Clinical Pharmacokinetics Flashcards
what provides the basis for “usual dose”
population pharmacokinetics which are derived from averages of healthy adults +/- pediatric population
what to consider when giving the drug topically, transdermally, or subcutaneously
- thick vs thin skin
- intact vs impaired skin
- lipophilic vs hydrophilic drug
- skin temp
calcium levels and serum albumin
- reported calcium levels measure calcium bound to albumin, so decr albumin can result in falsely low calcium level (80% bound)
- hypercalcemia can occur if the level isn’t interpreted correctly
- ionized calcium=nonbound calcium
metabolism basics
how a medication is broken down to less active, more water soluble by products
phase I metabolism reactions
-reduction, oxidation, hydrolysis with Cyp450
phase II metabolism reactions
- conjugation
- glucuronidation, acetylation, sulfation
most drugs undergo _____ elimination
renal
can overestimate renal function if using actual creatinine level if….
hemodialysis can filter out hydro-_____ drugs of ____ molecular weight
hydrophillic; small
acute renal failure causes
- dehydration
- dye
- medications
chronic renal failure causes
-diabetes, hypertension, lupus, transplant
What four questions should you ask to individualize drug therapy?
1) what is the best route to enhance absorption?
2) Will the drug get to where I want it? (target site, perfusion, obese vs wasting, and edematous vs dehydrated)
3) assessment of hepatic and renal function
4) concomitant medications
PK variations in neonates
- immature skin has increased skin hydration— incr absorption of topical products
- incr extracellular fluid— incr Vd of water soluble drugs
- metabolic paths mature at different times
- GFR, tubular secretion, and reabsorption are immature at birth
PK variations in the elderly
- skin thinning =incr absorption of topical products
- incr adipose tissue = incr Vd of fat soluble drugs
- decr extracellular fluid — decr Vd of water soluble drugs
- age related changes in renal function = decr GFR
Therapeutic drug monitoring
- check drug levels to modify the dose based on your pt because originally, you prescribe a dose based on population pharmacokinetics
- you should make adjustments when the patient is at steady state
- assess the test drawn in relation to when it was drawn in relation to the administered dose and from where it was drawn
Drug interactions and ADME
- absorption: drug A affects Drug B, pH changes, and chelation
- Distribution: binding site competition (albumin) and disease state alterations in plasma proteins, fluid status, and adipose
- Metabolism: hepatic= Cyp450 enzymes= induction or inhibition
- Elimination: competition for pathways= mainly renal
types of interactions
- drug-drug: drug A incr/decr drug B, drug A causes toxic effect of Drug B, or incr adverse drug reactions
- drug-nutrient reaction: primarily oral and bioavailabilyt/efficacy/metabolism
- Drug-Disease state: drug may worsen disease state or disease stay could affect drug
- interactions can be intentional or unintentional