Background and study aims: Routine colorectal cancer screening, utilizing optical colonoscopy, has been shown
to reduce the incidence and mortality rate of colorectal cancer. Despite its prevalence
as the “gold standard” for neoplasia detection, the quality of colonoscopy screening
is hindered by missed, undiagnosed lesions that may go undetected when located on
the proximal aspect of haustral folds, rectal valves, the ileocecal valve, and/or
flexures. The aim of this phase I feasibility trial is to assess the safety and efficacy
of a new retrograde auxiliary imaging device, Third Eye™ Retroscope (Avantis Medical
Systems, Inc., Sunnyvale, California, USA), used with optical colonoscopy to improve
diagnostic yield.
Patients and methods: A total of 29 consecutive patients were enrolled in this phase I single-institution
prospective series. Primary efficacy endpoint was identification of polyps in the
retrograde image that were not identified in the antegrade image during colonoscope
withdrawal.
Results: Of the 29 patients enrolled, 24 patients were treated and 34 out of a total of 38
polyps (classified as either adenoma or hyperplasia) were identified in the antegrade
image. An additional four polyps, three hyperplastic and one adenoma, were identified
in the retrograde image, and were detected on the proximal aspect of haustral folds
during the colonoscope withdrawal, resulting in an 11.8 % increase in diagnostic yield.
No adverse events were encountered during the study.
Conclusion: A retrograde auxiliary imaging device used in conjunction with a standard optical
colonoscope proved to be safe, technically feasible, and clinically promising. A phase
II multi-institutional study is currently underway to further evaluate this device.
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G. Triadafilopoulos, MD
Division of Gastroenterology and Hepatology
Stanford University School of Medicine
Alway Building, Room M 211
300 Pasteur Drive, MC: 5187
Stanford
CA 94305-5187
USA
Fax: +1-650-988-7486
Email: vagt@stanford.edu