Wischmann Patricia, Stern Manuel, Baasen Sven, Schillings Miriam, Schremmer Johanna, Oliver Stern Marc, Klein Kathrin, Jung Christian, Zeus Tobias, Heiss Christian, Kelm Malte, Busch Lucas
Division of Cardiology, Pulmonology, and Vascular Medicine, Medical Faculty, Heinrich-Heine University, Düsseldorf, Germany.
CARID, Cardiovascular Research Institute Düsseldorf, Medical Faculty, and University Hospital Düsseldorf, Heinrich-Heine-University Düsseldorf, Germany.
Vasa. 2025 Jan;54(1):50-58. doi: 10.1024/0301-1526/a001135. Epub 2024 Jul 17.
Bifemoral arterial access is common in patients undergoing transcatheter aortic valve implantation (TAVI), with a primary treatment access (TAVI access) and a secondary non-TAVI access. Pseudoaneurysm (PSA) is an important complication of femoral arterial puncture. Major vascular complications after TAVI are well described, but little is known about PSA. A total of 2063 patients underwent transfemoral TAVI between January 2014 and January 2020. Vascular ultrasound of the common femoral artery was assessed before and after TAVI. We compared patient characteristics, periprocedural risk scores, procedural characteristics, and access site bleeding events according to Valve Academic Research Consortium 3 (VARC-3) criteria, length of stay (LOS), and all-cause mortality at one year between patients with (46) and without (2017) PSA. The incidence of PSA after TAVI was 2.2% (46/2063). All PSA were successfully treated with ultrasound-guided manual compression (UGMC) or thrombin injection (UGTI) without complications. Patients with PSA had lower platelet counts (210×1000/μl vs. 234×1000/μl; p<0.05), more heart failure symptoms on admission (91% vs. 25%; p<0.05), were more often treated with (N)OACs for atrial fibrillation (AF; 54% vs. 38%; p <0.05), and were less often treated with aspirin (35% vs. 51%; p<0.03). Multivariate analysis identified secondary access site (odds ratio [OR] 8.11; p<0.001) and (N)OAC therapy (OR 1.31; p = 0.037) as risk factors for PSA development. PSA is associated with VARC-3 type 1-3 access site bleeding and longer LOS (15.2 ± 11.3 d vs. 11.6 ± 8.9 d; p<0.01), but this did not affect one year mortality (17% vs. 14%; p = 0.53). Pseudoaneurysms are an important complication after TAVI and are associated with access site bleeding and prolonged hospital stay. (N)OAC therapy and secondary access are important risk factors. Pseudoaneurysms can be safely and effectively treated with thrombin injection and do not affect one-year mortality.
双股动脉入路在接受经导管主动脉瓣植入术(TAVI)的患者中很常见,有一个主要治疗入路(TAVI入路)和一个次要非TAVI入路。假性动脉瘤(PSA)是股动脉穿刺的一种重要并发症。TAVI后的主要血管并发症已有充分描述,但关于PSA的了解甚少。2014年1月至2020年1月期间,共有2063例患者接受了经股动脉TAVI。在TAVI前后对股总动脉进行血管超声检查。我们根据瓣膜学术研究联盟3(VARC-3)标准、住院时间(LOS)以及有PSA(46例)和无PSA(2017例)患者的一年全因死亡率,比较了患者特征、围手术期风险评分、手术特征和入路部位出血事件。TAVI后PSA的发生率为2.2%(46/2063)。所有PSA均通过超声引导下手动压迫(UGMC)或凝血酶注射(UGTI)成功治疗,无并发症。有PSA的患者血小板计数较低(210×1000/μl对234×1000/μl;p<0.05),入院时心力衰竭症状更多(91%对25%;p<0.05),因心房颤动(AF)接受(新型)口服抗凝药(NOACs)治疗的频率更高(54%对38%;p<0.05),而接受阿司匹林治疗的频率更低(35%对51%;p<0.03)。多变量分析确定次要入路部位(比值比[OR]8.11;p<0.001)和(新型)口服抗凝药治疗(OR 1.31;p = 0.037)是PSA发生的危险因素。PSA与VARC-3 1-3型入路部位出血和更长的住院时间相关(15.2±11.3天对11.6±8.9天;p<0.01),但这并不影响一年死亡率(17%对14%;p = 0.53)。假性动脉瘤是TAVI后的一种重要并发症,与入路部位出血和住院时间延长有关。(新型)口服抗凝药治疗和次要入路是重要的危险因素。假性动脉瘤可以通过凝血酶注射安全有效地治疗,且不影响一年死亡率。