Lecture 9: Induction drugs (Exam 2) Flashcards

1
Q

What are the characteristics of the ideal injectable drug

A
  • Provide reliable sedation, analgesia, & muscle relaxation
  • Min changes in CV or respiratory fxn
  • Small vol needed
  • Wide safety index
  • Rapid onset & short duration of action
  • Reversible
  • Non-cumulative
  • Readily metabolized & excreted by the body
  • Long shelf life (stable in heat & light)
  • Inexpensive
  • Ava on the market
  • Low potential for human abuse (not a controlled substance)
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2
Q

Fill out the table:

A
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3
Q

Describe propofol

A
  • Milky white oil in water emulsion
  • No preservative (discard open vial w/in 6 hours)
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4
Q

Describe propofol28

A

has benzyl alcohol preservative but only approved for dogs

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5
Q

What is the MOA of propofol

A

Activates GABA(a) receptor -> increases Cl conduction & block Na channel -> hyperpolarization (brought in a lot of neg ions) -> CNS depression & loss of consciousness

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6
Q

What are the pharmacokinetics of propofol

A
  • Rapid distribution followed by a slower clearance phase
  • Rapid hepatic metabolism & excretion by kidneys (not in cats or greyhounds)
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7
Q

What are the pharmacodynamics of Propofol (CNS, CV, Resp, musculoskeletal, & fetal/neonatal)

A
  • CNS - Decreases intracranial pressure & cerebral metabolism of oxygen (anticonvulsant effects so good for px w/ head trauma)
  • CV - Decreases BP due to vasodilation
  • Resp - Dose dep respiratory depression & transient apnea (often w/ cyanosis)
  • Musculoskeletal - produced muscle relaxation (transient myoclonus can occur)
  • Fetal/neonatal - cross placenta but is rapidly cleared from neonate
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8
Q

What is the propofol species specific consideration for grey hounds

A

Need same dose for induction but the recovery time is longer

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9
Q

What is the propofol species specific consideration for cats

A
  • Caution w/ repeated daily use
  • Don’t use propofol28 (can’t process the preservative really well)
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10
Q

What is the propofol species specific consideration for horses

A
  • not really used b/c excitation & vol/cost
  • Can be used for CRI
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11
Q

What is the propofol species specific consideration for swine

A

Does not induce malignant hyperthermia (good drug to use for them)

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12
Q

What is the propofol species specific consideration for small ruminants

A
  • Smooth rapid induction w/ a good recovery
  • Possible cost considerations
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13
Q

Describe the clinical scenario of propofol

A
  • Give over 60 - 90 sec
  • Swift induction (20 to 30 sec)
  • Be ready to ventilate px
  • Recover in 2 to 12 mins
  • No analgesia
  • Possible pain when injecting
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14
Q

What is the characteristics dissociative anesthetics

A

Dissociation from thalamocortical (consciousness) & limbic (emotion & memory) systems to change awareness (decrease)

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15
Q

What are the two most common dissociative anesthetics

A
  • Ketamine
  • Tiltamine
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16
Q

What is the MoA of dissociative anesthetics

A
  • Mainly: via antagonist effects @ NMDA receptors
  • Others: AMPA, BDNF, opioid, etc receptors
  • Interacts w/ voltage-gated Ca channels
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17
Q

What are the PKs of dissociative anesthetics

A
  • Water soluble (can give in multi different ways)
  • Rapid onset
  • Short duration
  • Highly lipophilic (quickly crosses the BBB)
  • Metabolized by the liver & excreted by the kidneys
18
Q

What are the PDs on the CNS or dissociative anesthetics

A
  • Cataleptic state (not asleep but not responding to external stimuli)
  • Can see emergency delirium (ataxia, hyper-reflexive, sensitive to touch, & increased motor activity)
19
Q

What are the PDs on the CV or dissociative anesthetics

A
  • Direct neg cardia inotropic effects (usually overcomed by sympathomimetic effects)
  • Increased BP, HR, cardiac output, myocardial oxygen req, & cardiac work
  • Inhibition of NE reuptake (increased plasma catecholamines)
20
Q

What are the PDs on the resp sys or dissociative anesthetics

A
  • Doesn’t cause sign resp depression
  • Bronchial smooth muscle relaxant (bronchodilation & decreased airway resistance)
  • “apneustic” resp pattern (prolonged inspiration & rel short expiratory time w/ several shallow breaths taken
  • Increased salivation & respiratory tract secretion
21
Q

What are the PDs on the musculoskeletal sys or dissociative anesthetics

A
  • Can cause muscle rigidity & even spont movements
  • IOP can increase after admin (b/c of increased tone of extraocular muscles)
22
Q

What are the PDs on the Fetal/neonatal or dissociative anesthetics

A
  • Crosses the placenta
  • Can cause fetal depression
23
Q

What are some dissociative anesthetics species specific considerations for dogs

A

Combine ketamine w/ benzo for induction (can us a alpha 2 agonist or opiod)

24
Q

What are some dissociative anesthetics species specific considerations for cats

A
  • Can spray into the mouth of fractious cats (can increase salivation)
  • Caution w/ use of dissociative in tigers (seizure-like behavior possible)
  • ketamine + alpha 2 agonist, benzo, &/or ace for IM
25
Q

What are some dissociative anesthetics species specific considerations for horses

A
  • Adequately sedate before induction
  • Admin ketamine w/ benzo, alpha 2 agonist, or guaifenesin)
  • Telazol inductions are smooth but recovery is rough
26
Q

What are some dissociative anesthetics species specific considerations for ruminants

A
  • ketamine + benzo/guaifenesin
  • “ketamine stun” tech (sub anesthetic dose of ket & xylazine given to calves prior to castration
27
Q

What are some dissociative anesthetics species specific considerations for swine

A
  • Does not induce malignant hyperthermia
  • Telazol has a slow calm recovery but not rec for pot belly pigs
28
Q

Describe the clinical use of dissociative anesthetics

A
  • Typically ketamine + benzo ( or a2 agonist)
  • Ket can be given as CRI @ sub anesthetic doses to reduce inhalant req
  • Not reversible
  • Oral, ocular, & swallowing reflexes are still intact (nystagmus common)
  • Use caution w/ px that have hepatic or renal dysfxn
  • Scheule 3 controlled sub
  • Telazol usually used in shelter med
29
Q

Describe alfaxalone

A
  • Older formulation was poorly water soluble & caused histamine release in dogs
  • New formula w/ non-cremophor (no histamine release & better water solubility) & can give IM/IV
  • No antimicrobial preservative
  • P450 hepatic metabolism & elimination via kidneys & feces
30
Q

What is the MOA of alfaxalone

A

Neuroactive steroid molecule that binds to GABA(A) receptor to increase Cl condution into the cell -> hyperpolarization of postsynaptic membrane -> CNS depression

31
Q

What are the PDs of alfaxalone (CNS, CV, Resp, Musculoskeletal, & neonatal/fatal)

A
  • CNS - Decreases CBF, ICP, & CMRO2
  • CV - hemodynamic stability but can cause dose dep hypotension (b/c of vasodilation)
  • Resp - dose dep respiratory depression &/or apnea
  • MS - good muscle relaxation
  • N/F - Crosses placenta & causes dose dep fetal depression
32
Q

Describe the clinical use of alfaxalone

A
  • No analgesia
  • Used for induction but can also be used as CRI to maintain ax
  • Used for px undergoing c-section
  • Good induction for dogs that are a poor ax risk
  • Can increase IOP in dogs
  • No pain on IV injection
  • Schedule IV controlled sub
  • Transient paddling, excitement in cats, & vocalization in dogs may occur in recovery (rough recovery for horses)
33
Q

Describe etomidate

A
  • pH of 6.9
  • Insoluble in water
  • high osmolarity leads to adverse effects
34
Q

What is the MOA of etomidate

A

Enhances action of GABA (inhibitory neurotransmitter) @ the GABA(A) receptor -> increased Cl conduction into cell -> hyperpolarization of postsynaptic neuron -> CNS depression & hypnosis

35
Q

What are the PKs of etomidate

A
  • Rapid penetration of brain (quick induction)
  • Rapid redistribution to inactive tissue (fast recovery)
  • Large therapeutic index
  • Metabolism by liver & plasma esterases
  • Excreted in urine
36
Q

What are the PDs of etomidate (CNS, CV, Resp, Endocrine, MS, N/F)

A
  • CNS - cerebroprotective effects (vasoconstriction of cerebral vessels, reduces CBF, & CMRO2) which leads to cerebral perfusion maintained & decrease in ICP occurs. Decreases IOP
  • CV - Min to no change in HR, SV, CO, MAP, & CVP. Baroreceptor fxn & SNS response remain intact (hemodynamic stability)
  • Resp - min effects
  • Endo - Adrenocortical suppression for up to 5 to 6 H
  • MS - myoclonus or tremors
  • N/F - min effects
37
Q

What is the clinical effects of etomidate

A
  • Preferred induction agent for px w/ hemodynamic instability, increased ICP, or cirrhosis
  • No analgesia
  • Caution for px w/ addison’s or highly stressed px
  • Doesn’t appear to be cumulative but not recommended as a CRI b/c of adrenocortical suppression & possible RBC damage
  • Premed dose of benzo can decrease myoclonus
38
Q

What are the side effects of etomidate

A
  • Pain on injection
  • Vomiting
  • Excitement
  • Cats - drooling/salivation & concern for IV hemolysis
39
Q

When are mask/chamber inductions used

A
  • Exotics
  • Very aggressive px where injectable anesthetics are not possible
40
Q

What should be noted about mask or chamber inductions

A
  • Use caution b/c of exposure to personnel & potential to harm px
  • They are not considered the standard of care in most situations
41
Q

What are some other combos that can be used for induction

A
  • Opioid induction (fent + benzo)
  • Ket + propofol
  • Guaifenesin + ket
  • Guaifenesin + ket + xylazine
  • Guaifenesin + thiopental
  • Propofol + thiopental
  • Ket + xylanzine
  • Telazon + ket + xylazine/dexmed
  • Ket + alfaxalone