Department Surgery, Rollins School of Public Health, Emory University, Atlanta, Georgia 30322, USA.
Ann Thorac Surg. 2011 Jan;91(1):244-9. doi: 10.1016/j.athoracsur.2010.08.055.
Single-lung transplantation (SLT) and bilateral lung transplantation (BLT) are both good options for patients with end-stage lung disease secondary to idiopathic pulmonary fibrosis. It is, however, unclear whether BLT offers any survival advantage over SLT. The purpose of our study was to evaluate a large group of patients to determine if either SLT or BLT officered a long-term survival advantage for patients with IPF.
This was an Institutional Review Board-approved retrospective analysis of the United Network of Organ Sharing database from 1987 to 2008. Survival was determined using Kaplan-Meir estimates and the effect of laterality was determined by Cox proportional hazards and propensity analyses.
Lung transplantation for idiopathic pulmonary fibrosis was performed in 3,860 patients (2,431 SLTs and 1429 BLTs). Multivariate and propensity analysis failed to show any survival advantage for BLT (hazard ratio = 0.90, 95% confidence interval = 0.78 to 1.0, p = 0.11). One-year conditional survival favored BLT (hazard ratio 0.73, 95% confidence interval 0.60 to 0.87, p = 0.00064). Risk factors for early death included recipient age over 57 and donor age over 36 years.
Bilateral lung transplantation should be considered for younger patients with idiopathic pulmonary fibrosis and results may be optimized when younger donors are used.
对于特发性肺纤维化(IPF)等终末期肺病患者,单肺移植(SLT)和双肺移植(BLT)都是很好的选择。然而,尚不清楚 BLT 是否比 SLT 具有生存优势。本研究的目的是评估一大组患者,以确定 SLT 或 BLT 是否为 IPF 患者提供长期生存优势。
这是对 1987 年至 2008 年美国器官共享网络数据库进行的机构审查委员会批准的回顾性分析。使用 Kaplan-Meier 估计来确定生存情况,通过 Cox 比例风险和倾向分析来确定侧别影响。
对 3860 例特发性肺纤维化患者进行了肺移植(2431 例 SLT 和 1429 例 BLT)。多变量和倾向分析均未显示 BLT 具有生存优势(风险比=0.90,95%置信区间为 0.78 至 1.0,p=0.11)。1 年条件生存率有利于 BLT(风险比 0.73,95%置信区间 0.60 至 0.87,p=0.00064)。早期死亡的风险因素包括受体年龄大于 57 岁和供体年龄大于 36 岁。
对于特发性肺纤维化的年轻患者,应考虑进行双侧肺移植,当使用较年轻的供体时,结果可能会得到优化。