Vonoprazan causes symptomatic improvement in non-erosive gastroesophageal reflux disease: A systematic review and meta-analysis
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Date
2024-06-06
Journal Title
Journal ISSN
Volume Title
Publisher
Elsevier
Abstract
Objective: To evaluate the efficacy and safety of vonoprazan therapy as compared to conventional proton pump
inhibitors (PPIs) or no vonoprazan for non-erosive esophagitis.
Methods: A thorough search was conducted across databases. The primary outcome was to determine the mean
variance in the gastroesophageal reflux disease (GERD) score after vonoprazan treatment. Secondary outcomes
comprised alterations in the scores for epigastric pain and post-prandial distress, the proportion of patients
displaying improvement, and the occurrence of adverse events. Pooled mean differences and relative risks were
determined utilizing random effects models.
Results: A total of 1,944 articles were screened and nine of them were included. As compared to PPI or no
vonoprazan therapy, vonoprazan treatment led to a significant reduction in the GERD score [mean difference:
-3.88 (95 % CI: -5.48, -2.28), p < 0.01, i
2
=95 %]. As compared to PPI or no vonoprazan therapy, vonoprazan
treatment led to a significant reduction in the epigastric pain score [mean difference: -3.02 (95 % CI: -5.41,
-0.63), p = 0.01, i
2
=75 %] and post-prandial distress score [mean difference: -2.82 (95 % CI: -3.51, -2.12), p <
0.01, i
2
=0 %] (all moderate GRADE evidence). Vonoprazan therapy was found to be safe.
Conclusion: Treatment with vonoprazan could significantly improve symptoms in patients with non-erosive
esophagitis or non-erosive GERD.
Description
Keywords
Gastroesophageal reflux disease (GERD), Non-erosive esophagitis, Proton pump inhibitors (PPIs), Vonoprazan
Citation
Bandyopadhyay, S., Verma, P., Shambo Samrat Samajdar, & Das, S. (2024). Vonoprazan causes symptomatic improvement in non-erosive gastroesophageal reflux disease: A systematic review and meta-analysis. Clinics and Research in Hepatology and Gastroenterology, 102373–102373. https://doi.org/10.1016/j.clinre.2024.102373
