Test 1: Dexmedetomidine Flashcards

1
Q

How does Dexmedetomidine compare to Clonidine in terms of alpha 2 agonism?

A

Clonidine α2:α1 = 220:1
Dexmetomidine α2:α1 = 1620:1

Dex is a highly specific α2-adrenergic agonist
Drug class: Imidozalines (alpha agonists)

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2
Q

Can Dex be used as a sole agent for patients with neuromuscular blockade?

A

No, limited amnestic effect.

Has sedative effects, but does not produce GA even at high doses.
-Patients tend to be easily arousable
-Minimal effects on respiratory drive
-Can continue infusions throughout emergence and during weaning from mechanical ventilation.

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3
Q

What are the analgesic qualities of Dex?

A

-Augments the effects of opioids
-Spinal and supraspinal (locus coeruleus) mechanism
-Hypnosis results from stimulation of Alpha 2 receptors in the locus coeruleus
-Analgesic effects originate at the level of the spinal cord.

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4
Q

What is the MOA of Dexmedetomidine?

A

The alpha 2A subtype mediates the majority of the analgesic and sedative effects on the CNS.
-HIGHLY selective, centrally acting alpha2 agonist
-Hyperpolarization due to efflux of K+ ions, which leads to a subsequent decrease in neuronal firing as well as reduced norepinephrine release mediated by inhibitory presynaptic autoreceptors.
-Stimulation of Alpha 2 receptors = decreased catechol release
-Inhibits Adenylyl Cyclase = decreased cAMP
Overall effects are r/t decreased sympathetic outflow.

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5
Q

What is important to know regarding the administration of Dex in a patient with cardiac disease?

A

The sympatholytic effects of Dex lead to decreased HR and BP.
-Decreased myocardial demand in response to painful stimuli (!!Blue Box!) Anti-anginal effect.
-Associated with a mortality benefit

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6
Q

What is important to know regarding the administration of Dex in a patient with Heart Block?

A

-Bradycardia can be dangerous in the setting of heart block. Use Dex with caution.

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7
Q

What is important to know regarding the administration of Dex in a patient with high sympathetic tone (Diabetes, elderly, or Hypovolemic)?

A

Significant hypotension is more likely in the setting of high sympathetic tone.

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8
Q

What is important to know with Loading Dose administration of Dex? (Blue box!)

A

Typically, Dex will lead to decreased HR and decreased BP due to sympatholytic effects.

However, direct effects on peripheral Alpha 2B and 2A receptors can lead to hypertension.
-This is seen during loading doses.
-Avoid administering as a bolus.

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9
Q

What are the CNS effects of Dexmedetomidine?

A

-Supraspinal analgesia
-Spinal analgesia
-Sedation, but patients tend to be arousable
-Decrease in CBF without changes in ICP and CMRO2
-Synergistic effect when combined with other sedative-hypnotics
-Does not interfere with electrophysiologic monitoring

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10
Q

What are the CV effects of Dexmedetomidine?

A

-Bradycardia (40% of patients)
-Variable HTN or HoTN
-Hypotension responds well to fluid and/or vasopressors

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11
Q

What are the Respiratory effects of Dexmedetomidine?

A

-Preserved respiratory drive
-Possible small to moderate decrease in Vt (no change in RR)
-Decreased salivation
-Possibly beneficial to decrease airway reactivity in patients with COPD/asthma

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12
Q

What are the Misc. effects of Dexmedetomidine?

A

-Decreased salivation (presents an advantage over Ketamine for fiberoptic intubation)
-Decreased shivering
-Infusions should not exceed 24 hours
-Can facilitate extubation in patients that become agitated when sedation is held.
-Diuretic effect
-Renal, gastroprotective, and anti-inflammatory effects

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13
Q

What is the onset time for Dexmedetomidine?

A

10-20 minutes

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14
Q

What are the pharmacokinetics of Dex?

A

-Onset = 5-10 minutes
-94% protein bound
-Metabolism: Hepatic CYPs & glucuronidation
-1/2 life = 2-3 hours
-DOA = 1-2 hours

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15
Q

What is the DOA of Dexmedetomidine?

A

60 - 120 minutes (1-2 hours)

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16
Q

What is the ICU Infusion dose of Dex? (From Nagelhout)

A

-Loading: 1 mcg/kg IV over 10-20 minutes
-Maintenance: 0.2 - 0.7 mcg/kg/hr

17
Q

What is the sedation dose of Dex?

A

-Loading: 0.5 - 1 mcg/kg over 10 min
-Maintenance: 0.2 - 1.0 mcg/kg/hr (adjunct to propofol or as pain mgmt)
-Decreases dose requirements for inhaled and injected anesthetics

18
Q

What type of receptor is the Alpha 2 receptor?

A

GPCR
When activated, results in the inhibition of Ca Channels, activation of K+ channels, and direct modulation of the exocytic release of proteins.
-This produces hyperpolarization of the cells and thus inhibition.

19
Q

Avoid administration of what drug with Dexmedetomidine?

A

-Transient, profound HTN was noted when using glycopyrrolate to treat dexmedetomidine induced bradycardia in children.

20
Q

What is the main site of action for the sedative actions of Dex?

A

The main site of action for the sedative actions of dexmedetomidine is the pontine noradrenergic nucleus, the locus coeruleus.