Duke University Hospital, Durham, North Carolina, USA.
Duke University Hospital, Durham, North Carolina, USA.
JACC Heart Fail. 2024 Mar;12(3):438-447. doi: 10.1016/j.jchf.2023.11.015. Epub 2024 Jan 24.
Extended criteria donor (ECD) hearts available with donation after brain death (DBD) are underutilized for transplantation due to limitations of cold storage.
This study evaluated use of an extracorporeal perfusion system on donor heart utilization and post-transplant outcomes in ECD DBD hearts.
In this prospective, single-arm, multicenter study, adult heart transplant recipients received ECD hearts using an extracorporeal perfusion system if hearts met study criteria. The primary outcome was a composite of 30-day survival and absence of severe primary graft dysfunction (PGD). Secondary outcomes were donor heart utilization rate, 30-day survival, and incidence of severe PGD. The safety outcome was the mean number of heart graft-related serious adverse events within 30 days. Additional outcomes included survival through 2 years benchmarked to concurrent nonrandomized control subjects.
A total of 173 ECD DBD hearts were perfused; 150 (87%) were successfully transplanted; 23 (13%) did not meet study transplantation criteria. At 30 days, 92% of patients had survived and had no severe PGD. The 30-day survival was 97%, and the incidence of severe PGD was 6.7%. The mean number of heart graft-related serious adverse events within 30 days was 0.17 (95% CI: 0.11-0.23). Patient survival was 93%, 89%, and 86% at 6, 12, and 24 months, respectively, and was comparable with concurrent nonrandomized control subjects.
Use of an extracorporeal perfusion system resulted in successfully transplanting 87% of donor hearts with excellent patient survival to 2 years post-transplant and low rates of severe PGD. The ability to safely use ECD DBD hearts could substantially increase the number of heart transplants and expand access to patients in need. (International EXPAND Heart Pivotal Trial [EXPANDHeart]; NCT02323321; Heart EXPAND Continued Access Protocol; NCT03835754).
由于冷藏限制,脑死亡后供体(DBD)的可利用的扩展标准供体(ECD)心脏在移植中未得到充分利用。
本研究评估了体外灌注系统在 ECD DBD 心脏供体心脏利用和移植后结果中的作用。
在这项前瞻性、单臂、多中心研究中,如果心脏符合研究标准,接受成人心脏移植的患者将使用体外灌注系统接受 ECD 心脏。主要结局是 30 天存活率和无严重原发性移植物功能障碍(PGD)的复合结局。次要结局是供体心脏利用率、30 天存活率和严重 PGD 的发生率。安全性结局是 30 天内心脏移植物相关严重不良事件的平均数量。其他结局包括通过 2 年基准与同期非随机对照受试者的存活率。
共灌注了 173 个 ECD DBD 心脏;150 个(87%)成功移植;23 个(13%)不符合研究移植标准。在 30 天时,92%的患者存活且无严重 PGD。30 天存活率为 97%,严重 PGD 的发生率为 6.7%。30 天内心脏移植物相关严重不良事件的平均数量为 0.17(95%CI:0.11-0.23)。患者的存活率分别为移植后 6、12 和 24 个月时的 93%、89%和 86%,与同期非随机对照受试者相当。
使用体外灌注系统成功移植了 87%的供体心脏,患者在移植后 2 年的存活率高,严重 PGD 的发生率低。安全使用 ECD DBD 心脏的能力可以大大增加心脏移植的数量,并扩大有需要的患者的可及性。(国际 EXPAND 心脏关键试验 [EXPANDHeart];NCT02323321;心脏 EXPAND 持续准入方案;NCT03835754)。