TY - JOUR
T1 - Severity of Bronchopulmonary Dysplasia and Neurodevelopmental Outcome at 2 and 5 Years Corrected Age
AU - Katz, Trixie A.
AU - Vliegenthart, Roseanne J. S.
AU - Aarnoudse-Moens, Cornelieke S. H.
AU - Leemhuis, Aleid G.
AU - Beuger, Sabine
AU - Blok, Geert Jan
AU - van Brakel, Monique J. M.
AU - van den Heuvel, Maria E. N.
AU - van Kempen, Anne A. M. W.
AU - Lutterman, Claire
AU - Rijpert, Maarten
AU - Schiering, Irene A.
AU - Ran, Nicolien C.
AU - Visser, Fenna
AU - Wilms, Janneke
AU - van Kaam, Anton H.
AU - Onland, Wes
N1 - Publisher Copyright:
© 2021 The Author(s)
PY - 2022/4
Y1 - 2022/4
N2 - Objective: To evaluate the association between bronchopulmonary dysplasia (BPD) severity and risk of neurodevelopmental impairment (NDI) at 2 years and 5 years corrected age and to examine whether this association changes over time. Study design: This single-center retrospective cohort study included patients with a gestational age <30 weeks surviving to 36 weeks postmenstrual age, divided into groups according to BPD severity. NDI was defined as having cognitive or motor abilities below −1 SD, cerebral palsy, or a hearing or a visual impairment. The association was assessed using a multivariate logistic regression model analysis, adjusting for known confounders for NDI, and mixed-model analysis. Results: Of the 790 surviving infants (15% diagnosed with mild BPD, 9% with moderate BPD, and 10% with severe BPD), 88% and 82% were longitudinally assessed at 2 years and 5 years corrected age, respectively. The mixed-model analysis showed a statistically significant increase in NDI at all levels of BPD severity compared with infants with no BPD, and a 5-fold increased risk in NDI was seen from 2 years to 5 years corrected age in all degrees of BPD severity. The strength of this association between NDI and BPD severity did not change over time. Conclusions: Increased BPD severity is associated with increased risk of NDI at both 2 years and 5 years corrected age. The absolute incidence of NDI increased significantly from 2 years to 5 years corrected age for all BPD severity categories, but this increased risk was similar at both time points in each category.
AB - Objective: To evaluate the association between bronchopulmonary dysplasia (BPD) severity and risk of neurodevelopmental impairment (NDI) at 2 years and 5 years corrected age and to examine whether this association changes over time. Study design: This single-center retrospective cohort study included patients with a gestational age <30 weeks surviving to 36 weeks postmenstrual age, divided into groups according to BPD severity. NDI was defined as having cognitive or motor abilities below −1 SD, cerebral palsy, or a hearing or a visual impairment. The association was assessed using a multivariate logistic regression model analysis, adjusting for known confounders for NDI, and mixed-model analysis. Results: Of the 790 surviving infants (15% diagnosed with mild BPD, 9% with moderate BPD, and 10% with severe BPD), 88% and 82% were longitudinally assessed at 2 years and 5 years corrected age, respectively. The mixed-model analysis showed a statistically significant increase in NDI at all levels of BPD severity compared with infants with no BPD, and a 5-fold increased risk in NDI was seen from 2 years to 5 years corrected age in all degrees of BPD severity. The strength of this association between NDI and BPD severity did not change over time. Conclusions: Increased BPD severity is associated with increased risk of NDI at both 2 years and 5 years corrected age. The absolute incidence of NDI increased significantly from 2 years to 5 years corrected age for all BPD severity categories, but this increased risk was similar at both time points in each category.
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85122632780&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/34929243
U2 - 10.1016/j.jpeds.2021.12.018
DO - 10.1016/j.jpeds.2021.12.018
M3 - Article
C2 - 34929243
SN - 0022-3476
VL - 243
SP - 40-46.e2
JO - Journal of Pediatrics
JF - Journal of Pediatrics
ER -