US20170354402A1 - Braided medical devices - Google Patents

Abstract

A braided vaso-occlusive member formed out of first plurality of filaments interwoven with a second plurality of filaments, wherein filaments of the first plurality are helically wound in a first rotational direction along an elongate axis of the braided member, and filaments of the second plurality are wound in a second rotational direction opposite the first rotational direction, such that filaments of the first plurality cross over and/or under filaments of the second plurality at each of a plurality cross-over locations axially spaced along the elongate axis of the braided member, wherein at each cross-over location, the filaments of the first plurality cross over at least two consecutive filaments of the second plurality, then cross under only a single filament of the second plurality, and then cross over at least two additional consecutive filaments of the second plurality.

Description

RELATED APPLICATION DATA
• The present application claims the benefit under 35 U.S.C. §119 to U.S. Provisional Application Ser. No. 62/348,659, filed Jun. 10, 2016. The foregoing application is hereby incorporated by reference into the present application in its entirety.
FIELD
• The inventions disclosed herein relate to braided medical devices used for the treatment of vascular defects, such as aneurysms, and more particularly to woven braid patterns to be used in such braided medical devices.
BACKGROUND
• Medical devices such as stents, filters, thromboembolic capture devices, flow diverters, vaso-occlusive devices, collectively referred to herein as “embolic devices” are often composed of one or more elongate members (e.g., wires, drawn-filled tubes, threads, filaments and the like) that are woven into a braid or mesh pattern. Such braided embolic devices may be utilized for treating various types of vascular defects, such as aneurysms, and may be provided in a wide variety of respective delivery and deployed sizes and shapes; particularly, secondary shapes when the device is deployed in a targeted vasculature site. Some exemplary secondary shapes of braided embolic devices include spherical, ovoid, flat ribbon, helical braided ribbon, or combinations thereof, suitable for the treatment of vascular defects.
• Braided embolic devices are commonly made out of self-expanding materials, so that when the devices are deployed from a delivery system into the target site in a patient, the unconstrained devices expand without requiring assistance. Self-expanding embolic devices may be biased so as to cause the braided device to expand upon release from a delivery catheter and/or include a shape-memory component, which allows the device to expand upon exposure to a predetermined condition (e.g., in-vivo conditions). Some embolic devices may be characterized as hybrid devices which have some characteristics of both self-expandable materials and non-self-expandable materials.
• Additionally, the respective elongate members (wires, drawn-filled tubes, threads, filaments and the like) forming the braid may be made from a variety of materials, including both bio-erodible and non-bio-erodible polymers and metals. In some applications, bio-erodible polymer embolic devices are desirable due to their biodegradability and generally increased flexibility compared to metal embolic devices. Further, embolic devices can be made from shape memory or superelastic materials, such as shape memory metals, e.g., Nitinol, and polymers, e.g., polyurethane. Such shape memory embolic devices can be induced by known shape setting techniques, e.g., temperature, electrical, magnetic field and/or exposure to narrowband light to take on a secondary shape after delivery within a targeted vascular site. Superelastic embolic materials, such as superelastic Nitinol, may take on a shape after delivery without need for an inductive stimulus. Other materials used in the embolic devices can include stainless steel, titanium, platinum, nickel, chrome cobalt alloy, Elgiloy, or the like, and combinations thereof. In drug delivery embolic devices, the device can carry and/or the surface of the device can be coated with a bioactive or therapeutic agent, e.g., thrombosis inducing agent.
• In the treatment of vascular defects, such as aneurysms, the braided embolic device is typically loaded into (or onto) a delivery system in a collapsed or radially compressed delivery configuration. The delivery system—typically a so-called micro-catheter—is percutaneously introduced in a patient, generally by so called minimally invasive techniques. The braided embolic device is then distally advanced through the delivery system and introduced into a targeted vasculature site of the patient. As such the braided embolic device must have a suitable “pushability” that allows the translation of the device through the lumen of a delivery catheter. Further, in the treatment of certain vascular defects, the expanded configuration or secondary shape of the braided embolic device should be suitable to engage an embolic obstruction and/or the walls of a blood vessel without overcoming the resistive forces of the vessel.
• Particularly, the radial expansion forces of the braided embolic device should be suitable to engage the desired obstructions and/or the blood vessel walls, while being sufficiently flexible (e.g., soft) to avoid damaging the blood vessel at the target site. Therefore, the braided embolic device should have sufficient column strength in the collapsed or radially compressed delivery configuration, allowing the braided embolic devices to be pushed and translated through the delivery system into the target site without buckling, deforming or crumpling. Additionally, a suitable combination of stiffness and flexibility in the braided embolic device is desirable, for the device to be pulled, re-sheathed, or to pull an engaged obstruction from the vessel, while being sufficiently flexible when delivered into the target site.
• Some braided embolic devices achieve a desired flexibility by reducing the diameter or cross-sectional area of the elongate members (i.e., wires) forming the braid or by reducing the amount of elongate members in the braid. However, reducing the diameter of the wires in already low wire diameter limits for embolic devices is challenging to manufacture, and along with reducing the number of wires, these options tend to sacrifice on the needed stiffness of the device. Moreover, these options may negatively impact on the overall performance of the braided embolic device by either reducing the width of the device or decreasing the wire density required to effectively treat a vascular defect. Other braided embolic devices achieve a desired stiffness by having the wires of the braided device welded, bonded or otherwise engaged to each other at a certain angle, which in turn may sacrifice the needed flexibility of the device. Techniques addressing the above delivery and deployment concerns for braided embolic devices are described in U.S. Pat. Nos. 9,011,482 and 9,060,777, the entire disclosures of which are incorporated herein by reference, as though set forth in full.
• FIGS. 1A-B illustrate an exemplary prior art braided embolic device in the form of a tubularbraided stent10.FIG. 1A shows thebraided stent10 in a radially expanded delivered configuration, having aproximal portion12, adistal portion14 and alumen16 extending therebetween. The braidedstent10 is formed out of a plurality of elongate members (e.g., wires, drawn-filled tubes, threads, filaments and the like)20 that are woven together.FIG. 1B is a two-dimensional plan view of a section of awall18 of thebraided stent10, showing that theelongate braid members20 are woven in a standard repeating “one-over, one-under”pattern50, which is a common weave pattern used in known braided embolic devices. In the one-over, one-under braid pattern, each braid member of a first set ofelongate braid members22 cross over and under each braid member of a second set of braid members in an alternating manner, wherein the elongate braid members of the first set are substantially orthogonal to the elongate braid members of the second set (and vice versa). Similarly, theelongate braid members24 of the second set each extend over/under the respective braid members of thefirst set22 in the same alternating one-over, one-under pattern, “over” and “under” being relative terms that depend on which facing side of thewall section18 is being viewed. The repeating one-over, one-under braid pattern provides thestent10 with sufficient column strength in the radially compressed delivery configuration allowing the embolic devices to be pushed and translated through the delivery system. However, this standard braid pattern also reduces the flexibility and softness of thestent10 when deployed at a target site in the vasculature.
SUMMARY
• In an exemplary embodiment of one of the disclosed inventions, an implantable vaso-occlusive device is provided for occluding an aneurysm, the device comprising a braided member formed out of a first plurality of filaments interwoven with a second plurality of filaments, the braided member having a compressed configuration when constrained in a lumen of a delivery catheter, and an expanded configuration when not constrained. The braided member filaments of the first plurality are helically wound in a first rotational direction along an elongate axis of the braided member, and filaments of the second plurality are wound in a second rotational direction opposite the first rotational direction along the elongate axis of the braided member, such that filaments of the first plurality cross over and/or under filaments of the second plurality at each of a plurality cross-over locations axially spaced along the elongate axis of the braided member, wherein at each cross-over location, the filaments of the first plurality cross over at least two consecutive filaments of the second plurality, then cross under only a single filament of the second plurality, and then cross over at least two additional consecutive filaments of the second plurality.
• Without limitation, at each cross-over location, the filaments of the first plurality may be oriented substantially orthogonal to the filaments of the second plurality when the device is in an expanded, non-constrained configuration. Also, without limitation, the first rotational direction may be clockwise, and the second rotational direction may be counter-clockwise.
• In one embodiment, at each cross-over location, the filaments of the first plurality cross over exactly two consecutive filaments of the second plurality, then cross under only a single filament of the second plurality, and then cross over exactly two more consecutive filaments of the second plurality. In other embodiments, at each cross-over location, the filaments of the first plurality cross over at least three consecutive filaments of the second plurality, then cross under only a single filament of the second plurality, and then cross over at least three more consecutive filaments of the second plurality. By way of a non-limiting example, a braided device according to one embodiment may comprise a first body portion and a second body portion, and at each cross-over location in the first body portion, the filaments of the first plurality cross over two or three consecutive filaments of the second plurality, then cross under only a single filament of the second plurality, and then cross over at least two or three more consecutive filaments of the second plurality.
• In an exemplary embodiment of another one of the disclosed inventions, an implantable vaso-occlusive device is provided for occluding an aneurysm, the device comprising a braided member formed out of braid filaments, the braided member having an compressed configuration when constrained in a lumen of a delivery catheter, and a tubular expanded configuration when not constrained, wherein when the braid member is in the expanded configuration, the braid filaments are disposed circumferentially about an elongate axis of the braided member. The braid filaments comprising a plurality of filaments made out of a first material, and one or more marker filaments made of a second material having a higher stiffness and a higher radiopacity, respectively, than the first material filaments.
• By way of non-limiting examples, the vaso-occlusive device first material filaments may be made out of nickel-titanium alloy, and the marker filaments may be made out of platinum alloy. In one embodiment, the marker filaments include first and second marker filaments that are circumferentially offset approximately 180° from each other along at least a portion of the braided device when the braided device is in the tubular expanded configuration, wherein the first marker filament is made out of a different material and/or has a different diameter, respectively, than the second marker filament. In another embodiment, the marker filaments include four marker filaments that are circumferentially offset approximately 90° from each other along at least a portion of the braided device when the braided device is in the tubular expanded configuration, wherein at least one of the four marker filaments is made out of a different material and/or has a different diameter, respectively, than at least one other of the four marker filaments. In yet another embodiment, the marker filaments include six marker filaments that are be circumferentially offset approximately 60° from each other along at least a portion of the braided device when the braided device is in the tubular expanded configuration, wherein at least one of the six marker filaments is made out of a different material and/or has a different diameter, respectively, than at least one other of the six marker filaments.
• In various exemplary embodiments, the marker filaments of the vaso-occlusive device include a first set of adjacent maker elements and a second set of adjacent marker elements, wherein the first set of adjacent marker elements may be circumferentially offset approximately 180° from the second set of adjacent marker elements along at least a portion of the braided device when the braided device is in the tubular expanded configuration. The first set of adjacent marker filaments comprising first and second marker filaments disposed adjacent one another, wherein the first marker filament is made out of a different material and/or has a different diameter, respectively, than the second marker filament.
• Without limitation, the first marker filament may be made out of platinum alloy, and the second marker filament may be made out of nitinol and platinum drawn-filled tube. In one embodiment, the first set of adjacent marker filaments include first, second and third marker filaments disposed adjacent each other, wherein first marker filament is made out of a different material and/or has a different diameter, respectively, than one or both of the second and third marker filaments.
• In an exemplary embodiment of yet another one of the disclosed inventions, an implantable vaso-occlusive device is provided for occluding an aneurysm, the device comprising a braided member formed out of a plurality of interwoven braid filaments, the braided member having an compressed configuration when constrained in a lumen of a delivery catheter, and an expanded configuration when not constrained, in which the braid filaments are disposed circumferentially about an elongate axis of the braided member, wherein in the expanded configuration, the braided member defines a plurality of segments having enlarged cross-sections (referred to herein as “enlarged cross-section segments”) spaced apart along the elongate axis thereof, wherein adjacent enlarged cross-section segments of the plurality are connected by a respective reduced cross-section segment, and wherein the braid filaments are interwoven according to a first weave pattern to create the respective enlarged cross-section segments, and wherein the braid filaments are interwoven according to a second weave pattern different than the first weave pattern to create each reduced cross-section segments.
• By way of non-limiting example, in the second weave pattern, subsets of the plurality of interwoven braid filaments are wound into respective linking braids and/or wire bundles that span between adjacent enlarged cross-section segments. In the expanded configuration of the vaso-occlusive device, a respective reduced cross-section segment may be outwardly expanded into a fattened, ribbon-like configuration about the elongate axis, and the enlarged cross-section segments may be circumferentially expanded about the elongate axis.
• Other and further aspects and features of embodiments will become apparent from the ensuing detailed description in view of the accompanying figures.
BRIEF DESCRIPTION OF THE DRAWINGS
• FIGS. 1A and 1B are respective perspective and plan side views of a Prior Art braided embolic device having a standard repeating “one-over, one-under” braid pattern.
• FIG. 2 is a plan view of a repeating “two-over, one-under” braid pattern that may be used for constructing braided embolic devices, according to one embodiment of the disclosed inventions.
• FIG. 3 is a plan view of a repeating “two-over, two-under” braid pattern that may be used for constructing braided embolic devices, according to another embodiment of the disclosed inventions.
• FIGS. 4A and 4B are respective front and back plan views of a repeating “three-over, one-under” braid pattern that may be used for constructing braided embolic devices, according to yet another embodiment of the disclosed inventions.
• FIG. 5 is a plan view of a repeating “two-over, two-under” braid pattern that may be used for constructing braided embolic devices, according to other embodiment of the disclosed inventions.
• FIG. 6 is a plan view of a repeating “four-over, one-under” braid pattern that may be used for constructing braided embolic devices, according to other embodiment of the disclosed inventions.
• FIG. 7 is a plan view of a repeating “seven-over, one-under” braid pattern that may be used for constructing braided embolic devices, according to other embodiment of the disclosed inventions.
• FIG. 8 is a perspective view of an exemplary tubular embolic device having any of the braid patterns of previously disclosed embodiments.
• FIG. 9 is a perspective view of an exemplary tubular embolic device having the “two-over, one-under” braid pattern shown inFIG. 2.
• FIGS. 10A and 10B are respective perspective and cross-sectional views of an exemplary elongate braid member that may be used for constructing braided embolic devices, such as the device ofFIGS. 8-9.
• FIGS. 11A and 11B are respective perspective and cross-sectional views of an alternate exemplary elongate braid member that may be used for constructing braided embolic devices, such as the device ofFIGS. 8-9.
• FIGS. 12A and 12B are respective cross-sectional views of an alternate exemplary elongate braid member that may be used for constructing braided embolic devices, such as the device ofFIGS. 8-9.
• FIGS. 13-20 are cross-sectional views of exemplary braided embolic devices, constructed according to embodiments of the disclosed inventions.
• FIGS. 21A-C are perspective and cross-sectional views of another exemplary braided embolic devices, constructed according to embodiments of the disclosed inventions.
• FIGS. 22-25 are perspective views of exemplary elongate sets of plurality of elongate members, constructed according to embodiments of the disclosed inventions.
• FIGS. 26A-B are perspective side and top views of yet another exemplary braided embolic devices, constructed according to embodiments of the disclosed inventions
DETAILED DESCRIPTION OF THE ILLUSTRATED EMBODIMENTS
• Various embodiments are described hereinafter with reference to the figures. The figures are not necessarily drawn to scale, the relative scale of select elements may have been exaggerated for clarity, and elements of similar structures or functions are represented by like reference numerals throughout the figures. It should also be understood that the figures are only intended to facilitate the description of the embodiments, and are not intended as an exhaustive description of the invention or as a limitation on the scope of the invention, which is defined only by the appended claims and their equivalents. In addition, an illustrated embodiment needs not have all the aspects or advantages shown. An aspect or an advantage described in conjunction with a particular embodiment is not necessarily limited to that embodiment and can be practiced in any other embodiments even if not so illustrated.
• As used in this specification and the appended claims, the singular forms “a”, “an” and “the” include plural referents unless the content clearly dictates otherwise. As used in this specification and the appended claims, the term “or” is generally employed in its sense including “and/or” unless the content clearly dictates otherwise.
• FIG. 2 illustrates a two-dimensional plan view of anexemplary braid150 that may be used for constructing a braided embolic device, according to one embodiment of the disclosed inventions. Thebraid150 is formed by a plurality of inter-wovenelongate members200, including a first set ofelongate members200A-E inter-woven with a second set ofelongate members200a-e, wherein theelongate members200A-E are substantially orthogonally disposed with respect to theelongate members200a-e. In particular, theelongate members200A-E and200a-eare interwoven in a repeating “two-over, one under” pattern, wherein each elongate member of each set200A-E and200a-eextends over two successive elongate members, and then under the next successive elongate member, respectively, of the other set. For example, when viewed from the perspective shown inFIG. 2 (e.g., one/front side of the braid150), theelongate member200A of the first set extends over successiveelongate members200band200c, then under theelongate member200d, respectively, of the second set. Similarly, when viewed from the opposite side of thebraid150 that is depicted inFIG. 2, theelongate member200cof the second set extends over successiveelongate members200C and200D, then under the nextelongate member200E, respectively, of the first set.
• FIG. 3 illustrates a two-dimensional plan view of anexemplary braid150′ that may be used for constructing a braided embolic device, according to another embodiment of the disclosed inventions. Thebraid150′ is formed by a plurality of inter-wovenelongate members200′, including a first set ofelongate members200A′-E′ inter-woven with a second set ofelongate members200a′-e′, wherein theelongate members200A′-E′ are substantially orthogonally disposed with respect to theelongate members200a′-e′. As depicted inFIG. 3, theelongate members200A′-E′ and200a′-e′ are interwoven in a repeating “two-over, two under” pattern, wherein each elongate member of each set200A′-E′ and200a′-e′ extends over two successive elongate members, and then under the next two successive elongate members, respectively, of the other set. For example, when viewed from the perspective shown inFIG. 3 (e.g., one/front side of thebraid150′), theelongate member200C′ of the first set extends over successiveelongate members200a′ and200b′, then under theelongate members200c′ and200d′ of the second set. Similarly, when viewed from the opposite side of thebraid150′ that is depicted inFIG. 3, theelongate member200c′ of the second set extends over successiveelongate members200D′ and200E′, then underelongate members200B′ and200C′ of the first set.
• FIGS. 4A and 4B are plan views of analternative braid153 that may be used for constructing braided embolic devices according to further embodiments of the disclosed inventions. As was the case of thebraid150 shown inFIG. 2, thebraid153 shown inFIGS. 4A and 4B is formed out of two sets ofelongate braid members200 that are interwoven. But inbraid153, theelongate braid members200 are interwoven in a repeating “three-over, one-under” pattern. For example, when viewed from the perspective shown inFIG. 4A (e.g., one/front side of the braid153), theelongate member200D of the first set extends over successiveelongate members200a,200band200c, then under theelongate member200d, of the second set. Further, theelongate member200D of the first set continues to extend over successiveelongate members200e,200fand200g(FIG. 4A), then under theelongate member200h(not shown). Similarly, when viewed from the opposite side of thebraid153 that is depicted inFIG. 4B, theelongate member200dof the second set extends over successiveelongate members200A,200B and200C, then under the nextelongate member200D. Further, theelongate member200dof the second set continues to extend over successiveelongate members200E,200F and200G, then under theelongate member200H of the first set.
• FIG. 5 is a plan view of analternative braid152 that may be used for constructing braided embolic devices according to further embodiments of the disclosed inventions. As was the case of thebraid150′ shown inFIG. 3, thebraid152 shown inFIG. 5 is formed out of two sets ofelongate braid members200′ that are interwoven. But inbraid152, theelongate braid members200 are interwoven in a repeating and adjacently successive “two-over, two-under” pattern. For example, when viewed from the perspective shown inFIG. 5 (e.g., one/front side of the braid152), both of the adjacently disposedelongate member200c′ and200d′ of the second set extend over successiveelongate members200A′ and200B′, then underelongate members200C′ and200D′ of the first set. Similarly, when viewed from the opposite side of thebraid152 that is depicted inFIG. 5, both of the adjacently disposedelongate member200C′ and200D′ of the first set extend over successiveelongate members200e′ and200f, then under theelongate members200c′ and200d′ of the second set.
• FIG. 6 is a plan view of analternative braid154 that may be used for constructing braided embolic devices according to further embodiments of the disclosed inventions. As was the case of thebraid150 shown inFIG. 2, thebraid154 shown inFIG. 6 is formed out of two sets ofelongate braid members200 that are interwoven. But inbraid154, theelongate braid members200 are interwoven in a repeating “four-over, one-under” pattern. For example, theelongate member200eof the second set extends over successiveelongate members200A,200B,200C and200D, then under theelongate member200E of the first set. Similarly, when viewed from the opposite side of thebraid154 that is depicted inFIG. 6, theelongate member200E of the first set extends over successiveelongate members200i,200h,200gand200f, then under the nextelongate member200eof the second set.
• FIG. 7 is a plan view of analternative braid157 that may be used for constructing braided embolic devices according to further embodiments of the disclosed inventions. Thebraid157 shown inFIG. 7 is formed out of two sets ofelongate braid members200 that are interwoven, similarly to thebraid150 shown inFIG. 2. However inbraid157, theelongate braid members200 are interwoven in a repeating “seven-over, one-under” pattern. For example, when viewed from the perspective shown inFIG. 7 (e.g., one/front side of the braid157), theelongate member200gof the second set extends over successiveelongate members200A,200B,200C,200D,200E,200F and200G, then under theelongate member200H of the first set. Further, when viewed from the opposite side of thebraid157 that is depicted inFIG. 7, theelongate member200H of the first set extends over successiveelongate members200o,200n,200m,200l,200k,200jand200i, then under the nextelongate member200hof the second set.
• As shown inFIGS. 2-7, the braid for embolic devices may comprise a variety of braid patters. By way of non-limiting and additional examples, the braid patterns may include “five-over, one-under”, “six-over, one-under”, “eight-over, one-under” patterns, and/or “three-over, three-under”, “four-over, four-under” patterns (not shown) or the like or combinations thereof. The disclosed braid patterns or combination thereof incorporated into an embolic device provides the device (e.g., stent) with suitable stiffness (e.g., column strength), particularly, when the embolic device is in a radially compressed delivery configuration within a delivery system, allowing the device to be translated, pushed or moved through the lumen of the delivery system for deployment at a target site. Further, the embolic devices having a braid constructed with the disclosed braid patterns or combination thereof, allows the device to smoothly translate through the delivery system by providing lower surface area in the device which in turn lowers the frictional forces (e.g., resistance) from the delivery system into the embolic device. Moreover, the disclosed braid pattern provides for an increased flexibility and softness in the embolic device, as compared with a braid employing the standard one-over, one-under pattern (e.g.,FIGS. 1A-B). The increased flexibility and softness of the embolic device is particularly desirably after the device is deployed at a target site, conforming to the target site in a patient while avoiding injury or damage to the target site. The disclosed braid patterns or combination thereof (e.g.,FIGS. 2-7) provide an optimal balance between longitudinal and radial stiffness during delivery, and flexibility after delivery of the embolic device.
• FIG. 8 illustrates an exemplary braidedembolic device100 constructed according to one embodiment of the disclosed inventions, and incorporating one or a combination of the braid patterns of the disclosed inventions, such as inFIGS. 2-7. The braidedembolic device100 comprises a tubular configuration having adistal portion120, aproximal portion140 and alumen130 extending therebetween. Theembolic device100 has a radially compressed delivery configuration (not shown), and a radially expanded deployed configuration (shown inFIG. 8), and preferably comprises a length that ranges from approximately 2 centimeters up to approximately 40 centimeters in the deployed configuration, and more preferably from approximately 5 centimeters up to approximately 25 centimeters in the deployed configuration. The braidedembolic device100 may comprise anywhere from ten to ninety interwoven elongate members, wherein a first set ofelongate braid members200 are interwoven with a second set of elongate braid members in either of the repeating patterns disclosed or a combination thereof. Theembolic device100 may include a braid155 having theelongate braid members200 spaced apart in relatively even manner in the radially expanded deployed configuration, as shown inFIG. 8. The braid155elongate members200 define a plurality of openings orcells170 of similar dimensions, when theembolic device100 is in the radially expanded deployed configuration. The braid155 of theembolic device100 may be formed by any of the disclosed braid pattern, combinations thereof, and/or having a variety of elongate members200 (e.g., thickness, materials), that will be described in further detail below.
• FIG. 9 illustrates an exemplary braidedembolic device100′ constructed according to another embodiment of the disclosed inventions, and incorporating the repeating “two-over, one under” braid pattern depicted inFIG. 2. Theembolic device100′ depicted inFIG. 9 is similar to theembolic device100 depicted inFIG. 8. One difference is that theembolic device100′ comprises abraid159 havingelongate braid members200 with a plurality of openings or cells175 and177 of different dimensions, when theembolic device100′ is in the radially expanded deployed configuration. For example, the cells175 have a smaller dimension than the cells177 of thebraid159. The two-over, one under braid pattern allows the braidedembolic device100′ to radially expand into a non-symmetrical deployed configuration, as shown inFIG. 9.
• When expanded, the braidedembolic device100′ comprises a plurality of sections (or segments)210 and220 extending from theproximal portion120 to thedistal portion140. Each of thesections210 and220 comprises a plurality ofelongate braid members200, in whichsection210 comprises a less dense arrangement of theelongate braid members200, insection220. The repeating “two-over, one-under” pattern still provides suitable stiffness or column strength when thedevice100′ is in the radially compressed delivery configuration, thereby allowing thedevice100′ to be pushed through the lumen of a delivery system, while also allowing the device to smoothly translate through the delivery system by providing lower surface area in the device which in turn lowers the frictional forces (resistance) from the delivery system into the embolic device.
• It should be appreciated that any of the disclosed braided patterns or a combination thereof, which may have a variety of elongate members forming the braid of the embolic device, may comprise the radially expanded deployed configuration ofFIG. 9, or any other suitable expanded configuration. Additionally or alternatively, the radially expanded deployed configuration of the embolic device may comprise evenly-spaced and/or unevenly-spaced elongate members defining a plurality of cells having similar and/or different dimensions, or combinations thereof.
• FIGS. 10A and 10B illustrate theelongate member200 used for constructing braided embolic devices according to embodiments of the disclosed inventions. Theelongate member200 comprises a proximal portion252 and adistal portion254, and has a length L₁suitable for achieving a desired braided device length, and a width W₁that preferably is in a range from approximately 0.05 millimeters to approximately 1.00 millimeters, and more preferably in a range from approximately 0.1 millimeters to approximately to 0.4 millimeters. In some embodiments, the width and/or cross-sectional dimensions of theelongate member200 remain constant along its length. In other embodiments, one or more of the width and/or cross-sectional dimensions of theelongate member200 vary along its length, e.g., in a tapered configuration (not shown). It should be appreciated that theelongate braid members200 may have a variable dimensions, such as having a combination of larger and smaller diameter (or cross-section if not round) elongate members in a braid (e.g.,braid150,150′,152,153,154,155,157 and159).
• As shown inFIG. 10B, theelongate member200 comprises a substantially circular cross-section. Alternatively, theelongate member200 may have any other suitable cross-sections, such as, by way of non-limiting examples, ovoid or elliptical (shown inFIG. 12A), or theelongate member200 may comprise a ribbon-like configuration having a substantially rectangular cross-section (shown inFIGS. 11A and 11B), or other suitable cross-section, such as, flattened with rounded edges (shown inFIG. 12B), or combinations thereof. Eachelongate braid member200, or portions thereof, may be coated or otherwise formed with a layer of radiopaque material. Additionally, theelongate braid members200 may carry and/or be coated with a bioactive or therapeutic agent (e.g., thrombosis inducing agent). Additionally or alternatively, each of theelongated braid member200 may comprise a wire, drawn-filled-tube, threads, filaments or the like, composed by one or more suitable biocompatible materials.
• Theelongate braid members200 may be composed from any number of biocompatible, compressible, elastic materials or combinations thereof, including polymeric materials, metals, and metal alloys, such as stainless steel, tantalum, or a nickel titanium alloy such as a super-elastic nickel titanium alloy known as Nitinol. Certain super-elastic alloys may be desirable for their shape recoverable features, which tolerate significant flexing without deformation even when used for forming relatively small elongate braid members. Further when a braided embolic device comprises elongate braid members composed of self-expanding materials, the unconstrained embolic device can be made to be biased to expand into a predetermined deployed configuration, as shown withdevices100 or100′ ofFIGS. 8-9. Some super-elastic alloys that may be useful for this purpose include nickel/titanium alloys (48-58 atomic % nickel and optionally containing modest amounts of iron); copper/zinc alloys (38-42 weight % zinc); copper/zinc alloys containing 1-10 weight % of beryllium, silicon, tin, aluminum, or gallium; or nickel/aluminum alloys (36-38 atomic % aluminum).
• Further suitable metals and alloys for the elongate braid members include “platinum group” metals, such as, platinum, rhodium, palladium, rhenium, as well as tungsten, gold, silver, tantalum, and alloys of these metals, such as platinum/tungsten alloy, or the like and combinations thereof. These metals have significant radiopacity and in their alloys may be tailored to accomplish an appropriate blend of flexibility and stiffness. Moreover, a variety of different imaging methods can be used to ensure accurate positioning of the braided embolic devices within a delivery system and when deployed in a patient. Examples of suitable imaging methods include biplane fluoroscopy, digital subtraction angiography with road mapping technology, venous angiography with road mapping technology, and the like. The embolic devices may comprise radio-opaque materials or markers that allow viewing of the position of the device under fluoroscopy.
• FIGS. 13-16 illustrate cross-sectional views of braided embolic devices comprising radiolucent and radio-opaque members, according to the embodiments of the disclosed inventions. The braidedembolic devices100 ofFIGS. 13-16 compriseradiolucent members250 composed of stainless steel, Nitinol, biocompatible polymers or other suitable materials. As shown inFIG. 13, the braidedembolic device100 comprises two evenly-spaced radio-opaque members260 (cross-sectional views of elongate members200) along the diameter D₁of thedevice100. Alternatively, the braidedembolic device100 ofFIG. 14 comprises four evenly-spaced radio-opaque members260 along the diameter D₁, andFIG. 15 comprises six evenly-spaced radio-opaque members260 along the diameter D₁. The braidedembolic device100 ofFIG. 16 comprises foursets260′ of evenly-spaced radio-opaque members along the diameter D₁, where each set260′ comprises two adjacently disposed radio-opaque members260. The radio-opaque members260 comprise filaments composed of platinum. It should be appreciated that other radio-opaque materials may be used inmembers260.
• In alternative embodiments,FIGS. 17A-B comprise four evenly-spaced radio-opaque members260 along the diameter D₁composed of platinum and four evenly-spaced radio-opaque members270 along the diameter D₁composed of Nitinol, where each of themembers260 are adjacently disposed to arespective member270. Themembers260 and270 may comprise different diameters. By way of non-limiting example, themembers260 have a smaller diameter D₂than the diameter D₃ofmembers270 inFIG. 17A; conversely, themembers260 have a larger diameter D₄than the diameter D₅ofmembers270 inFIG. 17B.
• In another alternative embodiment,FIG. 18 comprises four evenly-spaced radio-opaque members260 along the diameter D₁composed of platinum, a first set of four evenly-spaced radio-opaque members270 along the diameter D₁, and a second set of four evenly-spaced radio-opaque members270′ along the diameter D₁. Themembers270 and270′ are composed of Nitinol. As shown inFIG. 18, each of themembers260 is disposed betweenrespective members270 and270′, themembers260 have a smaller diameter D₆than the diameter D₇ofmembers270 and270′.
• In yet another alternative embodiment,FIG. 19 comprises four evenly-spaced radio-opaque members260 along the diameter D₁₀composed of platinum, a first set of four evenly-spaced radio-opaque members270 along the diameter D₁₀, and a second set of four evenly-spaced radio-opaque members270′ along the diameter D₁₀. Themembers270 and270′ are composed of Nitinol. As shown inFIG. 19, each of themembers260 is disposed betweenrespective members270 and270′ and displaced towards thelumen130 of theembolic device100 in the radially expanded configuration, themembers260 have a smaller diameter D₁₂than the diameter D₁₃ofmembers270 and270′.
• In a further alternative embodiment,FIG. 20 comprises four evenly-spaced radio-opaque members260 along the diameter D₂₀composed of platinum, a first set of four evenly-spaced radio-opaque members270 along the diameter D₂₀, and a second set of four evenly-spaced radio-opaque members270′ along the diameter D₂₀. Themembers270 and270′ are composed of Nitinol. As shown inFIG. 20, each of themembers260 is disposed betweenrespective members270 and270′. The members207′ are displaced towards thelumen130 of theembolic device100 in the radially expanded configuration, and the members207 are displaced away from thelumen130. Further, themembers260 have a smaller diameter D₂₁than the diameter D₂₂ofmembers270 and270′. Particularly,FIG. 20 shows the cross-sectional view of the braidedembolic device100′ ofFIG. 9. Additionally, the elongated members of the braidedembolic devices100 ofFIGS. 13-16 may comprise filaments, wires, drawn-filled tube or their like, composed of one or more suitable biocompatible materials, for example, nitinol and platinum drawn-filled tubes.
• FIGS. 21A-26B illustrate further exemplary braided embolic devices comprising a variety of braid patterns portions, constructed according to the embodiments of the disclosed inventions. The embolic devices portions ofFIGS. 21A-C andFIGS. 26A-B may comprise one or more of the braid patterns of the disclosed inventions, such as the patterns ofFIGS. 2-7, or a combination of patterns thereof, or any other suitable braid pattern.
• As shown inFIG. 21A, a braidedembolic device110 comprises an elongated configuration having adistal portion122, aproximal portion144, and a plurality ofsuccessive portions180 extending therebetween. Similarly to theembolic device100 ofFIG. 8, theembolic device110 has a radially compressed delivery configuration (not shown), and a radially expanded deployed configuration (shown inFIG. 21A), and preferably comprises a length that ranges from approximately 2 centimeters up to approximately 40 centimeters in the deployed configuration, and more preferably from approximately 5 centimeters up to approximately 25 centimeters in the deployed configuration. Theembolic device110 further comprises a plurality ofelongate member200 forming thebraid151 of thedevice110, similarly to theembolic device100. The plurality ofportions180 include alternatingfirst portions182 andsecond portions184 of theembolic device110 in the radially expanded deployed configuration. Thefirst portions182 of theembolic device110 comprises a flat, ribbon-like configuration formed by a single layer ofbraid151. Alternatively, thefirst portions182 may be formed by more than one layer ofbraid151, such as, a flattened tubular braid. Thefirst portions182 of theembolic device110 comprising the ribbon-like configuration have rectangular cross-sections, as shown inFIG. 21B. Alternatively, thefirst portions182 may have any other suitable cross-sections, for example: ovoid or elliptical, such as a tubular braid that is flattened, single-layer ribbon with rounded edges cross-section or the like, or combinations thereof. Thesecond portions184 of theembolic device110 comprises a round or tube-like configuration formed by two or more of the plurality ofelongate members200 twisted, bundled, coupled together or the like. The two or more coupledelongate members200 form an elongate set ofmembers200 between two of thefirst portions182 of theembolic device110. As shown inFIGS. 21A and 21C, thesecond portions184 depicts elongate sets200-1,200-2,2003, and200-4 showing the tube-like configuration. Further, the round, tube-like configuration of thesecond portions184 may be better appreciated in the cross-sectional view ofFIG. 21C, further including elongated sets200-5, and200-6. By way of non-limited examples, each of the elongate sets200-1 to200-6 may be formed by having twoelongate members200 twisted together (FIG. 22), more than twoelongate members200 twisted together (FIG. 23), or by having the plurality ofelongate members200 bundled together (FIG. 24), or any other suitable coupling or combinations therefor (FIG. 25).
• FIGS. 26A-B depict perspective side and top views of anotherembolic device112, constructed according to the embodiments of the disclosed inventions.FIGS. 26A-B illustrate anembolic device112 that is similar to theembolic device110 depicted inFIGS. 21A-C. One difference is that theembolic device112 comprises abraid156 extending between theproximal portion144′ anddistal portion122′ of thedevice112 forming the plurality ofsuccessive portions180′. Another difference is that the plurality ofsuccessive portions180′ further includestransition portions183 between each of thefirst portions182′ andsecond portions184′ of theembolic device110 in the radially expanded deployed configuration. Similarly toembolic device110, thefirst portions182′ of theembolic device112 comprises a flat, ribbon-like configuration and thesecond portions184′ of theembolic device112 comprises a round or tube-like configuration. Further, thetransition portions183 may comprise tapered, cone-like configurations formed between the corresponding first182′ and second184′ portions of theembolic device112, as shown inFIG. 26A. Thebraid156 of theembolic device112 may vary in pitch, i.e., a distance between respectiveelongate members200, dimensions of the cells/openings, in pattern, and/or any other suitable configuration that allows for the formation of the plurality ofsuccessive portions180′.
• In the embodiments ofFIG. 21A andFIGS. 26A-B, each of thefirst portions182,182′ have respective length L₁that are larger than the respective lengths L₂of thesecond portions184,184′. The length L₁of thefirst portions182,182′ is approximately between 5 and 500 millimeters; preferably between 40 and 200 millimeters. The length L₂of thesecond portions184,184′ is approximately between 0.1 and 50 millimeters; preferably between 1 and 10 millimeters. The shorter length L₂and/or the configuration of thesecond portions184,184′ may form bending points that lower the axial and/or bending strength of theembolic devices110,112 at the correspondingsecond portions184,184′ when arespective device110,112 is under compression. For example, during the delivery of theembolic device110 from a delivery system into a target site in a patient (e.g., aneurysm sac), thedevice110 would be subjected to axial and/or bending stress due to the force/pressure exerted by the advancing force and by the target site (e.g., aneurysm inner wall) that the device comes in contact with. As the result, theembolic device110 bends or folds along thesecond portions184 assuming a three dimensional configuration within the target site (e.g., aneurysm sac).
• It should be appreciated that the embolic devices constructed according to the disclosed embodiments may be deployed at a target vascular site using devices and methods known in the art.
• Although particular embodiments have been shown and described herein, it will be understood by those skilled in the art that they are not intended to limit the present inventions, and it will be obvious to those skilled in the art that various changes, permutations, and modifications may be made (e.g., the dimensions of various parts, combinations of parts) without departing from the scope of the disclosed inventions, which is to be defined only by the following claims and their equivalents. The specification and drawings are, accordingly, to be regarded in an illustrative rather than restrictive sense. The various embodiments shown and described herein are intended to cover alternatives, modifications, and equivalents of the disclosed inventions, which may be included within the scope of the appended claims.

Claims (20)

What is claimed is:

1. An implantable vaso-occlusive device for occluding an aneurysm, comprising:

a braided member formed out of a first plurality of filaments interwoven with a second plurality of filaments, the braided member having a compressed configuration when constrained in a lumen of a delivery catheter, and an expanded configuration when not constrained;

wherein filaments of the first plurality are helically wound in a first rotational direction along an elongate axis of the braided member, and filaments of the second plurality are wound in a second rotational direction opposite the first rotational direction along the elongate axis of the braided member, such that filaments of the first plurality cross over and/or under filaments of the second plurality at each of a plurality cross-over locations axially spaced along the elongate axis of the braided member,

wherein at each cross-over location, the filaments of the first plurality cross over at least two consecutive filaments of the second plurality, then cross under only a single filament of the second plurality, and then cross over at least two additional consecutive filaments of the second plurality.

2. The vaso-occlusive device ofclaim 1, wherein at each cross-over location, the filaments of the first plurality are oriented substantially orthogonal to the filaments of the second plurality when the device is in an expanded, non-constrained configuration.

3. The vaso-occlusive device ofclaim 1, wherein the first rotational direction is clockwise, and the second rotational direction is counter-clockwise.

4. The vaso-occlusive device ofclaim 1, wherein at each cross-over location, the filaments of the first plurality cross over exactly two consecutive filaments of the second plurality, then cross under only a single filament of the second plurality, and then cross over exactly two more consecutive filaments of the second plurality.

5. The vaso-occlusive device ofclaim 1, wherein at each cross-over location, the filaments of the first plurality cross over at least three consecutive filaments of the second plurality, then cross under only a single filament of the second plurality, and then cross over at least three more consecutive filaments of the second plurality.

6. The vaso-occlusive device ofclaim 1, wherein the braided device comprises a first body portion and a second body portion, and wherein at each cross-over location in the first body portion, the filaments of the first plurality cross over two or three consecutive filaments of the second plurality, then cross under only a single filament of the second plurality, and then cross over at least two or three more consecutive filaments of the second plurality.

7. An implantable vaso-occlusive device for occluding an aneurysm, comprising:

a braided member formed out of braid filaments, the braided member having an compressed configuration when constrained in a lumen of a delivery catheter, and a tubular expanded configuration when not constrained, wherein when the braid member is in the expanded configuration, the braid filaments are disposed circumferentially about an elongate axis of the braided member,

the braid filaments comprising a plurality of filaments made out of a first material, and one or more marker filaments made of a second material having a higher stiffness and a higher radiopacity, respectively, than the first material filaments.

8. The vaso-occlusive device ofclaim 7, wherein the first material filaments are made out of nickel-titanium alloy, and the marker filaments are made out of platinum alloy.

9. The vaso-occlusive device ofclaim 7, the marker filaments including first and second marker filaments that are circumferentially offset approximately 180° from each other along at least a portion of the braided device when the braided device is in the tubular expanded configuration.

10. The vaso-occlusive device ofclaim 9, wherein the first marker filament is made out of a different material and/or has a different diameter or cross-section, respectively, than the second marker filament.

11. The vaso-occlusive device ofclaim 7, the marker filaments including four marker filaments that are circumferentially offset approximately 90° from each other along at least a portion of the braided device when the braided device is in the tubular expanded configuration.

12. The vaso-occlusive device ofclaim 11, wherein at least one of the four marker filaments is made out of a different material and/or has a different diameter or cross-section, respectively, than at least one other of the four marker filaments.

13. The vaso-occlusive device ofclaim 7, the marker filaments including six marker filaments that are circumferentially offset approximately 60° from each other along at least a portion of the braided device when the braided device is in the tubular expanded configuration, wherein at least one of the six marker filaments is made out of a different material and/or has a different diameter or cross-section, respectively, than at least one other of the six marker filaments.

14. The vaso-occlusive device ofclaim 7, the marker filaments including a first set of adjacent maker elements and a second set of adjacent marker elements, wherein the first set of adjacent marker elements are circumferentially offset approximately 180° from the second set of adjacent marker elements along at least a portion of the braided device when the braided device is in the tubular expanded configuration.

15. The vaso-occlusive device ofclaim 14, the first set of adjacent marker filaments comprising first and second marker filaments disposed adjacent one another, wherein the first marker filament is made out of a different material and/or has a different diameter or cross-section, respectively, than the second marker filament.

16. The vaso-occlusive device ofclaim 15, wherein the first marker filament is made out of platinum alloy and the second marker filament is made out of nitinol and platinum drawn-filled tubes.

17. The vaso-occlusive device ofclaim 14, the first set of adjacent marker filaments comprising first, second and third marker filaments disposed adjacent each other, wherein first marker filament is made out of a different material and/or has a different diameter or cross-section, respectively, than one or both of the second and third marker filaments.

18. An implantable vaso-occlusive device for occluding an aneurysm, comprising:

a braided member formed out of a plurality of interwoven braid filaments, the braided member having an compressed configuration when constrained in a lumen of a delivery catheter, and an expanded configuration when not constrained, in which the braid filaments are disposed circumferentially about an elongate axis of the braided member,

wherein in the expanded configuration, the braided member defines a plurality of enlarged cross-section segments spaced apart along the elongate axis thereof, wherein adjacent enlarged cross-section segments of the plurality are connected by a respective reduced diameter segment, and

wherein the braid filaments are interwoven according to a first weave pattern to create the respective enlarged cross-section segments, and wherein the braid filaments are interwoven according to a second weave pattern different than the first weave pattern to create each reduced diameter segment.

19. The vaso-occlusive device ofclaim 18, wherein in the second weave pattern, subsets of the plurality of interwoven braid filaments are wound into respective linking braids and/or wire bundles that span between adjacent enlarged cross-section segments.

20. The vaso-occlusive device ofclaim 18, wherein in the expanded configuration of the vaso-occlusive device, the reduced cross-section segment is outwardly expanded into a fattened, ribbon-like configuration about the elongate axis, and the enlarged cross-section segments are circumferentially expanded about the elongate axis.

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