The present invention relates to plates for generating, applying, and maintaining compression to a site in a human or animal body in order to facilitate healing of diseased or damaged tissue. The invention finds particular utility in the field of orthopedics and specifically for reducing fractures and maintaining compression between bone fragments. While the invention has application throughout the body, its utility will be illustrated herein in the context of the repair of fractured or displaced bone tissue, such as during a Calcaneal-Cuboid Arthrodesis, Metatarsal Shortening and/or Distal Radius Fixation. The present invention also finds utility as a cervical compression plate, and/or as other spinal compression plates.
In the field of orthopedic surgery it is common to rejoin broken bones. The success of the surgical procedure often depends on the ability to reapproximate the bone fragments, the amount of compression achieved between the bone fragments, and the ability to sustain that compression over a period of time. If the surgeon is unable to bring the bone fragments into close contact, a gap will exist between the bone fragments and the bone tissue will need to fill that gap before complete healing can take place. Furthermore, gaps between bone fragments that are too large allow motion to occur between the bone fragments, disrupting the healing tissue and thus slowing the healing process. Optimal healing requires that the bone fragments be in close contact with each other, and for a compressive load to be applied and maintained between the bone fragments. Compressive strain between bone fragments has been found to accelerate the healing process in accordance with Wolf's Law.
Broken bones can be rejoined using plates. These plates are generally formed from a sheet or ribbon of material with a plurality of holes formed therein. The plates are typically manufactured from either stainless steel alloys or titanium alloys. The plates are placed adjacent to a fracture so that the plate spans the fracture line, and then screws are inserted through the holes in the plate and into the bone fragments on either side of the fracture site so as to stabilize the bone fragments relative to one another.
While these plates are designed to stabilize a fracture, they do not always succeed in generating a compressive load between the bone fragments. It is widely reported that the compressive load of plates dissipates rapidly as the bone relaxes and remodels around the screws which hold the plate to the bone.
Thus there exists a clinical need for new and improved compression plates which are able to bring bone fragments into close proximity with each other, generate a compressive load, and maintain that compressive load for a prolonged period of time while healing occurs.
The present invention provides a novel compression plate which is able to bring bone fragments into close proximity with each other, generate a compressive load, and maintain that compressive load for a prolonged period of time while healing occurs.
Among other things, the present invention comprises the provision and use of a novel compression plate which is manufactured from a single piece of shape memory material (e.g., a material capable of exhibiting superelasticity and/or a temperature-induced shape change). The shape memory material may be a metal alloy (e.g., Nitinol) or a polymer (e.g., appropriately processed PEEK). The novel compression plate is designed to reduce fractures and generate and maintain more uniform compression between the cortical bone and cancellous bone of the bone fragments so as to aid in fracture healing.
In one form of the invention, the novel compression plate comprises two opposing regions joined together by a pair of elastic bridge members, and an opening in each of the two opposing regions for receiving screws. In the un-restrained state, the two elastic bridge members are bowed outwardly. Prior to implantation, the two elastic bridge members can be reversibly strained inwardly so that the two elastic bridge members are nearly parallel (i.e., the two elastic bridge members are stretched laterally inwardly). A delivery device may be used to accomplish this straining of the compression plate and to hold the compression plate in this strained state prior to implantation. Upon implantation, the constraint on the two elastic bridge members is removed, whereupon the two elastic bridge members attempt to return to their original unrestrained state, thereby generating a compressive load and maintaining that compressive load for a prolonged period of time while healing occurs.
In one preferred form of the invention, there is provided apparatus for providing compression within a body, said apparatus comprising:
a compression plate comprising first and second opposing regions connected together by at least one elastic bridge member, wherein said at least one elastic bridge member has a non-linear configuration when it is in its unbiased condition but is capable of being elastically deformed to a more linear configuration upon the application of force to said at least one elastic bridge member, and at least one opening formed in each of said first and second opposing regions, wherein said at least one opening in each of said first and second opposing regions is configured to receive a fastener;
such that said openings in said first and second opposing regions are separated by a first distance when said at least one elastic bridge member is in its said non-linear configuration, and said openings in said first and second opposing regions are separated by a second distance when said at least one elastic bridge member is in its said more linear configuration, and further wherein said second distance is greater than said first distance.
In another preferred form of the invention, there is provided a compression plate for providing compression to first and second bone fragments across a fracture line, said compression plate comprising:
first and second opposing regions connected together by at least one elastic bridge member, wherein said at least one elastic bridge member has a non-linear configuration when it is in its unbiased condition but is capable of being elastically deformed to a more linear configuration upon the application of force to said at least one elastic bridge member; and
at least one opening formed in each of said first and second opposing regions, wherein said at least one opening in each of said first and second opposing regions is configured to receive a fastener;
such that when said at least one elastic bridge member is elastically strained into its said more linear configuration, and said compression plate is positioned against bone so that one of said openings is positioned over the first bone fragment and one of said openings is positioned over the second bone fragment, with said at least one elastic bridge member spanning the fracture line, and when a fastener is passed through one opening and into the first bone fragment and another fastener is passed through the other opening and into the second bone fragment, and the strain on said at least one elastic bridge member is thereafter released, said compression plate will apply a compressive force across the fracture line.
In another preferred form of the invention, there is provided a method for applying compression to first and second bone fragments across a fracture line, said method comprising:
providing apparatus for providing compression within a body, said apparatus comprising:
elastically straining said at least one elastic bridge member into its said more linear configuration, and positioning said compression plate against the first and second bone fragments so that one of said openings is positioned over the first bone fragment and one of said openings is positioned over the second bone fragment, with said at least one elastic bridge member spanning the fracture line, and passing a fastener through one opening and into the first bone fragment and passing another fastener through the other opening and into the second bone fragment; and
releasing the strain on said at least one elastic bridge member so that said compression plate will apply a compressive force across the fracture line.
In another preferred form of the invention, there is provided a compression plate comprising:
first and second opposing regions connected together by at least one bridge member; and
at least one opening formed in each of said first and second opposing regions, wherein said at least one opening in each of said first and second opposing regions is configured to receive a fastener;
wherein said at least one bridge member is formed out of austenite but capable of forming stress-induced martensite;
and further wherein at least one of said opposing regions is formed out of fully annealed Nitinol or martensitic Nitinol with an austenite start temperature greater than body temperature.
In another preferred form of the invention, there is provided apparatus for providing distraction within a body, said apparatus comprising:
a distraction plate comprising first and second opposing regions connected together by at least one elastic bridge member, wherein said at least one elastic bridge member has a more linear configuration when it is in its unbiased condition but is capable of being elastically deformed to a less linear configuration upon the application of force to said at least one elastic bridge member, and at least one opening formed in each of said first and second opposing regions, wherein said at least one opening in each of said first and second opposing regions is configured to receive a fastener;
such that said openings in said first and second opposing regions are separated by a first distance when said at least one elastic bridge member is in its said more linear configuration, and said openings in said first and second opposing regions are separated by a second distance when said at least one elastic bridge member is in its said less linear configuration, and further wherein said first distance is greater than said second distance.
In another preferred form of the invention, there is provided a method for applying distraction to first and second bone segments, said method comprising:
providing apparatus for providing distraction to first and second bone segments, said apparatus comprising:
elastically straining said at least one elastic bridge member into its said less linear configuration, and positioning said distraction plate against the first and second bone segments so that one of said openings is positioned over the first bone segment and one of said openings is positioned over the second bone segment, and passing a fastener through one opening and into the first bone segment and passing another fastener through the other opening and into the second bone segment; and
releasing the strain on said at least one elastic bridge member so that said distraction plate will apply a distraction force to the first and second bone segments.
These and other objects and features of the present invention will be more fully disclosed or rendered obvious by the following detailed description of the preferred embodiments of the invention, which is to be considered together with the accompanying drawings wherein like numbers refer to like parts, and further wherein:
Looking first at
Novel compression plate 5 is preferably a structure manufactured from a single piece of shape memory material (e.g., a material capable of exhibiting superelasticity and/or a temperature-induced shape change). The shape memory material may be a metal alloy (e.g., Nitinol) or a polymer (e.g., appropriately processed PEEK). Compression plate 5 is designed to reduce fractures and generate and maintain compression between bone fragments in order to aid in fracture healing. Compression plate 5 generally comprises two opposing regions 10 joined together by a pair of elastic bridge members 15, and at least one opening 20 formed in each of the two opposing regions 10 for receiving fixation screws. Openings 20 may have a countersunk feature (e.g., a bore-counterbore configuration) so as to allow the heads of the fixation screws to sit substantially flat with the top surface of compression plate 5. Additionally, openings 20 may be threaded so as to allow for positive engagement between the openings and the threaded fixation screws. In the un-restrained state, elastic bridge members 15 are bowed outwardly, such as in the manner shown in
Prior to implantation, elastic bridge members 15 of compression plate 5 can be reversibly strained inwardly (i.e., bent laterally inwardly), thus increasing the distance 25 (
During implantation, the strained (i.e., elongated) compression plate 5 is positioned against the bone fragments and secured to those bone fragments by passing fixation screws through openings 20 and into the bone fragments.
Removal of the induced strain on compression plate 5 (provided by the delivery device, see below) results in compression plate 5 attempting to return to its original un-restrained state (
Thus it should be appreciated that compression plate 5 may be formed in a variety of linear and non-linear configurations, and may include two or more opposing regions 10 and one or more elastic bridge members 15. Thus, for example, in one form of the invention, compression plate 5 may comprise a linear configuration having two opposing regions 10 connected together by one or more elastic bridge members 15. In another form of the invention, compression plate 5 may comprise a linear configuration having three or more opposing regions 10, each pair of opposing regions being connected together by one or more elastic bridge members 15. In still another form of the invention, compression plate 5 may comprise a non-linear configuration (e.g., a curved configuration) having two opposing regions 10 connected together by one or more elastic bridge members 15. In still another form of the invention, compression plate 5 may comprise a non-linear configuration (e.g., a triangular configuration, a L-shaped configuration, etc.) having three or more opposing regions 10, each pair of opposing regions being connected together by one or more elastic bridge members 15. It will be appreciated that compression plate 5 may also comprise still other configurations, e.g., square, circular, etc., all of which are considered to be within the scope of the present invention.
It will be appreciated that the fixation screws used with compression plate 5 may be conventional fixation screws of the sort well known in the field of fracture fixation.
By way of example but not limitation, and looking now at
It will be appreciated that various delivery devices may be used to deploy compression plate 5 in the body.
By way of example but not limitation, and looking now at
Now next at
First, compression plate 5 is loaded onto the delivery device (e.g., delivery device 200 discussed above) and elastic bridge members 15 are compressed so that they are near-parallel (or at least more parallel). The constrained compression plate 5 is then placed over the fracture line 300 and holes 310 are drilled through openings 20. Screws (e.g., snap-off screws 120 of snap-off screw system 100) are installed (i.e., they are advanced through openings 20 and into bone fragments 305), thereby fixing compression plate 5 to the bone fragments 305. The constraining delivery device (e.g., delivery device 200) is then removed and the compression plate 5 is allowed to attempt to regain its original unconstrained shape, thereby generating and maintaining compression across the fracture site.
Note that compression plate 5 is configured so that the force which is generated as compression plate 5 reconfigures (i.e., as elastic bridge members 15 return outwardly) is less than the “tear through” force of the bone which receives screws 120, i.e., compression plate 5 is specifically engineered so as to not “tear through” the bone tissue when attempting to reconfigure to its original foreshortened configuration. The compressive forces of compression plate 5 can be controlled by (i) modulating the material properties of the compression plate, and/or (ii) varying the geometry of the compression plate.
The percentage of cold work in the shape memory material forming compression plate 5 affects the compressive force generated by the reconfiguring compression plate. As the percentage of cold work increases, the compression force declines. A Nitinol compression plate should, preferably, have between about 15% and 55% cold work to control the recovery force of the compression plate; however, other degrees of cold work may be used, and/or the material may not be cold worked at all.
Another material property that affects the plate's compression force is the temperature differential between the body that the compression plate will be implanted into (assumed to be 37° C., which is the temperature of a human body) and the austenite finish temperature of the shape memory material forming compression plate 5. A smaller temperature differential between the two will result in the compression plate generating a smaller compressive load; conversely, a larger temperature differential between the two will result in the compression plate generating a larger compressive load. When the compression plate is made out Nitinol, the compression plate should, preferably, have an austenite finish temperature of greater than about −10° C., resulting in a temperature differential of about 47° C. when the compression plate is implanted (assuming that the compression plate is implanted in a human body).
Plate geometry also affects the compression forces which are generated by the reconfiguring plate. More particularly, the cross-sectional area of elastic bridge members 15 affects the compression forces generated by the reconfiguring plate. As the cross-sectional areas increase, so do the compression forces that the reconfiguring plate will generate. It should be appreciated that the force generated as an elastic bridge member 15 attempts to recover from the constrained linear configuration (
In one preferred form of the invention, compression plate 5 and delivery device 200 are provided in the form of a sterilized kit. The kit may include additional instruments to aid in the implantation of the compression plate (e.g., k-wire, drill bit, plate size guide, screws, etc.). In one preferred form of the invention, compression plate 5 is provided with an associated delivery device (e.g., delivery device 200) in a sterile package, with elastic bridge members 15 being pre-constrained (e.g., so that elastic bridge members 15 are substantially straight, or at least more straight than when the elastic bridge members are in their unconstrained condition) in the sterile package by the delivery device (e.g., delivery device 200).
Static Elastic Bending: 25 mm interaxis width compression plates were tested. A 4-point bending load was applied on a tensile testing machine at a rate of 25.4 mm/min. Bending stiffness was calculated as the initial slope of load vs. displacement. The novel compression plate 5 had comparable Bending Strengths (16.33N/mm vs. 15.86N/mm p=0.818) to conventional fracture fixation plates.
Compression Force: Greater interfragmentary compression has been found to enhance the healing of fractured bones. The compression plates of the present invention utilize the unique superelastic properties of Nitinol to enhance and sustain compression across the fracture plane. The compressive force generated by the novel compression plates of the present invention generate and maintain 180N of compression over nearly 1 mm of bone resorption.
If desired, and looking now at
Additionally, it should be appreciated that plastic threaded insert 450 insulates the metallic fixation screw from compression plate 5, thereby limiting galvanic corrosion between the compression plate 5 and the metallic fixation screws.
In the foregoing disclosure, compression plate 5 is secured to bone fragments using threaded fixation screws. However, if desired, other types of fasteners may also be used to secure compression plate 5 to bone fragments. By way of example but not limitation, pins may be used to secure compression plate 5 to bone fragments.
In the foregoing disclosure, compression plate 5 has been discussed in the context of providing compression across a fracture. However, it should also be appreciated that, if desired, the apparatus can be modified so as to provide a distraction force to bone (e.g., to separate two bones or bone fragments, or to induce bone growth in a single bone, etc.).
By way of example but not limitation, and looking now at
Prior to implantation, elastic bridge members 515 of distraction plate 505 can be reversibly strained outwardly (i.e., forced outwardly), thus decreasing the distance 525 between opposing regions 510 (and hence openings 520) of distraction plate 505. A delivery device can be used to strain elastic bridge members 515 so as to force elastic bridge members 515 outwardly, e.g., a delivery device generally similar to the delivery device 200, or the delivery device 240, discussed above, except that the delivery device is configured to force elastic bridge members 515 apart when appropriate.
During implantation, the strained (i.e., the forcibly foreshortened) distraction plate 505 is secured to bone by passing fixation screws through openings 520 and into the bone.
Removal of the induced strain on distraction plate 505 (provided by the aforementioned delivery device) results in distraction plate 505 attempting to return to its original un-restrained state (i.e., with elastic bridge members 515 linearly aligned), thereby generating a distraction load on the bone to which distraction plate 505 is secured (i.e., through elastic bridge members 515, openings 520 and fixation screws extending through openings 520), and maintaining that distraction load on the bone for a prolonged period of time while healing occurs.
It should be understood that many additional changes in the details, materials, steps and arrangements of parts, which have been herein described and illustrated in order to explain the nature of the present invention, may be made by those skilled in the art while still remaining within the principles and scope of the invention.
This application is a continuation of U.S. patent application Ser. No. 14/658,009 filed on Mar. 13, 2015, which is claims benefit of U.S. Provisional Patent Application Ser. No. 61/952,524, filed Mar. 13, 2014.
Number | Date | Country | |
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61952524 | Mar 2014 | US |
Number | Date | Country | |
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Parent | 14658009 | Mar 2015 | US |
Child | 16830858 | US |