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[Long QT syndrome under cisapride in neonates and infants]

J M Lupoglazoff1, A Bedu, C Faure

  • 1Service de cardiologie, hôpital Robert-Debré, Paris, France.

Insights

High-dose cisapride in infants can cause QT prolongation, a reversible heart rhythm issue. Reducing the dosage or stopping the medication normalizes heart function, emphasizing caution with combined drug use.

Area of Science:

  • Pediatric Cardiology
  • Clinical Pharmacology

Context:

  • Cisapride is a common treatment for gastroesophageal reflux in neonates and infants.
  • QT prolongation and torsades de pointes are known risks in adults, but data in infants is limited.

Purpose:

  • To investigate the incidence and characteristics of QT prolongation in infants treated with cisapride.
  • To evaluate the reversibility of cisapride-induced QT prolongation upon dose adjustment or discontinuation.

Summary:

  • Seven infants (mean age 41.8 days) without prior cardiac abnormalities received cisapride at a mean dose of 1.31 mg/kg/d.
  • ECG and Holter monitoring revealed QT prolongation (mean QTc 486 ms) with a notched T-wave pattern.
  • Upon reducing cisapride dosage or stopping the drug, QTc normalized within 48 hours, with a mean QTc shortening of 74 ms.

Impact:

  • High-dose cisapride in preterm infants, newborns, and infants is associated with reversible QT prolongation.
  • Clinical use of cisapride, especially with other QT-prolonging drugs, requires extreme caution in this population.
Abstract

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