ABSTRACT: Peripheral artery disease (PAD) is a common condition encountered in primary care and subspecialty clinics. Despite guidelines recommending antiplatelet agents, statins, and in some cases cilostazol, many patients with PAD are not receiving appropriate medications. Interventionalists who evaluate and treat these patients have a unique opportunity to prescribe appropriate cardioprotective medications, and to educate the primary care provider. In this article we will review guidelines for prescribing antiplatelet agents (aspirin and clopidogrel), statins, and cilostazol in patients with PAD; review evidence behind the guidelines; and present a “report card” of healthcare provider compliance with these guidelines. We will also describe some of the barriers that reduce clinician compliance with guidelines and present some strategies to overcome these barriers.
VASCULAR DISEASE MANAGEMENT 2013:10(2):E37-E44
Key words: peripheral artery disease, medical treatment of peripheral artery disease
Peripheral artery disease (PAD) is commonly encountered in primary care and subspecialty clinics. Its prevalence — estimated to be 7.1 million in the United States1 — increases with increasing age (>40 years) and with independently associated risk factors of diabetes, smoking, and hyperlipidemia. These risk factors have an additive effect on the development and severity of the disease.2
Approximately 50% of patients with PAD are asymptomatic and diagnosed by screening Ankle Brachial Index (ABI), 10% to 35% have claudication, and 1% to 2% have critical limb ischemia (CLI), defined as rest pain, tissue loss, or gangrene.3 Patients with PAD (defined as ABI score <0.9) have lower survival (Figure 1)4 and higher rates of cardiovascular and cerebrovascular events as compared to patients without PAD.4,5-7 Symptom severity and lower ABI score have been correlated with greater functional decline and decreased survival (Figure 2).4,5,8,9 The annual mortality among patients with critical limb ischemia, defined as an ABI <0.4, is approximately 25%, with most of the morbidity and mortality related to myocardial infarction (MI) and stroke.10
Even with known high prevalence and associated high cardiovascular morbidity and mortality, PAD remains under-recognized and undertreated. The PARTNERS (PAD Awareness, Risk and Treatment: New Resources for Survival) study, which evaluated approximately 7,000 patients aged 70 years or older, or aged 50 through 69 years with history of cigarette smoking or diabetes in primary care practices across the United States, showed that of patients with known PAD, only 83% were aware of their diagnosis, and only 49% of their physicians were aware of the diagnosis.11
The National Cholesterol Education Program (NCEP) expert panel considers PAD an equivalent to coronary artery disease (CAD), and therefore recommends that patients with PAD receive the same cardioprotective medication regimen as patients with CAD.12 However, despite evidence from several studies showing that antiplatelet agents13-15 and statins16-18 reduce cardiovascular morbidity and mortality in patients with PAD, only 25% of the patients with PAD are receiving appropriate medical treatment.19 This alarmingly low number may stem from poor provider awareness about how to manage PAD.19 The recently published Performance Measures for Adults with PAD, which provide metrics for quality improvement and external reporting, recommend prescribing an antiplatelet and a statin.20
Interventionalists who treat patients with PAD have a unique opportunity to place patients on optimal cardioprotective therapy in accordance with the latest guidelines. The purpose of this article is to review guidelines for the use of antiplatelets (aspirin and clopidogrel), statins, and cilostazol; summarize evidence behind the guidelines; and present a “report card” of how we do as health care providers in adhering to these guidelines.
Aspirin, typically in daily doses of 75 to 325 mg, is recommended as safe and effective antiplatelet therapy to reduce the risk of MI, stroke, or vascular death in individuals with symptomatic atherosclerotic lower extremity PAD, including those with intermittent claudication or critical limb ischemia, prior lower extremity revascularization (endovascular or surgical), or prior amputation for lower extremity ischemia (class 1, level of evidence: B).21
Aspirin: evidence behind the guidelines
In 2002, the Antithrombotic Trialists’ Collaboration performed a meta-analysis examining the efficacy of antiplatelet agents on cardiovascular events (nonfatal MI, nonfatal stroke, and vascular death) in 135,000 patients (287 studies) with vascular disease (acute and previous MI, acute and previous stroke, or other high-risk conditions, such as lower extremity PAD).15 The authors found that patients receiving antiplatelet therapy experienced a 22% odds reduction for adverse cardiovascular events compared with patients not receiving an antiplatelet agent (P<.0001). In a subset analysis of 42 trials including 9,214 patients with PAD, there was a 23% reduction in serious vascular events (P<.004) compared with controls.15 Similar benefit was observed in patients with intermittent claudication as well as those undergoing peripheral bypass grafting and peripheral angioplasty.15 The rate of cardiovascular events was similar in patients taking high doses vs low doses of aspirin. More recently, the CLIPS (Critical Leg Ischemia Prevention Study) trial14 demonstrated reduction in cardiovascular events in patients randomized to aspirin versus placebo. This study involved patients with symptomatic (claudicant) or asymptomatic PAD (ABI <0.85) documented by angiography or ultrasound. The trial was stopped early because of poor patient recruitment.
Recent papers raised doubts regarding the benefits of aspirin in patients with PAD. A meta-analysis including 18 trials compared the effects of aspirin (with or without dipyridamole) vs controls in patients with PAD.22 Out of 5,269 patients in this trial, 2,823 of whom were taking aspirin (with or without dipyridamole) there was no statistically significant reduction in the primary end point of cardiovascular events (nonfatal MI, nonfatal stroke, and cardiovascular death) (pooled relative risk [RR] 0.88; P=.13). However, associations of aspirin therapy with the individual components of the primary end points showed that the risk of nonfatal stroke was significantly lower in the aspirin group than in the placebo group (RR 0.66; P=.02). One caveat about this trial is that it may have missed smaller but beneficial effects of aspirin as it was designed to detect a 25% or greater reduction in cardiovascular events.
The POPADAD (Prevention of Progression of Asymptomatic Diabetic Arterial Disease) trial23 evaluated the effects of aspirin versus placebo in 1,276 patients with diabetes and asymptomatic PAD (ABI <0.99). Aspirin therapy failed to show any benefits in reducing cardiovascular events and mortality. The AAA trial (Aspirin for Asymptomatic Atherosclerosis)24 randomized 3,350 asymptomatic patients with ABI <0.95 to receive either aspirin or placebo for mean duration of 8.2 years. Aspirin therapy failed to show any benefits in reduction of primary endpoint, a composite of initial fatal or nonfatal coronary event, stroke, or revascularization. One limitation of the study was that 40% of the patients were noncompliant with the medication regimen.
Because recent trials showed a neutral effect of aspirin, the level of evidence for prescribing aspirin in patients with PAD has been changed from A to B in the 2011 ACCF/AHA focused update guidelines.21
Clopidogrel (75 mg per day) is recommended as a safe and effective alternative antiplatelet therapy to aspirin to reduce the risk of MI, ischemic stroke, or vascular death in individuals with symptomatic atherosclerotic lower extremity PAD, including those with intermittent claudication or critical limb ischemia, prior lower extremity revascularization (endovascular or surgical), or prior amputation for lower extremity ischemia (class 1, level of evidence: B).21
Evidence behind the guidelines
Clopidogrel is a thienopyridine derivative that decreases platelet activation. The CAPRIE (Clopidogrel versus Aspirin in Patients at Risk of Ischemic Events) trial13 randomized 19,185 high-risk patients (recent MI, recent stroke, or PAD) to receive either clopidogrel or aspirin for a mean duration of 1.91 years. The primary endpoint was a composite of ischemic stroke, MI, or vascular death. Patients randomized to clopidogrel experienced an 8.7% relative risk reduction in vascular events (P=.043). In the subgroup of patients with PAD, patients randomized to clopidogrel had 23.8% relative risk reduction in vascular events (P=.0028) (Figure 3).
Combination Antiplatelet Therapy
The combination of aspirin and clopidogrel may be considered to reduce the risk of cardiovascular events in patients with symptomatic atherosclerotic lower extremity PAD, including those with intermittent claudication or critical limb ischemia, prior lower extremity revascularization (endovascular or surgical), or prior amputation for lower extremity ischemia and who are not at increased risk of bleeding and who are at high perceived cardiovascular risk (class IIb, level of evidence: B).21
Evidence behind the guidelines
The CHARISMA trial directly compared dual antiplatelet therapy (aspirin and clopidogrel) to aspirin alone in 15,603 patients who were at high risk for cardiovascular events.25 After a median of 28 months follow-up, no difference was seen in the primary endpoint, a composite of myocardial infarction, stroke, or death from cardiovascular causes between two treatment groups. In subgroup of patients with PAD, combination therapy failed to show any benefits. Two post-hoc analyses26,27 of the CHARSIMA trial identified potential benefits to combination antiplatelet therapy over aspirin alone. However, this observation needs to be validated with a well-designed, randomized control trial. Keeping these results in mind the 2011 focused updated ACCF/AHA guidelines included new recommendation for dual antiplatelet therapy.21
Treatment with a statin is indicated for all patients with PAD to achieve a target low density lipoprotein (LDL) cholesterol level of less than 100 mg/dL (class 1, level of evidence: B).3
Treatment with a statin medication to achieve a target LDL cholesterol level of less than 70 mg/dL is reasonable for patients with lower extremity PAD at very high risk of ischemic events (class IIa, level of evidence: B).3
Evidence behind the guidelines
The Heart Protection Study randomized 20,536 high risk patients with CAD, cerebrovascular, PAD, or diabetes to receive 40 mg of simvastatin daily or placebo.16 After 5 years of follow-up, patients allocated to the simvastatin group enjoyed a 24% relative risk reduction in the occurrence of MI, stroke, and coronary and noncoronary revascularization (P=.0001, Figure 4). Patients receiving simvastatin also had 17% proportional reduction in mortality due to vascular causes. A subgroup analysis found 22% reduction in the rate of first vascular events in 6,748 patients with PAD regardless of their presenting cholesterol levels.28
Statin use is associated with decreased mortality in CLI patients undergoing infrainguinal bypass graft surgery17 or endovascular repair.18 In the latter series, patients with CLI who underwent endovascular revascularization were categorized according to whether they were taking a statin at the time of revascularization. At 24 months after revascularization, patients who were prescribed a statin had significantly better primary patency, secondary patency, limb salvage, and overall survival than patients who were not taking a statin. Moreover, the beneficial effects of statins were independent of the total cholesterol and LDL levels.18
Cilostazol (100 mg orally 2 times per day) is indicated as an effective therapy to improve symptoms and increase walking distance in patients with lower extremity PAD and intermittent claudication (in the absence of heart failure) (class 1, level of evidence: A).3
A therapeutic trial of cilostazol should be considered in all patients with lifestyle-limiting claudication (in the absence of heart failure) (class 1, level of evidence: A).3
Evidence behind the guidelines
Cilostazol is a phosphodiesterase type 3 inhibitor that has antiplatelet and vasodilatory properties.29 Several trials have shown that cilostazol increases walking distance compared with placebo in patients with intermittent claudication.30-33 A cilostazol dose of 100 mg twice daily is more effective than 50 mg twice daily.33
Cilostazol also has been shown to reduce restenosis,34-37 decrease the rate of target vessel revascularization (TVR),34 and improve limb salvage35 in patients who have undergone infrainguinal intervention. In one trial, 80 patients with intermittent claudication due to femoropopliteal lesion (without an inflow lesion, with an outflow artery, and with symptoms that were not improved with pharmacological therapy or exercise) were randomized to cilostazol or placebo. Patients underwent either balloon angioplasty or stent placement (stent was placed if after 60 sec of balloon angioplasty the residual stenosis was >30%). The lesion length was 121 ± 67.3 mm and 131.5 ± 84.0 mm in patients who did and did not receive cilostazol, respectively. There was significant reduction in the primary end point of TVR at 2 years follow-up in the patients receiving cilostazol (84.6% vs 62.2%; P=.04, Figure 5). Patients receiving cilostazol also had better secondary outcomes, which included lower binary restenosis rate (43.6% vs 70.3%; P=.02), freedom from target lesion revascularization (87.2% vs 67.6%; P<.05) and freedom from major adverse cardiovascular events (MACE) defined as death, nonfatal MI, stroke, percutaneous or surgical revascularization, and leg amputation (79.5% vs 48.7%; P=.006).34
In another series, 618 patients (356 with and 262 without cilostazol) with CLI who underwent endovascular therapy were retrospectively analyzed. Patients who were receiving cilostazol had better amputation-free survival (47.7% vs 32.7%; log rank P<.001), limb salvage (86.6% vs 75.3%; log rank P=.004), and freedom from surgical conversion (91.0% vs 81.2%; log rank P=.001) than patients who were not taking cilostazol. However, no significant difference was observed between two groups in terms of overall survival and freedom from repeat revascularization.35
Pentoxifylline is used by some providers as a treatment for claudication. The data to support its use in patients with claudication are insufficient. Two meta-analyses of randomized, placebo controlled trials found only marginal benefit of pentoxifylline.38,39 ACC/AHA 2005 practice guidelines for management of patients with PAD concluded that clinical effectiveness of pentoxifylline as therapy for claudication is marginal and not well established and gave class IIB (level of evidence: C) recommendation for its use.3
Report Card of Physician Compliance and Conclusion
Table 1 shows a “report card” in terms of prescribing antiplatelet agents and statins in several major trials and case series. The trend for prescribing antiplatelet agents seems to be increasing in the recent trials but still remains around 80%. Except for the CASTLE trial, the use of statins in most trials remains disappointing, with utilization rates below 50%. Thus, even in highly controlled research settings, it appears that patients with PAD remain undertreated with cardioprotective medications.
Studies have suggested a variety of physician-related factors that could be responsible for nonadherence with the guidelines. These factors include lack of physician awareness or disagreement with the guidelines, lack of confidence that they could adhere to the guideline recommendations, and their belief that following guidelines will not change patient outcomes. Lack of motivation and physician habits are also postulated as a barrier to adhering to guidelines.40 Other external factors such as lack of time, lack of resources (e.g., computer reminder system), limited reimbursement and presence of contradictory guidelines also have been shown to decrease physician compliance.40,41 Table 2 summarizes potential barriers to compliance with the guidelines and suggests possible interventions. Table 3 provides a summary of the recommended medical treatment in patients with PAD.
Steps must be taken to improve physician awareness and compliance with PAD guidelines. First and foremost, primary care physicians need to be aware of the signs and symptoms of PAD, as well as recommendations for managing these patients. Specialists who see these patients in consultation whether in vascular medicine, interventional cardiology with special training in endovascular medicine, or vascular surgery should insure that each patient is on optimal cardioprotective therapy. Vascular specialists are uniquely positioned to educate referring providers on the latest recommendations for managing PAD.
The prevalence of PAD is going to increase with the aging of the United States population. Increased physician awareness of how to manage PAD not only will improve compliance with the guidelines, but also may help providers improve the lives of their patients.
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- Heart Protection Study Collaborative Group. MRC/BHF Heart Protection Study of cholesterol lowering with simvastatin in 20,536 high-risk individuals: a randomised placebo-controlled trial. Lancet. 2002;360(9326):7-22.
- Schanzer A, Hevelone N, Owens CD, Beckman JA, Belkin M, Conte MS. Statins are independently associated with reduced mortality in patients undergoing infrainguinal bypass graft surgery for critical limb ischemia. J Vasc Surg. 2008;47(4):774-781.
- Aiello FA, Khan AA, Meltzer AJ, Gallagher KA, McKinsey JF, Schneider DB. Statin therapy is associated with superior clinical outcomes after endovascular treatment of critical limb ischemia. J Vasc Surg. 2012;55(2):371-9; discussion 380.
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Editor’s Note: Disclosure: The authors have completed and returned the ICMJE Form for Disclosure of Potential Conflicts of Interest. Dr. Slovut discloses that he serves as a member of the Data Safety Monitoring Board for a study funded by Arteriocyte, Inc. Dr. Kumar has no disclosures to report in relation to the content of this article.
Manuscript received September 28, 2012; provisional acceptance given October 29, 2012; final version accepted November 5, 2012.
Address for correspondence: David Paul Slovut, MD, PhD, Division of Cardiology, and Division of Vascular and Endovascular Surgery, Montefiore Medical Center, Bronx, New York, USA, Email: firstname.lastname@example.org