在肺移植的静脉-动脉体外氧合过程中,白细胞计数增加与非分数肝素需求增加有关

Koichi Kashiwa, Hideo Kurosawa, Kazuki Fujishiro, Hitoshi Kubo, Ryota Inokuchi, Masahiko Bougaki, Gaku Kawamura, Masaaki Sato, C. Konoeda, Jun Nakajima, Kent Doi
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引用次数: 0

摘要

这项回顾性观察研究旨在探讨临床炎症指标是否与肺移植手术中静脉-动脉体外膜氧合(V-A ECMO)维持ACT范围所需的未分馏肝素(UFH)剂量有关。在 2021 年 1 月至 2022 年 5 月期间使用 V-A ECMO 进行肺移植手术的所有患者中,有 27 名患者入选。根据 UFH 输注率是否在初始输注率(7-8 单位/公斤/小时)的基础上增加(增加组,n = 10)或维持或减少输注率(未增加组,n = 17),这些患者被分为两组。输注速度以 160 至 200 秒的活化凝血时间 (ACT) 为目标进行调整。开始 ECMO 1-2 小时后,ACT 明显降低(179.0(166.5-188.5)秒对 224.0(193.0-242.0)秒,P=0.006),白细胞(WBC)计数在增加组更高(12.6±3.3 对 9.5±4.0×103/μL,P=0.046)。手术期间,增高组的 UFH 输注率更高。开始 ECMO 后 1-2 小时白细胞计数的临界值被确定为 10.2 × 103/μL(灵敏度 90.0%,特异度 58.8%,曲线下面积 0.712),该临界值的判别具有统计学意义(P=0.018)。这些数据表明,白细胞计数与肺移植手术期间 V-A ECMO 的 UFH 输注率要求增加有关。有必要进行进一步评估,以明确白细胞计数在确定最佳 UFH 剂量方面的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Increased white blood cell count is associated with an increased demand for unfractionated heparin during veno-arterial extracorporeal oxygenation in lung transplantation
This retrospective observational study aimed to examine whether clinical inflammatory parameters were associated with the requirement dosage of unfractionated heparin (UFH) to maintain the range of ACT in veno-arterial extracorporeal membrane oxygenation (V-A ECMO) during lung transplantation surgery. Among all patients who underwent lung transplantation using V-A ECMO from January 2021 to May 2022, 27 patients were included. These patients were divided into the two groups based on whether the infusion rate of UFH was increased from the initial infusion rate (7-8 units/kg/hr) (increased group, n = 10) or the infusion rate was maintained or decreased (non-increased group, n = 17). The infusion rate was adjusted with activated clotting time (ACT) target of 160 to 200 seconds. At 1-2 hours after starting ECMO, ACT was significantly lower (179.0 (166.5-188.5) versus 224.0 (193.0-242.0) sec, P=0.006) and white blood cell (WBC) counts were higher in the increased group (12.6±3.3 versus 9.5±4.0×103/μL, P=0.046). The UFH infusion rates were higher in the increased group during the surgery. The cutoff value of WBC count at 1-2 hours after starting ECMO for discriminating the need for increasing the UFH dosage was determined as 10.2 × 103/μL (sensitivity 90.0%, specificity 58.8%, area under the curve 0.712) and discrimination of this cut off value was confirmed as statistically significant (P=0.018). These data suggested that WBC count was associated with the requirement of increase in UFH infusion rate of V-A ECMO during lung transplantation surgery. Further evaluation is necessary to clarify the role of WBC count for determining the optimal UFH dosage.
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