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Published on: May 11, 2014
Endocytoscopic microvasculature evaluation is a reliable new diagnostic method for colorectal lesions (with video)
Shin-Ei Kudo1, Masashi Misawa1, Yoshiki Wada2
1Digestive Disease Center, Showa University, Northern Yokohama Hospital, Yokohama, Japan.
Background:
We previously reported on the efficacy of endocytoscopic classification (EC-C). However, the correlation of the endocytoscopic vascular (EC-V) pattern with diagnoses was unclear.
Objective:
To assess the diagnostic accuracy of the EC-V pattern for colorectal lesions.
Design:
Retrospective.
Setting:
A university hospital.
Patients:
Patients who underwent endocytoscopy between January 2010 and March 2013.
Intervention:
We evaluated 198 consecutive lesions according to the EC-V pattern (EC-V1, obscure surface microvessels; EC-V2, clearly observed surface microvessels of a uniform caliber and arrangement; and EC-V3, dilated surface microvessels of a nonhomogeneous caliber or arrangement).
Main Outcome Measurements:
The diagnostic accuracy for predicting hyperplastic polyps and invasive cancer were compared between the EC-V pattern and other modalities (narrow-band imaging, pit pattern, and EC-C).
Results:
The sensitivity, specificity, and accuracy of the EC-V1 pattern for diagnosing hyperplastic polyps were 95.5%, 99.4%, and 99.0%, respectively. The sensitivity, specificity, and accuracy of the EC-V3 pattern for diagnosing invasive cancer were 74.6%, 97.2%, and 88.6%, respectively. The diagnostic accuracy of the EC-V pattern for predicting hyperplastic polyps was comparable to the other modalities. For predicting invasive cancer, the EC-V pattern was comparable to narrow-band imaging and pit pattern, although EC-C was slightly more accurate (P = .04). In the substudy, the diagnosis time by using the EC-V pattern was shorter than that with the EC-C pattern (P < .001).
Limitations:
A single-center, retrospective study.
Conclusions:
The EC-V pattern saved more time than the EC-C pattern and had a diagnostic ability comparable to that of other optical biopsy modalities.
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