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首页> 外文期刊>European journal of gastroenterology and hepatology >Evaluation of a new biopsy urease test: Pronto Dry, for the diagnosis of Helicobacter pylori infection.
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Evaluation of a new biopsy urease test: Pronto Dry, for the diagnosis of Helicobacter pylori infection.

机译:新的活检尿素酶测试的评估:Pronto Dry,用于诊断幽门螺杆菌感染。

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摘要

BACKGROUND: The gastric biopsy urease test is the most frequently used test for the diagnosis of Helicobacter pylori infection in routine gastrointestinal endoscopy practice. In Malaysia up to recently, only one commercial biopsy urease test was available: the CLO test (Ballard Medical Products, Draper, Utah, USA). Large endoscopy units use their own 'homemade' unbuffered ultra rapid urease test for diagnosis of H. pylori infection. OBJECTIVE: To compare the accuracy and reaction time of a new biopsy urease test, Pronto Dry (Medical Instruments Corporation, Solothurn, Switzerland) and the CLO test in the diagnosis of H. pylori infection. METHODS: Consecutive patients presenting with dyspepsia to the endoscopy unit, University of Malaya Medical Centre were recruited for the study. Patients who were previously treated for H. pylori infection or who had received antibiotics, proton pump inhibitors or bismuth compounds in the preceding 4 weeks were excluded. H. pylori diagnosis was made based on the ultra rapid urease test and histological examination of gastric biopsies. Four antral and four corpus biopsies were taken for this purpose from all patients. A diagnosis of H. pylori infection was made when both the ultra rapid urease test and histology were positive in either the antral or corpus biopsies. A negative diagnosis of H. pylori was made when both tests from antral and corpus biopsies were all negative. Another four antral and four corpus biopsies (two each) were taken for the Pronto Dry and CLO tests. The Pronto Dry and CLO tests were stored and performed according to the manufacturer's instruction. RESULTS: Two hundred and eight patients were recruited in the study. Eighty-six of the patients were males and 122 were females. The mean age was 46.3 years with a range of 15-82 years. The results for both the Pronto Dry and the CLO tests were completely concordant with sensitivity, specificity, positive predictive value, negative predictive value and diagnostic accuracy of 98.1%, 100%, 100%, 98.1% and 99%, respectively. The Pronto Dry test showed a faster reaction time to positive compared with the CLO test, with 96.2% positive reaction by 30 min versus 70.8% and 100% positive reaction time by 55 min versus 83%. The colorimetric change was also more distinct with the Pronto Dry test compared with the CLO test. CONCLUSIONS: Both the Pronto Dry and the CLO tests were highly accurate for the diagnosis of H. pylori infection. The Pronto Dry test showed a quicker positive reaction time and the positive colour change was more distinct.
机译:背景:胃活检尿素酶测试是常规胃肠道内窥镜检查实践中最常用于诊断幽门螺杆菌感染的测试。在马来西亚,直到最近,只有一种商业活检尿素酶测试可用:CLO测试(Ballard Medical Products,Draper,美国犹他州)。大型内窥镜检查单位使用自己的“自制”无缓冲超快速尿素酶检测方法来诊断幽门螺杆菌感染。目的:为了比较新型活检尿素酶测试,Pronto Dry(瑞士索洛图恩市医疗器械公司)和CLO测试在幽门螺杆菌感染诊断中的准确性和反应时间。方法:招募到马来亚大学医学中心内镜科就诊的消化不良的连续患者进行研究。排除先前接受过幽门螺杆菌感染治疗或在前4周内接受过抗生素,质子泵抑制剂或铋化合物的患者。幽门螺杆菌的诊断是基于超快速尿素酶试验和胃活检组织学检查。为此目的,对所有患者进行了四次肛门窦活检和四次尸体活检。当肛门或活体活检中超快速脲酶试验和组织学均呈阳性时,可诊断为幽门螺杆菌感染。当来自肛门活检和尸体活检的检查均为阴性时,幽门螺杆菌诊断为阴性。另外进行了四次肛门窦和四次活体活检(每次两次)以进行Pronto Dry和CLO测试。按照制造商的说明存储和执行Pronto Dry和CLO测试。结果:该研究招募了208名患者。患者中有86例是男性,而122例是女性。平均年龄为46.3岁,范围为15-82岁。 Pronto Dry和CLO测试的结果分别与敏感性,特异性,阳性预测值,阴性预测值和诊断准确度完全一致,分别为98.1%,100%,100%,98.1%和99%。与CLO测试相比,Pronto Dry测试显示出更快的阳性反应时间,到30分钟时阳性反应为96.2%,而到70.8%时为100%,到55分钟时阳性反应时间为83%,而到100%则为100%。与CLO测试相比,Pronto Dry测试的色度变化也更为明显。结论:Pronto Dry和CLO测试对于幽门螺杆菌感染的诊断均非常准确。 Pronto Dry测试表明阳性反应时间更快,并且阳性颜色变化更明显。

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