Effect of cisapride on the QT interval in infants with gastroesophageal reflux
1West Jefferson Medical Center, New Orleans, Louisiana, USA. vkhoshoo@earthlink.net
Insights
Cisapride therapy for gastroesophageal reflux in infants showed a slight, not statistically significant, increase in QT interval. Cautious use at recommended doses is generally safe, with minimal risk of prolonged QT intervals.
Area of Science:
- Pediatric Cardiology
- Gastroenterology
- Pharmacology
Background:
- Gastroesophageal reflux (GER) is common in infants.
- Cisapride has been used to treat GER but carries potential cardiac risks.
- Assessing the cardiac safety of cisapride in infants is crucial.
Purpose of the Study:
- To prospectively evaluate the effect of cisapride on QT interval in infants (3-6 months) with GER.
- To determine if cisapride therapy leads to significant QT prolongation or cardiac events.
Main Methods:
- A prospective study involving two groups of infants with GER receiving cisapride.
- Group A: ECG before and after 2 weeks of cisapride (1 mg/kg/day).
- Group B: ECG after >1 month of cisapride therapy (0.8-1.1 mg/kg/day).
- Exclusion criteria included cardiopulmonary, renal, hepatic issues, apnea history, or concurrent use of macrolides/azoles.
Main Results:
- Cisapride therapy (1 mg/kg/day) caused a slight, non-significant increase in QT interval (pre: 390±18 ms, post: 400±20 ms).
- QT interval remained below the 440 ms upper limit.
- Two out of 100 infants (2%) showed QT prolongation (>450 ms), without arrhythmias or identifiable causes.
- Prolongation patterns were similar in short-term and long-term therapy groups.
Conclusions:
- Cautious cisapride use at modest doses (<1.2 mg/kg/day) appears safe in young infants with GER.
- Recommendations include precise dosing, parental education on administration and drug interactions.
- The benefits of cisapride may outweigh risks with careful monitoring and education.
Objective:
We prospectively studied the effect of cisapride per se on QT interval in young infants (3-6 months) with gastroesophageal reflux (GER) in a controlled setting.
Study Design:
The infants diagnosed with GER and deemed to require therapy with cisapride were divided into 2 groups. Group A comprised infants with GER who underwent an electrocardiogram (ECG) before initiation of therapy with cisapride in the dose of 1 mg per kg per 24 hours, divided into 3 doses. They were reweighed after 7 to 10 days, and the dose was adjusted for their new weight. A repeat ECG was performed after approximately 2 weeks (12-18 days) of therapy. The QT interval was measured in each ECG and then the corrected QT interval was calculated by Bazett's formula. Group B comprised infants with GER who had already been on therapy with cisapride for over 1 month. All infants in group B received cisapride in an approximate dose of 1 mg per kg per 24 hours (.8-1.1 mg/kg/24 hours) given in 3 divided doses. They underwent only 1 ECG, ie, at 1 to 4 months after initiation of therapy. The measurement of the actual dose of cisapride was demonstrated to every parent and a marked measuring syringe was provided. The following categories of infants were not included: those with any underlying cardiopulmonary, renal, or hepatic problem; those with a history of apnea; those using a macrolide antibiotic or azole antifungal at any stage during the study; and infants hospitalized for any reason during the course of the study.
Results:
Cisapride therapy in the dose of 1 mg/kg/day frequently resulted in a slight increase in the QT interval (pretreatment: 390 +/- 18 milliseconds; posttreatment: 400 +/- 20 milliseconds) but the increase was still below the accepted upper limit of 440 milliseconds and not statistically significant. Even with prolonged therapy, the pattern of change in QT interval was similar to that with therapy for 2 weeks. Overall, 2 of 100 (2%) infants developed a prolongation of corrected QT interval beyond the normal range (456 and 486 milliseconds). Neither infant had evidence of any arrhythmia or conduction defect on ECG. No additional factor could be identified in either infant to explain prolongation of the QT interval.
Conclusion:
Our experience suggests that cautious cisapride therapy in young infants in a modest dose does not result in arrhythmias or conduction defects. We recommend that: 1) the dose of cisapride in infants be <1.2 mg/kg/day and preferably between.8 and 1 mg/kg/day; 2) the right measure of the dose be actually demonstrated to the parents; and 3) parents be provided a list of drug interactions with cisapride. One should think twice before denying the use of an effective drug simply because of the need for closer monitoring and extra time spent for parent education.
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