The first North American use of the Pipeline Flex flow diverter.

Abstract:

:Flow diversion for the management of intracranial aneurysms represents a paradigm shift in how aneurysms are managed. The Pipeline embolization device (PED) is, to date, the only flow diverter approved for use in the USA by the Food and Drug Administration. Limitations and complications with new treatment strategies are inevitable, and with the PED there have been reports of complications, most commonly with challenging deployments. Once deployment has been initiated, the device is 'one-way'; it can only be deployed further or removed. Yet, situations arise in which the ability to recapture or reposition the device would be advantageous. A second-generation Pipeline has been developed that addresses these concerns. We report the first use in North America of this second-generation Pipeline device: the Pipeline Flex. We discuss our rationale for using the device, our impressions of its operation, and the relevant literature concerning the current state of flow diversion.

journal_name

J Neurointerv Surg

authors

Duckworth EA,Nickele C,Hoit D,Belayev A,Moran CJ,Arthur AS

doi

10.1136/neurintsurg-2014-011548.rep

subject

Has Abstract

pub_date

2016-02-01 00:00:00

pages

e8

issue

2

eissn

1759-8478

issn

1759-8486

pii

neurintsurg-2014-011548.rep

journal_volume

8

pub_type

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