Neuro Flashcards

1
Q

list the types of MS

A

relapsing-remitting, primary progressive, secondary progressive

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2
Q

which areas are most commonly affected by MS

A

optic nerve, cervical cord, periventricular areas

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3
Q

2 signs in MS

A

Lhermitte’s - neck flexion = paresthesia

uthoff’s - worse in heat

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4
Q

investigations in MS

A

MRI - demyelinating plaques
LP - oligoclonal bands
evoked potentials

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5
Q

diagnosis of anterior stroke (ie symptoms) and arteries affected

A

need 3/3 for total and 2/3 for partial
unilateral hemiparesis, hemianopia, dysphasia
middle cerebral (arm), anterior cerebral (leg)

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6
Q

diagnosis of poterior stroke (ie symptoms) and arteries affected

A
one of;
homonymous hemianopia
loss of consciousness
cerebellar syndrome 
vertebrobasilar arteries
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7
Q

diagnosis of lacunar stroke (ie symptoms) and arteries affected

A
1 of; 
unilateral weakness
ataxic hemiparesis
sensory change 
perforating arteries
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8
Q

long term management of stroke

A

aspirin for 2/52 then clopidogrel

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9
Q

management of TIA

A

do ABCDE2

warfarin if AF or clopidogrel if no AF

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10
Q

explain CHADS2Vasc

A

risk of stroke in AF

give warfarin

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11
Q

describe the presentation and CT findings of an extradural and vessel affected

A

lucid period then reduced LOC following temporal bone fracture
fixed dilated pupil due to CN III compression
biconvex lesion with midline shift
middle meningeal

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12
Q

describe the presentation and CT findings of a sub dural

A

fluctuating consciousness. can be chronic.
crescent shaped not limited by suture lines (bright/hyperdense in acute, dark/hypodense in chronic)
bridging veins

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13
Q

describe the presentation and CT findings of subarachnoid

A

sudden onset thunder clap headache, meningism, N&V
star sign, follows suture lines
circle of willis

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14
Q

investigations and management in subarachnoid

A

CT
Lp 12 hrs after onset - xanthochromia
nimodipine

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15
Q

presentation of parkinsons

A

rigidity, bradykinesia (slow intention, shuffling gait), tremor (resting, pill rolling, unilateral)

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16
Q

name the parkinson’s plus syndromes

A

multiple system atrophy - autonomic dysfunction
progressive supranuclear palsy - vertical gaze palsy, postural instability
lewey body dementia - visual hallucinations
vascular - risk factors
corticobasal degeneration - alien limb, sensory loss

trial of levodopa doesn’t help

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17
Q

what drugs are used in parkinsons

A
MAOi's (selegiline)
dopamine agonists (ropinirole) - domperidone as antiemetic is nausea and vomiting
l-dopa and madopar (decarboxylase inhibitor)
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18
Q

acute and chronic treatment of tension headache

A

short term analgesia/ amitriptyline

10 sessions acupuncture over 5-8 weeks

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19
Q

acute and chronic treatment of cluster headache

A

100% oxygen and SC/sublingual triptan

verapimil

20
Q

acute and chronic treatment of migraine

A

oral triptan and analgesia

if get >2 attacks a month give topiramate (can give propranolol)

21
Q

investigations in seizures

A

EEG, CT, glucose , U&E’s

22
Q

management of epilepsy

A
sodium valproate (generalised)
carbamazepine (focal)
23
Q

driving advice in seizures

A

cant drive for 6 months after seizure and cant drive for 1 year seizure free in epilepsy

24
Q

driving advice in TIA

A

at least 1 month off driving

25
management of status epilepticus
buccal midaz , repeat benzo, phenytoin, phenobarbital
26
signs in spinal cord compression
UMN signs BELOW level LMN signs at level of lesion contralateral loss of pain and temperature sensation sphincter disturbance
27
neuro deficits in brown sequard
ipsilateral loss of vibration, proprioception, and fine touch (dorsal columns) and motor function at the level of lesion contralateral loss of pain and temperature 1-2 levels below the lesion
28
management of MS
alemtuzumab beta interferon methylpred in flare up
29
criteria for MND
El escorial criteria UMN and LMN signs no sensory signs progressive course
30
investigations and management of MND
EMG creatinine kinase high riluzole and baclofen for spacisity
31
presentation of myasthenia gravis
``` diplopia/ptosis speech change peek sign snarl swallowing and breathing difficulties ```
32
investigations in myasthenia gravis
Ab's: anti Ach, anti-musk CT thorax for thymus hyperplasia EMG
33
management of myasthenia gravis (chronic and acute)
pyridostigmine, immunosuppression, thymectomy acute: plasma exchange and IVIg
34
triad in normal pressure hydrocephalus
gait abnormality dementia urinary incontinence
35
signs in a c5/6 radiculopathy
loss of biceps reflex (6 letters) | altered thumb sensation
36
signs in C7 radiculopathy
loss of triceps reflex (7 letters) | middle finger sensation
37
signs in L5 radiculopathy
cant stand on heels (dorsiflexion) | big toe sensation
38
signs in s1 radiculopathy
cant stand on toes | absent ankle reflex
39
what does a negative rinne's test mean
bone conduction = better than air conduction | conductive deafness
40
weber's test lateralized to left ear means?
conductive problem in left ear (if rinnes negative) | or sensorineural deafness in right ear (if rinnes positive .- ie. normal rinne's)
41
describe grading of muscle weakness (MRC)
0: no contraction 1: flicker 2: some active movement 3: active movement against gravity 4: active movement against some resistance 5: normal power
42
investigations in memory loss
AMT (out of 10) MMSE (out of 30. <24 = demantia) bloods: B12/folate, FBC, ESR, U&E, calcium, syphilis CT
43
management in dementia
psychosocial | anticholinesterase i's : donepezil, rivastigmine, memantine
44
causes of facial nerve palsy
``` bells (diagnosis of exclusion) ramsay hunt infection stroke tumour diabetes GBS parotid tumour ```
45
what is bells palsy
one half of face paralysed (LMN) CN VII palsy give prednisilone
46
what mononeuropathy gives you foot drop?
common peroneal
47
causes of polyneuropathy
``` diabetes Gbs b12/folate deficiency RA polyarteritis nodosa GPA polycythaemia HIV syphilis lymes disease charcot marie tooth drugs (alcohol, isoniazid, phenytoin, metronidazole, nitrofurantoin) ```