Comparison of Oral Acetaminophen Versus Ibuprofen in Premature Infants With Patent Ductus Arteriosus

Mohammad Mehdi Bagheri1, Pedram Niknafs1, Fatemeh Sabsevari1

  • 1Afzalipour Medical Center, Kerman University of Medical Sciences, Kerman, IR Iran.

Insights

Oral acetaminophen and ibuprofen show similar efficacy in closing patent ductus arteriosus (PDA) in preterm infants. Acetaminophen is recommended due to fewer complications, offering a safer alternative for PDA treatment.

Area of Science:

  • Neonatal Medicine
  • Pharmacology
  • Pediatric Cardiology

Background:

  • Patent ductus arteriosus (PDA) is a significant cause of morbidity in preterm infants.
  • Effective treatment of PDA is crucial for improving outcomes in premature neonates.

Purpose of the Study:

  • To compare the efficacy of oral acetaminophen versus oral ibuprofen for PDA closure in preterm neonates.
  • To evaluate acetaminophen as a potentially safer alternative to ibuprofen for PDA treatment.

Main Methods:

  • A randomized clinical trial involving 120 preterm infants (<37 weeks gestation) with echocardiographically confirmed PDA.
  • Infants received either oral acetaminophen (15mg/kg q6h for 3 days) or oral ibuprofen (20mg/kg initial, then 10mg/kg at 24 & 48h).
  • Treatment efficacy was assessed via repeat echocardiography after treatment completion.

Main Results:

  • After the first treatment course, PDA closure rates were 82.1% for acetaminophen and 75.8% for ibuprofen (P=0.38).
  • Following a second course, closure rates were 50% for acetaminophen and 73.3% for ibuprofen (P=0.21).
  • No statistically significant difference in efficacy was observed between the two drugs.

Conclusions:

  • Oral acetaminophen and ibuprofen demonstrate comparable efficacy in closing PDA in preterm neonates.
  • Acetaminophen is recommended as a preferred treatment option due to its favorable safety profile and minimal complications compared to ibuprofen.
  • Acetaminophen presents a viable alternative for managing PDA in preterm infants, potentially reducing adverse effects associated with ibuprofen.
Abstract

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