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46 Cards in this Set
- Front
- Back
What are the non-pharmacological treatments? |
Review the following (M.O.F.A.S.A.M):
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What do antacids do? |
'Neutralise' acid in the stomach |
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What do antacids usually contain? |
Alumium, Magnesium or BOTH |
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What else can antacids contain, but why is it unsuitable? |
Sodium bicarbonate, but it's unsuitable for regular use because of the high sodium content |
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What do antacids provide? |
Immediate symptom relief |
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How is the duration of antacids? |
It has a limited duration of action |
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When should antacids be taken? |
After meals and before bedtime |
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Can the administration of antacid be together with some drugs? |
NO |
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What can aluminium based antacids cause? |
Constipation |
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What can magnesium based antacids cause? |
Diarrhoea |
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Name examples of antacids |
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What can antacids that contain alginate do? |
Form a raft that 'floats' on the stomach contents to reduce reflux, and therefore protect the oesophageal mucosa |
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Give examples of antacids that contain alginate |
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What are histamine2 receptor antagonists? |
Structural analogues of histamine |
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What do histamine2 receptor antagonists do? |
Block the histamine receptors in gastric parietal cells, and therefore prevent acid secretion |
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Does HRA have any role in treating peptic ulcer disease? |
No, because it's less effective than proton pump inhibitors |
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The main role of HRA is in what? |
Dyspepsia - because patients with mild symptoms may not need proton pump inhibitors |
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Name examples of HRAs |
C.R.F.N-tidine:
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HRAs have lower risk of side effects than what? |
Proton Pump Inhibitors |
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What are the most COMMON side effects of HRAs? |
Diarrhoea and Headaches |
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What occasional side effects have been reported for HRAs? |
Confusion and Rashes |
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Which HRAs has the most drug interactions? |
Cimetidine |
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Which HRAs is the most commonly prescribed? |
Ranitidine |
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What do proton pump inhibitors do? |
Control gastric secretion by inhibiting proton pumps (H+,K+ -ATP ase) - the enzymes responsible for the final step in gastric secretion from parietal cells |
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When carried in the blood stream, are PPIs active? |
They are inactive pro-drugs |
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Which cell do PPIs get carried to? |
Parietal cells |
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When are PPIs active? |
When they are under acidic conditions, they are converted into their active form |
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How is the reversibility of PPI binding to proton pumps? |
Irreversible |
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What should be noted about how different PPIs bind? |
Different PPIs bind to different sites on the proton pump |
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Name proton pump inhibitors |
R.O.P.E.L-prazole:
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How many hours after administrations is the max plasma concentration reached for:
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Since PPIs irreversibly bind to the pumps, how is the duration of acid inhibition? |
It is a sustained duration, with a half life of approximately 48 hours |
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When are PPIs most effective to be taken? |
30 minutes before meals |
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What do PPIs only inhibit? |
ACTIVELY secreting proton pumps, because it only becomes active in acidic conditions |
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PPIs get metabolised where? |
In the liver |
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How is the safety of PPIs? |
It's relatively safe |
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What are the most common side effects of PPIs? |
Diarrhoea and headache |
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What has long term acid suppression been associated with? |
*more studies needed to confirm this* |
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What is eradication therapy in relation to dyspepsia? |
Eradication of H Pylori |
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What is usually used to eradicate H pylori? |
Antibiotics and Ulcer healing drugs together |
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What should be given in the first line of eradication therapy? |
PPI with amoxicillin and clarithromycin |
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For patients allergic to penicillin, what can be done for them? |
Replace amoxicillin with metronidazole |
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When choosing regimes for eradication, what should be a goal? |
Eradication rates of more than 80% |
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What can enhance the efficacy of eradication? |
Lowering acidity levels |
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What are the usual reasons for treatment failure by eradication therapy? |
N.A.R.I.U:
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Surgical operations for dyspepsia used to be common, but now when are they ever used? |
In emergencies when bleeding peptic ulcers:
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