Risk factors for toxicity
The toxicity of a local anaesthetic is influenced by:
- the specific local anaesthetic used (eg bupivacaine is more toxic than lidocaine)
- whether a coformulation with adrenaline has been used1
- route of administration (eg intravenous injection is more likely to cause toxicity than other routes)
- method of administration (eg an intravenous bolus injection is likely to result in a higher peak concentration than an infusion)
- site of administration (eg systemic absorption through skin is slower than through mucous membranes)
- vascularity of surrounding tissues (vascularity enhances absorption)
- patient-specific factors (eg pre-existing cardiac disease may compound drug toxicity).
A local anaesthetic block can cause toxic effects in itself, separate from the toxicity of the drug (eg hypotension due to a spinal or epidural block).
1 Adrenaline (epinephrine) is coformulated with some local anaesthetic drugs (eg bupivacaine, lidocaine) for parenteral use. Adrenaline’s vasoconstrictor effect slows systemic absorption of the local anaesthetic from the injection site. This prolongs the local anaesthetic effect and reduces the likelihood of systemic toxicity.Return