NMBA Dosages Flashcards

1
Q

Succinylcholine (alternate name):

A

Anectine

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2
Q

Succinylcholine structure:

A

2 Ach molecules
depolarizing neuromuscular blocking agent
highly ionized, water soluble

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3
Q

Succinylcholine MOA:

A
  1. Mimics Ach
  2. Produces a sustained depolarization of post junctional membrane causing a single contraction
  3. Causes skeletal muscle paralysis, inactivates Na+ channels
  4. Succ blocks Ach from being able to bind to receptor
  5. Will not be metabolized by acetylcholinesterase
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4
Q

Succinylcholine Onset:

A

IV: 30-60 sec IM: 1-3 min

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5
Q

Succinylcholine Duration of action:

A

IV: 3-10 min IM: 5-10 min

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6
Q

Succinylcholine Metabolism:

A

Plasma Cholinesterase

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7
Q

Succinylcholine IV intubation dose:

A

IV: 1 mg/kg (intubation)

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8
Q

Succinylcholine IM intubation dose:

A

1.5-3 mg/kg + anticholinergic

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9
Q

Succinylcholine side effects:

A
  1. Myalgias
  2. Increase IOP
  3. Increase ICP
  4. Hyperkalemia
  5. Bradycardia
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10
Q

Succinylcholine Contraindications / cautions

A
  1. Avoid in Neuro patients (upregulation of receptors)
  2. Avoid in high K
  3. Malignant Hyperthermia trigger
  4. Avoid in burn patients, sepsis
  5. No reversal
  6. Inhalational anesthetics decrease dose needed (25-50%)
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11
Q

Rocuronium (alternate name)

A

Zemuron

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12
Q

Rocuronium Structure:

A

Nondepolarizing neuromuscular blocking agent
Aminosteroid
Quaternary ammoinum group
Hydroxyl group

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13
Q

Rocuronium MOA:

A
  1. Competitive antagonist, binds to alpha subunit of nicotinic receptor
  2. Only needs to bind to 1 alpha subunit
  3. Channels will not open
  4. Action potential will not propagate
  5. Skeletal muscle paralysis
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14
Q

Rocuronium Onset:

A

30-60 sec (RSI dose)

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15
Q

Rocuronium Duration of action:

A

30-60 min

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16
Q

Rocuronium PB:

A

30%

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17
Q

Rocuronium Metabolism:

A

60% biliary unchanged
40% really unchanged,
Minimal hepatic

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18
Q

Rocuronium IV induction dose:

A

IV: 0.6-1 mg/kg (generally 1 mg/kg, induction)

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19
Q

Rocuronium IV RSI dose:

A

IV: 1.2 mg/kg (RSI)

20
Q

Rocuronium IV maintenance dose:

A

IV: 0.06-0.6 mg/kg (maintenance)

21
Q

Rocuronium IV defasiculating dose:

A

IV: 5-10 mg (defasiculating)

22
Q

Rocuronium Side effects:

A
  1. CV stable
  2. Does not cross placenta
  3. Does not cross BBB
  4. Paralysis
  5. Transient hypotension
23
Q

Rocuronium Contraindications / cautions:

A
  1. Previous Allergic rxn
  2. Do not administer without sedating patient
  3. Caution in renal disease
  4. Caution in hepatic disease
  5. Inhalational anesthetics decrease dose needed (25-50%)
24
Q

Vecuronium (alternate name):

A

Norcuron

25
Q

Vecuronium structure:

A

Nondepolarizing neuromuscular blocking agent
Amino steroid
Quaternary ammonium group

26
Q

Vecuronium MOA:

A
  1. Antagonist
  2. Competitively binds to alpha subunit of nicotinic receptor
  3. Blocks Ach from attaching
  4. Channels cannot open
  5. Action potential cannot occur
27
Q

Vecuronium Onset:

A

3 min

28
Q

Vecuronium duration of action:

A

30-60 min

29
Q

Vecuronium PB:

A

60%

30
Q

Vecuronium Metabolism:

A

40% hepatic,
40% in bile unchanged,
20% really

31
Q

Vecuronium IV induction dose:

A

IV: 0.08-0.1 mg/kg (up to 20 mg)

32
Q

Vecuronium IV maintenance dose:

A

IV: 0.01-0.05 mg/kg (maintenance)

33
Q

Vecuronium IV defasiculating dose:

A

IV: 0.5 mg (defasiculating)

34
Q

Vecuronium side effects:

A
  1. CV stable
  2. Does not cross placenta
  3. Does not cross BBB
  4. Paralysis
  5. ED95 = 0.03mg/kg
35
Q

Vecuronium Contraindications / cautions:

A
  1. Do not administer without sedation
  2. Do not give if previous allergic reaction
  3. Caution in hepatic disease
  4. Caution in renal disease
  5. Inhalational anesthetics decrease dose needed (25-50%)
36
Q

Cisatracurium (alternate name):

A

Nimbex

37
Q

Cisatracurium structure:

A

Benzoisoquinolinium
Quaternary ammonium group
Stereoisomer of atricurium

38
Q

Cisatracurium MOA:

A
  1. Antagonist
  2. Competitively binds to alpha subunit of nicotinic receptor
  3. Blocks Ach from attaching
  4. Channels cannot open
  5. Action potential cannot occur
39
Q

Cisatracurium Onset:

A

3 min

40
Q

Cisatracurium duration of action:

A

30-60 min

41
Q

Cisatracurium PB:

A

not successfully studied - rapid degredation

42
Q

Cisatracurium Metabolism:

A

Hoffman elimination and plasma esterases

43
Q

Cisatracurium IV intubation dose:

A

IV: 0.1-0.2 mg/kg (intubation)

44
Q

Cisatracurium IV maintenance dose:

A

IV: 0.05-0.1 mg/kg (maintenance)

45
Q

Cisatracurium IV defasiculating dose:

A

IV: 1-2 mg (defasiculating )

46
Q

Cisatracurium side effects:

A
  1. CV stable
  2. Does not cross placenta
  3. Does not cross BBB
  4. Paralysis
  5. Degrades without renal or hepatic intervention
47
Q

Cisatracurium Contraindications / cautions:

A
  1. Do not administer without sedating patient
  2. Do not give if previous allergic rxn
  3. pH important (hoffmans)
  4. Thermoregulation important (hoffmans)
  5. Inhalational anesthetics decrease dose needed (25-50%)