Endoscopy 2006; 38(5): 444-448
DOI: 10.1055/s-2006-925265
Original Article
© Georg Thieme Verlag KG Stuttgart · New York

Does Chromoendoscopy with Structure Enhancement Improve the Colonoscopic Adenoma Detection Rate?

M.-G.  Lapalus1 , T.  Helbert2 , B.  Napoleon3 , J.  F.  Rey4 , P.  Houcke5 , T.  Ponchon1 and the Société Française d’Endoscopie Digestive
  • 1Fédération des Spécialités Digestives, Hôpital E. Herriot, Lyon, France
  • 2Hôpital A. Paré, Marseille, France
  • 3Clinique Jeanne d’Arc, Lyon, France
  • 4Institut A. Tzanck, Saint-Laurent du Var, France
  • 5Clinique du Croisé Laroche, Marcq en Baroeul, France
Further Information

Publication History

Submitted 8 December 2005

Accepted after revision 22 January 2006

Publication Date:
09 May 2006 (online)

Background and Study Aims: Colonoscopy is still considered the standard investigation for the detection of colorectal adenomas, but the miss rate, especially for small and flat lesions, remains unacceptably high. Chromoscopy has been shown to increase the yield for lesion detection in inflammatory bowel disease. The aim of this randomized prospective study was to determine whether a combination of chromoscopy and structure enhancement could increase the adenoma detection rate in high-risk patients.
Patients and Methods: All patients included in the trial had a personal history of colorectal adenomas and/or a family history of colorectal cancer (but excluding genetic syndromes). They were randomized to one of two tandem colonoscopy groups, with the first pass consisting of conventional colonoscopy for both groups, followed by either chromoscopy and structure enhancement (the “study” group) or a second conventional colonoscopy (the control group) for the second-pass colonoscopy. All detected lesions was examined histopathologically after endoscopic resection or biopsy. The principal outcome parameter was the adenoma detection rate; the number, histopathology, and location of lesions was also recorded.
Results: A total of 292 patients were included in the study (146 patients in each group). The patients’ demographic characteristics, the indications for colonoscopy, and the quality of bowel preparation were similar in the two groups. There was a significant difference between the two groups with respect to the median duration of the examination (18.9 minutes in the control group vs. 27.1 minutes for the study group, P < 0.001). Although more hyperplastic lesions were detected throughout the colon in the study group (P = 0.033), there was no difference between the two groups in either the proportion of patients with at least one adenoma or in the total number of adenomas detected. Chromoscopy and structure enhancement diagnosed significantly more diminutive adenomas (< 5mm) in the right colon, compared with controls (P = 0.039).
Conclusions: On the basis of our results we cannot generally recommend the systematic use of chromoscopy and structure enhancement in a high-risk patient population, although the detection of small adenomas in the proximal colon was improved.

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M.-G. Lapalus, M. D.

Fédération des Spécialités Digestives

Pavillon H · Hôpital E. Herriot · 5 Place d’Arsonval · 69437 Lyon · France

Fax: +33-4-72-11-01-47

Email: marie-george.lapalus@chu-lyon.fr

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