SARS-CoV-2感染后病例对照肺移植队列的长期结局

Frontiers in transplantation Pub Date : 2025-05-21 eCollection Date: 2025-01-01 DOI:10.3389/frtra.2025.1583919
Sandrine Hanna, Rami Hallak, Susanna M Leonard, Samantha Morrison, Sarah Peskoe, Jordan Whitson, John M Reynolds, Cameron R Wolfe, Hakim Azfar Ali
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引用次数: 0

摘要

背景:呼吸道病毒可影响肺移植受者的同种异体移植物功能,但尚不清楚SARS-CoV-2感染是否会发生这种情况。我们研究了感染SARS-CoV-2的肺移植受者的长期预后。方法:这项单中心回顾性研究将2020年6月至2021年4月期间感染SARS-CoV-2的肺移植受体与匹配的对照组进行了比较。在SARS-CoV-2队列中,测试了临床因素与结果之间的单变量相关性。分析肺功能检查的变化。主要终点包括急性细胞排斥反应和12个月内的全因死亡率。结果:53例肺移植受者感染SARS-CoV-2。中位年龄为64岁。29例(54.7%)为门诊患者,24例(45.3%)需要住院治疗,其中13例入住重症监护病房。全因死亡率为24.5%。在SARS-CoV-2队列中,年龄与全因死亡率(p值0.017)、ICU入院率(p = 0.009)和A1C水平(p = 0.033)显著相关。与基线相比,FEV1的平均变化在3个月时为-1.1%,在6个月和12个月时变化最小(分别为-2.6%和-1%)。急性细胞排斥反应在13.7%的SARS-CoV-2队列中被发现,而在匹配的对照组中为11.8%;与感染状态无显著相关性(p = 0.706)。然而,全因死亡率与感染状况显著相关(p = 0.019)。结论:肺移植受者SARS-CoV-2的长期预后差异很大。在SARS-CoV-2队列中,全因死亡率为24.5%,年龄与死亡率显著相关。我们没有观察到该组FEV1的显著下降。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long-term outcomes of a case-control lung transplant cohort after SARS-CoV-2 infection.

Background: Respiratory viruses can impact the allograft function in lung transplant recipients, but it is unknown if this occurs with SARS-CoV-2 infection. We studied the long-term outcomes of lung transplant recipients infected with SARS-CoV-2.

Methods: This single-center retrospective study compared lung transplant recipients with SARS-CoV-2 between June 2020 and April 2021 with a matched control group. Within the SARS-CoV-2 cohort, univariable associations between clinical factors and outcomes were tested. Changes in pulmonary function tests were analyzed. Primary endpoints included acute cellular rejection and all-cause mortality within 12 months.

Results: Fifty-three lung transplant recipients were infected with SARS-CoV-2. The median age was 64 years. 29 (54.7%) were managed outpatient, and 24 (45.3%) required hospitalization, with 13 intensive care unit admissions. All-cause mortality was 24.5%. Within the SARS-CoV-2 cohort, older age was significantly associated with all-cause mortality (p-value 0.017) as was ICU admission (p = 0.009) and an A1C > 6.5 (p = 0.033). The mean change in FEV1 was -1.1% at 3 months with minimal change at 6 and 12 months (-2.6% and -1% respectively), all compared to baseline. Acute cellular rejection was identified in 13.7% of the SARS-CoV-2 cohort compared to 11.8% in the matched control group; it was not significantly associated with the infection status (p = 0.706). However, all-cause mortality was significantly associated with infection status (p = 0.019).

Conclusion: Long-term outcomes of SARS-CoV-2 in lung transplant recipients are widely variable. Within the SARS-CoV-2 cohort, all-cause mortality was 24.5%, and older age was significantly associated with mortality. We did not observe significant declines in FEV1 in this group.

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