Cargando…

No neurodevelopmental benefit of cerebral oximetry in the first randomised trial (SafeBoosC II) in preterm infants during the first days of life

AIM: Cerebral hypoxia has been associated with neurodevelopmental impairment. We studied whether reducing cerebral hypoxia in extremely preterm infants during the first 72 hours of life affected neurological outcomes at two years of corrected age. METHODS: In 2012‐2013, the phase II randomised Safeg...

Descripción completa

Detalles Bibliográficos
Autores principales: Plomgaard, Anne M., Alderliesten, Thomas, van Bel, Frank, Benders, Manon, Claris, Olivier, Cordeiro, Malaika, Dempsey, Eugene, Fumagalli, Monica, Gluud, Christian, Hyttel‐Sorensen, Simon, Lemmers, Petra, Pellicer, Adelina, Pichler, Gerhard, Greisen, Gorm
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585779/
https://www.ncbi.nlm.nih.gov/pubmed/29908039
http://dx.doi.org/10.1111/apa.14463
_version_ 1783428772249206784
author Plomgaard, Anne M.
Alderliesten, Thomas
van Bel, Frank
Benders, Manon
Claris, Olivier
Cordeiro, Malaika
Dempsey, Eugene
Fumagalli, Monica
Gluud, Christian
Hyttel‐Sorensen, Simon
Lemmers, Petra
Pellicer, Adelina
Pichler, Gerhard
Greisen, Gorm
author_facet Plomgaard, Anne M.
Alderliesten, Thomas
van Bel, Frank
Benders, Manon
Claris, Olivier
Cordeiro, Malaika
Dempsey, Eugene
Fumagalli, Monica
Gluud, Christian
Hyttel‐Sorensen, Simon
Lemmers, Petra
Pellicer, Adelina
Pichler, Gerhard
Greisen, Gorm
author_sort Plomgaard, Anne M.
collection PubMed
description AIM: Cerebral hypoxia has been associated with neurodevelopmental impairment. We studied whether reducing cerebral hypoxia in extremely preterm infants during the first 72 hours of life affected neurological outcomes at two years of corrected age. METHODS: In 2012‐2013, the phase II randomised Safeguarding the Brains of our smallest Children trial compared visible cerebral near‐infrared spectroscopy (NIRS) monitoring in an intervention group and blinded NIRS monitoring in a control group. Cerebral hypoxia was significantly reduced in the intervention group. We followed up 115 survivors from eight European centres at two years of corrected age, by conducting a medical examination and assessing their neurodevelopment with the Bayley Scales of Infant and Toddler Development, Second or Third Edition, and the parental Ages and Stages Questionnaire (ASQ). RESULTS: There were no differences between the intervention (n = 65) and control (n = 50) groups with regard to the mean mental developmental index (89.6 ± 19.5 versus 88.4 ± 14.7, p = 0.77), ASQ score (215 ± 58 versus 213 ± 58, p = 0.88) and the number of children with moderate‐to‐severe neurodevelopmental impairment (10 versus six, p = 0.58). CONCLUSION: Cerebral NIRS monitoring was not associated with long‐term benefits or harm with regard to neurodevelopmental outcome at two years of corrected age.
format Online
Article
Text
id pubmed-6585779
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-65857792019-06-27 No neurodevelopmental benefit of cerebral oximetry in the first randomised trial (SafeBoosC II) in preterm infants during the first days of life Plomgaard, Anne M. Alderliesten, Thomas van Bel, Frank Benders, Manon Claris, Olivier Cordeiro, Malaika Dempsey, Eugene Fumagalli, Monica Gluud, Christian Hyttel‐Sorensen, Simon Lemmers, Petra Pellicer, Adelina Pichler, Gerhard Greisen, Gorm Acta Paediatr Regular Articles AIM: Cerebral hypoxia has been associated with neurodevelopmental impairment. We studied whether reducing cerebral hypoxia in extremely preterm infants during the first 72 hours of life affected neurological outcomes at two years of corrected age. METHODS: In 2012‐2013, the phase II randomised Safeguarding the Brains of our smallest Children trial compared visible cerebral near‐infrared spectroscopy (NIRS) monitoring in an intervention group and blinded NIRS monitoring in a control group. Cerebral hypoxia was significantly reduced in the intervention group. We followed up 115 survivors from eight European centres at two years of corrected age, by conducting a medical examination and assessing their neurodevelopment with the Bayley Scales of Infant and Toddler Development, Second or Third Edition, and the parental Ages and Stages Questionnaire (ASQ). RESULTS: There were no differences between the intervention (n = 65) and control (n = 50) groups with regard to the mean mental developmental index (89.6 ± 19.5 versus 88.4 ± 14.7, p = 0.77), ASQ score (215 ± 58 versus 213 ± 58, p = 0.88) and the number of children with moderate‐to‐severe neurodevelopmental impairment (10 versus six, p = 0.58). CONCLUSION: Cerebral NIRS monitoring was not associated with long‐term benefits or harm with regard to neurodevelopmental outcome at two years of corrected age. John Wiley and Sons Inc. 2018-07-05 2019-02 /pmc/articles/PMC6585779/ /pubmed/29908039 http://dx.doi.org/10.1111/apa.14463 Text en ©2018 The Authors. Acta Pædiatrica published by John Wiley & Sons Ltd on behalf of Foundation Acta Pædiatrica This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Regular Articles
Plomgaard, Anne M.
Alderliesten, Thomas
van Bel, Frank
Benders, Manon
Claris, Olivier
Cordeiro, Malaika
Dempsey, Eugene
Fumagalli, Monica
Gluud, Christian
Hyttel‐Sorensen, Simon
Lemmers, Petra
Pellicer, Adelina
Pichler, Gerhard
Greisen, Gorm
No neurodevelopmental benefit of cerebral oximetry in the first randomised trial (SafeBoosC II) in preterm infants during the first days of life
title No neurodevelopmental benefit of cerebral oximetry in the first randomised trial (SafeBoosC II) in preterm infants during the first days of life
title_full No neurodevelopmental benefit of cerebral oximetry in the first randomised trial (SafeBoosC II) in preterm infants during the first days of life
title_fullStr No neurodevelopmental benefit of cerebral oximetry in the first randomised trial (SafeBoosC II) in preterm infants during the first days of life
title_full_unstemmed No neurodevelopmental benefit of cerebral oximetry in the first randomised trial (SafeBoosC II) in preterm infants during the first days of life
title_short No neurodevelopmental benefit of cerebral oximetry in the first randomised trial (SafeBoosC II) in preterm infants during the first days of life
title_sort no neurodevelopmental benefit of cerebral oximetry in the first randomised trial (safeboosc ii) in preterm infants during the first days of life
topic Regular Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585779/
https://www.ncbi.nlm.nih.gov/pubmed/29908039
http://dx.doi.org/10.1111/apa.14463
work_keys_str_mv AT plomgaardannem noneurodevelopmentalbenefitofcerebraloximetryinthefirstrandomisedtrialsafeboosciiinpreterminfantsduringthefirstdaysoflife
AT alderliestenthomas noneurodevelopmentalbenefitofcerebraloximetryinthefirstrandomisedtrialsafeboosciiinpreterminfantsduringthefirstdaysoflife
AT vanbelfrank noneurodevelopmentalbenefitofcerebraloximetryinthefirstrandomisedtrialsafeboosciiinpreterminfantsduringthefirstdaysoflife
AT bendersmanon noneurodevelopmentalbenefitofcerebraloximetryinthefirstrandomisedtrialsafeboosciiinpreterminfantsduringthefirstdaysoflife
AT clarisolivier noneurodevelopmentalbenefitofcerebraloximetryinthefirstrandomisedtrialsafeboosciiinpreterminfantsduringthefirstdaysoflife
AT cordeiromalaika noneurodevelopmentalbenefitofcerebraloximetryinthefirstrandomisedtrialsafeboosciiinpreterminfantsduringthefirstdaysoflife
AT dempseyeugene noneurodevelopmentalbenefitofcerebraloximetryinthefirstrandomisedtrialsafeboosciiinpreterminfantsduringthefirstdaysoflife
AT fumagallimonica noneurodevelopmentalbenefitofcerebraloximetryinthefirstrandomisedtrialsafeboosciiinpreterminfantsduringthefirstdaysoflife
AT gluudchristian noneurodevelopmentalbenefitofcerebraloximetryinthefirstrandomisedtrialsafeboosciiinpreterminfantsduringthefirstdaysoflife
AT hyttelsorensensimon noneurodevelopmentalbenefitofcerebraloximetryinthefirstrandomisedtrialsafeboosciiinpreterminfantsduringthefirstdaysoflife
AT lemmerspetra noneurodevelopmentalbenefitofcerebraloximetryinthefirstrandomisedtrialsafeboosciiinpreterminfantsduringthefirstdaysoflife
AT pelliceradelina noneurodevelopmentalbenefitofcerebraloximetryinthefirstrandomisedtrialsafeboosciiinpreterminfantsduringthefirstdaysoflife
AT pichlergerhard noneurodevelopmentalbenefitofcerebraloximetryinthefirstrandomisedtrialsafeboosciiinpreterminfantsduringthefirstdaysoflife
AT greisengorm noneurodevelopmentalbenefitofcerebraloximetryinthefirstrandomisedtrialsafeboosciiinpreterminfantsduringthefirstdaysoflife