Peripheral vascular disease
Classification and external resources
ICD-10	I73.9
ICD-9	443.9
DiseasesDB	31142
eMedicine	med/391 emerg/862
MeSH	D016491

Peripheral vascular disease (PVD), also known as peripheral artery disease (PAD) or peripheral artery occlusive disease (PAOD), includes all diseases caused by the obstruction of large arteries in the arms and legs; and it also includes a subset of diseases classified as microvascular diseases resulting from episodal narrowing of the arteries(raynauds), or widening thereof(erythromelalgia) i.e. vascular spasms. PVD can result from atherosclerosis, inflammatory processes leading to stenosis, an embolism, or thrombus formation. It causes either acute or chronic ischemia (lack of blood supply), typically of the legs.

[edit] Classification

Peripheral artery occlusive disease is commonly divided in the Fontaine stages, introduced by Dr René Fontaine in 1954:^[1] 1) mild pain when walking ("claudication"); 2) severe pain when walking relatively shorter distances (intermittent claudication); 3) pain while resting (rest pain); 4) biological tissue loss (gangrene);

[edit] Symptoms

• Claudication - pain, weakness, numbness, or cramping in muscles due to decreased blood flow
• Sores, wounds, or ulcers that heal slowly or not at all
• Noticeable change in color (blueness or paleness) or temperature (coolness) when compared to the other limb
• Diminished hair and nail growth on affected limb and digits.

[edit] Causes

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• Smoking - tobacco use in any form is the single most important modifiable cause of PVD internationally. Smokers have up to a tenfold increase in relative risk for PVD in a dose-related effect. Exposure to second-hand smoke from environmental exposure has also been shown to promote changes in blood vessel lining (endothelium) which is a precursor to atherosclerosis.

• Diabetes mellitus - between two and four times increased risk of PVD by causing endothelial and smooth muscle cell dysfunction in peripheral arteries. Diabetics account for up to 70% of nontraumatic amputations performed, and a known diabetic who smokes runs an approximately 30% risk of amputation within 5 years.

• Dyslipidemia - elevation of total cholesterol, LDL cholesterol, and triglyceride levels each have been correlated with accelerated PVD. Correction of dyslipidemia by diet and/or medication is associated with a major improvement in short-term rates of heart attack and stroke. This benefit is gained even though current evidence does not demonstrate a major reversal of peripheral and/or coronary atherosclerosis.

• Hypertension - elevated blood pressure is correlated with an increase in the risk of developing PVD, as well as in associated coronary and cerebrovascular events (heart attack and stroke).

• Other risk factors which are being studied include levels of various inflammatory mediators such as C-reactive protein, homocysteine, and an over active sex life may increase risk of contracting PVD

• Risk of PVD also increases if the patient is: over the age of 50, African American, male, obese, or has a personal history of vascular disease, heart attack, or stroke.

[edit] Diagnosis

Upon suspicion of PVD, the first-line study is the ankle brachial pressure index (ABPI/ABI) which is a measure of the fall in blood pressure in the arteries supplying the legs. A reduced ABPI (less than 0.9) is consistent with PVD. Values of ABPI below 0.8 indicate moderate disease and below 0.5 severe disease.ABPI less than 0.3 signifies "critical limb ischemia" where emergency measures are needed to save the limb. It is possible for conditions which stiffen the vessel walls (such as calcifications that occur in the setting of chronic diabetes) to produce incorrect readings and high values(>1.3), meriting further investigation regardless.

If ABPI's are abnormal the next step is generally a lower limb doppler ultrasound examination to look at site and extent of atherosclerosis at the femoral artery. Other imaging can be performed by angiography, where a catheter is inserted into the femoral artery and selectively guided to the artery in question and then used to inject radiodense contrast agent whilst an X-ray is taken. Any stenosis of the arteries can be identified and treated at the same time by balloon angioplasty if the stenosis is over a short segment (<3 cm). However if the artery is occluded or there is diffuse disease present, then arterial bypass surgery may be required.

Modern multislice computerized tomography (CT) scanners provide direct imaging of the arterial system as an alternative to angiography. CT provides complete evaluation of the aorta and lower limb arteries without the need for an angiogram's arterial injection of contrast agent.

[edit] Prevalence and Incidence

The prevalence of peripheral vascular disease in people aged over 55 years is 10%–25% and increases with age; 70%–80% of affected individuals are asymptomatic; only a minority ever require revascularisation or amputation^[2]. Peripheral vascular disease affects 1 in 3 diabetics over the age of 50.^[3]

In the USA peripheral arterial disease affects 12–20 percent of Americans age 65 and older. Approximately 10 million Americans have PVD. Despite its prevalence and cardiovascular risk implications, only 25 percent of PAD patients are undergoing treatment.^[4]

The incidence of symptomatic PVD increases with age, from about 0.3% per year for men aged 40–55 years to about 1% per year for men aged over 75 years. The prevalence of PVD varies considerably depending on how PAD is defined, and the age of the population being studied.^[2] Diagnosis is critical, as people with PAD have a four to five times higher risk of heart attack or stroke.

In Western Australia, the prevalence of symptomatic disease at around 60 years of age is about 5%.^[5]

A study from the NHANES 1999–2000 data found that PVD affects approximately 5 million adults.^[4]

The Diabetes Control and Complications Trial and U.K. Prospective Diabetes Study trials in people with type 1 and type 2 diabetes, respectively, demonstrated that glycemic control is more strongly associated with microvascular disease than macrovascular disease. It may be that pathologic changes occurring in small vessels are more sensitive to chronically elevated glucose levels than is atherosclerosis occurring in larger arteries.^[6]

[edit] Therapy

Dependent on the severity of the disease, the following steps can be taken:

• Conservative measures include Smoking cessation (cigarettes promote PVD and are a risk factor for cardiovascular disease). Regular exercise for those with claudication helps open up alternative small vessels (collateral flow) and the limitation in walking often improves. Medication with aspirin, clopidogrel and statins, which reduce clot formation and cholesterol levels, respectively, can help with disease progression and address the other cardiovascular risks that the patient is likely to have.^[7] Treadmill exercise has been reviewed as another treatment with a number of positive outcomes including reduction in cardiovascular events and improved quality of life ^[8]
• Angioplasty (PTA or percutaneous transluminal angioplasty) can be done on solitary lesions in large arteries, such as the femoral artery.
• Plaque excision, in which the plaque is scraped off of the inside of the vessel wall.
• Occasionally, bypass grafting is needed to circumvent a seriously stenosed area of the arterial vasculature. Generally, the saphenous vein is used, although artificial (Gore-Tex) material is often used for large tracts when the veins are of lesser quality.
• Rarely, sympathectomy is used - removing the nerves that make arteries contract, effectively leading to vasodilatation.
• When gangrene of toes has set in, amputation is often a last resort to stop infected dying tissues from causing septicemia.
• Arterial thrombosis or embolism has a dismal prognosis, but is occasionally treated successfully with thrombolysis.

[edit] Associations

Many PVD patients also have angina pectoris or have had myocardial infarction. There is also an increased risk for stroke.

The moderate consumption of alcohol has been found to be associated with a reduction of the risk of PVD by almost one-third compared to those who do not drink alcohol.^[9]

[edit] Guidelines

Several different guideline standards have been developed, including:

• TASC II Guidelines^[10][11][12]

• ACC/AHA Guidelines^[13]

[edit] See also

• Chronic venous insufficiency
• Vascular myelopathy
• Chronic cerebrospinal venous insufficiency

[edit] References

[edit] External links

• Peer Assisted Learning Guide (University of Manchester) - scribd.com
• Peripheral Arterial Disease at Merck Manual of Diagnosis and Therapy Professional Edition - Accessed on 27 March 2007
• Stem Cell Therapy for Peripheral Vascular Disease in India

This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Peripheral vascular disease".