GI Pharmacology Flashcards

1
Q

What are some of the symptoms of GORD?

A
  • Painful heart burn
  • Cough
  • Larygntitis
  • Astha
  • Dental erosion
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2
Q

What are some of the complications of GORD?

A
  • Oesophagitis
  • Ulceration
  • Haemorrhage (anaemia)
  • Stricure formation
  • Barret’s oesophagus
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3
Q

What medications can exacerbate the symptoms of GORD?

A

Anything that relaxes smooth muscle

  • alpha bockers
  • anticholinergics
  • benzodiazepines
  • beta blockers
  • CCBs
  • NSAIDs
  • Nitrates
  • Theophylline
  • TCAs
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4
Q

What are some risk factors for developing GORD?

A
  • Older age
  • Hiatus hernia (lower oesophageal sphinter into thorax)
  • Obesity
  • Pregnancy
  • Smoking
  • Alcohol consumption
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5
Q

What lifestyle changes would you recommend for someone experiencing GORD symptoms?

A
  • Weight loss
  • Avoid trigger food
  • Eat smaller meals
  • Eat earlier in the day
  • Reduce alcohol/ caggeine intake
  • Stop smoking (limited evidence)
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6
Q

What are the pharmacological steps for treating GORD?

A
  • Introduce proton pump inhibitor first line
  • If unsuccessful- add in H2 Receptor Antagonist
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7
Q

Name 2 proton pump inhibitors

A
  • Omeprazole
  • Lansoprazole
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8
Q

What is gastritis?

A

An inflammatory change in the gastric mucosa

Can be erosive/ non-erosive. Acute / chronic

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9
Q

What are some of the symptoms of gastritis?

A
  • Burning epigastric pain
    • Food may increase or decrease pain
  • Nausea
  • Vomiting
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10
Q

What are some of the risk factors for developing gastritis?

A
  • H. pylori infection
  • Chronic NSAID use
  • Bile reflux
  • Chronic alcohol use
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11
Q

How do you manage erosive gastritis?

A
  • Remove irritant (NSAID, alcohol, bile)
  • Add PPI or H2 Receptor antagonist
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12
Q

How do you eradicate H. pylori?

A

Triple therapy

  1. PPI
    • Amoxicillin
    • Clarithromycin or Metronidazole (effectove but has side effects)
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13
Q

How do PPIs work?

A
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14
Q

How do H2 receptor antagonists work?

A
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15
Q

Name a H2 receptor antagonist

A

Ranitidine

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16
Q

What is peptic ulcer disease?

A

A defect in the gastric or dueodenal mucosa that exptends through the muscularis mucosa

17
Q

What are some the symptoms of peptic ulcer disease?

A
  • Epigastric pain after meals
    • soon after meals (gastric ulcer)
    • 2-3 hours after (duodenal)
18
Q

What are some of the risk factors for developing peptic ulcer disease?

A
  • H pylori infection
  • NSAIDs
19
Q

How do manage peptic ulcer disease that is H.pylori negative?

A
  • Stop NSAIDs
    • consider switching to COX-2 selective NSAID e.g. celecoxib
    • doesn’t effect COX-1 prostaglandin synthesis which is protective for the GI tract
  • Add PPI (+ H2 RA if unresponsive)
20
Q

How do you test for H.pylori?

A
  • Carbon 13 urea breath test
  • Or stool antigen test
21
Q

What are the 2 different isoforms of COX enzymes and where are they distributed throughout the body?

A

COX-1

  • high concentration in platelets, vascular endothelial cells, stomach and kidney
  • produces prostaglandings necessary to maintain endocrine, renal function, gastric mucosa integrity and haemostasis

COX-2

  • normal conditions, very low levels
  • rapdily increases at time of tissue damage
22
Q

What are the benefits and disadvantages of COX-2 inhibitors

A

Benefit:

  • Gastric protection

Disadvantage:

  • not good for CVS if given long term
  • High levels of TXA2 → pro-thrombotic
23
Q

What factors of the stomach offer protection against mucosal injury?

A
  • Acid - innate defence against bacterial invasion
  • Mucus - lubricates, traps bacteria, barrier against pepsin (protease that can auto-digest stomach)
  • Epthelial replaced 2-4 days
  • Good mucosal blood flow- if epithelium damaged rapid repair can occur
24
Q

What are the two types of gastric prostalandins and what are their effects?

A

PGE2 & PGI2

  • Potent vasodilators
  • Decrease acid secretion (at high levels)
  • Stimulate mucus and bicarb secretion in stomach
  • Reduce permeability of epithelium to backflow of acid
  • Reduce release of inflammatory mediators
  • Promote ulcer healing
25
Q

Explain how parietal cells change from non-secreting state to secreting states

A
  • Non-secreting state: Proton pumps are in membrane bound compartments (tubovesicles)
    • lack K+ permeability blocking H-K ATPase activity
    • Apical membrane of parietal cell has involutions called canaliculi - v. acidic, have K+ channels
  • Secreting state: tubulovesicles fuse with canalicular membrane
    • proton pumps move to a position where they can exchange H+ for K+
    • Requires a lot of energy
26
Q

Proton pump inhibitors are pro-drugs. Explain how they are activated

A
  • Activated by the acidic conditions of the parietal cell canaliculus
  • PPIs are weak bases so accumulate in the acidic space of secreteory canaliculi
    • Gives them a high concentration in the luminal surface of parietal cell
27
Q

Explain the MoA of proton pump inhibitors

A
  • Bind covalently to the gastric H+/K+ ATPase to irreversibly block function
  • Prolonged and nearly complete suppression of acid secretion
  • Have long effect- takes time for de novo synthesis to produce more enzyme
28
Q

What are some of the side effects of proton pump inhibitors?

A
  • Generally well tolerated
  • Headache, nausea, GI tract issues, abdo pain
  • May decrease effectiveness of clopidogrel (anti-platelet)
  • Increased risk of infections if used in hosptials
  • Leads to an increased production of gastrin due to parietal cell and ECL hyperplasia
29
Q

Explain how H2 receptor antagonists work

A
  • Competitively and reversibly inhibit the binding of histamine to H2 receptors on patietal cells
  • Indirectly block the effects of gastrin and ACh on the parietal cell
  • Activate PKA to change shape of parietal cell → create cannaliculi
30
Q

What are some of the side effects of H2 receptor antagonists?

A
  • Diarrhoea
  • Constipation
  • Musche ache and fatigue
31
Q

Why is the H2 receptor antagonists Cimetidine not used as frequently?

A
  • Inhibitis several Cytochrome P450s
  • Decreases metabolism of lidocaine, phenytoin theophylline and warfarin
  • Potentially results in toxic levels
32
Q

Give an example of prostaglandin analogue

A

Misoprostol

33
Q

Explain how misoprostol works

A
  • Prostaglandin analgoue
  • Acts on PGE2 affecting similar pathway to H2 RA
  • Eventually inhibits PKA so there is no conformational change of parietal cell
34
Q

What are some of the side effects and contraindications of misoprostol?

A

Side effect:

  • Diarrhoea
  • Abdominal pain
  • Often result in non-compliance

Contra-indicated:

  • Pregnant women
  • Causes uterine contractions
  • useful in post-partum haemorrhage
35
Q

How to antacids work?

A
  • Neutralise HCl in stomach
  • React with acid to form water and salt
36
Q

Name 2 commonly used antacid preparations

A

Alginic acid

Aluminium hydroxide

37
Q

What is step up vs step down therapy for treating GORD?

A

Step up: Start on H2 RA then progress to PPI if necessary

(more economical)

Step down: start on PPI and lower to H2 RA to see if they can maintain symptoms

Continuous PPI therapy is the most effective

38
Q

What properties of helicobacter pylori mean it thrives in the upper GI tract?

A
  • Microaerophillic (stomach has perfect amount of O2)
  • Has flagellae- allows movement through mucus layer
  • Can attach to gastric epithelia
  • Produces urease. Converts urea→ ammonia + CO2
39
Q

How does helicobacter pylori damage the gastric epithelium

A
  • Promotes strong immune response
  • Ammonium hydroxide is toxic to gastric epthelia
  • Produces endotoxins