Division of Gastroenterology and Hepatology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
Department of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
Transplantation. 2022 Nov 1;106(11):2182-2192. doi: 10.1097/TP.0000000000004209. Epub 2022 Jun 16.
Immunosuppression is a critical aspect of post-transplant management, yet practices at intermediate and late time points after liver transplantation (LT) are poorly characterized.
A retrospective cohort of 11 326 adult first LT alone recipients between 2007 and 2016 was identified by linking United Network for Organ Sharing transplant data to Medicare administrative claims. The immunosuppression regimen was obtained from Medicare billing claims. Factors associated with calcineurin inhibitor (CNI) monotherapy at 1-, 3-, and 5-y post-LT were investigated using mixed-effects logistic regression. Center practice heterogeneity was evaluated. The association of immunosuppression regimen (time-updating) with patient and graft survival was studied.
CNI monotherapy was used in 51.9% at 1-y post-LT and 68.6% at 5-y post-LT. Center-specific rates ranged from 20.0%-79.9% to 15.4%-95.2%, respectively. CNI monotherapy at 1- and 3-y post-LT was less likely among Black recipients ( P = 0.027 and P = 0.015 versus White, respectively). CNI plus antimetabolite was associated with improved adjusted patient (hazard ratio, 0.59; P < 0.001) and graft (hazard ratio, 0.62; P < 0.001) survival versus CNI monotherapy. The benefit of CNI plus antimetabolite on patient and graft survival increased with older age.
In this first longitudinal analysis of LT immunosuppression practices among Medicare beneficiaries, a CNI plus antimetabolite approach led to improved outcomes. Significant center heterogeneity in practice was observed.
免疫抑制是肝移植(LT)后管理的一个关键方面,但 LT 后中期和晚期的实践情况描述较差。
通过将联合器官共享网络(UNOS)移植数据与医疗保险管理索赔相链接,确定了 2007 年至 2016 年间 11326 例单独接受成人首次 LT 的患者的回顾性队列。免疫抑制方案是从医疗保险计费索赔中获得的。使用混合效应逻辑回归分析了与 LT 后 1、3 和 5 年时使用钙调神经磷酸酶抑制剂(CNI)单药治疗相关的因素。评估了中心实践异质性。研究了免疫抑制方案(时间更新)与患者和移植物生存的关系。
LT 后 1 年和 5 年时,CNI 单药治疗分别为 51.9%和 68.6%。中心特异性比率分别为 20.0%-79.9%至 15.4%-95.2%。与白人相比,黑人患者接受 LT 后 1 年和 3 年时 CNI 单药治疗的可能性较小(P=0.027 和 P=0.015)。与 CNI 单药治疗相比,CNI 加抗代谢物治疗与调整后的患者(风险比,0.59;P<0.001)和移植物(风险比,0.62;P<0.001)生存率提高相关。随着年龄的增长,CNI 加抗代谢物对患者和移植物生存的获益增加。
在这项对医疗保险受益人的 LT 免疫抑制实践的首次纵向分析中,CNI 加抗代谢物方法改善了结果。观察到实践中存在显著的中心异质性。