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Outcomes following clonidine ingestions in children: an analysis of poison control center data
Kendra Amico1, Rolando Cabrera1, Latha Ganti2,3,4
1Emergency Medicine and Neurology, University of Central Florida College of Medicine, Orlando, FL, USA.
Insights
Pediatric clonidine ingestions increased significantly from 2002 to 2016, with a rise in intentional exposures among females and older children. Outcomes varied by age, with younger children more likely to require intensive care.
Area of Science:
- Toxicology
- Pediatric Emergency Medicine
- Public Health Surveillance
Background:
- Clonidine ingestions represent a significant concern in pediatric toxicology.
- Understanding trends and outcomes is crucial for prevention and management strategies.
Purpose of the Study:
- To characterize pediatric clonidine ingestions.
- To report incidence trends over a 15-year period (2002-2016).
- To evaluate associated outcomes and risk factors.
Main Methods:
- Retrospective analysis of pediatric clonidine exposure data from the Florida Poison Center.
- Examination of demographic, exposure type, and outcome variables.
- Statistical analysis to identify trends and significant associations.
Main Results:
- A total of 3444 exposures were recorded.
- Incidence increased from 4.8 to 9.1 per 100,000 children.
- Adolescent and female intentional ingestions rose significantly.
- Older age and higher clonidine dose correlated with major medical outcomes.
- Younger children were more likely to be admitted to the ICU; females were more likely to be admitted to the ICU.
Conclusions:
- Pediatric clonidine exposures have increased over time, exceeding population growth.
- Demographic shifts in ingestions, particularly among adolescents and females, warrant attention.
- Age and dose are critical factors influencing severity and ICU admission.
Background:
This paper sought to characterize pediatric clonidine ingestions, report trends in incidence, and evaluate outcomes using the Florida Poison Center's data over a period of 15 years, from 2002 to 2016.
Results:
There were 3444 total exposures. Forty percent of the cohort was female. The median age was 5 years. The age distribution changed over time to a higher proportion of teenagers exposed (p < 0.0001). From 2002 to 2016, exposures increased from 182 to 378 with a rise in incidence from 4.8 to 9.1 per 100,000 children. Acute on chronic exposures increased from 29.3% to 42.2% (p < 0.0001). Female intentional ingestions increased from 52 to 70% (p < 0.0001). Twenty-four percent were managed at home, 34% were discharged from the emergency department, 8% were admitted to the floor, and 25% were admitted to the intensive care unit (ICU). Major medical outcomes were associated with older age (p = 0.0043, 95% CI 0.0015 to 0.0080) and higher clonidine dose (p < 0.0001, 95% CI 0.0347 to 0.0600). Older children were more likely to ingest a larger dose of clonidine (p < 0.001, 95% CI 0.0531 to 0.0734), while younger children were more likely to be admitted to the ICU (p < 0.001, 95% CI - 0.0092 to - 0.0033). Males were more likely to have acute on chronic ingestions (p < 0.001, 95% CI - 0.1639 to - 0.0982); females were significantly more likely to be admitted to the ICU (p < 0.0001, 95% CI 0.0380 to 0.0969).
Conclusions:
Our analysis shows an increase in the incidence in pediatric clonidine exposures over time despite adjustment for population growth.
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