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From the trenches: A clinician’s perspective

From the trenches: A clinician’s perspective. Gogi Kumar,MD Assistant Professor WSUBSOM Medical Director Department of Child Neurology Dayton Children’s Hospital. My Trench. General Cope’s Trench. Case. 13 year old with first unprovoked seizure

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From the trenches: A clinician’s perspective

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  1. From the trenches: A clinician’s perspective GogiKumar,MD Assistant Professor WSUBSOM Medical Director Department of Child Neurology Dayton Children’s Hospital

  2. My Trench

  3. General Cope’s Trench

  4. Case • 13 year old with first unprovoked seizure • Mom hears a thud in the morning , finds her in the shower having a generalized tonic- clonic seizure • Seizure lasts for 2 minutes • Sleep deprived

  5. CT scan, urine pregnancy and drug screen is negative • EEG:

  6. I diagnose her with new onset primary generalized epilepsy • Suggest starting on Lamictal

  7. First Question What is Epilepsy?

  8. Definition of Epilepsy • 2005 ILAE definition: 2 unprovoked seizures >24 hours apart • Epilepsy is a disorder of the brain characterized by an enduring predisposition to generate epileptic seizures

  9. A practical clinical definition of epilepsyFisher et al Epilepsia,55(4):475-482,2014ILAE Task force Epilepsy is a disease of the brain defined by any one of the following: 1.Atleast 2 unprovoked (reflex seizures) occurring >24 hour apart 2.One unprovoked seizure(or reflex)seizure and a probability of further seizures similar to the general recurrence rate (at least 60%) after two unprovoked seizures occurring over the next 10 years 3.Diagnosis of an epilepsy syndrome

  10. 2nd Question • Can you do any other test to be sure? • Blood test? MRI? • Does epilepsy get better? • How will I know when epilepsy has resolved?

  11. Epilepsy BiomarkersEngel et al Epilepsia 2013 August;54(04)61-69 Biomarker is an objectively measured characteristic of a normal or pathological process. Uses in epilepsy include • Predict the development of epilepsy • Confirm the presence of epilepsy • Measure progression • Predict pharmaco-resistance • Confirm that the condition is resolved • Used to create animal models • Reduce the cost of the clinical trial

  12. Epilepsy Biomarkers Engel et al Epilepsia 2013 August;54(04)61-69

  13. 3rd Question • What kind of epilepsy does my child have? • I was reading about seizures while waiting for you to come and see us and read about focal and generalized seizures. Can you tell me more about this?

  14. The Organization of the Epilepsies: Report of the ILAE Commission on Classification and Terminology Ingrid E Scheffer et al • For each patient, we should aim to diagnose seizure type(s), electroclinical syndrome and etiology where possible.

  15. Organization of epilepsies Electro clinical syndrome: age of onset, seizure types, EEG patterns, imaging features and co-morbidities such as intellectual impairment Benign is replaced by ‘Self limited’ She has ‘Genetic generalized epilepsy’

  16. Organization of epilepsies Etiological (1) Genetic (2) Structural (3)Metabolic (4) Immune (5) Infectious (6) Unknown

  17. Organization of epilepsies Descriptors of focal seizures according to degree of impairment during seizure* Without impairment of consciousness or awareness • With observable motor or autonomic components – “Focal motor” and “autonomic” can be used • Involving subjective sensory or psychic phenomena only – “aura” can also be used • Replaces term “simple partial seizure” With impairment of consciousness or awareness • “Dyscognitive” can also be used. It is understood that dyscognitive may not always mean altered awareness but it is used here to denote altered consciousness or awareness which may be response tested • Replaces term “complex partial seizure” Evolving to a bilateral convulsive seizure • May include tonic, clonic or tonic and clonic components in any order • Replaces term “secondarily generalized seizure”

  18. Question no 4 • Are you sure it is generalized and not focal?

  19. Focal abnormalities in idiopathic generalized epilepsySeneviratne et al Epilepsia,55(8);1157-1169,2014 • Aura:25% to 54%, visual/epigastric/preictal prodromal symptoms • Focal semiology:35%to 46% include head version/eye version/focal myoclonic jerks • Absence seizures: Automatisms are common during hyperventilation • EEG: Focal interictal abnormalities found in 1/3rd

  20. Focal abnormalities in idiopathic generalized epilepsySeneviratne et al Epilepsia,55(8);1157-1169,2014 Cortical focus theory : Cortical focus within the perioral regions of somatosensory cortex led the thalamus by a mean of 8.1 m sec during the first 500ms of an absence seizure. Important to differentiate Idiopathic generalized epilepsy from focal frontal lobe epilepsy with secondary bilateral synchrony.

  21. Question no 5 • When will she grow out of this? • How will I know?

  22. Resolution of epilepsyFisher et al Epilepsia,55(4):475-482,2014ILAE Task force • Epilepsy is resolved for individuals who have an age dependent epilepsy syndrome and are now past the age • Seizure free for the last 10 years with no seizure medication for the last 5 years.

  23. Long-Term Outcome in Epilepsy with Grand Mal on Awakening: Forty Years ofFollow-upHoltkamp et al, Annals of Neurology Volume 75,Issue 2 February 2014 42 patients with Epilepsy with Grandmal on Awakening (EGMA) Follow up of 40.1 +/- 12.6 years(range=20-62).26 of 42 patients with EGMA (61.9%) were in 5 year terminal remission. Out of the 26 patients 21 were still taking AEDs and 5 had been completely off medications. Age at the time of investigation was the only independent predictor for seizure freedom. 35.7% in patients younger than 55 years,66.7% in patients between 56 and 65 years and 81.3% in patients older than 65 years. AED withdrawal was done in 45.2% patients and 63.2% of them had a relapse 47.6% had an university degree and 88.1% were regularly employed.

  24. Natural course and predictors of spontaneous seizure remission in idiopathic generalized epilepsy :7-27 years of follow up Podewelis et al Epilepsy Research (2014)108,1221-1227 • 15 IGE patients who refused treatment • Mean duration of follow up was 15.3 years • 5 patients had CAE,5 patients had EGCTS,4 patients had JAE (absence +GTCS), 1 patient had CAE • Mean age of onset of epilepsy was 15.3 years, mean duration of epilepsy was 18.3 years and mean duration of follow up was 15.3 years • Remission rate was 80% in CAE,60% EGTCS and 20% with IGE with ABS/GTCS. • Photoparoxysmal response was found in 20% of the patients and it was a poor prognostic factor

  25. Juvenile myoclonic epilepsy 25 years after seizure onset : A population based studyCamfield et al Neurology 2009,73;1041-1045 • 23 patients • Age at first seizure 10.4+/-4.3 years • Mean follow up of 25.8 years • Average age at follow up was 36 years • 11 (48%) no longer received AEDs, 6 of these were seizure free,3 had myoclonus only and 2 had rare seizures • 12 received AED treatment at the end of follow up • 1/3 rd grew out of their troublesome seizures.17% free of all seizures.

  26. Question no 6 • Will she have a normal life?

  27. Psychosocial complications in Adult Life Epidemiologic aspects: Lost in transition Camfield et al Epilepsia,55(Suppl.3):3-7,2014 Nova scotia cohort IGE • Psychiatric diagnosis (27%) • High school graduation (40%) • Pregnancy outside stable relationships (38%) • Living alone (23%) • Unemployment(33%) • Criminal conviction (7%)

  28. Behavioral changes in Pediatric epilepsy syndrome JME • Impaired abstract reasoning, cognitive speed and planning • Janznoted ‘an engaging but emotionally unstable, fairly immature personality, wavering between camaraderie and mistrust, which may lead to difficulties in social adaptation’

  29. Death in children with epilepsy • Children with an underlying neurological disorder sufficient to interfere with daily activities have a death rate of 25% (Nova scotia study) • Risk of SUDEP in children without neurological disorders is same as general reference population (Nova scotia study)

  30. Long-Term Mortality in Childhood-Onset EpilepsyMattiSillanpää, M.D., Ph.D., and ShlomoShinnar, M.D., Ph.D.N Engl J Med 2010; 363:2522-2529 December23,2010 • 245Finnish children with epilepsy, after 40 years of follow-up, 60 subjects had died (24%), a rate three times as high as the expected age- and sex-adjusted mortality in the general population. • A total of 33 of 60 deaths (55%) were related to epilepsy • A remote symptomatic cause of epilepsy associated with an increased risk of death as compared with an idiopathic or cryptogenic cause (37% vs. 12%, P<0.001). • Risk for SUDEP was 7% at 40 years overall and 12%not in long-term remission and not receiving medication.

  31. Cumulative Risk of All Epilepsy-Related Deaths and Sudden, Unexplained Deaths in Subjects with Epilepsy. Sillanpää M, Shinnar S. N Engl J Med 2010;363:2522-2529

  32. Cumulative Rate of Death According to Cause of Epilepsy. Sillanpää M, Shinnar S. N Engl J Med 2010;363:2522-2529

  33. Conclusions • Childhood-onset epilepsy was associated with a substantial risk of epilepsy-related death, including sudden, unexplained death. • The risk was especially high among children who were not in remission.

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