Aneurysms & Dissections

 

  • Background

    Definitions

    • Aneurysm: dilation of artery which is bound by all 3 walls of the vessel (intima, media, adventitia). At risk of dissection and/or rupture.
    • Pseudoaneurysm: bleed from an artery which pools in an enclosed compartment next to the vessel.
    • Dissection: intima tears and blood enters, separating it from the media and forming a false lumen, which can become aneurysmal and/or lead to reduction of distal blood flow.

    Aneurysm locations

    Can occur anywhere, but common sites are:

    • Aorta: abdominal (commonest) or thoracic. The former is more likely to rupture, and the latter is more likely to dissect (or dissection may come first and lead to aneurysm).
    • Major arteries: popliteal (commonest), femoral, axillary, carotid.
    • Circle of Willis (saccular/berry aneurysms).
  • Complications

    • Rupture
    • Dissection
    • Thrombosis or embolism.
    • Pressure on neighbouring structures.
    • Fistula into neighbouring structures.
    • Infection: mycotic aneurysm.
  • Abdominal aortic aneurysm (AAA)

    Location

    Usually below the level of the renal arteries ('infrarenal').

    Risk factors

    • Atherosclerosis and its risk factors: smoking, HTN, cholesterol.
    • Demographic: male, ↑age.
    • Family history.
    • Rarely, due to a specific inflammatory (e.g. Behcet's) or connective tissue (e.g. Marfan's) cause.

    Presentation

    Stable aneurysm:

    • Usually asymptomatic. May be detected through screening.
    • On examination, there may be a pulsatile mass visible or palpable in the abdomen. Pain on palpation suggests ↑risk of rupture.

    Rupture:

    • Abdominal, flank, or back pain.
    • Shock
    • Syncope. Consider ruptured AAA in all older men (>55) or women (>70) presenting with collapse.

    Investigations

    Bloods:

    • Basic bloods: FBC, coag, U&E, LFT.
    • Pre-op: cross-match.

    Imaging:

    • Diagnosis is usually with US. One off screening is offered to all men in the UK at age 65, and considered for women with risk factors at age 70.
    • CT contrast or MRI angio provide more information, and are used if US not clear or before planned surgery. CT may show 'high-attenuating crescent', a bleed within the aneurysmal wall suggesting imminent rupture.
    • If ruptured, may proceed to surgery without imaging (or just bedside US) if unstable, otherwise CT if stable.

    Management

    Conservative:

    • Regular US monitoring if small and asymptomatic.
    • Manage risk factors.
    • Contact DVLA if >6 cm.

    Surgery:

    • Indications: aneurysm ≥5.5 cm. At this point, the risk of rupture overtakes the risk of surgery for most, though this may differ in those who are not operatively fit.
    • Open repair involves clamping the artery and sewing a graft inside the aneurysm sac to replace it.
    • Endovascular aneurysm/aortic repair (EVAR) is a less invasive alternative, whereby stents are inserted through the femoral artery. Quicker recovery, lower short-term mortality, and no long-term mortality difference. Risk of endovascular leaks ('endoleaks'), which need to be monitored with regular CT or US. Preferred if patient has co-morbidities (esp. multiple previous abdo surgeries).
    • 1.5% in-hospital mortality risk after elective repair.

    Ruptured AAA:

    • Resuscitation with blood products.
    • Emergency repair: open repair or EVAR.
    • 80% mortality risk, 40% if operated.
  • Thoracic aortic aneurysm and aortic dissection

    Background

    Distinct but related pathologies:

    • Aneurysms are at increased risk of dissection.
    • Conversely, the false lumen of a dissection can become aneurysmal.

    Causes

    • CVD risk factors: hypertension, cholesterol, smoking.
    • Aortic regurgitation. This can also be a complication of TAA.
    • Marfan's or Ehlers-Danlos.
    • Familial
    • Mycotic aneurysm: cause by infection, usually bacterial (despite name sounding fungal).
    • Syphilitic aortitis. By convention, not considered a mycotic aneurysm.
    • Inflammatory: RA, Behcet's, Takayasu's, giant cell arteritis.

    Presentation

    Aneurysm:

    • Usually asymptomatic, with pain suggesting a high risk of rupture.
    • Unlike abdominal aneurysm, TAA's tend to dissect first rather than rupture. However, it can then progress to rupture.

    Dissection:

    • Tearing or sharp pain, maximal at onset (unlike MI, which builds), radiating to back. Anterior pain suggests ascending aorta, while posterior (infrascapular) pain suggests descending.
    • BP: hypotension, pulse deficit (unequal BP between arms, seen in 15%).
    • New murmur of aortic regurgitation.
    • May lead to MI through extension to coronary arteries.
    • Neurological deficits.
    • Defined as chronic if symptoms >2 weeks. Lower risk of complications.

    Rupture:

    • Shock, haemoptysis, or tamponade.

    Investigations

    • ECG: may show MI.
    • CXR may show widened mediastinum, but ↓sensitivity.
    • Definitive diagnosis usually on CT, though may also be seen on echo and MRI.

    Management

    Aneurysm:

    • Repair via open surgery or EVAR if: unstable, symptomatic, or >5.5 cm. Risk of paraplegia.

    Dissection:

    • Aggressive BP lowering with labetalol IV or esmolol IV.
    • Type A involves the Ascending aorta and requires surgery.
    • Type B involves the descending aorta, Beyond the left subclavian artery, and only requires surgery if there is rupture or worsening pain.
    • Chronic, stable dissections can often be managed medically with antihypertensives.
  • Popliteal aneurysm

    Presentation

    • Sign: easily palpable popliteal pulse.
    • May have co-morbid abdominal aneurysm.
    • More likely to cause thrombosis than rupture, leading to acute limb ischaemia.

    Management

    • Treat acute ischaemia with femoropopliteal bypass.
    • If aneurysm discovered before thrombosis occurs, treat with grafting.

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