Lidocaine, also called lignocaine, is an amide local anesthetic with additional class Ib antiarrhythmic activity. It is used for local and regional nerve blockade and for selected ventricular arrhythmias. Intravenous infusions also have adjunctive analgesic applications, particularly in dogs and horses, and a specialist role in management of equine postoperative ileus.
Group
Local anaesthetic and class Ib antiarrhythmic
Mechanism of Action
Lidocaine blocks voltage-gated sodium channels, particularly when they are open or inactivated. In peripheral nerves, this interrupts action-potential propagation and produces local anesthesia. In ventricular tissue, it suppresses abnormal automaticity and excitability, supporting antiarrhythmic action. Systemic analgesic effects include modulation of nociceptive signaling; proposed effects in equine ileus also involve inflammatory and pain pathways, with the full mechanism unresolved.
Dose Rates
Dogs
| Use / stage | Dose | Route | Schedule | Instructions |
|---|---|---|---|---|
| Ventricular arrhythmia bolus | 2–4 mg/kg | IV | Cumulative maximum 8 mg/kg over 10 minutes. Track the cumulative amount delivered within that 10-minute window. | |
| Ventricular arrhythmia infusion — Loading | 1 mg/kg | IV | ||
| Ventricular arrhythmia infusion — Maintenance | 50–75 mcg/kg/min | IV | Continuous | |
| Ventricular arrhythmia | 6 mg/kg | IM | Every 1.5 h | |
| Epidural anaesthesia | 4.4 mg/kg | EPIDURAL | Once | Use an appropriate 2% preservative-free solution. |
| Perioperative analgesia — Loading | 2 mg/kg | IV | ||
| Perioperative analgesia — Maintenance | 0.05 mg/kg/min | IV | Continuous | Up to 1 days |
| Ventricular arrhythmia infusion — Maintenance | 40–80 mcg/kg/min | IV | Continuous | Separate titration alternative, with ECG monitoring. |
| Ventricular arrhythmia infusion — Maintenance | 25–80 mcg/kg/min | IV | Continuous | Separate titration alternative, with ECG monitoring. |
| Ventricular arrhythmia infusion — Maintenance | 25–75 mcg/kg/min | IV | Continuous | Separate titration alternative, with ECG monitoring. |
| Ventricular arrhythmia | 4 mg/kg | IM | Do not use the IM alternative in shock; onset approximately 10-15 minutes. | |
| Analgesic infusion | 2–4 mg/kg/hour | IV | Continuous | |
| Analgesic infusion — Loading | 1–4 mg/kg | IV | ||
| Analgesic infusion — Maintenance | 1–5 mg/kg/hour | IV | Continuous | |
| Alternative perioperative analgesia — Loading | 2 mg/kg | IV | Give over 2-3 minutes. | |
| Alternative perioperative analgesia — Maintenance | 50–100 mcg/kg/min | IV | Continuous | |
| Epidural anaesthesia | 4–5 mg/kg | EPIDURAL | Once | Appropriate preservative-free formulation; effects start within about 10 minutes and last around 1.5 hours. |
Cats
| Use / stage | Dose | Route | Schedule | Instructions |
|---|---|---|---|---|
| Epidural anaesthesia | 4.4 mg/kg | EPIDURAL | Once | Use an appropriate 2% preservative-free solution. |
| Ventricular arrhythmia bolus — Initial | 0.1–0.4 mg/kg | IV | Administer slowly and reassess cardiovascular response. | |
| Ventricular arrhythmia bolus — Maintenance | 0.25–0.75 mg/kg | IV | Subsequent escalation only if there has been no response to the initial dose. | |
| Ventricular arrhythmia infusion — Loading | 0.5–1 mg/kg | IV | ||
| Ventricular arrhythmia infusion — Maintenance | 10–20 mcg/kg/min | IV | Continuous | Equivalent to 0.6-1.2 mg/kg/hour; cats have increased cardiotoxicity risk. |
| Epidural anaesthesia | 4–5 mg/kg | EPIDURAL | Once | Appropriate preservative-free formulation; effects start within about 10 minutes and last around 1.5 hours. |
| Ventricular arrhythmia bolus — Initial | 0.25–0.5 mg/kg | IV | Slow IV; subsequent 0.15-0.25 mg/kg in 5-20 minutes only according to response. Track cumulative exposure. |
Horses
| Use / stage | Dose | Route | Schedule | Instructions |
|---|---|---|---|---|
| Ventricular tachycardia — Initial | 0.25–0.5 mg/kg | IV | Administer over 5-10 minutes; refractory cases have received 1.3-1.5 mg/kg. | |
| Ventricular tachycardia — Maintenance | 30–50 mcg/kg/min | IV | Continuous | |
| Postoperative ileus — Loading | 1.3 mg/kg | IV | Administer over 15 minutes. | |
| Postoperative ileus — Maintenance | 50 mcg/kg/min | IV | Continuous | |
| Analgesia — Loading | 2 mg/kg | IV | ||
| Analgesia — Maintenance | 50 mcg/kg/min | IV | Continuous | |
| Ventricular tachycardia — Initial | 1–1.5 mg/kg | IV | Monitor ECG and follow with an individualized infusion if effective. | |
| Colic-associated ileus or pain — Loading | 1.4 mg/kg | IV | ||
| Colic-associated ileus or pain — Maintenance | 0.03–0.05 mg/kg/min | IV | Continuous |
Indications
- Local infiltration, topical mucosal anesthesia and regional nerve blockade for veterinary procedures.
- Epidural or other regional anesthesia with an appropriate formulation and technique.
- Treatment of selected ventricular tachyarrhythmias, particularly ventricular tachycardia or clinically significant ventricular premature complexes.
- Adjunctive perioperative or trauma-associated analgesia using a systemic infusion in selected patients.
- Specialist management of postoperative ileus in horses.
Contraindications
- Cats are especially susceptible to systemic cardiotoxicity.
- Reduced hepatic blood flow can decrease clearance.
- Avoid epinephrine-containing formulations for antiarrhythmic use.
- Major SA/AV/intraventricular block without pacing, or amide-local-anaesthetic hypersensitivity.
Interactions
- Alkaline storage mixtures can precipitate lidocaine hydrochloride; administer promptly if buffering is used.
Adverse effects
- Tremors, seizures, fasciculations, ataxia and vomiting
- Cardiovascular depression and arrhythmias
- Feline methaemoglobinaemia and haemolysis
Toxicity
Stop administration and support airway, ventilation and circulation; manage seizures and consider lipid-emulsion treatment for severe systemic local-anaesthetic toxicity.
Preparations
| Preparation | Form | Strength | Route |
|---|---|---|---|
| Lidocaine (Lignocaine) 5 mg/mL injection Plain lidocaine, without epinephrine; strength stated for the hydrochloride preparation. | Injection | 5 mg / mL | IV, IM |
| Lidocaine (Lignocaine) 10 mg/mL injection Plain lidocaine, without epinephrine; strength stated for the hydrochloride preparation. | Injection | 10 mg / mL | IV, IM |
| Lidocaine (Lignocaine) 15 mg/mL injection Plain lidocaine, without epinephrine; strength stated for the hydrochloride preparation. | Injection | 15 mg / mL | IV, IM |
| Lidocaine (Lignocaine) 20 mg/mL injection Plain lidocaine, without epinephrine; strength stated for the hydrochloride preparation. | Injection | 20 mg / mL | IV, IM |
| Lidocaine 20 mg/mL preservative-free epidural solution Preservative-free formulation only; no epinephrine. | Injection | 20 mg / mL | EPIDURAL |
Monitoring and Administration
Use continuous ECG for antiarrhythmic treatment and observe for neurologic toxicity, especially in cats.
For the described buffering method, 1 mEq sodium bicarbonate is added to 10 mL lidocaine and used immediately. Avoid prolonged storage of buffered mixtures.
Epidural use requires an appropriate preservative-free formulation.
Published guidance describes equine lidocaine 10 g added to 3 L LRS as approximately 0.33%; actual final volume must be established before a mixing calculation.
For refractory equine ventricular arrhythmias, magnesium sulfate may be added as a separate assessed treatment: published guidance describes 2.7 g in 1 L saline over 10 minutes, corresponding to approximately 2-6 mg/kg in its patient context. Do not mix magnesium into calcium-containing fluid.
The morphine-lidocaine-ketamine combination targets morphine 0.24, lidocaine 3 and ketamine 0.6 mg/kg/hour. The recipe amounts do not produce all target rates at a single common fluid rate; a validated combination recipe is required.
Topical lidocaine/EMLA may be applied as a thin layer every 3-4 hours as needed. Avoid eyes and unlabelled ear use, large areas and prolonged exposure; prilocaine increases methaemoglobinaemia risk. Wash hands or wear gloves. Topical concentration ranges alone do not establish an exact mass per mL or gram for every product.