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Treating EEG Seizures in Hypoxic Ischemic Encephalopathy: A Randomized Controlled Trial
Preethi Srinivasakumar1, John Zempel2, Shamik Trivedi3
1Departments of Pediatrics, preethi.srinivasakumar@UTSouthwestern.edu.
Pediatrics
|October 21, 2015
Summary
Treating electrographic seizures in neonatal hypoxic ischemic encephalopathy (HIE) reduces seizure burden. Lower seizure burden is linked to less severe brain injury and better neurodevelopmental outcomes in infants.
Area of Science:
- Neonatal neurology
- Pediatric critical care
- Neurodevelopmental disorders
Background:
- The impact of treating electrographic seizures in neonatal hypoxic ischemic encephalopathy (HIE) remains unclear.
- Early identification and management of seizures are crucial for improving outcomes in HIE.
Purpose of the Study:
- To investigate the effect of treating electrographic seizures alone versus clinical seizures on seizure burden and neurodevelopmental outcomes in neonates with HIE.
Main Methods:
- Randomized trial comparing treatment of electrographic seizures alone (ESG) versus clinical seizures (CSG) in neonates (≥36 weeks) with moderate to severe HIE.
- Continuous EEG monitoring for up to 96 hours to quantify electrographic seizure burden (SB).
- Assessment of brain injury severity via MRI and neurodevelopmental evaluation using the Bayley Scales of Infant and Toddler Development (BSID III) at 18-24 months.
Main Results:
- Treatment of electrographic seizures alone (ESG) resulted in a significantly lower median seizure burden (SB) compared to clinical seizure group (CSG) (P = .02).
- The ESG group experienced fewer seizures and shorter time to treatment (P = .04).
- Increased SB was significantly associated with more severe brain injury on MRI and lower BSID III performance scores across all domains (P < .03).
Conclusions:
- EEG monitoring and treatment of electrographic seizures in neonates with HIE significantly reduce seizure burden.
- Reduced seizure burden is associated with less severe brain injury and improved neurodevelopmental outcomes in infants with HIE.
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