Muscle relaxants and reversal agents Flashcards
Doses for muscle relaxants
Suxamethonium: 1.5mg/kg
Rocuronium: 0.6 mg/kg, 1.2 mg/kg for RSI
Vecuronium: 0.1mg/kg
Atracurium: 0.6 mg/kg
Onset for muscle relaxants
Suxamethonium: 30 seconds
Rocuronium: 2 minutes at 0.6mg/kg, 30-60 seconds at 1.2mg/kg
Vecuronium: 3 minutes
Atracurium: 3 minutes
Duration for muscle relaxants
Suxamethonium: 5 minutes
Rocuronium: 40 minutes
Vecuronium: 40 minutes
Atracurium: 40 minutes
Note with repeat dosing, non-depolarising agents duration of action is prolonged especially with aminosteroid agents that are organ dependent (vec and roc). For infusions its more common to see atracurium (and cisatracurium used)
Special features for the muscle relaxants
Suxamethonium: Fastest onset, fast offset, the only depolarising muscle relaxant in use so muscle fasciculations mark the onset of block
Rocuronium: Fastest onset at 1.2mg/kg, direct reversal agent suggamadex, no histamine release
Vecuronium: Intermediate onset, direct reversal agent suggamadex, no histamine release, very low anaphylaxis risk
Atracurium: Intermediate onset, non-organ dependent metabolism
Unique side effects of muscle relaxants
Suxamethonium: hyperkalaemia - arrest, higher anaphylaxis risk, malignant hyperthermia, sux apnoea = prolonged action, myalgias, second dose bradycardia
Rocuronium: Higher anaphylaxis risk, hepatic and renal metabolism
Vecuronium: Hepatic and renal metabolism
Atracurium: Histamine release/anaphylactoid reactions
Common side effects to all muscle relaxants
High anaphylaxis risk
Definitive muscle paralysis = apnoea (ventilation always required)
Needs reversal agent
2 categories of muscle relaxants
Depolarising (sux) and non-depolarising (all others)
Non-depolarising are divided in to aminosteroids (roc, vec) and benzylisoquinoliniums (atracurium, cisatrac)
Speed of onset
The less potent the drug, the faster the onset
The less potent, the more particles are needed to exert an effect. More particles mean a higher concentration gradient to drive the diffusion of drug molecule to the site of action.
Rocuronium is the least potent therefore with a dose of 1.2mg/kg dose it acts very quickly
= an application of Fick’s Law of Diffusion
What is sux apnoea
Describes prolonged muscle paralysis after the administration of sux due to pseudocholinesterase deficiency (which can be acquired or genetic)
Explain genetic pseudocholinesterase deficiency
96% of people have the normal gene with paralysis lasting about 5 minutes
4% may have a heterozygous mutation - paralysis lasting about 10 minutes
A very small number of people have a homozygous mutation whereby paralysis may last for hours
How can you acquire a pseudocholinesterase deficiency?
Pregnancy
Kidney and liver disease
Heart failure
Thyroid disease
Drugs (lithium, neostigmine, cytotoxic agents)