Digestive Endoscopy Unit, Catholic University, Rome, Italy.
Clin Gastroenterol Hepatol. 2010 Jun;8(6):516-22. doi: 10.1016/j.cgh.2010.02.018. Epub 2010 Mar 6.
BACKGROUND & AIMS: Colon capsule endoscopy (CCE) is a noninvasive and painless technique used to explore the colon without sedation or air insufflation. We performed a systematic review and meta-analysis to assess the accuracy of CCE in detecting colorectal polyps. METHODS: The MEDLINE, EMBASE, and SCOPUS databases were searched, from 2006 to 2009, for the terms "colon capsule" and "Pillcam colon"; searches included abstracts. Studies were included that focused on detecting colorectal polyps with CCE and that were verified using within-subject reference colonoscopy. The risk of bias within each study was ascertained according to Quality Assessment of Diagnostic Accuracy in Systematic Reviews recommendations. The per-patient sensitivity and specificity were calculated for polyps of any size and for significant findings (polyps, > or =6 mm in size or >3 in number). Forest plots were produced based on random-effect models. The risk of bias across studies was assessed using the interstudy heterogeneity statistic, meta-regression, and the Egger test. RESULTS: Eight studies provided data on 837 patients; the prevalences of polyps and significant findings were 57% and 27.4%, respectively. CCE sensitivity for polyps of any size and significant findings were 71% and 68%, respectively. CCE specificity for polyps of any size and significant findings were 75% and 82%, respectively. High levels of heterogeneity (interstudy heterogeneity, >75%) were not detected. Moderate heterogeneity partially was explained by the different design of individual studies. CCE identified 16 of the 21 cancerous lesions detected by colonoscopy (pooled sensitivity, 76%). CONCLUSIONS: CCE sensitivity for polyps and significant findings compares favorably with other noninvasive colorectal cancer screening strategies. CCE specificity is likely to be underestimated because reference colonoscopy examination results are blinded.
背景与目的:结肠胶囊内镜(CCE)是一种非侵入性、无痛的技术,无需镇静或注气即可探查结肠。我们进行了一项系统评价和荟萃分析,以评估 CCE 检测结直肠息肉的准确性。
方法:从 2006 年至 2009 年,我们在 MEDLINE、EMBASE 和 SCOPUS 数据库中使用“colon capsule”和“Pillcam colon”这两个术语进行了检索,并对摘要进行了搜索。我们纳入了专注于使用 CCE 检测结直肠息肉的研究,且这些研究使用了受试者内参考结肠镜检查进行了验证。根据系统评价中诊断准确性质量评估的建议,确定了每项研究的偏倚风险。计算了任意大小的息肉和有意义发现(息肉,>或=6mm 或>3 个)的每位患者的敏感性和特异性。根据随机效应模型生成了森林图。使用跨研究异质性统计量、meta 回归和 Egger 检验评估了研究间的偏倚风险。
结果:8 项研究共纳入 837 例患者的数据;息肉和有意义发现的患病率分别为 57%和 27.4%。CCE 对任意大小的息肉和有意义发现的敏感性分别为 71%和 68%。CCE 对任意大小的息肉和有意义发现的特异性分别为 75%和 82%。未检测到高度异质性(异质性>75%)。部分异质性是由个别研究设计的不同引起的。CCE 发现了结肠镜检查发现的 21 个癌性病变中的 16 个(汇总敏感性为 76%)。
结论:CCE 检测息肉和有意义发现的敏感性优于其他非侵入性结直肠癌筛查策略。CCE 特异性可能被低估,因为参考结肠镜检查结果是盲法的。
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