Author/Authors :
Abdia, Saeed Gastroenterology and Liver Diseases Research Center - Research Institute for Gastroenterology and Liver Diseases - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Sargashteh, Zahra Department of Clinical Pharmacy - School of Pharmacy - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Abbasinazari, Mohammad Department of Clinical Pharmacy - School of Pharmacy - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Salamzadeh, Jamshid Department of Clinical Pharmacy - School of Pharmacy - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Mortazavi, Alireza Department of Pharmaceutics - School of Pharmacy - Shahid Beheshti University of Medical Sciences, Tehran, Iran
Abstract :
Proton pump inhibitors (PPIs) are recommended as first line treatments for gastroesophageal
reflux disease (GERD). Failure to PPIs has been mentioned as a problem in pharmacotherapy
of GERD. The present study compared the symptom relief, quality of life (QoL) and adverse
drug reactions (ADRs) of omeprazole plus buccal buspirone with that of omeprazole alone.This
was a prospective, randomized trial between buccal buspirone (10 mg/d) plus omeprazole (20
mg/d) and omeprazole (20 mg/d) plus placebo administered for 4 weeks to patients with GERD
symptoms. Patients who had GERD symptoms enrolled in this study. 67 patients were randomly
assigned to either the buspirone plus omeprazole group (n = 33) or the placebo plus omeprazole
group (n = 34). Finally, 58 patients completed the study (29 in each group). Treatment response
rates in each drug group were evaluated according to the Frequency Scale for the Symptoms
of GERD (FFSG). The QoL and ADRs have been also evaluated too.The treatment score rates
for symptom relief according to the FFSG were 7.13 ± 5.13 in the buspirone group and 15.34 ±
8.17 in the placebo group. Regarding FFSG score, there is a significant difference between the
groups (p < 0.0001). QoL were 6.86 ± 6.65 and 27.2 ± 20.95 in placebo and buspirone group,
respectively after four weeks and there is a significant difference in two groups ( p < 0.0001).
The total incidence of ADRs were similar in the buspirone and placebo groups (p = 0.36).A
combination of buccal buspirone plus omeprazole may be a more effective treatment for GERD
than omeprazole alone.
Keywords :
Buspirone , GERD , Omeprazole , Trial , Buccal