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
Q

Define how drug elimination is related to drug withdrawal times in food animals

A

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
Q

List the 4 main factors affecting drug elimination

A

 Hydration status
 Age
 Health
 Blood pressure

27
Q

MEC

A

minimum effective concentration; minimum plasma drug level needed for the drug to work

28
Q

MTC

A

minimum toxic concentration; plasma drug level where we first see toxic effects

29
Q

Peak plasma levels

A

highest concentration of drug in the plasma after it is given

30
Q

therapeutic range

A

drug concentration in the animal that produces the desired effect without toxicity

31
Q

Loading dose

A

higher initial drug dose given to get the drug concentration up to the therapeutic range in a quicker amount of time

32
Q

Maintenance dose

A

dose of drug that maintains the drug in the therapeutic range

33
Q

Steady State

A

constant level of drug concentration in the plasma

34
Q

Half- life

A

time required for the amount of drug in the body to be reduced by half its original level

35
Q

ED50

A

effective dose 50; dose of a drug that causes the defined effect in 50% of animals that take it

36
Q

LD50

A

lethal dose 50; dose of a drug that will kill 50% of animals that take it

37
Q

Margin of safety

A

the difference between a drugs ed50 and ld50

38
Q

Affinity

A

strength of binding between a drug and it’s receptor

39
Q

Agonist

A

drug that binds to its receptor and causes an effect

40
Q

Antagonist

A

drug that inhibits or blocks the response of a cell when the drug is bound to the receptor

41
Q

Explain what a peak plasma level is and how the drugs plasma concentration affects this

A

when drug elimination rate equals absorption rate; increases with extent of absorption

42
Q

Contrast peak plasma levels in drugs given via different routes of administration

A

intravenous reaches peak plasma levels fastest

43
Q

Explain the difference between high and low affinity

A

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