wk 12-14 quiz Flashcards

1
Q

List good client communication skills and strategies

A

clear and concise, respectful, talk slowly, discuss important info without animal, go over entire prescription and demonstrate if necessary

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2
Q

pharmacokinetics

A

physiological movement of drugs within
the body and includes the mechanisms of drugs moving into, throughout, and out of the body

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3
Q

List the 4 steps of pharmacokinetics

A
  • Absorption
  • Distribution
  • Metabolism/ Biotransformation
  • Excretion
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4
Q

List 4 different mechanisms of drug transport across cell membranes

A
  • Passive diffusion
  • Facilitated diffusion
  • Active transport
  • Pinocytosis/Phagocytosis
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5
Q

passive diffusion

A

Movement of drug molecules from area of high concentration to an area of low concentration

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6
Q

facilitated diffusion

A

Uses carrier molecules within the cell membrane to passively carry drug molecules

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7
Q

active transport

A

Movement of drug molecules with a carrier molecule that pumps the molecule across a concentration gradient

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8
Q

pinocytosis/phagocytosis

A

Cell drinking/cell eating

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9
Q

List and briefly describe drug characteristics that affect absorption

A

 Solubility
 pH
 Molecule size
 Route of administration

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10
Q

List and briefly describe animal characteristics that affect absorption

A

 Age, Sex, Species
 Health status
 Metabolism and Genetics

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11
Q

bioavailability

A

The amount of given drug that is absorbed and reaches circulation

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12
Q

Describe the factors that affect bioavailability

A

 Route of administration
 Blood supply to the area the drug was given
 Surface area available for absorption
 Mechanism of drug absorption

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13
Q

Compare and contrast onset of action, duration of effect, and volumes given for each drug route of administration and how that can affect bioavailability

A

quicker onset = shorter duration of effect

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14
Q

distribution

A

Movement of drugs from the bloodstream to the target tissue or site of action

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15
Q

Describe how tissue perfusion affects drug distribution

A

 Amount of blood flow to an area
 Higher perfusion = quicker distribution
 Lower perfusion = slower distribution

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16
Q

Describe how membrane permeability affects drug distribution

A

Some larger molecules cannot easily pass through smaller vessels

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17
Q

Describe how protein binding affects drug distribution

A

If a drug binds to a larger protein in the blood, it may get stuck in the bloodstream and not able to leave the capillaries to be distributed

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18
Q

Define volume of distribution and list factors that can affect this

A

How well a drug is distributed; Concentration and volume of drug given can affect this; Can be affected by diseases with increased body fluid concentrations (ascites, edema, etc.) May need more drug

19
Q

List the primary site of Biotransformation and the name of the main enzyme association with this

A

liver; Cytochrome P450

20
Q

List the 4 main pathways of biotransformation

A

 Oxidation reactions
 Reduction reactions
 Hydrolysis
 Conjugation

21
Q

List the ways that drug interactions can occur during biotransformation

A

 Synergistically: Drugs given together will produce a greater individual response than if given separate
 Antagonistically: Drugs given together will produce a lessened individual response
 Altered absorption
 Competition for binding sites
 Altered excretion
 Altered metabolism

22
Q

Describe the main factors that affect biotransformation

A
  • plasma protein binding
  • storage in tissues and and fat depots
  • liver disease
  • age of patient
  • nutritional status of patient
  • species and individual variation
  • body temp
  • route of administration
23
Q

List the primary and secondary methods of drug elimination

A

kidney is primary; liver secondary

24
Q

List the lesser methods of drug elimination

A

Milk, saliva, lungs, sweat

25
Define how drug elimination is related to drug withdrawal times in food animals
Muscle, liver, kidney, milk, egg, etc. samples are taken and analyzed for drug residues when establishing withdrawal times depending on the use of the animal
26
List the 4 main factors affecting drug elimination
 Hydration status  Age  Health  Blood pressure
27
MEC
minimum effective concentration; minimum plasma drug level needed for the drug to work
28
MTC
minimum toxic concentration; plasma drug level where we first see toxic effects
29
Peak plasma levels
highest concentration of drug in the plasma after it is given
30
therapeutic range
drug concentration in the animal that produces the desired effect without toxicity
31
Loading dose
higher initial drug dose given to get the drug concentration up to the therapeutic range in a quicker amount of time
32
Maintenance dose
dose of drug that maintains the drug in the therapeutic range
33
Steady State
constant level of drug concentration in the plasma
34
Half- life
time required for the amount of drug in the body to be reduced by half its original level
35
ED50
effective dose 50; dose of a drug that causes the defined effect in 50% of animals that take it
36
LD50
lethal dose 50; dose of a drug that will kill 50% of animals that take it
37
Margin of safety
the difference between a drugs ed50 and ld50
38
Affinity
strength of binding between a drug and it’s receptor
39
Agonist
drug that binds to its receptor and causes an effect
40
Antagonist
drug that inhibits or blocks the response of a cell when the drug is bound to the receptor
41
Explain what a peak plasma level is and how the drugs plasma concentration affects this
when drug elimination rate equals absorption rate; increases with extent of absorption
42
Contrast peak plasma levels in drugs given via different routes of administration
intravenous reaches peak plasma levels fastest
43
Explain the difference between high and low affinity
A drug with a higher affinity for a receptor can compete with or displace another drug that binds the same receptor but has a lower affinity