Interventional procedure overview of Balloon cryoablation for treating Barrett's oesophagus
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Outcome measures
Safety and efficacy outcomes are included. Further details are provided below.
Patient safety
Identified outcomes relevant to safety include:
Pain/discomfort
Measured using either a 10-point Likert or visual analogue scale (VAS), with 0 indicating no pain and 10 indicating worst pain
Adverse events (AE)
Bleeding
Oesophageal perforation
Oesophageal stricture
Dysphagia
Device malfunction
Efficacy
Identified outcomes relevant to BE include:
Complete eradication or remission of dysplasia
Complete eradication of internal metaplasia
BE surface regression
Proportion of BE converted to squamous epithelium, measured by independent expert assessors comparing pre- and post-CBA images or videos
Disease progression
Progression to more advanced dysplasia or ImCA
Conversion to neo-squamous epithelium
Technical success
Treatment of all visible BE as intended
Treatment failure
Residual requiring further treatment (CBA or otherwise)
Prague classification
The Prague classification for BE is reported across some studies. This is a standardised system used during endoscopy to measure and describe the extent of BE. The classification includes both the maximal length (M) (including tongues) of BE, and the length of the circumferential Barrett segment (C).
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