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Lumbar Artery Branch in Treatment of Thoracoabdominal Aortic Aneurysm to Prevent Spinal Cord Ischemia. 腰动脉分支治疗胸腹主动脉瘤预防脊髓缺血。
IF 1.5 2区 医学 Q3 PERIPHERAL VASCULAR DISEASE Pub Date : 2026-01-08 DOI: 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。
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引用次数: 0
Central Venous Stenosis and Occlusion in Dialysis Patients: A Technical and Outcome-Based Analysis of Endovascular Intervention. 透析患者中心静脉狭窄和闭塞:血管内介入的技术和结果分析。
IF 1.5 2区 医学 Q3 PERIPHERAL VASCULAR DISEASE Pub Date : 2026-01-07 DOI: 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.
目的:本研究的目的是评估血液透析患者中心静脉狭窄(CVS)和闭塞(CVO)的血管内治疗的早期和长期技术和临床结果,并描述旨在优化血管通路保留的程序策略。材料和方法:对2020年1月至2024年12月期间所有接受上肢动静脉通道血管内重建术治疗症状性CVS/CVO的患者进行回顾性单中心分析。适应症包括严重静脉充血,透析后出血时间延长,通路成熟不良,透析效率不高。经双超声和计算机断层血管造影诊断;当无创成像不确定时,采用数字减影血管造影。记录手术细节、器械使用和围手术期结果。主要结局为原发性通畅;次要结局包括技术成功、手术安全、累积(次要)通畅和免于再干预。结果:治疗44例患者,平均年龄65.8±16.2岁,男性占59.1%,其中50%为完全性闭塞。最常见的病变部位为头臂静脉(70.4%)。高压球囊血管成形术占93.2%,支架植入术占45.5%(多为自膨胀镍钛诺)。技术成功率93.2%,无围手术期并发症。在36.7±32.2个月的中位随访中,20例(45.5%)患者因再狭窄(34.1%)或再闭塞(11.4%)进行了再干预;30%的再介入显示支架骨折。Kaplan-Meier分析显示,6个月时原发性通畅率为85.5%,12个月时为69.9%,18个月时为58.7%。6个月时累积通畅率为88.4%,12和24个月时为80.9%,36个月时为74.8%,60个月时为69.1%。先前的同侧中心静脉导管放置与再次干预的自由度降低有关。结论:血液透析患者血管内CVS/CVO血运重建术是安全的,技术成功率高。虽然初级通畅随着时间的推移而下降,但累积通畅仍然是有利的,这强调了及时的再干预和有组织的监测在延长可及寿命方面的作用。该研究强化了血管内血运重建术作为治疗血液透析患者中心静脉狭窄和闭塞的安全有效的一线策略,允许血管通道立即重用并避免透析中断。数据强调,长期成功较少依赖于单一的“完美”程序,而更多地依赖于有组织的监督和及时的再干预。先前的同侧中心静脉导管放置是失败的关键预测因素,强调需要尽量减少导管的使用并促进早期AVF的产生。从实用的角度来看,在长或容易反冲的病变中选择初级支架置入,并仔细注意支架的耐久性,可以有意义地延长这一脆弱人群的使用寿命。
{"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":"&lt;p&gt;&lt;strong&gt;Purpose: &lt;/strong&gt;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.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Materials and methods: &lt;/strong&gt;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.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;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.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusions: &lt;/strong&gt;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}
引用次数: 0
Systematic Review and Metanalysis on the Advanta V12/iCast Outcomes as Bridging Stent in Iliac Branch Devices. Advanta V12/iCast作为髂支支架桥接效果的系统评价与meta分析。
IF 1.5 2区 医学 Q3 PERIPHERAL VASCULAR DISEASE Pub Date : 2026-01-07 DOI: 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":"&lt;p&gt;&lt;strong&gt;Purpose: &lt;/strong&gt;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.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;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.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;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%; &lt;i&gt;I&lt;/i&gt;&lt;sup&gt;2&lt;/sup&gt; = 0%; certainty: very low). Regarding the 30-day outcomes, the occlusion/stenosis rate was 2% (95% CI = 0%-9%; &lt;i&gt;I&lt;/i&gt;&lt;sup&gt;2&lt;/sup&gt; = 0%), the endoleak Ic/IIIc rate was 0.3% (95% CI = 0%-3%; &lt;i&gt;I&lt;/i&gt;&lt;sup&gt;2&lt;/sup&gt; = 0%) and the reintervention rate was 1% (95% CI = 0%-3%; &lt;i&gt;I&lt;/i&gt;&lt;sup&gt;2&lt;/sup&gt; = 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%; &lt;i&gt;I&lt;/i&gt;&lt;sup&gt;2&lt;/sup&gt; = 19%; certainty: very low), the endoleak Ic/IIIc overall rate was 5% (95% CI = 3%-8%; &lt;i&gt;I&lt;/i&gt;&lt;sup&gt;2&lt;/sup&gt; = 0%; certainty: very low), and the reintervention rate was 5% (95% CI = 3%-9%; &lt;i&gt;I&lt;/i&gt;&lt;sup&gt;2&lt;/sup&gt; = 0%; certainty: very low).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusions: &lt;/strong&gt;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}
引用次数: 0
Endovascular Treatment for Patients With Isolated Internal Iliac Artery Aneurysm: A Single-Center Retrospective Study Over a 10-Year Period. 孤立髂内动脉瘤的血管内治疗:一项超过10年的单中心回顾性研究
IF 1.5 2区 医学 Q3 PERIPHERAL VASCULAR DISEASE Pub Date : 2026-01-03 DOI: 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.

目的:孤立性髂内动脉瘤(IIIAA)是一种罕见的疾病,约占所有腹内动脉瘤的0.3%至0.5%。本研究旨在通过一个相对较大的队列来评估血管内治疗IIIAA的结果。方法:回顾性分析我院2014年4月至2024年4月收治的45例IIIAA患者。收集和分析患者人口统计资料、干预结果和随访结果。结果:共纳入49例IIIAAs患者45例(女性2例),平均年龄70.4±9.2岁。该队列显示出高患病率的心脑血管危险因素,31.1%有恶性肿瘤病史。30例(66.7%)患者被诊断为偶发IIIAA,其余患者表现为腹部或腰部疼痛、排尿困难或动脉瘤破裂等症状。单纯支架植入3例,单纯线圈栓塞5例,其余37例采用联合入路。远端分支完全栓塞率为69.0%(29/42),技术成功44例。平均随访时间23.8±21.5个月。随访期间,5例患者死于癌症或心力衰竭。7例患者出现臀部跛行,保守治疗后1例仍未痊愈。4例远端分支栓塞不完全患者出现囊扩张;其中3个需要重新干预。12个月和24个月无再干预生存率分别为95.5%和88.2%。结论:血管内治疗,特别是支架植入和圈管栓塞联合治疗IIIAA是安全有效的,中期无再介入生存率为85.25%,盆腔缺血风险可接受。在某些情况下,完全栓塞流出支在技术上是具有挑战性的,而囊栓塞作为一种替代方法的有效性仍有争议。临床压入性髂内动脉瘤(IIIAA)是一种极为罕见的疾病。本回顾性研究纳入我院收治的45例IIIAA患者,以评价血管内治疗的安全性和疗效。大多数患者接受支架植入以封闭髂内动脉开口,同时对远端分支进行线圈栓塞。所有患者2年无再干预生存率为85.25%,表明血管内治疗效果良好。然而,在4例未接受完全远端分支栓塞的患者中观察到术后囊扩张,强调需要对这部分患者进行严格的随访。
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引用次数: 0
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. 选择性主动脉上主干支架植入术治疗慢性残余A型夹层的全主动脉弓修复
IF 1.5 2区 医学 Q3 PERIPHERAL VASCULAR DISEASE Pub Date : 2026-01-03 DOI: 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.

目的:探讨选择性主动脉主干支架置入术对慢性A型主动脉夹层(cTAAD)患者主动脉重构的影响。方法:回顾性分析2017年至2024年采用双开窗医师改良内移植物(PMEGs)修复主动脉弓治疗cTAAD的患者。目的是比较主动脉治疗和重塑,SAT演变,以及根据SAT剥离状态(前后),使用双开窗PMEG进行全主动脉弓修复的总体结果。结果:42例cTAAD患者中,30例有SAT夹层。35例患者接受了标准PMEG,而7例患者接受了额外的选择性SAT支架置入(3例LCCA, 1例头臂干(BT), 4例右锁骨下动脉(RSA)和3例右颈总动脉(RCCA))。技术上的成功率是100%。30 d时,1例死于中风,1例死于出院后肺炎。在18.5个月的中位随访期间(IQR: 38.8),未发生Ia型内漏。共观察到6个Ic型内漏;3名患者接受了再次干预,其余3名患者接受了随访CT扫描,未发现主动脉生长的证据。12例(40%)患者出现完全的SAT剥离,其中9例为标准PMEG。32例(76%)患者主动脉重构阳性,中位内径缩小-1% (IQR: 5.5%)。5例患者在中期随访期间死亡,无与手术相关的死亡。有和没有初始SAT剥离的患者主动脉重构阳性率分别为73%和83% (p=0.7),最初没有SAT剥离的患者和治愈的患者主动脉重构阳性率分别为83%和92% (p=1),持续SAT剥离的患者和其他患者主动脉重构阳性率分别为61%和88% (p=0.07)。接受治疗性抗凝治疗或双重抗血小板治疗的患者显示阳性重构减少。结论:双开窗pmeg治疗残余ctaad疗效显著,具有高的SAT愈合和良好的重构。持续的SAT剥离可能会阻碍重构,需要额外的干预。临床应用无系统SAT支架的开窗医师改良内移植物修复冲击主动脉弓可减少SAT操作,降低卒中风险,同时提高SAT和主动脉夹层的愈合率。对于持续存在的SAT夹层和报道的主动脉生长,可以进行二次辅助SAT干预以增强主动脉重塑。
{"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}
引用次数: 0
Low-Dose 4-Dimensional Computed Tomographic Angiography for Diagnosing Indeterminate Endoleak After Hybrid Arch Repair: A Case Report. 低剂量四维计算机断层血管造影诊断混合弓修复后不确定内漏1例报告。
IF 1.5 2区 医学 Q3 PERIPHERAL VASCULAR DISEASE Pub Date : 2026-01-03 DOI: 10.1177/15266028251409060
Kenta Masada, Reiko Katsuya, Katsukiyo Kitabayashi, Hajime Ichikawa

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.

目的:介绍一例低剂量4维计算机断层血管造影(4D-CTA)在常规CTA结果不确定的情况下,对慢性B型主动脉夹层混合弓修复后的II型内漏进行精确分类的病例。病例:一名74岁女性因慢性B型主动脉夹层接受左颈总动脉-锁骨下搭桥和胸椎血管内主动脉修复复合弓修复术。术后6年发现动脉瘤囊增大。常规CTA两期检查(早期动脉期和延迟静脉期)不能区分Ia型和II型内漏。低剂量4D-CTA(剂量长度产物:302.6 mGy·cm)显示动脉晚期囊内延迟造影剂增强,符合源自左锁骨下动脉(LSCA)的II型内漏。靶向线圈栓塞成功解决了内漏,术中血管造影证实了LSCA分支的造影剂流入。结论:低剂量4D-CTA可以精确分类内漏并指导适当的再干预。这种方式是一种有用和实用的内漏评估工具,特别是当标准成像不确定时。本病例强调了四维计算机断层血管造影(4D-CTA)在胸血管内主动脉修复(TEVAR)后对内溢进行分类的诊断价值,特别是在标准CTA不确定的情况下。4D-CTA鉴定出左侧锁骨下动脉II型内漏,使确诊和靶向线圈栓塞成为可能。值得注意的是,扫描使用低剂量方案(剂量长度乘积:302.6 mGy·cm),大大低于先前研究报道的bb0 1000 mGy·cm,同时保持了诊断质量。标准化的低剂量4D-CTA方案可能支持更广泛的临床应用。
{"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}
引用次数: 0
A Modified Transcarotid Artery Revascularization Technique for High-Risk Carotid Stenosis. 改良经颈动脉重建术治疗高危颈动脉狭窄。
IF 1.5 2区 医学 Q3 PERIPHERAL VASCULAR DISEASE Pub Date : 2025-12-31 DOI: 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}
引用次数: 0
Cracking the Calcium Barrier: Intravascular Lithotripsy for Peripheral Arterial Disease-1-year Outcomes From 50 Procedures in a Singapore Tertiary Hospital. 打破钙屏障:外周动脉疾病的血管内碎石术-新加坡三级医院50例手术的1年结果
IF 1.5 2区 医学 Q3 PERIPHERAL VASCULAR DISEASE Pub Date : 2025-12-30 DOI: 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.

本研究报告了我们在东南亚三级医疗中心采用血管内碎石术(IVL)治疗重度钙化外周动脉疾病(PAD)的经验。在2022年10月至2024年4月期间,49名患者共进行了50次手术。该队列有很高的合并症负担,94%的患者表现为慢性肢体威胁缺血,62%的患者被归类为伤口、缺血和足部感染(WIfI) 4期,31%的患者患有终末期肾功能衰竭。84%的病变存在严重的血管钙化(外周动脉钙化评分系统[PACSS] 4级)。IVL作为最终治疗前的血管准备策略,所有病例均采用辅助治疗。技术成功率100%,平均光增益为71.4%±21.8%。16%的病例需要置入术,没有远端栓塞事件。随访1年,目标病变血运重建率为6.1%,总体再干预率为14%,肢体保留率为84%,死亡率为31%。我们的研究结果表明,IVL是严重钙化PAD患者血管准备的一种安全有效的选择,在复杂的高风险人群中取得了很高的技术成功和良好的中期结果。临床影响钙化外周动脉疾病在血管内治疗中仍然是一个具有挑战性的分支,通常限制腔内增益,增加夹层风险,并损害药物传递。这项单中心研究表明,IVL是一种安全有效的血管制备策略,适用于现实世界中具有高合并症负担且主要为PACSS 4级疾病的人群。IVL技术成功率100%,光增益大,并发症发生率低;1年的肢体保留和再干预结果良好。这些发现支持IVL作为一种实用的方法来改善严重钙化和提高高危患者接受血管内治疗的程序可靠性。
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引用次数: 0
Pre-curved Fenestrated Endovascular Repair Versus Total Arch Replacement for Aortic Arch Aneurysm Repair. 预弯曲开窗血管内修复与全弓置换术修复主动脉弓动脉瘤。
IF 1.5 2区 医学 Q3 PERIPHERAL VASCULAR DISEASE Pub Date : 2025-12-29 DOI: 10.1177/15266028251400217
Kosuke Nakamae, Takashi Azuma, Satoru Domoto, Yoshihiko Yokoi, Masataka Hirota, Hiroshi Niinami

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。
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引用次数: 0
Optimizing PMEG Technique: Enhancing Endovascular Repair With Pre-Manufactured Fenestrated Endografts. 优化PMEG技术:利用预制开窗内移植物增强血管内修复。
IF 1.5 2区 医学 Q3 PERIPHERAL VASCULAR DISEASE Pub Date : 2025-12-27 DOI: 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.

目的:探讨COOK Medical公司预制定制装置(CMD)经医师改良的带一个强化开窗和预制减径系带的内移植物(PMEG)在复杂腹主动脉瘤治疗中的临床应用及效果。方法:所有采用PMEG技术治疗的患者均纳入研究。单个预制开窗位于距离近端边缘57毫米处。两个近端移植物直径(34 mm和36 mm)在远端逐渐变细至22 mm,从顶部开始变细至67 mm,延伸至40 mm。结果:共纳入10例患者,其中男性8例(80%),平均年龄74岁(IQR: 70 ~ 78)。适应症包括退行性腹主动脉瘤(n=6[60%])、穿透性主动脉溃疡(n=2[20%])和真菌性动脉瘤(n=2(20%))。3例(30%)表现为内源性破裂,6例(60%)无破裂症状,1例(10%)无症状。动脉瘤中位直径53mm (IQR 48.3-73.2 mm)。医生修改包括创建至少三个额外的开窗,所有用鹅网钢丝加固和缝合固定。所有目标船只均成功桥接。手术时间中位数为208.5 min (IQR: 161.3 ~ 290 min),修改时间中位数为71.5 min (IQR: 55 ~ 96 min)。住院死亡率为20%,均为真菌性动脉瘤破裂患者。其余8例患者均已恢复基线功能状态,目前正在接受随访(中位随访时间:4.5个月;IQR: 1-13个月),迄今所有靶血管保持通畅。术后CT示1例III型内漏,1例Ib型内漏,2例II型内漏。TEVAR和开窗主动脉瓣之间的III型内陷采用巨大Palmaz支架(一次血管内再干预)治疗,而其他患者仍在随访中。结论:使用一个预制开窗和减径系带的简化PMEG是可行的,并且在修改和部署方面具有技术优势,具有良好的早期效果。临床影响使用单个预制开窗的内移植物作为医生修改内移植物的开始移植物,通过减少定制时间和简化修改过程,提高了手术效率。这种方法降低了技术复杂性,提高了程序的可重复性,扩大了PMEG技术的适用性。因此,pmeg可以更容易地用于更大范围的复杂主动脉解剖,为那些可能有有限或高风险手术选择的患者扩大血管内治疗选择。
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引用次数: 0
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Journal of Endovascular Therapy
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