Neurology Flashcards

1
Q

How do we reduce ICP?

A

Head up 30 degrees
Hyperventilate –> low CO2 –> vasoconstriction

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2
Q

What kind of haemorrhage doesn’t tend to cause a midline shift?

A

Subarachnoid haemorrhage

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3
Q

How do we manage a non-traumatic (aneurysmal) subarachnoid haemorrhage?

A

CT angiogram to locate site of aneurysm

Nimodipine 60mg 5 per day

Minimise valsalvas (bed rest, codeine to stop coughing, laxatives to stop constipation, antiemetics to stop vomiting)

Don’t give antiepileptic unless prev. seizure

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4
Q

If a pt has a typical subarachnoid haemorrhage history but the CT head comes back normal, what should we consider?

A

Delayed lumbar puncture

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5
Q

What’s the most common brain tumour in adults?

A

Metastasis

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6
Q

How do we investigate an abscess?

A

Diffusion-weighted MRI

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7
Q

If a patient has back pain and insensate incontinence (wet/soiled without realising) then what do we suspect?

A

Cauda equina

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8
Q

How do we investigate cauda equina?

A

Lower limb neuro exam, PR exam

Pin-prick saddle exam

Pregnancy test if Female

Post-void bladder scan

MRI non-contrast of the lumbar spine

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9
Q

On a CT head, if we have “white” blood do we do a Burr hole or not?

A

No bc white blood = thick so Burr hole won’t relieve pressure

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10
Q

On a CT head, if we have “grey” blood do we do a Burr hole or not?

A

Yes, bc grey blood = thin

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11
Q

If we suspect early hydrocephalus, what can we do to manage it?

A

External ventricular drain in theatre

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12
Q

What does chorea mean?

A

Involuntary, random, irregular, purposeless movements

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13
Q

What does the hummingbird sign indicate?

A

Progressive supranuclear palsy

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14
Q

What does the hot cross bun sign indicate?

A

Multiple systems atrophy

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15
Q

What are three types of hyperkinetic movement disorders causing involuntary movements?

A

Tremor, chorea, dystonia

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16
Q

What does finger-thumb tapping getting smaller and slower indicate?

A

Parkinsonism

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17
Q

What do we need to include in a movement disorder history?

A

Tone
Power
Reflexes
Sensation
Co-ordination

18
Q

What’s the pathophysiology of Parkinson’s disease?

A

Depletion of dopamine in the basal ganglia

Reduction of dopamine-producing neurons in the substantia nigra

Inhibition of the thalamus –> bradykinesia

19
Q

What are six causes of seizures?

A

HIP SEA

Hypoglycaemia

Infection: HSV encephalitis

Psych

20
Q

If you have a left cerebellar infarct, where will you see the problem?

A

Left side

(Ipsilateral)

21
Q

Wasting, fasciculations, reflexes present. What are you thinking?

A

Motor Neurone Disease

22
Q

What does pronator drift indicate?

A

Weakness in that arm

23
Q

Does parkinsons have spastic or rigid tone?

A

Rigid

24
Q

What’s the difference between spastic and rigid?

A

Rigid: all the way through
Spastic: worse at the start

25
Q

What can cause promixal weakness?

A

Upper motor neurone lesion
Myopathy

26
Q

What can cause distal weakness?

A

Neuropathy

27
Q

If we just have pain in the dermatome of C7?

A

Radiculopathy - disc jutting out and compressing the nerve

28
Q

What kind of conditions can cause a glove and stocking distribution of sensory loss?

A

Diabetic neuropathy

Alcoholic neuropathy

29
Q

What could “tripping over small steps” indicate?

A

Foot drop (common peroneal nerve palsy)

30
Q

What looks like Guillian Barre but isn’t?

A

Chronic Inflammatory Demyelinating Polyradiculopathy
- polyphasic unlike GB, and milder symptoms, requires long-term treatment, whereas GB is self-limiting.

31
Q

Guess the diagnosis: 24M, high plantar arch, lower leg weakness and distal muscle wasting, peripheral sensory loss.

A

Charcot Marie Tooth disease

32
Q

What are the causes of peripheral neuropathy?

A

ABCDE

A – Alcohol
B – B12 deficiency
C – Cancer (e.g., myeloma) and Chronic kidney disease
D – Diabetes and Drugs (e.g., isoniazid, amiodarone, leflunomide and cisplatin)
E – Every vasculitis

33
Q

What’s characteristic of Myasthenia Gravis?

A

Variability

34
Q

What causes dyskinetic cerebral palsy? (slow, writhing movements of the limbs)

A

Damage to the basal ganglia and substantia nigra

35
Q

What kind of signs would MS show most? (UMN, LMN, mixed, etc.)

A

UMN
AKA Pyramidal
AKA Long tract

36
Q

What is Lhermitte’s sign?

A

Barber chair sign in MS
When neck is flexed (chin-to-chest), electric shock-like pain

37
Q

What is Uhthoff’s phenomenon?

A

In the context of MS, it is the worsening of vision following rise in body temperature

38
Q

What are the investigations for MS and what would positive results show?

A

Bloods –> HLAB-27

MRI –> demyelinated (white) T2 lesions, periventricular plaques, Dawson fingers

LP –> oligoclonal bands in the CSF, increased intrathecal synthesis of IgG

Delayed visual evoked potentials

39
Q

What do we need evidence of to diagnose MS?

A

Lesions that vary in location and are disseminated in time and space.
–>

Evidence of two or more relapses:

EITHER
objective evidence of =>2 lesions
OR
objective evidence of 1 lesion + history of previous relapse

40
Q

Parkinsonism + autonomic disturbance (postural hypotension, atonic bladder) = ?

A

Multiple System Atrophy