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1.
Clin Neuroradiol ; 32(4): 971-977, 2022 Dec.
Article in English | MEDLINE | ID: mdl-35416489

ABSTRACT

BACKGROUND: Mechanical thrombectomy is the standard of care for acute ischemic stroke due to large-vessel occlusion; however, mechanical thrombectomy fails to achieve adequate recanalization in nearly one third of these cases. Rescue therapy using two stentrievers simultaneously yields good results in clots refractory to single stentriever treatment. We aimed to determine the safety and efficacy of first-line double stentriever thrombectomy for acute occlusion of the M1 segment of the middle cerebral artery and/or terminal internal carotid artery (TICA). METHODS: This single-center study prospectively enrolled consecutive patients with a single M1/TICA occlusion to undergo double stentriever thrombectomy between May and October 2020. Outcomes included successful recanalization (modified thrombolysis in cerebral infarction, TICI 2b/3), first-pass effect, procedure times, number of device passes, symptomatic intracerebral hemorrhage, National Institutes of Health Stroke Scale Score (NIHSS) at discharge, 90-day functional independence (modified Rankin scale 0-2), and 90-day mortality. RESULTS: We analyzed 39 patients median age 79 years (range 42-96 years); 23 (58.9%) female; 19 (48.7%) with TICA occlusions; 5 (12.8%) with mRS 3-5 at admission; mean NIHSS at admission, 17 ± 4.39). Mean time from symptom onset to final angiogram was 238.0 ± 94.6 min; mean intervention duration was 36.0 ± 24.2 min. The mean number of device passes was 1.5 ± 1.07. All patients had final TICI 2b/3, and 27 (69%) had TICI 2c/3 after the first pass. We observed 3 (7.9%) cases of intracerebral symptomatic hemorrhages. At 90 days, 16 (41%) patients were functionally independent and 9 (23%) had died. The percentage of patients with good clinical outcome at 90 days was 55.5% in the first-pass subgroup. CONCLUSION: Our findings suggest that first-line double stentriever thrombectomy is safe and effective for M1/TICA occlusions.


Subject(s)
Brain Ischemia , Ischemic Stroke , Stroke , Humans , Female , Adult , Middle Aged , Aged , Aged, 80 and over , Male , Ischemic Stroke/etiology , Stroke/diagnostic imaging , Stroke/surgery , Stroke/etiology , Stents , Treatment Outcome , Retrospective Studies , Thrombectomy/methods , Brain Ischemia/etiology
2.
Front Neurol ; 12: 724811, 2021.
Article in English | MEDLINE | ID: mdl-34594298

ABSTRACT

Background: Mechanical thrombectomy (MT) has become the standard of care for acute ischemic stroke due to large vessel occlusion; however, its safety and efficacy in patients with distal strokes remains unclear. In this study, we investigated the safety and efficacy of MT for distal middle cerebral artery (MCA) occlusions using the CatchView Mini (CVM; Balt, Montmorency, France). Methods: This was a prospective single-center analysis of patients with a single MCA-M2 occlusion treated with the CVM device. Consecutive patients were prospectively enrolled from October 2018 to March 2020. Efficacy outcomes included successful recanalization [modified Thrombolysis in Cerebral Infarction (mTICI) 2b/3], procedure times, and number of device passes. Clinical outcomes included National Institutes of Health Stroke Scale Score (NIHSS) at discharge, 90-day functional independence (modified Rankin Scale 0-2) and safety outcomes included hemorrhagic complications, and 90-day mortality. Results: A total of 45 patients (mean age: 74.0 ± 12.6; 53.3% [24/45] female) were included in the study. Upon admission, 33.3% (15/45) of patients were mRS 3-5; and mean NIHSS was 13.2 ± 4.2 Mean time from symptom onset to final angiography was 250.0 ± 83.4 min with a mean intervention duration of 34.0 ± 12.6 min. The mean number of device passes was 1.8 ± 1.5 final mTICI 2b/3 was achieved in 91.1% (41/45) of patients. Eight hemorrhagic complications (17.8%, 8/34) occurred, none of which were symptomatic. At 90-days, 57.8% (26/45) patients were functionally independent and the rate of mortality was 15.6% (7/45). Conclusions: The present analysis demonstrates a low risk profile and high recanalization success for patients with distal M2 occlusions treated with the CVM device.

3.
Interv Neuroradiol ; 26(2): 222-230, 2020 Apr.
Article in English | MEDLINE | ID: mdl-31684785

ABSTRACT

BACKGROUND AND PURPOSE: Acute tandem occlusions often require carotid stenting. Combination of mechanical and pharmacologic therapies in addition to antiplatelet drugs administered to prevent acute stent thrombosis might increase the risk of intracerebral hemorrhage. We present a protocol of antiplatelet regimen based on early post-procedural dual-energy CT (DE-CT). MATERIAL AND METHODS: Fifty consecutive stroke patients with tandem occlusions treated with acute carotid stenting after intracranial thrombectomy and TICI 2b/3 were reviewed. All patients received intravenous lysine acetylsalicylate during the procedure. Dual (aspirin+clopidogrel with or without clopidogrel load, groups A and B, respectively) or mono (aspirin) antiplatelet regimen (group C) was administered 12-24 h later according to brain DE-CT findings. Carotid ultrasonography was performed at 24 h and before discharge. We evaluated the rate of subsequent symptomatic intracranial hemorrhage (SICH) and acute stent thrombosis in each group. RESULTS: Between June 2014 and December 2016, 50 patients were included (mean age 66 years, 76% men, baseline NIHSS 16, median time from symptom onset to recanalization 266 min). According to DE-CT, 24 patients were assigned to group A, 19 to group B and 7 to group C (4 of them had SICH at that time). One patient suffered a subsequent SICH (belonging to group B). There was only one stent thrombosis without clinical repercussions in group B. CONCLUSIONS: DE-CT may contribute to select antiplatelet regimen after acute carotid stenting in tandem occlusions.


Subject(s)
Carotid Stenosis/diagnostic imaging , Carotid Stenosis/drug therapy , Ischemic Stroke/diagnostic imaging , Ischemic Stroke/drug therapy , Platelet Aggregation Inhibitors/therapeutic use , Tomography, X-Ray Computed/methods , Adult , Aged , Aged, 80 and over , Aspirin/analogs & derivatives , Aspirin/therapeutic use , Carotid Stenosis/complications , Cerebral Hemorrhage/diagnostic imaging , Cerebral Hemorrhage/etiology , Clopidogrel/therapeutic use , Female , Humans , Ischemic Stroke/etiology , Lysine/analogs & derivatives , Lysine/therapeutic use , Magnetic Resonance Angiography , Male , Middle Aged , Retrospective Studies , Stents , Thrombectomy , Treatment Outcome
4.
Rev. neurol. (Ed. impr.) ; 66(1): 7-14, 1 ene., 2018. tab
Article in Spanish | IBECS | ID: ibc-170278

ABSTRACT

Introducción. La ampliación de las indicaciones de la trombectomía mecánica y su implementación en los hospitales españoles hacen necesario conocer los costes relacionados con este tratamiento para racionalizar los recursos económicos y permitir una adecuada distribución de éstos. Objetivos. Analizar los costes directos asociados a los pacientes con ictus isquémico agudo tratados con fibrinólisis intravenosa y con trombectomía mecánica, y valorar la efectividad y seguridad de ambos tratamientos durante los primeros 90 días de evolución en el Hospital Universitario Central de Asturias. Pacientes y métodos. Se realizó un análisis retrospectivo en el que se incluyó a 44 pacientes que recibieron fibrinólisis intravenosa y a 61 pacientes tratados con trombectomía mecánica, en los que se analizaron una serie de variables clínicas y económicas. Resultados. El coste total final medio por paciente fue de 16.059 euros en los tratados con trombectomía y de 8.169 euros en los que se administró fibrinólisis intravenosa. El porcentaje de pacientes con buen pronóstico funcional a los 90 días fue del 63,93% en los tratados de forma endovascular y del 56,82% en los que recibieron fibrinólisis intravenosa. Las tasas de mortalidad fueron del 18,03% y 11,36%, respectivamente. Conclusiones. El coste medio del tratamiento con trombectomía mecánica, así como el coste medio total por paciente durante la fase aguda de la enfermedad asociado a esta técnica, es mayor que en el caso de la fibrinólisis intravenosa. Tanto la fibrinólisis intravenosa como la trombectomía mecánica se configuran en nuestro medio como tratamientos efectivos y seguros (AU)


Introduction. The increase in the indications for mechanical thrombectomy and its implementation in Spanish hospitals makes it necessary to determine the costs related to this treatment so as to be able to streamline economic resources and allow them to be distributed in an appropriate manner. Aims. To analyse the direct costs associated with patients with acute ischaemic stroke who are treated with intravenous fibrinolysis and with mechanical thrombectomy, and to assess the effectiveness and safety of both treatments during the first 90 days of progression in the Hospital Universitario Central de Asturias. Patients and methods. A retrospective analysis was performed that included 44 patients who received intravenous fibrinolysis and 61 patients treated with mechanical thrombectomy, in whom a series of clinical and economic variables were analysed. Results. The mean final total cost per patient was 16,059 euros in treatments with thrombectomy and 8,169 euros in those in which intravenous fibrinolysis was administered. The percentage of patients with a good functional prognosis at 90 days was 63.93% in those treated by endovascular means and 56.82% in those who received intravenous fibrinolysis. Mortality rates were 18.03 and 11.36%, respectively. Conclusions. The mean cost of treatment with mechanical thrombectomy, as well as the total mean cost per patient during the acute phase of the disease associated with this technique, is higher than in the case of intravenous fibrinolysis. In our setting, both intravenous fibrinolysis and mechanical thrombectomy are considered to be effective and safe (AU)


Subject(s)
Humans , Thrombectomy/economics , Thrombolytic Therapy/economics , Stroke/therapy , Direct Service Costs/statistics & numerical data , Stroke Rehabilitation/economics , Cost-Benefit Analysis/statistics & numerical data , Treatment Outcome , Patient Safety
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