Bao Brian J, Kwon Ye In Christopher, Dunbar Emily G, Rollins Zachary, Patel Jay, Ambrosio Matthew, Bruno David A, Patel Vipul, Julliard Walker A, Kasirajan Vigneshwar, Hashmi Zubair A
Division of Cardiothoracic Surgery, Department of Surgery, Pauley Heart Center, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
Department of Biostatistics, Virginia Commonwealth University School of Population Health, Richmond, VA, USA.
Lung. 2025 Apr 25;203(1):57. doi: 10.1007/s00408-025-00811-9.
Combined lung-liver transplant (CLLT) is a complex yet life-saving procedure for patients with simultaneous end-stage lung and liver disease. Given the geographical allocation change to the lung allocation score (LAS) in 2017 and the recent SARS-CoV-2 outbreak in 2019, we aim to provide an updated analysis of the patient selection and outcomes of CLLTs.
The UNOS registry was used to identify all patients who underwent CLLT between January 2014 and June 2023. To account for the changes made to LAS in 2017, baseline characteristics and outcomes were compared between era 1 (before 2017) and era 2 (after 2017). Risk factors for mortality were analyzed using the Cox regression hazard models. Recipient survival of up to 3 years was analyzed using the Kaplan-Meier method.
117 CLLTs were performed (77.8% in era 2). Donor organs experienced significantly longer ischemic times (p = 0.039) and traveled longer distances (p = 0.025) in era 2. However, recipient (p = 0.79) and graft (p = 0.41) survival remained comparable at up to 3 years post-transplant between eras. CLLTs demonstrated similar long-term survival to isolated lung transplants (p = 0.73). Higher recipient LAS was associated with an increased mortality risk (HR 1.14, p = 0.034). Recipient diagnosis of idiopathic pulmonary fibrosis carried a 5.03-fold risk of mortality (p = 0.048) compared to those with cystic fibrosis.
In the post-2017 LAS change era, CLLTs are increasingly performed with comparable outcomes to isolated lung transplants. A careful, multidisciplinary approach to patient selection and management remains paramount to optimizing outcomes for this rare patient population.
联合肺肝移植(CLLT)对于同时患有终末期肺病和肝病的患者而言,是一项复杂但能挽救生命的手术。鉴于2017年肺分配评分(LAS)的地理分配变化以及2019年近期的新冠疫情爆发,我们旨在对CLLT的患者选择和治疗结果进行更新分析。
利用器官共享联合网络(UNOS)登记系统,确定2014年1月至2023年6月期间接受CLLT的所有患者。为了考虑2017年LAS的变化,对第1阶段(2017年之前)和第2阶段(2017年之后)的基线特征和治疗结果进行了比较。使用Cox回归风险模型分析死亡风险因素。采用Kaplan-Meier方法分析长达3年的受者生存率。
共进行了117例CLLT(第2阶段占77.8%)。在第2阶段,供体器官的缺血时间显著延长(p = 0.039),运输距离更远(p = 0.025)。然而,不同阶段之间,移植后长达3年的受者(p = 0.79)和移植物(p = 0.41)生存率仍相当。CLLT的长期生存率与单纯肺移植相似(p = 0.73)。较高的受者LAS与死亡风险增加相关(风险比1.14,p = 0.034)。与囊性纤维化患者相比,受者诊断为特发性肺纤维化的死亡风险高5.03倍(p = 0.048)。
在2017年LAS变化后的时代,CLLT的实施越来越多,其结果与单纯肺移植相当。对于这一罕见患者群体,采用谨慎的多学科方法进行患者选择和管理对于优化治疗结果仍然至关重要。