Enteral paracetamol or intravenous indomethacin for closure of patent ductus arteriosus in preterm neonates: A randomized controlled trial
Adult
Male
Indomethacin
Infant, Newborn
3. Good health
03 medical and health sciences
0302 clinical medicine
Humans
Infant, Very Low Birth Weight
Administration, Intravenous
Female
Ductus Arteriosus, Patent
Infant, Premature
Acetaminophen
DOI:
10.1007/s13312-015-0677-z
Publication Date:
2015-07-28T02:11:08Z
AUTHORS (6)
ABSTRACT
To compare the efficacy of enteral paracetamol and intravenous indomethacin for closure of patent ductus arteriosus (PDA) in preterm neonates.Randomized controlled trial.Level III neonatal intensive care unit.77 preterm neonates with birth weight ?1500 g and PDA size ?1.5 mm, with left to right ductal flow with left atrium to aortic root ratio >1.5:1; diagnosed by 2D-Echo within first 48 hours of life.Paracetamol drops through the infant feeding tube (15 mg/kg/dose 6 hourly for 7 days) or intravenous indomethacin (0.2 mg/kg/dose once daily for 3 days).Primary: PDA closure rate assessed by echocardiography. Secondary: need for surgical closure of PDA, renal impairment, gastrointestinal bleed, necrotising enterocolitis, hepatotoxicity, pulmonary hemorrhage, sepsis, hypothermia, retinopathy of prematurity, intraventricular hemorrhage, bronchopulmonary dysplasia and mortality.PDA closure rate was 100% (36/36) in enteral paracetamol group as compared to 94.6% (35/37) in intravenous indomethacin group (P=0.13). The secondary outcomes were also similar between the two groups. There was no occurrence of hepatotoxicity.Enteral paracetamol is safe but not superior to intravenous indomethacin in the treatment of PDA in preterm neonates.
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