Efficacy of vonoprazan for initial and maintenance therapy in reflux esophagitis, nonerosive esophagitis, and proton pump inhibitor-resistant gastroesophageal reflux disease.


Journal

Medicine
ISSN: 1536-5964
Titre abrégé: Medicine (Baltimore)
Pays: United States
ID NLM: 2985248R

Informations de publication

Date de publication:
Mar 2020
Historique:
entrez: 17 3 2020
pubmed: 17 3 2020
medline: 24 3 2020
Statut: ppublish

Résumé

Proton pump inhibitors (PPIs) have been the first line treatment for gastroesophageal reflux disease (GERD). The aim of this study was to evaluate the efficacy of vonoprazan (VPZ), a potassium-competitive acid blocker for reflux esophagitis (RE), nonerosive reflux disease (NERD), and PPI-resistant GERD patients.An open-label, single-center, observational study in our hospital was performed from August 2016 to August 2017. All patients diagnosed with GERD were asked to self-report a questionnaire of frequency scale for the symptoms of GERD (FSSG) and rate their degree of satisfaction with the treatment of GERD during outpatient visit. A total of 200 (RE 47, NERD 49, PPI-resistant GERD 104) patients were included in the present study. The primary endpoint was the change of FSSG and the proportion of degree of satisfaction with the treatment at the end of the initial therapy. A percentage of improvement (improvement rate) and resolution (resolution rate) at the end of the initial therapy were evaluated. Secondary endpoint included the proportion of patients with symptomatic relapse in the 24-week maintenance phase.FSSG and the degree of satisfaction were significantly improved after the initial therapy in every group. Improvement and resolution rate after the initial therapy were 83.0% and 67.0% in RE, 66.7% and 60.4% in NERD, and 76.0% and 60.4% in PPI-resistant group. There was no significance between after the initial therapy and 24 weeks in improvement and resolution rate. Thirty-two of the total 48 patients did not take VPZ at 24 weeks. Total FSSG score in each group was 1.67 ± 1.97, 2.71 ± 4.91, and 4.0 ± 4.93. The nonrelapse rate at 24 weeks in each group was 66.7%, 60.0%, and 50.0%. The resolution rate at 24 weeks in each group was 38.9%, 45.0%, and 30.0%.The VPZ therapy is effective for initial and maintenance therapy and improves heartburn and patient's satisfaction significantly in all 3 groups. Among patients who stopped taking VPZ during the maintenance period, 42.0% of RE and NERD group and 30% of PPI-resistant group experience complete remission from GERD at 24 weeks by introduction of VPZ.

Identifiants

pubmed: 32176102
doi: 10.1097/MD.0000000000019520
pii: 00005792-202003130-00079
pmc: PMC7440130
doi:

Substances chimiques

1-(5-(2-fluorophenyl)-1-(pyridin-3-ylsulfonyl)-1H-pyrrol-3-yl)-N-methylmethanamine 0
Proton Pump Inhibitors 0
Pyrroles 0
Sulfonamides 0

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

e19520

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Auteurs

Yasuhiko Gotoh (Y)

Department of Gastroenterology, Shin Beppu Hospital, Beppu.

Emiko Ishibashi (E)

Department of Gastroenterology, Shin Beppu Hospital, Beppu.

Shunichiro Honda (S)

Department of Gastroenterology, Shin Beppu Hospital, Beppu.

Tomohisa Nakaya (T)

Department of Gastroenterology, Shin Beppu Hospital, Beppu.

Chishio Noguchi (C)

Department of Gastroenterology, Shin Beppu Hospital, Beppu.

Koichi Kagawa (K)

Department of Gastroenterology, Shin Beppu Hospital, Beppu.

Kazunari Murakami (K)

Department of Gastroenterology, Oita University Hospital, Yufu, Oita, Japan.

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