Maximum Dose of Lidocaine for Local Anesthesia
For adults undergoing local infiltrative anesthesia, administer no more than 4.5 mg/kg of lidocaine without epinephrine or 7.0 mg/kg of lidocaine with epinephrine in a single treatment. 1
Adult Dosing Guidelines
Standard Local Infiltration
- Without epinephrine: Maximum 4.5 mg/kg 1
- With epinephrine: Maximum 7.0 mg/kg 1
- These doses are based on expert consensus and manufacturer recommendations, though the true maximum safe dose remains unknown 1
Special Circumstances
Multistage procedures (e.g., Mohs surgery):
- Maximum 500 mg (50 mL of 1% lidocaine solution) delivered incrementally over several hours 1
- This recommendation has stronger evidence (Level II) compared to standard dosing 1
Topical anesthesia for airway procedures:
- Maximum 9 mg/kg lean body weight 1
- This higher dose applies specifically to topical airway anesthesia, not infiltrative use 1
- Use lean body weight for calculation, not actual body weight 1
Intravenous regional anesthesia (Bier block):
- Dramatically reduced to 3-5 mg/kg only 2
- Long-acting agents (bupivacaine, ropivacaine) are contraindicated for IV use due to cardiac toxicity risk 2
Pediatric Dosing Guidelines
Children require substantially lower doses: 1
Infants under 6 months:
- Reduce all amide local anesthetic doses by 30% 2
- For example, a dose of 4.5 mg/kg becomes approximately 3.15 mg/kg 2
Critical Safety Measures to Prevent Toxicity
Before administration: 1
- Calculate the maximum allowable dose in milligrams before starting the procedure 1
- Use the lowest effective dose necessary 1
During injection: 1
- Aspirate before each injection to avoid intravascular administration 1
- Use incremental injections rather than bolus dosing 1
- Inject slowly to allow for early detection of toxicity 1
Monitoring: 1
- Continuously assess and communicate with the patient 1
- Watch for early signs: circumoral numbness, facial tingling, metallic taste, auditory changes, slurred speech 1
- Progressive toxicity manifests as seizures, CNS depression, cardiovascular collapse 1
Important Clinical Considerations
Epinephrine significantly increases safety margins:
- Adding epinephrine allows 55% higher doses (7.0 vs 4.5 mg/kg) by decreasing systemic absorption 1
- Use concentrations of 2.5-5 μg/mL when administering large doses 3
Highly vascular areas require dose reduction:
- Decrease doses when injecting into highly vascular tissues due to increased systemic absorption 2, 3
- No specific percentage reduction is defined, but use clinical judgment 3
Obese patients:
- Calculate doses using ideal body weight, not actual body weight 2
- This prevents overdosing in patients with excess adipose tissue 2
Common Pitfalls and How to Avoid Them
Calculation errors:
- Convert concentrations correctly: 1% lidocaine = 10 mg/mL 1
- For a 70 kg adult with epinephrine: maximum = 490 mg = 49 mL of 1% solution 1
Cumulative dosing in prolonged procedures:
- Track total dose administered over time 1
- For procedures lasting several hours, the 500 mg limit over 8 hours appears safe 1
Combining with other local anesthetics:
- Account for additive effects when using multiple agents 2
- Total dose of all local anesthetics must be considered 1
Drug interactions:
- Enhanced sedative effects occur when maximum doses are combined with opioids or sedatives 2
- Avoid IV lidocaine within 4 hours of other local anesthetic interventions 2
Context-Specific Variations
Tumescent anesthesia (specialized technique):
- Much higher doses up to 28 mg/kg without liposuction or 45 mg/kg with liposuction may be safe 4
- This applies only to dilute lidocaine (≤1 g/L) with epinephrine in large volumes 4
- Delayed systemic absorption allows these higher doses 4
Diluted solutions with epinephrine:
- Doses up to 21.6 mg/kg of 0.33% lidocaine with epinephrine for facelift procedures yielded peak levels well below toxic thresholds 5
- However, standard guidelines should be followed unless using established tumescent protocols 1
The evidence base for these recommendations is primarily expert consensus (Level III evidence), with the notable exception of the 500 mg limit for multistage procedures which has Level II evidence 1. Despite widespread clinical use for decades, randomized controlled trials establishing definitive maximum safe doses are lacking 3.