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30 vocabulary flashcards summarizing essential terms, complications, diagnostics, and management concepts for aortic aneurysm and dissection.
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Aortic Aneurysm
Permanent, localized out-pouching or dilation of the aortic wall that can occur in the thoracic or abdominal aorta.
Abdominal Aortic Aneurysm (AAA)
Aneurysm that develops in the abdominal aorta—75 % of all aortic aneurysms; most form below the renal arteries and are often asymptomatic.
Thoracic Aortic Aneurysm (TAA)
Aneurysm of the aortic arch or thoracic aorta; may cause angina, hoarseness, dysphagia, dyspnea, or JVD from pressure on nearby structures.
True Aneurysm
Dilation of all three layers of the arterial wall (intima, media, adventitia); the wall remains intact but weakened.
False (Pseudo) Aneurysm
Disruption of the arterial wall layers with bleeding that is contained by surrounding tissue, forming a hematoma that mimics an aneurysm.
Degenerative Cause
Age-related breakdown of collagen and elastin in the aortic wall leading to aneurysm formation.
Blue Toe Syndrome
Patchy cyanosis of toes caused by micro-emboli from an abdominal aortic aneurysm.
Grey Turner Sign
Flank ecchymosis indicating retroperitoneal bleeding, often seen with ruptured AAA.
Aneurysm Rupture
Life-threatening complication in which the aneurysm wall breaks, causing massive internal hemorrhage and hypovolemic shock.
Hypovolemic Shock
State of decreased blood volume marked by ↑HR, ↓BP, pallor, ↓urine output, ↓LOC—common after aneurysm rupture.
Retroperitoneal Rupture
AAA rupture limited by surrounding tissues; bleeding may be temporarily tamponaded, allowing time for surgical repair.
Endovascular Graft Procedure
Minimally invasive insertion of a stent-graft inside the aneurysm via femoral arteries to reinforce the aortic wall.
Graft Patency
The state of an inserted vascular graft remaining open and unobstructed, a primary postoperative nursing goal.
Aortic Dissection
Tear in the intimal layer of the aorta that allows blood to track between layers, creating a false channel and separating (dissecting) the wall.
Dissecting Aneurysm
Older term for aortic dissection emphasizing the presence of both dilation and wall separation.
Type A Dissection
Acute dissection involving the ascending aorta and/or arch; surgical emergency with high mortality.
Type B Dissection
Dissection confined to the descending thoracic aorta; often managed with endovascular repair or medical therapy.
Sharp “Tearing” Pain
Classic symptom of aortic dissection described as sudden, severe, ripping chest or back pain that follows the dissection path.
Aortic Valve Insufficiency
Regurgitation caused by Type A dissection that dilates the aortic root, producing a high-pitched murmur and possible heart failure.
Cardiac Tamponade
Compression of the heart by pericardial blood, a fatal complication of proximal aortic dissection rupture.
Spinal Cord Ischemia
Loss of blood flow to spinal arteries during dissection, leading to lower-extremity weakness or paralysis.
Endovascular Dissection Repair
Placement of a stent-graft across the dissection entry tear, commonly used for Type B dissections.
Conservative Therapy (Dissection)
ICU management focusing on pain relief, HR <60 bpm, SBP 100-120 mmHg, and CVD risk reduction when surgery is not immediate.
Beta Blockers
First-line drugs (e.g., esmolol) used to lower heart rate and aortic wall stress in acute aortic dissection.
Risk Factor Modification
Reduction of smoking, hypertension, hyperlipidemia, and other modifiable risks to slow aneurysm or dissection progression.
Transesophageal Echocardiogram (TEE)
Ultrasound probe in the esophagus providing real-time images of the thoracic aorta to diagnose aneurysm or dissection.
Computed Tomography (CT) Scan
Gold-standard imaging test to identify size, location, and extent of aneurysms and dissections.
Ultrasound Screening
Non-invasive abdominal imaging recommended for men ≥65 years with smoking history to detect asymptomatic AAA.
Superior Vena Cava (SVC) Compression
Pressure from a large TAA on the SVC causing facial and arm edema and jugular venous distension.
Connective Tissue Disorders
Genetic conditions (e.g., Marfan syndrome, Ehlers–Danlos) that weaken the aortic wall and increase aneurysm/dissection risk.