SIDE BRANCH STENT GRAFT
20220087836 · 2022-03-24
Assignee
Inventors
Cpc classification
A61F2220/0075
HUMAN NECESSITIES
A61F2002/828
HUMAN NECESSITIES
A61F2002/072
HUMAN NECESSITIES
A61F2002/075
HUMAN NECESSITIES
A61F2/89
HUMAN NECESSITIES
A61F2210/0014
HUMAN NECESSITIES
A61F2002/061
HUMAN NECESSITIES
A61F2/954
HUMAN NECESSITIES
International classification
Abstract
A joining arrangement between a main tube and a side arm (5) in a side arm stent graft (1). The side arm (5) is stitched into an aperture (11) in the main tube and is in fluid communication with it. The aperture is triangular, elliptical or rectangular and the side arm is cut off at an angle to leave an end portion having a circumferential length equal to the circumference of the aperture. The side arm can also include a connection socket (76) comprising a first resilient ring (79) around the arm at its end, a second resilient ring (80) spaced apart along the arm from the first ring and a zig zag resilient stent (82) between the first and second rings. The zig-zag resilient stent can be a compression stent. Both the main tube and the side arm are formed from seamless tubular biocompatible graft material.
Claims
1. A side arm stent graft comprising a main tube of a biocompatible material and a side arm tube of a biocompatible material extending from the main tube at an acute angle thereto and being stitched thereto and in fluid communication therewith, wherein the stent graft further comprises an elongate aperture in the main tube and having a periphery around which the side arm is stitched, the elongate aperture having a circumferential length and an end of the side arm tube including a beveled end portion having a circumferential length equal to the circumferential length of the elongate aperture, whereby the side arm tube is stitched to the main tube around the periphery of the elongate aperture.
2. A side arm stent graft as in claim 1 wherein the elongate aperture is substantially rectangular.
3. A side arm stent graft as in claim 1 wherein the elongate aperture is substantially elliptical.
4. A side arm stent graft as in claim 1 wherein the elongate aperture is substantially triangular.
5. A side arm stent graft as in claim 1 wherein the elongate aperture comprises a triangular aperture in the main tube around the periphery of which the side arm tube is stitched, the triangular aperture having a base and a pair of sides, wherein an angled inner end on the side arm tube comprises an end portion having a length equal to the length of the base of the triangular aperture and a beveled portion having a length equal to the length of the side of the triangular aperture, whereby the side arm tube is stitched to the main tube around the periphery of the triangular aperture with the end portion abutting the base of the triangular aperture and the beveled portions abutting the sides of the triangular aperture.
6. A side arm stent graft as in claim 1 wherein the side arm tube extends from the main tube at an acute angle thereto, the acute angle being in range of from 15 to 60 degrees.
7. A side arm stent graft as in claim 1 wherein the side arm tube extends from the main tube at an acute angle thereto, the acute angle being in the range of from 15 to 45 degrees.
8. A side arm stent graft as in claim 1 further comprising a plurality of self expanding stents along the main tube, one of the self expanding stents extending around both the main tube and the side arm tube.
9. A side arm stent graft as in claim 8 wherein the self expanding stent extending around both the main tube and the side arm tube comprises a bend adjacent to a proximal end of the stitching and struts extending down either side of the side arm tube.
10. A side arm stent graft comprising a main tube of a biocompatible material and a side arm tube of biocompatible material extending from the main tube at an angle thereto and stitched thereto and being in fluid communication therewith, wherein the side arm stent graft further comprises a triangular aperture in the main tube around the periphery of which the side arm tube is stitched, the triangular aperture having a base and a pair of sides, and an end of the side arm tube having a bevel to leave an end portion having a circumferential length equal to the length of the base of the triangular aperture and a length of the bevel equal to the length of the side of the triangular aperture, whereby the side arm tube is stitched to the main tube around the periphery of the triangular aperture with the end portion abutting the base of the triangular aperture and the bevel abutting the sides of the triangular aperture.
11. A side arm stent graft comprising a main tube of a biocompatible material and a side arm tube of a biocompatible material extending from the main tube and being stitched thereto and in fluid communication therewith, wherein the side arm stent graft further comprises an elongate aperture in the main tube and an angled inner end on the side arm tube, the periphery of the inner end on the side arm tube being stitched to the periphery of the aperture whereby the circumference of the joined region of the main tube and side arm tube increases along the length of the stitching at a first end of the joined region to the sum of the circumferences of the main tube and the side arm at the other end of the joined region.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0026] This then generally describes the invention but to assist with understanding reference will now be made to the accompanying drawings which show various embodiments of the invention.
[0027] In the drawings:
[0028]
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[0030]
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DETAILED DESCRIPTION
[0038] Now looking at the drawings and more particularly the first embodiment shown in
[0039] For the purpose of assisting in the explanation of the present invention the stent graft main tube 3 has a proximal end 7 and a distal end 9 and blood flow would normally be from the proximal end 7 to the distal end 9.
[0040] To join the branch tube 5 to the main tube 3, according to one embodiment of the invention, a triangular aperture or fenestration generally shown as 11 is cut into the main tube 3. The triangular aperture or fenestration 11 is in the shape of an isosceles triangle with the base 13 at the proximal end and the substantially equal length sides 15 more distal. The side arm 5 has a bevel cut in it at one of its ends such that the remainder 18 of the circumference of the side arm after the bevel 17 is cut into the side arm has a semi-circumference 19 which is substantially equal to the length of the base 13 of the triangular aperture or fenestration 11. The length of the bevel 17 is substantially equal to the length of the sides 15 of the triangular aperture or fenestration 11.
[0041]
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[0044]
[0045] Through
[0046] In practice a self-expanding stent 21 is placed on the outside of the stent graft at the branch or join region to assist with maintaining the side arm and main tube in a more circular cross section and as open as possible as shown in
[0047]
[0048] In this embodiment the side arm extends from the main tube 3 at an angle designated by the numeral 26. This angle may be in the region of from 15 to 45 degrees.
[0049] In one particular embodiment the main tube 3 may have a diameter of 12 mm and hence a circumference of 38 mm. The side tube may have a diameter of 8 mm and hence a circumference of 26 mm. The base of the triangular aperture or fenestration 11 may have a length of 13 mm and the sides of the triangular aperture or fenestration 11 may have a length of 20 mm. Hence the side arm 5 has a bevel cut into it leaving a semi circumference 19 of 13 mm and a length of the bevel 17 of 20 mm. The stent graft may have an overall length of 103 mm. In the case of a stent graft to be deployed into the common iliac artery with the side arm adapted to extend towards the internal iliac artery normally there may be a length of main tube of 16 mm proximal of the join to the side arm and up to 68 mm distal of the join to the side arm. The side arm may have a diameter of 8 mm and a length distally of the join region of up to 25 mm. It will be realised that for stent grafts to be deployed into the ascending or descending aorta with side arms to extend into their respective branch vessels, other lengths and diameters will be applicable.
[0050] One method by which the side arm stent graft according to the present invention may be assembled by stitching is as follows: [0051] The triangular aperture is cut out of the main tube and the bevel cut out of the side arm. [0052] The side arm is turned inside out and inserted into the main tube such that the remaining straight end at the bevelled end of the side arm is aligned with the base of the triangular aperture and the bevelled edges are aligned with the sides of the triangular aperture. [0053] The two tubes are temporarily tacked together. [0054] The bevelled edges are stitched to the sides of the triangular aperture. [0055] The bevelled end of the side arm is stitched to the base of the triangular aperture. [0056] The side arm is then pulled out through the aperture. [0057] The necessary stents are then stitched to the main tube and the side arm.
[0058] Both the side arm 5 and the main tube 3 are formed from a seamless tube of a biocompatible graft material. This means that when the stent graft is compressed into an endovascular delivery device seams along the length of the tube do not compromise the size of the stent graft.
[0059]
[0060] In this embodiment the stent graft 30 has an elongate elliptical fenestration or aperture 31 which is cut in the main body 32 and a side arm 34 has a angled and curved cut end 36 such that the circumference of the elliptical fenestration 31 is substantially the same length as the circumference of the angled and curved end 36.
[0061]
[0062]
[0063] In particular it can be noted that the stent 41 has a bend 43 between struts 44 and 45 adjacent to the proximal end of the stitching 38 and that the struts 44 and 45 extend on either side of the side arm 34.
[0064] By this arrangement the circumference of the main body and side arm increases from being the circumference of the main body at the proximal end of the join region until at the distal end of the join region, the total circumference is the circumference of the main body plus the circumference of the side arm and it is after this that the side arm actually exits.
[0065]
[0066]
[0067] The stent graft 70 has a main tubular body 72 and a side arm 74. Both the main tubular body and the side arm are formed from a seamless tube of a biocompatible graft material such as Dacron. A triangular aperture is formed in the main tube and a bevel cut into the inner end of the side arm and the side arm stitched into the triangular aperture with stitching 78 according to the method of the present invention. The side arm has a connection socket arrangement 76 at its distal end 77. The connection socket arrangement 76 comprises a first resilient ring 79 stitched to its terminal or distal end 77 and a second resilient ring 80 spaced apart from the first ring 79. Each ring 79 and 80 is formed from at least two turns and preferably three turns of nitinol wire and the ends of the nitinol wire terminate in loops 81. The use of the loops 81 prevents sharp ends from the nitinol wire from digging into the vasculature into which the stent graft is deployed. Between the first ring 79 and the second ring 80 is a stent 82 formed from a resilient material. The resilient stent 82 is formed from nitinol wire, for instance, and is made to be of a size which is at rest slightly smaller than the diameter of the side arm 74 and hence when sewn on to the outside of the side arm 74 it provides a diameter reducing effect on the side arm 74.
[0068] When a bridging stent such as a balloon expandable stent is placed into the socket 76 and expanded, the rings 79 and 80 provide firm locking for the balloon expanded stent and the resilient stent 82, which is expanded by the balloon expanded stent while it is being balloon expanded, provides a compressive effect to keep tension on the balloon expanded stent. By this means a firm connection can be obtained between the side arm and a bridging stent. A similar gripping effect can be obtained with the use of a bridging stent in the form of a self-expanding stent, a composite stent or other form of leg extension.
[0069]
[0070] In the case of each side arm a triangular aperture is formed in the main tube and a bevel cut into the inner end of the side arm and the side arm stitched into the triangular aperture with stitching 104 according to the method of the present invention. Each side arm has a connection socket arrangement 106 at its distal end. The connection socket arrangement 106 comprises a first ring 108 stitched to its terminal or distal end and a second ring 110 spaced apart from the first ring 108. Each ring 108 and 110 is formed from at least two turns and preferably three turns of nitinol wire and the ends of the nitinol wire terminate in loops. The use of the loops prevents sharp ends from the nitinol wire from digging into the vasculature into which the stent graft is deployed. Between the first ring 108 and the second ring 110 is a stent 112 formed from a resilient material. The resilient stent 112 is formed from nitinol wire, for instance, and is made to be of a size which is at rest slightly smaller than the diameter of the side arm 98 and hence when sewn on to the outside of the side arm 98 it provides a diameter reducing effect on the side arm 98.
[0071] The main stent graft has a series of self expanding stents 114 along its lengths and it will be particularly noted that self expanding stents extend over the junction regions of the side arms to assist with holding the side arms open to blood flow.
[0072] 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.
[0073] 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.