Pub Date : 2026-01-13DOI: 10.1136/jnis-2024-022896
Emmanuel C Ebirim, Ngoc Mai Le, Joseph N Samaha, Hussain Azeem, Ananya Iyyangar, Anjan N Ballekere, Saagar Dhanjani, Luca Giancardo, Eunyoung Lee, Sunil A Sheth
Background: Automated machine learning (ML)-based large vessel occlusion (LVO) detection algorithms have been shown to improve in-hospital workflow metrics including door-to-groin time (DTG). The degree to which care team engagement and interaction are required for these benefits remains incompletely characterized.
Methods: This analysis was conducted as a pre-planned post-hoc analysis of a randomized prospective clinical trial. ML-based LVO detection software was implemented at four comprehensive stroke centers (CSCs) from January 1, 2021, to February 27, 2022. Patients were included if they underwent endovascular thrombectomy for LVO acute ischemic stroke. ML software utilization was quantified as the total number of active users and the ratio of the number of comments to the number of patients analyzed by the software by site per week. Primary outcome was the reduction in DTG relative to pre-ML implementation by hospital utilization level. Data are expressed as median (IQR).
Results: Among 101 patients who met the inclusion criteria, the median age was 71 years (IQR 59-79), with 48.5% being female. CSC 4 had the greatest number of total active users per week (32.5 (27.5-34.5)), and comment-to-patient ratio per week (5.8 (4.6-6.9)). Increased ML software utilization was associated with improvements in DTG reduction. For every 1 unit increase in the comment-to-patient ratio, DTG time decreased by 2.6 (95% CI -5.09 to -0.13) min, while accounting for site-level random effects. Number of users-to-patient was not associated with a reduction in DTG time (β=-0.22, 95% CI -1.78 to 1.33).
Conclusions: In this post-hoc analysis, user engagement with software, rather than total number of users, was associated with site-specific improvements in DTG time.
背景:基于自动机器学习(ML)的大血管闭塞(LVO)检测算法已被证明可以改善医院工作流程指标,包括门到腹股沟时间(DTG)。护理团队参与和互动的程度对这些好处的要求仍然不完全明确。方法:本分析作为一项随机前瞻性临床试验的预先计划事后分析进行。基于ml的LVO检测软件于2021年1月1日至2022年2月27日在四家综合脑卒中中心(CSCs)实施。如果患者因左心室急性缺血性卒中而接受血管内血栓切除术,则纳入研究。ML软件利用率被量化为每周活跃用户总数和评论数与软件分析的患者数之比。主要结局是医院利用水平相对于ml实施前的DTG降低。数据以中位数(IQR)表示。结果:101例符合纳入标准的患者中位年龄为71岁(IQR 59 ~ 79),女性占48.5%。CSC 4每周总活跃用户数量最多(32.5(27.5-34.5)),每周评论与患者比率(5.8(4.6-6.9))。ML软件利用率的提高与DTG降低的改善有关。评论与患者比率每增加1个单位,DTG时间减少2.6分钟(95% CI -5.09至-0.13),同时考虑到部位水平的随机效应。使用者对患者的数量与DTG时间的减少无关(β=-0.22, 95% CI -1.78至1.33)。结论:在这个事后分析中,用户对软件的参与,而不是用户总数,与特定站点的DTG时间改善有关。
{"title":"Workflow improvements from automated large vessel occlusion detection algorithms are dependent on care team engagement.","authors":"Emmanuel C Ebirim, Ngoc Mai Le, Joseph N Samaha, Hussain Azeem, Ananya Iyyangar, Anjan N Ballekere, Saagar Dhanjani, Luca Giancardo, Eunyoung Lee, Sunil A Sheth","doi":"10.1136/jnis-2024-022896","DOIUrl":"10.1136/jnis-2024-022896","url":null,"abstract":"<p><strong>Background: </strong>Automated machine learning (ML)-based large vessel occlusion (LVO) detection algorithms have been shown to improve in-hospital workflow metrics including door-to-groin time (DTG). The degree to which care team engagement and interaction are required for these benefits remains incompletely characterized.</p><p><strong>Methods: </strong>This analysis was conducted as a pre-planned post-hoc analysis of a randomized prospective clinical trial. ML-based LVO detection software was implemented at four comprehensive stroke centers (CSCs) from January 1, 2021, to February 27, 2022. Patients were included if they underwent endovascular thrombectomy for LVO acute ischemic stroke. ML software utilization was quantified as the total number of active users and the ratio of the number of comments to the number of patients analyzed by the software by site per week. Primary outcome was the reduction in DTG relative to pre-ML implementation by hospital utilization level. Data are expressed as median (IQR).</p><p><strong>Results: </strong>Among 101 patients who met the inclusion criteria, the median age was 71 years (IQR 59-79), with 48.5% being female. CSC 4 had the greatest number of total active users per week (32.5 (27.5-34.5)), and comment-to-patient ratio per week (5.8 (4.6-6.9)). Increased ML software utilization was associated with improvements in DTG reduction. For every 1 unit increase in the comment-to-patient ratio, DTG time decreased by 2.6 (95% CI -5.09 to -0.13) min, while accounting for site-level random effects. Number of users-to-patient was not associated with a reduction in DTG time (β=-0.22, 95% CI -1.78 to 1.33).</p><p><strong>Conclusions: </strong>In this post-hoc analysis, user engagement with software, rather than total number of users, was associated with site-specific improvements in DTG time.</p>","PeriodicalId":16411,"journal":{"name":"Journal of NeuroInterventional Surgery","volume":" ","pages":"385-389"},"PeriodicalIF":4.3,"publicationDate":"2026-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143052687","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-13DOI: 10.1136/jnis-2025-023068
Christian Ferreira, Marcio Yuri Ferreira, Faith Singh, Tamika Wong, Sanskruti Bokil, Sara Massimo, Julianna Cavallaro, Olivia Albers, Randy D'Amico, David Langer, John Boockvar, Yafell Serulle
Background: Newly diagnosed glioblastoma (ndGBM) remains one of the most challenging malignancies to treat. Since the majority of patients experience tumor recurrence (rGBM) after first-line therapy, advancements in both initial and salvage treatments are essential.
Objective: We report our single-center experience on the feasibility and safety of superselective intra-arterial cerebral infusion (SIACI) with bevacizumab or cetuximab after osmotic blood-brain barrier disruption (oBBBd).
Methods: Partial results of three distinct trials (anonymized for blinded review) were analyzed. All patients were histopathologically confirmed to have either ndGBM or previously diagnosed ndGBM that progressed to rGBM despite standard therapy and had aKarnofsky Performance Status (KPS)≥70. All patients were admitted on the same day of the surgery, and the intervention followed similar steps in all included patients. Under general anesthesia, after oBBBd with mannitol, patients received SIACI.
Results: Between October 2014 and March 2024, 70 patients with a mean age of 56.2±12.4 years (range: 19-78) underwent successful treatment, encompassing 139 SIACIs and 246 infusions. All planned SIACIs were completed successfully. Forty-one patients with rGBM received bevacizumab-SIACI, 7 with ndGBM bevacizumab-SIACI, and 22 with ndGBM cetuximab-SIACI. In 133 of 139 SIACIs (95.7%), patients were discharged home with a length of stay of 1 day. The incidence of patients who experienced procedure-related and drug-related adverse events was 11.4% and 8.6%, respectively. No procedure-related deaths occurred.
Conclusion: In our single-center experience, comprising the largest cohort of bevacizumab or cetuximab SIACI treatment for rGBM and ndGBM, this promising and cutting-edge intervention is highly feasible and safe.
{"title":"Superselective intra-arterial cerebral infusion of chemotherapeutics after osmotic blood-brain barrier disruption in newly diagnosed or recurrent glioblastoma: technical insights and clinical outcomes from a single-center experience.","authors":"Christian Ferreira, Marcio Yuri Ferreira, Faith Singh, Tamika Wong, Sanskruti Bokil, Sara Massimo, Julianna Cavallaro, Olivia Albers, Randy D'Amico, David Langer, John Boockvar, Yafell Serulle","doi":"10.1136/jnis-2025-023068","DOIUrl":"10.1136/jnis-2025-023068","url":null,"abstract":"<p><strong>Background: </strong>Newly diagnosed glioblastoma (ndGBM) remains one of the most challenging malignancies to treat. Since the majority of patients experience tumor recurrence (rGBM) after first-line therapy, advancements in both initial and salvage treatments are essential.</p><p><strong>Objective: </strong>We report our single-center experience on the feasibility and safety of superselective intra-arterial cerebral infusion (SIACI) with bevacizumab or cetuximab after osmotic blood-brain barrier disruption (oBBBd).</p><p><strong>Methods: </strong>Partial results of three distinct trials (anonymized for blinded review) were analyzed. All patients were histopathologically confirmed to have either ndGBM or previously diagnosed ndGBM that progressed to rGBM despite standard therapy and had aKarnofsky Performance Status (KPS)≥70. All patients were admitted on the same day of the surgery, and the intervention followed similar steps in all included patients. Under general anesthesia, after oBBBd with mannitol, patients received SIACI.</p><p><strong>Results: </strong>Between October 2014 and March 2024, 70 patients with a mean age of 56.2±12.4 years (range: 19-78) underwent successful treatment, encompassing 139 SIACIs and 246 infusions. All planned SIACIs were completed successfully. Forty-one patients with rGBM received bevacizumab-SIACI, 7 with ndGBM bevacizumab-SIACI, and 22 with ndGBM cetuximab-SIACI. In 133 of 139 SIACIs (95.7%), patients were discharged home with a length of stay of 1 day. The incidence of patients who experienced procedure-related and drug-related adverse events was 11.4% and 8.6%, respectively. No procedure-related deaths occurred.</p><p><strong>Conclusion: </strong>In our single-center experience, comprising the largest cohort of bevacizumab or cetuximab SIACI treatment for rGBM and ndGBM, this promising and cutting-edge intervention is highly feasible and safe.</p>","PeriodicalId":16411,"journal":{"name":"Journal of NeuroInterventional Surgery","volume":" ","pages":"585-593"},"PeriodicalIF":4.3,"publicationDate":"2026-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143567195","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Studies have been conducted to explore the potential predictive indicators of unfavorable outcomes in patients with acute ischemic stroke (AIS) caused by large vessel occlusion (LVO). However, few studies have proposed a comprehensive predictive model combined with clinical baseline data and ancillary examination before surgery.
Method: In a retrospective study, we collected data on 823 patients with AIS-LVO who had undergone endovascular therapy (EVT); 562 patients who achieved successful revascularization with complete clinical and prognostic information were incorporated into the study. Those patients with a 90-day modified Rankin Scale (mRS) score of 0-2 were defined as having a favorable outcome, while a score of 3-6 represented an unfavorable outcome or futile reperfusion. To build up a predictive model, we applied multivariate logistic regression stepwise backward selection to decide which factors are supposed to be the components of the predictive model. Final model validity was testified by the variance inflation factor test and the Hosmer-Lemeshow (HL) goodness of fit test. The ultimate efficacy was supported by an area under the curve (AUC) value in both training groups and validation groups.
Results: 562 patients were enrolled in our study and divided into the training group and verification group in a ratio of 7:3. Factors of baseline data with P<0.1 in univariate logistic regression analysis were enrolled as the potential risk variables to conduct stepwise backward selection. The model was constructed by eight variables; higher mRS score (adjusted OR (aOR) 93.64, 95% CI 12.05 to 727.82, P<0.01), age >80 years (aOR 91.11, 95% CI 1.36 to 6116.36, P<0.05), National Institutes of Health Stroke Scale (NIHSS) >14 (aOR 0.15, 95% CI 0.02 to 0.99, P<0.05), operation history (aOR 8.13, 95% CI 1.32 to 50.20, P<0.05), creatinine (aOR 1.10, 95% CI 1.04 to 1.17, P<0.01), and neutrophil count (aOR 1.07, 95% CI 1.01 to 1.13, P<0.05) were associated with poor outcomes.
Conclusion: We established an estimation model for invalid reperfusion in AIS-LVO patients and constructed the nomogram for individualized predictions. The AUC of the training group and validation group were both 0.96, with excellent HL and decision curve analysis, presenting excellent clinical prediction efficiency and application potential.
{"title":"Clinical prediction model of invalid recanalization after complete reperfusion after thrombectomy in acute ischemic stroke patients: a large retrospective study.","authors":"Yuan Yuan, Shandong Jiang, Jingbo Li, Jing Zhang, Jingjing Ding, Sainan Liu, Jingyi Wang, Yanyan Zhang, Jianru Li, Gao Chen","doi":"10.1136/jnis-2025-023036","DOIUrl":"10.1136/jnis-2025-023036","url":null,"abstract":"<p><strong>Background: </strong>Studies have been conducted to explore the potential predictive indicators of unfavorable outcomes in patients with acute ischemic stroke (AIS) caused by large vessel occlusion (LVO). However, few studies have proposed a comprehensive predictive model combined with clinical baseline data and ancillary examination before surgery.</p><p><strong>Method: </strong>In a retrospective study, we collected data on 823 patients with AIS-LVO who had undergone endovascular therapy (EVT); 562 patients who achieved successful revascularization with complete clinical and prognostic information were incorporated into the study. Those patients with a 90-day modified Rankin Scale (mRS) score of 0-2 were defined as having a favorable outcome, while a score of 3-6 represented an unfavorable outcome or futile reperfusion. To build up a predictive model, we applied multivariate logistic regression stepwise backward selection to decide which factors are supposed to be the components of the predictive model. Final model validity was testified by the variance inflation factor test and the Hosmer-Lemeshow (HL) goodness of fit test. The ultimate efficacy was supported by an area under the curve (AUC) value in both training groups and validation groups.</p><p><strong>Results: </strong>562 patients were enrolled in our study and divided into the training group and verification group in a ratio of 7:3. Factors of baseline data with P<0.1 in univariate logistic regression analysis were enrolled as the potential risk variables to conduct stepwise backward selection. The model was constructed by eight variables; higher mRS score (adjusted OR (aOR) 93.64, 95% CI 12.05 to 727.82, P<0.01), age >80 years (aOR 91.11, 95% CI 1.36 to 6116.36, P<0.05), National Institutes of Health Stroke Scale (NIHSS) >14 (aOR 0.15, 95% CI 0.02 to 0.99, P<0.05), operation history (aOR 8.13, 95% CI 1.32 to 50.20, P<0.05), creatinine (aOR 1.10, 95% CI 1.04 to 1.17, P<0.01), and neutrophil count (aOR 1.07, 95% CI 1.01 to 1.13, P<0.05) were associated with poor outcomes.</p><p><strong>Conclusion: </strong>We established an estimation model for invalid reperfusion in AIS-LVO patients and constructed the nomogram for individualized predictions. The AUC of the training group and validation group were both 0.96, with excellent HL and decision curve analysis, presenting excellent clinical prediction efficiency and application potential.</p>","PeriodicalId":16411,"journal":{"name":"Journal of NeuroInterventional Surgery","volume":" ","pages":"348-355"},"PeriodicalIF":4.3,"publicationDate":"2026-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143811361","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-13DOI: 10.1136/jnis-2024-022870
Huanwen Chen, Rosy L Njonkou-Tchoquessi, Ananya Iyyangar, Paige Skorseth, Shyam Majmundar, Jacob Cherian, Timothy R Miller, Sunil A Sheth, Dheeraj Gandhi, Marco Colasurdo
Background: Complete recanalization (CR, modified Treatment in Cerebral Ischemia (mTICI) score of 2c or better) is associated with favorable outcomes after endovascular thrombectomy (EVT) for stroke patients. However, the degree of inter-proceduralist differences in CR rates is unknown, and whether higher CR rates are being achieved by performing more passes or by focusing on first-pass effectiveness is also unclear.
Methods: This was a multicenter retrospective study of anterior circulation large vessel occlusion stroke patients in the United States from 2016 to 2022. Patients treated by proceduralists with at least 50 cases were included. CR rates for each proceduralist were assessed and proceduralists were divided into tertiles. First-pass effect (FPE, defined as CR after one pass) and the number of passes for patients treated by the top tertile of proceduralists were compared with the bottom tertile. Mediation analyses were conducted to assess causal links between CR rates and number of passes or FPE.
Results: A total of 1096 EVTs performed by 11 proceduralists were identified. CR rates were highly variable across providers (43.1% to 75.3%, p<0.001). Patients treated by the top tertile were more likely to experience FPE (OR 1.99, 95% CI 1.49 to 2.67, p<0.001) and did not undergo more passes (p=0.69) compared with the bottom tertile. Higher rates of FPE among patients was a significant mediator of higher odds of CR among patients treated by the top tertile (p<0.001).
Conclusions: Angiographic outcomes among EVT proceduralists are highly variable. Proceduralists who achieve higher rates of CR are doing so with higher rates of FPE, not more passes.
{"title":"Inter-proceduralist variability in angiographic outcomes after stroke thrombectomy and the importance of quality over quantity of passes.","authors":"Huanwen Chen, Rosy L Njonkou-Tchoquessi, Ananya Iyyangar, Paige Skorseth, Shyam Majmundar, Jacob Cherian, Timothy R Miller, Sunil A Sheth, Dheeraj Gandhi, Marco Colasurdo","doi":"10.1136/jnis-2024-022870","DOIUrl":"10.1136/jnis-2024-022870","url":null,"abstract":"<p><strong>Background: </strong>Complete recanalization (CR, modified Treatment in Cerebral Ischemia (mTICI) score of 2c or better) is associated with favorable outcomes after endovascular thrombectomy (EVT) for stroke patients. However, the degree of inter-proceduralist differences in CR rates is unknown, and whether higher CR rates are being achieved by performing more passes or by focusing on first-pass effectiveness is also unclear.</p><p><strong>Methods: </strong>This was a multicenter retrospective study of anterior circulation large vessel occlusion stroke patients in the United States from 2016 to 2022. Patients treated by proceduralists with at least 50 cases were included. CR rates for each proceduralist were assessed and proceduralists were divided into tertiles. First-pass effect (FPE, defined as CR after one pass) and the number of passes for patients treated by the top tertile of proceduralists were compared with the bottom tertile. Mediation analyses were conducted to assess causal links between CR rates and number of passes or FPE.</p><p><strong>Results: </strong>A total of 1096 EVTs performed by 11 proceduralists were identified. CR rates were highly variable across providers (43.1% to 75.3%, p<0.001). Patients treated by the top tertile were more likely to experience FPE (OR 1.99, 95% CI 1.49 to 2.67, p<0.001) and did not undergo more passes (p=0.69) compared with the bottom tertile. Higher rates of FPE among patients was a significant mediator of higher odds of CR among patients treated by the top tertile (p<0.001).</p><p><strong>Conclusions: </strong>Angiographic outcomes among EVT proceduralists are highly variable. Proceduralists who achieve higher rates of CR are doing so with higher rates of FPE, not more passes.</p>","PeriodicalId":16411,"journal":{"name":"Journal of NeuroInterventional Surgery","volume":" ","pages":"371-376"},"PeriodicalIF":4.3,"publicationDate":"2026-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143432459","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-13DOI: 10.1136/jnis-2024-022792
Seyed Behnam Jazayeri, Omar M Al-Janabi, Aysha Alateya, Sara Muhammad, Sherief Ghozy, Alejandro A Rabinstein, Ramanathan Kadirvel, David F Kallmes
Background: Left ventricular assist devices (LVADs) are used as definitive therapy or as a bridge to heart transplant in patients with advanced heart failure. Thromboembolic complications such as acute ischemic stroke (AIS) are common among patients with LVAD support. This study aims to evaluate the current evidence on the efficacy and safety of mechanical thrombectomy (MT) in patients with AIS due to large vessel occlusions (LVO) and LVAD-support.
Methods: A comprehensive systematic review was conducted in PubMed, Embase, and Scopus to find observational studies with reports of ≥5 MTs in adult patients with LVAD support (PROSPERO registration code CRD42024597541). Rates of successful and complete reperfusion, favorable functional outcomes at 90 days (modified Rankin Scale (mRS) 0-2 or equal to pre-stroke mRS), mortality at 90 days, any intracerebral hemorrhage (ICH) and symptomatic ICH (sICH) were pooled using generalized linear mixed models.
Results: Eight studies were included with data from 51 patients and 62 MTs. The rate of successful reperfusion was 87.4% (95% CI 62.5% to 96.6%) and complete reperfusion rate was 57.3% (95% CI 35.1% to 76.9%). Rate of favorable functional recovery was 62.5% (95% CI 42.2% to 79.2%). Rate of sICH was 6.4% (95% CI 0.9% to 34.0%). Mortality rate was 16.7% (95% CI 7.1% to 34.7%). Between 25-40% of patients who were waiting for a heart transplant before their stroke received a heart transplant after MT.
Conclusions: MT for the emergent treatment of AIS in the setting of LVAD is relatively safe and efficacious for achieving successful reperfusion and good functional recovery.
背景:左心室辅助装置(lvad)被用作晚期心力衰竭患者的决定性治疗或心脏移植的桥梁。急性缺血性脑卒中(AIS)等血栓栓塞并发症在LVAD支持患者中很常见。本研究旨在评估机械取栓(MT)治疗大血管闭塞(LVO)和lvad支持的AIS患者的有效性和安全性。方法:在PubMed、Embase和Scopus中进行全面的系统评价,寻找在LVAD支持的成年患者(PROSPERO注册码CRD42024597541)中报告≥5个MTs的观察性研究。使用广义线性混合模型汇总再灌注成功率和完全再灌注率、90天时良好的功能结局(改良Rankin量表(mRS) 0-2或等于卒中前mRS)、90天死亡率、任何脑出血(ICH)和症状性ICH (sICH)。结果:纳入8项研究,51例患者和62例MTs的数据,再灌注成功率为87.4% (95% CI 62.5% ~ 96.6%),完全再灌注率为57.3% (95% CI 35.1% ~ 76.9%)。功能恢复良好率为62.5% (95% CI 42.2% ~ 79.2%)。siich发生率为6.4% (95% CI 0.9% ~ 34.0%)。死亡率为16.7% (95% CI 7.1% ~ 34.7%)。在卒中前等待心脏移植的患者中,有25-40%的患者在心脏移植后接受了心脏移植。结论:在LVAD的情况下,心脏移植用于AIS的紧急治疗是相对安全有效的,可以实现成功的再灌注和良好的功能恢复。
{"title":"Efficacy and safety of mechanical thrombectomy in patients with acute ischemic stroke and left ventricular assist device: review of the literature and meta-analysis.","authors":"Seyed Behnam Jazayeri, Omar M Al-Janabi, Aysha Alateya, Sara Muhammad, Sherief Ghozy, Alejandro A Rabinstein, Ramanathan Kadirvel, David F Kallmes","doi":"10.1136/jnis-2024-022792","DOIUrl":"10.1136/jnis-2024-022792","url":null,"abstract":"<p><strong>Background: </strong>Left ventricular assist devices (LVADs) are used as definitive therapy or as a bridge to heart transplant in patients with advanced heart failure. Thromboembolic complications such as acute ischemic stroke (AIS) are common among patients with LVAD support. This study aims to evaluate the current evidence on the efficacy and safety of mechanical thrombectomy (MT) in patients with AIS due to large vessel occlusions (LVO) and LVAD-support.</p><p><strong>Methods: </strong>A comprehensive systematic review was conducted in PubMed, Embase, and Scopus to find observational studies with reports of ≥5 MTs in adult patients with LVAD support (PROSPERO registration code CRD42024597541). Rates of successful and complete reperfusion, favorable functional outcomes at 90 days (modified Rankin Scale (mRS) 0-2 or equal to pre-stroke mRS), mortality at 90 days, any intracerebral hemorrhage (ICH) and symptomatic ICH (sICH) were pooled using generalized linear mixed models.</p><p><strong>Results: </strong>Eight studies were included with data from 51 patients and 62 MTs. The rate of successful reperfusion was 87.4% (95% CI 62.5% to 96.6%) and complete reperfusion rate was 57.3% (95% CI 35.1% to 76.9%). Rate of favorable functional recovery was 62.5% (95% CI 42.2% to 79.2%). Rate of sICH was 6.4% (95% CI 0.9% to 34.0%). Mortality rate was 16.7% (95% CI 7.1% to 34.7%). Between 25-40% of patients who were waiting for a heart transplant before their stroke received a heart transplant after MT.</p><p><strong>Conclusions: </strong>MT for the emergent treatment of AIS in the setting of LVAD is relatively safe and efficacious for achieving successful reperfusion and good functional recovery.</p>","PeriodicalId":16411,"journal":{"name":"Journal of NeuroInterventional Surgery","volume":" ","pages":"339-347"},"PeriodicalIF":4.3,"publicationDate":"2026-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143039206","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-13DOI: 10.1136/jnis-2024-022737
Guillaume Charbonnier, Nicole M Cancelliere, Alice B Brochu, Allison M Marley, Vitor M Pereira
Background: New generation flow-diverting stents have benefited from recent technological advances to reduce their thrombogenicity. This in vitro study is the first of its kind to compare multiple surface modified flow diverters with their bare metal counterparts.
Methods: A thrombin generation assay (TGA) was used to compare thrombin generation resulting from different stent types with glass beads (positive control) and plasma (negative control). Ten different stent types were studied, including a next-generation implant, Surpass Elite, with two different surface modifications. A thrombogram was generated from each of the 10 sample types, from which peak thrombin generation and time to peak (TTP) were obtained.
Results: Compared with the positive control and their bare metal counterparts, lower peak thrombin and longer TTP were obtained with most of the surface modified devices tested. Only the stent with an active heparin drug coating demonstrated lower peak thrombin and TTP than the negative control plasma.
Conclusion: Generally, surface modification resulted in lower thrombogenicity, as assessed by peak thrombin concentration and TTP, when compared with the unmodified version of the device. The device with an active heparin drug coating was significantly different from other surface modifications and plasma with respect to peak thrombin and TTP, though the implications of this should be investigated through future in vitro and in vivo studies.
{"title":"Thrombogenicity assessment of surface-modified flow diverters: the impact of different surface modification strategies on thrombin generation in an acute <i>in vitro</i> test.","authors":"Guillaume Charbonnier, Nicole M Cancelliere, Alice B Brochu, Allison M Marley, Vitor M Pereira","doi":"10.1136/jnis-2024-022737","DOIUrl":"10.1136/jnis-2024-022737","url":null,"abstract":"<p><strong>Background: </strong>New generation flow-diverting stents have benefited from recent technological advances to reduce their thrombogenicity. This in vitro study is the first of its kind to compare multiple surface modified flow diverters with their bare metal counterparts.</p><p><strong>Methods: </strong>A thrombin generation assay (TGA) was used to compare thrombin generation resulting from different stent types with glass beads (positive control) and plasma (negative control). Ten different stent types were studied, including a next-generation implant, Surpass Elite, with two different surface modifications. A thrombogram was generated from each of the 10 sample types, from which peak thrombin generation and time to peak (TTP) were obtained.</p><p><strong>Results: </strong>Compared with the positive control and their bare metal counterparts, lower peak thrombin and longer TTP were obtained with most of the surface modified devices tested. Only the stent with an active heparin drug coating demonstrated lower peak thrombin and TTP than the negative control plasma.</p><p><strong>Conclusion: </strong>Generally, surface modification resulted in lower thrombogenicity, as assessed by peak thrombin concentration and TTP, when compared with the unmodified version of the device. The device with an active heparin drug coating was significantly different from other surface modifications and plasma with respect to peak thrombin and TTP, though the implications of this should be investigated through future <i>in vitro</i> and <i>in vivo</i> studies.</p>","PeriodicalId":16411,"journal":{"name":"Journal of NeuroInterventional Surgery","volume":" ","pages":"493-499"},"PeriodicalIF":4.3,"publicationDate":"2026-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143573180","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Blood urea/creatinine (U/Cr) ratio is considered to be an ideal biomarker of dehydration. We investigated the association between the U/Cr ratio trajectory and delayed cerebral ischemia (DCI) as well as functional outcome in aneurysmal subarachnoid hemorrhage (aSAH). Additionally, we explored the role of DCI as a mediator and its interaction with dehydration.
Methods: Consecutive aSAH patients were reviewed. A latent class growth mixture model (LCGMM) was applied to classify the dehydration trajectory over 7 days. Multivariate logistic regression was conducted to examine associations between dehydration trajectories, DCI, and poor outcome. Furthermore, causal mediation analysis combined with a four-way decomposition approach was employed to quantify the extent to which DCI mediates or interacts with dehydration in influencing poor outcomes.
Results: A total of 519 aSAH patients were included. By applying the LCGMM method, we categorized participants into three dehydration trajectory groups: low group (n=353), decreasing group (n=97), and high group (n=69). Multivariate analysis demonstrated that dehydration trajectory was independently associated with both DCI and poor outcome. The effect of dehydration trajectory on poor outcome was partially mediated by DCI, involving both pure mediation and mediated interaction. Specifically, the excess relative risk of DCI was decomposed into four components: controlled direct effect (66.42%), mediation only (16.35%), interaction only (6.09%), and mediated interaction (11.16%).
Conclusion: Among aSAH patients, dehydration trajectory was significantly associated with poor functional outcome, with DCI serving as a partial mediator through both direct and interaction effects.
{"title":"Association between dehydration trajectory, delayed cerebral ischemia, and functional outcome in patients with aneurysmal subarachnoid hemorrhage: assessment of interaction and mediation.","authors":"Peng Zhang, Qi Tu, Minfeng Tong, Kefeng Shi, Tingyu Yang, Jiale Wang, Weizhong Zhang, Qi Pang, Zequn Li, Zhijian Xu","doi":"10.1136/jnis-2024-022953","DOIUrl":"10.1136/jnis-2024-022953","url":null,"abstract":"<p><strong>Background: </strong>Blood urea/creatinine (U/Cr) ratio is considered to be an ideal biomarker of dehydration. We investigated the association between the U/Cr ratio trajectory and delayed cerebral ischemia (DCI) as well as functional outcome in aneurysmal subarachnoid hemorrhage (aSAH). Additionally, we explored the role of DCI as a mediator and its interaction with dehydration.</p><p><strong>Methods: </strong>Consecutive aSAH patients were reviewed. A latent class growth mixture model (LCGMM) was applied to classify the dehydration trajectory over 7 days. Multivariate logistic regression was conducted to examine associations between dehydration trajectories, DCI, and poor outcome. Furthermore, causal mediation analysis combined with a four-way decomposition approach was employed to quantify the extent to which DCI mediates or interacts with dehydration in influencing poor outcomes.</p><p><strong>Results: </strong>A total of 519 aSAH patients were included. By applying the LCGMM method, we categorized participants into three dehydration trajectory groups: low group (n=353), decreasing group (n=97), and high group (n=69). Multivariate analysis demonstrated that dehydration trajectory was independently associated with both DCI and poor outcome. The effect of dehydration trajectory on poor outcome was partially mediated by DCI, involving both pure mediation and mediated interaction. Specifically, the excess relative risk of DCI was decomposed into four components: controlled direct effect (66.42%), mediation only (16.35%), interaction only (6.09%), and mediated interaction (11.16%).</p><p><strong>Conclusion: </strong>Among aSAH patients, dehydration trajectory was significantly associated with poor functional outcome, with DCI serving as a partial mediator through both direct and interaction effects.</p>","PeriodicalId":16411,"journal":{"name":"Journal of NeuroInterventional Surgery","volume":" ","pages":"450-459"},"PeriodicalIF":4.3,"publicationDate":"2026-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143670212","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-13DOI: 10.1136/jnis-2024-022842
Jin Eun, Seung Yoon Song, Sang Hyuk Im, Hae Kwan Park
Background: Transradial cerebral angiography (TRA) is a convenient but challenging procedure, particularly for selecting the left internal carotid artery (ICA) and vertebral artery.
Objective: To predict the selection of the left ICA using CT and MR images acquired before TRA.
Methods: Overall, 306 patients with TRA were enrolled and divided into either the group with success (264 patients) or the failure (42 patients) group. The following anatomical factors were measured: A1 (subclavian artery angle), A2 (right subclavian-innominate artery angle), A3 (innominate-left common carotid artery angle), D1 (aorta to right subclavian artery length), and D2 (innominate-to-left common carotid artery length).
Results: The median values for A1, A2, A3, D1, and D2 were 81.57° (IQR 69.26-94.14), 147.03° (125.73-161.09), 24.73 (15.85-37.72°), 34.73 mm (29.68-38.48), and 13.15 mm (11.33-15.64), respectively, with significant differences observed between the successful and failure groups in A3 (26.88° vs 15.50°; P<0.001), D1 (34.24 mm vs 37.62 mm; P<0.001), and D2 (12.78 mm vs 14.91 mm; P<0.001). The aortic arch type did not affect success (P=0.134), while patients in the failure group were significantly older (P<0.001). A predictive logistic regression model was developed, revealing differing factor impacts when controlling variables. The model (area under the curve 0.87) highlights data complexity and enables user-friendly prediction of left ICA-selective TRA success (https://je0000000342227505.shinyapps.io/icatra/).
Conclusion: This study demonstrated that the success of left ICA selective angiography can be predicted using aortic arch images, providing a basis for the extension of TRA.
{"title":"Transradial cerebral angiography: predicting left ICA selective angiography success using pre-diagnostic aortic arch factors.","authors":"Jin Eun, Seung Yoon Song, Sang Hyuk Im, Hae Kwan Park","doi":"10.1136/jnis-2024-022842","DOIUrl":"10.1136/jnis-2024-022842","url":null,"abstract":"<p><strong>Background: </strong>Transradial cerebral angiography (TRA) is a convenient but challenging procedure, particularly for selecting the left internal carotid artery (ICA) and vertebral artery.</p><p><strong>Objective: </strong>To predict the selection of the left ICA using CT and MR images acquired before TRA.</p><p><strong>Methods: </strong>Overall, 306 patients with TRA were enrolled and divided into either the group with success (264 patients) or the failure (42 patients) group. The following anatomical factors were measured: A1 (subclavian artery angle), A2 (right subclavian-innominate artery angle), A3 (innominate-left common carotid artery angle), D1 (aorta to right subclavian artery length), and D2 (innominate-to-left common carotid artery length).</p><p><strong>Results: </strong>The median values for A1, A2, A3, D1, and D2 were 81.57° (IQR 69.26-94.14), 147.03° (125.73-161.09), 24.73 (15.85-37.72°), 34.73 mm (29.68-38.48), and 13.15 mm (11.33-15.64), respectively, with significant differences observed between the successful and failure groups in A3 (26.88° vs 15.50°; P<0.001), D1 (34.24 mm vs 37.62 mm; P<0.001), and D2 (12.78 mm vs 14.91 mm; P<0.001). The aortic arch type did not affect success (P=0.134), while patients in the failure group were significantly older (P<0.001). A predictive logistic regression model was developed, revealing differing factor impacts when controlling variables. The model (area under the curve 0.87) highlights data complexity and enables user-friendly prediction of left ICA-selective TRA success (https://je0000000342227505.shinyapps.io/icatra/).</p><p><strong>Conclusion: </strong>This study demonstrated that the success of left ICA selective angiography can be predicted using aortic arch images, providing a basis for the extension of TRA.</p>","PeriodicalId":16411,"journal":{"name":"Journal of NeuroInterventional Surgery","volume":" ","pages":"508-512"},"PeriodicalIF":4.3,"publicationDate":"2026-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143523633","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-13DOI: 10.1136/jnis-2024-023014
Xin Su, Yongjie Ma, Zihao Song, Huiwei Liu, Chao Zhang, Huishen Pang, Yiguang Chen, Beichuan Zhao, Mingyue Huang, Liyong Sun, Peng Hu, Guilin Li, Tao Hong, Ming Ye, Hongqi Zhang, Peng Zhang
Background: Intracranial dural arteriovenous fistulas (DAVFs) are rare lesions, making it challenging to fully understand and improve their management. Globally, only two major large-scale studies have focused on DAVFs. This report outlines the design of the DREAM-INI (Dural arteriovenous fistula research and management in China) project and provides an overview of the 1101-patient cohort it includes.
Methods: Patient data were sourced from the DREAM-INI database, a retrospective, single-center observational study conducted from January 2001 to December 2022, encompassing a total of 1101 DAVF patients.
Results: The cohort consists of 367 patients diagnosed with Borden type I DAVFs, 172 patients with Borden type II fistulas, and 562 patients with Borden type III fistulas. 565 patients exhibited flow-related symptoms, 176 patients presented with intracranial hemorrhage, and 275 patients had non-hemorrhagic neurological deficits. A large proportion of patients (95.6%, 1053/1101) underwent treatment through endovascular embolization (83.7%, 922/1101), surgery (8.7%, 96/1101), or multimodal therapy (3.2%, 35/1101). The overall immediate angiographic cure rate was 85.2% (897/1053 treated cases), and the rate of treatment-related permanent neurological morbidity was 3.4% (45/1328 total procedures). The median duration from the final treatment to the last follow-up for DAVF was 39 months. The predictive factors for aggressive symptoms, initial angiographic cure, and complications in DAVFs have also been preliminarily explored.
Conclusions: With over 1100 patients, DREAM-INI represents a large and relatively well-documented registry of DAVF patient data in China and even globally. This database will enable numerous future studies, further advancing our understanding of this rare disease.
{"title":"Dural arteriovenous fistula research and management in China (DREAM-INI): initial characterization and patient cohort outcomes.","authors":"Xin Su, Yongjie Ma, Zihao Song, Huiwei Liu, Chao Zhang, Huishen Pang, Yiguang Chen, Beichuan Zhao, Mingyue Huang, Liyong Sun, Peng Hu, Guilin Li, Tao Hong, Ming Ye, Hongqi Zhang, Peng Zhang","doi":"10.1136/jnis-2024-023014","DOIUrl":"10.1136/jnis-2024-023014","url":null,"abstract":"<p><strong>Background: </strong>Intracranial dural arteriovenous fistulas (DAVFs) are rare lesions, making it challenging to fully understand and improve their management. Globally, only two major large-scale studies have focused on DAVFs. This report outlines the design of the DREAM-INI (Dural arteriovenous fistula research and management in China) project and provides an overview of the 1101-patient cohort it includes.</p><p><strong>Methods: </strong>Patient data were sourced from the DREAM-INI database, a retrospective, single-center observational study conducted from January 2001 to December 2022, encompassing a total of 1101 DAVF patients.</p><p><strong>Results: </strong>The cohort consists of 367 patients diagnosed with Borden type I DAVFs, 172 patients with Borden type II fistulas, and 562 patients with Borden type III fistulas. 565 patients exhibited flow-related symptoms, 176 patients presented with intracranial hemorrhage, and 275 patients had non-hemorrhagic neurological deficits. A large proportion of patients (95.6%, 1053/1101) underwent treatment through endovascular embolization (83.7%, 922/1101), surgery (8.7%, 96/1101), or multimodal therapy (3.2%, 35/1101). The overall immediate angiographic cure rate was 85.2% (897/1053 treated cases), and the rate of treatment-related permanent neurological morbidity was 3.4% (45/1328 total procedures). The median duration from the final treatment to the last follow-up for DAVF was 39 months. The predictive factors for aggressive symptoms, initial angiographic cure, and complications in DAVFs have also been preliminarily explored.</p><p><strong>Conclusions: </strong>With over 1100 patients, DREAM-INI represents a large and relatively well-documented registry of DAVF patient data in China and even globally. This database will enable numerous future studies, further advancing our understanding of this rare disease.</p>","PeriodicalId":16411,"journal":{"name":"Journal of NeuroInterventional Surgery","volume":" ","pages":"332-338"},"PeriodicalIF":4.3,"publicationDate":"2026-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143374303","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-13DOI: 10.1136/jnis-2024-022810
Franziska Dorn, Jan Borggrefe, Kai Kallenberg, Marielle Ernst, Daniel Behme, Annette Foerschler, Christoph Kabbasch, Thomas Liebig, Bernd Turowski, Hannes Nordmeyer
Background: Although recently presented randomized trials have failed to prove an overall benefit of mechanical thrombectomy (MT) for patients with medium vessel occlusions (MeVOs), questions remain unanswered, particularly regarding the technology and the role of dedicated small devices. This prospective multicenter, core lab reviewed registry study investigates the efficacy and safety of the APERIO Hybrid used as a first-line device for the treatment of MeVO patients.
Methods: Data from all MeVO patients who underwent MT with the APERIO or APERIO Hybrid17 as a first-line technique were prospectively included. The primary endpoint was the successful recanalization (Thrombolysis In Cerebral Infarction (TICI) 2b/3) after up to three passes with the APERIO without the use of a rescue technique and without any symptomatic intracranial hemorrhage (ICH).
Results: 134 patients were enrolled from 10 stroke centers. The primary endpoint was reached in 97 patients (81.5%, 95% CI 74.5% to 88.5%). In patients who failed the primary endpoint, TICI 2b/3 was reached with 4 to 6 APERIO passes in 4 patients (3.3%) and with other techniques in 18 patients (15%). Overall recanalization success was 95.8%. TICI 2b/3 with APERIO Hybrid was achieved after the first pass in 76 patients (63.9%), in 23 (19.3%) after 2 passes, and in 1 patient (0.8%) after 3 passes. Modified Rankin Scale (mRS) 0-2 at 90 days was reached by 79.0% of the patients. Symptomatic ICH occurred in no patients, asymptomatic ICH in 16 (13.5%), and subarachnoid hemorrhage in 15 patients (12.6%).
Conclusion: APERIO and APERIO Hybrid17 have been proven to be both safe and effective first-line devices for MT in MeVO stroke at different centers and with high rates of successful recanalization.
{"title":"REcanalization of Distal Cerebral Vessels In Acute Stroke Using ApeRio (REVISAR).","authors":"Franziska Dorn, Jan Borggrefe, Kai Kallenberg, Marielle Ernst, Daniel Behme, Annette Foerschler, Christoph Kabbasch, Thomas Liebig, Bernd Turowski, Hannes Nordmeyer","doi":"10.1136/jnis-2024-022810","DOIUrl":"10.1136/jnis-2024-022810","url":null,"abstract":"<p><strong>Background: </strong>Although recently presented randomized trials have failed to prove an overall benefit of mechanical thrombectomy (MT) for patients with medium vessel occlusions (MeVOs), questions remain unanswered, particularly regarding the technology and the role of dedicated small devices. This prospective multicenter, core lab reviewed registry study investigates the efficacy and safety of the APERIO Hybrid used as a first-line device for the treatment of MeVO patients.</p><p><strong>Methods: </strong>Data from all MeVO patients who underwent MT with the APERIO or APERIO Hybrid<sup>17</sup> as a first-line technique were prospectively included. The primary endpoint was the successful recanalization (Thrombolysis In Cerebral Infarction (TICI) 2b/3) after up to three passes with the APERIO without the use of a rescue technique and without any symptomatic intracranial hemorrhage (ICH).</p><p><strong>Results: </strong>134 patients were enrolled from 10 stroke centers. The primary endpoint was reached in 97 patients (81.5%, 95% CI 74.5% to 88.5%). In patients who failed the primary endpoint, TICI 2b/3 was reached with 4 to 6 APERIO passes in 4 patients (3.3%) and with other techniques in 18 patients (15%). Overall recanalization success was 95.8%. TICI 2b/3 with APERIO Hybrid was achieved after the first pass in 76 patients (63.9%), in 23 (19.3%) after 2 passes, and in 1 patient (0.8%) after 3 passes. Modified Rankin Scale (mRS) 0-2 at 90 days was reached by 79.0% of the patients. Symptomatic ICH occurred in no patients, asymptomatic ICH in 16 (13.5%), and subarachnoid hemorrhage in 15 patients (12.6%).</p><p><strong>Conclusion: </strong>APERIO and APERIO Hybrid<sup>17</sup> have been proven to be both safe and effective first-line devices for MT in MeVO stroke at different centers and with high rates of successful recanalization.</p>","PeriodicalId":16411,"journal":{"name":"Journal of NeuroInterventional Surgery","volume":" ","pages":"404-410"},"PeriodicalIF":4.3,"publicationDate":"2026-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144187185","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}