University of Pittsburgh Medical Center, Department of Cardiothoracic Surgery, Pittsburgh, Pennsylvania.
Columbia University Medical Center-New York Presbyterian Hospital, Department of Surgery, New York, New York.
Semin Thorac Cardiovasc Surg. 2019 Winter;31(4):783-793. doi: 10.1053/j.semtcvs.2019.05.006. Epub 2019 May 11.
Generation of plasma-free hemoglobin (pfHb) and activated complement during complex cardiac surgery contributes to end-organ dysfunction. This prospective, multicenter REFRESH I (REduction in FREe Hemoglobin) randomized controlled trial evaluated the safety and feasibility of CytoSorb hemoadsorption therapy to reduce these factors during prolonged cardiopulmonary bypass (CPB). Eligible patients underwent elective, nonemergent complex cardiac surgery with expected CPB duration ≥3 hours. Exclusions included single procedures including primary coronary artery bypass graft, single valves, transplant, and left ventricular assist device extraction. TREATMENT used 2 parallel 300 mL CytoSorb hemoadsorption cartridges in a side circuit during CPB. CONTROL was standard of care. Of 52 enrolled patients, 46 underwent surgery (Safety group, n = 23 vs Control, n = 23), and 38 were evaluated for pfHb reduction (EFFICACY group, n = 18 vs CONTROL, n = 20). Type and number of serious adverse events (44 vs 43 CONTROL) were similar, as was 30-day mortality. Transient reduction in platelets during CPB was observed in both groups, especially TREATMENT, but returned to pretreatment levels after CPB without bleeding. Peak pfHb was positively correlated with CPB length (P = 0.01) but the high variability of pfHb, due to the broad surgical procedure mix, prevented detection of changes in pfHb in the overall EFFICACY population. However, the valve replacement surgery subgroup (8 vs 10 CONTROL) had the highest peak pfHb levels, and TREATMENT demonstrated significant pfHb reductions vs CONTROL (P ≤ 0.05) in CPB ≥3 hours. In the EFFICACY group, C3a and C5a were significantly reduced by treatment throughout surgery. Intraoperative hemoadsorption with CytoSorb was safe and feasible in this randomized, controlled pilot study during complex cardiac surgery. Treatment with CytoSorb resulted in significant reductions in pfHb during valve replacement surgery and reductions in C3a and C5a in the overall EFFICACY group. Future studies will target complex cardiac surgery patients with prolonged CPB to assess hemoadsorption effect on end-organ dysfunction and outcomes.
在复杂心脏手术期间,血浆游离血红蛋白 (pfHb) 和激活的补体的产生会导致终末器官功能障碍。这项前瞻性、多中心 REFRESH I(减少游离血红蛋白)随机对照试验评估了 CytoSorb 血液吸附疗法在长时间体外循环 (CPB) 期间降低这些因素的安全性和可行性。符合条件的患者接受择期、非紧急复杂心脏手术,预计 CPB 时间≥3 小时。排除标准包括单次手术,包括原发性冠状动脉旁路移植术、单瓣膜、移植和左心室辅助装置提取。治疗中在 CPB 期间使用两个平行的 300ml CytoSorb 血液吸附盒。对照组为标准护理。52 名入组患者中,46 名接受手术(安全性组,n=23 与对照组,n=23),38 名评估 pfHb 降低(疗效组,n=18 与对照组,n=20)。严重不良事件的类型和数量(44 与 43 对照组)相似,30 天死亡率也相似。两组在 CPB 期间均观察到血小板短暂减少,尤其是治疗组,但 CPB 后血小板恢复到预处理水平,无出血。pfHb 峰值与 CPB 时间呈正相关(P=0.01),但由于手术程序广泛混合,pfHb 的高变异性阻止了在整个疗效人群中检测到 pfHb 的变化。然而,瓣膜置换手术亚组(8 与 10 对照组)的 pfHb 峰值最高,治疗组与对照组相比,CPB≥3 小时时 pfHb 显著降低(P≤0.05)。在疗效组中,整个手术过程中 C3a 和 C5a 通过治疗显著降低。在这项随机对照试验中,复杂心脏手术期间使用 CytoSorb 进行术中血液吸附是安全可行的。在瓣膜置换手术中,CytoSorb 治疗导致 pfHb 显著降低,在整个疗效组中,C3a 和 C5a 降低。未来的研究将针对 CPB 时间延长的复杂心脏手术患者,评估血液吸附对终末器官功能障碍和结局的影响。