Department of Thoracic and Cardiovascular Surgery, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.
Division of Infectious Disease, Department of Internal Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.
Yonsei Med J. 2021 Feb;62(2):164-171. doi: 10.3349/ymj.2021.62.2.164.
Calcineurin inhibitor (CNI) use has improved lung transplantation outcomes. However, significant perioperative complications in patients receiving CNI can deteriorate the early course of lung transplantation. To date, there is no consensus regarding the optimal agent for the induction regimen after lung transplantation. We aimed to determine the efficacy of basiliximab induction with delayed CNI initiation in the prevention of acute complications without compromising immunosuppression in high-risk patients.
Between January 2013 and December 2019, 236 patients at a single lung transplant center were retrospectively reviewed. Forty-one patients (17.4%) received basiliximab induction, and 195 patients (82.6%) received a routine triple-drug regimen without induction. The primary endpoint was postoperative acute kidney injury with several other postoperative outcomes as secondary end-points.
Preoperatively, the induction group had a higher proportion of patients who were admitted before transplantation (95.1% vs. 47.7%, <0.001) and received intensive unit care (90.2% vs. 33.8%, <0.001) and extracorporeal membrane oxygenation (ECMO) (87.8% vs. 20.0%, <0.001) compared to the non-induction group. No significant differences were observed in the incidence of acute rejection between groups (=0.657), although lower incidence of postoperative complications, including acute kidney injuries or culture-proven infections, were observed in the induction group. However, the differences were not statistically significant. A subgroup analysis of high-risk and preoperative ECMO support groups showed similar results.
Basiliximab induction with delayed CNI initiation for high-risk patients might decrease the incidence of perioperative complications, including acute renal failure, without increasing the risk of acute rejection.
钙调磷酸酶抑制剂(CNI)的使用改善了肺移植的结果。然而,接受 CNI 的患者在围手术期发生严重并发症会使肺移植的早期过程恶化。迄今为止,对于肺移植后诱导方案的最佳药物,尚无共识。我们旨在确定延迟 CNI 启动的巴利昔单抗诱导在预防高危患者的急性并发症而不影响免疫抑制的效果。
在 2013 年 1 月至 2019 年 12 月期间,对单个肺移植中心的 236 名患者进行了回顾性分析。41 名患者(17.4%)接受了巴利昔单抗诱导,195 名患者(82.6%)接受了常规三联药物治疗而无诱导。主要终点是术后急性肾损伤,其他术后结果为次要终点。
术前,诱导组中术前住院(95.1%对 47.7%,<0.001)和接受重症监护(90.2%对 33.8%,<0.001)和体外膜氧合(ECMO)(87.8%对 20.0%,<0.001)的患者比例较高。与非诱导组相比,两组之间急性排斥反应的发生率没有显著差异(=0.657),尽管诱导组术后并发症(包括急性肾损伤或培养阳性感染)的发生率较低。然而,这些差异没有统计学意义。高危和术前 ECMO 支持组的亚组分析也得出了相似的结果。
对于高危患者,延迟 CNI 启动的巴利昔单抗诱导可能会降低围手术期并发症(包括急性肾衰竭)的发生率,而不会增加急性排斥反应的风险。