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Effect of cisapride on corrected QT interval in neonates.
Artículo en Inglés | IMSEAR | ID: sea-44793
ABSTRACT

OBJECTIVE:

To evaluate the effect of cisapride on corrected QT (QTc) interval in neonates at the Queen Sirikit National Institute of Child Health.

METHOD:

A prospective study was performed to see the effects of cisapride on QTc interval in 20 neonates between 1st July 2001 and 31st January 2002. QTc interval was determined just before, 48 hours, 7 days and 15 days after the start of treatment with cisapride. QTc interval was calculated by averaging QT/square root(RR) values obtained from 5 consecutive beats in lead II of the EKG. Baseline electrolyte and calcium levels were drawn on all infants before treatment of cisapride. Drug dose ranged from 0.1-0.2 mg/kg every 6 to 8 hours.

RESULTS:

Twenty infants were enrolled in the survey but complete data was obtained on 18 infants only. QTc interval of > 0.45 seconds was not found in any neonate. There was no significant difference of QTc interval before and 48 hours, 7 days and 15 days after cisapride administration (p = 0.861). There were also no statistically significant effects of age at starting cisapride, weight, gestational age and dose on QTc interval (p = 0.581, 0.65, 0.8, and 0.497). There were no adverse effects such as diarrhea or jaundice during the study.

CONCLUSION:

Term and preterm infants using cisapride at the doses of 0.4-0.8 mg/kg/day did not develop QTc prolongation, arrhythmias or adverse effects. In the absence of risk factors, cisapride may be safe for use in neonates.
Asunto(s)
Texto completo: Disponible Índice: IMSEAR (Asia Sudoriental) Asunto principal: Fármacos Gastrointestinales / Femenino / Humanos / Masculino / Recién Nacido / Reflujo Gastroesofágico / Unidades de Cuidado Intensivo Neonatal / Estudios Prospectivos / Análisis de Varianza / Resultado del Tratamiento Tipo de estudio: Estudio observacional / Factores de riesgo Idioma: Inglés Año: 2003 Tipo del documento: Artículo

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Texto completo: Disponible Índice: IMSEAR (Asia Sudoriental) Asunto principal: Fármacos Gastrointestinales / Femenino / Humanos / Masculino / Recién Nacido / Reflujo Gastroesofágico / Unidades de Cuidado Intensivo Neonatal / Estudios Prospectivos / Análisis de Varianza / Resultado del Tratamiento Tipo de estudio: Estudio observacional / Factores de riesgo Idioma: Inglés Año: 2003 Tipo del documento: Artículo