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A novel one-step Helicobacter pylori saliva antigen test

机译:一种新型的一步式幽门螺杆菌唾液抗原检测

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Background: A rapid, reliable, and sufficiently accurate test for diagnosing Helicobacter pylori infection is required for screening dyspeptic patients before a referral for endoscopy. The purpose of this article is two-fold: first, to evaluate the accuracy of a one-step H. pylori saliva antigen (HPS) test; and second, to compare noninvasive and invasive H. pylori tests in Taiwanese population. Methods: A total of 104 consecutive dyspeptic patients admitted for gastroenterology into the outpatient department underwent a one-step HPS test, rapid urease test, histology, and 13C-urea breath test 13C-UBT (proto C-13 urea kit). The accuracy of the HPS test was compared with a gold standard defined by at least two positive H. pylori test results from three H. pylori tests (histology, rapid urease test, and 13C-UBT). Results: The 104 patients eligible for analysis (mean age: 58 years, range 22-87 years), 21 (20%) were gold standard positive. Among them, the positive of the one-step H. pylori saliva Ag test, rapid urease test, 13C-UBT, histology were (52; 50%), (17; 16%), (27; 25%) and (22; 21%) respectively. The sensitivity and specificity of the HPS tests, rapid urease test, 13C-UBTs, and histology were 71.43% and 55.42%, 76.19% and 98.80%, 100% and 92.77%, and 85.71% and 95.18%, respectively, relative to the gold standard. The one-step HPS test exhibited a sensitivity of 71.43%, nearly equivalent to that of the rapid urea test. Conclusion: The one-step HPS test exhibited a high sensitivity and low specificity compared with the other tests, indicating that it is not sufficiently accurate for use in a clinical setting for diagnosing H. pylori infection. However, the test is simple to use (requiring only a saliva sample), inexpensive, and noninvasive in its application, and thus appealing for use in population-based prevalence surveys of the epidemiology of H. pylori infection.
机译:背景:在转诊接受内窥镜检查之前,筛查消化不良患者需要快速,可靠且足够准确的诊断幽门螺杆菌感染的测试。本文的目的有两个方面:首先,评估一步一步幽门螺杆菌唾液抗原(HPS)测试的准确性;其次,比较台湾人群的非侵入性和侵入性幽门螺杆菌检测。方法:总共104例入院门诊的消化系统消化不良患者接受了一步一步HPS测试,快速尿素酶测试,组织学检查和13C-尿素呼气测试13C-UBT(C-13型原尿素试剂盒)。将HPS检测的准确性与由三个幽门螺杆菌检测(组织学,快速尿素酶检测和13C-UBT)中至少两个阳性幽门螺杆菌检测结果定义的金标准进行比较。结果:104例符合分析标准的患者(平均年龄:58岁,范围22-87岁),其中21例(20%)为金标准阳性。其中,一步法幽门螺杆菌唾液Ag试验,快速尿素酶试验,13C-UBT,组织学的阳性结果分别为(52; 50%),(17; 16%),(27; 25%)和(22) ; 21%)。 HPS检测,快速尿素酶检测,13C-UBT和组织学检测的敏感性和特异性分别为71.43%和55.42%,76.19%和98.80%,100%和92.77%,85.71%和95.18%。黄金标准。一步式HPS测试的灵敏度为71.43%,几乎与快速尿素测试的灵敏度相当。结论:一步式HPS检测与其他检测相比具有较高的敏感性和低特异性,这表明其在临床上诊断幽门螺杆菌感染的准确性不够。但是,该测试方法易于使用(仅需要唾液样本),价格低廉且在应用中无创,因此很适合用于幽门螺杆菌感染流行病学的基于人群的流行调查。

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