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No change in neurodevelopment at 11 years after extremely preterm birth.

Marlow, N; Ni, Y; Lancaster, R; Suonpera, E; Bernardi, M; Fahy, A; Larsen, J; Trickett, J; Hurst, JR; Morris, J; et al. Marlow, N; Ni, Y; Lancaster, R; Suonpera, E; Bernardi, M; Fahy, A; Larsen, J; Trickett, J; Hurst, JR; Morris, J; Wolke, D; Johnson, S (2021) No change in neurodevelopment at 11 years after extremely preterm birth. Arch Dis Child Fetal Neonatal Ed, 106 (4). pp. 418-424. ISSN 1468-2052 https://doi.org/10.1136/archdischild-2020-320650
SGUL Authors: Morris, Joan Katherine

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Abstract

OBJECTIVE: To determine whether improvements in school age outcomes had occurred between two cohorts of births at 22-25 weeks of gestation to women residents in England in 1995 and 2006. DESIGN: Longitudinal national cohort studies. SETTING: School-based or home-based assessments at 11 years of age. PARTICIPANTS: EPICure2 cohort of births at 22-26 weeks of gestation in England during 2006: a sample of 200 of 1031 survivors were evaluated; outcomes for 112 children born at 22-25 weeks of gestation were compared with those of 176 born in England during 1995 from the EPICure cohort. Classroom controls for each group acted as a reference population. MAIN OUTCOME MEASURES: Standardised measures of cognition and academic attainment were combined with parent report of other impairments to estimate overall neurodevelopmental status. RESULTS: At 11 years in EPICure2, 18% had severe and 20% moderate impairments. Comparing births at 22-25 weeks in EPICure2 (n=112), 26% had severe and 21% moderate impairment compared with 18% and 32%, respectively, in EPICure. After adjustment, the OR of moderate or severe neurodevelopmental impairment in 2006 compared with 1995 was 0.76 (95% CI 0.45 to 1.31, p=0.32). IQ scores were similar in 1995 (mean 82.7, SD 18.4) and 2006 (81.4, SD 19.2), adjusted difference in mean z-scores 0.2 SD (95% CI -0.2 to 0.6), as were attainment test scores. The use of multiple imputation did not alter these findings. CONCLUSION: Improvements in care and survival between 1995 and 2006 are not paralleled by improved cognitive or educational outcomes or a reduced rate of neurodevelopmental impairment.

Item Type: Article
Additional Information: This article has been accepted for publication in Archives of Disease in Childhood Fetal and Neonatal Edition, 2021 following peer review, and the Version of Record can be accessed online at http://dx.doi.org/10.1136/archdischild-2020-320650. © Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.
Keywords: epidemiology, neonatology, neurology, psychology, Academic Success, Child, Child Development, Child, Preschool, Developmental Disabilities, England, Female, Gestational Age, Humans, Infant, Infant, Extremely Premature, Infant, Newborn, Longitudinal Studies, Male, Neurodevelopmental Disorders, Premature Birth, Prospective Studies, Severity of Illness Index, Humans, Premature Birth, Severity of Illness Index, Longitudinal Studies, Prospective Studies, Child Development, Developmental Disabilities, Gestational Age, Child, Child, Preschool, Infant, Infant, Newborn, England, Female, Male, Infant, Extremely Premature, Neurodevelopmental Disorders, Academic Success, neonatology, epidemiology, neurology, psychology, epidemiology, neonatology, neurology, psychology, Academic Success, Child, Child Development, Child, Preschool, Developmental Disabilities, England, Female, Gestational Age, Humans, Infant, Infant, Extremely Premature, Infant, Newborn, Longitudinal Studies, Male, Neurodevelopmental Disorders, Premature Birth, Prospective Studies, Severity of Illness Index, Pediatrics, 1114 Paediatrics and Reproductive Medicine
SGUL Research Institute / Research Centre: Academic Structure > Population Health Research Institute (INPH)
Journal or Publication Title: Arch Dis Child Fetal Neonatal Ed
ISSN: 1468-2052
Language: eng
Dates:
DateEvent
July 2021Published
27 January 2021Published Online
15 December 2020Accepted
Publisher License: Creative Commons: Attribution-Noncommercial 4.0
Projects:
Project IDFunderFunder ID
MR/N024869/1Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
PubMed ID: 33504573
Web of Science ID: WOS:000670027100015
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/113727
Publisher's version: https://doi.org/10.1136/archdischild-2020-320650

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