Cargando…

Cohort study of growth patterns by gestational age in preterm infants developing morbidity

OBJECTIVES: To examine differences in growth patterns in preterm infants developing major morbidities including retinopathy of prematurity (ROP), bronchopulmonary dysplasia (BPD), necrotising enterocolitis (NEC) and intraventricular haemorrhage (IVH). STUDY DESIGN: Cohort study of 2521 infants born...

Descripción completa

Detalles Bibliográficos
Autores principales: Klevebro, S, Lundgren, P, Hammar, U, Smith, L E, Bottai, M, Domellöf, M, Löfqvist, C, Hallberg, B, Hellström, A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5128893/
https://www.ncbi.nlm.nih.gov/pubmed/27856479
http://dx.doi.org/10.1136/bmjopen-2016-012872
_version_ 1782470495370739712
author Klevebro, S
Lundgren, P
Hammar, U
Smith, L E
Bottai, M
Domellöf, M
Löfqvist, C
Hallberg, B
Hellström, A
author_facet Klevebro, S
Lundgren, P
Hammar, U
Smith, L E
Bottai, M
Domellöf, M
Löfqvist, C
Hallberg, B
Hellström, A
author_sort Klevebro, S
collection PubMed
description OBJECTIVES: To examine differences in growth patterns in preterm infants developing major morbidities including retinopathy of prematurity (ROP), bronchopulmonary dysplasia (BPD), necrotising enterocolitis (NEC) and intraventricular haemorrhage (IVH). STUDY DESIGN: Cohort study of 2521 infants born at a gestational age (GA) of 23–30 weeks from 11 level III neonatal intensive care units in USA and Canada, and 3 Swedish population-based cohorts. OUTCOMES: Birth weight and postnatal weight gain were examined relative to birth GA and ROP, BPD, NEC and IVH development. RESULTS: Among infants with a birth GA of 25–30 weeks, birth weight SD score and postnatal weight were lower in those developing ROP and BPD. Infants developing ROP showed lower growth rates during postnatal weeks 7–9 in the 23–24 weeks GA group, during weeks 4–6 in the 25–26 weeks GA group and during weeks 1–5 in the 27–30 weeks GA group. Infants with BPD born at 27–30 weeks GA showed lower growth rates during postnatal weeks 3–5. Infants with NEC had lower growth rates after postnatal week 6 in all GA groups, with no significant differences in birth weight SD score. IVH was not associated with prenatal or postnatal growth. CONCLUSIONS: In this cohort study of extremely preterm infants, we found that the postnatal growth pattern was associated with morbidities such as ROP, BPD and NEC as well as with gestational age at birth.
format Online
Article
Text
id pubmed-5128893
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BMJ Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-51288932016-12-02 Cohort study of growth patterns by gestational age in preterm infants developing morbidity Klevebro, S Lundgren, P Hammar, U Smith, L E Bottai, M Domellöf, M Löfqvist, C Hallberg, B Hellström, A BMJ Open Paediatrics OBJECTIVES: To examine differences in growth patterns in preterm infants developing major morbidities including retinopathy of prematurity (ROP), bronchopulmonary dysplasia (BPD), necrotising enterocolitis (NEC) and intraventricular haemorrhage (IVH). STUDY DESIGN: Cohort study of 2521 infants born at a gestational age (GA) of 23–30 weeks from 11 level III neonatal intensive care units in USA and Canada, and 3 Swedish population-based cohorts. OUTCOMES: Birth weight and postnatal weight gain were examined relative to birth GA and ROP, BPD, NEC and IVH development. RESULTS: Among infants with a birth GA of 25–30 weeks, birth weight SD score and postnatal weight were lower in those developing ROP and BPD. Infants developing ROP showed lower growth rates during postnatal weeks 7–9 in the 23–24 weeks GA group, during weeks 4–6 in the 25–26 weeks GA group and during weeks 1–5 in the 27–30 weeks GA group. Infants with BPD born at 27–30 weeks GA showed lower growth rates during postnatal weeks 3–5. Infants with NEC had lower growth rates after postnatal week 6 in all GA groups, with no significant differences in birth weight SD score. IVH was not associated with prenatal or postnatal growth. CONCLUSIONS: In this cohort study of extremely preterm infants, we found that the postnatal growth pattern was associated with morbidities such as ROP, BPD and NEC as well as with gestational age at birth. BMJ Publishing Group 2016-11-17 /pmc/articles/PMC5128893/ /pubmed/27856479 http://dx.doi.org/10.1136/bmjopen-2016-012872 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ 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 Paediatrics
Klevebro, S
Lundgren, P
Hammar, U
Smith, L E
Bottai, M
Domellöf, M
Löfqvist, C
Hallberg, B
Hellström, A
Cohort study of growth patterns by gestational age in preterm infants developing morbidity
title Cohort study of growth patterns by gestational age in preterm infants developing morbidity
title_full Cohort study of growth patterns by gestational age in preterm infants developing morbidity
title_fullStr Cohort study of growth patterns by gestational age in preterm infants developing morbidity
title_full_unstemmed Cohort study of growth patterns by gestational age in preterm infants developing morbidity
title_short Cohort study of growth patterns by gestational age in preterm infants developing morbidity
title_sort cohort study of growth patterns by gestational age in preterm infants developing morbidity
topic Paediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5128893/
https://www.ncbi.nlm.nih.gov/pubmed/27856479
http://dx.doi.org/10.1136/bmjopen-2016-012872
work_keys_str_mv AT klevebros cohortstudyofgrowthpatternsbygestationalageinpreterminfantsdevelopingmorbidity
AT lundgrenp cohortstudyofgrowthpatternsbygestationalageinpreterminfantsdevelopingmorbidity
AT hammaru cohortstudyofgrowthpatternsbygestationalageinpreterminfantsdevelopingmorbidity
AT smithle cohortstudyofgrowthpatternsbygestationalageinpreterminfantsdevelopingmorbidity
AT bottaim cohortstudyofgrowthpatternsbygestationalageinpreterminfantsdevelopingmorbidity
AT domellofm cohortstudyofgrowthpatternsbygestationalageinpreterminfantsdevelopingmorbidity
AT lofqvistc cohortstudyofgrowthpatternsbygestationalageinpreterminfantsdevelopingmorbidity
AT hallbergb cohortstudyofgrowthpatternsbygestationalageinpreterminfantsdevelopingmorbidity
AT hellstroma cohortstudyofgrowthpatternsbygestationalageinpreterminfantsdevelopingmorbidity