Abstract
Over the past decade, evidence has emerged that children growing up after neonatal critical illness, irrespective of underlying diagnosis, are at risk of memory impairment and academic problems. These difficulties are manifest even
when intelligence is within the normal range. In this Review, we propose a common neurodevelopmental pathway following neonatal critical illness by showing that survivors of preterm birth, congenital heart disease, and severe
respiratory failure share an increased risk of long-term memory deficits and associated hippocampal alterations. Rather than a consequence of underlying diagnosis, we suggest that this shared vulnerability is probably related to
common conditions associated with neonatal critical illness, including hypoxia, neuroinflammation, stress, exposure to anaesthetics, or a complex interplay of these factors at different postconceptional ages. Future work should be
aimed at improvement of early identification of patients at risk and evaluation of intervention modalities, such as
exercise or cognitive training.
when intelligence is within the normal range. In this Review, we propose a common neurodevelopmental pathway following neonatal critical illness by showing that survivors of preterm birth, congenital heart disease, and severe
respiratory failure share an increased risk of long-term memory deficits and associated hippocampal alterations. Rather than a consequence of underlying diagnosis, we suggest that this shared vulnerability is probably related to
common conditions associated with neonatal critical illness, including hypoxia, neuroinflammation, stress, exposure to anaesthetics, or a complex interplay of these factors at different postconceptional ages. Future work should be
aimed at improvement of early identification of patients at risk and evaluation of intervention modalities, such as
exercise or cognitive training.
Originalsprog | Engelsk |
---|---|
Tidsskrift | The Lancet Child & Adolescent Health |
Vol/bind | 2 |
Udgave nummer | 4 |
Sider (fra-til) | 281-289 |
Antal sider | 9 |
ISSN | 2352-4642 |
Status | Udgivet - apr. 2018 |