Epilepsy Flashcards

1
Q

How are ‘seizures’ and ‘epilepsy’ defined and how do they relate to one another?

A

Seizures are abnormal excessive neuronal activity in the brain. Caused by over expression of glutamate (excitatory neurotransmitter) or under expression of GABA (inhibitory neurotransmitter). Epilepsy is a condition that’s characterised by recurrent seizures.

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2
Q

Describe generalised seizures and partial seizures

A

Generalied seizures affects both sides of the brain from the start. They almost always impact on awareness so the terms ‘aware’ or ‘impaired awareness’ are not used for them
Partial/focal seizures originates in one side of the brain
If person remains alert and able to interact is called a focal onset aware seizure.
If person is not aware of surrounding its focal impared awareness seizure ( Complex partial seizure)

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3
Q

Diagnosis of epilepsy

A
  • at least two unprovoked (or reflex) seizures occurring more than 24 hours apart
  • one unprovoked seizure and a probability of further seizures (at least 60%)
  • diagnosis of an epilepsy syndrome.
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4
Q

Define absence seizures and its symptoms

A

Absence seizures is a generalised seizure occur most often in children. It is characterized by a very brief loss of awareness, commonly manifested as a blank stare with or without subtle body movements such as eye blinking, lip smacking or chewing.

People with absence seizures may not be aware that something is wrong for years.
Kids who start having absence seizures in early years stand a good chance of outgrowing them without treatment.

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5
Q

Define tonic seizures and its symptoms

A

They are a form of generalised seizures and associated with sudden stiffening of muscles and may cause the person to fall, often backwards.

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6
Q

Define atonic seizures and its symptoms

A

also known as drop attacks, are characterized by a sudden loss of muscle tone (loss of muscle strength), which may cause the person to collapse or drop down.

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7
Q

Define Clonic seizures and its symptoms

A

Symptoms are rhythmic jerking muscle movements. Most commonly affected are the muscles of the neck, face, arms and legs. Clonic seizures are rare.

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8
Q

Define myoclonic seizures and its symptoms

A

Myoclonic seizures are brief jerks or twitches of a muscle or a group of muscles. There can be one or many twitches occurring within a couple of seconds.

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9
Q

Define Tonic-clonic seizures and its symptoms

A

Generalised convulsive seizures, which are combinations of muscle stiffening and jerking. It also involves sudden loss of consciousness and sometimes loss of bladder control.
A tonic-clonic seizure that lasts longer than 5min requires immediate medical treatment.

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10
Q

Define simple partial seizures and symptoms

A

Simple partial: depending on the affected brain area, patients may have unusual feelings, strange sensations or uncontrollable jerky movements, but remain conscious and aware of the surroundings.

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11
Q

Define complex partial seizures and symptoms

A

involves a loss or changes in consciousness, awareness and responsiveness.

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12
Q

How do the main symptoms for each seizure type relate to the causes and parts of the brain that are affected?

A

a seizure that begins in the occipital cortex may result in flashing lights.
a seizure that affects the motor cortex may result in rhythmic jerking movements of the face, arm, or leg on the side of the body opposite to the involved cortex (Jacksonian seizure).
a seizure that begins in the parietal cortex may cause distortion of spatial perception.
a seizure that begins in the dominant frontal lobe may cause sudden speech difficulties.

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13
Q

What are the main consequences of uncontrolled or poorly controlled seizures?

A

When seizures continue unchecked, complications can arise including (Therapeutic Guidelines, 2019):
central nervous system injury
noncardiogenic pulmonary oedema
rhabdomyolysis, acidosis and kidney failure
hyperthermia
aspiration risk
trauma (falls, shoulder dislocation etc)
increased risk of sudden unexpected death in epilepsy (SUDEP)
poor quality of life/uncertainty (unable to drive, employment affected etc)

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14
Q

Explain the seizure mechanism

A

Seizures are caused by brain alterations that resulted in an underactivity of GABA neurons and/or an over activity of glutamatergic neurons.

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15
Q

Describe the process of an action potential

A

Action potential:

When there is stimulus, the voltage gated sodium channels open
Positively charged sodium ions rush into cell → thus causing depolarisation
Depolarisation leads to opening of voltage gated calcium channels, thereby calcium ions enter the cell
Calciums triggers release of glutamate from vesicles
Neuron releases glutamate (excitatory neurotransmitter) into synaptic cleft.
triggers action potential from next neuron.

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16
Q

Roles of GABA and glutamate

A

Glutamate binds to AMPA receptors → leads to entry of sodium ions
Glutamate also binds to NMDA receptors → leads to entry of calcium ions
Calcium can also enter via T type Ca channels causing depolarization.
Hyperactivity of glutamate can lead to seizures.

GABA is released into synaptic cleft and binds to GABA-A receptors on the excitatory neuron causes them to open and allow negatively charged Cl- ions to enter.
GABA is removed from synaptic cleft via reuptake through the GABA-transporter-1 (GAT1) and degraded by an enzyme gamma-aminobutyric acid (GABA-T)

17
Q

How does the alteration of neurotransmitters relate to the pharmacological effects of commonly used antiepileptic drugs in preventing or reducing the seizure occurrence?

A

Sodium channel actions ( effective at treating focal seizures)
voltage-gated sodium channels antiepileptics that block sodium channels and reduce the amount of sodium that enters the neuron.

Decrease high frequency discharge from neurons without decreasing low frequency neurons

Calcium channel actions
Blockade of high voltage-activated channel (P/Q type) This channel modulates the release of excitatory neurotransmitters such as glutamate. Therefore, inhibition of alpha-2-delta-1 containing calcium channels can reduce seizures.
Blockade of low voltage-activated (T type) is effective at treat absence seizures.

Modulation of SVA2**
Binds to SV2A protein that are found in the walls of vesicles that contain glutamate. → binding to SV2A impair the synaptic release of glutamate and thus decrease neuronal excitability

GABA-related actions
Blockade of GABA transporter (GAT1a selective)
Blocking GABA reuptake, thereby prolong GABA inhibitory actions in synaptic cleft. Inhibition of GABA transaminase (preventing break down of GABA)

Allosteric activation of GABAA receptors
Make GABA more able to bind
Benzodiazepines, topiramate (Topiromate can also inhibit excitatory neurotransmission by blocking AMPA receptors. )

18
Q

Define Drug Resistant Epilepsy

A

Drug resistant epilepsy may be defined as failure of trials of two tolerated, appropriately chosen anti-epileptic medicine schedules to achieve sustained seizure freedom.

19
Q

Define Drug responsive epilepsy

A

Drug‐responsive epilepsy is defined as seizure‐free for a minimum of three times the longest pre intervention inter-seizure interval or 12 months, whichever is longer

20
Q

What are common trigger factors for seizures

A

Trigger factors can directly cause a seizure (e.g. strong emotions, intense exercise, loud music, high dose alcohol, illicit stimulant drugs and flashing lights ).
OR
Lower seizure thresholds rather than directly causing a seizure (e.g. fever, menstrual period, lack of sleep, stress , medications etc.)

21
Q

What common medications lower seizure threshold?

A

Analgesics - opioids
Anticancer drugs
Antimicrobials - Cephalosporins (fourth generation), penicillin etc
Hypoglycaemic agents - any anti-diabetic
Psychiatric medications - Antipsychotics, SSRI, Lithium
Pulmonary drugs
Stimulant drugs
Sympathomimetics and decongestants - phenylephrine
Hormones