Tsiouris Athanasios, Wilson Lynn, Sekar Rajesh B, Mangi Abeel A, Yun James J
Section of Cardiac Surgery, Yale University School of Medicine, New Haven, Connecticut.
J Card Surg. 2016 Dec;31(12):772-777. doi: 10.1111/jocs.12861. Epub 2016 Oct 23.
A lack of donor hearts remains a major limitation of heart transplantation. Hearts from Centers for Disease Control (CDC) high-risk donors can be utilized with specific recipient consent. However, outcomes of heart transplantation with CDC high-risk donors are not well known. We sought to define outcomes, including posttransplant hepatitis and human immunodeficiency virus (HIV) status, in recipients of CDC high-risk donor hearts at our institution.
All heart transplant recipients from August 2010 to December 2014 (n = 74) were reviewed. Comparison of 1) CDC high-risk donor (HRD) versus 2) standard-risk donor (SRD) groups were performed using chi-squared tests for nominal data and Wilcoxon two-sample tests for continuous variables. Survival was estimated with Kaplan-Meier curves.
Of 74 heart transplant recipients reviewed, 66 (89%) received a SRD heart and eight (11%) received a CDC HRD heart. We found no significant differences in recipient age, sex, waiting list 1A status, pretransplant left ventricular assist device (LVAD) support, cytomegalovirus (CMV) status, and graft ischemia times (p = NS) between the HRD and SRD groups. All of the eight HRD were seronegative at the time of transplant. Postoperatively, there was no significant difference in rejection rates at six and 12 months posttransplant. Importantly, no HRD recipients acquired hepatitis or HIV. Survival in HRD versus SRD recipients was not significantly different by Kaplan-Meier analysis (log rank p = 0.644) at five years posttransplant.
Heart transplants that were seronegative at the time of transplant had similar posttransplant graft function, rejection rates, and five-year posttransplant survival versus recipients of SRD hearts. At our institution, no cases of hepatitis or HIV occurred in HRD recipients in early follow-up.
供体心脏短缺仍然是心脏移植的一个主要限制因素。疾病控制中心(CDC)高危供体的心脏在获得特定受体同意后可以使用。然而,CDC高危供体心脏移植的结果尚不清楚。我们试图确定在我们机构接受CDC高危供体心脏移植的受体的移植后结局,包括移植后肝炎和人类免疫缺陷病毒(HIV)状态。
回顾了2010年8月至2014年12月期间所有心脏移植受体(n = 74)。对1)CDC高危供体(HRD)组与2)标准风险供体(SRD)组进行比较,名义数据采用卡方检验,连续变量采用Wilcoxon双样本检验。采用Kaplan-Meier曲线估计生存率。
在回顾的74例心脏移植受体中,66例(89%)接受了SRD心脏,8例(11%)接受了CDC HRD心脏。我们发现HRD组和SRD组在受体年龄、性别、等待名单1A状态、移植前左心室辅助装置(LVAD)支持、巨细胞病毒(CMV)状态和移植物缺血时间方面无显著差异(p = 无统计学意义)。8例HRD在移植时均为血清学阴性。术后,移植后6个月和12个月时的排斥反应率无显著差异。重要的是,没有HRD受体感染肝炎或HIV。通过Kaplan-Meier分析,HRD受体与SRD受体在移植后5年的生存率无显著差异(对数秩检验p = 0.644)。
移植时血清学阴性的心脏移植与SRD心脏受体相比,移植后移植物功能、排斥反应率和移植后5年生存率相似。在我们机构,HRD受体在早期随访中未发生肝炎或HIV病例。