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Abdominal aortic aneurysm

An aortic aneurysm is a general term for any swelling (dilatation or aneurysm) of the aorta, usually representing an underlying weakness in the wall of the aorta at that location. While the stretched vessel may occasionally cause discomfort, it is the risk of rupture causing severe pain, massive internal hemorrhage and, without prompt treatment, resulting in a quick death. In addition the aneurysm may split (Aortic dissection) which may block vessels that branch off from the aorta or release blood clots (emboli) causing blockage to blood-flow elsewhere. more...

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Pathology

The physical change in the aortic diameter can occur secondary to an intrinsic defect in the protein construction of the aortic wall, trauma, infection, or due to progressive destruction of aortic proteins by enzymes. The last is the most common cause of aneurysmal disease although the origin of this enzymatic destruction is not known.

Signs, symptoms and diagnosis

  • Most intact aortic aneurysms do not produce any symptoms. Untreated, aneurysms tend to become progressively larger, although the rate of enlargement is unpredictable for any individual. Rarely, clotted blood which lines most aortic aneurysms can break off and result in an embolus. They may be found on physical examination. Medical imaging is necessary to confirm the diagnosis.

Abdominal Aortic Aneurysm

Aortic aneurysms are more common in the abdominal aorta, one reason for this is that elastin, the principle load bearing protein present in the wall of the aorta, is reduced in the abdominal aorta as compared to the thoracic aorta (nearer the heart). Most are true aneurysms that involve all three layers (tunica intima, tunica media and tunica adventitia), and are are generally asymptomatic before rupture.

The prevalence of AAAs increases with age, with an average age of 65-70 at the time of diagnosis. AAAs have been attributed to atherosclerosis, though other factors are involved in their formation.

An AAA may remain asymptomatic indefinitely. There is a large risk of rupture once the size has reached 5 cm, though some AAAs may swell to over 15 cm in diameter before rupturing. Before rupture, an AAA may present as a large, pulsatile mass above the umbilicus. A bruit may be heard from the turbulent flow in a severe atherosclerotic aneurysm or if thombosis occurs. Unfortunately, however, rupture is usually the first hint of AAA. Once an aneurysm has ruptured, it presents with a classic pain-hypotension-mass triad. The pain is classically reported in the abdomen, back or flank. It is usually acute, severe and constant, and may radiate through the abdomen to the back.

The diagnosis of an abdominal aortic aneurysm can be confirmed at the bedside by the use of ultrasound. Rupture could be indicated by the presence of free fluid in potential abdominal spaces, such as Morrison's pouch, the splenorenal space, subdiaphragmatic spaces and peri-vesical spaces. A contrast-enchanced abdominal CT scan is needed for confirmation.

Only 10-25% of patients survive rupture due to large pre- and post-operative mortality. Annual mortality from ruptured abdominal aneurysms in the United States alone is about 15 000. Another important complication of AAA is formation of a thrombus in the aneurysm.

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Repair of small abdominal aortic aneurysms - Tips from Other Journals
From American Family Physician, 9/15/02 by Bill Zepf

A study by the United Kingdom Small Aneurysm Trial participants showed no benefit in five-year survival from early repair of abdominal aortic aneurysms (AAAs) up to 5.5 cm in diameter, and this result has recently been confirmed by a large American trial. The United Kingdom investigators now report data on survival after an average of eight years of follow-up.

From 93 hospitals in the United Kingdom, the authors identified 1,276 patients with infrarenal AAAs that were 4.0 to 5.5 cm in diameter. Consent for randomization was obtained from 1,090 subjects, who were assigned to either early surgical repair or serial ultrasonographic surveillance. Those in the surveillance group were subsequently offered surgery if the aneurysm grew larger than 5.5 cm or expanded by more than 1 cm in a given year, if repair of a proximal or iliac aneurysm was scheduled, or if the aneurysm became symptomatic. More than one half of the surveillance group eventually had surgical repair. Rates of smoking cessation were monitored, and success rates after one year were verified by serum measurement of nicotine metabolite (cotinine).

Short-term (30 days postoperative) mortality rates were not significantly higher among patients in the surveillance group who later underwent surgical repair (7.2 percent mortality) versus those assigned to early repair (5.5 percent). As noted in the earlier report of this trial, after five years of follow-up there was no significant difference in survival with early aneurysm repair. With longer-term follow-up data available, a small mortality benefit was seen with early repair (53 percent in the early surgery group versus 45 percent in the surveillance and later repair group). The authors considered the possibility that the surveillance group's survival disadvantage could be due to increased rates of aneurysm rupture, but there was no strong evidence to support that hypothesis. Compared with men, women had almost three times the risk of death from aneurysm rupture (14 percent versus 5 percent).

The trial authors noted that after one year of follow-up, smoking rates in the surveillance group were substantially higher than rates in the early-surgery group (48 percent versus 28 percent). They postulated that the greater success with smoking cessation among those assigned to early surgery might explain their overall survival advantage. The authors concluded that with longer-term follow-up, a modest survival benefit became apparent for early surgical repair of small AAAs. Women had higher rates of death from aneurysm rupture than men did, and they may be less appropriate candidates for surveillance.

2002;346:1445-52.

COPYRIGHT 2002 American Academy of Family Physicians
COPYRIGHT 2002 Gale Group

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