کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6097722 1210292 2015 11 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Original articleClinical endoscopyMetachronous colorectal cancers result from missed lesions and non-compliance with surveillance
موضوعات مرتبط
علوم پزشکی و سلامت پزشکی و دندانپزشکی بیماری‌های گوارشی
پیش نمایش صفحه اول مقاله
Original articleClinical endoscopyMetachronous colorectal cancers result from missed lesions and non-compliance with surveillance
چکیده انگلیسی

BackgroundSeveral studies examined the rate of colorectal cancer (CRC) developed during colonoscopy surveillance after CRC resection (ie, metachronous CRC [mCRC]), yet the underlying etiology is unclear.ObjectiveTo examine the rate and likely etiology of mCRCs.DesignPopulation-based, multicenter study. Review of clinical and histopathologic records, including data of the national pathology database and The Netherlands Cancer Registry.SettingNational cancer databases reviewed at 3 hospitals in South-Limburg, The Netherlands.PatientsTotal CRC population diagnosed in South-Limburg from January 2001 to December 2010.InterventionsColonoscopy.Main Outcome MeasurementsWe defined an mCRC as a second primary CRC, diagnosed >6 months after the primary CRC. By using a modified algorithm to ascribe likely etiology, we classified the mCRCs into cancers caused by non-compliance with surveillance recommendations, inadequate examination, incomplete resection of precursor lesions (CRC in same segment as previous advanced adenoma), missed lesions, or newly developed cancers.ResultsWe included a total of 5157 patients with CRC, of whom 93 (1.8%) had mCRCs, which were diagnosed on an average of 81 months (range 7-356 months) after the initial CRC diagnosis. Of all mCRCs, 43.0% were attributable to non-compliance with surveillance advice, 43.0% to missed lesions, 5.4% to incompletely resected lesions, 5.4% to newly developed cancers, and 3.2% to inadequate examination. Age-adjusted and sex-adjusted logistic regression analyses showed that mCRCs were significantly smaller in size (odds ratio [OR] 0.8; 95% confidence interval [CI], 0.7-0.9) and more often poorly differentiated (OR 1.7; 95% CI, 1.0-2.8) than were solitary CRCs.LimitationsRetrospective evaluation of clinical data.ConclusionIn this study, 1.8% of all patients with CRC developed mCRCs, and the vast majority were attributable to missed lesions or non-compliance with surveillance advice. Our findings underscore the importance of high-quality colonoscopy to maximize the benefit of post-CRC surveillance.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Gastrointestinal Endoscopy - Volume 82, Issue 2, August 2015, Pages 325-333.e2
نویسندگان
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