoLab H. pylori and 0.16 for Premier Platinum HpSA, the sensitivity, specificity, positive predictive value, negative predictive value and diagnostic accuracy were 93%, 90%, 98%, 68% and 93% for the monoclonal test and 84%, 67%, 94%, 40% and 81% for the polyclonal test, respectively. The sensitivity, specificity, negative predictive value and diagnostic accuracy of the monoclonal test were significantly greater than those of the polyclonal test (chi(2) = 3.98; p < .05 for sensitivity and chi(2) = 15.67; p = .000 for specificity, chi(2) = 15.78; p = .000 for negative predictive value and chi(2) = 6.37; p = .012 for diagnostic accuracy). The bacterial load did not affect the sensitivity of either test.Conclusions. The monoclonal FemtoLab H pylori test, using a cut-off 0.19, is a very sensitive, specific and easy to perform diagnostic tool for the primary diagnosis of H. pylori infection in Turkish patients with dyspepsia.
机译:目标。为了评估两种不同的酶免疫法检测土耳其消化不良患者粪便样本中幽门螺杆菌状态的可靠性。材料和方法。 151名患者因消化不良而被上伊斯坦布尔胃肠大学内窥镜内镜科住院,其中[非溃疡性消化不良(NUD)74例,十二指肠溃疡(DU)64例,胃癌13例)被纳入研究。通过组织学,快速尿素酶测试和培养证实了所有患者中的幽门螺杆菌感染。如果单独的培养物或组织学和快速尿素酶测试均为阳性,则将患者分类为幽门螺杆菌阳性;仅当所有这些测试均保持阴性时,才将患者分类为阴性。从患者获得粪便样品,以评估单克隆(FemtoLab H. pylori)和多克隆(Premier Platinum HpSA)粪便抗原测试的可靠性,并比较这两种测试的诊断准确性。使用chi(2)检验进行统计比较。使用FemtoLab H. pylori的截断值0.19和Premier Platinum HpSA的截断值0.16,对于FemtoLab幽门螺杆菌HpSA的截断值为0.16,对于PemoriLab幽门螺杆菌HpSA的截断值为0.16,单克隆测试分别为84%,67%,94%,40%和81%。单克隆测试的灵敏度,特异性,阴性预测值和诊断准确性显着高于多克隆测试(chi(2)= 3.98; p <.05灵敏度和chi(2)= 15.67; p = .000对于特异性,chi(2)= 15.78;对于阴性预测值,p = .000;对于诊断准确性,chi(2)= 6.37; p = .012)。细菌载量不影响任何一项测试的敏感性。 FemtoLab幽门螺杆菌单克隆抗体检测的临界值为0.19,是一种非常灵敏,特异且易于执行的诊断工具,可用于对土耳其消化不良患者进行幽门螺杆菌感染的初步诊断。

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