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Using cluster analysis to describe phenotypical heterogeneity in extremely preterm infants: a retrospective whole-population study

OBJECTIVE: To use cluster analysis to identify discrete phenotypic groups of extremely preterm infants. DESIGN: Secondary analysis of a retrospective whole population study. SETTING: All neonatal units in England between 2014 and 2019. PARTICIPANTS: Infants live-born at less than 28 weeks of gestati...

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Autores principales: Dassios, Theodore, Williams, Emma E, Harris, Christopher, Greenough, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8886439/
https://www.ncbi.nlm.nih.gov/pubmed/35228290
http://dx.doi.org/10.1136/bmjopen-2021-056567
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author Dassios, Theodore
Williams, Emma E
Harris, Christopher
Greenough, Anne
author_facet Dassios, Theodore
Williams, Emma E
Harris, Christopher
Greenough, Anne
author_sort Dassios, Theodore
collection PubMed
description OBJECTIVE: To use cluster analysis to identify discrete phenotypic groups of extremely preterm infants. DESIGN: Secondary analysis of a retrospective whole population study. SETTING: All neonatal units in England between 2014 and 2019. PARTICIPANTS: Infants live-born at less than 28 weeks of gestation and admitted to a neonatal unit. INTERVENTIONS: K-means cluster analysis was performed with the gestational age, Apgar score at 5 min and duration of mechanical ventilation as input variables. PRIMARY AND SECONDARY OUTCOME MEASURES: Bronchopulmonary dysplasia, discharge on home oxygen, intraventricular haemorrhage, death before discharge from neonatal care. RESULTS: Ten thousand one hundred and ninety-seven infants (53% male) were classified into four clusters: Cluster 1 contained infants with intermediate gestation and duration of ventilation and had an intermediate mortality and incidence of bronchopulmonary dysplasia. Cluster 2 contained infants with the highest gestation, a shorter duration of ventilation and the lowest mortality. Cluster 3 contained infants with the lowest Apgar score and highest mortality and incidence of intraventricular haemorrhage. Cluster 4 contained infants with the lowest gestation, longest duration of ventilation and highest incidence of bronchopulmonary dysplasia. CONCLUSION: Clinical parameters can classify extremely preterm infants into discrete phenotypic groups with differing subsequent neonatal outcomes.
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spelling pubmed-88864392022-03-17 Using cluster analysis to describe phenotypical heterogeneity in extremely preterm infants: a retrospective whole-population study Dassios, Theodore Williams, Emma E Harris, Christopher Greenough, Anne BMJ Open Paediatrics OBJECTIVE: To use cluster analysis to identify discrete phenotypic groups of extremely preterm infants. DESIGN: Secondary analysis of a retrospective whole population study. SETTING: All neonatal units in England between 2014 and 2019. PARTICIPANTS: Infants live-born at less than 28 weeks of gestation and admitted to a neonatal unit. INTERVENTIONS: K-means cluster analysis was performed with the gestational age, Apgar score at 5 min and duration of mechanical ventilation as input variables. PRIMARY AND SECONDARY OUTCOME MEASURES: Bronchopulmonary dysplasia, discharge on home oxygen, intraventricular haemorrhage, death before discharge from neonatal care. RESULTS: Ten thousand one hundred and ninety-seven infants (53% male) were classified into four clusters: Cluster 1 contained infants with intermediate gestation and duration of ventilation and had an intermediate mortality and incidence of bronchopulmonary dysplasia. Cluster 2 contained infants with the highest gestation, a shorter duration of ventilation and the lowest mortality. Cluster 3 contained infants with the lowest Apgar score and highest mortality and incidence of intraventricular haemorrhage. Cluster 4 contained infants with the lowest gestation, longest duration of ventilation and highest incidence of bronchopulmonary dysplasia. CONCLUSION: Clinical parameters can classify extremely preterm infants into discrete phenotypic groups with differing subsequent neonatal outcomes. BMJ Publishing Group 2022-02-28 /pmc/articles/PMC8886439/ /pubmed/35228290 http://dx.doi.org/10.1136/bmjopen-2021-056567 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Paediatrics
Dassios, Theodore
Williams, Emma E
Harris, Christopher
Greenough, Anne
Using cluster analysis to describe phenotypical heterogeneity in extremely preterm infants: a retrospective whole-population study
title Using cluster analysis to describe phenotypical heterogeneity in extremely preterm infants: a retrospective whole-population study
title_full Using cluster analysis to describe phenotypical heterogeneity in extremely preterm infants: a retrospective whole-population study
title_fullStr Using cluster analysis to describe phenotypical heterogeneity in extremely preterm infants: a retrospective whole-population study
title_full_unstemmed Using cluster analysis to describe phenotypical heterogeneity in extremely preterm infants: a retrospective whole-population study
title_short Using cluster analysis to describe phenotypical heterogeneity in extremely preterm infants: a retrospective whole-population study
title_sort using cluster analysis to describe phenotypical heterogeneity in extremely preterm infants: a retrospective whole-population study
topic Paediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8886439/
https://www.ncbi.nlm.nih.gov/pubmed/35228290
http://dx.doi.org/10.1136/bmjopen-2021-056567
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