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GERICLINICS

GeriQBank · Paper III · Q1

Epilepsy in the Elderly — Definition, Pathophysiology, Clinical Features, Investigations and Treatment

Moderate YieldAsked ×115-mark essay
Chapter
Neurology, Neuro-ophthalmology & Environmental Emergencies
Years asked
Not recorded in the source
Frequency
Set 1× in Paper III (2009–2025)

As set in the university paper

  • Definition, pathophysiology, clinical features, investigations and treatment of epilepsy in the elderly.

    Paper III · Neurology — Stroke, Coma, Seizures & Neuromuscular · asked ×1 · 15-mark essay · see in paper list

Answer framework

  1. Definitions (ILAE) — seizure; epilepsy criteria; provoked seizures; status epilepticus; refractory epilepsy
  2. Epidemiology — third commonest; U-shaped incidence; prevalence; status epilepticus and NCSE
  3. Aetiology and pathophysiology — acute symptomatic causes; causes of epilepsy; mechanism; autoimmune causes
  4. Clinical features — focal onset; subtle presentation; atypical auras; prolonged postictal state; NCSE
  5. Investigations — eyewitness history; EEG limits; video-EEG; imaging and bloods; differential diagnosis
  6. Treatment — after the first unprovoked seizure; the ideal drug; start low; preferred and avoided drugs; comorbidity; frailty and bones; status epilepticus algorithm; prognosis
  7. Recent updates — newer ASMs; tolerability-driven choice; post-stroke seizures; ILAE 2017 and "ASM"; India

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Detailed answer

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Short revision answer

  • A seizure is a transient episode of signs or symptoms from abnormal excessive or synchronous neuronal activity. Epilepsy (ILAE): two unprovoked seizures >24 hours apart, one with ≥60% recurrence risk over 10 years, or an epilepsy syndrome; provoked seizures don't count. Status epilepticus: >30 minutes of seizure, or seizures without recovery between; refractory epilepsy: failure of two appropriate, tolerated drugs.
  • Epilepsy is the third commonest neurological disorder in old age; incidence is U-shaped and 25% of new seizures begin after 65. Active epilepsy affects about 1.5% at ≥75 (over 5% in nursing homes); status epilepticus is nearly twice as common as in the general population (86/100,000/year), and NCSE is commoner in the very old and critically ill.
  • Causes: acute symptomatic — stroke 30–54%, metabolic 10–15%, tumour, trauma and drugs about 10% each. Epilepsy — cryptogenic 48–50%, stroke 40–53% (the largest identifiable cause), dementia 5–20%, tumours 4–19%. A gliotic scar forms a hyperexcitable focus; amyloid-driven hyperexcitability raises risk in AD; consider autoimmune (LGI1) and Hashimoto's encephalopathy.
  • Presentation is subtle: focal onset in 62–68%; brief confusion, unexplained falls or stereotyped movements; non-specific auras (dizziness), often from extratemporal (frontal) foci; postictal states lasting hours to days (Todd's paresis mimics stroke). NCSE presents as altered mental state, odd behaviour or aphasia, often with acute illness, drug toxicity or withdrawal.
  • Investigations: diagnosis rests on an eyewitness account. EEG sensitivity falls with age (normal in a third; non-specific slowing is common) — add a sleep EEG; video-EEG is the gold standard (6–15% of "uncontrolled epilepsy" is psychogenic). MRI for everyone, plus ECG, glucose, electrolytes, calcium, renal and liver function and drug review. Differentials: syncope, limb-shaking TIA, transient global or epileptic amnesia, hypoglycaemia, RBD, PLMD, delirium, psychogenic attacks.
  • Treatment: treat after the first unprovoked seizure (recurrence is high), especially with a lesion or epileptiform EEG; start low, go slow, monotherapy (lower doses often work — valproate 30–40% less). Prefer lacosamide, lamotrigine or levetiracetam (best seizure freedom at 6 and 12 months); avoid phenytoin, carbamazepine, phenobarbital, primidone, valproate and benzodiazepines.
  • Tailor to comorbidity: in depression avoid levetiracetam, topiramate, phenobarbital, primidone and vigabatrin; in AD treat after a second episode and avoid polytherapy. Epilepsy is a top 10 frailty-related condition — assess falls, protect bones (ASMs raise fracture risk), and use STOPP/START and Beers.
  • Status epilepticus (treat within 5–10 minutes; glucose if hypoglycaemic): lorazepam 0.1 mg/kg IV, diazepam 10 mg or midazolam 10 mg IM, repeated once at 10 minutes; then phenytoin 15 mg/kg (with cardiac monitoring), valproate 15–30 mg/kg or levetiracetam 20–30 mg/kg; refractory → midazolam or propofol infusion and anaesthesia. Most become seizure-free on the first drug; failure in the first year predicts resistance; surgery or VNS (27–44% reduction) suit selected patients.
  • Updates: newer ASMs (lamotrigine, oxcarbazepine, levetiracetam, topiramate, zonisamide, lacosamide) match older ones with better tolerability, and ganaxolone is the newest; in people ≥65, choose by tolerability (Drugs & Aging 2026) — oxcarbazepine and eslicarbazepine cause hyponatraemia, avoid lacosamide in AV block, ECG before lamotrigine in heart disease. After stroke: no primary prophylaxis; early seizures (≤7 days) are acute symptomatic, late ones (>7 days) are epilepsy — treat with lamotrigine or levetiracetam.
  • The ILAE 2017 classification and the term "antiseizure medication" are now standard; operational status thresholds are t1 = 5 min and t2 = 30 min. India: the rural treatment gap is 50–70%; phenytoin and phenobarbital are still common although levetiracetam and lamotrigine are cheap generics; driving needs self-declaration and about a year seizure-free.

Condensed by GeriClinics from the detailed answer below, with no new facts added.

1.

Epilepsy in the Elderly — Definition, Pathophysiology, Clinical Features, Investigations and Treatment Definitions (ILAE / IBE)

1.

An epileptic seizure is a transient occurrence of signs and/or symptoms due to abnormal excessive or synchronous neuronal activity in the brain.

2.

Epilepsy exists when a seizure is confirmed and the brain shows an enduring tendency to recur. It is diagnosed with: two unprovoked or reflex seizures more than 24 hours apart; OR one unprovoked seizure with a ≥60% probability of another over the next 10 years; OR an epilepsy syndrome.

3.

A seizure provoked by a transient factor acting on an otherwise normal brain does not count towards a diagnosis of epilepsy.

4.

Status epilepticus (SE): more than 30 minutes of continuous seizure activity, or intermittent seizures without full recovery of consciousness between them. Shorter operational durations are now proposed.

5.

Refractory epilepsy: failure of adequate trials of two tolerated, appropriately chosen antiepileptic drug (AED) schedules to achieve sustained seizure freedom.

Epidemiology

6.

Epilepsy is the third most common neurological disorder in older age groups. Incidence follows a U-shaped curve, highest at both ends of life. 25% of new-onset seizures occur after age 65.

7.

Prevalence of active epilepsy at age ≥75 is about 1.5% (twice that of younger adults); in nursing homes it exceeds 5%.

8.

SE incidence in the elderly is almost double the general population (86/100,000/year), rising with age, highest at ≥85 years. Non-convulsive SE (NCSE) occurs more often in the very old and critically ill.

Aetiology and pathophysiology

9.

Acute symptomatic seizures: stroke 30–54%, metabolic/electrolyte imbalance 10–15%, tumours 10%, trauma 10%, drug-related 10%, CNS infection 2–3%.

10.

Epilepsy: cryptogenic 48–50%, stroke 40–53% (single largest identifiable cause), dementia 5–20%, tumours 4– 19%, trauma 1–3%.

11.

Mechanism: cortical/subcortical injury → gliotic scar → a hyperexcitable focus. In Alzheimer's disease, amyloid-driven network hyperexcitability raises seizure risk. Consider also autoimmune limbic encephalitis (VGKC/LGI1 antibodies) and Hashimoto's encephalopathy.

Clinical features

12.

Seizure onset is focal in 62–68% and generalised in 27–39%; for established epilepsy, focal 65%, generalised 13%, unknown 22%.

13.

Presentation is subtle — brief episodes of confusion, unexplained falls, or stereotyped movements, often misdiagnosed as non-specific confusional states.

14.

Typical auras (fear, epigastric rising sensation, déjà vu) are less common; non-specific auras such as dizziness predominate. The seizure focus is more often extratemporal, especially frontal.

15.

The postictal period is prolonged — lasting hours to days. Todd's paresis may mimic stroke.

16.

NCSE presents as altered mental status ranging from mild disorientation to confusion or coma, uncharacteristic behaviour or aphasia. More than half occur with acute medical illness — organ failure, drug toxicity, alcohol/benzodiazepine withdrawal, metabolic disturbance.

Investigations

17.

Diagnosis is clinical, based on an eyewitness description. The major difficulty is that older patients often cannot give an accurate history.

18.

EEG sensitivity falls with age: epileptiform transients occur less often, activation procedures add little, EEG is normal in about one-third, and non-specific focal slowing is common even without seizures. A sleep or nap EEG is advised if the awake study is negative.

19.

Inpatient video-EEG is the gold standard for characterising events and distinguishing epileptic from psychogenic non-epileptic attacks (6–15% of "uncontrolled epilepsy").

20.

Brain imaging in every patient — MRI preferred over CT as it is more sensitive for stroke, TBI and structural lesions. Add ECG (exclude arrhythmic syncope), glucose, electrolytes, calcium, renal and liver function, and drug review.

21.

Differential diagnosis: syncope, limb-shaking TIA, transient global amnesia, transient epileptic amnesia, hypoglycaemia, REM sleep behaviour disorder, periodic limb movement disorder, hypnic jerks, delirium, psychogenic attacks.

Treatment

22.

Because recurrence risk is high, treat after the first confirmed unprovoked seizure, especially with a brain lesion or epileptiform EEG.

23.

An ideal AED for the elderly has linear pharmacokinetics, minimal hepatic metabolism, minimal drug interaction and renal excretion, and minimal impact on cognition, memory or mood — no such drug exists.

24.

Start low, titrate slowly, use monotherapy first-line. Older patients often respond to lower doses (e.g. valproate dose reduced by 30–40%).

25.

Preferred agents: lacosamide, lamotrigine and levetiracetam — these have the greatest likelihood of seizure freedom at 6 and 12 months. Lamotrigine is better tolerated than carbamazepine.

26.

Avoid: phenytoin, carbamazepine, phenobarbital, primidone, valproate and benzodiazepines — chronic toxicity, interactions and neurotoxicity in hypoalbuminaemia.

27.

Match the drug to comorbidity: in depression avoid levetiracetam (irritability), topiramate, phenobarbital, primidone and vigabatrin. In Alzheimer's disease, treat after a second episode; avoid polytherapy, which impairs cognition.

28.

Epilepsy is one of the top 10 conditions related to frailty. Assess falls risk and provide bone protection — AEDs increase fracture risk. Use STOPP/START and Beers criteria to manage polypharmacy.

29.

SE algorithm (Pathy's Box 51.1): treat within 5–10 minutes; IV glucose if hypoglycaemic. First line — lorazepam 0.1 mg/kg IV (2 mg/min), or diazepam 10 mg over 2 min, or midazolam 10 mg IM; repeat once at 10 min. Second line (established SE) — phenytoin 15 mg/kg (max 20 mg/min, with cardiac and BP monitoring), or valproate 15–30 mg/kg if cardiovascular comorbidity, or levetiracetam 20–30 mg/kg over 15 min. Refractory — midazolam or propofol infusion, then general anaesthesia and ventilation.

30.

Prognosis is good — most newly diagnosed older patients become seizure-free on first AED monotherapy. Failure to become seizure-free within the first year predicts drug resistance. Epilepsy surgery and vagus nerve stimulation (27– 44% seizure reduction) are feasible in selected older patients.

Latest Updates (2023–Present)

Continuum "Update on Antiseizure Medications" (2025): lamotrigine, oxcarbazepine, levetiracetam, topiramate, zonisamide and lacosamide have efficacy equal to older agents with equal or better tolerability as first-line therapy for focal epilepsy; pregabalin is inferior to lamotrigine. Lacosamide, pregabalin and eslicarbazepine have successful conversion-to-monotherapy data. Ganaxolone is the newest FDA-approved ASM.

Drugs & Aging (2026) review of ASMs in adults ≥65: because most ASMs have comparable efficacy, tolerability and quality of life — not efficacy — should drive drug choice. Practical cautions: eslicarbazepine and oxcarbazepine cause hyponatraemia in the elderly; lacosamide should be avoided in AV block; lamotrigine needs slow titration and an ECG in cardiac disease; cenobamate, brivaracetam and perampanel are emerging options. Neurology (2025) network meta-analysis of ASMs in post-stroke seizures (Misra et al.) and Frontiers in Neurology (2025): lamotrigine and levetiracetam are favoured; primary ASM prophylaxis after stroke is not recommended; early seizures (≤7 days) are acute symptomatic, while late seizures (>7 days) define post-stroke epilepsy and warrant long-term treatment. Lacosamide is a promising option including for NCSE in stroke. The ILAE 2017 classification (focal / generalised / combined / unknown, with awareness and motor descriptors) remains the operative framework; the term "antiseizure medication (ASM)" has replaced "AED" in current literature. Indian context: the epilepsy treatment gap remains 50–70% in rural India; phenytoin and phenobarbital remain widely used because of cost, though both are on the STOPP/Beers avoid list for older adults. Levetiracetam and lamotrigine are now inexpensive generics and should be preferred. Driving requires self-declaration of epilepsy under the Central Motor Vehicles Rules; Indian epilepsy society practice advises at least one year of seizure freedom before resuming driving.

Current Practice Update

Textbook Position (Pathy's 6th ed.) Current Evidence-Based Practice (2023–2026)

Term "antiepileptic drug (AED)" Replaced by "antiseizure medication (ASM)" — reflects symptomatic rather than disease-modifying action Lacosamide, lamotrigine, levetiracetam are safe Confirmed. Choice now driven explicitly by tolerability and quality of life, since and first-line efficacy is comparable (Drugs & Aging 2026)

SE defined as >30 minutes; shorter durations Operationally accepted: t1 = 5 min (start treatment), t2 = 30 min (risk of neuronal "proposed" injury)

Eslicarbazepine listed as a useful newer agent Usable, but hyponatraemia risk in the elderly now explicitly flagged; monitor sodium Post-stroke seizure treatment not separately No primary prophylaxis after stroke. Late seizures = post-stroke epilepsy → treat addressed with lamotrigine or levetiracetam Edaravone/newer agents "need more study" Cenobamate, brivaracetam, perampanel and ganaxolone now have geriatric tolerability data Examiner's Tip — say these lines verbatim:

"Epilepsy is the third commonest neurological disorder in the elderly; incidence follows a U-shaped curve and 25% of new-onset seizures occur after 65."

"Stroke is the single largest identifiable cause, accounting for 40–53% of epilepsy in this age group." "Presentation is subtle — brief confusion, falls or stereotyped movements. Over- and under-diagnosis are equally common."

"EEG sensitivity falls with age; it is normal in one-third. Video-EEG is the gold standard; MRI is mandatory in all." "Treat after the first unprovoked seizure because of high recurrence — start low, go slow, monotherapy first." "Lacosamide, lamotrigine and levetiracetam are the drugs of choice; avoid phenytoin, carbamazepine, phenobarbital and valproate."

"Epilepsy is one of the top 10 conditions related to frailty — always assess falls risk and give bone protection."

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