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. Author manuscript; available in PMC: 2016 Sep 12.
Published in final edited form as: Gut. 2015 May 14;64(11):1816–1823. doi: 10.1136/gutjnl-2013-306706

Table 1.

Clinical performance for novel optical imaging technologies

Imaging technology Studies Sensitivity Specificity Type of lesion Level of evidence References
High definition white light endoscopy (HD-WLE) RCT 40%–64% 98%–100% LGD/HGD/EAC Ib 33,59
Chromoendoscopy
 Methylene blue RCT 49%–51% 48%–85% LGD/HGD/EAC Ib 25,26
 Acetic acid P 96% 81% IIa 28
Narrow band imaging (NBI) RCT, P, MA 47%–100% 72%–100% LGD/HGD/EAC Ib 3134
Autofluorescence imaging (AFI) P, RCT 42%–50% 61%–92% HGD/EAC Ib 36,38
Endoscopic trimodal imaging (ETMI) RCT NA NA LGD/HGD/EAC Ib 40,41
Optical coherence tomography (OCT) P 68%–83% 75%–82% LGD/HGD/EAC IIa 44,45
Optical frequency domain imaging (OFDI) P NA NA LGD/HGD/EAC IIa 46,47
Confocal laser endoscopy (CLE) RCT, P, MA 63%–100% 70%–98% LGD/HGD/EAC Ib 51,5659
Molecular imaging P 75% 94% HGD/EAC IIa 74

Performance and level of evidence for clinical studies performed using novel optical imaging technologies for BE surveillance.

Levels of evidence: Ib, evidence including at least one RCT; IIa, evidence including prospective, controlled, non-randomised studies.

BE, Barrett’s oesophagus; EAC, oesophageal cancer; HGD, high-grade dysplasia; LGD, low-grade dysplasia; MA, meta-analysis; NA, not available; P, prospective study; RCT, randomised control trial.