Abstract

Endoluminal reconstruction with flow-diverting stents represents a widely accepted technique for the treatment of complex intracranial aneurysms. This European registry study analyzed the initial experience of 15 neurovascular centers with the Flow-Redirection Intraluminal Device (FRED) system. Consecutive patients with intracranial aneurysms treated with the FRED between February 2012 and March 2015 were retrospectively reviewed. Complications and adverse events, transient and permanent morbidity, mortality, and occlusion rates were evaluated. During the defined study period, 579 aneurysms in 531 patients (median age, 54 years; range, 13-86 years) were treated with the FRED. Seven percent of patients were treated in the acute phase (≤3 days) of aneurysm rupture. The median aneurysm size was 7.6 mm (range, 1-36.6 mm), and the median neck size 4.5 mm (range, 1-30 mm). Angiographic follow-up of >3 months was available for 516 (89.1%) aneurysms. There was progressive occlusion witnessed with time, with complete occlusion in 18 (20%) aneurysms followed for up to 90 ± 14 days, 141 (82.5%) for 180 ± 20 days, 116 (91.3%) for 1 year ± 24 days, and 122 (95.3%) aneurysms followed for >1 year. Transient and permanent morbidity occurred in 3.2% and 0.8% of procedures, respectively. The overall mortality rate was 1.5%. This retrospective study in real-world patients demonstrated the safety and efficacy of the FRED for the treatment of intracranial aneurysms. In most cases, treatment with a single FRED resulted in complete angiographic occlusion at 1 year.

Highlights

  • BACKGROUND AND PURPOSEEndoluminal reconstruction with flow-diverting stents represents a widely accepted technique for the treatment of complex intracranial aneurysms

  • There was progressive occlusion witnessed with time, with complete occlusion in 18 (20%) aneurysms followed for up to 90 Ϯ 14 days, 141 (82.5%) for 180 Ϯ 20 days, 116 (91.3%) for 1 year Ϯ 24 days, and 122 (95.3%) aneurysms followed for Ͼ1 year

  • We report the results of the European Flow-Redirection Intraluminal Device (FRED) study (EuFRED), which included 15 European neurovascular centers and evaluated the safety and efficacy of this device in consecutive real-world patients with intracranial aneurysms treated with the FRED

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Summary

RESULTS

Baseline Patient and Aneurysm Characteristics A total of 531 patients with 579 aneurysms were enrolled. Male (No.) Female (No.) Age at time of treatment (median) (range) (yr) Presentation of patients (No.) Incidental Headaches Cranial nerve palsy Recanalization of previously treated aneurysm Subarachnoid hemorrhage. A total 579 aneurysms in 531 patients were treated in 534 procedures using a median of 1 FRED (range, 1–5). In 12 procedures, complete occlusion of the stent, parent artery, and aneurysm complex was registered periprocedurally and during fol-. After routine follow-up at 6 months, a paraophthalmic aneurysm and parent artery showed complete occlusion and the antiplatelet medication was stopped. One month later the patient died from a severe stroke caused by stent occlusion. Imaging Outcomes After a median follow-up time of 6.6 months (range, 0.03– 45.6 months), the overall complete occlusion rate was 69.2%. No significant predictors of aneurysm occlusion were identified in multivariable analysis

CONCLUSIONS
MATERIALS AND METHODS
DISCUSSION
Strengths and Limitations
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