University of Leicester
Browse

Two-Year Outcomes After Selective Early Treatment of Patent Ductus Arteriosus with Ibuprofen in Preterm Babies: Follow-Up of Baby-OSCAR - A Randomised Controlled Trial

Download (1.04 MB)
Version 2 2025-09-08, 15:24
Version 1 2025-08-13, 14:42
journal contribution
posted on 2025-09-08, 15:24 authored by Samir Gupta, Heather OConnor, Edmund Juszczak, Nimish V Subhedar, Ursula Bowler, Charlotte Clarke, David Field, Elizabeth Hutchison, Justine Pepperell, Wilf Kelsall, Tracy Roberts, Sunil Sinha, Kayleigh Stanbury, Jonathan Wyllie, Pollyanna Hardy, Samantha JohnsonSamantha Johnson, Baby-OSCAR Collaborative Group
<p dir="ltr">Background</p><p dir="ltr">Children born extremely preterm are at increased risk of developmental problems and respiratory morbidity due to patent ductus arteriosus (PDA). The objective of this study was to evaluate whether early treatment of a PDA ≥1.5 mm with ibuprofen improved neurodevelopmental and respiratory outcomes at 24 months of age, corrected for prematurity.</p><p dir="ltr">Methods</p><p dir="ltr">Baby-OSCAR was a UK multi-center placebo-controlled masked randomized clinical trial in infants born 23+0–28+6 weeks' gestation. The main long-term outcome was survival without moderate or severe neurodevelopmental impairment at 24 months’ corrected age, assessed using parent report primarily or classified by blinded end-point review committee where parent-reported data were not available. Other secondary outcomes included survival without respiratory morbidity and duration of oxygen supplementation. (ISRCTN Registry number ISRCTN84264977).</p><p dir="ltr">Findings</p><p dir="ltr">From July 2015 through December 2020, 653 infants underwent randomization. At 24 months’ corrected age, outcome data were available for 537 children: 263 in the ibuprofen group and 274 in the placebo group. Survival without moderate to severe neurodevelopmental impairment in the ibuprofen and placebo groups was 131/248 (53.0%) and 134/259 (51.9%) respectively; adjusted risk ratio 1.01 (95% confidence interval [CI] 0.86–1.18); p = 0.901. Survival without respiratory morbidity was 66/220 (30%) and 74/225 (32.9%) respectively; adjusted risk ratio 0.89 (95% CI 0.68–1.18). Median duration of oxygen supplementation from randomization was 76.0 and 78.0 days, respectively; adjusted median difference −1.5 (−13.8 to 10.9).</p><p dir="ltr">Interpretation</p><p dir="ltr">We found no evidence of an improvement in neurodevelopmental and respiratory outcomes at 24 months’ corrected age, after selective early treatment of a PDA ≥1.5 mm with ibuprofen in children born extremely preterm.</p><p dir="ltr">Funding</p><p dir="ltr">This study was funded by the National Institute for Health Research (NIHR) Health Technology Assessment Programme (11/92/15).</p>

Funding

NIHR Health Technology Assessment Program (reference number 11/92/15)

History

Author affiliation

College of Life Sciences Healthcare

Version

  • VoR (Version of Record)

Published in

EClinicalMedicine

Volume

87

Publisher

Elsevier

issn

2589-5370

eissn

2589-5370

Copyright date

2025

Available date

2025-08-13

Language

en

Deposited by

Professor Samantha Johnson

Deposit date

2025-08-04

Data Access Statement

All data requests should be submitted to the corresponding author for consideration. Access to de-identified patient data may be granted for secondary analysis following review. If approved, a data sharing agreement will be put in place. Data availability will begin with publication.

Usage metrics

    University of Leicester Publications

    Licence

    Exports

    RefWorks
    BibTeX
    Ref. manager
    Endnote
    DataCite
    NLM
    DC