878 Influence of Long-Term Treatment With Topical Corticosteroids on Natural Course of Eosinophilic Esophagitis and Correlation Between Symptoms and Endoscopy, Histology, and Blood Eosinophils

2013 ◽  
Vol 144 (5) ◽  
pp. S-154 ◽  
Author(s):  
Alain Schoepfer ◽  
Susanne Portmann ◽  
Ekaterina Safroneeva ◽  
Tanja Kuchen ◽  
Christian Bussmann ◽  
...  
2017 ◽  
Vol 112 (10) ◽  
pp. 1527-1535 ◽  
Author(s):  
Thomas Greuter ◽  
Christian Bussmann ◽  
Ekaterina Safroneeva ◽  
Alain M Schoepfer ◽  
Luc Biedermann ◽  
...  

2020 ◽  
Vol 13 ◽  
pp. 175628482092728
Author(s):  
Stephan Miehlke ◽  
Alfredo J. Lucendo ◽  
Alex Straumann ◽  
Albert Jan Bredenoord ◽  
Stephen Attwood

Eosinophilic esophagitis (EoE) is a chronic inflammatory disorder of the esophagus characterized by symptoms of esophageal dysfunction and eosinophil-predominant inflammation. The incidence of EoE has increased substantially over the past two decades in Europe and North America. The natural course of EoE appears to be progressive with a high risk of stricture formation. The current European guideline recommend swallowed topical corticosteroids, proton-pump inhibitors or dietary intervention for initial and long-term treatment of EoE. Swallowed topical corticosteroids can be considered to be the best studied drug class in EoE, with more than 1000 patients enrolled in randomized clinical trials worldwide. In most of them, fluticasone or budesonide formulations have been used that were originally designed for asthma therapy, thus presumably suboptimal for EoE treatment. The new orodispersible budesonide tablet with effervescent properties is the first approved esophageal-targeted formulation specifically developed for the treatment of EoE, which has become available in many European countries. This article gives an overview of the evolution of topical corticosteroids in EoE and provides an update on recent data from large-scale multicenter trials exploring the efficacy and safety of the orodispersible budesonide tablet with effervescent properties in adult EoE patients.


2020 ◽  
Vol 158 (6) ◽  
pp. S-825
Author(s):  
Matteo Ghisa ◽  
Giorgio Laserra ◽  
Brigida Barberio ◽  
Salvatore Tolone ◽  
Nicola de Bortoli ◽  
...  

2015 ◽  
Vol 357 ◽  
pp. e321
Author(s):  
A. Altintas ◽  
M. Nalbantoglu ◽  
U. Uygunoglu ◽  
G. Gozubatik-Celik ◽  
S. Akkas-Yazici ◽  
...  

Author(s):  
Evan S. Dellon ◽  
Margaret H. Collins ◽  
David A. Katzka ◽  
Vincent A. Mukkada ◽  
Gary W. Falk ◽  
...  

2018 ◽  
Vol 67 (2) ◽  
pp. 210-216 ◽  
Author(s):  
Carolina Gutiérrez-Junquera ◽  
Sonia Fernández-Fernández ◽  
M. Luz Cilleruelo ◽  
Ana Rayo ◽  
Luis Echeverría ◽  
...  

2010 ◽  
Vol 138 (5) ◽  
pp. S-123
Author(s):  
Alex Straumann ◽  
Lukas Degen ◽  
Christian Bussmann ◽  
Christoph Beglinger ◽  
Alain Schoepfer ◽  
...  

Endoscopy ◽  
2021 ◽  
Author(s):  
Sydney Greenberg ◽  
Nicole Chang ◽  
Stephanie Corder ◽  
Craig C Reed ◽  
Swathi Eluri ◽  
...  

Background & Aims: Little is known about esophageal dilation as a long-term treatment eosinophilic esophagitis (EoE). We examined the impact of a “dilate and wait” strategy on symptoms and safety of patients with EoE. Methods: This retrospective cohort study included two groups of EoE patients: those who underwent a dilation-predominant approach, defined as >3 dilations as EoE sole therapy or for histologically refractory disease (>15 eos/hpf); and those who had routine care, defined as <3 dilations or histologic response. Characteristics of the groups were compared and outcomes for the dilation-only group assessed. Results: Of 205 patients, 53 (26%) received the dilation-predominant strategy (n=408 dilations total), most commonly because of histologic treatment non-response (75%). These patients were younger (33 vs 41 yrs, p=0.003), had a narrower baseline esophageal diameter (9.8 vs 11.5mm, p=0.005), underwent more dilations (7.7 vs 3.4, p <0.001), but achieved a smaller final diameter (15.7 vs 16.7mm, p=0.01) compared to routine care. With this strategy, 30 patients (57%) had ongoing symptom improvement, with esophageal caliber change independently associated with symptom response (aOR 1.79; 95%CI 1.17-2.78); 26 (49%) used the strategy as a bridge to clinical trials. Over a median follow-up of 1001 days (IQR 581-1710), there were no deaths or dilation-related perforations, but there were 9 ER visits, including 1 for post-dilation bleeding and 4 for food impaction. Conclusions: A dilation-predominant long-term treatment strategy allows for symptom control or bridge to clinical trials for patients with difficult to treat EoE. Close follow-up and monitoring for complications is required.


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