Vascular And Transplant Flashcards

1
Q

Describe the pathophysiology of diabetic foot

A

Describe in terms of effects on vasculature, effects on neurology, and local effects of hyperglycaemia.

Vasculature

  • Microvascular disease
    • Hyperglycaemia causes vasoconstriction, inflammation, and thrombosis
    • Reduced endothelial NO, increased Reactive oxygen species, “advanced glycation products” all cause thickened capillaries
  • Macrovascular disease Diabetes often part of the metabolic syndrome that drives macrovascular disease

Neurology

  • Sensory neuropathy Disease of the vasa nervorum from microvascular disease
  • Autonomic neuropathy
    • Denervation of sweat glands causes dry skin and cracks
    • Inability to vasodilate in response to infection
  • Motor neuropathy Atrophy of small muscles causes change in weight distribution and eventual dislocation of MT heads; subluxation of the 1st MTP is classic
  • Visual impairment ​Contributes to trauma and ulceration

Tissue effects in hyperglycaemia

  • Impaired chemotaxis and phagocytosis due to chronic glycosylation of neutrophils
  • Ideal bacterial substrate
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2
Q

Causes of perepheral vascular disease

A

Commonest

  • Atherosclerosis

Rare

  • Burgers Disease (smokers)
  • Persistant sciatic artery
  • Popliteal entrapment (pop art in medial head of gastrocnemius)
  • Cystic adventitial disease (abnormL development of mucin producing mesenchymal cells cause cytic degeneration inadventitia)
  • Fibromuscular dysplasia
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3
Q

What are the common sited of atheroma deposit

A

Sites of stress/strain or high turbulence

  • Ostia
    • coronoary
    • Mesenteric
    • Renal
  • Bifurcation
    • Carotid
    • Aortic
    • Iliac
  • SFA
  • popliteal
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4
Q

How can you assess severity of Perepheral disease on history

A

This can be done with the Fontaine stage

1 = Asymptomatic

2 = Intermittent Claudication

3 - rest pain

4 - Tissue loss

Rutherford Scale can also be used but is more cumbersome than the Fonatine

0 = Asymptomatic

1 = mild claudcation

2 = moderate claudcation

3 = severe claudcation

4 = rest pain

5 = mild tissue loss

6 = major tissue loss

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5
Q

What are the important things to ask/exmine for PVD patient?

A

History

  • Claudication symptoms, distance, duration
  • Smoking
  • Cardiac risk assessment
  • Stroke
  • PMH - IHD, CAD, MI, CKD, DM, obesity, Hyperlipidemia

Exam -

  • Inspect for trophic changes - hair loss, shiny skin, hypertrophic nails
  • Tissue loss
  • exam all pulses and capillary refill
  • ABPI
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6
Q

What are normal values of ankle and toe pressures? When would you be worried about critical iscahemia?

A

ANKLE PRESSURE

Normal - 90% of systemic BP

60-80 mmHg needed for healing

50 mmHg - Critical ischaemia

ABPI

  • >1.2 -> ?calcification check toe pressure
  • 0.9-1.2 = normal
  • 0.6-0.9 = cludication
  • <0.5 = critical ischaemia
  • <0.3 = rest pain

TOE PRESSURE (normally about 30 mm Hg less than ankle)

  • pressure <30mmHg = critical
  • TBPI
    • >0.8 = normal
    • <.3 = critical
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7
Q

How does arterial flow velocity change with stenosis

A

Normal –> 150cm/s —-> triphasic

<50% stenosis —-> 200cm/s —–> triphasic

50-75% stenosis —> 200-400cm/s —> triphasic/biphasic

>75% stenosis —> >400cm/s —> monophasic, dampened

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8
Q

Outline the utility of common investigations for PVD

A

ABPI

  • cheap, can be done in clinic
  • good screenig for PVD

Duplex US (B/colour/power/spectral mode)

  • Cheap, noninvasive
  • good for superficial vessels - very good for common femoral and distal popliteal
  • sensitive and specific
  • not good for small vessels and large or deep vessels (supra-inguinal) or tortuous vessels.

CTA

  • Good for emergency situation and when MRA not appropriate
  • radiation involved
  • CT cannot reliably differentiate between contrast and organic narrowing particularly in small vessels.

MRA

  • better than CTA
  • Contrast toxicity particulalrly in CKD 3 and above (nephrogenic systemic fibrosis for whihc the nly treatment is renal transplant.

Angiography

  • Gold standard
  • used only when endovascualr intervention is planned
  • Complications
    • Procedure related - hematoma, dissection, AV fistula, Pseudoaneurysm
    • Contrast related - nausea, vomiting, alleric reaction, renal impairement
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9
Q

What are the types of endoleak and their usual management?

A

Type 1 endoleak

  • leak between the vessel wal and the graft
  • Intervene

Type 2

  • Back bleeding (lumbar, IMA, median sacral)
  • Intervene if expanding

Type 3

  • Fabric or metal failure
  • intervene

Type 4

  • Porous graft
  • Observe

Type 5

  • Serous leak (expansion by >5mm in absnce of leak)
  • observe
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10
Q

What size Aneurysm will you intervene on?

A

AAA

  • 5.5cm
  • enalrging >1cm /yr or symptomatic

Iliac = 3cm

Femoral = 3.5 cm

Pop = 2 cm

Splenic/Visceral - 2 or any size in women of child bearing age.

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11
Q

Criteria for EVAR of aortic aneurysm

A

EVAR has better short term outcome compared to open repair at cost of poorer long term result. Results of UK EVAR1 and DREAM trials show that by 4 years post op EVAR and open outcomes are comparable, and after that open outcomes are superior to EVAR.

For AAA, patients needd pre-op CT angio.

  • IMA should be expendable (rely on marginal vs re-implant)
  • Atleast 1 internal iliac should be patent
  • neck - >1cm landing zone
  • neck diamteer <3cm
  • Angle <60degree

For Iliac

  • neck >1cm long
  • Diamter >8mm - <24mm
  • not tortuous
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12
Q

Complication of EVAR

A

EVAR specific

  • Endoleak
  • graft migration
  • Kinking/occlusion
  • hematoma
  • pseudoaneurysm
  • AV fistula
  • Dissection

AAA realted

  • MI
  • stroke
  • ischaemic bowel
  • Acute renal failure
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