Neurology Flashcards

1
Q

Wernicke’s Encephalopathy triad

A

ophthalmoplegia: nystagmus/ lta rectus palsy, conjugate gaze palsy

ataxia, encephalopathy

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2
Q

Korsakoff’s syndrome

A

IRREVERSIBLE

ophthalmoplegia, ataxa, encephalopathy, antero/retrograde amnesia, confabulation

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3
Q

Mx Generalised Toni-clonic

A

M: sodium valporate
F: lamotrigine/levetiracetam

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4
Q

Focal seizure 1st line

A

lamotrigine/ levetiracetam

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5
Q

Focal seizure 2nd line

A

cabamazepine/ oxcarbazepine/ zonisamide

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6
Q

abscence seizure 1 st line

A

ethosuxide

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7
Q

abscence seizure 2nd line

A

M: sodium valporate
F: lamotrigine/ levetiracetam

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8
Q

myoclonic seizure Tx

A

M: sodium valporate
F: levetiracetam

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9
Q

Tonic/ Atonic seizures Tx

A

M: sodium valporate
F: lamotrigine

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10
Q

migraine prophylaxis

A

propranolol
topiramate avoid in women of childbearing ge
amitriptyline

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11
Q

Acute mx cluster headache

A

O2 100%
sc triptan

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12
Q

TIA mx

A

300mg aspirin stat unless taking low dose aspirin already

If more than 1 episode tia/ suspected cardio emboli’s or severe stenosis- referral for admission

If 1 tia within 7 days assessment within 24 hours

If tia >7d days refer r/v within 7d

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13
Q

Ix Parkinsons

A

I123-FP-CIT-SPECT=> DatScan

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14
Q

1st line Parkinsons tx

A

Levodopa

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15
Q

Parkinsons mx

A

1st line: Levodopa

2nd line: Levodopa + Dopamine AG/ MAO-Bi/ COMTi

DA-R AG: bromocriptine, ropinirole, cabergoline, apomorphine: younger pt/ mild sx

MAOB-i: selegiline

COMTi: entacapone, tolcapone

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16
Q

SE Dopamine R AG

A

ergot- derived DA-R AG: bromocriptine, cabergoline-> pulmonary/ retroperitoneal/ cardiac fibrosis

elderly pt: increased risk hallucinations

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17
Q

TACI (total anterior circulation infarcts)

A

involves middle and ant cerebral arteries
unilat hemiparesis +/- hemisensory loss face, arm, leg. Homonymous hemianopia, increased cognitive dysfunction

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18
Q

PACI (partial naterior circulation infarcts)

A

2 of the criteria
unilat hemiparesis +/- hemisensoryloss face/ arm/ leg. homonymous hemianopia. increased cognitive dysunfctionction

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19
Q

LACI (lcunar infarcts)

A

involves perforating arteries around internal capsule, thalamus and basal ganglia. 1 of follwing present. Unilateral weekness +/- sensory deficit of face and arm, arm and leg or all three. Pure sensory stroke. Ataxic hemiparesis

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20
Q

Posterior circulation infarcts (POCI)

A

vertebrobasilar arteries. Presens with 1 of following. Cerebellar or brainstem syndromes. Loss of consciousness. Isolated homonymous hemianopia. (Lateral medullary stndrome aka Wallenberg’s syndrome)

21
Q

Ischaemic stroke timing of thrombolysis + Mx
Mx stroke related to AFib when to start DOAC

A

4.5 hr
Aspirin 300mg ASAP
if DOAC- not started until r/o haemorrhage not until 14d passed from onset of ischaemicc stroke

22
Q

When to consider thrombectomy

A

Pre stroke functional status <3, modified rakin scale and score >5 NIHSS

Offer thrombectomy ASAP within 6hrs of onset with iv thrombolysis 4.5hr to pts with acute ischaemia.

Thrombectomy ASAP last known to be well 6-24hrs previously

23
Q

how long to give aspirin or clopidogrel in stroke

24
Q

GCS

A

EVM

E: spontaneous, command, pain, nil
V: orientate, confused, words non sense, incomprehensible sound

M: command, localises pain, withdraw from pain, flexion, extension, no motor response

25
Cranial nerve: which Sensory, motor, both
Some say marry money but my brother says big brain matters most
26
Central vs peripheral VII nerve palsy
Central contralateral droop of lower half of mouth to lesion as other half also innervated by ontralateral side Peripheral inability to wrinkle forehead and drop of half mouth on ipsilateral side of lesion
27
Hand position when damage to ulnar & radial nerve
Radial nerve: wrist drop Ulnar: claw hand
28
AFib related stroke when to start DoAC
14 days passed from ischaemic stroke due to high risk of haemorrhage
29
Timing of thombolysis and thrombectomy
Thrombolysis 4.5 hrs Thrombectomy 6hrs
30
Causes of SAH
Traumatic cause Spontaneous
31
Dx of SAH timing of LP
CT head within 6 hours of sx onset: if negative then Lp not needed If more than 6 hours sx onset & normal: do LP, needs to be perform at least 12 hours following sx onset as checking for xanthochromia. Norma, or high opening pressure
32
Mx of SAH
Supportive Vasospasm: po nifedipine Intracranial aneurysm: coil Can develop hyponatraemia: due to SIaDH
33
Acute to of migraine
Po triptan and NSAIDS or po triptan and paracetamol
34
Cluster headache mx and prophylactic
Acute oxygen 100% Subcutaneous triptan Prophylactic:verapamil , tapering dose of prednisone
35
Inheritance of essential tremor and mx
AD Propranolol 1st line Primidone sometimes used
36
Motor neuron investigation
Clinical but nerve conduction can help exclude neuropathy EMG: decreased number of action potential with increased amplitude MRI: exclude diff dx of cervical cord compression and myelopathy
37
Motor neuron disease mx
riluzol: prevents activation of glutamate receptor n-invasive bipap
38
GBS cause, Ix, is it ascending or descending
Peripheral nervous system demyelination, ascending paralysis. Campylobacter jejuni LP: increased protein with normal WBC Nerve conduction decreased motor nerve conduction velocity due to demyelination, prolonged distal motor latency, f wave latency increased
39
Miller fisher syndrome
Ophthalmoplegia, areflexia, ataxia: eye muscle affected first. Variant of GBS Anti GQ1b Ab
40
Huntington genetics
AD triculeitide repeat disorder CaG on chromosome 4 Anticipatory
41
Neuropathic pain mx
1St line: amitriptyline, duloxetine, gabapentin, pregabalin Reduce: tramadol- rescue tx
42
Causes of neuroleptic malignant syndrome
Pt taking antipsychotics Slower onset- hours to days
43
Mx of neuroleptic malignant syndrome
Stop antipsychotics Ivi Dantrolene decreases excitation contraction skim binding to ryanodine receptor. Decreases release of calcium from sarcoplasmic reticulum
44
Multiple sclerosis classification
1. Relapsing remitting 2. Secondary progressive 3. Primary progressive
45
Uhthoff’s phenomenon, most common findings in MS, Lhermitles syndrome, what kind of muscle weakness
Uhthoff: worsening vision after increased body temp in Ms Lhermitles : paraesthesia in limbs on neck flexion Most common eye signs: optic neuritis Motor spastic weakness due to demyelination along nerves of brain and spine
46
Dx of Ms
Demonstration of lesion disseminated in time and space MRI: initial test- increased signal T2 lesion, periventricular plaque, Dawson fingers often seen on FLAIR images hyperintense lesion perpendicular to corpus callous. 2. csf: oligoclonal bands and not in serum , increased intrathecal synthesis of IgG Visual field: visual evoked potential delayed but well preserved waveform
47
Dystrophies types, inheritance, classic findings
XR dystrophin xp21 Duchenne frameshit, severe form- calf pseudohypertrophy, growers sign Becker insertion less severe form
48
Herpes simplex encephalitis ix
CSF: lymphocytosis, increased protein Pcr for hsv Ct: medial temporal and inferior frontal changes MRI
49
Mx of migraine in children and adults and prophylaxis
Children: acute mx- ibuprofen more effective than paracetamol. >12 years triptan may be used but follow up needed. Sumatriptan nasal spray is the only proven triptan. Prophylaxis pizotifen + propranolol 1st line. 2nd line- valporate/ topiramate/ amitriptyline Adult: 1st line- oral triptan + nsaid OR po triptan + paracetamol If not effective than offer n-oral pre metoclopramide/ prochooperazine with or without n-oral nsaids. Triptan Prophylaxis- propranolol, topiramate not in female in childbearing age, amitriptyline