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Multicenter Experience with FRED Jr Flow Re-Direction Endoluminal Device for Intracranial Aneurysms in Small Arteries

dc.contributor.authorMoehlenbruch, M. A.
dc.contributor.authorKizilkilic, O.
dc.contributor.authorKiller-Oberpfalzer, M.
dc.contributor.authorBaltacioglu, F.
dc.contributor.authorIslak, C.
dc.contributor.authorBendszus, M.
dc.contributor.authorKocer, N.
dc.date.accessioned2026-10-09T21:52:19Z
dc.date.issued2017
dc.departmentYüksek İhtisas Üniversitesi
dc.description.abstractThe authors assessed the clinical safety and efficacy of the Flow Re-Direction Endoluminal Device Jr (FRED Jr) dedicated to small-vessel diameters between 2.0 and 3.0 mm in 42 patients with 47 aneurysms. The primary efficacy end point of complete or near complete occlusion was reached at 1 month in 27/41 (66%), at 6 months in 21/27 (78%), and at 12 months in 11/11 (100%) aneurysms. BACKGROUND AND PURPOSE: Flow diverters are emerging as an endovascular treatment alternative for proximally located intracranial aneurysms. However, treatment of aneurysms at and beyond the circle of Willis is not well-established. We assessed the clinical safety and efficacy of the Flow Re-Direction Endoluminal Device Jr (FRED Jr) dedicated to small-vessel diameters between 2.0 and 3.0 mm. MATERIALS AND METHODS: This was a multicenter observational clinical study of 42 patients with 47 aneurysms treated by a flow-direction technique with the FRED Jr. The primary end point for clinical safety was the absence of death, major or minor stroke, and TIA. The primary end point for treatment efficacy was complete and near-complete occlusion according to the O'Kelly-Marotta grading scale at follow-up after 1, 6, and 12 months. RESULTS: The FRED Jr deployment was technically successful in all cases. In 39/42 (93%) patients, the primary safety end point was reached; in the 3 remaining patients, 1 disabling ischemic stroke, 1 minor stroke with complete recovery at discharge, and 1 TIA were observed. Two asymptomatic, completely reversible side-branch occlusions occurred. Angiographic (DSA or flat panel CT) and clinical follow-up were available after 1 month in 41/47 (87%), 6 months in 27/47 (57%), and 12 months in 11/47 (23%) aneurysms. The primary efficacy end point was reached at 1 month in 27/41 (66%), at 6 months in 21/27 (78%), and at 12 months in 11/11 (100%) aneurysms. CONCLUSIONS: Deployment of the FRED Jr is safe and effective in the treatment of intracranial aneurysms located in small vessels.
dc.identifier.doi10.3174/ajnr.A5332
dc.identifier.endpage1965
dc.identifier.issn0195-6108
dc.identifier.issn1936-959X
dc.identifier.issue10
dc.identifier.orcid0000-0002-3626-6244
dc.identifier.orcid0000-0001-5572-7694
dc.identifier.orcid0000-0003-0884-6492
dc.identifier.orcid0000-0002-9094-6769
dc.identifier.orcid0000-0002-6620-8934
dc.identifier.orcid0000-0002-9090-6716
dc.identifier.pmid28798217
dc.identifier.startpage1959
dc.identifier.urihttps://doi.org/10.3174/ajnr.A5332
dc.identifier.urihttps://hdl.handle.net/20.500.12794/3897
dc.identifier.volume38
dc.identifier.wosWOS:000411955100028
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakPubMed
dc.indekslendigikaynak.digerScience Citation Index Expanded (SCI-EXPANDED)
dc.language.isoen
dc.publisherAmer Soc Neuroradiology
dc.relation.ispartofAmerican Journal of Neuroradiology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.relation.sdgGoal-03: Good Health and Well-Being
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20260922
dc.subjectPipeline Embolization Device
dc.subjectTerm Follow-Up
dc.subjectEndovascular Treatment
dc.subjectCerebral Aneurysms
dc.subjectDivertor Stent
dc.subjectSafety
dc.subjectEfficacy
dc.subjectCircle
dc.subjectWillis
dc.subjectDiversion
dc.titleMulticenter Experience with FRED Jr Flow Re-Direction Endoluminal Device for Intracranial Aneurysms in Small Arteries
dc.typeArticle

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