Early Use of Aspirin for Coronary Allograft Prophylaxis in Heart Transplant Recipients

医学 阿司匹林 危险系数 肺移植 内科学 心脏移植 回顾性队列研究 置信区间 移植 心脏病学 队列研究 比例危险模型 外科
作者
Cassia Kessler Iglesias,Jason Bloom,Xiaoman Xiao,Jeremy Moskovitch,H. Eckford,Sophie Offen,Eugene Kotlyar,Anne Keogh,Andrew Jabbour,Peter Bergin,Angeline Leet,James Hare,Andrew J. Taylor,Chris Hayward,P. Jansz,David M. Kaye,Peter S. Macdonald,K. Muthiah
出处
期刊:Transplantation [Wolters Kluwer]
卷期号:109 (2): 346-351 被引量:2
标识
DOI:10.1097/tp.0000000000005131
摘要

Background. Coronary allograft vasculopathy (CAV) remains a significant cause of morbidity and mortality after heart transplantation. The use of aspirin for CAV prophylaxis has recently garnered interest as a possible therapeutic adjunct in this setting. Methods. This 2-center retrospective cohort study included 372 patients who underwent heart transplantation between January 2009 and March 2018 and were stratified according to the commencement of aspirin during their index transplant admission. The primary outcome was the development of moderate or severe CAV (International Society for Heart and Lung Transplantation grade ≥2) at surveillance coronary angiography. Secondary endpoints included mortality at follow-up. Results. There were no differences in age, sex, and cause of heart failure. In the early aspirin group, the preponderant risk factors included use of ventricular assist devices, pretransplant smoking, and mild or moderate rejection. Multivariable analyses to assess for independent predictors of CAV development and mortality demonstrated that aspirin was associated with reduced mortality (adjusted hazard ratio = 0.19; 95% confidence interval, 0.08-0.47, P < 0.01) and a trend toward a protective effect against the development of moderate or severe CAV (adjusted hazard ratio = 0.24; 95% confidence interval, 0.54-1.19; P = 0.08). Conclusions. In this retrospective risk-adjusted 2-center cohort study, early aspirin administration was associated with reduced risk of death and a trend toward a protective effect against CAV development. These findings warrant validation in prospective randomized trials.
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