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Published on: September 20, 2019
Double-Blind, Randomized Clinical Trial Comparing One Percent Buffered Versus Two Percent Unbuffered Lidocaine
Suzanne D Baker1, Jessica Y Lee2, Raymond P White3
1Dr. Baker is in private practice, North Carolina State University, Raleigh, N.C., USA.
Insights
Buffered lidocaine in children demonstrated equal effectiveness to unbuffered formulations, but with significantly lower blood lidocaine levels. This buffered local anesthetic offers a safer alternative for pediatric pain management.
Area of Science:
- Pediatric Anesthesiology
- Pharmacology
- Pain Management
Background:
- Buffered local anesthetics are an alternative to conventional formulations.
- Limited evidence exists regarding their use in pediatric populations.
Purpose of the Study:
- To compare anesthetic and physiological differences between buffered 1% and unbuffered 2% lidocaine with epinephrine in children.
- To assess safety and efficacy in pediatric patients.
Main Methods:
- Randomized, double-blinded, crossover study involving 25 children aged 10-12 years.
- Inferior alveolar nerve blocks administered with either buffered 1% or unbuffered 2% lidocaine.
- Primary outcomes included blood lidocaine levels, onset, duration, and pain on injection.
Main Results:
- Buffered lidocaine resulted in a 63% lower mean blood lidocaine level compared to unbuffered lidocaine (P<0.05).
- No significant differences were observed in pain on injection, onset, or duration of anesthesia between the two formulations.
Conclusions:
- Buffered local anesthetic formulations are equally effective as higher-concentration unbuffered formulations.
- Buffered lidocaine significantly reduces systemic absorption, offering a potential advantage in preventing local anesthetic toxicity in children.
Abstract:
Purpose: Buffered local anesthetics offer an alternative to conventional, unbuffered anesthetic formulations; however, evidence about their use in children is scant. The purpose of this study was to determine the anesthetic and physiologic differences associated with the use of buffered one percent and unbuffered two percent lidocaine (both with 1:100,000 epinephrine) in children. Methods: In this randomized, double-blinded, crossover study, 25 children ages 10 to 12 years old received two inferior alveolar never blocks, at least one week apart, randomized to alternating sequences of two drug formulations: (1) formula A-three mL buffered one percent lidocaine (i.e., including 0.3 mL of 8.4 percent sodium bicarbonate); or (2) formula B-three mL unbuffered two percent lidocaine. Primary outcomes were mean blood lidocaine levels (15 minutes post-injection), timing of clinical signs onset, response to pain on injection, and duration of anesthesia. Analyses relied upon analysis of variance for crossover study designs and a P<0.05 statistical significance criterion. Results: The buffered formulation resulted in significantly lower mean blood lidocaine levels compared to unbuffered-a 63 percent (P<0.05) weight-adjusted relative decrease. The authors found no important differences in pain upon injection, onset, and duration of anesthesia. Conclusion: The buffered local anesthetic formulation showed equal effectiveness with a double-concentration unbuffered formulation while resulting in lower mean blood lidocaine levels-an important gain for the prevention of anesthetic toxicity.
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