Impact of Bronchopulmonary Dysplasia, Brain Injury, and Severe Retinopathy on the Outcome of Extremely Low-birth-weight Infants at 18 Months: Results from the Trial of Indomethacin Prophylaxis in Preterms
Overview
Authors
Affiliations
Context: Despite more than 2 decades of outcomes research after very preterm birth, clinicians remain uncertain about the extent to which neonatal morbidities predict poor long-term outcomes of extremely low-birth-weight (ELBW) infants.
Objective: To determine the individual and combined prognostic effects of bronchopulmonary dysplasia (BPD), ultrasonographic signs of brain injury, and severe retinopathy of prematurity (ROP) on 18-month outcomes of ELBW infants.
Design: Inception cohort assembled for the Trial of Indomethacin Prophylaxis in Preterms (TIPP).
Setting And Participants: A total of 910 infants with birth weights of 500 to 999 g who were admitted to 1 of 32 neonatal intensive care units in Canada, the United States, Australia, New Zealand, and Hong Kong between 1996 and 1998 and who survived to a postmenstrual age of 36 weeks.
Main Outcome Measures: Combined end point of death or survival to 18 months with 1 or more of cerebral palsy, cognitive delay, severe hearing loss, and bilateral blindness.
Results: Each of the neonatal morbidities was similarly and independently correlated with a poor 18-month outcome. Odds ratios were 2.4 (95% confidence interval [CI], 1.8-3.2) for BPD, 3.7 (95% CI, 2.6-5.3) for brain injury, and 3.1 (95% CI, 1.9-5.0) for severe ROP. In children who were free of BPD, brain injury, and severe ROP the rate of poor long-term outcomes was 18% (95% CI, 14%-22%). Corresponding rates with any 1, any 2, and all 3 neonatal morbidities were 42% (95% CI, 37%-47%), 62% (95% CI, 53%-70%), and 88% (64%-99%), respectively.
Conclusion: In ELBW infants who survive to a postmenstrual age of 36 weeks, a simple count of 3 common neonatal morbidities strongly predicts the risk of later death or neurosensory impairment.
Fontijn J, Engel C, Kreutzer K, Poets C, Bassler D BMC Pediatr. 2025; 25(1):172.
PMID: 40050762 PMC: 11887233. DOI: 10.1186/s12887-025-05512-z.
Presumed etiology of preterm birth: brain injury and neurodevelopmental outcomes.
El Shahed A, Chau V, Terry J, Whitehead C, Synnes A, Grunau R Pediatr Res. 2025; .
PMID: 40000858 DOI: 10.1038/s41390-025-03945-x.
Young K, Benny M, Schmidt A, Wu S Cells. 2025; 13(24.
PMID: 39768185 PMC: 11674922. DOI: 10.3390/cells13242094.
Intraventricular Hemorrhage and Survival, Multimorbidity, and Neurodevelopment.
Rees P, Gale C, Battersby C, Williams C, Carter B, Sutcliffe A JAMA Netw Open. 2025; 8(1):e2452883.
PMID: 39761048 PMC: 11704976. DOI: 10.1001/jamanetworkopen.2024.52883.
Dorner R, Li L, DeMauro S, Schmidt B, Zangeneh S, Vaucher Y J Pediatr. 2024; 278:114428.
PMID: 39643110 PMC: 11867846. DOI: 10.1016/j.jpeds.2024.114428.