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Analgesic responses to i.v. lignocaine
British Journal of Anaesthesia
|May 1, 1982
Summary
Intravenous lignocaine effectively reduced clinical neuralgic pain, particularly deafferentation pain, at lower doses. However, it showed limited effect on ischemic pain, even at higher concentrations.
Area of Science:
- Anesthesiology
- Neurology
- Pharmacology
Background:
- Neuralgic pain presents diverse etiologies.
- Intravenous lignocaine is a local anesthetic with potential systemic effects.
- Understanding lignocaine's differential analgesic effects is clinically relevant.
Purpose of the Study:
- To evaluate the analgesic efficacy of intravenous lignocaine in patients with neuralgic pain.
- To compare lignocaine's effect on clinical neuralgic pain versus experimentally induced ischemic pain.
- To investigate the dose-dependent and pain-type-specific actions of lignocaine.
Main Methods:
- Five patients with neuralgic pain were administered intravenous lignocaine.
- Pain intensity was assessed for both clinical neuralgic pain and concurrently induced ischemic pain.
- Lignocaine was administered in a high-dose infusion followed by lower doses, with corresponding blood concentrations monitored.
Main Results:
- High-dose lignocaine (3 mg kg-1) reduced both clinical and ischemic pain, with a significantly greater reduction in clinical pain.
- At lower doses, lignocaine effectively suppressed clinical neuralgic pain but had no significant effect on ischemic pain.
- Clinical neuralgic pain was almost totally suppressed at lower lignocaine concentrations compared to its lack of effect on ischemic pain.
Conclusions:
- Intravenous lignocaine exhibits a differential analgesic effect based on pain etiology.
- Lignocaine appears particularly effective for deafferentation pain and central neuralgias.
- Peripheral pain of origin is largely unaffected by lignocaine, except at potentially toxic concentrations.