Division of Thoracic Surgery, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Division of Pulmonary & Critical Care Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Ann Thorac Surg. 2019 Apr;107(4):1046-1052. doi: 10.1016/j.athoracsur.2018.10.034. Epub 2018 Nov 23.
Cytomegalovirus (CMV) infection has been associated with poor outcomes after solid organ transplantation. The long-term impact of donor and recipient CMV serological status on lung transplant outcomes remains unclear. Accordingly, we evaluated the impact of donor and recipient CMV status on long-term patients as well as allograft survival after single (SLT) and double lung transplantation (BLT).
The Scientific Registry of Transplant Recipients was used to track all adult lung transplants in United States from May 2005 to June 2016. Patient mortality and bronchiolitis obliterans syndrome were determined up to 5 years using Cox proportional hazards modeling. Additionally, landmark analysis was performed conditional on survival at 1 year.
Compared with donor negative-recipient CMV-IgG negative (D-R-), donor positive-recipient negative (D+R-) and donor positive-recipient positive (D+R+) groups had increased mortality at 1 and 5 years after BLT, with the former demonstrating highest risk. Although mortality was not increased with CMV seropositive donors after SLT at 1 year, both D+R- and D+R+ groups demonstrated greater mortality at 5 years. Risk of bronchiolitis obliterans syndrome was not affected by CMV serological status. Conditional landmark analysis confirmed that lungs from CMV seropositive donors conferred highest risk for long-term mortality.
CMV seronegative recipients undergoing either BLT or SLT from CMV seropositive donors have the highest risk of long-term mortality that extends beyond the first year. Further studies are needed to determine the causes of higher mortality observed in the CMV seronegative recipients and risks and benefits of extension of CMV prophylaxis, particularly in the high-risk group.
巨细胞病毒(CMV)感染与实体器官移植后不良结局有关。供体和受者 CMV 血清学状态对肺移植结局的长期影响尚不清楚。因此,我们评估了供体和受者 CMV 状态对长期患者以及单肺(SLT)和双肺移植(BLT)后同种异体移植物存活的影响。
使用移植受者科学登记处来跟踪 2005 年 5 月至 2016 年 6 月在美国进行的所有成人肺移植。使用 Cox 比例风险模型确定患者死亡率和闭塞性细支气管炎综合征,最长可达 5 年。此外,在 1 年时进行生存条件下的里程碑分析。
与供体阴性-受者 CMV-IgG 阴性(D-R-)相比,供体阳性-受者阴性(D+R-)和供体阳性-受者阳性(D+R+)组在 BLT 后 1 年和 5 年时死亡率增加,前者风险最高。虽然在 SLT 后 1 年时 CMV 血清阳性供体不会增加死亡率,但 D+R-和 D+R+组在 5 年时死亡率更高。闭塞性细支气管炎综合征的风险不受 CMV 血清学状态的影响。条件性里程碑分析证实,CMV 血清阳性供体的肺移植物具有最高的长期死亡率风险。
CMV 血清阴性接受者接受 CMV 血清阳性供体的 BLT 或 SLT 均具有最高的长期死亡率风险,这种风险超出了第 1 年。需要进一步研究以确定在 CMV 血清阴性接受者中观察到的更高死亡率的原因,以及延长 CMV 预防的风险和益处,特别是在高危组。