US20070016233A1 - Vasoocclusive device for treatment of aneurysms - Google Patents

Abstract

The three-dimensional device is adapted to be inserted into a portion of a vasculature for occluding the portion of the vasculature for use in interventional therapy and vascular surgery. The device is formed from a multi-stranded micro-cable having a plurality of flexible strands of a shape memory material and at least one radiopaque strand. The flexible strands in a multi-stranded micro-cable of the device can be helically wound, or can be configured as parallel, longitudinal strands, and can also be formed to have a secondary, three-dimensional therapeutic configuration, such as helical, conical, spherical, or other geometric shapes. The strands can be made of a shape memory nickel titanium alloy, that is highly flexible at a temperature appropriate for introduction into the body via a catheter, and that after placement will take on the therapeutic shape. The device can also include a therapeutic agent, and can be bundled by an outer cover to constrain the strands of the micro-cable about a longitudinal axis to produce a composite banded cable. The radiopaque strand can have a core strand with a plurality of intermittently spaced apart enlarged radiopaque portions that may be a plurality of beads of radiopaque material spaced apart and mounted on the core strand, or a plurality of coils intermittently wound about and spaced apart on the core strand. A polyhedral occlusive device is also provided, adapted to be inserted into a portion of a vasculature for occluding a portion of the vasculature, for use in interventional therapy and vascular surgery. One or more therapeutic fibers can also be woven into the coil to enhance treatment of the side after placement of the device.

Description

RELATED APPLICATIONS
• This is a continuation-in-part of Ser. No. 09/019,841 filed Feb. 6, 1998, which was a continuation-in-part of Ser. No. 08/986,004 filed Dec. 5, 1997.
BACKGROUND OF THE INVENTION
• 1. Field of the Invention
• This invention relates generally to implantable devices for interventional therapeutic treatment or vascular surgery, and concerns a stranded micro-cable with enhanced radiopacity that can be used to fabricate a vascular device, a stent, a guidewire or the like. More particularly, the invention relates to three dimensional microcoil vasoocclusive devices fabricated from stranded micro-cable.
• 2. Description of Related Art
• The art and science of interventional therapy and surgery has continually progressed towards treatment of internal defects and diseases by use of ever smaller incisions or access through the vasculature or body openings, in order to reduce the trauma to tissue surrounding the treatment site. One important aspect of such treatments involves the use of catheters to place therapeutic devices at a treatment site by access through the vasculature. Examples of such procedures include transluminal angioplasty, placement of stents to reinforce the walls of a blood vessel or the like and the use of vasoocclusive devices to treat defects in the vasculature. There is a constant drive by those practicing in the art to develop new and more capable systems for such applications. When coupled with developments in biological treatment capabilities, there is an expanding need for technologies that enhance the performance of interventional therapeutic devices and systems.
• One specific field of interventional therapy that has been able to advantageously use recent developments in technology is the treatment of neurovascular defects. More specifically, as smaller and more capable structures and materials have been developed, treatment of vascular defects in the human brain which were previously untreatable or represented unacceptable risks via conventional surgery have become amenable to treatment. One type of non-surgical therapy that has become advantageous for the treatment of defects in the neurovasculature has been the placement by way of a catheter of vasoocclusive devices in a damaged portion of a vein or artery.
• Vasoocclusion devices are therapeutic devices that are placed within the vasculature of the human body, typically via a catheter, either to block the flow of blood through a vessel making up that portion of the vasculature through the formation of an embolus or to form such an embolus within an aneurysm stemming from the vessel. The vasoocclusive devices can take a variety of configurations, and are generally formed of one or more elements that are larger in the deployed configuration than when they are within the delivery catheter prior to placement. One widely used vasoocclusive device is a helical wire coil having a deployed configuration which may be dimensioned to engage the walls of the vessels. One anatomically shaped vasoocclusive device that forms itself into a shape of an anatomical cavity such as an aneurysm and is made of a pre-formed strand of flexible material that can be a nickel-titanium alloy is known from U.S. Pat. No. 5,645,558, which is specifically incorporated by reference herein. That vasoocclusive device comprises one or more vasoocclusive members wound to form a generally spherical or ovoid shape in a relaxed state. The vasoocclusive members can be a helically wound coil or a co-woven braid formed of a biocompatible material, and the device is sized and shaped to fit within a vascular cavity or vesicle, such as for treatment of an aneurysm or fistula. The vasoocclusive member can be first helically wound or braided in a generally linear fashion, and is then wound around an appropriately shaped mandrel or form, and heat treated to retain the shape after removal from the heating form. Radiopacity can be provided in the vasoocclusive members by weaving in synthetic or natural fibers filled with powdered radiopaque material, such as powdered tantalum, powdered tungsten, powdered bismuth oxide or powdered barium sulfate, which can potentially be released during vascular surgery.
• Another occlusion device for closing defects in vascular walls is known that is formed by a pair of distinct sections of varying configuration, which may be parabolic or conical bodies oriented to flare outward. Yet another implantable vasoocclusive device is known that is formed by a complex, helically wound coil adapted to take on a secondary shape suitable for snugly fitting within a given vascular cavity upon deployment, that can be formed by winding the coil on a mandrel having radially extending poles.
• The delivery of such vasoocclusive devices can be accomplished by a variety of means, including via a catheter in which the device is pushed through the catheter by a pusher to deploy the device. The vasoocclusive devices, which can have a primary shape of a coil of wire that is then formed into a more complex secondary shape, can be produced in such a way that they will pass through the lumen of a catheter in a linear shape and take on a complex shape as originally formed after being deployed into the area of interest, such as an aneurysm. A variety of detachment mechanisms to release the device from a pusher have been developed and are known in the art.
• For treatment of areas of the small diameter vasculature such as a small artery or vein in the brain, for example, and for treatment of aneurysms and the like, micro-coils formed of very small diameter wire are used in order to restrict, reinforce, or to occlude such small diameter areas of the vasculature. A variety of materials have been suggested for use in such micro-coils, including nickel-titanium alloys, copper, stainless steel, platinum, tungsten, various plastics or the like, each of which offers certain benefits in various applications. Nickel-titanium alloys are particularly advantageous for the fabrication of such micro coils, in that they can have super-elastic or shape memory properties, and thus can be manufactured to easily fit into a linear portion of a catheter, but attain their originally formed, more complex shape when deployed. Although various materials are more or less kink resistant when nickel-titanium alloys are dimensioned into wire smaller than approximately 0.010 inches in diameter, they can have low yield strength and can kink more easily, thus severely limiting the applications for such finely drawn wire in the fabrication of vasoocclusive devices. As a further limitation to such applications, nickel-titanium alloys are also not radiopaque in small diameters, and a single nickel-titanium wire would need to be approximately 0.012 inches in diameter to be even slightly radiopaque. However, such a thickness of a single nickel-titanium wire would unfortunately also be relatively stiff and possibly traumatic to the placement site, particularly if used for treatment of delicate and already damaged areas of the small diameter vasculature such as an aneurysm in an artery or vein in the brain, for example.
• One conventional guidewire for use in a catheter is known that is made of a high elasticity nickel-titanium alloy, and is useful for accessing peripheral or soft tissue targets. The distal tip of the guidewire is provided with a radiopaque flexible coil tip, and a radiopaque end cap is attached to the guidewire by a radiopaque ribbon. Such a construction is complex to manufacture, fragile and can potentially break off during use with undesirable results. A stretch resistant vasoocclusive coil is also known that can be made of a primary helically wound coil of platinum wire, with a stretch-resisting wire attached within the primary coil between two end caps. Unfortunately, such a construction is relatively difficult to fabricate and also fragile, allowing for the possibility of the fracture of the central radiopaque wire, the coil, the welds or some combination of them, and it can also potentially break off during use. Also, such a construction has a complex and nonlinear bending characteristic, dependent on the spacing of the coils and central wire and the radius of the bend of the coil.
• From the above, it can be seen that vasoocclusive devices and their attendant deployment systems provide important improvements in the treatment of damaged neurovascular areas. However, there remain important limitations in the technology presently available to fabricate these devices. It would therefore be desirable to provide a structural element that can be incorporated into a stent, guidewire, micro-coil or the like, which offers the advantages of a shape memory alloy such as a nickel-titanium alloy, and that incorporates radiopaque material in a stable configuration that is not subject to breaking during use of the device, so that the device can be visualized under fluoroscopy. It would also be desirable to be able to create a variety of three dimensional vasoocclusive shapes that can be deployed from a catheter into an aneurysm or other defect and to thereby provide an efficient therapy for treatment of the defect. The present invention meets these and other needs.
SUMMARY OF THE INVENTION
• Significant advances have been made in the treatment of neurovascular defects without resolution to surgery. More specifically, micro catheters have been developed which allow the placement of vasoocclusive devices in an area of the vasculature which has been damaged. In presently used techniques, the vasoocclusive devices take the form of spiral wound wires that can take more complex three dimensional shapes as they are inserted into the area to be treated. By using materials that are highly flexible, or even super-elastic and relatively small in diameter, the wires can be installed in a micro-catheter in a relatively linear configuration and assume a more complex shape as it is forced from the distal end of the catheter.
• In order to gain the advantages presently being realized with micro-catheter therapies and procedures to repair damage to the vasculature in the brain and other vessels, shape memory materials such as nickel-titanium alloys have been incorporated in vasoocclusive devices to be placed by the catheters. However, the range of diameters of wire and the configurations of the resulting geometry ofboth the coils and the devices developed which can be used have been limited by both the relatively small diameter of wire that must be used to avoid trauma and allow housing within the catheter prior to deployment, and the requirement for larger diameters to provide for radiopaque markers and mechanical robustness. In many cases this has resulted in primary wire characteristics in the coil that are unacceptably stiff, very delicate, or subject to kinking. The present invention obtains significant advantages over such prior art devices by providing a cable of multiple strands of an alloy adapted to be used in catheters, stents, vasoocclusive devices, guidewires and the like, thus providing a kink resistant, high strength material with highly desirable performance characteristics which can be altered by construction details to suit a variety of interventional therapeutic procedures.
• More specifically, it has been found that single strands of small diameter nickel-titanium alloys, as well as other metal alloys, used to form vasoocclusive devices can be kinked if twisted and pulled as can occur during or after deployment from a catheter, especially if the doctor wishes to withdraw a partially deployed coil because it is somehow incorrect in size, shape or length to repair the damage to the vessel. Also, single wire coils are more likely to cause trauma to the area to be treated if the wire is of a sufficient diameter to provide adequate tensile strength. Furthermore, such small diameter wires of some of these materials such as nickel-titanium, stainless steel and the like, are not generally radiopaque with currently available equipment, necessitating the use of radiopaque markers attached to the device, with the resultant possible diminution of functionality and increased diameter.
• The present invention solves these and other problems by providing, in its broadest aspect, a micro-cable which includes at least one radiopaque strand to offer a continuous indication under fluoroscopy of the deployed configuration of the device incorporating the micro-cable. When combined with the benefits of a material such as nickel-titanium in the other strands of the micro-cable, numerous advantages are available from the use of this basic construction in interventional medicine.
• Briefly, and in general terms, a presently preferred embodiment of the present invention provides for a multi-stranded micro-cable made of a suitable material such as stainless steel or a nickel-titanium alloy, with the cable including at least one radiopaque strand, made of platinum, tungsten or gold, in order to serve as a marker during a procedure. The multi-stranded micro-cable can be configured into a stent, guidewire, micro-coil or the like used in micro-catheters, for example, to restrict, reinforce, or to occlude areas of the small diameter vasculature such as an artery or vein in the brain, for example, for treatment of aneurysms and the like.
• In one presently preferred embodiment, the invention accordingly provides for a multi-stranded micro-cable formed of a plurality of flexible strands of a super elastic material, and at least one radiopaque strand. In one presently preferred embodiment, the multi-stranded micro-cable comprises a plurality of flexible strands of nickel-titanium alloy, the micro-cable having at least one central axially disposed radiopaque wire, such as platinum, tungsten or gold, for example, in order to provide a radiopaque marker during vascular procedures. In this preferred embodiment, the construction of the invention places the lowest tensile strength and highest flexibility member, the radiopaque marker strand, in a position in the cable which results in minimum stress on that member, at the same time, the super elastic material is in the outer strands, which have the dominant affect on performance parameters, thus enhancing the benefits of the material. Another benefit associated with the invention compared to prior art devices is that the multiple stranded cable configuration, in addition to providing a highly flexible and resilient structure, eliminates the necessity of a safety wire, since the failure of a single strand will not cause a severing of the cable. Also, the construction prevents stretching of the cable in the event of failure of a single strand, which is a significant benefit compared to constructions which have a coil around a central safety wire.
• In a second presently preferred embodiment, the invention includes a multi stranded cable constructed of multiple twisted strands of a suitable material such as a shape memory alloy or super elastic alloy of nickel-titanium, with one or more of the twisted strands consisting of a radiopaque material. The radiopaque strand may be one or more of the peripheral twisted strands and may also include one or more central strands of the cable. In a preferred aspect of the embodiment, the cable consists of six peripheral twisted strands and a central linear core strand, one or more of which can be of radiopaque material.
• In a third aspect of the invention, the cable can be of linear strands that are arranged in a bundle and fastened or bound at intervals, or continuously, in order to maintain contact among the strands as the cable is bent. One or more of the strands may be radiopaque. This construction is adaptable to guidewires and other structures that must be pushable and/or torqueable, but still remain highly flexible and include radiopacity. Variations on this embodiment can include an outer sheath which consists of a solid or helically wound cover to provide enhanced torqueability and pushability. More specifically, the outer sheath can vary in thickness, stiffness of material or spring of the sheath members to provide desired variations in bending or stiffness of the cable. Such a construction is particularly adaptable to guidewires and the like, and can be varied in terms of the binding or outer layer to alter the torqueability of the cable, and the flexibility of the cable can be varied along its length by the number and sizes of the stranded members in the cable.
• In a fourth aspect of the invention, one or more of the strands can be of a therapeutic material used to enhance treatment of the site after placement of the device. In one presently preferred embodiment of the invention, the cable includes twisted strands of wire around the periphery of the cable, at least one of which is radiopaque. The core of the cable contains a therapeutic agent such as human growth hormone, genetic material, antigens or the like that are intended to become active after placement. Such a construction can be adapted to a variety of interventional therapeutic treatments. In one aspect of this embodiment, one of the strands can have multiple functions, such as providing both a therapeutic effect and also contributing to the structural integrity of the cable. By using copper in such a micro-cable, for instance, the copper can enhance the use of a device made from the cable as an intra-uterine device, with the copper also contributing to the radiopacity and structural integrity of the micro-cable. In the event that such an effect is desired, the therapeutic strand can be placed on the exterior of the cable to enhance contact with the site to be treated.
• In a fifth aspect of the invention, a three dimensional occlusive device is provided that is adapted to be inserted into a portion of a vasculature for occluding the portion of the vasculature for use in interventional therapy and vascular surgery, that comprises at least one multi-stranded micro-cable having a plurality of flexible strands of a resilient material, with at least one radiopaque strand to provide a radiopaque marker of the deployed configuration of a device made of the cable during vascular surgery. The occlusive device is configured to have a primary, collapsed coil configuration or shape, and an expanded, or secondary three dimensional coil configuration or shape, that can be generally helical, conical, or spherical shapes. The flexible strands in a multi-stranded micro-cable of the occlusive device can be helically wound, or can be configured as parallel, longitudinal strands. In a currently preferred embodiment, at least one of the strands comprises a super-elastic material. In another currently preferred embodiment, a plurality of the strands comprises a super-elastic material. One presently preferred super-elastic material comprises a nickel titanium alloy, that can be heat treated such that the alloy is highly flexible at a temperature appropriate for introduction into the body via a catheter, and after placement, the device will seek its minimum energy shape as originally formed and thereby take on a shape designed to optimize the therapeutic purposes desired for the device.
• In another aspect of the invention, at least one of the strands comprises a shape memory material. In another currently preferred embodiment, a plurality of the strands are comprised of a shape memory material. One presently preferred shape memory material comprises a shape memory polymer. In one configuration, the strands of the micro-cable are arranged as exterior strands surrounding at least one interior strand, or core, and at least one radiopaque strand is disposed in the micro-cable, either centrally, axially disposed in the bundle of strands, or in the exterior strands surrounding the central core. The micro-cable can include a plurality of radiopaque strands, such as platinum, gold, or tungsten.
• In the fifth aspect of the invention, at least one of the strands in the core or exterior strands can comprise a therapeutic agent, such as a copper or copper alloy wire or any of a variety of therapeutically active metals, alloys or components, a fiber such as Dacron (polyester), polyglycolic acid, polylactic acid, fluoropolymers, nylon, polyaramid fiber (e.g. Kevlar®), or silk chosen for thrombogenicity. Since the micro-cable consists of stranded parts, one or more strands may be longer than others, or even intermittently terminated, to thereby extend beyond the diameter of the remaining strands and thereby increase the therapeutic effect of that strand. Alternatively, at least one of the strands can be coated with or impregnated with a therapeutic material, which can include, but is not limited to, any one or combination of human growth hormone, genetic material, antigens, hydrogels, collagen, bio-absorbable polymers such as lactic acids/glycolic acids, caprolactam or microcellular foam. In addition, the therapeutic element can comprise a means to conduct energy, such as an optical fiber to conduct light energy.
• In the fifth aspect of the invention, the strands of the micro-cable can also be bundled by at least one outer cover or sheath to constrain the strands of the micro-cable about a longitudinal axis to produce a composite banded cable. The outer sheath can comprise a containment strand wound about the strands and made of a low friction material, such as a fluoropolymer, for example, or a heat shrinkable plastic tube. In one feature of the fifth aspect of the invention, a plurality of heat shrink plastic covers are placed over the strands of the micro-cable to provide bending stiffness in the cable. The strands of the micro-cable can be banded at intervals by a plurality of bands. In another variation, a plurality of micro-cables that are arranged as parallel, longitudinal micro-cables or a helically wound micro-cables to form a composite cable can have an exterior wrapped cover that can be wound at greater or lesser intervals along the outside to provide variations in the torqueability and stiffness of the composite cable. Also, the thickness and width of the wrapping cover, as well as its material composition along the composite cable can vary in cross section along the length of the composite cable to provide bending stiffness of said cable which varies with the position on said cable. Also, the number of strands and the degree to which they extend along the composite cable can be varied within the sheath, and the outer sheath itself can be multi-layered with different materials in order to provide a graduated bending and stiffness characteristic over the length of the cable. The occlusive device thus can be formed of a plurality of micro-cables in order to provide desired bending and strength characteristics, either as helically wound micro-cables, or parallel longitudinal micro-cables having a collapsed composite cable configuration and an expanded composite cable configuration with a secondary shape. In another feature of the fifth aspect of the invention, the composite cable can further comprise at least one longitudinal sensing element for sensing a parameter, such as an optical imaging element, i.e., where the sensing element can comprises an optical fiber. Alternatively, the sensing element can comprise a thermal imaging element, or an ultrasound imaging element, for example.
• In a further aspect of the invention, the form about which the three dimensional shape is wound is formed from metal, ceramic or other heat resistant material and has formed within it the path desired for the micro-cable corresponding to the shape. For example, the form can be of a spherical configuration, with the surface containing channels into which the cable is laid prior to heat treating. The channels can be arranged so that the resultant shape is kink resistant and relatively easy to withdraw without kinking. The form can also contain passages through which the cable can pass to advantageously form the shape.
• After the cable is wound around the form, the form and cable can be heat treated to cause the cable material to adopt the shape of the form as a low energy shape. The cable can then be removed from the form and put into a catheter-introducer prior to use in intravascular therapy.
• In another presently preferred embodiment, the invention comprises a device for use in interventional therapy and vascular surgery, adapted to be inserted into a portion of a vasculature, comprising a shape memory coil having an outer coil portion and an inner core portion, the shape memory coil having a collapsed primary coil configuration and an expanded secondary configuration with a three dimensional shape; and a radiopaque strand extending through the core of the shape memory coil to provide a radiopaque marker of the deployed configuration of the device. In one presently preferred embodiment, the shape memory coil comprises a multi-stranded coil having a plurality of flexible strands of a resilient material, and in an alternate preferred embodiment, the shape memory coil comprises a single stranded coil, such as of a nickel titanium alloy, or a shape memory polymer, for example. The radiopaque strand enhances the radiopacity of a multi-stranded coil as well as a single stranded coil of pure nickel titanium alloy, which will advantageously not fray upon stretching, and is stretch resistant. With such an inner radiopaque strand, the coil can also be made of other materials, such as a shape memory polymer such as polyurethane, for example.
• In a presently preferred embodiment, the radiopaque strand comprises a core strand having a plurality of intermittently spaced apart enlarged radiopaque portions that can comprise a radiopaque material selected from the group consisting of platinum and gold, for example. The core strand can comprise a material selected from the group consisting of platinum, gold, a shape memory polymer having a glass transition temperature (T_g) below 25° C., a hydrogel, an amorphous gel, and a fiber. In one presently preferred aspect, the enlarged radiopaque portions can comprise a plurality of beads of radiopaque material spaced apart and mounted on a core strand of material, and the beads may comprise a radiopaque material selected from the group consisting of platinum, gold and tungsten. In another presently preferred aspect, one or more of the plurality of beads can optionally be bonded to a segment of the shape memory coil, such as an end bead bonded to an end segment of the shape memory coil, for example.
• In another presently preferred aspect, the enlarged radiopaque portions may comprise a plurality of coils intermittently wound about and spaced apart on the core strand, and the core strand can comprise a radiopaque material selected from the group consisting of platinum and gold. The spaced apart coils can comprise a radiopaque material selected from the group consisting of platinum and gold.
• In another presently preferred embodiment, a polyhedral occlusive device is provided, adapted to be inserted into a portion of a vasculature for occluding a portion of the vasculature, for use in interventional therapy and vascular surgery. The occlusive device can be formed with multiple coils centrally connected together at their inner ends to a central coil body and radiating outward from the central coil body. When inserted within a vessel at a treatment site, such as within an aneurysm, the radiating coil arms of the occlusive device extend to fill the vessel in three dimensions, allowing the occlusive device to accommodate the shape of the vessel.
• In another presently preferred embodiment, the device for use in interventional therapy and vascular surgery includes a micro-cable or coil formed of one or more flexible strands of a resilient material, having a collapsed primary coil configuration and an expanded secondary configuration with a three dimensional shape; and one or more therapeutic fibers woven into the coil to enhance treatment of the site after placement of the device. The coil can also be formed to include one or more radiopaque strands to provide a radiopaque marker of the deployed configuration of the device. The one or more therapeutic fibers can be woven about adjacent or non-adjacent loops of the coil, or can be woven through multiple strands of adjacent loops of the coil. The one or more therapeutic fibers are made of a material that will provide a timed release of a therapeutic agent intended to become active after placement of the device, such as human growth hormone, collagen, a modified polymer with growth factor, genetic material for gene therapy, antigens, or the like. A plurality of therapeutic fibers can be provided so that the different fibers in the coil can provide different therapeutic agents to provide a range of therapies.
• These and other aspects and advantages of the invention will become apparent from the following detailed description and the accompanying drawings, which illustrate by way of example the features of the invention.
BRIEF DESCRIPTION OF THE DRAWINGS
• FIG. 1 is a perspective of a radiopaque microstrand cable constructed according to the invention.
• FIG. 2 is a cross-section at2-2 ofFIG. 1.
• FIG. 3 is a helical vasoocclusive coil formed of the cable of the invention.
• FIG. 4 is a spherical vasoocclusive structure formed using the cable of the invention.
• FIG. 5 is a stacked coil vasoocclusive device formed using the cable of the invention.
• FIG. 6 is a cross section of a vascular member with an aneurysm illustrating the approach of a vasoocclusive coil towards the aneurysm.
• FIG. 7 is an illustration of a vasoocclusive coil which has been introduced into an aneurysm preparatory to being deployed within the aneurysm.
• FIG. 8 is an illustration of a spherical vasoocclusive coil formed with cable of the invention deployed within an aneurysm.
• FIG. 9 is an alternate in a preferred embodiment of the invention including a plurality of radiopaque strands within the cable.
• FIG. 10 is an alternate preferred embodiment incorporating a therapeutic member within the radiopaque cable of the invention.
• FIG. 11 is an alternate preferred embodiment of the present invention wherein strands of the cable are arranged within an exterior binding consisting of multiple straps about the cable.
• FIG. 12 is a perspective view of the embodiment ofFIG. 11.
• FIG. 13 is an alternative embodiment to the embodiment ofFIG. 12 wherein the external binding of the cable represents a sheath wound about the cable.
• FIGS. 14aand14bare perspectives of alternative embodiments of the embodiment ofFIG. 13.
• FIG. 15 is a cross-section of an alternative embodiment in which a plurality of multi-strand cables are included within an external sheath surrounding the cable.
• FIG. 16 is a perspective view of the embodiment ofFIG. 14.
• FIG. 17 is a plan view of a beaded radiopaque strand according to another preferred embodiment of the invention.
• FIG. 18 is a sectional view of the beaded radiopaque strand ofFIG. 17 inserted in a shape memory coil.
• FIG. 19 is a plan view of an alternate preferred embodiment of a radiopaque strand with intermittent spaced apart coils.
• FIG. 20 is a plan view of an alternate preferred embodiment of the radiopaque strand having spaced apart enlarged radiopaque portions.
• FIG. 21 is a schematic diagram of a preferred three dimensional radiating coil configuration of a primary wind polyhedral occlusion device according to the principles of the invention.
• FIG. 22 is a schematic diagram of an alternate preferred embodiment of a primary wind polyhedral occlusive device according to the principles of the invention.
• FIG. 23 is a perspective view of a mandrel for forming the polyhedral occlusive device ofFIG. 22.
• FIG. 24 is a schematic diagram of an alternate preferred embodiment of a secondary wind polyhedral occlusive device according to the principles of the invention.
• FIG. 25 is a perspective view of another preferred alternate embodiment of a helical vasoocclusive coil according to the principles of the invention, with a therapeutic fiber woven around adjacent loops of the coil.
• FIG. 26 is a perspective view of another preferred alternate embodiment of a helical vasoocclusive coil according to the principles of the invention, with a plurality of therapeutic fibers woven around adjacent loops of the coil.
• FIG. 27 is a perspective view of another preferred alternate embodiment of a helical multi-stranded vasoocclusive coil according to the principles of the invention, with a therapeutic fiber woven through strands of adjacent loops of a multi-stranded coil.
• FIG. 28 is a perspective view of another preferred alternate embodiment of a helical multi-stranded vasoocclusive coil according to the principles of the invention, with a plurality of therapeutic fibers woven through strands of adjacent loops of a multi-stranded coil.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
• While nickel-titanium alloys are useful in forming super-elastic or shape memory interventional devices, micro-coils formed of very small diameter wires of nickel-titanium alloy material for treatment of areas of the small diameter vasculature such as an artery or vein in the brain, for treatment of aneurysms and the like, for example, can have relatively low yield strengths and are somewhat subject to kinking, even if made of super-elastic alloy. This can create problems if the coil is to be withdrawn after being emplaced by the doctor, as for instance, if the device is too small to effectively fill the cavity to be treated. Furthermore, even solid wires of a size suitable for use in interventional devices are not very radiopaque.
• As is illustrated in the drawings, which are provided for the purposes of illustration and not by way of limitation, the invention is embodied in a multi-stranded micro-cable formed of a plurality of flexible strands of a resilient material with the cable including at least one radiopaque strand. In a presently preferred embodiment of the invention illustrated inFIG. 1, the multi-stranded micro-cable10 is approximately from 0.0015 to 0.009 inches in diameter, and comprises a plurality offlexible strands12 of nickel-titanium alloy, with at least one centrally, axially disposedradiopaque wire14 which is approximately from 0.0005 to 0.003 inches in diameter. While the above stated diameters represent those presently known to be compatible with the invention, larger or smaller diameters may be useful for particular applications. The centralradiopaque wire14 can be formed of platinum or gold, for example, or other similar suitable radiopaque metals, in order to provide a radiopaque marker of the deployed configuration of a device made of the cable during vascular surgery.
• There are numerous benefits to the novel construction of the invention for use in interventional devices and the like. By using the stranded or micro-cable construction of the invention, a device made from the micro-cable becomes virtually kink resistant compared to the single strand wires now commonly used in micro-coils. The multi-strand cable construction of the invention allows the micro-wires of the cable to slip across each other and reinforce each other rather than break or take a set. Also, by incorporating a stranded radiopaque material such as platinum, tungsten or gold into the cable construction, the device is radiopaque in sizes much smaller than with other constructions. The micro-cable construction of the invention can be used to produce soft, kink resistant, radiopaque stents, guidewires, guidewire distal tips, and micro-coils.
• FIG. 2 is a cross-section of the micro-cable ofFIG. 1 at2-2 illustrating one presently preferred arrangement of the strands within the cable. In this embodiment, theexterior strands12 are formed of a resilient material chosen to provide the characteristics desired for a specific application in interventional therapies. In a presently preferred embodiment, this material is a nickel titanium super-elastic alloy which is heat treated such that the alloy is highly flexible at a temperature appropriate for introduction into the body via a catheter. By choosing such a material for micro-coils and the like, the devices formed from the micro-cable can be relatively easily placed into the appropriate body cavity and after placement, the device will take on a shape designed to optimize the therapeutic purposes desired for the device. As illustrated inFIG. 2, such a cable can have acentral core14 of a radiopaque material such as gold or platinum, thus dramatically enhancing the radiopacity of the cable. Even a solid super-elastic wire of the same diameter as the cable would have substantially less radiopacity than the cable of the invention with the central gold or platinum wire and the construction of the invention provides numerous other highly desirable characteristics. Among these characteristics is the relative flexibility and resistance to kinking of the cable compared to an equivalent single wire and substantially greater accommodation of the cable to bending, etc., with resultant lessening of trauma to the surrounding tissue and ease of placement in a small body cavity.
• One advantageous application of the invention is to vasoocclusive devices formed of the micro-cable for insertion into aneurysms and other vascular defects for the purpose of occluding flow to the aneurysm.FIG. 3 illustrates ahelically wound coil16 of micro-cable10 which is formed to fit within a micro-catheter for insertion into an area upon which a therapeutic procedure is to be performed. While a helical coil is illustrated, it will be appreciated that numerous other secondary shapes can be formed from the cable of the invention, as will be described further below. More specifically, as illustrated inFIG. 4, a three dimensional, essentially spherical,device18 can be formed of thecable10, (or even of a coil of the cable, if appropriate) at a temperature sufficient to heat treat the material and thereby create a memory of the desired shape. The device is then inserted into a catheter from which it may be deployed into an aneurysm or the like. The teachings of U.S. Pat. No. 5,645,558 describe the construction of such a device out of flexible wire and are incorporated by referenced herein.FIG. 5 illustrates acollapsed coil configuration20 for a vasoocclusive device which also can be formed from the cable of the invention and is used for the purposes of insertion into aneurysms and other defects that have relatively large entry necks compared to their internal volume.
• FIG. 6 is an illustration of acatheter22 using acoil16 as a vasoocclusive device made of the present invention and used for insertion into ananeurysm24 projecting laterally from ablood vessel26. Thecoil16 is contained within theouter housing28 of a micro-catheter that is used to house the coil prior to deployment. The end of thecatheter housing28 is introduced into theopening30 of theaneurism24 by use of a guide wire (note shown). Thereafter, thevasoocclusive coil16, and apusher32 are introduced into the catheter to provide for insertion of the vasoocclusive device into the aneurysm. In a presently preferred embodiment, thecoil16 formed of the cable of the invention is retained to anoptical fiber pusher32 which is attached to the coil by a collar of shapememory plastic material34 as described in co-pending application Ser. No. 08/986,004 the disclosure of which are incorporated herein by reference. As shown inFIG. 7, the coil is introduced into the aneurysm and is then pushed from the micro-catheter until it fills the cavity.
• Those skilled in the art will recognize that it is sometimes the case that the vasoocclusive device must be withdrawn after it is fully or partly inserted into the aneurysm. In such a case, there is a danger that the coil will be stretched beyond its elastic range or kink, or otherwise deform and make withdrawal difficult. Those skilled in the art will also recognize that it is sometimes advantageous to form vasoocclusive devices of secondary shapes which are based upon a basic configuration of a coil or the like. The present invention includes such applications within the scope of the invention. However, when vasoocclusive devices made of even super-elastic material are used, it is sometimes the case that the devices will be stretched or kinked when withdrawal is attempted. The cable of the present invention substantially reduces the probability that kinking or stretching beyond yield will occur in a given instance, while at the same time providing radiopacity not available with other constructions. Thus, the present invention represents an important forward step in the technology of interventional therapy.
• In one presently preferred embodiment, theshape memory collar34 is heated to a temperature which allows it to be shrunk ontocoil16. The collar is attached tooptical fiber pusher32 by an adhesive36 which retains high strength at temperatures beyond the shape memory material transition point. After insertion, and when the operator is satisfied that the device is properly deployed, light energy from a source of coherent light is introduced into the proximal end of the optical fiber (not shown) and propagated in thedistal end38 of the fiber to cause the shapememory material collar34 to return to its previous shape andrelease coil16. Those skilled in the art will recognize that the invention can also be used with a variety of other placement catheter systems, and it is not intended that the invention be limited to the placement concepts illustrated by way of example.
• Those skilled in the art will recognize that a number of shaped devices may be introduced into an area to be treated depending upon its geometry and the number of devices to be inserted.FIG. 8 illustrates an essentiallyspherical device18 which has been deployed into such an aneurysm but it will commonly be found that a device such as that shown would then be supplemented by a further coiled device inserted within the space inside the spherical device to completely occlude flow from the artery to the aneurysm.
• While one presently preferred implementation of the micro-cable of the invention has been illustrated, those skilled in the art will appreciate that other variations of the invention may have advantages for certain purposes.FIG. 9 is an example of onesuch construction40 in which radiopacity is more desirable than in other forms and for that reason a number ofradiopaque strands42, in this illustration four in number, are formed into the cable along with threeresilient material strands44. It will also be appreciated that a larger or smaller number of strands may be incorporated into a given cable and the cables may be formed of multiple cables in order to provide desired bending and strength characteristics. It will also be appreciated by those skilled in the art that the invention is adaptable to the use of a variety of materials which by themselves would not have been easily adaptable to micro devices for interventional therapies. For instance, materials such as copper are useful for intrauterine devices and the like, but copper wire, even when heavily alloyed, has certain limitations for use in such devices. By use of the present invention, composite cables incorporating one or more strands of a desired material can be configured with other strands providing strength, flexibility, shape memory, super-elasticity, radiopacity or the like for previously unavailable characteristics in micro devices.
• The invention is also adaptable to numerous other purposes.FIG. 10 illustrates a cross-section of a further preferred embodiment in whichradiopaque strands42 andresilient strands44 form a portion of the cable and atherapeutic agent48 is contained in one of the strands. Such a therapeutic agent can include human growth hormone, hydrogels, or a variety of other agents which will serve to provide desired therapeutic capabilities when placed within a specific area of the body being treated by use of the micro-catheter. Depending upon the application of the therapeutic agent, its method of action and the delay, if any, in the time after placement in which the therapeutic action is desired, the agent strand may be placed in any of a variety of positions with the cable, from core wire outward. Also, it may be desirable to coat one or more strands with a therapeutic material for certain purposes. Such constructions are contemplated within the scope of the invention.
• It is also contemplated within the scope of the invention that one or more of the strands of the micro-cable is longer than the others, and perhaps intermittently terminated, to thereby produce a micro-cable in which the therapeutic strands extend to a greater diameter than the other strands to thus increase the therapeutic effect of the therapeutic stand. Such a construction is particularly advantageous if increased thrombogenicity is desired, while maintaining structural continuity and radiopacity for the micro-cable.
• FIG. 11 illustrates a cross-section of an additional presently preferred embodiment of the invention in which thestrands12,14 of the micro-cable10 are bundled and banded at intervals bybands50 to produce a composite bandedcable52 in order to provide increased flexibility without unraveling or dislocation of the strands in the cable.FIG. 12 is a perspective view of the bandedcable50 of this embodiment. While the illustrated configuration shows the strands being laid parallel within the cable, it is also possible in this construction to include both twisted cables as theprimary cables10 within theouter bands50 to form thecomposite cable52. This configuration can use one or morelongitudinal strands14 which are radiopaque, thus providing a continuous indication of radiopacity within the cable. As a further alternative embodiment, it is possible for thelongitudinal cable52 to be formed of a singleinner cable10 withbands50.
• FIG. 13 illustrates a further embodiment of the invention in which longitudinal strands of cables are contained within awound cover56 for the purposes of providing a composite guide wire or the like58 having improved torqueability. Such a construction has particular advantages for guidewire designs having improved radiopacity in very small diameters. It will be appreciated that in this configuration, as well as the other longitudinally arranged multi-stranded cables, the number of strands and the degree to which they extend along the cable within the sheath is a variable which can be used to provide increased stiffness, pushability and torqueability in some sections with greater flexibility in others. Additionally, composite cables according to the invention can incorporate additional elements normally not available in solid guide wires, such as optical, thermal or ultrasound imaging elements, therapeutic agent delivery catheters, and can take advantage of materials which are not readily adaptable to prior art catheter or guide wire designs incorporating a primary wire structured element.FIGS. 14aand14billustrate a further variable available because of the invention; the exterior wrappedcover56 can be wound at greater orlesser intervals60 along the outside to provide variations in the torqueability and stiffness of the composite cable. Also, the thickness and width of the wrappingcover56, as well as its material composition along thecomposite guide wire58, can offer further capabilities for customizing the design for various applications. These advantages can be combined with the benefits of shape memory or super-elastic alloys to create guidewires and other devices with heretofore unavailable capabilities.
• FIG. 15 illustrates a cross-section of a micro-cable according to the invention which has at least one overall exterior sheath to contain the micro-cable. The micro-cable may be made of one or more multiple strand elements which may further include twisted or longitudinal strands within their construction. The sheath may also be used to control the torqueability characteristics of the cable and as discussed in co-pending application Ser. No. 08/986,004, the sheath may be multi-layered with different materials in order to provide a graduated bending and stiffness characteristic over the length of the cable.
• Referring to FIGS.17 to20, in another presently preferred embodiment, a nickel titanium alloy coil, such as the multi-stranded micro-cable described above, can be made radiopaque by the insertion of a radiopaque strand having spaced apart enlarged radiopaque portions into the core of a primary and/or secondary wind. The radiopaque material preferably has a desired degree of stiffness so as not to compromise the desired degree of softness of the coil. The material may comprise a beaded core of platinum, gold, shape memory polymer having a glass transition temperature (T_g) below 25° C., polymer, hydrogel, and the like, or a flexible strand, rod, amorphous gel, fiber, and the like. The radiopaque strand can be used to enhance the radiopacity of the multi-stranded coil, as indicated above, as well as a pure nickel titanium alloy coil, which will advantageously not fray upon stretching, and is stretch resistant. With such an inner radiopaque strand, the coil can also be made of other materials, such as a polyurethane shape memory polymer, for example.
• In a presently preferred embodiment illustrated inFIGS. 17 and 18, theradiopaque strand70 may comprise a plurality ofbeads72 of radiopaque material, such as platinum, gold or tungsten, spaced apart and mounted, such as by soldering, welding, or adhesive bonding such as by cyanoacrylate adhesive, on a core strand74 of material that can be platinum, gold or tungsten, or a shape memory polymer having a glass transition temperature (T_g) below 25° C. The beaded radiopaque strand can form the central core of a multi-stranded micro-cable, and as is shown inFIG. 18, the beadedradiopaque strand70 may form a core of a pure nickeltitanium alloy coil76 wound around the beaded radiopaque strand, and having aproximal stem77 bonded to the coil by soldering, welding, adhesive or the like, that can also be formed as a radiopaque marker, of such materials as platinum, gold or tungsten, for example. In a preferred aspect, one or more beads, such as anend bead78, may optionally be bonded to asegment80 of the coil, such as bycyanoacrylate adhesive81, for example.
• In another presently preferred embodiment illustrated inFIG. 19, the radiopaque strand can comprise aradiopaque wire82, such as platinum or gold, for example, intermittently wound with a plurality of spaced apart coils84 of radiopaque material, such as platinum or gold, for example, to form an inner radiopaque core for a multi-stranded micro-cable, or in an alternate preferred embodiment, the intermittently wound radiopaque strand may form a core of a pure nickel titanium alloy coil wound around the intermittently wound radiopaque strand.
• Referring toFIG. 20, in another presently preferred embodiment, the radiopaque strand can comprise aradiopaque wire86, such as platinum or gold, for example, with intermittently spaced apart enlargedradiopaque portions88, to form an inner radiopaque core for a multi-stranded micro-cable, or for a pure nickel titanium alloy coil wound around the radiopaque strand.
• It will be appreciated that a three dimensional occlusive device adapted to be inserted into a portion of a vasculature for occluding the portion of the vasculature for use in interventional therapy and vascular surgery, can be formed as described above, from at least one multi-stranded micro-cable having a plurality of flexible strands of a resilient material, with at least one radiopaque strand to provide a radiopaque marker for the device during vascular surgery. The occlusive device is configured to have a primary coil shape, as illustrated inFIG. 5, and an expanded secondary three dimensional coil configuration or shape, that can be generally helical, conical, or spherical shapes, such as the spherical shapes illustrated inFIGS. 4 and 8. A mandrel suitable for making such three dimensionally shaped occlusive devices can be formed of a refractory material, such as alumina or zirconia, for example. The mandrel typically has the general three dimensional shape that the occlusive device will be given, and can have a generally helical, conical, or spherical shape, or can have a unique shape designed to provide such a form to the occlusive device to fit a particular vascular structure to be treated. The mandrel forms a support for the winding and heat treatment of the micro-cable, plurality of microcables, or composite micro-cable occlusive device as described above, and ideally will not contaminate the occlusive device during heat treatment of the device. The surface of the mandrel preferably has a plurality of circumferential grooves for aligning the occlusive device as it is wound on the mandrel. The surface of the mandrel may also have one or more apertures for receiving one or more ends of the micro-cable, plurality of microcables, or composite micro-cable, to assist winding into the desired form.
• The wound occlusive device is then heat treated at a suitable temperature and a sufficient period of time to impart the form to the shape memory material included in the device. While heat treatment at a temperature of about 1100° F. for approximately 4 hours or more is typically sufficient to impart the form to the occlusive device when the shape memory material is a nickel titanium super-elastic alloy, but when the occlusive device includes fibers or a therapeutic agent that can be affected by heat, the temperature utilized can be substantially lowered, and the duration of heat treatment adjusted accordingly, as will be appreciated by those skilled in the art. Alternatively, if the therapeutic agent is not amenable to elevated temperatures, it may be added after formation of the three dimensional shape. After the heat treatment, the occlusive device is removed from the mandrel, and cold worked into the desired collapsed primary configuration for placement into a catheter or cannula for use. It will be appreciated that those techniques can also be used for a variety of cables produced according to the invention, including those which use shape memory materials other than nickel-titanium alloys. When the occlusive device reaches its destination in the vasculature during vascular therapy, it assumes the secondary relaxed and expanded three dimensional shape imparted from the heat treatment on the mandrel.
• In another presently preferred embodiment, a three dimensional, polyhedral occlusive device is provided, adapted to be inserted into a portion of a vasculature for occluding a portion of the vasculature, for use in interventional therapy and vascular surgery. The occlusive device can be formed as described above, from at least one multi-stranded micro-cable having a plurality of flexible strands of a resilient material, with at least one radiopaque strand to provide a radiopaque marker for the device during vascular surgery, with multiple coils, preferably four or more coils, centrally connected together at their inner ends, and in a presently preferred aspect, connected at their inner ends to a central coil body and radiating outward from the central coil body. When inserted with a vessel at a treatment site, such as within an aneurysm, the radiating coil arms of the occlusive device extend to fill the vessel in three dimensions, allowing the occlusive device to accommodate the shape of the vessel. In a preferred aspect, the radiating coils of the occlusive device can thus form a tetrahedral, pentahedral, hexahedral, or other polyhedral shape, symmetrical or unsymmetrical, and are preferably formed from conically shaped coil arms that have an expanding diameter as they radiate outward from the central coil body, with the radiating coil arms having soft larger diameter outer ends. The central coil body may be spherical or rounded, or may be correspondingly cubical, tetrahedral, pentahedral, or otherwise appropriately polyhedral. A typical aneurysm may have a diameter of approximately 10 mm., and the coil arms will also typically have an outer diameter of approximately 10 mm.
• As is illustrated inFIG. 21, one presently preferred three dimensionalradiating coil configuration90 is a primary wind coil having a hexahedral configuration with six conically shapedcoil arms92 radiating from acentral coil junction94 in the three x, y and z axes of a three dimensional pattern of coordinates. Such a three dimensional radiating coil configuration can be formed by individually winding the radiating arms of the hexahedral configuration on conically shaped mandrel, and bonding the inner apical ends96 of the coils together by welding, solder, adhesive such as cyanoacrylate, or the like. Acentral coil body98 such as the spherical coil described above is also preferably similarly bonded to the inner ends of the coil arms.
• Referring toFIG. 22, in another presently preferred embodiment, a three dimensional radiatinghexahedral coil configuration100 for the occlusive device is also a primary wind coil with six conically shaped coils orcoil arms102 radiating from a central coil ball or sphere104 in the three x, y and z axes forming a three dimensional pattern of coordinates. The central ball may also alternatively have the shape of a cube, for example. The outer diameter of the coil arms typically can be approximately 10 mm., and the diameter of the central coil ball or sphere typically can be 3 mm. in diameter. The hexahedral coil can be formed by winding the central spherical coil about a mandrel as described above and then joining the six radiating conical coil arms at their inner apical ends106 to the centralspherical coil108, as described above, such as by welding, solder, adhesive such as cyanoacrylate, or the like. Alternatively, the hexahedral coil configuration can be formed as a continuous primary wind of the coil by winding the central spherical coil, and forming the radiating arms by a double winding of the radiating conical coil arms, first up from the center and then back down, with each of the radiating conical coil arms being wound in turn about the central spherical at the appropriate location.
• Referring toFIG. 23, such a hexahedral configuration with six conically shaped coils radiating from a common central coil ball or sphere can be formed by winding the coils about amandrel110 formed of a refractory material, such as alumina or zirconia, for example, and having invertedconical coil arms112 radiating from acentral body114, such as a spherical, rounded, cubical, tetrahedral, pentahedral or otherwise polyhedral central body, for example. The mandrel forms a support for the winding and heat treatment of the three dimensional radiating hexahedral coil occlusive device as described above, and ideally will not contaminate the occlusive device during heat treatment of the device. The surface of the central body of the mandrel preferably has a plurality ofcircumferential grooves116 for aligning the occlusive device as it is wound on the mandrel. The surface of the mandrel may also have one ormore apertures118 for receiving one or more ends of the micro-cable, plurality of microcables, or composite micro-cable forming the hexahedral occlusive device, to assist winding into the desired form.
• In another configuration illustrated inFIG. 24, a another presently preferred alternate three dimensionalradiating coil configuration120 is a secondary wind coil of a primary wind coil, such as a helical wind, for example, the secondary wind coil having a hexahedral configuration with six conically shaped-coil arms122 radiating from the commoncentral coil124, which is illustrated as having a cubical shape, in the three x, y and z axes of a three dimensional pattern of coordinates. The outer diameter of the coil arms typically can be approximately 10 mm., and the diameter of the central coil ball or sphere typically can be 3 mm. in diameter. The hexahedral secondary wind configuration can be formed by winding the primary helical wind coil about an appropriate mandrel, and then joining the six radiating conical coil arms at their inner apical ends126 to the commoncentral coil128, as described above, such as by welding, solder, adhesive such as cyanoacrylate, or the like. Alternatively, the hexahedral coil configuration can be formed as a continuous primary wind of the coil by winding the central coil body, and forming the radiating arms by a double winding of the radiating conical coil arms, first up from the center and then back down, with each of the radiating conical coil arms being wound in turn about the central spherical at the appropriate location.
• As is described above, the tetrahedral, pentahedral, hexahedral or other polyhedral wound occlusive device radiating from the common central coil is then preferably heat treated upon the mandrel at a suitable temperature and for a sufficient period of time to impart the relaxed form to the shape memory material forming the device. The occlusive device can then be cold worked into a shape suitable for delivery through a catheter to a desired treatment site, and when the occlusive device reaches its destination in the vasculature during vascular therapy, it assumes the relaxed and expanded three dimensional shape imparted from the heat treatment on the mandrel.
• In another presently preferred embodiment illustrated inFIGS. 25 and 26, ahelical microcoil130 that can be formed of one or more flexible strands of nickel-titanium alloy, has one or moretherapeutic fibers136 advantageously woven about adjacent loops of the coil, used to enhance treatment of the site after placement of the device. The helical microcoil can also be formed to include one or more axially disposed radiopaque wires, as described above. Alternatively, the one or more therapeutic fibers can be woven about non-adjacent loops of the coil as well. The therapeutic fibers are preferably made of a material that will provide a timed release of a therapeutic agent, such as human growth hormone, collagen, a modified polymer with growth factor, genetic material for gene therapy, antigens or the like, that are intended to become active after placement. When multiple fibers are provided, as is shown inFIG. 26, different fibers can be provided in the same coil with different therapeutic agents to provide different therapies. The fibers are preferably woven into the coil by hand after the heat setting of the coil shape.
• In another presently preferred embodiment illustrated inFIGS. 27 and 28, ahelical microcoil140 formed of a plurality offlexible strands142 of nickel-titanium alloy, with at least one centrally, axially disposedradiopaque wire144 as described above, has one or moretherapeutic fibers136 as described above, advantageously woven through the multiple strands of adjacent loops of the coil, to enhance treatment of the site after placement of the device. Alternatively, the one or more therapeutic fibers can be woven through the strands of non-adjacent loops of the coil as well. When multiple fibers are provided, as is shown inFIG. 28, the different fibers can be provided in the same coil with different therapeutic agents to provide different therapies. The one or more fibers are preferably woven through the strands of the multiply-stranded microcoil by hand during winding of the multiply-stranded microcoil.
• 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 (147)

1. A multi-stranded micro-cable for use in interventional therapy and vascular surgery, comprising:

a plurality of flexible strands of a resilient material; said micro-cable including at least one radiopaque strand to provide a radiopaque marker.

2. The multi-stranded micro-cable ofclaim 1, wherein at least one radiopaque strand comprises an axially disposed radiopaque wire.

3. The multi-stranded micro-cable ofclaim 1 wherein at least one of said plurality of flexible strands of a resilient material are comprised of a super-elastic material.

4. The multi-stranded micro-cable ofclaim 3 wherein at least one of said super-elastic material comprises a nickel titanium alloy.

5. The multi-stranded micro-cable ofclaim 1 wherein at least one of said plurality of flexible strands of a resilient material are comprised of a shape memory material.

6. The multi-stranded micro-cable ofclaim 5 wherein said shape memory material comprises a nickel-titanium alloy.

7. The multi-stranded micro-cable ofclaim 5 wherein said shape memory material comprises a shape memory polymer.

8. The multi-stranded micro-cable ofclaim 1 wherein said plurality of flexible strands further comprise a central core wire, said plurality of flexible strands are twisted about said central core wire, and at least one of said twisted strands comprising a radiopaque strand.

9. The multi-stranded micro-cable ofclaim 1 wherein said plurality of flexible strands further comprises a plurality of flexible strands twisted about a central core wire, said central core wire being made of a radiopaque material.

10. The multi-stranded micro-cable ofclaim 1 wherein said radiopaque strand comprises a material selected from the group consisting of platinum, gold, and tungsten.

11. The multi-stranded micro-cable ofclaim 5 wherein said radiopaque strands comprise a plurality of strands of said micro-cable, at least one of said plurality of radiopaque strands arrayed in the outer twisted strands of said cable.

12. The multi-stranded micro-cable ofclaim 1, further comprising at least one strand of a therapeutic material.

13. The multi-stranded micro-cable ofclaim 12 wherein said strand of therapeutic material is selected from the group consisting of hydrogel and human growth hormone.

14. The multi-stranded micro-cable ofclaim 1, further comprising a sheath to constrain said strands of said micro-cable about a longitudinal axis.

15. The multi-stranded micro-cable ofclaim 14 wherein said sheath comprises a containment strand wound about said longitudinal strands.

16. The multi-stranded micro-cable ofclaim 14 further comprising an outer flexible sheath of low friction material.

17. The multi-stranded micro-cable ofclaim 16 wherein said outer sheath comprises a fluoropolymer.

18. The multi-stranded micro-cable ofclaim 14 wherein said sheath comprises a heat shrinkable plastic tube.

19. A multi-stranded micro-cable for use in interventional therapy and vascular surgery comprising:

a plurality of flexible strands made of a resilient material helically wound around a central core, said central core comprising an axially placed therapeutic substance.

20. The multi-stranded micro-cable ofclaim 19 wherein said therapeutic substance includes one or more of components from the group of hydro-gel, collagen, bio-absorbable polymers such as lactic acids/glycolic acids and capro lactam.

21. The multi-stranded micro-cable ofclaim 19 wherein said cable further comprises at least one of said strands of resilient material being a radiopaque strand to provide a radiopaque marker during a therapeutic procedure.

22. The multi-stranded micro-cable ofclaim 19 wherein at least one of said flexible strands of the wire made of resilient material further comprises a shaped memory or super-elastic material.

23. The multi-stranded micro-cable ofclaim 19 wherein said shaped memory or super-elastic material further comprises a nickel titanium alloy.

24. The multi-stranded micro-cable ofclaim 19 wherein said therapeutic material further comprises material to promote human cell growth.

25. The multi-stranded micro-cable ofclaim 19 wherein said therapeutic substance core is a fiber such as Dacron (polyester), polyglycolic acid, polylactic acid, fluoropolymers, nylons, polyaramid fiber kevlar or silk chosen for thrombogenicity.

26. The multi-stranded micro-cable ofclaim 19 further comprising replacing at least one strand in said outer wound strands with a strand of a therapeutic material.

27. The multi-stranded micro-cable ofclaim 14 wherein said sheath further comprises a plurality of heat shrink plastic covers placed to provide bending stiffness in said cable which varies with the position on said cable.

28. The multi-stranded micro-cable ofclaim 14 wherein said sheath further comprises a sheath which varies in cross section along its length to provide bending stiffness of said cable which varies with the position on said cable.

29. The multi-stranded micro-cable ofclaim 14 further comprising at least one longitudinal element for sensing a parameter.

30. The multi-stranded micro-cable ofclaim 14 further comprising at least one longitudinal element for providing a therapeutic effect at a location near the distal end of said cable.

31. The multi-stranded micro-cable ofclaim 29 wherein said sensing element comprises an optical fiber.

32. The multi-stranded micro-cable ofclaim 30 wherein said therapeutic element comprises means to conduct energy.

33. The multi-stranded micro-cable ofclaim 32 wherein said means to conduct energy comprises an optical fiber to conduct light energy.

34. A device for use in interventional therapy and vascular surgery, adapted to be inserted into a portion of a vasculature, comprising:

at least one multi-stranded micro-cable having a collapsed primary coil configuration and an expanded secondary configuration with a three dimensional shape, each said multi-stranded micro-cable having a plurality of flexible strands of a resilient material and at least one radiopaque strand to provide a radiopaque marker of the deployed configuration of the device.

35. The device ofclaim 34, wherein said secondary three dimensional shape is selected from the group consisting of generally spherical, generally helical, and generally conical shapes.

36. The device ofclaim 34, wherein said plurality of strands are helically wound.

37. The device ofclaim 34, wherein said plurality of flexible strands are parallel longitudinal strands.

38. The device ofclaim 34, wherein at least one of said plurality of strands comprises a super-elastic material.

39. The device ofclaim 38, wherein said super-elastic material comprises a nickel titanium alloy.

40. The device ofclaim 34, wherein at least one of said strands comprises a shape memory material.

41. The device ofclaim 34, wherein said shape memory material comprises a nickel-titanium alloy.

42. The device ofclaim 41, wherein said shape memory nickel-titanium alloy is heat treated such that the alloy is highly flexible at a temperature appropriate for introduction into the body via a catheter, and after placement, the device will take on a shape designed to optimize the therapeutic purposes desired for the device.

43. The device ofclaim 34, wherein at least one of the strands comprises a therapeutic agent.

44. The device ofclaim 43 wherein said strand comprising a therapeutic agent is wound into said micro-cable so that at least a portion of said strand projects beyond the diameter of the other strands in said cable.

45. The device ofclaim 43, wherein said therapeutic agent comprises a fiber selected from the group consisting of Dacron (polyester), polyglycolic acid, polylactic acid, fluoropolymers, nylons, polyaramid fiber, keviar, silk chosen for thrombogenicity, human growth hormone, genetic material, antigens, hydrogel, collagen, and bio-absorbable polymers including lactic acids, glycolic acids, caprolactam and microcellular foams.

46. The device ofclaim 43, wherein said therapeutic agent comprises means to conduct energy.

47. The device ofclaim 46, wherein said means to conduct energy comprises an optical fiber to conduct light energy.

48. The device ofclaim 43, wherein said therapeutic agent is disposed axially in a central core

49. The device ofclaim 34, wherein said plurality of strands comprises a plurality of exterior strands surrounding at least one interior strand.

50. The device ofclaim 34, wherein said plurality of strands comprises a plurality of exterior strands surrounding a central core.

51. The device ofclaim 34, wherein said radiopaque strand comprises at least one centrally, axially disposed radiopaque wire.

52. The device ofclaim 34, wherein said radiopaque wire comprises a radiopaque material selected from the group consisting of platinum, tungsten, and gold.

53. The device ofclaim 34, wherein said micro-cable comprises a plurality of radiopaque strands.

54. The device ofclaim 34, wherein said strands of the micro-cable are bundled by at least one outer cover to produce a composite banded cable.

55. The device ofclaim 54, wherein said outer cover comprises a sheath to constrain said strands of said micro-cable about a longitudinal axis.

56. The device ofclaim 54, wherein said outer cover comprises an outer sheath of material to provide bending stiffness and constrain said longitudinal strands about said longitudinal axis.

57. The device ofclaim 55, wherein said sheath comprises a containment strand wound about said longitudinal strands.

58. The device ofclaim 55, wherein said sheath is made of low friction material.

59. The device ofclaim 55, wherein said sheath is made of a fluoropolymer.

60. The device ofclaim 55, wherein said sheath comprises a heat shrinkable plastic tube.

61. The device ofclaim 55, wherein said sheath comprises a plurality of heat shrink plastic covers placed to provide bending stiffness in said cable which varies with the position on said cable.

62. The device ofclaim 54, wherein said strands of the micro-cable are bundled by a plurality of bands disposed at intervals along said micro-cable to produce a composite banded cable.

63. The device ofclaim 61, wherein said strands are laid parallel within the composite banded cable.

64. The device ofclaim 55, wherein said strands are twisted within the composite banded cable.

65. The device ofclaim 56, wherein said outer cover is wound at varying intervals along the outside to provide variations in the torqueability and stiffness of the composite cable.

66. The device ofclaim 56, wherein the width of the outer cover is varied along the composite cable.

67. The device ofclaim 54, wherein said outer covering varies in cross section along its length to provide bending stiffness of said composite cable which varies along said composite cable.

68. The device ofclaim 54, wherein the number of strands and the degree to which they extend along said composite cable within the outer covering varies along said composite cable.

69. The device ofclaim 54, wherein said outer covering comprises a plurality of layers formed of different materials in order to provide a graduated bending and stiffness characteristic over the length of the cable.

70. The device ofclaim 54, wherein said composite microcable comprises a plurality of micro-cables disposed within said outer cover in order to provide desired bending and strength characteristics.

71. The device ofclaim 70, wherein said plurality of micro-cables are helically wound within said outer cover.

72. The device ofclaim 70, wherein said plurality of micro-cables extend parallel and longitudinally within said outer cover.

73. The device ofclaim 70, wherein said composite cable has a collapsed primary configuration and an expanded secondary configuration with a secondary shape.

74. The device ofclaim 73, wherein said secondary shape is three dimensional.

75. The device ofclaim 73, wherein said secondary shape is selected from the group consisting of spherical, helical, and conical shapes.

76. The device ofclaim 70, wherein said plurality of micro-cables are bundled by at least one outer cover to produce said composite banded cable.

77. The device ofclaim 76, wherein said plurality of micro-cables are banded at intervals by a plurality of bands.

78. The device ofclaim 34, further comprising at least one longitudinal element for sensing a parameter.

79. The device ofclaim 68, wherein said longitudinal element for sensing a parameter is selected from the group consisting of an optical imaging element, an optical fiber, a thermal imaging element, and an ultrasound imaging element.

80. A three dimensional composite device having a collapsed coil configuration with a primary shape and an expanded coil configuration with a secondary three dimensional shape for use in interventional therapy and vascular surgery, the device adapted to be inserted into a portion of a vasculature for occluding the portion of the vasculature, comprising:

a plurality of multi-stranded micro-cables having a collapsed coil configuration with a primary shape and an expanded coil configuration with a secondary three dimensional shape, each said multi-stranded micro-cable having a plurality of flexible strands of a resilient material, and at least one said strand being a radiopaque strand to provide a radiopaque marker of the deployed configuration of a device made of the cable during vascular surgery.

81. The three dimensional composite device ofclaim 80, said micro-cable further comprising at least one outer cover disposed over at least a portion of said plurality of multi-stranded micro-cables to produce a composite banded cable.

82. The three dimensional composite device ofclaim 81, wherein said secondary three dimensional shape is selected from the group consisting of generally spherical, generally helical, and generally conical shapes.

83. The three dimensional composite device ofclaim 81, wherein said plurality of strands are helically wound.

84. The three dimensional composite device ofclaim 81, wherein said plurality of flexible strands are parallel longitudinal strands.

85. The three dimensional composite device ofclaim 81, wherein at least one of said plurality of strands comprises a super-elastic material.

86. The three dimensional composite device ofclaim 81, wherein a plurality of said flexible strands are comprised of a super-elastic material.

87. The three dimensional composite device ofclaim 81, wherein said super-elastic material comprises a nickel titanium alloy.

88. The three dimensional composite device ofclaim 81, wherein at least one of said strands comprises a shape memory material.

89. The three dimensional composite device ofclaim 81, wherein a plurality of said flexible strands of a resilient material are comprised of a shape memory material.

90. The three dimensional composite device ofclaim 89, wherein said shape memory material comprises a nickel-titanium alloy.

91. The three dimensional composite device ofclaim 89, wherein said shape memory nickel-titanium alloy is heat treated such that the alloy is highly flexible at a temperature appropriate for introduction into the body via a catheter, and after placement, the device will take on a shape designed to optimize the therapeutic purposes desired for the device.

92. The three dimensional composite device ofclaim 89, wherein said shape memory material comprises a shape memory polymer.

93. The three dimensional composite device ofclaim 81, wherein at least one of the strands comprises a therapeutic agent selected from the group consisting of a fiber selected from the group consisting of Dacron (polyester), polyglycolic acid, polylactic acid, fluoropolymers, nylons, polyaramid fiber kevlar and silk chosen for thrombogenicity, human growth hormone, genetic material, antigens and hydrogels.

94. The three dimensional composite device ofclaim 93, wherein at least a portion of said strand of therapeutic agent projects beyond the diameter of the remaining strands on said cable.

95. The three dimensional composite device ofclaim 93, wherein said therapeutic agent comprises at least one component selected from the group consisting of hydrogel, collagen, and bio-absorbable polymers including lactic acids, glycolic acids and caprolactam.

96. The three dimensional composite device ofclaim 81, wherein said outer cover comprises a sheath to constrain said strands of said micro-cable about a longitudinal axis.

97. The three dimensional composite device ofclaim 81, wherein said outer cover comprises an outer sheath of material to provide bending stiffness and constrain said longitudinal strands about said longitudinal axis, said sheath being formed of a low friction material selected from the group consisting of a fluoropolymer and a heat shrinkable plastic tube.

98. The three dimensional composite device ofclaim 96, wherein said sheath comprises a containment strand wound about said longitudinal strands.

99. The three dimensional composite device ofclaim 96, wherein said sheath comprises a plurality of heat shrink plastic tubes placed to provide bending stiffness in said cable which varies with the position on said cable.

100. The three dimensional composite device ofclaim 81, wherein said strands of the micro-cable are bundled by a plurality of bands disposed at intervals along said micro-cable to produce a composite banded cable.

101. The three dimensional composite device ofclaim 100, wherein said strands are laid parallel within the composite banded cable.

102. The three dimensional composite device ofclaim 100, wherein said exterior wrapped cover is wound at varying intervals along the outside to provide variations in the torqueability and stiffness of the composite cable.

103. The three dimensional composite device ofclaim 100, wherein the width of the outer cover is varied along the composite cable.

104. The three dimensional composite device ofclaim 81, wherein said outer covering varies in cross section along its length to provide bending stiffness of said composite cable which varies along said composite cable.

105. The three dimensional composite device ofclaim 81, wherein the number of strands and the degree to which they extend along said composite cable within the outer covering varies along said composite cable.

106. The three dimensional composite device ofclaim 97, wherein outer covering comprises a plurality of layers formed of different materials in order to provide a graduated bending and stiffness characteristic over the length of the cable.

107. A device for use in interventional therapy and vascular surgery, adapted to be inserted into a portion of a vasculature, comprising:

a shape memory coil having an outer coil portion and an inner core portion, said shape memory coil having a collapsed primary coil configuration and an expanded secondary configuration with a three dimensional shape; and

a radiopaque strand extending through the core of the shape memory coil to provide a radiopaque marker of the deployed configuration of the device.

108. The device ofclaim 107, wherein said shape memory coil comprises a multi-stranded coil having a plurality of flexible strands of a resilient material.

109. The device ofclaim 107, wherein said shape memory coil comprises a single stranded coil.

110. The device ofclaim 109, wherein said single stranded coil comprises a nickel titanium alloy.

111. The device ofclaim 109, wherein said single stranded coil comprises a shape memory polymer.

112. The device ofclaim 107, wherein said radiopaque strand comprises a core strand having a plurality of intermittently spaced apart enlarged portions.

113. The device ofclaim 112, wherein said enlarged portions comprise a radiopaque material selected from the group consisting of platinum and gold.

114. The device ofclaim 112, wherein said enlarged portions comprise a plurality of beads of radiopaque material spaced apart and mounted on a core strand of material.

115. The device ofclaim 114, wherein said beads comprise a radiopaque material selected from the group consisting of platinum, gold and tungsten.

116. The device ofclaim 114, wherein at least one of said plurality of beads is bonded to a segment of the shape memory coil.

117. The device ofclaim 114, wherein an end bead is bonded to a segment of the shape memory coil.

118. The device ofclaim 112, wherein said enlarged portions comprise a plurality of coils intermittently wound about and spaced apart on said core strand.

119. The device ofclaim 118, wherein said core strand comprises a radiopaque material selected from the group consisting of platinum and gold.

120. The device ofclaim 118, wherein said spaced apart coils comprise a radiopaque material selected from the group consisting of platinum and gold.

121. The device ofclaim 112, wherein said core strand comprises a material selected from the group consisting of platinum, gold, a shape memory polymer having a glass transition temperature (T_g) below 25° C., a hydrogel, an amorphous gel, and a fiber.

122. An occlusive device for use in interventional therapy and vascular surgery, adapted to be inserted into a portion of a vasculature, said occlusive device comprising:

a plurality of coil arms formed of shape memory material having a collapsed primary coil configuration and a three dimensional, polyhedral expanded secondary configuration, said coil arms having inner and outer ends, said inner ends of said coil arms being connected together, and

a central coil body connected to said inner ends of said coil arms.

123. The occlusive device ofclaim 122, wherein said plurality of coil arms further comprises at least four coil arms.

124. The occlusive device ofclaim 122, wherein said plurality of coil arms comprise six radiating coil arms forming a hexahedral configuration.

125. The occlusive device ofclaim 122, wherein said plurality of coil arms are formed from conically shaped coils each having an inner apical end, and said inner apical ends being connected to said central body, said conically shaped coils having an expanding diameter as they radiate outward.

126. The occlusive device ofclaim 123, wherein said central body comprises a central three dimensional coil connecting said inner ends of said at least four coil arms together.

127. The occlusive device ofclaim 126, wherein said at least four coil arms comprise six radiating coil arms forming a hexahedral configuration.

128. The occlusive device ofclaim 126, wherein said plurality of coil arms are formed from conically shaped coils each having an inner apical end, and said inner apical ends being connected to said central body, said conically shaped coils having an expanding diameter as they radiate outward.

129. The occlusive device ofclaim 126, wherein said central three dimensional coil has a shape selected from the group consisting of spherical, rounded, and cubical shapes.

130. The occlusive device ofclaim 126, wherein said central three dimensional coil is tetrahedral.

131. The occlusive device ofclaim 130, wherein said at least four coil arms comprise four radiating coil arms forming a tetrahedral configuration.

132. The occlusive device ofclaim 127, wherein said central three dimensional coil is pentahedral.

133. The occlusive device ofclaim 132, wherein said at least four coil arms comprise five radiating coil arms forming a pentahedral configuration.

134. The occlusive device ofclaim 123, wherein said at least four coil arms comprise at least one multi-stranded micro-cable having a plurality of flexible strands of a resilient material, with at least one radiopaque strand to provide a radiopaque marker.

135. The occlusive device ofclaim 123, wherein said at least four coil arms comprise at least one secondary wind coil of a primary helical wind coil.

136. The occlusive device ofclaim 126, wherein said central three dimensional coil comprises a secondary wind coil of a primary helical wind coil.

137. A device for use in interventional therapy and vascular surgery, adapted to be inserted into a portion of a vasculature, comprising:

a coil having a collapsed primary coil configuration and an expanded secondary configuration with a three dimensional shape, said coil being formed from at least one flexible strand of a resilient material; and

at least one therapeutic fiber woven into the coil to enhance treatment of the site after placement of the device.

138. The device ofclaim 137 wherein said at least one flexible strand comprises a plurality of flexible strands of a resilient material, and at least one radiopaque strand to provide a radiopaque marker of the deployed configuration of the device.

139. The device ofclaim 137 wherein said at least one therapeutic fiber is woven about adjacent loops of the coil.

140. The device ofclaim 137 wherein said at least one therapeutic fiber is woven about non-adjacent loops of the coil.

141. The device ofclaim 138, wherein said at least one therapeutic fiber is woven through the multiple strands of adjacent loops of the coil.

142. The device ofclaim 138, wherein said at least one therapeutic fiber is woven through the multiple strands of non-adjacent loops of the coil.

143. The device ofclaim 137 wherein said at least one therapeutic fiber is made of a material that will provide a timed release of a therapeutic agent intended to become active after placement of the device.

144. The device ofclaim 143, wherein said therapeutic agent selected from the group consisting of human growth hormone, collagen, a modified polymer with growth factor, genetic material for gene therapy, and antigens.

145. The device ofclaim 143, wherein said at least one therapeutic fiber comprises a plurality of therapeutic fibers, with different fibers provided in the coil with different therapeutic agents to provide different therapies.

146. The device ofclaim 137 wherein said coil secondary three dimensional configuration is helical.

147. The device ofclaim 137 wherein said at least on flexible strand comprises a nickel-titanium alloy.

Images