Target concentration intervention Flashcards
Why do the PK and PD vary?
Systematic/ predictably: body size, disease state, genotype
Random/ not predictable: between subject variability, within subject variability
What are the three ways we can dose?
Population: every one gets the same dose, most convenient
Group: Same dose for a similar group, e.g. same wight, CrCL, genotype
Individual: dose determined by an individuals response
What are the two reasons for TCI?
1) usefulness of a drug is hard to measure (the drug is working when the clinical outcome is not easily observable). Examples: anti-arrythmics, anti-convulsants
2) Big unpredictable variability.
TCI step 1
Choose target concentration
TCI step 2
Determine V and CL
estimates?
V: size and body composition
CL: size, renal + hepatic function
TCI step 3
Calculate LD(V) and maintenance dose (CL)
TCI step 4 and when?
Measure response.
TCI step 5
Measure conc. Goal is to estimate PK e.g CL
Take one sample typically (gentamicin 2), and take it during the middle of the dosing interval. (usually closer to the Css)
(gentamicin peak and trough) (The conc varies a lot over the day)
Therapeutic drug monitoring
Is imprecise, and sub-optimal at borders of the range. Drugs concentrations are measured, and if within the normal range it is okay. leads to if towards bottom of range, more likely to be ineffective or vice versa, toxic
TCI strong points
Is accurate and focuses on the individual. is accurate and focuses on the PK and PD principles to show how patients are different