Toxic Drug Monitoring

DEFINITION OF TERMS:

  • Pharmacodynamics: what the drugs do to the body
  • Pharmacokinetics: what the body does to the drug (biotransformation, distribution, metabolism and elimination)
  • First pass metabolism: drugs enter the hepatic route first before entering the general circulation
  • Half-life: time needed for a drug’s concentration in serum to decrease into
    half
  • Peak specimen: collection of this is done 30-60 mins after the administration of drug
  • Trough specimen: this is collected before administration of the succeeding dose
CLASSIFICATION OF DRUGS REPRESENTATIVE DRUGS
Antibiotics Aminoglycosides, chloramphenicol, vancomycin
Anticonvulsants Ethosuximide, Carbamazepine, Phenytoin,
Phenobarbital, Valproic acid
Antidepressants Lithium, Fluoxetine and tricyclic antidepressants
Anti
inflammatory/analgesics
Aspirin, acetaminophen
Anti-neoplastic Busulfan, methotrexate
Bronchodilators Theohylline
Cardioactive Digoxin, Procainamide, Lidocaine, Propanolol,
Quinidine
Immunosuppressives Tacrolimus (FK-506), Prednisone, Cyclosporine

GOOD TO KNOW FOR THE DRUGS:

  • Aspirin: drug that inhibits cyclooxygenase
  • Acetaminophen: hepatotoxic drug
  • Lithium: for treatment of bipolar disorder or manic depression
  • Phenobarbital: used for treatment of grand-mal
  • Valproic acid: for treatment of petit mal
  • Vancomycin: cause of red man syndrome
CONVERSION FACTORS
ANALYTES CONVENTIONAL UNITS TO SI UNITS CONVERSION
FACTOR
ALBUMINg/dL to g/L

10
PHOSPHOLIPID 0.01
TOTAL PROTEIN 10
AMMONIA μg/dL to μmol/L 0.587
THYROXINE μg/dL to nmol/L 12.9
BICARBONATEmEq/L to mmol/L

1.0
CHLORIDE 1.0
MAGNESIUM 0.5
POTASSIUM 1.0
SODIUM 1.0
LITHIUM mEq/L to μmol/L 1.0
BUNmg/dL to mmol/L

0.357
CALCIUM 0.25
CHOLESTEROL 0.026
GLUCOSE 0.0555
PHOSPHORUS 0.323
TRIGLYCERIDE 0.0113
URIC ACID 0.0595
BILIRUBINmg/dL to μmol/L


17.1
CREATININE 88.4
IRON 0.179
pCO2 mm/Hg to kPa

0.133
pO2 0.133