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dc.contributor.authorKuhn, Anna Luisa
dc.contributor.authorGounis, Matthew J
dc.contributor.authorPuri, Ajit S
dc.date2022-08-11T08:10:49.000
dc.date.accessioned2022-08-23T17:20:54Z
dc.date.available2022-08-23T17:20:54Z
dc.date.issued2020-01-01
dc.date.submitted2020-01-08
dc.identifier.citation<p>Neurosurgery. 2020 Jan 1;86(Supplement_1):S3-S10. doi: 10.1093/neuros/nyz307. <a href="https://doi.org/10.1093/neuros/nyz307">Link to article on publisher's site</a></p>
dc.identifier.issn0148-396X (Linking)
dc.identifier.doi10.1093/neuros/nyz307
dc.identifier.pmid31838534
dc.identifier.urihttp://hdl.handle.net/20.500.14038/48405
dc.description.abstractThe introduction of flow diverter technology to the field of neurointervention has revolutionized the treatment of intracranial aneurysms. The therapy approach has shifted from intrasaccular aneurysm treatment to exclusion of the aneurysm from the blood circulation with remodeling of the parent artery. Previously, "difficult"-to-treat aneurysms including fusiform and blister aneurysms, but also aneurysms arising from a diseased vessel segment, can now be safely and permanently treated with flow diverters. A little over a decade ago, after extensive bench testing and refinement of the flow diverter concept, the device was eventually available for clinical use and today it has become a standard treatment for intracranial aneurysms. Currently, United States Food and Drug Administration (FDA)-approved flow diverters are the Pipeline Embolization Device (Medtronic) and the Surpass Streamline Flow Diverter (Stryker). The devices can either be delivered or deployed via a standard femoral artery approach or a radial artery approach. Other considerations for catheter setup and device deployment strategies depending on aneurysm location or vessel anatomy are described.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=31838534&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://doi.org/10.1093/neuros/nyz307
dc.subjectAneurysm
dc.subjectDevice technology
dc.subjectFlow diverter
dc.subjectPipeline Embolization Device
dc.subjectRupture
dc.subjectSurpass
dc.subjectaneurysm embolization devices
dc.subjectmedical military deployment fluid flow
dc.subjectAnalytical, Diagnostic and Therapeutic Techniques and Equipment
dc.subjectCardiovascular Diseases
dc.subjectNeurology
dc.subjectRadiology
dc.subjectSurgery
dc.titleIntroduction: History and Development of Flow Diverter Technology and Evolution
dc.typeJournal Article
dc.source.journaltitleNeurosurgery
dc.source.volume86
dc.source.issueSupplement_1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/radiology_pubs/514
dc.identifier.contextkey16139757
html.description.abstract<p>The introduction of flow diverter technology to the field of neurointervention has revolutionized the treatment of intracranial aneurysms. The therapy approach has shifted from intrasaccular aneurysm treatment to exclusion of the aneurysm from the blood circulation with remodeling of the parent artery. Previously, "difficult"-to-treat aneurysms including fusiform and blister aneurysms, but also aneurysms arising from a diseased vessel segment, can now be safely and permanently treated with flow diverters. A little over a decade ago, after extensive bench testing and refinement of the flow diverter concept, the device was eventually available for clinical use and today it has become a standard treatment for intracranial aneurysms. Currently, United States Food and Drug Administration (FDA)-approved flow diverters are the Pipeline Embolization Device (Medtronic) and the Surpass Streamline Flow Diverter (Stryker). The devices can either be delivered or deployed via a standard femoral artery approach or a radial artery approach. Other considerations for catheter setup and device deployment strategies depending on aneurysm location or vessel anatomy are described.</p>
dc.identifier.submissionpathradiology_pubs/514
dc.contributor.departmentRadiology
dc.source.pagesS3-S10


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