Lecture 8 - PRINCIPLES OF PHARMACOTHERAPEUTICS Flashcards
What happens to the plasma concentration during repeated administration?
If a drug that is eliminated by first-order kinetics, is administered repeatedly, the average plasma concentration of the drug will increase until a mean steady-state level is reached.
When is the different levels of steady state achived?
- Levels will be at the high point of the steady state range shortly after a dose is administered.
- Levels will be at the low point immediately before administration of the next dose.
How is the mean of plasma concentration during steady state?
The mean of plasma concentration during steady-state (Cpss) is 1.44 times higher then the Cmax after the first application.
When is a large loading dose needed?
-A large loading dose may be needed initially when the therapeutic concentration of a drug in the plasma must be achieved rapidly.
What is the :Maintenance dose rate?
-Maintenance dose rate is the dose of a drug required per unit time to maintain the wanted steady-state level in the plasma to sustain a specific therapeutic effect.
How can the magnitude of fluctuations (shifts/changes) at the steady state can be controlled?
- The magnitude of fluctuations can be controlled by the dosing interval.
- A shorter dosing interval decreases fluctuations, and a longer dosing interval increases them.
What can may hurt the steady-state level?
Too long intervals between application of doses may hurt the steady-state level.
How do you calculate the loading dose?
- To calculate the loading dose, select the desired plasma concentration of drug and multiply by the Vd.
- After administration of the loading dose , one administers the drug at the maintenance dose rate to maintain the drug concentration at the desired steady-state level.
To remain at steady state, the dose rate must equal the ….
To remain at steady state, the dose rate must equal the elimination rate; that is, the rate at which the drug is added to the body must equal the rate at which it is eliminated.
elimination rate = Cl × Drugplasma.