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Development, testing, and findings of a pediatric-focused trigger tool to identify medication-related harm in US
Glenn S Takata1, Wilbert Mason, Carol Taketomo
1Division of General Pediatrics, Department of Pediatrics, University of Southern California School of Medicine, Los Angeles, California, USA.
Insights
A new pediatric trigger tool effectively detected adverse drug events (ADEs) in children
Area of Science:
- Pediatric patient safety
- Pharmacovigilance
- Health informatics
Background:
- Adverse drug events (ADEs) are a significant concern in pediatric healthcare.
- Existing methods for ADE detection may not adequately capture the scope of ADEs in children.
- There is a need for specialized tools to improve ADE identification in pediatric populations.
Purpose of the Study:
- To develop a pediatric-specific trigger tool for ADE detection.
- To determine the incidence and characteristics of ADEs in children's hospitals using the developed tool.
Main Methods:
- A pediatric-specific trigger tool was developed and validated.
- Retrospective chart review of 960 patients across 12 children's hospitals.
- Evaluation of identified ADEs for severity, preventability, and reporting.
Main Results:
- The tool identified 107 unique ADEs, with rates significantly higher than previously reported.
- Common ADEs included pruritus and nausea, often linked to opioid analgesics and antibiotics.
- 22% of ADEs were preventable, with most causing mild, temporary harm.
Conclusions:
- Pediatric ADE rates are higher than previously understood.
- The developed pediatric trigger tool is effective for identifying ADEs in hospitalized children.
- Most ADEs resulted in temporary harm, but a significant portion were preventable and missed by traditional reporting.
Objectives:
The purposes of this study were to develop a pediatric-focused tool for adverse drug event detection and describe the incidence and characteristics of adverse drug events in children's hospitals identified by this tool.
Methods:
A pediatric-specific trigger tool for adverse drug event detection was developed and tested. Eighty patients from each site were randomly selected for retrospective chart review. All adverse drug events identified using the trigger tool were evaluated for severity, preventability, ability to mitigate, ability to identify the event earlier, and presence of associated occurrence report. Each trigger and the entire tool were evaluated for positive predictive value.
Results:
Review of 960 randomly selected charts from 12 children's hospitals revealed 2388 triggers (2.49 per patient) and 107 unique adverse drug events. Mean adverse drug event rates were 11.1 per 100 patients, 15.7 per 1000 patient-days, and 1.23 per 1000 medication doses. The positive predictive value of the trigger tool was 3.7%. Twenty-two percent of all adverse drug events were deemed preventable, 17.8% could have been identified earlier, and 16.8% could have been mitigated more effectively. Ninety-seven percent of the identified adverse drug events resulted in mild, temporary harm. Only 3.7% of adverse drug events were identified in existing hospital-based occurrence reports. The most common adverse drug events identified were pruritus and nausea, the most common medication classes causing adverse drug events were opioid analgesics and antibiotics, and the most common stages of the medication management process associated with preventable adverse drug events were monitoring and prescribing/ordering.
Conclusions:
Adverse drug event rates in hospitalized children are substantially higher than previously described. Most adverse drug events resulted in temporary harm, and 22% were classified as preventable. Only 3.7% were identified by using traditional voluntary reporting methods. Our pediatric-focused trigger tool is effective at identifying adverse drug events in inpatient pediatric populations.
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