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Aneurysm

An aneurysm (or aneurism) (from Greek ανευρυσμα, a dilatation) is a localized dilation or ballooning of a blood vessel by more than 50% of the diameter of the vessel. Aneurysms most commonly occur in the arteries at the base of the brain (the circle of Willis) and in the aorta (the main artery coming out of the heart) - this is an aortic aneurysm. more...

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The layer of the artery that is in direct contact with the flow of blood is the tunica intima, commonly called the intima. This layer is made up of mainly endothelial cells. Adjacent to this layer is the tunica media, known as the media. This "middle layer" is made up of smooth muscle cells and elastic tissue. The outermost layer (farthest from the flow of blood) is known as the tunica adventitia or the adventitia. This layer is composed of connective tissue.

Types

Aneurysms are also described according to their shape: Saccular or fusiform. Aneurysms can be broken down into two groups: true aneurysms and false aneurysms. A true aneurysm involves an outpouching of all three layers of a blood vessel: the intima, the media, and the adventitia. True aneurysms can be due to congenital malformations, infections, or hypertension. A false aneurysm, also known as a pseudoaneurysm, involves an outpouching of only the adventitia. Pseudoaneurysms can be due to trauma involving the intima of the blood vessel, and are a known complication of percutaneous arterial procedures.

Locations

Aneurysms can occur anywhere where there is a blood vessel, although they are most common in arteries. Most non-intracranial aneurysms (95%) arise distal to the origin of the renal arteries at the infrarenal abdominal aorta, a condition mostly caused by atherosclerosis. The thoracic aorta can also be involved. One common form of thoracic aortic aneurysm involves widening of the proximal aorta and the aortic root, which leads to aortic insufficiency. Aneurysms occur in the legs also, particularly in the deep vessels (e.g., the popliteal vessels in the knee). Arterial aneurysms are much more common, but venous aneurysms do happen (for example, the popliteal venous aneurysm).

  • While most aneurysms occur in an isolated form, the occurrence of berry aneurysms of the anterior communicating artery of the circle of Willis is associated with autosomal dominant polycystic kidney disease (ADPKD).
  • The third stage of syphilis also manifests as aneurysm of the aorta, which is due to loss of the vasa vasorum in the tunica adventitia.

Risks

Rupture and blood clotting are the risks involved with aneurysms. Rupture leads to drop in blood pressure, rapid heart rate, and lightheadedness. The risk of death is high except for rupture in the extremities. Blood clots from popliteal arterial aneurysms can travel downstream and suffocate tissue. Only if the resulting pain and/or numbness are ignored over a significant period of time will such extreme results as amputation be needed. Clotting in popliteal venous aneurysms are much more serious as the clot can embolise and travel to the heart, or through the heart to the lungs (a pulmonary embolism).

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Does ultrasound screening for abdominal aortic aneurysm improve mortality in men over 65? - Patient Oriented Evidence That Matters: practice recommendations
From Journal of Family Practice, 4/1/03 by David Fisher

Ashton HA, Buxton MJ, Day NE, et al. The Multicentre Aneurysm Screening Study (MASS) into the effect of abdominal aortic aneurysm screening on mortality in men: a randomized controlled trial. Lancet 2002; 360:1531-1539.

* PRACTICE RECOMMENDATIONS

Screening for abdominal aortic aneurysm (AAA) in men over age 65 years reduced their mortality related to AAA, but did not affect overall mortality. Therefore, population-based screening for AAA cannot be recommended.

* BACKGROUND

Emergency surgery following ruptured AAA is seldom successful, though surgical intervention before rupture occurs may prevent significant morbidity and mortality. Ultrasound can often detect AAAs at a size when rupture is still unlikely to occur, providing an opportunity for early intervention.

* POPULATION STUDIED

More than 70,000 men, aged 65 years and over, were recruited from 4 outpatient health centers in the United Kingdom. Patients were excluded if they had a previous AAA repair, terminal illness, or other serious health problem. Of the 67,800 men who qualified, 33,839 men were randomly chosen to receive an invitation for an abdominal ultrasound to screen for AAA, and the remaining 33,961 men acted as controls.

* STUDY DESIGN AND VALIDITY

Patients were randomized in a concealed fashion to receive abdominal ultrasound to screen for AAA or to receive routine health care. Those among the scanned group whose aorta measured 3 cm or greater were assigned to follow-up: yearly scans for an aortic diameter of 3.0-4.4 cm, quarterly scans for a diameter of 4.5-5.4 cm, or referral to surgery for diameters of 5.5 cm or greater. Follow-up ranged from 3 to 5 years.

Mortality was assessed through review of death certificates by an independent party, and additional information was collected to confirm cause of death. Quality of life was measured with 4 standardized scales. Quality assurance of ultrasound scanning was monitored throughout the study.

* OUTCOMES MEASURED

The primary outcome measured was death related to AAA. Other outcomes measured included all-cause mortality, frequency of ruptured AAA, 30-day surgical mortality, and the effect of screening and surgery on quality of life.

* RESULTS

The group that was scanned had a significantly lower rate of aneurysm-related mortality (0.19%) than the group not scanned (0.33%), yielding a relative risk reduction of 42% (P=.0002, number needed to screen=710). However, there was no difference in all-cause mortality between the 2 groups, likely due to the relatively low prevalence of AAA.

Death rates from surgery did not differ much between the groups. Quality of life--including anxiety, depression, and perception of health status--did not differ between men who had positive scans and those who had negative scans. Cost-effectiveness data were gathered but have not yet been published.

David Fisher, MD, MPH, and Richard Lord, MD, Department of Family and Community Medicine, Wake Forest University, Winston-Salem, NC. E-mail: rlord@wfubmc.edu.

COPYRIGHT 2003 Dowden Health Media, Inc.
COPYRIGHT 2003 Gale Group

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