Lower extremity arterial disease vs. coronary artery disease: mortality differences after revascularization

医学 冠状动脉疾病 内科学 血运重建 心脏病学 入射(几何) 置信区间 泊松回归 优势比 死亡率 比率 外科 心肌梗塞 人口 物理 环境卫生 光学
作者
Mitsuyoshi Takahara,Yoshimitsu Soga,Osamu Iida
出处
期刊:European Heart Journal [Oxford University Press]
卷期号:45 (18): 1634-1643 被引量:7
标识
DOI:10.1093/eurheartj/ehae207
摘要

Abstract Background and Aims Patients undergoing revascularization for lower extremity arterial disease (LEAD) may face a higher risk of mortality than those with coronary artery disease (CAD). This study aimed to characterize the difference in mortality risk between patients undergoing revascularization for LEAD and CAD and identify associated factors. Methods The 1-year database of 10 754 patients undergoing revascularization for CAD (n = 6349) and LEAD (n = 4405) was analysed. Poisson regression models were used to characterize interpopulation differences in mortality, adjusting for baseline clinical features, including age, sex, polyvascular disease, comorbidities, medications, and vulnerabilities. Results Individuals with LEAD were older, were more likely to have polyvascular disease, had more comorbidities, and received fewer cardioprotective drugs than those with CAD. Vulnerabilities remained more common in the LEAD group even after adjusting for these clinical features. The crude risk ratio of mortality incidence for LEAD vs. CAD was 2.91 (95% confidence interval, 2.54–3.34), attenuated to 2.14 (1.83–2.50) after controlling for age, sex, and polyvascular disease. The percentage attenuation in the excessive mortality associated with LEAD was 29%. The stepwise addition of comorbidities, medications, and vulnerabilities as adjusting factors attenuated the incidence risk ratio to 1.48 (1.26–1.72), 1.33 (1.12–1.58), and 1.17 (0.98–1.39), respectively, and increased the percentage attenuation to 64%, 73%, and 86%, respectively. Conclusions Mortality risk was almost three-fold higher in patients undergoing revascularization for LEAD than in those with CAD. The excessive mortality was considerably attributable to inter-group differences in baseline characteristics, including potentially clinically or socially modifiable factors.
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