2023
DOI: 10.1111/jir.13021
|View full text |Cite
|
Sign up to set email alerts
|

Intellectual functioning in survivors of extremely low birthweight: Cognitive outcomes in childhood and adolescence

Abstract: BackgroundInfants born at extremely low birthweight (ELBW: ≤1000 g) are vulnerable to intellectual disabilities, but the factors that may distinguish between ELBW survivors with and without these impairments are not well understood. In this study, prospective associations between neonatal factors and functional outcomes in childhood and adolescence were compared in ELBW survivors with and without borderline intellectual functioning (BIF).MethodsBorderline intellectual functioning was defined by IQ < 85, ass… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2023
2023
2024
2024

Publication Types

Select...
3

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(1 citation statement)
references
References 99 publications
0
1
0
Order By: Relevance
“…This is consistent with the results of Paananen et al [33], who studied 128 very premature infants and found that infants with inflammation and high concentrations of inflammatory cytokines were at high risk of BPD. Thus, in addition to the neurological impairment associated with BPD [34], it is now recognized that the exposition of the immature brain to inflammation contributes to significant cerebral injury and adversely affects brain development, leading to subsequent neurological impairment [35]. The role of inflammation in the development of BPD may also be responsible for part of the poor neurodevelopment outcomes of the infants who had presented severe RDS and subsequent BPD in the neonatal period.…”
Section: Discussionmentioning
confidence: 99%
“…This is consistent with the results of Paananen et al [33], who studied 128 very premature infants and found that infants with inflammation and high concentrations of inflammatory cytokines were at high risk of BPD. Thus, in addition to the neurological impairment associated with BPD [34], it is now recognized that the exposition of the immature brain to inflammation contributes to significant cerebral injury and adversely affects brain development, leading to subsequent neurological impairment [35]. The role of inflammation in the development of BPD may also be responsible for part of the poor neurodevelopment outcomes of the infants who had presented severe RDS and subsequent BPD in the neonatal period.…”
Section: Discussionmentioning
confidence: 99%