• Dig. Dis. Sci. · Mar 2019

    Randomized Controlled Trial Multicenter Study Comparative Study

    Short-Term Symptomatic Relief in Gastroesophageal Reflux Disease: A Comparative Study of Esomeprazole and Vonoprazan.

    • Kouichi Sakurai, Hiroko Suda, Satomi Fujie, Takayuki Takeichi, Ayako Okuda, Tetsuya Murao, Kiwamu Hasuda, Masahiro Hirano, Kiyoharu Ito, Katsuie Tsuruta, and Masahiro Hattori.
    • Hattori Clinic, 2-12-35 Shin-machi, Chuo-ku, Kumamoto City, Kumamoto, 860-0004, Japan. sakuraiko@jcom.zaq.ne.jp.
    • Dig. Dis. Sci. 2019 Mar 1; 64 (3): 815-822.

    Background And AimProton pump inhibitors and vonoprazan (a potassium-competitive acid blocker) are recommended as first-line treatments for gastroesophageal reflux disease (GERD). However, few reports have investigated the onset of action of these agents for GERD symptom relief. The present study compared the symptom relief of esomeprazole with that of vonoprazan via monitoring self-reported GERD symptoms after treatment initiation.MethodsThis was a prospective, multicenter, randomized, open-label, parallel group, comparative clinical study between esomeprazole (20 mg/day) and vonoprazan (20 mg/day) administered for 4 weeks to patients with GERD symptoms. Patients who had scores ≥ 8 on the Gastroesophageal Reflux Disease Questionnaire (GerdQ) were defined as having GERD and enrolled in this study. Sixty patients were randomly assigned to either the esomeprazole group (n = 30) or the vonoprazan group (n = 30). Treatment response rates in each drug group were evaluated according to the GerdQ. The Frequency Scale for the Symptoms of GERD (FSSG) scores from the 1st day after treatment initiation and the Global Overall Symptom (GOS) scale scores during treatment were also evaluated.ResultsAt 4 weeks, the treatment response rates for symptom relief according to the GerdQ were 88.0% in the esomeprazole group and 81.8% in the vonoprazan group. The GOS scales, which reflect the impact of GERD symptoms, were similar for both groups. The FSSG scores decreased from the 1st to the 14th day in both groups.ConclusionsThere were no substantial differences in the symptom relief between the two groups at any time point in this short-term study.

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