Anesthetic Pharmacology 2 Flashcards
Pharmacokinetics of inahlation
Absoprtion phase - uptake
Metabolic - biotransformation
Excretion - elmination
NO and xenon are true gases but all others are vapors of volatile liquids
Volatile anesthetics
Exist in liquid form in ambient pressure and temp
Vapor pressure
If system is in closed container, will equilibrate between liquid and gas phases
Boiling point
Point at which VP exceeds atmospheric temp
How is anesthetic effect acheieved
Deliver a specific PP of agent to the brain
All phases are minimal relative to rate at which delivered or removed from the lungs
INhaled anesthetics transferred
From lungs to blood to brain…all pressures will equilibrate
Anesthetic inhalation…how do we control
Plasma and tissues havbe low capacity to absorb the inhaled relative to amount we can deliver to lungs…allows use ot rapidly change concentration in BS and brain
Anesthetic uptake
Rate of rise of partial pressure of the inhalational agfent at the alveolus (Fa/Fi) correlates best with onset
Blood gas sloubility best used to describe the speed of onset
Low blood gas solubility causes a fadster rise in Fa/Fi and induces faster anesthesia
Low, medium and high solubility
Low - desflurane, sevoflurane
Med - isoflurane
High - halothane
If you want to increase speed of induction
CHoose low solubility agent
Increase inspired ocncentration
Increase minute ventilation (hyperventilation)
How to induce a child
Mix sevoflurane and N2)
Turn dials to maximum
Crying baby helps speed up
Anesthesia termination
Biotransformation plays little role in termination of anesthesia
Halothane is major exception and up to 20% is biotransforemd in liver
Effects are primarily terminated by excretion (nearly exclusively throug hthe lungs)
Wakeup occurs when
PP of volatile agents drops below MAC(awake)
Depot
Amount of anesthetic abosrbed in fat once the vaporizer has been turned off and inspired concentration drops
Speedy wake up
Choose low blood/gas solubility agent
Low fat solubility
Increase minute ventilation