Therapeutic drug monitoring Flashcards

1
Q

What are the 4 main principles of pharmacokinetics

A
  1. Absorption
  2. Distribution
  3. Metabolism
  4. Excretion
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What are the 6 factors that affect the pharmokinetics of a drug

A
  1. Age
  2. Weight
  3. Sex
  4. Genetrics
  5. Diseases
  6. Drug interactions
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is pharmacokinetics

A

studies how drugs move through the body, covering four primary processes: absorption, distribution, metabolism, and excretion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What is the MEC

A

Minimum Effective Concentration: This is the minimum concentration of the drug above which therapeutic value of the drug is seen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What is the MTC

A

Minimum Toxic Concentration: upper concentration above which the rate and severity of adverse effects become
unacceptable

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What could be the 4 possible causes of a lower than expected conc. of a drug in a patient

A
  1. Incorrect dose given to the patient
  2. Patient is non adherent to the patient
  3. Rapid elimination of the drug
  4. Time when the sample was taken is incorrect
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What are the possible causes of a higher than normal conc. of the drug 4

A
  1. Error in the dose regimen
  2. Decreased renal or hepatic function
  3. Timing of the sampling
  4. No response despite therapeutic conc. [tolerance]
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

When can you safely say that you have reached the steady state

A

This occurs after at least 5 half lives after the last dose change

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is therapeutic drug monitoring

A

Measurement of drug concentration in the body fluids

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Why is it important to do TDM 4

A
  1. Avoid toxicity
  2. Optimize the dose of the drug
  3. Detect any changes in pharmacokinetics
  4. Monitor adherence to the drugs
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What are the 6 main factors that influence pharmacokinetics

A
  1. Age
  2. Weight
  3. Sex
  4. Genetics
  5. Disease
  6. Drug interaction
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Which drugs are suitable for TDM 4

A
  1. High interpatient variability in the plasma concentration
  2. Narrow therapeutic range
  3. When there is a high correlation between the plasma conc. and then clinical effect
  4. There is availability and it is cost effective
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What are the factors related to a patient that indicate TDM 3

A
  1. Lack of a clinical response
  2. To monitor the adherence to drugs
  3. Suspected toxicity
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What are the co morbidities that would indicate TDM in patients 3

A
  1. Drug- drug interactions
  2. Renal and hepatic disease
  3. GIT issues that could result in decreased absorption
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What are the possible causes of lower concentrations than what is expected

A
  1. Incorrect dose was given
  2. Patient is non adherent
  3. Rapid elimination of the drug is present [Induction, genetics, increased renal excretion]
  4. Timing of the sample was taken at the incorrect time
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What are the causes of higher than normal concentration

A
  1. Error in the dose regimen
  2. There is a decrease in renal and hepatic function
  3. Slowed elimination
  4. Timing of the sampling is incorrect
17
Q

When is the steady state achieved

A

At least 5 half lives after the last dose change

18
Q

What is zero order kinetics

A

The body eliminates a fixed amount of the drug per unit of time. The elimination is linear irrespective of the conc. of the drug

19
Q

What is first order kinetics

A

This is where the rate of elimination is proportional to the drug conc..Elimination is exponential on a concentration vs. time graph.

20
Q

What is meant by a Capacity-saturable metabolism

A

This is where the drug elimination become saturated at higher drug concentrations and so there is a transition from a first order