Neuro Flashcards

1
Q

Where do the demyelinating plaques occur in MS? and what symptoms does this give?

A

Occurs:

  • Optic nerves: optic neuropathy & pain on movement
  • Paraventricular regions: slow gait speed and mental ability
  • Brainstem: sudden diplopia and nystagmus
  • Spinal cord: spastic paraparesis + urinary symptoms
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2
Q

Explain Unthoffs phenomena

A

Unthoffs phenomena - symptoms worse on heat and exercise

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3
Q

What investigations could you do to someone with MS and what would they show?

A

MRI - multiple plaques seen in paraventricular regions, corpus callosum, cerebellar peduncles, brainstem and cervical cord

LP - Oligoclonal bands IgG electrophoresis

EV - evoked potentials

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4
Q

What do you have to have to make a diagnosis of MS?

A

Lesions disseminated in time and space

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5
Q

What treatment can you give for

a) acute relapses
b) Active relapsing and remitting
c) Severe relapsing and remitting

A

a) Acute relapses = steroids: methylprednisolone
b) Active relapsing and remitting = beta interferons,
c) Severe relapsing and remitting = monoclonal antibodies: Natalizumab

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6
Q

What are the different types of MS?

A

Relapsing and remitting
Rapdily progressive
Primary progressive
Secondary progressive

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7
Q

What are the differentials for MS?

A

SLE

CNS sarcoidosis

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8
Q

Describe Gillian-barre syndrome

A

= acute inflammatory demyelinating polyneuropathy

Trigger = infection
Progressive symmetrical weakness/numbness of the distal muscles which can eventually progress to the proximal muscles
Areflexia
Autonomic neuropathy: arrhytmias, increased HR, Sweating and urinary retention

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9
Q

What are the diagnostic features of GBS?

A

Required: progressive weakness of all 4 limbs & areflexia
Supportive: progressive over 4 weeks, symmetrical, mild sensory impairment, autonomic dysfunction, no fever at onset
Recovery 2 weeks after the period of progression has stopped

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10
Q

How do you treat BGS?

A
Suportive AAAA 
Airway support 
Analgesia: NSAID 
Autonomic: catheters 
Antithrombin: LMWH 

Iv Immunoglobulin
Plasma exchange

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11
Q

Which gland is associated with MG?

A

Thymus

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12
Q

What type of medication is pyridostrigmine?

A

Anticholinesterase

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13
Q

What are the treatment options for MG?

A

Symptoms: anti cholinesterase = pyridostigmine
Immunosuppression: Prednisolone/methotrexate
Thymectomy

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14
Q

Which nerve is involved in carpal tunnel syndrome?

What movement does this nerve do?

A

Median nerve - C6-T1

Pincer grip

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15
Q

What is dysphonia?

Give some causes

A

Dysphonia = difficulty producing sound of the voice - hoarse/whispered speech
Causes: laryngitis, CNX lesions, Parkinsonism

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16
Q

What is dysarthria?

Give some causes

A

Difficulty speaking - poorly articulated/slurred
Basal ganglia - parkinsonism, dystonic
Motor-end plate - MG
Brainstem- bulbar

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17
Q

What is dysphagia?

A

Disorder of language content

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18
Q

What are the two different types of aphasias?

A

1) Fluent/receptive aphasia
Problem understanding - werkicke’s aphasia

2) Non-fluent/expressive aphasia
Problem articulating
Broca’s aphasia

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19
Q

Contralateral homonymous hemianopia with macular sparing
Visual agnosia
a) ACA
b) MCA
c) PCA
d) Retinal/opthalamic artery
e) Basilar Artery
f) Weber’s syndrome (branches of the PCA that supply the mid brain)
g) PICA (lateral medullary syndrome, Wallenberg syndrome)

A

Contralateral homonymous hemianopia with macular sparing

Visual agnosia

c) PCA

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20
Q

Amaurosis fugax

a) ACA
b) MCA
c) PCA
d) Retinal/opthalamic artery
e) Basilar Artery
f) Weber’s syndrome (branches of the PCA that supply the mid brain)
g) PICA (lateral medullary syndrome, Wallenberg syndrome)

A

Amaurosis fugax

d) retinal/opthalamic artery

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21
Q

‘Locked-in’ syndrome

a) ACA
b) MCA
c) PCA
d) Retinal/opthalamic artery
e) Basilar Artery
f) Weber’s syndrome (branches of the PCA that supply the mid brain)
g) PICA (lateral medullary syndrome, Wallenberg syndrome)

A

‘Locked-in’ syndrome

e) Basilar artery

22
Q

Contralateral hemiparesis and sensory loss, lower extremity > upper

a) ACA
b) MCA
c) PCA
d) Retinal/opthalamic artery
e) Basilar Artery
f) Weber’s syndrome (branches of the PCA that supply the mid brain)
g) PICA (lateral medullary syndrome, Wallenberg syndrome)

A

Contralateral hemiparesis and sensory loss, lower extremity > upper
a) ACA

23
Q

Contralateral hemiparesis and sensory loss, upper extremity > lower
Contralateral homonymous hemianopia
Aphasia
a) ACA
b) MCA
c) PCA
d) Retinal/opthalamic artery
e) Basilar Artery
f) Weber’s syndrome (branches of the PCA that supply the mid brain)
g) PICA (lateral medullary syndrome, Wallenberg syndrome)

24
Q

Ipsilateral: facial pain and temperature loss
Contralateral: limb/torso pain and temperature loss
Ataxia, nystagmus
a) ACA
b) MCA
c) PCA
d) Retinal/opthalamic artery
e) Basilar Artery
f) Weber’s syndrome (branches of the PCA that supply the mid brain)
g) PICA (lateral medullary syndrome, Wallenberg syndrome)

25
Q

Ipsilateral CN III palsy
Contralateral weakness of upper and lower extremity
a) ACA
b) MCA
c) PCA
d) Retinal/opthalamic artery
e) Basilar Artery
f) Weber’s syndrome (branches of the PCA that supply the mid brain)
g) PICA (lateral medullary syndrome, Wallenberg syndrome)

A

Webbers syndrome

26
Q

What is menieres disease?

A

Disorder of the inner ear - intermittent endoolymph HTN

Attacks of severe vertigo, N&V, low frequency hearing loss, tinnitus and a feeling of a full ear

27
Q

How do you diagnose benign paroxysmal positional vertigo?

A

Hallpikes Manoeuvre

28
Q

How do you diagnose menieres disease?

A

Audiomety documented low to medium frequency sensioneural hearing loss
>2 episodes of vertigo between 20m-12 hours long
Fluctuating aural symptoms

29
Q

How do you treat menieres disease?

A

Low sodium diet
Thiazide diuretic - bendroflumethiazide
Surgical - endolymphatic sac removal

30
Q

What spinal cord disorders can cause dizziness?

A

MS

B12 deficiency

31
Q

What are the 3 parts of GCS and what are they out off?

What is the value for a comatose patient and a totally unresponsive patient?

A
Eye opening /4
Verbal /5
Motar /6 
Comatose = 8/15 
Totally unresponsive = 3/15
32
Q

Give some causes of coma

A

V = cerebrovascular disease, hypoxic-ischamic injury
I = meningitis, encephalitis, sepsis
T = trauma
A
M = Hypoglycemia, DKA, hyperglycaemia hyperosmolar state, hypothyroid, acute renal failure, hepatic encephalopathy
I = Opioid (give naloxone) Benzodiazepine (flumazenil)

33
Q

How can you tell if someone is brain stem dead?

A

Eyes: 1) pupil 2) blink 3) move side-side
Ears: Eye movement to temp
Gag, cough and pain

Pupillary light reflex
Corneal reflex - V & VII
Oculocephalic reflex - eyes move side to side when head is move to remain looking at a fixed position

Caloric reflex - eyes move to ear when warm/cold water is added

Pharyngeal gag reflex, laryngeal cough reflex
Response to pain in the trigeminal distribution

34
Q

What is a apnea test?

A

This is mandatory to diagnose someone as brain stem dead - ventilatory support is slowly turned off and their co2 levels are monitored
+ve - if they rise and there is no response/increased respiratory effort made

35
Q

What is Guillian-Barre syndrome?

A

It is an acute demyelinating polyneuropathy with absent reflexes

36
Q

What can trigger GBS?

A

Campylobacter jejuni
EBV
CMV
HIV

37
Q

What are the signs that you might see with GBS?

A
Observation - fasciculations 
T: Hypotonia 
P: reduced power 
S: Altered sensation 
R: absent or reduced reflexes
38
Q

What might you see in LP of GBS?

A

Increase in CSF proteins but not cells

39
Q

How do you treat GBS?

A

Supportive - analgesia, catheters or LMW heparin (DVT prophylaxis is essential)

  • Plasma Exchange (remove the abs)
    or//
  • IV immunoglobulins (reduce to immune response)
40
Q

What are the complications of GBS?

A

Persistent paralysis
Resp failure (measure FVC 4 hourly)
VTE
Cardiac arrhythmias

41
Q

What is MG?

A

Its an AI disease with auto-abs to the ACh receptors at the NMJ

42
Q

Which drugs can exacerbate MG?

A
BB 
Aminoglycoside abs (gentamicin)
43
Q

What is Lambert-eaton syndrome and what conditions is it associated with?

A

It is opposite to MG
Repeated muscle contractions leads to increased muscle strength (less fatiguability following repetition)
Its due to abs against the pre-synaptic voltage gated calcium channels in the peripheral NS

Associated with SCLC, breast and ovarian ca

44
Q

The Revised El Escorial Criteria is used to make sure other possible causes have been ruled out before making a diagnosis on MND.
What pointers are suggestive of MND?

A

Asymmetrical distal weakness
Brisk reflexes in a wasted limb
No major sensory/pain
Relentless progression of signs and symptoms

45
Q

What are the SE of levodopa?

A

Dyskinesia
“on/off” effects
Postural hypotension
Psychosis

46
Q

Give examples of the dopamine receptor agonists

& SE

A

Bromocriptine, ropinirole + cabergoline

SE: impulse control, excessive daytime sleeping, hallucination, postural hypotension

47
Q

What can you give for prophalaxis of cluster headaches?

48
Q

What are the red flags of headaches?

A

Signs of raised ICP (worse in the morning, vomiting)
Headache with new onset seizure/focal neurological deficit
Thunderclap
Jaw claudication/visual disturbances
Signs of meningism - neck stiffness/photophobia
Progressively worsening

49
Q

What are SAH associated with?

A

HTN + Poly cystic kidney disease

50
Q

What would you see on a LP of SAH?

A

Xathnochromia

51
Q

How would you treat SAH?

A

A–>E
Prevent vasospasm = Nimodipine
Prevent re-bleeding = endovascular clipping and coiling