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Comparison of Adenosine Administration Utilizing a Single-Syringe Versus a Double-Syringe Method in a Simulated
Brianna Schafer1, Kelly E Steidl1,2, Jeni L Burgess1
1Department of Pharmacy, Upstate University Hospital.
The single syringe (SS) method for adenosine administration was significantly faster than the double syringe (DS) method in a simulated pediatric emergency setting. Most participants preferred the SS method, finding it easier to administer.
Area of Science:
- Emergency Medicine
- Pediatric Critical Care
- Pharmacology
Background:
- Adenosine is crucial for treating supraventricular tachycardia in pediatric emergencies.
- Current administration methods, like the double syringe (DS) technique, may be time-consuming.
- Optimizing adenosine delivery is vital for improving patient outcomes in critical care settings.
Purpose of the Study:
- To compare the adenosine administration time between the single syringe (SS) and double syringe (DS) methods.
- To evaluate preparation time, errors, and participant preferences in a simulated pediatric emergency department (ED).
Main Methods:
- A prospective, randomized, crossover simulation study involving pharmacist-physician pairs.
- Adenosine doses were prepared by pharmacists and administered by physicians.
- Primary outcome was adenosine administration time; secondary outcomes included preparation metrics and participant feedback.
Main Results:
- The SS method demonstrated significantly shorter administration times compared to the DS method (13s vs. 26s, P<0.001).
- No significant differences were observed in preparation times or pharmacist-rated ease of administration.
- Physicians rated the SS method easier to administer, and 68.8% of participants preferred it.
Conclusions:
- The SS method offers a faster adenosine administration time compared to the DS method in a simulated ED environment.
- The SS method was perceived as easier to administer and was preferred by the majority of participants.
- Further clinical studies are needed to validate these findings and assess impact on patient outcomes, given the simulation design limitations.
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