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Risk of metachronous advanced neoplasia in patients with multiple diminutive adenomasoa mark
  • Kim, Jung Yoon ;
  • Kim, Tae Jun ;
  • Baek, Sun Young ;
  • Ahn, Soohyun ;
  • Kim, Eun Ran ;
  • Hong, Sung Noh ;
  • Chang, Dong Kyung ;
  • Kim, Young Ho
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dc.contributor.authorKim, Jung Yoon-
dc.contributor.authorKim, Tae Jun-
dc.contributor.authorBaek, Sun Young-
dc.contributor.authorAhn, Soohyun-
dc.contributor.authorKim, Eun Ran-
dc.contributor.authorHong, Sung Noh-
dc.contributor.authorChang, Dong Kyung-
dc.contributor.authorKim, Young Ho-
dc.date.issued2018-01-01-
dc.identifier.urihttps://dspace.ajou.ac.kr/dev/handle/2018.oak/30336-
dc.description.abstractObjectives: Individuals with advanced adenomas or three or more adenomas have a higher risk of metachronous advanced neoplasia (AN) and are recommended to undergo surveillance colonoscopy at shorter intervals. However, it is questionable whether patients with multiple (three or more) non-advanced diminutive adenomas should be considered as high-risk. Methods: We analyzed 5482 patients diagnosed with one or more adenomas during their first colonoscopy screening and who underwent a follow-up colonoscopy. Patients were categorized into four groups based on adenoma characteristics at baseline: Group 1, 1-2 non-advanced adenomas; Group 2, ≥3 non-advanced, diminutive (1 to 5 mm) adenomas; Group 3, ≥3 non-advanced, small (6-9 mm) adenomas; and Group 4, advanced adenomas. Results: During a median follow-up of 38 months, the incidence of metachronous AN at surveillance colonoscopy was 5.6%. The incidence of AN was 3.9% in group 1, 5.9% in group 2, 10.6% in group 3, and 22.1% in group 4. The adjusted hazard ratios (HRs) [95% confidence intervals (CIs)] for metachronous AN between group 2, group 3, and group 4, and low risk group 1 were 1.71 (0.99- 2.94), 2.76 (1.72-4.44), and 5.23 (3.57-7.68), respectively. Compared with group 4, the adjusted HRs (95% CIs) for group 1, group 2, and group 3 were 0.19 (0.13-0.28), 0.32 (0.18-0.59), and 0.52 (0.31-0.89), respectively. Conclusions: We found that patients with three or more non-advanced diminutive adenomas had a borderline increased risk of metachronous AN compared with patients with low risk adenomas.-
dc.language.isoeng-
dc.publisherWolters Kluwer Health-
dc.subject.meshAdenoma-
dc.subject.meshAged-
dc.subject.meshColonic Polyps-
dc.subject.meshColonoscopy-
dc.subject.meshColorectal Neoplasms-
dc.subject.meshFemale-
dc.subject.meshFollow-Up Studies-
dc.subject.meshHumans-
dc.subject.meshIncidence-
dc.subject.meshMale-
dc.subject.meshMiddle Aged-
dc.subject.meshNeoplasm Staging-
dc.subject.meshNeoplasms, Second Primary-
dc.subject.meshPractice Guidelines as Topic-
dc.subject.meshProportional Hazards Models-
dc.subject.meshRepublic of Korea-
dc.subject.meshRetrospective Studies-
dc.subject.meshRisk Assessment-
dc.subject.meshRisk Factors-
dc.subject.meshTime Factors-
dc.subject.meshTumor Burden-
dc.titleRisk of metachronous advanced neoplasia in patients with multiple diminutive adenomas-
dc.typeArticle-
dc.citation.endPage1861-
dc.citation.startPage1855-
dc.citation.titleAmerican Journal of Gastroenterology-
dc.citation.volume113-
dc.identifier.bibliographicCitationAmerican Journal of Gastroenterology, Vol.113, pp.1855-1861-
dc.identifier.doi10.1038/s41395-018-0210-9-
dc.identifier.pmid30072776-
dc.identifier.scopusid2-s2.0-85052311579-
dc.identifier.urlhttps://journals.lww.com/ajg/pages/default.aspx-
dc.description.isoatrue-
dc.subject.subareaHepatology-
dc.subject.subareaGastroenterology-
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Ahn, Soohyun안수현
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