Darling Jeremy D, Caron Elisa, Park Jemin, van Galen Isa, Guetter Camila R, Gomez-Mayorga Jorge, Sanders Andrew P, Stangenberg Lars, Schermerhorn Marc L
Division of Vascular and Endovascular Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA.
Division of Vascular and Endovascular Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA.
J Vasc Surg. 2025 Apr;81(4):830-838. doi: 10.1016/j.jvs.2024.12.037. Epub 2024 Dec 17.
Ongoing innovations in the minimally invasive management of complex abdominal aortic aneurysms, including physician-modified endografts (PMEG) and, more recently, Fiber Optic RealShape (FORS) technology, have allowed vascular surgeons to expand the surgical indications for and complexity of care to this multifaceted patient population. Prior analyses have demonstrated intraoperative advantages of Fiber Optic RealShape in the management of complex abdominal aortic aneurysms for lower total procedural radiation and cannulation tasks; however, few analyses have evaluated the technology's effect on perioperative and postoperative outcomes.
All PMEGs performed at our institution between 2020 and 2024 were reviewed retrospectively. Primary intraoperative and perioperative outcomes included fluoroscopy time and dose, target vessel cannulation failure, target vessel dissection or perforation, and perioperative complications. Primary postoperative (6-month) outcomes included target vessel related (type Ic or IIIc) endoleak and target vessel instability, defined as any branch-related complication leading to aneurysm rupture, death, occlusion, component separation, or reintervention. Inverse probability of treatment weighting was used to account for factors of clinical significance. The χ test, logistic regression, and Cox regression were used to evaluate perioperative outcomes in the weighted cohort.
Between 2020 and 2024, 118 patients received a PMEG: 49 with Fiber Optic RealShape (FORS) and 69 using standard fluoroscopy. Baseline characteristics were similar between groups. After weighting, use of FORS exhibited lower fluoroscopy time (38 minutes vs 56 minutes; P < .01) and air Kerma (429 mGy vs 655 mGy; P = .01). Between FORS and standard fluoroscopy, there were no differences noted in target vessel cannulation failure (4.7% vs 1.0%) or in intraoperative or perioperative target vessel perforation (1.9% vs 1.0%) or dissection (6.7% vs 2.1%) (all P > .05). Perioperative complications were similar between groups (22% vs 21%), including spinal cord ischemia (temporary, 8.4% vs 6.1%; permanent, 2.0% vs 3.9%) and bowel ischemia (0% vs 2.6%). FORS use did demonstrate lower rates of target vessel instability (1.2% vs 10%; P = .02) at 6 months; however, this difference did not persist on multivariable analysis.
Since the implementation of FORS at our institution, when compared with standard fluoroscopy, there have been significantly lower intraoperative fluoroscopy times and total radiation doses, with no difference in target vessel cannulation failure, dissection, perforation, perioperative complications, or target vessel instability at 6 months after a PMEG. Although these data may represent our institution's gradual improvement in expertise with this new technology, our results underscore the importance of additional analyses on this evolving technology as it becomes more integrated into the standard practice of the management of complex aortic pathologies.
复杂腹主动脉瘤微创治疗方面的持续创新,包括医生改良型腔内移植物(PMEG)以及最近的光纤实时塑形(FORS)技术,使血管外科医生能够扩大对这类多方面患者群体的手术适应症并增加护理的复杂性。先前的分析表明,在复杂腹主动脉瘤治疗中,光纤实时塑形技术在降低总手术辐射和插管任务方面具有术中优势;然而,很少有分析评估该技术对围手术期和术后结果的影响。
回顾性分析2020年至2024年在本机构进行的所有PMEG手术。主要术中及围手术期结果包括透视时间和剂量、靶血管插管失败、靶血管夹层或穿孔以及围手术期并发症。主要术后(6个月)结果包括靶血管相关(Ic型或IIIc型)内漏和靶血管不稳定,靶血管不稳定定义为任何导致动脉瘤破裂、死亡、闭塞、组件分离或再次干预的分支相关并发症。采用治疗权重的逆概率来考虑具有临床意义的因素。使用χ检验、逻辑回归和Cox回归来评估加权队列中的围手术期结果。
2020年至2024年期间,118例患者接受了PMEG手术:49例使用光纤实时塑形技术(FORS),69例使用标准透视。两组的基线特征相似。加权后,使用FORS的透视时间较短(38分钟对56分钟;P <.01),空气比释动能较低(429 mGy对655 mGy;P =.01)。在FORS组和标准透视组之间,靶血管插管失败率(4.7%对1.0%)、术中或围手术期靶血管穿孔率(1.9%对1.0%)或夹层率(6.7%对2.1%)均无差异(所有P >.05)。两组的围手术期并发症相似(22%对21%),包括脊髓缺血(暂时性,8.4%对6.1%;永久性,2.0%对3.9%)和肠缺血(0%对2.6%)。使用FORS在6个月时确实显示出较低的靶血管不稳定率(1.2%对10%;P =.02);然而,在多变量分析中这种差异并未持续存在。
自本机构实施FORS以来,与标准透视相比,术中透视时间和总辐射剂量显著降低,PMEG术后6个月时靶血管插管失败、夹层、穿孔、围手术期并发症或靶血管不稳定方面无差异。尽管这些数据可能代表了本机构对这项新技术专业知识的逐步提高,但我们的结果强调了随着这项不断发展的技术越来越多地融入复杂主动脉病变管理的标准实践,对其进行更多分析的重要性。