1. Phenobarbitone in Rh Hemolytic Disease of the Newborn: A Randomized Double-Blinded Placebo-Controlled Trial
- Author
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Mari Jeeva Sankar, Ashok K. Deorari, Kannan Venkatnarayan, Vinod K. Paul, and Ramesh Agarwal
- Subjects
Male ,Double blinded ,Placebo-controlled study ,Gestational Age ,Tertiary care ,Drug Administration Schedule ,law.invention ,Erythroblastosis, Fetal ,Rh hemolytic disease ,Double-Blind Method ,Randomized controlled trial ,Cholestasis ,law ,medicine ,Humans ,business.industry ,Infant, Newborn ,Bilirubin ,Phototherapy ,medicine.disease ,Treatment Outcome ,Infectious Diseases ,Phenobarbital ,Anesthesia ,Pediatrics, Perinatology and Child Health ,Gestation ,Female ,business ,medicine.drug - Abstract
Objective To evaluate the efficacy of prophylactic oral phenobarbitone (PB) in neonates with Rh hemolytic disease of the newborn. Study design In this double-blind randomized trial conducted in a tertiary care unit, we randomly allocated neonates with Rh hemolytic disease of the newborn born at or after 32 weeks' gestation to PB (10 mg/kg/day on day 1 followed by 5 mg/kg/day on days 2-5) (n = 23) or oral glucose (n = 21). The primary outcome was the duration of phototherapy. Results Baseline variables were comparable. There was no difference in the median duration of phototherapy [54 (range: 0-180) vs. 35 h (0-127); p = 0.39] and in the incidences of failure of phototherapy or significant rebounds of serum bilirubin. However, the proportion of infants with cholestasis was significantly lower in the PB group (0 vs. 19%; p = 0.04). Conclusions PB does not reduce duration of phototherapy or its episodes. Its potential to reduce cholestasis needs validation in larger studies.
- Published
- 2013
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