首页> 外文期刊>Journal of cystic fibrosis: official journal of the European Cystic Fibrosis Society >Increased risk of PTLD in lung transplant recipients with cystic fibrosis
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Increased risk of PTLD in lung transplant recipients with cystic fibrosis

机译:肺移植受者的PTLD风险增加,囊性纤维化

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Abstract Background Post-transplant lymphoproliferative disease (PTLD) is an important cause of morbidity and mortality following lung transplantation. Recipients with cystic fibrosis (CF) may have an increased risk of PTLD although the literature is limited to single center cohorts. Our primary aim is to examine PTLD in an adult lung transplant population by utilizing the International Society for Heart and Lung Transplantation Registry. Methods We studied 30,598 adult recipients of lung transplants performed between 1999 and 2011. The primary outcome was development of and time to PTLD. In addition to indication for transplant, other predictors examined included Epstein–Barr virus (EBV) and cytomegalovirus (CMV) serostatus, gender, and age. Outcomes were assessed with univariable and multivariable Cox proportional hazard models to obtain hazard ratios (HR). Results 17% of the cohort had a diagnosis of CF. PTLD developed in 2% of CF recipients compared to 1% for non-CF recipients ( p Conclusions CF recipients have a higher risk for PTLD compared to non-CF recipients. Further studies are needed to account for additional risk factors and management in this population post-transplant.
机译:摘要背景后移植后淋巴抑制剂(PTLD)是肺移植后发病率和死亡率的重要原因。囊性纤维化(CF)的受者可能具有增加的PTLD风险,尽管文献仅限于单中心队列。我们的主要目标是通过利用国际心脏和肺移植登记处的国际社会来检查成人肺移植人群的PTLD。方法研究了1999年至2011年间肺移植成年人的30,598名成人受者。主要结果是开发和时间到PTLD。除了用于移植的指示外,还检查了其他预测因子,包括Epstein-Barr病毒(EBV)和患有细胞病毒(CMV)的血清肿,性别和年龄。使用单变性和多变量的Cox比例危害模型评估结果,以获得危害比率(HR)。结果17%的队列诊断了CF. PTLD在2%的CF受体中开发的,而非CF受试者的1%相比(P结论CF受体与非CF受体相比,PTLD的风险较高。需要进一步研究,以考虑该人群的额外危险因素和管理后移植。

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