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Standardized approach to direct first pass aspiration technique for endovascular thrombectomy: Description and initial experience with CANADAPT. 用于血管内血栓切除术的直接首过抽吸技术的标准化方法:CANADAPT 的描述和初步经验。
IF 1.7 4区 医学 Q3 Medicine Pub Date : 2024-02-08 DOI: 10.1177/15910199241230360
I R Macdonald, V Linehan, B Sneek, David Volders

Background: Endovascular thrombectomy (EVT) is standard of care for acute ischemic stroke. Stent assisted EVT with aspiration (SOLUMBRA) technique has remained a mainstay approach. There is growing evidence that A Direct Aspiration First Pass Technique (ADAPT) is a safe, efficient and effective approach for EVT, offering several advantages. This study describes and reports initial institutional experience in the use of a standardized scientific based aspiration only technique: CANADAPT.

Methods: Single center prospective cohort study was performed on consecutive patients treated for large/medium vessel ischemic stroke with CANADAPT. Intravenous thrombolytics were administered according to routine practice, independent of the decision to proceed with EVT. A sequential stepwise aspiration only technique was then applied, CANADAPT, consisting of three maneuvers, A, B and C. The reperfusion success rate, number of passes, use of rescue technique, complication rate and procedural cost were determined.

Results: Twenty-two patients were included in this case series representing M1 (17, 77%), M1/2 (2, 9%), carotid-T (2, 9%) and basilar (1, 5%) occlusions. First pass recanalization was achieved in 11 (50%) of patients. A further four patients had successful reperfusion with a second pass of CANADAPT (total 68% success rate). Only one patient had successful reperfusion with the aspiration catheter at the clot interface (CANADAPT A). All others required some withdrawal of the aspiration catheter for reperfusion (CANADAPT B and C). Seven patients had SOLUMBRA rescue. Of these, five patients (22% of total patients) had further successful reperfusion. Overall median procedural time was 23 min for first recanalization and 30 min for final recanalization. The cost per procedure was $6630 ± 1069 for CANADAPT, and $13,530 ± 2706 for SOLUMBRA techniques.

Conclusions: CANADAPT represents a standardized scientific-based approach to aspiration only thrombectomy intervention. This initial study demonstrates the safety, efficiency and efficacy of this technique for use in EVT.

背景:血管内血栓切除术(EVT)是治疗急性缺血性脑卒中的标准方法。支架辅助吸栓术(SOLUMBRA)一直是主流方法。越来越多的证据表明,直接抽吸首次通过技术(ADAPT)是一种安全、高效、有效的 EVT 方法,具有多种优势。本研究描述并报告了使用基于科学的标准化抽吸技术的初步机构经验:方法:对使用 CANADAPT 治疗大/中血管缺血性卒中的连续患者进行了单中心前瞻性队列研究。静脉溶栓按照常规方法进行,与是否进行 EVT 的决定无关。结果显示,22 名患者的再灌注成功率、通过次数、抢救技术的使用、并发症发生率和手术费用均有所提高:本病例系列包括 22 例患者,分别代表 M1(17 例,77%)、M1/2(2 例,9%)、颈动脉-T(2 例,9%)和基底动脉(1 例,5%)闭塞。11名患者(50%)实现了首次再通畅。另有四名患者在第二次使用 CANADAPT 时成功实现了再灌注(总成功率为 68%)。只有一名患者在血块界面处使用抽吸导管(CANADAPT A)成功实现了再灌注。其他所有患者都需要抽吸导管进行再灌注(CANADAPT B 和 C)。七名患者接受了 SOLUMBRA 抢救。其中,5 名患者(占患者总数的 22%)进一步成功进行了再灌注。首次再通畅的中位手术时间为 23 分钟,最终再通畅的中位手术时间为 30 分钟。CANADAPT的每次手术费用为6630美元±1069美元,SOLUMBRA技术的每次手术费用为13530美元±2706美元:结论:CANADAPT 是一种基于科学的标准化抽吸式血栓切除术干预方法。这项初步研究证明了该技术用于 EVT 的安全性、高效性和有效性。
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引用次数: 0
A rare dissecting anterior inferior cerebellar artery aneurysm treated with flow diversion using a silk vista baby device. 使用丝绸 Vista Baby 装置进行血流分流,治疗了一个罕见的小脑前下动脉剥脱性动脉瘤。
IF 1.7 4区 医学 Q3 Medicine Pub Date : 2024-01-24 DOI: 10.1177/15910199241227467
Omar Kass-Hout, Ziad Darkhabani, Tibor Becske

Background: Dissecting intracranial pseudoaneurysms represent a challenge for treatment both endovascularly and surgically.

Methods: We review the treatment course of a ruptured anterior inferior cerebellar artery (AICA) dissecting pseudoaneurysm in a 50-year-old patient and review the history of dissecting aneurysms and AICA aneurysms treatment.

Results: An aneurysm cure was achieved using flow diversion in the AICA. The recent introduction of flow diversion devices that can be deployed through 0.017" microcatheters represents a new avenue for treatment of aneurysms.

Conclusion: To the best of our knowledge this is the first published case of flow diversion in the(?) AICA to treat a dissecting aneurysm. The introduction of Silk Vista Baby and similar future devices is likely to widen the scope of aneurysm treatment utilizing flow diversion in distal distribution with small parent arteries.

背景:颅内剥离性假动脉瘤是血管内治疗和手术治疗的难题:方法:我们回顾了一名 50 岁患者的小脑前下动脉(AICA)破裂剥离性假动脉瘤的治疗过程,并回顾了剥离性动脉瘤和 AICA 动脉瘤治疗的历史:结果:通过对 AICA 进行血流分流,动脉瘤得以治愈。最近推出的可通过 0.017 英寸微导管部署的血流分流装置是治疗动脉瘤的新途径:据我们所知,这是第一例发表的在 AICA(?)Silk Vista Baby 和未来类似设备的问世,很可能会拓宽在母动脉较小的远端分布区利用血流分流治疗动脉瘤的范围。
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引用次数: 0
A technical guide to robotic-assisted carotid angioplasty and stenting with the Corindus CorPath GRX system. 使用Corindus CorPath GRX系统进行机器人辅助颈动脉血管成形术和支架植入术的技术指南。
IF 1.7 4区 医学 Q3 Medicine Pub Date : 2024-01-17 DOI: 10.1177/15910199241226856
Anzhela D Moskalik, Buqing Liang, Branden J Cord, Ben Waldau

Robotic-assisted carotid artery angioplasty and stenting is becoming more popular due to its precision and radiation safety. In this video, we present a case using the CorPath GRX Robotic System (Corindus, a Seimens Healthineers Company, Waltham, Massachusetts, USA) with step-by-step procedure process and technical nuances (video 1). We demonstrate that cervical carotid angioplasty and stenting can be safely performed using the robotic system with efficiency and accuracy.

机器人辅助颈动脉血管成形术和支架植入术因其精确性和辐射安全性而越来越受欢迎。在这段视频中,我们展示了一个使用 CorPath GRX 机器人系统(Corindus,Seimens Healthineers 公司,美国马萨诸塞州沃尔瑟姆市)的病例,并逐步介绍了手术过程和技术细节(视频 1)。我们证明了颈动脉血管成形术和支架植入术可以使用机器人系统安全、高效、准确地进行。
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引用次数: 0
Effect of sarcopenia on mortality in acute stroke patients receiving endovascular treatment. 肌肉疏松症对接受血管内治疗的急性中风患者死亡率的影响。
IF 1.7 4区 医学 Q3 Medicine Pub Date : 2024-01-17 DOI: 10.1177/15910199241227465
Muhammed Said Beşler, Nurdan Çay, Bige Sayın

Background: To investigate the effect of sarcopenia on mortality in patients with acute ischemic stroke caused by anterior circulation large artery occlusion who underwent endovascular treatment.

Methods: Acute ischemic stroke patients (n = 194) treated with mechanical thrombectomy who underwent chest computed tomography between 2019 and 2022 (median age, 69 [interquartile range: 61-77], 95 females, 99 males) were evaluated retrospectively. The cross-sectional area and density of the pectoralis muscle [pectoralis muscle area (PMA) and pectoralis muscle density (PMD)] at the level of the aortic arch and the erector spinae muscle at the T12 level [erector spinae muscle area (ESMA) and erector spinae muscle density (ESMD)] were measured. The association between skeletal muscle parameters and mortality outcomes was investigated using the receiver operating characteristic (ROC) curve and multivariable logistic regression analyses.

Results: The 90-day mortality rate was 32% in the study population (n = 62). The ROC analysis revealed that ESMD [area under the curve (AUC): 0.765] and PMD (AUC: 0.759) performed best in the prediction of 90-day mortality. In the multivariable logistic regression analysis, PMD [odds ratio (OR): 0.896; 95% confidence interval (CI): 0.846-0.948; p < 0.001], ESMA (OR: 0.929; 95% CI: 0.878-0.983; p = 0.011), and ESMD (OR: 0.947; 95% CI: 0.913-0.983; p = 0.004), but not PMA, were independent risk factors for 90-day mortality.

Conclusion: PMD, ESMA, and ESMD may be risk factors for 90-day mortality after mechanical thrombectomy for acute ischemic stroke.

背景:研究肌肉疏松症对接受血管内治疗的前循环大动脉闭塞所致急性缺血性脑卒中患者死亡率的影响:目的:研究肌肉疏松症对接受血管内治疗的前循环大动脉闭塞引起的急性缺血性卒中患者死亡率的影响:对2019年至2022年期间接受胸部计算机断层扫描的接受机械取栓术治疗的急性缺血性卒中患者(n = 194)(中位年龄69岁[四分位间范围:61-77],女性95人,男性99人)进行回顾性评估。研究人员测量了主动脉弓水平的胸肌横截面积和密度[胸肌面积(PMA)和胸肌密度(PMD)]以及T12水平的竖脊肌横截面积和密度[竖脊肌面积(ESMA)和竖脊肌密度(ESMD)]。采用接收器操作特征曲线(ROC)和多变量逻辑回归分析研究了骨骼肌参数与死亡率之间的关系:研究对象(n = 62)的 90 天死亡率为 32%。ROC分析显示,ESMD[曲线下面积(AUC):0.765]和PMD(AUC:0.759)在预测90天死亡率方面表现最佳。在多变量逻辑回归分析中,PMD[几率比(OR):0.896;95% 置信区间(CI):0.846-0.948;P = 0.011]和ESMD(OR:0.947;95% CI:0.913-0.983;P = 0.004)是90天死亡率的独立危险因素,而不是PMA:结论:PMD、ESMA 和 ESMD 可能是急性缺血性卒中机械取栓术后 90 天死亡率的风险因素。
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引用次数: 0
Safety and efficacy of the Woven Endo-Bridge-17 device for intracranial aneurysm treatment: A systematic review and meta-analysis. 用于治疗颅内动脉瘤的 Woven Endo-Bridge-17 装置的安全性和有效性:系统回顾和荟萃分析。
IF 1.7 4区 医学 Q3 Medicine Pub Date : 2024-01-17 DOI: 10.1177/15910199231226294
Sherief Ghozy, Ahmed Sallam Motawei, Charbel Moussalem, Amro Elrefaei, Hassan Kobeissi, Alzhraa S Abbas, Adam A Dmytriw, David F Kallmes, Ramanathan Kadirvel

Background: The Woven Endo-Bridge (WEB) device revolutionized the treatment of wide-necked bifurcation aneurysms by intrasaccular flow diversion. The latest advancement is the WEB-17 system, offering greater flexibility with fewer wires, enabling treatment of smaller distal aneurysms using smaller microcatheters than the WEB-21 system.

Methods: We conducted a systematic review following preferred reporting items for systematic reviews and meta-analyses guidelines, analyzing data from seven retrospective cohort studies involving 483 aneurysms treated with the WEB-17 device. Statistical analysis computed pooled prevalence rates and 95% confidence intervals using appropriate models for each outcome and R software version 4.3.1 (R Foundation for Statistical Computing, Vienna, Austria).

Results: Technical success was achieved in 475 out of 483 aneurysms treated with the WEB-17 device, with a success rate of 98.34% (95% confidence interval (CI) = 96.72-99.17). Among the successful cases, 4.97% (95% CI = 1.60-14.39) required adjunctive devices. Adequate occlusion, defined as complete occlusion or neck remnants, was observed in 94.41% (95% CI = 88.17-97.46) of cases. Periprocedural complications were infrequent, with thromboembolic complications occurring in 4.93% (95% CI = 3.29-7.30) of cases, hemorrhagic complications in 1.28% (95% CI = 0.58-2.83), and postprocedural neurologic complications in 0.99% (95% CI = 0.31-3.14). Procedure-related morbidity was observed in 1.71% (95% CI = 0.86-3.39) of cases, and there was one procedure-related mortality reported at 0.21% (95% CI = .03-1.50). Mortality unrelated to the procedure occurred in 1% (95% CI = 0.23-4.15).

Conclusion: Our findings suggest that the WEB-17 device is associated with a high rate of technical success, favorable angiographic outcomes, and a low rate of periprocedural complications. Further research, including prospective trials, is needed to confirm these findings and establish its safety and efficacy definitively.

背景:编织内桥(WEB)设备通过肌内血流分流彻底改变了宽颈分叉动脉瘤的治疗方法。与 WEB-21 系统相比,WEB-17 系统具有更大的灵活性和更少的导线,可以使用更小的微导管治疗更小的远端动脉瘤:我们按照系统综述和荟萃分析指南的首选报告项目进行了系统综述,分析了来自七项回顾性队列研究的数据,这些研究涉及使用 WEB-17 设备治疗的 483 个动脉瘤。统计分析针对每种结果使用适当的模型和 R 软件 4.3.1 版(奥地利维也纳 R 统计计算基金会)计算了汇总患病率和 95% 置信区间:在使用 WEB-17 设备治疗的 483 例动脉瘤中,有 475 例获得了技术成功,成功率为 98.34%(95% 置信区间 (CI) = 96.72-99.17)。在成功的病例中,4.97%(95% 置信区间 = 1.60-14.39)需要辅助装置。94.41%(95% CI = 88.17-97.46)的病例观察到充分闭塞,即完全闭塞或颈部残留。围手术期并发症并不常见,血栓栓塞并发症发生率为 4.93% (95% CI = 3.29-7.30),出血并发症发生率为 1.28% (95% CI = 0.58-2.83),术后神经系统并发症发生率为 0.99% (95% CI = 0.31-3.14)。1.71%(95% CI = 0.86-3.39)的病例出现了与手术相关的发病率,0.21%(95% CI = 0.03-1.50)的病例出现了与手术相关的死亡率。与手术无关的死亡率为 1%(95% CI = 0.23-4.15):我们的研究结果表明,WEB-17 装置的技术成功率高,血管造影结果良好,围手术期并发症发生率低。需要进一步的研究,包括前瞻性试验,来证实这些发现,并最终确定其安全性和有效性。
{"title":"Safety and efficacy of the Woven Endo-Bridge-17 device for intracranial aneurysm treatment: A systematic review and meta-analysis.","authors":"Sherief Ghozy, Ahmed Sallam Motawei, Charbel Moussalem, Amro Elrefaei, Hassan Kobeissi, Alzhraa S Abbas, Adam A Dmytriw, David F Kallmes, Ramanathan Kadirvel","doi":"10.1177/15910199231226294","DOIUrl":"https://doi.org/10.1177/15910199231226294","url":null,"abstract":"<p><strong>Background: </strong>The Woven Endo-Bridge (WEB) device revolutionized the treatment of wide-necked bifurcation aneurysms by intrasaccular flow diversion. The latest advancement is the WEB-17 system, offering greater flexibility with fewer wires, enabling treatment of smaller distal aneurysms using smaller microcatheters than the WEB-21 system.</p><p><strong>Methods: </strong>We conducted a systematic review following preferred reporting items for systematic reviews and meta-analyses guidelines, analyzing data from seven retrospective cohort studies involving 483 aneurysms treated with the WEB-17 device. Statistical analysis computed pooled prevalence rates and 95% confidence intervals using appropriate models for each outcome and R software version 4.3.1 (R Foundation for Statistical Computing, Vienna, Austria).</p><p><strong>Results: </strong>Technical success was achieved in 475 out of 483 aneurysms treated with the WEB-17 device, with a success rate of 98.34% (95% confidence interval (CI) = 96.72-99.17). Among the successful cases, 4.97% (95% CI = 1.60-14.39) required adjunctive devices. Adequate occlusion, defined as complete occlusion or neck remnants, was observed in 94.41% (95% CI = 88.17-97.46) of cases. Periprocedural complications were infrequent, with thromboembolic complications occurring in 4.93% (95% CI = 3.29-7.30) of cases, hemorrhagic complications in 1.28% (95% CI = 0.58-2.83), and postprocedural neurologic complications in 0.99% (95% CI = 0.31-3.14). Procedure-related morbidity was observed in 1.71% (95% CI = 0.86-3.39) of cases, and there was one procedure-related mortality reported at 0.21% (95% CI = .03-1.50). Mortality unrelated to the procedure occurred in 1% (95% CI = 0.23-4.15).</p><p><strong>Conclusion: </strong>Our findings suggest that the WEB-17 device is associated with a high rate of technical success, favorable angiographic outcomes, and a low rate of periprocedural complications. Further research, including prospective trials, is needed to confirm these findings and establish its safety and efficacy definitively.</p>","PeriodicalId":49174,"journal":{"name":"Interventional Neuroradiology","volume":null,"pages":null},"PeriodicalIF":1.7,"publicationDate":"2024-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139486637","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Single-center outcomes of Onyx Frontier™ and Resolute Onyx™ drug-eluting balloon-mounted stents for rescue stenting for acute large vessel occlusion. Onyx Frontier™ 和 Resolute Onyx™ 药物洗脱球囊支架用于急性大血管闭塞抢救性支架置入术的单中心疗效。
IF 1.7 4区 医学 Q3 Medicine Pub Date : 2024-01-17 DOI: 10.1177/15910199231226285
Shyle H Mehta, Timothy G White, Kevin A Shah, Daniel G Lynch, Cassidy D Werner, Ina Teron, Thomas Link, Athos Patsalides, Henry H Woo

Background: In cases where mechanical thrombectomy (MT) fails, rescue stenting may be necessary to achieve reperfusion; however, the lack of standardized techniques or devices poses a challenge. This series aims to present our early experience with the Onyx Frontier™ and Resolute Onyx™ balloon-mounted drug-eluting stents for rescue stenting.

Methods: A retrospective chart review was performed of all patients who underwent rescue stenting, in the setting of failed MT, using Onyx Frontier™ or Resolute Onyx™ stents at a single institution. Technical details, procedural complications, and patient outcomes were recorded for each case.

Results: Twenty-two Onyx Frontier™ and Resolute Onyx™ stents were deployed in 18 patients undergoing rescue stenting. Stent locations included the middle cerebral artery (36.4%), internal carotid artery (18.2%), vertebral artery (22.7%), and basilar artery (22.7%). The average National Institutes of Health Stroke Scale score before MT was 13.8 (range 0-31). The median initial modified Rankin Scale (mRS) score was zero, while the median mRS score at follow-up was three. Successful reperfusion, as assessed by TICI scores, was achieved in 43.8% of patients for TICI 3, 43.8% for TICI 2C, and 12.5% for TICI 2B. Post-revascularization, 16.7% of patients experienced hemorrhage, of which one patient (5.6%) had symptomatic hemorrhage.

Conclusions: Onyx Frontier™ and Resolute Onyx™ stents are well suited for rescue stenting in cases of failed MT. These balloon-mounted drug-eluting stents exhibit excellent navigability, rendering them appropriate for rescue revascularization procedures. Our findings demonstrate that these stents confer a high degree of technical success.

背景:在机械血栓切除术(MT)失败的病例中,可能需要使用救援支架来实现再灌注;然而,标准化技术或设备的缺乏带来了挑战。本系列旨在介绍我们使用 Onyx Frontier™ 和 Resolute Onyx™ 球囊安装药物洗脱支架进行抢救性支架置入的早期经验:对一家医疗机构使用 Onyx Frontier™ 或 Resolute Onyx™ 支架对 MT 失败的所有患者进行了回顾性病历审查。记录了每个病例的技术细节、手术并发症和患者预后:18名接受抢救性支架植入术的患者使用了22枚Onyx Frontier™和Resolute Onyx™支架。支架位置包括大脑中动脉(36.4%)、颈内动脉(18.2%)、椎动脉(22.7%)和基底动脉(22.7%)。MT 前美国国立卫生研究院卒中量表平均评分为 13.8(0-31 分不等)。初始改良朗肯量表(mRS)评分的中位数为零,而随访时mRS评分的中位数为3分。根据 TICI 评分评估,43.8% 的患者成功实现了再灌注,TICI 为 3,43.8% 的患者 TICI 为 2C,12.5% 的患者 TICI 为 2B。血管重建后,16.7%的患者出现出血,其中一名患者(5.6%)出现症状性出血:结论:Onyx Frontier™ 和 Resolute Onyx™ 支架非常适合用于 MT 失败病例的抢救性支架植入。这些球囊安装的药物洗脱支架具有极佳的可操作性,因此非常适合用于抢救性血管重建手术。我们的研究结果表明,这些支架具有很高的技术成功率。
{"title":"Single-center outcomes of Onyx Frontier™ and Resolute Onyx™ drug-eluting balloon-mounted stents for rescue stenting for acute large vessel occlusion.","authors":"Shyle H Mehta, Timothy G White, Kevin A Shah, Daniel G Lynch, Cassidy D Werner, Ina Teron, Thomas Link, Athos Patsalides, Henry H Woo","doi":"10.1177/15910199231226285","DOIUrl":"https://doi.org/10.1177/15910199231226285","url":null,"abstract":"<p><strong>Background: </strong>In cases where mechanical thrombectomy (MT) fails, rescue stenting may be necessary to achieve reperfusion; however, the lack of standardized techniques or devices poses a challenge. This series aims to present our early experience with the Onyx Frontier™ and Resolute Onyx™ balloon-mounted drug-eluting stents for rescue stenting.</p><p><strong>Methods: </strong>A retrospective chart review was performed of all patients who underwent rescue stenting, in the setting of failed MT, using Onyx Frontier™ or Resolute Onyx™ stents at a single institution. Technical details, procedural complications, and patient outcomes were recorded for each case.</p><p><strong>Results: </strong>Twenty-two Onyx Frontier™ and Resolute Onyx™ stents were deployed in 18 patients undergoing rescue stenting. Stent locations included the middle cerebral artery (36.4%), internal carotid artery (18.2%), vertebral artery (22.7%), and basilar artery (22.7%). The average National Institutes of Health Stroke Scale score before MT was 13.8 (range 0-31). The median initial modified Rankin Scale (mRS) score was zero, while the median mRS score at follow-up was three. Successful reperfusion, as assessed by TICI scores, was achieved in 43.8% of patients for TICI 3, 43.8% for TICI 2C, and 12.5% for TICI 2B. Post-revascularization, 16.7% of patients experienced hemorrhage, of which one patient (5.6%) had symptomatic hemorrhage.</p><p><strong>Conclusions: </strong>Onyx Frontier™ and Resolute Onyx™ stents are well suited for rescue stenting in cases of failed MT. These balloon-mounted drug-eluting stents exhibit excellent navigability, rendering them appropriate for rescue revascularization procedures. Our findings demonstrate that these stents confer a high degree of technical success.</p>","PeriodicalId":49174,"journal":{"name":"Interventional Neuroradiology","volume":null,"pages":null},"PeriodicalIF":1.7,"publicationDate":"2024-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139486639","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Carotid stenting for symptomatic carotid artery web: Multicenter experience. 颈动脉支架治疗无症状颈动脉网:多中心经验。
IF 1.7 4区 医学 Q3 Medicine Pub Date : 2024-01-17 DOI: 10.1177/15910199231226293
Christopher R Pasarikovski, Jeremy Lynch, Michael Corrin, Jerry C Ku, Ashish Kumar, Vitor M Pereira, Timo Krings, Leodante da Costa, Sandra E Black, Ronit Agid, Victor Xd Yang

Objective: Carotid artery webs are an underappreciated cause of recurrent ischemic stroke, and may represent a significant portion of cryptogenic stroke. Evidence-based guidelines for the management of symptomatic carotid webs do not exist. The goal of this study is to audit our local experience for patients with symptomatic carotid artery webs undergoing carotid stenting as a treatment option, along with describing the hypothesized dynamic physiology of carotid webs.

Methods: All patients undergoing stenting for symptomatic carotid artery web at two comprehensive regional stroke centers with high endovascular thrombectomy volume from January 1, 2012 to March 1, 2021 were included. The modified Rankin Scale (mRS) score was used to define functional outcome at 3 months after stenting.

Results: Fourteen consecutive patients with symptomatic carotid artery webs underwent stenting. Twelve patients were female (86%), with a median age of 54 (IQR, 48-64) years across all patients. Stroke was the qualifying event in 12 (86%) patients and TIA in 2. Eleven patients (11/14, 79%) achieved a mRS score of 0-2 at 90 days, 2 (14%) were mRS 3-5, and one patient was lost to follow-up. The median follow-up was 12 months (IQR, 10-12). There was no recurrent stroke or TIA like symptoms in any patients.

Conclusions: Carotid stenting appears to be safe at preventing recurrent stroke/TIA with a median follow-up of 12 months in this retrospective multicenter observational study.

目的:颈动脉网是导致复发性缺血性卒中的一个未被重视的原因,可能占隐源性卒中的很大一部分。目前尚无以证据为基础的无症状颈动脉网治疗指南。本研究的目的是总结我们当地对无症状颈动脉蛛网膜患者进行颈动脉支架置入术治疗的经验,同时描述颈动脉蛛网膜的假设动态生理学:方法:纳入2012年1月1日至2021年3月1日期间在两个综合性区域卒中中心接受支架植入术治疗症状性颈动脉网的所有患者。采用改良Rankin量表(mRS)评分来确定支架植入术后3个月的功能预后:14名无症状颈动脉蹼患者连续接受了支架植入术。12名患者为女性(86%),所有患者的中位年龄为54岁(IQR,48-64岁)。有 11 名患者(11/14,79%)在 90 天后的 mRS 评分为 0-2,2 名患者(14%)的 mRS 评分为 3-5,1 名患者失去随访。中位随访时间为 12 个月(IQR,10-12 个月)。所有患者均未出现中风复发或类似 TIA 的症状:在这项回顾性多中心观察研究中,中位随访时间为 12 个月的颈动脉支架植入术在预防复发性卒中/TIA 方面似乎是安全的。
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引用次数: 0
An updated meta-analysis on the safety and effectiveness of the Contour Neurovascular system. 关于 Contour 神经血管系统安全性和有效性的最新荟萃分析。
IF 1.7 4区 医学 Q3 Medicine Pub Date : 2024-01-15 DOI: 10.1177/15910199231226280
Pemla Jagtiani, Georgios S Sioutas, Juan Vivanco-Suarez, Jan-Karl Burkhardt, Visish M Srinivasan
{"title":"An updated meta-analysis on the safety and effectiveness of the Contour Neurovascular system.","authors":"Pemla Jagtiani, Georgios S Sioutas, Juan Vivanco-Suarez, Jan-Karl Burkhardt, Visish M Srinivasan","doi":"10.1177/15910199231226280","DOIUrl":"https://doi.org/10.1177/15910199231226280","url":null,"abstract":"","PeriodicalId":49174,"journal":{"name":"Interventional Neuroradiology","volume":null,"pages":null},"PeriodicalIF":1.7,"publicationDate":"2024-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139473012","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Metal allergy and neurovascular stenting: A systematic review. 金属过敏与神经血管支架植入术:系统综述。
IF 1.7 4区 医学 Q3 Medicine Pub Date : 2024-01-15 DOI: 10.1177/15910199231226283
Dhrumil Vaishnav, Muhammed Amir Essibayi, Aureliana Toma, Genesis Liriano, Raja Sandeep Perkash, Ariel Stock, Ryan Holland, Adam A Dmytriw, Stacey Q Wolfe, Sami Al Kasab, Alejandro Spiotta, Neil Haranhalli, David J Altschul

Background: Intracranial stents and flow diverters contain significant amounts of metals, notably nickel, which can cause allergic reactions in a considerable portion of the population. These allergic responses may lead to complications like in-stent stenosis (ISS) and TIA/Stroke in patients receiving stents or flow diverters for intracranial aneurysms.

Methods: We conducted a systematic review of studies from inception until July 2023, which reported outcomes of patients with metal allergy undergoing neurovascular stenting. The skin patch test was used to group patients into those with positive, negative, or absent patch test results but with a known history of metal allergy.

Results: Our review included seven studies with a total of 39 patients. Among them, 87% had a history of metal allergy before treatment. Most aneurysms (89%) were in the anterior circulation and the rest (11%) were in the posterior circulation. Skin patch tests were performed in 59% of patients, with 24% showing positive results and 33% negative. Incidental ISS was observed in 18% of patients, and the rate of TIA/Stroke was reported in 21%. The pooled rates of ISS and TIA/Stroke were higher in the first group (43% and 38%) compared to the second (18% and 9%) and third groups (15% and 15%), but these differences were not statistically significant.

Conclusions: The current neurosurgical literature does not provide a conclusive association between metal allergy and increased complications among patients undergoing neurovascular stenting. Further studies are necessary to gain a more comprehensive understanding of this topic.

背景:颅内支架和血流分流器含有大量金属,尤其是镍,这可能导致相当一部分人发生过敏反应。这些过敏反应可能导致接受支架或血流分流术治疗颅内动脉瘤的患者出现支架内狭窄(ISS)和 TIA/中风等并发症:我们对从开始到 2023 年 7 月的研究进行了系统回顾,这些研究报告了接受神经血管支架治疗的金属过敏患者的结果。采用皮肤斑贴试验将患者分为斑贴试验结果为阳性、阴性或不存在斑贴试验结果但已知有金属过敏史的患者:我们的综述包括七项研究,共涉及 39 名患者。其中,87%的患者在治疗前有金属过敏史。大多数动脉瘤(89%)位于前循环,其余(11%)位于后循环。59%的患者进行了皮肤斑贴试验,其中24%呈阳性结果,33%呈阴性结果。在 18% 的患者中观察到偶然的 ISS,21% 的患者报告了 TIA/中风的发生率。与第二组(18% 和 9%)和第三组(15% 和 15%)相比,第一组(43% 和 38%)的 ISS 和 TIA/Stroke 合并率较高,但这些差异并无统计学意义:目前的神经外科文献并未提供金属过敏与神经血管支架植入术患者并发症增加之间的确凿关联。为了更全面地了解这一问题,有必要开展进一步的研究。
{"title":"Metal allergy and neurovascular stenting: A systematic review.","authors":"Dhrumil Vaishnav, Muhammed Amir Essibayi, Aureliana Toma, Genesis Liriano, Raja Sandeep Perkash, Ariel Stock, Ryan Holland, Adam A Dmytriw, Stacey Q Wolfe, Sami Al Kasab, Alejandro Spiotta, Neil Haranhalli, David J Altschul","doi":"10.1177/15910199231226283","DOIUrl":"10.1177/15910199231226283","url":null,"abstract":"<p><strong>Background: </strong>Intracranial stents and flow diverters contain significant amounts of metals, notably nickel, which can cause allergic reactions in a considerable portion of the population. These allergic responses may lead to complications like in-stent stenosis (ISS) and TIA/Stroke in patients receiving stents or flow diverters for intracranial aneurysms.</p><p><strong>Methods: </strong>We conducted a systematic review of studies from inception until July 2023, which reported outcomes of patients with metal allergy undergoing neurovascular stenting. The skin patch test was used to group patients into those with positive, negative, or absent patch test results but with a known history of metal allergy.</p><p><strong>Results: </strong>Our review included seven studies with a total of 39 patients. Among them, 87% had a history of metal allergy before treatment. Most aneurysms (89%) were in the anterior circulation and the rest (11%) were in the posterior circulation. Skin patch tests were performed in 59% of patients, with 24% showing positive results and 33% negative. Incidental ISS was observed in 18% of patients, and the rate of TIA/Stroke was reported in 21%. The pooled rates of ISS and TIA/Stroke were higher in the first group (43% and 38%) compared to the second (18% and 9%) and third groups (15% and 15%), but these differences were not statistically significant.</p><p><strong>Conclusions: </strong>The current neurosurgical literature does not provide a conclusive association between metal allergy and increased complications among patients undergoing neurovascular stenting. Further studies are necessary to gain a more comprehensive understanding of this topic.</p>","PeriodicalId":49174,"journal":{"name":"Interventional Neuroradiology","volume":null,"pages":null},"PeriodicalIF":1.7,"publicationDate":"2024-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139473016","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Balloon-assisted U-turn Technique to Access Cortical Vein for Transvenous Embolization of Mixed Dural-pial Arteriovenous Malformation. 经静脉栓塞硬脊膜-皮质混合动静脉畸形的球囊辅助 U 形转弯技术。
IF 1.7 4区 医学 Q3 Medicine Pub Date : 2024-01-15 DOI: 10.1177/15910199231226288
Muhammed Amir Essibayi, Dhrumil Vaishnav, Ryan Holland, David J Altschul

Cerebral arteriovenous malformations can be classified into pure pial, mixed dural-pial, and pure dural types. Mixed pial-dural AVMs (DPAVM) are rare and often receive blood supply from dural meningeal arteries, including branches of the internal carotid, external carotid, and vertebral arteries.1- 6 DPAVMs, which are usually large and complex, require delicate endovascular and surgical treatment methods. The cure rate is low, and recurrence is very common, leading to high morbidity and mortality. In this case video, we present a case of PDAVM that recurred after initial endovascular onyx embolization, requiring additional endovascular coiling which resulted in obliteration of the DPAVM.

脑动静脉畸形可分为纯硬膜型、硬膜-硬膜混合型和纯硬膜型。硬脑膜混合型动静脉畸形(DPAVM)较为罕见,通常由硬脑膜动脉供血,包括颈内动脉、颈外动脉和椎动脉的分支。1- 6 DPAVM 通常较大且复杂,需要精细的血管内治疗和手术治疗方法,治愈率低,复发率高,导致高发病率和高死亡率。在本病例视频中,我们介绍了一例 PDAVM 病例,该病例在最初的血管内缟玛瑙栓塞术后复发,需要进行额外的血管内卷绕术,最终导致 DPAVM 闭塞。
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Interventional Neuroradiology
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