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Published on: October 11, 2019
Unintentional artenimol/piperaquine overdose in two children occurring without evidence of subsequent cardiotoxicity
Alexandra Tielli1, Vincent Jullien2, Lauren Pull1
1Hôpital Robert-Debré, Service d'Accueil des Urgences pédiatriques, Assistance Publique-Hôpitaux de Paris, 48 boulevard Sérurier, 75019 Paris, France.
Insights
Two children accidentally received a 3-day dose of artemisin/piperaquine (AP) antimalarial treatment. Despite the overdose, both children showed no adverse effects on their cardiac health or QTc interval.
Area of Science:
- Pharmacology
- Clinical Medicine
- Pediatrics
Background:
- Artemisinin/piperaquine (AP) is a first-line antimalarial treatment in Paris.
- Standard protocol involves hospital observation for 1 hour post-first dose to monitor for vomiting.
Observation:
- Two pediatric patients accidentally received the full 3-day AP treatment course instead of a single dose.
- Serum piperaquine levels and corrected QT (QTc) intervals were monitored post-ingestion.
Findings:
- Despite the AP overdose, neither patient experienced adverse electrophysiological events.
- Cardiac function and QTc intervals remained unaffected in both children following the accidental overdose.
Implications:
- This case suggests a potentially wider safety margin for AP overdose than previously reported.
- Further investigation into AP overdose effects in pediatric populations may be warranted.
- Clinical management guidelines for AP administration may need review based on these findings.
Abstract:
At the emergency department of the Robert-Debré children's hospital in Paris, France, artenimol/piperaquine (AP) has been the first-line antimalarial treatment since September 2012. Most children receive the first dose at the hospital and return home if, after 1 hour's observation, there have been no episodes of vomiting. Here we report the case of two children, aged 11 years and 5 years, respectively, in whom the entire cumulative 3 days' treatment course combined was accidentally administered instead of just the first-day treatment dose. Serum piperaquine levels were measured between Hour 40 (H40) and Day 29 (D29) post-ingestion for the first patient, and between H17 and D7 for the second patient. Corrected QT (QTc) values were measured between H12 and D20 for the first patient and between H17 and H64 for the second patient. Despite reports of adverse electrophysiological events, AP overdose occurred without consequence on the QTc interval or clinical cardiac state in these two children.
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