Abstract

Purpose CAV has an immunological component and continues to limit long term outcomes in heart transplantation (HT). Smaller single center studies have suggested that induction with r-ATG may reduce development of CAV. We evaluated the association of induction with r-ATG, Basiliximab (BxB), or ‘no induction’ and CAV in HT recipients, traditionally considered not highly sensitized [pre-transplant panel reactive antibody (PRA) class 1 and class 2 ≤ 10%]. Methods Between 6/2004 and 03/2015, we identified 4,654 adult HT recipients in UNOS who either had induction with r-ATG, BxB or ‘no induction’ at the time of HT, and had information on pre-HT PRA levels and CAV. Donor age above 55 years or structural abnormalities, multi-organ or repeat transplants were excluded. The 3 groups: r-ATG (n=644), BxB (n=991), no induction (n=3019) were compared for baseline donor/recipient characteristics and CAV. Results Overall, pre-transplant PRA 1 and 2 levels were 0.5±1.7% and 0.3±1.3% respectively. Compared to no induction or BxB, HT recipients in r-ATG group were slightly younger (53 vs 55 vs 56 yrs), more black race (23% vs 16% vs 22%), less Status 1A (49% vs 59 vs 62%). BxB group had more recipients with creatinine >1.5 (24% vs 23% in r-ARG vs 17% no-induction) (all p Conclusion Although rates of CAV were higher in our specific cohort than previously reported for the overall HT population, r-ATG was associated with lower CAV in HT recipients who are traditionally considered to be not highly sensitized.

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