January 26, Montgomery County Regional Outpatient Center Dietary Therapies Program (Main Hospital) Comprehensive Pediatric Epilepsy Program

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First time Seizure and New onset Epilepsy Stirred not shaken January 26, 2017 First time Seizure and New onset Epilepsy Amy Kao, MD Children s National Health System Center for Neuroscience and Behavioral Medicine Division of Neurophysiology and Epilepsy akao@childrensnational.org Montgomery County Regional Outpatient Center Dietary Therapies Program (Main Hospital) Comprehensive Pediatric Epilepsy Program No disclosures (editor for Medscape Child Neurology section)

New onset Seizure: Objectives Discuss general approach to evaluation and treatment of new onset seizure Review terminology in seizures/epilepsy Understand classification of seizures and epilepsy by onset, etiology, syndrome Discuss management approach, process, and resources at Children s National Health System Definitions A seizure Sudden, transient signs/symptoms due to abnormal excessive or hypersynchronous electrical discharges of neurons (the event) Epilepsy Enduring predisposition to generate epileptic seizures (the tendency for recurrence) At least 2 unprovoked seizures > 24 hours apart Consistent with particular epilepsy syndrome One seizure and 60% risk of recurrence within 10 years

Definitions Status epilepticus Seizure lasting 30 minutes OR A series of seizures lasting 30 minutes without full consciousness regained between OR Seizure >5 minutes (practical definition) Medically refractory epilepsy Seizures unresponsive to 2 or 3 antiseizure medications Impact of Seizures/Epilepsy Risk of having a seizure by age 20: > 4% Risk of epilepsy by age 20: > 1% Risk of epilepsy by age 74: 3% Peak occurrence in childhood and over 65 Approx 1/3 epilepsy patients do not respond to 2 or 3 antiseizure medications (Kwan P, Brodie M 2000) 47% seizure free on 1 st AED 14% seizure free on 2 nd or 3 rd AED 3% seizure free on 2 drugs

Classification of Seizures by Onset Generalized onset GTC Absence Myoclonic Tonic Atonic Partial/Focal Onset Simple partial Complex partial Secondarily generalized Seizure Semiology (Focal Seizures) Temporal lobe abdominal aura, psychic aura, olfactory aura, distal motor or oral automatisms, post ictal nose wipe (ipsilateral) Frontal lobe nocturnal, shorter than temporal, tonic (fencing supplementary sensorimotor cortex contralat to extended arm), versive (forced turning), hypermotor (orbital/mesial, but also temp, insular) Occipital visual hallucinations (Brodmann 17/18), emesis, autonomic Parietal focal tingling/numbness (sensory cortex) Insular gustatory aura, autonomic Gelastic hypothalamic hamartoma

Classification of Seizures by Syndromes Cluster of symptoms, signs, EEG findings, which is consistent, implies diagnosis, treatment, prognosis Epileptic encephalopathies ( catastrophic ) vs. Self limited/pharmacoresponsive ( benign, idiopathic/genetic ) Infantile spasms Childhood absence Lennox Gastaut syndrome Benign rolandic Genetic eg Dravet syndrome Juvenile myoclonic Structural eg TS, diffuse migrational disorders First Question Was it a Seizure? Loss of tone or consciousness Abnormal heart rhythm Vasovagal syncope Attention deficit disorder Disorders of breathing Breathholding spells Hyperventilation Other medical conditions Hypoglycemia Gastroesophageal reflux

More in Differential Diagnosis Movements Benign sleep myoclonus Dystonia/poor motor control or hyperreflexia Tics Nonepileptic seizures ( Pseudoseizures ) Sleep disorder (parasomnias) Night terrors Sleep walking Behavioral or Self stimulation Evaluation of First Seizure History Is it a seizure? What type? Cause? Exam Remote or acute symptomatic cause? Bloodwork infection, electrolytes Lumbar puncture? Head CT vs brain MRI Hsieh DT et al 2010 (prospective, 0 24 months) 57% brain MRIs abnl (16% of all MRIs had dysgenesis, more in 1 6 mos) 35% head CTs abnormal (9% of all CTs required acute mgmt) Singh RK et al 2010 (prospective, status epilepticus) Acute symptomatic=cns infection; Remote symptomatic=dysgenesis CT acute vascular lesions and acute edema MRI subtle abnormalities, dysplasia, MTS (remote) EEG postictal vs 2 weeks after

First Unprovoked Seizure Predict recurrence risk Idiopathic/cryptogenic: 30 to 50% by 2 years EEG for prognosis and findings of epilepsy syndrome if abnormal, ~50% recurrence risk Remote symptomatic: >50% If focal onset, abnormal exam, abnormal development, focal EEG abnormality MRI Not different if status epilepticus Seizure remission no different if AED initiated after 1 st or 2 nd seizure Treatment after First Seizure Reassurance Safety No unsupervised baths or swimming alone Biking with helmet, and on sidewalk Baby monitor Discuss SUDEP Counseling Appearance of seizures (e.g. complex partial) First aid during seizure Rescue med if prolonged seizure

Drugs which may lower seizure threshold http://www.epilepsy.com/information/professionals/resourcelibrary/tables/drugs may lower seizure threshold Antihistamines (diphenhydramine) Stimulants (more theoretical than in reality) Pseudoephedrine Bupropion Meperidine New Onset Seizure: Take Home Points Goals of the approach to new onset seizure Rule out/address acute symptomatic cause (especially infants) Determine likelihood of recurrence (i.e. epilepsy) Features consistent with an epilepsy syndrome? EEG findings MRI abnormalities Provide education Safety precautions Management of future seizures ( seizure first aid ) Seizure action plan for school RE: the child s risk of epilepsy

New Onset Seizure: Take Home Points Initiate process as inpatient or outpatient? parental anxiety education can be provided in ED or PCP office? access to scheduling systems ease of follow up (proximity, socioeconomic factors) Systems at Children s National Update your info if not receiving notification of admissions Phone call after discharge (Epilepsy NP) Follow up visit with Neurology within 6 weeks of discharge MRI high resolution with thin slices (nonurgent, sedation/anesthesia if needed) Helpful References www.epilepsy.com (Epilepsy Foundation of America) www.health.nih.gov www.talkaboutit.org

Outpatient Contact Numbers Current access approx 3 days 1 888 884 BEAR (2327) May need to drive for soonest appointment (but parking easier than at hospital) ROC appointment lines Children s National Health System: 202 476 3611 Montgomery County Regional Outpatient Center (Rockville): 301 765 5400 Laurel Regional Outpatient Center: 240 568 7000 Frederick Regional Outpatient Center: 301 682 6661 Annapolis Regional Outpatient Center: 410 266 6582 Urgent headache/concussion appointments 202 476 HEAD akao@childrensnational.org

Register Now for the 27 th Annual Pediatric Neurology Update Movement Disorders Wednesday, April 19, 2017 7:45 am 5 pm This year s course will be focused on the new understandings, molecular biology, and novel treatments of childhood movement disorders ranging from Tourette s syndrome to incapacitating neuro genetic and auto immune conditions. We invite you to join us for presentations from renowned experts in the field in this full day, CME accredited event. Learn more and register now at ChildrensNational.org/NeurologyUpdate.