About this trial
Patent ductus arteriosus (PDA), the most common cardiovascular complication of prematurity, is associated with higher mortality and morbidities in extremely low gestational age neonates (ELGANs, \< 27+0 weeks). Ibuprofen and acetaminophen, which act by reducing prostaglandin synthesis, are the most commonly used first and second line agents for PDA treatment across Canada. However, initial treatment failure with monotherapy is a major problem, occurring in \>60% ELGANs. Treatment failure is associated with worsening rates of mortality and bronchopulmonary dysplasia (BPD), while early treatment success can achieve rates comparable to neonates without PDA. Treatment failure resulting in prolonged disease exposure is thought to be a major contributor. Recently, combination therapy with acetaminophen and ibuprofen has emerged as a new treatment regime. Acetaminophen exerts anti-prostaglandin effect through a different receptor site than ibuprofen, providing a biological rationale for their synergistic action.
The objective of this study is to evaluate the clinical impact, efficacy and safety of combination regime (Ibuprofen + IV Acetaminophen) for the first treatment course for PDA in ELGANs vs. Ibuprofen alone (current standard treatment).
The study will also evaluate the effects of combination regime vs. ibuprofen alone on neurodevelopmental outcomes at 18-30 months corrected age.
Eligibility criteria
Qualifiers
Preterm infants born <27+0 weeks gestational age
Permission given by the attending clinician to approach and then consent obtained from parents
Diagnosis of PDA ≥ 1.5 mm on echocardiography with unrestrictive predominantly left to right shunt
Designated to receive first treatment course with intravenous or enteral ibuprofen, as decided by the attending team.
Disqualifiers
Chromosomal anomaly
Pre-treatment renal dysfunction defined as urine output < 1ml/kg/hour for the previous 24 hours or serum creatinine > 100 micromol/L
Pre-treatment hepatic dysfunction defined as serum aminotransferase (ALT) > 100 units/L94
Platelet count <50,000 per microliter
Trial design
Treatments tested in this trial
- Acetaminophen Injection
- Ibuprofen 20 mg/mL oral suspension or Ibuprofen lysine 10 mg/mL injection solution (Neoprofen)
- Sodium chloride 0.9% injection
Treatment groups
Sponsors and collaborators
Mount Sinai Hospital, Canada
Lead sponsor
Sunnybrook Health Sciences Centre
Collaborator
McMaster Children's Hospital
Collaborator
The Rotunda Hospital
Collaborator
John Hunter Hospital
Collaborator
Royal Alexandra Hospital
Collaborator
Centre de Recheche du Centre Hospitalier Université Laval
Collaborator
Royal North Shore Hospital
Collaborator
Prince of Wales Hospital, Shatin, Hong Kong
Collaborator