Lidocaine: Difference between revisions
| Line 29: | Line 29: | ||
==Special Populations== | ==Special Populations== | ||
*[[Drug Ratings in Pregnancy|Pregnancy Rating]]: | *[[Drug Ratings in Pregnancy|Pregnancy Rating]]: American B, Australia A | ||
*Lactation: Not expected to cause any adverse effect <ref>https://www.ncbi.nlm.nih.gov/books/NBK501230/</ref> | *Lactation: Not expected to cause any adverse effect <ref>https://www.ncbi.nlm.nih.gov/books/NBK501230/</ref> | ||
*Renal Dosing | *Renal Dosing | ||
Revision as of 15:21, 17 March 2019
See critical care quick reference for drug doses by weight.
General
- Also known internationally as lignocaine
- Type: Local anesthetics; Antiarrhythmics
- Dosage Forms: Local injection, transdermal, intravenous, inhaled, viscous
- Common Trade Names: Xylocaine, P-Care, ReadySharp Lidocaine, Xylocard [1]
Adult Dosing
Local Anesthetic
- Maximum without epinepherine: 5mg/kg (max 300mg)
- Maximum with epinepherine: 7mg/kg (max 500mg)
Antiarrhythmic
- Loading dose = 1-1.5mg/kg
- Additional boluses of 0.5-0.75mg/kg q5-10min up to max of 3mg/kg
- If effective start infusion of 2mg/min
- Indications
- Treatment of ventricular arrhythmias and ectopy
- Considered 2nd-line to amiodarone for treatment of V-fib and pulseless v-tach
- Treatment of ventricular arrhythmias and ectopy
Pediatric Dosing
Local Anesthetic
- Without epinepherine: 5mg/kg (max 300mg)
- With epinepherine: 7mg/kg (max 500mg)
Antiarrhythmic
See critical care quick reference for drug doses by weight.
Special Populations
- Pregnancy Rating: American B, Australia A
- Lactation: Not expected to cause any adverse effect [2]
- Renal Dosing
- Hepatic Dosing
Contraindications
- Allergy to class/drug or agents with same chemical classification (amide/ester)
- High SA or AV block
Adverse Reactions
Serious
- Local Anesthetic Systemic Toxicity (LAST)
- Rare during infiltration of local anesthetic
- CNS toxicity
- Metallic taste, tinnitus, tingling of lips, dizziness, anxiety, confusion, lethargy, loss of consciousness, seizures
- Cardiovascular toxicity
- Bradycardia, decreased myocardial contractility, atrioventricular block, vasodilation, ventricular arrhythmias, cardiac arrest
Pharmacology
- Half-life:
- Onset of action = 45-90s
- Duration of action = 10-20min (antiarrythmic IV); 30-90 min (subcutaneous)
- Metabolism:
- Excretion:
- Mechanism of Action:
- Class Ib antiarrythmic
- Binds to fast Na channels in inactive state thereby inhibiting recovery after repolarization
- Acts preferentially on ischemic tissue
- Elevates V-fib threshold
- Suppresses ventricular ectopy
- Little effect on vascular tone, contractility or cardiac output
- Class Ib antiarrythmic
Comments
- For wounds, may use HCO3 (1cc to 10cc Lido) to decrease pain
- Inject through wound edges NOT intact skin
See Also
References
- ↑ Lidocaine. Lexicomp. Wolters Kluwer Health, Inc. Riverwoods, IL. Accessed March 15, 2019
- ↑ https://www.ncbi.nlm.nih.gov/books/NBK501230/
- ↑ Lidocaine. Lexicomp. Wolters Kluwer Health, Inc. Riverwoods, IL. Accessed March 15, 2019
- ↑ Lidocaine. Lexicomp. Wolters Kluwer Health, Inc. Riverwoods, IL. Accessed March 15, 2019
- ↑ Lidocaine. Lexicomp. Wolters Kluwer Health, Inc. Riverwoods, IL. Accessed March 15, 2019
- ↑ Lidocaine. Lexicomp. Wolters Kluwer Health, Inc. Riverwoods, IL. Accessed March 15, 2019
