UT Southwestern, Department of Pediatrics, Division of Critical Care, Dallas, Texas, USA.
Duke University Hospital, Department of Pediatrics, Division of Critical Care, Durham, North Carolina, USA.
Transfusion. 2021 Jan;61(1):42-51. doi: 10.1111/trf.16164. Epub 2020 Dec 2.
Factor consumption is common during ECMO complicating the balance of pro and anticoagulation factors. This study sought to determine whether transfusion of coagulation factors using fresh frozen plasma (FFP) increased ECMO circuit life and decreased blood product transfusion. Secondly, it analyzed the association between FFP transfusion and hemorrhagic and thrombotic complications.
Thirty-one pediatric ECMO patients between October 2013 and January 2016 at a quaternary care institution were included. Patients were randomized to FFP every 48 hours or usual care. The primary outcome was ECMO circuit change. Secondary outcomes included blood product transfusion, survival to decannulation, hemorrhagic and thrombotic complications, and ECMO costs.
Median (interquartile range [IQR]) number of circuit changes was 0 (0, 1). No difference was seen in percent days without a circuit change between intervention and control group, P = .53. Intervention group patients received median platelets of 15.5 mL/kg/d IQR (3.7, 26.8) vs 24.8 mL/kg/d (12.2, 30.8) for the control group (P = .16), and median packed red blood cells (pRBC) of 7.7 mL/kg/d (3.3, 16.3) vs 5.9 mL/kg/d (3.4, 18.7) for the control group, P = .60. FFP transfusions were similar with 10.2 mL/kg/d (5.0, 13.9) in the intervention group vs 8.8 (2.5, 17.7) for the control group, P = .98.
In this pilot randomized study, scheduled FFP did not increase circuit life. There was no difference in blood product transfusion of platelets, pRBCs, and FFP between groups. Further studies are needed to examine the association of scheduled FFP with blood product transfusion.
在体外膜肺氧合(ECMO)过程中,因子消耗很常见,这会影响促凝和抗凝因子之间的平衡。本研究旨在确定使用新鲜冷冻血浆(FFP)输注凝血因子是否会延长 ECMO 回路的使用寿命并减少血液制品的输注。其次,分析 FFP 输注与出血和血栓并发症之间的关系。
2013 年 10 月至 2016 年 1 月期间,在一家四级医疗机构纳入 31 例儿科 ECMO 患者。患者被随机分为 FFP 每 48 小时输注组或常规治疗组。主要结局是 ECMO 回路变化。次要结局包括血液制品输注、脱机存活、出血和血栓并发症以及 ECMO 成本。
中位数(四分位距 [IQR])无回路变化天数为 0(0,1)。干预组和对照组之间无回路变化的天数百分比无差异,P = 0.53。干预组患者接受的中位数血小板量为 15.5 毫升/公斤/天 IQR(3.7,26.8),而对照组为 24.8 毫升/公斤/天(12.2,30.8)(P = 0.16),接受的中位数浓缩红细胞(pRBC)量为 7.7 毫升/公斤/天(3.3,16.3),而对照组为 5.9 毫升/公斤/天(3.4,18.7)(P = 0.60)。FFP 输注量相似,干预组为 10.2 毫升/公斤/天(5.0,13.9),对照组为 8.8 毫升/公斤/天(2.5,17.7)(P = 0.98)。
在这项初步的随机研究中,计划的 FFP 输注并未延长回路寿命。两组之间血小板、pRBC 和 FFP 的血液制品输注量无差异。需要进一步的研究来检查计划的 FFP 与血液制品输注之间的关系。