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      International veterinary epilepsy task force consensus proposal: diagnostic approach to epilepsy in dogs

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          Abstract

          This article outlines the consensus proposal on diagnosis of epilepsy in dogs by the International Veterinary Epilepsy Task Force. The aim of this consensus proposal is to improve consistency in the diagnosis of epilepsy in the clinical and research settings. The diagnostic approach to the patient presenting with a history of suspected epileptic seizures incorporates two fundamental steps: to establish if the events the animal is demonstrating truly represent epileptic seizures and if so, to identify their underlying cause. Differentiation of epileptic seizures from other non-epileptic episodic paroxysmal events can be challenging. Criteria that can be used to make this differentiation are presented in detail and discussed. Criteria for the diagnosis of idiopathic epilepsy (IE) are described in a three-tier system. Tier I confidence level for the diagnosis of IE is based on a history of two or more unprovoked epileptic seizures occurring at least 24 h apart, age at epileptic seizure onset of between six months and six years, unremarkable inter-ictal physical and neurological examination, and no significant abnormalities on minimum data base blood tests and urinalysis. Tier II confidence level for the diagnosis of IE is based on the factors listed in tier I and unremarkable fasting and post-prandial bile acids, magnetic resonance imaging (MRI) of the brain (based on an epilepsy-specific brain MRI protocol) and cerebrospinal fluid (CSF) analysis. Tier III confidence level for the diagnosis of IE is based on the factors listed in tier I and II and identification of electroencephalographic abnormalities characteristic for seizure disorders. The authors recommend performing MRI of the brain and routine CSF analysis, after exclusion of reactive seizures, in dogs with age at epileptic seizure onset <6 months or >6 years, inter-ictal neurological abnormalities consistent with intracranial neurolocalisation, status epilepticus or cluster seizure at epileptic seizure onset, or a previous presumptive diagnosis of IE and drug-resistance with a single antiepileptic drug titrated to the highest tolerable dose.

          This consensus article represents the basis for a more standardised diagnostic approach to the seizure patient. These recommendations will evolve over time with advances in neuroimaging, electroencephalography, and molecular genetics of canine epilepsy.

          Electronic supplementary material

          The online version of this article (doi:10.1186/s12917-015-0462-1) contains supplementary material, which is available to authorized users.

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          Most cited references36

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          Uncovering the neurobehavioural comorbidities of epilepsy over the lifespan.

          Epilepsy is a common neurological disorder that is complicated by psychiatric, cognitive, and social comorbidities that have become a major target of concern and investigation in view of their adverse effect on the course and quality of life. In this report we define the specific psychiatric, cognitive, and social comorbidities of paediatric and adult epilepsy, their epidemiology, and real life effects; examine the relation between epilepsy syndromes and the risk of neurobehavioural comorbidities; address the lifespan effect of epilepsy on brain neurodevelopment and brain ageing and the risk of neurobehavioural comorbidities; consider the overarching effect of broader brain disorders on both epilepsy and neurobehavioural comorbidities; examine directions of causality and the contribution of selected epilepsy-related characteristics; and outline clinic-friendly screening approaches for these problems and recommended pharmacological, behavioural, and educational interventions. Copyright © 2012 Elsevier Ltd. All rights reserved.
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            Paroxysmal dyskinesias revisited: a review of 500 genetically proven cases and a new classification.

            Paroxysmal movement disorders are a heterogeneous group of conditions manifesting as episodic dyskinesia with sudden onset and lasting a variable duration. Based on the difference of precipitating factors, three forms are clearly recognized, namely, paroxysmal kinesigenic (PKD), non-kinesigenic (PNKD), and exercise induced (PED). The elucidation of the genetic cause of various forms of paroxysmal dyskinesia has led to better clinical definitions based on genotype-phenotype correlations in the familial forms. However, it has been increasingly recognized that (1) there is a marked pleiotropy of mutations in such genes with still expanding clinical spectra; and (2) not all patients clinically presenting with either PKD, PNKD, or PED have mutations in these genes. We aimed to review the clinical features of 500 genetically proven cases published to date. Based on our results, it is clear that there is not a complete phenotypic-genotypic correlation, and therefore we suggest an algorithm to lead the genetic analyses. Given the fact that the reliability of current clinical categorization is not entirely valid, we further propose a novel classification for paroxysmal dyskinesias, which takes into account the recent genetic discoveries in this field.
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              Behavioral changes in dogs associated with the development of idiopathic epilepsy.

              The aim of the study was to demonstrate behavioral changes with the development of epilepsy in dogs, a species proposed as a naturally occurring animal model for human epilepsy. Owners of dogs diagnosed with idiopathic epilepsy (n=80) completed a modified, previously-validated behavioral and seizure questionnaire. Principal axis factor analysis identified behavioral factors, the scores for which were compared before and after the development of epilepsy. Drug-naïve dogs showed an increase in the behavior factors Fear/Anxiety, Defensive Aggression, and Abnormal Perception. In dogs receiving antiepileptic medication, there were still increases in Fear/Anxiety and Abnormal Perception, but no longer in Defensive Aggression. Additional increases were observed in Abnormal Reactivity, Attachment Disorder, Demented Behavior, and Apathetic Behavior. Pharmacoresistant dogs had larger increases in Controlling Aggression, Abnormal Perception, and Demented Behavior than drug responders. Our data suggest that dogs, like humans and rodents, exhibit neurobehavioral comorbidities with the development of epilepsy. Copyright © 2011 Elsevier Inc. All rights reserved.
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                Author and article information

                Contributors
                luisa.derisio@aht.org.uk
                sofie.bhatti@ugent.be
                krmunana@ncsu.edu
                jacques.penderis@vet-neurology.co.uk
                Veronika.Stein@tiho-hannover.de
                Andrea.Tipold@tiho-hannover.de
                mbe@sund.ku.dk
                robyn.fernside@googlemail.com
                andreafischer@lmu.de
                snlong@unimelb.edu.au
                P.J.J.Mandigers@uu.nl
                matiasek@patho.vetmed.uni-muenchen.de
                rpacker@rvc.ac.uk
                akos.pakozdy@vetmeduni.ac.at
                patte037@umn.edu
                srplatt@uga.edu
                mpodell@comcast.net
                potschka@pharmtox.vetmed.uni-muenchen.de
                marti.pumarola@uab.cat
                ClareR@fitzpatrickreferrals.co.uk
                hvolk@rvc.ac.uk
                Journal
                BMC Vet Res
                BMC Vet. Res
                BMC Veterinary Research
                BioMed Central (London )
                1746-6148
                28 August 2015
                28 August 2015
                2015
                : 11
                : 148
                Affiliations
                [ ]Animal Health Trust, Lanwades Park, Kentford, Newmarket, CB8 7UU Suffolk, UK
                [ ]Department of Small Animal Medicine and Clinical Biology, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, Merelbeke, 9820 Belgium
                [ ]Department of Clinical Sciences, College of Veterinary Medicine, North Carolina State University, 1052 William Moore Drive, Raleigh, NC 27607 USA
                [ ]Vet Extra Neurology, Broadleys Veterinary Hospital, Craig Leith Road, Stirling, FK7 7LE Stirlingshire UK
                [ ]Department of Small Animal Medicine and Surgery, University of Veterinary Medicine Hannover, Bünteweg 9, 30559 Hannover, Germany
                [ ]Department of Veterinary and Clinical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Frederiksberg C, Denmark
                [ ]Fernside Veterinary Centre, 205 Shenley Road, Borehamwood, SG9 0TH Hertfordshire UK
                [ ]Centre for Clinical Veterinary Medicine, Ludwig-Maximilians-University, Veterinärstr. 13, 80539 Munich, Germany
                [ ]University of Melbourne, 250 Princes Highway, Weibee, 3015 VIC Australia
                [ ]Department of Clinical Sciences of Companion Animals, Utrecht University, Yalelaan 108, 3583 CM Utrecht, The Netherlands
                [ ]Section of Clinical & Comparative Neuropathology, Centre for Clinical Veterinary Medicine, Ludwig-Maximilians-University, Veterinärstr. 13, 80539 Munich, Germany
                [ ]Department of Clinical Science and Services, Royal Veterinary College, Hatfield, AL9 7TA Hertfordshire UK
                [ ]Clinical Unit of Internal Medicine Small Animals, University of Veterinary Medicine, Veterinärplatz 1, 1210 Vienna, Austria
                [ ]University of Minnesota College of Veterinary Medicine, D426 Veterinary Medical Center, 1352 Boyd Avenue, St. Paul, MN 55108 USA
                [ ]College of Veterinary Medicine, University of Georgia, 501 DW Brooks Drive, Athens, GA 30602 USA
                [ ]Chicago Veterinary Neurology and Neurosurgery, 3123 N. Clybourn Avenue, Chicago, IL 60618 USA
                [ ]Department of Pharmacology, Toxicology and Pharmacy, Ludwig-Maximillians-University, Königinstr. 16, 80539 Munich, Germany
                [ ]Department of Animal Medicine and Surgery, Veterinary Faculty, Universitat Autònoma de Barcelona, Campus UAB, Bellaterra, 08193 Barcelona, Spain
                [ ]Fitzpatrick Referrals, Halfway Lane, Eashing, Godalming, GU7 2QQ Surrey UK
                [ ]School of Veterinary Medicine, Faculty of Health & Medical Sciences, University of Surrey, Guildford, GU2 7TE Surrey UK
                Article
                462
                10.1186/s12917-015-0462-1
                4552251
                26316175
                bcfe5489-8395-4cc1-ac33-87a6a6698af7
                © De Risio et al. 2015

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 4 June 2015
                : 29 June 2015
                Categories
                Correspondence
                Custom metadata
                © The Author(s) 2015

                Veterinary medicine
                dog,seizure,epilepsy,idiopathic epilepsy,diagnosis
                Veterinary medicine
                dog, seizure, epilepsy, idiopathic epilepsy, diagnosis

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