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      Mechanical Thrombectomy of the Fetal Posterior Cerebral Artery

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          Abstract

          Background

          Fetal posterior cerebral artery (FPCA) occlusion is a rare but potentially disabling cause of stroke. While endovascular treatment is established for acute large vessel occlusion stroke, FPCA occlusions were excluded from acute ischemic stroke trials. We aim to report the feasibility, safety, and outcome of mechanical thrombectomy in acute FPCA occlusions.

          Methods

          We performed a multicenter retrospective review of consecutive patients who underwent mechanical thrombectomy of acute FPCA occlusion. Primary FPCA occlusion was defined as an occlusion that was identified on the pre‐procedure computed tomography angiography or baseline angiogram whereas a secondary FPCA occlusion was defined as an occlusion that occurred secondary to embolization to a new territory after recanalization of a different large vessel occlusion. Demographics, clinical presentation, imaging findings, endovascular treatment, and outcome were reviewed.

          Results

          There were 25 patients with acute FPCA occlusion who underwent mechanical thrombectomy, distributed across 14 centers. Median National Institutes of Health Stroke Scale on presentation was 16. There were 76% (19/25) of patients who presented with primary FPCA occlusion and 24% (6/25) of patients who had a secondary FPCA occlusion. The configuration of the FPCA was full in 64% patients and partial or “fetal‐type” in 36% of patients. FPCA occlusion was missed on initial computed tomography angiography in 21% of patients with primary FPCA occlusion (4/19). The site of occlusion was posterior communicating artery in 52%, P2 segment in 40% and P3 in 8% of patients. Thrombolysis in cerebral infarction 2b/3 reperfusion was achieved in 96% of FPCA patients. There were no intraprocedural complications. At 90 days, 48% (12/25) were functionally independent as defined by modified Rankin scale≤2.

          Conclusions

          Endovascular treatment of acute FPCA occlusion is safe and technically feasible. A high index of suspicion is important to detect occlusion of the FPCA in patients presenting with anterior circulation stroke syndrome and patent anterior circulation.

          Novelty and significance

          This is the first multicenter study showing that thrombectomy of FPCA occlusion is feasible and safe.

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          Most cited references33

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          Endovascular thrombectomy after large-vessel ischaemic stroke: a meta-analysis of individual patient data from five randomised trials.

          In 2015, five randomised trials showed efficacy of endovascular thrombectomy over standard medical care in patients with acute ischaemic stroke caused by occlusion of arteries of the proximal anterior circulation. In this meta-analysis we, the trial investigators, aimed to pool individual patient data from these trials to address remaining questions about whether the therapy is efficacious across the diverse populations included.
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            A randomized trial of intraarterial treatment for acute ischemic stroke.

            In patients with acute ischemic stroke caused by a proximal intracranial arterial occlusion, intraarterial treatment is highly effective for emergency revascularization. However, proof of a beneficial effect on functional outcome is lacking. We randomly assigned eligible patients to either intraarterial treatment plus usual care or usual care alone. Eligible patients had a proximal arterial occlusion in the anterior cerebral circulation that was confirmed on vessel imaging and that could be treated intraarterially within 6 hours after symptom onset. The primary outcome was the modified Rankin scale score at 90 days; this categorical scale measures functional outcome, with scores ranging from 0 (no symptoms) to 6 (death). The treatment effect was estimated with ordinal logistic regression as a common odds ratio, adjusted for prespecified prognostic factors. The adjusted common odds ratio measured the likelihood that intraarterial treatment would lead to lower modified Rankin scores, as compared with usual care alone (shift analysis). We enrolled 500 patients at 16 medical centers in The Netherlands (233 assigned to intraarterial treatment and 267 to usual care alone). The mean age was 65 years (range, 23 to 96), and 445 patients (89.0%) were treated with intravenous alteplase before randomization. Retrievable stents were used in 190 of the 233 patients (81.5%) assigned to intraarterial treatment. The adjusted common odds ratio was 1.67 (95% confidence interval [CI], 1.21 to 2.30). There was an absolute difference of 13.5 percentage points (95% CI, 5.9 to 21.2) in the rate of functional independence (modified Rankin score, 0 to 2) in favor of the intervention (32.6% vs. 19.1%). There were no significant differences in mortality or the occurrence of symptomatic intracerebral hemorrhage. In patients with acute ischemic stroke caused by a proximal intracranial occlusion of the anterior circulation, intraarterial treatment administered within 6 hours after stroke onset was effective and safe. (Funded by the Dutch Heart Foundation and others; MR CLEAN Netherlands Trial Registry number, NTR1804, and Current Controlled Trials number, ISRCTN10888758.).
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              Randomized Assessment of Rapid Endovascular Treatment of Ischemic Stroke

              Among patients with a proximal vessel occlusion in the anterior circulation, 60 to 80% of patients die within 90 days after stroke onset or do not regain functional independence despite alteplase treatment. We evaluated rapid endovascular treatment in addition to standard care in patients with acute ischemic stroke with a small infarct core, a proximal intracranial arterial occlusion, and moderate-to-good collateral circulation. We randomly assigned participants to receive standard care (control group) or standard care plus endovascular treatment with the use of available thrombectomy devices (intervention group). Patients with a proximal intracranial occlusion in the anterior circulation were included up to 12 hours after symptom onset. Patients with a large infarct core or poor collateral circulation on computed tomography (CT) and CT angiography were excluded. Workflow times were measured against predetermined targets. The primary outcome was the score on the modified Rankin scale (range, 0 [no symptoms] to 6 [death]) at 90 days. A proportional odds model was used to calculate the common odds ratio as a measure of the likelihood that the intervention would lead to lower scores on the modified Rankin scale than would control care (shift analysis). The trial was stopped early because of efficacy. At 22 centers worldwide, 316 participants were enrolled, of whom 238 received intravenous alteplase (120 in the intervention group and 118 in the control group). In the intervention group, the median time from study CT of the head to first reperfusion was 84 minutes. The rate of functional independence (90-day modified Rankin score of 0 to 2) was increased with the intervention (53.0%, vs. 29.3% in the control group; P<0.001). The primary outcome favored the intervention (common odds ratio, 2.6; 95% confidence interval, 1.7 to 3.8; P<0.001), and the intervention was associated with reduced mortality (10.4%, vs. 19.0% in the control group; P=0.04). Symptomatic intracerebral hemorrhage occurred in 3.6% of participants in intervention group and 2.7% of participants in control group (P=0.75). Among patients with acute ischemic stroke with a proximal vessel occlusion, a small infarct core, and moderate-to-good collateral circulation, rapid endovascular treatment improved functional outcomes and reduced mortality. (Funded by Covidien and others; ESCAPE ClinicalTrials.gov number, NCT01778335.).
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                Author and article information

                Contributors
                (View ORCID Profile)
                (View ORCID Profile)
                Journal
                Stroke: Vascular and Interventional Neurology
                SVIN
                Ovid Technologies (Wolters Kluwer Health)
                2694-5746
                November 2021
                November 2021
                : 1
                : 1
                Affiliations
                [1 ]Department of Radiology Boston Medical Center Boston University‐School of Medicine Boston MA
                [2 ]Department of Neurology, Boston Medical Center Boston University‐School of Medicine Boston MA
                [3 ]Neuroendovascular Program Massachusetts General Hospital ‐ Harvard Medical School Boston MA
                [4 ]Department of Radiology, Mayo Clinic Rochester MN
                [5 ]Interventional Neuroradiology Miami Cardiac &amp; Vascular Institute and Baptist Neuroscience Center Miami FL
                [6 ]Department of Radiology New York University Langone Medical Center New York NY
                [7 ]Interventional Neuroradiology Unit University Hospital Careggi Firenze Toscana Italy
                [8 ]Department of Neurology Texas Tech University Health Sciences Center El Paso El Paso TX
                [9 ]Interventional Neuroradiology/Endovascular Neurosurgery Hospital Clínico Universitario de Valladolid Valladolid Spain
                [10 ]Department of Neurosurgery Westchester Medical Center at New York Medical College Valhalla NY
                [11 ]Division of Interventional Neuroradiology Goodman Campbell Brain and Spine, Ascension St. Vincent Medical Center Indianapolis IN
                [12 ]Department of Neurosurgery Icahn School of Medicine at Mount Sinai New York NY
                [13 ]Department of Neurosurgery Rutgers University Newark NJ
                [14 ]Division of Neurosurgery Beth Israel Deaconess Medical Center Boston MA
                [15 ]Department of Neurology, Radiology and Neurosurgery The University of Iowa Hospitals and Clinics Iowa City IA
                [16 ]Department of Neurology University of Texas Rio Grande Valley, Valley Baptist Medical Center Harlingen TX
                [17 ]Cooper Neurological Institute Cooper University Hospital Camden NJ
                [18 ]Department of Neurology University Hospital Heidelberg Heidelberg Germany
                [19 ]Neuroscience Institute St Vincent Mercy Hospital Toledo OH
                [20 ]Department of Neurosurgery, Boston Medical Center Boston University‐School of Medicine Boston MA
                Article
                10.1161/SVIN.121.000115
                57b4109b-ae48-4006-97aa-c9d725387182
                © 2021
                History

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