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首页> 外文期刊>The British Journal of Surgery >Systematic review of the impact of registration and screening on colorectal cancer incidence and mortality in familial adenomatous polyposis and Lynch syndrome
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Systematic review of the impact of registration and screening on colorectal cancer incidence and mortality in familial adenomatous polyposis and Lynch syndrome

机译:系统地审查登记和筛查对家族性腺瘤性息肉病和林奇综合征的结直肠癌发病率和死亡率的影响

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Background The British Society of Gastroenterology recommends that all familial adenomatous polyposis (FAP) and Lynch syndrome (LS) families are screened in the context of a registry. This systematic review was performed to appraise the published evidence for registration and screening in relation to colorectal cancer (CRC) incidence and mortality. Methods Five electronic databases were searched using a combination of medical subject heading terms and free-text keywords. Titles and abstracts were scrutinized by two independent reviewers. Inclusion criteria were English-language studies describing CRC incidence and/or mortality in patients with FAP or LS, with comparison of either: screened and unscreened patients, or time periods before and after establishment of the registry. Results Of 4668 abstracts identified, 185 full-text articles were selected; 43 studies fulfilled the inclusion criteria. No randomized clinical trial evidence was identified. For FAP, 33 of 33 studies described a significant reduction of CRC incidence and mortality with registration and screening. For LS, nine of ten studies described a reduction of CRC incidence and mortality with registration and screening. Five studies (FAP, 2; LS, 3) provided evidence for complete prevention of CRC-related deaths during surveillance. Clinical and statistical heterogeneity prevented pooling of data for meta-analysis. Conclusion Studies consistently report that registration and screening result in a reduction of CRC incidence and mortality in patients with FAP and LS (level 2a evidence, grade B recommendation). Funding and managerial support for hereditary CRC registries should be made available. Presented to the Association of Surgeons of Great Britain and Ireland 2013 Congress, Glasgow, UK, May 2013, and to the Annual Meeting of the Association of Coloproctology of Great Britain and Ireland, Liverpool, UK, July 2013; published in abstract form as Br J Surg 2013; 100(Suppl 7): 123-124 and as Colorectal Dis 2013; 15(Suppl 1): 4 Registration and screening of benefit
机译:背景英国胃肠病学会建议对所有家族性腺瘤性息肉病(FAP)和林奇综合征(LS)家庭进行筛查。进行了这项系统的评估,以评估已发表的有关结直肠癌(CRC)发病率和死亡率的注册和筛查证据。方法使用医学主题词和自由文本关键字的组合来检索五个电子数据库。标题和摘要由两名独立的审阅者进行审查。入选标准为描述FAP或LS患者的CRC发生率和/或死亡率的英语研究,并比较以下因素:筛查和未筛查患者,或建立登记之前和之后的时间段。结果共检索到4668篇摘要,选择全文文章185篇; 43项研究符合纳入标准。没有发现随机临床试验证据。对于FAP,33项研究中的33项描述了通过注册和筛查可显着降低CRC发生率和死亡率。对于LS,十项研究中的九项描述了通过注册和筛查可降低CRC发生率和死亡率。五项研究(FAP,2; LS,3)为完全预防监视期间CRC相关死亡提供了证据。临床和统计异质性阻止了汇总分析的数据。结论研究一致报告称,注册和筛查可降低FAP和LS患者的CRC发生率和死亡率(2a级证据,B级推荐)。应该为遗传性CRC登记处提供资金和管理支持。于2013年5月在英国格拉斯哥举行的2013年大不列颠及爱尔兰外科医生协会大会上发表,并于2013年7月在英国利物浦的大不列颠及爱尔兰结肠直肠病协会年会上作了介绍;以Br J Surg 2013的抽象形式出版; 100(增刊7):123-124,如结肠直肠疾病2013年; 15(Suppl 1):4利益的登记和筛选

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