Gisbert Javier P, de la Morena Felipe, Abraira Víctor
Department of Gastroenterology, "La Princesa" University Hospital, Universidad Autónoma, Madrid, Spain.
Am J Gastroenterol. 2006 Aug;101(8):1921-30. doi: 10.1111/j.1572-0241.2006.00668.x. Epub 2006 Jun 16.
To perform a systematic review and a meta-analysis of accuracy of monoclonal stool antigen test (SAT) for the diagnosis of Helicobacter pylori infection.
assessing the accuracy of monoclonal SAT for the diagnosis of H. pylori infection.
electronic and manual bibliographical searches.
independently done by two reviewers.
meta-analyses combining the sensitivities, specificities, and likelihood ratios (LRs) of the individual studies.
Twenty-two studies, including 2,499 patients, evaluated the monoclonal SAT before eradication therapy. Pooled sensitivity, specificity, LR+, and LR- were: 0.94 (95% CI 0.93-0.95), 0.97 (0.96-0.98), 24 (15-41), and 0.07 (0.04-0.12). The accuracy of both monoclonal and polyclonal SAT was evaluated together in 13 pretreatment studies, and higher pooled sensitivity was demonstrated with the monoclonal technique (0.95 vs 0.83). Twelve studies, including 957 patients, assessed the monoclonal SAT to confirm eradication after therapy. Pooled sensitivity, specificity, LR+, and LR- were 0.93 (0.89-0.96), 0.96 (0.94-0.97), 17 (12-23), and 0.1 (0.07-0.15). Both tests were evaluated together in eight post-treatment studies and, again, the monoclonal technique showed higher sensitivity (0.91 vs 0.76). Heterogeneity among studies disappeared when a single outlier study was excluded. Subanalysis depending on the reference method, the study population, or the study quality showed similar results.
Monoclonal SAT is an accurate noninvasive method both for the initial diagnosis of H. pylori infection and for the confirmation of its eradication after treatment. The monoclonal technique has higher sensitivity than the polyclonal one, especially in the post-treatment setting.
对单克隆粪便抗原检测(SAT)诊断幽门螺杆菌感染的准确性进行系统评价和荟萃分析。
评估单克隆SAT诊断幽门螺杆菌感染的准确性。
电子和手工文献检索。
由两名评价者独立完成。
对各研究的敏感性、特异性和似然比(LR)进行荟萃分析。
22项研究(包括2499例患者)在根除治疗前对单克隆SAT进行了评估。合并敏感性、特异性、阳性似然比和阴性似然比分别为:0.94(95%CI 0.93 - 0.95)、0.97(0.96 - 0.98)、24(15 - 41)和0.07(0.04 - 0.12)。13项治疗前研究同时评估了单克隆和多克隆SAT的准确性,单克隆技术显示出更高的合并敏感性(0.95对0.83)。12项研究(包括957例患者)在治疗后评估单克隆SAT以确认根除情况。合并敏感性、特异性、阳性似然比和阴性似然比分别为0.93(0.89 - 0.96)、0.96(0.94 - 0.97)、17(12 - 23)和0.1(0.07 - 0.15)。8项治疗后研究同时评估了两种检测方法,单克隆技术再次显示出更高的敏感性(0.91对0.76)。排除一项异常值研究后,各研究间的异质性消失。根据参考方法、研究人群或研究质量进行的亚组分析显示了相似的结果。
单克隆SAT是一种准确的非侵入性方法,可用于幽门螺杆菌感染的初始诊断及其治疗后根除情况的确认。单克隆技术比多克隆技术具有更高的敏感性,尤其是在治疗后情况下。