Epilepsy: the Disorder
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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. -
EEG in the Diagnosis, Classification, and Management of Patients With
EEG IN THE DIAGNOSIS, J Neurol Neurosurg Psychiatry: first published as 10.1136/jnnp.2005.069245 on 16 June 2005. Downloaded from CLASSIFICATION, AND MANAGEMENT ii2 OF PATIENTS WITH EPILEPSY SJMSmith J Neurol Neurosurg Psychiatry 2005;76(Suppl II):ii2–ii7. doi: 10.1136/jnnp.2005.069245 he human electroencephalogram (EEG) was discovered by the German psychiatrist, Hans Berger, in 1929. Its potential applications in epilepsy rapidly became clear, when Gibbs and Tcolleagues in Boston demonstrated 3 per second spike wave discharge in what was then termed petit mal epilepsy. EEG continues to play a central role in diagnosis and management of patients with seizure disorders—in conjunction with the now remarkable variety of other diagnostic techniques developed over the last 30 or so years—because it is a convenient and relatively inexpensive way to demonstrate the physiological manifestations of abnormal cortical excitability that underlie epilepsy. However, the EEG has a number of limitations. Electrical activity recorded by electrodes placed on the scalp or surface of the brain mostly reflects summation of excitatory and inhibitory postsynaptic potentials in apical dendrites of pyramidal neurons in the more superficial layers of the cortex. Quite large areas of cortex—in the order of a few square centimetres—have to be activated synchronously to generate enough potential for changes to be registered at electrodes placed on the scalp. Propagation of electrical activity along physiological pathways or through volume conduction in extracellular spaces may give a misleading impression as to location of the source of the electrical activity. Cortical generators of the many normal and abnormal cortical activities recorded in the EEG are still largely unknown. -
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 -
The Approach to Patients with ''Non-Epileptic Seizures''
498 Postgrad Med J: first published as 10.1136/pgmj.2004.029785 on 5 August 2005. Downloaded from REVIEW The approach to patients with ‘‘non-epileptic seizures’’ J D C Mellers ............................................................................................................................... Postgrad Med J 2005;81:498–504. doi: 10.1136/pgmj.2004.029785 Up to one fifth of patients who present to specialist clinics with loose shorthand to refer to the psychological attacks alone.12 The terms psychogenic NES and seizures do not have epilepsy. The majority of such patients functional seizures overcome some of these suffer from psychologically mediated episodes; dissociative objections but formal psychiatric classification seizures, often referred to as ‘‘non-epileptic seizures’’. This systems provide clearly defined labels. Unfor- tunately, though, there are still inconsistencies: paper describes the diagnostic evaluation of seizure thus, within DSM IV13 such attacks are classified disorders, including clinical assessment and the role of special under somatoform disorder and in ICD 1014 the investigations. The organic and psychiatric imitators of diagnostic label ‘‘dissociative convulsions’’, is classified within the group of conversion dis- epilepsy are outlined and findings on psychiatric assessment orders. It is the latter terminology that will be are reviewed. This group of patients often proves difficult to adopted here. engage in appropriate treatment and an approach to As we have seen, dissociative convulsions or seizures (DS) are common, the diagnosis is often explaining the diagnosis is described. As yet there are no missed, and when it is patients not only fail to controlled trials of treatment in this disorder but preliminary receive appropriate treatment but are subject to evidence suggests cognitive behavioural therapy is both a unnecessary, costly,15 and potentially harmful medical interventions. -
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. -
Signs of Teen Drug Abuse 14 EDITS
Signs of Teen Drug Abuse SoberCollege.com Teen Drug Abuse Are you concerned that your child is using drugs or alcohol? Whether you are concerned about changes in appearance or behavior Sober College can help you find out more about a range of symptoms associated with drug use. Table of Contents: Symptoms Drug Types ......................................................................................................................................................... 2 Red eyes ...................................................................................................................................................... 3 Weight loss ...................................................................................................................................................... 4 Cuts, sores or bruises...................................................................................................................................... 5 Deterioration of physical appearance .......................................................................................................... 6 Shakes and tremors ........................................................................................................................................ 7 Anger issues ..................................................................................................................................................... 8 Financial difficulties ...................................................................................................................................... -
An Overview of Psychogenic Non-Epileptic Seizures: Etiology, Diagnosis and Management
REVIEW ARTICLE COPYRIGHT © 2018 THE CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES INC. An Overview of Psychogenic Non-Epileptic Seizures: Etiology, Diagnosis and Management Ángela Milán-Tomás, Michelle Persyko, Martin del Campo, Colin M. Shapiro, Karl Farcnik ABSTRACT: The purpose of this review is to provide an update of the research regarding the etiology, diagnosis and management of psychogenic non-epileptic seizures (PNES). A literature search using Pubmed, Ovid MEDLINE and EMBASE database was performed from 2000 up to August 2017. We have evaluated the different factors leading to PNES as well as the diagnostic approach and management of this disorder which continue to be very difficult. The coexistence of epilepsy and PNES poses special challenges and requires the coordinated efforts of the family physicians, psychiatrists, psychologists and neurologists. Although this condition has an overall poor prognosis, a multidisciplinary approach in the diagnosis and management of this disorder would likely improve the outcomes. We have proposed a diagnostic and treatment algorithm for PNES and suggested a national registry of patients suffering from this condition. The registry would contain data regarding treatment and outcomes to aid in the understanding of this entity. RÉSUMÉ: Vue d’ensemble des crises psychogènes non-épileptiques: étiologie, diagnostic et prise en charge. L’objectif de cet article est de présenter une mise à jour des activités de recherche qui concernent l’étiologie, le diagnostic et la prise en charge des crises psychogènes non-épileptiques (CPNE). Pour ce faire, nous avons mené de 2000 à août 2017 une recherche bibliographique au moyen des bases de données suivantes : PubMed, Ovid MEDLINE et Embase. -
Part Ii – Neurological Disorders
Part ii – Neurological Disorders CHAPTER 4 EPILEPSY Dr William P. Howlett 2012 Kilimanjaro Christian Medical Centre, Moshi, Kilimanjaro, Tanzania BRIC 2012 University of Bergen PO Box 7800 NO-5020 Bergen Norway NEUROLOGY IN AFRICA William Howlett Illustrations: Ellinor Moldeklev Hoff, Department of Photos and Drawings, UiB Cover: Tor Vegard Tobiassen Layout: Christian Bakke, Division of Communication, University of Bergen E JØM RKE IL T M 2 Printed by Bodoni, Bergen, Norway 4 9 1 9 6 Trykksak Copyright © 2012 William Howlett NEUROLOGY IN AFRICA is freely available to download at Bergen Open Research Archive (https://bora.uib.no) www.uib.no/cih/en/resources/neurology-in-africa ISBN 978-82-7453-085-0 Notice/Disclaimer This publication is intended to give accurate information with regard to the subject matter covered. However medical knowledge is constantly changing and information may alter. It is the responsibility of the practitioner to determine the best treatment for the patient and readers are therefore obliged to check and verify information contained within the book. This recommendation is most important with regard to drugs used, their dose, route and duration of administration, indications and contraindications and side effects. The author and the publisher waive any and all liability for damages, injury or death to persons or property incurred, directly or indirectly by this publication. CONTENTS EPILEPSY 79 EPILEPSY SYNDROMES � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � 79 CLASSIFICATION� -
Investigation of Seizures in Infants
Chapter 23 Investigation of seizures in infants RICHARD E. APPLETON1 and AILSA McLELLAN2 1The Roald Dahl EEG Unit, Paediatric Neurosciences Foundation, Alder Hey Children’s NHS Foundation Trust, Liverpool, and 2Department of Paediatric Neurosciences, Royal Hospital for Sick Children, Edinburgh The investigation of seizures in infancy (i.e. within the first year of life) begins with establishing whether the seizures are epileptic or non-epileptic in origin. The ‘broad’ differential diagnosis of possible seizures and ‘epilepsy’ is multiple and is particularly difficult under the age of 12 months and includes: Gastro-oesophageal reflux (Sandifer’s syndrome) Pallid syncopal attacks (reflex anoxic seizures) Cyanotic breath-holding attacks Cardiac arrhythmias Münchausen syndrome by proxy (passive or active both representing a form of child abuse) Shuddering spells and jitteriness Hyperekplexia Benign neonatal sleep myoclonus Benign myoclonus of infancy Tonic reflex activity and involuntary movements (seen in children with neurological impairment including cerebral palsy or hydrocephalus). Once a non-epileptic disorder has been excluded or the episodes are considered to be obviously epileptic, then the following conditions/investigations should be considered on a chronological basis. Perinatal (first week of life) and neonatal (first month of life) seizures The newborn period is the time of life with the highest risk of seizures1-3. This is because of the relative lack, and immature development of inhibitory neurotransmitters and their pathways. The immature and developing brain is susceptible to a large number of both cerebral and systemic insults including: Asphyxia (hypoxic-ischaemic encephalopathy) the most common and also most serious cause of neonatal seizures – particularly in term infants Intra- and periventricular haemorrhage – particularly in pre-term infants Metabolic dysfunction (e.g. -
Fostering Epilepsy Care in Europe All Rights Reserved
EPILEPSY IN THE WHO EUROPEAN REGION: Fostering Epilepsy Care in Europe All rights reserved. No part of this publication may be reproduced, stored in a database or retrieval system, or published, in any form or any way, electronically, mechanically, by print, photoprint, microfilm or any other means without prior written permission from the publisher. Address requests about publications of the ILAE/IBE/WHO Global Campaign Against Epilepsy: Global Campaign Secretariat SEIN P.O. Box 540 2130 AM Hoofddorp The Netherlands e-mail: [email protected] ISBN NR. 978-90-810076-3-4 Layout/ Printing: Paswerk Bedrijven, Cruquius, Netherlands Table of contents Foreword ................................................................................................................................................. 4 Preface ................................................................................................................................................. 5 Acknowledgements ........................................................................................................................................ 6 Tribute ................................................................................................................................................. 7 Abbreviations ................................................................................................................................................. 8 Background information on the European Region ......................................................................................... -
First Responders
(067UDLQLQJ (SLOHSV\DQG 6HL]XUH0DQDJHPHQW 3$57,&,3$17·6*8,'( 7KH(SLOHSV\)RXQGDWLRQOHDGVWKHÀJKWWRVWRSVHL]XUHVÀQGDFXUHDQGRYHUFRPHWKHFKDOOHQJHV created by epilepsy. 7KH(SLOHSV\)RXQGDWLRQLVWKHQDWLRQDOYROXQWDU\DJHQF\VROHO\GHGLFDWHGWRWKHZHOIDUHRIWKHQHDUO\ PLOOLRQSHRSOHZLWKHSLOHSV\LQWKH86DQGWKHLUIDPLOLHV7KHRUJDQL]DWLRQZRUNVWRHQVXUHWKDW SHRSOHZLWKVHL]XUHVDUHDEOHWRSDUWLFLSDWHLQDOOOLIHH[SHULHQFHVWRLPSURYHKRZSHRSOHZLWKHSLOHSV\ DUHSHUFHLYHGDFFHSWHGDQGYDOXHGLQVRFLHW\DQGWRSURPRWHUHVHDUFKIRUDFXUH,QDGGLWLRQWR SURJUDPVFRQGXFWHGDWWKHQDWLRQDOOHYHOHSLOHSV\FOLHQWVWKURXJKRXWWKH8QLWHG6WDWHVDUHVHUYHGE\ (SLOHSV\)RXQGDWLRQDIÀOLDWHVDURXQGWKHFRXQWU\ )RUPRUHLQIRUPDWLRQYLVLWWKH(SLOHSV\)RXQGDWLRQZHEVLWHZZZHSLOHSV\IRXQGDWLRQRUJ or call 800-332-1000. Table of Contents Introduction .....................................................................................................................1 About this Training .........................................................................................................1 What is a Seizure? ..........................................................................................................2 Typical Causes for Seizures ............................................................................3 What is Epilepsy? ...........................................................................................................4 Causes of Epilepsy ..........................................................................................4 Danger of Prolonged Seizure ..........................................................................5