Prosthesis delivery systems and methods
AssigneeAptus Endosystems, Inc.
InventorsAndrew L. Chiang, Lee Bolduc
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AssigneeAptus Endosystems, Inc.
InventorsAndrew L. Chiang, Lee Bolduc
Estimating the term…
Apparatus and method deliver a prosthesis into a hollow body organ or blood vessel. The systems and methods make use of a catheter. A carrier on the distal end of the catheter is sized and configured to carry the prosthesis. A release mechanism and an enclosure mechanism on the distal end are operable to retain and enclose the prosthesis on the carrier. The release mechanism and the enclosure mechanism are also operable to selectively expose and release the prosthesis from the carrier for deployment in the hollow body organ or blood vessel.
A method for deploying an endovascular prosthesis comprising
Dependencies are inferred from the claim text.
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Blood vessels: stent-grafts
Instruments specially adapted for placement or removal of stents or stent-grafts: for placing stents or stent-grafts in a bifurcation
With relative longitudinal movement between outer sleeve and prosthesis, e.g. using a push rod: the proximal portion of the stent or stent-graft…
Instruments specially adapted for placement or removal of stents or stent-grafts: handle assemblies therefor
Term ended 13 Jun 2024 (estimated)
This application claims the benefit of United States Provisional Patent Application Ser. No. 60/488,753, filed Jul. 21, 2003, and entitled “Endoprosthesis Deliveiy Systems and Methods.”
The invention relates generally to the delivery of a prosthesis to a targeted site within the body, e.g., for the repair of diseased and/or damaged sections of a hollow body organ and/or blood vessel.
The weakening of a vessel wall from damage or disease can lead to vessel dilatation and the formation of an aneurysm. Left untreated, an aneurysm can grow in size and may eventually rupture.
The invention will be understood from the following detailed description of preferred embodiments, taken in conjunction with the accompanying drawings, wherein:
FIG. 1A is a perspective view of a prosthesis delivery catheter embodies features of the invention.
FIG. 1B is an enlarged perspective view, with portions broken away and in section, of the distal end of the prosthesis delivery catheter shown in FIG. 1A.
I. Prosthesis Delivery Catheter
FIGS. 1A and 1B show a prosthesis delivery catheter 10. The purpose of the catheter 10 is to (i) contain and/or restrain a prosthesis 14 prior to its deployment (see FIG. 1B), (ii) deliver the prosthesis 14 through the vasculature to a desired location within the body, e.g., a hollow body organ or a blood vessel (see FIG. 2), and (iii) controllably deploy the prosthesis 14 in the desired location (see FIG. 3).
In the illustrated arrangement (see FIG. 3), the prosthesis 14 takes the form of an endovascular, self-expanding stent prosthesis. In this respect, the prosthesis or prostheses 14 may have a wide variety of conventional configurations. It can typically comprise a fabric or some other blood semi-impermeable flexible barrier which is supported by a structure formed by stents 48. The stent structure can have any conventional stent configuration, such as zigzag, serpentine, expanding diamond, or combinations thereof. The stent structure may extend the entire length of the prosthesis, and in some instances can be longer than the fabric components of the prosthesis. Alternatively, the stent structure can cover only a small portion of the prosthesis, e.g., being present at the ends. The stent structure may have three or more ends when it is configured to treat bifurcated vascular regions, such as the treatment of abdominal aortic aneurysms, when the stent prosthesis extends into the iliac arteries. In certain instances, the stent structures can be spaced apart along the entire length, or at least a major portion of the entire length, of the stent-prosthesis, where individual stent structures are not connected to each other directly, but rather connected to the fabric or other flexible component of the prosthesis. Still, it is contemplated that the stent structures could be attached to one another at discrete locations, e.g., in the proximal neck region. Such stent structures could comprise individual stents that are connected together when incorporated into the prosthesis, or stents that are manufactured in a joined condition prior to incorporation into the prosthesis.