Clinical & Experimental Cardiology

Clinical & Experimental Cardiology
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Editorial - (2012) Volume 3, Issue 11

Therapy of Lower Extremity Peripheral Arterial Disease

Wilbert S. Aronow*
Cardiology Division, New York Medical College, USA
*Corresponding Author: Wilbert S. Aronow, MD, FACC, FAHA, Professor of Medicine, Cardiology Division, New York Medical College, Macy Pavilion, Room 138, Valhalla, NY 10595, USA, Tel: (914) 493-5311, Fax: (914) 235-6274 Email:

Peripheral arterial disease (PAD) is chronic arterial occlusive disease of the lower extremities caused by atherosclerosis. An anklebrachial index of less than 0.90 or 1.4 or higher is diagnostic of PAD. Duplex ultrasonography, computed tomographic angiography, and magnetic resonance angiography are useful in assessing the anatomic location and severity of PAD and in selecting suitable candidates for endovascular or surgical revascularization [1].

Risk factors that predispose to PAD include age, cigarette smoking, diabetes mellitus, hypertension, dyslipidemia, increased plasma homocysteine levels, and hypothyroidism [1-4]. PAD coexists with other atherosclerotic disorders [5]. Persons with PAD are at increased risk for all-cause mortality, cardiovascular mortality, and cardiovascular events [6,7].

Smoking cessation reduces progression of PAD to critical leg ischemia and reduces the risk of myocardial infarction and death from cardiovascular causes. Smokers should be referred to a smoking cessation program [1]. Hypertension should be adequately controlled to reduce cardiovascular mortality and morbidity in persons with PAD [1,8]. The blood pressure should be reduced to less than140/90 mm Hg [8]. The higher the hemoglobin A1c levels in patients with diabetes mellitus and PAD, the higher the prevalence of severe PAD [9]. Diabetes mellitus should be treated with the hemoglobin A1c level decreased to less than 7.0% [1].

Treatment of dyslipidemia with statins has been demonstrated to reduce the incidence of mortality, cardiovascular events, and stroke in persons with PAD with and without coronary artery disease [10,11]. Double-blind, randomized, placebo-controlled studies have also demonstrated that statins improve exercise time until intermittent claudication [12,13]. Persons with PAD should have their serum lowdensity lipoprotein cholesterol reduced to less than 70 mg/dl [1].

Antiplatelet drugs have been shown to reduce the incidence of vascular death, nonfatal myocardial infarction, and nonfatal stroke in persons with PAD [14]. Persons with PAD should be treated with aspirin or clopidogrel [1]. Persons with PAD should also be treated with angiotensin-converting enzyme inhibitors to reduce cardiovascular events [1,15]. Beta blockers should be used to reduce coronary events in persons with PAD and coronary artery disease in the absence of contraindications to these drugs [16].

Cilostazol should be given to patients with PAD to increase walking distance [1,17]. Contraindications to the use of cilostazol include heart failure, a creatinine clearance less than 25 ml/min, a known predisposition for bleeding, or co-administration of CYP3A4 or CYP2C19 inhibitors such as cimetidine, diltiazem, erythromycin, ketoconazole, lansoprazole, omeprazole, and HIV-1 protease inhibitors.

The optimal exercise program for improving claudication pain distance in persons with PAD uses intermittent walking to near-maximal pain during a program of at least 6 months [18]. The American College of Cardiology/American Heart Association guidelines recommends a supervised exercise program for patients with intermittent claudication [1]. These guidelines also state that persons with PAD must have proper foot care [1].

Indications for lower extremity percutaneous transluminal angioplasty or bypass surgery are 1) incapacitating claudication in persons interfering with work or lifestyle; 2) limb salvage in persons with limb-threatening ischemia as manifested by rest pain, nonhealing ulcers, and/or infection or gangrene; and 3) vasculogenic impotence [1,19]. Amputation of lower extremities should be performed if tissue loss has progressed beyond the point of salvage, if surgery is too risky, if life expectancy is very low, or if functional limitations diminish the benefit of limb salvage [20].

References

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  2. Ness J, Aronow WS, Ahn C (2000) Risk factors for peripheral arterial disease in an academic hospital-based geriatrics practice. J Am Geriatr Soc 48: 312-314.
  3. Aronow WS, Ahn C (1998) Association between plasma homocysteine and peripheral arterial disease in older persons. Coronary Artery Dis 9: 49-50.
  4. Mya MM, Aronow WS (2003) Increased prevalence of peripheral arterial disease in older men and women with subclinical hypothyroidism. J Gerontol A Biol Sci Med Sci 58: 68-69.
  5. Aronow WS, Ahn C (1994) Prevalence of coexistence of coronary artery disease, peripheral arterial disease, and atherothrombotic brain infarction in men and women > or = 62 years of age. Am J Cardiol 74: 64-65.
  6. Criqui MH, Ninomiya JK, Wingard DL, Ji M, Fronek A (2008) Progression of peripheral arterial disease predicts cardiovascular disease morbidity and mortality. J Am Coll Cardiol 52: 1736-1742.
  7. Aronow WS, Ahmed MI, Ekundayo OJ, Allman RM, Ahmed A (2009) A propensity-matched study of the association of peripheral arterial disease with cardiovascular outcomes in community-dwelling older adults. Am J Cardiol 103: 130-135.
  8. Aronow WS, Fleg JL, Pepine CJ, Artinian NT, Bakris G, et al. (2011) ACCF/AHA 2011 Expert Consensus Document on Hypertension in the Elderly. A Report of the American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents. Developed in collaboration with the American Academy of Neurology, American Geriatrics Society, American Society for Preventive Cardiology, American Society for Hypertension, American Society of Nephrology,Association of Black Cardiologists, and European Society of Hypertension. J Am Coll Cardiol 57: 2037-2114.
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  10. Aronow WS, Ahn C (2002) Frequency of new coronary events in older persons with peripheral arterial disease and serum low-density lipoprotein cholesterol ³125 mg/dl treated with statins versus no lipid-lowering drug. Am J Cardiol 90: 789-791.
  11. Heart Protection Study Collaborative Group (2007) Randomized trial of the effects of cholesterol-lowering with simvastatin on peripheral vascular and other major vascular oputcomes in 20,536 people with peripheral arterial disease and other high-risk conditions. J Vasc Surg 45: 645-654.
  12. Aronow WS, Nayak D, Woodworth S, Ahn C (2003) Effect of simvastatin versus placebo on treadmill exercise time until the onset of intermittent claudication in older patients with peripheral arterial disease at 6 months and at 1 year after treatment. Am J Cardiol 92: 711-712.
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  14. Antithrombotic Trialists’ Collaboration (2002) Collaborative meta-analyis of randomised trials of antiplatelet therapy for prevention of death, myocardial infarction, and stroke in high risk patients. BMJ 324: 71-86.
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  16. Aronow WS, Ahn C (2001) Effect of beta blockers on incidence of new coronary events in older persons with prior myocardial infarction and symptomatic peripheral arterial disease. Am J Cardiol 87: 1284-1286.
  17. Thompson PD, Zimet R, Forbes WP, Zhang P (2002) Meta-analysis of results from eight randomized, placebo-controlled trials on the effect of cilostazol on patients with intermittent claudication. Am J Cardiol 90: 1314-1319.
  18. Gardner AW, Poehlman ET (1995) Exercise rehabilitation programs for the treatment of claudication pain. A meta-analysis. JAMA 274: 975-980.
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  20. Fujitani RM, Gordon IL, Perera GB, Wilson SE (2003) Peripheral vascular disease in the elderly. In: Aronow WS, Fleg JL, eds. Cardiovascular Disease in the Elderly Patient, 3rd ed. New York City: Marcel Dekker, Inc: 707-763.
Citation: Aronow WS (2012) Therapy of Lower Extremity Peripheral Arterial Disease. J Clin Exp Cardiolog 3:e115.

Copyright: © 2012 Aronow WS, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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