Fentanyl Flashcards

Please note that the drug card information is for Educational Use ONLY, and the source is from Carrie Bowman's glossary of drug cards permitted by use of Georgetown NAP students. No permission is given to use these cards for anything other than as a study resource for our program.

1
Q

What is the drug class of Fentanyl?

A

synthetic phenylpiperidine opioid agonist, analgesic

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2
Q

What are the uses of Fentanyl?

A
  • Analgesia intraop and postop
  • administered as premed to blunt hemodynamic responses to airway manipulation and reduce inhalation agent dosage requirements
  • provides GA either administered as sole anesthetic or in combo with IV sedatives/hypnotics
  • administered in the epidural and subarachnoid spaces to augment the effectiveness of RA
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3
Q

What is the MOA of Fentanyl?

A
  • Binds to mu opioid receptors in the brain, brainstem, spinal cord, and primary afferent peripheral terminals producing analgesia
  • mimics the actions of enkephalins, endorphins, dynorphins causing the action of antinocioceptive systems resulting in cellular hyperpolarization and inhibition of NT release
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4
Q

How is Fentanyl metabolized?

A

primarily in the liver by N-dealkylation and Hydroxylation

-dependent on liver blood flow/ high hepatic extraction ratio

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5
Q

Does metabolism of Fentanyl produce metabolites?

A

-minimally pharmacologically active metabolites: Norfentanil, hydroxyproprionyl-fentanyl, and hydroxyproprionyl-norfentanyl

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6
Q

How is Fentanyl redistributed?

A
  • Fentanyl is highly lipid soluble allowing rapid crossing of biological membranes and uptake by highly perfused tissue groups including the brain, heart, lungs
  • Rapidly redistributed to inactive tissue sites such as fat and muscle
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7
Q

What is important about the lungs and Fentanyl?

A

The lungs serve as a large inactive storage site, with an estimated 75% of the initial dose undergoing 1st pass pulmonary uptake

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8
Q

What is the Volume of Distribution?

A

Vd is 4L/kg

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9
Q

What is the distribution time? redistribution time?

A

Distrib time: 1.7 minutes

Redistribution time: 13 minutes

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10
Q

What is the termination elimination 1/2 time of Fentanyl?

A

3.1 - 6.6 hours

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11
Q

How is Fentanyl eliminated?

A

Norfentanyl (principle metabolite) excreted by the kidneys and can be detected in the urine 48 - 72 hours after administration

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12
Q

Is Fentanyl protein bound?

A

approx 80% protein bound to plasma proteins

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13
Q

What are the CNS side effects of Fentanyl?

A
  • increase in ICP in head injury patients if respiration is not controlled
  • seizure like activity and muscle rigidity
  • Dizziness, blurred vision
  • Miosis
  • Pruritis
  • Drowsiness, Sedation, Confusion
  • CNS depression
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14
Q

What are the CV effects of Fentanyl?

A
  • Bradycardia
  • Elevated CVP, PAP, and PVR associated with opioid induced muscle rigidity, hypotension, peripheral vasodilation, arrythmia
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15
Q

What are the respiratory effects of Fentanyl?

A
  • Respiratory depression
  • depression of airway reflexes
  • decreased lung compliance, FRC, hypercapnia, and hypoxemia associated with opioid induced muscle rigidity
  • Bronchospasm
  • Laryngospasm
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16
Q

What are the GI effects of Fentanyl?

A
  • increased common bile duct pressure
  • N/V
  • Delayed gastric emptying and intestinal transit
17
Q

What are the endocrine/metabolic effects of Fentanyl?

A

ADH release

18
Q

What are the contraindications to use of Fentanyl?

A

-use with caution in patients with impaired hepatic and/or renal function, head trauma, elevated ICP, and bradyarrhythmias

19
Q

What synergistic effect occurs with Fentanyl and ____________ and __________?

A

Benzodiazepines and other CNS depressants cause marked opioid synergism with respect to hypnosis and respiratory depression

20
Q

What drug interaction can occur between Fentanyl and Nitrous Oxide?

A

cardiovascular depression

21
Q

Adminstration with _________ and Fentanyl may cause?

A

Droperidol

may cause hypotension or HTN

22
Q

What is the anesthetic premedication dose of Fentanyl?

A

25 - 100 mcg

23
Q

What is the analgesia (including post-op bolus) dose of Fentanyl?

A

1 - 2 mcg/kg (usually 0.5-1 mcg/kg)

24
Q

What is the infusion dose of Fentanyl?

A

0.01 - 0.05 mcg/kg/min

25
Q

What is the GA IV dose for a sole agent, for Fentanyl?

A

50 - 150 mcg/kg

26
Q

What is the regional anesthesia dose for Fentanyl?

A

Epidural: 50 - 100 mcg (loading)
Spinal: 10 - 25 mcg

27
Q

What is the reversal/ antagonist of Fentanyl and the dose of it?

A

Naloxone (Narcan) at 0.1 - 2 mg IV incremental doses; 10 mg max

28
Q

Is Fentanyl more or less lipid soluble than morphine with a longer or shorter DOA?

A

MORE lipid soluble than Morphine with SHORTER DOA- 75% of initial dose undergoing first pass pulmonary uptake

29
Q

_______ redistribution to _________ tissue sites as ______, _________ _________, and ________

A

rapid redistribution to inactive tissue sites as fat, skeletal muscle, and lungs

30
Q

What can multiple IV doses or continuous infusion produce?

A

progressive saturation of inactive tissue->leads to 2nd peak b/c comes back to plasma

31
Q

Does plasma concentration decrease rapidly?

A

Plasma concentration does NOT decrease rapidly and DOA is prolonged-> 2dary peak in plasma levels

32
Q

What is the clinical significance of Fentanyl?

A
  • Used as analgesic adjunct for surgery
  • as adjuvant to blunt stimulation of incision, laryngoscopy
  • as sole anesthetic in large doses due to hemodynamic stability
  • 100 x more potent than morphine
  • wide range of doses given: 1-20 mcg/kg
  • Lozenges (fent lollipop) 5-20 mcg/kg 45 min prior to induction