Neurology Flashcards

1
Q

Absolute contraindications to thrombolysis

A
  • Known hypersensitivity/anaphylaxis reactions to the medication or related excipients (increased risk with ACEi use)
  • Active internal bleeding
  • Current intracranial haemorrhage
  • Intracranial neoplasm, arteriovenous malformation, aneurysm, or other conditions that may increase haemorrhage
  • Bleeding diathesis (e.g. von Willebrand disease, haemophilia, advanced liver disease etc.)
  • Recent (i.e. within 3 months) intracranial or intraspinal surgery, major surgery
  • Recent (i.e. within 3 months) serious head trauma
  • Recent (i.e. within 3 months) stroke, for patients with acute myocardial infarction or pulmonary embolism
  • Severe uncontrolled hypertension
  • Subarachnoid haemorrhage
  • Active peptic ulcer disease
  • Prolonged CPR
  • Active seizure
  • Patient <18yo
  • BSL <2.8 or >22.2
  • Already anticoagulated
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2
Q

Antiepileptics in acute seizure management incl. doses

A

Levetiracetam
- 10-40mg/kg max 3g paeds
- 20-60mg/kg max 4.5g adults
- Best choice in females due to lower risk pregnancy category

Sodium valproate
- 10-40mg/kg, max 3g
- Contra-indicated in: prgenancy, drug tox seizures, children <2 years, known urea cycle disorders

Phenytoin
- 15-20mg/kg max 1-1.5g
- Poorly effective in alcohol withdrawal seizures, partial seizures
- Contraindicated in Na channel tox-related seizures
- Incompatible with glucose, most other drugs

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3
Q

Uthoff’s phenomenon

A

Reduced vision secondary to:
- Exercise
- Hot meal
- Hot bath
Seen in MS

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4
Q

Lhermitte’s sign

A

Sudden “electric” sensation down back on neck flexion.
Classically associated with MS

Also seen in transverse myelitis, Behcet’s, osteogenesis imperfecta, trauma, radiation myelopathy, B12 deficiency

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5
Q

Optic neuritis features

A
  • ​decreasing visual acuity over days
  • ​central scotoma, usually unilateral
  • ​visual field deficits
    *​ associated with pain on eye movement
    *​ disturbed colour perception an early sign
    *​ 50% have papillitis on fundoscopy
    *​ 40% go on to have multiple sclerosis
    • occurs in 40% at some stage of disease
    • presenting symptom in 20%
      *​ prognosis
      -​ 1/3 completely recover
    • ​1/3 partially recover
      -​ 1/3 not at all
  • ​visual evoked potentials delayed in 80%
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6
Q

Diagnostic criteria for multiple sclerosis

A

Clinical attacks and MRIB+spine-confirmed lesions disseminated in time (DIT) and space (DIS)

i.e.
>=2 clinical attacks with >=2 lesions with objective clinical evidence
>=2 clinical attacks with 1 lesion with objective clinical evidence + clinical history suggestive of previous lesion
>=2 clinical attacks with 1 lesion disseminated in space evident of MRI
1 clinical attack with >=2 lesions on MRI
1 clinical attack with 1 lesion on MRI, disseminated in space

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7
Q

MS management

A

In acute attacks:
- High dose methylpred - 500-1000mg IV for 3-7 days
- Pred 75mg daily with wean for milder attacks
- Plasma exchange in steroids ineffective

Prevention:
- Azathioprine
- Cyclophosphamide
- Plasmapharesis
- Natalizumab - 300mg IV monthly ( expensive)
- Glatiramer acetate - 20mg subcut daily
- Interferon
- Copolymer I

Lifestyle
- Low saturated fat diet
- Omega 3 fatty acid supplementation
- Vit D via sunlight or supplementation
- Meditation and exercise

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8
Q

MS epidemiology

A

*​ commonest chronic neurological condition
*​ first onset most commonly in patients 30 - 40 years of age
* ​about 60% of cases are women
*​ rare in children
*​ temperate zone prevalence
*​ higher incidence in Tasmania, lower in QLD
*​ loss of suppressor T cells prior to attacks

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9
Q

MS vs ADEM

A

Age group
- ADEM typically <10yo
- MS rare in children, age typically 3rd-4th decade of life
ADEM monophasic demyelination
Sudden-onset multiple defects rare in MS
Seizures, meningism rare in MS
ADEM typically following a febrile illness or vaccination

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10
Q

FVC treatment thresholds in GBS with suspected diaphragmatic involvement

A
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11
Q

Components of Ottawa SAH rule for headache evaluation

A

Age >= 40
Neck pain or stiffness
Limited neck flexion on examination
Witnessed LOC
Onset during exertion
Thunderclap headache

Only used in patient >=15yo with new, severe, atraumatic headache without focal neurology, prior aneurysm, SAH, brain tumour or chronic recurrent headache

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12
Q

LP vs CTA for SAH >6 hours post-onset - pros and cons

A
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13
Q

Two major vessels involved in blunt cerebrovascular injury and their clinical features

A

Internal carotid artery dissection
- Unilateral headache, typically frontotemporal; severity may mimic SAH/migraine
- Anterior neck pain
- Partial Horner syndrome: miosis and ptosis
- Cranial nerve palsies

Vertebral artery dissection
- Headache, typically occipital
- Posterior neck pain
- Facial paraesthesias
- Lateral medullary syndrome
- Diplopia, ataxia

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14
Q

Tool for evaluating possibility of blunt traumatic cerebrovascular injury

A

Denver screening criteria
Broken down into signs and symptoms and risk factors

Signs and symptoms
- Focal neurological defecit
- Cervical bruit
- Infarct on CTB
- Expending neck haematoma
- Neuro exam inconsistent with CTB

Risk factors
- Neck trauma with cervical spine injury
- Severe facial injuries; Le Fort II or III
- Base of skull fractures
- Cervical manipulation
- Connective tissue disease
- Near hanging with anoxic brain injury
- Scalp degloving

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15
Q

Hunt and Hess classification for SAH

A

Grade I
- Asymptomatic or minimal headache
- Mild nuchal rigidity
Grade II
- Moderate to severe headache
- Nuchal rigidity
- Cranial nerve palsy only
Grade III
- Drowsiness or confusion
- Mild focal deficit
Grade IV
- Stupor
- Hemiparesis
- Vegetative disturbance
Grade V
- Deep coma
- Decerebrate
- Moribund

Outcomes:
Grade I-II - independent 90-95%, death 1-2%
Grade IV-V - independent 10%, death 80%

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16
Q

World Federation of Neurological Surgeons grading for SAH

A

Grade I - GCS 15 w/ no motor deficit
Grade II - GCS 13-14 w/ mo motor deficit
Grade III - GCS 13-14 w/ motor deficit
Grade IV - GCS 7-12, w/ or w/o motor deficit
Grade V - GCS <7, w/ or w/o motor deficit

17
Q

Fischer scale for CT evaluation of SAH

A

Grade I - No blood detected
Grade II - Diffuse deposition of blood without clots or layers of blood >1mm
Grade III - Localised clots and/or layers of blood >1mm thick; no IVH (highest risk of vasospam; 37%)
Grade IV - Intracerebral or intraventricular clots present

18
Q

Components of cerebellar exam

A

Nystagmus
Speech
Past-pointing/dysmetria
Dysdiadochokinesis
Intention tremor
Ataxia
Romberg’s

19
Q

Rinne vs Weber’s

A

Rinne’s test
- Place 256Hz tuning fork on mastoid
- When no longer audible, place over external auditory meatus
- Positive: air conduction > bone (normal or sensorineural loss)
- Negative: bone > air conduction (conductive hearing loss)

Weber’s test
- Place 256 Hz tuning fork on middle of forehead
- If sound midline, normal
- Heard loudest in:
* Normal ear in sensory deficit
* Abnormal ear in conductive deficit

20
Q

Features of oculomotor nerve palsy

A

Motor
- Ptosis
- Eye in “down and out” position
- Inability to elevate, depress or turn medially

Pupillary
- Mydriasis
- Absent direct light reflex
- Absent accommodation reflex

Motor features predominate in intrinsic disease (e.g. diabetic neuropathy, arteritis, MS, GBS/MFv)
Pupillary features predominate in extrinsic compression (e.g. raised ICP, tumour, aneurysm)

21
Q

Associated symptoms with CN III palsy at varying sites of lesion

22
Q

Features and causes of facial nerve palsy

A

Features
- Weakness of facial musculature including forehead
- Decreased taste ipsilateral anterior 2/3rds tongue
- Ipsilateral hyperacusis
- Ipsilateral reduced tear production

Causes
- Malignancy: Acoustic neuroma, facial neuroma, meningioma, cholesteatoma etc.
- Trauma: Temporal bone fracture, facial laceration, mastoid surgery
- Infectious: Acute or chronic supperative otitis media, Lyme disease, HIV, syphillis, EBV
- Guillain-Barre
- Bell’s palsy
- Ramsay Hunt
- Diabetes
- Botulism

23
Q

Bell’s Palsy - Prognosis and prognostic factors

A

86% complete recovery at 2 months

Poorer outcome in:
- Complete paralysis
- Pregnancy
- Diabetes
- Taste disorder
- Older age

24
Q

Indications for clot retrieval

A

Requires all the following:

  • Potentially disabling stroke (NIHSS score ≥ 5)

*​ Adult with pre-stroke modified Rankin Scale score ≤ 2
- ​patients with mRS 3 or more do not benefit

*​ Acute ischaemic stroke from occlusion of major named vessel
-​ e.g. internal carotid, M1, dominant vertebral, basilar
- Can be M2 if NIHSS >10 and if ineligible for thrombolysis
- Unclear if posterior cerebral artery occlusions benefit

*​ Alberta Stroke Program Early Computed Tomography Score (ASPECTS) ≥ 6

  • ​Thrombolyisis (if used) able to be given within 4.5 hours after stroke onset

*​ Arterial access can occur within 24 hours of stroke onset

25
Q

Rate of decrease in BP for hypertensive emergency

A

Decrease MAP by 15-25% within 1-2 hours

OR

Decrease MAP by 20% in first hour, aim 160/100 mmHg in 4-6 hours

26
Q

Features of nystagmus that suggest a central cause

A

Bi-directional
Direction-changing
Vertical or purely rotational
Non-fatiguable
No latency to onset post-Dix-Hallpike
Fixation does not inhibit or worsens
Spontaneous

27
Q

HINTS in central vs peripheral vertigo

28
Q

Antibiotics for VP shunt-associated ventriculitis

A

Vancomycin 25mg/kg
+
Meropenem 2g q8hrly
OR cefepime 2g q8hrly

29
Q

CTB: 24M prev hydrocephalus with VP shunt in situ, intermittent severe headaches

A

Slit ventricle syndrome

Often presents with waxing and waning symptoms. Secondary to over-drainage, tissues occlude the orifices of the proximal shunt apparatus. As ICP increases, occluding tissue disengages with resolution of symptoms until drainage and occlusion may occur again.

30
Q

Potential sites for venticular shunt drainage

A

Peritoneum (VP shunt)
Pleural cavity
Right atrium
Ureter
Gall bladder

31
Q

Components and use of of ABCD2 score

A

Predicts risk of stroke following suspected TIA

Age >=60 +1
BP >140/90 (initial; either) +1
Clinical features
- Speech disturbance w/o motor +1
- Unilateral weakness +2
Duration
- <10 mins +0
- 10-59 mins +1
- >=60 mins +2
Diabetes +1

32
Q

Differentials for ring-enhancing lesion on CTB

A

Primary malignancy (Glioblastoma Multiforme most likely, others include anaplastic astrocytoma)
Cerebral metastasis (Lung, Breast)
Cerebral abscess
Primary CNS lymphoma
Cerebral toxoplasmosis
Cerebral Tuberculosis
Subacute cerebral infarction
Tumefactive dymeylination

33
Q

List of unstable cervical spine fractures

A

Jefferson’s fracture (C1 burst)
Bilateral Cervical facet dislocation
Odontoid fracture, type II or III
Atlanto-occipital dissociation
Hangman’s fracture (bilateral C2 pedicle fracture)
Flexion teardrop

Mnemonic: “Jefferson Bit Off A Hangman’s Thumb”

34
Q

Triptans contra-indicated in…

A

Coronary artery disease
PVD
Cerebrovascular disease
Uncontrolled hypertension
Migraine with hemiplegia