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体外膜肺氧合患者使用重组凝血因子VIIa的安全性。

Safety of recombinant factor VIIa in patients under extracorporeal membrane oxygenation.

作者信息

Anselmi Amedeo, Guinet Patrick, Ruggieri Vito Giovanni, Aymami Marie, Lelong Bernard, Granry Solène, Malledant Yannick, Le Tulzo Yves, Gueret Pierre, Verhoye Jean-Philippe, Flecher Erwan

机构信息

Division of Thoracic and Cardiovascular Surgery, Pontchaillou University Hospital, Rennes, France INSERM (French National Institution for Healthcare and Medical Research) Unit 1099, University of Rennes 1, Rennes, France.

Division of Cardiac Anesthesia, Pontchaillou University Hospital, Rennes, France.

出版信息

Eur J Cardiothorac Surg. 2016 Jan;49(1):78-84. doi: 10.1093/ejcts/ezv140. Epub 2015 Apr 23.

Abstract

OBJECTIVES

To address the safety (rate of thromboembolic events and circuit complications) and efficacy (rate of bleeding control) of recombinant activated coagulation factor VII (rFVIIa) to treat severe bleeding refractory to all surgical and medical treatments in patients under veno-arterial (VA) or veno-venous (VV) extracorporeal membrane oxygenation (ECMO) support.

METHODS

In a tertiary referral University Cardiothoracic Surgery Centre including three intensive care units, 30 patients received the rFVIIa during ongoing VA or VV ECMO support (8.6% of ECMO activity from 2005 to 2014; N = 347). Early and late clinical results were analysed (retrospective analysis of prospectively collected data). In a substudy, a case-matching procedure was performed among ECMO patients who received (Group A) or did not receive (Group B) rFVIIa treatment.

RESULTS

The mediastinum was the most common site of refractory bleeding (after heart transplantation or other cardiac surgery; 90%); 90% (n = 27) of patients were on VA ECMO and the remainder on VV ECMO. The survival rate at ECMO explantation and at the 30th post-implantation day was 67 and 50%, respectively. The final efficacy rate of rFVIIa in stopping bleeding was 93.3%. The rate of thromboembolic events was 3.3% (1 case) and the rate of circuit change was 16.7% (without instances of overt circuit clotting). After case-matching, Group A comprised 23 patients and Group B included 43 patients. No statistically significant differences were observed among groups in terms of thromboembolic events (P = 0.99), circuit change, ventilation time (P = 0.71), infectious complications (P = 06) and survival at both ECMO explantation and the 30th post-implantation day. Late survival was comparable (Kaplan-Meier analysis; P = 0.42).

CONCLUSIONS

In case of life-threatening bleeding refractory to all conventional therapies, rFVIIa presents an acceptable safety profile in patients under ECMO support. No circuit dysfunctions and limited rates of thromboembolism are observed.

摘要

目的

探讨重组活化凝血因子VII(rFVIIa)治疗在静脉-动脉(VA)或静脉-静脉(VV)体外膜肺氧合(ECMO)支持下,对所有手术和内科治疗均难治的严重出血的安全性(血栓栓塞事件发生率和体外循环并发症)和有效性(出血控制率)。

方法

在一家拥有三个重症监护病房的三级转诊大学心胸外科中心,30例患者在进行VA或VV ECMO支持期间接受了rFVIIa治疗(占2005年至2014年ECMO治疗活动的8.6%;N = 347)。分析早期和晚期临床结果(对前瞻性收集的数据进行回顾性分析)。在一项子研究中,对接受(A组)或未接受(B组)rFVIIa治疗的ECMO患者进行病例匹配程序。

结果

纵隔是难治性出血最常见的部位(心脏移植或其他心脏手术后;90%);90%(n = 27)的患者接受VA ECMO支持,其余接受VV ECMO支持。ECMO撤除时和植入后第30天的生存率分别为67%和50%。rFVIIa止血的最终有效率为93.3%。血栓栓塞事件发生率为3.3%(1例),体外循环更换率为16.7%(无明显体外循环凝血情况)。病例匹配后,A组包括23例患者,B组包括43例患者。在血栓栓塞事件(P = 0.99)、体外循环更换、通气时间(P = 0.71)、感染并发症(P = 0.6)以及ECMO撤除时和植入后第30天的生存率方面,各组之间未观察到统计学显著差异。晚期生存率相当(Kaplan-Meier分析;P = 0.42)。

结论

在所有传统治疗均难治的危及生命的出血情况下,rFVIIa在接受ECMO支持的患者中具有可接受的安全性。未观察到体外循环功能障碍,血栓栓塞发生率有限。

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