Patent Application
20110313512
This disclosure relates to a medical device and more particularly to a stent graft deployed by endovascular techniques.
In recent years endovascular implantable devices have been developed for treatment of aortic aneurysms. These devices are delivered to the treatment site through the vascular system of the patient rather than by open surgery. The devices include a tubular or cylindrical framework or scaffolding of one or more stents to which is secured a tubular shape of graft material such as woven Dacron, polyester polytetrafluoroethylene or the like. The devices are initially reduced to a small diameter, placed into the leading or proximal end of a catheter delivery system. The delivery system is inserted into the vascular system of the patient such as through a femoral incision. The leading end of the delivery system is maneuvered to the treatment site over a previously positioned guide wire. Through manipulation of a control system that extends to the proximal end of the catheter from the distal end of the system outside the patient the implantable device is then deployed by holding the device as its location and withdrawing a surrounding sheath. The stent graft or implantable device can then self expand or is expanded through the use of a balloon which is introduced with the stent graft implantable device. The stent graft becomes anchored into position to healthy wall tissue in the aorta after which the delivery system is removed leaving the device in position thereby bypassing an aneurysm in the aorta in a manner that channels all blood flow through the stent graft so that no blood flow enters the aneurysm, such that not only does the aneurysm no longer continue to grow and possibly rupture but the aneurysm actually begins to shrink and commonly disappears entirely.
Where there are branch vessels from the aorta then provision may need to be made to supply blood to the branch vessels. This is done by fenestrations and where necessary side branch extension stent grafts.
This disclosure will be generally discussed in relation to treatment of aortic aneurysms in the thoraco-abdominal region of the aorta but the disclosure is not so limited and can be used where there are branch vessels from a main vessel.
For treatment of thoracic aortic aneurysms in particular it is necessary to introduce the implantable device high up in the aorta and in a region of the aorta which is curved and where there can be strong blood flow.
In the thoracic aorta there are major branch vessels, the brachiocephalic, the left carotid and the left subclavian and for treatment of an aneurysm in the region of the thoracic arch provision must be made for blood supply to continue to these arteries while an operation is in progress and after completion of the operation. For this purpose fenestrations or side branches are provided into a stent graft in that region. Access is generally obtained to these fenestrations to deploy side arms into the stent graft via the left or right brachial arteries or less commonly via the left or right carotid arteries.
Catheterisation of a branch vessel from a main vessel can be difficult and to assist pre-catheterised fenestrations or side branches have been used.
Throughout this specification the term distal with respect to a portion of the aorta, a deployment device or a prosthesis means 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 the disclosure is said to reside in a stent graft comprising a tubular body comprising a wall of a biocompatible graft material and at least one tubular side arm received in the wall, the wall in the vicinity of the side arm comprising a loose fold of the graft material, the side arm being fastened to the loose fold of graft material such that the tubular side arm can be angled proximally and distally and from side to side.
Preferably the tubular side arm comprises an inner end and an outer end and is fastened into the loose fold of graft material by a circumferential fastening around the tubular side arm between the inner end and the outer end.
Preferably the tubular side arm extends partially within the tubular body of the stent graft and partially outside the tubular body of the stent graft.
Preferably the tubular side arm comprises a reinforcing ring at each end thereof and a plurality of zig zag reinforcing struts extending between the reinforcing rings.
Preferably the loose fold of graft material is provided proximally and distally of the tubular side arm and the side arm can be angled proximally and distally. Alternatively the loose fold of graft material can be provided circumferentially to each side of the tubular side arm and the side arm can be angled laterally or from side to side. Alternatively the loose fold of graft material is provided both proximally and distally of the tubular side arm and circumferentially to each side of the tubular side arm and the side arm can be angled proximally and distally and angled laterally from side to side.
In an alternative form the disclosure comprises a stent graft comprising a tubular body comprising a wall of a biocompatible graft material, the tubular body being supported by a plurality of zig zag stents, a portion of graft material between two adjacent stents of the plurality of zig zag stents comprising a loose fold region of the graft material, and at least one tubular side arm received in the loose fold region of the graft material, the side arm being fastened to the loose fold of graft material such that the loose fold of material is proximally and distally of the tubular side arm and wherein the tubular side arm can be angled proximally and distally.
In an alternative form the disclosure comprises a stent graft comprising a tubular body comprising a wall of a biocompatible graft material, the tubular body being supported by a plurality of zig zag stents, a portion of graft material between two adjacent stents of the plurality of zig zag stents comprising a loose fold region of the graft material, and at least one tubular side arm received in the loose fold region of the graft material, the side arm being fastened to the loose fold of graft material such that the loose fold of material is provided circumferentially to each side of the tubular side arm and the side arm can be angled laterally from side to side.
In an alternative form the disclosure comprises a stent graft comprising a tubular body comprising a wall of a biocompatible graft material, the tubular body being supported by a plurality of zig zag stents, a portion of graft material between two adjacent stents of the plurality of zig zag stents comprising a loose fold region of the graft material, and at least one tubular side arm received in the loose fold region of the graft material, the side arm being fastened to the loose fold of graft material such that the loose fold of material is provided both proximally and distally of the tubular side arm and circumferentially to each side of the tubular side arm and the side arm can be angled proximally and distally and angled laterally from side to side.
In an alternative form the disclosure comprises a stent graft comprising;
at least a first stent and an adjacent second stent, the first and second stents having at least a pair of adjacent bends on the first stent aligned with an adjacent pair of bends on the second stent, whereby a first pair of adjacent struts of the first stent and a second pair of adjacent struts of the second adjacent stent together define a diamond shaped region;
In this embodiment of the disclosure the recess portion of the biocompatible graft material provides a loose fold of the biocompatible graft material around the tubular side arm.
Preferably the stent graft further comprises a third adjacent stent, the third adjacent stent having at least a pair of bends adjacent to the second stent whereby a third pair of adjacent stents of the third strut defines a second diamond shaped region,
a second recess in the second diamond shaped region, the second recess extending into the lumen of the tubular body, the second recess being defined by a second recess portion of a biocompatible graft material;
In an alternative form the disclosure comprises a stent graft comprising a tubular body comprising a wall of a biocompatible graft material and at least one tubular side arm received in the wall, the tubular side arm comprising an inner end and an outer end, the wall in the vicinity of the side arm comprising a loose fold of the graft material when the side arm is extending substantially at right angles to the tubular body of the stent graft, the tubular side arm being fastened to the loose fold of graft material by a circumferential fastening around the tubular side arm between the inner end and the outer end such that the tubular side arm can be angled proximally at its outer end wherein to facilitate cathertisation of a branch vessel and distally at is outer end wherein to facilitate placement of a side arm extension stent graft and the tubular side arm remaining in its proximal or distal position without tension in the previously loose fold of graft material unless acted upon by an external force.
In an alternative form the disclosure comprises a stent graft comprising a tubular body comprising a wall of a biocompatible graft material and at least one tubular side arm received in the wall, the wall in the vicinity of the side arm comprising sufficient graft material such that the tubular side arm can be angled proximally to a proximal position and distally to a distal position without inducing sufficient tension in the graft material that would otherwise bias the tubular side arm away from the respective proximal and distal positions.
This then generally describes the disclosure but to assist with understanding reference will now be made to the accompanying drawings which show preferred embodiments of the disclosure.
In the drawings:
In
In this embodiment the zig zag stents 14 are formed from nitinol and therefore have a relatively wide included angle 20 such that a pair of stents, where the points of the stents align, form substantially diamond shaped regions 22 and 24.
Into each of the regions 22 and 24 a recess 25, 23 respectively is formed and lined or defined by graft material 26 to form the recess. The graft material 26 includes folded regions 28 which are adjacent to a tubular side arm 30 which is received into the recess and stitched as at 32 into the recess.
As can be seen particularly in
In
In this embodiment the tubular side arm 44 includes a reinforcing ring 52 at each end and a zig zag stent reinforcement 54 between the ends.
Immediately to each side of the side arm 44 there is a loose fold of the material of the recess 42a and 42b and this loose fold enables the tubular side arm to be angled as shown by the dotted lines 56a and 56b.
The arrangement angled to 56a is shown in
The arrangement of the angled side arm at 56b is shown in
The existence of the loose fold of material to each side of the tubular side arm when it is in the position extending substantially at right angles to the stent graft means that when the tubular side arm is toggled or angled to one side or the other, the side arm stays in the toggled or angled position with out the previously loose folds being tensioned to the extent that they provide a returning force. If an external force is applied such as by a guide wire passing through the side arm then the side arm can be toggled or angles to an different position.
As can be seen in
The schematically illustrated thoracic arch 70 includes an ascending aorta 72 ascending from an aortic valve 74 of the heart up to a thoracic arch 76 from which extends the brachiocephalic artery 78, the left common carotid artery 80 and the left subclavian artery 82. Generally when providing side branches into these arteries an anastomosis is provided between the left carotid artery and the left subclavian artery as shown as 84 and two side arms are used. The aorta has a descending aorta portion 86 which has an aneurism 88.
A particular problem that exists with catheterization of the great vessels and deploying side arms from the great vessels into a stent graft is to obtain access from a partially deployed stent graft into those vessel. In
Once catheterization has occurred the stent graft can be further advanced so that its proximal end 90a extends further down the ascending aorta 72. At this stage the guide wires 96 and 98 that have been used for catheterization of the side arms 92 and 94 or further guide wires replacing them can be used to deploy side branch extensions and in doing this the side arms 92 and 94 can be angled so that their outer ends can extend distally which facilitates the placement of the side arm stent graft extension and which facilitates blood flow into the vessels after they have been grafted.
The reinforcing rings 52 and the zig zag stent 54 on the side arm stent graft enable a good seal to be obtained between a side arm stent graft and the respective side branches.
The distal end 90b of the stent graft extends down the descending aorta 86 and into the aneurism 88 and hence a further stent graft 104 has been deployed to provide a seal at the other end of the aneurism 88 (not shown).
It can be seen that by this disclosure there is provided an arrangement by which a side arm of a stent graft can be toggled in one direction for instance for facilitating catheterization and into another direction to facilitate alignment with a side branch vessel.
Although the disclosure has generally been discussed in relation to the thoracic arch and to proximal or distal angulations of the side arm it will be realized that the arrangement can be used in other side branch situations in the aorta or other vessels of the human or animal body and can be angled from side to side to facilitate alignment with other side branch vessels such as the renal arteries the celiac artery or the mesenteric arteries.
Throughout the specification various indications have been given as to the scope of the disclosure but the disclosure is not limited to any one of these but may reside in two or more combined together. Examples are given for illustration only and not for limitation.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2010202544 | Jun 2010 | AU | national |
