Amy Yang1, Daniel H Arndt2, Robert A Berg3, Jessica L Carpenter4, Kevin E Chapman5, Dennis J Dlugos6, William B Gallentine7, Christopher C Giza8, Joshua L Goldstein9, Cecil D Hahn10, Jason T Lerner8, Tobias Loddenkemper11, Joyce H Matsumoto8, Kendall B Nash12, Eric T Payne10, Iván Sánchez Fernández11, Justine Shults1, Alexis A Topjian3, Korwyn Williams13, Courtney J Wusthoff14, Nicholas S Abend15. 1. Department of Biostatistics and Epidemiology, Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine at The University of Pennsylvania, United States. 2. Departments of Pediatrics and Neurology, Beaumont Children's Hospital and Oakland University William Beaumont School of Medicine, Royal Oak, MI, United States. 3. Department of Anesthesia and Critical Care Medicine, The Children's Hospital of Philadelphia and The Perelman School of Medicine at The University of Pennsylvania, Philadelphia, PA, United States. 4. Department of Neurology, Children's National Medical Center, Washington, DC, United States. 5. Department of Pediatrics and Neurology, Children's Hospital Colorado and University of Colorado School of Medicine, Aurora, CO, United States. 6. Departments of Neurology and Pediatrics, The Children's Hospital of Philadelphia and The Perelman School of Medicine at The University of Pennsylvania, Philadelphia, PA, United States. 7. Division of Neurology, Duke Children's Hospital and Duke University School of Medicine, Durham, NC, United States. 8. Division of Neurology, Department of Pediatrics Mattel Children's Hospital and UCLA Brain Injury Research Center, Department of Neurosurgery, David Geffen School of Medicine at UCLA, Los Angeles, CA, United States. 9. Division of Neurology, Children's Memorial Hospital and Northwestern University Feinberg School of Medicine, Chicago, IL, United States. 10. Division of Neurology, The Hospital for Sick Children and University of Toronto, Toronto, ON, United States. 11. Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Boston Children's Hospital and Harvard Medical School, Boston, MA, United States. 12. Department of Neurology, University of California San Francisco, San Francisco, CA, United States. 13. Department of Pediatrics, University of Arizona College of Medicine and Barrow's Neurological Institute at Phoenix Children's Hospital, Phoenix, AZ, United States. 14. Division of Child Neurology, Stanford University, Palo Alto, CA, United States. 15. Departments of Neurology and Pediatrics, The Children's Hospital of Philadelphia and The Perelman School of Medicine at The University of Pennsylvania, Philadelphia, PA, United States. Electronic address: abend@chop.edu.
Abstract
PURPOSE: Electrographic seizures are common in encephalopathic critically ill children, but identification requires continuous EEG monitoring (CEEG). Development of a seizure prediction model would enable more efficient use of limited CEEG resources. We aimed to develop and validate a seizure prediction model for use among encephalopathic critically ill children. METHOD: We developed a seizure prediction model using a retrospectively acquired multi-center database of children with acute encephalopathy without an epilepsy diagnosis, who underwent clinically indicated CEEG. We performed model validation using a separate prospectively acquired single center database. Predictor variables were chosen to be readily available to clinicians prior to the onset of CEEG and included: age, etiology category, clinical seizures prior to CEEG, initial EEG background category, and inter-ictal discharge category. RESULTS: The model has fair to good discrimination ability and overall performance. At the optimal cut-off point in the validation dataset, the model has a sensitivity of 59% and a specificity of 81%. Varied cut-off points could be chosen to optimize sensitivity or specificity depending on available CEEG resources. CONCLUSION: Despite inherent variability between centers, a model developed using multi-center CEEG data and few readily available variables could guide the use of limited CEEG resources when applied at a single center. Depending on CEEG resources, centers could choose lower cut-off points to maximize identification of all patients with seizures (but with more patients monitored) or higher cut-off points to reduce resource utilization by reducing monitoring of lower risk patients (but with failure to identify some patients with seizures).
PURPOSE: Electrographic seizures are common in encephalopathic critically illchildren, but identification requires continuous EEG monitoring (CEEG). Development of a seizure prediction model would enable more efficient use of limited CEEG resources. We aimed to develop and validate a seizure prediction model for use among encephalopathic critically illchildren. METHOD: We developed a seizure prediction model using a retrospectively acquired multi-center database of children with acute encephalopathy without an epilepsy diagnosis, who underwent clinically indicated CEEG. We performed model validation using a separate prospectively acquired single center database. Predictor variables were chosen to be readily available to clinicians prior to the onset of CEEG and included: age, etiology category, clinical seizures prior to CEEG, initial EEG background category, and inter-ictal discharge category. RESULTS: The model has fair to good discrimination ability and overall performance. At the optimal cut-off point in the validation dataset, the model has a sensitivity of 59% and a specificity of 81%. Varied cut-off points could be chosen to optimize sensitivity or specificity depending on available CEEG resources. CONCLUSION: Despite inherent variability between centers, a model developed using multi-center CEEG data and few readily available variables could guide the use of limited CEEG resources when applied at a single center. Depending on CEEG resources, centers could choose lower cut-off points to maximize identification of all patients with seizures (but with more patients monitored) or higher cut-off points to reduce resource utilization by reducing monitoring of lower risk patients (but with failure to identify some patients with seizures).
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