US20140188208A1 - Self-expanding pseudo-braided intravascular device - Google Patents

Abstract

A self-expanding, pseudo-braided device embodying a high expansion ratio and flexibility as well as comformability and improved radial force. The pseudo-braided device is particularly suited for advancement through and deployment within highly tortuous and very distal vasculature. Various forms of the pseudo-braided device are adapted for the repair of aneurysms and stenoses as well as for use in thrombectomies and embolic protection therapy.

Description

BACKGROUND OF THE INVENTION
• The present invention relates to self-expanding, knitted devices and more particularly, to a self-expanding knitted device for intravascular repair of distal and tortuous vasculature.
• The vasculature of an animal or a human characteristically suffers from a variety of maladies. Vessel walls can weaken and become distended over time in response to blood flow and pressures, thereby resulting in formation of aneurysms. Such aneurysms can take on a myriad of forms. In particular, aneurysms may form at or near bifurcated vessels creating enlarged areas about the bifurcation, or may form a pocket, for example, in side walls of vessels. Due to the complications associated with aneurysms that rupture or otherwise fail, it is critical that an aneurysm be treated expeditiously and effectively. Intravascular treatment procedures include placing grafts within the aneurysm in a manner to ensure that blood flows through the graft rather than through the weakened vessel. Additionally, in the event that the aneurysm is in the form of a pocket in the side wall of a vessel, a stent might first be placed at the repair site then the pocket filled with material such as coils.
• Stenoses also typically form in vasculature of humans and animals. Specifically, thrombotic or atherotic stenoses can form nearly anywhere in the vasculature. Such narrowing of the vessel is, of course, highly dangerous to the patient where the afflicted vessel provides the sole blood flow access to critical parts of the body. To treat such stenoses, a supporting structure can be placed at the diseased site for the purpose of enlarging and holding open the vessel. It is known in the art to employ stents for this purpose.
• Vessel occlusions can also be treated by employing devices which are actuated to debulk and remove vessel occluding thrombi. This procedure is generally referred to as a thrombectomy. Typically, such devices are intravascularly advanced to the repair site and manipulated to remove the unwanted material from the vessel by physically engaging the thrombus and severing the same from the vessel wall.
• Due to procedures such as thrombectomies or due to the natural, albeit undesirable, function of a patient's vasculature, emboli may be found traveling through a blood vessel. Embolic material can cause unwanted blockages or otherwise facilitate the formation of an occlusion in a vessel which too, can be highly dangerous to a patient. To address this problem, emboli-catching filters can be intravascularly placed within vasculature to thereby provide embolic protection. Such devices are often implanted temporarily within vasculature and removed upon being satisfied that the undesirable embolic material has been captured.
• In certain situations, it is desirable to aid the formation of thrombus. For example, devices may be placed within aneurysmal spaces to slow and eventually cease blood flow therethrough. This procedure is sometimes referred to as embolic therapy, the basic thrust of which is to minimize or eliminate exposure of weakened sections of vasculature to blood flow and pressure.
• Unfortunately, many areas of vasculature are inaccessible by a conventional intravascular repair means because the repair devices typically employed are often too large or rigid to be effectively advanced through tortuous vasculature or to vasculature that is very distal to the site through which the vasculature is accessed. Alternatively, in the event that there is success in advancing the repair devices to the diseased portion or repair site of the vasculature, conventional repair devices sometimes lack a large enough expansion ratio and/or radial stiffness to accomplish the necessary repair. Moreover, conventional devices can lack a profile suited to avoid traumatic engagement with a vessel wall or sufficient radiopacity so that remote observation is impossible.
• Thus, where an intravascular approach is not available to the physician, invasive surgical techniques must be applied. To wit, a patient's chest, abdomen or cranium, for example, must be directly traversed in a major surgical procedure.
• Hence, those concerned with repair of diseased vasculature have recognized the need for devices that can be employed to effectively repair distal and highly tortuous vasculature. The present invention fulfills these needs.
SUMMARY OF THE INVENTION
• Briefly, and in general terms, the present invention provides devices contemplated for the repair of highly tortuous and distal vasculature. Basically, the invention is directed to a self-expanding, pseudo-braided structure that is characterized by having a large expansion ratio and high flexibility as well as an improved radial strength accomplished through the advantageous utilization of deflection energy.
• In one preferred embodiment, the devices of the present invention are fabricated from a single filament configured into a repeating helical pattern that is interlaced into a mesh or pseudo-braided tubular shape. The filament may embody an elongate highly elastic and shape settable material. A reversal of direction that the filament undergoes presents a blunt, rounded surface that is atraumatic to vessel walls. The structure in the present application is referred to as pseudo-braided. Braiding is the interlacing of at least three wires at various angles to each other to form a braid, whereas the present invention uses a single filament that is interlaced with itself along the length of the structure at various angles. It is within the scope of the invention to interlace another filament or a plurality of other filaments into the pseudo-braid formed by the single filament.
• In another aspect of the invention, the pseudo-braided or interlaced structure has a high expansion ratio with a low metal to space ratio. A large expansion ratio is accomplished by the unique single filament construction that provides additional springback forces.
• In other aspects of the invention, there are various methods for terminating the filaments. Additionally, various methods are contemplated for adjusting the radiopacity as well as the expansion and spring characteristics of the pseudo-braided devices. Various methods are also contemplated for improving coverage of the pseudo-braided devices and enhancing the anchoring of the same within distal and tortuous vasculature.
• The self-expanding, pseudo-braided devices disclosed are intended for use in addressing various maladies effecting vasculature. In particular, the self-expanding, pseudo-braided devices can be configured specifically to facilitate the repair of aneurysms and stenoses as well as to act as filter or thrombectomy devices.
• These and other objects and advantages of the invention will become apparent from the following more detailed description, when taken in conjunction with the accompanying drawings of illustrative embodiments.
BRIEF DESCRIPTION OF THE DRAWINGS
• FIG. 1 is a side view of a pseudo-braided device of the present invention;
• FIG. 2 is an end view of the pseudo-braided device shown inFIG. 1;
• FIG. 3 is a side view of a pseudo-braided device of the present invention, depicting a device with a flared end;
• FIG. 4 depicts a first embodiment of a filament reversal;
• FIG. 5 depicts a second embodiment of a filament reversal;
• FIG. 6 depicts a third embodiment of a filament reversal;
• FIG. 7 depicts a fourth embodiment of a filament reversal;
• FIG. 8 depicts a fifth embodiment of a filament reversal;
• FIG. 9 depicts a first embodiment of a method for joining ends of a filament;
• FIG. 10 depicts a second embodiment of a method for joining ends of a filament;
• FIG. 11 depicts a third embodiment of a method for joining ends of a filament;
• FIG. 12 depicts a fourth embodiment of a method for joining ends of a filament;
• FIG. 13 depicts a fifth embodiment of a method for joining ends of a filament;
• FIG. 14 depicts a sixth embodiment of a method for joining ends of a filament;
• FIG. 15 depicts a seventh embodiment of a method for joining ends of a filament;
• FIG. 16 depicts a eighth embodiment of a method for joining ends of a filament;
• FIG. 17 is a perspective view of a first alternative method of forming a pseudo-braided device of the present invention;
• FIG. 18 is a perspective view of a second alternative method of forming a pseudo-braided device of the present invention;
• FIG. 19 is a side view of a sectioned portion of a blood vessel suffering from an aneurysm and a pseudo-braided device of the present invention being deployed from a catheter;
• FIG. 20 depicts the implantation of the device ofFIG. 19 within a vessel;
• FIG. 21 is a side view of a sectioned portion of a blood vessel suffering from an aneurysm and a pseudo-braided device of the present invention being deployed from an alternative embodiment of a delivery catheter;
• FIG. 22 is a side view of a sectioned portion of a blood vessel suffering from a stenosis and a pseudo-braided device of the present invention being deployed from a catheter;
• FIG. 23 depicts the implantation of the pseudo-braided device ofFIG. 22 within a vessel;
• FIG. 24 is a side view of a pseudo-braided device of the present invention configured as an embolic protection device;
• FIG. 25 depicts a side view of an alternate embodiment of the pseudo-braided device of the present invention configured as an embolic protection device;
• FIG. 26 is a side view of a pseudo-braided device of the present invention configured as a thrombectomy device;
• FIG. 27 depicts a side view of an alternate embodiment of the pseudo-braided device of the present invention configured as a thrombectomy device;
• FIG. 28 depicts a side view of yet another embodiment of the pseudo-braided device of the present invention configured as a thrombectomy device; and
• FIG. 29 is a side view of a sectional portion of a portion of a blood vessel suffering from an aneurysm and a pseudo-braided device of the present invention configured to be placed within the aneurysm.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
• Turning now to the drawings, and particularly toFIGS. 1 and 2, there is shown a self-expandingpseudo-braided structure50 of the present invention. Thepseudo-braided device50 is contemplated for use in highly tortuous and very distal vasculature of an animal or human. Due to its novel structure, thepseudo-braided device50 is flexible in a compressed configuration and conformable to tortuous anatomy in a relaxed condition. Moreover, the device embodies high flexibility and a large expansion capability while providing sufficient radial force (i.e., hoop stiffness).
• In a presently preferred embodiment, thepseudo-braided device50 of the present invention is formed from thesingle filament52. Thefilament52 is configured into a repeating helical pattern that is interlaced upon itself by passing the end of the filament over then under the filament forming the helix as the end of the filament is wound down and back up the length of the structure to thereby form a generallytubular body54. At the crossings of the filament there can be local deformations formed as the top wire is bent over the bottom wire however it has been discovered that for most applications deformations are not necessary to add spring force and resistance against fraying because of the ends formed by the reversal of winding. Thetubular body54 defines aninterior lumen56 and includes afirst end58 andsecond end60.
• It is also contemplated that the self-expanding pseudo-braided structure can embody modified tubular configurations. That is, as shown inFIG. 3, one end of the self-expandingpseudo-braided structure50 can include an increased diameter section orflare61. Alternatively, both ends of the device can include aflare61, such flares can have the same general shape or one flare may be greater than the other.
• Thefilament52 is preferably an elongate, highly elastic and shape settable member. In one preferred embodiment, thefilament52 has a circular cross-sectional profile and can comprise nickel titanium alloy, eligiloy™, steel or other suitable materials.
• In order to assemble thepseudo-braided device50, it is contemplated that thefilament52 can be wrapped about a mandrel in a first direction and in a helical fashion for a desired length along the mandrel (not shown). Once the desired length is achieved, the direction of winding is reversed.
• Reversal of winding can be accomplished in a number of ways. It is contemplated, however, that the reversal of winding present a smooth, blunt surface that would be atraumatic to a vessel wall. As shown inFIG. 4, such an atraumatic reversal can be accomplished employing asimple arc62. Atraumatic reversal can also be provided by single64 or double66 loop backs as well as a figure-8reversal68 or a full-turnhelical reversal69 as shown inFIGS. 5-8, respectively.
• Various radii of curvature and length of loops can be employed according to the application. The loops or hoops of the various reversals contemplated can have a constant or irregular radii of curvature and the loops can have an acute radius of curvature (not shown). It is believed that minimizing stress concentrations in the reversals may have the added benefit of optimizing springback forces. Thus, stress concentration in the reversals can also be varied for a particular application. Moreover, in order to facilitate the reversal of direction of thefilament52, the mandrel can have pegs extending therefrom at desired intervals, about which the filament can be routed.
• Once a reversal direction is made, the filament is interlaced in an over/under fashion about itself in a helical pattern in the reverse axial direction but same rotational direction. The desired density of thewall70 defining thetubular body54 is accomplished by altering the number of reversals and thelongitudinal spacing72 of adjacent members wrapped in the helical pattern. That is, the number of traversals, which is defined as the portion of thefilament52 between two reversals of direction, can be varied as can the number of revolutions per traversal. Typically, the number of reversals at eachend58,60 of thetubular body70 number from six (6) to twelve (12) and as much as twenty (20).
• Upon achieving a desired pseudo-braided pattern and wall density, the ends74,76 of thefilament52 are joined. There are a myriad of ways in which the ends74,76 can be joined. While the figures illustrate such joining as occurring generally at the middle of thepseudo-braided device50, it is also contemplated that such joining can occur at the ends of the structure or anywhere in between. Ultimately, however, it is desired that the joining of theends74,76 of thefilament52 be accomplished in a manner such that the vessel wall is presented with as atraumatic a surface as necessary for a particular application, there is a low profile, and no compromise in device function.
• As shown inFIGS. 9 and 10, one way of joining theend74,76 of thefilament52 is to twine them together. The ends74,76 of the filament can also be joined by soldering or welding to form a welded joint78 as shown inFIG. 11. A preferred method of welding is laser welding.
• Alternatively, the ends74,76 of thefilament52 can be joined utilizing pottedtantalum powder80, as depicted inFIG. 12. In order to do so, the tantalum powder is first mixed with an epoxy. Thereafter, thefilament50 is coated with the tantalum/epoxy compound and left to cure.
• Moreover, the ends74,76 of thefilament52 can be configured into a linear slide arrangement82 (seeFIG. 13). In such an arrangement, onefilament end74 is wrapped around the other filament end76 which remains straight or undeformed. This means for joining theend74,76 of thefilaments52 has the advantage of compensating for length mismatches. To wit, one wire can move relative to the other.
• The ends74,76 of the filament can also be formed with flattened welding surfaces84 (FIG. 14). These weld surfaces84 are then aligned and thereafter welded together by conventional methods.
• Finally, the ends74,76 of thefilament52 can be crimped together using asleeve86 or are otherwise joined by way of a ball member88 (FIGS. 15 and 16). In both instances, a bore is provided to receive both ends74,76 of thefilament52. In the case of thesleeve86 embodiment, the outer surface of thesleeve86 can be crimped to retain thesleeve86 on theends74,76 of thefilament52. A press fit is contemplated for theball88 and configuration.
• The assembledpseudo-braided device50 embodies a number of unique features. In particular, the reversal of the knit direction provides a resilient response at theends58,60 of thepseudo-braided device50 compared to that of other conventional braided structures that have unconnected wire ends. That is, reversals of direction act as a spring and tend to attempt to return to pseudo-braided device to its original expanded shape. This feature allows thepseudo-braided device50 to be compressed to smaller than ten (10) percent of its original diameter and once released, to spring back to its original uncompressed configuration. Accordingly, thepseudo-braided device50 of the present invention is characterized by having a very large expansion ratio.
• Embodying a very large expansion ratio provides thepseudo-braided device50 of the present invention with a number of advantages. In particular, thepseudo-braided device50 can be delivered within vasculature using very small diameter catheters or microcatheters. This in turn allows for the placement of thepseudo-braided device50 within very distal vasculature. Thus, using microcatheters to deliver thepseudo-braided device50 facilitates advancement through highly tortuous as well as very narrow vessels such as in the cerebral vasculature.
• Furthermore, the reversals of direction of thefilament50 tend to improve radial force (i.e., hoop stiffness) by forcing deflection energy to bend the reversal arc as well as displace the same. With particular reference toFIG. 4, reversals defined bysimple bends62 embody relatively high stress concentrations at thebend62. Such high stress concentrations may be suitable for a purpose requiring a particular deflection energy. In contrast, reversals defined by full-turn helixes (FIG. 8), for example, tend to distribute stress concentrations throughout thehelix69 and therefore provide a different deflection energy. By comparison, braided devices that lack reversals deflect in response to a load much more readily than theends58,60 of the pseudo-braided device of the present invention and those braided devices only rely on pivots at the crossings of the wires whereas the present invention embodies crossings plus spring ends.
• The crossingangle90 can also be varied for a particular application. The crossingangle90 is defined by two portions of the filament that cross each other. It is presently contemplated that the crossing angle can range up to approximately90 degrees or more. It has been found that the braid angle directly affects radial stiffness and conformability which can thus be optimized for a particular application.
• It has also been recognized that joining theends74,76 of the filament maintains filament alignment. Filament alignment is important particularly when deploying thepseudo-braided device50 in extremely tortuous vessels for a number of reasons. First, in the event thefilaments52 were permitted to slide out of place, weaker areas would be created in thepseudo-braided device50. Those weaker areas would have an increased propensity to buckle. Secondly, iffilaments52 were to slide out of place, the mesh openings can become variable. As a result, there would be larger openings in the mesh or interlaced structure in some places that would reduce functionality of the device. Finally, if filaments were permitted to slide out of place, catheter distortion during deployment will likely increase. Thus, when thefilaments52 of the pseudo-braided device maintain good alignment while in the compressed condition, the individual radial forces of eachfilament52 add together to form a consistent radial force in all directions along the length of thepseudo-braided device50.
• It is also possible to produce apseudo-braided device50 that is comprised of one wire, where that one wire has variations along its length that corresponds to specific pseudo-braiding processes of a particular desired configuration. To wit, a wire could be masked and chemically etched to produce a variable diameter wire that corresponds to thepseudo-braided device50 design of choice, such that for example, the bends of thefilament52 that comprise the ends of thepseudo-braided device50 can be of a smaller diameter than the wire that comprises the remainder of thepseudo-braided device body70. Additionally, the bends could be of a larger diameter for providing a greater expansion rate and radial force. These variations may advantageously create apseudo-braided device50 with a desired strength, without increasing its resistance to being pushed through a catheter lumen in a compressed configuration.
• This kind of design variation could be followed for other attributes as well. For example, such as for non-thrombogenic coatings, coatings laced with therapeutic drugs, plating processes to selectively increase radiopacity, and plating processes to selectively increase stiffness.
• Alternatively, rather than a round profile, thefilament52 can be formed from a filament having various other cross-sectional profiles. That is, the filament can comprise an oval, triangular, rectangular, square, bowed, crescent moon, or tapered profiles. Thefilament52 itself can also be formed from a small diameter tube or be configured into a coil along its length.
• It is also recognized that the desired pseudo-braided structure can be made from a plurality offilaments52. Such plurality offilaments52 can be configured with a number of reversals of varying types, so that the benefits associated therewith can be used advantageously. The ends of these filaments can also be joined together to provide atraumatic engagement with vessel walls as discussed above.
• When deploying thepseudo-braided device50 of the present invention within a patient's vasculature, it is desirable to be able to remotely observe the placement thereof. Thus, it is important that thepseudo-braided device50 be sufficiently radiopaque so that such remote observation is possible by conventional methods such as fluoroscopy.
• Referring now toFIGS. 15 and 16, the radiopacity of thepseudo-braided device50 can be enhanced by employing platinum or other sufficiently radiopaque materials as the crimpingsleeve86 or theball end88. Platinum coils (not shown) could similarly be wrapped about portions of thefilament52 to act as radiopaque markers. Additionally, thefilament52 can be twined with one or more platinum filaments along its length, thereby providing apseudo-braided device50 that is radiopaque from one end to the other.
• Additionally, it is contemplated that in certain applications, it may be desirable to plate the filament with gold or platinum. The entirety of thetubular body70 can be plated or the reversals could be masked and the remainder of thebody70 be plated. By thus masking the reversals, the desirable spring characteristics of thepseudo-braided device50 of the present invention can be preserved.
• Referring now toFIGS. 17 and 18, there is shown methods of manufacturing thepseudo-braided device50 of the present invention in a manner to optimize vessel coverage for particular applications. As shown inFIG. 17, a particular configuration of thepseudo-braided device50 can be formed by wrapping afilament52 about a formingmandrel92 such that there is tight winding at an inferior end portion94 and relatively looser winding at asuperior end portion96. The tightly wound portion being contemplated to provide the resultantpseudo-braided device50 with structure for anchoring and for increasing surface area for vessel coverage. The more loosely wound portion provides a gradual transition to the more tightly wound portion as well as a means for more easily deploying thepseudo-braided device50 when it is released from a catheter.
• FIG. 18 additionally depicts awavy midsection98 which is contemplated for use in also increasing coverage when the pseudo-braided device is deployed within a vessel. The waves can generally resemble a sinusoidal path and can also take on an undulating serpentine pattern.Such waves98 can alternatively extend the length of the filament thereby providing the pseudo-braided device with increased coverage throughout its length. Such waveforms are created by threading the filament through a mesh setting shape then again wrapping the filament about a mandrel again setting the shape.
• It has also been recognized that the waveforms like those shown inFIG. 18 can be spanned with a highly elastic material for the purpose of again improving coverage. As with the closely wound filament embodiment, the waves can additionally improve anchoring capabilities by enhancing in a circumferential direction, the traction between the vessel wall and thepseudo-braided device50.
• Thepseudo-braided device50 of the present invention has applications in a number of areas including operating as an aneurysm cover, in conjunction with thrombotic and artherotic stenosis therapy, as an embolic protector, as a thrombectomy device and in embolic therapy. As stated, due to its high expansion ratio and superior flexibility, thepseudo-braided device50 can be placed within vasculature and advanced deep within the patient's anatomy to a repair site. Once there, thepseudo-braided device50 can be deployed within highly tortuous vascular for the purpose of addressing the particular malady effecting the vessel. As shown inFIGS. 19 and 20, thepseudo-braided device50 of the present invention can be advanced within ablood vessel100 using adelivery catheter102. Due to the ability to reduce thepseudo-braided device50 to less than 10 percent of the expanded diameter, microcatheters can be utilized for this purpose. In a preferred embodiment, the delivery catheter is contemplated to include or cooperate with apusher103 that operates to facilitate relative movement between thepseudo-braided device50 and thedelivery catheter102.
• In an alternate configuration (SeeFIG. 21), a compressed stent has a lumen that astandard guidewire201 can freely pass through. This allows improved access. When ready, theguidewire201 can be withdrawn and replaced with the push wire200 or theguidewire201 can have a proximally placed pushingring202 that accomplishes the ejection of the pseudo-braided device from thedelivery catheter102.
• Upon advancing thedelivery catheter102 to arepair site104, the pseudo-braided device is deployed from adistal end106 of the delivery catheter102 (FIG. 20). It is contemplated that any number of conventional means may be employed to eject the pseudo-braided device from thedelivery catheter102, including but not limited to a pusher device (not shown) configured coaxially within thedelivery catheter102 which operates to engage aproximal end58 of thepseudo-braided device50 while withdrawing thedelivery catheter102 proximally.
• As stated, thepseudo-braided device50 of the present invention is also particularly suited to operate as an aneurysm cover. As shown in the figures, thepseudo-braided device50 can be deployed to overlay anopening108 to ananeurysm110 formed in a sidewall of a vessel. By being so positioned, thepseudo-braided device50 can redirect flow from entering the aneurysm, become covered with endothelium cells and seal off the opening into the aneurysm, or retainembolic coils112 or other thrombus producing materials inserted in theaneurysm sack110. It is to be noted that it is preferred to implace thepseudo-braided device50 prior to embolic material as the same prevents prolapse of material into the parent vessel.
• Using similar methods, thepseudo-braided device50 of the present invention could additionally be employed to repair thrombotic or artherotic stenoses14 found in a blood vessel100 (SeeFIGS. 22 and 23). Due to its high expansion ratio and enhanced radial strength (i.e., hoop strength), thepseudo-braided device50 can be deployed across thestenosis114 and be allowed to self-expand to thereby press the thrombotic or artherotic material forming the stenoses against the walls of thevessel100. By doing so, the pseudo-braided device operates to hold open and enlarge thevessel100 at the repair site.
• By reconfiguring the basic structure of thepseudo-braided device50, as previously mentioned, the advantages provided by the present invention can be used to address other maladies effecting vessels. More specifically, thepseudo-braided device50 can be reconfigured as anembolic protection device120. With reference toFIGS. 24 and 25, asuperior end portion122 of the contemplated embolic protection devices can be necked down so as to form a generally conical profile. Such necking could be accomplished by way of altering the manufacturing process or thesuperior end122 of the pseudo-braided structure can simply be restrained to a relatively smaller cross-sectional profile by way of adhesion or mechanical devices. It is contemplated that thesuperior end120 of theembolic protection device120 be affixed by conventional means to anelongate member124 that is positionable within a delivery catheter similar to that depicted inFIGS. 19-23. Theinferior end126 of theembolic protection device120, in its expanded form, provides a generally circular, cross-sectional profile, opening for receiving blood flow.
• In one embodiment of the embolic protection device120 (FIG. 25), a plurality of proximally extending filaments orwire loops128 are routed about portions of the filament defining theinferior end126 of theembolic protection device120. Proximal ends129 of the loops can be affixed to a collar that is intended to slide along theelongate member124. Independent control of the collar is also contemplated such that a separate actuator (not shown) which extends to the operator can be supplied to manipulate the position of the collar along theelongate member124. In either case, theloops128 are provided in the event additional control of the opening and closing of theembolic protection device120 is desired.
• Upon advancing theembolic protection device122 to a desirable location within a patient's vasculature, theelongate member124 is held stationary while the delivery catheter (not shown) is withdrawn proximally. Theinferior end portion26 and atubular midsection130 of theembolic protection device122 are then permitted to self-expand against the walls of the vessel into which the device is deployed. The fully openedembolic protection device120 permits blood to flow into its interior and through its pseudo-braided walls but acts as a barrier to emboli passing through the blood. That is, emboli entering theembolic protection device120 are captured by its pseudo-braided structure. The captured emboli can thereafter be removed from the patient's vasculature when theembolic protection device120 is removed or other conventional means such as suction devices can be employed to remove the emboli.
• Turning now toFIGS. 26-28, there are shown various embodiments of the present invention configured asthrombectomy devices148.Such thrombectomy devices148 can be advanced and deployed within a patient's vasculature using the delivery catheter depicted inFIGS. 19-23. With specific reference toFIG. 26, the pseudo-braided device of the present invention can be attached at itsends140,142 by way ofcollars144 to anelongate member146 to thereby form one embodiment of athrombectomy device148. Upon deployment and expansion within a target vessel, thethrombectomy device assembly148 provides a mid-section150 that is well-suited for engaging and, upon rotation of the device, shearing thrombus from a vessel wall. In order to facilitate self-expansion, onecollar144 is permitted to slide along theelongate member146, while the other collar is longitudinally fixed thereto.
• As shown inFIGS. 27 and 28, thethrombectomy devices148 may also embody pseudo-braided portions of varied density. For example, the more denselypseudo-braided midsection152 of the device depicted inFIG. 27 is particularly suited for accomplishing the thrombectomy whereas its less densely pseudo-braidedsuperior end portion154 is intended for capture of emboli. Thethrombectomy device148 ofFIG. 28 embodies a less densely pseudo-braided midsection contemplated for macerating a thrombus adhering to a blood vessel wall whereas itssuperior end portion160, being more densely pseudo-braided, is configured for removal and capture of emboli.
• Thepseudo-braided device50 of the present invention can also be closed at each of its ends to form an expandable spherical shape that is suited as anembolic therapy device170. With reference toFIG. 29, such an embolic therapy device can be advanced within a vessel using adelivery catheter102. Theembolic therapy device170 can then be deployed within ananeurysm sack110 and permitted to self-expand to thereby facilitate thrombus formation. Aconventional releasable connection172 to an elongatedelivery assembly sub-component174 is contemplated so that theembolic therapy device170 can remain in theaneurysm110 when the delivery assembly is removed from the patient.
• In view of the foregoing, it is clear that the pseudo-braided device of the present invention is useful in numerous of applications. Moreover, due to its high expansion ratio and flexibility, the pseudo-braided device of the present invention can be employed to repair very distal as well as tortuous portions of a patient's vasculature.
• It will be apparent from the foregoing that, while particular forms of the invention have been illustrated and described, various modifications can be made without departing from the spirit and scope of the invention. Accordingly, it is not intended that the invention be limited, except as by the appended claims.

Claims (12)

1-42. (canceled)

43. A method involving employing a device for use in embolic therapy within vasculature having an opening to an aneurysm sac, comprising:

gaining access to vasculature;

placing thrombus producing materials within the aneurysm sac; and

placing a device including an elongate filament configured into a pseudo-braided pattern and formed to define a generally tubular body with a first end and a second end into the vasculature to cover the opening to the aneurysm sac.

44. The method ofclaim 43, wherein each of the first and second ends are defined by a plurality of endless reversals of direction.

45. The method ofclaim 43, wherein at least one of said plurality of reversals embody loops having a variable radius of curvature.

46. The method ofclaim 43, wherein said pseudo-braided pattern is uniform along a length of said tubular body.

47. The method ofclaim 43, wherein the thrombus producing material includes embolic coils.

48. The method ofclaim 43, further including:

placing the device into a microcatheter;

advancing the microcatheter into the vasculature; and

ejecting the device into the vasculature.

49. The method ofclaim 43, wherein the device can be reduced to less than 10 percent of its expanded diameter.

50. The method ofclaim 43, wherein said device can be delivered into a patient's vasculature by a microcatheter.

51. The method ofclaim 43, wherein the device is self-expanding.

52. The method ofclaim 43, wherein at least some of the thrombus producing materials are self-expanding.

53. The method ofclaim 43, wherein the device is implanted into the vasculature before the thrombus producing materials are placed into the aneurysm sac.

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