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How safe are paediatric emergency departments? A national prospective cohort study
Amy C Plint1,2, Amanda S Newton3, Antonia Stang4,5
1Pediatric Emergency, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada plint@cheo.on.ca.
Insights
Approximately 1 in 33 children experience adverse events after paediatric emergency care. Most of these patient safety events are preventable, often stemming from management or diagnostic issues.
Area of Science:
- Pediatric Emergency Medicine
- Patient Safety Research
- Healthcare Quality Improvement
Background:
- Patient safety risks in pediatric emergency departments are not well-quantified.
- High numbers of children receive care in these settings, necessitating risk assessment.
Purpose of the Study:
- To estimate the risk, type, preventability, and severity of adverse events in children treated in a pediatric emergency department.
- To identify specific patient populations at higher risk for adverse events.
Main Methods:
- Prospective, multicenter cohort study across nine pediatric emergency departments.
- Enrolled 6376 children, with 94% completing 21-day follow-up via telephone interviews and health record review.
- Adverse events were identified using flagged outcomes and a validated trigger tool, with independent reviewer confirmation.
Main Results:
- 3.0% (1 in 33) of children experienced at least one adverse event related to their emergency department visit.
- 187 adverse events were identified; 76.5% were deemed preventable.
- Management (52.4%) and diagnostic issues (19.3%) were the most common causes, leading to return visits, admissions, or critical care transfers.
Conclusions:
- A significant proportion of children treated in pediatric emergency departments experience preventable adverse events.
- Focusing on improving management and diagnostic processes can enhance patient safety.
- Further research should target high-risk populations to mitigate adverse event occurrence.
Background:
Despite the high number of children treated in emergency departments, patient safety risks in this setting are not well quantified. Our objective was to estimate the risk and type of adverse events, as well as their preventability and severity, for children treated in a paediatric emergency department.
Methods:
Our prospective, multicentre cohort study enrolled children presenting for care during one of 168 8-hour study shifts across nine paediatric emergency departments. Our primary outcome was an adverse event within 21 days of enrolment which was related to care provided at the enrolment visit. We identified 'flagged outcomes' (such as hospital visits, worsening symptoms) through structured telephone interviews with patients and families over the 21 days following enrolment. We screened admitted patients' health records with a validated trigger tool. For patients with flags or triggers, three reviewers independently determined whether an adverse event occurred.
Results:
We enrolled 6376 children; 6015 (94%) had follow-up data. Enrolled children had a median age of 4.3 years (IQR 1.6-9.8 years). One hundred and seventy-nine children (3.0%, 95% CI 2.6% to 3.5%) had at least one adverse event. There were 187 adverse events in total; 143 (76.5%, 95% CI 68.9% to 82.7%) were deemed preventable. Management (n=98, 52.4%) and diagnostic issues (n=36, 19.3%) were the most common types of adverse events. Seventy-nine (42.2%) events resulted in a return emergency department visit; 24 (12.8%) resulted in hospital admission; and 3 (1.6%) resulted in transfer to a critical care unit.
Conclusion:
In this large-scale study, 1 in 33 children treated in a paediatric emergency department experienced an adverse event related to the care they received there. The majority of events were preventable; most were related to management and diagnostic issues. Specific patient populations were at higher risk of adverse events. We identify opportunities for improvement in care.
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