新一代超快速脲酶检测幽门螺杆菌感染的准确性和可行性评价

IF 0.9 Q4 GASTROENTEROLOGY & HEPATOLOGY
Marco Cagnoni, C. Pagnini, M. Crovaro, A. Aucello, R. Urgesi, L. Pallotta, G. Fanello, M. D. Di Paolo, M. Graziani
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引用次数: 1

摘要

幽门螺杆菌(Hp)感染可通过侵入性和非侵入性方法诊断,其中快速脲酶试验(RUTs)是一种重要的选择。结果的准确性和快速性是RUTs的基础。本研究的目的是前瞻性评估新一代超快速脲酶试验(iNatal duo试验)检测Hp的敏感性、特异性和阳性时间,并将结果与其他可用的RUTs [CLO试验(弯曲杆菌样生物试验)、CP试验(幽门螺旋弯曲杆菌试验)和Pronto Dry试验]进行比较。连续接受上胃镜检查的患者进行胃活检:胃窦2个,体内2个用于组织学检查,胃窦各1个,体内1个。在活检组织插入试剂后1、5、15、30和60分钟、3小时和24小时读取RUTs。组织学被认为是“金标准”。在未服用质子泵抑制剂(PPI)的患者(n = 924)中,通过计算敏感性、特异性和阳性和阴性预测值来评估这些试验的性能。计算各RUT和组织学的一致性率(κ)并进行比较。在服用PPI的患者亚组(n = 198)中也测试了atal duo测试的表现。未服用PPIs的924例患者中有225例(24.3%)Hp阳性,服用PPIs的198例患者中有56例(28.3%)Hp阳性。在每个时间点,新生儿二联试验对Hp的检测均较其他rut灵敏。未服用PPIs的患者5分钟的敏感性为96.2%,服用PPIs的患者为92.2%。在iNatal duo试验中,κ与组织学的关系高于其他RUT (30 min时:iNatal duo 0.99, CLO 0.60, CP 0.78, Pronto 0.85, 15 min时:iNatal duo 0.99, CLO 0.46, CP 0.63, Pronto 0.71)。在一项前瞻性研究中,在接受和未接受PPI治疗的患者中,iNatal duo试验都显示出Hp检测的准确性和快速性。这种新一代的超快速脲酶试验可用于快速、正确地处理疑似Hp感染的上消化道内镜患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of Accuracy and Feasibility of a New-Generation Ultra-Rapid Urease Test for Detection of Helicobacter pylori Infection
Helicobacter pylori (Hp) infection can be diagnosed by invasive and noninvasive methods, and, among the former, Rapid Urease Tests (RUTs) are an important option. Accuracy and rapidity of results are fundamental for RUTs. The aim of the study is to prospectively evaluate the sensitivity, specificity and time to positivity of a new-generation ultra-rapid urease test (iNatal duo test) for Hp detection and compare the results with other available RUTs [CLO Test (Campylobacter-Like Organism Test), CP Test (Campylobacter pylori Test) and Pronto Dry]. Gastric biopsies were taken in consecutive patients undergoing upper endoscopy: two in the antrum and two in the body for histology, and one in the antrum and one in the body for each RUT. RUTs were read at 1, 5, 15, 30 and 60 min, 3 h and 24 h after biopsy insertion into the reagent. Histology was considered as “gold standard”. The performance of the tests was evaluated in patients not taking proton pump inhibitors (PPI) (n = 924) by calculation of sensitivity, specificity and positive and negative predictive value. Agreement rate (κ) for every RUT and histology was calculated and compared. The performance of the iNatal duo test was also tested in a subgroup of patients taking PPI (n = 198). Hp was positive in 225/924 patients (24.3%) not taking PPIs and in 56/198 (28.3%) who were taking PPIs. The iNatal duo test was more sensitive than the other RUTs for detecting Hp at every time point. The sensitivity at 5 min was 96.2% in patients not taking PPIs and 92.2% in patients taking PPIs. κ with histology was higher for the iNatal duo test than any other RUT (at 30 min: iNatal duo 0.99, CLO 0.60, CP 0.78, Pronto 0.85, at 15 min: iNatal duo 0.99, CLO 0.46, CP 0.63, Pronto 0.71). In a prospective study, the iNatal duo test demonstrated high accuracy and rapidity for Hp detection, both in patients with and without PPI therapy. This new generation of ultra-rapid urease test could be useful for the rapid and correct management of patients undergoing upper GI endoscopy for suspected Hp infection.
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