from the trenches: a clinician’s perspective gogi kumar,md assistant professor wsubsom medical...
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From the trenches: A clinician’s perspective
Gogi Kumar,MDAssistant Professor
WSUBSOMMedical Director
Department of Child NeurologyDayton Children’s Hospital
My Trench
General Cope’s Trench
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
• CT scan, urine pregnancy and drug screen is negative
• EEG:
• I diagnose her with new onset primary generalized epilepsy
• Suggest starting on Lamictal
First Question
What is Epilepsy?
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
A practical clinical definition of epilepsyFisher et al Epilepsia,55(4):475-482,2014
ILAE 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 apart2.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 years3.Diagnosis of an epilepsy syndrome
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?
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
Epilepsy BiomarkersElectrophysiology Imaging
Ictal patterns and interictal spikesFrequencies, duration, source localization, morphology, field size
Routine MRI Measures Enhancement (BBB)Functional (FMRI) Spectroscopy (MRS)Diffusion Tensor (DTI) Susceptibility (SWI)
High frequency oscillationsActivation proceduresPhotic Stimulation Hyperventilation Sleep Deprivation Drug Induction
PET (Positron Emission Tomography)FDG (Deoxyglucose) FMZ (Flumazanil)AMT (alphamethyltryptophane) PK (Inflammation)
Excitability TMS(Transcranial Magnetic Stimulation)Direct Electrical Stimulation(Part of Surgical Workup)
SPECT (Single Photon Emission Computed Tomography)
Engel et al Epilepsia 2013 August;54(04)61-69
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?
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.
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’
Organization of epilepsies
Etiological(1) Genetic (2) Structural (3)Metabolic (4) Immune (5) Infectious (6) Unknown
Organization of epilepsiesDescriptors 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”
Question no 4
• Are you sure it is generalized and not focal?
Focal abnormalities in idiopathic generalized epilepsy
Seneviratne 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
Focal abnormalities in idiopathic generalized epilepsy
Seneviratne 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.
Question no 5
• When will she grow out of this?• How will I know?
Resolution of epilepsyFisher et al Epilepsia,55(4):475-482,2014
ILAE 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.
Long-Term Outcome in Epilepsy with Grand Mal on Awakening: Forty Years ofFollow-up
Holtkamp 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.
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
Juvenile myoclonic epilepsy 25 years after seizure onset : A population based study
Camfield 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.
Question no 6
• Will she have a normal life?
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%)
Behavioral changes in Pediatric epilepsy syndrome
JME• Impaired abstract reasoning, cognitive speed
and planning• Janz noted ‘an engaging but emotionally
unstable, fairly immature personality, wavering between camaraderie and mistrust, which may lead to difficulties in social adaptation’
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)
Long-Term Mortality in Childhood-Onset EpilepsyMatti Sillanpää, M.D., Ph.D., and Shlomo Shinnar, M.D., Ph.D.
N Engl J Med 2010; 363:2522-2529 December23,2010
• 245 Finnish 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.
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
Cumulative Rate of Death According to Cause of Epilepsy.
Sillanpää M, Shinnar S. N Engl J Med 2010;363:2522-2529
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.