1/15
Dr. Johnson - Exam 2
Name | Mastery | Learn | Test | Matching | Spaced | Call with Kai |
|---|
No analytics yet
Send a link to your students to track their progress
What are the advantages of inhalant anesthetics?
predictable & rapid adjustment of effect (better control)
part of a complete delivery system
precision vaporizer (simple), O2 source, control of ventilation, CO2 removal
inexpensive after initial investment
What are the disadvantages of inhalant anesthetics?
naroow therapeutic index (2-4)
expensive initial investment
don’t block nociceptive input → hyperalgesia
side effects → cardiovascular, respiratory
What is the primary advantage of isoflurane over sevoflurane?
less expensive (sevo 10x more $$)
What is the primary advantage of of sevoflurane over isoflurane?
less soluble
Both isoflurane and sevoflurane are administered as what?
both are stored as a liquid and administered in a gaseous state
Why does an inhalant anesthetic with a high vapor pressure poses a risk to a patient?
can very rapidly administer a lethal dose to the patient
What is the clinically useful way to record the amount of inhalant being administered to a patient?
volume % = concentration of one gas in a mixture
administer anesthetic then observe to decide clinical effect
What is partial pressure?
the pressure exerted by one gas in a mixture of gases if occupying the space alone
What controls the clinical effect of inhalants on the patient?
partial pressure in the brain
How do changes in partial pressure can affect inhalant anesthetics & what is the clinical application?
lower partial pressure in the brain = less likely to be unconscious
anesthestic vaporizer setting IS NOT CHANGING
ex 1: surgery on top of a mountain = lower atm pressure = lower partial pressure
ex 2: surgery at sea level = higher atm pressure = higher partial pressure
What clinical property is dictated by the blood:gas solubility?
determines induction and recovery time!
What are the predicted clinical effects between 2 inhalants based on blood:gas partition coefficients (PC)?
more soluble = slower induction & recovery
ex 1: Sevo PC = 0.6 → less soluble = fast induction/recovery
ex 2: Iso PC = 1.4 → more soluble = slow induction/recovery
If given PC of 2 inhalants in relation to the blood:gas partition, what can you calculate?
how much time it takes to absorb (rate of induction/recovery)
What clinical property is predicted by the oil:gas solubility?
determines potency
What are the predicted clinical effects between 2 inhalants based on oil:gas partition coefficients (PC)?
more lipid soluble = more potent = less concentration required for clinical effect
*ex 1: Sevo PC = 50 → less potent = great conc. of drug required
ex 2: Iso PC = 99 → more potent = less conc of drug required
If given PC of 2 inhalants in relation to the oil:gas partition, what can you calculate?
concentration required to see clinical effect