Exercise Rehabilitation for Patients With Critical Limb Ischemia After Revascularization

Background: Peripheral arterial disease (PAD) refers to narrowing and occlusion of arteries supplying oxygenated blood to non-coronary and non-intracranial circulatory systems. This term is typically used to describe disease in the legs though it also affects upper extremities, renal and mesenteric vessels. Symptomatic patients typically experience leg pain with walking or physical activity which is referred to as intermittent claudication (IC). In more advanced chronic disease states with severely compromised blood flow to the tissues, patients may have leg pain at rest or even non healing wounds that can lead to tissue loss which is defined as critical limb ischemia (CLI).

Risk factor management is critical for PAD patients with the goal of improving symptoms and preventing disease progression. This includes smoking cessation as well as appropriate management for hypertension, dyslipidemia and diabetes. Antiplatelet therapy should be initiated in symptomatic patient or when other risk factors are present. Exercise interventions should be encouraged in all patients with PAD. In patients who have progressed to critical limb ischemia, treatment goals are to relieve pain, heal wounds and prevent limb loss. In addition to risk factor management and medical therapy, these patients require revascularization procedures. Depending on the extent and location of disease, the techniques used may be endovascular/interventional (minimally invasive), surgical, or a hybrid combination of the two.

There has been minimal research examining exercise rehabilitation after revascularization. There are no studies that have focused on exercise rehabilitation exclusively in patients with CLI.

Purpose/Objectives: The aim of this study is to develop a better understanding of the role for supervised exercise rehabilitation programs (SEP) in PAD-CLI patients after revascularization. This pilot study will assess the feasibility for expanding this research to a larger randomized controlled trial.

Study Design:

This is a two-phase, single-center, non-blinded randomized controlled trial.

Objectives:

In phase 1, the investigators will assess feasibility. Specifically, the investigators will assess rate of enrollment, barriers to participation and any methodological challenges that may require changes. If phase 1 of this study shows reasonable rates of enrollment and no methodological challenges, we will proceed to phase 2.

Key objectives for phase 2 are as follows:

1. The primary objective is to show how SEP affects functional capacity and quality of life in patients with PAD-CLI after revascularization.
2. The secondary objective is to show how SEP affects the rate of major adverse limb events (MALE) and improve survival in patients with PAD-CLI after revascularization.

Hypotheses: 1) PAD-CLI patients who have undergone revascularization will have a greater improvement in functional capacity and quality of life compared with patients treated with best medical therapy alone.

1. PAD-CLI patients who have undergone revascularization will have fewer MALE and improved survival compared with patients treated with best medical therapy alone.

Methodology: Patients included in the study will be identified in the vascular surgery outpatient clinic or through emergency department as requiring revascularization secondary to critical limb ischemia. Patients will be approached regarding study participation prior to the revascularization procedure. After eligibility is confirmed and patients have signed informed consent, patients will be randomized to one of two groups:

1. Best Medical Therapy (BMT): Appropriate risk factor management, encouragement to mobilize.
2. Supervised Exercise Program (SEP): consist of BMT plus a supervised exercise program.

Patients will undergo evaluation of functional capacity assessment using a graded treadmill test at the outset of the study and after 12 weeks of either BMP or SEP. The investigators will also administer a validated quality of life (QoL) questionnaire to the two different groups at the outset and completion of the study. Patients will be followed annually to monitor for MALE and survival.

Statistics: Normally distributed data will be presented as mean ± SD. Results at baseline and 12 weeks will be compared using a paired t-test. For data that is not normally distributed, comparisons will be performed using a non-parametric Mann-Whitney test. Comparisons will be accepted as statistically significant at 95% confidence level (p≤0.05). STATA software will be used for statistical analysis.