Gross Benjamin D, Zhu Jerry, Rao Ajit, Ilonzo Nicole, Storch Jason, Faries Peter L, Marin Michael L, George Justin M, Tadros Rami O
Division of Vascular Surgery, Department of Surgery, The Icahn School of Medicine at Mount Sinai, New York, NY.
Division of Vascular Surgery, Department of Surgery, The Icahn School of Medicine at Mount Sinai, New York, NY.
Ann Vasc Surg. 2024 Feb;99:242-251. doi: 10.1016/j.avsg.2023.08.017. Epub 2023 Oct 5.
The purpose of this study was to assess outcomes after spinal anesthesia (SA) versus general anesthesia (GA) in patients undergoing thoracic endograft placement and to evaluate the adjunctive use of cerebrospinal fluid drainage (CSFD) placement.
A single-center retrospective review of patients that underwent thoracic endograft placement from 2001 to 2019 was performed. Patients were stratified based on the type of anesthesia they received: GA, SA or epidural, GA with CSFD, and SA with CSFD. Primary outcomes included 30-day mortality and length of stay (LOS). Baseline characteristics were analyzed with Student's t-test and Pearson's chi-squared test. Multivariate logistic regression analysis was performed to identify risk factors for 30-day mortality and longer LOS.
A total of 333 patients underwent thoracic endograft placement; 104 patients received SA, 180 patients received GA, 30 patients received GA and CSFD, and 19 patients received SA and CSFD. Of the total patients, 16.2% underwent thoracic endograft placement for type B aortic dissection, 3.3% for type A aortic dissection, and 12.3% for penetrating ulcer. The mean age of the study population was 68.7 years old. Patients undergoing SA were older with a mean age of 73.4 years versus 64.7 years for patients undergoing GA (P < 0.001). Spinal anesthesia (SA) was preferred in patients at high risk for GA (>75 years old: 52.9% vs. 33.3%, P < 0.001; renal comorbidities: 20.6% vs. 10.6%, P = 0.03, and current smokers: 26.7% vs. 9.6%, P < 0.001). Length of stay (LOS) was decreased in the SA group (4.29 days vs. 9.70 days, P < 0.001). There was a lower incidence of spinal cord ischemia in the SA group (1.0% vs. 2.2%, P = 0.44), as well as significantly decreased 30-day mortality (0% vs. 5.6%, P = 0.01), reintervention (19.2% vs. 26.8%, P = 0.02), and return to the operating room (6.8% vs. 12.7%, P = 0.02). Of the 19 patients that had SA + CSFD, there were no signs and symptoms of spinal cord ischemia and decreased incidence of perioperative complications (0% vs. 33.3%, P = 0.01). There was no difference in the risk for intraoperative complications, neurologic complications, or 30-day mortality between GA + CSFD patients versus SA + CSFD patients. Age >75 (P = 0.002), intraoperative complications (P < 0.001), and perioperative complications (P = 0.02) were associated with increased mortality after thoracic endograft placement per multivariate logistic regression analysis.
Spinal anesthesia (SA) in select high-risk patients was associated with reduced 30-day mortality, neurologic complications, and LOS compared to GA. The concurrent use of spinal drainage and SA had satisfactory results compared to spinal drainage and GA.
本研究旨在评估接受胸主动脉腔内修复术的患者行脊髓麻醉(SA)与全身麻醉(GA)后的结局,并评估脑脊液引流(CSFD)的辅助使用情况。
对2001年至2019年接受胸主动脉腔内修复术的患者进行单中心回顾性研究。根据患者接受的麻醉类型进行分层:GA、SA或硬膜外麻醉、GA联合CSFD、SA联合CSFD。主要结局包括30天死亡率和住院时间(LOS)。采用Student t检验和Pearson卡方检验分析基线特征。进行多因素logistic回归分析以确定30天死亡率和更长住院时间的危险因素。
共有333例患者接受了胸主动脉腔内修复术;104例患者接受SA,180例患者接受GA,30例患者接受GA联合CSFD,19例患者接受SA联合CSFD。在所有患者中,16.2%因B型主动脉夹层接受胸主动脉腔内修复术,3.3%因A型主动脉夹层,12.3%因穿透性溃疡。研究人群的平均年龄为68.7岁。接受SA的患者年龄较大,平均年龄为73.4岁,而接受GA的患者平均年龄为64.7岁(P<0.001)。GA高风险患者(>75岁:52.9%对33.3%,P<0.001;合并肾脏疾病:20.6%对10.6%,P=0.03;当前吸烟者:26.7%对9.6%,P<0.001)更倾向于选择脊髓麻醉(SA)。SA组的住院时间(LOS)缩短(4.29天对9.70天,P<0.001)。SA组脊髓缺血的发生率较低(1.0%对2.2%,P=0.44),30天死亡率也显著降低(0%对5.6%,P=0.01),再次干预(19.2%对26.8%,P=0.02)以及返回手术室的比例(6.8%对12.7%,P=0.02)。在19例接受SA+CSFD的患者中,没有脊髓缺血的体征和症状,围手术期并发症的发生率降低(0%对33.3%,P=0.01)。GA+CSFD患者与SA+CSFD患者在术中并发症、神经并发症或30天死亡率方面没有差异。根据多因素logistic回归分析,年龄>75岁(P=0.002)、术中并发症(P<0.001)和围手术期并发症(P=0.02)与胸主动脉腔内修复术后死亡率增加相关。
与GA相比,选择性高风险患者行脊髓麻醉(SA)可降低30天死亡率、神经并发症和住院时间。与脊髓引流联合GA相比,脊髓引流联合SA的效果令人满意。