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Fits, Faints and Funny Turns Anne Grover CN1 Neurology Objectives To appreciate the wide range of disorders that present with ‘clinical events’ To discuss epileptic ‘lookalikes’ To outline history taking Seizures Are characterized by a sudden change in movement, behaviour, sensation or consciousness produced by a sudden burst of excessive electrical activity in brain cells causing a chemical (neurotransmitter) imbalance. Causes of seizures Brain infection Brain Tumour Fever Heart disease High BP Medications Seizures Drug/ alcohol abuse Stroke Metabolic/ endocrine Head injury Epilepsy Epilepsy – refers to a group of different neurological conditions characterised by recurrent, unprovoked epileptic seizures A manifestation(s) of epileptic excessive usually self-limiting activity of neurons in the brain Epilepsy Affects 1 in 115 people Prevalence in Ireland <42 000 people with epilepsy Approximately 50 million worldwide One of the most common serious chronic neurological conditions 1. Joint Epilepsy Council. Epilepsy prevalence, incidence and other statistics. 2011; 2. Brainwave 2009 SEIZURE CLASSIFICATION INTERNATIONAL LEAGUE AGAINST EPILEPSY (ILAE) 2010 Focal Generalised Focal discharges Some loss of awareness Discharges coming from both hemispheres Complete loss of consciousness Tonic clonic Convulsion Absence ‘Blank spell’ ‘Aura’ Motor/sensory Change in awareness and behaviour Secondary generalised Usually tonic clonic convulsion Myoclonic jerk Twitch/jerk Atonic Drop attack Tonic Stiffness Copyright © 123Rf Ltd. or their partners. Images may not be copied or downloaded without permission from 123RF Limited IE/BUC/12/0304 Electroclinical syndromes Defined as an ‘electroclinical’ pattern of clinical features and investigation findings may have different aetiologies. Common electroclinical syndromes eg- Childhood absence epilepsy - Juvenile absence epilepsy - Juvenile myoclonic epilepsy - Lennox Gastaut Generalised Tonic Clonic Seizure Prodromes – non-epileptic clinical alteration prior to onset of an epileptic seizure Aura – “warning sign” – epileptic seizure experienced prior to GTCS Initial tonic phase -Epileptic cry, eyes open, roll upwards, jaw clamps shut Limbs stiff & extended, arms may flex, cyanosis Clonic Phase Rhythmic jerking of all 4 limbs, jaw & facial muscles May froth at the mouth, bite tongue, urinary incontinence Jerking gradually slows before stopping Itcal phase Followed by flaccidity of muscles Consciousness slowly regained, may lapse into deep sleep minutes to hours after GTCS generally self-limiting, last 1-2 minutes ACTION A Assess the situation, ABC’s. Get assistance. Remove any object that could cause harm C Cushion patient’s head to protect from injury T Time, note the time the seizure started I Identify possible cause O Over, put patient into recovery position when possible, note what happened, time seizure ended. N Never restrain the patient, or put anything into their mouth. Provoking factors Illness or fever Sleep deprivation Missing doses AED’s Alcohol Stress Prolonged acute epileptic seizures Definition of status epilepticus: A seizure lasting >5 minutes, or Two or more seizures without a return of consciousness between seizures1 Immediate treatment is recommended for: Prolonged seizures ≥5 minutes, or Repeated convulsive seizures (≥3 in an hour)2 Treatment delay lessens the chance of successful response to a single medication3 Women’s issues Menstrual cycle Fertility Contraception Pregnancy Lifestyle implications • • • • • • • Social issues Driving Working Personal safety Good nutrition, special diets Memory problems Mood changes Seizure imitators Syncope Psychogenic non-epileptic seizures (PNES) Transient ischaemic attack Narcolepsy/cataplexy/sleep apnea Sleep-walking, night terrors Panic attack Complex migraines. Cardiac arrhythmias. Syncope LOC & postural tone Brief stiffening or spasms & irregular jerks of the limbs Eyes open, roll upwards Urinary incontinence & trauma Generally less than 10 seconds Convulsive syncope - 70-90% Psychogenic non-epileptic seizures Appear to lose consciousness & fall Eyes closed Often lack stereotypical characteristics Jerking may be asymmetric, asynchronous, wax and wane Pelvic thrust, flailing & tremors Vocalise throughout Consciousness may be retained Diagnosis History History History History Obtain a detailed account of the event from the patient and a witness Where, when, what happened? Any warning sign? Any triggers? First event? Other events? Progression- How did it start? After the event? Useful features Conclusion Epilepsy is one of the most serious, chronic neurological conditions Can be difficult to distinguish between imitators 20-30% of patients misdiagnosed A detailed history can assist with diagnosis References Brainwave The Irish Epilepsy Association. Shedding Light on Epilepsy. A nurses information pack. Epilepsy Ireland. (2009).The prevalence of Epilepsy in Ireland Study. www.epilepsy.ie Murphy, S., Epilepsy-definitions, diagnosis and treatment. Nursing in General Practice. Nizam, S., Spencer, S.S. (2004). An approach to the evaluation of a patient for seizures and epilepsy. Wisconsin Medical Journal. 103:1. British Paediatric Neurology Association. (2013). Paediatric Epilepsy Training Level One Handbook. United Kingdom. Thank you