Pediatric ergot alkaloid exposures reported to the California Poison Control System: 1997-2008
1Department of Emergency Medicine, University of California , San Francisco-Fresno, Fresno, CA , USA.
Pediatric ergot alkaloid exposures rarely cause severe toxicity but lead to frequent hospitalizations. Current guidelines should favor home management and shorter emergency department stays for these cases.
Area of Science:
- Pediatric Toxicology
- Pharmacovigilance
- Clinical Pharmacology
Background:
- The toxicity risk of ergot alkaloid medications in children is not well-defined.
- Historical ergot alkaloid toxicity and ergotism necessitate careful triage for pediatric exposures.
- Current triage recommendations for pediatric ergot alkaloid exposures may be inconsistent.
Purpose of the Study:
- To characterize the clinical effects of unintentional ergot alkaloid exposures in pediatric patients.
- To determine the necessity of hospitalization following pediatric ergot alkaloid exposures.
Main Methods:
- Retrospective cohort study of pediatric (< 7 years) ergot alkaloid exposures reported to the California Poison Control System (CPCS) from 1997 to 2008.
- Analysis of case narratives for demographics, agent, dose, exposure route, symptoms, treatment, hospitalization, and outcomes.
- Inclusion criteria applied to 353 out of 374 reported cases.
Main Results:
- The majority of exposures (99%) were oral in route, with a median patient age of 24 months.
- Most common effects were transient gastrointestinal distress (16%) and lethargy (5%).
- Despite few serious outcomes (similar to other poisonings), hospitalizations were disproportionately high (OR 13.8) compared to other pediatric poisonings.
Conclusions:
- Pediatric ergot alkaloid exposures typically result in minor, transient adverse effects.
- A small number of severe toxicity cases were linked to methylergonovine.
- Poison control and ED guidelines should be revised to recommend home management and brief ED observation over extensive critical care admissions.
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