Liu M, Mallory G B, Schecter M G, Worley S, Arrigain S, Robertson J, Elidemir O, Danziger-Isakov L A
The Children's Hospital at Cleveland Clinic, Cleveland, OH 44195, USA.
Pediatr Transplant. 2010 May;14(3):431-6. doi: 10.1111/j.1399-3046.2010.01296.x. Epub 2010 Mar 4.
To evaluate the epidemiology and to investigate the impact of RVI on chronic allograft rejection after pediatric lung transplantation, a retrospective study of pediatric lung transplant recipients from 2002 to 2007 was conducted. Association between RVI and continuous and categorical risk factors was assessed using Wilcoxon rank-sum tests and Fisher's exact tests, respectively. Association between risk factors and outcomes were assessed using Cox proportional hazards models. Fifty-five subjects were followed for a mean of 674 days (range 14-1790). Twenty-eight (51%) developed 51 RVI at a median of 144 days post-transplant (mean 246; range 1-1276); 41% of infections were diagnosed within 90 days. Twenty-five subjects developed 39 LRI, and eight subjects had 11 URI. Organisms recovered included rhinovirus (n = 14), adenovirus (n = 10), parainfluenza (n = 10), influenza (n = 5), and RSV (n = 4). Three subjects expired secondary to their RVI (two adenovirus, one RSV). Younger age and prior CMV infection were risks for RVI (HR 2.4 95% CI 1.1-5.3 and 17.0; 3.0-96.2, respectively). RVI was not associated with the development of chronic allograft rejection (p = 0.25) or death during the study period. RVI occurs in the majority of pediatric lung transplant recipients, but was not associated with mortality or chronic allograft rejection.
为评估小儿肺移植术后呼吸道病毒感染(RVI)的流行病学特征并调查其对慢性移植物排斥反应的影响,我们对2002年至2007年的小儿肺移植受者进行了一项回顾性研究。分别使用Wilcoxon秩和检验和Fisher精确检验评估RVI与连续性和分类风险因素之间的关联。使用Cox比例风险模型评估风险因素与结局之间的关联。55名受试者的随访时间平均为674天(范围14 - 1790天)。28名(51%)受试者在移植后中位数144天(平均246天;范围1 - 1276天)发生了51次RVI;41%的感染在90天内被诊断出来。25名受试者发生了39次下呼吸道感染(LRI),8名受试者发生了11次上呼吸道感染(URI)。分离出的病原体包括鼻病毒(n = 14)、腺病毒(n = 10)、副流感病毒(n = 10)、流感病毒(n = 5)和呼吸道合胞病毒(RSV,n = 4)。3名受试者因RVI死亡(2例腺病毒感染,1例RSV感染)。年龄较小和既往巨细胞病毒(CMV)感染是发生RVI的风险因素(风险比[HR]分别为2.4,95%置信区间[CI] 1.1 - 5.3;以及17.0;3.0 - 96.2)。在研究期间,RVI与慢性移植物排斥反应的发生(p = 0.25)或死亡无关。大多数小儿肺移植受者会发生RVI,但它与死亡率或慢性移植物排斥反应无关。