Histamine-2 Receptor Antagonist
- Their onset is slower than that of antacids, but their duration is longer.
- In large heartburn studies the earliest onset of symptom relief occurs around 30 minutes and peak effects are 1-1.5 hours after treatment.
- The anti-secretory effect, even with low doses, is prolonged and lasts for around 10-12 hours. This means dosing frequency compared to antacids can be reduced and many subjects require only one dose per day.
Antacid
- Acid in the oesophagus and stomach may be partly or completely neutralised for rapid relief of symptoms but further gastric acid production will occur and may be stimulated via a gastrin-mediated response to a rise in gastric pH.
- The consumption of further food will contribute to the termination of activity as gastric acid production is stimulated.
- By virtue of their mode of action, antacids cannot be used to prevent symptoms associated with ‘trigger’ foods.
- For these reasons antacids require regular re-dosing as symptoms return.
HISTAMINE-2 RECEPTOR ANTAGONISTS
(Ranitidine)
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ANTACIDS
(Magnesium Trisilicate)
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Mechanism of Action
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Inhibit acid secretion by blocking H2 receptors on the parietal cell
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Antacids can neutralize gastric acid and reduce acid delivery to the duodenum. They may also stimulate the defensive systems in the stomach by increasing bicarbonate and mucus secretion.
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Side Effects
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Side effects of H2RAs are rare
A common side effect associated with ranitidine is headache, occurring in about 3% of people who take it.
Confusion: Rare cases of reversible confusion have been associated with ranitidine; usually elderly or severely ill patients, or in patients with renal or hepatic impairment.
Hepatic effects: Elevation in ALT levels has occurred with higher doses (≥100 mg) or prolonged IV therapy (≥5 days); monitor ALT levels daily for the remainder of treatment.
Vitamin B12 deficiency: Prolonged treatment (≥2 years) may lead to vitamin B12 malabsorption and subsequent vitamin B12 deficiency
Rebound acid hypersecretion has been reported after discontinuation of therapy.
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Antacid side effects depend upon the quantity consumed and the duration of therapy.
Magnesium-containing antacids cause diarrhea and hypermagnesemia; the latter only becomes important in patients with renal insufficiency. Long-term, excessive use has been associated with the development of silica-based renal calculi. |
Special Precautions
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Relief of symptoms does not preclude the presence of a gastric malignancy.
Use with caution in patients with hepatic impairment (ranitidine undergoes hepatic metabolism).
Ranitidine is primarily excreted renally; dosage adjustment is recommended in patients with renal impairment.
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May alter absorption of other drugs, therefore antacids, tetracyclines or iron salts should be given 1-2 hours apart.
At high dosage, magnesium salts not only cause diarrhoea but also possible CNS depression. Magnesium trisilicate mixture has a sodium content of 6.4 mmol equivalent to 73.4 mg/5 ml or 147mg/10 ml dose. This must be taken into consideration for patients on a controlled sodium diet. Used with caution in patients with fluid retention There is a risk of metabolic alkalosis when oral magnesium salts are given with polystyrene sulphonate resins. |
Effectiveness
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Hotz et al, 1994
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References
- https://www.uptodate.com.
- http://www.kck.usm.my/husm/pharmacy/formulary/5.htm#5a
- https://www.uspharmacist.com/article/updates-in-nonprescription-therapy-for-heartburn-and-gerd
- https://www.ncbi.nlm.nih.gov/pubmed/8164599
- http://selfcarejournal.com/article/self-care-of-heartburn/
- https://www.drugs.com/ppa/ranitidine.htm
- https://www.medicines.org.uk/emc/medicine/25289
- http://www.nytimes.com/health/guides/disease/gastroesophageal-reflux-disease/medications.html
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