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[Pediatric poisoning with triptans: review of cases in the Lille poison center between 2000 and 2010]
I Larivière1, A Garat, P Nisse
1Centre antipoison, CHRU de Lille, 5, avenue Oscar-Lambret, 59037 Lille cedex, France.
Insights
Pediatric triptan poisoning is generally well-tolerated, with few symptoms and no severe complications. Hospitalization for children ingesting triptans should be based on individual factors, not automatic.
Area of Science:
- Pediatric Toxicology
- Clinical Pharmacology
- Emergency Medicine
Context:
- Triptans are first-line acute migraine treatments.
- Limited pediatric data exists for triptan poisoning.
- Precautionary hospitalizations are common for young children with triptan ingestion.
Purpose:
- To estimate the risks of triptan poisoning in young children.
- To inform clinical decision-making regarding pediatric triptan ingestions.
- To reduce unnecessary hospitalizations for triptan poisoning in children.
Summary:
- A review of 84 children under 6 years with triptan ingestion found most cases were well-tolerated.
- Symptoms occurred in 13% of cases and were mild, with no severe complications reported.
- Hospitalization decisions should consider patient history, dose, and symptoms, rather than being systematic.
Impact:
- Updated clinical guidelines suggest a less alarmist approach to pediatric triptan poisoning.
- Focus hospitalization on high-risk patients, considering cardiac history and presenting symptoms.
- Home management with adsorbing treatment and phone monitoring is a viable option for asymptomatic children.
Background And Objective:
Triptans are recommended to treat acute migraine. Pediatric data remain insufficient for making decisions in cases of triptan poisoning. Consequently, hospitalization is often warranted as a precautionary measure. This study aims to more accurately estimate the risks incurred when a young child ingests triptan tablets.
Main Outcome Measures:
This study reviewed all cases of acute triptan poisoning listed by the Lille poison center between January 2000 and December 2009 in children younger than 6 years. Cases with certain ingestion, no drug interactions, and no other known etiology were selected. The gravity of each case was estimated by the poisoning severity score and follow-up was conducted by phone.
Results:
A cohort of 84 patients was collected: 6% were lost to follow-up. The mean intake was 1.22 tablets (range, 0.25-6), for the most part zolmitriptan (64.2%), eletriptan (14.3%) and naratriptan (14.3%). Fifty-nine children (74.5%) were admitted to the hospital and 20 children monitored at home. The majority received evacuation or adsorbing treatment. Symptoms were not frequent (13%) and were well tolerated, in particular on the hemodynamic level (ten cases of PSS1). The adverse events observed were tachycardia (4 cases), arterial hypertension (1 case), dyspnea (2 cases), drowsiness (2 cases), marbling of the extremities (1 case), vomiting (3 cases), and digestive pain (1 case). The 2 cases of dyspnea, induced by 2.5mg and 7.5mg of zolmitriptan, respectively, were associated with cardiovascular symptoms and were left untreated. According to its pharmacological action, the potential risk of a serotoninergic syndrome is a concern with triptan intake. No severe complication was recorded, so based on this study, our guidelines were updated. The response should be less alarmist, but a watchful attitude should be retained. Hospitalization should not be systematic, but focused on the patient's cardiac history, the dose, and the symptomatology. If the child remains at home, specific action should be managed: an adsorbing treatment and close monitoring by phone remain essential.
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