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Scalene block as a predictor of surgical success for treatment of thoracic outlet syndrome 斜角肌烯阻滞作为胸廓出口综合征手术治疗成功的预测因子
Pub Date : 2026-01-01 DOI: 10.1016/j.jvsvi.2025.100343
Dorcie Ann Gillette MD , Linda Peng BS , Maen Aboul Hosn MD

Background

Neurogenic thoracic outlet syndrome (TOS) is a difficult pathology to accurately diagnose given the overlap between multiple causes of neuralgias of the upper extremity. Although scalene blocks are often used as diagnostic tools for brachial plexus compression at the level of the thoracic outlet, they can also be predictive of symptomatic relief after thoracic outlet decompression. Our objective is to evaluate the predictive value of preoperative scalene block for postoperative symptom improvement.

Methods

A retrospective review was performed for all patients who underwent a scalene block before first rib resection and at our institution between 2018 and 2023. Data on demographics, presenting symptoms, and preoperative workup were collected. Symptom resolution after scalene block and surgical decompression was assessed through chart review and direct patient contact. These were classified into three categories: complete resolution, partial resolution, and no resolution.

Results

A total of 98 patients were referred to the pain clinic for diagnostic scalene blocks after evaluation for TOS. Of these patients, 80 underwent diagnostic scalene block. A total of 63 patients who underwent a scalene block proceeded to undergo first rib resection. All patients experienced partial or complete improvement after the scalene block. Of these patients, 32 (63%) had complete improvement, 18 (35%) had partial improvement, and one patient (2%) had no improvement after first rib resection.

Conclusions

Neurogenic TOS is a complex pathology whose diagnosis can be challenging in patients presenting with nonclassical symptoms. Based on our findings, preoperative scalene block is an effective tool to accurately predict postoperative symptomatic improvement after first rib resection. The extent of predicted improvement remains variable and a harder measure to quantify given its subjective nature.
背景神经源性胸廓出口综合征(TOS)是一种难以准确诊断的病理,因为上肢神经痛的多种原因存在重叠。虽然斜角肌阻滞常被用作胸廓出口水平臂丛压迫的诊断工具,但它们也可以预测胸廓出口减压后症状的缓解。我们的目的是评估术前斜角肌阻滞对术后症状改善的预测价值。方法回顾性分析2018年至2023年在我院第一肋骨切除术前行斜角肌阻滞的所有患者。收集了人口统计学、出现症状和术前检查的数据。通过图表回顾和患者直接接触来评估斜角肌阻滞和手术减压后的症状缓解情况。这些被分为三类:完全分辨率,部分分辨率和无分辨率。结果98例患者经TOS评估后转诊至疼痛门诊诊断斜角肌阻滞。在这些患者中,80例诊断为斜角肌阻滞。共有63名接受斜角肌阻滞的患者接受了第一肋骨切除术。所有患者在斜角肌阻滞后均有部分或完全改善。在这些患者中,32例(63%)患者完全改善,18例(35%)患者部分改善,1例(2%)患者在第一肋骨切除术后没有改善。结论神经源性TOS是一种复杂的病理,在出现非典型症状的患者中诊断具有挑战性。基于我们的研究结果,术前斜角肌阻滞是准确预测第一肋骨切除术后症状改善的有效工具。预测改善的程度仍然是可变的,而且由于其主观性质,很难量化。
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引用次数: 0
Design of the RadFree randomized controlled study comparing LumiGuide, powered by Fiber Optic RealShape Technology, with conventional fluoroscopy guidance in fenestrated endovascular aortic repair RadFree随机对照研究的设计,比较光纤RealShape技术驱动的LumiGuide与传统透视引导在开窗血管内主动脉修复中的作用
Pub Date : 2026-01-01 DOI: 10.1016/j.jvsvi.2026.100354
Andres Schanzer MD , Darren B. Schneider MD , Carlos Timaran MD , Adam W. Beck MD , Marc Schermerhorn MD , Geert Willem Schurink MD , Joost van Herwaarden MD, PhD , Bijan Modarai MD, PhD , Nathalie Moreels MD , Frédéric Cochennec MD , Tim Resch MD, PhD , Tilo Kölbel MD

Objective

To evaluate whether the use of LumiGuide, a novel real-time three-dimensional navigation system powered by Fiber Optic RealShape technology (Philips), reduces procedure fluoroscopy time compared with conventional fluoroscopic guidance during fenestrated endovascular aortic repair (FEVAR).

Methods

The RadFree study is a prospective, randomized, unblinded, multicenter clinical trial conducted at 11 vascular centers in Europe and the United States. Adults undergoing primary FEVAR with at least two target visceral vessels suitable for LumiGuide are randomized 1:1 to LumiGuide or conventional fluoroscopy. Stratification is performed by aneurysm extent. The primary endpoint is total procedure fluoroscopy time. Secondary outcomes include radiation exposure metrics (fluoroscopy time and rate, dose area product, and air kerma during navigation), cumulative procedural radiation dose, adverse LumiGuide device-related effects, and device deficiencies. Tertiary end points assess navigation efficiency and total procedure duration (first catheter/wire in to last catheter/wire out). The planned sample size of 182 subjects provides ≥80% power to detect a significant reduction in fluoroscopy time at a two-sided α of 0.05. Analyses follow an intention-to-treat approach.

Results

This report details the trial rationale, methods, and planned analyses. Enrollment is currently ongoing; interim analysis will occur at 50% recruitment to assess safety and efficacy signals.

Conclusions

RadFree is the first prospective, randomized multicenter trial evaluating the impact of LumiGuide on fluoroscopy time, radiation exposure and procedural efficiency in FEVAR. Its results will inform whether advanced three-dimensional navigation can safely and effectively reduce fluoroscopy dependence, improving safety for patients and endovascular teams.
目的评价采用光纤RealShape技术(Philips)的新型实时三维导航系统LumiGuide在开窗血管内主动脉修复(FEVAR)中,与传统透视引导相比,是否减少了手术透视时间。RadFree研究是一项前瞻性、随机、非盲、多中心临床试验,在欧洲和美国的11个血管中心进行。至少有两根靶血管适合使用LumiGuide的原发性FEVAR成人按1:1随机分配至LumiGuide或常规透视。分层是根据动脉瘤的范围进行的。主要终点是整个过程的透视时间。次要结果包括辐射暴露指标(透视时间和频率、剂量面积积和导航过程中的空气密度)、累积程序辐射剂量、LumiGuide设备相关的不良影响和设备缺陷。第三终点评估导航效率和总手术时间(第一个导管/导线插入到最后一个导管/导线取出)。182名受试者的计划样本量提供≥80%的能力来检测显着减少透视时间,双侧α为0.05。分析遵循意向治疗方法。结果本报告详细介绍了试验的基本原理、方法和计划分析。注册目前正在进行中;中期分析将在50%的招募时进行,以评估安全性和有效性信号。结论radfree是首个评估LumiGuide对FEVAR透视时间、辐射暴露和程序效率影响的前瞻性、随机多中心试验。其结果将为先进的三维导航是否可以安全有效地减少透视依赖,提高患者和血管内团队的安全性提供信息。
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引用次数: 0
Medications modulating the risk of prolonged length of stay after transcarotid artery revascularization 调节经颈动脉重建术后延长住院时间风险的药物
Pub Date : 2026-01-01 DOI: 10.1016/j.jvsvi.2025.100332
Arjun Kumar BS , Patrick D. Conroy MD , Alec Schubert MD , Shivani Raizada BA , Aakanksha Gupta MD , Mikael Fadoul MD , Joseph V. Lombardi MD, MBA , Philip M. Batista MD

Objective

Transcarotid artery revascularization (TCAR) is an increasingly used alternative to carotid endarterectomy. Although the expected length of stay (LOS) after TCAR is typically 1 day, a subset of patients experience prolonged LOS (pLOS), which has important implications for cost, complication risk, and patient recovery. Previous investigations have identified various demographic and clinical risk factors for pLOS after TCAR. However, the role of a preoperative medication regimen is unclear. Our study aims to evaluate the association between specific medication classes, including antihypertensives and antidiabetic agents, and pLOS after TCAR.

Methods

We performed a retrospective, single-institution cohort analysis for all patients who underwent TCAR between 2019 and 2024. Of the 194 patients identified, 131 (67.5%) were stratified into normal LOS (≤1 day) and 63 (32.5%) into pLOS (≥2 days). Demographics, comorbidities, and detailed medication profiles were collected. Logistic regression analyses, adjusted for key covariates, were used to determine associations among medication class, dosage, and pLOS. Statistical significance was set at P < .05.

Results

The rate of pLOS was 32.5% (63/194). Baseline demographics and comorbidities were similar between normal LOS and pLOS groups, with the exception that a history of cerebrovascular accident, stroke, transient ischemic attack, or amaurosis fugax was significantly associated with increased odds of pLOS (odds ratio: 1.89, P < .05). No individual class of antihypertensive, antidiabetic, or diuretic medication was independently associated with pLOS. However, subgroup analyses demonstrated that patients on a low-dose β-blocker had significantly lower odds of pLOS (adjusted odds ratio: 0.82, P = .02). In addition, use of a cardioselective β-blocker was found to be protective against pLOS (adjusted odds ratio: 0.87, P = .04). Other classes of antihypertensives, including angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, and calcium channel blockers, showed no significant associations with pLOS.

Conclusions

In this single-center, retrospective analysis, preoperative use of a β-blocker, specifically at a low dose with cardioselective agents, was associated with decreased odds of pLOS after TCAR. These findings suggest that medication management may represent a modifiable factor to optimize perioperative outcomes of TCAR. Further prospective studies are warranted to confirm these associations and inform perioperative risk stratification strategies.
目的经颈动脉重建术(TCAR)是一种越来越多的替代颈动脉内膜切除术的方法。虽然TCAR后的预期住院时间(LOS)通常为1天,但一部分患者会经历延长的LOS (pLOS),这对成本、并发症风险和患者康复具有重要意义。先前的调查已经确定了TCAR后pLOS的各种人口统计学和临床危险因素。然而,术前用药方案的作用尚不清楚。我们的研究旨在评估特定药物类别(包括降压药和降糖药)与TCAR后pLOS之间的关系。方法:对2019年至2024年间接受TCAR治疗的所有患者进行回顾性单机构队列分析。194例患者中,131例(67.5%)分为正常LOS组(≤1天),63例(32.5%)分为pLOS组(≥2天)。收集了人口统计学、合并症和详细的用药资料。对关键协变量进行调整后的逻辑回归分析用于确定药物类别、剂量和pLOS之间的关联。差异有统计学意义,P < 0.05。结果pLOS患病率为32.5%(63/194)。基线人口统计学和合并症在正常LOS组和pLOS组之间相似,除了脑血管意外、中风、短暂性脑缺血发作或烟性黑朦的病史与pLOS的发病率增加显著相关(优势比:1.89,P < 0.05)。没有单独的降压、降糖或利尿药物与pLOS独立相关。然而,亚组分析显示,使用低剂量β受体阻滞剂的患者发生pLOS的几率明显较低(调整后的优势比:0.82,P = 0.02)。此外,发现使用心脏选择性β受体阻滞剂对pLOS有保护作用(校正优势比:0.87,P = 0.04)。其他类型的抗高血压药物,包括血管紧张素转换酶抑制剂、血管紧张素受体阻滞剂和钙通道阻滞剂,与pLOS无显著相关性。结论:在这项单中心回顾性分析中,术前使用β受体阻滞剂,特别是低剂量的心脏选择性药物,与TCAR后pLOS的发生率降低有关。这些发现表明,药物管理可能是优化TCAR围手术期预后的一个可改变的因素。需要进一步的前瞻性研究来证实这些关联,并为围手术期风险分层策略提供信息。
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引用次数: 0
Paclitaxel-based devices in subintimal versus intraluminal angioplasty for chronic total occlusion of the femoropopliteal artery 基于紫杉醇的装置用于慢性股腘动脉全闭塞的内膜下血管成形术与腔内血管成形术
Pub Date : 2026-01-01 DOI: 10.1016/j.jvsvi.2025.100329
Taro Kimura MD, Toshitaka Okabe MD, PhD, Hirotoshi Sato MD, Toshihiko Matsuda MD, Daiki Kato MD, Yui Koyanagi MD, Takeshi Okura MD, Yuma Gibo MD, Yuki Ito MD, Shigehiro Ishigaki MD, Tatsuki Fujioka MD, Suguru Shimazu MD, Yuji Oyama MD, PhD, Naoei Isomura MD, PhD, Masahiko Ochiai MD, PhD

Objective

Chronic total occlusion (CTO) of the femoropopliteal artery lesion is a common manifestation of symptomatic lower limb atherosclerosis. However, femoropopliteal chronic total occlusion (FP-CTO) lesions remain a major challenge in endovascular treatment (EVT). Although drug-coated balloons and drug-eluting stents have demonstrated superior outcomes compared with plain old balloon angioplasty and bare nitinol stents in treating femoropopliteal lesions, the optimal strategy for subintimal approaches in FP-CTO remains unclear.

Methods

We retrospectively analyzed 62 patients with FP-CTO who underwent EVT using paclitaxel-based devices (drug-eluting stent or drug-coated balloon) at our institution. Patients were assigned to subintimal (n = 15) or intraluminal (n = 47) groups. At 18 months, the primary end point was freedom from clinically driven target lesion revascularization (CD-TLR), and secondary end points included freedom from reocclusion and the composite of CD-TLR and reocclusion.

Results

At 18 months, freedom from CD-TLR was higher in the intraluminal group than in the subintimal group (76.6% vs 53.3%, P = .045). Freedom from reocclusion was also higher in the intraluminal group (87.2% vs 53.3%, P = .003) than in the subintimal group. In multivariable Cox proportional hazards analysis, the subintimal approach and lesion length were independent risk factors for CD-TLR.

Conclusions

In EVT for FP-CTO, intraluminal paclitaxel-based device therapy was superior to subintimal therapy, with significantly higher rates of freedom from retreatment.
目的股腘动脉慢性全闭塞(CTO)是下肢动脉粥样硬化的常见症状。然而,股腘静脉慢性全闭塞(FP-CTO)病变仍然是血管内治疗(EVT)的主要挑战。尽管药物包被球囊和药物洗脱支架与普通球囊血管成形术和裸镍钛诺支架相比,在治疗股腘动脉病变方面表现出更好的效果,但在FP-CTO中,内膜下入路的最佳策略仍不清楚。方法回顾性分析我院62例使用紫杉醇基装置(药物洗脱支架或药物包被球囊)行EVT的FP-CTO患者。患者被分为内膜下组(n = 15)和腔内组(n = 47)。在18个月时,主要终点是无临床驱动的靶病变血运重建(CD-TLR),次要终点包括无牙合和CD-TLR和牙合的复合。结果18个月时,腔内组的CD-TLR自由度高于内膜下组(76.6%比53.3%,P = 0.045)。腔内组的再闭塞自由度也高于内膜下组(87.2% vs 53.3%, P = 0.003)。在多变量Cox比例风险分析中,内膜下入路和病变长度是CD-TLR的独立危险因素。结论在治疗FP-CTO的EVT中,腔内紫杉醇为基础的装置治疗优于内膜下治疗,且再次治疗的成功率显著高于内膜下治疗。
{"title":"Paclitaxel-based devices in subintimal versus intraluminal angioplasty for chronic total occlusion of the femoropopliteal artery","authors":"Taro Kimura MD,&nbsp;Toshitaka Okabe MD, PhD,&nbsp;Hirotoshi Sato MD,&nbsp;Toshihiko Matsuda MD,&nbsp;Daiki Kato MD,&nbsp;Yui Koyanagi MD,&nbsp;Takeshi Okura MD,&nbsp;Yuma Gibo MD,&nbsp;Yuki Ito MD,&nbsp;Shigehiro Ishigaki MD,&nbsp;Tatsuki Fujioka MD,&nbsp;Suguru Shimazu MD,&nbsp;Yuji Oyama MD, PhD,&nbsp;Naoei Isomura MD, PhD,&nbsp;Masahiko Ochiai MD, PhD","doi":"10.1016/j.jvsvi.2025.100329","DOIUrl":"10.1016/j.jvsvi.2025.100329","url":null,"abstract":"<div><h3>Objective</h3><div>Chronic total occlusion (CTO) of the femoropopliteal artery lesion is a common manifestation of symptomatic lower limb atherosclerosis. However, femoropopliteal chronic total occlusion (FP-CTO) lesions remain a major challenge in endovascular treatment (EVT). Although drug-coated balloons and drug-eluting stents have demonstrated superior outcomes compared with plain old balloon angioplasty and bare nitinol stents in treating femoropopliteal lesions, the optimal strategy for subintimal approaches in FP-CTO remains unclear.</div></div><div><h3>Methods</h3><div>We retrospectively analyzed 62 patients with FP-CTO who underwent EVT using paclitaxel-based devices (drug-eluting stent or drug-coated balloon) at our institution. Patients were assigned to subintimal (n = 15) or intraluminal (n = 47) groups. At 18 months, the primary end point was freedom from clinically driven target lesion revascularization (CD-TLR), and secondary end points included freedom from reocclusion and the composite of CD-TLR and reocclusion.</div></div><div><h3>Results</h3><div>At 18 months, freedom from CD-TLR was higher in the intraluminal group than in the subintimal group (76.6% vs 53.3%, <em>P</em> = .045). Freedom from reocclusion was also higher in the intraluminal group (87.2% vs 53.3%, <em>P</em> = .003) than in the subintimal group. In multivariable Cox proportional hazards analysis, the subintimal approach and lesion length were independent risk factors for CD-TLR.</div></div><div><h3>Conclusions</h3><div>In EVT for FP-CTO, intraluminal paclitaxel-based device therapy was superior to subintimal therapy, with significantly higher rates of freedom from retreatment.</div></div>","PeriodicalId":74034,"journal":{"name":"JVS-vascular insights","volume":"4 ","pages":"Article 100329"},"PeriodicalIF":0.0,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146173351","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Rethinking advance care planning in chronic limb-threatening ischemia: A narrative review of the literature 对慢性肢体缺血预先护理计划的反思:文献综述
Pub Date : 2026-01-01 DOI: 10.1016/j.jvsvi.2025.100325
Olivia Fuson MD , Michelle Yi BS , Ann Gaffey MD

Objective

Although patients with chronic limb-threatening ischemia (CLTI) who undergo major amputation experience greater 1-year mortality risks, data on advance care planning (ACP) in this population are limited. The aim of this review was to summarize the current and evidence-based implementation of ACP among patients with CLTI.

Methods

A literature review of ACP among patients with CLTI was performed. The Pubmed and Google Scholar databases were queried for articles on frequency, quality, and outcomes of ACP for patients with CLTI.

Results

Among patients who undergo major amputation for CLTI, reported mortality is 30% to 50% at the 1-year follow-up. Reported ACP completion rates before surgical intervention for patients with CLTI ranged from 5% to 30%. Palliative care use was limited, with only 1% to 3% of patients with CLTI receiving palliative care referrals before surgery, and <30% of patients receiving palliative care consultations before death. Advance directives for patients with CLTI were similarly lacking, with 14% to 30% of vascular patients completing advance directives before death.

Conclusions

Although ACP has been shown to enhance quality of life for both patients and caregivers and lower health care costs in similar populations, ACP remains underused and poorly characterized in the vascular patient population. Further research is needed to evaluate ACP implementation for patients with CLTI and other life-limiting vascular pathologies.
虽然接受主要截肢的慢性肢体威胁性缺血(CLTI)患者1年死亡风险更高,但该人群的提前护理计划(ACP)数据有限。本综述的目的是总结目前在CLTI患者中ACP的循证实施情况。方法回顾性分析CLTI患者ACP的相关文献。在Pubmed和谷歌Scholar数据库中查询有关CLTI患者ACP的频率、质量和结果的文章。结果在因CLTI而接受大截肢的患者中,在1年随访中报告的死亡率为30%至50%。据报道,CLTI患者手术前ACP完成率从5%到30%不等。姑息治疗的使用是有限的,只有1% - 3%的CLTI患者在手术前接受了姑息治疗转诊,30%的患者在死亡前接受了姑息治疗咨询。CLTI患者的预先指示同样缺乏,14%至30%的血管患者在死亡前完成了预先指示。结论:虽然ACP已被证明可以提高患者和护理人员的生活质量,并降低类似人群的医疗保健费用,但ACP在血管患者群体中仍未得到充分利用,且特征不明确。需要进一步的研究来评估ACP在CLTI和其他限制生命的血管病变患者中的实施情况。
{"title":"Rethinking advance care planning in chronic limb-threatening ischemia: A narrative review of the literature","authors":"Olivia Fuson MD ,&nbsp;Michelle Yi BS ,&nbsp;Ann Gaffey MD","doi":"10.1016/j.jvsvi.2025.100325","DOIUrl":"10.1016/j.jvsvi.2025.100325","url":null,"abstract":"<div><h3>Objective</h3><div>Although patients with chronic limb-threatening ischemia (CLTI) who undergo major amputation experience greater 1-year mortality risks, data on advance care planning (ACP) in this population are limited. The aim of this review was to summarize the current and evidence-based implementation of ACP among patients with CLTI.</div></div><div><h3>Methods</h3><div>A literature review of ACP among patients with CLTI was performed. The Pubmed and Google Scholar databases were queried for articles on frequency, quality, and outcomes of ACP for patients with CLTI.</div></div><div><h3>Results</h3><div>Among patients who undergo major amputation for CLTI, reported mortality is 30% to 50% at the 1-year follow-up. Reported ACP completion rates before surgical intervention for patients with CLTI ranged from 5% to 30%. Palliative care use was limited, with only 1% to 3% of patients with CLTI receiving palliative care referrals before surgery, and &lt;30% of patients receiving palliative care consultations before death. Advance directives for patients with CLTI were similarly lacking, with 14% to 30% of vascular patients completing advance directives before death.</div></div><div><h3>Conclusions</h3><div>Although ACP has been shown to enhance quality of life for both patients and caregivers and lower health care costs in similar populations, ACP remains underused and poorly characterized in the vascular patient population. Further research is needed to evaluate ACP implementation for patients with CLTI and other life-limiting vascular pathologies.</div></div>","PeriodicalId":74034,"journal":{"name":"JVS-vascular insights","volume":"4 ","pages":"Article 100325"},"PeriodicalIF":0.0,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145925584","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Cadaveric models for vascular surgery training 血管外科训练用尸体模型
Pub Date : 2026-01-01 DOI: 10.1016/j.jvsvi.2025.100330
Koyal K. Ansingkar MS , Maham Rahimi MD, PhD

Objective

This review aims to provide a methodology for cadaveric model creation and detail various cadaveric models that have been used in vascular surgery education and can be adapted for further use.

Methods

The vascular anatomy of the cadavers was first assessed with diagnostic angiography to ensure adequacy for use in creating a cadaveric training model. Pulsatile flow with a motorized pump was established by accessing the left common carotid artery with an open approach for the inflow and accessing the left common femoral artery using a percutaneous approach to establish an outflow. Models for training various common vascular surgery procedures were then created. The residents themselves were involved in the creation of the models to maximize teaching.

Results

These models created include an angiogram model, an infrarenal abdominal aortic aneurysm model, a ruptured abdominal aortic aneurysm model, a Type B aortic dissection model, and a pulmonary embolism model, all with pulsatility that can simulate normal arterial hemodynamics. Angiography, endovascular aneurysm repair, complete proximal balloon control and supraceliac aortic cross-clamping, thoracic endovascular aortic repair, the Provisional Extension to Induce Complete Attachment (PETTICOAT) technique, the Knickerbocker technique, the STABILISE technique, the candy-plug technique, and mechanical thrombectomy in the pulmonary artery were all successfully performed on these models.

Conclusions

Cadaveric models have become increasingly important in vascular surgery training, providing realistic environments for procedural practice and team-based learning, with ongoing improvements to enhance their applicability and use. The life-like simulation allows trainees to learn the intricacies of each procedure that may not be thoroughly discussed during real clinical scenarios.
目的为建立人体模型提供一种方法,并详细介绍血管外科教学中使用的各种人体模型。方法首先用诊断性血管造影对尸体的血管解剖进行评估,以确保在创建尸体训练模型时使用的充分性。通过开放入路进入左颈总动脉,通过经皮入路进入左股总动脉,建立电动泵的脉动血流。然后创建了训练各种常见血管手术程序的模型。住院医生自己也参与了模型的创建,以最大限度地提高教学效果。结果建立的模型包括血管造影模型、肾下腹主动脉瘤模型、腹主动脉瘤破裂模型、B型主动脉夹层模型和肺栓塞模型,均具有模拟正常动脉血流动力学的搏动性。血管造影、血管内动脉瘤修复、完全近端球囊控制和腹腔上主动脉交叉夹紧、胸段血管内主动脉修复、临时延伸诱导完全附着(PETTICOAT)技术、Knickerbocker技术、稳定技术、糖塞技术、机械肺动脉取栓等均在这些模型上成功实施。结论三维模型在血管外科培训中的作用越来越重要,为程序实践和团队学习提供了逼真的环境,并不断改进,以提高其适用性和实用性。逼真的模拟允许受训者学习每个程序的复杂性,在真实的临床场景中可能不会被彻底讨论。
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引用次数: 0
Artificial intelligence assessment of the jugular venous pulse from ultrasound high-resolution B-mode clips: A proof of concept 高分辨率b型超声片段颈静脉脉搏的人工智能评估:概念验证
Pub Date : 2026-01-01 DOI: 10.1016/j.jvsvi.2025.100349
Paolo Zamboni MD , Anselmo Pagani MSc , Giulia Baldazzi MD , Saverio Farsoni MSc, PhD , Pietro Busi MD , Chiara Marchesin MD , Antonino Proto MSc , Alessandro Bertagnon MSc, PhD

Objective

The jugular venous pulse (JVP) is a pivotal clinical parameter that currently can only be invasively measured through jugular catheterization and subsequent central venous pressure measurement. The ultrasound B-mode clip of the internal jugular vein cross-sectional area modifications allows to build a JVP curve that significantly correlates with the central venous pressure. However, this process is time-consuming and not suitable for clinical use. The aim of the present study is to verify whether artificial intelligence (AI) allows a rapid and reliable JVP waveform assessment as compared with a human operator.

Methods

High-resolution B-mode internal jugular vein clips (558 frames) of a cohort of six human subjects have been blindly analysed in post-processing by three different researchers and a neural network. Agreement was quantified using two complementary measures: Dice similarity coefficient (Dice) and the Hausdorff distance at the 95th percentile (HD95). Furthermore, a noninferiority test was performed comparing the model with the human raters. The null hypothesis (H0) was that the model performs worse than human raters by at least Δ = 0.055 Dice, a difference that is considered clinically negligible.

Results

The average processing time per frame was 19.80 ± 5.08 seconds for human operators, compared with 0.03404 seconds ± 0.01806 seconds for the AI model running on a standard consumer-grade laptop. This represents a difference of nearly three orders of magnitude (a difference that could be quantitatively described as 580 times faster). Agreement between human raters was very high, with median Dice 0.959 (95% confidence interval, 0.958-0.960). Agreement between the model and each rater was slightly lower, with a median Dice of approximately 0.907 (95% confidence interval, 0.904-0.909). Human raters had median HD95 values of <5 pixels, reflecting very small boundary differences. The model-vs-rater comparisons showed somewhat higher HD95 values, with medians or approximately 8 to 10 pixels, but still within a clinically acceptable range given the resolution of the images. The Wilcoxon paired test rejected the null hypothesis H0 (P = .004169), showing that the model is not inferior to human raters within this clinically acceptable margin.

Conclusions

Our study demonstrates an amazing time efficiency of the entire AI segmentation process, with a precision quite comparable with the human researchers' assessment. Our findings, in perspective, support the clinical introduction of ultrasound AI JVP waveform assessment in a variety of potentially interested medical specialties, including cardiology, critical care, neurosciences, and vascular surgery.
目的颈静脉脉冲(JVP)是一项关键的临床参数,目前只能通过颈静脉导管插入和随后的中心静脉压测量来测量。b型超声对颈内静脉横截面积的修改可以建立与中心静脉压显著相关的JVP曲线。但该方法耗时长,不适合临床使用。本研究的目的是验证与人类操作员相比,人工智能(AI)是否允许快速可靠的JVP波形评估。方法对6名受试者的558帧高分辨率b模式颈内静脉片段进行了后处理,由3位不同的研究者和神经网络进行了盲法分析。一致性使用两个互补的度量来量化:Dice相似系数(Dice)和第95百分位的Hausdorff距离(HD95)。此外,将该模型与人类评分者进行了非劣效性检验。零假设(H0)是该模型的表现比人类评分者差至少Δ = 0.055 Dice,这一差异在临床上被认为可以忽略不计。结果人工操作平均每帧处理时间为19.80±5.08秒,而在标准消费级笔记本电脑上运行的人工智能模型平均每帧处理时间为0.03404±0.01806秒。这表示了近三个数量级的差异(可以用快580倍来定量描述这种差异)。人类评分者之间的一致性非常高,Dice的中位数为0.959(95%置信区间为0.958-0.960)。模型与每个评分者之间的一致性略低,Dice的中位数约为0.907(95%置信区间为0.904-0.909)。人类评分者的HD95中位数为5像素,反映了非常小的边界差异。模型与评分者的比较显示HD95值略高,中位数约为8至10像素,但考虑到图像的分辨率,仍在临床可接受的范围内。Wilcoxon配对检验拒绝原假设H0 (P = 0.004169),表明该模型在临床可接受的范围内并不逊于人类评分者。我们的研究证明了整个人工智能分割过程具有惊人的时间效率,其精度与人类研究人员的评估相当。从这个角度来看,我们的研究结果支持在各种潜在感兴趣的医学专业(包括心脏病学、重症监护、神经科学和血管外科)中临床引入超声AI JVP波形评估。
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引用次数: 0
Quality of life among patients with carotid body tumors in a retrospective matched-pair observational study 颈动脉体肿瘤患者生活质量的回顾性配对观察研究
Pub Date : 2026-01-01 DOI: 10.1016/j.jvsvi.2025.100328
Hoda Alimohamad MD , Wienand A. Omta MSc, PhD , Maaike Verheij BSc , Jeroen Jansen MD, PhD , Jaap F. Hamming MD, PhD , Abbey Schepers MD, PhD

Background

The quality of life (QoL) in patients with head and neck paragangliomas, including carotid body tumors (CBTs), is known to be reduced. Currently, there are only a few studies performed on the QoL among patients diagnosed with CBTs during follow-up and after surgery.

Objective

This study aims to assess QoL in patients with CBT in follow-up and after surgery and to compare both groups with a control group.

Methods

In this retrospective study, patients with CBT who underwent surgery were matched using Euclidean distance scoring with patients in follow-up based on age, gender, tumor size, tumor laterality, and follow-up duration. All matched patients completed the World Health Organization Quality of Life-Brief, Sickness Impact Profile 68, and Short-Form Survey-36 questionnaires. A control group was recruited through an open online survey distributed via public channels.

Results

No statistically significant QoL differences were found between resected and non-resected patients with CBT. Comparing non-resected, resected, and control groups, the Short-Form Health Survey-36 showed significant differences in physical function, role-physical, and general health (P = .00). The Sickness Impact Profile 68 indicated a significant difference in mobility between resected and control groups, and the World Health Organization Quality of Life-Brief showed a significant difference in physical function (P < .02). Comorbidities and postoperative complications may contribute to reduced QoL in this population.

Conclusions

No significant QoL differences between matched patients with CBT in follow-up and those who underwent resection. Both groups had lower QoL compared with controls in the subscales for physical function, role-physical, and general health. These findings suggest a personalized approach may be more appropriate than assuming surgery improves QoL.
研究背景头颈部副神经节瘤患者的生活质量(QoL),包括颈动脉体肿瘤(CBTs),已知会降低。目前,对诊断为cbt的患者随访期间和术后生活质量的研究较少。目的评价CBT患者术后随访的生活质量,并与对照组进行比较。方法在本回顾性研究中,基于年龄、性别、肿瘤大小、肿瘤侧边性和随访时间,采用欧氏距离评分法将接受CBT手术的患者与随访患者进行匹配。所有匹配的患者都完成了世界卫生组织生活质量简介、疾病影响概况68和简短调查问卷36。通过公开的在线调查招募了一个对照组。结果CBT手术切除与未手术切除患者的生活质量差异无统计学意义。与未切除组、切除组和对照组相比,简短健康调查-36显示身体功能、角色-身体和一般健康状况有显著差异(P = .00)。疾病影响概况68显示切除组和对照组之间的活动能力有显著差异,世界卫生组织生活质量简报显示身体功能有显著差异(P < .02)。合并症和术后并发症可能导致该人群生活质量降低。结论配合CBT治疗的患者与手术切除患者的生活质量无显著差异。与对照组相比,两组在身体功能、角色-身体和一般健康的子量表上的生活质量都较低。这些发现表明,个性化的方法可能比假设手术可以改善生活质量更合适。
{"title":"Quality of life among patients with carotid body tumors in a retrospective matched-pair observational study","authors":"Hoda Alimohamad MD ,&nbsp;Wienand A. Omta MSc, PhD ,&nbsp;Maaike Verheij BSc ,&nbsp;Jeroen Jansen MD, PhD ,&nbsp;Jaap F. Hamming MD, PhD ,&nbsp;Abbey Schepers MD, PhD","doi":"10.1016/j.jvsvi.2025.100328","DOIUrl":"10.1016/j.jvsvi.2025.100328","url":null,"abstract":"<div><h3>Background</h3><div>The quality of life (QoL) in patients with head and neck paragangliomas, including carotid body tumors (CBTs), is known to be reduced. Currently, there are only a few studies performed on the QoL among patients diagnosed with CBTs during follow-up and after surgery.</div></div><div><h3>Objective</h3><div>This study aims to assess QoL in patients with CBT in follow-up and after surgery and to compare both groups with a control group.</div></div><div><h3>Methods</h3><div>In this retrospective study, patients with CBT who underwent surgery were matched using Euclidean distance scoring with patients in follow-up based on age, gender, tumor size, tumor laterality, and follow-up duration. All matched patients completed the World Health Organization Quality of Life-Brief, Sickness Impact Profile 68, and Short-Form Survey-36 questionnaires. A control group was recruited through an open online survey distributed via public channels.</div></div><div><h3>Results</h3><div>No statistically significant QoL differences were found between resected and non-resected patients with CBT. Comparing non-resected, resected, and control groups, the Short-Form Health Survey-36 showed significant differences in physical function, role-physical, and general health (<em>P</em> = .00). The Sickness Impact Profile 68 indicated a significant difference in mobility between resected and control groups, and the World Health Organization Quality of Life-Brief showed a significant difference in physical function (<em>P</em> &lt; .02). Comorbidities and postoperative complications may contribute to reduced QoL in this population.</div></div><div><h3>Conclusions</h3><div>No significant QoL differences between matched patients with CBT in follow-up and those who underwent resection. Both groups had lower QoL compared with controls in the subscales for physical function, role-physical, and general health. These findings suggest a personalized approach may be more appropriate than assuming surgery improves QoL.</div></div>","PeriodicalId":74034,"journal":{"name":"JVS-vascular insights","volume":"4 ","pages":"Article 100328"},"PeriodicalIF":0.0,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146173326","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
RECONSTRUCT study protocol for real-world outcomes of covered endovascular reconstruction of the aortic bifurcation using the GORE VIABAHN VBX balloon-expandable endoprosthesis to treat aortoiliac occlusive disease 重建研究方案:使用GORE VIABAHN vx球囊可扩张腔内假体治疗主动脉髂闭塞性疾病的主动脉分叉覆盖血管内重建的真实结果
Pub Date : 2026-01-01 DOI: 10.1016/j.jvsvi.2025.100342
Leigh Ann O’Banion MD , Michele Antonello MD , Hector Novoa , Rizwan Afzal , Jean Bismuth MD
Aortoiliac occlusive disease (AIOD) is a common manifestation of peripheral artery disease (PAD) and contributes substantially to global morbidity and mortality. Although open surgical repair provides durable outcomes, its risks have led to a shift toward endovascular-first strategies. The covered endovascular reconstruction of the aortic bifurcation (CERAB) technique has emerged as a promising option for complex AIOD. The objective of this manuscript is to describe the methodology of the RECONTSRUCT study, designed to evaluate the safety and effectiveness of the GORE VIABAHN VBX balloon-expandable endoprosthesis (VBX stent graft) in the CERAB procedure for AIOD. The RECONSTRUCT study is a multicenter, single-arm, retrospective study enrolling at least 158 patients across 35 sites in the United States and Europe. Data collection includes demographics, medical history, procedural details, device characteristics, and clinical follow-up from electronic health records. The primary effectiveness endpoint is 1-year primary patency, defined as uninterrupted blood flow (<50% binary restenosis) through the CERAB devices without target lesion revascularization (TLR). The primary safety endpoint is 30-day morbidity, defined as any major adverse cardiovascular event or procedure-related reintervention. Secondary endpoints include technical success, 30-day mortality, freedom from device fracture, primary assisted and secondary patency, freedom from TLR and clinically driven TLR, and overall survival. The study will provide real-world, multicenter evidence on VBX stent graft use in CERAB for AIOD. Standardized data collection with independent review and adjudication will enhance data reliability, and findings may address an important evidence gap in managing complex aortoiliac disease.
主动脉髂闭塞性疾病(AIOD)是外周动脉疾病(PAD)的常见表现,是全球发病率和死亡率的重要组成部分。尽管开放手术修复提供了持久的结果,但其风险已导致转向血管内优先策略。覆盖主动脉分叉血管内重建(CERAB)技术已成为复杂AIOD的一种很有前途的选择。本文的目的是描述重构研究的方法,旨在评估GORE VIABAHN VBX球囊可膨胀内假体(VBX支架)在CERAB手术治疗AIOD的安全性和有效性。rebuild研究是一项多中心、单臂、回顾性研究,在美国和欧洲的35个地点招募了至少158名患者。数据收集包括来自电子健康记录的人口统计、病史、程序细节、设备特征和临床随访。主要有效性终点为1年原发性通畅,定义为不间断血流(50%二元再狭窄)通过CERAB装置,无靶病变血运重建术(TLR)。主要安全终点是30天的发病率,定义为任何主要不良心血管事件或手术相关的再干预。次要终点包括技术成功、30天死亡率、无器械骨折、原发性辅助和继发性通畅、无TLR和临床驱动TLR以及总生存期。该研究将为在CERAB中使用vx支架治疗AIOD提供真实的、多中心的证据。具有独立审查和裁决的标准化数据收集将提高数据的可靠性,并且研究结果可能解决复杂主动脉髂疾病管理中的重要证据空白。
{"title":"RECONSTRUCT study protocol for real-world outcomes of covered endovascular reconstruction of the aortic bifurcation using the GORE VIABAHN VBX balloon-expandable endoprosthesis to treat aortoiliac occlusive disease","authors":"Leigh Ann O’Banion MD ,&nbsp;Michele Antonello MD ,&nbsp;Hector Novoa ,&nbsp;Rizwan Afzal ,&nbsp;Jean Bismuth MD","doi":"10.1016/j.jvsvi.2025.100342","DOIUrl":"10.1016/j.jvsvi.2025.100342","url":null,"abstract":"<div><div>Aortoiliac occlusive disease (AIOD) is a common manifestation of peripheral artery disease (PAD) and contributes substantially to global morbidity and mortality. Although open surgical repair provides durable outcomes, its risks have led to a shift toward endovascular-first strategies. The covered endovascular reconstruction of the aortic bifurcation (CERAB) technique has emerged as a promising option for complex AIOD. The objective of this manuscript is to describe the methodology of the RECONTSRUCT study, designed to evaluate the safety and effectiveness of the GORE VIABAHN VBX balloon-expandable endoprosthesis (VBX stent graft) in the CERAB procedure for AIOD. The RECONSTRUCT study is a multicenter, single-arm, retrospective study enrolling at least 158 patients across 35 sites in the United States and Europe. Data collection includes demographics, medical history, procedural details, device characteristics, and clinical follow-up from electronic health records. The primary effectiveness endpoint is 1-year primary patency, defined as uninterrupted blood flow (&lt;50% binary restenosis) through the CERAB devices without target lesion revascularization (TLR). The primary safety endpoint is 30-day morbidity, defined as any major adverse cardiovascular event or procedure-related reintervention. Secondary endpoints include technical success, 30-day mortality, freedom from device fracture, primary assisted and secondary patency, freedom from TLR and clinically driven TLR, and overall survival. The study will provide real-world, multicenter evidence on VBX stent graft use in CERAB for AIOD. Standardized data collection with independent review and adjudication will enhance data reliability, and findings may address an important evidence gap in managing complex aortoiliac disease.</div></div>","PeriodicalId":74034,"journal":{"name":"JVS-vascular insights","volume":"4 ","pages":"Article 100342"},"PeriodicalIF":0.0,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146022801","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Peroneal-only runoff after endovascular revascularization and the impact on limb salvage outcomes 血管内血管重建术后仅腓骨径流及其对肢体保留结果的影响
Pub Date : 2026-01-01 DOI: 10.1016/j.jvsvi.2025.100351
Francisco Lasanta-Gorbea MD , Jose Ortiz-Fullana MD, MPH , Sebastian Castañer-Colberg MD , Van Acevedo-Vargas MD , Jorge Martinez-Trabal MD, FACS, RPVI, FSVS , Rafael Santini-Dominguez MD, FACS, RPVI, FSVS

Background

Hispanic patients with chronic limb-threatening ischemia (CLTI) have more advanced infrapopliteal arterial disease compared with other ethnic groups. This pattern often results in fewer available target vessels for revascularization and a greater dependence on a single runoff artery to achieve limb salvage. Among the infrapopliteal vessels, the peroneal artery, typically terminating above the ankle and supplying the foot through collateral branches, has traditionally been considered the least favorable target due to its indirect contribution to pedal perfusion. This study evaluated outcomes of peroneal-only runoff after endovascular revascularization in an exclusively Hispanic CLTI cohort.

Methods

A retrospective cohort study was conducted at a tertiary medical center in Puerto Rico, including all limbs with post-revascularization arteriograms demonstrating sole peroneal artery runoff (January 2020 to July 2025). Demographics, comorbidities, and outcomes were analyzed. The primary endpoint was limb salvage; secondary outcomes included amputation-free survival (AFS), limb event-free survival (LEFS), and reintervention. The predictive utility of Rutherford classification; Wound, Ischemia, and foot Infection (WIfI) score; and Global Limb Anatomic Staging System (GLASS) staging was assessed.

Results

A total of 120 limbs from 117 Hispanic patients (median age, 74 years; 87.5% with diabetes) were included. At 1 year, limb salvage was 78.3%, AFS was 69.2%, and LEFS was 55.8%; 32.5% required reintervention. Rutherford classification, WIfI score, and GLASS stage were not significantly associated with outcomes (all P > .05). In multivariable Cox regression, no variable independently predicted major amputation. Patients with a reintervention in the first year were 2.35 times more likely to have a major amputation or death (hazard ratio, 2.35; P = .031).

Conclusions

In this high-risk Hispanic CLTI cohort, peroneal-only runoff revascularization achieved acceptable limb salvage and survival outcomes. Conventional risk stratification systems (Rutherford, WIfI, GLASS) were not good predictors of outcomes, suggesting limited utility in patients with isolated peroneal perfusion. These findings support the peroneal artery as a viable revascularization target when other tibial vessels are unavailable.
背景:西班牙裔慢性肢体威胁缺血(CLTI)患者与其他族裔相比,有更多的晚期腘下动脉疾病。这种模式通常导致可用于血运重建的靶血管较少,并且更依赖于单一的径流动脉来实现肢体保留。在腘下血管中,腓动脉通常终止于踝关节以上,并通过侧支供应足部,由于其间接贡献足部灌注,传统上被认为是最不利的目标。本研究评估了西班牙裔CLTI队列中血管内血管重建术后仅腓骨径流的结果。方法在波多黎各的一家三级医疗中心进行了一项回顾性队列研究,包括所有血管重建术后动脉造影显示腓骨动脉径流的肢体(2020年1月至2025年7月)。分析了人口统计学、合并症和结果。主要终点是肢体保留;次要结局包括无截肢生存期(AFS)、肢体无事件生存期(LEFS)和再干预。卢瑟福分类的预测效用;伤口、缺血和足部感染(WIfI)评分;评估整体肢体解剖分期系统(GLASS)分期。结果117例西班牙裔患者(中位年龄74岁,糖尿病患者占87.5%)共纳入120条肢体。1年时肢体保留率为78.3%,AFS为69.2%,LEFS为55.8%;32.5%需要再干预。Rutherford分类、WIfI评分和GLASS分期与结果无显著相关(均P >; 0.05)。在多变量Cox回归中,没有变量独立预测主要截肢。第一年再次干预的患者发生主要截肢或死亡的可能性是前者的2.35倍(风险比,2.35;P = 0.031)。结论:在这个高风险的西班牙裔CLTI队列中,仅腓骨径流血运重建术获得了可接受的肢体挽救和生存结果。传统的风险分层系统(Rutherford, WIfI, GLASS)不能很好地预测预后,这表明在孤立腓骨灌注患者中的应用有限。这些发现支持腓动脉作为一个可行的目标,当其他胫骨血管不可用时。
{"title":"Peroneal-only runoff after endovascular revascularization and the impact on limb salvage outcomes","authors":"Francisco Lasanta-Gorbea MD ,&nbsp;Jose Ortiz-Fullana MD, MPH ,&nbsp;Sebastian Castañer-Colberg MD ,&nbsp;Van Acevedo-Vargas MD ,&nbsp;Jorge Martinez-Trabal MD, FACS, RPVI, FSVS ,&nbsp;Rafael Santini-Dominguez MD, FACS, RPVI, FSVS","doi":"10.1016/j.jvsvi.2025.100351","DOIUrl":"10.1016/j.jvsvi.2025.100351","url":null,"abstract":"<div><h3>Background</h3><div>Hispanic patients with chronic limb-threatening ischemia (CLTI) have more advanced infrapopliteal arterial disease compared with other ethnic groups. This pattern often results in fewer available target vessels for revascularization and a greater dependence on a single runoff artery to achieve limb salvage. Among the infrapopliteal vessels, the peroneal artery, typically terminating above the ankle and supplying the foot through collateral branches, has traditionally been considered the least favorable target due to its indirect contribution to pedal perfusion. This study evaluated outcomes of peroneal-only runoff after endovascular revascularization in an exclusively Hispanic CLTI cohort.</div></div><div><h3>Methods</h3><div>A retrospective cohort study was conducted at a tertiary medical center in Puerto Rico, including all limbs with post-revascularization arteriograms demonstrating sole peroneal artery runoff (January 2020 to July 2025). Demographics, comorbidities, and outcomes were analyzed. The primary endpoint was limb salvage; secondary outcomes included amputation-free survival (AFS), limb event-free survival (LEFS), and reintervention. The predictive utility of Rutherford classification; Wound, Ischemia, and foot Infection (WIfI) score; and Global Limb Anatomic Staging System (GLASS) staging was assessed.</div></div><div><h3>Results</h3><div>A total of 120 limbs from 117 Hispanic patients (median age, 74 years; 87.5% with diabetes) were included. At 1 year, limb salvage was 78.3%, AFS was 69.2%, and LEFS was 55.8%; 32.5% required reintervention. Rutherford classification, WIfI score, and GLASS stage were not significantly associated with outcomes (all <em>P</em> &gt; .05). In multivariable Cox regression, no variable independently predicted major amputation. Patients with a reintervention in the first year were 2.35 times more likely to have a major amputation or death (hazard ratio, 2.35; <em>P</em> = .031).</div></div><div><h3>Conclusions</h3><div>In this high-risk Hispanic CLTI cohort, peroneal-only runoff revascularization achieved acceptable limb salvage and survival outcomes. Conventional risk stratification systems (Rutherford, WIfI, GLASS) were not good predictors of outcomes, suggesting limited utility in patients with isolated peroneal perfusion. These findings support the peroneal artery as a viable revascularization target when other tibial vessels are unavailable.</div></div>","PeriodicalId":74034,"journal":{"name":"JVS-vascular insights","volume":"4 ","pages":"Article 100351"},"PeriodicalIF":0.0,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146022898","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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JVS-vascular insights
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