Epilepsy I Flashcards

1
Q

What are the important features of taking a history in a patient who has fallen down?

A

Get patient experience before, during and after event

Eye witness is critical = ask for demonstration of movements

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2
Q

What questions do you ask about the onset of someone falling?

A

What were they doing, environment, light headedness or syncope, pallor, breathing, posturing of limbs, head turning

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3
Q

What types of movements may someone exhibit when they fall down?

A

Tonic phase, clonic movements, corpopedal spasms, rigor

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4
Q

What are the important parts of the aftermath of a falling incident?

A

Speed of recovery, sleepiness, disorientation, deficits

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5
Q

What are the risk factors for epilepsy?

A

Birth and development, seizures in past (including febrile), head injury (especially loss of consciousness), drugs, family history

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6
Q

What is done in a seizure clinic?

A

Don’t examine patient in first visit = take history only

If diagnosis of syncope = CV examination and take lying and standing BP

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7
Q

What are high risk drugs for causing epilepsy?

A

Tramadol, prochloperazine, morphine and other opioids

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8
Q

What is the most important investigation to do in someone who has collasped?

A

ECG = must exclude long QT syndrome as it can present with syncopal seizures which mimic epilepsy

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9
Q

What imaging is done in clinic?

A

MRI = better than CT for imaging brain and doesn’t give dose of radiation

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10
Q

Which patients get a CT scan done acutely?

A

Skull fracture, deteriorating GCS, focal signs, head injury with seizures, failure of GCS to be 15 after 4hrs, suggestion of other pathology

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11
Q

What are the indications for doing an EEG?

A

To determine if someone is in non-convulsant status
To classify type of epilepsy
To confirm non-epileptic attacks
For surgical evaluation

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12
Q

Are EEGs always abnormal in epileptics?

A

No = EEG can be normal in epilepsy, and abnormal in non-epileptics

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13
Q

What are the differentials of epilepsy?

A

Syncope, panic attacks, TIA, hypoglycaemia, cataplexy, tonic spasm of MS, non-epileptic attack disorder, sleep phenomena, migraine, parasomnias, periodic paralysis

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14
Q

What are some features of seizure counselling?

A

Reassure patient = seizures don’t always mean epilepsy

Risk of recurrences and of sudden unexplained death in epilepsy (SUDEP)

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15
Q

What are the rules for driving with a history of seizures?

A
Seizures = must be free of seizure for 6 months or 5 years for HGV
Epilepsy = clear for 1 year or 3 years during sleep, 10 years off medication for HGV
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16
Q

What safety advice is given to patients with seizures and epilepsy?

A

Avoid using deep far friers, baths and climbing ladders

Rock climbing and open water swimming not advised

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17
Q

What is epilepsy?

A

Tendancy to recurrent, usually spontaneous epileptic seizures

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18
Q

What causes epilepsy?

A

Abnormal synchronisation of neuronal activity = usually excitatory with high frequency AP, sometimes inhibitory

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19
Q

What occurs in epilepsy?

A

Interruption of normal brain activity = focally or generalised, usually brief (seconds-minutes)

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20
Q

What is the incidence of epilepsy?

A

Most common in infancy and old age
Occurs in 50-80/100,000
Mortality = 1/400 per annum, 1/100 in young people

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21
Q

What causes focal epilepsy?

A

Part of the brain is structurally abnormal = can cause both focal and generalised seizures (irritates cortical pathways)

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22
Q

What occurs in generalised epilepsy?

A

Cortical networks involved so only generalised seizures occur

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23
Q

What are the categories of focal deficits?

A

Motor, sensory and psychic

24
Q

What are some motor focal deficits?

A

Rhythmic jerking, posturing, head and eye deviation, automatisms, vocalisations

25
Q

What are some types of focal sensory deficits?

A

Olfactory, gustatory, somatosensory, visual, auditory

26
Q

What are some focal psychic deficits?

A

Memory issues, deja vu, depersonalisation, aphasia, complex visual hallucinations

27
Q

What are the kinds of generalised seizures?

A

Absence, myoclonic, atonic, tonic, tonic clonic

28
Q

What is the epidemiology of generalised seizures?

A

Most are genetic

Present in childhood and adolescence

29
Q

What are some features of primary generalised epilepsy?

A

Generalised spike wave abnormalities on EEG

Often presents in childhood or teens

30
Q

What is the treatment for primary generalised epilepsy?

A

Sodium valporate is first line = teratogenic

Lamotrigine is second line

31
Q

What is an example of a primary generalised epilepsy?

A

Juvenile myoclonic epilepsy = early morning jerks, generalised seizures, risk factors are sleep deprivation and flashing lights

32
Q

What are some features of focal onset epilepsy?

A

Underlying structural cause
Onset at any age = more common with increasing age
Complex partial seizures with hippocampal sclerosis

33
Q

How is focal onset epilepsy treated?

A

Carbamazepine or lamotrigine

34
Q

How effective are anti-epileptic drugs?

A

55% are seizure free after starting monotherapy

85% have drug resistant epilepsy

35
Q

What areas do anti-epileptic drugs target?

A

Pre-synaptic exitability and neurotransmitter release

The GABA system

36
Q

What are the only two anti-epileptic drugs that can be used in combination?

A

Sodium valproate and lamotrigine

37
Q

How are absences treated?

A

Sodium valproate or ethosuximide

38
Q

How are myoclonic seizures treated?

A

Sodium valproate, levetiracetem or clonazepam

Lamotrigine may make it worse

39
Q

How are atonic, tonic and tonic-clonic seizures treated?

A

Sodium valproate

40
Q

What are some examples of anti-convulsants?

A

Phenytoin, sodium valproate, carbamazepine, lamotrigine, levetiracetam, topiramide, gabapentin/pregabalin

41
Q

What is phenytoin used for?

A

Acute management only = emzyme inducer

42
Q

What are some of the side effects of sodium valproate?

A

Weight gain, hair loss and fatigue

43
Q

What are some features of carbamazepine?

A

Effective but poorly tolerated

May make generalised epilepsy worse

44
Q

What are the side effects of topiramide?

A

Sedation, dysphagia and weight loss = poorly tolerated by patients

45
Q

What are some issues with prescribing anti-convulsants in women?

A

Some induce hepatic enzymes with alter the efficacy of the pill
Dose of the morning after pill must be increased
Shouldn’t use progesterone only pill = progesterone implants no longer effective

46
Q

What is status epilepticus?

A

Recurrent epileptic seizures without full recovery of consciousness = continuous activity >30mins

47
Q

What are the types of status epilepticus?

A

Generalised convulsant = non-convulsant status, conscious but in altered state
Epilepsia partialis continua = continued focal seizures, consciousness preserved

48
Q

What are the precipitants of status epilepticus?

A

Severe metabolic disorders = hyponatraemia
Infection and head trauma
Subarachnoid haemorrhage
Abrupt withdrawl of anti-convulsants
Treating absence seizures with carbamazepine

49
Q

What is convulsive status?

A

Generalised convulsions without cessation = excess cerebral energy demand and poor substrate delivery cause lasting damage

50
Q

What can convulsant status lead to?

A

Respiratory insufficiency and hypoxia, hypotension, hyperthermia, rhabdomyolysis

51
Q

What are some features of uncontrolled status epilepticus?

A

Glutamate release, excitotoxicity, neuronal death

52
Q

What is the initial management of status epilepticus?

A

Stabilise patient and investigate cause = blood test, CT
Anti-convulsants = phneytoin, kappa valproate
Never give benzodiazepines

53
Q

What is the treatment for prolonged/serial status epilepticus at home?

A

Diazepam 10-20mg rectal

Miodazolam 10-20mg buccal (not licensed)

54
Q

What is the treatment for sustained control of status epilepticus in patients with established epilepsy?

A

Re-establish usual AED treatment by nasogastric tube/orally or IV for phenytoin

55
Q

What is the treatment for sustained control of status epilepticus in patients with new or continuing seizures?

A

Fosphenytoin = 18mg/kg IV with EEG monitoring
Phenytoin = 18mg/kg IV with EEG monitoring
Phenobarbital = 15mg/kg (above options preferred)
Maintain drug levels

56
Q

What is the management of a patient with status epilepticus that persists after initial treatment?

A

Transfer to ITU within 1hr of admission
Control status with general anaesthesia = thiopentone or propfol
Monitor control with full EEGs or cerebral function monitor

57
Q

What are some features of partial status epilepticus?

A

Suspect in any patient presenting with an acute confusional state = confirm with EEG
Treatment the same as for status epilepticus