Injectable induction agents Flashcards

1
Q

propofol

A

it’s its own class
ultra short-acting (nonbarbiturate)
wide dosing margin
can use for induction and total IV anesthesia
also used for uncontrolled seizures
can be used CRI

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2
Q

propofol solubility

A

minimally water soluble

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3
Q

what is in propofol?

A

can be egg, glycerin, or soy based
base makes it not bacteriostatic

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4
Q

propofol appearance

A

milky appearance

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5
Q

propofol storage

A

once open lasts 6-24 hours refrigerated

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6
Q

propofol mode of action

A

appears to affect GABA receptors

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7
Q

propofol onset, duration, and metabolization

A

rapid onset, short duration, rapidly metabolized

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8
Q

is propofol fat soluble?

A

highly fat soluble
it’s taken up by vessel rich tissues and quickly redistributed to muscle and fat

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9
Q

propofol complete recovery

A

dog: 20 min
cat: 30 min

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10
Q

what does propofol cause?

A

dose dependent CNS depression, sedation, anesthesia
may also cause muscle twitching, sneezing, yawning, head shaking, apnea, hypotension, excitement, arrhythmias

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11
Q

etomidate

A

not controlled
used for induction in cardiac patients
also an emetic
IV
inhibits GABA
ultra short-acting (redistributed away from brain and rapidly metabolized)
not used CRI

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12
Q

what does etomidate cause?

A

causes hypnosis, vomiting, insignificant analgesia
may also cause brief hypotension, brief apnea, muscle twitching, pain at injection site, RBC hemolysis, adrenal suppression

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13
Q

alfaxolone

A

old drug (1970s) - discontinued cause of histamine release and anaphylactic reactions
neuroactive steroids, binds to GABA receptors
Alfaxan is now a water-soluble neuroanesthetic (metabolized by liver, no histamine release)

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14
Q

Alfaxan

A

C-IV controlled
no preservative
discard after 6 hours of 1st puncture
shelf life of 56 days after 1st puncture for multidose
synergistic
dose: dog- 1-3 mg/kg, cat- 2-5 mg/kg
CRI okay
administer slow
IM or IV

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15
Q

barbiturates history

A

developed in 1930s-1950s
derivatives of barbituric acid
classes: ultra short-acting, short-acting, intermediate-acting, long-acting

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16
Q

ultra short-acting barbiturates

A

ex: thiopental sodium, methohexital
used for induction of dogs, cats, horses
C-III controlled

17
Q

short-acting barbiturates

A

ex: pentobarbital
induces/maintains anesthesia in lab animals
concentrated doses used as euthanasia
C-II (fatal plus) or C-III (Euthasol)

18
Q

intermediate/long-acting

A

phenobarbital
anticonvulsant and sedative (increases seizure threshold)
not commonly used for sedation anymore
C-IV controlled

19
Q

barbiturate mode of action

A

inhibits GABA, depresses CNS

20
Q

ionized vs nonionized barbiturates

A

nonionized passes through cell membranes
acidosis = increased nonionized = increase sedation
alkalosis = decreased nonionized = decreased sedation

21
Q

what do barbiturates cause?

A

causes mild sedation, hypnosis, unconsciousness, CNS depression (excitement at low doses)
may also cause cardiac depression, hypotension, cardiac arrhythmias and blocks, decreased RR and apnea, coughing, sneezing, laryngospasms

22
Q

dissociatives

A

ex: telazol (tiletamine + zolazepam), ketamine
C-III controlled
IV, IM, po
often combined with other drugs - Benzos (ketval) and opioids

23
Q

dissociatives mode of action

A

cause disruption of nerve transmission in parts of the brain and stimulation in others
N-methyl-D-aspartate (NMDA) inhibitors so responsible for windup and respond to low-intensity pain stimuli

24
Q

dissociatives onset, duration, excretion

A

1-2 min IV, 10 min IM
duration: 20-30 min
redistributed and metabolized by liver
excreted by kidneys

25
Q

what does dissociatives cause?

A

causes sedation, anesthesia, analgesia
may also cause catalepsy, tachycardia, hypertension, excitement, arrhythmias