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Updated: Aug 15, 2026

Methods for ECG Evaluation of Indicators of Cardiac Risk, and Susceptibility to Aconitine-induced Arrhythmias in Rats Following Status Epilepticus
Published on: April 5, 2011
[Syncope with long QT interval in a 39 day-old infant treated with cisapride]
Insights
Cisapride (a medication for gastrointestinal issues) may cause heart problems, especially in infants. Combining it with ranitidine could increase this risk due to potential drug interactions.
Area of Science:
- Pediatric Pharmacology
- Clinical Toxicology
- Drug Safety
Background:
- Cisapride is a prokinetic agent used for gastrointestinal motility disorders.
- Ranitidine is a histamine H2 receptor antagonist.
- Potential drug interactions and adverse effects, particularly cardiotoxicity, require careful consideration.
Observation:
- A 37-day-old infant treated with high-dose cisapride (1.2 mg/kg/d) and ranitidine presented with malaise.
- The infant exhibited a prolonged QT interval and ventricular extrasystoles upon admission.
- Cardiac abnormalities resolved after discontinuation of cisapride.
Findings:
- The observed cardiotoxicity, including prolonged QT interval, was likely linked to cisapride.
- High dosage of cisapride and potential metabolism inhibition by ranitidine may have contributed to the adverse event.
- Plasma concentration of cisapride was not measured, limiting definitive pharmacokinetic conclusions.
Implications:
- This case highlights the critical importance of appropriate cisapride dosing in infants.
- The potential for a drug interaction between cisapride and ranitidine, leading to cardiotoxicity, warrants further investigation.
- Healthcare providers should exercise caution when co-prescribing these medications in pediatric populations.
Unlabelled:
Cardiotoxicity of cisapride may increase when this drug is associated with ranitidine.
Case Report:
A 37-day old term infant, treated with cisapride (1.2 mg/kg/d) and ranitidine for regurgitations, was hospitalized for malaise. A prolonged QT interval (with isolate ventricular extrasystoles), noted at admission, disappeared rapidly after cisapride withdrawal. Linkage to cisapride was probable, promoted by high dosage and cisapride metabolism inhibition by ranitidine, but its plasma concentration was not measured.
Conclusion:
This case report stresses the problem of cisapride dosage in infants and the question of an interaction between cisapride and ranitidine.
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