MODULAR CENTER PEGGED GLENOID
A glenoid prosthetic is provided and may include a first component having an articulating surface engaged by the head of a humeral component or a natural humerus and an engagement surface formed on an opposite side of the first component than the articulating surface. A second component may be attached to the first component proximate to the engagement surface and may be attached to a resected glenoid of a scapula. The second component may be formed from a different material than the first component and may include at least one coupling stem received within an aperture formed in the resected glenoid.
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This application is a continuation of U.S. patent application Ser. No. 12/835,223, filed on Jul. 13, 2010, which is a continuation-in-part of U.S. patent application Ser. No. 11/385,035, filed on Mar. 20, 2006 (now U.S. Pat. No. 7,753,959). The entire disclosures of each of the above applications are incorporated herein by reference.
FIELDThe present disclosure relates to a prosthetic device and, more particularly, to a modular glenoid prosthetic.
BACKGROUNDThe statements in this section merely provide background information related to the present disclosure and may not constitute prior art. A natural shoulder joint may undergo degenerative changes due to a variety of etiologies. When these degenerative changes become so far advanced and irreversible, it may ultimately become necessary to replace a natural shoulder joint with a prosthetic shoulder joint. When implantation of such a shoulder joint prosthesis becomes necessary, the natural head portion of the humerus can be resected and a cavity is created in the intramedullary canal of the host humerus for accepting a humeral component. The humeral component includes a head portion used to replace the natural head of the humerus. Once the humeral component has been implanted, the glenoid cavity positioned at the lateral edge of the scapula may also be resurfaced and shaped to accept a glenoid component. The glenoid component generally includes an articulating surface which is engaged by the head portion of the humeral component.
It is generally known in the art to provide a shoulder joint prosthesis having a glenoid component, as discussed above. However, the current prior art glenoid components along with the associated surgical components and instruments utilized during shoulder arthroplasty suffer from many disadvantages.
For example, since the glenoid component is subject to various types of loading by the head portion of the humeral component, the glenoid component must offer a stable and secure articulating surface. To achieve this, some glenoid components provide pegs that are inserted and cemented into holes bored into the glenoid cavity. However, such existing pegged glenoid components also exhibit several disadvantages. For example, some of the pegged glenoid components utilize up to five pegs to stabilize and secure the glenoid component to the scapula. Such glenoid components increase the amount of bone tissue removed, while also increasing the labor and complexity of the shoulder arthroplasty. Other pegged glenoid components may offer one or two larger diameter pegs that reduce the complexity of the shoulder arthroplasty. However, the larger diameter pegs also requires excess bone tissue to be removed that may not be practical in some patients. Furthermore, the use of one or two pegs may potentially reduce overall stability of the glenoid component, similar to a keeled glenoid.
Additionally, most prior art glenoid components only rely on the keel or pegs to secure the glenoid component to the scapula, via a cement mantle. These systems are typically rigid in fixation methods. In this regard, the prior art systems fail to provide a selection of coupling mechanisms which may best be used to address varying degenerative changes or specific muscular needs of a patient.
What is needed then is a glenoid component and associated surgical components for use in shoulder arthroplasty that does not suffer from the above-mentioned disadvantages. This in turn, will provide a glenoid component which is stable and secure, reduces the overall amount of bone tissue required to be removed, reduces inventory, reduces the overall surgical time and complexity, increases overall medial surface area, enhances and increases attachment strength and adaptivity without increasing overall peg diameter, provides a fully enhanced coupling mechanism and increased overall stability, and provides increased tensile and shear strength. It is, therefore, an object of the present invention to provide such a glenoid component and associated surgical components for use in shoulder arthroplasty.
SUMMARYThis section provides a general summary of the disclosure, and is not a comprehensive disclosure of its full scope or all of its features.
A glenoid prosthetic is provided and may include a first component having an articulating surface engaged by the head of a humeral component or a natural humerus and an engagement surface formed on an opposite side of the first component than the articulating surface. A second component may be attached to the first component proximate to the engagement surface and may be attached to a resected glenoid of a scapula. The second component may be formed from a different material than the first component and may include at least one coupling stem received within an aperture formed in the resected glenoid.
In another configuration, a glenoid prosthetic is provided and may include a first component having an articulating surface engaged by the head of a humeral component or a natural humerus and an engagement surface formed on an opposite side of the first component than the articulating surface. A second component may be attached to the first component proximate to the engagement surface and may be attached to a resected glenoid of a scapula. The second component may be attached to the first component via a snap-fit and may include at least one coupling stem received within an aperture formed in the resected glenoid.
Further areas of applicability will become apparent from the description provided herein. The description and specific examples in this summary are intended for purposes of illustration only and are not intended to limit the scope of the present disclosure.
The drawings described herein are for illustration purposes only and are not intended to limit the scope of the present disclosure in any way.
The following description is merely exemplary in nature and is not intended to limit the present disclosure, application, or uses.
Referring generally to
The coupling stems 28 can be configured to include a first superior fixed peg 28 and a pair of second inferior fixed pegs 28, each fixed peg 28 positioned on the coupling side 26 to form the corners of a triangle and, preferably, an isosceles triangle. The coupling stems 28 can take on various forms. In this regard, the fixed stems 28 can have a relatively smooth profile which define annular and/or longitudinal grooves 33. As described below, the grooves 33 can be configured to accept bone cement to fixably couple the peg to apertures 35 defined within a resected glenoid 37. As shown in
As best seen in
As shown, the central stem 48 can have various surface treatments. It is envisioned the stem can be formed of a biocompatible polymer, metallic or ceramic. Additionally, the central pegs can have surface treatment such as powder metal spray coating or other porous structures to facilitate the ingrowth of bone. As shown in
Shown in
After the resection, a plurality of fixed peg accepting holes 59 are machined into the resected glenoid 37.
As shown in
Referring generally to
The coupling stems 28 can be configured to include a first superior removable peg 28 and a pair of second inferior removable pegs 28. Each removable peg 28 is positioned on the coupling side 26 to form the corners of a triangle and, optionally, an isosceles triangle. The coupling pegs 28 can take on various forms. In this regard, the pegs 28 can have a relatively smooth profile which define annular and/or longitudinal grooves 33. As described above, the grooves 33 can be configured to accept bone cement to fixably couple the peg to apertures 35 defined within a resected glenoid 37. As shown in
It is envisioned that the pegs 28 can be coupled to the coupling side via a threaded member or a locking taper. The threaded member 60 can have a self tapping thread configured to engage a threaded hole formed in the coupling side 26. Additionally, the threaded member 60 can be coupled to a bushing integrally molded into the glenoid prosthetic 20. Optionally, the threaded bushing can have a textured exterior surface or retaining flange to facilitate the integration thereof. Each peg has a flat bearing surface configured to bear against a flat bearing surface on the medial side or the bushing.
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Example embodiments are provided so that this disclosure will be thorough, and will fully convey the scope to those who are skilled in the art. Numerous specific details are set forth such as examples of specific components, devices, and methods, to provide a thorough understanding of embodiments of the present disclosure. It will be apparent to those skilled in the art that specific details need not be employed, that example embodiments may be embodied in many different forms and that neither should be construed to limit the scope of the disclosure. In some example embodiments, well-known processes, well-known device structures, and well-known technologies are not described in detail.
The terminology used herein is for the purpose of describing particular example embodiments only and is not intended to be limiting. As used herein, the singular forms “a,” “an” and “the” may be intended to include the plural forms as well, unless the context clearly indicates otherwise. The terms “comprises,” “comprising,” “including,” and “having,” are inclusive and therefore specify the presence of stated features, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, integers, steps, operations, elements, components, and/or groups thereof. The method steps, processes, and operations described herein are not to be construed as necessarily requiring their performance in the particular order discussed or illustrated, unless specifically identified as an order of performance. It is also to be understood that additional or alternative steps may be employed.
When an element or layer is referred to as being “on,” “engaged to,” “connected to” or “coupled to” another element or layer, it may be directly on, engaged, connected or coupled to the other element or layer, or intervening elements or layers may be present. In contrast, when an element is referred to as being “directly on,” “directly engaged to,” “directly connected to” or “directly coupled to” another element or layer, there may be no intervening elements or layers present. Other words used to describe the relationship between elements should be interpreted in a like fashion (e.g., “between” versus “directly between,” “adjacent” versus “directly adjacent,” etc.). As used herein, the term “and/or” includes any and all combinations of one or more of the associated listed items.
Although the terms first, second, third, etc. may be used herein to describe various elements, components, regions, layers and/or sections, these elements, components, regions, layers and/or sections should not be limited by these terms. These terms may be only used to distinguish one element, component, region, layer or section from another region, layer or section. Terms such as “first,” “second,” and other numerical terms when used herein do not imply a sequence or order unless clearly indicated by the context. Thus, a first element, component, region, layer or section discussed below could be termed a second element, component, region, layer or section without departing from the teachings of the example embodiments.
Spatially relative terms, such as “inner,” “outer,” “beneath,” “below,” “lower,” “above,” “upper” and the like, may be used herein for ease of description to describe one element or feature's relationship to another element(s) or feature(s) as illustrated in the figures. Spatially relative terms may be intended to encompass different orientations of the device in use or operation in addition to the orientation depicted in the figures. For example, if the device in the figures is turned over, elements described as “below” or “beneath” other elements or features would then be oriented “above” the other elements or features. Thus, the example term “below” can encompass both an orientation of above and below. The device may be otherwise oriented (rotated 90 degrees or at other orientations)
Claims
1. A glenoid prosthetic comprising:
- a first component having an articulating surface operable to be engaged by the head of a humeral component or a natural humerus and an engagement surface formed on an opposite side of said first component than said articulating surface; and
- a second component attached to said first component proximate to said engagement surface and operable to be attached to a resected glenoid of a scapula, said second component being formed from a different material than said first component and including at least one coupling stem operable to be received within an aperture formed in said resected glenoid.
2. The glenoid prosthetic of claim 1, wherein said second component is attached to said first component via a snap-fit.
3. The glenoid prosthetic of claim 1, wherein said second component is attached to said first component at a perimeter surface of said first component, said perimeter surface being disposed substantially perpendicular to said engagement surface.
4. The glenoid prosthetic of claim 1, wherein said first component includes a radial groove formed in a perimeter surface thereof, said perimeter surface being disposed substantially perpendicular to said engagement surface.
5. The glenoid prosthetic of claim 4, wherein said second component includes a flange received by said radial groove to attach said second component to said first component.
6. The glenoid prosthetic of claim 5, wherein said second component includes at least one peg extending into a bore formed in said first component at said engagement surface to attach said second component to said first component.
7. The glenoid prosthetic of claim 6, wherein said second component is attached to said first component via a snap-fit at said radial groove.
8. The glenoid prosthetic of claim 4, wherein said second component is attached to said first component via a snap-fit at said radial groove.
9. The glenoid prosthetic of claim 1, wherein said second component is molded onto said first component.
10. The glenoid prosthetic of claim 1, wherein said first component is formed from a polymer material and said second component is formed from metal.
11. A glenoid prosthetic comprising:
- a first component having an articulating surface operable to be engaged by the head of a humeral component or a natural humerus and an engagement surface formed on an opposite side of said first component than said articulating surface; and
- a second component attached to said first component proximate to said engagement surface and operable to be attached to a resected glenoid of a scapula, said second component being attached to said first component via a snap-fit and including at least one coupling stem operable to be received within an aperture formed in said resected glenoid.
12. The glenoid prosthetic of claim 11, wherein said second component at least partially surrounds a perimeter surface of said first component, said perimeter surface being disposed substantially perpendicular to said engagement surface.
13. The glenoid prosthetic of claim 11, wherein said second component is attached to said first component at a perimeter surface of said first component, said perimeter surface being disposed substantially perpendicular to said engagement surface.
14. The glenoid prosthetic of claim 11, wherein said first component includes a radial groove formed in a perimeter surface thereof, said perimeter surface being disposed substantially perpendicular to said engagement surface.
15. The glenoid prosthetic of claim 14, wherein said second component includes a flange received by said radial groove to attach said second component to said first component.
16. The glenoid prosthetic of claim 15, wherein said second component includes at least one peg extending into a bore formed in said first component at said engagement surface to attach said second component to said first component.
17. The glenoid prosthetic of claim 16, wherein said second component is attached to said first component via said snap-fit at said radial groove.
18. The glenoid prosthetic of claim 14, wherein said second component is attached to said first component via said snap-fit at said radial groove.
19. The glenoid prosthetic of claim 11, wherein said first component is formed from a polymer material and said second component is formed from metal.
Type: Application
Filed: Mar 12, 2013
Publication Date: Jul 25, 2013
Applicant: BIOMET MANUFACTURING CORP. (Warsaw, IN)
Inventor: Biomet Manufacturing Corp. (Warsaw, IN)
Application Number: 13/795,980
International Classification: A61F 2/40 (20060101);