Pub Date : 2024-01-01DOI: 10.1016/j.ejvsvf.2024.07.012
V. Dabravolskaite ∗ , H. Hakovirta , F. Schoenhoff , D. Kotelis , V. Makaloski , M. Lescan
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Pub Date : 2024-01-01DOI: 10.1016/j.ejvsvf.2024.05.006
Alexandre Oliny , Côme Bosse , Philippe Charbonneau , Stephan Haulon , Dominique Fabre
Introduction
Acute limb ischaemia resulting from foreign body embolisation is an infrequent yet critical complication associated with vascular closure devices (VCDs). Despite the widespread use of VCDs, rare complications such as fragment emboli pose unique challenges, necessitating heightened clinical awareness. This case report presents a case of acute limb ischaemia caused by a VCD malfunction following an endovascular procedure.
Report
A 70 year old male who was diagnosed with a severe claudication of the lower extremity (Rutherford III) due to right common iliac stenosis, underwent angioplasty using a FemoSeal (Terumo Ltd., Surrey, UK) to close the right femoral artery access. Two weeks later, the patient presented with acute lower limb ischaemia due to a right popliteal–tibial occlusion. Emergency surgical thrombo-embolectomy was successfully performed from a medial popliteal approach, and the thrombus, which contained a polymer disc from the VCD at its distal end, was completely removed.
Discussion
Despite VCDs being proven safe and efficient, rare complications such as fragment emboli can occur, and physicians should be aware of the possible delayed onset of symptoms. Moreover, the radiolucent nature of the polymer disc in a FemoSeal complicates diagnostic imaging. While endovascular approaches exist, open surgery is a safe and effective strategy for retrieving fragments and treating the patient in acute limb ischaemia cases.
Conclusion
Physicians should remain vigilant for embolic risks associated with vascular closure devices, even with suitable anatomy and following guidelines, especially considering the trend toward early ambulation and discharge.
{"title":"Closure Device Migration: An Unusual Cause of Acute Limb Ischaemia Following a Simple Endovascular Procedure","authors":"Alexandre Oliny , Côme Bosse , Philippe Charbonneau , Stephan Haulon , Dominique Fabre","doi":"10.1016/j.ejvsvf.2024.05.006","DOIUrl":"10.1016/j.ejvsvf.2024.05.006","url":null,"abstract":"<div><h3>Introduction</h3><p>Acute limb ischaemia resulting from foreign body embolisation is an infrequent yet critical complication associated with vascular closure devices (VCDs). Despite the widespread use of VCDs, rare complications such as fragment emboli pose unique challenges, necessitating heightened clinical awareness. This case report presents a case of acute limb ischaemia caused by a VCD malfunction following an endovascular procedure.</p></div><div><h3>Report</h3><p>A 70 year old male who was diagnosed with a severe claudication of the lower extremity (Rutherford III) due to right common iliac stenosis, underwent angioplasty using a FemoSeal (Terumo Ltd., Surrey, UK) to close the right femoral artery access. Two weeks later, the patient presented with acute lower limb ischaemia due to a right popliteal–tibial occlusion. Emergency surgical thrombo-embolectomy was successfully performed from a medial popliteal approach, and the thrombus, which contained a polymer disc from the VCD at its distal end, was completely removed.</p></div><div><h3>Discussion</h3><p>Despite VCDs being proven safe and efficient, rare complications such as fragment emboli can occur, and physicians should be aware of the possible delayed onset of symptoms. Moreover, the radiolucent nature of the polymer disc in a FemoSeal complicates diagnostic imaging. While endovascular approaches exist, open surgery is a safe and effective strategy for retrieving fragments and treating the patient in acute limb ischaemia cases.</p></div><div><h3>Conclusion</h3><p>Physicians should remain vigilant for embolic risks associated with vascular closure devices, even with suitable anatomy and following guidelines, especially considering the trend toward early ambulation and discharge.</p></div>","PeriodicalId":36502,"journal":{"name":"EJVES Vascular Forum","volume":"61 ","pages":"Pages 113-115"},"PeriodicalIF":0.6,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2666688X24000868/pdfft?md5=e20c3267aa0d7c7adcec3e31a721aac3&pid=1-s2.0-S2666688X24000868-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141042618","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}
Pub Date : 2024-01-01DOI: 10.1016/j.ejvsvf.2024.01.054
Arshia Javidan , Muralie Vignarajah , Matthew W. Nelms , Fangwen Zhou , Yung Lee , Faysal Naji , Ahmed Kayssi
Objective
Due to its video based approach, YouTube has become a widely accessed educational resource for patients and trainees. This systematic review characterised and evaluated the peer reviewed literature investigating YouTube as a source of patient or trainee education in vascular surgery.
Data sources
A comprehensive literature search was conducted using EMBASE, MEDLINE, and Ovid HealthStar from inception until 19 January 2023. All primary studies and conference abstracts evaluating YouTube as a source of vascular surgery education were included.
Review methods
Video educational quality was analysed across several factors, including pathology, video audience, and length.
Results
Overall, 24 studies were identified examining 3 221 videos with 123.1 hours of content and 37.1 million views. Studies primarily examined YouTube videos on diabetic foot care (7/24, 29%), peripheral arterial disease (3/24, 13%), carotid artery stenosis (3/24, 13%), varicose veins (3/24, 13%), and abdominal aortic aneurysm (2/24, 8%). Video educational quality was analysed using standardised assessment tools, author generated scoring systems, or global author reported assessment of quality. Six studies assessed videos for trainee education, while 18 studies evaluated videos for patient education. Among the 20 studies which reported on the overall quality of educational content, 10/20 studies deemed it poor, and 10/20 studies considered it fair, with 53% of studies noting poor educational quality for videos intended for patients and 40% of studies noting poor educational quality in videos intended for trainees. Poor quality videos had more views than fair quality videos (mean 27 348, 95% CI 15 154–39 543 views vs. 11 372, 95% CI 3 115–19 629 views, p = .030).
Conclusion
The overall educational quality of YouTube videos for vascular surgery patient and trainee education is suboptimal. There is significant heterogeneity in the quality assessment tools used in their evaluation. A standardised approach to online education with a consistent quality assessment tool is required to better support online patient and trainee education in vascular surgery.
{"title":"YouTube as a Source of Patient and Trainee Education in Vascular Surgery: A Systematic Review","authors":"Arshia Javidan , Muralie Vignarajah , Matthew W. Nelms , Fangwen Zhou , Yung Lee , Faysal Naji , Ahmed Kayssi","doi":"10.1016/j.ejvsvf.2024.01.054","DOIUrl":"10.1016/j.ejvsvf.2024.01.054","url":null,"abstract":"<div><h3>Objective</h3><p>Due to its video based approach, YouTube has become a widely accessed educational resource for patients and trainees. This systematic review characterised and evaluated the peer reviewed literature investigating YouTube as a source of patient or trainee education in vascular surgery.</p></div><div><h3>Data sources</h3><p>A comprehensive literature search was conducted using EMBASE, MEDLINE, and Ovid HealthStar from inception until 19 January 2023. All primary studies and conference abstracts evaluating YouTube as a source of vascular surgery education were included.</p></div><div><h3>Review methods</h3><p>Video educational quality was analysed across several factors, including pathology, video audience, and length.</p></div><div><h3>Results</h3><p>Overall, 24 studies were identified examining 3 221 videos with 123.1 hours of content and 37.1 million views. Studies primarily examined YouTube videos on diabetic foot care (7/24, 29%), peripheral arterial disease (3/24, 13%), carotid artery stenosis (3/24, 13%), varicose veins (3/24, 13%), and abdominal aortic aneurysm (2/24, 8%). Video educational quality was analysed using standardised assessment tools, author generated scoring systems, or global author reported assessment of quality. Six studies assessed videos for trainee education, while 18 studies evaluated videos for patient education. Among the 20 studies which reported on the overall quality of educational content, 10/20 studies deemed it poor, and 10/20 studies considered it fair, with 53% of studies noting poor educational quality for videos intended for patients and 40% of studies noting poor educational quality in videos intended for trainees. Poor quality videos had more views than fair quality videos (mean 27 348, 95% CI 15 154–39 543 views <em>vs.</em> 11 372, 95% CI 3 115–19 629 views, <em>p</em> = .030).</p></div><div><h3>Conclusion</h3><p>The overall educational quality of YouTube videos for vascular surgery patient and trainee education is suboptimal. There is significant heterogeneity in the quality assessment tools used in their evaluation. A standardised approach to online education with a consistent quality assessment tool is required to better support online patient and trainee education in vascular surgery.</p></div>","PeriodicalId":36502,"journal":{"name":"EJVES Vascular Forum","volume":"61 ","pages":"Pages 62-76"},"PeriodicalIF":0.6,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2666688X24000558/pdfft?md5=cf93b94fb75ababa525384f5cd25e1f5&pid=1-s2.0-S2666688X24000558-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139636778","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}
The physical impact of the application of Heli-FX EndoAnchors (EA; Medtronic, Minneapolis, USA) on endograft (EG) material is unclear. This study aimed to examine the possible EG membrane alterations after EA implantation.
Methods
Heli-FX EndoAnchors were applied in vitro into four aortic endocuffs: AFX2 (Endologix Inc., Irvine, USA); Endurant II (Medtronic, Minneapolis, USA); Gore Excluder (W.L. Gore and Assoc., Flagstaff, USA); and Zenith Renu (Cook Aortic Interventions, Bloomington, USA). Two of these, Endurant II and Renu, are made of polyethylene terephthalate (PET), while Excluder and AFX2 are made of expanded polytetrafluoroethylene (ePTFE). The penetration angle was measured for each EA. The EAs were then carefully removed, and perforations examined with digital and fluorescent microscopy. The area and perimeter of the holes were digitally calculated, and material alterations were analysed.
Results
Of the 13 EAs applied, 12 remained in place. The mean penetration angle was 79°. The ePTFE perforations had oval openings, while PET perforations were round. After EA removal, comparisons between ePTFE and PET material perforations suggested a larger hole area (p = 0.011) and perimeter (p = 0.003) in the former. The ePTFE perforations in the AFX2 were the largest compared with the holes in other endocuffs (p = 0.050). The perforation channel of the ePTFE membrane of the Excluder cuff retained its form after EA removal. Local dissection like layer damage extended further. The perforations in both the Endurant II and the Renu endocuffs shared similar characteristics, with multiple fibres of PET elongated, distorted, or ruptured.
Conclusion
During EA placement, the EG membrane undergoes local alteration and or destruction. Expanded PTFE, particularly AFX2 endocuffs (for which EA use is not recommended), are characterised by a more extensive degree of material alteration compared with PET. Additional studies are required to chronologically supplement these findings in fatigue tests.
目的应用 Heli-FX EndoAnchors(EA;美敦力,美国明尼阿波利斯)对内膜移植物(EG)材料的物理影响尚不清楚。本研究旨在检查 EA 植入后 EG 膜可能发生的变化。方法在体外将 Heli-FX EndoAnchors 应用于四种主动脉内膜腔:AFX2 (Endologix Inc., Irvine, USA);Endurant II (Medtronic, Minneapolis, USA);Gore Excluder (W.L. Gore and Assoc., Flagstaff, USA);Zenith Renu (Cook Aortic Interventions, Bloomington, USA)。其中 Endurant II 和 Renu 由聚对苯二甲酸乙二醇酯 (PET) 制成,而 Excluder 和 AFX2 则由膨体聚四氟乙烯 (ePTFE) 制成。测量了每种 EA 的穿透角度。然后小心地取出 EA,用数码显微镜和荧光显微镜检查穿孔。对穿孔的面积和周长进行了数字计算,并对材料的变化进行了分析。平均穿透角度为 79°。ePTFE 穿孔为椭圆形,而 PET 穿孔为圆形。去除 EA 后,ePTFE 和 PET 材料穿孔的比较结果表明,前者的穿孔面积更大(p = 0.011),周长更大(p = 0.003)。与其他内塞相比,AFX2 的 ePTFE 穿孔面积最大(p = 0.050)。切除 EA 后,Excluder 袖套 ePTFE 膜的穿孔通道仍保持原样。局部剥离层损伤进一步扩大。Endurant II 和 Renu 内充气罩囊的穿孔具有相似的特征,PET 的多条纤维拉长、扭曲或破裂。与 PET 相比,膨胀聚四氟乙烯,尤其是 AFX2 内塞(不建议使用 EA),具有更广泛的材料变化特征。需要进行更多的研究,以按时间顺序补充这些疲劳测试结果。
{"title":"The Impact of Heli-FX EndoAnchor Application on Endograft Material: An Experimental Study","authors":"Damir Vakhitov , Nabil Chakfé , Frédéric Heim , Arindam Chaudhuri","doi":"10.1016/j.ejvsvf.2024.09.001","DOIUrl":"10.1016/j.ejvsvf.2024.09.001","url":null,"abstract":"<div><h3>Objective</h3><div>The physical impact of the application of Heli-FX EndoAnchors (EA; Medtronic, Minneapolis, USA) on endograft (EG) material is unclear. This study aimed to examine the possible EG membrane alterations after EA implantation.</div></div><div><h3>Methods</h3><div>Heli-FX EndoAnchors were applied <em>in vitro</em> into four aortic endocuffs: AFX2 (Endologix Inc., Irvine, USA); Endurant II (Medtronic, Minneapolis, USA); Gore Excluder (W.L. Gore and Assoc., Flagstaff, USA); and Zenith Renu (Cook Aortic Interventions, Bloomington, USA). Two of these, Endurant II and Renu, are made of polyethylene terephthalate (PET), while Excluder and AFX2 are made of expanded polytetrafluoroethylene (ePTFE). The penetration angle was measured for each EA. The EAs were then carefully removed, and perforations examined with digital and fluorescent microscopy. The area and perimeter of the holes were digitally calculated, and material alterations were analysed.</div></div><div><h3>Results</h3><div>Of the 13 EAs applied, 12 remained in place. The mean penetration angle was 79°. The ePTFE perforations had oval openings, while PET perforations were round. After EA removal, comparisons between ePTFE and PET material perforations suggested a larger hole area (<em>p</em> = 0.011) and perimeter (<em>p</em> = 0.003) in the former. The ePTFE perforations in the AFX2 were the largest compared with the holes in other endocuffs (<em>p</em> = 0.050). The perforation channel of the ePTFE membrane of the Excluder cuff retained its form after EA removal. Local dissection like layer damage extended further. The perforations in both the Endurant II and the Renu endocuffs shared similar characteristics, with multiple fibres of PET elongated, distorted, or ruptured.</div></div><div><h3>Conclusion</h3><div>During EA placement, the EG membrane undergoes local alteration and or destruction. Expanded PTFE, particularly AFX2 endocuffs (for which EA use is not recommended), are characterised by a more extensive degree of material alteration compared with PET. Additional studies are required to chronologically supplement these findings in fatigue tests.</div></div>","PeriodicalId":36502,"journal":{"name":"EJVES Vascular Forum","volume":"62 ","pages":"Pages 72-77"},"PeriodicalIF":1.4,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142421592","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}