Publikasi Scopus 2024 per tanggal 31 Mei 2024 (409 artikel)

Simadibrata D.M.; Lesmana E.; Fass R.
Simadibrata, Daniel Martin (57202134322); Lesmana, Elvira (57208440285); Fass, Ronnie (7103304557)
57202134322; 57208440285; 7103304557
A systematic review and meta-analysis of the efficacy of vonoprazan for proton pump inhibitor-resistant gastroesophageal reflux disease
2024
Journal of Gastroenterology and Hepatology (Australia)
39
5
796
805
9
1
Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, United States; Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom; Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia; Division of Gastroenterology and Hepatology, MetroHealth Medical System, Case Western Reserve University, Cleveland, OH, United States
Simadibrata D.M., Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, United States, Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom; Lesmana E., Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, United States, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia; Fass R., Division of Gastroenterology and Hepatology, MetroHealth Medical System, Case Western Reserve University, Cleveland, OH, United States
Background and Aim: Up to 40% of gastroesophageal reflux disease (GERD) patients experience inadequate symptom relief with a proton pump inhibitor (PPI), termed PPI-resistant or refractory GERD. Vonoprazan, a potassium-competitive acid blocker, has better efficacy than PPI in suppressing gastric acid secretion. This meta-analysis summarizes the efficacy and safety of vonoprazan for treating PPI-resistant GERD (both erosive esophagitis [EE] and non-erosive reflux disease [NERD]). Methods: Four electronic databases (Medline, Embase, SCOPUS, and CENTRAL) were searched for studies indexed until August 1, 2023. Both observational studies and clinical trials assessing the efficacy and safety of vonoprazan in PPI-resistant GERD were included. Efficacy outcomes included healing and maintenance rates of EE and improvement of the Frequency Scale for Symptoms of GERD (FSSG) scores. Serious adverse events (SAEs) were considered a safety outcome. The modified Newcastle-Ottawa Scale (NOS) was used to assess study quality. Results: Twelve studies were included in this meta-analysis. Healing rates of PPI-resistant EE with vonoprazan 20 mg were 91.7% (95% CI 86.8–94.8%) and 88.5% (95% CI 69.7–96.2%) at weeks 4 and 8, respectively. For healed PPI-resistant EE, the overall maintenance rates with vonoprazan 10 mg were 82.6% (95% 61.2–95.0%) at week 8, 86.0% (95% CI 72.1–94.7%) at week 24, and 93.8% (95% CI 69.8–99.8%) at week 48. FSSG scores were improved in 74.6% (95% CI 65.8–81.7%) and 51.9% (95% CI 37.8–65.7%) of patients at weeks 4 and 8. Overall, no SAE was reported. Conclusion: Vonoprazan demonstrated high efficacy in the healing and maintenance of PPI-resistant EE and moderate efficacy for the improvement of FSSG score. Vonoprazan was well tolerated in PPI-resistant GERD patients. © 2024 Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd.
Gastroesophageal reflux disease; Meta-analysis; PPI-resistant GERD; Refractory GERD; vonoprazan
Drug Resistance; Gastroesophageal Reflux; Humans; Proton Pump Inhibitors; Pyrroles; Sulfonamides; Treatment Outcome; esomeprazole; lansoprazole; omeprazole; rabeprazole; vonoprazan; 1-(5-(2-fluorophenyl)-1-(pyridin-3-ylsulfonyl)-1H-pyrrol-3-yl)-N-methylmethanamine; proton pump inhibitor; pyrrole derivative; sulfonamide; adult; aged; Article; digestive system disease assessment; drug efficacy; drug safety; female; Frequency Scale for Symptoms of GERD; healing rate; human; male; meta analysis; Newcastle-Ottawa scale; non erosive reflux disease; randomized controlled trial (topic); reflux esophagitis; systematic review; treatment duration; unspecified side effect; drug resistance; gastroesophageal reflux; treatment outcome
John Wiley and Sons Inc
08159319
38263507
Article
Q1
1067
3778