Department of Cardiovascular Surgery, Inselspital, University Hospital Bern, University of Bern, Bern, Switzerland.
Department of Cardiovascular Surgery, Inselspital, University Hospital Bern, University of Bern, Bern, Switzerland.
Ann Vasc Surg. 2021 Aug;75:341-348. doi: 10.1016/j.avsg.2021.01.096. Epub 2021 Feb 5.
The administration of unfractionated heparin (UFH) during endovascular repair of blunt traumatic aortic injury (BTAI) is controversial. The aim of the study is to report the early outcomes of patients undergoing thoracic endovascular aortic repair (TEVAR) for BTAI, and to assess the individualized intraoperative use and dose of UFH.
This is a retrospective analysis including consecutive patients treated with TEVAR for BTAI of the descending aorta between January 1st, 2005 and December 31st, 2018. Intraoperative use and doses of UFH were analyzed. Primary outcome included a reintervention because of new onset bleeding and/or thromboembolic complication and 30-day mortality. Technical success, injury severity score (ISS), timing of treatment, and neurologic deterioration were secondary outcome.
Thirty-six patients with a mean age of 47 ± 18 years, 30 males (83%), were included. Intraoperative administration of UFH was recorded in 30/36 patients (83%) with a mean dose of 4750 ± 2180 IU. Two patients had no UFH because of extensive intracranial hemorrhage or suspected relevant liver laceration, respectively; 1 died in theatre, 1 was already anticoagulated having a mechanical aortic valve, and in 2 no information about heparin use was found. During 30 days of follow-up, 3 patients died (8%; 3/36): 1 patient with completely transected aorta died on-table and 2 on the fifth postoperative day, 1 from trauma-associated brain injury and 1 with multi organ failure. No bleeding or thromboembolic complication requiring reintervention occurred in any patient during 30 days follow-up. In 3 patients partial unintentional coverage of the left common carotid artery occurred, resulting in technical success of 89% (32/36). Mean ISS was 43 ± 15. Thirty-five patients (97%) were severely injured having an ISS ≥ 25. Twenty-nine patients (81%) were treated within 24 hr and 6 patients (17%) within 1 week. No stroke or spinal cord ischemia was observed.
Systemic heparinization in different doses during TEVAR for BTAI can be safe with no intraoperative bleeding or thromboembolic complications in early postoperative period.
在钝性创伤性主动脉损伤(BTAI)的血管内修复过程中,使用未分级肝素(UFH)存在争议。本研究旨在报告接受胸主动脉腔内修复术(TEVAR)治疗的 BTAI 患者的早期结果,并评估术中 UFH 的个体化使用和剂量。
这是一项回顾性分析,纳入了 2005 年 1 月 1 日至 2018 年 12 月 31 日期间接受 TEVAR 治疗的降主动脉 BTAI 连续患者。分析术中 UFH 的使用和剂量。主要结局包括新发出血和/或血栓栓塞并发症需要再次干预以及 30 天死亡率。技术成功率、损伤严重程度评分(ISS)、治疗时机和神经功能恶化是次要结局。
36 例患者的平均年龄为 47±18 岁,30 例男性(83%),其中 30 例(83%)术中使用了 UFH,平均剂量为 4750±2180IU。有 2 例患者因广泛颅内出血或疑似相关肝裂伤而未使用 UFH;1 例患者在术中死亡,1 例患者因患有机械主动脉瓣而已经抗凝,2 例患者未发现肝素使用信息。在 30 天的随访期间,有 3 例患者死亡(8%;3/36):1 例完全性主动脉撕裂患者在术中死亡,2 例患者在术后第 5 天死亡,1 例患者死于创伤相关脑损伤,1 例患者死于多器官功能衰竭。在 30 天的随访期间,没有任何患者发生需要再次干预的出血或血栓栓塞并发症。在 3 例患者中,左颈总动脉部分非故意覆盖,导致技术成功率为 89%(32/36)。平均 ISS 为 43±15。35 例(97%)患者严重受伤,ISS≥25。29 例(81%)患者在 24 小时内接受治疗,6 例(17%)患者在 1 周内接受治疗。未观察到卒中或脊髓缺血。
在 BTAI 的 TEVAR 过程中,使用不同剂量的全身肝素化是安全的,在术后早期没有术中出血或血栓栓塞并发症。