US20030153969A1 - Methods and apparatus for intraluminal placement of a bifurcated intraluminal graft - Google Patents

Abstract

Methods and apparatus for placing a bifurcated aortic graft, with extensions, into a body lumen. An aortic graft is provided with a unique combination of self-expanding a balloon expandable wires. The aortic graft is bifurcated and includes ipsilateral and contralateral legs. Two extension grafts are provided for frictional engagement with the legs of the aortic graft. For placement of the bifurcated aortic graft with extensions, an introducer assembly including a dilator and a sheath assembly provides access for the introduction of a main catheter and a directional catheter. The main catheter is provided for deployment of the bifurcated aortic graft within the lumen of a vessel. A balloon is provided on the main catheter for expanding the balloon-expandable wires of the aortic graft. The directional catheter, which includes a deflecting spring portion, permits placement of a guidewire through the ipsilateral leg and into the contralateral leg of the aortic graft. In turn, a second introducer sheath and a second catheter assembly are provided contralaterally for introduction of a graft extension. Upon balloon-expansion, the graft extension is frictionally engaged with the contralateral leg of the aortic graft. A third catheter assembly including a second extension graft is provided for introduction of the extension graft and balloon-expansion thereof for frictional engagement with the ipsilateral leg of the graft.

Description

RELATED APPLICATIONS
• The present application is a continuation of co-pending allowed patent application Ser. No. 09/819,539, which is a divisional patent application of issued U.S. Pat. No. 6,368,345, filed Apr. 9, 2002, which is a continuation-in-part application of abandoned U.S. application Ser. No. 09/163,580, filed Sep. 30, 1998.[0001]
BACKGROUND OF THE INVENTION
• 1. Field of the Invention[0002]
• The present invention is directed generally to methods and apparatus for positioning an intraluminal graft. More specifically the present invention is related to methods and apparatus for positioning an intraluminal graft into a bifurcating vessel such as an artery.[0003]
• 2. Discussion of Related Technology[0004]
• An artery or other vessel that is weakened by disease, injury, or congenital defect, can become distended due to the pressure of blood or other fluid flowing through the weakened area. In the vasculature, this distended weakening is called an aneurysm. An aneurysm typically occurs in the arterial vessels of the head, chest, or abdomen. The distension may cause the vessel to rupture, which can have serious, even life-threatening consequences.[0005]
• Aneurysms in the abdominal aorta are typically distended around the circumference of the aorta and tapered at both ends. Most aneurysms of the abdominal aorta are caused by atherosclerotic weakening of a segment of the wall. Abdominal aneurysms may cause backache and severe pain, and may be visible as a throbbing swelling. If an abdominal aorta ruptures, it is seriously life threatening.[0006]
• Traditionally, aneurysms have been treated by radical surgical graft replacement. This approach is risky for the patient and is sometimes not feasible due to other pre-existing disease states of the patient. More recently, aneurysms have been treated by placement of an intraluminal or endovascular graft. These intraluminal or endovascular grafts may be of various types, including grafts having stents, wireforms, or other attachment means attached to or integrated into the graft structure.[0007]
• In general, intraluminal grafts and their respective support and/or attachment means fall into two major categories, self-expanding and pressure expandable. Self-expanding intraluminal grafts, are supported and/or attached via resilient or shape-memory material such as spring steel or Nitinol™. Self-expanding material is capable of being formed in a configuration from which it may be compressed to a radially compact diameter for placement within a damaged vessel. At the time of use, the memory feature of these materials causes them to self-expand from the radially compact diameter to the expanded operative diameter.[0008]
• Pressure-expandable intraluminal grafts are supported and/or attached via plastically deformable material such as stainless steel that is initially formed in its radially compact diameter. This type of material does not have memory, and will remain in the radially compact diameter until manually expanded. Typically, outwardly directed pressure is exerted upon the graft through use of a balloon so as to cause radial expansion and resultant plastic deformation of the material to its operative diameter.[0009]
• Careful positioning and firm implantation of the intraluminal graft is critical to the successful treatment of the underlying medical condition. This is particularly difficult to accomplish when the aneurysm extends from an artery into one or more divergent arteries. A “trouser graft” has been suggested for use in a first main artery and a pair of divergent arteries by White et al. in PCT Application Nos. WO 97/17910; WO 97/17911; WO 97/18006; WO 97/26936; and WO 97/26938; all of which are hereby incorporated herein by reference in their entireties. A trouser graft comprises a first tubular body that bifurcates into two smaller tubular bodies. In the referenced disclosures, the first tubular body is placed in first artery and the two smaller tubular bodies are placed so as to extend within the two divergent arteries.[0010]
• Notwithstanding the important teachings of the foregoing references, features of the aforementioned device have recognized shortcomings that make them less than complete solutions to the treatment of aneurysms in the vasculature, or to the treatment of similar damage to other vessels. The present invention provides substantial improvements to the methods and apparatus of the prior art.[0011]
SUMMARY OF THE INVENTION
• It is an object of the present invention to provide an improved intraluminal graft and method for placement of same that diminishes deleterious kinking and twisting of the graft during and after placement thereof in a vessel.[0012]
• It is another object of the present invention to provide an improved intraluminal graft and method for placement of same that provides control over inadvertent longitudinal movement within a vessel.[0013]
• Another object of the present invention is to provide an improved intraluminal “trouser” graft and method for placement of same that precludes inadvertent separation of the legs of the trouser.[0014]
• These and other objects and features of the present invention will become more fully apparent from the following description and appended claims, or may be learned by the practice of the invention as set forth hereinafter.[0015]
• To achieve the forgoing objects, and in accordance with the invention as embodied and broadly described herein, the present invention relates to new and useful apparatus and methods for placing a bifurcated graft at the site of a damaged vessel. In a preferred embodiment, the methods and apparatus of the present invention are directed to placement of a bifurcated graft within an aneurysm located in the abdominal aorta downstream of the renal arteries. Preferably, placement of the graft is through the right femoral artery of a patient.[0016]
• An introducer assembly is provided which is configured for placement over a guidewire and for facilitating the advancement of various catheter assemblies required in connection with the practice of the invention. The introducer assembly includes a sheath, valve head, and a dilator. The sheath is preferably cylindrical in shape and is formed so as to have an appropriate flexibility and an outer diameter suitable for placement at the location of an aneurysm to be repaired. The valve head permits insertion and removal of various catheters during the method of the present invention without significant loss of blood from the femoral artery. The proximal end of the valve head is provided with a threaded connector which facilitates connection of the valve head to other catheters. The dilator, which includes a tapered tip, is placed during use through the valve head and the sheath so that the tapered tip portion protrudes from the sheath. The dilator tip portion is capable of being advanced gently through the tortuous pathway of the vasculature without causing undue trauma or a perforation, yet is also sufficiently stiff to cause the blood vessels to assume a less tortuous path.[0017]
• Another component of the present invention is a bifurcated aortic graft. The preferred bifurcated aortic graft includes both self-expanding and balloon-expandable wireforms along its length. The balloon-expandable wires permit precision in placement of the aortic graft. The self-expanding wires open within the vessel immediately upon deployment from the main catheter assembly, which allows insertion of other modular components, opens a removal path for the inflatable balloons, and reduces kinking. The self-expanding wires also increase the anchoring force between the bifurcated graft and modular extension grafts used to extend the bifurcated graft into communication with non-distended vessel walls.[0018]
• One of the self-expanding wireforms is located at a septum region of the bifurcated graft. The septum region separates an ipsilateral leg from a contralateral leg (“ipsilateral” and “contralateral” referring to opposite lateral sides of the patient depending on the surgical approach). This septum wire prevents and helps eliminate the kinks that are typically encountered with conventional bifurcated grafts. In addition, the self-expanding wireform at the septum region includes crimps functioning as radiopaque markers generally pointing to the septum region, which aids in identifying the location of the septum under fluoroscopy. Two additional self-expanding wireforms are located at the ends of each leg of the bifurcated graft. These wireforms facilitate opening the legs immediately upon deployment from the main catheter assembly to allow for the insertion of modular components. These leg wireforms also contain crimps as radiopaque markers which aid in identifying the ends of the bifurcated graft legs. All crimps on the self-expanding wireforms are placed on the anterior side of the graft, thus aiding in orientation of the graft under fluoroscopy.[0019]
• The main catheter assembly is utilized to place the aortic graft described above, which is compressed and loaded onto the distal end of the main catheter assembly. The main catheter assembly is sized such that it will fit inside the introducer sheath.[0020]
• The components of the main catheter assembly include the following: a rigid loader configured for connection to the valve head of the sheath assembly; a proximal connector assembly including a distal pusher connector; an elongate, tubular pusher body; an elongate catheter with a coaxial tube construction; and an inflatable catheter balloon.[0021]
• In addition to the aortic graft, two additional graft portions are adapted to extend into the respective iliac arteries to form a frictional engagement with the ipsilateral and contralateral legs of the aortic graft. These extension grafts typically comprise straight cylindrical tubes, with an upstream end having a common diameter. The upstream ends interlock with the respective downstream portions of the aortic graft.[0022]
• The present invention may further include a directional catheter which permits placement of the graft extensions. The directional catheter includes a deflecting spring portion, a knob used to deflect the spring portion, and a connector nut for connection with the sheath assembly.[0023]
• The preferred method for using the aforementioned components of the present invention includes the following steps. An incision is made and a primary guidewire is placed in conventional fashion in the ipsilateral side, that is, for example, through the right femoral artery and the right common iliac artery so as to extend well upstream of the aneurysm. The introducer assembly is advanced over and along the primary guidewire into a position upstream of the renal arteries. Once the sheath of the introducer assembly has been properly placed, the dilator is retracted along the guidewire and then completely removed from within the sheath assembly and from primary guidewire. The main catheter assembly is inserted over the primary guidewire and into the sheath assembly, and then connected thereto. The pusher body is distally advanced to push the aortic graft and main catheter through to the end of the introducer sheath. The sheath containing the aortic graft is then retracted slowly to approximately a desired deployment position in the abdominal aorta. The introducer sheath is then retracted to a position just below the septum region, freeing the aortic graft and exposing it to blood flow.[0024]
• The balloon-expandable, upstream portion of the aortic graft remains in a substantially compressed configuration. The catheter balloon is inflated which facilitates the concurrent radial expansion of the balloon-expandable portions of the graft from the initial, collapsed orientation, to the second, expanded orientation. In one embodiment of the present invention, the graft is slightly over-sized to optimize engagement of the aortic graft with the aortic wall. When the graft is fully expanded, the upstream end thereof frictionally engages the luminal surfaces of unaffected regions of the aorta just below the renal arteries. After the graft has been radially expanded in the aforementioned manner, the balloon is deflated, longitudinally stretched to prevent snagging on the graft, and then removed. The main catheter is then withdrawn slowly and carefully, with the introducer sheath and the primary guidewire remaining in place.[0025]
• For placement of the graft extensions, the directional catheter is first inserted over the primary guidewire through the ipsilateral side, that is, for example, through the right femoral artery and the right common iliac artery. The spring portion of the directional catheter is positioned such that it is above the septal region of the aortic graft. The spring portion is deflected by pulling proximally on the knob. A supplemental guidewire is then advanced through the directional catheter and out the deflected spring portion such that the supplemental guidewire extends down the contralateral leg and through the left common iliac artery. The supplemental guidewire is extended until it is in the left femoral artery, at which time the left femoral artery is cross-clamped and a cut-down or percutaneous incision is performed to retrieve the supplemental guidewire. Once the guidewire is retrieved, a stiffer guidewire is exchanged through the left femoral artery until it is within the first graft and reaches the contralateral side of the aortic graft. A second introducer assembly is then introduced over the stiff guidewire.[0026]
• A second catheter assembly on which is packaged a tubular graft extension is then introduced through the second sheath assembly until the introducer sheath extends through the left iliac artery and terminates at the bifurcation point of the aortic graft. The sheath followed by the pusher of the second catheter assembly are then pulled back proximally to release the tubular graft extension. The balloon on the second catheter assembly is then inflated such that the upstream end of the extension graft is frictionally engaged with the downstream contralateral leg of the aortic graft. In one embodiment of the present invention, the extension graft is slightly over-sized such that it optimally engages with the self-expanding downstream contralateral leg. The balloon is then deflated and the second catheter assembly is removed in the manner previously described hereinabove with respect to the main catheter.[0027]
• The directional catheter is also removed such that a second catheter assembly, on which is packaged a tubular graft extension, and which may be identical to the second catheter assembly, can be introduced over the primary guidewire and through the first introducer sheath assembly. This third catheter assembly is advanced until the distal end of the extension graft is at the bifurcation point of the aortic graft. In like manner to that previously described hereinabove, a third graft extension positioned on the third catheter assembly is deployed such that its upstream end is in contact with the ipsilateral leg of the aortic graft, and its downstream end is in contact with the right iliac artery. Also in like manner to that described hereinabove, the balloon on third catheter assembly is inflated to expand the balloon expandable extension graft in the ipsilateral side. In one embodiment of the present invention, the extension graft is slightly over-sized such that it optimally engages with the self-expanding downstream ipsilateral leg. In like manner to that previously described above, the balloon is deflated, extended proximally and then the third catheter assembly is withdrawn.[0028]
• In an alternate embodiment both the ipsilateral and contralateral balloon catheters could be positioned simultaneously and inflated sequentially. While maintaining the position of the third catheter balloon the second catheter balloon is deflated and stretched and the second catheter is removed. The third catheter balloon is subsequently deflated, stretched, and removed.[0029]
• The second sheath assembly and the stiff guidewires are withdrawn and the contralateral incision or puncture is sutured. An angiographic examination may take place to determine if the grafts are correctly placed and functioning. The first introducer sheath assembly is withdrawn and the right femoral incision is sutured. The result is a functioning trouser graft bridging an aneurysm.[0030]
BRIEF DESCRIPTION OF THE DRAWINGS
• To more fully understand the manner in which the above-recited and other advantages and objects of the invention are obtained, a more particular description of the invention will be rendered by reference to a specific embodiment thereof which is illustrated in the appended drawings. Understanding that these drawings depict only a typical embodiment of the invention and are not therefore to be considered to be limiting of its scope, the invention in its presently understood best mode for making and using the same will be described and explained with additional specificity and detail through the use of the accompanying drawings in which:[0031]
• FIG. 1 is a front view of an aortic graft in accordance with the present invention;[0032]
• FIG. 1A is a perspective view of a cylindrical mandrel for forming the self-expanding wires of FIG. 1;[0033]
• FIG. 1B is a partial plan view of an alternate configuration for a balloon-expandable wireform in accordance with the present invention;[0034]
• FIG. 2 is front view of a graft extension in accordance with the present invention;[0035]
• FIG. 2A is an internal cross-sectional view of the graft extension from FIG. 2;[0036]
• FIG. 2B is a front view of an embodiment of the aortic graft of the present invention having a tapered trunk region;[0037]
• FIG. 2C is a front view of the untapered aortic graft of FIG. 1;[0038]
• FIG. 2D is a front view of another embodiment of the aortic graft of the present invention having a tapered trunk region;[0039]
• FIG. 2E is a front view of an embodiment of the graft extension of the present invention having a tapered downstream end;[0040]
• FIG. 2F is a front view of the untapered graft extension of FIG. 2;[0041]
• FIG. 2G is a front view of another embodiment of the graft extension of the present invention having a tapered downstream end;[0042]
• FIG. 3 is an exploded perspective view of an introducer assembly of the present invention;[0043]
• FIG. 4 is a perspective view of a main catheter assembly of the present invention;[0044]
• FIG. 5 is a front perspective view of a directional catheter assembly of the present invention;[0045]
• FIG. 6 is a side view of the main catheter assembly of FIG. 4 with the expandable balloon shown exposed and in an expanded configuration;[0046]
• FIG. 7A is a partial perspective view of the main catheter assembly being inserted into the introducer assembly;[0047]
• FIG. 7B is a partial perspective view of the main catheter assembly connected to the introducer assembly;[0048]
• FIG. 8A is a schematic cutaway view of the abdominal region of the human body (“schematic abdominal view”) having a guidewire positioned therein;[0049]
• FIG. 8B is a sectional view of an abdominal aorta and aneurysm (“sectional aneurysmic view”) having a guidewire positioned therethrough;[0050]
• FIG. 9A is a schematic abdominal view having an introducer assembly positioned therein;[0051]
• FIG. 9B is a sectional aneurysmic view having an introducer assembly positioned therethrough;[0052]
• FIG. 9C is a schematic abdominal view with an introducer sheath positioned above the renal arteries and the dilator removed therefrom;[0053]
• FIG. 10A is a schematic abdominal view with the balloon of the main catheter assembly and aortic graft advanced within the introducer sheath to the renal arteries;[0054]
• FIG. 10B is a sectional aneurysmic view similar to FIG. 10A;[0055]
• FIG. 10C is a detailed view of the introducer sheath being withdrawn to expose the aortic graft therein;[0056]
• FIG. 10D is a sectional aneurysmic view with the introducer sheath withdrawn to a position downstream of the aortic graft;[0057]
• FIG. 11A is a schematic abdominal view with the balloon of the main catheter assembly expanded within a trunk portion of the aortic graft;[0058]
• FIG. 11B is a schematic abdominal view with the balloon of the main catheter assembly over-expanded within the aortic graft trunk portion;[0059]
• FIG. 12A is a schematic abdominal view with the balloon of the main catheter assembly deflated within the aortic graft;[0060]
• FIG. 12B is a sectional aneurysmic view with the deflated balloon on the main catheter assembly being stretched to facilitate removal from inside the aortic graft;[0061]
• FIG. 12C is a schematic abdominal view with the main catheter assembly being withdrawn therefrom and only the main guidewire extending through the aortic graft;[0062]
• FIG. 13A is a schematic abdominal view with the directional catheter connected to the sheath assembly and positioned within the aortic graft;[0063]
• FIG. 13B is a detailed view of the directional catheter being deflected around the septum region of the aortic graft;[0064]
• FIG. 13C is a sectional aneurysmic view with the directional catheter advanced to a position above the renal arteries and a second guidewire positioned within the contralateral side;[0065]
• FIG. 14A is a schematic abdominal view with a second catheter assembly positioned within the contralateral side;[0066]
• FIG. 14B is a sectional aneurysmic view with a second introducer sheath positioned at the septum region and the dilator removed therefrom;[0067]
• FIG. 15A is a sectional aneurysmic view of a balloon of the second catheter assembly and an associated first extension graft advanced within the second introducer sheath to the septum region;[0068]
• FIG. 15B is a sectional aneurysmic view with the second introducer sheath withdrawn to a position downstream of the now exposed first extension graft;[0069]
• FIG. 15C is a sectional aneurysmic view with the first extension graft from FIG. 15B being expanded from inflation of the balloon on the second catheter assembly;[0070]
• FIG. 16A is a sectional aneurysmic view with a balloon of a third catheter assembly and an associated second extension graft advanced within the first introducer sheath on the ipsilateral side to the septum region of the aortic graft;[0071]
• FIG. 16B is a sectional aneurysmic view with the first introducer sheath withdrawn to a position downstream of the now exposed second extension graft;[0072]
• FIG. 16C is a cross-section along[0073]line16C-16C of FIG. 16B; and
• FIG. 16D is a sectional aneurysmic view with a fully deployed aortic graft and first and second graft extensions.[0074]
DESCRIPTION OF THE PREFERRED EMBODIMENTS
• The present invention enables placement of a bifurcated graft at a site of a damaged vessel, such as an artery, by minimally invasive techniques rather than an open surgical access route. Although the methods and apparatus of the present invention are applicable for various types of body lumens, the description herein will be directed to placement of a bifurcated graft within an aneurysm located in the abdominal aorta downstream of the renal arteries for purposes of brevity and simplicity.[0075]
• In addition, a particular procedure is described herein showing placement of the graft through the right femoral artery of a patient. This method is presently preferred for several reasons. For example, it is contemplated that the bifurcated graft of the present invention will be placed by a vascular surgeon, interventional radiologist or a cardiologist. As a practical matter, physicians are accustomed to placing catheters through a femoral artery entry point, and are less accustomed to other entry points. Further, since most physicians are right handed, the preferred insertion will be in the right femoral artery. By describing this type of insertion, however, it is not intended to exclude other insertion locations, such as the left subclavian artery, or the initiation of the procedure through the left femoral artery. Those of ordinary skill will be able to take the teachings herein and apply them to other body lumens, other lumen locations, and other insertion sites.[0076]
• As the terms are used herein with reference to the human body, “upstream” pertains to the direction towards the heart while “downstream” pertains to the direction away from the heart. When referring to catheters, “distal” refers to the tip of catheter that is inserted into a patient and “proximal” refers to the end of the catheter outside the body of a patient. The orientation of the graft of the present invention will be referenced with respect to whether it is carried by the catheter or implanted at the aneurysm site. Specifically, upstream and downstream will be used to refer to the portions of the implanted graft closer and farther from the heart, respectively. Alternatively, when the graft is still carried on the catheter, distal and proximal will be used to refer to portions of the graft in accordance with the aforementioned catheter orientation. Finally, ipsilateral refers to the side of the patient in which the primary guidewire and main catheter are inserted (the right femoral artery in the present embodiment), while contralateral refers to the opposite side.[0077]
• Aneurysms frequently form in the abdominal aorta at a location between the renal arteries and immediately proximal to the common iliac arteries. FIG. 8A, for example, illustrates the anatomy of the abdomen in the location of an aortic aneurysm. The[0078]abdominal aorta100 can be seen branching distally into the common iliac arteries, the right commoniliac artery102 and the left commoniliac artery104. The right and leftrenal arteries106,108 and the right and leftkidneys110,112 are located proximal from thecommon iliacs102,104. In between the common iliacs and the renal arteries, anaortic aneurysm114 can be seen as a bulging section of theabdominal aorta100. Although not depicted in the present figure, such an aneurysm may even extend down one or both iliac arteries. The right and left commoniliac arteries102,104 become the right and leftfemoral arteries116,118 in the region of thepelvis98.
• A. Introducer Assembly[0079]
• It is important to introduce the bifurcated aortic graft of the present invention without causing damage to the patient's vasculature, without undue loss of blood, without dislodging plaque, and with minimum effort. It is a feature of the present invention to utilize an “introducer assembly” to achieve these objectives.[0080]
• The “introducer assembly” of the present invention is preferably configured for placement over a guidewire. Portions of the introducer assembly are thereafter used to facilitate the advancement of various catheter assemblies required in connection with the practice of the invention as described below. An introducer assembly useful in the practice of the present invention is described in co-pending U.S. patent application Ser. No. 08/713,070 filed on Sep. 12, 1996, incorporated herein by reference (the '070 application).[0081]
• The primary components of[0082]introducer assembly130 may be observed by reference to FIG. 3. FIG. 3 depicts asheath assembly132.Sheath assembly132 is comprised generally of asheath134 and avalve head136.Sheath134 is preferably cylindrical in shape along those portions of its length to be inserted into a patient.Sheath134 is formed so as to have an appropriate flexibility and an outer diameter suitable for placement at the location of an aneurysm to be repaired.Sheath134 is provided with a lumen having a diameter suitable to permit insertion of the graft sections and the various catheters described below.Tip portion138 ofsheath134 is preferably curved so as to minimize any trauma to tissue or tendency to dislodge plaque when the sheath is advanced upstream into a patient's vasculature. As mentioned in the '070 application,tip portion138 is preferably fitted with a radiopaque marker to assist in proper placement during use.
• The femoral artery is a relatively high-pressure lumen.[0083]Sheath134 is fitted withvalve head136 in a fluid-tight fashion.Valve head136 permits insertion and removal of various catheters during the method of the present invention without significant loss of blood from the femoral artery.
• FIG. 3 additionally illustrates a[0084]dilator140 used initially during the insertion ofsheath134 and during any subsequent upstream movement ofsheath134.Dilator140 is placed during use throughvalve head136 andsheath134 so that tapereddilator tip portion142 protrudes fromsheath tip portion138.Dilator tip portion142 is formed of a somewhat resilient material that is capable of being advanced gently through the tortured pathway of the vasculature without causing undue trauma or a perforation. Yet, it is desired that the tip portion be sufficiently stiff to cause the blood vessels to assume a less tortuous path. In other words, it is intended that the tip portion straighten the vasculature so as to facilitate placement of the sheath.Dilator140 is provided with a lumen therethrough capable of fitting over a guidewire.
• The proximal end of[0085]valve head136 is provided with a threadedconnector144. This threaded connector facilitates fluid-tight connection of the valve head to other catheters during the practice of the method of the invention, as discussed in greater detail below.
• The method for insertion of the introducer assembly will now be described. As illustrated in FIGS. 8A and 8B, an[0086]incision120 is made and aprimary guidewire128 is placed in conventional fashion in the rightfemoral artery116 and right commoniliac artery102 so as to extend well upstream of theaneurysm114.
• As illustrated in FIGS. 3 and 9A, the introducer assembly[0087]130 (comprising thesheath assembly132 and the dilator140) is advanced over and along theprimary guidewire128. As the introducer assembly is advanced,dilator tip portion142 gently straightens the patient's vasculature in preparation forsheath134. As seen in FIG. 9B, the introducer assembly is advanced to the point wheretip portion138 of thesheath134 is upstream from the desired site of graft placement. Specifically, thetip portion138 is advanced upstream of one of the tworenal arteries106 and108 located most proximal to the heart. Under fluoro-visualization, aradiopaque marker139 insheath tip portion138 confirms proper placement with respect to the anatomical landmark of the renal arteries.
• Once the sheath has been properly placed, the dilator[0088]140 (FIG. 3) is retracted along the guidewire and then completely removed from within thesheath assembly132 and fromprimary guidewire128. As illustrated in FIG. 9C, once thedilator140 has been removed, the lumen ofsheath134 is available for placement of other catheters. Valve head136 (FIG. 7A) prevents substantial blood loss fromsheath assembly132.
• B. Aortic Graft[0089]
• The aortic graft is designed for introduction into the abdominal aorta with the use of the main loading catheter, which will be described in more detail below. First, the preferred structure of the aortic graft will be described with reference to FIG. 1.[0090]
• As illustrated in FIG. 1, one presently preferred embodiment of the aortic graft is designated generally at[0091]10. Such a bifurcated graft, sometimes referred to as a “trouser graft,” is adapted for insertion transfemorally to the situs of an aortic aneurysm in the region where the iliac arteries branch from the abdominal aorta.
• The[0092]aortic graft10 includes aproximal trunk portion12 and is bifurcated to define two proximal legs, acontralateral leg14 and anipsilateral leg16. In this preferred embodiment, theipsilateral leg16 extends longer than thecontralateral leg14 to facilitate loading of both legs into a smaller diameter loader when self expanding wireforms are attached to the end of each leg. The length difference between the two legs corresponds to the height of the self-expanding wireform, so that the self-expanding wireforms are not side by side within the loader. This reduces the overall bulk of the graft and permits loading into a smaller diameter loader. One of skill in the art will appreciate, however, that the relative lengths of the two graft legs may be adjusted depending on the particular application for which the graft is to be used. This difference in leg lengths also aids in orientation of the bifurcated graft under fluoroscopy.
• The[0093]aortic graft10 is configured from a flexibletubular structure18 which is reinforced by wireforms20 extending circumferentially around or woven into thetubular structure18. The flexibletubular structure18 is foldable, and thewireforms20 are radially compressible and expandable. Thus, the graft is configured to move between an insertion diameter, in which state the graft may be inserted intraluminally into the aorta, and a larger, expanded diameter (illustrated in FIG. 1) in which state the graft may be secured within the aorta.
• In the expanded state illustrated in FIG. 1, the[0094]trunk portion12 is generally cylindrical and has atrunk diameter22 corresponding generally to the diameter of an average aorta. In this preferred embodiment, thetrunk portion12 may be configured to be a variety of sizes, one of which is selected according to the size of the abdominal aorta of the patient into which the graft is to be implanted. It is presently preferred to make grafts in which the trunk portion is sized to an expansion diameter of 19, 21, 23, 25, 27, and 29 mm. These sizes, of course, are not limiting of the sizes which may be utilized in accordance with the teachings of the present invention
• As can readily be seen upon inspection of the graft of FIG. 1, the[0095]trunk portion12 defines a cylindrical tube through which fluid may flow. At aseptum region28, the graft bifurcates into the twoleg portions14,16. The cylindrical tubes defined by the two leg portions are in fluid communication with thetrunk portion12, thereby approximating the internal configuration of the bifurcated junction of the aortic artery. Thelegs14,16 are cylindrical and have diameters which, in their expanded state, correspond to a fixed diameter to insure a constant interface between the legs and the upstream end of the extension grafts which will be described later. In this embodiment, thecontralateral leg14 and theipsilateral leg16 have expanded diameters of 13 mm. Again, the magnitude of the expanded diameter of thelegs14,16 may be varied according to the desired interface between the legs and the extension grafts. However the diameter of the legs is not dependent on the diameter of the trunk region. In prior art bifurcated woven grafts, the leg diameter is one half the diameter of the trunk. For example, a 26 mm trunk would always bifurcate into two 13 mm legs, a 28 mm graft would bifurcate into two 14 mm legs, a 24 mm graft would bifurcate into two 12 mm legs, etc. This is a function of how bifurcated grafts are typically woven.
• In the present invention, as shown in FIGS. 2B and 2D, the lower portion of the trunk region can be tapered either out (see FIG. 2B) or in (see FIG. 2D) to insure a constant diameter of the legs regardless of the trunk diameter. For example, as shown in FIG. 2D, a 28 mm trunk would taper down to 26 mm in its lower region prior to being bifurcated into two 13 mm legs. Similarly, as shown in FIG. 2B, a 24 mm trunk would taper out to 26 mm prior to being bifurcated into two 13 mm legs. This provides for a standard leg diameter regardless of the trunk diameter and insures a constant interface and interlock between the bifurcated graft and the extension grafts (see FIGS. 2E through 2G) regardless of the relative diameters of the trunk and the downstream ends of the extension grafts.[0096]
• An alternative embodiment of this invention would be to maintain a straight trunk through the bifurcation region and then taper the legs either out or in to maintain a constant downstream diameter.[0097]
• The flexible[0098]tubular structure18 is preferably made of a tube of woven polyester fabric. Although polyester is presently preferred, other materials may be utilized for the flexibletubular structure18. Such materials include but are not limited to expanded polytetrafluoroethylene (ePTFE), coated polyester, porous polyurethane, silicone, and spun or woven polymeric fibers. One of skill in the art of biocompatible grafts will readily identify other materials suitable for application in the construction of the flexibletubular structure18. It is preferred that the tubular structure be made of a material which is porous, thereby allowing tissue ingrowth into the graft material and/or formation of an intimal layer, although for some applications it may be desirable to make the tubular structure of a fluid impervious material.
• Preferably, the fabric is woven into the tubular configuration, thereby eliminating seams or other internal protrusions which could interfere with blood flow or form locations for thrombi to occur. By employing a flexible fabric for the[0099]tubular structure18, the fabric will readily fold to accommodate radial contraction of the graft, such as is necessary for intraluminal introduction of the graft.
• In a preferred embodiment of the present invention, the fabric tubing of the graft and the wireforms therein can be over-sized with respect to the first balloon used to expand the balloon-expandable wireforms. Due to the fact that there is a small amount of recoil that occurs in the balloon-expandable wireforms after expansion, it may be desirable to re-expand these wireforms to more accurately retain the graft within the vessel. If the fabric tubing of the graft and the wireforms have a diameter which is larger than the post-recoil diameter of the wireforms after their first expansion, the physician can use a second, larger balloon to re-expand or over-expand the balloon-expandable wireforms such that upon recoil of the wireforms their diameters are of the proper size for optimum retention of the graft within the vessel.[0100]
• This feature enables a surgeon to optimize the fit of a graft within a vessel without having to remove it and replace it with another. That is, a graft which upon first balloon-expansion may not sufficiently engage with the wall of the vessel, may be subsequently over-expanded to optimize the fit therein. For example, the fabric tubing of the graft may have a diameter of 24 mm, while the balloon-expandable wireforms have a diameter of 24 mm. The graft is first inflated to 23 mm and the wireforms will recoil to 22 mm. If the physician chooses to further expand the wireforms and more optimally retain the graft in the vessel, the physician will bring in a larger balloon which inflates to 25 mm. After recoil, the final wireform diameter will be 24 mm and the graft will be in its fully opened state.[0101]
• In accordance with a presently preferred embodiment of the invention, a number of[0102]wireforms20 are provided to furnish structural rigidity to the graft and to secure the graft within the body lumen. As illustrated in FIG. 1,aortic graft10 includes two different types of wireforms: balloon-expandable wireforms30 and self-expandingwireforms32. This preferred embodiment includes three balloon expandable wireforms34,36, and38, which are woven into the fabric but positioned primarily on the interior of the fabric in thetrunk region12 and a single balloon-expandable wireform40 positioned on the exterior of the fabric at the distal end of thetrunk region12. A self-expandingwireform42 is attached to the outside of the fabric at theseptum region28 with a self-expandingwireform44 positioned on the distal end of thecontralateral leg14 and another self-expandingwireform46 at the distal end of theipsilateral leg16.
• The balloon-[0103]expandable wireforms30 of the present invention are preferably made of an alloy of carbon, silicon, phosphorus, sulphur, chromium, nickel, beryllium, cobalt, iron, manganese and molybdenum which is sold under the ELGILOY trade name by Elgiloy, L. P. of Elgin, Ill., U.S.A. Other materials which may be utilized in making thewireforms30 include a nickel and titanium alloy sold under the NITINOL trade name, stainless steel, and other biocompatible, implantable metals. The wires used in manufacturing the balloon-expandable wireforms30 of the present invention are preferably about 0.012 inches in diameter.
• Preferably, each of the balloon-[0104]expandable wireforms30 is similarly configured with a curvilinear geometry such as the closed sinusoidal-like wave geometry illustrated in FIG. 1, with alternatingcrests50 andvalleys52 which define an amplitude54. The amplitude54 of a wireform is thus defined as the longitudinal distance between acrest50 and anadjacent valley52. In this preferred embodiment, the amplitude54 of theproximal wireform34 in its expanded state is approximately 0.103 inches.
• The balloon-[0105]expandable wireforms30 are preferably configured with a plurality ofintermediate segments56 which are connected by correspondingcrests50 andvalleys52. Thecrests50 andvalleys52 are formed with a radius which, in this preferred embodiment, is about 0.025 inches.
• Preferably, the intermediate segments are positioned at an angle with respect to each other of greater than about 90 degrees in order to provide greater wireform rigidity, reduced wireform recoil and increased anchoring force. To those ends the intermediate segments are more preferably positioned at an angle with respect to each other from a range of about 100 degrees to about 135 degrees. Most preferably, the intermediate segments are positioned at an angle with respect to each other from a range of about 120 degrees to about 125 degrees.[0106]
• For example, in the most preferred embodiment, the[0107]crests50 andvalleys52 of the balloon-expandable wireforms30 are configured by obtaining annealed ELGILOY wire having a diameter of preferably about 0.012 inches and wrapping the wire around a pin having a diameter of 0.050 inches, thereby defining a plurality of adjacent,intermediate segments56 positioned at an angle with respect to each other of from about 120 to 125 degrees. Thus, the amplitude of theintermediate segments56 of theproximal wireform34 in its expanded state (i.e., excluding the radius which defines the crests and valleys) is about 0.103 inches. In this presently preferred embodiment, each balloon-expandable wireform40 has eight crests50.
• An alternative method for constructing the balloon-[0108]expandable wireforms30 is to configure the wireforms in a true sinusoidal-like pattern. By constructing thewireforms30 according to this alternative method, the angle between adjacent intermediate portions is about 120 to 125 degrees, thereby maintaining the number of crests on the wireform to eight. Alternatively, the balloon-expandable wireforms are configured such that they are continuously curvilinear as illustrated by FIG. 1B. This continuouslycurvilinear shape48 primarily serves to reduce stress on the wireforms when the aortic graft is in its first, compressed state. One of skill in the art will be familiar with other methods for manufacturing balloon-expandable wireforms without departing from the teachings of the present invention.
• Because the wire has been annealed, it will readily plastically deform to maintain its configuration. Thus, the wireform may be plastically deformed between the radially collapsed position and the radially expanded position of FIG. 1. The wireforms are, therefore, not resilient to any substantial extent, requiring them to be physically expanded into contact with the internal wall of the aorta via a force other than their own resilience. Further, there is some amount of recoil after balloon-expansion of the wireforms, which will be discussed in more detail below.[0109]
• The balloon-[0110]expandable wireforms34,36, and38 which are positioned along the proximal portion of thetrunk12 of the graft are preferably secured to the fabric graft material by weaving the wireform through the fabric material. The wire is woven through the fabric such that the distal tip of the valley of each wireform extends through the graft and is positioned on the outside of thefabric structure18. The weaving is accomplished by initially configuring an elongated piece of wire into the predetermined curvilinear configuration. With the wire so configured, it may be manually woven through thefabric structure18 until the wire extends around the entire circumference of thefabric structure18. The wire is woven such that it is primarily positioned along the interior of the fabric tube, with only small segments of wire exposed to the outside of the tube.
• The wireform is woven into the fabric tube such that when the wire extends around the entire periphery of the fabric tube, the free ends of the wire protrude from the tube at positions adjacent to each other, thereby enabling a[0111]tail segment62 to be defined by the free ends. The loose ends are preferably held together with a crimping sleeve64 positioned over them. After crimping the sleeve to secure the ends to each other and thereby complete the circular configuration of the wireform, any portion of the wires extending beyond the ends of the sleeve may be trimmed to cleanly finish thetail segment62. It is preferable that no portion of the wire extend beyond the edge of the crimping sleeve to eliminate the possibility of the wire cutting or piercing the lumen wall.
• As illustrated in FIG. 1, the tail segments are positioned on the outside of the[0112]fabric layer18 and extend below the longitudinal position of theother valleys52 of the wireform. Thus, the mostproximal wireform34 of FIG. 1 includes atail segment62 extending in the distal direction below the level ofadjacent valleys52. Although this configuration is preferred, one of skill in the art will appreciate that thewireforms30 may be formed in two parts with two tails positioned on opposite sides of the graft.
• The[0113]tail segments62 of the balloon-expandable wireforms30 are preferably configured to extend substantially flat against thefabric layer18, i.e., substantially parallel to the longitudinal axis60 of the graft. With the tail segments so configured, the risk that the tail segments will penetrate or damage the wall of a lumen with which it comes into contact will be substantially reduced.
• The[0114]proximal wireform34 is positioned with respect to the upper edge of the fabric layer such that approximately one-third of the wireform extends beyond the edge of the fabric layer. The wireform is positioned to extend above the edge of the fabric layer to prevent any portion of the fabric layer from oscillating, or “flapping,” in response to the flow of blood past the edge of the graft. As an additional measure to prevent such fabric oscillation in the blood stream, the edge of the fabric is configured with V-shaped notches corresponding generally to thevalleys52 of theproximal wireform34. Thus, the risk of the existence of any loose fabric which could potentially be affected by the passing flow of blood is substantially reduced.
• In an alternate embodiment of the present invention, the proximal-most balloon-expandable wireform is preferably configured to have a diameter in its expanded state which is slightly larger than that of the portion of the fabric tubular structure into which it is weaved. Thus, in the illustrated embodiment in which the proximal opening of the fabric portion of the graft has a diameter of 22 mm, the[0115]proximal wireform34 is configured with a diameter of 24 mm. By configuring the wireform to be slightly larger than the fabric into which it is woven, the fabric will be maintained in a constant state of slight tension upon expansion of the wireform, thereby reducing the possibility of the fabric folding or oscillating in response to blood flow through the graft.
• Wireforms[0116]36,38 are positioned adjacent theproximal wireform34 and are spaced apart from each other such that the wireforms do not interfere with each other in either a radially expanded or contracted state. Thus, for example, in a preferred embodiment the valleys ofwireform34 are located proximal of the crests ofwireform36. Thewireforms34,36,38 are also aligned “in phase,” with peaks along one longitudinal line and adjacent valleys aligned along a second longitudinal line, thereby further reducing the possibility of overlap of adjacent wireforms. (While there may be some overlapping of thetail segments62 with an adjacent wireform, because the tail segments extend on the outside of the fabric layer and the adjacent wireform is primarily on the inside of the fabric layer, a small degree of overlap with an adjacent wireform does not pose a problem.)
• In addition, adjacent balloon-expandable wireforms are not connected to one another. This coupled with the in-phase configuration of the wireforms maximizes flexibility of the aortic graft without permitting deleterious kinking, which is of primary importance in the often tortuous paths of the abdominal aorta and iliac arteries.[0117]
• The proximal three[0118]wireforms34,36,38 are preferably positioned as close to each other as possible without overlapping. In this embodiment, thewireforms34,36,38 are positioned along the length of the graft about every 4.0 mm. By minimizing the space between the proximal threewireforms34,36,38, the force exerted against the wall of the body lumen is enhanced. Thus, to the extent that the lumen surrounding these three wireforms is healthy and not expanded due to the aneurysm, thewireforms34,36,38 will all assist in achieving a frictional interface with the proximal end of the graft in the lumen.
• The distal balloon-[0119]expandable wireform40 is configured similarly to the other balloon-expandable wireforms34,36, and38 in that all are generally circular in cross section.
• The distal balloon-[0120]expandable wireform40 is attached to thefabric structure18 in a different manner from the other balloon-expandable wireforms. Instead of being woven into thefabric structure18,distal wireform40 is attached to the fabric by tying it to the fabric with polyester thread. Other biocompatible threads may also be employed for securing thedistal wireform40 to thefabric tubular structure18. In this preferred embodiment, eachcrest50 ofdistal wireform40 is secured to the fabric. Eachintermediate segment56 ofdistal wireform40 is also preferably tied to the fabric at a point approximately midway between thecrest50 and anadjacent valley52. Although in this preferred embodiment,wireform40 is tied to the fabric structure with a thread, one of skill in the art will readily identify other attachment methods. Adhesives, for example, may be successfully employed in accordance with the teachings of the present invention.
• [0121]Distal wireform40 is preferably positioned in thetransition region66 to aid in keeping the graft open. In this preferred embodiment, thedistal wireform40 is located approximately 15 mm below the proximallyadjacent wireform38. By positioning thedistal wireform40 in thetransition region66, it will generally be located within the aneurysmic sack when the graft is properly implanted within the lumen of a patient. Consequently, thedistal wireform40 will not engage the wall of the lumen and serves only to provide structural rigidity to maintain the graft open at thetransition region66. Thus, it is preferable that thedistal wireform40 be positioned along the outside of the fabric structure whereas the other balloon-expandable wireforms are primarily located inside of the fabric structure. With thewireform40 on the outside of the fabric structure, the wireform does not interfere with blood flow through the graft. In addition, it can not be inadvertently snagged from the inside as modular components are introduced into the lumen of the bifurcated graft.
• In addition to the balloon-[0122]expandable wireforms30 discussed above, thegraft10 of the present invention also includes a number of self-expandingwireforms32. The configuration of each of the self-expandingwireforms32 is naturally biased towards an expanded state, such as that illustrated in FIG. 1. The self-expandingwireforms32 may be made of the same base material used in the construction of the balloon-expandable wireforms30, although the method of manufacturing may differ. Thus, ELGILOY wire is preferred, with a number of other materials acceptable for such use.
• As illustrated in FIG. 1, the self-expanding[0123]wireforms32 employed in thegraft10 of the present invention have a generally curvilinear configuration having loops which define crests70 andvalleys72. Further, theintermediate sections74 are not straight, but have an “S” shape along their length.
• The self-expanding[0124]wireforms32 are constructed by obtaining cold worked ELGILOY wire having a diameter of preferably about 0.012 inches and wrapping it around acylindrical form78, such as that illustrated in FIG. 1A, havingprimary pins80 positioned to form the loops which define thecrests70 andvalleys72 of the wireform. Twosecondary pins82 are positioned adjacent eachprimary pin80 to aid in defining the loops and configuring the “S” shape in theintermediate region74 of the wireform.
• The wireform is thus positioned about the entire circumference of the[0125]form78 and the ends may be fitted with a crimping sleeve while positioned in an overlapping configuration. With the wireform thus configured on theform78, the wireform and form are placed in an oven heated to about 500 degrees centigrade for about 3.5 to about 5.0 hours. By thus heat treating the self-expandingwireform32, the wireform will develop a memory corresponding to the shape in which it is positioned on the form. Thus, the wireform may be elastically deformed, such as by radially compressing the wireform for intraluminal insertion into a patient, and, when released, will resiliently return to the shape it had during the heat treatment.
• As an alternative method for constructing the self-expanding[0126]wireforms32 of the present invention, a form comprising a flat surface (not illustrated) with a similar pin configuration may be utilized. After heat treating the wireform, the ends of the wireform may be attached, thereby forming the wireform into its cylindrical configuration, according to any of those methods described above.
• As the self-expanding wireforms resiliently move between their expanded and contracted positions, tension is applied to the outer portion of the resulting wireform loop and a corresponding compression results on the inner portion of the wireform loop. Thus, the[0127]pins80,82 of theform78 are selected to have a radius such that the resulting tension and compression on the loop stay below the yield point of the wire. It has been found that for the preferred embodiment of the self-expandingwireforms32 illustrated in FIG. 1, a pin diameter of about 0.070 inches is satisfactory and presently preferred.
• The self-expanding[0128]wireforms32 are advantageously configured such that theintermediate regions74 of the wireforms are in an “S” shape. As the wireform moves between its expanded and contracted positions, the elastic deformation which occurs to accommodate such movement is spread substantially evenly throughout the entire length of the wireform. Consequently, the entire length of the wireform acts as a spring to help restore the wireform to its original configuration after radial compression. Thus, the elastic deformation is not concentrated solely in the loops defining the crests and valleys of the wireform, but is also absorbed by the intermediate segments. This reduces the potential for exceeding the yield point of the wire at the crest and valleys of the wireform, which would cause plastic deformation and prevent the wireform from functioning as intended.
• With the self-expanding[0129]wireforms32 formed according to one of the methods described above, they may be attached to thefabric tubular structure18 of thegraft10. Attachment of the self-expandingwireforms32 is preferably accomplished by tying thecrests70 andvalleys72 to the fabric, as illustrated in FIG. 1. It is presently preferred that each crest and valley be tied in five separate locations around the perimeter of the loop defining the respective crest or valley.
• The self-expanding[0130]wireforms32 are designed to have an initial expanded diameter which is slightly larger than the diameter of that portion of the graft where they are to be positioned. It is presently preferred that the wireform be about 2.0 mm larger in diameter than the cross section of fabric to which it is attached. By configuring the wireform with such a relative diameter, the self-expandingwireforms32, when fully expanded, maintain the fabric structure to which they are attached in a state of slight tension, thereby ensuring that the fabric structure (defining the artificial lumen) is fully open.
• Further, the distal self-expandable wireforms exert a radially inward force against the balloon-expandable portions of the graft extensions engaged therewith, as will be described in more detail below with respect to the discussion of placement of the graft extensions.[0131]
• When designing the wireform, it must also be recognized that the wireform will lose about five percent of its recoil ability after being radially compressed into its state of reduced diameter and subsequently expanded. Thus, for a wireform which is to be positioned at the distal end of either the 13 mm diameter[0132]contralateral leg14 oripsilateral leg16, the wireform will initially be designed to have a diameter of about 15.7 mm. After the wireform has been radially compressed and subsequently expanded in a body lumen, it will expand to a diameter of about 14.5 mm—slightly larger than the 13 mm fabric lumen provided at the leg, as desired.
• The most proximal self-expanding[0133]wireform42 is positioned at theseptum region28 of the graft.Wireform42 thus acts to maintain theseptum region28 of the graft open as blood flows through the graft. In this preferred embodiment, the proximal self-expandingwireform42 is located about 6 to 10 mm distal of the adjacent balloon-expandable wireform40.
• As illustrated in FIG. 1, at the[0134]septum region28 of the aortic graft, the ends of self-expandingseptum wireform42 are secured in crimping sleeves84,85. These crimping sleeves are of an outer diameter such that they provide a second function as radiopaque markers. It has been found that for the preferred embodiment of the crimps84,85 illustrated in FIG. 1, an outer diameter of at least 0.036 inches is satisfactory and presently preferred. The configuration of these crimping sleeves aids in proper orientation of the aortic graft and confirmation of the location of the septum within the abdominal aorta. Thewireform44 oncontralateral leg14 andwireform46 onipsilateral leg16, similarly include crimpingsleeve86.
• Each of the self-expanding[0135]wireforms32 is positioned exteriorly of thefabric tubular structure18, thereby avoiding interference with blood flow within the graft, and preventing the wireforms from being inadvertently snagged from the inside as modular components are introduced into the lumen of the bifurcated graft. Additionally, the attachment of graft extensions tocontralateral leg14 and ipsilateral leg16 (explained below) is facilitated by having the wireform positioned on the outside portion of the fabric leg.
• The[0136]graft10 is further configured with laterally extendingreinforcement wires90, disposed on eachleg14,16. Thewires90 are preferably made of the same base material as the wireforms. Thewires90 are positioned on eachleg14,16 and extend generally from avalley72 onwireform42 to acorresponding crest70 on a respective one ofwireforms44 and46. As illustrated in FIG. 1, thereinforcement wires90 are tied onto thefabric structure18 in a similar manner as are wireforms32, taking care that thewire90 does not longitudinally cross into any of the wireforms. Thereinforcement wire90 keeps the legs of the wireform from folding or buckling.
• These two[0137]longitudinal wireforms90 are also provided withradiopaque crimps91 which assist in the placement of the extension grafts withinlegs14 and16.
• C. Main Catheter Assembly[0138]
• The main catheter assembly is utilized to place the aortic graft described above, which is compressed and loaded onto the distal end of the main catheter assembly as will be described in more detail below. A main catheter assembly useful in the practice of the present invention is described in co-pending U.S. patent application Ser. No. 08/713,070 filed on Sep. 12, 1996, previously incorporated herein by reference hereinabove (the '070 application).[0139]
• The[0140]sheath assembly132 is utilized to facilitate the operative placement of the main catheter assembly. As such, the main catheter assembly is sized such that it will fit inside theintroducer sheath134.
• The primary components of the[0141]main catheter assembly180 may be observed by reference to FIGS. 4 and 6. The catheter assembly of the present invention comprises arigid loader200 which is used to facilitate the operative coupling of the catheter assembly to the introducer assembly during use of the present endovascular delivery system, as will be described in more detail with reference to FIGS. 9B and 9C. The loader comprises anelongate tube202 including a lumen, a proximal end, and a distal end which is defined by a reduced diameter distal section. An internally threadedconnector nut204 is attached to the distal portion of the elongate tube.
• The catheter assembly is cooperatively engaged and secured to the head of the introducer sheath assembly by initially inserting the distal section of the loader into the valve head of the sheath assembly subsequent to the removal of the dilator from therewithin. FIG. 7A illustrates insertion of the main catheter assembly into the valve head of the sheath assembly. More particularly, the distal section of the[0142]loader200 is extended into the threadedconnector144 of thevalve head136 with the connector nut being threadably engaged to the externally threaded proximal portion of the threadedconnector144. FIG. 7B illustrates theconnector nut204 connected to thevalve head136 of thesheath assembly132.
• The loader and corresponding receiving portion of the valve head are preferably formed of rigid material such that the loader will seat correctly within the interfacing portion of the valve head without flexing or distortion thereof. This ensures proper positioning and registry of the loader and the valve head relative to each other. Furthermore, the ability of the loader to be positively engaged, that is, locked by threadable engagement of the nut to the valve head of the introducer assembly, also facilitates and maintains proper registry and positioning of the loader relative to the introducer assembly.[0143]
• The catheter assembly of the present invention further includes a proximal connector assembly[0144]206 (FIGS. 4 and 6). The proximal connector assembly includes apusher connector182, which is preferably a Y-connector. Theproximal connector assembly206 further includes atubular body210 having a lumen extending longitudinally therethrough that is ultimately in fluid communication with the interior of theballoon194. Atubular side arm214, which communicates with the lumen of the tubular body, is connected to the tubular body and extends angularly therefrom. Astopcock218 on the end of thetubular side arm214 permits valving of the balloon inflation lumen. The proximal connector additionally comprises a Y-connector208 and acontrast connector212.
• The[0145]main catheter assembly180 further comprises an elongate,tubular pusher body184. Thepusher body184 includes adistal end186, aproximal end188, and a lumen extending longitudinally therethrough. The outer diameter of the distal section slightly exceeds that of the remainder of the pusher body. Theproximal end188 is operatively connected to thepusher connector182, which along with the pusher body, will expel the loaded aortic graft to leave it in place within the aorta as will be described in more detail below with respect to the preferred method of the present invention.
• The main catheter assembly of the present invention further comprises an elongate catheter with a coaxial tube construction. As illustrated in FIG. 6, the elongate coaxial tube catheter comprises an elongate[0146]outer tube190 and an elongateinner tube192. The outer catheter defines a distal end, a proximal end, and hollow lumen extending longitudinally therethrough. The inner tube is smaller in diameter than the outer tube and extends through the lumen thereof. The inner tube defines a distal end, a proximal end, and hollow lumen extending longitudinally therethrough. The inner tube is slidably extensible distally and retractable proximally relative to the outer tube.
• The main catheter assembly further comprises an elongate,[0147]inflatable catheter balloon194, illustrated in its inflated configuration in FIG. 6. This inflatable balloon serves to expand the balloon-expandable reinforcement wires of the aortic graft. When fully inflated, the balloon of the catheter assembly has a generally uniform, cylindrical configuration.
• The balloon includes a distal end which is attached to a[0148]tubular sleeve portion196 of theinner tube192, and a proximal end which is attached to theouter tube190. In turn, the extension of the inner tube distally relative to the outer tube facilitates the longitudinal stretching of the balloon. The catheter also includes aspacer clip198 which allows the balloon to be extended or lengthened after deflation thereof to facilitate withdrawal of the balloon and catheter from the expanded aortic graft. The inner tube is initially oriented in a first retracted position relative to the outer tube. The balloon is inflated only when the inner tube is in its retracted orientation.
• Subsequent to being deflated, the balloon is preferably stretched longitudinally by the distal advancement of the inner tube of the catheter relative to the outer tube thereof. More particularly, the inner tube is moved from its first, retracted position to its second extended position. The movement of the inner tube from its retracted position to its extended position to stretch the balloon is facilitated by tightly grasping the balloon and contrast connectors of the proximal connector assembly, and subsequently pushing the contrast connector distally toward the balloon connector. Since the outer tube is rigidly attached to the balloon connector and the inner tube is rigidly attached to the contrast connector via the sheath, movement of the contrast connector toward the balloon connector results in a slideable advancement of the inner tube distally within the outer tube. As a result, the attachment of the spacer clip to the exposed portion of the sheath prevents the contrast connector from being moved distally toward the balloon connector. While the spacer clip is in its operative position upon the sheath, the balloon cannot be longitudinally stretched in that the inner tube is prevented from moving from its first, retracted position to its second, extended position. Once the spacer clip is detached from the sheath, the balloon and contrast connectors are no longer maintained in spaced relation to each other so that the contrast connector can be pushed distally toward the balloon connector, thereby facilitating the distal advancement of the inner tube to its extended position and the resultant stretching of the deflated balloon.[0149]
• The downstream end of the graft ipsilateral leg is trapped between the distal section of the pusher body and the balloon catheter shaft. This facilitates reorientation of the graft during deployment, if desired.[0150]
• D. Main Graft Deployment[0151]
• The method for using the main catheter assembly following the withdrawal of the dilator from within the sheath assembly will now be described. Initially, with reference to FIG. 10A, the[0152]main catheter assembly180 is inserted over theprimary guidewire128 and into thesheath assembly132. Thedistal connector nut204 is connected to the threaded sleeve portion of thevalve head136.
• With reference to FIGS. 10A and 10B, the main catheter is then advanced over the[0153]guidewire128 and within thesheath134 such that the distal-most portion extends from thesheath tip portion138, and above therenal arteries106,108. To accomplish this, the pusher body184 (FIG. 4) is distally advanced through the lumen of theintroducer sheath134 until such time as thecollapsed graft10 protrudes from the distal end of thesheath138. More specifically, as seen in FIG. 10B, the distal end194aofballoon194 and theinner catheter192 protrude from thesheath134. The precise positioning of the main catheter in this manner is facilitated by observing under fluoroscopy the relative positions of a contrast marker associated with the balloon distal end194aand theradiopaque marker139 insheath tip portion138. The tworadiopaque markers139,194aare brought together, with the combination being relatively located with respect to the renal arteries.
• The position of the[0154]sheath134 across theaneurysm114 permits the shielded introduction of the main catheter withballoon194 andgraft10 thereon into the proper implantation position. In other words, the surroundingsheath134 shields the advancing catheter and the otherwise expanded and irregularly shapedgraft10 from blood flow resistance. Moreover, thesheath134 protects the graft assembly from contacting the vessel walls to prevent potential snags. In short, the initial positioning of the sheath upstream of the location at which the graft will be finally implanted ensures that, the expanded graft will only have to be displaced downstream into its final location, which is in the direction of blood flow and thus this operation is substantially easier to effectuate and is also less prone to inflict damage on the vessel walls.
• Once the[0155]graft10, still within thesheath134, is positioned upstream from its final location the sheath is removed. FIGS. 10C and 10D illustrate this operation. To accomplish this, the pusher body184 (FIG. 4) is held stationary as thesheath134 is withdrawn from the main catheter to a position just downstream from thegraft10. Desirably, as seen in FIG. 10D, thesheath134 is withdrawn so that thetip portion138 is just downstream from the longer of thecontralateral leg14 oripsalateral leg16. In the case of anenlarged aneurysm114 as shown, thetip portion138 will still be within the aneurysm. As the introducer sheath assembly is withdrawn, the self-expandingwireforms42,44, &46 (FIG. 1) in the aortic graft expand within the aneurysm sack, while the balloon-expandable wireforms30 maintain a substantially compressed configuration.
• A final step of positioning of the[0156]graft10 may be required. That is, removal of thesheath134 from over thegraft10, as seen in FIG. 10C, may leave the distal end of the graft (and distal end of balloon194a) upstream of therenal arteries106,108. (In some instances, removal of thesheath134 will, by friction, pull the main catheter andgraft10 along with it, though the surgeon is instructed to maintain the catheter position with thepusher body184. In this respect, the initial positioning of the distal end of the entire assembly upstream of the renal arteries is intended to provide some margin for downstream movement of the catheter). If the contrast marker at the balloon distal end194aremains upstream of or adjacent to therenal arteries106,108, the main catheter is then withdrawn further downstream to reposition the balloon distal end just downstream of the renal arteries. This final position is seen in FIG. 10D. Theinflation balloon194 can be seen in outline inside of theaortic graft10. The final displacement of the expandedgraft10 downstream is with the blood flow and thus does not require much force.
• As seen in FIG. 10D, the[0157]graft10 is sized such that the distal end (as carried on the catheter) thereof protrudes beyond the upstream boundary of the aortic aneurysm and into unaffected region of theabdominal aorta100. Locating the distal end of thegraft10 just below (downstream from) therenal arteries106,108 ensures the maximum length of contact between the eventually expandedgraft10 and the unaffected abdominal aortic wall. Thecontralateral leg14 andipsalateral leg16 of thegraft10 extend into theaneurysm114, and, as will be detailed below, extensions thereto are used to continue their respective lumens at least to the unaffected regions of theiliac arteries102,104.
• As seen in FIGS. 11A and 11B, the[0158]balloon194 is then inflated via the balloon connector. The inflation/pressurization of the balloon causes radial expansion of thetrunk portion12 of thegraft10 from its initial, collapsed orientation, to its second, expanded orientation. Due to the configuration of the balloon when fully inflated, the radial expansion of thetrunk portion12 to its second, expanded orientation is uniform. In this respect, the expansion forces applied to the opposed ends of thetrunk portion12 by the balloon are equal to those applied to the remainder thereof. This uniform application of expansion forces to thetrunk portion12 facilitates the tight engagement of the opposed ends thereof to the luminal surface of the aorta. Preferably, the balloon is inflated for 30 seconds to a pressure of about 2 atmospheres. FIG. 11A, for example, illustratesinflated balloon194 within the expanded aortic graft10 (in outline). Further, as illustrated in more detail in FIG. 11B,balloon194 may be slightly over-sized (represented by the arrows pointing outwardly from the balloon) to forceaortic graft10 into optimal engagement with the aortic wall, especially given the tendency of the wireforms to recoil inwardly slightly after expansion. When the graft is fully expanded, the opposed ends thereof frictionally engage the luminal surfaces of unaffected regions of the aorta.
• After the graft has been radially expanded in the aforementioned manner the balloon is deflated and removed from within the[0159]sheath134. As illustrated in FIG. 12A, theballoon194 is deflated and thestopcock218 is left open to room air to equalize negative pressure. When theballoon194 is deflated it may not return to its initial, uninflated orientation due to rigidity of the balloon material. Rather, the diameter of the main body portion of the deflated balloon may remain substantially the same as when the balloon is fully inflated, or may otherwise continue to protrude in a manner that could complicate subsequent retraction and removal of the delivery catheter.
• To prevent the deflated[0160]balloon194 from inadvertently catching on or interfering with the radially expandedgraft10 during the withdrawal of the balloon from within, the balloon is longitudinally stretched prior to the withdrawal of the main catheter from within the graft as seen in FIG. 12B. As previously explained, such stretching of the deflated balloon is accomplished by distally advancing theinner tube192 of the main catheter relative to theouter tube190 thereof. Such movement of the inner tube is facilitated by tightly grasping the balloon and contrast connectors of the proximal connector assembly with the spacer clip removed, and subsequently pushing the contrast connector distally toward the balloon connector, which pushes the distal end of the balloon in the direction indicated by thearrow216 in FIG. 12B. A vacuum may be pulled throughstopcock218 to completely deflate theballoon194.
• The main catheter with the now deflated and stretched[0161]balloon194 is then withdrawn slowly and carefully from the aortic graft and into the introducer sheath as illustrated in FIG. 12C. Once the main catheter assembly has been proximally retracted into theintroducer sheath134, it is withdrawn from within the patient's body as indicated byarrow217. Theaortic graft10 remains in place within the abdominal aorta with theintroducer sheath134 still in position just downstream thereof, and theprimary guidewire128 extending therethrough. It should be noted that the blood flow down theabdominal artery100 now flows completely through thegraft10; that is, through thetrunk12 and twolegs14 and16. Attachment of the extensions inside the legs must adapt to this flow, as will be described below.
• E. Extension Grafts[0162]
• As previously described hereinabove, the downstream end of the[0163]aortic graft10 is bifurcated with aseptum region28 separating theipsilateral leg16 from thecontralateral leg14. Two additional graft portions are adapted to extend into the respective iliac arteries and to form a frictional engagement with the ipsilateral and contralateral legs of the aortic graft.
• These extension grafts typically comprise straight or tapered cylindrical tubes, with an upstream end having a common diameter, while the diameter of the downstream ends can vary depending on the anatomy of the patient (see FIGS. 2E through G). The upstream ends interlock with the respective downstream portions of the aortic graft. By fixing the diameter of the upstream ends of the extension graft and the downstream ends of the bifurcated aortic graft as shown in FIGS. 2B through 2G, a consistent interface and interlock can be achieved regardless of the patients anatomy. The diameter of the downstream end of the graft extensions can be provided in varying diameters so as to suit the diameter of the iliac artery into which graft portions are being implanted. The change in diameter can be provided by a short step-down portion as shown in FIG. 2G, or a step-up portion, as shown in FIG. 2E, or by a region of taper extending along a length of the graft portion.[0164]
• Turning now to FIG. 2, one preferred embodiment of a[0165]graft extension170 is depicted. The graft extension comprises anupstream portion172, adownstream portion174, and a lumen running the length thereof.
• In a preferred embodiment the[0166]graft extension170 is configured from aflexible tubular175 structure which is reinforced bywireforms176 extending circumferentially around the tubular structure. The flexible tubular structure is foldable and the wireforms are radially compressible and expandable. Thus, the extension graft is configured to move between an insertion diameter, in which state the graft may be inserted through a femoral and iliac artery and into one of the bifurcated legs of the aortic graft, and a larger, expanded diameter (illustrated in FIG. 2) in which state the graft may be secured within the aortic graft.
• In the expanded state illustrated in FIG. 2, the[0167]extension graft170 is generally cylindrical and may be configured to be a variety of sizes, one of which is selected according to the size of the iliac artery of the patient into which the extension graft is to be implanted.
• The flexible[0168]tubular structure175 is preferably made of a tube of woven polyester fabric. Although polyester is presently preferred, other materials may be utilized for the flexibletubular structure175. Such materials include but are not limited to expanded polytetrafluoroethylene (ePTFE), coated polyester, porous polyurethane, silicone, and spun or woven polymeric fibers. One of skill in the art of biocompatible grafts will readily identify other materials suitable for application in the construction of the flexibletubular structure175. It is preferred that the tubular structure be made of a material which is porous, thereby allowing tissue ingrowth into the graft material and/or formation of an intimal layer, although for some applications it may be desirable to make the tubular structure of a fluid impervious material.
• Preferably, the fabric is woven into the tubular configuration, thereby eliminating seams or other internal protrusions which could interfere with blood flow or form locations for thrombi to occur. By employing a flexible fabric for the tubular structure, the fabric will readily fold to accommodate radial contraction of the graft, such as is necessary for intraluminal introduction of the graft.[0169]
• In one preferred embodiment of the present invention, the diameter of the fabric tubing of the graft is over-sized with respect to the wire-forms therewithin. Upon balloon-expansion of the balloon-expandable wireforms, there is a small amount of recoil that occurs in the wireforms. The fabric tubing of the graft therefore can have a diameter which is larger than the post-recoil diameter of the wireforms. In turn, the wireforms can be over-expanded with a second balloon of a different size such that upon recoil, the diameter of the wireforms is of the proper size for optimum retention of the graft within the vessel. This feature enables a surgeon to optimize the fit of a graft within a vessel without having to remove a too-small graft and replace it with another. That is, a graft which upon first balloon-expansion may not sufficiently engage with wall of vessel, may be subsequently over-expanded by a second balloon of a larger size to optimize the fit therein.[0170]
• In accordance with a presently preferred embodiment of the invention, a number of balloon-[0171]expandable wireforms176 are provided to furnish structural rigidity to the graft and to secure the graft within the body lumen. Each of the balloon-expandable wireforms is similarly configured with a curvilinear geometry such as the closed sinusoidal-like wave geometry illustrated in FIG. 2A, with alternatingcrests150 andvalleys152 which define anamplitude154. Theamplitude154 of a wireform is thus defined as the longitudinal distance between acrest150 and anadjacent valley152.
• Alternatively, the balloon-expandable wireforms are configured such that they are continuously curvilinear, such as the configuration of the wireform illustrated by FIG. 11B. As noted above, this continuously[0172]curvilinear shape48 reduces stress on the wireforms when the graft is in its first, compressed state.
• An alternative method for constructing the balloon-expandable wireforms is to configure the wireforms in a true sinusoidal pattern. One of skill in the art will be familiar with other methods for manufacturing balloon-expandable wireforms without departing from the teachings of the present invention.[0173]
• The balloon-[0174]expandable wireforms176 are preferably configured with a plurality ofintermediate segments156 which are connected by correspondingcrests150 andvalleys152. Thecrests150 andvalleys152 are formed with a radius which, in this preferred embodiment, is about 0.025 inches.
• Preferably, the intermediate segments are positioned at an angle with respect to each other of greater than about[0175]90 degrees in order to provide greater wireform rigidity, reduced wireform recoil, and increased anchoring force. To those ends the intermediate segments are more preferably positioned at an angle with respect to each other from a range of about 100 degrees to about 135 degrees. Most preferably, the intermediate segments are positioned at an angle with respect to each other from a range of about 120 degrees to about 125 degrees.
• The balloon-[0176]expandable wireforms176 of the present invention are preferably made of an alloy of carbon, silicon, phosphorus, sulphur, chromium, nickel, beryllium, cobalt, iron, manganese and molybdenum which is sold under the ELGILOY trade name by Elgiloy, L. P. of Elgin, Ill., U.S.A. Other materials which may be utilized in making the wireforms include a nickel-titanium shape memory alloy sold under the NITINOL trade name, stainless steel, and other biocompatible, implantable metals. The wires used in manufacturing the balloon-expandable wireforms of the present invention are preferably about 0.012 inches in diameter.
• Because the wire has been annealed, it will readily plastically deform to maintain its configuration. Thus, the wireform may be plastically deformed between the radially collapsed position and the radially expanded position of FIG. 2. The wireforms are, therefore, not resilient to any substantial extent, requiring them to be physically expanded into contact with the internal wall of the iliac artery and downstream legs of the aortic graft via an external force rather than expanding by virtue of their own resilience.[0177]
• The balloon-expandable wireforms which are positioned along the graft extension are preferably secured to the fabric graft material by weaving the wireform through the fabric material. The wire is weaved through the fabric such that the distal tip of the valley of each wireform extends through the graft and is positioned on the outside of the fabric structure. The weaving is accomplished by initially configuring an elongated piece of wire into the predetermined curvilinear configuration. With the wire so configured, it may be manually woven through the fabric structure until the wire extends around the entire circumference of the fabric structure. The wire is woven such that it is primarily positioned along the interior of the fabric tube, with only small segments of wire exposed to the outside of the tube.[0178]
• The wireform is woven into the fabric tube such that when the wire extends around the entire periphery of the fabric tube, the free ends of the wire protrude from the tube at positions adjacent to each other, thereby enabling a[0179]tail segment177 to be defined by the free ends. The loose ends are preferably held together with a crimpingsleeve178 positioned over them. After crimping the sleeve to secure the ends to each other and thereby complete the circular configuration of the wireform, any portion of the wires extending beyond the ends of the sleeve may be trimmed to cleanly finish the tail segment.
• As illustrated in FIG. 2, the crimping sleeves extend outwardly along the external surface of the extension graft and are radially spaced apart. Preferably, the crimping sleeves on the[0180]upstream portion172 of the extension graft face in a downstream direction, thus frictionally engaging with the wall of the aortic graft body which helps to hold the extension into place. In fact, these upstream crimping sleeves can actually hook on the interior surface of the primary bifurcated graft, thus ensuring no longitudinal movement or separation of the extension graft from the primary aortic graft. The crimping sleeves on thedownstream portion174 face upstream and may frictionally engage, but not penetrate, the wall of the vessel lumen within which the device is placed. The crimping sleeves act as radiopaque markers, particularly for aiding in the placement and positioning of the graft extensions.
• The most[0181]proximal wireform168 and the mostdistal wireform166 are positioned with respect to the upper and lower edge of the fabric layer such that approximately one-third of the wireform extends beyond the respective edge of the fabric layer. In particular, the proximal-most wireform is positioned to extend above the edge of the fabric layer to prevent any portion of the fabric layer from oscillating, or “flapping,” in response to the flow of blood past the edge of the graft. As an additional measure to prevent such fabric oscillation in the blood stream, the proximal and distal edges of the fabric are configured with V-shaped notches corresponding generally to thevalleys152 of the proximal and distal wireforms. Thus, the risk of the existence of any loose fabric which could potentially be affected by the passing flow of blood is substantially reduced.
• In an alternate embodiment of the present invention, the proximal-most balloon-expandable wireform is preferably configured to have a diameter in its expanded state which is slightly larger than that of the portion of the fabric tubular structure into which it is weaved. By configuring the wireform to be slightly larger than the fabric into which it is woven, the fabric will be maintained in a constant state of slight tension upon expansion of the wireform, thereby reducing the possibility of the fabric folding or oscillating in response to blood flow through the graft.[0182]
• Additionally, the proximal balloon-expandable wireforms on the graft extension work in concert with the distal self-expandable wireforms on the aortic graft to hold the graft extensions in place. The balloon-expandable wires can be expanded slightly beyond the diameter of the distal self-expandable wireforms. This will cause the distal self-expandable wireforms to exert a radially inward pressure against the balloon-expandable portions of the graft extensions, thereby enhancing the frictional interface between them and providing a tighter seal.[0183]
• In a preferred embodiment of the present invention, the wireforms are positioned adjacent one another and are spaced apart from each other such that the wireforms do not interfere with each other in either a radially expanded or contracted state. Thus, for example, the valleys of one wireform are located proximal of the crests of the next adjacent wireform. Preferably, the wireforms are also aligned “in phase,” with peaks along one longitudinal line and adjacent valleys aligned along a second longitudinal line, thereby further reducing the possibility of overlap of adjacent wireforms. (While there may be some overlapping of the tail segments with an adjacent wireform, because the tail segments extend on the outside of the fabric layer and the adjacent wireform is primarily on the inside of the fabric layer, a small degree of overlap with an adjacent wireform does not pose a problem.)[0184]
• In addition, adjacent balloon-expandable wireforms are not connected to one another. This coupled with the in-phase configuration of the wireforms maximizes flexibility of the aortic graft without permitting deleterious kinking, which is of primary importance in the often tortuous paths of the abdominal aorta and iliac arteries.[0185]
• An important feature of the extension grafts of the present invention is the spacing distance between adjacent wireforms. It has been discovered in accordance with the investigations of the present invention that optimizing the spacing distance between the wireforms improves the balance between kink resistance and flexibility in the graft extensions. Too much space promotes kinking, while too little space detracts from flexibility. These are important features in the often tortuous path of the iliac arteries and abdominal aorta in which the graft extensions are to be placed.[0186]
• FIG. 2A, for example, illustrates in cross-section balloon-[0187]expandable wireforms176. Preferably the length “L” or separation distance between adjacent wireforms is measured from the closest point on each neighboring wire. For example, in FIG. 2A, L is the distance betweencrest150 andvalley152.
• Further, the graft extensions have a diameter “D” which varies according to the differently sized extensions. In one embodiment the length L between adjacent wireforms is preferably less than 2D. In a preferred embodiment the length L between adjacent wireforms will be less than D. In another preferred embodiment the length between adjacent wireforms will be less than D and greater than zero. Therefore, the preferred separation distance depends on the diameter of the graft.[0188]
• In a 14 mm graft a preferred separation distance between adjacent wireforms that has been found to be acceptable during use is 2.4 to 2.5 mm.[0189]
• Further, as discussed above, the interface between the upstream portion of the extension graft and the downstream leg of the aortic graft is preferably standardized such that the downstream legs and the upstream extensions have the same dimension at their interface, regardless of the diameter of the aorta above the aneurysm and the diameters of the iliac arteries below the aneurysm.[0190]
• F. Directional Catheter[0191]
• The present invention further includes a directional catheter. The structure of this catheter is substantially disclosed in WO 97/26936, which was previously incorporated by reference hereinabove. Specifically, the directional catheter facilitates guidewire access to the contralateral leg of the bifurcated graft to allow placement of a contralateral extension graft into the bifurcated graft.[0192]
• The primary components of[0193]directional catheter220 may be observed by reference to FIG. 5. The directional catheter includes a deflectingspring portion222, (illustrated substantially deflected).Knob224 is used to deflect the spring portion.Connector nut226 is provided such that the directional catheter can be operatively connected with the sheath assembly.
• G. Extension Graft Deployment[0194]
• The procedure for attaching the extension tubes will now be described. With reference to FIGS. 13A and 13B, the[0195]sheath134 stiffened by a dilator (not shown) is advanced over theguidewire128 until thedistal tip138 is located approximately at theseptum region28. The location of thedistal tip138 is again facilitated by fluoro-visualization of themarker139 with respect to the radiopaque crimping sleeves84,85 (FIG. 1) on thegraft10. The dilator is then proximally withdrawn from within thesheath134, and thedirectional catheter220 advanced distally over theguidewire128 and within thesheath134 to project a short distance from the distal tip138 (FIG. 13B).
• More particularly, the[0196]directional catheter220 is first inserted over the primary guidewire through the ipsilateral side, for example, through the rightfemoral artery116 and the right commoniliac artery102 in the present case. FIG. 13A illustrates thedirectional catheter220 operatively connected to thesheath assembly132. Thespring portion222 of thedirectional catheter220 is positioned such that it is above theseptal region28 of theaortic graft10. Proper positioning of the spring portion to the contralateral side is adjusted by rotating or advancing forwards or backwards the wholedirectional catheter220 while under fluoro-visualization. Thespring portion222 is deflected by pullingknob224 in the direction of the arrow in FIG. 13A. FIG. 13B illustrates the deflectedspring portion222 positioned within thecontralateral leg14.
• A[0197]supplemental guidewire228 is then advanced through thedirectional catheter220 and out the deflectedspring portion222 to extend down thecontralateral leg14 and through the left commoniliac artery104. Thesupplemental guidewire228 is extended until it is in the leftfemoral artery118, at which time the left femoral artery is cross-clamped and a cut-down or percutaneous incision is performed to retrieve the supplemental guidewire. If the guidewire has not been guided fully along the femoral artery a snare or similar device can be introduced through the left femoral artery to grab the guidewire and draw it back to the puncture or incision site for retrieval.
• As seen in FIG. 13C, once the[0198]supplemental guidewire228 is in place through the left commoniliac artery104 thedirectional catheter220 is advanced distally through thebifurcated graft10 and into a position above therenal arteries106,108. Thespring portion222 remains deflected to present a curvilinear upstream profile. This curved profile enables advancement of thedirectional catheter220 without risk of the distal end of thespring portion222 snagging on the openings to therenal arteries106,108. Thedirectional catheter220 remains in this position while thetubular graft extension170 is attached to thecontralateral leg14. Astiffer guidewire228ais then exchanged with thesupplemental guidewire228 by conventional methods to extend through the leftiliac artery104 and within thecontralateral leg14 of the aortic graft.
• As illustrated in FIGS. 14A and 14B, a[0199]second introducer assembly230 is introduced with the help of adilator240 over thestiff guidewire228ain the manner previously described for thefirst introducer assembly130. Thedilator240 is removed leaving asecond sheath270 in position with itsdistal tip272 adjacent thegraft septum region28. Again, aradiopaque marker274 on thedistal tip272 aligns with theseptum region28 and its radiopaque markers84,85 (FIG. 1).
• As seen in FIG. 15A, a second catheter assembly, on which is packaged the[0200]tubular graft extension170 is then introduced through thesheath270. A pusher body, (not shown but similar to that described above) pushes thetubular graft extension170 distally within thesheath270. Again, this procedure for advancing a graft upstream with respect to theaneurysm114 while housed within thesheath270 is necessary to avoid difficulties associated with displacing an irregularly shaped object against the blood flow. It is especially significant given that thetrunk portion12 has been expanded into contact with theabdominal aorta100, and thus the entire blood flow through the abdominal aorta continues through thegraft legs14,16. Ultimately, adistal portion286 of the inflation balloon extends from thedistal tip272 ofsheath270.
• Once the[0201]tubular graft extension170 is in place, thesecond introducer sheath270 is withdrawn (as seen by thearrow276 in FIG. 15B) to a position within the left commoniliac artery104. After displacing thesecond introducer sheath270, the pusher body is retracted slightly to release the proximal end of thegraft extension170. FIG. 15B illustrates the compressed balloon-expandabletubular graft extension170 in proper position for expansion and implantation.
• As illustrated in FIG. 15C, the balloon on the second catheter assembly is then inflated forcing the upstream portion of the[0202]graft extension170 into contact with the inner surface of thecontralateral leg14, and downstream portion of the graft extension into contact with the inner surface of the left commoniliac artery104. As with theinflation balloon194 for thetrunk portion12 the inflation balloon for thetubular graft extension170 is first deflated and then stretched to remove it from within graft without snagging.
• After the[0203]tubular graft extension170 on the contralateral side has been expanded, thedirectional catheter220 in thefirst introducer sheath134 is withdrawn. First, however, thespring portion222 is straightened to its home position (FIG. 15C) to enable thecatheter220 to be retracted within thesheath134.
• As seen in FIG. 16A, a third catheter assembly on which is packaged another[0204]tubular graft extension170′ is then advanced over theprimary guidewire128 and through the lumen of thesheath134 until adistal end296 of the inflation balloon projects slightly from thedistal tip138. Again, a radiopaque marker on the distal end of the balloon catheter is used to place it in registry with themarker139 on thedistal tip138, which was previously registered with the marker at thegraft septum region28.
• The[0205]first introducer sheath134 is slightly larger than thesecond sheath270 because it is sized for passage of theballoon194 of the first catheter assembly on which thetrunk portion12 is wrapped. For example, the inner diameter of theintroducer sheath134 may be 19 French, while the inner diameter of thesecond sheath270 may be 16 French. As a result, there is some acceptable clearance between passage of the third catheter assembly andtubular graft extension170′ thereon and the inner lumen of theintroducer sheath134. In this manner theintroducer sheath134 need not be removed and replaced with a smaller one.
• In the same manner as on the contralateral side, and as illustrated in FIG. 16B, first the[0206]sheath134 and then the pusher body (not shown) are withdrawn proximally to release thetubular graft extension170′ such that its upstream end is inside theipsilateral leg16 of theaortic graft10 and its downstream end is within the right commoniliac artery102. The catheter balloon is inflated to force the upstream end of thegraft extension170′ into contact with the inner surface of theipsalateral leg16. At the same time, the balloon forces the downstream end of thegraft extension170′ into contact with the inner surface of the right commoniliac artery102. The final expanded position of thetubular graft extension170′ is seen in FIG. 16D.
• FIG. 16C illustrates a cross-section of the left common[0207]iliac artery104 with the firsttubular graft extension170 expanded into contact therewith. As was described with respect to FIG. 2A, thewireforms176 terminate in ends which are secured outside theextension wall175 withcrimps178. Thecrimps178 as shown project outward from thewall175 at a slight angle and provide additional friction to locate theextension170 within theartery104. Advantageously, thecrimps178 are riot sharp and do not penetrate the vessel wall, as with some prior art grafts. Instead, the irregular surface formed by themultiple crimps178 prevents migration of thetubular graft extension170 without damage to the wall of theartery104.
• Subsequently, the inflation balloon is deflated and then stretched before removing it along with the third catheter assembly from within the[0208]graft extension170′.
• In one embodiment of the present invention, the upstream portions of either of the[0209]graft extensions170,170′ may be slightly over-sized to maximize the frictional engagement with the downstream portions of the respective contralateral oripsilateral legs14,16. In particular, the over-expansion of the balloon-expandable wireforms slightly beyond the diameter of the distal self-expandable wireforms causes the distal self-expandable wireforms of the contralateral or ipsilateral legs to exert a radially inward force against the balloon-expandable portions of the graft extension. This resistance selves to improve the frictional engagement between the contralateral downstream leg and the graft extension. Furthermore, the respective wireforms and associated crimps tend to hook together to more securely couple thegraft extensions170,170′ to the respective contralateral oripsilateral legs14,16.
• In an alternate embodiment, colloquially known as the “kissing” technique, both the ipsilateral and contralateral balloon catheters could remain in place during implantation of both[0210]leg extensions170,170′. In this technique, the third catheter balloon for theipsalateral leg extension170′ is inflated while the second catheter balloon remains within thecontralateral leg extension170. In other words, while the third catheter balloon inflates, the second catheter balloon remains in place in thecontralateral leg extension170, and is preferably deflated to ambient pressure but is not stretched or reduced by a vacuum. The third catheter balloon is subsequently deflated, stretched and removed, followed by deflation, stretching and removal of the second catheter balloon. The use of the kissing technique or the more common sequential contralateral-ipsalateral extension implantation technique is up to the preference of the surgeon.
• An angiographic examination may take place to determine if the grafts are correctly placed and functioning. The second sheath assembly and the stiff guidewires are withdrawn and the contralateral incision or puncture is sutured. The first introducer sheath assembly is then withdrawn and the right femoral incision is sutured. The result is a functioning trouser graft bridging an aneurysm as illustrated in FIG. 16D.[0211]
• The operation may be carried out using a general anaesthetic, an epidural anaesthetic, or in suitable cases, using only a local anaesthetic.[0212]
• The present invention may be embodied in other specific forms without departing from its spirit or essential characteristics. The described embodiments are to be considered in all respects only as illustrative and not restrictive. The scope of the invention is, therefore, indicated by the appended claims rather than by the foregoing description. All changes which come within the meaning and range of equivalency of the claims are to be embraced within their scope.[0213]

Claims (24)

What is claimed is:

1. An intraluminal prosthesis comprising:

a trouser graft having a trunk and two trunk legs diverging in a downstream direction from the trunk at a septum region, wherein the trouser graft is attachable at its upstream end to an aorta;

wherein the trouser graft is of a specified length and at least a first trunk leg is of a specified length so that upon attachment of the trouser graft to the aorta the septum region and the first trunk leg are locatable upstream from the aortic bifurcation;

wherein the trunk comprises a first trunk diameter at its upstream end conformable to the diameter of the aorta where it will be attached and a second trunk diameter at its downstream end which is different from the first trunk diameter and wherein each trunk leg has a trunk leg diameter; and

a tubular extension overlappingly connectable to a downstream end of the first trunk leg, at least a portion of the tubular extension having a tubular extension diameter conformable to the first trunk leg diameter to provide a consistent interface therewith.

2. The intraluminal prosthesis ofclaim 1 wherein the first trunk diameter is greater than the second trunk diameter and the trunk steps down between its upstream and downstream ends.

3. The intraluminal prosthesis ofclaim 1 wherein the first trunk diameter is greater than the second trunk diameter and the trunk tapers at least along a portion of its length between its upstream and downstream ends.

4. The intraluminal prosthesis ofclaim 1 wherein the first trunk diameter is less than the second trunk diameter and the trunk steps up between its upstream and downstream ends.

5. The intraluminal prosthesis ofclaim 1 wherein the first trunk diameter is less than the second trunk diameter and the trunk tapers at least along a portion of its length between its upstream and downstream ends.

6. The intraluminal prosthesis ofclaim 1 wherein the tubular extension diameter is substantially uniform throughout its length.

7. The intraluminal prosthesis ofclaim 1 wherein the tubular extension has a first tubular extension diameter at an upstream end which is conformable to the trunk leg diameter to provide a consistent interface therewith and a second tubular extension diameter at a downstream end which is conformable to the diameter of a vessel to which it will be attached.

8. The intraluminal prosthesis ofclaim 7 wherein the first tubular extension diameter is greater than the second tubular extension diameter and the tubular extension steps down between the upstream and downstream ends.

9. The intraluminal prosthesis ofclaim 7 wherein the first tubular extension diameter is greater than the second tubular extension diameter and the tubular extension tapers at least along a portion of its length between the upstream and downstream ends.

10. The intraluminal prosthesis ofclaim 7 wherein the first tubular extension diameter is less than the second tubular extension diameter and the tubular extension steps up between the upstream and downstream ends.

11. The intraluminal prosthesis ofclaim 7 wherein the first tubular extension diameter is less than the second tubular extension diameter and the tubular extension tapers at least along a portion of its length between the upstream and downstream ends.

12. The intraluminal prosthesis ofclaim 1 wherein the two trunk legs are circular in cross-section and the combined diameters of their respective trunk leg diameters is equal to the second trunk diameter.

13. The intraluminal prosthesis ofclaim 12 wherein the second trunk diameter is 26 mm and the trunk leg diameter of each trunk leg is 13 mm.

14. The intraluminal prosthesis ofclaim 1 wherein the trouser graft further comprises one or more expandable wireforms at its upstream end attachable to an aorta.

15. An intraluminal prosthesis comprising:

a trouser graft having a trunk and two trunk legs diverging in a downstream direction from the trunk at a septum region, wherein the trouser graft is formed of a graft body having an external surface and an internal surface and comprises one or more expandable wireforms at its upstream end attachable to an aorta;

wherein the trouser graft is of a specified length so that upon attachment of the trouser graft to the aorta the septum region is locatable upstream from an aortic bifurcation and at least a first trunk leg is of a specified length so that upon attachment of the trouser graft to the aorta the first trunk leg is locatable upstream from the aortic bifurcation;

wherein the trunk has a circular cross-section and comprises a first trunk diameter at its upstream end conformable to the diameter of the aorta to which it will be attached and a second trunk diameter at its downstream end which is different from the first trunk diameter and wherein each trunk leg has a trunk leg diameter; and

a tubular extension overlappingly connectable to a downstream end of the first trunk leg, the tubular extension having a first tubular extension diameter at an upstream end which is conformable to the trunk leg diameter to provide a consistent interface therewith and a second tubular extension diameter at a downstream end which is conformable to the diameter of a vessel to which it will be attached.

16. A method of implanting a modular intraluminal prosthesis while providing for a consistent interface between the modular components of the prosthesis comprising the following steps:

determining a main vessel diameter and a branch vessel diameter;

providing a bifurcated graft comprising a first trunk diameter at an upstream end which will conform to the main vessel diameter and a second trunk diameter at a downstream end which is different from the first trunk diameter, the bifurcated graft further comprising two trunk legs diverging in a downstream direction from the trunk at a septum region, each trunk leg having a standardized trunk leg diameter;

endoluminally delivering the bifurcated graft to an implantation site and expanding the bifurcated graft so that the upstream end of the bifurcated graft is in contact with the main vessel;

providing a tubular extension with at least a portion of the tubular extension having a standardized tubular extension diameter which will conform to the standardized trunk leg diameter;

endoluminally delivering the tubular extension into position to overlappingly fit into a downstream end of one of the two trunk legs; and

expanding the tubular extension so that the portion of the tubular extension having the standardized tubular extension diameter overlappingly connects to the downstream end of the one of the two trunk legs to provide a consistent interface therewith.

17. The method ofclaim 16 wherein the step of expanding the tubular extension further comprises expanding the tubular extension with a balloon catheter.

18. The method ofclaim 16 wherein the bifurcated graft provided has a first trunk diameter which is greater than the second trunk diameter and the trunk steps down between the upstream and downstream ends.

19. The method ofclaim 16 wherein the bifurcated graft provided has a first trunk diameter which is greater than the second trunk diameter and the trunk tapers at least along a portion of its length between the upstream and downstream ends.

20. The method ofclaim 16 wherein the bifurcated graft provided has a first trunk diameter which is less than the second trunk diameter and the trunk steps up between the upstream and downstream ends.

21. The method ofclaim 16 wherein the bifurcated graft provided has a first trunk diameter which is less than the second trunk diameter and the trunk tapers at least along a portion of its length between the upstream and downstream ends.

22. The method ofclaim 16:

wherein the step of providing a tubular extension further comprises providing a tubular extension having a first tubular extension diameter at a first end which will conform to the standardized trunk leg diameter and a second tubular extension diameter at a second end which will conform to the branch vessel diameter; and

wherein the step of expanding the tubular extension further comprises expanding the tubular extension so that the first end of the tubular extension overlappingly connects to the downstream end of the one of the two trunk legs and the second end of the tubular extension is in contact with the branch vessel.

23. The method ofclaim 22 wherein the step of expanding the tubular extension comprises expanding the tubular extension with a balloon catheter.

24. A method of implanting a modular intraluminal prosthesis while providing for a consistent interface between the modular components of the prosthesis comprising the following steps:

determining a main vessel diameter and a branch vessel diameter;

providing a bifurcated graft comprising a first trunk diameter at an upstream end which will conform to the main vessel diameter and a second trunk diameter at a downstream end which is different from the first trunk diameter, the bifurcated graft further comprising two trunk legs diverging in a downstream direction from the trunk at a septum region, each trunk leg having a standardized trunk leg diameter and at least a first trunk leg being of a specified length;

endoluminally delivering the bifurcated graft to an implantation site and expanding the bifurcated graft so that the upstream end of the bifurcated graft is in contact with the main vessel while the septum region and the first trunk leg of the bifurcated graft are located upstream from a bifurcation of the main vessel into the branch vessel;

providing a tubular extension having a first standardized tubular extension diameter at a first end which will conform to the standardized trunk leg diameter and a second tubular extension diameter at a second end which will conform to the branch vessel diameter;

endoluminally delivering the tubular extension to an implantation site and expanding the tubular extension such that the first end of the tubular extension with the standardized tubular extension diameter overlappingly connects to the downstream end of the first trunk leg with the standardized trunk leg diameter and the second end of the tubular extension is in contact with the branch vessel.

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