Division of Pediatric Critical Care Medicine, Children's National Hospital, Washington, District of Columbia, USA.
Division of Cardiology and Cardiac Transplant, Children's National Hospital, Children's National Heart Institute, Washington, District of Columbia, USA.
J Clin Apher. 2023 Oct;38(5):514-521. doi: 10.1002/jca.22053. Epub 2023 Apr 12.
Cardiac transplants increasingly occur following placement of ventricular assist devices (VADs). A strong association exists between human leukocyte antigen (HLA) sensitization and VAD placement; however, desensitization protocols that utilize therapeutic plasma exchange (TPE) are fraught with technical challenges and are at increased risk of adverse events. In response to increased VAD utilization in our pre-transplant population, we developed a new institutional standard for TPE in the operating room.
Through a multidisciplinary effort, we developed an institutional protocol for intraoperative TPE immediately prior to cardiac transplantation after cannulation onto cardiopulmonary bypass (CPB). All procedures used the standard TPE protocol on the Terumo Optia (Terumo BCT, Lakewood, CO, USA), but incorporated multiple modifications to limit patients' bypass times, and to coordinate with the surgical teams. These modifications included deliberate misidentification of replacement fluid and maximization of the citrate infusion rate.
These adjustments allowed the machine to run at maximal inlet speeds, minimizing duration of TPE. To date, 11 patients have been treated with this protocol. All survived their cardiac transplantation operation. Hypocalcemia and hypotension were noted; however, none of these adverse events appeared to have clinical impact. Technical complications included unexpected fibrin deposition in the TPE circuit and air in the inlet line due to surgical manipulation of the CPB cannula. No thromboembolic complications occurred in any patient.
We feel that this procedure can be rapidly and safely performed in HLA sensitized pediatric patients on CPB to limit the risk of antibody mediated rejection of their heart transplant.
心脏移植越来越多地发生在心室辅助装置(VAD)放置之后。人类白细胞抗原(HLA)致敏与 VAD 放置之间存在很强的关联;然而,利用治疗性血浆置换(TPE)的脱敏方案存在技术挑战,并且发生不良事件的风险增加。为了应对我们移植前人群中 VAD 使用量的增加,我们制定了一项新的手术室 TPE 机构标准。
通过多学科努力,我们制定了一种机构方案,即在心肺旁路(CPB)插管后,在心脏移植前立即进行术中 TPE。所有程序均使用 Terumo Optia(Terumo BCT,Lakewood,CO,USA)的标准 TPE 方案,但进行了多项修改,以限制患者的旁路时间,并与手术团队协调。这些修改包括故意错误识别替代液和最大程度地增加柠檬酸盐输注率。
这些调整使机器能够以最大入口速度运行,最大限度地减少 TPE 的持续时间。迄今为止,已有 11 名患者接受了该方案治疗。所有患者均在心脏移植手术后幸存。虽然注意到低钙血症和低血压,但这些不良事件均无临床影响。技术并发症包括由于 CPB 插管的手术操作,TPE 回路中意外出现纤维蛋白沉积和入口线中出现空气。任何患者均未发生血栓栓塞并发症。
我们认为,该程序可以在 CPB 上的 HLA 致敏儿科患者中快速安全地进行,以限制其心脏移植发生抗体介导排斥的风险。