Mandell Daniel, Planinsic Raymond, Melean Fernando, Hughes Christopher, Tevar Amit D, Humar Abhinav, Cassidy Benjamin J, Simmons Richard, Dewolf Andre, Sakai Tetsuro
1 Anesthesiology, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
2 Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
Semin Cardiothorac Vasc Anesth. 2018 Dec;22(4):376-382. doi: 10.1177/1089253218760221. Epub 2018 Feb 28.
Tissue plasminogen activator (tPA) has been reported to treat intraoperative pulmonary thromboembolism (PTE) during liver transplantation (LT). However, tPA administration is often delayed due to fear of uncontrolled bleeding and storage in a refrigerator outside of operating rooms. Various dosages of tPA were used. We hypothesize that a policy of tPA storage and low dosage use improves patient outcomes. At a transplantation center, a multidisciplinary committee has implemented a tPA policy since April 2014, which includes the following: (1) timely administering of low-dose tPA (0.5-4 mg) for intraoperative PTE; (2) keeping 2 vials of tPA (2 mg/vial) in the operating room at room temperature; and (3) transferring unused tPA vials to the cardiology catheterization laboratory for next-day use. A prospective observational study was conducted to record the incidence and outcome of PTE during LTs. Over the next 19 months, 99 adult deceased donor LTs were performed with 1 (1.0%) intraoperative PTE. A 45-year-old woman with hepatitis C developed PTE within 5 minutes after graft reperfusion. A 2-mg tPA was immediately administered via a central venous line with hemodynamic improvement and clot lysis. Thromboelastography was normalized in 90 minutes. Five LT cases developing intraoperative PTE have been reported to receive "standard" dosages of tPA (20-110 mg) or urokinase (4400 IU/kg), which were administered more than 20 minutes after the diagnosis of PTE. One intraoperative death and one later mortality were noted with intracranial hemorrhages/infarction of 3 cases. The multidisciplinary low-dose tPA policy for PTE was suggested to be effective.
据报道,组织型纤溶酶原激活剂(tPA)可用于治疗肝移植(LT)术中的肺血栓栓塞症(PTE)。然而,由于担心出血无法控制以及tPA需在手术室之外的冰箱中储存,tPA的给药常常延迟。tPA使用了各种不同剂量。我们假设,tPA储存和低剂量使用的策略可改善患者预后。在一个移植中心,自2014年4月起,一个多学科委员会实施了一项tPA策略,该策略包括以下内容:(1)对术中PTE及时给予低剂量tPA(0.5 - 4毫克);(2)在手术室室温下保存2瓶tPA(每瓶2毫克);(3)将未使用的tPA瓶转移至心脏导管插入实验室供次日使用。进行了一项前瞻性观察研究,以记录肝移植术中PTE的发生率和预后情况。在接下来的19个月里,共进行了99例成人尸体供肝肝移植手术,其中1例(1.0%)发生术中PTE。一名45岁的丙型肝炎女性在移植肝再灌注后5分钟内发生PTE。立即通过中心静脉导管给予2毫克tPA,血流动力学得到改善,血栓溶解。血栓弹力图在90分钟内恢复正常。据报道,有5例肝移植术中发生PTE的病例接受了“标准”剂量的tPA(20 - 110毫克)或尿激酶(4400国际单位/千克),这些药物在PTE诊断后20多分钟才给药。3例出现颅内出血/梗死,记录到1例术中死亡和1例后期死亡。提示多学科的低剂量tPA治疗PTE策略是有效的。