1/268
Looks like no tags are added yet.
Name | Mastery | Learn | Test | Matching | Spaced | Call with Kai |
|---|
No analytics yet
Send a link to your students to track their progress
anesthetic agent
any drug used to induce a loss of sensation with/without unconciousness
adjunct
drugs that are not true anesthetics (used during anesthesia to produced other desired effects), used as part of BALANCED anesthesia
sedation, muscle relaxation, analgesia, reversal, neuromuscular blockade, parasympathetic blockade
list 7 effects that adjuncts can provide
route of administration, time of administration, principle effect, chemistry
list four classifications of anesthetic agents and adjuncts
not true analgesics
most commonly used general anesthesia have little to no pain control:
halogenated inhalent agents (iso, sevo), propofol
list two examples of general anesthesia we may use
true analgesics
general anesthesia must be accompanied by administration of ___ ___ if pain control is necessary
opioids, alpha-2 agonists, dissociatives
list 3 examples of true anesthetics we can use if pain control is necessary
calm/sedate fractious animal, minimize adverse effects, reduce required dose of concurrent drugs, smoother induction, decrease pain, muscle relaxation
list 6 reasons we would use preanesthetic medications
SQ
slow onset, long duration
IM
faster onset, shorter duration
IV
fastest onset, shortest duration, dose usually ½ the dose of SQ/IM
PO/OTM
slowest onset, longest duration, rarely used, given to patients too aggressive to be handled
intramuscular
which route of administration is most common to balance onset of time/duration
water -soluble
most anesthetic agents and adjuncts are ___-___
diazepam, propofol
what two drugs are NOT water-soluble?
diazepam with ketamine
what two drugs can be mixed even though only one of them is water-soluble?
agonist
drug that binds to and stimulates tissue receptors (what most anesthetic agents and adjuncts are!)
antagonist
drug that competitively binds to target receptors and displace corresponding agonist, blocking further action (Reversal agents!)
partial agonist (opioid)
drug that binds to and partially stimulates tissue receptors
agonist-antagonist (opiods)
drug that binds to more than one receptor type and simultaneously stimulate at least one and block at least one
parasympatholytic drug
drugs that prevent and treat bradycardia (decreases salivary secretions
atropine, glycopyrrolate
list two examples of anticholinergics
atropine
faster onset, shorter peak, shorter duration anticholinergic
glycopyrrolate
slower onset, longer peak, longer duration anticholinergic
atropine, glycopyrrolate
these two drugs will NOT work well in hypothermic patients
5 minutes
onset of action of atropine via IM
1 minute
onset of action of atropine via IV
30-45 minutes
onset of action of glycopyrrolate via IM
up to 5 minutes
onset of action of glycopyrrolate via IV
60-90 minutes
duration of action of atropine via IM
30 minutes
duration of action of atropine via IV
60-90 minutes
duration of action of glycopyrrolate via IM
up to 1 hour
duration of action of glycopyrrolate via IV
central nervouse system
anticholinergics have little impact and is NOT a sedative on this region of body
cardiovascular system
anticholinergics help prevent and treat bradycardia in this region of body, may treat hypotension, and may induce temporary cardiac arrhythmias
respiratory system
anticholinergics help reduction and thickening of respiratory secretions in this region of body
GI motility, secretions
anticholinergics help reduce ___ ___ and salivary/lacrimal ___ (this is why we keep eyes lubricated!)
intestinal peristalsis inhibition
anticholinergics may lead to colic in horses of bloat in ruminants (___ ___ ___)
tranquilizer
drug group that reduces anxiety, does not decrease awareness or wakefulness
sedative
drug group that reduces mental awareness, causes sleepiness
pre-anesthetic period
tranquilizers and sedatives are terms often used interchangeably and are commonly used in ___-anesthetic period
phenothiazines, benzos, alpha 2-agonist
list 3 drug classes that are commonly used for sedation/tranquility
acepromazine
drug example of phenothiazines
no
is acepromazine controlled?
pre-anesthetic/tranquilizer
acepromazine is a ___-anesthetic and a ____
decrease
acepromazine helps ___ dose of general anesthesia needed
opiods
acepromazine may be used with ___ for minor procedures
IV, IM, PO
acepromazine can be administered via these 3 routes:
no antagonist agent
acepromazine has no ___ agent
liver
acepromazine is metabolized by the ___
placenta
acepromazine can slowly cross the ___
yellow
acepromazine is commonly this distinct color:
calming, sedation, reluctant movement, decreased interest
list 4 effects that acepromazine can have on the central nervous system
no
is acepromazine an analgesic?
peripheral vasodilation
to cause hypotension and hypothermia
peripheral vasodilation, antiarrhythmic efffect
list two effects that acepromazine has on cardiovascular system
up to 30 minutes
onset of action of acepromazine via IM
5-15 minutes
onset of action of acepromazine via IV
45-60 minutes
peak effect of acepromazine via IM
30-45 minutes
peak effect of acepromazine via IV
4-8 hours
duration of action of acepromazine via IM or IV for dogs
1-3 hours
duration of action of acepromazine via IV or IM for horses
respiratory system
acepromazine has no significant affect to this body system
antiemetic
acepromazine causes this effect to the GI system
antihistamine effect
acepromazine has a ___ effect; prevents histamine release (decreases allergic response)
allergey-testing patients
acepromazine should be avoided in these types of patients
penile prolapse
acepromazine can cause ___ ___ in horses and other large animals, and is best to avoid using this in breeding stallions
decreased PCV
acepromazine causes decreased ___ in horses and dogs. it drops within 30 minutes
bradycardia and hypotension
acepromazine can cause these two effects in giant breeds
increased excitement
acepromazine causes this main effect in boxers
terriers
this breed of dog is commonly resistant to acepromazine
neonates, geriatrics, liver/cardiac dysfunction, debilitated patient
acepromazine can have increased potency/duration in these 4 types of special patients:
vein
ensure IV injections of acepromazine in horses enter the ___
severe CNS excitement/depression, seizure, death
what are 3 things that can happen if we give acepromazine in the artery of a horse?
midazolam, diazepam, zolazepam
list 3 examples of benzodiazepines
benzodiazepines
drug class that is controlled, reversible, and often used with other agents for their muscle relaxant and anticonvulsant properties
young, healthy patients
benzos can have unpredictable sedation for ___,___ patients causing dysphoria, excitement, or ataxia
15 minutes or less
onset of action of benzos via IM
1-3 minutes
onset of action of benzos via IV
15-30 minutes
peak effect of benzos via IM
5-20 minutes
peak effect of benzos via IV
1-2 hours
duration of action of benzos via IM
1-4 hours
duration of action of benzos via IV
midazolam, diazepam
two most commonly used benzos in vet anesthesia
anticonvulsent
midazolam or diazepam commonly used for its ___ effects
light sensitive
midazolam and diazepam are ___ sensitive
flumazenil
the antagonist for midazolam and diazepam
midazolam
this benzo is water-soluble, can be given IV or IM, faster onset of action, and shorter duration of action
diazepam
this benzo is NOT water-soluble, hurts via IM, slower onset of action, longer duration of action
viscid
painful with IM injection
antianxiety and calming
benzos cause ___ and ___ effecrts only in old or ill animals
disorientation and excitment
benzos cause ___ and ___ in young, healthy animals
dysphoria and aggression
benzos cause ___ and ___ in cats
involuntary muscle twitching
benzos cause ___ ___ ___ in horses
ataxia or recumbent
benzos cause ___ or ___ in large animals
minimal, high
benzos have ___ effect and ___ margin of safety on the cardiovascular and respiratory systems
slowly IV
diazepam must be given ___ IV
dexmedetomidine, xylazine
list two examples of alpha 2-agonists
alpha 2-agonist
this drug class is uncontrolled, reversible, and decreases sympathetic nervous system causing sedation, analgesia, and muscle relaxation