Seizures post Stroke
Transcription
Seizures post Stroke
Contents Ø Epidemiology Seizures post Stroke Elizabeth Dempsey C.N.S. Neurology Mater Misericordiae University Hospital post Stroke Seizures Ø Classification of Seizures Ø Possible Causes of Post Stroke Seizures Ø Early & Late post Stroke Seizures Ø Recording of Seizures Ø Management /Pharmacology Ø Psychosocial Impact/Education/lifestyle Epidemiology of Seizures post Stroke Ø Stroke; leading cause of symptomatic Epilepsy in Adults, (Neurology,2006,Ryvlin et al) Ø Ø Ø Ø Prevalence & incidence Epilepsy rises with age, 1/3 new Seizures 2nd Stroke (Sander,1996 &Panayiotopoulos 2008) Stroke 30%new Dx Epilepsy> 60 years 10-15% with acute Stroke/TIA: present Seizure.>30% seizure/48hrs (Crino/Delanty2002) 54-66% single seizure,2-4%develop epilepsy (Ryvlin et al Seizure/Epilepsy Ø Ø 2006) Ø 5% seizures are marker for Stroke ((Manford Manford 2003) Ø Epilepsy,3rd most common Neurology disorder after Stroke, Dementia (Tallis,2002) Ø Seizure is a sudden, paroxysmal, synchronous repetitive discharge of Cerebral Neurons that interrupt brain function (Brainwave 2009) +/- alteration of consciousness Epilepsy is the tendency to have recurrent unprovoked seizures.37,000 people in Ireland with Epilepsy (Linehan et al 2009) Post Stroke Epilepsy recurrent unprovoked late onset seizures(Cavazos,2004) Neurological Complication post Stroke: Seizures Cause of Seizures Ø Ø Ø Ø Ø Ø Ø Ø Ø Previous Stroke 30-40% 1% patients >65yrs; 20-40% 2nd Stroke Asymptomatic Cerebral infarction (Brodie,Kwan 2005) Alzheimer's & Dementia risk of seizures Brain Tumors, Head trauma Alcohol withdrawal seizures Systemic Disorders; Metabolic, Electrolyte, C.N.S.infections, C.N.S.infections, Medications:antipsychotics Medications:antipsychotics,, antidepressants,antibiotics Alcohol/Substance Abuse Ø Ø Ø Ø Ø Ø Ø Ø Early post Stroke seizures; (E.P.S.) Acute Symptomatic, 6%<7/7 Late post Stroke Seizures (L.P.S.);>7/-7/months L.P.S.;3% year1,4.7% year 2,7.4%year 5, 8.9%10 yrs Onset, E.P.S.: simple partial,complex-partial,2nd generalized tonic clonic (G.T.C.) Early seizures>post stroke epilepsy,2nd structural brain abnormalities/focus (Crino,Delanty,2002) L.P.S., Post Stroke Epilepsy, recurrent unprovoked late onset seizuresG.T.C.(Cavazos,2004) Immediately Ø Partial type seizures in Ischaemic or haemorrhagic Stroke (Stroke 1998) Ø No correlation of acute Seizures with size of lesion,functional outcome mortality (Crino,delanty,2002) Early or Late post Stroke Seizures Ø Acute Stroke most common cause of seizures in the elderly Risks; Early seizure, location; cerebral cortex & severity of stroke 8% Haemorrhagic Stroke( Stroke(I.C.H),develop seizures after 2/52 5% Ischaemic Stroke.(BMJ,2005,Brodie,Kwan) ?Ischaemic Stroke Rx Partial/focal Epilepsy Ø Ø Ø Ø Ø Ø Ø Ø 63% Partial seizures not recognised Limb jerking, tingling Atypical features, memory lapses, confusion, inattention (Brodie, Brodie, Kwan 2005) Symptoms in seconds-minutes Spread – adjacent areas Resolve minutes-hours Partial/aura – C.P.S. -2nd generalisation ? persistent Neurological signs Differential Diagnosis Ø Ø Ø Ø Ø Ø Ø Ø Funny Turns Syncope Hypoglycaemia /Hyperglycaemia /Hyperglycaemia T.I.A. Migraine Trans Global Amnesia Vertigo/non specific dizziness(Shorovon,2000) Todd’ Todd’ s paresis (temporary reduction in motor function activated at onset of attack, resolves approx 30 mins,Manford2003) Risks for Seizures in Stroke Ø Ø Ø Ø Ø Ø Ø Ø Ø Ø Age Cocaine Abuse>rise Stroke/I.C.H/seizures Alcohol Cerebro Autosomal Dominant Arteriopathy with Subcortical Infarcts & Leukoencephalopathy(C.A.D.A.S.I.L.) Leukoencephalopathy(C.A.D.A.S.I.L.) Arterial-Venous Malformation (A.V.M.) Cerebral Amyloid Angiopathy (C.A.A.) Mitochondrial Encephalomyopathy, Encephalomyopathy, Lactic Acidosis & Stroke (M.E.L.A.S.) Stroke like episodes & seizures Rheumatic heart disease, Endocarditis, Endocarditis, Mitral valve prolapse Reperfusion syndrome, Carotid Endarterectomy, Endarterectomy, Sickle Cell Disease Diagnostic Considerations E.E.G. Changes Ø 1st Ø Elderly; Ø ? 2nd Ø Slow seizure illness Ø History, witnessed account Ø Vital signs Ø Laboratory/toxicology Ø C.T. scan/M.R.I. Ø E.E.G. variety of changes activity, normal variant after 50 years Ø Sharp spikes, sleeping, drowsy with >age To Treat or not to Treat ?? Ø Ø Prophylactic Rx ? if seizure onset< 24hrs Prophylactic Rx in I.C.H. with cortex, beneficial (Crino/Delanty,2002) Ø Ø Ø Ø Ø Treat if seizure>7/7 post stroke, late onset seizures; long term treatment (A.C.N.R.2011) Single seizure/classification/E.E.G. Women, Acceptance, Contraception, Folic Acid Treatment aim; seizure control with no side effects Start low, dose & titrate slowly to avoid toxicity Pharmacokinetics • • • • • • • Biological age V’ V’s chronological age Complex pharmacokinetics, Protein Binding reduced, Albumen concentrations lowered ½ life increased as metabolism slower Interaction of other medications complicates absorption, clearance, elimination Limited drug trials for elderly population with seizures post Stroke Compliance; memory, cognition, intellect, Adverse effects, drug toxicity, lower serum levels(Shorvon,2000) Seizure Medication Concerns for Rx Ø Bone Mineral density reduced after Stroke, hemiplegic side, Ø Fracture Risk increased: duration of immobility, severity of hemiplegia, hemiplegia, time after menopause Ø Influencing factors; recovery, hemiplegia Ø vitamin D, warfarin ( Kenneth,Poole et al,Stroke 2002) (Anti Epileptic Drugs/A.E.D.’ Drugs/A.E.D.’S) Ø Ø Ø Ø Phenytoin PHT Phenobarbital PHB Sodium valproate VPA Carbamazepamine CBZ Ø Mysoline PMD Ø Ø Ø Ø Ø Ø Ø Ø Ø Concerns of A.E.D. for Stroke & Epilepsy Ø Ø Ø Ø Ø Use of aed’ aed’s,# risk; CBZ,PHB,OXC,VAL Enzyme inducing PHT,CBZ,&PHB Continued AED use higher risk of bone loss @ hip – # x 5 yrs Epilepsy # 2-6 >gen >gen population, chronic steroid use (Neurology 2004) Falls common in epilepsy 2nd C.N.S. effects >seizures, ataxia, altered sensation, cognitive impairment Immobility, inactivity, few weight bearing activities, residential care, focal weakness osteopenia A.E.D. options in Stroke Ø Ø Ø Ø Psychosocial Implications Ø Ø Ø Ø Ø Ø Impact of Seizures/misconceptions Injuries, osteoporotic fracture Quality of Life Driving Employment Drug payment/Medical Card/Long term Illness/Drug refund scheme Lamotrigine LTG Levetiracetam LEV Topiramate TPM Oxycarbazepine OXC Zonisamide ZNG Gabapentin GBT TiagabineTGB Rufinamide Lacosamide I.L.A.E. Gabapentin(GBT) Gabapentin(GBT) & Lamotrigine(LTG),1ts line monotherapy for partial Epilepsy Gbt 81%seizure free @ 30/12 e.g.(9001200/od) Lct 100-150/od ?Oxcarbazepine & Levetiracetam benefit elderly post Stroke patients Education Ø Ø Ø Ø Ø Ø Ø Ø Collaborative decision re Rx Information re medications/benefits/potential side effects/documentation of titration Written instructions, careful explanation, Blister packs Advice re Seizure Safety Reduce Seizure triggers: Adequate sleep/hydration/nutrition/compliance with a.e.d’ a.e.d’s. Avoid heights/use shower instead of baths/ avoid swimming alone/reduce c2H5oH Support Group, Irish Epilepsy Assocation;Brainwave, Assocation;Brainwave, www.epilepsy.ie Conclusion Ø Seizures in Stroke patients, Challenging/Ambiguities Ø Minimal research on Elderly patients with A.E.D.’ A.E.D.’S Ø Risk/Benefit options Ø Continuous Observation of Stroke patients Thank You