GI mc3 Flashcards

1
Q

lithium is the treatment of choice in

A

acute mania and in prophylaxis of manic depression

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2
Q

lithium and toxicity outcome

A

producing dose-dependent and dose-independent side effects

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3
Q

how is lithium distributed

A

unevenly, -0.7L/kg volume distribution

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4
Q

Volume distribution

A

the theoretical volume that would be necessary to contain the total amount of an administered drug at the same concentration that is observed in the blood plasma.

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5
Q

lithium distribution model

A

two-compartment model

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6
Q

lithium distriibution time

A

8 hours

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7
Q

lithiu half life

A

20-24 hours

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8
Q

how long does it take lithium to reach a steady state

A

5-6 days

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9
Q

how many half lives does it take lithium to reach steady state

A

5

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10
Q

digoxin half life

A

36

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11
Q

digoxin reaches steady state in how many days

A

5-7

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12
Q

why do a loading dose

A

steady state plasma concentration must be reached more rapidly

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13
Q

how do you do a loading dose

A

big dose on the innitiation of treatment

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14
Q

Volume of distribution of digoxin =

A

7.3 L/kg

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15
Q

what does Volume of distribution of digoxin suggest

A

widely distributed outside the water compartment and is also protein bound or distributed by some other tissue type

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16
Q

what places does digoxin have a high affinity for

A

skeletal and cardiac muscles, intestines and kidneys

17
Q

what should digoxin dosing be based on

A

estimated lean body mass

18
Q

where are lipid soluble drugs stored

A

fat

19
Q

which drugs have a high volume of distribution

A

drugs that accumulate in organs either by active transport or by specific binding to tissue molecules

20
Q

what drugs is bone a resevoir for

A

tetracycline and heavy metals

21
Q

where is digoxin excreted

A

Most digoxin is eliminated unchanged by the kidneys

22
Q

patients w renal impairment and digoxin vod

A

vod reduced

23
Q

what mediates tubular digoxin secretion

A

p-glycoprotein

24
Q

what can inhibit p-glycoprotein

A

spironolactone, quinidine, verapamil and amiodarone

25
Q

renal failure affect on clearance of digoxin

A

decreases

26
Q

where can digoxin be metabolised

A

tiny bit in the liver

8% undergoes an enterohepatic cycle.

27
Q

is dogoxin absorbed in the gut

A

ye but poorly

28
Q

oral bioavailability of digoxin level

A

high

29
Q

Bioavailability

A

fraction of a dose of drug that is absorbed from its site of administration and reaches in an unchanged from the systemic circulation.

30
Q

what happens to digoxin in the gut

A

metabolised

31
Q

how is digoxin metablised in the gut

A

hydrolysed by acid in stomach

bacteria in the intestines

32
Q

what does the bioavailability of a drug depend on

A

absorption across the intestinal wall.
Decomposition of the drug in the lumen.
pH and perfusion of the small intestine.
Surface and time available for absorption.
Competing reactions in the lumen (for example of the drug with food).
Hepatic first-pass effect.

33
Q

whats more bioavailable liquid digoxin or tablet

A

liquid