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Reducing Unnecessary Penicillin Allergy Labels in the Pediatric Surgical Population
Ann M Hefel1, Laura A Wang, Maureen Bauer
1Author Affiliations: Department of Pediatrics, University of Colorado, Aurora, Colorado.
Insights
A quality improvement project reduced penicillin allergy labels in pediatric surgical patients by using oral provocation testing. This improved access to allergy evaluations and decreased unnecessary labeling without adverse events.
Area of Science:
- Pediatric Allergy and Immunology
- Quality Improvement in Healthcare
- Surgical Patient Management
Background:
- Up to 10% of children are labeled with penicillin allergy, often inaccurately, leading to adverse outcomes and increased costs.
- Unnecessary penicillin allergy labels can result in suboptimal antibiotic selection and treatment failures.
- At a pediatric surgical center, 7% of patients carried a penicillin allergy label prior to the intervention.
Purpose of the Study:
- To decrease the rate of penicillin allergy labeling in pediatric surgical patients.
- To improve timely access to penicillin allergy evaluations.
- To assess the safety and efficacy of oral provocation testing (OPT) in this population.
Main Methods:
- A pre/postimplementation study design was employed.
- Pediatric surgical patients with a penicillin allergy label were identified and risk-stratified.
- A single-dose oral provocation test (OPT) with amoxicillin was administered to eligible patients.
Main Results:
- The percentage of patients with a penicillin allergy label decreased from 7% to 6.4% post-intervention (P=.045).
- Median wait time for allergy evaluation significantly reduced from 102 days to 42 days (P<.0001).
- Forty-two patients successfully completed the oral provocation test without adverse events.
Conclusions:
- This quality improvement initiative effectively reduced penicillin allergy labeling rates in pediatric surgical patients.
- The project enhanced access to allergy evaluations, shortening wait times considerably.
- Oral provocation testing proved to be a safe and effective method for de-labeling penicillin allergy in this cohort.
Background:
Up to 10% of children report having a penicillin allergy; however many of these are misdiagnoses or the allergy resolves over time. Having an unnecessary penicillin allergy label increases risk of adverse clinical outcomes and increased health care costs.
Local Problem:
At our local pediatric surgical center, the percentage of patients with a penicillin allergy label was 7%.
Methods:
A pre/postimplementation design was used.
Interventions:
Pediatric surgical patients with a penicillin allergy label were identified and risk-stratified to undergo a single-dose oral provocation test (OPT) to amoxicillin.
Results:
Forty-two patients underwent an OPT. The percentage of patients with a penicillin allergy label decreased to 6.4% after 6 months ( P = .045). Median wait time for an allergy evaluation decreased from 102 to 42 days ( P < .0001).
Conclusions:
This quality improvement project decreased penicillin allergy labeling rates in pediatric surgical patients, improved access to penicillin allergy evaluation, and had no adverse outcomes.
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