Induction Drugs - Ketamine Exam 2 Flashcards

1
Q

What type of drug is ketamine?

A
  • Phenycyclidine derivative
  • NMDA receptor antagonist (PCP; “angel dust”)
  • amnestic and intense analgesic
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2
Q

What type of anesthesia does ketamine produce?

A
  • Dissociative anesthesia (psychedelic)
  • cataleptic state
  • slow nystagmus
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3
Q

What two properties does ketamine possess?

A
  • Amnestic
  • intense analgesia
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4
Q

What signs and symptoms does dissociative anesthesia (ketamine) produce?

A
  • “Zonked” state
  • Non-communicative but awake,
  • Hypertonus & purposeful movements
  • Eyes open but “no one’s home”
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5
Q

What are ketamine’s two greatest advantages over propofol and etomidate?

A
  • No pain at injection (no propylene glycol)
  • Profound analgesia at sub-anesthetic doses
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6
Q

What are the two greatest disadvantages of ketamine?

A
  • Emergence delirium
  • Abuse potential
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7
Q

What is Benzethonium Chloride? What is its relevance?

A

Ketamine preservative that inhibits ACh receptors

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8
Q

Differentiate S(+)Ketamine vs R(-)Ketamine.

A

S-Ketamine (left-handed isomer) is essentially better
More intense analgesia, ↑metabolism & recovery, Less salivation, Lower emergence delirium

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9
Q

which ketamine isomer has cocaine like effects?

A

Racemic ketamine
inhibits reuptake of catecholamines in nerve endings

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10
Q

What benefits does a racemic ketamine mixture offer?

A

Less fatigue & cognitive impairment
Inhibits catecholamine reuptake at nerve endings (like cocaine)

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11
Q

What is Ketamine’s main mechanism of action?

A
  • Non-competitive inhibition of NMDA (N-methyl-D-aspartate) receptors
  • decreases pre-synaptic release of glutamate
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12
Q

What are Ketamine’s secondary receptor sites?

A
  • Weak GABA_A effects
  • Opioid (Mu μ, Delta δ, and Kappa κ, weak gamma σ)
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13
Q

what is the most abundant excitatory neurotransmitter in the CNS?

A

Glutamate

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14
Q

What is Ketamine’s time of onset? (IV & IM)

A

IV: 1 min
IM: 5 min (mostly for pediatric patients)

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15
Q

What is Ketamine’s duration of action?

A

10-20 min

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16
Q

What about ketamine’s lipid solubility?

A

Highly lipid soluble (5-10x greater than thiopental)

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17
Q

What is the result of ketamine’s lipid solubility?

A

Brain → non plasma bound → peripheral tissue

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18
Q

What is the Vd and E½ time of ketamine?

A

Vd = 3L/kg, E ½ = 2-3 hours

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19
Q

Name the pharmacokinetic profile of ketamine: Clearance, Metabolism, Excretion.

A

Clearance: high hepatic clearance (1L/min), Metabolism: CYP450’s, Excretion: kidneys

20
Q

What is the primary metabolite of ketamine and what is its significance?

A

Norketamine is metabolite (⅓ potency and prolongs analgesia)

21
Q

In what patient population is ketamine tolerance most often seen?

A

Burn patients

22
Q

What is the induction dose of ketamine IV? What if it is given IM?

A

0.5 - 1.5 mg/kg IV, 4 - 8 mg/kg IM

23
Q

What is the maintenance dosing of ketamine?

A

0.2 - 0.5 mg/kg IV, 4 - 8 mg/kg IM

24
Q

What is the subanesthetic/analgesic dose of ketamine?

A

0.2 - 0.5 mg/kg IV

25
Q

What is the post-operative sedation and analgesia dosing for ketamine in pediatric cardiac surgery cases?

A

1-2 mg/kg/hour

26
Q

What is the neuraxial epidural analgesia dosing of ketamine? What about intrathecal route?

A

30mg epidural, 5 - 50 mg via intrathecal/spinal/subarachnoid

27
Q

Ketamine is a potent sialagogue. What does this mean for your clinical practice?

A

Manage excessive secretions during intubation & watch for coughing/laryngospasm

28
Q

What drug and dosing should be used to treat excessive salivary secretions from ketamine administration?

A

Glycopyrrolate: 0.2mg

29
Q

You gave ketamine and the patient fell asleep within 30 seconds. When would you expect the patient to: Wake up? Be fully conscious? Start remembering things?

A

Wake up in 10-20 minutes, Full consciousness in 60 - 90 min, Amnestic effects should also wear off in 60 - 90 min

30
Q

What patient populations is ketamine best used for?

A

Acutely hypovolemic patients, Asthmatics, Mental health patients

31
Q

When would you do an IM induction of a patient?

A

Uncooperative and difficult-to-manage mentally challenged patients

32
Q

Though ketamine has many indications, when should it be avoided?

A

Patients with pulmonary HTN and ↑ICP

33
Q

What are Ketamine’s effects on ICP? Why?

A

↑ICP via ↑CBF by 60%, Potent cerebral vasodilator

34
Q

At what dosing will the ICP increasing effects of ketamine plateau?

35
Q

Due to ketamine’s increased excitatory EEG activity, how much does seizure potential increase with administration?

A

Trick question. No increase in seizure potential with ketamine

36
Q

What does the cardiovascular profile of ketamine look like? How can this side effect profile be blunted?

A

SNS stimulation ( ↑ in sBP, PAP, HR, CO, etc.)
Blunted via pre-med with benzo’s, volatiles, or nitrous

37
Q

Say you just gave ketamine and you have an unexpected drop in systolic BP and CO. What happened? How do you treat it?

A

Depleted catecholamine stores
Treat with direct-acting SNS agents (ex. phenylephrine) vs indirect (ex. ephedrine)

38
Q

What is the Pulmonary profile of ketamine?

A

No depression of ventilation with CO₂ response maintained, ↑ salivary excretion, Intact upper airway tone & reflexes, Bronchodilator with no histamine release

39
Q

What does emergence delirium present like with ketamine?

A

Visual, auditory, proprioceptive illusions. Morbid & vivid dreams up to 24 hours

40
Q

What is the proposed physiologic mechanism of action for emergence delirium occurrence with ketamine?

A

Depression of inferior colliculus & medial geniculate nucleus

41
Q

What percentage of patients will develop ketamine induced emergence delirium? How can it be prevented?

A

Psychedelic effects in 5 - 30% of patients
Pre-med with benzos

42
Q

What “other system” effect does ketamine have?

A

PLT aggregation inhibition

43
Q

What are ketamine’s most common drug interactions?

A

Volatiles → hypotension, Non-depolarizing NMBs → enhancement, Succinylcholine → prolongation

44
Q

Why does ketamine prolong succinylcholine’s effects?

A

Ketamine is a plasma cholinesterase inhibitor

45
Q

Which induction agent has the highest analgesic properties?

46
Q

Why would ketamine be a decent induction drug for an OSA patient? Why not?

A

Preservation of upper airway reflexes & ventilatory function
Sialagogue