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Examination on factors affecting symptom change after drug withdrawal in patients with erosive gastroesophageal reflux disease undergoing symptom-controlled maintenance therapy with acid-secretion inhibition drugs

Authors :
Hironori Tanaka
Toshihisa Takeuchi
Shinya Nishida
Hitosi Hongo
Michiaki Takii
Takeshi Higashino
Makoto Sanomura
Hirota Miyazaki
Masahiro Hoshimoto
Tsuguhiro Kimura
Masahiro Sakaguchi
Takashi Abe
Akitoshi Hakoda
Noriaki Sugawara
Taro Iwatsubo
Shinpei Kawaguchi
Kazuhiro Ota
Yuichi Kojima
Kazuhide Higuchi
Publication Year :
2022
Publisher :
Research Square Platform LLC, 2022.

Abstract

Background: In patients with gastroesophageal reflux disease (GERD) on maintenance therapy with acid-suppressive drugs, it is not clear what background factors allow patients to discontinue the drugs. The aim is to examine the relationship of the changes in the frequency and severity of gastrointestinal symptoms after discontinuation of acid-secretion inhibitors for erosive GERD (eGERD) with possible patient background factors, and to identify factors that influence these changes.Methods: This is a multicenter, open-label, interventional, exploratory study. eGERD patients with mild mucosal injury whose symptoms were under control and who were on maintenance therapy with acid-suppressive drugs were withdrawn from the drug treatment for 4 weeks. We examined the relationship of patient background (sex, age, body mass index, alcohol consumption, smoking habits), esophageal hiatal hernia, H. pylori infection, pepsinogen I and II concentrations and I/II ratios, blood gastrin levels before and after drug discontinuation with total score change in Frequency Scale for the symptoms of GERD (FSSG) .Results: Of the 92 patients whose symptoms could be assessed before and after drug withdrawal, 66 patients (71.7% of the total) had FSSG Conclusions: Consideration of background factors is unlikely to be required in the discontinuation of maintenance therapy for eGERD. There was no significant difference in the extent of disease or frequency of recurrence during the discontinuation period, regardless of whether the drug before discontinuation was a PPI or VPZ.Trial registration: The study was registered in the UMIN Clinical Trial Registry (UMIN000029957).

Details

Database :
OpenAIRE
Accession number :
edsair.doi...........021fe8581d1bd8bdb3809ad87627568c