Clinical Pharmacokinetics Flashcards

1
Q

what provides the basis for “usual dose”

A

population pharmacokinetics which are derived from averages of healthy adults +/- pediatric population

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2
Q

what to consider when giving the drug topically, transdermally, or subcutaneously

A
  • thick vs thin skin
  • intact vs impaired skin
  • lipophilic vs hydrophilic drug
  • skin temp
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3
Q

calcium levels and serum albumin

A
  • 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
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4
Q

metabolism basics

A

how a medication is broken down to less active, more water soluble by products

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5
Q

phase I metabolism reactions

A

-reduction, oxidation, hydrolysis with Cyp450

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6
Q

phase II metabolism reactions

A
  • conjugation

- glucuronidation, acetylation, sulfation

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7
Q

most drugs undergo _____ elimination

A

renal

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8
Q

can overestimate renal function if using actual creatinine level if….

A
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9
Q

hemodialysis can filter out hydro-_____ drugs of ____ molecular weight

A

hydrophillic; small

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10
Q

acute renal failure causes

A
  • dehydration
  • dye
  • medications
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11
Q

chronic renal failure causes

A

-diabetes, hypertension, lupus, transplant

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12
Q

What four questions should you ask to individualize drug therapy?

A

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

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13
Q

PK variations in neonates

A
  • 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
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14
Q

PK variations in the elderly

A
  • 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
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15
Q

Therapeutic drug monitoring

A
  • 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
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16
Q

Drug interactions and ADME

A
  • 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
17
Q

types of interactions

A
  • 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