Abstract | PURPOSE: To provide additional efficacy data in patients treated with rabeprazole through week 4, and to validate sustained relief of gastroesophageal reflux disease symptoms through week 8 as well as to further analyze rabeprazole safety in patients with wide-ranging demographic and clinical characteristics. RESULTS: Patients in this study (N = 2,449) demonstrated significant overall improvement versus baseline (P < 0.001). Substantial symptom relief was seen throughout 8 weeks of treatment. By week 4, complete relief of daytime and nighttime heartburn, belching, regurgitation, and dysphagia was observed in 87.5, 90.7, 50.7, 77.6, and 75.1% of patients, respectively. Improvements were seen in rabeprazole-treated patients (<65 or >or=65 years) with a range of baseline symptom severities and across different racial groups. Rabeprazole was well tolerated. CONCLUSIONS:
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Authors | Alan Cutler, Malcolm Robinson, Anita Murthy, Byron Delemos |
Journal | Digestive diseases and sciences
(Dig Dis Sci)
Vol. 55
Issue 2
Pg. 338-45
(Feb 2010)
ISSN: 1573-2568 [Electronic] United States |
PMID | 19557517
(Publication Type: Comparative Study, Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- 2-Pyridinylmethylsulfinylbenzimidazoles
- Enzyme Inhibitors
- Rabeprazole
- Proton-Translocating ATPases
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Topics |
- 2-Pyridinylmethylsulfinylbenzimidazoles
(administration & dosage)
- Aged
- Dose-Response Relationship, Drug
- Endoscopy, Gastrointestinal
- Enzyme Inhibitors
(administration & dosage)
- Esophagitis, Peptic
(complications, diagnosis, drug therapy)
- Female
- Follow-Up Studies
- Heartburn
(drug therapy, epidemiology, etiology)
- Humans
- Incidence
- Male
- Middle Aged
- Proton-Translocating ATPases
(antagonists & inhibitors)
- Rabeprazole
- Time Factors
- Treatment Outcome
- United States
(epidemiology)
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