NMBs, Reversal Agents, and Antimuscarinic agents Flashcards

1
Q

What drugs can decrease pseudocholinesterase activity?

A
  1. Echothiopate (glaucoma drug)
  2. Neostigmine/pyridostigmine (Cholinesterase inhibitors)
  3. Phenelzine (MAO inhibitor)
  4. Cyclophosphamide (antineoplastic agent)
  5. Metoclopramide (Antiemetic)
  6. Esmolol (B-Blocker)
  7. Pancuronium (NDMR)
  8. Oral contraceptives (Various agents)
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2
Q

Bibucaine number

A

The percentage of inhibition of pseudocholinesterase activity.

Normal activity = 80

Homozygote with abnormal allele = 20

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3
Q

What are some cardiovascular effects of succinylcholine administration?

A

Act at all Ach receptors causing:

  • Possible bradycardia, more likely with second dose. Can be pretreated with antimuscarinic.
  • Higher doses can increase heart rate and blood pressure
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4
Q

Absolute contraindications to succinylcholine

A

Patients with already elevated potassium levels such as burn patients, massive trauma, neurological disorders, stroke, spinal cord injury, Parkinson’s disease, tetanus, cerebral aneurysm, polyneuropathy, Guillain-Barre syndrome, intraabdominal infection, risk of malignant hyperthermia, allergy to succ, [K] > 5.5mEq/L

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5
Q

What are the special considerations of atracurium?

A
  • Metabolized quickly by Ester/Hoffman degradation
  • Triggers dose-dependent histamine release, especially >0.5mg/kg
  • Avoid in asthmatics
  • Laudanosine, a metabolite is associated with precipitation of seizure activity
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6
Q

What are special considerations with cisatracurium?

A
  • Hoffman elimination, 4X more potent than atracurium
  • Extenstively less side effects compared to atracurium, does not alter heart rate or have any autonomic effects
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7
Q

What are special considerations with mivacurium?

A
  • Metabolized by pseudocholinesterase similar to succ, so patients with low pseudocholinesterase activity will have prolonged blockade
  • Releases histamine to about the same extent as atracurium
  • Advantage is a shorter duration of action (20-30min)
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8
Q

What are special considerations of pancuronium?

A
  • Metabolized mainly by the liver, and some of the metabolites are active
  • Prolonged in patients with kidney failure, because that is where (40%) is eliminated
  • 1 to 2 hours of duration, longest acting NMB
  • Causes hypertension and tachycardia because of vagal blockade and sympathetic stimulaiton (avoid in patients with heart disease of any sort)
  • Arrythmias can occur, especially with patients on tricyclic antidepresants
  • Patients with allergies to bromide may exhibit allergic reactions
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9
Q

What are special considerations of vecuronium?

A
  • Structure is basically pancuronium, minus a methyl group that doesn’t affect potency and reduces the side effects of pancuronium
  • Equipotency of pancuronium, and women are 30% more sensitive
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10
Q

What are special considerations of rocuronium?

A
  • No metabolism, eliminated by liver/kidney
  • Modestly prolonged by severe liver failure and pregnancy, and elderly due to smaller liver mass
  • Better choice for the rare patient in ICU needing prolonged muscle relaxant
  • Speedy onset, can be used for RSI
  • Has slight vagolytic tendencies
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11
Q

How do you monitor a neuromuscular block?

A

Use a peripheral nerve stimulator:

  • Tetany, twitch, TOF
  • Fade - reduction of evoked response indicative of ND block
  • Clinical recovery correlates with absence of fade
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12
Q

Recovery index?

A

Offset speed to recovery from 25% to 75% twitch

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13
Q

Train of four tells you:

A

-Progressive fade as relaxation increases
Disappearance of:
-4th = 75% block
-3rd = 80-85% block
-2nd = 85-90% block
-1st = 90-98% block

Clinical relaxation requires 75-95% block

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14
Q

A single twitch stimulation tells you:

A
  • The amount of blockage
  • Height remains normal until 75% Ach receptors are occupied
  • Completely disapears when 90-95% receptors are occupied
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15
Q

When should you administer your NMB reversal?

A

Recovery of the first twitch

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16
Q

Tachycardic effects of antimuscarinics:

A

Atropine > Glycopyrrolate > Scopolamine

17
Q

Bronchodilation effects of antimuscarinics:

A

Atropine/Glycopyrrolate > Scopolamine

18
Q

Sedative effect of antimuscarinics:

A

Scopolamine > Atropine > Glycopyrrolate (no effect)

19
Q

Anisialagogue effects of antimuscarinics:

A

Scopolamine/Glycopyrrolate > Atropine

  • Salivary secretions, gastric secretions, are markedly reduced
  • Decreased intestinal motility and peristalsis prolong gastric emptying time
  • Lower esophogeal sphincter pressure is reduced