MODULAR PROSTHESIS FOR AT LEAST PARTIAL REPLACEMENT OF A TUBULAR BONE ADJOINING A JOINT
20220401219 · 2022-12-22
Assignee
Inventors
Cpc classification
A61F2002/3674
HUMAN NECESSITIES
A61F2/30767
HUMAN NECESSITIES
A61F2002/30772
HUMAN NECESSITIES
A61F2310/00544
HUMAN NECESSITIES
A61F2/30734
HUMAN NECESSITIES
A61F2310/00293
HUMAN NECESSITIES
A61F2002/30332
HUMAN NECESSITIES
A61F2250/0024
HUMAN NECESSITIES
A61F2002/30736
HUMAN NECESSITIES
A61F2/3607
HUMAN NECESSITIES
A61F2002/30339
HUMAN NECESSITIES
A61F2310/00796
HUMAN NECESSITIES
A61F2002/3092
HUMAN NECESSITIES
A61F2002/30331
HUMAN NECESSITIES
A61F2220/0033
HUMAN NECESSITIES
A61F2002/30616
HUMAN NECESSITIES
A61L27/306
HUMAN NECESSITIES
A61L2430/02
HUMAN NECESSITIES
International classification
Abstract
Modular endoprosthesis for at least partial replacement of a tubular bone, comprising, as module components, a stem for insertion into a bone cavity of the tubular bone, and an end piece comprising a support body with a neck part arranged on the medial aspect thereof. Said module components being able to be coupled to each other and released from each other along a longitudinal axis of the shaft. The end piece has at least two different surface configurations on its support body, namely a closed surface (6′) on a medial aspect, and a porous configuration of the surface on the opposite, lateral aspect. The latter permits and positions the adhesion of muscle tissue, specifically without suturing. The muscle trauma caused by suturing, and the peak loads that occur at the respective suture points, can thus be avoided by virtue of the invention, by means of the location-specific direct adhesion of the muscle. It is thus possible to achieve quicker and reliable mobilization of the patient, and this with a reduced risk of complications.
Claims
1. A modular endoprosthesis for at least partial replacement of a long bone, comprising as module components: a stem for insertion into a bone cavity of the long bone, an end piece comprising a supporting body with an anterior, posterior, medial and lateral side, and a neck part arranged on the medial side having a receptacle for a joint device, and at least one intermediate piece, wherein the module components can be coupled to and detached from each other along a longitudinal axis of the stem, characterized in that the end piece has at least two differently designed surface formations on its supporting body: a closed surface (6′) on a medial side, and a porous formation of the surface on the lateral side.
2. The modular endoprosthesis of claim 1, wherein the porous formation of the surface is designed as an open-cell porous lattice structure.
3. The modular endoprosthesis of claim 2, wherein the unit cells are designed as an assembled structure and each consist of an interior space and a plurality of interconnected bars surrounding the interior space.
4. The modular endoprosthesis of claim 2, wherein the porous formation of the surface is designed as a unit with the supporting body.
5. The modular endoprosthesis of claim 1, wherein the porous formation is provided with a coating which promotes growth.
6. The modular endoprosthesis of claim 1, wherein the porous formation extends from the lateral side in the manner of a half shell to the anterior and to the posterior side.
7. The modular endoprosthesis of claim 1, wherein a rounding with a lateral flattening is provided at the transition between the lateral side to the anterior side and/or to the posterior side.
8. The modular endoprosthesis of claim 7, wherein the rounding has a radius of curvature (r) which is at most a quarter of the distance (d) from the anterior to the posterior side of the supporting body.
9. The modular endoprosthesis of claim 7, wherein the lateral flattening is flat or has a minimum radius of curvature (R) of twice the distance (d) from the anterior to the posterior side of the supporting body.
10. The modular endoprosthesis of claim 1, wherein the supporting body has the porous formation of the surface exclusively on its lateral side.
11. The modular endoprosthesis of claim 10, wherein the porous formation also extends to an upper side of the supporting body, but exclusively in a lateral region.
12. The modular endoprosthesis of claim 1, wherein the lower region of the end piece does not have the porous formation.
13. The modular endoprosthesis of claim 1, wherein a plurality of passage holes provided in the lateral region, and these passage holes extend from the anterior to the posterior side of the supporting body.
14. The modular endoprosthesis of claim 13, wherein one or more passage holes open into the region having the porous formation, and each of their openings is provided with a non-porous border, which in turn is completely surrounded by the porous formation.
15. The modular endoprosthesis of claim 14, wherein the porous formation has pores with a width in the range between 0.4 and 2 mm, preferably 0.7 to 1.5 mm.
16. The modular endoprosthesis of claim 1, wherein modular components can be connected by means of matching connections, and has an exchangeable end piece (3*) (6*).
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0022] The invention is explained in more detail below with reference to the attached drawing by way of example, using an embodiment, wherein:
[0023]
[0024]
[0025]
[0026]
[0027]
DETAILED DESCRIPTION
[0028] A modular endoprosthesis according to the embodiment shown in the figures is designed as a modular femoral component of a hip joint endoprosthesis for implantation on a femur 9. It comprises a stem part 1, an intermediate piece 2 and an end piece 3 as essential components. In this particular embodiment, the individual components 1, 2, 3 are connected to each other in a rotationally fixed manner, for example via plug-in connections 5.
[0029] The stem part 1 comprises an anchoring region 11 tapering conically in the lower portion, with several anchoring ribs 13 running in the longitudinal direction of the stem part 1. The anchoring region 11 is designed to be implanted in a bone cavity (intramedullary canal) 91 of the femur 9.
[0030] In its upper region, the stem part 1 also includes a coupling part 12 with a larger cross section. It has a cylindrical shell surface and is connected to the intermediate piece 2 via a conical plug-in connection (not visible in
[0031] The end piece 3 is divided into two regions: on the one hand, it comprises as its main component a supporting body 31 with a female cone as part of the plug-in connection 5 to the intermediate piece 2, and comprises a neck part 32 which comprises a retaining pin 33 shaped as a truncated cone for receiving a joint ball 34 as part a joint device of an artificial hip joint, the joint ball 34 being pivotably mounted in a socket of an acetabular component (not shown) of the artificial hip joint when in the implanted state. The retaining pin 33 of the neck part 32 is arranged on a medial side 36 of the end piece 3, and the lateral side 38 of the end piece 3 is situated opposite therefrom; the two are connected via an anterior side 35 and a rear (posterior) side 37. The distance between the anterior side 35 and the posterior side 37 determines the thickness d of the supporting body 31. On the other hand, the end piece 3 has, as a further main component, a porous formation 6 of its surface, which is provided in an upper region of the supporting body 31 on the lateral side, and only there. This will be explained in more detail later.
[0032] Further components of the modular endoprosthesis are shown in
[0033] For a more detailed explanation of the end piece 3 and its porous surface formation 6, reference is now made to
[0034] The porous formation 6 is located approximately in the upper half of the supporting body 31 of the end piece 3. The porous formation 6 forms a defined starting point for soft tissue, specifically for the adhesion of the gluteus medius (not shown). By virtue of the porous formation 6, the muscle can attach precisely on the surface marked by the porous formation 6, and not in other regions. In this way, a precisely defined connection of the muscle to the modular endoprosthesis is achieved. This effectively prevents attachment in undesired regions.
[0035] An exemplary structure of the porous formation 6 is shown schematically in
[0036] As can also be seen in
[0037] To further improve the ingrowth behavior, a flattening 39 is preferably provided on the lateral side 38 (see the area highlighted by the bold dashed lines in
[0038] Furthermore, one or more passage holes 8 can be arranged in the lateral region of the supporting body 31, extending transversely to the central axis 30 and opening into the region of the porous formation 6. In this case, their respective openings 80 are surrounded by a border 81 which surrounds each opening 80 like a wall. In this region, the surface is closed, i.e., not porous.
[0039] A further expedient supplementary part for the modular endoprosthesis is shown in