Electroencephalographic seizures in critically ill children: Management and adverse events.
France W Fung, Marin Jacobwitz, Lisa Vala...
https://pubmed.ncbi.nlm.nih.gov/31538340Actively Recruiting
Led by Children's Hospital of Philadelphia · Updated on 2025-02-04
2500
Participants Needed
1
Research Sites
N/A
Total Duration
C
Children's Hospital of Philadelphia
Lead Sponsor
N
National Institute of Neurological Disorders and Stroke (NINDS)
Collaborating Sponsor
Electrographic seizures frequently occur in critically ill children and often require continuous EEG monitoring, which uses significant resources. Researchers are studying these seizures to identify risk factors and improve management strategies, as current data on the best anti-seizure medications and approaches is limited. This single-center observational study takes place at the Children's Hospital of Philadelphia and aims to create prediction models to guide EEG monitoring and evaluate the safety of current seizure management. Participants in this study are critically ill children in the Pediatric ICU undergoing clinically indicated continuous EEG monitoring. The study observes their electrographic seizure management practices following the hospital's ICU EEG Monitoring Pathway. There are no experimental treatments; instead, the study tracks EEG monitoring and seizure interventions as they naturally occur to collect data on risk factors and safety. During the study, children receive clinically required EEG monitoring and seizure management as part of their care. Researchers collect data on seizure occurrence over three days and monitor safety outcomes such as mortality, cardiopulmonary effects, organ dysfunction, and hospital-acquired infections over five days. The study does not interfere with treatment and focuses on understanding seizure risks and management outcomes over the observation period.
CONDITIONS
Electrographic Seizure Management and Neurobehavioral Outcomes in Critically Ill Children
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 5 days
Participants undergo clinically indicated continuous EEG monitoring to identify electrographic seizures and assess seizure risk factors.
Continuous monitoring during ICU stay
Duration - Up to 5 days
Participants are observed for safety outcomes including mortality, cardiopulmonary adverse effects, organ dysfunction, and hospital-acquired infections.
Total: 1 location
1
Children's Hospital of Philadelphia
Philadelphia, Pennsylvania, United States, 19104
Actively Recruiting
N
Nicholas S Abend, MD
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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