Hofer Markus, Benden Christian, Inci Ilhan, Schmid Christoph, Irani Sarosh, Speich Rudolf, Weder Walter, Boehler Annette
Division of Pulmonary Medicine, University Hospital Zurich, Zurich, Switzerland.
J Heart Lung Transplant. 2009 Apr;28(4):334-9. doi: 10.1016/j.healun.2008.12.025.
Lung transplantation is the ultimate therapy for end-stage cystic fibrosis (CF) lung disease; however, the debate continues as to whether lung transplantation improves survival. We report post-transplant outcome in CF at our institution by comparing 5-year post-transplant survival with a calculated 5-year survival without lung transplantation, using a predictive 5-year survivorship model, and describe pre-transplant parameters influencing transplant outcome.
CF patients undergoing lung transplantation at our center were included (1992 to 2007). Survival rates were calculated and compared, and univariate and multivariate Cox regression analyses were used for statistical assessment.
Eighty transplants were performed in CF patients, 11 (13.8%) of whom were children. Mean age at transplant was 26.2 years (95% confidence interval: 24.4 to 28.0). The Liou raw score at transplant was -20 (95% confidence interval: -16 to -24), resulting in an estimated 5-year survival without transplantation of 33 +/- 14%, compared with a 5-year post-transplant survival of 68.2 +/- 5.6%. Further improvement was noted in the recent transplant era (since 2000), with a 5-year survival of 72.7 +/- 7.3%. Univariate analysis revealed that later year of transplant and diagnosis of diabetes influenced survival positively. Pediatric age had no negative impact. In the multivariate analysis, only diabetes influenced survival, in a positive manner.
Lung transplantation performed at centers having experience with the procedure can offer a true survival benefit to patients with end-stage CF lung disease.
肺移植是终末期囊性纤维化(CF)肺病的最终治疗方法;然而,关于肺移植是否能提高生存率的争论仍在继续。我们通过使用预测性5年生存模型,将移植后5年生存率与计算得出的未进行肺移植的5年生存率进行比较,报告了我们机构CF患者的移植后结局,并描述了影响移植结局的移植前参数。
纳入在我们中心接受肺移植的CF患者(1992年至2007年)。计算并比较生存率,并使用单因素和多因素Cox回归分析进行统计评估。
对CF患者进行了80例移植,其中11例(13.8%)为儿童。移植时的平均年龄为26.2岁(95%置信区间:24.4至28.0)。移植时的Liou原始评分为-20(95%置信区间:-16至-24),导致估计未移植的5年生存率为33±14%,而移植后5年生存率为68.2±5.6%。在最近的移植时代(自2000年以来)生存率有进一步提高,5年生存率为72.7±7.3%。单因素分析显示,移植年份较晚和糖尿病诊断对生存率有积极影响。儿童年龄没有负面影响。在多因素分析中,只有糖尿病以积极方式影响生存率。
在有该手术经验的中心进行肺移植可为终末期CF肺病患者带来真正的生存益处。