Modular endo-aortic device for endovascular aortic repair of dissections and being configured for adaptability of organs of various anatomical characteristics and method of using the same
First Claim
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1. A kit comprising:
- a stent device for placement in the aorta arch of a patient, wherein a diameter of the stent device may be modified by translation of an end of the stent device to thereby alter a length thereof causing modification of the diameter of the stent device,wherein the stent device comprises;
a distal stent portion that is permeable,wherein the distal stent portion is a wireframe assembly that defines a circumferential periphery that spans but does not extend into the brachiocephalic artery, left common carotid artery, and left subclavian artery when placed within the aortic arch of a patient; and
a proximal portion that is impermeable and having a constraining member for constraining a diameter thereof,wherein the proximal portion engages the distal stent portion at respective ends thereof such that the proximal portion is spaced-apart from the distant stent portion; and
a deployment apparatus comprising a sheath for housing the stent device and having a guide rod passing through a center therethrough for deploying the stent device at an operational site,wherein the sheath constrains the distal portion of the stent device in a compressed state,wherein the constraining member constrains the proximal portion of the stent device in a compressed state after removal of the sheath until release of the constraining member, andwherein the guide rod carries the stent device and is removable through a center of the stent device when the stent device is in an expanded state and positioned within the aortic arch of the patient upon removal of the sheath.
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Abstract
A device for placement in the aortic arch of a patient is provided. The device includes a distal portion for being engageably received in an aortic arch of a patient beyond the left subclavian artery and a stent portion fluidly engaged with the distal portion, the stent portion being permeable and configured to span a portion of the aortic arches to which the brachiocephalic trunk, left common carotid artery, and left subclavian artery attach to the aortic arch. A diameter of the stent portion may be modified by translation of the proximal portion to thereby alter a length of the stent portion thus causing modification of the diameter of the stent portion to fit anatomical features of differing dimensions.
19 Citations
11 Claims
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1. A kit comprising:
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a stent device for placement in the aorta arch of a patient, wherein a diameter of the stent device may be modified by translation of an end of the stent device to thereby alter a length thereof causing modification of the diameter of the stent device, wherein the stent device comprises; a distal stent portion that is permeable, wherein the distal stent portion is a wireframe assembly that defines a circumferential periphery that spans but does not extend into the brachiocephalic artery, left common carotid artery, and left subclavian artery when placed within the aortic arch of a patient; and a proximal portion that is impermeable and having a constraining member for constraining a diameter thereof, wherein the proximal portion engages the distal stent portion at respective ends thereof such that the proximal portion is spaced-apart from the distant stent portion; and a deployment apparatus comprising a sheath for housing the stent device and having a guide rod passing through a center therethrough for deploying the stent device at an operational site, wherein the sheath constrains the distal portion of the stent device in a compressed state, wherein the constraining member constrains the proximal portion of the stent device in a compressed state after removal of the sheath until release of the constraining member, and wherein the guide rod carries the stent device and is removable through a center of the stent device when the stent device is in an expanded state and positioned within the aortic arch of the patient upon removal of the sheath. - View Dependent Claims (2, 3, 4, 5, 6, 7, 8, 9, 10, 11)
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Specification