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Published on: June 20, 2020
[Effects of cisapride on QT interval in children]
Amalia Tamariz-Martel Moreno1, Antonio Baño Rodrigo, Marciano Sánchez Bayle
1Sección de Cardiología Pediátrica. Hospital Universitario Niño Jesús. Universidad Autónoma de Madrid. Madrid. Spain. amtamariz@yahoo.es
Insights
Cisapride treatment did not significantly prolong the corrected QT interval (QTc) in infants and children without risk factors. This study found no significant QTc changes in pediatric patients receiving cisapride.
Area of Science:
- Pediatric Cardiology
- Clinical Pharmacology
Background:
- Gastrointestinal motility disorders are common in infants and children.
- Cisapride is a prokinetic agent used to treat such conditions.
- Concerns exist regarding potential cardiac side effects, specifically QT interval prolongation.
Purpose of the Study:
- To prospectively evaluate the effects of cisapride on the corrected QT interval (QTc) in pediatric patients.
- To determine if therapeutic doses of cisapride prolong QTc in infants and children.
Main Methods:
- A prospective study involving 175 children aged 1.5 months to 16.8 years.
- Electrocardiograms (ECGs) were obtained before and after 15 days of cisapride treatment (0.2 mg/kg/dose, 3-4 times/day).
- A subset of 24 patients also had a posttreatment ECG.
Main Results:
- No statistically significant difference was observed in the mean QTc interval before (0.390 ± 0.018 s) and after cisapride treatment (0.391 ± 0.018 s).
- The mean QTc interval in patients with only a posttreatment ECG was 0.399 ± 0.018 s.
- No patient exhibited a QTc interval exceeding 0.450 s.
Conclusions:
- Therapeutic doses of cisapride do not appear to significantly prolong the QTc interval in infants and children.
- In the absence of associated risk factors, cisapride can be used with a low risk of QTc prolongation in pediatric populations.
- Further monitoring may be warranted in children with pre-existing cardiac risk factors.
Abstract:
This prospective study evaluated the effects of cisapride on corrected QT interval (QTc) in infants and children. From October 2000 to March 2003 two electrocardiograms (ECG) were obtained for 175 children (ranging in age from 1.5 months to 16.8 years), before and after 15 days of treatment with cisapride (0.2 mg/kg/dose, 3-4 times/day). A single posttreatment ECG was also obtained for 24 patients (ranging in age from 1.5 month to 15.8 years). No statistically significant differences were found between the mean QTc interval before (0.390 [0.018 s]) and after treatment (0.391 [0.018 s]). In patients for whom only a posttreatment ECG recording was performed, mean QTc interval was 0.399 (0.018 s). The QTc interval was never longer than 0.450 s in any of the children. In our experience the use of cisapride at therapeutic doses in infants and children who have no associated risk factors does not significantly prolong QTc interval.
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