Epilepsy Study Guide
Study Guide
📖 Core Concepts
Epilepsy – a set of brain disorders marked by ≥ 2 unprovoked seizures > 24 h apart (or a single seizure with ≥60 % 10‑yr recurrence risk).
Seizure – sudden, excessive, synchronized neuronal firing that may cause loss of awareness, motor jerks, or convulsions.
Seizure classification (ILAE 2025) – Focal, Generalized, Unknown onset, Unclassified.
Ictogenesis – the moment the balance of excitation ↔ inhibition collapses, producing a paroxysmal depolarizing shift and a seizure.
Epileptogenesis – progressive changes (cell loss, gliosis, network re‑organization) that turn a once‑normal brain into a seizure‑prone one.
Status epilepticus – seizure activity lasting ≥5 min (or repeated seizures without full recovery).
Post‑ictal state – recovery period after a seizure; can last minutes to days and may include confusion, headache, Todd’s paralysis, or psychosis.
Drug‑resistant epilepsy – failure of ≥2 appropriately chosen, tolerated antiseizure meds at optimal doses.
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📌 Must Remember
Diagnostic criteria:
≥2 unprovoked (or reflex) seizures >24 h apart, or
1 unprovoked seizure + ≥60 % 10‑yr recurrence risk, or
A defined epilepsy syndrome.
First‑line meds:
Generalized seizures: Valproate (first line), Lamotrigine (2nd line).
Absence seizures: Ethosuximide or Valproate.
Focal seizures: Levetiracetam or Valproate (cost/side‑effect considerations).
Teratogenic hierarchy (lowest → highest risk):
Leviteracetam ≈ Lamotrigine < Valproate > Phenytoin > Carbamazepine > Phenobarbital > Gabapentin.
Driving eligibility: seizure‑free for 3 months–3 years depending on jurisdiction; risk of motor‑vehicle collisions ≈ 2× the general population.
SUDEP risk factors: uncontrolled generalized tonic‑clonic seizures, nocturnal seizures, sleeping alone, refractory epilepsy.
Seizure clusters: ≥2 seizures within 24 h (or a noticeable rise over baseline).
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🔄 Key Processes
Seizure onset → propagation (ictogenesis)
Loss of inhibitory control → paroxysmal depolarizing shift → rapid, synchronous firing → clinical seizure.
Epileptogenesis timeline (after an insult)
Acute injury → neuronal loss & gliosis → synaptic re‑organization → chronic hyper‑excitable network → spontaneous seizures.
Acute management of a generalized tonic‑clonic seizure
Stay calm, clear hazards.
Gently guide to ground; turn to recovery position.
No restraints, no objects in mouth.
Time seizure; >5 min → call EMS (possible status).
Status epilepticus treatment algorithm
Step 1: Benzodiazepine (IV lorazepam or buccal midazolam).
Step 2: If still seizing, give levetiracetam, phenytoin, or valproate (levetiracetam preferred).
Pre‑surgical epilepsy evaluation
Detailed seizure semiology → long‑term video EEG → high‑resolution MRI → neuropsych testing → (optional) PET/SPECT/invasive monitoring → multidisciplinary decision.
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🔍 Key Comparisons
Focal vs. Generalized seizures
Onset: one brain region → may spread vs. bilateral simultaneous onset.
Consciousness: often preserved in focal‑aware; usually impaired in generalized tonic‑clonic.
Valproate vs. Lamotrigine (generalized seizures)
Efficacy: Valproate > Lamotrigine.
Teratogenicity: Valproate high risk; Lamotrigine low risk.
Ethosuximide vs. Valproate (absence seizures)
Target: Ethosuximide blocks T‑type Ca²⁺ channels → ideal for pure absence.
Broadness: Valproate works on multiple seizure types but higher side‑effect profile.
Ketogenic diet vs. Modified Atkins
Efficacy: Classic ketogenic ≈ 3× higher seizure‑freedom in children.
Tolerability: Modified Atkins better tolerated, slightly less effective.
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⚠️ Common Misunderstandings
“All seizures are epilepsy.” – Provoked (e.g., fever, hypoglycemia) seizures are not epilepsy.
“You must put something in the mouth to stop a seizure.” – This is dangerous; never force the mouth open.
“If a patient is seizure‑free for 1 year, epilepsy is resolved.” – Resolution requires ≥10 years seizure‑free and ≥5 years off meds.
“Valproate is safe in pregnancy.” – It has the highest teratogenic risk; avoid if possible.
“All patients need routine drug‑level monitoring.” – Not necessary when seizures are controlled and no toxicity concerns.
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🧠 Mental Models / Intuition
“Excitation‑Inhibition Scale” – Visualize the brain as a seesaw; epilepsy tips the balance toward excitation. Anything that lowers the seizure threshold (sleep loss, stress) pushes the seesaw down.
“Seizure spread as a fire” – Focal seizures are a spark; if the fire jumps across the corpus callosum it becomes generalized (focal‑to‑bilateral).
“Epilepsy as a “broken circuit” – Structural lesions are “short‑circuits” that bypass normal inhibition, creating a loop of runaway firing.
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🚩 Exceptions & Edge Cases
Reflex epilepsy (≈ 6 %): seizures reliably provoked by specific stimuli (flashing lights, reading). Standard classification may list as “unknown onset” if not recognized.
Autoimmune encephalitis – May present with seizures but requires antibody testing; conventional antiseizure meds often insufficient alone.
Drug‑induced hormonal contraception failure – Enzyme‑inducing ASMs (e.g., carbamazepine) raise contraceptive failure to 3‑6 %; lamotrigine levels can drop, reducing seizure control.
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📍 When to Use Which
Choose medication based on seizure type
Focal: start with levetiracetam (good tolerability) → consider carbamazepine/oxcarbazepine if cost is key.
Generalized tonic‑clonic: valproate (unless pregnancy risk) → lamotrigine or levetiracetam as alternatives.
Absence: ethosuximide first → valproate if mixed seizure types.
Surgery vs. Diet
Drug‑resistant focal epilepsy with a clear MRI lesion: prioritize surgery.
Drug‑resistant generalized or multifocal epilepsy, especially in children: consider ketogenic diet or neurostimulation.
Pregnancy planning
Switch to lamotrigine or levetiracetam before conception; supplement folic acid 4 mg daily.
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👀 Patterns to Recognize
Jacksonian march → focal seizure spreading sequentially → think cortical motor area involvement.
Auras preceding a seizure → indicate focal onset; ask patient about sensory or psychic phenomena.
Sudden loss of tone (atonic) → high risk of falls & injury; often part of generalized epilepsy syndromes.
Post‑ictal Todd’s paralysis – focal weakness that resolves within 24 h; clues to seizure focus (contralateral hemisphere).
Clusters – multiple seizures <24 h with incomplete recovery → may need rescue medication plan.
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🗂️ Exam Traps
“Any seizure after a head injury is epilepsy.” – Acute symptomatic seizures are not epilepsy unless they become unprovoked.
“Valproate is safe for all women of child‑bearing age.” – High teratogenicity; contraindicated when safer alternatives exist.
“All focal seizures impair consciousness.” – Focal aware (preserved consciousness) seizures exist; don’t assume impairment.
“EEG alone confirms epilepsy.” – Diagnosis requires clinical seizure description plus EEG; a normal EEG does not rule out epilepsy.
“If a patient has a single seizure, give antiseizure medication immediately.” – Treatment is usually deferred unless high recurrence risk or specific syndrome.
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