therapeutic drug monitoring Flashcards

1
Q

what is TDM

A

measure [drug] and [metabolites] to investigate the dosing to specific patients

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2
Q

when to perform TDM (4 reasons)

A
  1. low/narrow therapeutic range
  2. low patient compliance with drugs
  3. symptoms and toxicity of drug is hard to distinguish
  4. has pharmacokinetic variability
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3
Q

what pharmocokinetic variability can be measured by TDM

A
  1. inter-individual
  2. non-linear order drug kinetics
  3. drug-drug interactions
  4. physiological conditions (e.g. pregnancy) or underlying diseases
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4
Q

specimens for TDM

A
  1. serum/plasma
  2. EDTA-whole blood
  3. urine
  4. saliva/oral fluid
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5
Q

TDM measurements

A
  1. trough levels, prior to next dose to evaluate therapeutic effect
  2. peak levels at varying times to avoid toxic risks
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6
Q

methotrexate is monitored because

A

toxicity is common in high dose therapy
immune suppression, renal failure, myelosuppression, liver toxicity, neurological toxicity, GI toxicity, death

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7
Q

digoxin (heart failure drug) monitored because

A

low therapeutic index
GI distress, confusion, visual impairment, hyperkalemia, cardiac toxicity

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8
Q

phenytoin (anticonvulsant) monitored for

A

non-linear kinetics and inter-individual ability
ataxia, tremor, lethargy, seizure exacerbation, neuropsychiatric changes

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9
Q

lithium (bipolar disorder)

A

narrow therapeutic index, wide inter-individual variations
lethargy, weakness, slurred speech, ataxia, tremor, myoclonic jerks

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10
Q

aspirin monitored for

A

likely to overdose
nausea, vomiting, increased respiratory rate (alkalosis)

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11
Q

respiratory acidosis

A
  1. increased CO2
  2. unable to remove via respiration
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12
Q

metabolic acidosis

A
  1. increased acid
  2. kidney unable to clear
  3. underlying: diabetes, lactic acidosis, aspirin toxicity, dehydration
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13
Q

respiratory alkalosis

A
  1. decreased CO2
  2. hyperventillation, lack O2, high alttitude, aspirin poisoning
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