CEMENT-DIRECTING ORTHOPEDIC IMPLANTS
20170156777 ยท 2017-06-08
Inventors
- Andrew R. Sennett (Hanover, MA, US)
- William Harwick Gruber (Southborough, MA, US)
- Joseph Ernest Richard (Bedford, MA, US)
Cpc classification
A61B17/8811
HUMAN NECESSITIES
A61F2002/30092
HUMAN NECESSITIES
A61F2002/30019
HUMAN NECESSITIES
A61F2002/30243
HUMAN NECESSITIES
A61F2/4455
HUMAN NECESSITIES
A61F2/0063
HUMAN NECESSITIES
A61F2/30907
HUMAN NECESSITIES
A61B17/8822
HUMAN NECESSITIES
A61B17/7098
HUMAN NECESSITIES
International classification
A61B17/88
HUMAN NECESSITIES
A61B17/70
HUMAN NECESSITIES
A61F2/00
HUMAN NECESSITIES
Abstract
A cement-directing structure for use in cement-injection bone therapy includes a collapsible, self-restoring braided structure with regions of differential permeability to the bone cement. The regions of differential permeability may be provided by areas where the braided mesh density is greater or lesser than surrounding areas and/or by means of a baffle. After the structure is placed in a void within a bony structure, cement is injected into the interior of the structure then oozes out in preferred directions according to the locations of the regions of differential permeability.
Claims
1. A device for use in treating orthopedic defects in a procedure, said device comprising: a collapsible, expandable mesh structure configured to have a first, collapsed configuration and a second, expanded configuration, wherein said mesh structure comprises co-braided primary members and secondary members occupying interstices between said primary members, and wherein said mesh structure has regions of different permeability or flow resistance configured to control the direction of bone cement or other orthopedic filler material through said mesh structure.
2. The device of claim 1, wherein said mesh structure is elastic and capable of self-expansion.
3. The device of claim 1, wherein said mesh structure includes a coating on at least a portion of said mesh structure.
4. The device of claim 1, wherein the primary and secondary members comprise wire members.
5. The device of claim 1, wherein the primary and secondary members are different from one another.
6. The device of claim 1, wherein the secondary members are smaller than the primary members.
7. The device of claim 1, wherein the first, collapsed configuration is maintained by a sheath.
8. The device of claim 1, wherein said mesh structure has at least one region in which the mesh opening size of said region is greater than the mesh opening size of surrounding regions.
9. The device of claim 8, wherein said mesh structure is configured such that bone cement flows preferentially out of the device through said at least one region of greater mesh opening size.
10. The device of claim 3, wherein the coating defines a flow-retarding baffle member.
11. The device of claim 10, wherein the flow-retarding baffle is formed on select regions of said mesh structure.
12. The device of claim 1, wherein said device is generally hollow and has first and second ends, both of which are closed.
13. The device of claim 1, wherein said device is generally hollow and has first and second ends, said first end is fastener closed and said second end is unrestrained.
14. A device for use in treating orthopedic defects in a procedure comprising inserting the device into a cavity within a bony member and injecting bone cement or other orthopedic filler material into an interior region of the device, said device comprising: a flexible mesh structure configured to move between a collapsed position and an expanded position, wherein the flexible mesh structure has sufficient rigidity to maintain walls of the cavity apart from each other in the expanded position; wherein the mesh structure is a co-braided structure including primary members and secondary members occupying interstices between said primary members.
15. The device of claim 14, wherein said mesh structure has regions of different permeability or flow resistance.
16. The device of claim 14, wherein said structure includes a coating on a portion of outer surface of the mesh structure to control the direction of the bone cement or other orthopedic filler material through the mesh structure.
17. The device of claim 14, wherein the mesh structure is elastic and capable of self-expanding.
18. The device of claim 14, wherein the primary and secondary members are wire and are different from one another.
19. The device of claim 17, wherein the secondary members are smaller than the primary members.
20. The device of claim 14, wherein the first, collapsed configuration is maintained by a sheath.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0019] These and other features and advantages of the invention will become clearer from the description below and the figures, in which:
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DETAILED DESCRIPTION
[0030] A first embodiment 100 of a cement-directing structure according to the invention is illustrated in
[0031] The core member 102 is formed from a multiplicity of elastic, heat-setting monofilament wire members (e.g., Nitinol wires) that are braided together in a plain braid fashion to form a collapsible, self-expanding, generally tubular structure using techniques that are known in the art. Other metallic or polymeric monofilament wires may also be used. The shape-memory /shape-restoring properties of alloys (particularly Nitinol), however, make them preferred. The core member 102 has sufficient mechanical strength and elasticity to assume its nominal shape upon complete insertion into a bone cavity and to contact opposed fractured surfaces, thereby providing some support to the surfaces and maintaining patency of the cavity.
[0032] As illustrated in
[0033] The cement flow windows 108 are regions of the core structure 102 where the secondary members have been removed from the meshwork formed by the primary wire members 112, thus leaving areas of increased permeability to cement flow relative to the surrounding regions of the core structure 102. The rest of the surface of the structure, however, remains co-braided. Thus, cement will tend to flow preferentially out of the cement flow windows 108 when it is injected into the interior of the cement-directing structure 100. The secondary members may be removed from the structure of the core member 102 by laser or mechanical cutting after the core member has been formed and heat-set in its desired configuration.
[0034] The specific location of the cement flow window(s) 108 will, of course, depend on clinical intent. According to a presently preferred configuration, however, two cement flow windows 108 are provided. Lengthwise speaking, as best illustrated in
[0035] The baffle 110, on the other hand, provides a region or regions of decreased permeability to cement flow as compared to the surrounding regions of the core structure 102. In other words, the baffle 110 blocks or severely restricts the flow of cement out of cement-directing structure 102 in specific locations when cement is injected into the interior of the structure 102. In this regard, the baffle 110 may be formed as an impermeable, flexible polymeric sheet or coating that is attached or bonded to either the inside or the outside of the core braided structure 102. The flexible polymeric coating may be silicone or other biocompatible materials such as EPTFE (expanded polytetroflouroethylene) or polyurethane, or it may comprise a tightly woven fabric such as polyester or other biocompatible or degradable suture material. The coating may be attached or adhered to the structure by a number of manufacturing processes known in the art, such as dip coating or electrospinning. The approximate thickness of the baffle coating is 0.0005 to 0.003 inches, so the coating will not preclude elastic deformation of the overall braided structure.
[0036] As is the case with respect to the cement window(s) 108, the precise location of the baffle 110 will depend on clinical intent. According to the presently preferred embodiment, however, the baffle 110 extends all the way from one end 104 of the device to the opposite end 106 and covers the ends, as illustrated in
[0037] Basic construction of a structure 100 according to the invention is illustrated in
[0038] Insertion and cement-directing operation of a structure 100 within a vertebral body VB is illustrated in
[0039] As illustrated in
[0040] Once the sheath-covered structure 102 is fully inserted into the cavity formed within the bone structure being treated, the sheath 132 is retracted, as illustrated in
[0041] A filling portal (not shown) on the other end of the rod is then connected to a cement injection syringe via a luer lock fitting (not shown). Cement can then be injected into the center of the structure, as indicated by directional arrows shown in the cannula 134. It is preferable that the open end of the structure be collapsed around the hollow push rod 132, thereby forming a slideable connection that assures lengthwise positioning and targeting of the flow portal of the push rod 132 within the center axis of the self-restoring device and easy removal of the push rod after filling with cement.
[0042] (Alternatively, a separate filling needle (shown in phantom in
[0043] As illustrated in
[0044] In particular, a greater amount of cement will flow out of the cement flow windows 108, as represented by the relatively thick, large arrows, than will flow out of the remainder of the structure 100, as represented by the relatively thin, small arrows. For the given orientation of the structure 100 within the vertebral body, with the cement flow windows 108 facing anterior-superior and anterior-inferior and the baffle 100 facing posterior, significant masses M of cement will be directed anterior-superior and anterior-inferior into the forward third of the vertebral body, thereby forming mantles of cement which cross the plane of the vertebral fracture. The cement mantles will be located adjacent to the vertebral endplates and thus will form a load-bearing column of cement.
[0045] Where other flow of cement out of the structure 100 exists, smaller volumes or masses m of cement will form. These smaller masses m of cement will beneficially interdigitate with the surrounding healthy bone tissue, thereby helping to anchor the structure of the invention in place within the vertebral body VB.
[0046] Conversely, the baffle 110, which is impermeable to cement, will block the flow of cement out of the structure 100 in the posterior direction. Advantageously, this helps prevent cement from flowing posteriorly, e.g., into the posterior venous complex, spinal canal, etc.
[0047] A modified embodiment 200 of a cement-directing structure according to the invention is illustrated in
[0048] Other variations in the invention are also possible. For example, using a variant of the manufacturing method described above, a multi-layered braided structure can be formed. For example, it is known that braids can be formed in multiple layers over a mandrel. Alternatively, the original braided tube structure may be folded back on itself prior to heat-setting, as illustrated in
[0049] Another multi-layered variation 300 of a cement-directing structure according to the invention is shown in
[0050] If the stacked, multi-layer structure is too thick to fit in a sheath in the collapsed state for deployment, then a layered structure may be constructed in vivo by deploying individual self-restoring structures sequentially into the original expanded structure. In that specific instance, the outer layer 306 would have an opening sufficient to accept the second layer 304 such that when assembled in vivo the second layer occupies the opening of the first layer. The inner expandable structures 302, 304 may or may not have a baffling component, supplementary filaments, or coatings, yet would provide enhanced mechanical strength as each layer expands and contacts the outer layer. Each consecutive device would be pre-assembled in the collapsed state into a cannula and then deployed through the cannula in sequence (not shown). The plurality of layers defined in this alternate embodiment has the secondary benefit of reinforcement to the cement mantle.
[0051] In addition to these variant embodiments, shapes other than the ovoid or football shape shown in the Figures above may be desirable. For example, oblong or pear-shaped cement-directing structures 400 might be desired where, for example, when it is clinically indicated to approach the vertebral body bilaterally, through each pedicle, as illustrated in
[0052] These and other variations to the embodiments disclosed and described above will occur to those having skill in the art. To the extent such variations incorporate the inventive concepts disclosed herein, they are deemed to fall within the scope of the following claims.