Brain damage in the preterm infant (clinics in developmental medicine no.131)

1995 ◽  
Vol 37 (5) ◽  
pp. 417-417
Author(s):  
M. V. Squier
Keyword(s):  
Neonatology ◽  
2021 ◽  
pp. 1-4
Author(s):  
Viktoria Engert ◽  
Celine Siauw ◽  
Annika Stock ◽  
Monika Rehn ◽  
Achim Wöckel ◽  
...  

Current evidence from the COVID-19 pandemic suggests that neonatal SARS-coronavirus-2 infections usually have a mild course. Data on how maternal infection during pregnancy affects fetal development are scarce. We present the unique case of a moderate preterm infant with intracranial bleeding and periventricular leukomalacia as a potential consequence of post-COVID-19 hyperinflammation during pregnancy.


The Lancet ◽  
1986 ◽  
Vol 328 (8504) ◽  
pp. 460 ◽  
Author(s):  
Gorm Greisen ◽  
Hanne Munck ◽  
Hans Lou

2021 ◽  
Vol 22 (4) ◽  
pp. 1671
Author(s):  
Nathanael Yates ◽  
Alistair J. Gunn ◽  
Laura Bennet ◽  
Simerdeep K. Dhillon ◽  
Joanne O. Davidson

Preterm birth is associated with a high risk of morbidity and mortality including brain damage and cerebral palsy. The development of brain injury in the preterm infant may be influenced by many factors including perinatal asphyxia, infection/inflammation, chronic hypoxia and exposure to treatments such as mechanical ventilation and corticosteroids. There are currently very limited treatment options available. In clinical trials, magnesium sulfate has been associated with a small, significant reduction in the risk of cerebral palsy and gross motor dysfunction in early childhood but no effect on the combined outcome of death or disability, and longer-term follow up to date has not shown improved neurological outcomes in school-age children. Recombinant erythropoietin has shown neuroprotective potential in preclinical studies but two large randomized trials, in extremely preterm infants, of treatment started within 24 or 48 h of birth showed no effect on the risk of severe neurodevelopmental impairment or death at 2 years of age. Preclinical studies have highlighted a number of promising neuroprotective treatments, such as therapeutic hypothermia, melatonin, human amnion epithelial cells, umbilical cord blood and vitamin D supplementation, which may be useful at reducing brain damage in preterm infants. Moreover, refinements of clinical care of preterm infants have the potential to influence later neurological outcomes, including the administration of antenatal and postnatal corticosteroids and more accurate identification and targeted treatment of seizures.


ASHA Leader ◽  
2010 ◽  
Vol 15 (7) ◽  
pp. 22-23 ◽  
Author(s):  
Steven M. Barlow ◽  
Meredith A. Poore ◽  
Emily A. Zimmerman ◽  
Don S. Finan

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