Session 9: Cortical Dysfunction Flashcards

1
Q

What is Dementia?

A
  • Progressive deterioration of higher cortical function.
  • Dementia overall results in neuronal degeneration throughout the cortex which accounts for its wide variety of symptoms and clinical picture.
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2
Q

What is the presentation of dementia generally?

A
  • Memory Deficit: struggle to learn new information, short term memory loss
  • Behavioural: altered personality, disinhibition, labile emotions, wandering
  • Physical: incontinence, reduced oral intake, difficulty swallowing
  • Language disorder: anomic aphasia, difficulty understanding language
  • Visuospatial disorder: unable to identify visual and spatial relationships between objects
  • Apraxia: difficulty with motor planning resulting in inability to perform learned purposeful movements
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3
Q

What investigations are done for Dementia?

A
  • Full history + MMSE (assess the degree of cognitive impairment and rate of progression of disease)
  • Full neurological examination
  • Blood Test
  • CT/MRI head (rule out other causes such as tumour and check for features of dementia)
  • Memory Clinic follow up
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4
Q

What are features of dementia on CT/MRI head?

A
  • Dilatation
  • Generalised Atrophy
  • Hippocampal Atrophy
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5
Q

What does a CAM Score assess?

A
  1. Acute change or fluctuating mental status
  2. Altered consciousness – hypo (refusing food or drink) /hyperactive (rambling)
  3. Inattention
  4. Disorganised thinking
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6
Q

What CAM score describe delirium?

A

Combination of 1+2 and either 3 or 4 shows Delirium

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7
Q

What are the common non reversible causes of Dementia?

A
  • Alzheimer’s Disease (commonest cause of dementia. Account for 60-80% of cases)
  • Dementia with Lewy-Bodies
  • Fronto-temporal Dementia
  • Vascular Dementia
  • Crutzfeldt-Jacob disease
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8
Q

What are the common reversible causes of Dementia?

A
  • Depression
  • Trauma
  • Vitamin Deficiency
  • Alcohol
  • Thyroid Disorder
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9
Q

What is the macroscopic pathology of Alzheimer’s disease?

A

-Loss of cortical and subcortical white matter causing gyri atrophy with narrow gyri and wide sulci along with mark ventricular dilation reflecting loss of white matter

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10
Q

What is the microscopic pathology of Alzheimers disease?

A

Formation of

  • Amyloid-beta plaques (proteolytic break down from amyloid precursor protein)
  • Neurofibrillary tangles

Causes degeneration

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11
Q

What is the Clinical picture of Alzheimer’s disease?

A
  • Starts with minor memory loss which may not be initially noticed or impact on their life
  • Progression to development of problems with visuospatial awareness and apraxia making it difficult to carry out daily tasks such as getting dressed and cooking.
  • In Alzheimer’s disease, there is a slowly linear decline over many years with no recovery, until the patient is incontinent, unable to recognize loved ones and loses a sense of self
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12
Q

What is the microcopid pathology of Dementia with Lewy bodies?

A

-Lewy Bodies in the cortex and Substantia nigra

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13
Q

What is the clinical picture of Dementia with Lewy bodies?

A
  • Substantial fluctuating decline in cognition over time which may improve for a while and then drop back down.
  • Parkinson’s symptoms (Bradykinesia, Tremor, Rigidity, Postural instability resulting in falls, Visual hallucination)
  • Unresponsive to dopamine agonist treatment in the same way Parkinson’s disease would be
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14
Q

What is the pathology involved in Vascular Dementia?

A
  • Arteriosclerosis of the blood vessels supplying the brain

- Diffuse small vessel disease vs infarcts (large vessel disease)

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15
Q

What is the clinical picture in Vascular Dementia?

A
  • Abrupt, step wise decline in cognitive function related to vascular episode.
  • Following insult, the patient will retain that current level of cognition until another episode occurs.
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16
Q

What is the management of Vascular Dementia?

A

-Assess cardiovascular risk and treat hypertension/high cholesterol

17
Q

What are the pathologies associated with Fronto-tempoal dementia?

A
  • Frontotemporal lobar degeneration with tau pathology
  • Pick’s disease
  • Familial tauopathies
18
Q

How is Dementia Holistically managed?

A
  1. Therapies
    - Pets, Babies
  2. Memory aids
    - Orientation boards, Remembrance Therapy, Life stories
  3. Social care
    - Risk Assessment, Care Needs, Mental Capacity Act
    - More important to manage the social implications and concerns of the family.
    - Need to make sure the patient is safe and act in their best interest which may require care at home or a permanent nursing home placement
  4. Drugs
    - Cholinesterase inhibitors(group of drugs shown to slow progress of disease temporarily in some patients with mild-moderate Alzheimer’s but this is only temporary)
    - Memantine
19
Q

What is a seizure?

A

-A sudden irregular discharge of electrical activity in the brain causing a physical manifestation such as sensory disturbance, unconsciousness or convulsion.


20
Q

What is a convulsion?

A

-Uncontrolled shaking movements of the body due to rapid and repeated contraction and relaxation of muscles

21
Q

What is an aura?

A

A perpetual disturbance experienced by some prior to a seizure e.g. strange light, unpleasant smell, confusing thoughts 


22
Q

What is epilepsy?

A

Neurological disorder marked by sudden recurrent episodes of sensory disturbance, LOC or convulsions, associated with abnormal electrical activity in the brain

23
Q

What is Status Epilepticus?

A
  • Epileptic seizures occurring continuously without recovery of consciousness in between
  • Medical emergency
24
Q

What are the types of Partial Seizures?

A
  • Simple (same consciousness)

- Complex (consciousness is impaired)

25
Q

What are the types of Generalised Seizures?

A
  • Absence (daydreaming)
  • Myoclonic (brief shock-like muscle jerks)
  • Tonic clonic (1st tonic so muscles tense, 2nd clonic convulsions)
  • Tonic (increased tone)
  • Atonic (without tone so drip attacks occur)
26
Q

What are common examples of partial seizures?

A
  • Temporal lobe epilepsy – 1st/2nd decade in most following seizure with fever or an early injury to the brain
  • Aura e.g. auditory hallucination, rush of memories
  • Frontal lobe epilepsy
  • Abnormal movement when motor area affected
27
Q

What are the investigations done in epilepsy?

A
  • Clinical history
  • EEG
  • MRI (all patients with new-onset seizures)
  • ECG (in all adults)
28
Q

Why is EEG used in Epilepsy?

A
  • Not diagnostic but supports the diagnosis
  • Assess risk of seizure recurrence in there first unprovoked seizure
  • Standard assessment involves photic stimulation and hyperventilation and patient has to be warned that may induce a seizure
29
Q

When shouldn’t you use EEG?

A
  • Probably syncope
  • Clinical presentation support diagnosis of non-epileptic event
  • In isolation to make epilepsy diagnosis
30
Q

What should you do if EEG is unclear?

A
  • Repeat standard EEGs
  • Sleep EEGs
  • Long term video or ambulatory EEG
31
Q

What part of the history before the seizure are you concerned about?

A
  • PMH, FH
  • Triggers
  • Aura
  • First sign/symptom
32
Q

What part of the history during the seizure are you concerned about?

A
  • Description of Seizure
  • Duration
  • Abrupt/gradual end
33
Q

What part of the history after the seizure are you concerned about?

A
  • Post ictal state
  • Tongue biting
  • Incontinence
  • Neurological deficit
34
Q

What are differential diagnosis for Epilepsy?

A
  • Vascular: Stroke, TIA
  • Infection: Abscess, Meningitis
  • Trauma: Intracerebral haemorrhage
  • Autoimmune: Systemic Lupus Erythematous
  • Metabolic: Hypoxia, Electrolyte imbalance, Hypoglycaemia, Thyroid dysfunction
  • Iatrogenic: Drugs, Alcohol Withdrawal
  • Neoplastic: Intracerebral mass

-Congenital

35
Q

What is the management of Epilepsy?

A
  • Lorazepam

- Midazolam

36
Q

What has to be considered with epilepsy and driving?

A
  • If suffers epilepsy when awake, licence is taken away until 1-year seizure-free
  • If due to medication change: 6 months seizure-free
  • Seizures whilst asleep or don’t affect driving or consciousness – assessment of case by DVLA
  • If one-off seizure, then can apply when 6 months seizure-free and assessment by DVLA