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控制性循环死亡后肺移植供体的选择:包括原位腹部常温区域灌注和体外肺灌注的法国方案结果。

Controlled donation after circulatory death lung transplantation: Results of the French protocol including in situ abdominal normothermic regional perfusion and ex vivo lung perfusion.

机构信息

Department of Thoracic Surgery and Lung Transplantation, Hôpital Foch, Suresnes, France.

Department of Thoracic Surgery and Lung Transplantation, Centre Hospitalier Universitaire de Strasbourg Strasbourg, France.

出版信息

J Heart Lung Transplant. 2023 Aug;42(8):1093-1100. doi: 10.1016/j.healun.2023.03.003. Epub 2023 Mar 13.

DOI:10.1016/j.healun.2023.03.003
PMID:37019731
Abstract

BACKGROUND

The French national protocol for controlled donation after circulatory determination of death (cDCD) includes normothermic regional perfusion (NRP) in case of abdominal organ procurement and additional ex-vivo lung perfusion (EVLP) before considering lung transplantation (LT).

METHODS

We made a retrospective study of a prospective registry that included all donors considered for cDCD LT from the beginning of the program in May 2016 to November 2021.

RESULTS

One hundred grafts from 14 donor hospitals were accepted by 6 LT centers. The median duration of the agonal phase was 20 minutes [2-166]. The median duration from circulatory arrest to pulmonary flush was 62 minutes [20-90]. Ten lung grafts were not retrieved due to prolonged agonal phases (n = 3), failure of NRP insertion (n = 5), or poor in situ evaluation (n = 2). The remaining 90 lung grafts were all evaluated on EVLP, with a conversion rate of 84% and a cDCD transplantation rate of 76%. The median total preservation time was 707 minutes [543-1038]. Seventy-one bilateral LTs and 5 single LTs were performed for chronic obstructive pulmonary disease (n = 29), pulmonary fibrosis (n = 21), cystic fibrosis (n = 15), pulmonary hypertension (n = 8), graft-versus-host disease (n = 2), and adenosquamous carcinoma (n = 1). The rate of PGD3 was 9% (n = 5). The 1-year survival rate was 93.4%.

CONCLUSION

After initial acceptance, cDCD lung grafts led to LT in 76% of cases, with outcomes similar to those already reported in the literature. The relative impacts of NRP and EVLP on the outcome following cDCD LT should be assessed prospectively in the context of comparative studies.

摘要

背景

法国国家循环确定死亡后控制性捐献协议(cDCD)包括腹部器官获取时的常温区域灌注(NRP)和考虑肺移植(LT)前的额外离体肺灌注(EVLP)。

方法

我们对一个从 2016 年 5 月项目开始就纳入所有 cDCD-LT 供者的前瞻性注册进行回顾性研究。

结果

来自 14 个供者医院的 100 个移植物被 6 个 LT 中心接受。濒死期的中位数持续时间为 20 分钟[2-166]。从循环停止到肺冲洗的中位数持续时间为 62 分钟[20-90]。由于濒死期延长(n=3)、NRP 插入失败(n=5)或原位评估不佳(n=2),10 个肺移植物未被取出。其余 90 个肺移植物均在 EVLP 上进行评估,转化率为 84%,cDCD 移植率为 76%。中位总保存时间为 707 分钟[543-1038]。71 例双侧 LT 和 5 例单肺 LT 用于慢性阻塞性肺疾病(n=29)、肺纤维化(n=21)、囊性纤维化(n=15)、肺动脉高压(n=8)、移植物抗宿主病(n=2)和腺鳞癌(n=1)。PGD3 的发生率为 9%(n=5)。1 年生存率为 93.4%。

结论

初始接受后,cDCD 肺移植物在 76%的病例中导致 LT,结果与文献中已报道的相似。NRP 和 EVLP 对 cDCD-LT 后结果的相对影响应在比较研究的背景下进行前瞻性评估。

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