Hollow endoprosthesis

Details Hollow endoprosthesis Hollow endoprosthesis

2002-01-08

2003-11-04

Robert, Eduardo C. (Department: 3732)

Prosthesis (i.e., artificial body members), parts thereof, or ai

Implantable prosthesis

Bone

Reexamination Certificate

active

06641616

ABSTRACT:

FIELD OF THE INVENTION
This invention concerns a hollow endoprosthesis for use in a tubular bone.
Endoprostheses for use in a tubular bone have been known for a long time in many designs. They are set in the bones surgically after the medullary space is routed out and are anchored there either without cement or with bone cement.
DESCRIPTION OF THE RELATED ART
This invention concerns an endoprosthesis in the first class mentioned, i.e., an endoprosthesis that can be fixed in tubular bones without cement. A number of different implants are also known from this class. The only examples referred to here are implants that are produced by the method described in DE-A-41 06 971. Variations are described in DE-A-195 43 530, for example. The implants mentioned are characterized by the fact that they basically have a basic solid metal body, which is covered, at least partly, by a three-dimensional, open-mesh spatial network structure, into which and through which bone material of the bone tissue surrounding the implant grows after implantation to achieve a permanent secondary fixation of the implant in the tubular bone.
These known implants have major advantages compared to implants fixed with cement. Thus, after complete organization at a number of bone trabeculae, the implant is embedded almost hanging free in the surrounding spongiosa, so it can make stress-dependent equalizing movements in the medullary space, but this is not possible in practice for an implant that is cemented in, since then discrete layers (bone-cement implant) hit and work against one another. In this case, the layer of bone cement that connects the implant is on the layer of spongiosa. Equalizing movements under stress cause loosening of the bone cement and hence loosening of the seat of the implant in the bone.
But there can also be problems with the implants fixed without cement described due to the solidity of the basic body, because the implants, on one hand, and the bone, on the other, have very different moduluses of electricity. Thus, the modulus of electricity of the implant is much higher than that of the bone, which, despite the favorable free suspension in the spongiosa, can lead to problems with the loosening of the implant.
SUMMARY OF THE INVENTION
On this background, it is the purpose of this invention to propose an implant which has much less of a tendency to be loosened in its seat in tubular bones.
This purpose is accomplished, in general, with a hollow endoprosthesis, which consists mainly of a metal grid network, which has metal particles at least at its junctions, which is made of a basic body and at least three pins projecting radially from it which are integral parts of the material forming the grid network, and part of which is also composed of solid metal.
The design as a hollow implant by the grid network causes a significant adaptation of the modulus of electricity of the endoprosthesis and of the bone.
In other words, despite its load-bearing structure, the implant is given a certain elasticity which allows it to react in a quasi-bone-like way to the stresses that occur.
Metal particles are used to stimulate the growth of the bone material surrounding the endoprosthesis, and they give the endoprosthesis an aggressive exterior, whereby the surrounding bone material is stimulated to bleed and thus to build and organize bone trabeculae into the structures.
To maintain sufficient stability of the endoprosthesis, it is provided that part consist of solid metal, but a smaller part than out of the grid network. This other solid part assumes a guide function for the endoprosthesis, in the area where only small forces must be introduced from the endoprosthesis into the bone material. If the hollow endoprosthesis in the invention is designed as a hip shaft of an artificial hip joint, the solid part made of metal forms the distal end of the hip shaft.
It is especially preferred if at least 60% of it is composed of the metal grid network. Accordingly, the remaining 40% is solid, and in the case of a hip shaft, on the distal part and to a smaller degree in the proximal area for coupling an artificial joint cavity. This endoprosthesis therefore has at least a 60% area in which the corresponding modulus of electricity approximates that of the bone.
To increase mechanical stability while only slightly increasing the modulus of electricity of the section of the endoprosthesis consisting of the grid network, it may an advantage to provide reinforcing braces made with the grid network. In the case of a hip shaft prosthesis, for example, they would run parallel from proximal to distal to the solid metal distal section.
In summary, it should once more be emphasized that designing a large part of the endoprosthesis as a metal grid network is essential in terms of equalizing the modulus of electricity, and mounting it with the particles described is essential in terms of stimulating the growth of the bone material surrounding the endoprosthesis for fast, permanent organization in and through the plane of the surface structure, which is made of particles and then into the inside of the endoprosthesis.


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