Optimal Omeprazole Dosing and Symptom Control: A Randomized Controlled Trial (OSCAR Trial)
Autor: | Adam T. Perzynski, Nisheet Waghray, M. Michael Wolfe, Mark Votruba, Abhijeet Waghray |
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Rok vydání: | 2018 |
Předmět: |
Adult
Male medicine.medical_specialty Time Factors Physiology Disease Severity of Illness Index Drug Administration Schedule Article law.invention 03 medical and health sciences 0302 clinical medicine Heartburn Patient Education as Topic Randomized controlled trial law Internal medicine medicine Humans Symptom control Dosing Omeprazole Aged Ohio Hepatology business.industry Remission Induction Gastroenterology Reflux Proton Pump Inhibitors Middle Aged medicine.disease Treatment Outcome 030220 oncology & carcinogenesis Gastroesophageal Reflux GERD Female 030211 gastroenterology & hepatology medicine.symptom business medicine.drug |
Zdroj: | Digestive Diseases and Sciences. 64:158-166 |
ISSN: | 1573-2568 0163-2116 |
DOI: | 10.1007/s10620-018-5235-9 |
Popis: | Proton pump inhibitors (PPIs) are potent inhibitors of acid secretion and are the mainstay of therapy for gastroesophageal reflux disease (GERD). Initially designed to be taken 30 min before the first daily meal, these agents are commonly used suboptimally, which adversely affects symptom relief. No study to date has assessed whether correcting dosing regimens would improve symptom control. The objective of this study was to determine whether patients with persistent GERD symptoms on suboptimal omeprazole dosing experience symptomatic improvement when randomized to commonly recommended dosing regimen and to evaluate the economic impact of suboptimal PPI dosing in GERD patients. Patients with persistent heartburn symptoms ≥ 3 times per week treated with omeprazole 20 mg daily were enrolled and randomized to commonly recommended dosing or continued suboptimal dosing of omeprazole. The primary outcomes were changes in symptom, frequency, and severity, as determined using the Gastroesophageal Reflux Disease Symptom Assessment Scale (GSAS) 4 weeks after the intervention was administered. In secondary analysis, an alternative measure of symptom load was used to infer potential costs. Sixty-four patients were enrolled. GSAS symptom, frequency, and severity scores were significantly better when dosing was optimized for overall and heartburn-specific symptoms (P |
Databáze: | OpenAIRE |
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