Shimauchi T, Yamaura K, Higashi M, Abe K, Yoshizumi T, Hoka S
Department of Anaesthesiology and Critical Care Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Operating Rooms, Kyushu University Hospital, Fukuoka, Japan; Department of Anaesthesiology, Fukuoka University School of Medicine, Fukuoka, Japan.
Transplant Proc. 2017 Nov;49(9):2117-2121. doi: 10.1016/j.transproceed.2017.09.025.
Inadequate hemostasis during living donor liver transplantation (LDLT) is mainly due to coagulopathy but may also include fibrinolysis. The purpose of this study was to determine the incidence of fibrinolysis and assess its relevance to mortality in LDLT.
The incidence and prognosis of fibrinolysis were retrospectively studied in 76 patients who underwent LDLT between April 2010 and February 2013. Fibrinolysis was evaluated and defined by maximum lysis (ML) >15% within a 60-minute run time using thromboelastometry (ROTEM).
Fibrinolysis was observed in 19 of the 76 (25%) patients before the anhepatic (pre-anhepatic) phase and was developed in 24 (32%) patients during and after the anhepatic (post-anhepatic) phase. In these 43 patients who had fibrinolysis, spontaneous recovery occurred in 29 patients (73%) within 3 hours after reperfusion of the liver graft. Recovery with tranexamic acid was noted in 2 patients with fibrinolysis in the post-anhepatic phase. Thrombosis in the portal vein and liver artery was noted in 14 patients, and the incidence was significantly greater in patients with post-anhepatic fibrinolysis than in those with pre-anhepatic fibrinolysis (P = .0017). Fibrinolysis that developed in the pre-anhepatic phase was associated with increased 30-day and 6-month mortalities (P = .0003 and .0026, respectively).
Fibrinolysis existed and developed in a large percentage of patients during LDLT. Thrombosis in the portal vein and hepatic artery was more common in patients with fibrinolysis in the post-anhepatic phase. Fibrinolysis that developed in the pre-anhepatic phase was associated with increased 30-day and 6-month mortalities.
活体肝移植(LDLT)过程中止血不充分主要归因于凝血功能障碍,但也可能包括纤溶亢进。本研究旨在确定纤溶亢进的发生率,并评估其与LDLT患者死亡率的相关性。
回顾性研究2010年4月至2013年2月期间接受LDLT的76例患者的纤溶亢进发生率及预后情况。采用血栓弹力图(ROTEM)在60分钟运行时间内评估并定义纤溶亢进为最大溶解率(ML)>15%。
76例患者中,19例(25%)在无肝前期出现纤溶亢进,24例(32%)在无肝期及无肝后期出现纤溶亢进。在这43例发生纤溶亢进的患者中,29例(73%)在肝移植再灌注后3小时内自发恢复。2例无肝后期纤溶亢进患者使用氨甲环酸后恢复。14例患者出现门静脉和肝动脉血栓形成,无肝后期纤溶亢进患者的发生率显著高于无肝前期纤溶亢进患者(P = 0.0017)。无肝前期发生的纤溶亢进与30天和6个月死亡率增加相关(分别为P = 0.0003和0.0026)。
LDLT期间,很大比例的患者存在并发生纤溶亢进。无肝后期纤溶亢进患者门静脉和肝动脉血栓形成更为常见。无肝前期发生的纤溶亢进与30天和6个月死亡率增加相关。