The technical field of this disclosure is medical implantation devices, particularly, a branch vessel suture stent system and method.
Wide ranges of medical treatments have been developed using endoluminal prostheses, which are medical devices adapted for temporary or permanent implantation within a body lumen, such as naturally occurring or artificially made lumens. Examples of lumens in which endoluminal prostheses may be implanted include arteries such as those located within coronary, mesentery, peripheral, or cerebral vasculature; veins; gastrointestinal tract; biliary tract; urethra; trachea; hepatic shunts; and fallopian tubes. Various types of endoluminal prostheses have also been developed with particular structure to modify the mechanics of the targeted luminal wall.
A number of vascular devices have been developed for replacing, supplementing, or excluding portions of blood vessels. These vascular devices include endoluminal vascular prostheses and stent grafts. Aneurysm exclusion devices, such as abdominal aortic aneurysm (AAA) devices, are used to exclude vascular aneurysms and provide a prosthetic lumen for the flow of blood. Vascular aneurysms are the result of abnormal dilation of a blood vessel, usually from disease or a genetic predisposition, which can weaken the arterial wall and allow it to expand. Aneurysms can occur in any blood vessel, but most occur in the aorta and peripheral arteries, with the majority of aneurysms occurring in the abdominal aorta. An abdominal aortic aneurysm typically begins below the renal arteries and extends into one or both of the iliac arteries.
Aneurysms, especially abdominal aortic aneurysms, have in the past been treated using open surgical procedures in which the diseased vessel segment is bypassed and repaired using a sewn in artificial vascular graft. While open surgery is an effective surgical technique in light of the risk of a fatal abdominal aortic aneurysm rupture, the open surgical technique suffers from a number of disadvantages. The surgical procedure is complex, requires a long hospital stay, requires a long recovery time, and has a high morbidity and mortality rates. Less invasive devices and techniques have been developed to avoid these disadvantages. Tubular endoluminal prostheses that provide a conduit or conduits for blood flow while excluding blood flow to the aneurysm site are introduced into the blood vessel using a catheter in a less or minimally invasive technique. The tubular endoluminal prosthesis is introduced in a small diameter crimped condition and expanded at the aneurysm. Although often referred to as stent grafts, these tubular endoluminal prostheses differ from covered stents in that they are not used to mechanically prop open natural blood vessels. Rather, they are used to secure an artificial conduit in a sealing engagement with the vessel wall without further opening the abnormally dilated natural blood vessel.
Stent grafts for use in abdominal aortic aneurysms typically include a support structure supporting woven or interlocked graft material. Examples of woven graft materials are woven polymer materials, e.g., Dacron, or polytetrafluoroethylene (PTFE). Interlocked graft materials include knit, stretch, and velour materials. The graft material is secured to the inner or outer diameter of the support structure, which supports the graft material and/or when functioning as a seal holds it in place against a surrounding vessel wall. In this configuration the stent graft is secured to a vessel wall above and below the aneurysm. A proximal spring stent of the stent graft can be located above the aneurysm to provide a radial force which engages the vessel wall and provides an outward force to seal the proximal end of the stent graft to the vessel wall. The proximal spring stent can include anchor pins to puncture the vessel wall and further secure the stent graft in place.
One impediment in using stent grafts high in the abdominal aorta is the need to maintain blood flow to the renal arteries and superior mesenteric artery when the only region suitable for sealing the proximal end of the stent graft to the wall of the aorta is superior to these visceral arteries. An estimated ten percent of AAA cases amenable to endovascular repair require suprarenal fixation, potentially cutting off blood to the kidneys and intestine. One proposed solution to this problem has been to provide branched conduits from the stent graft whose main body covers these branches to perfuse the renal arteries and superior mesenteric artery.
In such arrangements, a joint created in situ between the stent graft and the branched conduit is prone to leakage, reducing flow to the branch vessels and continuing to pressurize the aneurysmal sac. One approach to this problem has been to custom make a stent graft with branched conduits for a particular patient, so that the branch conduit seal is fabricated before the stent graft is deployed in the patient. This approach has its own problems, however, since each stent graft is different, requiring a customized stent graft constructed using individualized personal measurements and construction. In addition, the bulky customized stent grafts are difficult to deploy, since the branch conduits are attached before deployment and thus make the device so much more bulky. The efficacy of such branched customized stent grafts is yet to be proven.
Another approach to the problem of branch conduit joint leakage has been to fenestrate the graft material in situ after the stent has been deployed, deploy a covered branch vessel stent in the fenestration to provide a flow path (conduit) between the main stent graft lumen and the visceral artery, and form the seal in place. This approach has problems because complicated sealing mechanisms are required and limited working space is available in the vessel. One approach has been to flare the end of the branch vessel stent. Flaring is however technically complex and time consuming to implement. Another approach has been to use a grommet or fitting crimped across the graft material, but such fittings are complex and difficult to deploy.
Another problem is fixation of the branch vessel stent at the visceral artery. If the stent graft shifts after being implanted, the branch vessel stent may no longer be aligned with the visceral artery and the length of the branch vessel stent in the visceral artery may be reduced. The patency of the branch vessel stent may be reduced if twisting of the branch vessel stent causes it to partially collapse.
It would be desirable to have a branch vessel suture stent system and method that would overcome the above disadvantages.
One aspect according to the present invention provides a branch vessel suture stent having a stent body having a first end, a second end, and a central axis, the first end having a first periphery; and shape memory hooks disposed about the first periphery, each of the shape memory hooks being attached to the first periphery at an attachment point, the shape memory hooks being elongated in a stressed state and looped in a parent state, each of the shape memory hooks defining a loop plane in the parent state. The shape memory hooks are substantially parallel to the central axis in the stressed state, and the first periphery at the attachment point for each of the shape memory hooks is substantially orthogonal to the loop plane for each of the shape memory hooks in the parent state.
Another aspect according to the present invention provides a branch vessel suture stent system including a suture stent delivery catheter; and a branch vessel suture stent operably attached to the suture stent delivery catheter, the branch vessel suture stent having a stent body having a first end, a second end, and a central axis, the first end having a first periphery; and shape memory hooks disposed about the first periphery, each of the shape memory hooks being attached to the first periphery at an attachment point, the shape memory hooks being elongated in a stressed state and looped in a parent state, each of the shape memory hooks defining a loop plane in the parent state. The shape memory hooks are substantially parallel to the central axis in the stressed state, and the first periphery at the attachment point for each of the shape memory hooks is substantially orthogonal to the loop plane for each of the shape memory hooks in the parent state.
Another aspect according to the present invention provides a method of stenting a branch vessel off a main vessel, the method including providing a main vessel stent graft having main vessel stent graft material and a main vessel stent graft lumen; deploying the main vessel stent graft in the main vessel; providing a branch vessel suture stent in a stressed state, the branch vessel suture stent having a stent body and shape memory hooks, the stent body having a first end including a first periphery, the shape memory hooks being disposed about the first periphery; advancing the branch vessel suture stent through a fenestration in the main vessel stent graft to locate the stent body in the branch vessel and the shape memory hooks in the main vessel stent graft lumen; and allowing the seal portion of the stent to expand and then relaxing each of the shape memory hooks to engage the main vessel stent graft material and form a loop.
Another aspect according to the present invention provides a branch vessel suture stent for use in a branch vessel with a main vessel stent graft having main vessel stent graft material, the branch vessel suture stent including means for stenting the branch vessel, the stenting means having a central axis; and means for hooking the main vessel stent graft material, the hooking means being connected to the stenting means and having a stressed state and a parent state. Each of the hooking means is substantially parallel to the central axis in a compressed state and then as the stent reaches its initial deployment configuration in the stressed state the hooking means are released to form a loop in the parent state.
The foregoing and other features and advantages according to the invention will become further apparent from the following detailed description read in conjunction with the accompanying drawings. The detailed description and drawings are merely illustrative, rather than limiting in scope.
The outer shaft 28 can be operably connected to a catheter handle 30 for advancing the branch vessel suture stent to the deployment site. In one embodiment, the outer shaft 28 has an outer shaft lumen 37 for receiving the inner shaft 32. The inner shaft 32 can be operably connected to a sheath handle 36 to move the sheath 34 axially and release the distal portion of branch vessel suture stent 40. In one embodiment, the inner shaft 32 has a guidewire lumen 38 for receiving the guidewire 26. The guidewire 26 can be advanced to the deployment site, such as a branch vessel, and the suture stent delivery catheter 22 advanced to the deployment site over the guidewire 26. The proximal portion of the suture stent 40, i.e., its hook portions are sleeved with separate hypotubes 35 (shown with dashed lines) when a handle element (not shown) attached to the hypotubes is retracted, the hook elements are released.
The branch vessel suture stent system 20 can be used to deploy a branch vessel suture stent at the ostium of a branch vessel connected to a main vessel. Exemplary deployment of a branch vessel suture stent in an abdominal aortic aneurysm proceeds as follows.
The main vessel stent graft is deployed in the main vessel. The steerable catheter is advanced to the abdominal aortic aneurysm through the femoral artery, the carotid artery, or the subclavian artery. The catheter is guided to the location of the aneurysm with X-ray or fluoroscopic data and a main vessel stent graft is advanced to the aneurysm. A guidewire is prepositioned in the vessel to guide the catheter to aid in deployment of the main vessel stent graft. A main vessel stent graft is initially deployed in and spanning the aneurysm. The distal end of the suture stent delivery catheter 22 is advanced to the branch vessel, such as a renal artery, over a pre-positioned guidewire 26. The branch vessel can be approached through a fenestration in the main vessel stent graft material of the main vessel stent graft. In one embodiment, the fenestration is made in the main vessel stent graft before the main vessel stent graft is inserted in the patient. In another embodiment, the fenestration is made in situ after the main vessel stent graft is deployed in the main vessel. The branch vessel suture stent 40 has a stent body and a number of shape memory hooks at the proximal end of the stent body. The sheath 34 is positioned through the fenestration so that the stent body is within the branch vessel and the shape memory hooks are still within the main vessel stent graft lumen. The sheath 34 is moved distally so that as the branch vessel suture stent 40 is released from the constraint of the sheath it (expands) changes from the stressed state to the parent state. The stent body expands in diameter and the shape memory hooks if unrestrained would loop toward the branch vessel to engage the main vessel stent graft material of the main vessel stent graft or the main vessel stent graft material of the main vessel stent graft and the ostium of the branch vessel. In the parent state, the shape memory hooks form loops. However, since the branch vessel suture stent 40 is transported to the delivery site in a compressed (small delivery catheter) diameter, looping of the memory hooks at the small diameter would cause the tips of the hooks to engage at a related small diameter. So in this instance a bundle (array) of hypotubes (one hypotube 35 for each hook) spaced around a tubular perimeter, each hypotube 35 individually having been slipped over (as a sleeve) or surrounding a respective corresponding hook loop to restrain (prevent) the hook loop from turning into a loop, while still in small body diameter. As the sheath 34 is moved off the stent 40 to allow it to fully radially expand and the main body portion of the stent establishes a deployed position as it expands and contacts the surrounding vessel and branch opening of the main stent graft body. Once the sheath has been removed and the body of the stent 40 has fully expanded the ends of the hypotubes still holding the hooks substantially straight, also expand to the full diameter of the branch vessel. Then the outer shaft to which the radially expanded hypotubes are articulably connected is retracted to release the hook loops to from their restraint and allow the loops to engage and secure themselves in the surrounding tissues and graft material. Once the branch vessel suture stent 40 is expanded fully and released to its parent state, the sheath 34 can be pulled back through the lumen of the branch vessel suture stent 40, and the suture stent delivery catheter 22, the guidewire 26, and the steerable catheter 24 removed from the patient.
Those skilled in the art will appreciate that the approach for deployment of the branch vessel suture stent can be made via externally accessible branch vessel, such as carotid, to the main vessel for particular applications, rather than the approach from the main vessel toward the branch vessel described above. For example, when a main vessel stent graft is deployed in the aortic arch as the main vessel, the suture stent delivery catheter can deliver the branch vessel suture stent through the right common carotid artery, the left common carotid artery, or the left subclavian artery as the branch vessels. When the approach is from the branch vessel, the shape memory hooks and hypotube mechanism holding them are disposed toward the distal end of the suture stent delivery catheter and the sheath is retracted toward the proximal end to release the branch vessel suture stent, while the hypotube mechanism is moved forward to be released.
The branch vessel suture stent 40 can be made of any shape memory material having a stressed state and a parent state, such as a shape memory metal and/or shape memory polymer. Examples of shape memory metals include nickel titanium alloys (Nitinol), and the like. The shape memory materials have an Af transformation temperature below body temperature at which the branch vessel suture stent 40 is released from the stressed state and relaxes into the parent state.
The branch vessel suture stent 40 can be formed from a single workpiece or assembled from multiple pieces. In one example, the branch vessel suture stent 40 is laser cut from a single piece of Nitinol tubing, and then the shape memory hooks are formed into loops, treated to set the parent shape, and then elongated into the stressed shape for delivery. In another example, the stent body of the branch vessel suture stent 40 is formed of braided strands of Nitinol woven into a tubular lattice and the shape memory hooks are made of shape set Nitinol tubing sharpened to form the sharp tip and crimped onto one end of the lattice. In another example, the stent body of the branch vessel suture stent 40 is made of one material, such as shape memory polymer, and the shape memory hooks are made of another material, such as shape memory metal. In yet another example, the body stent is balloon expandable and is made of a deformable material, such as steel, stainless steel, cobalt chromium alloys, titanium, polymers, copolymers, or combinations thereof, and the shape memory hooks are made of a shape memory material. Those skilled in the art will appreciate that the pattern of the body stent of the branch vessel suture stent 40 can be any pattern supporting a compressed configuration and an expanded configuration. The pattern can be diamond-shaped, slotted, rectangular, or any other pattern suitable for the desired application.
The hypotubes are made of a stiff, yet thin walled material, such as nitinol or stainless steel, or polymer tubes, which prevent the hooks from bending, but allow the hypotube bundle to expand radially as the proximal sheath 34′ is removed from around it.
The branch vessel suture stent 40 can support suture stent graft fabric material to prevent flow across the stent body and to form a seal with the main vessel stent graft material of the main vessel stent graft deployed in the main vessel. In one embodiment, the suture stent graft fabric material is disposed over and supported by the stent body and the elongated shape memory hooks. The suture stent graft fabric material can include gussets to accommodate motion of the shape memory hooks as required to allow motion of the shape memory hooks between the stressed state and the parent state. If desired for a particular application, the sharp tips of the shape memory hooks can extend through the suture stent graft fabric material when the branch vessel suture stent 40 is in the stressed state. In another embodiment, the suture stent fabric graft material is disposed over the stent body and not disposed over the elongated shape memory hooks. In yet another embodiment, the branch vessel suture stent 40 does not include suture stent graft material. Those skilled in the art will appreciate that the suture stent fabric graft material can be any woven or interlocked graft material suitable for stent grafts, such as woven polymer materials, e.g., Dacron, or polytetrafluoroethylene (PTFE), or interlocked graft materials including knit, stretch, and velour materials.
The branch vessel suture stent 40 can include radiopaque markers as desired to improve visibility on X-ray and fluoroscopic images. The radiopaque markers can be made of platinum, iridium, or any other radiopaque material. In one embodiment, radiopaque marker (disks, or sleeves or coatings) 47 are provided the second end 46 of the stent body 42. Radiopaque marker elements 47 can be provided at other or additional places on the branch vessel suture stent 40, such as at the first end 44.
Referring to
The providing a main vessel stent graft 202 includes providing a main vessel stent graft having main vessel stent graft material and a main vessel stent graft lumen. In one embodiment, the main vessel stent graft also has a fenestration pre-formed in the main vessel stent graft material at the anticipated axial location of the branch vessel. The fenestration can be located based on measurements of the anatomy of the particular patient.
The deploying the main vessel stent graft 204 includes deploying the main vessel stent graft in the main vessel. In one embodiment, the main vessel stent graft is advanced to the deployment site in the main vessel through the femoral artery, the carotid artery, or the subclavian artery. In one embodiment, the deploying the main vessel stent graft 204 further includes fenestrating the main vessel stent graft to form the fenestration at the location of the ostium of the branch vessel.
The providing a branch vessel suture stent having shape memory hooks 206 includes providing a branch vessel suture stent in a stressed state, the branch vessel suture stent having a stent body and shape memory hooks, the stent body having a first end including a first periphery, and the shape memory hooks being disposed about the first periphery. An exemplary branch vessel suture stent is illustrated in
Referring to
The expanding the main body of the branch vessel suture stent while holding the shape memory hooks substantially straight as the main body expands 209 involves the radial expansion of the hypotube buddle (array) to position the hooks adjacent to their points of engagement with the adjacent structures prior to deployment. The relaxing the shape memory hooks 210 includes relaxing each of the shape memory hooks to engage the main vessel stent graft material and form a loop. The shape memory hooks 210 relax from a stressed state to a parent state when the shape memory is above the transformation temperature. The shape memory hooks 210 are restrained by hypotubes and/or dissolvable restraining bands until the branch vessel suture stent is in place for deployment.
While specific embodiments are disclosed herein, various changes and modifications can be made without departing from the spirit and scope thereof.