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DOI 10.1111/j.1365-2036.2004.02217.x

Медицинская библиотека · Alimentary pharmacology & therapeutics · 2004

A single dose of ranitidine 150 mg modulates oesophageal acid sensitivity in patients with functional heartburn.

Rodriguez-Stanley S, Ciociola A A, Zubaidi S, Proskin H M, Miner P B

Клиническое исследованиеСтатьяРандомизированное исследованиеПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

The rapid onset and symptomatic response to histamine-2 receptor antagonists prior to the pharmacological effect on acid secretion suggests a different mechanism of action.

AIM: To determine if ranitidine decreases oesophageal sensitivity to chemical and mechanical stimulation, potentially via oesophageal histamine receptors.

METHODS

A total of 18 patients with functional heartburn received oral ranitidine 150 mg b.d. or placebo for 7 consecutive days in a double-blind randomized crossover design and underwent Barostat balloon distention and Bernstein acid infusion on study day 1 (90 min postdose) and study day 7. First sensation and pain were recorded and pain severity was rated on a 5-point Likert scale and a 100 mm visual analogue scale. Least square mean values were generated and one-tailed t-tests were performed.

RESULTS

After a single dose of ranitidine 150 mg, time to pain with oesophageal acid infusion was increased by 29% (P < 0.05) and visual analogue scale and Likert scores were decreased by 20% (P < 0.06) and 23% (P < 0.02), respectively compared with placebo. After 1 week of ranitidine, positive alterations in sensory parameters persisted. Balloon distention sensory parameters were not altered by ranitidine.

CONCLUSIONS

Ranitidine significantly decreased oesophageal sensitivity to acid. Failure of ranitidine to improve balloon sensory parameters supports existence of multiple sensory pathways in the oesophagus.

Для цитирования: Rodriguez-Stanley S, Ciociola A A, Zubaidi S, Proskin H M, Miner P B. A single dose of ranitidine 150 mg modulates oesophageal acid sensitivity in patients with functional heartburn.. Alimentary pharmacology & therapeutics. 2004. DOI: 10.1111/j.1365-2036.2004.02217.x.

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