Neuro Flashcards

(51 cards)

1
Q

Dermatome = ?

A

= area of skin supplied by a single spinal nerve/root

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2
Q

Myotome = ?

A

= volume of muscle supplied by a single spinal motor nerve

most muscles have more than one myotome

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3
Q

What does the lateral corticospinal tract control

A

rapid, skilled, voluntary movement

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4
Q

what does the anterior corticospinal tract control

A

rapid skilled voluntary movement

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5
Q

vestibulospinal tract role?

A

facilitates extensors, inhibits flexors (controls dizziness) and balance

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6
Q

rubrospinal tract role

A

facilitates flexors and and inhibits extensors

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7
Q

tectospinal tract role

A

truncal reflexes from sigths

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8
Q

Define TIA

A

= transient and reversible episode of sudden onset neurological dysfunction caused by ischaemia without acute infarction
symps usually resolve within 24 hours

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9
Q

Where do most TIAs occur

A

in the anterior circulation (carotid territory)

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10
Q

what are the most rapid acting antihypertensives used in acute BP lowering after stroke/haemorrhage

A
  • IV labetamol (BB)

- IV GTN

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11
Q

define syncope attack

A

= paroxysmal event where changes in behaviour, sensation and cognitive processes are caused by insufficient blood/oxygen supply to the brain

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12
Q

3 causes of blackouts

A

syncope
epilepsy
non-epileptic seizures

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13
Q

precipitating factors for status epilepticus

A

alcohol abuse
abruptly stopping AEDs
intercurrent illness
poor compliance with tx

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14
Q

define myotonia

A

= delayed relaxation of muscle after contraction

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15
Q

characteristic pathology/general symptoms of MG

A

weakness and fatiguability of occular, bulbar and proximal limb muscles

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16
Q

4 conditions assoc w MG

A

RA
thyroid disease
pernicious anaemia
SLE

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17
Q

Ab involved in MG

A

anti-AChR and anti-MuSK

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18
Q

histology of MG

A

See AChR Ig and complement deposited at post synaptic membranes

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19
Q

occular symptoms of MG

A

diplopia, ptosis

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20
Q

What worsens the weakness experienced in MG

A
pregnancy
hypokalaemia
emotion
infection
exercise
drugs
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21
Q

Mx of MG

A

PYRIDOSTIGMINE (= acetyl-cholinesterase inhibitor)
if not controlled, add steroids, gradually decrease prednis dose
if not controlled still, add MTX/azathioprine
thymectomy if difficult to control
plasmapharesis in severe exacerbation

22
Q

what is the most common form of MND and what neurones are involved

A

Amyotrophic lateral sclerosis (ALS) - UMN & LMN

23
Q

different patterns of onset in MND

A
limb onset (most common)
bulbar onset (worse prognosis - 20%)
resp onset (least common)
24
Q

how would you distinguish MND from MS, MG and GBS

A

in MND:

  • bladder and rectal sphincters usually spared
  • no sensory symps
25
MND (ALS) general symps
eventually weakness and atrophy of all 4 extremities, trunk and bulbar muscles
26
characteristic sign in MND
fasciculations
27
what is Guillain barre syndrome (GBS)
= acute inflammatory demyelinating ascending polyneuropathy of PNS
28
what is GBS normally triggered by
an upper respt tract/GIT infection
29
common causative agents of GBS
CAMPYLOBACTER JEJUNI, CMV, | others: mycoplasma, zoster, EBV, HIV - 40% no infectious cause found
30
clinical presentation of GBS
1-3 wks post-inf: ascending symmetrical weakness, starting in distal muscles and progressing to more proximal ones over ~4wks followed by recovery see: loss of reflexes, neuropathic pain and autonomic dysfunction
31
signs of autonomic dysfunction
sweating, tachycardia, arrhythmias
32
what may lead to an ITU admission with GBS
involvement of resp muscles, | therefore must monitor FVC regularly in these pts
33
Mx of GBS
IV Ig plasmapharesis (effective but rarely used) MONITOR VENTILATION
34
3 cardinal symptoms/signs of brain tumour
symps of raised ICP progressive neurological deficit epilepsy
35
signs of raised ICP
headache, drowsiness, N&V
36
cardinal physical sign of brain tumour
papilloedema
37
cell origin of most primary brain tumours
glial cell (mainly astrocytomas)
38
what is dexamethasomes action
decreases cerebral oedema
39
Mx of GBM
TEMOZOLOMIDE = chemo has radically improved survival in pts with MGMT mutant other mx: surgical resection (w. post-op chemo), RT,
40
mx of secondary brain tumours
surgery not often poss but surgery and chemo have best outcome BSC often as effective as RT and prolongs QOL
41
causes of meningitis in neonates
E coli, group B B-haemolytic strep
42
causes of meningitis in adults
n. meningitidis, strep. pneumoniae, (h. influenzae)
43
causes of meningitis in eldery
n. meningitidis, strep. pneumoniae, listeria
44
causes of meningitis in immunocompromised
CMV, cryptococcus (stains with INDIA INK), TB
45
S&S of meningitis
``` headache meningism = neck stiffness and photophobia Kernig's and Brudinski sign Non-blanching petechial rash altered mental state (oedema) fever seizures ```
46
Mx of meningitis
if suspect bacterial - start ABX immediately IV cefotaxime (if community benzylpenicillin) if >50 add ampicillin to cover for listeria dexamethasome - decrease cerebral oedema Notify PHE!!
47
prophylaxis of meningitis
rifampicin/ciprofloxacin
48
what is encephalitis
inflam of brain parenchyma | affects frontal and temporal lobes --> decreased consciousness, confusion and focal signs
49
what causes encephalitis
viral infection - most commonly HSV1 and 2 others: varicella zoster, EBV, mumps, measles, CMV, HIV non-viral - secondary to bacterial meningitis, TB, toxoplasma
50
S&S of encephalitis
features of viral inf DECREASED CONSCIOUSNESS behavioural change, focal neurological deficit, coma, seizures
51
mx of encephalitis
if viral URGENT ACYCLOVIR | if meningitis suspected, emergency IM benzylpenicillin