Overview of Aortic Aneurysm
- Definition: Aortic aneurysm refers to a segmental, full-thickness dilation of the aorta, exceeding 50% of its normal diameter due to weakening of the vessel wall.
Pathophysiology
- Wall weakening: Aneurysms form when structural changes occur in the aortic wall, including degradation of elastin and collagen.
- Types:
- Abdominal Aortic Aneurysm (AAA): Typically below the renal arteries; more common than TAA.
- Thoracic Aortic Aneurysm (TAA): Involves the thoracic aorta, often associated with genetic disorders.
- Causes:
- AAA: Primarily caused by atherosclerosis.
- TAA: Related to connective tissue diseases (e.g., Marfan syndrome, Ehlers-Danlos syndrome) or chronic hypertension.
Risk Factors
- Smoking: Strongest modifiable risk factor for AAA.
- Hypertension: Increases wall stress, contributing to aneurysm formation.
- Genetic predispositions: Marfan syndrome, bicuspid aortic valve, and other connective tissue disorders elevate the risk for TAA.
- Age and gender: Aneurysms are more common in men over 60 years of age.
Symptoms and Signs
- Asymptomatic: Aneurysms often grow silently and are discovered incidentally on imaging.
- Symptoms:
- AAA: Abdominal or back pain, pulsatile mass in the abdomen.
- TAA: Chest pain, hoarseness, dysphagia (compression of surrounding structures).
- Complications:
- Rupture: Sudden, severe pain with hypotension and shock.
- Aortic dissection: Tearing chest or back pain, commonly in TAA.
- Thrombosis and embolism: Distal ischemia due to thrombus formation in the aneurysm.
Diagnostic Workup
- Ultrasound: First-line screening for AAA in at-risk populations (e.g., men aged 65-75 who have smoked).
- CT angiography: Gold standard for detailed visualization of both AAA and TAA for preoperative planning.
- MRI: Alternative for patients with contrast allergies or for follow-up in genetically predisposed individuals (e.g., Marfan syndrome).
Management
- Conservative:
- Regular imaging surveillance for small, asymptomatic aneurysms (e.g., <5.5 cm).
- Smoking cessation, hypertension control, statin therapy.
- Surgical indications:
- AAA >5.5 cm or TAA >5.5-6.0 cm (depending on location).
- Rapid growth (>0.5 cm over 6 months).
- Symptomatic aneurysms or those showing signs of impending rupture.
- Surgical options:
- Endovascular Aneurysm Repair (EVAR): Minimally invasive; preferred for anatomically suitable AAAs.
- Open surgical repair: Necessary for large or complex aneurysms, particularly for TAA.
Postoperative Care
- Imaging surveillance: Lifelong follow-up after EVAR to monitor for endoleaks or graft complications.
- Medications:
- Antihypertensives, especially for TAA, to reduce wall stress and prevent further aneurysm expansion.
- Statins for underlying atherosclerosis.
Essential Points
- AAA screening is crucial for men aged 65-75 with a history of smoking, using abdominal ultrasound.
- Rupture risk increases with aneurysm size, and AAA rupture is a medical emergency with high mortality.
- Surgical repair is recommended for aneurysms larger than 5.5 cm or those growing rapidly.
- Genetic syndromes like Marfan syndrome require careful monitoring, as they predispose to TAA.