Technical feasibility, clinical effectiveness, and safety of esophageal stricture dilation using a novel endoscopic attachment cap in adults with eosinophilic esophagitis - 13/10/21
Abstract |
Background and Aims |
The BougieCap (Ovesco Endoscopy AG, Tübingen, Germany) is a new device that allows optical and tactile feedback during stricture dilation of the upper GI tract. We evaluated the technical feasibility, clinical efficacy, and safety of a 1-time esophageal stricture dilation using the BougieCap in adults with eosinophilic esophagitis (EoE).
Methods |
EoE patients prospectively included in the Swiss EoE Cohort were dilated with the BougieCap for esophageal strictures (esophageal diameter, ≤14 mm) and stricture-related symptoms. Symptoms were assessed before and 2 weeks after a single dilation session using the validated Eosinophilic Esophagitis Activity Index Patient Reported Outcomes instrument (score ranges from 0 to 100 points).
Results |
Fifty patients (70% men; median age, 41 years; median disease duration, 4 years; 50% treated with swallowed topical corticosteroids, 10% with proton pump inhibitors, 14% with combined swallowed topical corticosteroids plus proton pump inhibitors, 14% with elimination diet, 12% without antieosinophil therapy) were evaluated. Endoscopic bougienage was technically successful in 100%. The median esophageal diameter increased from 12 mm (interquartile range [IQR], 12-13) to 16 mm (IQR, 16-16; P < .001). Median symptom severity dropped from 32 points (IQR, 27-41) to 0 (IQR, 0-10; P < .001) at 2 weeks postdilation. In 1 patient the BougieCap was temporarily lost after stricture dilation in the hypopharynx but could be retrieved. No severe adverse events were reported.
Conclusions |
In adults with EoE, endoscopic treatment of esophageal strictures using the BougieCap is technically feasible and safe and offers significant symptomatic improvement in the short term.
Le texte complet de cet article est disponible en PDF.Graphical abstract |
Abbreviations : EoE, EEsAI PRO, SEECS
Plan
| DISCLOSURE: The following authors received research support for this study from the Swiss National Science Foundation: A. M. Schoepfer (grant 32003B_160115/1), E. Safroneeva (185008). All other authors disclosed no financial relationships. Research support for this study (A. Schoepfer) was provided by the Swiss EoE foundation and grants from Sanofi-Genzyme, Astra-Zeneca, and Dr Falk Pharma. |
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| If you would like to chat with an author of this article, you may contact Dr Schoepfer at alain.schoepfer@chuv.ch. |
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| See CME section, p. 998. |
Vol 94 - N° 5
P. 912 - novembre 2021 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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