Department of Cardiology, Children's Hospital Boston, Boston, Massachusetts 02115, USA.
J Heart Lung Transplant. 2010 May;29(5):517-22. doi: 10.1016/j.healun.2009.11.601. Epub 2010 Jan 12.
Long-term oral corticosteroids have been a mainstay of maintenance immunosuppression in pediatric heart transplantation. In this study, we report early clinical outcomes in a cohort of pediatric heart transplant recipients managed using a steroid-avoidance protocol.
Of the 70 patients who underwent heart transplantation during the study period, 55 eligible recipients, including 49 non-sensitized and 6 sensitized (all 55 with negative crossmatch) patients, entered a steroid-avoidance immunosuppression protocol consisting of thymoglobin induction followed by a 2-drug, tacrolimus-based, corticosteroid-free regimen. The primary outcome variable was freedom from moderate rejection (International Society for Heart and Lung Transplantation [ISHLT] Grade 2R/3A or antibody-mediated rejection).
The median age at transplant was 7.1 years (range 2 weeks to 22 years) and median follow-up was 19 months (range 2 to 46 months). Fifty patients survived to discharge after transplantation. Of these patients, 2 (4%) were discharged on steroids and 8 (16%) started on maintenance steroids at follow-up. Rejection was diagnosed in 8 patients (Grade 2R cellular rejection in 3 and antibody-mediated rejection in 5). Freedom from rejection was 92% at 6 months (95% confidence interval [CI] 80% to 97%) and 87% at 1 year (CI 73% to 94%). Post-transplant survival was 91% at 6 months (CI 79% to 96%) and 88% at 12 and 24 months (CI 75% to 95%). There was 1 death due to rejection (antibody-mediated) 8 months after transplantation.
An immunosuppression protocol consisting of induction followed by corticosteroid avoidance appears to achieve acceptable rejection rates during the first year post-transplant in pediatric heart transplant recipients.
长期口服皮质类固醇一直是小儿心脏移植中维持免疫抑制的主要方法。在这项研究中,我们报告了一组使用类固醇避免方案治疗的小儿心脏移植受者的早期临床结果。
在研究期间,70 名接受心脏移植的患者中,有 55 名符合条件的受者,包括 49 名非致敏者和 6 名致敏者(所有 55 名均为阴性交叉配型),进入了一种类固醇避免免疫抑制方案,包括胸腺球蛋白诱导,然后是 2 种药物、他克莫司为基础、无皮质类固醇的方案。主要结局变量是无中度排斥反应(国际心肺移植协会[ISHLT]2R/3A 级或抗体介导的排斥反应)。
移植时的中位年龄为 7.1 岁(范围为 2 周至 22 岁),中位随访时间为 19 个月(范围为 2 至 46 个月)。50 名患者在移植后存活出院。这些患者中,有 2 名(4%)出院时使用类固醇,8 名(16%)在随访时开始使用维持类固醇。8 名患者(3 例细胞排斥 2R 级,5 例抗体介导排斥)诊断为排斥反应。6 个月时的无排斥率为 92%(95%置信区间[CI]为 80%至 97%),1 年时为 87%(CI 为 73%至 94%)。6 个月时的移植后存活率为 91%(CI 为 79%至 96%),12 个月和 24 个月时为 88%(CI 为 75%至 95%)。移植后 8 个月,有 1 例因排斥反应(抗体介导)死亡。
在小儿心脏移植受者中,诱导后使用皮质类固醇避免的免疫抑制方案在移植后第一年似乎可达到可接受的排斥反应率。