移植前输血对肺移植后原发性移植物功能障碍的风险

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摘要

背景主要移植物功能障碍(PGD)是肺移植短期和长期死亡的主要原因。方法这是对 2018 年 1 月至 2022 年 7 月期间在一个学术中心(伊利诺伊州芝加哥市西北大学范伯格医学院)进行的 206 例连续肺移植手术的回顾性研究。收集了患者特征、移植前实验室值、输血需求、术中和术后结果等数据。结果13.2%的患者(n = 28)出现PGD 3级(PGD 3)。共有 33 名患者在 4 周内接受了输血,21 名患者在肺移植前一周接受了输血。移植前输血与较高的 PGD 3 发生率密切相关(48.5% vs 6.9%;P < .001)。移植前输血组与未输血组的 1 年存活率无明显差异(77.7% vs 88.0%; P = .478)。与未使用 PGD 3 的受者相比,使用 PGD 3 的受者 1 年存活率降低(63.5% vs 89.9%; P = .0012)。在单变量分析中,移植前和移植内预测 PGD 3 的因素包括年龄较小(P < .01)、移植前使用体外膜肺氧合(ECMO)(P < .001)、肺分配评分较高(P < .001)、冠状病毒病 2019 (COVID-19) 相关急性呼吸窘迫综合征(P < .结论移植前输血可能与较高的 PGD 发生率有关。研究结果表明,肺移植受者移植前输血存在潜在风险。
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The Risk of Pretransplant Blood Transfusion for Primary Graft Dysfunction After Lung Transplant

Background

Primary graft dysfunction (PGD) is the leading cause of short- and long-term mortality associated with lung transplantation. The impact of pretransplantation blood transfusions for recipients is not fully elucidated.

Methods

This is a retrospective review of 206 consecutive lung transplantations performed at a single academic center (Northwestern University Feinberg School of Medicine, Chicago, IL) from January 2018 to July 2022. Data on patient characteristics, pretransplantation laboratory values, transfusion requirements, and intraoperative and postoperative outcomes were collected.

Results

PGD grade 3 (PGD 3) occurred in 13.2% of the cohort (n = 28). A total of 33 patients received a blood transfusion within 4 weeks, whereas 21 patients received a blood transfusion a week before their lung transplant. Pretransplantation transfusions were strongly associated with a higher incidence of PGD 3 (48.5% vs 6.9%; P < .001). There was no significant difference in 1-year survival between the pretransplantation transfused group and the nontransfused group (77.7% vs 88.0%; P = .478). The 1year survival was reduced in recipients with PGD 3 compared with recipients without PGD 3 (63.5% vs 89.9%; P = .0012). In univariate analysis, pretransplant and intratransplant predictors of PGD 3 included younger age (P < .01), pretransplant extracorporeal membrane oxygenation (ECMO) use (P < .001), higher lung allocation score (P < .001), coronavirus disease 2019 (COVID-19)–related acute respiratory distress syndrome (P < .01), blood transfusion within 4 weeks (P < .001), longer operative time (P < .001), intratransplant blood transfusion (P < .001), and intratransplant venoarterial ECMO use (P < .001).

Conclusions

Pretransplantation blood transfusions could be associated with a higher rate of PGD. The findings indicated the potential risks of pretransplantation blood transfusions in lung transplant recipients.

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