Narrow-band imaging with magnification in Barrett’s esophagus: validation of a simplified grading system of mucosal morphology patterns against histology
R. Singh1
, G. K. Anagnostopoulos1
, K. Yao1
, H. Karageorgiou1
, P. J. Fortun1
, A. Shonde1
, K. Garsed1
, P. V. Kaye2
, C. J. Hawkey1
, K. Ragunath1
1Wolfson Digestive Diseases Centre, Queen’s Medical Centre, Nottingham, UK
2Department of Histopathology, Queen’s Medical Centre, Nottingham, UK
Background and study aims: Validation of a simplified classification of mucosal morphology in prediction of histology in Barrett’s esophagus using narrow-band imaging with magnification (NBI-Z) and assessing its reproducibility by endoscopists experienced in the use of NBI (NBI-experts) and by endoscopists who were new to NBI (non-NBI-experts).
Patients and methods: In a prospective cohort study of 109 patients with Barrett’s esophagus at a single tertiary referral center, mucosal patterns visualized in Barrett’s esophagus on NBI-Z were classified into four easily distinguishable types: A, round pits with regular microvasculature; B, villous/ridge pits with regular microvasculature; C, absent pits with regular microvasculature; D, distorted pits with irregular microvasculature. The NBI-Z grading was compared with the final histopathological diagnosis, and positive (PPV) and negative predictive values (NPV) were calculated. The reproducibility of the grading was then assessed by NBI-expert and non-NBI-expert endoscopists, and interobserver and intraobserver agreement were calculated using κ statistics.
Results:Per-biopsy analysis: In 903 out of 1021 distinct areas (87.9 %) the NBI-Z grading corresponded to the histological diagnosis. Per-patient analysis: The PPV and NPV for type A pattern (columnar mucosa without intestinal metaplasia) were 100 % and 97 % respectively; for types B and C (intestinal metaplasia) they were 88 % and 91 % respectively, and for type D (high-grade dysplasia) 81 % and 99 % respectively. Inter- and intraobserver agreement: The mean κ values in assessing the various patterns were 0.71 and 0.87 in the non-expert group; 0.78 and 0.91 in the expert group.
Conclusions: This study has validated a simplified classification of the various morphologic patterns visualized in Barrett’s esophagus and confirmed its reproducibility when used by NBI-expert and non-NBI-expert endoscopists.
References
1
Devesa S S, Blot W J, Fraumeni Jr J F.
Changing patterns in the incidence of esophageal and gastric carcinoma in the United States.
Cancer.
1998;
83
2049-2053
2
Jankowski J, Provenzale D, Moayyedi P.
Oesophageal adenocarcinoma arising from Barrett’s metaplasia has regional variations in the West.
Gastroenterology.
2002;
122
588-590
7
Cameron A, Carpenter H A.
Barrett’s esophagus, high grade dysplasia, and early adenocarcinoma: a pathological study.
Am J Gastroenterol.
1997;
92
586-591
9
Hamamoto Y, Endo T, Nosho K. et al .
Usefulness of narrow band imaging endoscopy for diagnosis of Barrett’s oesophagus.
J Gastroenterol.
2004;
39
14-20
10
Anagnostopoulos G K, Yao K, Kaye P. et al .
Novel endoscopic observation in Barrett’s oesophagus using high resolution magnification endoscopy and narrow band imaging.
Aliment Pharmacol Ther.
2007;
26
501-507
11
Sharma P, Bansal A, Mathur S. et al .
The utility of a novel narrow band imaging endoscopy system in patients with Barrett’s esophagus.
Gastrointest Endosc.
2006;
64
167-175
12
Kara M A, Ennahachi M, Fockens P. et al .
Detection and classification of the mucosal and vascular patterns (mucosal morphology) in Barrett’s esophagus by using narrow band imaging.
Gastrointest Endosc.
2006;
64
155-166
13
Playford R J.
New British Society of Gastroenterology (BSG) guidelines for the diagnosis and management of Barrett’s oesophagus.
Gut.
2006;
55
442-443
15
Sharma P, Dent J, Armstrong D. et al .
The development and validation of an endoscopic grading system for Barrett’s esophagus: the Prague C & M criteria.
Gastroenterology.
2006;
131
1392-1399
17
Skacel M, Petras R E, Granlich T L. et al .
The diagnosis of low grade dysplasia in Barrett’s esophagus and its implication for disease progression.
Am J Gastroenterol.
2000;
95
3383-3387
20
Canto M I, Setrakian S, Willis J. et al .
Methylene blue-directed biopsies improve detection of metaplasia and dysplasia in Barrett’s oesophagus.
Gastrointest Endosc.
2000;
51
560-568
21
Sharma P, Weston A P, Topalovski M. et al .
Magnification chromoendoscopy for detection of intestinal metaplasia and dysplasia in Barrett’s oesophagus.
Gut.
2003;
52
24-27
22
Fortun P J, Anagnostopoulos G K, Kaye P. et al .
Acetic acid-enhanced magnification endoscopy in the diagnosis of specialised intestinal metaplasia, dysplasia and early cancer in Barrett’s oesophagus.
Aliment Pharmacol Ther.
2006;
23
735-742
23
Olliver J R, Wild C P, Sahay P. et al .
Chromoendoscopy with methylene blue and associated DNA damage in Barrett’s esophagus.
Lancet.
2003;
362
373-374