Stroke and acute neurological complaints Flashcards

1
Q

Where are the pain receptors that cause headaches as a symptom?

A

Brain tissue is insensate.

Traction or dilatation of intracranial vessels.
Traction of large extra cranial veins.
Compression, traction or inflammation of cranial and spinal nerves.
Meningeal irritation and raised intracranial pressure.
Spasm or trauma to cranial or cervical muscles.
Disturbance of serotonergic projections.

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2
Q

What is the purpose of headache assessment?

A

Diagnose headache subtype.
Determine cause (exclude secondary cause).
To explain diagnosis and rationale for treatment.
Optimise treatment.

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3
Q

How are headaches classified?

A
Primary headache (no causative disorder): migraine, tension type, cluster headache, other primary headaches.
Secondary headache (causative disorder): head or neck trauma, vascular disorder, CNS infection, intracranial pressure disorder, metabolic disorders, drug withdrawal disorders, headache psychiatric disorder, dental, ENT or ocular problem.
Cranial neuralgias.
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4
Q

Case 1:
27y/o man, right-handed, presents with sudden onset severe occipital headache while at work, sitting in from of computer for 2hrs, stressed with deadlines, drinking too much coffee.
No N or V or LOC. Stopped work, went home and rested (early bed).
History of migraine.
Examination: in A&E normal examination, no focal signs, apyrexial, obs stable.
What is your plan?
a) reassure and send home
b) present case and go home “I am year 3”
c) suggest CT, if normal send home
d) suggest CT head then LP
e) sumatriptan 50mg and await response

A

Suggest CT, if normal send home.

Thunderclap? could be subarachnoid haemorrhage, need to rule out.

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5
Q

How do patients present with subarachnoid haemorrhage?

A

1/3 present with acute onset severe headache as the only symptom.
5-11% misdiagnosed, most commonly as migraine.
Headache onset: abrupt, sudden, acute, thunderclap over seconds or minutes.

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6
Q

What are the headache red flags?

A

Age of onset: always consider secondary headache at any age with new headache or headache that differs from their normal; middle-aged to elderly (>50) GCA.
Type of onset: abrupt and severe (thunderclap).
Temporal: progressively severe or increasing frequency.
Pattern: significant change in headache pattern.
Neurological signs: meningioma (stiff neck), focal signs, confusion, altered LOC.
Systemic signs: abnormal examination, fever, weight loss.
Triggers: posture, valsalvar, coughing, exertion.
Secondary risk factors: systemic disease, cancer, HIV, 3rd trimester pregnancy/postpartum, recent head injury.

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7
Q

What are the causes of thunderclap headache?

A

Intracranial infection: meningitis.
CSF pressure related: 3rd ventricle colloid; cyst; spontaneous intracranial hypotension (SIH).
Vascular: ischaemic and haemorrhagic stroke; SAH; cerebral venous thrombosis; cervical arterial dissection; reversible cerebral vasoconstriction syndrome (RCVS); cerebral vasculitis; pituitary apoplexy; posterior reversible encephalopathy syndrome.
Others: acute hypertensive crisis; idiopathic thunderclap headache.

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8
Q

List secondary headache conditions which may have normal CT head scans.

A
Meningitis.
SAH.
Ischaemic stroke.
Cerebral venous thrombosis.
Cervical arterial dissection.
Reversible cerebral vasoconstriction syndrome.
Cerebral vasculitis and temporal arteritis.
Pituitary apoplexy.
Malignant hypertension.
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9
Q

What are the peripheral parts of the vestibular system?

A

Semicircular canals.

Vestibular nerve.

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10
Q

What are the central parts of the vestibular system?

A

Brainstem.

Cerebellum.

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11
Q

What conditions cause dizziness in the peripheral vestibular system?

A

BPPV.
Meniere’s.
Vestibular neuritis.

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12
Q

What conditions cause dizziness in the central vestibular system?

A

Isolated vertigo.
4% of isolated nystagmus is caused by stroke.
Other CNS deficits.

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13
Q

Where might the level of the lesion be in the nervous system in an upper motor neurone lesion?

A

Brain
Brain stem
Spinal cord

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14
Q

Where might the level of the lesion be in the nervous system in a lower motor neurone lesion?

A

Low motor neurone
Neuromuscular junction
Muscle

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15
Q

What is fatigability and what condition might it be seen in?

A

Ptosis develops, eye alignment changes vertically, causes diplopia as eyes are disconjugated.
Myasthenia gravis.

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16
Q

In a 3rd nerve palsy, what is the level of lesion in the nervous system?

A

Neuromuscular junction.

17
Q

What is Horner’s syndrome?

A

Ptosis, miosis, and anhydrosis.

Enophthalmos.

18
Q

What is the epidemiology of stroke?

A

A developing problem.
1 in 10 deaths is caused by a stroke.
3rd most common cause of death.
Worldwide 15m people suffer a stroke each year, 1/3 die and 1/3 disabled.

19
Q

What is a stroke?

A

The sudden death of brain cells due to blockage of blood flow or rupture of an artery to the brain parenchyma.
Ischaemic (85%) or haemorrhagic (12%) or SAH (3%).

20
Q

How does an intra-cerebral haemorrhage cause symptoms of stroke?

A
Pressure of increasing amounts of blood.
Blood itself (blood is irritating to the brain tissue, causing it to swell.
21
Q

What are some causes of haemorrhagic stroke?

A
Hypertension.
Rupture of an aneurysm or AVM.
Haemorrhagic necrosis (e.g. tumour, infection).
Venous outflow obstruction (CVT).
Trauma.
Altered haemostasis.
22
Q

What are the types of causes of ischaemic stroke?

A

Cryptogenic (30%).
Large vessel atherosclerosis (20%).
Small vessel disease (25%).
Cardio-embolic (20%).

23
Q

What causes ischaemic stroke?

A
Thrombus blocks artery to brain, prevents oxygen delivery.
Intracranial atherosclerosis.
Carotid plaque with emboli.
Aortic arch plaque.
Cardiogenic emboli.
Small artery disease.
Carotid stenosis.
Atrial fibrillation.
Valve disease.
Ventricular thrombi.
24
Q

What are the types of large artery atherosclerosis?

A

Intracranial stenosis.
Carotid stenosis (>50%).
Aortic arch plaque.

25
Q

What are the modifiable/ non-modifiable risk factors for large artery atherosclerosis leading to ischaemic stroke?

A
HT.
DM.
CAD.
Smoking.
Cholesterol.
BMI.
Age.
FMHx.
26
Q

What is the management plan for patients with large artery atherosclerosis or ischaemic stroke prevention?

A

Modify lifestyle factors.
Antiplatelet (e.g. aspirin, clopidogrel).
Duplex scan looking for stenosis.
Carotid endarterectomy is of additional benefit for symptomatic carotid disease.

27
Q

What are the cardioembolic causes of ischaemic stroke?

A

Atrial fibrillation and paroxysmal AF.
Valve disease.
Ventricular thrombi.

28
Q

What are the various complaints in acute stroke?

A

Alteration in consciousness: stupor or coma; confusion or agitation/memory loss; seizures; delirium.
Vision and eyes: monocular or binocular; visual field (hemianopia); vertigo, diplopia.
Ataxia: poor balance, clumsiness, or difficulty walking.
Speech and swallow: slurring of speech or difficulty understanding or expressing language; swallowing problems.
Headache: abrupt intense or unusually severe; associated with decreased level of consciousness/neurological deficit; unusual/severe neck or facial pain.
Facial weakness or asymmetry: paralysis of facial muscles (e.g. when patients speak or smile); may be on same side (ipsilateral) or opposite side (contralateral) to limb paralysis.
Weakness and paralysis.
Sensory loss.
Unilateral hearing loss, nausea, vomiting.

29
Q

What neuromuscular syndromes occur in left (dominant) hemisphere stroke?

A
Aphasia.
Right hemiparesis.
Right-sided sensory loss.
Right visual field defect.
Poor right conjugate gaze.
Dysarthria.
Difficulty reading, writing, or calculating.
30
Q

What neuromuscular syndromes occur in right (non-dominant) hemisphere stroke?

A
Neglect of left visual field.
Extinction of left-sided stimuli.
Left hemiparesis.
Left-sided sensory loss.
Left visual field defect.
Poor left conjugate gaze.
Dysarthria.
Spatial disorientation.
31
Q

What neuromuscular syndromes occur in brainstem/ cerebellum/ posterior hemisphere stroke?

A
Motor or sensory loss in all 4 limbs.
Crossed signs.
Limb or gait ataxia.
Dysarthria.
Disconjugate gaze (diplopia).
Nystagmus (vertigo).
Bilateral visual field defects.
32
Q

What neuromuscular syndromes occur in small subcortical hemisphere or brain stem stroke (lacunar syndromes)?

A
Pure motor.
Pure sensory.
Sensory motor.
Ataxic hemiparesis.
Dysarthria clumsy hand syndrome. 
(Without abnormalities of higher brain function, sensation, or vision).
33
Q

What is bright on a CT scan?

A
Blood
Contrast
Bone
Calcium
Metal
34
Q

What is dark on a CT scan?

A

Air
CSF/water
Oedema

35
Q

Case 1:
24y/o female from Somalia.
Gradual onset generalised headache with some nausea and lightheadedness eases with eating.
Has had 3-4 attacks in the last month.
PMHx: DM (insulin dependent); depression.
SHx: refugee, orphaned aged 6.
O/E: left homonymous hemianopia.
Metal artefact seen on CT.
What is the likely cause of the headache?

A

Hypoglycaemia.

Metal artefact caused hemianopia- bullet remained from genocide as a child.

36
Q

What is the ischaemic cascade?

A

When brain cells are deprived of sufficient oxygen, a biochemical cascade is initiated, involving several pathways known as the ischaemic cascade, leading towards cell death: necrosis, apoptosis and inflammation.

37
Q

What are the dynamic changes following ischaemic stroke?

A

Necrosis and apoptosis.
Inflammation.
Repair and remodelling (angiogenesis and neurogenesis).
Increased density (&darkness) on CT brain.

38
Q

What is the ischaemic penumbra window of opportunity?

A

Ischaemic zone surrounds a central core of infarction.
Viability of brain tissue is preserved if perfusion is restored within a critical time period.
Tissue surrounding the infarct that is salvageable, but at risk.

39
Q

Case 2:
History: sudden onset of diplopia and left-sided weakness of the face, arm and leg.
On examination: right eye failure of abduction on right lateral gaze, weakness of CN VII with forehead sparing on the left, tone and reflexes increased on the left, weakness of arm and leg on left side, up going plantar on left.
What is this syndrome?

A

Millard Gilbert syndrome.