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Wake up! This is the 21st century! 醒醒吧!这是21世纪!
Pub Date : 2025-09-30 DOI: 10.1016/j.jvsvi.2025.100308
Darwin Eton MD, FACS, DFSVS
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引用次数: 0
Popliteal artery adventitial disease: A case report and understanding the pathophysiology and management 腘动脉外膜病变1例,病理生理及治疗体会
Pub Date : 2025-01-01 DOI: 10.1016/j.jvsvi.2025.100221
Dirk A. Le Roux MBChB(Pret), FCS(SA), CVS(SA) , Pradeep P. Mistry MBChB(Pret), MMed Surgery(Pret), FCS(SA), CVS(SA) , Lewis J. Levien MBBCh, FCS(SA), PhD(MED) , Hideaki Obara MD, PhD , Rahul Agarwal MBBS, DNB(General Surgery), DrNB(Vascular Surgery)
Popliteal artery adventitial disease (PAAD) underlies a significant portion of vascular conditions of the lower extremities, often culminating in critical limb ischemia and warranting a greater clinical understanding for effective management. Characterized by the cystic degeneration of the adventitia of the popliteal artery, PAAD remains a challenging condition both in terms of diagnosis and treatment. This review seeks to explore the complex pathophysiology, diagnostic criteria, and current management strategies, as well as discussing emerging therapies and future outlook for patients with PAAD.
腘动脉外膜疾病(PAAD)是下肢血管疾病的重要组成部分,通常以严重肢体缺血为高潮,需要更好的临床理解以进行有效的治疗。PAAD以腘动脉外膜囊性变性为特征,在诊断和治疗方面仍然是一个具有挑战性的疾病。本文旨在探讨复杂的病理生理学、诊断标准和当前的管理策略,并讨论新的治疗方法和未来对PAAD患者的展望。
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引用次数: 0
Role of private equity in vascular care 私募股权在血管护理中的作用
Pub Date : 2025-01-01 DOI: 10.1016/j.jvsvi.2025.100223
Bhagwan Satiani MD, MBA, DFSVS, FACHE, FACS , Jessica L. Bailey–Wheaton JD , Todd A. Zigrang MBA, MHA, FACHE, CVA, ASA , Hiranya A. Rajasinghe MD, FACS

Objective

Private Equity (PE) investors have been rapidly expanding their presence in the health care industry, including investments in physician practices, asserting that this will benefit patients, physicians, and the health care system.

Methods

We summarize the literature related to PE partnering with physicians, discuss the pros and cons, illustrate the financial implications through a case study, and offer glimpses into the future clouded by governmental pushback.

Results

In a time of increasing regulatory burdens and decreasing reimbursement, PE offers vascular surgeons (VS) options for private practice, and corporate employment. PE contends that this relationship adds value by reducing inefficiencies and waste, and the capital infusion allows procurement of the latest technology and tools for better outcomes. Furthermore, PE management will negotiate with insurance companies to increase reimbursement, manage human resources tasks, billing, and accounting and allow the VS to concentrate on quality patient care. Management will also prepare the practice for new models of care (eg, whether value-based reimbursement or accountable care organizations). PE projects to expand market share and have VS partners share profits, based on a formula, when the entity is later sold to another buyer in the future.

Conclusions

Although there may be some advantages for VS to partner with PE entities, it may not be ideal for all career stages and requires considerable expertise in negotiations and vigilance for unfavorable regulatory actions.
私募股权(PE)投资者一直在迅速扩大他们在医疗保健行业的存在,包括对医生实践的投资,声称这将使患者、医生和医疗保健系统受益。方法我们总结了与PE与医生合作的相关文献,讨论了利弊,通过案例研究说明了财务影响,并提供了对政府阻力笼罩的未来的一瞥。结果在监管负担增加和报销减少的时代,PE为血管外科医生提供了私人执业和企业就业的选择。PE认为,这种关系通过减少低效率和浪费来增加价值,并且资本注入允许采购最新技术和工具以获得更好的结果。此外,私募股权管理层将与保险公司谈判,以增加报销,管理人力资源任务,计费和会计,并允许私募股权公司专注于高质量的患者护理。管理层还将为新的护理模式(例如,无论是基于价值的报销还是负责任的护理组织)的实践做好准备。PE项目扩大市场份额,并根据公式让VS合伙人分享利润,当实体在未来出售给另一个买家时。尽管VS与PE实体合作可能有一些优势,但这可能不是所有职业阶段的理想选择,并且需要在谈判方面具有相当的专业知识,并对不利的监管行动保持警惕。
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引用次数: 0
Spontaneous superior mesenteric artery dissection due to idiopathic large vessel vasculitis-report of a case and review of the literature 特发性大血管炎所致自发性肠系膜上动脉夹层1例报告及文献复习
Pub Date : 2025-01-01 DOI: 10.1016/j.jvsvi.2025.100224
Natarajan Sekar MS, MNAMS, MCh (Vascular Surgery), DSc, FRCS (Glas) , Rohit Mehra MS, DrNB (Peripheral vascular Surgery), FACS , Prem Chand Gupta MS

Background

Spontaneous isolated superior mesenteric artery dissection (SISMAD) is defined as superior mesenteric artery (SMA) dissection without the presence of aortic dissection. SISMAD can be asymptomatic or present with acute abdominal pain. Diagnosis is usually by computed tomography angiography (CTA). The exact etiology of SISMAD is not known. Atherosclerosis, hypertension, and high convexity of SMA have been implicated in the development of SISMAD. The majority can be managed by conservative measures. Endovascular stenting is advised when medical management fails. Open surgery has a limited role in this condition. Nonspecific large vessel vasculitis can cause inflammation around the visceral aorta, celiac artery, and SMA, leading to dissection in these vessels. Recognizing mesenteric artery vasculitis as a potential cause of abdominal pain can be challenging. Usually, they show only elevated nonspecific inflammatory markers and no features of systemic vasculitis. Addition of steroids can help to resolve the inflammation and avoid unnecessary intervention.

Methods

We are reporting here of a successful conservative management of a 55-year-old male patient with SISMAD due to isolated large vessel vasculitis involving the SMA. He had no systemic vasculitis, and the CTA showed typical features of SMA vasculitis and dissection. In addition to traditional medical management, he was given an infusion of methyl prednisolone followed by oral steroids.

Results

He had complete relief of symptoms and was discharged after 5 days. Follow-up CTA showed flow in the true lumen though the true lumen showed stenosis.

Conclusions

Isolated mesenteric artery vasculitis without systemic involvement is rarely reported in the literature, which can be the cause for dissection not being recognized. Patients diagnosed with SISMAD should undergo routine checks for inflammatory markers and vasculitis. If the markers are high, steroids may be added to the conservative measures to reduce the inflammation, which can help in remodeling of the SMA and thereby improving the outcome. The majority of patients with SISMAD could be initially managed by medical treatment. Persistent pain and fear of missing the diagnosis of bowel ischemia have been the most important causes for early conversion to intervention. The addition of a short course of steroids, especially for those with elevated inflammatory markers, can help in early resolution of the inflammation with relief of pain. This would help to avoid unnecessary intervention.
自发性孤立性肠系膜上动脉夹层(SISMAD)被定义为肠系膜上动脉(SMA)夹层,但不存在主动脉夹层。SISMAD可无症状或伴有急性腹痛。诊断通常通过计算机断层血管造影(CTA)。SISMAD的确切病因尚不清楚。动脉粥样硬化、高血压和SMA的高凸度与SISMAD的发展有关。大多数人可以通过保守措施来管理。当医疗管理失败时,建议血管内支架植入术。在这种情况下,开放手术的作用有限。非特异性大血管炎可引起内脏主动脉、腹腔动脉和SMA周围的炎症,导致这些血管剥离。认识到肠系膜动脉血管炎是腹痛的潜在原因是具有挑战性的。通常,它们仅表现为非特异性炎症标志物升高,而无全身性血管炎的特征。添加类固醇可以帮助消除炎症,避免不必要的干预。方法:我们在此报告一例55岁男性患者,因孤立性大血管炎累及SMA,成功地进行了保守治疗。无全身性血管炎,CTA显示典型的SMA血管炎及夹层特征。除了传统的医疗管理外,他被给予甲基强的松龙输注,然后口服类固醇。结果患者症状完全缓解,5天后出院。随访CTA显示真管腔有血流,但真管腔狭窄。结论单纯性肠系膜动脉血管炎不累及全身的病例在文献中很少报道,这可能是未被识别的解剖原因。被诊断为SISMAD的患者应接受炎症标志物和血管炎的常规检查。如果标记物较高,可以在保守治疗中加入类固醇以减少炎症,这有助于SMA的重塑,从而改善预后。大多数SISMAD患者最初可以通过药物治疗来控制。持续的疼痛和害怕错过肠缺血的诊断是早期转向干预的最重要原因。添加短期类固醇治疗,特别是对于那些炎症标志物升高的患者,可以帮助早期解决炎症并减轻疼痛。这将有助于避免不必要的干预。
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引用次数: 0
Ex vivo evaluation of the clinical performance of an elastic crepe or support bandage for the treatment of varicose veins 弹性绉或支撑绷带治疗静脉曲张临床性能的体外评价
Pub Date : 2025-01-01 DOI: 10.1016/j.jvsvi.2025.100226
Rathnaganpathi Thulasikumar Dr med , Manoj Prabakar Ravichandran Dr med , Ferdinand Tamoue PhD , Thulasikumar Ganapathy Dr med

Background

Varicose vein is a progressive disease that does not have remission except after pregnancy and delivery. It is a type of venous insufficiency that presents with dilated, tortuous, elongated veins owing to the permanent loss of the valvular efficiency. The aim of the study is to demonstrate the health care professionals can consistently achieve a sub-bandage interface pressure of 30 ± 10 mm Hg using an Elastic Crepe Bandage, ECB-394, or its derivatives, which has similar viscoelastic properties, to treat patients with varicose veins.

Methods

This study was conducted among the varicose vein patients attending Sree Parthas Multispecialty Hospital and the Department of Vascular Surgery over a period of 3 months. Patients were screened for the study from November 2023 to February 2024. Based on the inclusion and exclusion criteria, study participants were recruited. The final sample size was 35. Demographic details were recorded. Sub-bandage pressure was measured with the Pico Press sensor. The data collected were entered in Excel Sheet and analysis were done by SPSS 23. A P value of less than .05 was considered as statistically significant.

Results

The mean age of the study participants was 42.37 ± 12.09 years, with a minimum age of 22 years and a maximum of 72 years. Males were predominant in our study, accounting for 27 participants (77.1%). Systemic hypertension, present in six patients (17.1%), was the most common comorbidity. A statistically significant difference was observed between the initial and final pressure measurements. Compliance and safety were found to be 100% among the study participants. Efficacy was observed in 80% of the participants, although adherence was only noted in 60%.

Conclusions

The study demonstrates the effectiveness and safety of the intervention, with a high compliance rate and a statistically significant improvement in pressure outcomes. However, adherence remains a key area for further improvement.
背景:静脉曲张是一种进行性疾病,除非在怀孕和分娩后才有缓解。这是一种静脉功能不全的类型,由于瓣膜效率的永久丧失,静脉扩张,扭曲,拉长。本研究的目的是证明医疗保健专业人员可以使用弹性皱纹绷带(ECB-394)或其衍生物(具有类似的粘弹性特性)持续地达到30±10毫米汞柱的绷带界面压力,以治疗静脉曲张患者。方法本研究对在Sree Parthas多专科医院血管外科就诊的静脉曲张患者进行为期3个月的研究。患者从2023年11月到2024年2月进行了研究筛选。根据纳入和排除标准,招募研究参与者。最终样本量为35。记录了人口统计细节。用Pico Press传感器测量绷带下压力。收集的数据在Excel表格中输入,并使用SPSS 23进行分析。P值小于0.05认为有统计学意义。结果研究对象平均年龄42.37±12.09岁,最小年龄22岁,最大年龄72岁。男性在我们的研究中占主导地位,占27名参与者(77.1%)。6例患者(17.1%)出现全身性高血压,是最常见的合并症。在初始和最终压力测量之间观察到统计学上显著的差异。研究参与者的依从性和安全性均为100%。80%的参与者观察到疗效,尽管只有60%的参与者注意到依从性。结论本研究证明了干预的有效性和安全性,依从率高,压力结局有统计学意义上的改善。然而,依从性仍然是进一步改善的关键领域。
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引用次数: 0
Plumber, scientist, entrepreneur, teacher: can one really do all? 水管工、科学家、企业家、教师:一个人真的能做到一切吗?
Pub Date : 2025-01-01 DOI: 10.1016/j.jvsvi.2024.100169
Trisha L. Roy MD, PhD
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引用次数: 0
0.35-mm lead-equivalent aprons provide similar protection to interventionalists compared to 0.5-mm lead-equivalent aprons during fluoroscopically guided interventions 在透视引导下,0.35毫米铅当量围圈与0.5毫米铅当量围圈相比,为介入治疗人员提供了类似的保护
Pub Date : 2025-01-01 DOI: 10.1016/j.jvsvi.2024.100154
Antonio Solano MD , Alejandro Pizano MD , Bala Ramanan MBBS, MS , Michael C. Siah MD , Khalil Chamseddin MD , Gerardo Gonzalez-Guardiola MD , Vivek Prakash MD , Michael Shih MD , M. Shadman Baig MD , Carlos H. Timaran MD , Jeffrey Guild PhD , Melissa L. Kirkwood MD

Objective

Protective garments are part of the routine radiation safety equipment used during fluoroscopically guided interventions (FGIs). New elements and lead equivalences have been introduced by manufacturers, which may influence protection for interventionalists from ionizing radiation. We sought to determine the performance of different lead-equivalent apron vests during FGIs in clinical and simulated scenarios.

Methods

Our primary endpoint was to evaluate the effectiveness of radiation dose attenuation of two different protective leaded apron vests, one with nominal 0.5-mm lead equivalence and a second with 0.35-mm lead equivalence, which were evaluated in clinical and simulated settings. In the clinical setting, optically stimulated luminescence nanoDot™ detectors were placed at the upper outer quadrant (UOQ) chest wall (CW) position, both over and under the apron vests on one vascular surgeon performing FGIs over a 21-month period. All interventions were performed in hybrid rooms with Allura Clarity (Phillips Healthcare) C-arms with state of-the-art software for vessel navigation, digital subtraction angiography, digital magnification, and collimation. Dosimeters were placed on either side of the primary operator’s body, located on the side closest to the X-ray source. In the simulation, fluorography was performed on a 30-inch-thick acrylic scatter phantom at 68, 80, 100, and 120 kVp for an exposure of 2000 mGy reference air kerma. Experiments were performed on the 0.35-mm and 0.5-mm lead-equivalent aprons. Paired Wilcoxon, χ2, and analysis of variance tests were performed to identify statistical significance of radiation attenuation dose rates.

Results

Operator UOQ CW radiation dose was measured during 32 FGIs: 16 were performed with the 0.5-mm lead-equivalent apron and 16 with the 0.35-mm lead-equivalent apron. Median procedure reference air kerma was 167 mGy (interquartile range, 99-437 mGy) when the 0.5-mm apron vest was worn vs 250 mGy (interquartile range, 144-410 mGy) with the 0.35-mm vest. There was no significant difference in UOQ CW radiation dose attenuation between the two lead equivalencies: thick 89% vs thin 86%; P = .2. In the simulated scenario, radiation dose attenuation was similar for all measured kVp, with no significant differences for both apron vests (94% thick vs 95% thin; P = .49).

Conclusions

Heavier leaded aprons do not offer clinically significant increased protection over thinner lead. Due to the long-term musculoskeletal strain on interventionalists, it is safe to consider lightweight lead protection.
目的防护服是荧光透视引导干预(FGIs)中常规辐射安全设备的一部分。制造商引入了新的元素和铅当量,这可能会影响对介入人员的电离辐射保护。我们试图在临床和模拟场景中确定不同铅当量围裙背心在fgi中的性能。方法本研究的主要终点是评估两种不同的铅围裙防护背心的辐射剂量衰减效果,一种是标称的0.5 mm铅当量,另一种是0.35 mm铅当量,并在临床和模拟环境中进行评估。在临床环境中,在21个月的时间里,将光刺激发光nanoDot™探测器放置在一名血管外科医生进行fgi的上外象限(UOQ)胸壁(CW)位置,在围裙背心上方和下方。所有干预均在混合室进行,采用Allura Clarity (Phillips Healthcare) c型臂,配备最先进的血管导航、数字减影血管造影、数字放大和准直软件。剂量计放置在主要操作者身体的两侧,位于最靠近x射线源的一侧。在模拟中,对30英寸厚的丙烯酸散射模体在68、80、100和120 kVp下进行荧光成像,暴露于2000 mGy的参考空气克玛。实验分别在0.35 mm和0.5 mm铅当量围裙上进行。采用配对Wilcoxon、χ2和方差分析检验确定辐射衰减剂量率的统计学意义。结果测量32例fgi过程中操作者UOQ连续辐射剂量,其中16例使用0.5 mm铅当量围裙,16例使用0.35 mm铅当量围裙。穿0.5 mm围裙背心时的中位手术参考空气当量为167 mGy(四分位数范围,99-437 mGy),而穿0.35 mm围裙背心时的中位手术参考空气当量为250 mGy(四分位数范围,144-410 mGy)。两种铅当量在UOQ连续辐射剂量衰减方面无显著差异:厚铅89% vs薄铅86%;p = .2。在模拟情景中,辐射剂量衰减对所有测量的kVp都是相似的,两种围裙背心没有显著差异(94%厚vs 95%薄;p = .49)。结论含铅护圈与薄铅护圈相比,在临床上并没有明显的保护作用。由于介入治疗者长期的肌肉骨骼劳损,考虑轻量铅保护是安全的。
{"title":"0.35-mm lead-equivalent aprons provide similar protection to interventionalists compared to 0.5-mm lead-equivalent aprons during fluoroscopically guided interventions","authors":"Antonio Solano MD ,&nbsp;Alejandro Pizano MD ,&nbsp;Bala Ramanan MBBS, MS ,&nbsp;Michael C. Siah MD ,&nbsp;Khalil Chamseddin MD ,&nbsp;Gerardo Gonzalez-Guardiola MD ,&nbsp;Vivek Prakash MD ,&nbsp;Michael Shih MD ,&nbsp;M. Shadman Baig MD ,&nbsp;Carlos H. Timaran MD ,&nbsp;Jeffrey Guild PhD ,&nbsp;Melissa L. Kirkwood MD","doi":"10.1016/j.jvsvi.2024.100154","DOIUrl":"10.1016/j.jvsvi.2024.100154","url":null,"abstract":"<div><h3>Objective</h3><div>Protective garments are part of the routine radiation safety equipment used during fluoroscopically guided interventions (FGIs). New elements and lead equivalences have been introduced by manufacturers, which may influence protection for interventionalists from ionizing radiation. We sought to determine the performance of different lead-equivalent apron vests during FGIs in clinical and simulated scenarios.</div></div><div><h3>Methods</h3><div>Our primary endpoint was to evaluate the effectiveness of radiation dose attenuation of two different protective leaded apron vests, one with nominal 0.5-mm lead equivalence and a second with 0.35-mm lead equivalence, which were evaluated in clinical and simulated settings. In the clinical setting, optically stimulated luminescence nanoDot™ detectors were placed at the upper outer quadrant (UOQ) chest wall (CW) position, both over and under the apron vests on one vascular surgeon performing FGIs over a 21-month period. All interventions were performed in hybrid rooms with Allura Clarity (Phillips Healthcare) C-arms with state of-the-art software for vessel navigation, digital subtraction angiography, digital magnification, and collimation. Dosimeters were placed on either side of the primary operator’s body, located on the side closest to the X-ray source. In the simulation, fluorography was performed on a 30-inch-thick acrylic scatter phantom at 68, 80, 100, and 120 kVp for an exposure of 2000 mGy reference air kerma. Experiments were performed on the 0.35-mm and 0.5-mm lead-equivalent aprons. Paired Wilcoxon, χ<sup>2</sup>, and analysis of variance tests were performed to identify statistical significance of radiation attenuation dose rates.</div></div><div><h3>Results</h3><div>Operator UOQ CW radiation dose was measured during 32 FGIs: 16 were performed with the 0.5-mm lead-equivalent apron and 16 with the 0.35-mm lead-equivalent apron. Median procedure reference air kerma was 167 mGy (interquartile range, 99-437 mGy) when the 0.5-mm apron vest was worn vs 250 mGy (interquartile range, 144-410 mGy) with the 0.35-mm vest. There was no significant difference in UOQ CW radiation dose attenuation between the two lead equivalencies: thick 89% vs thin 86%; <em>P</em> = .2. In the simulated scenario, radiation dose attenuation was similar for all measured kVp, with no significant differences for both apron vests (94% thick vs 95% thin; <em>P</em> = .49).</div></div><div><h3>Conclusions</h3><div>Heavier leaded aprons do not offer clinically significant increased protection over thinner lead. Due to the long-term musculoskeletal strain on interventionalists, it is safe to consider lightweight lead protection.</div></div>","PeriodicalId":74034,"journal":{"name":"JVS-vascular insights","volume":"3 ","pages":"Article 100154"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143135728","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Systematic review and meta-analysis of cardiovascular events after endovascular aneurysm repair vs open surgical repair 血管内动脉瘤修复与开放手术修复后心血管事件的系统回顾和荟萃分析
Pub Date : 2025-01-01 DOI: 10.1016/j.jvsvi.2025.100208
Catherine Boudreau MD , Graham McClure MD, MSc , Julien D’Astous MD , Kamil Polok MD, PhD , Jakub Fronczek MD, PhD , Augustin Toma MD , Stephen Yang MD, MSc , Fadi Elias MD, MSc , Wojciech Szczeklik MD, PhD , Emmanuelle Duceppe MD, PhD

Objective

Randomized controlled trials (RCTs) have shown a reduction in short-term mortality with endovascular aneurysm repair (EVAR) compared with open surgical repair (OSR) but failed to demonstrate a long-term mortality advantage. Our study aims to determine whether this loss of mortality benefit could be attributed to differences in cardiovascular events.

Methods

We searched MEDLINE, PubMed, Embase, and Web of Science for RCTs comparing EVAR and OSR for abdominal aortic aneurysm treatment. Title and abstracts, full texts, and study quality were assessed by two independent reviewers. Risk of bias was assessed using the Cochrane Collaboration tool for RCTs. Pooled risk ratios (RR) with 95% confidence intervals (CI) were calculated using the random-effects method, and heterogeneity was assessed using the I2 statistics.

Results

Our search identified 5204 manuscripts, of which 99 full texts were screened, and 40 manuscripts included. Nine individual RCTs met the eligibility criteria. Inter-rater agreement was excellent for final study inclusion (k = 0.88). Overall, the risk of bias was low. Patients treated with EVAR had a significantly lower short-term mortality (RR: 0.65, 95% CI: 0.43-0.99). The totality of evidence on cardiovascular mortality (3 studies; 1265 patients, RR: 0.61, 95% CI: 0.16-2.25) did not rule out large differences in mortality in either direction. There were no statistically significant differences in long-term all-cause mortality (6 studies; 3436 patients, RR: 1.00, 95% CI: 0.95-1.06) and cardiovascular mortality (4 studies; 3097 patients, RR 1.09, 95% CI: 0.92-1.30), although for the later, the point estimate shifted in the other direction.

Conclusions

Postoperative cardiovascular complications are frequent after abdominal aortic aneurysm repair, and most events are asymptomatic. More data are needed to inform whether the loss of mortality benefit at long-term follow-up with EVAR compared with OSR could be explained by prognostically important undetected cardiac events.
目的随机对照试验(RCT)显示,与开放性手术修复(OSR)相比,血管内动脉瘤修复(EVAR)可降低短期死亡率,但未能显示长期死亡率的优势。我们的研究旨在确定这种死亡率优势的丧失是否可归因于心血管事件的差异。方法我们检索了MEDLINE、PubMed、Embase和Web of Science中比较EVAR和OSR治疗腹主动脉瘤的RCT。由两名独立审稿人对标题和摘要、全文以及研究质量进行评估。采用 Cochrane 协作工具评估 RCT 的偏倚风险。采用随机效应法计算汇总风险比 (RR) 及 95% 置信区间 (CI),并采用 I2 统计法评估异质性。其中有 9 项研究符合资格标准。对于最终纳入的研究,评分者之间的一致性非常好(k = 0.88)。总体而言,偏倚风险较低。接受EVAR治疗的患者短期死亡率明显较低(RR:0.65,95% CI:0.43-0.99)。有关心血管死亡率的全部证据(3 项研究;1265 名患者,RR:0.61,95% CI:0.16-2.25)均不能排除死亡率存在较大差异的可能性。在长期全因死亡率(6 项研究;3 436 名患者,RR:1.00,95% CI:0.95-1.06)和心血管死亡率(4 项研究;3097 名患者,RR 1.09,95% CI:0.92-1.30)方面没有统计学意义上的显著差异,尽管后者的点估计值向另一个方向移动。需要更多的数据来说明,与OSR相比,EVAR在长期随访中丧失的死亡率益处是否可以用预后重要的未发现的心脏事件来解释。
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引用次数: 0
Aortic remodeling and survival for chronic post dissection thoracoabdominal aneurysm following physician-modified endograft 医师改良内移植术治疗慢性胸腹动脉瘤后夹层的主动脉重塑和生存率
Pub Date : 2025-01-01 DOI: 10.1016/j.jvsvi.2025.100195
Guangmin Yang MD , Yuang Jiang MD , Guangjin Gao MD , Guangyan Wu MD , Yepeng Zhang MD , Min Zhou PhD

Objective

This study aimed to evaluate the midterm outcomes of aortic remodeling, clinical results, and reinterventions following the use of physician-modified endografts (PMEGs) in patients with post dissection thoracoabdominal aneurysms (PD-TAAAs).

Methods

From January 1, 2017, to December 31, 2020, a cohort of 62 patients underwent fenestrated and branched endovascular aortic repair with PMEGs for residual type A and type B aortic dissection. The true lumen (TL) diameter and false lumen statues were assessed at four aortic levels. Data on aortic remodeling, survival rate, and reintervention were collected and analyzed.

Results

Among the 62 patients treated with PMEGs, the overall survival rate and the freedom from reintervention were 94.5% and 79.4% at 5 years, respectively. The mean TL diameter at four levels before surgery was 27.09 ± 4.65 mm, 23.16 ± 5.58 mm, 18.04 ± 4.64 mm, and 15.41 ± 6.79 mm, respectively. The mean diameter of the TL at four levels after 1-year follow-up was 29.3 ± 4.92 mm, 27.47 ± 5.46 mm, 21.79 ± 3.62 mm, and 19.10 ± 4.41 mm, respectively, showing significant increase in TL diameter at all levels (P ≤ .05). The mean follow-up was 5.09 ± 0.71 years, with an overall survival rate of 96.4% (95% confidence interval [CI], 85.9%-99.1%) at 1 year and 94.5% (95% CI, 84.0%-98.2%) at 5 years. The freedom from reintervention rate was 92.7% (95% CI, 81.8%-97.2%) at 1 year and 79.4% (95% CI, 79.4%-96.0%) at 5 years.

Conclusions

PMEGs for chronic dissection TAAAs can complete entry tears exclusion, resulting in satisfactory results. Aortic remodeling is favorable at the downstream aorta. Comprehensive pre-planning and strict follow-up protocol should be adopted to guarantee long-term outcomes.
目的:本研究旨在评估胸腹动脉瘤(pd - taaa)夹层后使用医师改良内移植物(PMEGs)后主动脉重构的中期结局、临床结果和再干预。方法2017年1月1日至2020年12月31日,62例a型和B型主动脉夹层残留患者行pmeg开窗和分支血管内主动脉修复术。在四个主动脉水平评估真管腔直径和假管腔雕像。收集并分析主动脉重塑、存活率和再干预的数据。结果62例pmeg患者5年总生存率为94.5%,无再干预率为79.4%。术前4个节段TL直径平均分别为27.09±4.65 mm、23.16±5.58 mm、18.04±4.64 mm、15.41±6.79 mm。随访1年后,4个级别的TL直径平均分别为29.3±4.92 mm、27.47±5.46 mm、21.79±3.62 mm和19.10±4.41 mm,各级别TL直径均有显著增加(P≤0.05)。平均随访5.09±0.71年,1年总生存率为96.4%(95%可信区间[CI], 85.9% ~ 99.1%), 5年总生存率为94.5% (95% CI, 84.0% ~ 98.2%)。1年无再干预率为92.7% (95% CI, 81.8%-97.2%), 5年无再干预率为79.4% (95% CI, 79.4%-96.0%)。结论spmeg对慢性夹层TAAAs可完全排除进入性撕裂,效果满意。主动脉重塑在下游主动脉是有利的。应采取全面的前期规划和严格的后续方案,以保证长期效果。
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引用次数: 0
Efficacy of minimally invasive vascular interventions assessed with mobile multispectral near-infrared spectroscopy 移动多光谱近红外光谱评估微创血管干预的疗效
Pub Date : 2025-01-01 DOI: 10.1016/j.jvsvi.2025.100216
Alisha Roberta Oropallo MD , Amit Rao MD , Jo Ann Eisinger PA , Larry Leonardi PhD

Background

The adoption of minimally invasive techniques for treating chronic venous insufficiency has surged. Techniques such as foam sclerotherapy and radiofrequency ablation (RFA) are now widely used to address incompetent great saphenous veins. Duplex ultrasound examination has become the gold standard for diagnosing venous insufficiency and evaluating the effectiveness of these treatments. However, venous reflux ultrasound studies remain some of the most time-consuming tasks to obtain.

Objective

The objective of this study was to evaluate the effectiveness of minimally invasive vascular interventions, such as foam sclerotherapy and/or RFA, using mobile multispectral near-infrared spectroscopic (NIRS) imaging. By measuring changes in tissue oxygenation (StO2) before and after treatment, this study aims to provide insights into the utility of NIRS imaging as a noninvasive tool for assessing treatment outcomes.

Methods

This quasi-experimental pre-post-test design study included 14 patients treated for chronic venous insufficiency with either foam sclerotherapy or RFA between November 2022 and February 2024. The patient population presented with significant great saphenous vein insufficiency and normal deep venous pathology, with no evidence of deep vein thrombosis or superficial vein thrombosis, except for one case with partial chronic and deep venous thrombosis. NIRS images of the lower extremities were collected before and immediately after the treatment. The images were acquired from various anatomical locations including the dorsum and plantar aspects of the foot, the medial and lateral leg, and the wound area if present.

Results

The results demonstrated a statistically significant increase in mean StO2 in lower extremities after foam sclerotherapy and RFA, indicating an improved microcirculatory function in the treated limb. These improvements in StO2 in the lower extremities were consistent with the vascular examination results, which confirmed successful vein ablation or closure.

Conclusions

The study demonstrates that NIRS imaging effectively tracks treatment-related changes, providing a noninvasive and reliable method for the real-time assessment of StO2. By visualizing changes in microcirculation, this technology offers clinicians valuable insights, enabling earlier detection of treatment success or failure and facilitating timely interventions. As such, NIRS imaging holds promise as a valuable tool in clinical practice for evaluating the efficacy of minimally invasive vascular treatments. However, the small sample size limits the ability to draw definitive conclusions.
背景微创技术在慢性静脉功能不全治疗中的应用越来越广泛。泡沫硬化疗法和射频消融(RFA)等技术现在被广泛用于治疗功能不全的大隐静脉。双重超声检查已成为诊断静脉功能不全和评估这些治疗效果的金标准。然而,静脉反流超声研究仍然是一些最耗时的任务获得。目的本研究的目的是评估微创血管干预的有效性,如泡沫硬化治疗和/或RFA,使用移动多光谱近红外光谱(NIRS)成像。通过测量治疗前后组织氧合(StO2)的变化,本研究旨在深入了解近红外成像作为评估治疗结果的无创工具的实用性。方法:这项准实验前-后试验设计研究纳入了2022年11月至2024年2月期间接受泡沫硬化疗法或RFA治疗的14例慢性静脉功能不全患者。患者总体表现为大隐静脉明显不全,深静脉病理正常,除1例部分慢性深静脉血栓形成外,无深静脉血栓形成或浅静脉血栓形成的证据。在治疗前和治疗后立即收集下肢近红外光谱图像。图像来自不同的解剖位置,包括足背和足底,腿内侧和外侧,以及伤口区域(如果存在)。结果结果显示,泡沫硬化治疗和RFA治疗后下肢平均StO2有统计学意义的增加,表明治疗后肢体微循环功能得到改善。下肢StO2的改善与血管检查结果一致,证实静脉消融或关闭成功。结论近红外成像可有效跟踪治疗相关变化,为实时评估StO2提供了一种无创、可靠的方法。通过观察微循环的变化,这项技术为临床医生提供了有价值的见解,能够更早地发现治疗的成功或失败,并促进及时的干预。因此,近红外成像有望成为临床实践中评估微创血管治疗疗效的宝贵工具。然而,样本量小限制了得出明确结论的能力。
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JVS-vascular insights
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