Abstract | OBJECTIVE: STUDY DESIGN AND METHODS: Prospective, double-blind, randomized, placebo-controlled study. Sixty-two patients with a reflux finding score (RFS)>7 and a reflux symptom index (RSI)>13 were enrolled and received either esomeprazole 20 mg twice daily or placebo for three months. RSI and RFS were assessed at baseline, after six weeks, and after three months. RESULTS: Reductions of total RSI and RFS as well as of several subscores were significantly higher in the treatment group compared to placebo after three months (P<0.05 each). The difference between study groups was most pronounced for posterior commissure hypertrophy (P<0.01). CONCLUSION: In the treatment of LPR-related symptoms a high placebo effect can be observed. However, compared to control, twice-daily PPI treatment for three months demonstrated a significantly greater improvement in laryngeal appearance and LPR symptoms.
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Authors | Oliver Reichel, Holger Dressel, Katrin Wiederänders, Wolfgang J Issing |
Journal | Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery
(Otolaryngol Head Neck Surg)
Vol. 139
Issue 3
Pg. 414-20
(Sep 2008)
ISSN: 0194-5998 [Print] England |
PMID | 18722223
(Publication Type: Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- Anti-Ulcer Agents
- Proton Pump Inhibitors
- Esomeprazole
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Topics |
- Adult
- Aged
- Anti-Ulcer Agents
(administration & dosage, therapeutic use)
- Double-Blind Method
- Esomeprazole
(administration & dosage, therapeutic use)
- Female
- Gastroesophageal Reflux
(drug therapy)
- Humans
- Hypertrophy
- Hypopharynx
(drug effects, pathology, physiopathology)
- Male
- Middle Aged
- Prospective Studies
- Proton Pump Inhibitors
(administration & dosage, therapeutic use)
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