Pub Date : 2026-01-08DOI: 10.1177/15266028251413517
Stephanie Rodriguez, Mathew Wooster
Purpose: This article describes the modification of an iliac limb to incorporate a lumbar artery branch to decrease risk of spinal cord ischemia (SCI) in a patient with a symptomatic extent III thoracoabdominal aortic aneurysm (TAAA).
Case report: A 59-year-old female with a history of zone 3 to 5 thoracic endovascular aortic repair 6 weeks prior for chronic type B3-10 dissection with 6.5 cm aneurysmal degeneration presented with sudden onset chest and abdominal pain. Imaging revealed rapid growth to 9.8 cm with a new stent graft-induced entry tear and associated fat stranding. Not medically fit for open repair, the patient was taken for an emergent fenestrated/branched endovascular aortic repair (F/BEVAR). A 32×24×150 TX2 Zenith thoracic tube graft was modified with 4 fenestrations. A 13×11×56 Z SLE Cook iliac limb was modified to create a custom iliac fenestrated endoprosthesis, as this patient's right iliac anatomy was not suitable for off-the-shelf products. After deployment of the custom iliac fenestrated device and fenestrated thoracic device, an aortogram revealed a large L5 lumbar artery we felt was amenable to fenestration to help preserve spinal perfusion. A 13×16×39 Z SLE Cook iliac limb was modified with a branch for an L5 lumbar artery. Post-operative course was uneventful without ischemic-related complications. One-month follow-up imaging reveals stable sac size with type II endoleak and patent hypogastric and lumbar artery stents.
Conclusion: Preservation of collateral pathways is understood to be critical in prevention of SCI, although the precise branches necessary are not clear. Lumbar fenestration and hypogastric preservation to reduce risk of SCI is a feasible and valid technique that should be considered when anatomy allows.Clinical ImpactThis case validates the efficacy and safety of using a physician-modified iliac limb to salvage an L5 lumbar artery after endovascular exclusion of a symptomatic extent III thoracoabdominal aortic aneurysm (TAAA). This interventional approach allows for the maintenance of perfusion to the spine and preservation of potentially hemodynamically significant collateral pathways. Our results suggest that this technique to mitigate the risk of spinal cord ischemia is safe and effective and thus may be considered for appropriately-selected cases.
目的:这篇文章描述了在症状程度为III型胸腹主动脉瘤(TAAA)的患者中,髂肢体的修改以纳入腰动脉分支以降低脊髓缺血(SCI)的风险。病例报告:一名59岁女性,6周前因慢性B3-10型夹层行3- 5区胸腔血管内主动脉修复术,并发6.5 cm动脉瘤变性,并发突发性胸腹疼痛。成像显示快速生长至9.8厘米,伴有新支架诱导的进入性撕裂和相关的脂肪搁浅。医学上不适合开放修复,患者被送往紧急开窗/分支血管内主动脉修复(F/BEVAR)。将32×24×150 TX2胸顶管移植物改良为4个开窗。由于该患者的右髂解剖结构不适合现成的产品,因此对13×11×56 Z SLE Cook髂肢体进行了修改,以创建定制的髂开窗内假体。在使用定制的髂骨开窗装置和胸骨开窗装置后,主动脉造影显示一条大的L5腰动脉,我们认为可以开窗以帮助保持脊柱灌注。用L5腰动脉分支改造13×16×39 Z SLE Cook髂肢体。术后过程顺利,无缺血性并发症。一个月的随访影像显示囊腔大小稳定,伴有II型内漏和未闭的胃下动脉和腰动脉支架。结论:侧支通路的保护被认为是预防脊髓损伤的关键,尽管所需的确切分支尚不清楚。腰椎开窗和胃下保存降低脊髓损伤的风险是一种可行和有效的技术,在解剖允许的情况下应予以考虑。临床影响:本病例验证了在血管内排除症状程度为III的胸腹主动脉瘤(TAAA)后,使用医师改良的髂肢体挽救L5腰动脉的有效性和安全性。这种介入方法可以维持脊柱的灌注,并保留潜在的血流动力学意义重大的侧支通路。我们的结果表明,这种技术减轻脊髓缺血的风险是安全有效的,因此可以考虑适当选择的病例。
{"title":"Lumbar Artery Branch in Treatment of Thoracoabdominal Aortic Aneurysm to Prevent Spinal Cord Ischemia.","authors":"Stephanie Rodriguez, Mathew Wooster","doi":"10.1177/15266028251413517","DOIUrl":"https://doi.org/10.1177/15266028251413517","url":null,"abstract":"<p><strong>Purpose: </strong>This article describes the modification of an iliac limb to incorporate a lumbar artery branch to decrease risk of spinal cord ischemia (SCI) in a patient with a symptomatic extent III thoracoabdominal aortic aneurysm (TAAA).</p><p><strong>Case report: </strong>A 59-year-old female with a history of zone 3 to 5 thoracic endovascular aortic repair 6 weeks prior for chronic type B<sub>3-10</sub> dissection with 6.5 cm aneurysmal degeneration presented with sudden onset chest and abdominal pain. Imaging revealed rapid growth to 9.8 cm with a new stent graft-induced entry tear and associated fat stranding. Not medically fit for open repair, the patient was taken for an emergent fenestrated/branched endovascular aortic repair (F/BEVAR). A 32×24×150 TX2 Zenith thoracic tube graft was modified with 4 fenestrations. A 13×11×56 Z SLE Cook iliac limb was modified to create a custom iliac fenestrated endoprosthesis, as this patient's right iliac anatomy was not suitable for off-the-shelf products. After deployment of the custom iliac fenestrated device and fenestrated thoracic device, an aortogram revealed a large L5 lumbar artery we felt was amenable to fenestration to help preserve spinal perfusion. A 13×16×39 Z SLE Cook iliac limb was modified with a branch for an L5 lumbar artery. Post-operative course was uneventful without ischemic-related complications. One-month follow-up imaging reveals stable sac size with type II endoleak and patent hypogastric and lumbar artery stents.</p><p><strong>Conclusion: </strong>Preservation of collateral pathways is understood to be critical in prevention of SCI, although the precise branches necessary are not clear. Lumbar fenestration and hypogastric preservation to reduce risk of SCI is a feasible and valid technique that should be considered when anatomy allows.Clinical ImpactThis case validates the efficacy and safety of using a physician-modified iliac limb to salvage an L5 lumbar artery after endovascular exclusion of a symptomatic extent III thoracoabdominal aortic aneurysm (TAAA). This interventional approach allows for the maintenance of perfusion to the spine and preservation of potentially hemodynamically significant collateral pathways. Our results suggest that this technique to mitigate the risk of spinal cord ischemia is safe and effective and thus may be considered for appropriately-selected cases.</p>","PeriodicalId":50210,"journal":{"name":"Journal of Endovascular Therapy","volume":" ","pages":"15266028251413517"},"PeriodicalIF":1.5,"publicationDate":"2026-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145935930","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-07DOI: 10.1177/15266028251408988
Edoardo Pasqui, Giuseppe Galzerano, Elisa Lazzeri, Manfredi Giuseppe Anzaldi, Bruno Gargiulo, Leonardo Pasquetti, Michele Giubbolini, Gianmarco de Donato
<p><strong>Purpose: </strong>The purpose of the study is to evaluate the early and long-term technical and clinical outcomes of endovascular treatment for central venous stenosis (CVS) and occlusion (CVO) in hemodialysis patients, and to describe procedural strategies aiming at optimizing vascular access preservation.</p><p><strong>Materials and methods: </strong>A retrospective single-center analysis was performed including all patients with an upper-limb arteriovenous access undergoing endovascular revascularization for symptomatic CVS/CVO between January 2020 and December 2024. Indications comprised severe venous congestion, prolonged bleeding after dialysis, poor access maturation, and inadequate dialysis efficiency. Diagnosis was established by duplex ultrasound and computed tomography angiography; digital subtraction angiography was used when noninvasive imaging was inconclusive. Procedural details, device use, and perioperative outcomes were recorded. Primary outcome was primary patency; secondary outcomes included technical success, procedural safety, cumulative (secondary) patency, and freedom from reintervention.</p><p><strong>Results: </strong>Forty-four patients (mean age 65.8±16.2 years; 59.1% male) were treated, 50% for complete occlusions. The most frequent lesion site was the brachiocephalic vein (70.4%). High-pressure balloon angioplasty was performed in 93.2% of cases, and stents were implanted in 45.5% (mostly self-expanding nitinol). Technical success was achieved in 93.2% with no perioperative complications. Over a median follow-up of 36.7±32.2 months, 20 patients (45.5%) underwent reintervention for restenosis (34.1%) or reocclusion (11.4%); 30% of reinterventions revealed stent fractures. Kaplan-Meier analysis showed primary patency rates of 85.5% at 6 months, 69.9% at 12 months, and 58.7% at 18 months. Cumulative patency was 88.4% at 6 months, 80.9% at 12 and 24 months, 74.8% at 36 months, and 69.1% at 60 months. Prior ipsilateral central venous catheter placement was associated with reduced freedom from reintervention.</p><p><strong>Conclusions: </strong>Endovascular revascularization of CVS/CVO in hemodialysis patients is safe and offers high technical success. While primary patency declines over time, cumulative patency remains favorable, underscoring the role of timely reinterventions and structured surveillance in prolonging access life.Clinical ImpactThis study reinforces endovascular revascularization as a safe and effective first-line strategy for managing central venous stenosis and occlusion in hemodialysis patients, allowing immediate reuse of the vascular access and avoiding dialysis interruption. The data highlight that long-term success depends less on a single "perfect" procedure and more on structured surveillance and timely reintervention. Prior ipsilateral central venous catheter placement emerges as a key predictor of failure, underscoring the need to minimize catheter use and promote early AVF creation.
{"title":"Central Venous Stenosis and Occlusion in Dialysis Patients: A Technical and Outcome-Based Analysis of Endovascular Intervention.","authors":"Edoardo Pasqui, Giuseppe Galzerano, Elisa Lazzeri, Manfredi Giuseppe Anzaldi, Bruno Gargiulo, Leonardo Pasquetti, Michele Giubbolini, Gianmarco de Donato","doi":"10.1177/15266028251408988","DOIUrl":"https://doi.org/10.1177/15266028251408988","url":null,"abstract":"<p><strong>Purpose: </strong>The purpose of the study is to evaluate the early and long-term technical and clinical outcomes of endovascular treatment for central venous stenosis (CVS) and occlusion (CVO) in hemodialysis patients, and to describe procedural strategies aiming at optimizing vascular access preservation.</p><p><strong>Materials and methods: </strong>A retrospective single-center analysis was performed including all patients with an upper-limb arteriovenous access undergoing endovascular revascularization for symptomatic CVS/CVO between January 2020 and December 2024. Indications comprised severe venous congestion, prolonged bleeding after dialysis, poor access maturation, and inadequate dialysis efficiency. Diagnosis was established by duplex ultrasound and computed tomography angiography; digital subtraction angiography was used when noninvasive imaging was inconclusive. Procedural details, device use, and perioperative outcomes were recorded. Primary outcome was primary patency; secondary outcomes included technical success, procedural safety, cumulative (secondary) patency, and freedom from reintervention.</p><p><strong>Results: </strong>Forty-four patients (mean age 65.8±16.2 years; 59.1% male) were treated, 50% for complete occlusions. The most frequent lesion site was the brachiocephalic vein (70.4%). High-pressure balloon angioplasty was performed in 93.2% of cases, and stents were implanted in 45.5% (mostly self-expanding nitinol). Technical success was achieved in 93.2% with no perioperative complications. Over a median follow-up of 36.7±32.2 months, 20 patients (45.5%) underwent reintervention for restenosis (34.1%) or reocclusion (11.4%); 30% of reinterventions revealed stent fractures. Kaplan-Meier analysis showed primary patency rates of 85.5% at 6 months, 69.9% at 12 months, and 58.7% at 18 months. Cumulative patency was 88.4% at 6 months, 80.9% at 12 and 24 months, 74.8% at 36 months, and 69.1% at 60 months. Prior ipsilateral central venous catheter placement was associated with reduced freedom from reintervention.</p><p><strong>Conclusions: </strong>Endovascular revascularization of CVS/CVO in hemodialysis patients is safe and offers high technical success. While primary patency declines over time, cumulative patency remains favorable, underscoring the role of timely reinterventions and structured surveillance in prolonging access life.Clinical ImpactThis study reinforces endovascular revascularization as a safe and effective first-line strategy for managing central venous stenosis and occlusion in hemodialysis patients, allowing immediate reuse of the vascular access and avoiding dialysis interruption. The data highlight that long-term success depends less on a single \"perfect\" procedure and more on structured surveillance and timely reintervention. Prior ipsilateral central venous catheter placement emerges as a key predictor of failure, underscoring the need to minimize catheter use and promote early AVF creation.","PeriodicalId":50210,"journal":{"name":"Journal of Endovascular Therapy","volume":" ","pages":"15266028251408988"},"PeriodicalIF":1.5,"publicationDate":"2026-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145913763","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-07DOI: 10.1177/15266028251408018
George Apostolidis, Konstantinos Dakis, José I Torrealba, Giuseppe Panuccio, Konstantinos Spanos, Tilo Kölbel, Petroula Nana
<p><strong>Purpose: </strong>Iliac branch devices (IBDs) are indicated for the preservation of internal iliac artery (IIA) perfusion. Data on bridging stent choice in IBD are limited. The aim of this meta-analysis was to assess Advanta V12/iCast outcomes when used as bridging stent during IBD procedures.</p><p><strong>Methods: </strong>The English medical literature was systematically searched through PubMed, Scopus, and Cochrane Library (last search: 03.01.2025). The Preferred Reporting Items for Systematic Reviews and Meta-analyses statement was followed, and a predefined protocol was registered to PROSPERO. Randomized controlled trials and observational studies (2000--2025) reporting on the Advanta V12/iCast-related outcomes were eligible. The ROBINS-I tool and Grading of Recommendations Assessment, Development and Evaluations (GRADE) were used to assess the risk of bias and quality of evidence. Primary outcomes were technical success, stenosis/occlusion, endoleak Ic/IIIc, and reintervention rates during follow-up. Data on the outcomes of interest were synthesized using proportional meta-analysis.</p><p><strong>Results: </strong>From 2698 study reports, 10 observational studies (510 targeted IIAs, 467 IIAs bridged with Advanta V12/iCast) were included. According to ROBINS-I, eight studies were of low and two were of moderate quality. Technical success was 98% (95% confidence interval (CI) = 93%-100%; <i>I</i><sup>2</sup> = 0%; certainty: very low). Regarding the 30-day outcomes, the occlusion/stenosis rate was 2% (95% CI = 0%-9%; <i>I</i><sup>2</sup> = 0%), the endoleak Ic/IIIc rate was 0.3% (95% CI = 0%-3%; <i>I</i><sup>2</sup> = 0%) and the reintervention rate was 1% (95% CI = 0%-3%; <i>I</i><sup>2</sup> = 0%). The mean follow-up among studies was 23.4 months (95% CI = 14.2-32.7). During follow-up, the occlusion/stenosis rate was 4% (95% CI = 1%-11%; <i>I</i><sup>2</sup> = 19%; certainty: very low), the endoleak Ic/IIIc overall rate was 5% (95% CI = 3%-8%; <i>I</i><sup>2</sup> = 0%; certainty: very low), and the reintervention rate was 5% (95% CI = 3%-9%; <i>I</i><sup>2</sup> = 0%; certainty: very low).</p><p><strong>Conclusions: </strong>The Advanta V12/iCast balloon-expandable covered stent showed low occlusion/stenosis, endoleak, and reintervention rates at 30 days and follow-up and appeared to be a reliable bridging stent choice in IBDs.Clinical ImpactThe available literature on iliac branch devices does not provide adequate evidence supporting bridging stent selection. This systematic review and meta-analysis on the use of Advanta V12/iCast as bridging stent showed a high technical success rate of 98%, along with low occlusion/stenosis, endoleak Ic/IIIc and reintervention rates at 30 days, which were maintained below 5% during the total follow-up. These results reflect on the reliability of Advanta V12/iCast when used as bridging stent in iliac branch devices. However, the low quality of evidence should be considered upon result interpr
目的:髂分支装置(IBDs)适用于保留髂内动脉(IIA)灌注。关于IBD患者桥接支架选择的数据有限。本荟萃分析的目的是评估在IBD手术中作为桥接支架使用的Advanta V12/iCast的结果。方法:系统检索PubMed、Scopus和Cochrane Library的英文医学文献(最近检索时间:03.01.2025)。遵循系统评价和荟萃分析声明的首选报告项目,并向PROSPERO注册预定义的方案。报告Advanta V12/ icast相关结果的随机对照试验和观察性研究(2000- 2025)符合条件。使用ROBINS-I工具和分级推荐评估、发展和评价(GRADE)来评估偏倚风险和证据质量。主要结果是技术成功、狭窄/闭塞、内漏Ic/IIIc和随访期间的再干预率。相关结果的数据采用比例荟萃分析进行综合。结果:从2698项研究报告中,纳入了10项观察性研究(510项靶向IIAs, 467项与Advanta V12/iCast桥接的IIAs)。根据ROBINS-I, 8项研究为低质量,2项为中等质量。技术成功率为98%(95%置信区间(CI) = 93%-100%;I2 = 0%;确定性:非常低)。对于30天的结果,闭塞/狭窄率为2% (95% CI = 0%-9%; I2 = 0%),内漏Ic/IIIc率为0.3% (95% CI = 0%-3%; I2 = 0%),再干预率为1% (95% CI = 0%-3%; I2 = 0%)。研究的平均随访时间为23.4个月(95% CI = 14.2-32.7)。随访期间,闭塞/狭窄率为4% (95% CI = 1% ~ 11%; I2 = 19%;确定性极低),内漏Ic/IIIc总率为5% (95% CI = 3% ~ 8%; I2 = 0%;确定性极低),再干预率为5% (95% CI = 3% ~ 9%; I2 = 0%;确定性极低)。结论:Advanta V12/iCast球囊可膨胀覆膜支架在30天和随访中显示出低闭塞/狭窄、内漏和再干预率,似乎是ibd患者可靠的桥接支架选择。临床影响现有的关于髂分支装置的文献没有提供足够的证据支持桥式支架的选择。本系统综述和荟萃分析显示,使用Advanta V12/iCast作为桥接支架的技术成功率高达98%,并且在30天内闭塞/狭窄、内漏Ic/IIIc和再干预率较低,在总随访期间保持在5%以下。这些结果反映了Advanta V12/iCast作为髂分支装置桥接支架的可靠性。然而,在解释结果时应考虑到证据的低质量。
{"title":"Systematic Review and Metanalysis on the Advanta V12/iCast Outcomes as Bridging Stent in Iliac Branch Devices.","authors":"George Apostolidis, Konstantinos Dakis, José I Torrealba, Giuseppe Panuccio, Konstantinos Spanos, Tilo Kölbel, Petroula Nana","doi":"10.1177/15266028251408018","DOIUrl":"https://doi.org/10.1177/15266028251408018","url":null,"abstract":"<p><strong>Purpose: </strong>Iliac branch devices (IBDs) are indicated for the preservation of internal iliac artery (IIA) perfusion. Data on bridging stent choice in IBD are limited. The aim of this meta-analysis was to assess Advanta V12/iCast outcomes when used as bridging stent during IBD procedures.</p><p><strong>Methods: </strong>The English medical literature was systematically searched through PubMed, Scopus, and Cochrane Library (last search: 03.01.2025). The Preferred Reporting Items for Systematic Reviews and Meta-analyses statement was followed, and a predefined protocol was registered to PROSPERO. Randomized controlled trials and observational studies (2000--2025) reporting on the Advanta V12/iCast-related outcomes were eligible. The ROBINS-I tool and Grading of Recommendations Assessment, Development and Evaluations (GRADE) were used to assess the risk of bias and quality of evidence. Primary outcomes were technical success, stenosis/occlusion, endoleak Ic/IIIc, and reintervention rates during follow-up. Data on the outcomes of interest were synthesized using proportional meta-analysis.</p><p><strong>Results: </strong>From 2698 study reports, 10 observational studies (510 targeted IIAs, 467 IIAs bridged with Advanta V12/iCast) were included. According to ROBINS-I, eight studies were of low and two were of moderate quality. Technical success was 98% (95% confidence interval (CI) = 93%-100%; <i>I</i><sup>2</sup> = 0%; certainty: very low). Regarding the 30-day outcomes, the occlusion/stenosis rate was 2% (95% CI = 0%-9%; <i>I</i><sup>2</sup> = 0%), the endoleak Ic/IIIc rate was 0.3% (95% CI = 0%-3%; <i>I</i><sup>2</sup> = 0%) and the reintervention rate was 1% (95% CI = 0%-3%; <i>I</i><sup>2</sup> = 0%). The mean follow-up among studies was 23.4 months (95% CI = 14.2-32.7). During follow-up, the occlusion/stenosis rate was 4% (95% CI = 1%-11%; <i>I</i><sup>2</sup> = 19%; certainty: very low), the endoleak Ic/IIIc overall rate was 5% (95% CI = 3%-8%; <i>I</i><sup>2</sup> = 0%; certainty: very low), and the reintervention rate was 5% (95% CI = 3%-9%; <i>I</i><sup>2</sup> = 0%; certainty: very low).</p><p><strong>Conclusions: </strong>The Advanta V12/iCast balloon-expandable covered stent showed low occlusion/stenosis, endoleak, and reintervention rates at 30 days and follow-up and appeared to be a reliable bridging stent choice in IBDs.Clinical ImpactThe available literature on iliac branch devices does not provide adequate evidence supporting bridging stent selection. This systematic review and meta-analysis on the use of Advanta V12/iCast as bridging stent showed a high technical success rate of 98%, along with low occlusion/stenosis, endoleak Ic/IIIc and reintervention rates at 30 days, which were maintained below 5% during the total follow-up. These results reflect on the reliability of Advanta V12/iCast when used as bridging stent in iliac branch devices. However, the low quality of evidence should be considered upon result interpr","PeriodicalId":50210,"journal":{"name":"Journal of Endovascular Therapy","volume":" ","pages":"15266028251408018"},"PeriodicalIF":1.5,"publicationDate":"2026-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145913686","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-03DOI: 10.1177/15266028251408977
Hao Liu, Lingwei Zou, Xiaolang Jiang, Bin Chen, Zhihui Dong, Weiguo Fu
Objectives: Isolated internal iliac artery aneurysm (IIIAA) is a rare condition, accounting for approximately 0.3% to 0.5% of all intra-abdominal aneurysms. This study aimed to evaluate the outcomes of endovascular treatment for IIIAA using a relatively large cohort.
Methods: A retrospective analysis was conducted on 45 patients diagnosed with IIIAA who were admitted to our hospital between April 2014 and April 2024. Patient demographics, intervention outcomes, and follow-up results were collected and analyzed.
Results: A total of 45 patients (only 2 female) with 49 IIIAAs were included, with a mean age of 70.4±9.2 years. The cohort exhibited a high prevalence of cardiovascular and cerebrovascular risk factors, and 31.1% had a history of malignancy. Thirty patients (66.7%) were diagnosed with an incidental IIIAA, while the remaining patients presented with symptoms such as abdominal or lumbar pain, dysuria, or aneurysm rupture. Stent-graft placement alone was performed in 3 patients, coil embolization alone in 5 patients, and the remaining 37 patients underwent a combined approach. The rate of complete distal branch embolization was 69.0% (29/42), and technical success was achieved in 44 patients. The mean follow-up duration was 23.8±21.5 months. During follow-up, 5 patients died from cancer or heart failure. Buttock claudication was observed in 7 patients, with only 1 case remaining unresolved after conservative treatment. Sac dilation was noted in 4 patients who had incomplete distal branch embolization; of these, 3 required re-intervention. The 12-month and 24-month re-intervention-free survival rates were 95.5% and 88.2%, respectively.
Conclusion: Endovascular treatment, particularly the combination of stent-graft implantation and coil embolization, is both safe and effective for IIIAA, with a mid-term re-intervention-free survival rate of 85.25% and an acceptable risk of pelvic ischemia. Complete embolization of the outflow branches is technically challenging in some cases, and the efficacy of sac embolization as an alternative remains debatable.Clinical ImpactIsolated internal iliac artery aneurysm (IIIAA) is an exceedingly rare condition. This retrospective study identified and included 45 patients with IIIAA who were treated at our institution to evaluate the safety and therapeutic efficacy of endovascular treatment. The majority of patients underwent stent-graft implantation to seal the internal iliac artery ostium, along with coil embolization of the distal branches. The 2-year reintervention-free survival rate for all patients was 85.25%, demonstrating the favorable efficacy of endovascular treatment. However, postoperative sac dilation was observed in 4 patients who did not receive complete distal branch embolization, emphasizing the need for rigorous follow-up in this subset of patients.
{"title":"Endovascular Treatment for Patients With Isolated Internal Iliac Artery Aneurysm: A Single-Center Retrospective Study Over a 10-Year Period.","authors":"Hao Liu, Lingwei Zou, Xiaolang Jiang, Bin Chen, Zhihui Dong, Weiguo Fu","doi":"10.1177/15266028251408977","DOIUrl":"https://doi.org/10.1177/15266028251408977","url":null,"abstract":"<p><strong>Objectives: </strong>Isolated internal iliac artery aneurysm (IIIAA) is a rare condition, accounting for approximately 0.3% to 0.5% of all intra-abdominal aneurysms. This study aimed to evaluate the outcomes of endovascular treatment for IIIAA using a relatively large cohort.</p><p><strong>Methods: </strong>A retrospective analysis was conducted on 45 patients diagnosed with IIIAA who were admitted to our hospital between April 2014 and April 2024. Patient demographics, intervention outcomes, and follow-up results were collected and analyzed.</p><p><strong>Results: </strong>A total of 45 patients (only 2 female) with 49 IIIAAs were included, with a mean age of 70.4±9.2 years. The cohort exhibited a high prevalence of cardiovascular and cerebrovascular risk factors, and 31.1% had a history of malignancy. Thirty patients (66.7%) were diagnosed with an incidental IIIAA, while the remaining patients presented with symptoms such as abdominal or lumbar pain, dysuria, or aneurysm rupture. Stent-graft placement alone was performed in 3 patients, coil embolization alone in 5 patients, and the remaining 37 patients underwent a combined approach. The rate of complete distal branch embolization was 69.0% (29/42), and technical success was achieved in 44 patients. The mean follow-up duration was 23.8±21.5 months. During follow-up, 5 patients died from cancer or heart failure. Buttock claudication was observed in 7 patients, with only 1 case remaining unresolved after conservative treatment. Sac dilation was noted in 4 patients who had incomplete distal branch embolization; of these, 3 required re-intervention. The 12-month and 24-month re-intervention-free survival rates were 95.5% and 88.2%, respectively.</p><p><strong>Conclusion: </strong>Endovascular treatment, particularly the combination of stent-graft implantation and coil embolization, is both safe and effective for IIIAA, with a mid-term re-intervention-free survival rate of 85.25% and an acceptable risk of pelvic ischemia. Complete embolization of the outflow branches is technically challenging in some cases, and the efficacy of sac embolization as an alternative remains debatable.Clinical ImpactIsolated internal iliac artery aneurysm (IIIAA) is an exceedingly rare condition. This retrospective study identified and included 45 patients with IIIAA who were treated at our institution to evaluate the safety and therapeutic efficacy of endovascular treatment. The majority of patients underwent stent-graft implantation to seal the internal iliac artery ostium, along with coil embolization of the distal branches. The 2-year reintervention-free survival rate for all patients was 85.25%, demonstrating the favorable efficacy of endovascular treatment. However, postoperative sac dilation was observed in 4 patients who did not receive complete distal branch embolization, emphasizing the need for rigorous follow-up in this subset of patients.</p>","PeriodicalId":50210,"journal":{"name":"Journal of Endovascular Therapy","volume":" ","pages":"15266028251408977"},"PeriodicalIF":1.5,"publicationDate":"2026-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145893481","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-03DOI: 10.1177/15266028251410777
Christoph Bacri, Kheira Hireche, Pierre Alric, Ludovic Canaud
Objective: To assess the impact of selective supra-aortic trunk (SAT) stenting on aortic remodeling in patients with chronic type A aortic dissection (cTAAD).
Methods: Patients treated from 2017 to 2024 with aortic arch repair using double-fenestrated physician-modified endografts (PMEGs) for cTAAD were retrospectively analyzed. The objectives are to compare aortic treatment and remodeling, SAT evolution, and overall outcomes according to SAT dissection status (before and after), total aortic arch repair using a double-fenestrated PMEG.
Results: Among 42 cTAAD patients treated, 30 had SAT dissection. Thirty-five patients received a standard PMEG, while 7 underwent additional selective SAT stenting (3 LCCA, 1 brachiocephalic trunk (BT), 4 right subclavian artery (RSA), and 3 right common carotid artery (RCCA)). Technical success was 100%. At 30 days, 1 patient died from stroke, 1 from pneumonia post-discharge. During a median follow-up of 18.5 months (IQR: 38.8), no type Ia endoleaks occurred. Six type Ic endoleaks were observed; 3 patients underwent reintervention, while the remaining 3 were monitored with follow-up CT scans showing no evidence of aortic growth. Complete SAT dissection resolution occurred in 12 patients (40%), including 9 with standard PMEG. Positive aortic remodeling was seen in 32 patients (76%) with a median diameter reduction of -1% (IQR: 5.5%). Five patients died during mid-term follow-up, with no deaths related to the procedure. Positive aortic remodeling rates are 73% vs. 83% (p=0.7) between patients with and without initial SAT dissection, 83% vs 92% (p=1) between patients with initially no SAT dissection and those who healed, 61% vs 88% (p=0.07) between patients with persistent SAT dissection and the others. Patients on curative anticoagulation or dual antiplatelet therapy showed reduced positive remodeling.
Conclusion: Double-fenestrated PMEGs are effective for treating residual cTAADs, with high SAT healing and favorable remodeling. Persistent SAT dissection may hinder remodeling and require additional intervention.Clinical ImpactAortic arch repair using fenestrated physician-modified endografts without systematic SAT stenting reduces SAT manipulation and may lower stroke risk, while promoting a high rate of SAT and aortic dissection healing. In cases where SAT dissection persists and aortic growth is reported, secondary complementary SAT intervention can be performed to enhance aortic remodeling.
{"title":"Selective Supra-Aortic Trunk Stenting During Endovascular Total Aortic Arch Repair in Patients With Residual Chronic Type A Dissection Treated With Double-Fenestrated Physician-Modified Endografts.","authors":"Christoph Bacri, Kheira Hireche, Pierre Alric, Ludovic Canaud","doi":"10.1177/15266028251410777","DOIUrl":"https://doi.org/10.1177/15266028251410777","url":null,"abstract":"<p><strong>Objective: </strong>To assess the impact of selective supra-aortic trunk (SAT) stenting on aortic remodeling in patients with chronic type A aortic dissection (cTAAD).</p><p><strong>Methods: </strong>Patients treated from 2017 to 2024 with aortic arch repair using double-fenestrated physician-modified endografts (PMEGs) for cTAAD were retrospectively analyzed. The objectives are to compare aortic treatment and remodeling, SAT evolution, and overall outcomes according to SAT dissection status (before and after), total aortic arch repair using a double-fenestrated PMEG.</p><p><strong>Results: </strong>Among 42 cTAAD patients treated, 30 had SAT dissection. Thirty-five patients received a standard PMEG, while 7 underwent additional selective SAT stenting (3 LCCA, 1 brachiocephalic trunk (BT), 4 right subclavian artery (RSA), and 3 right common carotid artery (RCCA)). Technical success was 100%. At 30 days, 1 patient died from stroke, 1 from pneumonia post-discharge. During a median follow-up of 18.5 months (IQR: 38.8), no type Ia endoleaks occurred. Six type Ic endoleaks were observed; 3 patients underwent reintervention, while the remaining 3 were monitored with follow-up CT scans showing no evidence of aortic growth. Complete SAT dissection resolution occurred in 12 patients (40%), including 9 with standard PMEG. Positive aortic remodeling was seen in 32 patients (76%) with a median diameter reduction of -1% (IQR: 5.5%). Five patients died during mid-term follow-up, with no deaths related to the procedure. Positive aortic remodeling rates are 73% vs. 83% (p=0.7) between patients with and without initial SAT dissection, 83% vs 92% (p=1) between patients with initially no SAT dissection and those who healed, 61% vs 88% (p=0.07) between patients with persistent SAT dissection and the others. Patients on curative anticoagulation or dual antiplatelet therapy showed reduced positive remodeling.</p><p><strong>Conclusion: </strong>Double-fenestrated PMEGs are effective for treating residual cTAADs, with high SAT healing and favorable remodeling. Persistent SAT dissection may hinder remodeling and require additional intervention.Clinical ImpactAortic arch repair using fenestrated physician-modified endografts without systematic SAT stenting reduces SAT manipulation and may lower stroke risk, while promoting a high rate of SAT and aortic dissection healing. In cases where SAT dissection persists and aortic growth is reported, secondary complementary SAT intervention can be performed to enhance aortic remodeling.</p>","PeriodicalId":50210,"journal":{"name":"Journal of Endovascular Therapy","volume":" ","pages":"15266028251410777"},"PeriodicalIF":1.5,"publicationDate":"2026-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145893459","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Aim: To present a case in which low-dose 4-dimensional computed tomographic angiography (4D-CTA) enabled precise classification of a type II endoleak following hybrid arch repair for chronic type B aortic dissection, in the setting of inconclusive findings on conventional CTA.
Case: A 74-year-old woman underwent hybrid arch repair with left common carotid-subclavian bypass and thoracic endovascular aortic repair for chronic type B aortic dissection. Six years postoperatively, aneurysm sac enlargement was noted. Conventional CTA with a 2-phase protocol (early arterial and delayed venous phases) could not distinguish between type Ia and type II endoleaks. Low-dose 4D-CTA (dose-length product: 302.6 mGy·cm) revealed delayed contrast enhancement within the sac during the late arterial phase, consistent with a type II endoleak originating from the left subclavian artery (LSCA). Targeted coil embolization was successfully performed to resolve the endoleak, and contrast inflow from a branch of the LSCA was confirmed by intraprocedural angiography.
Conclusion: Low-dose 4D-CTA allowed for precise classification of the endoleak and guided appropriate reintervention. This modality represents a useful and practical tool for endoleak evaluation, especially when standard imaging is inconclusive.Clinical ImpactThis case highlights the diagnostic value of 4-dimensional computed tomographic angiography (4D-CTA) in classifying endoleaks after thoracic endovascular aortic repair (TEVAR), particularly when standard CTA is inconclusive. The 4D-CTA identified a type II endoleak from the left subclavian artery, enabling definitive diagnosis and targeted coil embolization. Notably, the scan was performed using a low-dose protocol (dose-length product: 302.6 mGy·cm), substantially lower than the >1000 mGy·cm reported in prior studies while preserving diagnostic quality. Standardized low-dose 4D-CTA protocols may support broader clinical adoption for endoleak evaluation.
{"title":"Low-Dose 4-Dimensional Computed Tomographic Angiography for Diagnosing Indeterminate Endoleak After Hybrid Arch Repair: A Case Report.","authors":"Kenta Masada, Reiko Katsuya, Katsukiyo Kitabayashi, Hajime Ichikawa","doi":"10.1177/15266028251409060","DOIUrl":"https://doi.org/10.1177/15266028251409060","url":null,"abstract":"<p><strong>Aim: </strong>To present a case in which low-dose 4-dimensional computed tomographic angiography (4D-CTA) enabled precise classification of a type II endoleak following hybrid arch repair for chronic type B aortic dissection, in the setting of inconclusive findings on conventional CTA.</p><p><strong>Case: </strong>A 74-year-old woman underwent hybrid arch repair with left common carotid-subclavian bypass and thoracic endovascular aortic repair for chronic type B aortic dissection. Six years postoperatively, aneurysm sac enlargement was noted. Conventional CTA with a 2-phase protocol (early arterial and delayed venous phases) could not distinguish between type Ia and type II endoleaks. Low-dose 4D-CTA (dose-length product: 302.6 mGy·cm) revealed delayed contrast enhancement within the sac during the late arterial phase, consistent with a type II endoleak originating from the left subclavian artery (LSCA). Targeted coil embolization was successfully performed to resolve the endoleak, and contrast inflow from a branch of the LSCA was confirmed by intraprocedural angiography.</p><p><strong>Conclusion: </strong>Low-dose 4D-CTA allowed for precise classification of the endoleak and guided appropriate reintervention. This modality represents a useful and practical tool for endoleak evaluation, especially when standard imaging is inconclusive.Clinical ImpactThis case highlights the diagnostic value of 4-dimensional computed tomographic angiography (4D-CTA) in classifying endoleaks after thoracic endovascular aortic repair (TEVAR), particularly when standard CTA is inconclusive. The 4D-CTA identified a type II endoleak from the left subclavian artery, enabling definitive diagnosis and targeted coil embolization. Notably, the scan was performed using a low-dose protocol (dose-length product: 302.6 mGy·cm), substantially lower than the >1000 mGy·cm reported in prior studies while preserving diagnostic quality. Standardized low-dose 4D-CTA protocols may support broader clinical adoption for endoleak evaluation.</p>","PeriodicalId":50210,"journal":{"name":"Journal of Endovascular Therapy","volume":" ","pages":"15266028251409060"},"PeriodicalIF":1.5,"publicationDate":"2026-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145893437","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-31DOI: 10.1177/15266028251400566
Zuanbiao Yu, Songjie Hu, Dehai Lang, Di Wang, Chunbo Xu, Xiaoliang Yin, Yafang Shao, Tiequan Yang
Introduction: Although transcarotid arterial revascularization (TCAR) may offer several advantages, the first commercial TCAR system (EnRoute; Boston Scientific, Marlborough, Massachusetts) is not available in many countries. Therefore, a suitable and simple technique for transcarotid treatment of high-risk carotid stenosis is needed.
Case report: We report a hybrid approach to carotid stenosis treatment: stenting with surgical exposure of the carotid artery, forming a flow reversal circuit, with a feasibility to add a distal filter. Sheaths are placed in the carotid artery and femoral vein to accomplish cerebral protection, forming a flow reversal circuit. In addition, a distal filter device was placed for cerebral protection. Technical success was achieved and the patient experienced no complications.
Conclusion: Our modified TCAR technique may be effective in patients with high-risk carotid stenosis.Clinical ImpactThis research work is aimed at high-risk patients with carotid artery stenosis who need surgical treatment. When there are no commercialized devices similar to Tcar but surgical treatment is urgently needed, This modified surgical approach can be adopted to reduce the incidence of ischemic stroke caused by intraoperative embolus detachment. The innovative significance of this research lies in using local materials and simple, practical instruments to reduce the risk of stroke caused by embolus detachment during surgery.
虽然经颈动脉血管重建术(TCAR)可能有几个优点,但第一个商业化的TCAR系统(EnRoute; Boston Scientific, Marlborough, Massachusetts)在许多国家都不可用。因此,需要一种合适而简单的经颈动脉治疗高危颈动脉狭窄的技术。病例报告:我们报告了颈动脉狭窄治疗的混合方法:手术暴露颈动脉支架置入,形成血流逆转回路,并可添加远端过滤器。将鞘置于颈动脉和股静脉内,起到脑保护作用,形成血流逆转回路。此外,还放置了远端过滤装置以保护大脑。技术上取得了成功,患者没有出现并发症。结论:我们改良的TCAR技术在高危颈动脉狭窄患者中是有效的。临床意义本研究针对颈动脉狭窄的高危患者,需要手术治疗。当没有类似Tcar的商业化装置,但迫切需要手术治疗时,可以采用这种改良的手术入路,降低术中栓子脱离引起缺血性脑卒中的发生率。本研究的创新意义在于使用局部材料和简单实用的器械,降低术中栓塞脱离引起脑卒中的风险。
{"title":"A Modified Transcarotid Artery Revascularization Technique for High-Risk Carotid Stenosis.","authors":"Zuanbiao Yu, Songjie Hu, Dehai Lang, Di Wang, Chunbo Xu, Xiaoliang Yin, Yafang Shao, Tiequan Yang","doi":"10.1177/15266028251400566","DOIUrl":"https://doi.org/10.1177/15266028251400566","url":null,"abstract":"<p><strong>Introduction: </strong>Although transcarotid arterial revascularization (TCAR) may offer several advantages, the first commercial TCAR system (EnRoute; Boston Scientific, Marlborough, Massachusetts) is not available in many countries. Therefore, a suitable and simple technique for transcarotid treatment of high-risk carotid stenosis is needed.</p><p><strong>Case report: </strong>We report a hybrid approach to carotid stenosis treatment: stenting with surgical exposure of the carotid artery, forming a flow reversal circuit, with a feasibility to add a distal filter. Sheaths are placed in the carotid artery and femoral vein to accomplish cerebral protection, forming a flow reversal circuit. In addition, a distal filter device was placed for cerebral protection. Technical success was achieved and the patient experienced no complications.</p><p><strong>Conclusion: </strong>Our modified TCAR technique may be effective in patients with high-risk carotid stenosis.Clinical ImpactThis research work is aimed at high-risk patients with carotid artery stenosis who need surgical treatment. When there are no commercialized devices similar to Tcar but surgical treatment is urgently needed, This modified surgical approach can be adopted to reduce the incidence of ischemic stroke caused by intraoperative embolus detachment. The innovative significance of this research lies in using local materials and simple, practical instruments to reduce the risk of stroke caused by embolus detachment during surgery.</p>","PeriodicalId":50210,"journal":{"name":"Journal of Endovascular Therapy","volume":" ","pages":"15266028251400566"},"PeriodicalIF":1.5,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145866261","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-30DOI: 10.1177/15266028251399111
Sean Yao Zu Kong, Anton Amirthanathan Jenil, Enhui Yong, Li Zhang, Lester Rhan Chaen Chong, Malcolm Han Wen Mak, Qiantai Hong, Glenn Wei Leong Tan, Yi-Wei Wu, Gabriel Chan, Gavin Lim, Lawrence Han Hwee Quek, Uei Pua, Justin Kwan, Enming Yong
This study reports our experience with intravascular lithotripsy (IVL) in managing heavily calcified peripheral arterial disease (PAD) at a tertiary center in Southeast Asia. A total of 50 procedures were performed in 49 patients between October 2022 and April 2024. The cohort had a high burden of comorbidities, with 94% presenting with chronic limb-threatening ischemia, 62% classified as wound, ischemia, and foot infection (WIfI) stage 4, and 31% having end-stage renal failure. Severe vascular calcification (Peripheral Artery Calcification Scoring System [PACSS] grade 4) was present in 84% of lesions. IVL was employed as a vessel preparation strategy prior to definitive treatment, with adjunctive therapies used in all cases. Technical success was achieved in 100% of procedures, with a mean luminal gain of 71.4%±21.8%. Bailout stenting was required in 16% of cases, and there were no incidents of distal embolization. At 1-year follow-up, the target lesion revascularization rate was 6.1%, the overall reintervention rate was 14%, limb salvage was 84%, and mortality was 31%. Our findings suggest that IVL is a safe and effective option for vessel preparation in patients with severely calcified PAD, achieving high technical success and favorable mid-term outcomes in a complex, high-risk population.Clinical ImpactCalcified peripheral arterial disease remains a challenging subset in endovascular therapy, often limiting luminal gain, increasing dissection risk, and impairing drug delivery. This single-center experience demonstrates that IVL is a safe and effective vessel-preparation strategy in a real-world population with high comorbidity burden and predominantly PACSS grade 4 disease. IVL achieved 100% technical success, substantial luminal gain, low complication rates; and favorable 1-year limb salvage and reintervention outcomes. These findings support IVL as a practical method for modifying severe calcification and improving procedural reliability in high-risk patients undergoing endovascular treatment.
{"title":"Cracking the Calcium Barrier: Intravascular Lithotripsy for Peripheral Arterial Disease-1-year Outcomes From 50 Procedures in a Singapore Tertiary Hospital.","authors":"Sean Yao Zu Kong, Anton Amirthanathan Jenil, Enhui Yong, Li Zhang, Lester Rhan Chaen Chong, Malcolm Han Wen Mak, Qiantai Hong, Glenn Wei Leong Tan, Yi-Wei Wu, Gabriel Chan, Gavin Lim, Lawrence Han Hwee Quek, Uei Pua, Justin Kwan, Enming Yong","doi":"10.1177/15266028251399111","DOIUrl":"https://doi.org/10.1177/15266028251399111","url":null,"abstract":"<p><p>This study reports our experience with intravascular lithotripsy (IVL) in managing heavily calcified peripheral arterial disease (PAD) at a tertiary center in Southeast Asia. A total of 50 procedures were performed in 49 patients between October 2022 and April 2024. The cohort had a high burden of comorbidities, with 94% presenting with chronic limb-threatening ischemia, 62% classified as wound, ischemia, and foot infection (WIfI) stage 4, and 31% having end-stage renal failure. Severe vascular calcification (Peripheral Artery Calcification Scoring System [PACSS] grade 4) was present in 84% of lesions. IVL was employed as a vessel preparation strategy prior to definitive treatment, with adjunctive therapies used in all cases. Technical success was achieved in 100% of procedures, with a mean luminal gain of 71.4%±21.8%. Bailout stenting was required in 16% of cases, and there were no incidents of distal embolization. At 1-year follow-up, the target lesion revascularization rate was 6.1%, the overall reintervention rate was 14%, limb salvage was 84%, and mortality was 31%. Our findings suggest that IVL is a safe and effective option for vessel preparation in patients with severely calcified PAD, achieving high technical success and favorable mid-term outcomes in a complex, high-risk population.Clinical ImpactCalcified peripheral arterial disease remains a challenging subset in endovascular therapy, often limiting luminal gain, increasing dissection risk, and impairing drug delivery. This single-center experience demonstrates that IVL is a safe and effective vessel-preparation strategy in a real-world population with high comorbidity burden and predominantly PACSS grade 4 disease. IVL achieved 100% technical success, substantial luminal gain, low complication rates; and favorable 1-year limb salvage and reintervention outcomes. These findings support IVL as a practical method for modifying severe calcification and improving procedural reliability in high-risk patients undergoing endovascular treatment.</p>","PeriodicalId":50210,"journal":{"name":"Journal of Endovascular Therapy","volume":" ","pages":"15266028251399111"},"PeriodicalIF":1.5,"publicationDate":"2025-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145858870","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: This study compares the outcomes of endovascular repair using pre-curved fenestrated endografts and open surgery with total arch replacement for aortic arch aneurysm repair.
Methods: Patients who underwent aortic arch aneurysm repair with fenestrated endograft or total arch replacement between 2009 and 2021 were retrospectively analyzed. Subjects were limited to true aortic arch aneurysms, and cases with a history of thoracic aortic surgery, connective tissue disorder, or concomitant procedure were excluded. The Kaplan-Meier method was used to calculate cumulative survival and freedom from aorta-related death, and the Fine and Grey methods were used for re-intervention rates.
Results: A total of 106 cases were included, with fenestrated endografts (F group, n=58) and total arch replacement (T group, n=48). The median follow-up times were 48.0 (25.5, 94.8) and 62.5 (46.0, 110.8) months (p=0.038) in the F and T group, respectively. The median age (76.5 [71.3, 80.0] vs 71.5 [66.0, 77.0], p<0.001) and European System for Cardiac Operative Risk Evaluation II (11.0 [10.0, 14.0] vs 8.5 [6.0, 11.0], p<0.001) were higher in the F group. Intraoperative blood transfusions (19 [32.8%] vs 48 [100%], p<0.001), operative times (145.0 [113.3, 191.0] vs 464.5 [413.8, 531.5], p<0.001), postoperative intubation times (0 [0, 0] vs 68.0 [20.0, 150.0], p<0.001), intensive care unit stays (1.0 [1.0, 2.0] vs 6.5 [5.0, 11.0], p<0.001) and in-hospital stays (10.0 [8.0, 12.0] vs 27.0 [22.0, 41.3], p<0.001) were significantly reduced in the F group. In-hospital mortality (2.0 [3.5%] vs 0 [0%], p=0.50), perioperative cerebral infarction (2 [3.5%] vs 3 [6.3%], p=0.66), and spinal cord injury (1 [1.7%] vs 0 [0%], p>1) were comparable between the 2 groups. The 5-year survival rates were 68.9% (standard error [SE]=6.85) and 81.5% (SE=6.00) in the F and T groups, respectively (p=0.003); however, freedom from aorta-related death rate (100% vs 100%, p=0.32) and the re-intervention rates (19.0% vs 6.30%, p=0.08) at 5-year showed no significant difference.
Conclusions: Fenestrated endovascular aortic repair reduces operative time, postoperative intubation, intensive care unit and in-hospital stays, and blood transfusions. The 5-year freedom from aorta-related death and re-intervention rates were comparable to those of total arch replacement.Clinical ImpactPre-curved fenestrated endografts provide a less-invasive yet effective option for aortic arch aneurysm repair, compared to total arch replacement. They offer shorter operative and intubation times, reduced transfusion rate, and shorter ICU stays, without increasing aorta-related mortality or reintervention during follow-up. This approach expands treatment opportunities for elderly and high-risk patients who previously could not undergo conventional arch repair.
背景:本研究比较了采用预弯曲开窗血管内移植物和全弓置换术修复主动脉弓动脉瘤的结果。方法:回顾性分析2009年至2021年间接受开窗内移植物或全弓置换术修复主动脉弓动脉瘤的患者。受试者仅限于真主动脉弓动脉瘤,排除有胸主动脉手术史、结缔组织疾病或伴随手术的病例。Kaplan-Meier法用于计算累积生存率和无主动脉相关死亡,Fine和Grey法用于计算再干预率。结果:共纳入106例患者,F组(n=58)和T组(n=48)全弓置换术。F组和T组的中位随访时间分别为48.0(25.5,94.8)和62.5(46.0,110.8)个月(p=0.038)。两组患者的中位年龄(76.5 [71.3,80.0]vs 71.5 [66.0, 77.0], p1)具有可比性。F组和T组5年生存率分别为68.9%(标准误差[SE]=6.85)和81.5% (SE=6.00) (p=0.003);5年无主动脉相关死亡率(100% vs 100%, p=0.32)和再干预率(19.0% vs 6.30%, p=0.08)差异无统计学意义。结论:开窗主动脉腔内修复术减少了手术时间、术后插管时间、重症监护病房和住院时间以及输血时间。5年无主动脉相关死亡和再干预率与全弓置换术相当。临床影响:与全弓置换术相比,预弯曲开窗内移植物为主动脉弓动脉瘤修复提供了一种微创但有效的选择。它们提供更短的手术和插管时间,更低的输血率,更短的ICU住院时间,在随访期间不增加主动脉相关死亡率或再干预。这种方法为以前不能进行常规弓修复的老年人和高危患者扩大了治疗机会。
{"title":"Pre-curved Fenestrated Endovascular Repair Versus Total Arch Replacement for Aortic Arch Aneurysm Repair.","authors":"Kosuke Nakamae, Takashi Azuma, Satoru Domoto, Yoshihiko Yokoi, Masataka Hirota, Hiroshi Niinami","doi":"10.1177/15266028251400217","DOIUrl":"https://doi.org/10.1177/15266028251400217","url":null,"abstract":"<p><strong>Background: </strong>This study compares the outcomes of endovascular repair using pre-curved fenestrated endografts and open surgery with total arch replacement for aortic arch aneurysm repair.</p><p><strong>Methods: </strong>Patients who underwent aortic arch aneurysm repair with fenestrated endograft or total arch replacement between 2009 and 2021 were retrospectively analyzed. Subjects were limited to true aortic arch aneurysms, and cases with a history of thoracic aortic surgery, connective tissue disorder, or concomitant procedure were excluded. The Kaplan-Meier method was used to calculate cumulative survival and freedom from aorta-related death, and the Fine and Grey methods were used for re-intervention rates.</p><p><strong>Results: </strong>A total of 106 cases were included, with fenestrated endografts (F group, n=58) and total arch replacement (T group, n=48). The median follow-up times were 48.0 (25.5, 94.8) and 62.5 (46.0, 110.8) months (p=0.038) in the F and T group, respectively. The median age (76.5 [71.3, 80.0] vs 71.5 [66.0, 77.0], p<0.001) and European System for Cardiac Operative Risk Evaluation II (11.0 [10.0, 14.0] vs 8.5 [6.0, 11.0], p<0.001) were higher in the F group. Intraoperative blood transfusions (19 [32.8%] vs 48 [100%], p<0.001), operative times (145.0 [113.3, 191.0] vs 464.5 [413.8, 531.5], p<0.001), postoperative intubation times (0 [0, 0] vs 68.0 [20.0, 150.0], p<0.001), intensive care unit stays (1.0 [1.0, 2.0] vs 6.5 [5.0, 11.0], p<0.001) and in-hospital stays (10.0 [8.0, 12.0] vs 27.0 [22.0, 41.3], p<0.001) were significantly reduced in the F group. In-hospital mortality (2.0 [3.5%] vs 0 [0%], p=0.50), perioperative cerebral infarction (2 [3.5%] vs 3 [6.3%], p=0.66), and spinal cord injury (1 [1.7%] vs 0 [0%], p>1) were comparable between the 2 groups. The 5-year survival rates were 68.9% (standard error [SE]=6.85) and 81.5% (SE=6.00) in the F and T groups, respectively (p=0.003); however, freedom from aorta-related death rate (100% vs 100%, p=0.32) and the re-intervention rates (19.0% vs 6.30%, p=0.08) at 5-year showed no significant difference.</p><p><strong>Conclusions: </strong>Fenestrated endovascular aortic repair reduces operative time, postoperative intubation, intensive care unit and in-hospital stays, and blood transfusions. The 5-year freedom from aorta-related death and re-intervention rates were comparable to those of total arch replacement.Clinical ImpactPre-curved fenestrated endografts provide a less-invasive yet effective option for aortic arch aneurysm repair, compared to total arch replacement. They offer shorter operative and intubation times, reduced transfusion rate, and shorter ICU stays, without increasing aorta-related mortality or reintervention during follow-up. This approach expands treatment opportunities for elderly and high-risk patients who previously could not undergo conventional arch repair.</p>","PeriodicalId":50210,"journal":{"name":"Journal of Endovascular Therapy","volume":" ","pages":"15266028251400217"},"PeriodicalIF":1.5,"publicationDate":"2025-12-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145858944","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-27DOI: 10.1177/15266028251397850
Jan Stana, Laurence Bertrand, Baban Assaf, David Bijan Khangholi, Nikolaos Konstantionou, Nikolaos Tsilimparis
Objective: To evaluate the clinical application and outcomes of physician-modified endografts (PMEG) made from a prefenestrated custom-made device (CMD) from COOK Medical with one reinforced fenestration and prefabricated diameter-reducing ties for the treatment of complex abdominal aortic aneurysms.
Methods: All patients treated with this adapted PMEG technique were included in the study. The single prefabricated fenestration was located 57 mm from the proximal edge. Two proximal graft diameters (34 mm and 36 mm) tapered to 22 mm distally, with tapering beginning 67 mm from the top and extending 40 mm were used. All grafts had a fixed length of 160 mm.
Results: Ten patients, of which 8 male (80%) and with a mean age of 74 (IQR: 70-78 y) were included. Indications included degenerative abdominal aortic aneurysms (n=6 [60%]), penetrating aortic ulcers (n=2 [20%]), and mycotic aneurysms (n=2 (20%). Three (30%) presented with contained rupture, six (60%) were symptomatic without rupture, and one (10%) was asymptomatic. Median diameter of the aneurysm was 53mm (IQR 48.3-73.2 mm). Physician modification involved creation of at least three additional fenestrations, all reinforced with Goose Snare wires and secured with sutures. All target vessels were successfully bridged. The median operating time was 208.5 min (IQR: 161.3-290 min), while the median modification time was 71.5 min (IQR 55-96 min). The in-hospital mortality rate was 20 %, both were patients with ruptured mycotic aneurysms. The remaining eight patients have all regained their baseline functional status and are currently undergoing follow-up (median follow-up time: 4.5 months; IQR: 1-13 months), with maintained patency of all target vessels to date. Postoperative CT revealed one type III endoleak, one type Ib, and two type II endoleaks. The type III endoleak between the TEVAR and the fenestrated aortic graft was treated with a giant Palmaz stent (one endovascular reintervention), while the others remain under follow-up.
Conclusions: Use of a simplified PMEG with one prefabricated fenestration and diameter-reducing ties is feasible and offers favorable early outcomes with technical advantages in modification and deployment.Clinical ImpactUsing an endograft with a single prefabricated fenestration as the outset graft for physician-modified endografts enhances procedural efficiency by reducing customisation time and simplifying the modification process. This approach lowers technical complexity, improves procedural reproducibility, and broadens the applicability of PMEG techniques. Consequently, PMEGs can be more readily used across a wider range of complex aortic anatomies, expanding endovascular treatment options for patients who might otherwise have limited or higher-risk surgical alternatives.
{"title":"Optimizing PMEG Technique: Enhancing Endovascular Repair With Pre-Manufactured Fenestrated Endografts.","authors":"Jan Stana, Laurence Bertrand, Baban Assaf, David Bijan Khangholi, Nikolaos Konstantionou, Nikolaos Tsilimparis","doi":"10.1177/15266028251397850","DOIUrl":"https://doi.org/10.1177/15266028251397850","url":null,"abstract":"<p><strong>Objective: </strong>To evaluate the clinical application and outcomes of physician-modified endografts (PMEG) made from a prefenestrated custom-made device (CMD) from COOK Medical with one reinforced fenestration and prefabricated diameter-reducing ties for the treatment of complex abdominal aortic aneurysms.</p><p><strong>Methods: </strong>All patients treated with this adapted PMEG technique were included in the study. The single prefabricated fenestration was located 57 mm from the proximal edge. Two proximal graft diameters (34 mm and 36 mm) tapered to 22 mm distally, with tapering beginning 67 mm from the top and extending 40 mm were used. All grafts had a fixed length of 160 mm.</p><p><strong>Results: </strong>Ten patients, of which 8 male (80%) and with a mean age of 74 (IQR: 70-78 y) were included. Indications included degenerative abdominal aortic aneurysms (n=6 [60%]), penetrating aortic ulcers (n=2 [20%]), and mycotic aneurysms (n=2 (20%). Three (30%) presented with contained rupture, six (60%) were symptomatic without rupture, and one (10%) was asymptomatic. Median diameter of the aneurysm was 53mm (IQR 48.3-73.2 mm). Physician modification involved creation of at least three additional fenestrations, all reinforced with Goose Snare wires and secured with sutures. All target vessels were successfully bridged. The median operating time was 208.5 min (IQR: 161.3-290 min), while the median modification time was 71.5 min (IQR 55-96 min). The in-hospital mortality rate was 20 %, both were patients with ruptured mycotic aneurysms. The remaining eight patients have all regained their baseline functional status and are currently undergoing follow-up (median follow-up time: 4.5 months; IQR: 1-13 months), with maintained patency of all target vessels to date. Postoperative CT revealed one type III endoleak, one type Ib, and two type II endoleaks. The type III endoleak between the TEVAR and the fenestrated aortic graft was treated with a giant Palmaz stent (one endovascular reintervention), while the others remain under follow-up.</p><p><strong>Conclusions: </strong>Use of a simplified PMEG with one prefabricated fenestration and diameter-reducing ties is feasible and offers favorable early outcomes with technical advantages in modification and deployment.Clinical ImpactUsing an endograft with a single prefabricated fenestration as the outset graft for physician-modified endografts enhances procedural efficiency by reducing customisation time and simplifying the modification process. This approach lowers technical complexity, improves procedural reproducibility, and broadens the applicability of PMEG techniques. Consequently, PMEGs can be more readily used across a wider range of complex aortic anatomies, expanding endovascular treatment options for patients who might otherwise have limited or higher-risk surgical alternatives.</p>","PeriodicalId":50210,"journal":{"name":"Journal of Endovascular Therapy","volume":" ","pages":"15266028251397850"},"PeriodicalIF":1.5,"publicationDate":"2025-12-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145844274","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}