Impact of Remdesivir on long-term outcomes in lung transplant recipients with SARS-CoV-2 infection: a retrospective cohort analysis.

IF 1.8 4区 医学 Q3 RESPIRATORY SYSTEM
Damiana-Maria Vulturar, Gaëlle Dauriat, Anne Gigandon, Pauline Pradère, Pierre Gazengel, Samuel Dolidon, Chahine Medraoui, Amir Hanna, Adrian Crutu, Liviu-Stefan Moaca, Laurène Cachera, Delphine Mitilian, Dominique Fabre, Elie Fadel, Olaf Mercier, Alban Le Monnier, Jérôme Le Pavec, Benoît Pilmis
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Abstract

Background: The COVID-19 pandemic has presented considerable challenges for lung transplant (LTx) recipients, a population inherently at high risk for severe complications. Although early data from the pandemic indicated worrisome outcomes for these patients, understanding the current context of SARS-CoV-2 infections is essential to inform ongoing management strategies. The efficacy of anti-viral treatments, including Remdesivir (RDV), remains uncertain. This study aims to evaluate the effect of RDV on clinical outcomes in LTx recipients infected with SARS CoV-2, primarily those with a clinically significant disease course.

Methods: A single-center retrospective cohort study was conducted, including LTx recipients with confirmed SARS-CoV-2 infection diagnosed between January 2022 and December 2023. Patients were classified as treated with RDV if they received at least three consecutive days of therapy, typically initiated in the context of symptomatic infection with increased oxygen requirements (RDV group). The primary outcome was all-cause mortality. Secondary outcomes were ICU admission, longitudinal changes in lung function, at 3-, 6-, and 12-months post-infection, incidence of COVID-19-associated pulmonary aspergillosis (CAPA) and bacterial co-infections. A multivariable logistic regression model was used to control for cofounding factors.

Results: Among the 130 LTx infected with SARS CoV-2, 61% (80/130) received at least 3 days of RDV. All cause of mortality was lower in the RDV group (4% 2/50) compared to the non-RDV group (15%, 12/80) (p= 0.05). Non-RDV group experienced a significant decline in forced expiratory volume in 1 second (FEV1) at 3 months post-infection compared to those in the RDV group (6% vs 3%, p = 0.04). ICU admission rates, bacterial coinfection, and CAPA were similar between groups.

Conclusion: RDV treatment appears to improve survival and may mitigate the long-term deterioration of lung function in lung transplant recipients infected with SARS CoV-2. These findings underscore the potential of RDV as a beneficial therapy in this high-risk population and highlight the need for further investigation in larger studies.

瑞德西韦对SARS-CoV-2感染肺移植受者长期预后的影响:回顾性队列分析
背景:COVID-19大流行给肺移植(LTx)受者带来了相当大的挑战,这一人群本身就是严重并发症的高风险人群。尽管大流行的早期数据表明这些患者的结局令人担忧,但了解SARS-CoV-2感染的当前背景对于为持续的管理策略提供信息至关重要。包括Remdesivir (RDV)在内的抗病毒治疗的疗效仍不确定。本研究旨在评估RDV对SARS CoV-2感染LTx受体临床结局的影响,主要是那些有临床显著病程的患者。方法:采用单中心回顾性队列研究,纳入2022年1月至2023年12月诊断为确诊的SARS-CoV-2感染的LTx接受者。如果患者接受了至少连续三天的治疗,通常是在有症状的感染和氧气需求增加的情况下开始的(RDV组),则将其归类为RDV治疗。主要结局为全因死亡率。次要结局是ICU住院情况、感染后3、6、12个月肺功能的纵向变化、covid -19相关肺曲霉病(CAPA)和细菌合并感染的发生率。采用多变量logistic回归模型控制共同影响因素。结果:在感染SARS CoV-2的130例LTx中,61%(80/130)接受了至少3 d的RDV。RDV组的全因死亡率(4% 2/50)低于非RDV组(15%,12/80)(p= 0.05)。与RDV组相比,非RDV组在感染后3个月的1秒用力呼气量(FEV1)显著下降(6%对3%,p = 0.04)。ICU住院率、细菌合并感染及CAPA组间比较相似。结论:RDV治疗可提高SARS CoV-2感染肺移植受者的生存率,并可能减轻肺功能的长期恶化。这些发现强调了RDV在这一高危人群中作为一种有益疗法的潜力,并强调了在更大规模研究中进一步调查的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Respiratory Medicine and Research
Respiratory Medicine and Research RESPIRATORY SYSTEM-
CiteScore
2.70
自引率
0.00%
发文量
82
审稿时长
50 days
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