lidocaine hydrochloride: prescribing and clinical use
Focused clinical detail for use alongside current product information, local policy and patient-specific assessment.
lidocaine hydrochloride: clinical details
Prescribing considerations
- Use only where resuscitation equipment, emergency medicines and appropriately skilled personnel are immediately available.
- Reduce systemic-toxicity risk through individual assessment, careful injection technique and vigilance for early neurological or cardiovascular symptoms.
- Use additional caution with hepatic or severe renal impairment, cardiac failure, impaired conduction, bradycardia, respiratory impairment, epilepsy, myasthenia gravis, shock, pregnancy and frailty.
- Inflamed or infected tissue can increase systemic absorption while reducing local anaesthetic effectiveness.
Contraindications and cautions
- Hypersensitivity to lidocaine, another amide local anaesthetic or a formulation excipient.
- For spinal or epidural anaesthesia: uncorrected hypovolaemia, coagulopathy, increased intracranial pressure, or intracranial or intraspinal haemorrhage.
- For antiarrhythmic use: severe conduction disorders; recent myocardial infarction or markedly reduced cardiac output unless a life-threatening ventricular arrhythmia is present.
Monitoring
- During systemic antiarrhythmic administration, continuously monitor ECG, blood pressure, consciousness and respiration.
- During prolonged parenteral treatment, monitor fluid balance, electrolytes and acid–base status.
- Monitor closely for early toxicity, particularly with impaired hepatic perfusion, severe renal impairment, interacting medicines or administration near highly vascular tissue.
Clinical pharmacology
Lidocaine reversibly blocks sodium channels in excitable membranes. It is extensively metabolised in the liver. Reduced hepatic blood flow or function can prolong exposure, while active metabolites may accumulate in severe renal impairment or during prolonged administration.
Formulation and product differences
- The selected product is a clear, colourless, single-use solution for injection.
- It contains sodium chloride, sodium hydroxide and water for injections, without a vasoconstrictor.
- Injectable lidocaine is not interchangeable in administration or licensed use with skin creams, gels, sprays or medicated plasters.
- It must not be mixed with sodium bicarbonate, specified incompatible injectable medicines or other alkaline solutions.
lidocaine hydrochloride preparations and strengths
Injection
Route: Parenteral
Strengths: 0.5% w/v, 1.0% w/v, 1% w/v, 2.0% w/v, 2% w/v
lidocaine hydrochloride interactions
Clinicians should review all medicines because systemic exposure and cardiac or neurological effects can be altered.
Other local anaesthetics
Cardiovascular and central nervous system effects can be additive.
Class I antiarrhythmics
Combined use should generally be avoided because serious cardiac adverse effects may occur.
Beta blockers or calcium-channel blockers
Cardiac conduction and contractility may be further suppressed; some beta blockers can also reduce lidocaine clearance.
Sources
These sources were used to prepare and review this medicine page.
Prepared and reviewed by the iatroX editorial team.