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Journal of Vascular Surgery Cases Innovations and Techniques最新文献

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Information for Readers
IF 0.7 Q4 SURGERY Pub Date : 2024-12-01 DOI: 10.1016/S2468-4287(24)00253-3
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引用次数: 0
Events of Interest
IF 0.7 Q4 SURGERY Pub Date : 2024-12-01 DOI: 10.1016/S2468-4287(24)00254-5
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引用次数: 0
Outcome of primary closure following carotid endarterectomy with a novel technique: An 8-year multicenter cohort study 采用新技术进行颈动脉内膜剥脱术后初次闭合的效果:一项为期 8 年的多中心队列研究
IF 0.7 Q4 SURGERY Pub Date : 2024-10-28 DOI: 10.1016/j.jvscit.2024.101662
Amir Ahmad Arabzadeh MD , Mohammadreza Kalantarmotamedi MD , Babak Sabet MD , Niki Tadayon MD
This study evaluated the safety and efficacy of a novel primary closure technique in carotid endarterectomy compared with traditional methods. Conducted over 8 years at three university hospitals, this study included 184 patients. Early complications (8.7%) included hematoma, transient ischemic attack, myocardial infarction, stroke, and death. Late complications involved myocardial infarction, death, transient ischemic attack, stroke, and reintervention. The 1-year follow-up showed a significant (>70%) restenosis rate of only 1.9%. The novel technique in carotid endarterectomy seems to be a safe and effective alternative to patch angioplasty, offering advantages for selected patients. Further studies are required.
这项研究评估了颈动脉内膜切除术中新型初级闭合技术与传统方法相比的安全性和有效性。这项研究在三所大学医院进行,历时8年,共纳入184名患者。早期并发症(8.7%)包括血肿、短暂性脑缺血发作、心肌梗死、中风和死亡。晚期并发症包括心肌梗死、死亡、短暂性脑缺血发作、中风和再次介入。1年的随访结果显示,再狭窄率仅为1.9%。颈动脉内膜切除术的新技术似乎是补片血管成形术的一种安全有效的替代方法,为特定患者提供了优势。还需要进一步研究。
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引用次数: 0
Endovascular salvage of renal and common iliac artery malperfusion following inadvertent hybrid arch dissection stent deployment in the false lumen during repair of type A dissection
IF 0.7 Q4 SURGERY Pub Date : 2024-10-28 DOI: 10.1016/j.jvscit.2024.101659
Rudra Pandya BSc , Luc Dubois MSc , Oonagh Scallan MD
This case report describes the endovascular management of a hybrid arch dissection stent inadvertently deployed in the false lumen during acute type A aortic dissection repair, resulting in renal and lower extremity malperfusion. Prompt identification and intervention are essential to minimize the morbidity and mortality associated with malperfusion. Various endovascular strategies exist to restore perfusion, and this case highlights a unique approach given the obliteration of the true lumen proximally and anatomy of the visceral ostia predominantly originating from the false lumen.
{"title":"Endovascular salvage of renal and common iliac artery malperfusion following inadvertent hybrid arch dissection stent deployment in the false lumen during repair of type A dissection","authors":"Rudra Pandya BSc ,&nbsp;Luc Dubois MSc ,&nbsp;Oonagh Scallan MD","doi":"10.1016/j.jvscit.2024.101659","DOIUrl":"10.1016/j.jvscit.2024.101659","url":null,"abstract":"<div><div>This case report describes the endovascular management of a hybrid arch dissection stent inadvertently deployed in the false lumen during acute type A aortic dissection repair, resulting in renal and lower extremity malperfusion. Prompt identification and intervention are essential to minimize the morbidity and mortality associated with malperfusion. Various endovascular strategies exist to restore perfusion, and this case highlights a unique approach given the obliteration of the true lumen proximally and anatomy of the visceral ostia predominantly originating from the false lumen.</div></div>","PeriodicalId":45071,"journal":{"name":"Journal of Vascular Surgery Cases Innovations and Techniques","volume":"11 1","pages":"Article 101659"},"PeriodicalIF":0.7,"publicationDate":"2024-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142743777","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
Endovascular repair with the Gore thoracoabdominal multibranch endoprosthesis for proximal degeneration after prior fenestrated endovascular aortic repair 使用戈尔胸腹多支主动脉内膜修复术进行血管内修复,治疗先前的栅栏式主动脉内膜修复术后的近端退变
IF 0.7 Q4 SURGERY Pub Date : 2024-10-26 DOI: 10.1016/j.jvscit.2024.101664
Lauren Cralle MD, Kathryn DiLosa MD, MPH, Steven Maximus MD
Degeneration of the thoracoabdominal aorta proximal to a prior fenestrated endovascular aortic repair represents a complex issue with limited options for repair. Previously, modified endografts or open conversion with endograft explant offered the only options for management. Here we describe use of the Gore Thoracoabdominal Multibranch Endoprosthesis for exclusion of an extent III thoracoabdominal aneurysm in the setting of degeneration proximal to a previously placed fenestrated device.
胸腹主动脉近端曾进行过开孔血管内主动脉修复术,其变性是一个复杂的问题,且修复方案有限。以前,治疗的唯一选择是改良的内移植物或通过内移植物剥离进行开放式转换。在此,我们描述了使用戈尔胸腹腔多支内支架在先前放置的开孔装置近端发生变性的情况下排除 III 度胸腹腔动脉瘤的方法。
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引用次数: 0
Hybrid repair of type A aortic dissection after infrarenal endovascular aortic repair and bilateral iliac branched grafts
IF 0.7 Q4 SURGERY Pub Date : 2024-10-26 DOI: 10.1016/j.jvscit.2024.101666
Quynh-Anh L. Dang BS, BBA , Ciaran S. O'Brien MD , William Rothstein MD , Chase Brown MD , Venkat Kalapatapu MD
Type A dissection is infrequently reported after infrarenal endovascular aortic repair (EVAR). Here, we present a case of an EVAR with iliac branch endoprosthesis complicated by type A dissection requiring ascending arch repair. After hemiarch repair, the patient was noted to have residual type B dissection, malperfusion of the left renal artery, and compression of the EVAR with left external iliac limb occlusion. These were treated successfully with iliac thrombectomy and dissection stent placement.
{"title":"Hybrid repair of type A aortic dissection after infrarenal endovascular aortic repair and bilateral iliac branched grafts","authors":"Quynh-Anh L. Dang BS, BBA ,&nbsp;Ciaran S. O'Brien MD ,&nbsp;William Rothstein MD ,&nbsp;Chase Brown MD ,&nbsp;Venkat Kalapatapu MD","doi":"10.1016/j.jvscit.2024.101666","DOIUrl":"10.1016/j.jvscit.2024.101666","url":null,"abstract":"<div><div>Type A dissection is infrequently reported after infrarenal endovascular aortic repair (EVAR). Here, we present a case of an EVAR with iliac branch endoprosthesis complicated by type A dissection requiring ascending arch repair. After hemiarch repair, the patient was noted to have residual type B dissection, malperfusion of the left renal artery, and compression of the EVAR with left external iliac limb occlusion. These were treated successfully with iliac thrombectomy and dissection stent placement.</div></div>","PeriodicalId":45071,"journal":{"name":"Journal of Vascular Surgery Cases Innovations and Techniques","volume":"11 1","pages":"Article 101666"},"PeriodicalIF":0.7,"publicationDate":"2024-10-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142743778","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
A rare case of May-Thurner syndrome due to external compression of the right and left common iliac veins
IF 0.7 Q4 SURGERY Pub Date : 2024-10-24 DOI: 10.1016/j.jvscit.2024.101658
Logan Schwarzman MD , Jack Aguilar MD , Nichelle Megowan MD
May-Thurner syndrome, also known as external iliac compression syndrome, is a rare but commonly underdiagnosed cause of asymmetric lower extremity edema. Here we describe a case of May-Thurner syndrome owing to external compression of the right and left common iliac veins presenting as chronic worsening asymmetric right greater than left lower extremity edema. Initial etiology workup was unremarkable, and further diagnostics revealed compression of the right common iliac vein at the bifurcation of the right common iliac artery between the right external and internal iliac arteries with concomitant compression of the left common iliac vein. Stenting of the right common iliac vein was completed, with significant symptomatic improvement at 30-day follow-up. This case documents a unique variant of May-Thurner syndrome rarely described in the literature.
{"title":"A rare case of May-Thurner syndrome due to external compression of the right and left common iliac veins","authors":"Logan Schwarzman MD ,&nbsp;Jack Aguilar MD ,&nbsp;Nichelle Megowan MD","doi":"10.1016/j.jvscit.2024.101658","DOIUrl":"10.1016/j.jvscit.2024.101658","url":null,"abstract":"<div><div>May-Thurner syndrome, also known as external iliac compression syndrome, is a rare but commonly underdiagnosed cause of asymmetric lower extremity edema. Here we describe a case of May-Thurner syndrome owing to external compression of the right and left common iliac veins presenting as chronic worsening asymmetric right greater than left lower extremity edema. Initial etiology workup was unremarkable, and further diagnostics revealed compression of the right common iliac vein at the bifurcation of the right common iliac artery between the right external and internal iliac arteries with concomitant compression of the left common iliac vein. Stenting of the right common iliac vein was completed, with significant symptomatic improvement at 30-day follow-up. This case documents a unique variant of May-Thurner syndrome rarely described in the literature.</div></div>","PeriodicalId":45071,"journal":{"name":"Journal of Vascular Surgery Cases Innovations and Techniques","volume":"11 1","pages":"Article 101658"},"PeriodicalIF":0.7,"publicationDate":"2024-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142743779","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
Thoracic endovascular aortic repair (TEVAR) for an acute type A aortic dissection following transcatheter aortic valve replacement (TAVR) 胸腔内血管主动脉修复术(TEVAR)治疗经导管主动脉瓣置换术(TAVR)后的急性A型主动脉夹层
IF 0.7 Q4 SURGERY Pub Date : 2024-10-24 DOI: 10.1016/j.jvscit.2024.101653
Vy C. Dang BS , Paul Haddad MD , Ross G. McFall MD , Jennifer Klopfenstein MD , Michael J. Reardon MD , Maham Rahimi MD, PhD
An 86-year-old male with multiple medical comorbidities was referred for an elective transcatheter aortic valve replacement (TAVR) for severe symptomatic aortic stenosis with an ejection fraction of 35%. A self-expanding valve was deployed successfully, but intraoperative transesophageal echocardiography (TEE) confirmed an acute type A aortic dissection (ATAAD), necessitating immediate intervention. Multiple intraoperative imaging modalities were utilized for deployment of a conformable GORE TAG (cTAG) stent graft for thoracic endovascular aortic repair (TEVAR). This case demonstrates TEVAR as an effective, minimally invasive option for immediate repair of ATAAD as a complication of TAVR in a high-risk surgical patient.
一位86岁的男性患者患有多种并发症,因射血分数为35%的严重症状性主动脉瓣狭窄而转诊接受经导管主动脉瓣置换术(TAVR)。虽然成功置入了自扩张瓣膜,但术中经食道超声心动图(TEE)确诊为急性A型主动脉夹层(ATAAD),必须立即进行干预。利用多种术中成像模式部署了可适形 GORE TAG(cTAG)支架移植物,用于胸腔内主动脉修复术(TEVAR)。该病例表明,TEVAR 是一种有效的微创选择,可立即修复高风险手术患者因 TAVR 并发症引起的 ATAAD。
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引用次数: 0
Endovascular repair and management of a ruptured inferior pancreaticoduodenal artery aneurysm: A case report and literature review 胰十二指肠下动脉瘤破裂的血管内修复和治疗:病例报告和文献综述
IF 0.7 Q4 SURGERY Pub Date : 2024-10-23 DOI: 10.1016/j.jvscit.2024.101650
Pavel Kibrik DO, Jerry Zhu BS, Ajit Rao MD, Daniel Han MD, Peter Faries MD, James Cornwall MD
Inferior pancreaticoduodenal artery aneurysm (IPDA) with the stenosis of the celiac axis is rare and may cause rupture. A unique etiology of IPDAs with celiac stenosis is median arcuate ligament syndrome. These aneurysms develop as a result of the dilation of the arteries from the retrograde blood flow into the pancreaticoduodenal arches because of celiac artery compression by the median arcuate ligament. We describe a 39-year-old man whose ruptured IPDA was associated with celiac artery stenosis and who was managed with coil embolization. The patient has agreed to have their case details and images published.
伴有腹腔轴狭窄的胰十二指肠下动脉瘤(IPDA)非常罕见,可能会导致破裂。腹腔轴狭窄的胰十二指肠动脉瘤的一个独特病因是弓状韧带正中综合征。由于腹腔动脉受到弓状韧带的压迫,血液逆流进入胰十二指肠弓导致动脉扩张,从而形成这些动脉瘤。我们描述了一名 39 岁男子的病例,他的 IPDA 破裂伴有腹腔动脉狭窄,我们对他进行了线圈栓塞治疗。患者已同意将其病例详情和图像公布于众。
{"title":"Endovascular repair and management of a ruptured inferior pancreaticoduodenal artery aneurysm: A case report and literature review","authors":"Pavel Kibrik DO,&nbsp;Jerry Zhu BS,&nbsp;Ajit Rao MD,&nbsp;Daniel Han MD,&nbsp;Peter Faries MD,&nbsp;James Cornwall MD","doi":"10.1016/j.jvscit.2024.101650","DOIUrl":"10.1016/j.jvscit.2024.101650","url":null,"abstract":"<div><div>Inferior pancreaticoduodenal artery aneurysm (IPDA) with the stenosis of the celiac axis is rare and may cause rupture. A unique etiology of IPDAs with celiac stenosis is median arcuate ligament syndrome. These aneurysms develop as a result of the dilation of the arteries from the retrograde blood flow into the pancreaticoduodenal arches because of celiac artery compression by the median arcuate ligament. We describe a 39-year-old man whose ruptured IPDA was associated with celiac artery stenosis and who was managed with coil embolization. The patient has agreed to have their case details and images published.</div></div>","PeriodicalId":45071,"journal":{"name":"Journal of Vascular Surgery Cases Innovations and Techniques","volume":"11 1","pages":"Article 101650"},"PeriodicalIF":0.7,"publicationDate":"2024-10-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142704800","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
“What can go wrong during thoracic endovascular aortic repair for type B aortic dissection” "B 型主动脉夹层胸腔内血管主动脉修补术中可能出现的问题
IF 0.7 Q4 SURGERY Pub Date : 2024-10-23 DOI: 10.1016/j.jvscit.2024.101657
Zachary Rengel MD, Gregory Magee MD, MSc, FACS, FSVS
{"title":"“What can go wrong during thoracic endovascular aortic repair for type B aortic dissection”","authors":"Zachary Rengel MD,&nbsp;Gregory Magee MD, MSc, FACS, FSVS","doi":"10.1016/j.jvscit.2024.101657","DOIUrl":"10.1016/j.jvscit.2024.101657","url":null,"abstract":"","PeriodicalId":45071,"journal":{"name":"Journal of Vascular Surgery Cases Innovations and Techniques","volume":"11 1","pages":"Article 101657"},"PeriodicalIF":0.7,"publicationDate":"2024-10-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142704797","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
期刊
Journal of Vascular Surgery Cases Innovations and Techniques
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