Induction Agent - Propofol Flashcards
What is the typical induction dose range of Propofol for adults?
A. 1-1.5 mg/kg
B. 2-2.5 mg/kg
C. 2.5-3.5 mg/kg
D. 3-4 mg/kg
B. 2-2.5 mg/kg
For pediatric patients, what is the recommended intravenous induction dose range of Propofol?
A. 1-2 mg/kg
B. 2-2.5 mg/kg
C. 2.5-3.5 mg/kg
D. 3.5-4.5 mg/kg
C. 2.5-3.5 mg/kg
What is the range of Propofol infusion doses for** sedation** in micrograms per kilogram per minute (mcg/kg/min)?
A. 10-50 mcg/kg/min
B. 15-60 mcg/kg/min
C. 25-75 mcg/kg/min
D. 50-100 mcg/kg/min
C. 25-75 mcg/kg/min
What is the infusion dose range for Propofol when used for general anesthesia (GA)?
A. 25-50 mcg/kg/min
B. 50-100 mcg/kg/min
C. 100-200 mcg/kg/min
D. 200-300 mcg/kg/min
C. 100-200 mcg/kg/min
What is the concentration of Propofol typically provided in its injectable form?
A. 1 mg/mL
B. 5 mg/mL
C. 10 mg/mL
D. 20 mg/mL
10 mg/mL
What is the primary mechanism of action (MOA) of Propofol?
A. NMDA receptor antagonist
B. GABAA receptor agonist
C. Dopamine receptor antagonist
D. Serotonin reuptake inhibitor
B. GABAA receptor agonist
How does Propofol’s activation of the GABAA receptor affect postsynaptic neurons?
A. Increases calcium conductance
B. Increases sodium conductance
C. Increases chloride conductance
D. Increases potassium conductance
C. Increases chloride conductance
What is the onset time of Propofol when administered intravenously?
A. 10 seconds
B. 30 seconds
C. 1-2 minutes
D. 3-5 minutes
B. 30 seconds
What is the typical duration of action for Propofol?
A. 1-3 minutes
B. 5-10 minutes
C. 15-20 minutes
D. 30 minutes
B. 5-10 minutes
What causes Propofol’s rapid onset and short duration of action?
A. Rapid metabolism in the liver
B. Uptake into the brain and redistribution to fat/muscle
C. Renal excretion
D. Slow absorption into the bloodstream
B. Uptake into the brain and redistribution to fat/muscle
not d/t metabolism!
What is the effect of Propofol on chloride conductance in postsynaptic neurons?
A. It decreases chloride conductance
B. It increases chloride conductance
C. It has no effect on chloride conductance
D. It blocks chloride channels
B. It increases chloride conductance
What is the typical elimination half-life of Propofol?
A. 0.1-0.5 hours
B. 0.5-1.5 hours
C. 1-3 hours
D. 3-5 hours
B. 0.5-1.5 hours
What is the context-sensitive half-time of Propofol?
A. About 5 minutes for every 1 hour infused
B. About 10 minutes for every 1 hour infused
C. About 15 minutes for every 2 hours infused
D. About 30 minutes for every 2 hours infused
C. About 15 minutes for every 2 hours infused
Which factor is the primary mechanism for Propofol’s clearance from plasma?
A. Renal excretion
B. Hepatic metabolism
C. Pulmonary uptake
D. Plasma protein binding
C. Pulmonary uptake
Clearance from plasma (pulmonary uptake) > hepatic blood flow (CYP)
How is Propofol eliminated from the body?
A. As active compounds via the liver
B. As inactive water-soluble compounds via the kidneys
C. Through unchanged excretion in the bile
D. Through biotransformation in the plasma
B. As inactive water-soluble compounds via the kidneys