11.1 The Brainstem EEG and Epilepsy Flashcards

1
Q

Describe where the brainstem starts and finishes anatomically

A

Begins at the foramen magnum and extends to the thalamus

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2
Q

How is the brainstem attached to the cerebellum anteriorly?

A

by 3 peduncles

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3
Q

What is the Reticular activating system (RAS)?

What is the main neurotrasmitter released here?

A

Network of neurons connecting the central core of the brainstem to extensive cortical areas: controls level of consciousness and alertness!!

It receives widespread sensory input and controls ascending information. It also has decending projections which control sensitivity of motor nuclei

Cholinergic neurons near junction of pons and midbrain

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4
Q

What can an fMRI show us?

A

RAS activity alters in REM, non-REM sleep and wakefulness

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5
Q

Describe the sleep-wake transition of RAS, when it is used clinically and what may occur when this goes wrong

A
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6
Q
# Define sleep
Define Coma
A

Sleep: a state of unconsciousness from which a person can be aroused

Coma: a state of unconsciousness from which a person cannot be aroused

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7
Q

Give 3 things important about sleep

A

Essential for normal human well-being

1) Memory consolidation
2) Repair of oxidative stress–restorative functions
3) Chronic sleep problems a/w neurodegeneration and mental health

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8
Q

What is Insomnia and give 4 causes

A

Failure to obtain the acquired amount or quality of sleep to function normally through the day

Causes: Mental health, drugs, pain, old age, technology

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9
Q

Give 4 ways to manage insomnia?

A

1) Sleep hygiene
2) Hypnotics
3) Z-drugs and benzodiazepines
4) Muscles relaxation, amnesic, anxiolytic, anticonvulsant
5) Enhance GABA-mediated neurotransmission

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10
Q

Give 4 issues with drugs given to treat insomnia

A

Addiction, dependence, day time sedation, tolerance

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11
Q

What is Hypersomnia and give 4 causes

A

Excessive daytime sleepiness

Causes: OSA, drugs, ETOH, depression/anxiety

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12
Q

What is Narcolepsy?

What symptom and what brain structure it is a/w

A

Irresistible sleep episodes lasting 5-30 minutes during the day

a/w cataplexy (loss of muscle tone/paralysis) and linked to abnormalities in the RAS

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13
Q

What is Parasomnia?

A

Sleep paralysis, sleep walking/talking, night terrors, confusional arousal

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14
Q

What is an EEG?

A

Electrodes on the scalp ➞ voltage recorded between 2 electrodes

Allows us to look at the brain activity of neurons and is best for sleep studies and epilepsy ➞ demonstrates several stages of sleep

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15
Q

What are the 4 basic waves seen on an EEG and which is seen during each stage of sleep

A

1) Beta – >14Hz = mental activity – frontal lobes
2) Alpha – 8-13Hz = relaxed and awake, occipital region and alters with eye opening/closing
3) Theta – 4-7Hz = drowsy, first stages of sleep
4) Delta – <4Hz = deep sleep

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16
Q

Compare our REM vs non-REM sleep (3)

A

REM:

  • Increases in length throughout the night – 10mins first cycles to 50mins last
  • Heart rate and respiration increase to awake levels
  • Dreams

Non-REM:

  • Restorative
  • Decreased cerebral blood flow, reduced O2 consumption
  • Reduced heart rate and breathing
17
Q

What is Epilepsy?

A

Umbrella term for many different seizure types/syndromes

It is a brain disorder that is characterised by periodic, unpredictable seizures, caused by the rhythmic, excessive and disorganised firing of groups of neurons

18
Q

List 4 ways in which epilepsy can present and describe these

A

1) Partial (focal) – remains within one small CNS site e.g. temporal lobe epilepsy (concious)
2) Complex – impairment of consciousness
3) Generalised – spread throughout both hemispheres and usually loss of consciousness
4) Secondary generalisation – when a partial seizure progresses into a generalized seizure

19
Q

Give 2 symptoms which may occur following a seziure and describe these

A

1) Postictal – state of reduced consciousness following a seizure
2) Todd’s paralysis – focal weakness in part or all of the body following a seizure (mins-hrs)

20
Q

Give 3 treatments of epilepsy

A

Treatments are aimed at suppression of the excitable focus

1) Medications- suppress neuronal membrane excitability by…

  • Increase inhibitory neurons – GABA agonists
  • Reduce excitatory neurons – Glutamate antagonists
  • Stabilise membranes to prevent re-firing – ion channels

2) Surgical – removal of the epileptogenic focus
3) Diet – ketogenic diets

21
Q

Give 4 causes of Epilepsy

A

Anything that damages or disrupts normal neuronal transmission such as: Trauma, haemorrhage, ischaemia, hypoxia, infection, hyperthermia, scar tissues,

NOTE: it is idiopathic 2/3rd of the time

22
Q

Describe Partial (focal) epilepsy (5)

A

We have consciousness preserved!!

Begins with motor/ sensory/ autonomic phenomena depending on cortical area affected

Motor, sensory, visual, olfactory, auditory/vestibular, frontal

May become secondary generalized

Mimic TIA/stroke symptoms or migranous aura

23
Q

Describe Complex partial epilepsy

A

Consciousness and memory impaired!!

Typically temporal lobe in origin e.g. temporal lobe epilepsy (due to temporal lobe scaring from insults early on in life) thus usually presents during late adolescence

Features: sensory, autonomic, motor, déjà vu, hallucinations and often a postictal phase and poor recall of events

24
Q

Describe generalised epilepsy

A

Generalised seizures involve both cortices and usually loss of consciousness with or without convulsions

25
Q

Describe Tonic/clonic or ‘Grand mal’ seizures

A

Initial phase of Tonic ➞ muscles go stiff and Clonic ➞ muscles jerk… followed by a period of unconsciousness

26
Q

Describe Absence or ‘petit mal’ seizures

What specific EEG change may be observed

A

Usually diagnosed in childhood and generally grow out of it ➞ those that don’t may go onto convulsive epilepsy

Seizures typically a few seconds hence go unnoticed for some time.

Patient has no memory and no postictal state

EEG highly specific – 3Hz spike and wave pattern (NB hyperventilation)

27
Q

Describe Juvenile myoclonic epilepsy

Is there a genetic link?

A

This is a form of generalised epilepsy (5-10%)

Onset in early adolescence and sometimes overlooked as clumsy… Eventually turn to generalized convulsion

Seizures consist of involuntary jerky movements mostly in the morning

T6 genes identified and great outcomes with specific anti epileptic drugs such as sodium valproate or lamotrigine (lifelong)

28
Q

Describe Status epilepticus

A

Consists of continual seizure with no or little interictal period typically >5mins

This is a Medical emergency because there is a high risk of hypoxia, thermal damage, muscle damage, lactic acidosis, electrolyte imbalance, shock