eISSN: 1897-4317
ISSN: 1895-5770
Gastroenterology Review/Przegląd Gastroenterologiczny
Current issue Archive Manuscripts accepted About the journal Editorial board Abstracting and indexing Subscription Contact Instructions for authors Publication charge Ethical standards and procedures
Editorial System
Submit your Manuscript
SCImago Journal & Country Rank
3/2023
vol. 18
 
Share:
Share:
Letter to the Editor

Esoxx added to standard therapy accelerates the healing of esophagitis

Anna Maria Pietrzak
1, 2

  1. II Gastroenterology Department, Centre of Postgraduate Medical Education, Warsaw, Poland
  2. Gastroenterology Department, Bielanski Hospital, Warsaw, Poland
Gastroenterology Rev 2023; 18 (3): 350–352
Online publish date: 2023/09/22
Article file
- Esoxx added.pdf  [0.16 MB]
Get citation
 
PlumX metrics:
 

Although proton pump inhibitors (PPI) remain the mainstay of peptic ulcer disease (PUD) treatment, their role in severe reflux esophagitis is less significant. It is because of multifactorial causes of gastroesophageal reflux disease (GERD) with acid toxicity being only one of them. The healing process takes time which is important in severe cases when rapid healing is crucial in the prevention of complications.

Thus we present a 62-year-old male, who presented to the emergency department with abdominal pain, heartburn, nausea and vomiting, and lastly with blood. Symptoms started after he had been treated with non-steroidal anti-inflammatory drugs for acute viral infection for three days. His past history was relevant for hypertension and type 2 diabetes. Laboratory tests were within normal ranges. Urgent gastroscopy revealed a large duodenal ulcer and severe esophagitis with a circumferential ulcer 15 cm in length (Figure 1 A). During the procedure further mucosal damage with bleeding caused by severe nausea and vomiting occurred. We hypothesized that the most probable cause of nausea and vomiting leading to esophagitis with impending perforation was functional sub-occlusion in the course of PUD. The intravenous proton pump inhibitor was implemented at a dose of 40 mg b.i.d. and also we added an Esoxx sachet three times daily. Prophylactically, the patient received antiemetic drugs. At first fluid diet was allowed, and in the following days, the diet was extended. After 4 days we decided to perform a second look gastroscopy with the intention of an intervention procedure in case of threatening duodenal ulcer bleeding. There has been significant improvement concerning ulcer disease. Surprisingly also esophageal ulcers were almost healed with much shallower erosions with filling epithelium. There were no signs of active or past bleeding (Figure 1 B). Endoscopy performed after 6 weeks confirmed sustained improvement (Figure 2).

Figure 1

A – Esophageal changes before treatment. B – Improvement of esophageal changes after 4 days of treatment

/f/fulltexts/PG/51444/PG-18-51444-g001_min.jpg
Figure 2

Sustained improvement after 6 weeks of treatment

/f/fulltexts/PG/51444/PG-18-51444-g002_min.jpg

Such rapid mucosal healing was unexpected given the efficacy data of PPIs. The largest meta-analysis showed that the weekly percentage of mucosal healing is 11.5%, which means that almost 90% of patients after a week of PPI use still have active inflammatory changes in the esophagus [1]. In a prospective multicenter analysis, it was proved that in grades C and D, esophagitis (LA classification) heals after 8 weeks only in 67.5% of cases [2]. Therefore, the reason for such rapid improvement and healing was considered to be the effect of adding Esoxx to the treatment. It is consistent with results of a recent study assessing symptom relief and mucosal healing in patients with radiation esophagitis [3]. Authors found that more than 92% of patients experienced symptoms’ improvement which lad to completion of oncologic treatment without delay.

Esoxx is a topical agent acting protective and healing esophageal mucosa. It is a combination preparation containing chondroitin sulfate (SC) and hyaluronic acid (HA) suspended in a bioadhesive carrier adapted to adhere to the esophageal mucosa – poloxamer 407 [4]. Esoxx makes a complex protective layer covering the mucosa, constituting a mechanical protective barrier against irritants, which has been proved in experimental and clinical studies [5]. It has a liquid form, easy to apply, in specially prepared sachets with one dose of the drug. It is not absorbed from the gastrointestinal tract, and therefore is safe for the patient. It does not interact with drugs or food.

In conclusion, the example discussed above shows that the addition of Esoxx to the treatment of esophagitis improves the effectiveness of therapy and shortens the healing time of the mucosa.

Conflict of interest

Served as a speaker for Alfasigma and BerlinChemie.

References

1 

Chiba N, De Gara C, Wilkinson M, Hunt R. Speed of healing and symptom relief in grade II to IV gastroesophageal reflux disease: a meta-analysis. Gastroenterology 1997; 112: 1798-810.

2 

Mizuno H, Matsuhashi N, Sakaguchi M, et al. Recent effectiveness of proton pump inhibitors for severe reflux esophagitis: the first multicenter prospective study in Japan. J Clin Biochem Nutr 2015; 57: 233-8.

3 

Carrasco E, López-Campos F, Sastre-Gallego S, et al. How efficacious is Ziverel® for symptomatic relief of acute radiation-induced esophagitis? Retrospective study of patients receiving oncologic treatment. Canc Therapy Oncol Int J 2017; 7: CTOIJ.MS.ID.555724.

4 

Palmieri B, Merighi A, Corbascio D, et al. Fixed combination of hyaluronic acid and chondroitin-sulphate oral formulation in a randomized double blind, placebo controlled study for the treatment of symptoms in patients with non-erosive gastroesophageal reflux. Eur Rev Med Pharmacol Sci 2013; 17: 3272-8.

5 

Savarino V, Pace F, Scarpignato C; Esoxx Study Group. Randomised clinical trial: mucosal protection combined with acid suppression in the treatment of non-erosive reflux disease–efficacy of Esoxx, a hyaluronic acid-chondroitin sulphate based bioadhesive formulation. Aliment Pharmacol Ther 2017; 45: 631-42.

Copyright: © 2023 Termedia Sp. z o. o. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
 
Quick links
© 2024 Termedia Sp. z o.o.
Developed by Bentus.