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Adenosine Administration With a Stopcock Technique Delivers Lower-Than-Intended Drug Doses
Nathaniel T Weberding1, Richard A Saladino1, M Beth Minnigh2
1Department of Pediatrics, Division of Pediatric Emergency Medicine, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Insights
Adenosine administration via stopcock may deliver lower doses in infants under 10 kg, potentially explaining their reduced response to acute supraventricular tachycardia treatment.
Area of Science:
- Pediatric Cardiology
- Pharmacology
- Medical Device Engineering
Background:
- Adenosine is the standard treatment for pediatric acute supraventricular tachycardia.
- Infants often show a diminished response to the initial adenosine dose.
- The stopcock method for adenosine administration is widely used in pediatric care.
Purpose of the Study:
- To investigate if the stopcock method delivers sub-therapeutic adenosine doses in pediatric patients weighing less than 10 kg.
- To correlate adenosine delivery efficacy with patient weight.
Main Methods:
- An in vitro model simulating adenosine delivery through a stopcock was developed.
- Adenosine doses were calculated for weights ranging from 2 to 25 kg (0.1 mg/kg).
- Adenosine concentration in the output was quantified using mass spectrometry and spectrophotometry.
Main Results:
- Delivered adenosine doses increased proportionally with patient weight.
- Mean delivered dose was 0.08 mg/kg for weights 2-9 kg and 0.1 mg/kg for 10-25 kg.
- Median delivered doses were significantly lower for infants under 10 kg compared to older children.
Conclusions:
- The stopcock method results in underdosing of adenosine in pediatric patients weighing less than 10 kg.
- This sub-therapeutic dosing may explain the observed decreased efficacy of adenosine in infants.
- Clinical practice may need adjustment for adenosine administration in low-weight infants.
Study Objective:
Adenosine administration with a stopcock is the recommended treatment for pediatric patients with acute supraventricular tachycardia. Recent reports suggest that many infants do not respond to the first dose of adenosine administered. Our aim is to determine whether administration of adenosine with a stopcock delivers lower-than-expected drug doses in patients weighing less than 10 kg, corresponding to weights of infants.
Methods:
We developed an in vitro model of adenosine delivery. Doses of adenosine corresponding to weights 2 to 25 kg were calculated, using a dose of 0.1 mg/kg, and administered through one port of a stopcock. Distilled water was administered through the second port. The adenosine concentration of the output was measured with mass spectrometry and results were confirmed with spectrophotometry of Evans blue.
Results:
The mean doses of adenosine delivered through the stopcock increased as weight increased. The mean dose of adenosine delivered was 0.08 mg/kg for weights 2 to 9 kg and 0.1 mg/kg for weights 10 to 25 kg (95% confidence interval for difference of means -0.03 to -0.009). The median dose of adenosine delivered was 0.07 mg/kg (interquartile range [IQR] 0.06 to 0.07 mg/kg), 0.09 mg/kg (IQR 0.08 to 0.09 mg/kg), and 0.1 mg/kg (IQR 0.09 to 0.1 mg/kg) for weights 2 to 5, 6 to 9, and 10 to 25 kg, respectively (rank difference=100; P<.05 for 2 to 5 kg versus 10 to 25 kg). Similar results were obtained with spectrophotometry.
Conclusion:
Administration of adenosine through a stopcock delivers doses lower than intended in patients weighing less than 10 kg, which may account for the decreased response of infants to the first dose of adenosine.
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