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Published on: July 7, 2016
Combination pharmacotherapy for patent ductus arteriosus: Rationale and evidence
Bonny Jasani1, Dany E Weisz2, Jeff Reese3
1Division of Neonatology, Hospital for Sick Children, Toronto, Canada; Department of Pediatrics, University of Toronto, Toronto, Canada.
Insights
Combination therapy with acetaminophen and ibuprofen shows promise for treating patent ductus arteriosus (PDA) in extremely low gestational age neonates (ELGANs). This novel approach may offer higher closure rates compared to ibuprofen alone, warranting further research.
Area of Science:
- Neonatal Medicine
- Pharmacology
- Pediatric Cardiology
Background:
- Patent ductus arteriosus (PDA) is common in preterm infants, particularly extremely low gestational age neonates (ELGANs).
- Current treatments like cyclooxygenase inhibitors have limitations including adverse effects and low efficacy in ELGANs.
- There is a critical need for alternative and more effective PDA treatment strategies in this vulnerable population.
Conclusions:
- Combination therapy with acetaminophen and ibuprofen presents a promising novel strategy for PDA treatment in ELGANs.
- Further adequately powered clinical trials are urgently needed to confirm the efficacy and safety of this combination therapy.
- Optimizing PDA treatment in ELGANs is crucial to reduce associated morbidities in neonatal intensive care settings.
Abstract:
While cyclooxygenase inhibitors have been the most common medications used to facilitate earlier closure of patent ductus arteriosus in preterm infants, adverse effects and low efficacy in extremely low gestational age neonates (ELGANs) have highlighted a need for alternative options. Combination therapy with acetaminophen and ibuprofen is a novel strategy for PDA treatment in ELGANs, as it may facilitate higher ductal closure rates via additive action on two separate pathways inhibiting prostaglandin production. Initial small observational studies and pilot randomized clinical trials indicate potentially higher efficacy of the combination regime to induce ductal closure in comparison to treatment with ibuprofen alone. In this review, we examine the potential clinical impact of treatment failure in ELGANs with significant PDA, highlight the biological rationale in support of studying combination therapy, and review the randomized and non-randomized studies to date. With the rising number of ELGANs receiving neonatal intensive care, who are vulnerable to PDA-related morbidities, there is an urgent need for adequately powered clinical trials to systematically investigate the efficacy and safety of combination therapy for PDA treatment.
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