Osteotomy gap filling implants such as implants for filling bone gaps resulting from craniotomies, cranial fixation systems of bone flaps and fractures, and related methods.
Osteotomy procedures can leave bone gaps. In many instances it is desirable to fill those bone gaps. For example, cranial osteotomy procedures often involve cutting a cranial bone flap that leaves a kerf that needs to be filled in order to facilitate reconnecting the blood supply and osteointegration to the cranial flap as well as to improve patient post-procedure cosmesis. Gap with fixation plating provides the surgeon with a novel system that address both the kerf width created when the bone is cut and fixation. See the abandoned patent application US 2010/0036413 A1 as an example of a prior art gap filling device.
The present invention solves the problems associated with the gap filling device freely articulating in segments that allow for smooth transition.
The implants that have been used in the past for cranial osteotomy kerfs leave room for improvement. For instance, Medpor porous polyethylene implants have been considered previously for filling cranial osteotomy kerfs. See Duck-Ho Goh, M. D. et al., “Medpor Craniotomy Gap Wedge Designed to Fill Small Bone Defects along Cranial Bone Flap” J Korean Neurosug Soc 46: 195-198, 2009. Problematically, when these previous implants are bent to fit the kerf's curvature, the implants buckle, reducing aesthetic results and otherwise negatively impacting on post-operative results. These and other previous implants may also be prone to breaking in the operating room when bent. The current state of the art leaves significant room for improvement.
Described herein are examples of osteotomy gap filling implants and methods. The osteotomy gap filling implant may include several implant segments, at least some of which are formed of a porous body, with a non-porous flexible spine extending through the plurality of implant segments.
In at least some implementations, the implant may be freely bent in several directions without the undesirable buckling that occurs in earlier implant designs. In some implementations, segments of the implants described herein bend about weakened joints that align with the center of nested radial plates.
In at least some implementations, the non-porous flexible spine strengthens the implant while remaining small enough not to prevent tissue and vascular structures from integrating through the implant to facilitate reconnecting the blood supply and osteointegration.
In one example an osteotomy gap filling implant includes implant segments, with at least some of the implant segments including a porous body. The implant also includes a non-porous flexible spine extending through the implant segments.
In this example the adjacent implant segments may be configured to flex relative to one another about at least one axis.
In this example the adjacent implant segments may be configured to flex relative to one another about multiple axes.
In this example the porous bodies of at least some of the implant segments may each include a top plate and a lower body descending from the top plate.
In this example the top plates of the porous bodies may be a series of radially nested top plates.
In this example the non-porous flexible spine may extend through the lower bodies.
In this example a first top plate of one of the implant segments and a second top plate of an adjacent implant segment may be at least partially separated by a curved gap defined by a first curved edge of the first top plate and a second curved edge of the second top plate.
In this example the first curved edge may be a convex curved edge and the second curved edge may be a concave curved edge corresponding in shape to the convex curved edge.
In this example a first lower body of one of the implant segments and a second lower body of an adjacent implant segment may be at least partially separated by a vertical break.
In this example the vertical break between the first and second lower bodies may define a flexural gap between the first and second lower bodies.
In this example at least one of the lower bodies at a first end of the implant may have a narrower width relative to one of the lower bodies at a second end of the implant.
In this example the lower bodies may taper in width from a first end of the implant to a second end of the implant.
In this example the flexible spine may be a single piece spine.
In this example the flexible spine may be a multi-piece spine.
In this example the multi-piece spine may include several rigid spine segments joined at articular joints.
In this example the articular joints may include ball and socket joints.
In this example at least one of the implant segments may also include an insert.
In this example the segment with the insert may have either a porous body or a non-porous body.
In this example the insert may be either entirely embedded in the segment or partially embedded in the segment.
In this example the insert may have holes or not have holes.
In this example the insert may be metal and the implant segment may be plastic.
In this example at least one of the implant segments may include a burr hole cover with a top plate that is larger than top plates of adjacent implant segments.
In this example at least some of the implant segments may be a sintered material molded to the non-porous flexible spine.
In this example the implant may be a cranial osteotomy gap filling implant.
In this example the spine may be configured to be elongated in length by at least 100% without breaking.
In this example the spine may be configured to be elongated in length by at least 300% without breaking.
In another example an osteotomy gap filling method may include steps of: (a) performing a cranial osteotomy in a cranial bone to form a kerf in the cranial bone; and (b) implanting an osteotomy gap filling implant into the kerf, the implant including: (i) several implant segments, at least some of the segments including a porous body; and (ii) a non-porous flexible spine extending through the implant segments.
In this example forming the kerf may constitute forming a curved kerf in the cranial bone.
In this example adjacent implant segments may be configured to flex relative to one another about multiple axes such that the implant can be curved to match the curved kerf in the cranial bone.
In this example the porous bodies of at least some of the implant segments each may include a top plate and a lower body descending from the top plate, the top plates of the porous bodies constituting a series of radially nested top plates.
In this example, during curving the implant to match the curved kerf, the spine may be configured to be elongated in length by at least 100% without breaking.
In this example, during curving the implant to match the curved kerf, the spine may be configured to be elongated in length by at least 300% without breaking.
In this example, prior to implanting the osteotomy gap filling implant into the kerf, the method may include repositioning a portion of the cranial bone such that the kerf tapers from a wider end to a narrower end.
In this example the porous bodies of at least some of the implant segments each may include a top plate and a lower body descending from the top plate, at least one of the lower bodies at a first end of the implant having a narrower width relative to one of the lower bodies at a second end of the implant. The method may be performed such that the implant is implanted into the kerf such that the first end of the implant is proximate the narrower end of the kerf and the second end of the implant is proximate the wider end of the kerf.
In the examples presented herein, the implants are cranial osteotomy gap filling implants. In other implementations, the implants may be configured for use in other craniotomy procedures, surgery of the orbit, surgery of the craniomaxillofacial areas, and other areas of the body where bone is cut and reconnection is needed.
In the examples presented herein, the adjacent implant segments are configured to flex relative to one another about at least one axis, and in these particular examples, they are configured to flex relative to one another about multiple axes.
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In some implementations, the implant's spine may be configured to elongate, in some instances up to 100%, up to 200%, up to 300%, or more, which may enhance the implant's ability to flex and conform to a wide range of shapes and fits.
The examples of implants described above are configured to allow for significant amounts of flexion in multiple degrees of freedom without buckling of the implant, allowing the implant to conform to an extremely wide range of shapes to fit a wide range of bone gaps created by osteotomy procedures.
Examples of the present invention have been described herein, including the best mode known to the inventors for carrying out the invention. The invention is susceptible to various modifications and alternative constructions, and exemplary embodiments have been shown and described in detail. Variations of those embodiments, within the spirit of the present invention, may become apparent to those of ordinary skill in the art upon reading the foregoing description. The inventors expect skilled artisans to employ such variations as appropriate, and the inventors intend for the invention to be practiced otherwise than as specifically described herein. Accordingly, it should be understood that there is no intention to limit the invention to the specific form or forms disclosed, but on the contrary, this invention includes all modifications and equivalents of the subject matter recited in the claim appended hereto as permitted by applicable law. Moreover, any combination of the above-described elements in all possible variations thereof is encompassed by the invention unless otherwise indicated herein or otherwise clearly contradicted by context. The foregoing description, for purposes of explanation, used specific nomenclature to provide a thorough understanding of the described embodiments. However, it will be apparent to one skilled in the art that the specific details are not required in order to practice the described embodiments. Thus, the foregoing descriptions of specific embodiments are presented for purposes of illustration and description. They are not intended to be exhaustive or to limit the described embodiments to the precise forms disclose. It will be apparent to one of ordinary skill in the art that many modifications and variations are possible in view of the above teachings.
This patent application claims priority to and the benefit of the filing date of U.S. provisional patent application Ser. No. 63/383,564 filed Nov. 14, 2022 for “Osteotomy Gap Filling Implant And Methods,” the entire contents of which are hereby incorporated by this reference.
Number | Date | Country | |
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63383564 | Nov 2022 | US |