This invention relates to a medical device and more particularly to the construction and deployment of a stent graft for the iliac artery
The invention will be generally discussed with reference to a branched stent graft which can be deployed so that its branch is directed towards an internal iliac artery from the common iliac but is not so limited and may be used with deployment into any branched vessel but is particularly applicable where the vessel into which the device is deployed is a blind vessel, that is, access is not available from an end of the vessel remote from the bifurcation from a main vessel.
Stent grafts are used for treatment of vasculature in the human or animal body to bypass a repair or defect in the vasculature. For instance, a stent graft may be used to span an aneurism which has occurred in or associated with the iliac artery. In many cases, however, such a damaged or defective portion of the vasculature may include a branch vessel such as an internal iliac artery. Bypassing such a branch vessel without providing blood flow into it can cause problems and hence it has been proposed to provide a side branch on a stent graft which when deployed is positioned over the opening to the internal iliac artery and then another stent graft can be deployed through the side branch into the internal iliac artery to provide a blood flow path to the internal iliac artery.
Generally, when deploying an endovascular stent graft into a body lumen, it is possible to obtain access to such a body lumen from each end of the lumen where necessary, thereby facilitating placement of a device in the lumen. The internal iliac artery which extends from the common iliac artery below the aortic bifurcation is for all intents and purposes a blind vessel because there is no practical way of performing an endovascular minimally invasive procedure into that vessel other than by entry from the common iliac artery. The term blind vessel is used herein to describe such a vessel.
There have been proposals to deploy a branched stent graft into the common iliac artery via a femoral artery from a femoral incision with the branched stent graft having a side arm to extend into or at least adjacent the internal iliac artery, however, the use of such devices is very dependent upon favourable layout of the arteries and in many cases, access is extremely difficult. Access over the aortic bifurcation has been proposed but as there is limited distance between the aortic bifurcation and the iliac bifurcation special construction of a stent graft for this region is desirable.
It is the object of this invention therefore to provide a stent graft for deployment particularly into the iliac arteries or at least to provide a physician with a useful alternative.
Throughout this specification the term distal with respect to a portion of the aorta, a deployment device or a prosthesis is the end of the aorta, deployment device or prosthesis further away in the direction of blood flow away from the heart and the term proximal means the portion of the aorta, deployment device or end of the prosthesis nearer to the heart. When applied to other vessels similar terms such as caudal and cranial should be understood.
In one form therefore the invention is said to reside in a side branch stent graft comprising a main tubular body of a biocompatible graft material and having a main lumen therethrough, a tubular side branch having a side branch lumen therethrough, the tubular side branch being affixed into the main tubular body so that the side branch lumen is in fluid communication with the main lumen, at least one external zig-zag stent on the main tubular body proximal of the tubular side branch, at least one external zig-zag stent on the main tubular body distal of the tubular side branch, one internal zig-zag stent at the distal end of the main tubular body, and a reinforcing ring around the proximal end of the main tubular body and stitched thereto.
Preferably there are one or two external zig-zag stents proximal of the tubular side branch and from one to three external zig-zag stents distal of the tubular side branch.
The reinforcing ring around the proximal end of the tubular body can comprise at least two turns of nitinol wire, each end of the nitinol wire terminating in a loop.
Preferably the tubular side branch comprises a connection socket for an extension stent. In one embodiment the connection socket comprises a first resilient ring around the tubular side branch at a distal end thereof, a second resilient ring spaced apart along the tubular side branch from the first ring and a zig zag resilient stent between the first and second rings. The zig zag resilient stent and the first and second rings are preferably on the outside of the tubular body and the first and second rings preferably comprise shape memory wire. The first and second rings preferably comprise at least two turns of wire with each end terminating in a loop.
The zig zag resilient stent of the connection socket preferably comprises a shape memory wire and the zig zag resilient stent defines a cylindrical form having a diameter less than that of the tubular side branch whereby to define a self contracting stent.
In a further form the invention comprises a side arm stent graft comprising a main tubular body of a biocompatible material, a fenestration in the main tubular body defined by a peripheral edge and a side arm being a tube of biocompatible material being joined around the peripheral edge at a joined region by stitching and extending from the main tube at an acute angle thereto and being in fluid communication with the main tubular body, at least one external zig-zag stent on the main tubular body proximal of the side arm, at least one external zig-zag stent on the main tubular body distal of the side arm, one internal zig-zag stent at the distal end of the main tubular body, and a reinforcing ring around the proximal end of the main tubular body and stitched thereto.
Preferably the fenestration is selected from the group comprising an elongate aperture, a substantially rectangular aperture, a substantially elliptical aperture and a substantially triangular aperture. The acute angle may be in the range of from 15 to 60 degrees and preferably 15 to 45 degrees.
The or each external zig-zag stents proximal of the tubular side branch can have a length of 14 mm and are spaced apart by about 2 mm and the or each external zig-zag stents distal of the tubular side branch has a length of 12 mm and are spaced apart by about 5 mm.
There may be further a central external zig-zag stent around the main tubular body and the tubular side branch. The central external zig-zag stent can have a length of 14 mm and is spaced apart from the stent proximal to it by about 2 mm and from the stent distal of it by about 5 mm.
The main tubular body can have a diameter of from 12 mm in a central portion and remaining at 12 mm or expanding to 20 mm at a proximal end with a frustoconical portion between the 12 mm and 20 mm portions and the tubular side branch has a diameter of about 8 mm. Alternatively the main tubular body can have a diameter of about 12 mm proximal of the tubular side branch and in a central portion and a diameter distal of the tubular side branch of from about 10 mm to 16 mm frustoconical portion between the 12 mm and 16 mm portions.
The main tubular body can have a length of about 69 mm to 119 mm and the tubular side branch has a length of about 25 mm. The stent graft can have a length from its proximal end to the distal end of the side arm of about 45 mm to 61 mm. The stent graft can have a length from its distal end to the distal end of the side arm of about 24 mm to 58 mm.
This then generally describes the invention but to assist with the understanding, reference will now be made to the accompanying drawings which show preferred embodiments of the invention.
In the drawings;
Now looking more closely at the drawings and in particular
PCT Patent Publication WO 2006/034276 entitled “Side Branch Stent Graft” includes discussion of one method of connection of a side arm to a main tubular body in a stent graft and the disclosure of this patent specification is incorporated herewith in its entirety.
On the side arm 5 there is a connection socket arrangement 19. The connection socket arrangement includes a self-expanding stent 21 between two reinforcing rings 22 and 23.
PCT Patent Publication WO 2006/034340 entitled “Stent Graft Connection Arrangement” discloses a stent graft connection arrangement of the type suitable for the side arm of the stent graft of the present invention, and the disclosure of that patent application is included herewith by reference in its entirety.
In the side arm stent graft shown in
The stent graft depicted in
For placement of a side branch stent graft into the internal iliac artery, the critical dimension is the distance from the proximal end 11 of the stent graft to the end 25 of the side arm 5 as this is the distance which must fit between the aortic bifurcation and the entrance to the internal iliac artery as will be discussed below.
Similarly in
Similarly in
Table 1 shows a range of sizes of stent grafts and numbers and sizes of stents as depicted in
As discussed above, the proximal length is important as a stent graft must be able to be deployed with its distal end below the aortic bifurcation and the distal end of its side arm proximal of the iliac bifurcation between the internal and external iliac arteries.
Similarly
Table 2 shows a range of sizes of stent grafts as depicted in
Table 3 shows a range of sizes of stent grafts as depicted in
The Nitinol™ reinforcing ring 9 provides reinforcement for the proximal end of the stent graft so that when a catheter or other device is being deployed into the proximal end of the stent graft the end of the stent graft cannot be damaged. The Nitinol™ reinforcing ring 9 provides a fixed diameter into which another self expanding or balloon expandable stent graft can expand or be expanded within the proximal end of the stent graft 1.
The vasculature illustrated generally consists of a descending aorta 152 extending down to renal arteries 153 and further extending as the infra-renal aorta 150 down to an aortic bifurcation 178 and into the iliac and contra-iliac arteries 154 and 187. The common iliac artery 154 further bifurcates into an external iliac artery 164 and an internal iliac artery 168. It is this internal iliac artery 168 which is described above as a blind artery as endovascular access is only available via the common iliac artery. An aneurysed region 151 of the aorta 150 extends down into the common iliac artery 154.
In
The general order of placement of such a stent graft assembly for an aneurised aorta is first that the iliac branch stent graft 160 is placed first with its distal end 162 placed into a non-aneurised region of the external iliac artery 164. The side arm 166 extends towards the internal iliac artery 168. Subsequent to placement of the iliac branched stent graft 160 a covered leg extension 170 is placed extending from the side branch 166 so that it extends into and seals in the internal iliac artery 168. The covered leg extension 170 can be a covered balloon expandable stent or a covered self expanding stent.
The main bifurcated stent graft 157 is then deployed through the contra-lateral iliac artery 187 so that its longer leg 176 extends down the contra-lateral iliac artery 187 and its shorter leg 172 terminates proximal of the reinforcing ring 174 on the iliac stent graft 160 and proximal of the aortic bifurcation 178. The proximal end of the bifurcated stent graft 157 seals into a landing zone in the region of aorta 182 just distal of the renal arteries 153 and the proximally extending supra-renal external stent 156 extends over the renal arteries to the aorta region 152 to provide good support for the bifurcated stent graft. A leg extension 190 can then be deployed to connect the shorter leg 172 of the main bifurcated stent graft 157 to the reinforcing ring 174 on the iliac stent graft 160. In a final deployment stage a leg extension 185 can deployed into the longer leg 176 to seal into a non-aneurised portion of the contra-lateral common iliac artery 187 if the longer leg does not already seal onto such a zone.
By this arrangement a stent graft is effectively bridging the aneurised region by sealing in the non-aneurised portion of the aorta as well as in the non-aneurised portions of the iliac arteries.
The critical dimension in relation to deployment of a stent graft into an aneurised iliac artery 154 is the distance shown as 135 in
The length of the distal portion 162 of the stent graft 160 must be such that it can extend to non-aneurised region of the external iliac artery 164 so that a seal may be obtained with the distal end of the stent graft 160. Where the aneurism extends some distance down the external iliac artery a further leg extension may be placed so that the stent graft assembly extends through non-aneurised region of the external iliac artery.
Throughout this specification various indications have been given as to the scope of this invention but the invention is not limited to any one of these but may reside in two or more of these combined together. The examples are given for illustration only and not for limitation.
Throughout this specification and the claims that follow, unless the context requires otherwise, the words ‘comprise’ and ‘include’ and variations such as ‘comprising’ and ‘including’ will be understood to imply the inclusion of a stated integer or group of integers but not the exclusion of any other integer or group of integers.
This application claims priority of provisional application Ser. No. 60/686,252, filed Jun. 1, 2005.
Number | Name | Date | Kind |
---|---|---|---|
5755778 | Kleshinski | May 1998 | A |
6811566 | Penn et al. | Nov 2004 | B1 |
6949121 | Laguna | Sep 2005 | B1 |
7018400 | Lashinski et al. | Mar 2006 | B2 |
7326242 | Eidenschink | Feb 2008 | B2 |
20020193873 | Brucker et al. | Dec 2002 | A1 |
20030097169 | Brucker et al. | May 2003 | A1 |
20030158594 | Kang et al. | Aug 2003 | A1 |
20040054403 | Israel | Mar 2004 | A1 |
20040138732 | Suhr et al. | Jul 2004 | A1 |
20050119731 | Brucker et al. | Jun 2005 | A1 |
20050171598 | Schaeffer | Aug 2005 | A1 |
20060136031 | Gallo et al. | Jun 2006 | A1 |
Number | Date | Country | |
---|---|---|---|
20060287704 A1 | Dec 2006 | US |
Number | Date | Country | |
---|---|---|---|
60686252 | Jun 2005 | US |