Aortic Wellness Center, Lenox Hill Hospital, 130 East 77th street, 4th Floor, New York, NY 10075, USA.
J Thorac Cardiovasc Surg. 2012 May;143(5):1198-204. doi: 10.1016/j.jtcvs.2012.01.004. Epub 2012 Jan 27.
Postoperative bleeding is a major cause of morbidity and mortality after complex aortic surgery. Intraoperative coagulopathy is a well-known culprit in this process. Recombinant activated factor VII is increasingly used for the postoperative management of such bleeding. We report our experience with the intraoperative use of this agent.
We performed a propensity-matched analysis on 376 retrospectively identified patients who underwent aortic root, arch, or ascending aortic replacement surgeries from 1999 to 2010. We matched a total of 58 patients: recombinant activated factor VII-treated group (n = 29) and nonrecombinant activated factor VII-treated group (n = 29). We compared the matched patients on re-exploration, mortality, bleeding-related events, use of blood and blood products, length of intensive care unit stay, duration of hospitalization, and thrombotic complications.
Propensity-matched patients had similar preoperative and intraoperative characteristics. The mean dose of recombinant activated factor VII group was 23 ± 12 μg/kg. We found significantly lower rates of surgical re-exploration (P = .004), fewer prolonged intubations (P = .004), less total chest tube output (P = .01), and fewer units of packed red blood cells (P = .01) and fresh-frozen plasma (P = .04) transfused postoperatively in the recombinant activated factor VII group. There was no significant difference in mortality (P = 1), duration of intensive care unit stay (P = .44) or hospital stay (P = .32), or thrombotic complications between the groups (P = .5).
We recommend the intraoperative administration of low-dose recombinant activated factor VII but limited to the management of persistent, nonsurgical, mediastinal bleeding in aortic surgery. Further prospective randomized studies and larger cohorts are needed to verify these findings.
术后出血是复杂主动脉手术后发病率和死亡率的主要原因。术中凝血功能障碍是该过程中的一个已知罪魁祸首。重组活化因子 VII 越来越多地用于此类出血的术后管理。我们报告了我们在术中使用该药物的经验。
我们对 1999 年至 2010 年间接受主动脉根部、弓部或升主动脉置换手术的 376 例回顾性识别患者进行了倾向匹配分析。我们共匹配了 58 例患者:重组活化因子 VII 治疗组(n = 29)和非重组活化因子 VII 治疗组(n = 29)。我们比较了匹配患者的再次探查、死亡率、出血相关事件、血液和血液制品的使用、重症监护病房住院时间、住院时间和血栓并发症。
倾向匹配患者具有相似的术前和术中特征。重组活化因子 VII 组的平均剂量为 23 ± 12 μg/kg。我们发现手术再次探查的发生率显著降低(P =.004),延长插管的时间更少(P =.004),总胸管引流量更少(P =.01),术后输血量更少红细胞单位(P =.01)和新鲜冷冻血浆(P =.04)。两组死亡率(P = 1)、重症监护病房住院时间(P =.44)或住院时间(P =.32)或血栓并发症无显著差异(P =.5)。
我们建议术中给予低剂量重组活化因子 VII,但仅限于主动脉手术中持续、非手术性纵隔出血的治疗。需要进一步的前瞻性随机研究和更大的队列来验证这些发现。