Neuromuscular Blocking Agents (Barash Ch 11) Flashcards

(18 cards)

1
Q

Only depolarizing NMBA

A

Succinylcholine

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2
Q

Succinylcholine side effects

A
  • Bradycardia and asystole
  • Fasciculations (80-90%) pretreat with non-depol to prevent
  • Myalgias (50-60%) prevent with NSAID pretreatment
  • Increased ICP (not as bad as DL with light sedation) and IOP
  • Hyperkalemia (0.5 mEq/L), avoid in kids burns, paraplegics, infection, sepsis, etc
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3
Q

What drug is responsible for more anaphylactic reactions than any other anesthetic drug (1 in 10,000)?

A

Succinylcholine

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4
Q

Clinical indications for succinylcholine

A

Biggest is RSI

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5
Q

Succinylcholine dosing for RSI, adults and kids…

A

Adults: 1.0 mg/kg, children: 1.5-2.0 mg/kg (kids more resistant)

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6
Q

Contraindications for succinylcholine

A
  • Pseudocholinesterase deficiency
  • History of malignant hyperthermia (SCh + inhaled anesthetic = 20x risk)
  • Critical care patients, immobilized patients, paraplegic pts, acidotic and hypovolemic patients (those at risk for lethal hyperkalemia)
  • NOTE: renal failure is not a contraindication if K+ is normal
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7
Q

Benzylisoquinolinium non-depolarizing NMBAs

A

Atracurium, cisatricurium, mivacurium

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8
Q

Aminosteroid non-depolarizing NMBAs

A

pancuronium, vecuronium, rocuronium

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9
Q

Dosing change of non-depolarizing NMBAs in hypervolemic state, why

A

Increase the dose initially. Due to positive charge the are distributed in ECF meaning lower concentrations will be present.

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10
Q

Pancuronium, short or long acting?

A

Long (1-2 hours), not used much any more because of potential for residual post-operative neuromuscular weakness.
- Accumulates due to active metabolite (50% potency of parent drug)

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11
Q

Vecuronium, duration of action?

A
  • Intermediate duration, no CV effects
  • More potent than rocuronium, thus slower onset
  • Metabolite has 60% potency of parent drug so can accumulate similar to pancuronium
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12
Q

Redeeming properties of Rocuronium?

A

Low potency means high plasma to active site gradient and quick onset. Given rapid onset and very few allergic reactions as well as lack of CV side effects it is now a good choice for RSI.

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13
Q

Rocuronium is used in high doses 1.0-1.2 mg/kg for RSI, what are some things to be aware of when giving Rocuronium at high doses?

A
  • Onset is fast ~60 seconds but is quite variable so may have difficult intubating conditions due to incomplete effect at 60 sec.
  • Duration is long at high doses >1 hr
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14
Q

What is suggammadex and why is it important?

A

Drug that forms complex with NMBA, reducing binding availability to nicotinic receptors. Can Give after Rocuronium if a failed RSI to decrease the duration of paralysis.

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15
Q

Why is atracurium not optimal for induction/intubation?

A

At high doses it causes histamine release causing skin flushing, tachycardia, and hypotension.

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16
Q

Why was CIS-atracurium developed?

A

To decrease the propensity for histamine release

17
Q

Cisatracurium’s positive qualities?

A
  • intermediate duration
  • no renal clearance
  • higher potency than atracurium so lower doses mean no histamine release
18
Q

What affect does propofol have on NMBAs? And local anesthetics?

A
  • Propofol has no effect on NMBAs

- Local causes increased duration (minimal) but no change to onset time