Huang H J, Yusen R D, Meyers B F, Walter M J, Mohanakumar T, Patterson G A, Trulock E P, Hachem R R
Division of Pulmonary and Critical Care Medicine, Washington University School of Medicine, St. Louis, MO, USA.
Am J Transplant. 2008 Nov;8(11):2454-62. doi: 10.1111/j.1600-6143.2008.02389.x. Epub 2008 Sep 10.
Primary graft dysfunction (PGD) is a common early complication after lung transplantation. We conducted a retrospective cohort study of 334 recipients to evaluate the impact of PGD graded at 24, 48 and 72 h on the risk of bronchiolitis obliterans syndrome (BOS) development (stage 1) and progression (stages 2 and 3). We constructed multivariable Cox proportional hazards models to determine the risk of BOS attributable to PGD in the context of other potential risk factors including acute rejection, lymphocytic bronchitis and respiratory viral infections. All grades of PGD at all time points were significant risk factors for BOS development and progression independent of acute rejection, lymphocytic bronchitis and respiratory viral infections. Specifically, PGD grade 1 at T24 was associated with a relative risk of BOS stage 1 of 1.93, grade 2 with a relative risk of 2.29 and grade 3 with a relative risk of 3.31. Furthermore, this direct relationship between the severity of PGD and the risk of BOS persisted at all time points. We conclude that all grades of PGD at all time points are independent risk factors for BOS development and progression. Future strategies that might attenuate the severity of PGD may mitigate the risk of BOS.
原发性移植肺功能障碍(PGD)是肺移植后常见的早期并发症。我们对334例受者进行了一项回顾性队列研究,以评估在24、48和72小时时分级的PGD对闭塞性细支气管炎综合征(BOS)发生(1期)和进展(2期和3期)风险的影响。我们构建了多变量Cox比例风险模型,以确定在包括急性排斥反应、淋巴细胞性支气管炎和呼吸道病毒感染等其他潜在风险因素的背景下,PGD导致BOS的风险。所有时间点的所有等级的PGD都是BOS发生和进展的显著风险因素,与急性排斥反应、淋巴细胞性支气管炎和呼吸道病毒感染无关。具体而言,T24时的1级PGD与BOS 1期的相对风险为1.93,2级为2.29,3级为3.31。此外,PGD严重程度与BOS风险之间的这种直接关系在所有时间点均持续存在。我们得出结论,所有时间点的所有等级的PGD都是BOS发生和进展的独立风险因素。未来可能减轻PGD严重程度的策略可能会降低BOS的风险。