2006B04 Describe the advantages and disadvantages of rocuronium for rapid sequence induction.

 

List:

·      Intro: rapid sequence introduction

·      Ideal kinetics

·      Ideal dynamics

 

Intro:

Rapid sequence induction

·  What: minimise time between hypnosis and intubation

·  Why: reduced risk of aspiration if

o Recent meal

o Impaired gastric emptying

o Otherwise at risk of regurgitation

·  How:

o Rapid hypnotic (thiopentone – highly lipid soluble)

o Rapid relaxant (suxamethonium classically)

o Pre-oxygenate

o Cricoid pressure

o Suction ready

Rocuronium

·  Fast onset non-depolarising neuromuscular blocker

·  Used in modified RSI

·  Large dose produces onset time similar to suxamethonium, but at the expense of long duration

 

Ideal pharmaceutics:

 

Rocuronium (ROC)

 

Suxamethonium (SUX) or other

Cheap

$20

$2

Compatibile with induction drugs

Thio (pH 11) + roc (pH 3.5) -> precipitation

pH 3.5 -> same

Doesn’t need refrigeration

Does

Does

Long life at room temp (90% potency)

2/12

2/52

Doesn’t need reconstitution

Doesn’t

Doesn’t

(Vecuronium does)

 

Ideal kinetics:

 

Rocuronium

Suxamethonium or other

Admin:

 

 

Can maintain paralysis by infusion

Y (but prolonged effect)

No (phase 2 blockade)

(Gantacurium: Y (fast offset))

Can give IM if IV cannula fails

No

Yes

Time course:

 

 

Rapid onset intubating conditions

(Bowman principle: ↓potency -> speed)

2x ED95 = 0.6mg/kg: 1-1.5min

4xED95 = 1.2mg/kg: 0.75-1min

4xED95 = 1.2 mg/kg: 0.5-1min

Rapid offset TOF 0.9

-Quick wake up after short procedure

-Safer if CICO

2xED95: 30-40mins

4xED95: 45-60 mins

4xED95: 5 mins

(Gantacurium 10 mins max)

Absorption

N/A

 

Distribution:

 

 

-Rapid distribution

i.e. fast offset after single bolus (e.g. gastroscopy)

Fast?

Fast?

-VDSS

 

 

Metabolism/excretion

 

 

-Rapid metabolism

i.e. fast offset after long infusion

t1/2β 70 mins (slow)

t1/2β 1-2 mins (fast)

-Organ-independent metabolism

(ok if liver/kidney failure)

5% metabolized

60% bile excretion

35% renal excretion

Plasma cholinesterase (produced by liver but rarely affected by liver disease)

(Gantacurium: cysteine adduction)

-No active metabolites

(ok if liver/kidney failure)

17-desacetylrocuronium less active

Hepatic elimination

Nil

(Gantacurium: Nil)

-No significant polymorphism

 

Sux apnoea rare

(pseudocholinesterase polymorphism)

 

Ideal dynamics:

 

Rocuronium

Suxamethonium or other

Effect:

 

 

-Non-depolarising

Depolarizing

(ion flux -> ↑plasma K+)

-No desensitisation

Y

(Phase 2 blockade, prolonged)

-Antidote for deep blockade

 i.e. fast offset after short case

 i.e. Safer if CICO

γ-cyclodextrin 16mg/kg if CICO

N

 

 

 

Side effects:

 

 

No histamine release

Does not

Does

No anaphylaxis

1 in 2500

1 in 2000

(Gantacurium: very low)

No ↑K+

Y (depolarisation)

↑↑↑ if denervated e.g. burns

No cardiac mAChr effect

Agonist -> sinus bradycardia, AV block, asystole, esp children

No malignant hyperthermia

Does

(activate abnormal ryanodine receptor)

No myalgia

(depolarisation)

No ↑IOP

(depolarisation)

No ↑IGP

(depolarisation)

↑risk aspiration (but also ↑lower oesophageal sphincter pressure)

No ganglion blockade

dTC does

 

 

 

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