The present disclosure relates generally to an implantable orthopaedic prosthesis, and more particularly to an implantable knee prosthesis.
During the lifetime of a patient, it may be necessary to perform a joint replacement procedure on the patient as a result of, for example, disease or trauma. The joint replacement procedure may involve the use of a prosthesis which is implanted into one or more of the patient's bones. In the case of a knee replacement procedure, a tibial tray is implanted into the patient's tibia. A bearing is then secured to the tibial tray. The condyle surfaces of the patient's femur, or the condyle surfaces of a replacement femoral component, bear against the tibial bearing.
One type of knee prosthesis is a fixed-bearing knee prosthesis. As its name suggests, the bearing of a fixed-bearing knee prosthesis does not move relative to the tibial tray. Fixed-bearing designs are commonly used when the condition of the patient's soft tissue (i.e., knee ligaments) does not allow for the use of a knee prosthesis having a mobile bearing.
According to one aspect, a fixed-bearing knee prosthesis includes a femoral component having a medial condyle surface and a lateral condyle surface. The knee prosthesis also includes a bearing having a medial bearing surface configured to articulate with the medial condyle surface of the femoral component, and a lateral bearing surface configured to articulate with the lateral condyle surface of the femoral component. A tibial tray is secured to the bearing. The tibial tray has a platform with an elongated stem extending downwardly from a lower surface thereof. A peripheral rail extends along at least an anterior section of the perimeter of the tray's platform. The peripheral rail extends upwardly from an upper surface of the platform. A retaining rail extends posteriorly away from the peripheral rail.
In some embodiments, the retaining rail has posterior width defined by the distance between a lateral end and a posterior end of a posterior-most edge of the retaining rail and a length defined by the distance of an imaginary center line segment extending from the anterior edge of the tibial tray to a midpoint located along the posterior-most edge halfway between the lateral end and the medial end. The posterior width of the retaining rail is less than, or equal to, the length of the retaining rail.
In certain embodiments, the peripheral rail extends along the entire perimeter of the platform. Moreover, the retaining rail may be contiguous with the peripheral rail.
The peripheral rail may have at least one undercut slot formed therein, with the bearing having at least one tab positioned in the at least one undercut slot of the peripheral rail.
The lower surface of the platform may have a recess formed therein, with the retaining rail being positioned in the recess. Illustratively, the recess is bounded by a sidewall which contacts the retaining rail.
According to another aspect, an implantable orthopaedic component includes a tibial tray configured to be secured to a surgically prepared tibia of a patient. The tibial tray has a platform with an elongated stem extending downwardly from a lower surface thereof. A peripheral rail extends along at least an anterior section of the perimeter of the tray's platform. The peripheral rail extends upwardly from an upper surface of the platform. A retaining rail extends posteriorly away from the peripheral rail.
In some embodiments, the retaining rail has posterior width defined by the distance between a lateral end and a posterior end of a posterior-most edge of the retaining rail and a length defined by the distance of an imaginary center line segment extending from the anterior edge of the tibial tray to a midpoint located along the posterior-most edge halfway between the lateral end and the medial end. The posterior width of the retaining rail is less than, or equal to, the length of the retaining rail.
In certain embodiments, the peripheral rail extends along the entire perimeter of the platform. Moreover, the retaining rail may be contiguous with the peripheral rail.
The peripheral rail may have at least one undercut slot formed therein, with the bearing having at least one tab positioned in the at least one undercut slot of the peripheral rail.
The lower surface of the platform may have a recess formed therein, with the retaining rail being positioned in the recess. Illustratively, the recess is bounded by a sidewall which contacts the retaining rail.
According to one aspect, a fixed-bearing knee prosthesis includes a femoral component having a medial condyle surface and a lateral condyle surface. The knee prosthesis also includes a bearing having a medial bearing surface configured to articulate with the medial condyle surface of the femoral component, and a lateral bearing surface configured to articulate with the lateral condyle surface of the femoral component. A tibial tray is secured to the bearing. The tibial tray has a platform with an elongated stem extending downwardly from a lower surface thereof. A peripheral rail extends along at least an anterior section of the perimeter of the tray's platform. The peripheral rail extends upwardly from an upper surface of the platform. A retaining rail extends posteriorly away from the peripheral rail.
In some embodiments, the peripheral rail has a posterior-most edge that includes a lateral end and a medial end, a lateral-most edge extending linearly from a first point on the peripheral rail to the lateral end of the posterior-most edge, and a medial-most edge extending linearly from a second point on the peripheral rail to the medial end of the posterior-most edge.
In certain embodiments, the peripheral rail extends along the entire perimeter of the platform. Moreover, the retaining rail may be contiguous with the peripheral rail.
The peripheral rail may have at least one undercut slot formed therein, with the bearing having at least one tab positioned in the at least one undercut slot of the peripheral rail.
The lower surface of the platform may have a recess formed therein, with the retaining rail being positioned in the recess. Illustratively, the recess is bounded by a sidewall which contacts the retaining rail.
The detailed description particularly refers to the following figures, in which:
While the concepts of the present disclosure are susceptible to various modifications and alternative forms, specific exemplary embodiments thereof have been shown by way of example in the drawings and will herein be described in detail. It should be understood, however, that there is no intent to limit the concepts of the present disclosure to the particular forms disclosed, but on the contrary, the intention is to cover all modifications, equivalents, and alternatives falling within the spirit and scope of the invention as defined by the appended claims.
Terms representing anatomical references, such as anterior, posterior, medial, lateral, superior, inferior, etcetera, may be used throughout this disclosure in reference to both the orthopaedic implants described herein and a patient's natural anatomy. Such terms have well-understood meanings in both the study of anatomy and the field of orthopaedics. Use of such anatomical reference terms in the specification and claims is intended to be consistent with their well-understood meanings unless noted otherwise.
Referring now to
The bearing 16 includes a lateral bearing surface 26 and a medial bearing surface 28. The bearing surfaces 26, 28 are configured to articulate with a lateral condyle surface 30 and a medial condyle surface 32, respectively, of the femoral component 12. Specifically, the femoral component 12 is configured to be implanted into a surgically prepared end of the patient's femur (not shown), and is configured to emulate the configuration of the patient's natural femoral condyles. As such, the lateral condyle surface 30 and the medial condyle surface 32 are configured (e.g., curved) in a manner which mimics the condyles of the natural femur. The lateral condyle surface 30 and the medial condyle surface 32 are spaced apart from one another thereby defining an intercondylar notch therebetween.
The components of the knee prosthesis 10 that engage the natural bone, such as the femoral component 12 and the tibial tray 14, may be constructed with a biocompatible metal, such as a cobalt chrome alloy, although other materials may also be used. The bone engaging surfaces of these components may be textured to facilitate cementing the component to the bone. Such surfaces may also be porous coated to promote bone ingrowth for permanent fixation.
The bearing 16 may be constructed with a material that allows for smooth articulation between the bearing 16 and the femoral component 12, such as a polymeric material. One such polymeric material is polyethylene such as ultrahigh molecular weight polyethylene (UHMWPE).
As shown in
As shown in
To secure the tibial bearing 16 to the tibial tray 14, the posterior tabs 38 of the bearing 16 are positioned in the posterior undercuts 46 of the tibial tray 14. Thereafter, the anterior portion of the tibial bearing 16 is then advanced downwardly toward the tibial tray 14 such that the pedestal 34 of the bearing's lower surface 36 is captured within the peripheral rail 42. As the anterior portion of the bearing 16 is advanced in such a manner, the anterior tabs 40 of the tibial bearing 16 are deflected by the peripheral rail 42 and thereafter snapped into the anterior undercuts 48 of the peripheral rail thereby securing the bearing 16 to the tray 14.
The upper surface 24 of the tray's platform 18 has a retaining rail 50 extending upwardly therefrom. In the illustrative embodiment described herein, the retaining rail 50 is embodied as an elongated tongue or flange which extends posteriorly from the anterior edge 52 of the tibial tray 14. In the illustrative embodiment described herein, the retaining rail 50 is contiguous with the peripheral rail 42, although the two rails 50, 42 could be embodied separately. Moreover, the retaining rail 50 is herein described as being of a similar height to the peripheral rail, although the components could be embodied has having dissimilar heights.
The lower surface 36 of the bearing 16 has a complimentary-shaped recess 54 defined therein. The recess 54 is bounded by a sidewall 56. As shown in the cross-sectional views of
As alluded to above, in the illustrative embodiment described herein, the retaining rail 50 is embodied as an elongated tongue or flange which extends posteriorly from the anterior edge 52 of the tibial tray 14 in a direction toward the center of the tray's platform 18. As shown in
As also shown in
As shown in
As shown in
In each of the embodiments shown in
As shown in
In addition to variations of the retaining rail 50, other modifications of the fixed-bearing knee prosthesis 10 are also contemplated. For example, as shown in
As described herein, the retaining rail 50 functions to restrict relative rotational motion between the bearing 16 and the tibial tray 14. The center of this rotation coincides approximately with the instantaneous center of torque exerted by the femoral component 12 on the bearing 16. Positioning the retaining rail 50 on the anterior portion of the peripheral rail 42 (as opposed to the posterior portion) effectively increases the distance from this center of rotation, thereby enhancing the ability of the retaining rail 50 to restrict rotation. The retaining rail 50 also functions to prevent substantial loading on the anterior holding elements (e.g., the anterior tabs 40).
The retaining rail 50 also functions as an alignment guide to facilitate assembly of the bearing 16 to the tibial tray 14. A user may assemble the bearing 16 to the tibial tray 14 entirely from the front (i.e., anterior to posterior), as described above. Alternatively, the user may load the bearing 16 from the front, but with the posterior lateral side engaged and the bearing 16 subsequently rotated into its locked position.
While the disclosure has been illustrated and described in detail in the drawings and foregoing description, such an illustration and description is to be considered as exemplary and not restrictive in character, it being understood that only illustrative embodiments have been shown and described and that all changes and modifications that come within the spirit of the disclosure are desired to be protected.
There are a plurality of advantages of the present disclosure arising from the various features of the apparatus, system, and method described herein. It will be noted that alternative embodiments of the apparatus, system, and method of the present disclosure may not include all of the features described yet still benefit from at least some of the advantages of such features. Those of ordinary skill in the art may readily devise their own implementations of the apparatus, system, and method that incorporate one or more of the features of the present invention and fall within the spirit and scope of the present disclosure as defined by the appended claims.
Number | Name | Date | Kind |
---|---|---|---|
4257129 | Volz | Mar 1981 | A |
4673407 | Martin | Jun 1987 | A |
4714474 | Brooks, Jr. et al. | Dec 1987 | A |
4795468 | Hodorek et al. | Jan 1989 | A |
4822362 | Walker et al. | Apr 1989 | A |
4944757 | Martinez et al. | Jul 1990 | A |
5271737 | Baldwin et al. | Dec 1993 | A |
5344460 | Turanyi et al. | Sep 1994 | A |
5370699 | Hood et al. | Dec 1994 | A |
5405396 | Heldreth et al. | Apr 1995 | A |
5413604 | Hodge | May 1995 | A |
5480446 | Goodfellow et al. | Jan 1996 | A |
5824103 | Williams | Oct 1998 | A |
5871545 | Goodfellow et al. | Feb 1999 | A |
5879394 | Ashby et al. | Mar 1999 | A |
5957979 | Beckman et al. | Sep 1999 | A |
5964808 | Blaha et al. | Oct 1999 | A |
6039764 | Pottenger et al. | Mar 2000 | A |
6068658 | Insall et al. | May 2000 | A |
6090144 | Letot et al. | Jul 2000 | A |
6162254 | Timoteo | Dec 2000 | A |
6280476 | Stanley et al. | Aug 2001 | B1 |
6299646 | Chambat et al. | Oct 2001 | B1 |
6379388 | Ensign et al. | Apr 2002 | B1 |
6869448 | Tuke et al. | Mar 2005 | B2 |
6986791 | Metzger | Jan 2006 | B1 |
20030139817 | Tuke et al. | Jul 2003 | A1 |
20040186583 | Keller | Sep 2004 | A1 |
20040215345 | Perrone, Jr. et al. | Oct 2004 | A1 |
20050021147 | Tarabichi | Jan 2005 | A1 |
20050055102 | Tornier et al. | Mar 2005 | A1 |
20050203631 | Daniels et al. | Sep 2005 | A1 |
20050209702 | Todd et al. | Sep 2005 | A1 |
20060036329 | Webster et al. | Feb 2006 | A1 |
Number | Date | Country |
---|---|---|
0 495 340 | Dec 1991 | EP |
2 653 992 | Oct 1991 | FR |
2293109 | Mar 1996 | GB |
WO 9966864 | Dec 1999 | WO |
Entry |
---|
Johnson & Johnson Orthopaedics, “Primary Cruciate-Retaining & Cruciate-Substituting Procedure”, Reference Guide for Use with P.F.C. Sigma Knee Systems, 1998. |
European Search Report for European Patent Application No. 08164944.4-2310 / 2042131, Mar. 16, 2009, 12 pgs. |
Number | Date | Country | |
---|---|---|---|
20090082873 A1 | Mar 2009 | US |