DEVICES AND METHODS FOR VASCULAR RECANALIZATION
First Claim
1. An apparatus, comprising:
- an elongate member; and
an expandable member coupled to a distal portion of the elongate member and configured to be inserted into a blood vessel, the expandable member defining a plurality of openings in a wall of the expandable member,the expandable member having a collapsed configuration for insertion into the blood vessel and an expanded configuration, the expandable member when in the expanded configuration defining an interior volume in fluid communication with the plurality of openings and configured to receive therein at least a first portion of a bodily tissue,the expandable member including a first portion having a first outer perimeter, a second portion having a second outer perimeter and a third portion having a third outer perimeter, the second outer perimeter being smaller than the first outer perimeter and smaller than the third outer perimeter such that the expandable member defines a capture region between the first portion and the third portion configured to receive at least a second portion of the bodily tissue.
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Accused Products
Abstract
In some embodiments, a medical device for recanalizing a vessel having a blockage and restoring blood flow through an obstructed blood vessel includes an expandable member coupled to a core wire and a hypotube that are movable relative to each other to manipulate the expandable member between various configurations. The expandable member having a capture structure in an expanded configuration. The expandable member can include multiple interstices formed by woven mesh filaments or braided strands through which the material blocking the vessel can pass. The capture structure can include a shape on its external surface that facilitates dislodgement and capture of the material within capture spaces created by the expandable member. Some embodiments include a capture sack or cap for capturing material and preventing material from migrating down stream of the blockage. Superoxygenated blood can be infused distal to the blockage to minimize loss of function during an ischemic event.
296 Citations
19 Claims
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1. An apparatus, comprising:
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an elongate member; and an expandable member coupled to a distal portion of the elongate member and configured to be inserted into a blood vessel, the expandable member defining a plurality of openings in a wall of the expandable member, the expandable member having a collapsed configuration for insertion into the blood vessel and an expanded configuration, the expandable member when in the expanded configuration defining an interior volume in fluid communication with the plurality of openings and configured to receive therein at least a first portion of a bodily tissue, the expandable member including a first portion having a first outer perimeter, a second portion having a second outer perimeter and a third portion having a third outer perimeter, the second outer perimeter being smaller than the first outer perimeter and smaller than the third outer perimeter such that the expandable member defines a capture region between the first portion and the third portion configured to receive at least a second portion of the bodily tissue. - View Dependent Claims (2, 3, 4, 5, 6)
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7. An apparatus, comprising:
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an elongate member; a first expandable member coupled to a distal portion of the elongate member; and a second expandable member coupled to the distal portion of the elongate member at a non-zero distance from the first expandable member, the first expandable member defining a plurality of openings in a wall of the first expandable member, the first expandable member and the second expandable member each configured to be inserted into a blood vessel when in a collapsed configuration, the first expandable member and the second expandable member each being movable to an expanded configuration when disposed within the blood vessel, the first expandable member when in its expanded configuration defining an interior volume in fluid communication with the plurality of openings and configured to receive at least a first portion of a bodily tissue within the blood vessel through the openings and within the interior volume of the first expandable member; the second expandable member when in its expanded configuration configured to prevent at least a second portion of the bodily tissue from migrating within the blood vessel past the second expandable member, the first expandable member and the second expandable member defining a capture region between the first expandable member and the second expandable member, the capture region configured to receive at least one of the second portion of the bodily tissue or a third portion of the bodily tissue, the first expandable member and the second expandable member being movable to their collapsed configurations while within the blood vessel such that the capture region moves from a first configuration to a second configuration in which the capture region substantially inhibits passage of at least one of the second portion of the bodily tissue or the third portion of the bodily tissue to an area outside the capture region. - View Dependent Claims (8, 9, 10, 11, 12)
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13. A method, comprising:
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inserting a distal portion of a medical device into a blood vessel, the medical device including an elongate member and an expandable member coupled to a distal portion of the elongate member, the expandable member defining a plurality of openings in a wall of the expandable member and being in a collapsed configuration during the inserting; positioning the distal portion of the medical device adjacent a blood clot within the blood vessel; actuating the medical device at a first time period to move the expandable member from the collapsed configuration to a first expanded configuration in which the expandable member defines an interior region in fluid communication with the plurality of openings and such that the expandable member contacts the blood clot and at least a first portion of the blood clot enters through at least one opening from the plurality of openings and into the interior region of the expandable member; and actuating the medical device at a second time period to move the expandable member from the first expanded configuration to a second expanded configuration in which the expandable member defines at least one capture region configured to receive a second portion of the blood clot therein. - View Dependent Claims (14, 15, 16, 17, 18, 19)
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Specification