World regional differences in outcomes for patients with peripheral artery disease: Insights from the EUCLID trial

Author:

Norgren Lars1ORCID,North Rebecca2,Baumgartner Iris3,Berger Jeffrey S4ORCID,Blomster Juuso I5,Hiatt William R6,Jones W Schuyler78,Katona Brian G9,Mahaffey Kenneth W10,Mulder Hillary7,Patel Manesh R78,Rockhold Frank W7ORCID,Fowkes F Gerry R11

Affiliation:

1. Faculty of Medicine and Health, Örebro University, Örebro, Sweden

2. Department of Statistics, North Carolina State University, Raleigh, NC, USA

3. Division of Angiology, Swiss Cardiovascular Centre, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland

4. Departments of Medicine and Department of Surgery, New York University School of Medicine, New York, NY, USA

5. Turku University Hospital, University of Turku, Turku, Finland

6. Division of Cardiology, Department of Medicine, University of Colorado School of Medicine, Aurora, CO, USA

7. Duke Clinical Research Institute, Durham, NC, USA

8. Division of Cardiology, Department of Medicine, Duke University School of Medicine, Durham, NC, USA

9. AstraZeneca Gaithersburg, Gaithersburg, MD, USA

10. Stanford Center for Clinical Research, Stanford University School of Medicine, Stanford, CA, USA

11. Usher Institute of Population Health Sciences and Informatics, University of Edinburgh, Edinburgh, UK

Abstract

Regional variations exist in the epidemiology of peripheral artery disease (PAD), in comorbidities, use of secondary prevention, and outcomes. Large studies of these variations in worldwide populations are rare. The EUCLID (Examining Use of tiCagreLor In peripheral artery Disease) trial included 13,885 patients with PAD from four geographical regions (Central/South America, Europe, Asia, North America) and compared monotherapy with ticagrelor and clopidogrel. Inclusion criteria were either an ankle–brachial index < 0.80 or a prior revascularization. The primary efficacy endpoint was time to first occurrence of any event in the composite of cardiovascular death, myocardial infarction, or ischemic stroke and did not differ between the study arms. This post hoc analysis of EUCLID confirmed that regional differences occurred in the inclusion criteria with more prior revascularization in North America (73.9%) and Asia (72.5%) compared with Central/South America (34.0%) and Europe (51.6%). The characteristics of patients also differed. Prior amputation at baseline was most frequent in Central/South America (6.3%) compared with other regions (1.6–2.8%). A history of stroke was most common in Asia, coronary heart disease in North America, and diabetes in Central/South America compared with other regions. The incidence of outcomes in patients with PAD varied by region. North America had the highest rate of the primary combined endpoint (5.97 events/100 patient-years). Corresponding rates were 4.80, 3.95, and 3.87 for Asia, Europe, and Central/South America, respectively. Hospitalization for acute limb ischemia (events/100 patient-years) was most frequent in Europe (0.75) and North America (0.74) compared with Asia (0.60) and Central/South America (0.33). Adjustment for inclusion criteria and relevant PAD characteristics did not have a major impact on these regional differences. Further adjustment for concomitant disease, risk factors, and preventive medication modified the regional differences only marginally. In conclusion, substantial regional differences were found in cardiovascular and limb outcomes in patients with PAD and were not explained by variation in the category of included patients, concomitant disease, risk factors, and prevention. Such differences, which may be due to variation in other factors such as background population rates or clinical care, need to be considered when designing and interpreting large international studies (ClinicalTrials.gov Identifier: NCT01732822).

Funder

astrazeneca

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine

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