2. Applied Pharmacokinetics Flashcards

1
Q

If digoxin has a t1/2 of roughly 40hrs, how long does it take to reach a steady state in the body?

A

Roughly a week (3x40hrs - 5x40hrs = 5 - 8.3 days)

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2
Q

Does digoxin have a large or small Vd?

A

Large (~200L, or 7.5L/kg)

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3
Q

Where is digoxin predominantly excreted?

A

The kidneys

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4
Q

What does the long t1/2 mean for initiating treatment?

A

A loading dose is needed

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5
Q

What should happen if the pt on digoxin developes renal failure? Why?

A

Maintenance dose should be decreased, because clearance of the drug will be decreased.

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6
Q

What happens in the digitoxic patient?

A

Bradycardia, vomiting, xanthopsia

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7
Q

How should a digitoxic pt be treated?

A

Hydrate with IV fluids
O2
Discontinue drug
Give activated charcoal for GI tract symptoms

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8
Q

How much paracetamol is generally considered an overdose?

A

~10g

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9
Q

How many pathways is paracetamol usually metabolised via?

A

3

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10
Q

How is 60% of paracetamol usually metabolised?

A

Conjugation with glutathione -> Glucoronide

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11
Q

How is 30% of paracetamol usually metabolised?

A

Conjugation -> Paracetamol sulphate

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12
Q

How is 10% of paracetamol usually metaolised?

A

P450 oxidation -> NAPQI, then conjugated with glutathione -> inactive metabolite

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13
Q

What is depleted in paracetamol overdose?

A

Glutathione

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14
Q

What is the significance of glutathione depletion in paracetamol overdose?

A

NAPQI buildup to toxic levels

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15
Q

How is paracetamol overdose treated?

A
Take blood paracetamol levels 4hrs after the initial overdose.
Activated charcoal (to reduce utake in GI tract)
N-acetlycysteine to replenish glutathione
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16
Q

How is loading dose calculated?

A

LD = Vd x target [Drug]

17
Q

How is target [Drug] calculated?

A

Usually by weight of pt

18
Q

What else should be taken into account when formulating loading dose?

A
  1. Drug formulation eg salt formation

2. Upper limit of LD regardless of weight