6. Physiology of Local
Anaesthetics
Implications
Acidic environments will have a greater proportion
of LA in the ionised (less active) form
Buffered LA will be more unionised and thus more
active
Consider metabolism when devising a dosage
10. Lignocaine
Widely used and highly familiar
Onset <5 min
Duration 30-90 min (half life up to triple in
severe liver disease)
Various formulations for easy use
Use of adrenaline in end artery territory?
11. Ropivacaine
Successor to bupivacaine as less cardiotoxic
with more predictable toxicity syndrome
Long duration of action (up to 20 hours)
Longer onset time (10-30 minutes)
12. Prilocaine
Least cardiotoxic of the amide local
anaesthetics
Metabolised by hepatic amidases to
aminophenols
These oxidise haemoglobin to form
methemoglobin
Management
1-2mg/kg (up to 50mg) in 50mL in NS over 3-5
minutes
Can repeat every 30 minutes, up to 7mg/kg with
16. Treatment options
Standard toxicology Na channel blockade
treatment
Sodium Bicarbonate
Hyperventilate
IV lipid emulsion
1.5mL/kg over ONE minute followed by
0.25mL/kg/minute until haemodynamically stable
>10min.
Note 0.25mL/kg/min = 1050mL/hr for a 70kg patient
Can rebolus a further 1.5mL/kg after ~30min and
increase rate to 0.5mL/kg/min.
Where is it kept?