Syncope and Seizures*
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Consciousness and Unconsciousness: Cross-Cultural Experience
Consciousness and Unconsciousness: Cross-Cultural Experience . In the West, consciousness was a topic of considerable interest in 19th-century philosophy and the early development of psychology. The philosopher John Locke, in his Essay Concerning Human Understanding, defined consciousness as "the perception of what passes in a man's own mind." William James in The Principles of Psychology, spoke of the "stream of consciousness," emphasizing the continuous and variable nature of mental content, thus viewing consciousness as a process. James also distinguished "normal, waking" or "rational" consciousness from other types. To study consciousness, 19th-century psychologists proceeded by means of "introspection." This method, deemed unscientific and unreliable because it produced inconsistent findings, was rejected by J. B. Watson and other American psychologists of the behaviorist school in the early 1900s. Consciousness was not a topic of psychological study in the United States for more than forty years. In the 1950s diverse factors emerged in American life and science that made consciousness again a significant area of research in psychology, neurobiology, and philosophy. These factors included the development of psychoactive drugs in psychiatry and in the counterculture; experiments in psychological warfare and brainwashing as a result of the Korean War and the Cold War; studies in cybernetics and artificial intelligence; and developments in brain and sleep research, as well as interest in Eastern religions (Yoga, Zen Buddhism and others). Intensive comparative and experimental research, some under secret governmental auspices, was carried on for some years, beginning in the 1950s. This included work with hallucinogens, particularly LSD-25, also sensory deprivation, biofeedback, sleep research, etc. -
Status Epilepticus: Pathophysiology, Epidemiology, and Outcomes
Arch Dis Child 1998;79:73–77 73 CURRENT TOPIC Arch Dis Child: first published as 10.1136/adc.79.1.73 on 1 July 1998. Downloaded from Status epilepticus: pathophysiology, epidemiology, and outcomes Rod C Scott, Robert A H Surtees, Brian G R Neville Convulsive status epilepticus (CSE) is the most consciousness being regained between the sei- common neurological medical emergency and zures. This gives the impression that status epi- continues to be associated with significant lepticus is always convulsive and is a single morbidity and mortality. Our approach to the entity. There are, however, as many types of epilepsies in childhood has been clarified by the status epilepticus as there are types of seizures, broad separation into benign and malignant and this definition is now probably outdated. syndromes. The factors that suggest a poorer To show that status epilepticus is a complex outcome in terms of seizures, cognition, and disorder, Shorvon has proposed the following behaviour include the presence of multiple sei- definition. Status epilepticus is a disorder in zure types, an additional, particularly cognitive which epileptic activity persists for 30 minutes disability, the presence of identifiable cerebral or more, causing a wide spectrum of clinical pathology, a high rate of seizures, an early age symptoms, and with a highly variable patho- of onset, poor response to antiepileptic drugs, physiological, anatomical, and aetiological and the occurrence of CSE.1 basis.2 CSE needs diVerent definitions for Convulsive status epilepticus is not a syn- diVerent purposes. Many seizures that last for drome in the same sense as febrile convulsions, five minutes will continue for at least 20 benign rolandic epilepsy, and infantile poly- minutes, and so treatment is required for most morphic epilepsy. -
Status Epilepticus: Initial Management
DATE: July 2018 TEXAS CHILDREN’S HOSPITAL EVIDENCE-BASED OUTCOMES CENTER Initial Management of Status Epilepticus Evidence-Based Guideline Definition: Status Epilepticus (SE) is a disease process Diagnostic Evaluation resulting in prolonged seizures of longer than 5 minutes. (1) The NOTE: Central nervous system (CNS) infection should be cause of SE can stem from the malfunction of the response to excluded. terminate a seizure or from the commencement of the mechanisms that result in prolonged seizures. (2) If SE History: Assess for continues for longer than 30 minutes, there can be permanent Seizure onset neurological damage, including neuronal death, neuronal Known seizure disorder injury, and alteration of neuronal networks. (2,3) Ingestion Fever (e.g., signs of serious infection) Epidemiology: Convulsive status epilepticus (CSE) is the Medications (4) most common neurological emergency seen in childhood. It o Received prior to presentation (e.g., type, dose, is also among the top five reasons for admission to the PICU at dosage, route) Texas Children’s Hospital and is the third most common o Current anticonvulsant medications reason for transport calls. SE is a medical emergency and is o Use of psychopharmacologic medications associated with an overall mortality rate of 8% in children and Toxic/Subtherapeutic anticonvulsant levels (4,5) o 30% in adults. Among children, the overall incidence of SE Nonadherence and/or recent change (4-6) o is approximately 1 to 6 per 10,000/year. The incidence Vagus Nerve Stimulation (VNS) appears to be higher in children under 1 year of age with over Metabolic abnormalities 50% of cases occurring in children under 3 years. -
Is It a Convulsion Or Dopamine Deficiency? a Case of Epilepsy in Dihydropteridine Reductase Deficiency
Letter to the editor pISSN 2635-909X • eISSN 2635-9103 Ann Child Neurol 2020;28(2):72-74 https://doi.org/10.26815/acn.2019.00304 Is It a Convulsion or Dopamine Deficiency? A Case of Epilepsy in Dihydropteridine Reductase Deficiency Jisu Ryoo, MD, Eun Sook Suh, MD, Jeongho Lee, MD Department of Pediatrics, Soonchunhyang University Seoul Hospital, Soonchunhyang University College of Medicine, Seoul, Korea Received: December 20, 2019 Dihydropteridine reductase (DHPR) deficiency A 15-year-old man was admitted to Soon- Revised: February 13, 2020 Accepted: March 2, 2020 is a severe form of hyperphenylalaninemia due chunhyang University Seoul Hospital. At the age to impaired renewal of a substance known as tet- of 3 months, he experienced the first seizure, Corresponding author: rahydrobiopterin (BH4), caused by mutations in characterized by brief psychomotor arrest and Jeongho Lee, MD the quinoid dihydropteridine reductase (QDPR) right hand tremor. He had no family history of Department of Pediatrics, gene [1]. If little or no BH4 is available to facili- seizures or genetic disorders. Brain magnetic res- Soonchunhyang University Seoul tate processing phenylalanine (Phe), this amino onance imaging (MRI) and EEG showed nor- Hospital, Soonchunhyang University College of Medicine, 59 acid can accumulate in the blood and other tis- mal results. The seizures were not controlled by Daesagwan- ro, Yongsan-gu, Seoul sues, and the levels of neurotransmitters (dopa- antiepileptic drugs, including topiramate, val- 04401, Korea mine, serotonin) and the folate in cerebrospinal proate, and lamotrigine; therefore, he discontin- Tel: +82-2-709-9341 fluid also decrease [1]. Symptoms such as mental ued the medication. -
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. -
Supplementary Table Term* Revised Term** Focal Seizure Without Impairment of a Subjective Sensory Or Psychic Experience As Part of Migraine Or Epilepsy
Supplementary table Term* Revised term** Focal seizure without impairment of A subjective sensory or psychic experience as part of migraine or epilepsy. In epilepsy it is a focal consciousness or awareness Aura seizure without loss of consciousness (a simple partial seizure). It may or may not be followed by involving subjective sensory or other seizure manifestations. psychic phenomena only Automatic behaviour associated with loss of awareness, such as lip smacking or hand wringing, Automatism Focal dyscognitive seizure occurring as part of a complex partial seizure. Convulsion (previously "grand Tonic-clonic seziure, convulsive Seizure with involuntary, irregular myoclonic, clonic or tonic–clonic movements of one or more mal") seizure limbs. Onset may be focal or primary generalised. Literally ‘already seen’, this refers to a false impression that a present experience is familiar. It is used to refer to something heard, experienced or seen. It can be the aura of a temporal lobe Déjà vu seizure, but also happens in other settings (normal experience, intoxication, migraine, psychiatric). Focal seizure (previously "partial, Focal seizure A seizure originating in a specific cortical location. May be due to a structural lesion. localization related") Literally a ‘blow’. Usually used for an epileptic seizure (but can refer to other paroxysmal events, Ictus such as migraine, transient neurological events and stroke). Similarly pre- and post-ictal are used may for the period before and after a seizure. Idiopathic Genetic In relation to epilepsy, this implies that there is an underlying genetic cause. Literally ‘never seen’, this refers to a false impression that a present experience is unfamiliar. It is Jamais vu used for something seen, heard or experienced. -
What Makes a Simple Partial Seizure Complex.Pdf
Epilepsy & Behavior 22 (2011) 651–658 Contents lists available at SciVerse ScienceDirect Epilepsy & Behavior journal homepage: www.elsevier.com/locate/yebeh Review What makes a simple partial seizure complex? Andrea E. Cavanna a,b,⁎, Hugh Rickards a, Fizzah Ali a a The Michael Trimble Neuropsychiatry Research Group, Department of Neuropsychiatry, University of Birmingham and BSMHFT, Birmingham, UK b National Hospital for Neurology and Neurosurgery, Institute of Neurology, and UCL, London, UK article info abstract Article history: The assessment of ictal consciousness has been the landmark criterion for the differentiation between simple Received 26 September 2011 and complex partial seizures over the last three decades. After review of the historical development of the Accepted 2 October 2011 concept of “complex partial seizure,” the difficulties surrounding the simple versus complex dichotomy are Available online 13 November 2011 addressed from theoretical, phenomenological, and neurophysiological standpoints. With respect to con- sciousness, careful analysis of ictal semiology shows that both the general level of vigilance and the specific Keywords: contents of the conscious state can be selectively involved during partial seizures. Moreover, recent neuroim- Epilepsy fi Complex partial seizures aging ndings, coupled with classic electrophysiological studies, suggest that the neural substrate of ictal Consciousness alterations of consciousness is twofold: focal hyperactivity in the limbic structures generates the complex Experiential phenomena psychic phenomena responsible for the altered contents of consciousness, and secondary disruption of the Limbic system network involving the thalamus and the frontoparietal association cortices affects the level of awareness. These data, along with the localization information they provide, should be taken into account in the formu- lation of new criteria for the classification of seizures with focal onset. -
DIAGNOSIS and TREATMENT of the NARCOLEPSY SYNDROME Analysis of Seventy-Five Case Records
DIAGNOSIS AND TREATMENT OF THE NARCOLEPSY SYNDROME Analysis of Seventy-Five Case Records GERALD BOWLING, M.D.,* Department of Internal Medicine and NELSON G. RICHARDS, M.D. Department of Neurology HE narcolepsy syndrome is known also as Gelineau's disease, the Gelineau- Redlich syndrome, paroxysmal sleep, and sleep epilepsy. Because of the compara- tive rarity of the disease and our lack of understanding of the term narcolepsy, we recently had difficulty in diagnosing several cases of the syndrome. This report undertakes to clarify the meaning of the term, to discuss the entity, and to report an analysis of 75 case records of narcoleptics treated at the Cleveland Clinic in the last nine years. In the past it has been alleged that the sleep of the narcoleptic is paroxysmal in onset.1 Hypersomnolence has frequently been used to describe the condition in which the patient is persistently drowsy without having actual sleeping spells, or in which he falls asleep perhaps only once a day while engaged in some activity. Yoss and Daly2 recently defined narcolepsy as consisting of four components: (1) narcolepsy proper — "excessive and persistent sleepiness"; (2) cataplexy — muscular weak- ness induced by emotion; (3) sleep paralysis — transient, benign loss of muscle tone at the beginning or end of sleep; (4) hypnagogic hallucinations — usually vivid auditory or visual hallucinations or illusions occurring during day or night drowsiness, usually with sleep paralysis. We are essentially in agreement with their definition. In our 75 patients, excessive and persistent sleepiness occurred alone or in combination with other symptoms. Figure 1 illustrates the incidence of the four components of the narcolepsy syndrome in our patients. -
The Neural Basis of the Dynamic Unconscious
Neuropsychoanalysis, 2011, 13 (1) 5 The Neural Basis of the Dynamic Unconscious Heather A. Berlin (New York) A great deal of complex cognitive processing occurs at the unconscious level and affects how humans behave, think, and feel. Sci- entists are only now beginning to understand how this occurs on the neural level. Understanding the neural basis of consciousness requires an account of the neural mechanisms that underlie both conscious and unconscious thought, and their dynamic interac- tion. For example, how do conscious impulses, thoughts, or desires become unconscious (e.g., repression) or, conversely, how do unconscious impulses, desires, or motives become conscious (e.g., Freudian slips)? Research taking advantage of advances in technologies, like functional magnetic resonance imaging, has led to a revival and re-conceptualization of some of the key concepts of psychoanalytic theory, but steps toward understanding their neural basis have only just commenced. According to psychoanalytic theory, unconscious dynamic processes defensively remove anxiety-provoking thoughts and impulses from consciousness in re- sponse to one’s conflicting attitudes. The processes that keep unwanted thoughts from entering consciousness include repression, suppression, and dissociation. In this literature review, studies from psychology and cognitive neuroscience in both healthy and patient populations that are beginning to elucidate the neural basis of these phenomena are discussed and organized within a con- ceptual framework. Further studies in this emerging field at the intersection of psychoanalytic theory and neuroscience are needed. Keywords: unconscious; psychodynamic; repression; suppression; dissociation; neural “Nothing is so difficult as not deceiving oneself.” 1998a). Early psychodynamic theorists attempted to Ludwig Wittgenstein [1889–1951] explain phenomena observed in the clinic, but lat- er cognitive scientists used computational models of the mind to explain empirical data. -
Epilepsy & My Child Toolkit
Epilepsy & My Child Toolkit A Resource for Parents with a Newly Diagnosed Child 136EMC Epilepsy & My Child Toolkit A Resource for Parents with a Newly Diagnosed Child “Obstacles are the things we see when we take our eyes off our goals.” -Zig Ziglar EPILEPSY & MY CHILD TOOLKIT • TABLE OF CONTENTS Introduction Purpose .............................................................................................................................................5 How to Use This Toolkit ....................................................................................................................5 About Epilepsy What is Epilepsy? ..............................................................................................................................7 What is a Seizure? .............................................................................................................................8 Myths & Facts ...................................................................................................................................8 How is Epilepsy Diagnosed? ............................................................................................................9 How is Epilepsy Treated? ..................................................................................................................10 Managing Epilepsy How Can You Help Manage Your Child’s Care? ...............................................................................13 What Should You Do if Your Child has a Seizure? ............................................................................14 -
Clinical Decision Making in Seizures and Status Epilepticus
January 2015 Clinical Decision Making Volume 17, Number 1 Authors In Seizures And Felipe Teran, MD Department of Emergency Medicine, Icahn School of Medicine at Mount Sinai, New York, NY; Faculty, Emergency Department, Clínica Status Epilepticus Alemana, Santiago, Chile Katrina Harper-Kirksey, MD Abstract Anesthesia Critical Care Fellow, Department of Anesthesia, Stanford Hospital and Clinics, Stanford, CA Andy Jagoda, MD, FACEP Seizures and status epilepticus are frequent neurologic emergen- Professor and Chair, Department of Emergency Medicine, Icahn cies in the emergency department, accounting for 1% of all emer- School of Medicine at Mount Sinai, New York, NY; Medical Director, Mount Sinai Hospital, New York, NY gency department visits. The management of this time-sensitive and potentially life-threatening condition is challenging for both Peer Reviewers prehospital providers and emergency clinicians. The approach to J. Stephen Huff, MD Professor of Emergency Medicine and Neurology, University of seizing patients begins with differentiating seizure activity from Virginia, Charlottesville, VA mimics and follows with identifying potential secondary etiolo- Jason McMullan, MD gies, such as alcohol-related seizures. The approach to the patient Assistant Professor, Department of Emergency Medicine, University of in status epilepticus and the patient with nonconvulsive status Cincinnati, Cincinnati, OH epilepticus constitutes a special clinical challenge. This review CME Objectives summarizes the best available evidence and recommendations Upon completion of this article, you should be able to: regarding diagnosis and resuscitation of the seizing patient in the 1. Describe the diagnostic approach to patients who have recovered from a seizure and patients in status epilepticus. emergency setting. 2. Recognize and treat patients with alcohol withdrawal seizures. -
Electroencephalogram Abnormality and High-Dose Busulfan in Conditioning Regimens for Stem Cell Transplantation
Bone Marrow Transplantation, (1998) 21, 217–220 1998 Stockton Press All rights reserved 0268–3369/98 $12.00 Electroencephalogram abnormality and high-dose busulfan in conditioning regimens for stem cell transplantation R Kobayashi, N Watanabe, A Iguchi, Y Cho, M Yoshida, H Arioka, H Naito, T Shikano and Y Ishikawa Department of Pediatrics, Hokkaido University School of Medicine, Sapporo, Japan Summary: Patients and methods High-dose busulfan (BU) is widely used in combined Between June 1989 and November 1996, a total of 22 chemotherapy before allogeneic or autologous bone patients with various hematological malignancies or marrow transplantation. Convulsions are reported as a immunodeficiencies received allogeneic BMT (14 cases) or side-effect of high-dose BU. We recorded electroence- autologous peripheral blood stem cell transplants (eight phalograms (EEGs) before and on the third day of BU cases) after preparation with high-dose BU (Table 1). Thir- administration in 22 patients. Abnormal EEGs were teen patients had acute lymphoblastic leukemia (ALL): observed on the third day in 13 cases (59%). These eight were in first complete remission (CR) and five were patients were older (P , 0.05) and had had larger doses in second CR. Five patients had acute non-lymphoblastic of BU (P , 0.025) than the nine patients with normal leukemia (ANLL): three were in first CR and two were EEGs. Convulsions occurred in two of the 22 patients, in second CR. Five patients had other diseases: two non- one of whom was receiving prophylaxis with phenytoin. Hodgkin’s lymphoma (NHL), one Wiskott Aldrich syn- Gamma aminobutyric acid (GABA), a natural mediator drome (WAS), and one chronic myelogenous leukemia of defense against epileptic activity, concentrations in (CML).