Cargando…

Neurodevelopmental outcomes following late and moderate prematurity: a population-based cohort study

OBJECTIVE: There is a paucity of data relating to neurodevelopmental outcomes in infants born late and moderately preterm (LMPT; 32(+0)–36(+6) weeks). This paper present the results of a prospective, population-based study of 2-year outcomes following LMPT birth. DESIGN: 1130 LMPT and 1255 term-born...

Descripción completa

Detalles Bibliográficos
Autores principales: Johnson, Samantha, Evans, T Alun, Draper, Elizabeth S, Field, David J, Manktelow, Bradley N, Marlow, Neil, Matthews, Ruth, Petrou, Stavros, Seaton, Sarah E, Smith, Lucy K, Boyle, Elaine M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4484499/
https://www.ncbi.nlm.nih.gov/pubmed/25834170
http://dx.doi.org/10.1136/archdischild-2014-307684
_version_ 1782378678033842176
author Johnson, Samantha
Evans, T Alun
Draper, Elizabeth S
Field, David J
Manktelow, Bradley N
Marlow, Neil
Matthews, Ruth
Petrou, Stavros
Seaton, Sarah E
Smith, Lucy K
Boyle, Elaine M
author_facet Johnson, Samantha
Evans, T Alun
Draper, Elizabeth S
Field, David J
Manktelow, Bradley N
Marlow, Neil
Matthews, Ruth
Petrou, Stavros
Seaton, Sarah E
Smith, Lucy K
Boyle, Elaine M
author_sort Johnson, Samantha
collection PubMed
description OBJECTIVE: There is a paucity of data relating to neurodevelopmental outcomes in infants born late and moderately preterm (LMPT; 32(+0)–36(+6) weeks). This paper present the results of a prospective, population-based study of 2-year outcomes following LMPT birth. DESIGN: 1130 LMPT and 1255 term-born children were recruited at birth. At 2 years corrected age, parents completed a questionnaire to assess neurosensory (vision, hearing, motor) impairments and the Parent Report of Children's Abilities-Revised to identify cognitive impairment. Relative risks for adverse outcomes were adjusted for sex, socio-economic status and small for gestational age, and weighted to account for over-sampling of term-born multiples. Risk factors for cognitive impairment were explored using multivariable analyses. RESULTS: Parents of 638 (57%) LMPT infants and 765 (62%) controls completed questionnaires. Among LMPT infants, 1.6% had neurosensory impairment compared with 0.3% of controls (RR 4.89, 95% CI 1.07 to 22.25). Cognitive impairments were the most common adverse outcome: LMPT 6.3%; controls 2.4% (RR 2.09, 95% CI 1.19 to 3.64). LMPT infants were at twice the risk for neurodevelopmental disability (RR 2.19, 95% CI 1.27 to 3.75). Independent risk factors for cognitive impairment in LMPT infants were male sex, socio-economic disadvantage, non-white ethnicity, preeclampsia and not receiving breast milk at discharge. CONCLUSIONS: Compared with term-born peers, LMPT infants are at double the risk for neurodevelopmental disability at 2 years of age, with the majority of impairments observed in the cognitive domain. Male sex, socio-economic disadvantage and preeclampsia are independent predictors of low cognitive scores following LMPT birth.
format Online
Article
Text
id pubmed-4484499
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher BMJ Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-44844992015-07-10 Neurodevelopmental outcomes following late and moderate prematurity: a population-based cohort study Johnson, Samantha Evans, T Alun Draper, Elizabeth S Field, David J Manktelow, Bradley N Marlow, Neil Matthews, Ruth Petrou, Stavros Seaton, Sarah E Smith, Lucy K Boyle, Elaine M Arch Dis Child Fetal Neonatal Ed Original Article OBJECTIVE: There is a paucity of data relating to neurodevelopmental outcomes in infants born late and moderately preterm (LMPT; 32(+0)–36(+6) weeks). This paper present the results of a prospective, population-based study of 2-year outcomes following LMPT birth. DESIGN: 1130 LMPT and 1255 term-born children were recruited at birth. At 2 years corrected age, parents completed a questionnaire to assess neurosensory (vision, hearing, motor) impairments and the Parent Report of Children's Abilities-Revised to identify cognitive impairment. Relative risks for adverse outcomes were adjusted for sex, socio-economic status and small for gestational age, and weighted to account for over-sampling of term-born multiples. Risk factors for cognitive impairment were explored using multivariable analyses. RESULTS: Parents of 638 (57%) LMPT infants and 765 (62%) controls completed questionnaires. Among LMPT infants, 1.6% had neurosensory impairment compared with 0.3% of controls (RR 4.89, 95% CI 1.07 to 22.25). Cognitive impairments were the most common adverse outcome: LMPT 6.3%; controls 2.4% (RR 2.09, 95% CI 1.19 to 3.64). LMPT infants were at twice the risk for neurodevelopmental disability (RR 2.19, 95% CI 1.27 to 3.75). Independent risk factors for cognitive impairment in LMPT infants were male sex, socio-economic disadvantage, non-white ethnicity, preeclampsia and not receiving breast milk at discharge. CONCLUSIONS: Compared with term-born peers, LMPT infants are at double the risk for neurodevelopmental disability at 2 years of age, with the majority of impairments observed in the cognitive domain. Male sex, socio-economic disadvantage and preeclampsia are independent predictors of low cognitive scores following LMPT birth. BMJ Publishing Group 2015-07 2015-04-01 /pmc/articles/PMC4484499/ /pubmed/25834170 http://dx.doi.org/10.1136/archdischild-2014-307684 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/
spellingShingle Original Article
Johnson, Samantha
Evans, T Alun
Draper, Elizabeth S
Field, David J
Manktelow, Bradley N
Marlow, Neil
Matthews, Ruth
Petrou, Stavros
Seaton, Sarah E
Smith, Lucy K
Boyle, Elaine M
Neurodevelopmental outcomes following late and moderate prematurity: a population-based cohort study
title Neurodevelopmental outcomes following late and moderate prematurity: a population-based cohort study
title_full Neurodevelopmental outcomes following late and moderate prematurity: a population-based cohort study
title_fullStr Neurodevelopmental outcomes following late and moderate prematurity: a population-based cohort study
title_full_unstemmed Neurodevelopmental outcomes following late and moderate prematurity: a population-based cohort study
title_short Neurodevelopmental outcomes following late and moderate prematurity: a population-based cohort study
title_sort neurodevelopmental outcomes following late and moderate prematurity: a population-based cohort study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4484499/
https://www.ncbi.nlm.nih.gov/pubmed/25834170
http://dx.doi.org/10.1136/archdischild-2014-307684
work_keys_str_mv AT johnsonsamantha neurodevelopmentaloutcomesfollowinglateandmoderateprematurityapopulationbasedcohortstudy
AT evanstalun neurodevelopmentaloutcomesfollowinglateandmoderateprematurityapopulationbasedcohortstudy
AT draperelizabeths neurodevelopmentaloutcomesfollowinglateandmoderateprematurityapopulationbasedcohortstudy
AT fielddavidj neurodevelopmentaloutcomesfollowinglateandmoderateprematurityapopulationbasedcohortstudy
AT manktelowbradleyn neurodevelopmentaloutcomesfollowinglateandmoderateprematurityapopulationbasedcohortstudy
AT marlowneil neurodevelopmentaloutcomesfollowinglateandmoderateprematurityapopulationbasedcohortstudy
AT matthewsruth neurodevelopmentaloutcomesfollowinglateandmoderateprematurityapopulationbasedcohortstudy
AT petroustavros neurodevelopmentaloutcomesfollowinglateandmoderateprematurityapopulationbasedcohortstudy
AT seatonsarahe neurodevelopmentaloutcomesfollowinglateandmoderateprematurityapopulationbasedcohortstudy
AT smithlucyk neurodevelopmentaloutcomesfollowinglateandmoderateprematurityapopulationbasedcohortstudy
AT boyleelainem neurodevelopmentaloutcomesfollowinglateandmoderateprematurityapopulationbasedcohortstudy