医师改良的内移植物治疗涉及主动脉弓的胸主动脉病变。

IF 1.5 2区 医学 Q3 PERIPHERAL VASCULAR DISEASE
Journal of Endovascular Therapy Pub Date : 2025-10-01 Epub Date: 2023-10-30 DOI:10.1177/15266028231207023
Qinshu Wen, Guangyan Wu, Ye Ji, Guangmin Yang, Yepeng Zhang, Wendong Li, Xiaolong Du, Xiaoqiang Li, Min Zhou
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引用次数: 0

摘要

目的:本研究旨在评估医生改良的腔内移植物(PMEG)治疗涉及主动脉弓的胸主动脉病变的效果。方法:对2018年2月至2022年5月期间连续接受PMEG治疗的胸主动脉病变患者进行回顾性单中心研究。收集有关基线特征、手术程序和随访信息的数据。终点包括技术成功率、并发症、死亡率、总生存率、再干预和靶血管不稳定。结果:本研究包括173名患有胸主动脉病变的患者(平均年龄=58±13,范围=28-83148男性),包括44个胸主动脉瘤、113个主动脉夹层(9个A型,4个残余A型,75个B型,32个非A非B型)、3个主动脉壁内血肿和13个穿透性主动脉溃疡。35例患者有3个开窗的PMEG,32例有2个开窗,106例有1个开窗。技术成功率为98%(170/173),30天死亡率为2%(3/173)。围手术期并发症包括中风(n=3.2%)、逆行性A型夹层(RTAD)和肾损伤(n=3,2%)。在中位随访11个月(范围=1-52)期间,发现7例死亡(4%)。11例再次介入治疗与支架相关。来自无名动脉(Ia)的Ia型内漏5例(3%),III型内漏2例(1%),来自左锁骨下动脉的Ic型内泄漏3例(2%)。一例IA支架移植物(SG)狭窄是由于附壁血栓引起的。2年时的总生存率、无二次干预和无靶血管不稳定的估计率分别为93.4%(95%置信区间[CI]=88.7%-98.1%)、80.7%(95%CI=77.3%-88.1%)和89.0%(95%CI=80.4%-97.6%)。结论:医生改良的内移植物在治疗涉及主动脉弓的胸主动脉病变方面显示出有希望的即时治疗效果。我们的研究表明,该技术是可行的,并产生了可接受的结果。需要长期的结果来进一步完善这种技术方法,以确认随着时间的推移,技术的成功性和耐用性是专业中心血管内主动脉弓修复的一个有价值的选择。临床影响:与其他分支/开窗技术相比,我们对173名患者进行的医生改良的内移植物的短期和中期结果显示出有希望的结果,并支持主动脉弓的血管内修复。同时,我们在稿件中指出的技术专长,包括预载导丝、减径丝和内部迷你袖口,为同行提供了参考和技术指导。最重要的是,它证明了PMEG作为一种组件都可以商业化的设备,可能是紧急手术和无法获得定制设备的中心的更好选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Physician-Modified Endografts for the Treatment of Thoracic Aortic Pathologies Involving the Aortic Arch.

Objective: This study aimed to evaluate the outcomes of physician-modified endografts (PMEGs) for the treatment of thoracic aortic pathologies involving the aortic arch.

Methods: A retrospective single-center study was performed on consecutive patients with thoracic aortic pathologies treated by PMEGs between February 2018 and May 2022. Data on baseline characteristics, operative procedure, and follow-up information were collected. The endpoints included technical success, complications, mortality, overall survival, re-intervention, and target vessel instability.

Results: This study comprised 173 patients (mean age=58±13, range=28-83, 148 men) with thoracic aortic pathologies, including 44 thoracic aortic aneurysms, 113 aortic dissections (9 type A, 4 residual type A, 75 type B, 32 non-A non-B), 3 aortic intramural hematomas, and 13 penetrating aortic ulcers. Thirty-five of the patients had PMEGs with 3 fenestrations, 32 had 2 fenestrations, and 106 had 1 single fenestration. Technical success was 98% (170/173), and the 30-day mortality was 2% (3/173). Perioperative complications included stroke (n=3, 2%), retrograde type A dissection (RTAD; n=3, 2%) and renal injury (n=3, 2%). Seven deaths (4%) were noted during a median follow-up of 11 (range=1-52) months. Eleven cases of re-intervention were stent-related. There were 5 type Ia endoleaks (3%), 2 type III endoleaks (1%) from the innominate artery (IA), and 3 type Ic endoleaks (2%) from the left subclavian arteries. One case of IA stent-graft (SG) stenosis was noted because of mural thrombus. Estimate rates of overall survival, freedom from secondary intervention, and freedom from target vessel instability at 2 years were 93.4% (95% confidence interval [CI]=88.7%-98.1%), 80.7% (95% CI=73.3%-88.1%), and 89.0% (95% CI=80.4%-97.6%), respectively.

Conclusions: Physician-modified endografts showed promising immediate therapeutic results in the treatment of thoracic aortic pathologies involving the aortic arch. Our study demonstrates that the technique is feasible and produces acceptable results. Long-term outcomes are required for further refinement of this technical approach to confirm technical success and durability over time as a valuable option for endovascular aortic arch repair in specialized centers.Clinical impactOur short- and mid-term outcomes of physician-modified endografts in 173 patients showed promising results compared to other branched/fenestrated techniques and backed up the endovascular repair of the aortic arch. Meanwhile, the technical expertise pointed out in our manuscript, including preloaded guidewire, diameter-reducing wire and inner mini-cuffs, provided reference and technical guidance for our peers. Most importantly, it demonstrated that the PMEG, as a device whose components were all commercially available, might be a better option for emergency surgery and for centers who had no access to custom-made devices.

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来源期刊
CiteScore
5.30
自引率
15.40%
发文量
203
审稿时长
6-12 weeks
期刊介绍: The Journal of Endovascular Therapy (formerly the Journal of Endovascular Surgery) was established in 1994 as a forum for all physicians, scientists, and allied healthcare professionals who are engaged or interested in peripheral endovascular techniques and technology. An official publication of the International Society of Endovascular Specialists (ISEVS), the Journal of Endovascular Therapy publishes peer-reviewed articles of interest to clinicians and researchers in the field of peripheral endovascular interventions.
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