Expandable Ring Intervertebral Fusion Device
20170172754 ยท 2017-06-22
Assignee
Inventors
- William Frasier (New Bedford, MA, US)
- Narendren Renganathan (Burlington, MA, US)
- Glen Presbrey (Mapleville, RI, US)
- Michael A. Fisher (Lawrenceville, GA, US)
- John Riley Hawkins (Cumberland, RI, US)
Cpc classification
A61F2002/30291
HUMAN NECESSITIES
A61F2002/30092
HUMAN NECESSITIES
A61F2/441
HUMAN NECESSITIES
A61F2002/30677
HUMAN NECESSITIES
A61F2002/2817
HUMAN NECESSITIES
A61F2002/30062
HUMAN NECESSITIES
A61F2230/0091
HUMAN NECESSITIES
A61F2002/30583
HUMAN NECESSITIES
A61F2/446
HUMAN NECESSITIES
A61F2210/0014
HUMAN NECESSITIES
A61F2002/30131
HUMAN NECESSITIES
A61F2002/3052
HUMAN NECESSITIES
A61F2002/30594
HUMAN NECESSITIES
A61F2002/30579
HUMAN NECESSITIES
A61F2220/0025
HUMAN NECESSITIES
A61F2230/0013
HUMAN NECESSITIES
A61F2/4465
HUMAN NECESSITIES
International classification
Abstract
An expandable tube having a substantially semicircular unexpanded shape is inserted into the disc space after the disc material has been removed therefrom. A plurality of expandable lockable rings are passed over this tube in their unexpanded states and positioned along the anterior edge of the endplates. The tube is then expanded, thereby forcing the rings to expand. The rings hold their final expanded configuration via a one-way locking mechanism. Once sufficient distraction is achieved and the rings locked, the tube is collapsed and removed, thereby leaving the expanded, locked rings behind to support the disc space.
Claims
1. A method of distracting a disc space having opposing vertebral endplates, comprising the steps of: a) inserting a tube having a throughbore into the disc space, b) passing a plurality of rings having a one-way locking mechanism over the tube in a first unexpanded state, c) positioning the plurality of rings along an anterior edge of the endplates, d) expanding the tube to force the rings to a second expanded locked state, e) collapsing the expanded tube to leave the locked rings behind to support the disc space, and f) removing the tube.
2. The method of claim 1 wherein each ring in its expanded locked state has a diameter substantially corresponding to a height of the disc space.
3. The method of claim 1 wherein each ring in its expanded locked state has a first row of gripping teeth extending outwards for gripping a first vertebral endplate.
4. The method of claim 1 wherein each ring in its expanded locked state has a second row of gripping teeth extending outwards for gripping a second vertebral endplate.
5. The method of claim 1 wherein the expansion step comprises providing a fluid in the throughbore of the flexible tube.
6. The method of claim 1 wherein each ring has a first and second end, the first end having a first mating tooth, the second end having a second mating tooth, wherein the first and second mating teeth mate with each other in the expanded locked state to prevent return of the ring to its unexpanded state.
7. A method of distracting a disc space having opposed vertebral endplates, comprising the steps of: a) inserting a tube into the disc space, the tube carrying a plurality of rings thereon, wherein the rings are in a first unexpanded state and have a one-way locking mechanism, b) positioning the rings along an anterior edge of the endplates, c) expanding the tube to force the rings to expand and lock, d) collapsing the expanded tube to leave behind the rings to support the disc space, and e) removing the tube.
8. A method of making an in-situ formed intervertebral fusion cage, comprising the steps of: a) inserting an assembly into a disc space, the assembly comprising an expandable balloon having a plurality of expandable rings thereon, b) expanding the expandable balloon to expand the expandable rings.
9. A method of making an in-situ formed intervertebral fusion cage, comprising the steps of: a) inserting into a disc space a fusion ring in an unexpanded state, b) expanding the ring to an expanded state.
10. A method of making an in-situ formed intervertebral fusion cage, comprising the steps of: a) inserting into a disc space a spiral-shaped fusion ring having an inner end and a outer end, wherein the ends overlap, b) expanding the ring so that the first end abuts the second end.
11. An assembly for inserting an intervertebral fusion device, comprising: a) a first flexible tube having an outer radius and a throughbore, a first unexpanded state and a second expanded state, b) a plurality of bladder rings having a first unexpanded state and a second expanded, locked state, wherein each bladder ring surrounds the outer radius of the tube and is filled with a curable component, wherein the plurality of rings are in their unexpanded states when the tube is initially in its unexpanded state, and wherein the plurality of bladder rings are in their expanded states once the tube has been placed in its expanded state.
12. An intervertebral fusion device comprising an assembly for inserting an intervertebral fusion device, comprising: a) a first flexible tube having an outer radius and a throughbore, a first unexpanded state and a second expanded state, b) a plurality of expandable rings having a first unexpanded state and a second expanded, locked state, wherein each ring comprises; i) upper and lower plates, each plate having an outer surface adapted for gripping a vertebral endplate and an inner surface adapted for bearing against the outer radius of the first flexible tube, and ii) a pair of elongatable struts connecting the upper and lower plates, each strut adapted to resist recession, wherein each expandable ring surrounds the outer radius of the tube, wherein the plurality of rings are in their unexpanded states when the tube is initially in its unexpanded state, and wherein the plurality of rings are in their expanded states once the tube has been placed in its expanded state.
13. An intervertebral fusion device comprising: a) first U-shaped component having first and second legs and an intermediate curved region comprising a convex surface and a concave surface, b) second U-shaped component having first and second legs and an intermediate curved region comprising a convex surface and a concave surface, wherein the concave surfaces oppose each other, and the convex surfaces are adapted for gripping respective opposed vertebral endplates, and wherein the first legs of each component are adapted to nest with each other to form a first keyway, and wherein the second legs of each component are adapted to nest with each other to form a second keyway.
14. The device of claim 13 further comprising a securement pin, wherein the first legs of each component further comprise a throughhole, and wherein the securement pin passes through each throughhole.
15. The device of claim 13 wherein the first legs of each component further comprise ratchet teeth adapted for one way movement.
Description
DESCRIPTION OF THE FIGURES
[0022]
[0023]
[0024]
[0025]
[0026]
[0027]
[0028]
[0029]
[0030]
[0031]
[0032]
[0033]
[0034]
[0035]
[0036]
[0037]
[0038]
DETAILED DESCRIPTION OF THE INVENTION
[0039]
[0040] Therefore, in accordance with the present invention, there is provided a method of distracting a disc space having opposing vertebral endplates, comprising the steps of : [0041] a) inserting a tube having a throughbore into the disc space,
[0042] b) passing a plurality of rings having a one-way locking mechanism over the tube in a first unexpanded state, [0043] c) positioning the plurality of rings along an anterior edge of the endplates, [0044] d) expanding the tube to force the rings to a second expanded locked state , [0045] e) collapsing the expanded tube to leave behind the locked rings to support the disc space, and [0046] f) removing the tube.
[0047] Also in accordance with the present invention, there is provided an intervertebral fusion device for supporting a disc space, comprising: [0048] a) a substantially semicircular array of rings having a first unexpanded state and a second expanded, locked state,
wherein each ring in its expanded, locked state has a diameter corresponding substantially to a height of the disc space.
[0049] In some embodiments, and now referring to
[0050]
[0051] Therefore, in accordance with the present invention, there is provided a method of making an in-situ formed intervertebral fusion cage, comprising the steps of: [0052] a) inserting an assembly into a disc space, the assembly comprising an expandable balloon having a plurality of expandable rings thereon, [0053] b) expanding the expandable balloon to expand the expandable rings.
[0054] Also in accordance with the present invention, there is provided a method of making an in-situ formed intervertebral fusion cage, comprising the steps of: [0055] a) inserting into a disc space a fusion ring in an unexpanded state, [0056] b) expanding the ring to an expanded state.
[0057] Also in accordance with the present invention, there is provided a method of making an in-situ formed intervertebral fusion cage, comprising the steps of: [0058] a) inserting into a disc space a spiral-shaped fusion ring having an inner end and a outer end, wherein the ends overlap, [0059] b) expanding the ring so that the first end abuts the second end.
[0060] The rings of the present invention could be continuous spiral coils that uncoil as they are distracted. The coils could have mechanical features that enable its shape to be fixed in space (crimp zones, interference fits, adhesives, keys, etc.). The coils could be nested. The nesting could be produced by deploying the first coil, sliding a second coil down the flexible tube and deploying that second coil, etc. The nested coils would exert progressively higher distraction strength. Theoretically, a predetermined interbody distraction load could be applied by concentric sequential deployment of spring coils. The coils could be made of a memory metal that deploys upon contact with the body's heat.
[0061] In some embodiments, each ring comprises chain links forming a linked chain. These links enable limited excursion but provide very high tensile strength once they are distracted. These chain links would require a fixation meansadhesives, crimps, keys, interference fits, stakes, etc.
[0062] In some embodiments, the expansion member (inner balloon) could be left in place to act as a delivery catheter for chemicals, energy, or diagnostic information as a quasi-chronic implant that is preferably removed before twenty eight days. In particular, the inner balloon may be adapted to deliver at least one of red or near infrared light, dissolved oxygen or nitric oxide, profound hypothermia, hyperthermia, electrical stimulation, mechanical stimulation, or growth factors.
[0063] Without wishing to be tied to a theory, it is believed that leaving a quasi-chronic catheter in the disc space to be fused is desirable because a significant amount of the bone graft placed in the disc space often necrotizes before vascularization and engraftment takes place, and the delivery catheter described above can alleviate some problems associated with ischemia and delayed engraftment.
[0064] Similarly, irradiation of the graft with red/NIR light might improve cell survival in the graft.
[0065] Likewise, since oxygen therapy has been shown to be beneficial in dermal wounds, catheter-based delivery of oxygen should be expected to improve the acute phase of hard tissue engraftment.
[0066] In some embodiments, mechanical energy is transferred through the catheter in order to drive bulk flow and thereby promote diffusion of metabolic products and wastes. One example of such mechanical energy is ultrasonic stimulation of graft tissues and bone remodeling.
[0067] In some embodiments, the expandable rings could comprise a part of an outer balloon or bladder that cures after hydraulic deployment. The outer bladder could allow the instrument-based flexible inner balloon (that expands the rings) to pass through it. Upon expansion, the implant-based outer bladder forms a soft ring of material surrounding the instrument-based flexible inner balloon that substantially conforms to the endplate geometry while preserving a near-ideal load-bearing circular void in the middle of the bladder. The outer bladder could cure on exposure to heat, light or well-timed chemical reaction. The instrument-based flexible inner balloon could be used to deliver the curing queue.
[0068] Now referring to
[0069] Preferably, the curable bladders of
[0075] In other embodiments, the plurality of curable bladder rings are inserted into the disc space prior to the insertion of the inner balloon into the disc space. In still other embodiments, the plurality of curable bladder rings are inserted into the disc space after the insertion of the inner balloon into the disc space.
[0076] Now referring to
[0077] Now referring to
[0078] In some embodiments, the inner balloon preferably comprises either PTFE or PET. When these materials are selected. this inner balloon can be made to have a very small outer dimension prior to expansion. In some embodiments. the bladder ring comprises either a fabric, ePTFE, or another plastic. More preferably, the bladder ring further has an osteo-integrating or high friction outer surface to assist in fusion or stabilization.
[0079] Therefore, in accordance with the present invention, there is provided an assembly for inserting an intervertebral fusion device, comprising: [0080] a) a first flexible tube 61 having an outer radius 63 and a throughbore, a first unexpanded state and a second expanded state, [0081] b) a plurality of bladder rings 65 having a first unexpanded state and a second expanded, locked state, [0082] wherein each bladder ring surrounds the outer radius of the tube and is filled with a curable component, [0083] wherein the plurality of rings are in their unexpanded states when the tube is initially in its unexpanded state, and [0084] wherein the plurality of bladder rings are in their expanded states once the tube has been placed in its expanded state.
[0085] Preferably, the first flexible tube has an arcuate expanded shape.
[0086] Now referring to
[0087] Therefore, in accordance with the present invention, there is provided an intervertebral fusion device comprising an assembly for inserting an intervertebral fusion device, comprising: [0088] a) a first flexible tube (not shown) having an outer radius and a throughbore, a first unexpanded state and a second expanded state, [0089] b) a plurality of expandable rings 71 having a first unexpanded state (
[0095] In some embodiments, the rings consist of multiple components connected by sliding keyways. Once distracted, the keyways could be fixed relative to one another by the various means described above. The keyway would replace the toothed irreversible fixation system described in
[0096] Now referring to
[0097] In particular, in accordance with the present invention, there is provided an intervertebral fusion device comprising: [0098] a) first U-shaped component 81 having first 82 and second 83 legs and a curved intermediate region 84 comprising a convex surface 85 and a concave surface 86, [0099] b) second U-shaped component 91 having first 92 and second 93 legs and a curved intermediate region 94 comprising a convex surface 95 and a concave surface 96,
wherein the concave surfaces oppose each other, and the convex surfaces are adapted for gripping respective opposing vertebral endplates, and
wherein the first legs of each component are adapted to nest with each other to form a first keyway, and
wherein the second legs of each component are adapted to nest with each other to form a second keyway.
[0100] In some embodiments, and now referring to
[0101] In some embodiments, and now referring to
[0102] As shown, each leg comprises a pair of parallel plates that nest with the parallel plates of the opposing leg. Adhesives could be applied between the sliding plates of each leg. The ultimate bond would be primarily loaded in shear. The adhesive could contain particulate or fiber reinforcement to withstand the shear.
[0103] In some embodiments, the faces on each plate could be textured or contoured to support load bearing. One-way ratchet and pawl mechanisms could be placed on the faces of each plate to prevent the plate from sliding after deployment.
[0104] The ring geometry could be modified to a different shape or to accommodate mechanical keys to prevent collapse.
[0105] In one embodiment, a hardenable, resorbable, bone fusion-promoting composition is delivered into the disc space by first providing a resorbable, expandable balloon to the disc space, and then filling the balloon with the fusion-promoting composition.
[0106] Preferred resorbable, expandable balloons include inflatable bags, thin-walled balloons, and fabric jackets.
[0107] In some embodiments, a mesh balloon is selected. The mesh nature of the bags provides for enhanced osteogenic connection between the internal cavity and the patient's tissue.
[0108] In some embodiments, the balloons are perforated to provide osteogenic avenues between the bone fusion-promoting composition and the patient's tissue.
[0109] Preferably, the balloon is resorbable. When the balloon is resorbable, its eventual resorption after fusion has taken place eliminates problems associated with permanent implants. More preferably, the resorbable balloon is made from a resorbable polymers as discussed below. However, in other embodiments, the balloon may include non-resorbable components or be completely non-resorbable.
[0110] Compositions for filling the balloon of this invention are known in the art. Hardenable, resorbable compositions include setting ceramics, polymerizable monomers and polymers, polymers flowable at temperatures above body temperature, and polymers solubilized in a biocompatible solvent. Examples of resorbable setting ceramics include calcium phosphates, hydroxyapatites and calcium sulfates. Examples of polymerizable resorbable monomers and polymers include poly(propylene fumarate), polyoxaesters, polyurethanes and polyanhydrides. In one preferred embodiment, the hardenable composition is a photopolymerized polyanhydride. In this embodiment, irradiation can be used to control the polymerization process, therefore, a partially polymerized putty can be made, then hardened by continuing the polymerization with irradiation after the composition has been placed. Examples of resorbable polymers flowable at temperatures above body temperature include polymers and copolymers of lactic acid, glycolic acid, carbonate, dioxanone, and trimethylene carbonate. An example of a biocompatible solvent that can be used to solubilize the aforementioned polymers include dimethyl sulfoxide.
[0111] In order to improve the osteoconductivity of the aforementioned hardenable, resorbable compositions, they may be delivered to the site as an in-situ formed porous scaffold. Techniques of in situ forming porous scaffolds are known in the art and include porogen leaching and foaming with gas-producing elements.
[0112] In preferred embodiments of this invention, the hardenable, resorbable compositions incorporate an osteoinductive component. Osteoinductive components include growth factors such as bone morphogenetic proteins that can be grafted onto or mixed into said hardenable compositions. The term growth factors encompasses any cellular product that modulates the growth or differentiation of other cells, particularly connective tissue progenitor cells. The growth factors that may be used in accordance with the present invention include, but are not limited to, members of the fibroblast growth factor family, including acidic and basic fibroblast growth factor (FGF-1 and FGF-2) and FGF-4; members of the platelet-derived growth factor (PDGF) family, including PDGF-AB, PDGF-BB and PDGF-AA; EGFs; members of the insulin-like growth factor (IGF) family, including IGF-I and -II; the TGF- superfamily, including TGF-1, 2 and 3 (including MP-52); osteoid-inducing factor (OIF), angiogenin(s); endothelins; hepatocyte growth factor and keratinocyte growth factor; members of the bone morphogenetic proteins (BMP's) BMP-1, BMP-3; BMP-2; OP-1; BMP-2A, BMP-2B, and BMP-7, BMP-14; HBGF-1 and HBGF-2; growth differentiation factors (GDF's), members of the hedgehog family of proteins, including indian, sonic and desert hedgehog; ADMP-1; members of the interleukin (IL) family, including IL-1 thru IL-6; GDF-5 and members of the colony-stimulating factor (CSF) family, including CSF-1, G-CSF, and GM-CSF; and isoforms thereof.
[0113] In addition, bone-producing cells, such as mesenchymal stem cells (MSCs), can be delivered with the hardenable compositions by first encapsulating the cells in hydrogel spheres then mixing in.
[0114] MSCs provide a special advantage because it is believed that they can more readily survive relatively harsh environments; that they have a desirable level of plasticity; and that they have the ability to proliferate and differentiate into the desired cells.
[0115] In some embodiments, the mesenchymal stem cells are obtained from bone marrow, preferably autologous bone marrow. In others, the mesenchymal stem cells are obtained from adipose tissue, preferably autologous adipose tissue.
[0116] In some embodiments, the mesenchymal stem cells used in an unconcentrated form. In others, they are provided in a concentrated form. When provided in concentrated form, they can be uncultured. Uncultured, concentrated MSCs can be readily obtained by centrifugation, filtration, or immuno-absorption. When filtration is selected, the methods disclosed in U.S. Pat. No. 6,049,026 (Muschler), the specification of which is incorporated by reference in its entirety, are preferably used. In some embodiments, the matrix used to filter and concentrate the MSCs is also administered into the container.
[0117] In another embodiment of the invention, the hardenable, resorbable, bone fusion-promoting composition is delivered to the disc space as a partially hardened, shapable putty. The putty can then be pressed into the disc space. Following shaping, the partially hardened composition will completely harden to provide a rigid fixation of the spine.