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Contemporary Profile of Seizures in Neonates: A Prospective Cohort Study - 24/06/16

Doi : 10.1016/j.jpeds.2016.03.035 
Hannah C. Glass, MDCM, MAS 1, 2, Renée A. Shellhaas, MD, MS 3, Courtney J. Wusthoff, MD 4, Taeun Chang, MD 5, Nicholas S. Abend, MD 6, Catherine J. Chu, MD 7, M. Roberta Cilio, MD, PhD 1, David V. Glidden, PhD 2, Sonia L. Bonifacio, MD, MAS 8, Shavonne Massey, MD 6, Tammy N. Tsuchida, MD, PhD 5, Faye S. Silverstein, MD 3, Janet S. Soul, MDCM 9
on behalf of the

Neonatal Seizure Registry Study Group

  List of additional members of Neonatal Seizure Registry Study Group is available at www.jpeds.com (Appendix).
Ann Marie Bergin, MB, ScM, MRCP (UK), Dennis Dlugos, MD, MSCE, Donna M. Ferriero, MD, MS, UCSF, Kevin Staley, MD

1 Departments of Neurology & Pediatrics, University of California, San Francisco Benioff Children's Hospital, University of California San Francisco, San Francisco, CA 
2 Department of Epidemiology & Biostatistics, University of California San Francisco, San Francisco, CA 
3 Department of Pediatrics & Communicable Diseases, University of Michigan, Ann Arbor, MI 
4 Departments of Neurology & Pediatrics, Stanford University, Palo Alto, CA 
5 Department of Neurology, Children's National Health System, George Washington University School of Medicine, Washington, DC 
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 
7 Department of Neurology, Massachusetts General Hospital, Boston, MA 
8 Division of Neonatal and Developmental Medicine, Department of Pediatrics, Stanford University, Palo Alto, CA 
9 Department of Neurology, Boston Children's Hospital, Boston, MA 

Abstract

Objective

To determine the contemporary etiology, burden, and short-term outcomes of seizures in neonates monitored with continuous video-electroencephalogram (cEEG).

Study design

We prospectively collected data from 426 consecutive neonates (56% male, 88% term) ≤44 weeks' postmenstrual age with clinically suspected seizures and/or electrographic seizures. Subjects were assessed between January 2013 and April 2015 at 7 US tertiary care pediatric centers following the guidelines of the American Clinical Neurophysiology Society for cEEG for at-risk neonates. Seizure etiology, burden, management, and outcome were determined by chart review by the use of a case report form designed at study onset.

Results

The most common seizure etiologies were hypoxic-ischemic encephalopathy (38%), ischemic stroke (18%), and intracranial hemorrhage (11%). Seizure burden was high, with 59% having ≥7 electrographic seizures and 16% having status epilepticus; 52% received ≥2 antiseizure medications. During the neonatal admission, 17% died; 49% of survivors had abnormal neurologic examination at hospital discharge. In an adjusted analysis, high seizure burden was a significant risk factor for mortality, length of hospital stay, and abnormal neurological examination at discharge.

Conclusions

In this large contemporary profile of consecutively enrolled newborns with seizures treated at centers that use cEEG per the guidelines of the American Clinical Neurophysiology Society, about one-half had high seizure burden, received ≥2 antiseizure medications, and/or died or had abnormal examination at discharge. Greater seizure burden was associated with increased morbidity and mortality. These findings underscore the importance of accurate determination of neonatal seizure frequency and etiology and a potential for improved outcome if seizure burden is reduced.

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Keywords : neonatal seizures, EEG, electroencephalogram, epilepsy, neurocritical care, infant, critical care, neonatal encephalopathy, hypoxic-ischemic encephalopathy

Abbreviations : ACNS, cEEG, EEG, HIE, ICH


Plan


 Supported by the Pediatric Epilepsy Research Foundation (Multi-center Neonatal Seizure Registry/A120625). H.G. is supported by the National Institutes of Health (NIH)/National Institute of Neurological Disorders and Stroke (K23NS066137) and the Neonatal Brain Research Institute at University of California, San Francisco. J.S. is supported by Boston Children's Hospital Intellectual and Developmental Disabilities Research Center (P30 HD18655). REDCap (Research Electronic Data Capture) tools is supported by University of California, San Francisco. The contents of this article are solely the responsibility of the authors and do not necessarily represent the official views of the NIH. The authors declare no conflicts of interest.


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Vol 174

P. 98 - juillet 2016 Retour au numéro
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