EEG in the Diagnosis, Classification, and Management of Patients With
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1 ILAE Classification & Definition of Epilepsy Syndromes in the Neonate
ILAE Classification & Definition of Epilepsy Syndromes in the Neonate and Infant: Position Statement by the ILAE Task Force on Nosology and Definitions Authors: Sameer M Zuberi1, Elaine Wirrell2, Elissa Yozawitz3, Jo M Wilmshurst4, Nicola Specchio5, Kate Riney6, Ronit Pressler7, Stephane Auvin8, Pauline Samia9, Edouard Hirsch10, O Carter Snead11, Samuel Wiebe12, J Helen Cross13, Paolo Tinuper14,15, Ingrid E Scheffer16, Rima Nabbout17 1. Paediatric Neurosciences Research Group, Royal Hospital for Children & Institute of Health & Wellbeing, University of Glasgow, Member of European Reference Network EpiCARE, Glasgow, UK. 2. Divisions of Child and Adolescent Neurology and Epilepsy, Department of Neurology, Mayo Clinic, Rochester MN, USA. 3. Isabelle Rapin Division of Child Neurology of the Saul R Korey Department of Neurology, Montefiore Medical Center, Bronx, NY USA. 4. Department of Paediatric Neurology, Red Cross War Memorial Children’s Hospital, Neuroscience Institute, University of Cape Town, South Africa. 5. Rare and Complex Epilepsy Unit, Department of Neuroscience, Bambino Gesu’ Children’s Hospital, IRCCS, Member of European Reference Network EpiCARE, Rome, Italy 6. Neurosciences Unit, Queensland Children's Hospital, South Brisbane, Queensland, Australia. Faculty of Medicine, University of Queensland, Queensland, Australia. 7. Clinical Neuroscience, UCL- Great Ormond Street Institute of Child Health, London, UK. Department of Clinical Neurophysiology, Great Ormond Street Hospital for Children NHS Foundation Trust, Member of European Reference Network EpiCARE London, UK 8. Université de Paris, AP-HP, Hôpital Robert-Debré, INSERM NeuroDiderot, DMU Innov-RDB, Neurologie Pédiatrique, Member of European Reference Network EpiCARE, Paris, France. 9. Department of Paediatrics and Child Health, Aga Khan University, East Africa. 1 10. Neurology Epilepsy Unit “Francis Rohmer”, INSERM 1258, FMTS, Strasbourg University, France. -
Title in All Caps
Epilepsy Syndromes: Where does Dravet Syndrome fit in? Scott Demarest MD Assistant Professor, Departments of Pediatrics and Neurology University of Colorado School of Medicine Children's Hospital Colorado Disclosures Scott Demarest has consulted for Upsher-Smith on an unrelated subject matter. No conflicts of interest Objectives • What is an Epilepsy Syndrome? • How do we define epilepsy syndromes? • Genetic vs Phenotype (Features) • So what? Why do we care about Epilepsy Syndromes? • How do we organize and categorize Epilepsy Syndromes? • What epilepsy syndromes are similar to Dravet Syndrome and what is different about them? Good Resource International League Against Epilepsy Epilepsydiagnosis.org https://www.epilepsydiagnosis.org/syndrome/epilepsy- syndrome-groupoverview.html What is an Epilepsy Syndrome? A syndrome is a collection of common clinical traits. For Epilepsy this is usually about: • What type of seizures occur? • Age seizure start? Electroclinical • Development? Features or • What does the EEG look like? Phenotype • Other Co-morbidities… Course of an Epilepsy Syndrome Developmental Trajectories - Theoretical Model Normal Previously Normal with Epileptic Encephalopathy Development Never Normal Gray represents Epilepsy Onset the intensity of Age Epilepsy How distinct are Epilepsy Syndromes? A B C Many features might overlap, but the hope is that the cluster of symptoms are “specific” to that epilepsy syndrome…this is often better in theory than practice. How does the individual patient fit? A B C Is this patient at type A,B or C? What about Syndromes Defined by Genes? Is SCN1A the same as Dravet Syndrome? …I don’t have a perfect answer for this… many diseases are being defined by the gene (CDKL5, SCN8A, CHD2). -
Epilepsy Syndromes E9 (1)
EPILEPSY SYNDROMES E9 (1) Epilepsy Syndromes Last updated: September 9, 2021 CLASSIFICATION .......................................................................................................................................... 2 LOCALIZATION-RELATED (FOCAL) EPILEPSY SYNDROMES ........................................................................ 3 TEMPORAL LOBE EPILEPSY (TLE) ............................................................................................................... 3 Epidemiology ......................................................................................................................................... 3 Etiology, Pathology ................................................................................................................................ 3 Clinical Features ..................................................................................................................................... 7 Diagnosis ................................................................................................................................................ 8 Treatment ............................................................................................................................................. 15 EXTRATEMPORAL NEOCORTICAL EPILEPSY ............................................................................................... 16 Etiology ................................................................................................................................................ 16 -
Using Amplitude-Integrated EEG in Neonatal Intensive Care
Journal of Perinatology (2010) 30, S73–S81 r 2010 Nature America, Inc. All rights reserved. 0743-8346/10 www.nature.com/jp REVIEW Using amplitude-integrated EEG in neonatal intensive care JD Tao and AM Mathur Department of Pediatrics, Washington University School of Medicine, St Louis, MO, USA monitoring can be applied, for example, to infants admitted with The implementation of amplitude-integrated electroencephalography encephalopathy, seizures or other brain malformations. Both term (aEEG) has enhanced the neurological monitoring of critically ill infants. and preterm infants may benefit from the clinical application of Limited channel leads are applied to the patient and data are displayed in a aEEG findings. Much similar to continuous monitoring of vital semilogarithmic, time-compressed scale. Several classifications are currently signs, bedside aEEG can help guide decision-making in real time in use to describe patient tracings, incorporating voltage criteria, pattern for infants admitted to the NICU. This article will review the recognition, cyclicity, and the presence or absence of seizures. In term history, classification and application of aEEG in both term and neonates, aEEG has been used to determine the prognosis and treatment for preterm infants. those affected by hypoxic–ischemic encephalopathy, seizures, meningitis and even congenital heart disease. Its application as inclusion criteria for therapeutic hypothermia remains controversial. In preterm infants, Background normative values and patterns corresponding to gestational age are being 2 established. As these standards emerge, the predictive value of aEEG Starting in the 1960s, Maynard et al., developed the first use of increases, especially in the setting of preterm brain injury and an instrument to study cerebral activity in resuscitated patients with intraventricular hemorrhage. -
ILAE Classification and Definition of Epilepsy Syndromes with Onset in Childhood: Position Paper by the ILAE Task Force on Nosology and Definitions
ILAE Classification and Definition of Epilepsy Syndromes with Onset in Childhood: Position Paper by the ILAE Task Force on Nosology and Definitions N Specchio1, EC Wirrell2*, IE Scheffer3, R Nabbout4, K Riney5, P Samia6, SM Zuberi7, JM Wilmshurst8, E Yozawitz9, R Pressler10, E Hirsch11, S Wiebe12, JH Cross13, P Tinuper14, S Auvin15 1. Rare and Complex Epilepsy Unit, Department of Neuroscience, Bambino Gesu’ Children’s Hospital, IRCCS, Member of European Reference Network EpiCARE, Rome, Italy 2. Divisions of Child and Adolescent Neurology and Epilepsy, Department of Neurology, Mayo Clinic, Rochester MN, USA. 3. University of Melbourne, Austin Health and Royal Children’s Hospital, Florey Institute, Murdoch Children’s Research Institute, Melbourne, Australia. 4. Reference Centre for Rare Epilepsies, Department of Pediatric Neurology, Necker–Enfants Malades Hospital, APHP, Member of European Reference Network EpiCARE, Institut Imagine, INSERM, UMR 1163, Université de Paris, Paris, France. 5. Neurosciences Unit, Queensland Children's Hospital, South Brisbane, Queensland, Australia. Faculty of Medicine, University of Queensland, Queensland, Australia. 6. Department of Paediatrics and Child Health, Aga Khan University, East Africa. 7. Paediatric Neurosciences Research Group, Royal Hospital for Children & Institute of Health & Wellbeing, University of Glasgow, Member of European Refence Network EpiCARE, Glasgow, UK. 8. Department of Paediatric Neurology, Red Cross War Memorial Children’s Hospital, Neuroscience Institute, University of Cape Town, South Africa. 9. Isabelle Rapin Division of Child Neurology of the Saul R Korey Department of Neurology, Montefiore Medical Center, Bronx, NY USA. 10. Programme of Developmental Neurosciences, UCL NIHR BRC Great Ormond Street Institute of Child Health, Department of Clinical Neurophysiology, Great Ormond Street Hospital for Children, London, UK 11. -
Clinical Approach to Burst-Suppression Pattern in an Intensive Care Unit: Basic and Updates
MICU ROUNDS Clinical approach to burst-suppression pattern in an intensive care unit: basic and updates Jie Pan MD, PhD, Amputch Karukote MD, Eri Shoji MD ABSTRACT A burst-suppression pattern is an electroencephalographic pattern characterized by a quasi-periodic high amplitude “burst” alternating with periods of low or flatline “suppression.” Recognizing and understanding this pattern is helpful for clinical management in intensive care units. Pathological burst-suppression is commonly seen in post cardiac arrest comatose patients. It can also be induced by anesthetics or hypothermia. A burst-suppression pattern in anoxic brain injury generally predicts a poor prognosis; however, exceptions do occur. Inducing burst- suppression by general anesthetics can be used to abort super-refractory status epilepticus. This article will discuss this unique EEG pattern, including basic mechanisms, related clinical conditions, and recent research updates. Keywords: EEG, burst-suppression, anoxic encephalopathy INTRODUCTION this EEG pattern is important for both neurologists and critical care specialists. A burst-suppression pattern (BSP) is a unique electroencephalography pattern commonly encoun- DESCRIPTION AND DISTINGUISHING FEATURES tered in intensive care units. The BSP occurs in the context of diffuse cerebral dysfunction with coma and The BSP is an electroencephalography pattern con- indicates a clinical severity that is greater than gener- sisting of a quasi-periodic high amplitude “burst” alternat- alized slowing but is less severe than electrocerebral ing with periods of low or absent activity “suppression.” inactivity. It is typically associated with a comatose This pattern is unique due to the abrupt change of ampli- state secondary to several pathophysiological etiolo- tude between burst and suppression periods.1,2 gies, including anoxic brain injury, induced hypother- mia, end stage status epilepticus, severe epileptic 1. -
Dictionary of Epilepsy
DICTIONARY OF EPILEPSY PART I: DEFINITIONS .· DICTIONARY OF EPILEPSY PART I: DEFINITIONS PROFESSOR H. GASTAUT President, University of Aix-Marseilles, France in collaboration with an international group of experts ~ WORLD HEALTH- ORGANIZATION GENEVA 1973 ©World Health Organization 1973 Publications of the World Health Organization enjoy copyright protection in accord ance with the provisions of Protocol 2 of the Universal Copyright Convention. For rights of reproduction or translation of WHO publications, in part or in toto, application should be made to the Office of Publications and Translation, World Health Organization, Geneva, Switzerland. The World Health Organization welcomes such applications. PRINTED IN SWITZERLAND WHO WORKING GROUP ON THE DICTIONARY OF EPILEPSY1 Professor R. J. Broughton, Montreal Neurological Institute, Canada Professor H. Collomb, Neuropsychiatric Clinic, University of Dakar, Senegal Professor H. Gastaut, Dean, Joint Faculty of Medicine and Pharmacy, University of Aix-Marseilles, France Professor G. Glaser, Yale University School of Medicine, New Haven, Conn., USA Professor M. Gozzano, Director, Neuropsychiatric Clinic, Rome, Italy Dr A. M. Lorentz de Haas, Epilepsy Centre "Meer en Bosch", Heemstede, Netherlands Professor P. Juhasz, Rector, University of Medical Science, Debrecen, Hungary Professor A. Jus, Chairman, Psychiatric Department, Academy of Medicine, Warsaw, Poland Professor A. Kreindler, Institute of Neurology, Academy of the People's Republic of Romania, Bucharest, Romania Dr J. Kugler, Department of Psychiatry, University of Munich, Federal Republic of Germany Dr H. Landolt, Medical Director, Swiss Institute for Epileptics, Zurich, Switzerland Dr B. A. Lebedev, Chief, Mental Health, WHO, Geneva, Switzerland Dr R. L. Masland, Department of Neurology, College of Physicians and Surgeons, Columbia University, New York, USA Professor F. -
Nocturnal Epilepsy and Parasomnias Dr.Ram Sankaraneni 10/02/2020
10/2/2020 Nocturnal Epilepsy and Parasomnias Dr.Ram Sankaraneni 10/02/2020 1 CREIGHTON UNIVERSITY Disclosures • None 2 1 10/2/2020 CREIGHTON UNIVERSITY Epilepsy and Sleep • 7.5 to 45 percent of people who have epilepsy have seizures mostly during sleep • Sleep disorders more prevalent in epileptic population 3 CREIGHTON UNIVERSITY • Diagnosis of complex nocturnal behaviors is difficult 4 2 10/2/2020 CREIGHTON UNIVERSITY Differential Diagnosis • Nocturnal Seizures • Non Epileptic Motor Disorders 5 CREIGHTON UNIVERSITY Non Epileptic Motor Disorders • NREM Parasomnias • REM parasomnias • Sleep related movement disorders • Psychogenic 6 3 10/2/2020 CREIGHTON UNIVERSITY When to Suspect an Epileptic etiology • Stereotyped nature • High frequency/Clusters • Timing of the events • Duration • Age of onset 7 CREIGHTON UNIVERSITY Nocturnal Seizures • Clinical manifestation of seizures vary based on location and involved network 8 4 10/2/2020 CREIGHTON UNIVERSITY Seizures in various stages of sleep 70 60 50 40 %seizures 30 %sleep 20 10 0 stage 1 stage 2 SWS REM Herman et al, Neurology 2001;56:1453-9. 9 Percentage of partial seizures arising during sleep from various seizure onset zones. S.T. Herman et al. Neurology 2001;56:1453-1459 ©2001 by Lippincott Williams & Wilkins 10 5 10/2/2020 CREIGHTON UNIVERSITY Frontal Lobe Epilepsy •2nd most common epilepsy ( 18% of adults) • Often misdiagnosed 11 CREIGHTON UNIVERSITY Challenges in Diagnosis • Dramatic/complex movements • No postictal state • Often no Aura • EEG – excessive artifacts • EEG – can be normal -
Nocturnal Epilepsies in Adults
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector Seizure 1997; 6: 145-149 Nocturnal epilepsies in adults BASIM A YAQUB, GHAZALA WAHEED & MOHAMMAD MU KABIRAJ Division of Neurology and Neurophysiology, King Khalid University Hospital, PO Box 7805, Riyadh 11472, Saudi Arabia Correspondence to: Dr. Basim A. Yaqub, Consultant Neurologist, Department of Clinical Neurosciences. Armed Forces Hospital, P.O. Box 7897 (X1006), Riyadh 11159, Kingdom of Saudi Arabia We evaluated the clinical characteristics and the electroencephalographic (EEG) findings by long video-EEG monitoring in 64 successive patients with definite nocturnal seizures. Mental state, neurological examination, neuroimaging and EEG background were normal in all patients. Classification of epilepsies was possible in 42 out of 64 (66%) patients according to the revised Classification of Epilepsies and Epileptic Syndromes by the Commission on Classification and Terminology of International League Against Epilepsy (1989). Out of those 42 patients, 33 (79%) had partial epilepsies, while 9 (21%) had generalized epilepsies. Response to antiepileptic drugs was excellent and only 4 (6%) patients had one seizure attack per year, two of them were on two antiepileptic drugs while the others were free of seizure on a single drug during the 2 years of follow-up. It seems that nocturnal seizuresin adults form a new distinctive partial epileptic syndrome of a benign entity. Key words: nocturnal seizures: epileptic syndromes: video-EEG monitoring: benign childhood epilepsy with centro-temporal spikes:antiepileptic drugs. INTRODUCTION EEG (VEEG) monitoring, has become an essential technique in most sleep laboratories, The pattern of seizure occurrence in most also it is an important technique for the epileptics is random without cycling or clustering identification and classification of unusual sei- so they can occur during the daytime or sleep’. -
The Relationship Between the Characteristics of Burst Suppression Pattern and Different Etiologies in Epilepsy
www.nature.com/scientificreports OPEN The relationship between the characteristics of burst suppression pattern and diferent etiologies in epilepsy Haipo Yang, Pan Gong, Xianru Jiao, Qiujun Zhou, Yuehua Zhang, Yuwu Jiang & Zhixian Yang* To analyze the relationship between the characteristics of burst suppression (BS) pattern and diferent etiologies in epilepsy. Patients with a BS pattern who were younger than 6 months old were screened from our electroencephalogram (EEG) database. The synchronized and symmetric BS patterns under diferent etiologies in epilepsy were analyzed. A total of 32 patients had a BS pattern on EEG. The etiologies included genetic disorders (37.5%), cortical malformations (28.1%), inborn errors of metabolism (12.5%), and unknown (21.9%). Twenty-fve patients were diagnosed with Ohtahara syndrome, one as early myoclonic encephalopathy, and one as epilepsy of infancy with migrating focal seizure. Five cases could not be classifed into any epileptic syndrome. Asynchronous BS pattern was identifed in 18 cases, of which 13 (72%) patients had genetic and/or metabolic etiologies. Synchronous BS pattern was identifed in 14 cases, of which 8 (57%) patients had structural etiologies. Twenty-three patients had symmetric BS patterns, of which 15 (65%) patients had genetic etiologies. Nine patients had asymmetric BS patterns, of which 8 (89%) patients had structural etiologies. Patients with genetic epilepsies tended to have asynchronous and symmetric BS patterns, whereas those with structural epilepsies were more likely to have synchronous and asymmetric BS patterns. Burst suppression (BS) is an abnormal electroencephalogram (EEG) pattern characterized by the alternating appearance of depressed background activity and bursts of mixed-frequency paroxysmal activity1. -
C1 PAGE.Indd
Neurology.org/N Child Neurology: A Case-Based Approach Cases from the Neurology® Resident & Fellow Section Child Neurology: A Case-Based Approach Cases from the Neurology® Resident & Fellow Section Editors John J. Millichap, MD Att ending Epileptologist Ann & Robert H. Lurie Children’s Hospital of Chicago Associate Professor of Pediatrics and Neurology Northwestern University Feinberg School of Medicine Chicago, IL Jonathan W. Mink, MD, PhD Frederick A. Horner, MD Endowed Professor in Pediatric Neurology Professor of Neurology, Neuroscience, and Pediatrics Chief, Division of Child Neurology Vice Chair, Department of Neurology University of Rochester Medical Center Rochester, NY Phillip L. Pearl, MD Director of Epilepsy and Clinical Neurophysiology William G. Lennox Chair, Boston Children’s Hospital Professor of Neurology Harvard Medical School Boston, MA Roy E. Strowd III, MEd, MD Assistant Professor Neurology and Oncology Wake Forest School of Medicine Winston Salem, NC © 2019 American Academy of Neurology. All rights reserved. All articles have been published in Neurology®. Opinions expressed by the authors are not necessarily those of the American Academy of Neurology, its affi liates, or of the Publisher. Th e American Academy of Neurology, its affi liates, and the Publisher disclaim any liability to any party for the accuracy, completeness, effi cacy, or availability of the material contained in this publication (including drug dosages) or for any damages arising out of the use or non-use of any of the material contained in this publication. TABLE OF CONTENTS Neurology.org/N Section 2. Pediatric stroke and cerebrovascular disorders 25 Introduction Robert Hurford, Laura L. Lehman, Behnam Sabayan, and Mitchell S.V. -
Recovery of Amplitude Integrated Electroencephalographic Background Patterns Within 24 Hours of Perinatal Asphyxia
F245 Arch Dis Child Fetal Neonatal Ed: first published as 10.1136/adc.2004.064964 on 21 April 2005. Downloaded from ORIGINAL ARTICLE Recovery of amplitude integrated electroencephalographic background patterns within 24 hours of perinatal asphyxia L G M van Rooij, M C Toet, D Osredkar, A C van Huffelen, F Groenendaal, L S de Vries ............................................................................................................................... Arch Dis Child Fetal Neonatal Ed 2005;90:F245–F251. doi: 10.1136/adc.2004.064964 Objective: To assess the time course of recovery of severely abnormal initial amplitude integrated electroencephalographic (aEEG) patterns (flat trace (FT), continuous low voltage (CLV), or burst suppression (BS)) in full term asphyxiated neonates, in relation to other neurophysiological and neuroimaging findings and neurodevelopmental outcome. Methods: A total of 190 aEEGs of full term infants were reviewed. The neonates were admitted within See end of article for 6 hours of birth to the neonatal intensive care unit because of perinatal asphyxia, and aEEG recording was authors’ affiliations started immediately. In all, 160 infants were included; 65 of these had an initial FT or CLV pattern and 25 ....................... an initial BS pattern. Neurodevelopmental outcome was assessed using a full neurological examination Correspondence to: and the Griffiths’ mental developmental scale. Dr de Vries, Department of Results: In the FT/CLV group, the background pattern recovered to continuous normal voltage within Neonatology, Wilhelmina 24 hours in six of the 65 infants (9%). All six infants survived the neonatal period; one had a severe Children’s Hospital, KE 04. disability, and five were normal at follow up. In the BS group, the background pattern improved to normal 123.1, PO Box 85090, 3508 AB Utrecht, the voltage in 12 of the 25 infants (48%) within 24 hours.