Association of Aspirin Treatment With Cardiac Allograft Vasculopathy Progression and Adverse Outcomes After Heart Transplantation

被引:9
作者
Asleh, Rabea [1 ,2 ]
Briasoulis, Alexandros [3 ]
Smith, Byron [1 ]
Lopez, Camden [1 ]
Alnsasra, Hilmi [1 ]
Pereira, Naveen L. [1 ]
Edwards, Brooks S. [1 ]
Clavell, Alfredo L. [1 ]
Stulak, John M. [1 ]
Locker, Chaim [1 ]
Kremers, Walter K. [1 ]
Daly, Richard C. [1 ]
Lerman, Amir [1 ]
Kushwaha, Sudhir S. [1 ]
机构
[1] Mayo Clin, Dept Cardiovasc Dis, Rochester, MN 55905 USA
[2] Hebrew Univ Jerusalem, Hadassah Hebrew Univ, Fac Med, Heart Inst,Med Ctr, IL-90000 Jerusalem, Israel
[3] Univ Iowa Hosp & Clin, Div Cardiovasc Dis, Iowa City, IA 52242 USA
关键词
Cardiac allograft vasculopathy; aspirin; heart transplantation; coronary intravascular ultrasound; INTERNATIONAL SOCIETY; PLATELET-FUNCTION; CYCLOSPORINE; CLOPIDOGREL; ARTERIOSCLEROSIS; IMMUNOSUPPRESSION; RECIPIENTS; SIROLIMUS; MECHANISM; CELLS;
D O I
10.1016/j.cardfail.2021.01.019
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Enhanced platelet reactivity may play a role in cardiac allograft vasculopathy (CAV) progression. The use of antiplatelet agents after heart transplantation (HT) has been inconsistent and although aspirin (ASA) is often a part of the medication regimen after HT, limited evidence is available on its benefit. Methods and Results: CAV progression was assessed by measuring the difference in plaque volume and plaque index between the last follow-up and the baseline coronary intravascular ultrasound examination. Overall, 529 HT recipients were retrospectively analyzed (337 had >2 intravascular ultrasound studies). The progression in plaque volume (P = .007) and plaque index (P = .002) was significantly attenuated among patients treated with early ASA (within the first year after HT). Over a 6.7-year follow-up, all-cause mortality was lower with early ASA compared with late or no ASA use (P < .001). No cardiac deaths were observed in the early ASA group, and the risk of CAV-related graft dysfunction was significantly lower in this group (P = .03). However, the composite of all CAV-related events (cardiac death, CAV-related graft dysfunction, or coronary angioplasty) was not significantly different between the groups (P = .16). Conclusions: Early ASA use after HT may delay CAV progression and decrease mortality and CAVrelated graft dysfunction, but does not seem to affect overall CAV-associated events.
引用
收藏
页码:542 / 551
页数:10
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