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A randomised trial of granulocyte-macrophage colony-stimulating factor for neonatal sepsis: childhood outcomes at 5 years
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F320.full.pdf | Published version | 571.54 kB | Adobe PDF | View/Open |
Title: | A randomised trial of granulocyte-macrophage colony-stimulating factor for neonatal sepsis: childhood outcomes at 5 years |
Authors: | Marlow, N Morris, T Brocklehurst, P Carr, R Cowan, F Patel, N Petrou, S Redshaw, M Modi, N Dore, CJ |
Item Type: | Journal Article |
Abstract: | Objective: We performed a randomised trial in very preterm, small for gestational age (SGA) babies to determine if prophylaxis with granulocyte macrophage colony stimulating factor (GM-CSF) improves outcomes (the PROGRAMS trial). GM-CSF was associated with improved neonatal neutrophil counts, but no change in other neonatal or 2-year outcomes. As subtle benefits in outcome may not be ascertainable until school age we performed an outcome study at 5 years. Patients and methods: 280 babies born at 31 weeks of gestation or less and SGA were entered into the trial. Outcomes were assessed at 5 years to determine neurodevelopmental and general health status and educational attainment. Results: We found no significant differences in cognitive, general health or educational outcomes between 83 of 106 (78%) surviving children in the GMCSF arm compared with 81 of 110 (74%) in the control arm. Mean mental processing composite (equivalent to IQ) at 5 years were 94 (SD 16) compared with 95 (SD 15), respectively (difference in means −1 (95%CI −6 to 4), and similar proportions were in receipt of special educational needs support (41% vs 35%; risk ratio 1.2 (95% CI 0.8 to 1.9)). Performance on Kaufmann-ABC subscales and components of NEPSY were similar. The suggestion of worse respiratory outcomes in the GM-CSF group at 2 years was replicated at 5 years. Conclusions: The administration of GM-CSF to very preterm SGA babies is not associated with improved or more adverse neurodevelopmental, general health or educational outcomes at 5 years. |
Issue Date: | 28-Apr-2015 |
Date of Acceptance: | 15-Mar-2015 |
URI: | http://hdl.handle.net/10044/1/49416 |
DOI: | https://dx.doi.org/10.1136/archdischild-2014-307410 |
ISSN: | 1359-2998 |
Publisher: | BMJ Publishing Group |
Start Page: | F320 |
End Page: | F326 |
Journal / Book Title: | Archives of Disease in Childhood. Fetal and Neonatal Edition |
Volume: | 100 |
Issue: | 4 |
Copyright Statement: | © 2015 The Author(s). Published by the BMJ Publishing Group Limited. 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/ |
Sponsor/Funder: | Wellcome Trust |
Funder's Grant Number: | 068499/Z/02/Z |
Keywords: | Science & Technology Life Sciences & Biomedicine Pediatrics EXTREMELY PRETERM BIRTH DEVELOPMENTAL-DISABILITY FOLLOW-UP CHILDREN NEUTROPENIA INFANTS AGE Child Psychology Haematology Neonatology Neurodevelopment Child Development Female Granulocyte-Macrophage Colony-Stimulating Factor Hematologic Agents Humans Infant, Extremely Premature Infant, Newborn Infant, Small for Gestational Age Leukocyte Count Male Neuropsychological Tests Neutrophils Outcome Assessment (Health Care) Sepsis Time 1114 Paediatrics And Reproductive Medicine |
Publication Status: | Published |
Appears in Collections: | Department of Medicine (up to 2019) |