Pulmonary, Allergy, and Critical Care Division, University of Pennsylvania School of Medicine, Philadelphia, PA; Center for Clinical Epidemiology and Biostatistics, University of Pennsylvania School of Medicine, Philadelphia, PA.
Pulmonary, Allergy, and Critical Care Division, University of Pennsylvania School of Medicine, Philadelphia, PA; Center for Clinical Epidemiology and Biostatistics, University of Pennsylvania School of Medicine, Philadelphia, PA.
Chest. 2013 Aug;144(2):616-622. doi: 10.1378/chest.12-1480.
There is significant heterogeneity within the primary graft dysfunction (PGD) syndrome. We aimed to identify distinct grade 3 PGD phenotypes based on severity of lung dysfunction and patterns of resolution.
Subjects from the Lung Transplant Outcomes Group (LTOG) cohort study with grade 3 PGD within 72 h after transplantation were included. Latent class analysis (LCA) was used to statistically identify classes based on changes in PGD International Society for Heart & Lung Transplantation grade over time. Construct validity of the classes was assessed by testing for divergence of recipient, donor, and operative characteristics between classes. Predictive validity was assessed using time to death.
Of 1,255 subjects, 361 had grade 3 PGD within the first 72 h after transplantation. LCA identified three distinct phenotypes: (1) severe persistent dysfunction (class 1), (2) complete resolution of dysfunction within 72 h (class 2), and (3) attenuation, without complete resolution within 72 h (class 3). Increased use of cardiopulmonary bypass, greater RBC transfusion, and higher mean pulmonary artery pressure were associated with persistent PGD (class 1). Subjects in class 1 also had the greatest risk of death (hazard ratio, 2.39; 95% CI, 1.57-3.63; P < .001).
There are distinct phenotypes of resolution of dysfunction within the severe PGD syndrome. Subjects with early resolution may represent a different mechanism of lung pathology, such as resolving pulmonary edema, whereas those with persistent PGD may represent a more severe phenotype. Future studies aimed at PGD mechanism or treatment may focus on phenotypes based on resolution of graft dysfunction.
原发性移植物功能障碍(PGD)综合征存在显著的异质性。我们旨在根据肺功能障碍的严重程度和恢复模式确定不同严重程度 3 级 PGD 的表型。
纳入肺移植结局组(LTOG)队列研究中在移植后 72 小时内出现 3 级 PGD 的患者。采用潜在类别分析(LCA)根据 PGD 国际心肺移植学会分级随时间的变化来对类别进行统计学分析。通过测试各类别之间受者、供者和手术特征的差异来评估类别的构建效度。采用死亡时间来评估预测效度。
在 1255 例患者中,361 例患者在移植后 72 小时内出现 3 级 PGD。LCA 确定了三种不同的表型:(1)严重持续功能障碍(1 类),(2)72 小时内功能障碍完全恢复(2 类),和(3)功能减弱但 72 小时内未完全恢复(3 类)。体外循环的使用增加、红细胞输注增加和平均肺动脉压升高与持续 PGD(1 类)相关。1 类患者的死亡风险最高(风险比,2.39;95%CI,1.57-3.63;P <.001)。
在严重 PGD 综合征中,功能障碍的恢复有不同的表型。早期恢复的患者可能代表不同的肺病理机制,例如肺水肿的消退,而那些持续存在 PGD 的患者可能代表更严重的表型。未来针对 PGD 机制或治疗的研究可能会根据移植物功能障碍恢复的表型来进行。