8 research outputs found

    Abstract 1122‐000138: De Novo Intracranial Stenosis after Mechanical Thrombectomy with Stent Retrievers

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    Introduction: Increased vascular damage with the use of stent‐retrievers (SR) has been shown on histopathological analysis of the vascular tissue immediately after mechanical thrombectomy (MT) in animal models. We hypothesized that intraoperative endovascular damage‐intimal injury could result in fibrosis and de novo vascular stenosis (dnVS). The purpose of the study is to identify de novo or worsening intracranial stenosis (wICS) of the treated vessel(s) on patients who underwent MT for the treatment of acute ischemic stroke with SR, on follow‐up vascular imaging (FVI). Methods: This was a retrospective chart review. Patients who underwent MT with SR at two centers from January 2015‐December 2020, who had FVI (CTA, MRA or cerebral angiogram) were included. Patient characteristics, procedural details, timing for FVI and clinical outcomes were collected. Two neuroradiologists reviewed baseline angiograms and FVI to assess for the presence of dnVS or wICS, and graded each stenosis and collateral scores (CS), when stenosis was present. CS were calculated using the multiphase CT angiography collateral score (mCTA). Fischer exact test and Mann‐Whitney U test were used to assess for differences in categorical and continuous variables, respectively. Statistical analysis was performed using SPSS 28.0 (IBM Corp.). Results: Forty‐six patients within this cohort had FVI with 9 patients developing dnVS or wICS in the follow‐up period (19.6%) with a median follow‐up of 113 days. Five of these patients demonstrated a complete occlusion of the target vessel on FVI. Of the remaining 4 patients, mean degree of stenosis was 55%. Only 2 of these patients had underlying stenosis on baseline post‐treatment angiogram: one with 44% stenosis which progressed to 95% in 2 months. Another with mild stenosis that progressed to complete occlusion in 50 days. Adequate revascularization, defined as TICI score >2b was achieved in 88.8% of patients with dnVS or wICS, and in 89.2% of patients with stable FVI. No significant differences were observed in baseline demographics, NIHSS score at presentation or initial ASPECTS. Median number of passes was identical between patients who developed dnVS or wICS (median 1, IQR [1, 2], p = 0.683). Mean CS for dnVS or wICS was 3. No significant differences were observed in discharge or follow‐up NIHSS scores, mRS, mortality, or recurrent stroke or TIA between the two cohorts. Conclusions: MT with SR can be associated with dnVS or wICS in some patients. The number of passes with SR did not seem to have an impact on this. Patients with dnVS or wICS did not have a higher incidence of recurrent stroke or TIA. This could be due to the development of new collaterals in this population. Our study is limited by a small cohort, however, larger studies might be challenging as standardized radiological follow up of these patients has not been implemented

    Predictors of Decompressive Hemicraniectomy in Successfully Recanalized Patients With Anterior Circulation Emergency Large‐Vessel Occlusion

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    Background Mechanical thrombectomy (MT) has been shown to improve functional outcome in patients with anterior circulation strokes and emergent large‐vessel occlusion (ELVO). Despite successful recanalization, some of these patients require decompressive hemicraniectomy (DHC). We aimed to study the predictors of DHC in successfully recanalized anterior circulation ELVO patients. Methods Consecutive patients with anterior circulation ELVO treated with MT during a 6‐year period were evaluated. Only successfully recanalized patients (modified Thrombolysis in Cerebral Infarction grades 2b, 2c, or 3) after MT were included in the analysis. Baseline demographic, clinical, and procedural variables were compared between patients requiring DHC after successful recanalization versus those who did not. Results Of 453 successfully recanalized patients with ELVO, 47 who underwent DHC had higher admission blood glucose levels (170±88 versus 142±66 mg/dL; P=0.008), lower median Alberta Stroke Program Early CT Scores (9 [interquartile range, 8–10] versus 10 [interquartile range, 9–10]; P=0.002), higher prevalence of poor collaterals on pretreatment computed tomography angiogram (75% versus 26%; P<0.001), and required more passes during MT (median, 3 [interquartile range, 3–4] versus 2 [interquartile range, 1–2]; P=0.001) compared with those who did not undergo DHC. In a multivariable model after adjusting for multiple confounders, higher admission blood glucose levels (P=0.031), poor collaterals on computed tomography angiography (P<0.001), and higher number of passes during MT (P<0.001) emerged as independent predictors of DHC in successfully recanalized patients with ELVO. Conclusions Higher admission blood glucose levels, poor collateral pattern on computed tomography angiography, and higher number of passes during MT were independently associated with DHC in patients with anterior circulation ELVO achieving successful recanalization following MT

    Pivotal Trial of the Neuroform Atlas Stent for Treatment of Anterior Circulation Aneurysms

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    Background and purposeStent-assisted coil embolization using the new generation Neuroform Atlas Stent System has shown promising safety and efficacy. The primary study results of the anterior circulation aneurysm cohort of the treatment of wide-neck, saccular, intracranial, aneurysms with the Neuroform Atlas Stent System (ATLAS trial [Safety and Effectiveness of the Treatment of Wide Neck, Saccular Intracranial Aneurysms With the Neuroform Atlas Stent System]) are presented.MethodsATLAS IDE trial (Investigational Device Exemption) is a prospective, multicenter, single-arm, open-label study of wide-neck (neck ≄4 mm or dome-to-neck ratio &lt;2) intracranial aneurysms in the anterior circulation treated with the Neuroform Atlas Stent and approved coils. The primary efficacy end point was complete aneurysm occlusion (Raymond-Roy class 1) on 12-month angiography, in the absence of retreatment or parent artery stenosis (&gt;50%) at the target location. The primary safety end point was any major stroke or ipsilateral stroke or neurological death within 12 months. Adjudication of the primary end points was performed by an independent Imaging Core Laboratory and the Clinical Events Committee.ResultsA total of 182 patients with wide-neck anterior circulation aneurysms at 25 US centers were enrolled. The mean age was 60.3±11.4 years, 73.1% (133/182) women, and 80.8% (147/182) white. Mean aneurysm size was 6.1±2.2 mm, mean neck width was 4.1±1.2 mm, and mean dome-to-neck ratio was 1.2±0.3. The most frequent aneurysm locations were the anterior communicating artery (64/182, 35.2%), internal carotid artery ophthalmic artery segment (29/182, 15.9%), and middle cerebral artery bifurcation (27/182, 14.8%). Stents were placed in the anticipated anatomic location in all patients. The study met both primary safety and efficacy end points. The composite primary efficacy end point of complete aneurysm occlusion (Raymond-Roy 1) without parent artery stenosis or aneurysm retreatment was achieved in 84.7% (95% CI, 78.6%-90.9%) of patients. Overall, 4.4% (8/182, 95% CI, 1.9%-8.5%) of patients experienced a primary safety end point of major ipsilateral stroke or neurological death.ConclusionsIn the ATLAS IDE anterior circulation aneurysm cohort premarket approval study, the Neuroform Atlas stent with adjunctive coiling met the primary end points and demonstrated high rates of long-term complete aneurysm occlusion at 12 months, with 100% technical success and &lt;5% morbidity. Registration: URL: https://www.clinicaltrials.gov. Unique identifier: NCT02340585
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