L.17 Immunoassay Applications Flashcards
What is Therapeutic Drug Monitoring (TDM)?
The clinical practice of measuring specific drugs at designated intervals to maintain a constant concentration in a patient’s bloodstream
What is the primary goal of TDM?
To optimize individual dosage regimens
How is drug therapy usually monitored?
Clinically, by assessing if the patient is getting better
For which types of drugs is TDM commonly carried out?
Drugs with a narrow benefit-to-risk ratio and/or a narrow therapeutic range
What is the therapeutic window?
The range of drug concentrations in the blood that produces the desired effect without causing toxicity
Is the therapeutic window fixed?
No, it can change with time, age, disease state, etc.
When is TDM required? (1)
When dose regimen at start of therapy needs establishing/optimising
When is TDM required? (2)
In cases of polypharmacy (multiple drugs) due to drug-drug interactions
When is TDM required? (3)
In renal-/hepatic impairment due to altered pharmacokinetics
When is TDM required? (4)
When there is non-compliance, meaning the patient is not taking the drug as prescribed
When is TDM required? (5)
In cases of toxicity, especially when adverse drug reactions (ADRs) resemble the disease being treated
When is TDM required? (6)
When there is a narrow therapeutic range
When is TDM required? (7)
When the drug itself can alter hepatic or renal function (e.g. gentamicin)
What does ADME stand for in pharmacokinetics?
Absorption, Distribution, Metabolism, Excretion
ADME represents the four key processes that affect the pharmacokinetics of a drug.
Define absorption in the context of pharmacokinetics.
The process by which a drug enters the bloodstream.
Absorption is crucial for determining the onset of a drug’s effects.
What is distribution in pharmacokinetics?
The dissemination of substances throughout the fluids and tissues of the body.
Distribution is influenced by factors such as drug solubility and blood flow.
What factors affect the distribution of a drug?
- Drug’s solubility
- Binding to plasma proteins
- Blood flow to tissues
These factors determine how well a drug spreads in the body.
Define metabolism in pharmacokinetics.
The process by which the body breaks down medication into active chemical substances.
Metabolism often occurs in the liver and affects drug efficacy.
What does excretion refer to in pharmacokinetics?
The process of eliminating drugs from the body (urine or feces).
Excretion is key for clearing drugs from the system and preventing toxicity.
What is TDM in pharmacokinetics?
Therapeutic Drug Monitoring.
TDM helps ensure drug levels remain within a therapeutic range.
What is peak concentration?
The highest concentration of a drug in the bloodstream after administration.
Monitoring peak concentration is important to avoid toxicity.
What is trough concentration?
The lowest concentration of a drug in the bloodstream before the next dose is administered.
Ensuring adequate trough concentration is vital for therapeutic effects.
What is Gentamicin?
An aminoglycoside antibiotic used to treat serious infections caused by Gram-negative bacteria.
Gentamicin is effective against specific bacterial infections.
Name two other aminoglycosides used in TDM.
- Amikacin
- Tobramycin
These antibiotics are monitored similarly to Gentamicin.