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Prognostic value of quantitative EEG in early hours of life for neonatal encephalopathy and neurodevelopmental outcomes.
Kota, Srinivas; Kang, Shu; Liu, Yu-Lun; Liu, Hanli; Montazeri, Saeed; Vanhatalo, Sampsa; Chalak, Lina F.
Afiliação
  • Kota S; Division of Neonatal-Perinatal Medicine, Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Kang S; Department of Bioengineering, University of Texas at Arlington, Arlington, TX, USA.
  • Liu YL; Peter O'Donnell Jr. School of Public Health, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Liu H; Department of Bioengineering, University of Texas at Arlington, Arlington, TX, USA.
  • Montazeri S; Department of Physiology, University of Helsinki, Helsinki, Finland.
  • Vanhatalo S; Department of Physiology, University of Helsinki, Helsinki, Finland.
  • Chalak LF; Division of Neonatal-Perinatal Medicine, Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX, USA. Lina.chalak@utsouthwestern.edu.
Pediatr Res ; 96(3): 685-694, 2024 Aug.
Article em En | MEDLINE | ID: mdl-39039325
ABSTRACT

BACKGROUND:

The ability to determine severity of encephalopathy is crucial for early neuroprotective therapies and for predicting neurodevelopmental outcome. The objective of this study was to assess a novel brain state of newborn (BSN) trend to distinguish newborns with presence of hypoxic ischemic encephalopathy (HIE) within hours after birth and predict neurodevelopmental outcomes at 2 years of age.

METHOD:

This is a prospective cohort study of newborns at 36 weeks' gestation or later with and without HIE at birth. The Total Sanart Score (TSS) was calculated based on a modified Sarnat exam within 6 h of life. BSN was calculated from electroencephalogram (EEG) measurements initiated after birth. The primary outcome at 2 year of age was a diagnosis of death or disability using the Bayley Scales of Infant Development III.

RESULTS:

BSN differentiated between normal and abnormal neurodevelopmental outcomes throughout the entire recording period from 6 h of life. Additionally, infants with lower BSN values had higher odds of neurodevelopmental impairment and HIE. BSN distinguished between normal (n = 86) and HIE (n = 46) and showed a significant correlation with the concomitant TSS.

CONCLUSION:

BSN is a sensitive real-time marker for monitoring dynamic progression of encephalopathy and predicting neurodevelopmental impairment. IMPACT This is a prospective cohort study to investigate the ability of brain state of newborn (BSN) trend to predict neurodevelopmental outcome within the first day of life and identify severity of encephalopathy. BSN predicts neurodevelopmental outcomes at 2 years of age and the severity of encephalopathy severity. It also correlates with the Total Sarnat Score from the modified Sarnat exam. BSN could serve as a promising bedside trend aiding in accurate assessment and identification of newborns who may benefit from additional neuroprotection therapies.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hipóxia-Isquemia Encefálica / Eletroencefalografia Limite: Child, preschool / Female / Humans / Male / Newborn Idioma: En Revista: Pediatr Res Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hipóxia-Isquemia Encefálica / Eletroencefalografia Limite: Child, preschool / Female / Humans / Male / Newborn Idioma: En Revista: Pediatr Res Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos
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