Arterial Disease Flashcards

1
Q

What is carotid artery disease? How will it present?

A

Build up of atherosclerotic plaques 1+ common & internal carotid arteries -> stenosis/ occlusion

  • Mostly asymptomatic
  • Causes 10-15% of ischaemic strokes due plaque rupture/ atheroembolism
  • TIA (<24hrs)

May Carotid bruit neck auscultation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Pathophysiology of atheromas

A

Fatty streak -> lipid core -> fibrous cap

Proliferation SM cells, foam cells -> EC lipid -> fibrosis, necrosis, inflammatory cells, cholesterol clefts -> disruption internal lamina then media -> in growth BVs -> plaque fissuring (cracking cap)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

How is carotid artery disease classified?

A

Radiologically - degree of stenosis

Mild - <50% diameter reduction
Moderate - 50-69%
Severe - 70-99%
Total occlusion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Differentials for carotid artery disease

A
  • carotid dissection - <50yrs, CT disorder, precipitated trauma
  • thrombotic occlusion CA - imaging different
  • fibromuscular dysplasia - stenosis angiopathy hypertrophy vessel wall, <50yrs, females, focal neurological deficit
  • vasculitis - giant cell arteritis/ Takayasu’s arteritis, systemic
    Hypoglycaemia, Todd’s paresis, subdural haematomma, SOL, VST, MS
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

How would you investigate someone suspected of carotid artery disease?

A

Suspected stroke - UrGeNT non-contrast CT head

Also:

  • bloods (FBC, U&Es, clotting, lipid profile, glucose)
  • ECG (A fib)

Thrombectomy to my considered CT contrast angiography

Post diagnosis I stroke/ TIA:
Duplex USS - degree stenosis
Lesions within CA - Ct angiography

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Acute management of carotid artery disease/ suspected stroke

A

High flow O2
Blood glucose optimised (4-11mmol)
Swallowing screen assessment

  • I stroke IV alteplase (admitted <4.5hrs symptoms onset + meet inclusion criteria), 300mg aspirin
    ✅thrombectomy + consider IV thrombolysis
  • H stroke correction coagulate the + neurosurgery referral (potential clot evacuation)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Long term management stroke/ TIA

A

Anti-platelets (aspirin 300mg OD 2 weeks -> clopidogrel 75mg OD)

Statin (atorvastatin)

Management hypertension/ DM/ smoking

Exercise

WL

Speech and language therapy
Physiotherapy
Occupation t

Carotid endarterectomy - all acute non-disabling with symptomatic carotid stenosis 50-99% ~ remove atheroma + damaged intima

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Oxford stroke classification

A

Classification Description Signs and Symptoms
Total Anterior Circulation Stroke (TACS) (20%) Large cortical stroke in middle or anterior cerebral artery areas Must have all of:
Motor weakness or sensory deficit of -‰¥2/3 areas (face, arm, leg)
Homonymous hemianopia
High cortical dysfunction (dysphasia, dyspraxia, or neglect)

Partial Anterior Circulation Stroke (PACS) (35%) Cortical stroke in middle or anterior cerebral artery areas Will present with either:
2/3 TACS criteria
Limited motor or sensory deficit (1 of leg, arm or face)
High cortical dysfunction alone

Lacunar Stroke (LACS) (20%) Occlusion of the deep penetrating arteries Will present with any of:
Pure motor -‰¥2/3 areas (face, arm, leg)
Pure sensory -‰¥2/3 areas (face, arm, leg)
Pure sensorimotor -‰¥2/3 areas (face, arm, leg)
Ataxic hemiparesis

Posterior Circulation Stroke (POCS) (25%) Occlusion of vertebrobasilar or PCA circulation, affecting brainstem, cerebellum, or occipital lobe Variety of presentations can occur, typically:
Ipsilateral CN palsy with contralateral motor or sensory defects
Bilateral motor or sensory deficits
Isolated homonymous hemianopia
Cerebellar dysfunction

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is an AAA? Risk factors?

A

Dilation abdominal aorta >3cm
(Aneurysm dilation >50%)
1/70 men >65yrs

RFs:
Atherosclerosis
Trauma
Infection 
CT disorder
Inflammatory disease
Smoking 
Hypertension 
Hyperlipidemia
FH
Male
Older
(DM negative)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Most AAAs are asymptomatic, how are they picked up? If they do have symptoms what would they be?

A

Incidental finding or screening (NAAASP) abdo USS men 65yrs (>5.5cm -> CT contrast)

Symptomatic:
Abdo pain 
Back/ loin pain 
Distal embolisation -> limb ischaemia 
Aortoenteric fistula 
Pulsatile mass 
Retroperitoneal haemorrhage signs rare

Rupture - abdo/ back/ lion pain, shock, syncope

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Management of AAAs

A

<5.5cm monitored duplex USS
3-4.4cm yearly scan
4.5-5.4 3 monthly

Reduce cvs factors

Surgery >5.5cm / expanding >1cm yr / symptomatic

  • open repair clamping, segment removed, prosthetic graft
  • endovascular repair graft via femoral arteries & fixing stent across (higher rates reintervention & rupture)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is the most important complication of an endovascular repair for AAAs? How can you classify it?

A

Endovascular leaking
Incomplete seal around aneurysm -> blood leaks around graft
Often asymptomatic - regular surveillance
-> rupture

Type 1 - leak graft end, inadequate seal
Type 2 - sac filling from branch vessel, most resolve
Type 3 - leak through defect in graft, resolves cessation anticoags
Type 5 - continued expansion aneurysm without leak imaging

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Complications of AAA

A

Rupture - pain, syncope, vomiting, pulsatile mass
Retroperitoneal leak
Classic triad (50%): flank/ back pain, hypotension, pulsatile mass
80% rupture posteriorly retroperitoneal space
Embolisation
Aortoduodenal fistula

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Management of ruptured AAA

A
Suspected:
High flow O2
IV access 
Urgent bloods (FBC U&amp;Es clotting crossmatch min 6U)
Shock treated carefully (BP <100mmHg)
Transferred vascular unit 
Unstable - open surgical repair 
Stable - ct angiogram
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What does the wall of an artery consist of? Where is the tear in an arterial dissection? How might it spread?

A

Tunica intima- endothelium, elastic membrane
Tunica media - smooth muscle
Tunica adventitia - external elastic membrane

Tear intima layer -> blood flow between & split intima & media
Can progress distally/ proximal/ both - anterograde -> iliac arteries, retrograde -> aortic valve (cardiac tamponade)
Chronic >14days

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

How can aortic dissections be classified?

A

Anatomically 2 systems

Debakey:
Type 1 - originates ascending aorta -> aortic arch
<65yrs, highest mortality (1% per hr)

Type 2 - confined ascending aorta
Elderly, atherosclerotic disease + hypertension

Type 3 - distal subclavian artery in descending aorta

a. Extends distally -> diaphragm
b. Extends beyond diaphragm into abdo aorta

Stanford classification:
A - debakey types 1 + 2, ascending aorta can propagate aortic arch + descending aorta

B - not involving ascending aorta, includes debakey type 3

17
Q

Risk factors for aortic dissection?

A
Hypertension 
Atherosclerotic disease
Male 
Ct disorders (Marfan’s, Ehler’s-danios syndrome) 
Bicuspid aortic valve 
50-70yrs
18
Q

A man presents with testing chest pain radiating to the back. Clinical sings include tachycardia, hypotension, new aortic regurgitation murmur & reduced urine output. What are your differentials? What other signs might there be? How would you investigate?

A

Aortic dissection
Signs end-organ hypoperfusion (reduced urine output, paraplegia, lower limb ischaemia, abdo pain secondary ischaemia, deterioration consciousness)
- CT angiogram
Transoesophageal echo maybe

MI - ECG, troponin
PE - dyspnoea, ABG hypoxia, CTPA/ V/Q scan
Pericarditis - ECG ST⬆️, pericardial rub auscultation
MSK back pain

19
Q

How would you manage aortic dissection?

A

✅urgent initial assessment
✅ high flow O2
✅IV access (2 large bore cannulas)
✅fluid resus cautiously (110mmGh, rupture just for cerebral perfusion)

Type A - surgically, removal ascending aorta & synthetic graft

Type B uncomplicated - medically, IV beta blockers (labetalol) Or CCB
Type B + rupture/renal,visceral,limb ischaemia/refectory pain/ uncontrollable hypertension - surgery

Lifelong antihypertensives + imaging (1,3,12 months -> 6-12 month intervals)

20
Q

What is the most common complication of chronic type B aortic dissections?
What are other complications of aortic dissections?

A

Aneurysm
✅ endovascular repair

- rupture
Regurgitation
MI
Cardiac tamponade
Stroke/ paraplegia
Mortality 20% before hospital
21
Q

Define a thoracic aortic aneurysm

What segments of the aorta can they involve?

A

Aneurysm - persistent, abnormal dilation of an artery to 1.5X normal diameter

Ascending aorta/ aortic root 60%
Aortic arch 10%
Descending aorta 40%
Thoracoacromial aorta 10%

Rarer, higher mortality - abdo aort aneurysms

22
Q

Aetiology of thoracic aortic aneurysms

A

Degradation of tunica media -> dilates -> wall tension rises -> dilates

  • CT disorders e.g. MS, EDS
  • bicuspid aortic valve (tuners)
  • trauma
  • aortic dissection
  • aortic arteritis
  • tertiary syphilis

Mean rate 1-2mm/yr

23
Q

Typically thoracic aneurysms are asymptomatic and found incidentally. If they are symptomatic what is the most common presentation and how does it change depending on site of aneurysm? What are some other potential symptoms?

A

Pain

Ascending aorta - anterior chest
Aortic arch - neck
Descending aorta - between scapulae

Back pain, hoarse voice, distempered neck veins, ❤️F symptoms, dyspnoea/ cough

-> rupture/ dissection

24
Q

How would you diagnose a thoracic aneurysm?

A

CXR - widened mediastinal silhouette, enlarged aortic knob, tracheal deviation?

  1. CT chest + contrast

Transoesophageal echocardiograohy (TOE) - concurrent aortic insufficiency/ dissection, routine marfan’s & susoected THoracic aortic disease

Pre-op: routine bloods, G&S, ECG, CXR

25
Q

Management of thoracic aneurysm

A
Confirmed - medical  (ramipril, atorvastatin, aspirin) + investigations 
- statin
Antiplatelet 
BP controlled
Smoking cessation 

Surgical: depends location

26
Q

What is the name for the condition causing syncope or neurological deficits (vertigo, diplopia, dysphagia, dysarthria, visual loss) when blood supply to the affected arm is increased through exercise?
Explain the pathophysiology of it

A

Subclavian steal syndrome - rare

  • Secondary proximal stenosing lesion*/ occlusion in subclavian artery (typically left 3X)
  • to compensate increased O2 demand in arm blood is drawn from collateral circulation -> reversed blood flow in ipsilateral vertebral artery (or internal thoracic)
  • > cerebral + upper limb features (arm claudication)

*atherosclerosis, vasculitis, thoracic outlet syndrome, complications surgery

27
Q

You suspect subclavian steal syndrome, how will you investigate?

A

Duplex USS - retrograde flow affected vertebral artery with exercise
- routine CXR

Definitive:
- CT angiography or MR angiography

28
Q

What are the three grades of disease severity for subclavian steal syndrome?

A

Pre-subclavian steal - reduced anterograde vertebral flow

Intermittent alternating flow - antegrade flow occurs in diastolic phase & retrograde in systolic

Advanced disease - permanent retrograde flow

29
Q

How to manage subclavian steal syndrome

A
Conservative:
Anti-platelet
Statin 
Smoking 
WL
Diabetic control 

Surgical:
Endovascular
bypass - longer/ distal occlusion
Percutaneous angioplasty

30
Q

From which artery does the right subclavian A branch from.

A

Brachiocephalic