Detalle Publicación

ARTÍCULO

Efficacy of proton pump inhibitor therapy for eosinophilic oesophagitis in 630 patients: results from the eoe connect

Autores: Laserna-Mendieta, E. J.; Casabona, S.; Guagnozzi, D.; Savarino, E.; Perello, A .; Guardiola-Arevalo, A.; Barrio, J .; Perez-Martinez, I.; Krarup, A. L.; Alcedo, J .; de la Riva Onandía, Susana Rosa; Rey-Iborra, E.; Santander, C.; Arias, A.; Lucendo, A. J. (Autor de correspondencia)
Título de la revista: ALIMENTARY PHARMACOLOGY AND THERAPEUTICS
ISSN: 1365-2036
Volumen: 52
Páginas: 798 - 807
Fecha de publicación: 2020
Resumen:
Background Proton pump inhibitors (PPIs) are the most commonly used first-line therapy for patients with eosinophilic oesophagitis (EoE). However, many aspects related to PPIs in EoE are still unknown. Aims To assess the effectiveness of PPI therapy for EoE in real-world practice. Methods This cross-sectional study collected data on PPI efficacy from the multicentre EoE CONNECT database. Clinical remission was defined as a decrease >= 50% in dysphagia symptom score; histological remission was defined as a peak eosinophil count below 15 eosinophils per high-power field. Factors associated with effectiveness of PPI therapy were identified by binary logistic regression multivariate analyses. Results Overall, 630 patients (76 children) received PPI as initial therapy (n = 600) or after failure to respond to other therapies (n = 30). PPI therapy achieved eosinophil density below 15 eosinophils per high-power field in 48.8% and a decreased symptom score >= 50% from baseline in 71.0% of patients. More EoE patients with an inflammatory rather than stricturing phenotype accomplished clinico-histological remission after PPI therapy (OR 3.7; 95% CI, 1.4-9.5); as well as those who prolonged treatment length from 8 to 12 weeks (OR 2.7; 95% CI, 1.3-5.3). After achieving clinico-histological remission of EoE, PPI dosage reduction was effectively maintained in 69.9% of cases, but tended to be less effective among patients with a stricturing phenotype. Conclusions Inflammatory EoE phenotype a