Variability in drug response
[RD5:p712-p723]
- Types of variability
* Pharmacokinetics
* Pharmadynamic
* Idiosyncratic
- Main causes of variability
* Ethnicity
* Age
* Pregnancy
* Genetic factors
* Idiosyncratic reactions
* Disease
* Drug interaction
Ethnicity
[RD5:p712]
Examples in ethnic differences:
Ethanol
- Chinese metabolise ethanol differently
--> Higher plasma concentration of acetaldehyde
--> Flushing and palpitation
Propranolol
- Chinese are more sensitive to CVS effects of propranolol than Caucasians
* But metabolise propranolol faster than Caucasians
--> Pharmacodynamic reasons for the sensitivity
- Afro-Caribbean individuals are less sensitive
Age
[RD5:p713-p714]
- Main reason: Drug elimination is less efficient in neonates and in elderly
- Other factors:
* Pharmacodynamic sensitivity
* Physiological factors (e.g. CVS reflexes)
* Pathological factors (e.g. CVS diseases)
* Body composition
* Concurrent drug administration
Effect of age on renal excretion
Paediatrics
- GFR in the newborn is about 20% of adult value
- Tubular function in the newborn is also reduced
- In term babies, renal function increases to adult values in less than a week
--> Continues to increase up to double the adult values at 6 months of age
* [RD5:p713]
- Increase in renal function occurs slowly in premature babies
Example:
- Gentamicin
* Halflife > 18 hours in premature babies
* Halflife = 10 hours in term babies
* Halflife = 1-4 hours in adults
Elderly
- GFR declines slowly from 20 years of age
* Falling by 25% at 50 years old
* Falling by 50% at 75 years old
- Plasma creatinine level may remain normal
* Creatinine synthesise is reduced in elderly due to reduced muscle mass
Example:
- Chronic administration of digoxin may lead to progressive increase in plasma concentration
--> A common cause of glycoside toxicity in the elderly
===
Placental transfer of drugs increases in late pregnancy
[MCQ, Wood and Wood apparently is the source]
Lipid soluble drugs cross placenta with increasing difficulty up to 1000 Da [BGK9:p1025]