Society for Vascular Surgery practice guidelines for atherosclerotic occlusive disease of the lower extremities: management of asymptomatic disease and claudication - PubMed
Review
. 2015 Mar;61(3 Suppl):2S-41S.
doi: 10.1016/j.jvs.2014.12.009. Epub 2015 Jan 28.
Michael S Conte 1 , Frank B Pomposelli 2 , Daniel G Clair 3 , Patrick J Geraghty 4 , James F McKinsey 5 , Joseph L Mills 6 , Gregory L Moneta 7 , M Hassan Murad 8 , Richard J Powell 9 , Amy B Reed 10 , Andres Schanzer 11 , Anton N Sidawy 12 ; Society for Vascular Surgery
Affiliations
- PMID: 25638515
- DOI: 10.1016/j.jvs.2014.12.009
Free article
Review
Society for Vascular Surgery practice guidelines for atherosclerotic occlusive disease of the lower extremities: management of asymptomatic disease and claudication
Society for Vascular Surgery Lower Extremity Guidelines Writing Group et al. J Vasc Surg. 2015 Mar.
Free article
Erratum in
- J Vasc Surg. 2015 May;61(5):1382
Abstract
Peripheral arterial disease (PAD) continues to grow in global prevalence and consumes an increasing amount of resources in the United States health care system. Overall rates of intervention for PAD have been rising steadily in recent years. Changing demographics, evolution of technologies, and an expanding database of outcomes studies are primary forces influencing clinical decision making in PAD. The management of PAD is multidisciplinary, involving primary care physicians and vascular specialists with varying expertise in diagnostic and treatment modalities. PAD represents a broad spectrum of disease from asymptomatic through severe limb ischemia. The Society for Vascular Surgery Lower Extremity Practice Guidelines committee reviewed the evidence supporting clinical care in the treatment of asymptomatic PAD and intermittent claudication (IC). The committee made specific practice recommendations using the GRADE (Grades of Recommendation Assessment, Development and Evaluation) system. There are limited Level I data available for many of the critical questions in the field, demonstrating the urgent need for comparative effectiveness research in PAD. Emphasis is placed on risk factor modification, medical therapies, and broader use of exercise programs to improve cardiovascular health and functional performance. Screening for PAD appears of unproven benefit at present. Revascularization for IC is an appropriate therapy for selected patients with disabling symptoms, after a careful risk-benefit analysis. Treatment should be individualized based on comorbid conditions, degree of functional impairment, and anatomic factors. Invasive treatments for IC should provide predictable functional improvements with reasonable durability. A minimum threshold of a >50% likelihood of sustained efficacy for at least 2 years is suggested as a benchmark. Anatomic patency (freedom from restenosis) is considered a prerequisite for sustained efficacy of revascularization in IC. Endovascular approaches are favored for most candidates with aortoiliac disease and for selected patients with femoropopliteal disease in whom anatomic durability is expected to meet this minimum threshold. Conversely, caution is warranted in the use of interventions for IC in anatomic settings where durability is limited (extensive calcification, small-caliber arteries, diffuse infrainguinal disease, poor runoff). Surgical bypass may be a preferred strategy in good-risk patients with these disease patterns or in those with prior endovascular failures. Common femoral artery disease should be treated surgically, and saphenous vein is the preferred conduit for infrainguinal bypass grafting. Patients who undergo invasive treatments for IC should be monitored regularly in a surveillance program to record subjective improvements, assess risk factors, optimize compliance with cardioprotective medications, and monitor hemodynamic and patency status.
Copyright © 2015 Society for Vascular Surgery. Published by Elsevier Inc. All rights reserved.
Comment in
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Screening, Evaluation, and Treatment of Peripheral Arterial Disease.
Skelly CL, Cifu AS. Skelly CL, et al. JAMA. 2016 Oct 11;316(14):1486-1487. doi: 10.1001/jama.2016.11103. JAMA. 2016. PMID: 27727372 No abstract available.
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