Intravenous Lidocaine Administration Guidelines
Dosing Protocol
For IV lidocaine administration, give a loading dose of 1.5 mg/kg over 10 minutes, followed by a continuous infusion at 1.5 mg/kg/hour, with duration not exceeding 24 hours in most cases. 1
Loading Dose
- Maximum loading dose: 1.5 mg/kg infused over 10 minutes 1
- Calculate using ideal body weight (IBW): Men = height in cm - 100; Women = height in cm - 105 2
- Do not use in patients weighing less than 40 kg 2
- Too rapid infusion increases toxicity risk 1
- Complete the initial infusion before skin incision when possible 1
Maintenance Infusion
- Standard rate: 1.5 mg/kg/hour 1
- Maximum hourly dose: 120 mg/hour regardless of weight 2
- This dosing typically maintains plasma concentrations below 5 μg/mL 1
- Only consultant anaesthetists or intensivists should alter infusion rates 1
- Frequent rate changes should be discouraged 1
Duration
- Do not exceed 24 hours in most patients 1
- If extension beyond 24 hours is necessary, reduce infusion rate to 50% 1
- Decision to extend must be made by consultant anaesthetist/intensivist or acute pain team 1
- Note that lidocaine exhibits time-dependent pharmacokinetics, with half-life prolonging from 100 minutes to 3.22 hours after 24 hours of infusion 3
Administration Technique
Equipment Requirements
- Use dedicated, labelled, lockable, tamperproof infusion pumps with fixed rate and upper rate limits 1
- Pumps must have anti-siphon and anti-reflux mechanisms 1
- Use commercially prepared syringes/bags when available to reduce concentration errors 1
- Maintain standard concentration throughout the hospital per protocol 1
IV Access and Line Management
- Deliver through a separate, dedicated cannula 1, 2
- Co-infuse minimum 10 mL/hour sodium chloride 0.9% from dedicated bag to flush lidocaine and reduce vein tracking 1
- Line must have one-way valve to prevent retrograde tracking into other infusions 1
- Label infusion line with ISO-standard grey 'lidocaine' label 1
- Maintain separate lidocaine monitoring chart 1
Monitoring Requirements
Initial Monitoring (Operating Theatre/Recovery)
- Anaesthetist must be present during initial dose 1
- Continuous ECG and pulse oximetry throughout 1
- Blood pressure every 5 minutes during initial infusion and first 15 minutes thereafter 1, 2
Post-Operative Monitoring
- Ideally manage in high dependency unit (level 2 care) 1
- Observations every 15 minutes for first hour, then hourly minimum 1
- Continue ECG monitoring (though cardiovascular changes are late signs) 1
- Nurses must be trained in toxicity recognition 1
- Acute pain team should be involved in monitoring and follow-up 1
Toxicity Recognition and Management
Early Warning Signs (Plasma 5-10 μg/mL)
- Neurological symptoms appear first: peri-oral tingling, tinnitus, light-headedness, restlessness 1
- Circumoral numbness, facial tingling, slurred speech 4, 2
- Tingling of tongue/lips 4, 2
Severe Toxicity Signs (Plasma >10 μg/mL)
- Muscle twitching, loss of consciousness 1, 4
- Respiratory arrest 1, 4
- Cardiac arrhythmias, myocardial depression 1, 4
- Ventricular arrest 4, 2
Emergency Preparedness
- Lipid emulsion 20% must be readily available wherever IV lidocaine is used 1
- Staff must know storage location 1
- Follow Association of Anaesthetists' management guideline for treatment 1
- Discontinue all lidocaine immediately if toxicity signs appear 4, 2
Drug Interactions and Contraindications
Local Anesthetic Interactions
- Remove topical 5% lidocaine plasters before starting IV infusion 1, 2
- No nerve or fascial plane blocks until 4 hours after completing IV lidocaine 1, 2
- No boluses into wound/epidural catheters until 4 hours after completion 1
- Infusions (without boluses) through wound/epidural catheters may start 30 minutes after stopping IV lidocaine 1
- Single-shot spinal blockade is acceptable due to small local anesthetic dose 1, 2
- Intrathecal opioids can be used concurrently 1
Concurrent Medications
- Concurrent ketamine administration is acceptable 1
- Ketamine is often tried before lidocaine in difficult-to-manage pain 1
High-Risk Populations (Use with Caution)
- Cardiac disease, electrolyte disorders 4, 2
- Seizure disorders 4, 2
- Renal or hepatic impairment 4, 2
- Pregnancy/breastfeeding 4, 2
- Neurological disorders 4, 2
- Advanced liver failure (contraindicated due to decreased clearance) 4
Critical Safety Considerations
Common Pitfalls to Avoid
- Never calculate dose using actual body weight in obese patients—use ideal body weight 2
- Never combine with other local anesthetics without appropriate waiting periods 1, 2
- Never assume cardiovascular signs will appear before neurological signs—they are late manifestations 1
- Never extend infusion beyond 24 hours without consultant approval and rate reduction 1
- Particular vigilance needed in patients with existing comorbidity 1