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Published on: October 14, 2014
Epinephrine absorption in children with a history of anaphylaxis
F E Simons1, J R Roberts, X Gu
1Department of Pediatrics and Child Health, Faculty of Medicine, University of Manitoba, Winnipeg, Canada.
Insights
Subcutaneous epinephrine absorption is delayed in children, potentially impacting anaphylaxis treatment. Intramuscular injection offers faster absorption and is the preferred method for allergic emergencies.
Area of Science:
- Pediatric Allergy and Immunology
- Clinical Pharmacology
- Emergency Medicine
Background:
- Epinephrine injection is crucial for treating systemic anaphylaxis.
- The absorption rate of epinephrine via subcutaneous injection in allergic children remains understudied.
Purpose of the Study:
- To investigate the clinical pharmacology of epinephrine absorption in children with a history of anaphylaxis.
- To compare the absorption rates of subcutaneous versus intramuscular epinephrine administration.
Main Methods:
- A prospective, randomized, blinded, parallel-group study involving 17 children with anaphylaxis history.
- Administration of epinephrine via subcutaneous injection (0.01 ml/kg) or intramuscular autoinjector (0.3 mg).
- Monitoring of plasma epinephrine concentrations, vital signs, and adverse effects.
Main Results:
- Subcutaneous epinephrine showed a delayed mean time to maximum plasma concentration (34 minutes) compared to intramuscular (8 minutes).
- Only 2 of 9 children achieved peak concentrations by 5 minutes with subcutaneous injection, versus 6 of 8 with intramuscular.
- No serious adverse effects were reported for either administration route.
Conclusions:
- Delayed epinephrine absorption via subcutaneous injection in children necessitates reevaluation of current recommendations.
- The intramuscular route of epinephrine administration is clinically preferable for faster absorption during anaphylaxis.
- Faster epinephrine absorption is critical for effective management of severe allergic reactions.
Background:
Prompt injection of epinephrine is the cornerstone of systemic anaphylaxis treatment. The rate of epinephrine absorption has not been reported previously in allergic children.
Objective:
Our objective was to study the clinical pharmacology of epinephrine in this population.
Methods:
We performed a prospective, randomized, blinded, parallel-group study in 17 children with a history of anaphylaxis to food, Hymenoptera venom, or other substances. We injected 0.01 ml/kg epinephrine solution (maximum 0.3 ml [0.3 mg]) subcutaneously, or 0.3 mg epinephrine intramuscularly from an autoinjector. Plasma epinephrine concentrations, heart rate, blood pressure, and adverse effects were monitored.
Results:
In nine children who received epinephrine subcutaneously, the mean maximum plasma epinephrine concentration (+/- SEM) was 1802 +/- 214 pg/ml, achieved at a mean time of 34 +/- 14 minutes (range, 5 to 120 minutes). Only two of the nine children achieved maximum plasma concentrations by 5 minutes. In eight children who received epinephrine intramuscularly, the mean maximum plasma concentration was 2136 +/- 351 pg/ml, achieved at a mean time of 8 +/- 2 minutes, which was significantly faster than the mean time at which maximum plasma concentrations were achieved after subcutaneous epinephrine injection (p < 0.05). Six of the eight children achieved maximum plasma concentrations by 5 minutes. The terminal elimination half-life was 43 +/- 15 minutes. No serious adverse effects were noted in any child.
Conclusions:
In children, recommendations for subcutaneous epinephrine injection are based on anecdotal experience, and should be reevaluated in view of our finding of delayed epinephrine absorption when this route is used. This delay might have important clinical implications during an episode of systemic anaphylaxis. The intramuscular route of injection is preferable.
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