Hayes Don, McConnell Patrick I, Galantowicz Mark, Whitson Bryan A, Tobias Joseph D, Black Sylvester M
Department of Pediatrics, Ohio State University College of Medicine, Columbus, Ohio; Department of Internal Medicine, Ohio State University College of Medicine, Columbus, Ohio; Section of Pulmonary Medicine, Nationwide Children's Hospital, Columbus, Ohio.
Department of Surgery, Ohio State University College of Medicine, Columbus, Ohio; Department of Cardiothoracic Surgery, Nationwide Children's Hospital, Columbus, Ohio.
Ann Thorac Surg. 2015 Apr;99(4):1184-91. doi: 10.1016/j.athoracsur.2014.12.008. Epub 2015 Feb 20.
Clinical practice in the United States has no restrictions in allocating lungs from adult donors to pediatric recipients.
The United Network for Organ Sharing database was queried from 1987 to 2013 for pediatric lung transplant recipients (aged less than 18 years) to assess survival using continuous donor age in years and two donor age groups, ≥ 18 years and > 30 years, for analysis.
Of 930 pediatric lung transplants, basic survival analysis identified a mortality hazard when adult lung allografts were transplanted into pediatric recipients; however, multivariate Cox models demonstrated that continuous donor age (hazard ratio [HR] 1.004, 95% confidence interval [CI]: 0.992-1.015, p = 0.524) as well as both categoric age groups, donor 18 years or older (HR 0.967, 95% CI: 0.714-1.309, p = 0.827) and donor older than 30 years (HR 1.168, 95% CI: 0.815-1.673, p = 0.398), did not significantly influence the risk for death. Moreover, propensity score matching analysis confirmed a lack of association of mortality risk with donor age ≥ 18 years (HR 1.129, 95% CI: 0.696-1.831, p = 0.623) and donor age > 30 years (HR 1.050, 95% CI: 0.569-1.937, p = 0.876). Bronchiolitis obliterans syndrome (BOS) was found to be a significant predictor of mortality in univariate analysis (HR 2.033, 95% CI: 1.639-2.521, p < 0.001), but the hazard of BOS did not vary across donor age categories.
Adult donor lung allografts appear not to negatively affect survival in pediatric lung transplant recipients when considering confounders, and do not influence survival through an increased hazard for the development of BOS.
在美国的临床实践中,将成年供体的肺分配给儿科受者没有限制。
查询器官共享联合网络数据库1987年至2013年期间的儿科肺移植受者(年龄小于18岁),使用供体年龄(以年为单位)的连续变量以及两个供体年龄组(≥18岁和>30岁)进行生存分析。
在930例儿科肺移植中,基本生存分析发现成年肺移植到儿科受者时存在死亡风险;然而,多变量Cox模型显示,供体年龄的连续变量(风险比[HR]1.004,95%置信区间[CI]:0.992 - 1.015,p = 0.524)以及两个分类年龄组,即18岁及以上的供体(HR 0.967,95%CI:0.714 - 1.309,p = 0.827)和30岁以上的供体(HR 1.168,95%CI:0.815 - 1.673,p = 0.398),均未显著影响死亡风险。此外,倾向评分匹配分析证实,死亡风险与18岁及以上的供体(HR 1.129,95%CI:0.696 - 1.831,p = 0.623)和30岁以上的供体(HR 1.050,95%CI:0.569 - 1.937,p = 0.876)缺乏关联。在单变量分析中,闭塞性细支气管炎综合征(BOS)被发现是死亡的重要预测因素(HR 2.033,95%CI:1.639 - 2.521,p < 0.001),但BOS的风险在不同供体年龄类别中没有差异。
在考虑混杂因素时,成年供体的肺移植似乎不会对儿科肺移植受者的生存产生负面影响,也不会通过增加BOS发生的风险来影响生存。