Recommended Conferences

PHYSIOTHERAPY 2022

Paris, France
Related Subjects
 

Prevalence and clinical implications of newly revealed, asymptomatic abnormal ankle-brachial index in patients with significant coronary artery disease

Author(s): Lee JY, Lee SW, Lee WS, Han S, Park YK, et al.

Abstract

Objectives: This study sought to evaluate the association between newly revealed abnormal ankle-brachial index (ABI) and clinical outcomes in patients with significant coronary artery stenosis.

Background: Little is known about the prevalence and clinical implications of ABI in patients with no claudication or previous history of peripheral artery disease who undergo diagnostic coronary angiography.

Methods: Between January 1, 2006, and December 31, 2009, ABI was evaluated in 2,543 consecutive patients with no clinical history of claudication or peripheral artery disease who underwent diagnostic coronary angiography. Abnormal ABI was defined as ≤0.9 or ≥1.4. The primary endpoint was the composite of death, myocardial infarction, and stroke over 3 years.

Results: Of the 2,543 patients, 390 (15.3%) had abnormal ABI. Of the 2,424 patients with at least 1 significant stenosis (≥50%) in a major epicardial coronary artery, 385 (15.9%) had abnormal ABI, including 348 (14.4%) with ABI ≤0.9 and 37 (1.5%) with ABI ≥1.4. During a median follow-up of 986 days, the 3-year major adverse event rate was significantly higher in patients with abnormal than normal ABI (15.7% vs. 3.3%, p < 0.001). After multivariate analysis, abnormal ABI was identified as a predictor of primary endpoint (hazard ratio [HR]: 1.87; 95% confidence interval [CI]: 1.23 to 2.84; p = 0.004). After adjustment by propensity-score matching, abnormal ABI could predict adverse clinical events in patients with established coronary artery disease (HR: 2.40; 95% CI: 1.41 to 4.10; p = 0.001).

Conclusions: The prevalence of newly revealed abnormal, asymptomatic ABI among patients who have significant CAD on coronary angiography was 15.9%. The presence of abnormal ABI was associated with a higher incidence of adverse clinical outcomes over 3 years.

Similar Articles

Epidemiology of peripheral artery disease

Author(s): Criqui MH, Aboyans V

Mortality over a period of 10 years in patients with peripheral arterial disease

Author(s): Criqui MH, Langer RD, Fronek A, Feigelson HS, Klauber MR, et al.

Functional decline in peripheral arterial disease: associations with the ankle brachial index and leg symptoms

Author(s): McDermott MM, Liu K, Greenland P, Guralnik JM, Criqui MH, et al.

Health ABC Collaborative Research Group

Author(s): Newman AB, Haggerty CL, Kritchevsky SB, Nevitt MC, Simonsick EM

The long-term prognostic value of the resting and postexercise ankle-brachial index

Author(s): Feringa HH, Bax JJ, van Waning VH, Boersma E, Elhendy A, et al.

Heinz Nixdorf Recall Study Investigative Group

Author(s): Gronewold J, Hermann DM, Lehmann N, Kröger K, Lauterbach K, et al.

Physical activity during daily life and mortality in patients with peripheral arterial disease

Author(s): Garg PK, Tian L, Criqui MH, Liu K, Ferrucci L, et al.

Walking exercise in patients with intermittent claudication

Author(s): Bartelink ML, Stoffers HE, Biesheuvel CJ, Hoes AW

Supervised exercise therapy versus non-supervised exercise therapy for intermittent claudication

Author(s): Fokkenrood HJ, Bendermacher BL, Lauret GJ, Willigendael EM, Prins MH, et al.

Supervised vs unsupervised exercise for intermittent claudication: A systematic review and meta-analysis

Author(s): Vemulapalli S, Dolor RJ, Hasselblad V, Schmit K, Banks A, et al.

Supervised exercise therapy for intermittent claudication in daily practice

Author(s): Kruidenier LM, Nicolaï SP, Hendriks EJ, Bollen EC, Prins MH, et al.

Supervised exercise therapy for intermittent claudication in a community-based setting is as effective as clinic-based

Author(s): Bendermacher BL, Willigendael EM, Nicolaï SP, Kruidenier LM, Welten RJ, et al.

Experimental model of pain-free treadmill training in patients with claudication

Author(s): Mika P, Spodaryk K, Cencora A, Unnithan VB, Mika A