therapeutic drug monitoring
TRANSCRIPT
Therapeutic drug Monitoring
What is therapeutic drug monitoring (TDM)?
Individualization of drug doses by maintaining plasma/blood drug concentrations within a target range---- therapeutic range therapeutic window.
Takes care of inter-individual variability.
Therapeutic Window
Therapeutic failure results when either the concentration is too low, ineffective therapy, or is too high, producing unacceptable toxicity. Between these limits of concentration lies a region associated with therapeutic success – regarded as a Therapeutic window.
Efficacy Toxicity
Drug concentration (log scale)
Res
pons
eWide therapeutic window
A B
Narrow therapeutic window
Efficacy Toxicity
Drug concentration (log Scale)
Res
pons
e
Major sources of Variability:
•Compliance
•Age- neonates, children, elderly
•Physiology- gender, pregnancy
•Disease- Hepatic, renal, cardiovascular, respiratory
•Drug interactions
•Environmental influences on drug metabolism
•Genetic polymorphisms
For which drugs is monitoring helpful?
•Marked pharmacokinetic variability
•Concentration related therapeutic and adverse effects
•Narrow therapeutic index
•Defined therapeutic (target) concentration range
•Desired therapeutic effect difficult to monitor
TDM useful in 2 major situations:
• Drugs used prophylactically to maintain absence of a condition--- seizures, cardiac arrhythmias. depressive/manic episodes, transplant rejection
• To avoid serious toxicity--- Aminoglycoside antibiotics
Sampling and drug analysis:
Plasma/ serum; cyclosporin- whole blood.
Timing: least variable point in dosing interval– predose/trough concentration.
Wait for steady state to be achieved---at least 5 half-lives. Exceptions are there! Drugs with long half-life.
HPLC, GLC, Immunoassays- sensitivity, specificity.
Information required for interpretation:
•Timing of sample in relation to last dose
•Duration of treatment in with current dose
•Age, gender
•Other drug therapy
•Relevant disease states
•Reason for TDM- lack of effect, routine monitoring, suspected toxicity.
Plasma protein binding:
Free drug vs total drug concentration.
Importance of plasma protein binding.
Remember that only total drug concentration is measured but only the free drug is active!
Drugs commonly monitored:Drug Therapeutic range (mg/L)Amiodarone 1.0-2.5Digoxin 0.5-2.1microgram/LQuinidine 2.0-5.0Theophylline 10-20Phenytoin 10-20Carbamazepine 5.0-12Sodium valproate 50-100Phenobarbitone 15-40Gentamicin peak>5, trough<2Amikacin peak>15, trough<5Vancomycin peak20-40, trough<10Lithium 0.6-1.2mmol/L
ESTIMATE INITIAL DOSE
Target Dose
Loading Dose
Maintenance Dose
BEGIN THERAPY
ASSESS THERAPY
Patient Response
Drug Level
REFINE DOSE ESTIMATE
ADJUST DOSE
Target concentration intervention
High Performance Liquid Chromatography