A141 在检测到近端增生性息肉、腺瘤及其合并症后,发生全部晚期肿瘤的风险

W. Safih, D. von Renteln, I. Popescu Crainic, C. Haumesser, B. Noyon, F. Mubaid, C. Rekkabi, P. Marques, Y Li, R. Djinbachian
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The primary outcome was the presence of T-MAN (comprising advanced adenomas or high-risk SL) during the follow-up colonoscopy depending on the presence of proximal HP, adenoma, or their combination at index colonoscopy. Secondary outcomes included assessing the risk of T-MAN at follow-up depending on index findings characteristics. Results 2014 patients were screened and 764 were included in the final analysis (44.1% male vs 55.9% female; mean age, 63y; median follow-up, 3.46 years). Patients with both proximal hyperplastic polyps and colonic adenomas during their initial colonoscopy had a significantly higher risk of developing T-MAN than patients with a combination of adenomas and distal HP or with only adenomas at index colonoscopy (30.5% vs 19%) [Hazard-ratio (HR)=1.95 (95% confidence interval (CI)1.3-2.9)]. A combination of proximal hyperplastic polyps and colonic adenomas is associated with a higher risk of T-MAN during follow-up than proximal HP alone (30.5% vs 13.9%) [HR=3.4 (95% CI 1.3-8.7)]. No statistically significant evidence was found to identify an increased risk of developing T-MAN at follow-up in patients presenting adenomas alone vs those with only proximal HP (19.1% vs 13.9%) [HR=1.9 (95% CI 0.75-4.7)]. Conclusions Patients with proximal hyperplastic polyps have an increased risk of presenting a T-MAN at the follow-up colonoscopy. Presenting a combination of hyperplastic polyps and adenomas indicates a higher risk of developing T-MAN than presenting an HP or adenoma alone. Funding Agencies Daniel von Renteln is supported by a \"Fonds de Recherche du Québec Santé\" career development award. He has also received research funding from ERBE Elektromedizin GmbH, Ventage, Pendopharm, Fujifilm and Pentax, and has received consultant or speaker fees from Boston Scientific Inc., ERBE Elektromedizin GmbH, and Pendopharm. Roupen Djinbachian is supported by a “Fonds de Recherche du Québec Santé/Ministère de la Santé et des Services Sociaux” clinical research award. The remaining authors declare that they have no conflict of interest.","PeriodicalId":508018,"journal":{"name":"Journal of the Canadian Association of Gastroenterology","volume":"126 ","pages":"108 - 109"},"PeriodicalIF":0.0000,"publicationDate":"2024-02-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A141 RISK OF TOTAL METACHRONOUS ADVANCED NEOPLASIA AFTER DETECTION OF PROXIMAL HYPERPLASTIC POLYPS, ADENOMAS, AND THEIR COMBINATION\",\"authors\":\"W. Safih, D. von Renteln, I. Popescu Crainic, C. Haumesser, B. Noyon, F. 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引用次数: 0

摘要

摘要 背景 最近的研究发现,近端无柄锯齿状病变(SSL)与晚期间变性肿瘤的风险增加有关,而远端 SSL 没有明显影响。目的 本研究的主要目的是评估在初次结肠镜检查中发现近端增生性息肉(HP)、腺瘤及其合并症后,在后续结肠镜检查中发生全晚期肿瘤(T-MAN)的风险。方法 回顾2014年和2015年接受结肠镜检查的45至74岁患者的医疗记录。主要结果是随访结肠镜检查时是否出现T-MAN(包括晚期腺瘤或高危SL),取决于首次结肠镜检查时是否出现近端HP、腺瘤或它们的组合。次要结果包括根据索引结果特征评估随访时出现 T-MAN 的风险。结果 2014 例患者接受了筛查,764 例纳入最终分析(男性占 44.1%,女性占 55.9%;平均年龄 63 岁;中位随访时间 3.46 年)。在初次结肠镜检查中同时发现近端增生性息肉和结肠腺瘤的患者,其罹患T-MAN的风险明显高于同时发现腺瘤和远端HP或在初次结肠镜检查中仅发现腺瘤的患者(30.5% vs 19%)[危险比(HR)=1.95(95% 置信区间(CI)1.3-2.9)]。在随访期间,近端增生性息肉和结肠腺瘤的组合与较高的 T-MAN 风险相关,而仅近端 HP 的组合则与较高的 T-MAN 风险相关(30.5% 对 13.9%)[HR=3.4(95% 置信区间 1.3-8.7)]。对于仅有腺瘤的患者与仅有近端HP的患者(19.1% vs 13.9%)[HR=1.9 (95% CI 0.75-4.7)],没有发现有统计学意义的证据表明随访期间发生T-MAN的风险增加。结论 患有近端增生性息肉的患者在后续结肠镜检查中出现 T-MAN 的风险增加。同时患有增生性息肉和腺瘤的患者比单纯患有增生性息肉或腺瘤的患者患 T-MAN 的风险更高。资助机构 丹尼尔-冯-伦特恩(Daniel von Renteln)获得了 "魁北克健康研究基金会"(Fonds de Recherche du Québec Santé)的职业发展奖。他还从 ERBE Elektromedizin GmbH、Ventage、Pendopharm、Fujifilm 和 Pentax 获得研究经费,并从 Boston Scientific Inc.、ERBE Elektromedizin GmbH 和 Pendopharm 获得顾问费或演讲费。Roupen Djinbachian 得到了 "魁北克卫生研究基金/卫生和社会服务部 "临床研究奖的支持。其余作者声明不存在利益冲突。
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A141 RISK OF TOTAL METACHRONOUS ADVANCED NEOPLASIA AFTER DETECTION OF PROXIMAL HYPERPLASTIC POLYPS, ADENOMAS, AND THEIR COMBINATION
Abstract Background Recent research findings have identified an association between proximal sessile serrated lesions (SSL) and a greater risk of advanced metachronous neoplasia, without significant impact of distal SSL. Aims The principal aim of this study was to assess the risk of total metachronous advanced neoplasia (T-MAN) at the follow-up (fu) colonoscopy after detection of proximal hyperplastic polyps (HP), adenomas and their combination at the initial colonoscopy. Methods Medical records for patients aged 45 to 74 who underwent colonoscopies in both 2014 and 2015 were reviewed. The primary outcome was the presence of T-MAN (comprising advanced adenomas or high-risk SL) during the follow-up colonoscopy depending on the presence of proximal HP, adenoma, or their combination at index colonoscopy. Secondary outcomes included assessing the risk of T-MAN at follow-up depending on index findings characteristics. Results 2014 patients were screened and 764 were included in the final analysis (44.1% male vs 55.9% female; mean age, 63y; median follow-up, 3.46 years). Patients with both proximal hyperplastic polyps and colonic adenomas during their initial colonoscopy had a significantly higher risk of developing T-MAN than patients with a combination of adenomas and distal HP or with only adenomas at index colonoscopy (30.5% vs 19%) [Hazard-ratio (HR)=1.95 (95% confidence interval (CI)1.3-2.9)]. A combination of proximal hyperplastic polyps and colonic adenomas is associated with a higher risk of T-MAN during follow-up than proximal HP alone (30.5% vs 13.9%) [HR=3.4 (95% CI 1.3-8.7)]. No statistically significant evidence was found to identify an increased risk of developing T-MAN at follow-up in patients presenting adenomas alone vs those with only proximal HP (19.1% vs 13.9%) [HR=1.9 (95% CI 0.75-4.7)]. Conclusions Patients with proximal hyperplastic polyps have an increased risk of presenting a T-MAN at the follow-up colonoscopy. Presenting a combination of hyperplastic polyps and adenomas indicates a higher risk of developing T-MAN than presenting an HP or adenoma alone. Funding Agencies Daniel von Renteln is supported by a "Fonds de Recherche du Québec Santé" career development award. He has also received research funding from ERBE Elektromedizin GmbH, Ventage, Pendopharm, Fujifilm and Pentax, and has received consultant or speaker fees from Boston Scientific Inc., ERBE Elektromedizin GmbH, and Pendopharm. Roupen Djinbachian is supported by a “Fonds de Recherche du Québec Santé/Ministère de la Santé et des Services Sociaux” clinical research award. The remaining authors declare that they have no conflict of interest.
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