EP0172883A1

EP0172883A1 - Apparatus for affixing a prosthesis to bone

Info

Publication number: EP0172883A1
Application number: EP85901207A
Authority: EP
Inventors: Douglas G. Noiles
Original assignee: Joint Medical Products Corp
Current assignee: Joint Medical Products Corp
Priority date: 1984-02-09
Filing date: 1985-02-08
Publication date: 1986-03-05
Also published as: WO1985003426A1; CA1262602A; CA1262602C

Abstract

Procédé et dispositif de fixation d'une prothèse sur un os, permettant de transférer les efforts de la prothèse à la partie dure de l'os d'une manière correspondant aux transferts d'efforts se produisant dans l'os naturel. Le dispositif comprend un corps (18) possédant une surface externe dont au moins une partie présente un contour lui permettant de s'adapter à une partie de la surface interne de la partie dure de l'os sur lequel la prothèse est fixée, de sorte que dans la région des parties correspondantes, une fraction considérable de la partie dure de l'os est à proximité étroite ou en contact avec la surface externe du corps, cette surface externe (22) dans la région correspondante étant texturée (46) de manière à augmenter l'engagement par frottement de la surface avec la partie dure de l'os. Dans certains modes préférés de réalisation, une prothèse composée d'un matériau contenant du titane et possédant une flexibilité et une résistance globale élevées comprend une partie possédant un revêtement en métal poreux dans lequel l'os peut croître.Method and device for fixing a prosthesis on a bone, making it possible to transfer the forces from the prosthesis to the hard part of the bone in a manner corresponding to the force transfers occurring in natural bone. The device comprises a body (18) having an external surface of which at least one part has a contour allowing it to adapt to a part of the internal surface of the hard part of the bone on which the prosthesis is fixed, so that in the region of the corresponding parts, a considerable fraction of the hard part of the bone is in close proximity or in contact with the external surface of the body, this external surface (22) in the corresponding region being textured (46) to increase the engagement by friction of the surface with the hard part of the bone. In certain preferred embodiments, a prosthesis composed of a material containing titanium and having high flexibility and overall resistance comprises a part having a coating of porous metal in which the bone can grow.

Description

APPARATϋS FOR AFFIXING A PROSTHESIS TO BONE BACKGROUND OF THE INVENTION

1. Field of the Invention

This invention relates to a method and apparatus for affixing a prosthesis to bone an ,^ in particular, to a method and apparatus for affixing a prosthesis to bone so as to produce stress transfers between the prosthesis and the bone which generally correspond to the stress transfers which occur in natural bone.

2. Description of the Prior Art The bony portion of human and animal bones consists of two types of tissue: hard or compact bone which is dense in texture, and soft or cancellous bone which consists of fibers and lamellae joined together to form a reticular network. The hard bone makes up the outer wall of the bone and provides most of the bone's overall strength. Cross-sections at all levels through a bone will include some hard bone.. The thickness of the hard bone will vary with the level of the cross-section, being smallest near the ends of the bone and greatest at the middle.

Soft bone, where present, forms the inner core of, the bone. This type of bone is primarily found near the ends of bone where the hard bone is thinnest. Current understanding is that, in these regions, the soft bone contributes to the overall strength of the bone by transferring at least some of the applied stresses from the thin portions of the hard bone to relatively large areas of the thicker portions of the hard bone located closer to the middle of the bone. In these regions of stress transfer, the fibers making up soft bone appear to have a regular, equipotential-like, arrangement wherein fibers intersect the hard bone at spaced intervals of approximately 1-2 mm. It is believed that this arrangement, at least in part, is responsible for the efficient transfer of applied stress from one part of hard bone to another.

To date, the methods and apparatus used to attach prostheses to bone have not adequately taken into account the detailed anatomy of bone described above. Specifically, the prior art approaches have failed to provide stress transfer to large areas of the thicker portions of hard bone as occurs, in nature through the interaction of soft bone with hard bone. Similarly, the fact that soft bone transfers stress to hard bone at spaced intervals of approximately 1-2 mm has also been ignored.

SUMMARY OF THE INVENTION

In view of the above state of the art, it is an object of the present invention to provide a method and apparatus for attaching a prosthesis to bone wherein stresses are transferred from the prosthesis to the bone in a manner which corresponds to the stress transfers which occur in natural bone. More specifically, it is an object of the invention to provide a method and apparatus for attaching a prosthesis to bone whereby stress is transferred from the prosthesis to relatively large areas of hard bone. It is a further object of the invention to provide a method and apparatus for attaching a prosthesis to bone whereby maximal stress is transferred to hard bone at spaced intervals separated by distances comparable to those at which fibers of soft bone intersect hard bone.

To achieve these and other objects, the invention, in accordance with one of its aspects, provides apparatus for affixing a prosthesis to bone, wherein said bone has an outer wall of hard bone and may have an inner core of soft bone, comprising a body having an outer surface at least a portion of which is contoured to mate with a portion of the inner surface of the hard bone so that, in the region of said mating portions, a substantial fraction of the hard bone is in close proximity to or in contact with the outer surface of the body, said outer surface in said mating region being textured to increase the frictional engagement of the surface with the hard bone.

In accordance with another of its aspects, the invention provides a method for affixing a prosthesis to bone, wherein said bone has an outer wall of hard bone and may have an inner core of soft bone, comprising the steps of:

(a) contouring a portion of the outer surface of the prosthesis to mate with a portion of the inner surface of the hard bone;

(b) providing the contoured portion with a textured surface designed to increase the coefficient of friction between the mating portions of the prosthesis and the hard bone; (c) reaming some, but not necessarily all, of the soft bone, if present, from the core of the bone; and (d) inserting the prosthesis into the reamed core so '. as to bring the mating portions of the prosthesis and the hard bone into engagement so that a substantial fraction of the mating portion of the hard bone is in close proximity to or in contact with the mating portion of the prosthesis, and so that, in the the region of the mating portions, some of the unreamed soft bone, if present, is crushed between the prosthesis and the hard bone.

In certain preferred embodiments of the invention, the textured surface of the prosthesis is formed from a plurality of spaced, outwardly extending shoulders, the distance between the shoulders being between approximately 0.5 and 5.0 mm so as to generally correspond to the observed spacing between the points of intersection of fibers of soft bone with hard bone. ^"In other preferred embodiments, the shoulders have sharp outer edges capable of cutting into the inner surface of the hard bone so that as the prosthesis is implanted, portions of the hard bone can be shaved away to produce an increased area of engagement between the prosthesis and the hard bone, while at the same time producing bone chips which will stimulate regenerative bone growth.

In further preferred embodiments, the apparatus is constructed in the form of a hollow collar to which other components of the prosthesis are attached.

In connection with each of these embodiments, parts of the outer surface of the prosthesis can be composed of porous metal into which bone can grow. The use of porous metal is especially preferred with regard to the embodiments in the form of collars because the processes normally used to make metal porous generally weaken the metal and for the collar embodiment this weakening effect can be limited to the collar which typically is subjected to smaller stresses than other parts of the prosthesis.

The accompanying drawings, which are incorporated in and constitute part of the specification, illustrate the preferred embodiments of the invention, and together with the description, serve to explain the principles of the invention. It is to be understood, of course, that both the drawings and the description are explanatory only and are not restrictive of the invention. BRIEF DESCRIPTION OF THE DRAWINGS

Figure 1 is a perspective , view of the femur portion of an artificial hip joint employing a collar constructed in accordance with the present invention. Figure 2 is a side view of the collar of Figure 1. Figure 3 is a top view of the collar of Figure 1. Figure 4 is a bottom view of the collar of Figure 1. Figure 5 is a front view of the collar of Figure 1. Figure 6 is a side view partially in section of a femur into which has been implanted the apparatus of Figure 1.

Figure 6A is an exploded view of the indicated portion of Figure 6 showing the relationship between the outer surface of the collar and the hard and soft bone of the femur.

Figure 7 is an exploded view of an artificial knee joint employing a tibia sleeve whose outer surface is constructed in accordance with the present invention.

Figure 8 is a top view of the tibia sleeve of Figure 7. Figure 9 is a front view of the tibia sleeve of Figure 7. Figure 10 is a bottom view of the tibia sleeve of Figure 7. Figure 11 is a cross-sectional view of the tibia sleeve of Figure 7 along lines 11-11 in Figure 9.

Figures 12 and 13 are exploded views of the outer surface of the tibia sleeve of Figure 7 showing, respectively, a porous coating and a texture designed to increase frictional engagement between the prosthesis and the bone in two directions.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

As discussed above, the present invention relates to a method and apparatus for affixing a prosthesis to bone so as to transfer stresses from the prosthesis to the bone in a manner which generally corresponds to the types of stress transfers which occur in natural bone.

To achieve this result, the prosthesis is provided with an outer surface at least a portion of which is both contoured to mate with a portion of the inner surface of the hard bone to which the prosthesis is being affixed, and provided with a texture which increases the frictional engagement between the outer surface and the hard bone. In this way, applied stresses are effectively transferred from the prosthesis to relatively large areas of hard bone in a manner similar to that which occurs in natural bone through the interaction of soft bone ^"with hard bone. Moreover, by providing the texture with a plurality of spaced regions having high coefficients of friction and by adjusting the spacing between those regions to be on the order of a few millimeters, the anatomical details of the interaction of soft bone with hard bone, wherein fibers of soft bone intersect hard bone every few millimeters, are also approximated.

Figures 1-6 and 7-13 illustrate the application of the invention to an artificial hip joint and an artificial knee joint, respectively. It is to be understood that the invention is equally applicable to other artificial joints, including, without limitation, artificial shoulder joints, artificial finger joints, artificial elbow joints, and the like. Along these same lines, in the discussion which appears below, certain features of the invention are described in detail with regard to only one of the two illustrated embodiments, e.g., the artificial hip joint. It is to be understood that these features can be used with both embodiments, as well as with the various other types of artificial joints listed above.

Also, for both the artificial hip joint and the artificial knee joint, the contoured and textured outer surface is shown associated with a separable component of the prosthesis, i.e., collar 18 in Figures 1-6 and tibia sleeve 38 in Figures 7-13. It is to be under¬ stood that this surface need not be carried by a separable component but can form part of the overall outer surface of a unitary prosthetic component, e.g., part of the outer surface of stem 12 in Figures 1-6.

Referring specifically to Figure 1, this figure shows a construction for femur portion 10 of an artificial hip joint. This portion includes a stem 12 to which is attached arm 14 and ball 16. Stem 12, arm 14 and ball 16 can be constructed in a variety of ways known to the art. Particularly preferred constructions for these components are described in U.S. Patents 3,820,167, 3,943,576, 3,996,625 and 4,077,070, the pertinent portions of which are included herein by reference.

Femur portion 10 also includes collar 18 which is constructed in accordance with the present invention. Collar 18 includes body 20 having outer surface 22. It also includes walled aperture 24 for receiving stem 12. The walls of aperture 24 taper inwardly from the top to the bottom of collar 18 and mate with a complementary taper on the outside of stem 12. The slopes of these tapers are chosen so that the stem and the collar lock together as the stem is pushed into the collar. To further secure stem 12 to collar 18, the stem is pro¬ vided with pins 28 which are received in recesses 26 formed in the collar. The pins and recesses prevent rotation of stem 12 within aperture 24.

As can best be seen in Figures 6 and 6A, outer surface 22 of collar 18 is contoured to mate with inner surface 30 of the hard bone portion 32 of bone 34. That is, outer surface 22 is given a shape such that, when collar 18 is implanted in a suitably prepared bone, e.g., the upper part of the femur for a hip prosthesis, a substantial fraction of the hard bone's inner surface 30 is in close proximity to or in contact with the prosthesis' outer surface 22.

Because the size and shape of particular human and animal bones varies from individual to individual, to achieve this close fit generally means that the surgeon must be supplied with a family of prostheses having outer surfaces of different sizes and shapes. In this regard, it is preferable to apply the contoured outer surfaces to a small piece, such as collar 18, rather than to a large piece, such as stem 12, since it is substantially less expensive to the manufacturer and much more convenient and economical to the user to provide, store and have available in the operating room a family of small pieces rather than large pieces.

In addition to having a contour which mates with the inner surface of the hard bone into which the prosthesis is to be implanted, outer surface 22 of collar 18 is also provided with a texture which increases the frictional engagement of the surface with the hard bone.

In Figures 1-6, the texture comprises a plurality of outwardly extending shoulders 36 oriented to increase the frictional engagement of surface 22 with the hard bone in the direction of the longitudinal axis of bone 34. Similar shoulders are used on tibia sleeve 38 of the artificial knee embodiment shown in Figures 7-11.

In Figure 12, in addition to shoulders 36, the outer surface of the prosthesis is provided with a porous surface into which bone can grow.^" As known in the art, such a surface can be obtained, among other ways, by coating the surface of the component with small balls 40 composed of the same metal as that used to form the component, e.g., a titanium alloy such as one containing 6% aluminum and 4% vanadium (see ASTM Spec. No. F136), and then heating the coated component to fuse the balls and the component together. An appro¬ priate size for the balls relative to the size of the prosthetic component is illustrated in Figure 12 wherein the distance represented by the longitudinal spacing (S) between shoulders 36 includes on the order of 2-10 balls. As discussed in detail below, this spacing is preferably on the order of between approximately 0.5 and 5.0 mm.

The presence of the porous coating not only allows bone to grow into the prosthesis over time, but, since the roughness of outer surface 22 is increased, also enhances the initial frictional engagement between the prosthesis and the hard bone which occurs at the time of implantation. This initial increase in frictional engagement occurs both in the direction of the longitudinal axis of the bone as well as in the direction corresponding to rotation of the prosthesis about the longitudinal axis of the bone. Although, in accordance with the invention, porous coatings can be used in combination with a mating contour applied directly to a component which is subjected to high stresses, e.g., stem 12, this approach is believed to entail a risk of failure of the prosthesis with extended periods of use unless the component is substantially redesigned in view of the.weakened material. This is so because the heating process used to form the porous coating, as well as the surface characteristics produced by the coating, can significantly reduce the component's fatigue strength.

For some prosthesis materials, e.g., cobalt-chromium alloys, this fatigue strength reduction can be compensated for by formulating or processing the alloy so that it has such a high initial strength that even significant strength reductions do not weaken the component to a point where it will not withstand the stresses associated with long periods of use. However, for other materials, in particular, titanium-containing materials such as the titanium alloy described above, the fatigue problem cannot be overcome by increasing the initial strength of the material. Moreover, for these materials, the reduction in strength caused by porous coating can be as high as 60% or more, e.g., from approximately 90,000 p.s.i. to about 30,000 p.s.i. for the titanium-aluminum-vanadium alloy described above.

In the past, this fatigue strength problem with porous coated, titanium-containing prostheses has been overcome, at least in part, by increasing the cross-sectional dimensions of the prosthesis. Unfortunately, this approach has the significant drawback that to a great extent, it leads to the loss of one of the primary advantages resulting from the use of titanium-containing materials in prostheses, namely, the fact that finished prostheses made from titanium-containing materials have a flexibility closer to that of natural bone than the flexibility achieved with other prosthesis materials, e.g., cobalt-chromium alloys.

In accordance with the present invention, it has now been found that a titanium-containing prosthesis can be porous coated while still maintaining both its overall strength and its flexibility. Specifically, this result is achieved by separating the prosthesis into components, some of which are subjected to relatively high stress, e.g., stem 12, and others of which are subjected to relatively low stress, e.g., collar 18, and then porous coating only the relatively low stress components. In this way, the finished prosthesis can have all three characteristics considered desirable by the art, namely, porous coating, strength, and flexibility.

Figure 13 shows an alternate surface texture designed to increase the frictional engagement of the prosthesis with the hard bone both in the direction of the longitudinal axis of the bone and in direction corresponding to rotation of the prosthesis about the longitudinal axis of the bone. In accordance with this embodiment, cutouts 42 are formed in shoulders 36 so as to produce surface discontinuities 44 which help prevent rotation of the prosthesis about its longitudinal axis. The un-cutout portions of shoulders 36 continue to function as a texture which increases the coefficient of friction between the prosthesis and the bone in the direction of the longitudinal axis of the bone. Most preferably, the spacing between surface discontinuities 44 is on the order of a few millimeters to correspond generally to the spacing observed between the points of intersection of fibers of soft bone with hard bone.

It should be noted that both tibia sleeve 38 and collar 18, as well as the inner surfaces of the hard bone portions of the tibia and femur with which these components mate, have non-circular cross-sections. These cross-sections in and of themselves tend to resist rotation so that in many cases texture enhancement in the direction corresponding to rotation of the prosthesis about the longitudinal axis of the bone may not be required.

As shown in the figures, contoured outer surface 22 of the prosthesis is made up of a plurality of segments 46. Within each segment, the perimeter of the outer surface is constant in both size and shape. Between segments, however, the sizes and/or shapes of the perimeters change so as to produce the contour which mates with the inner surface of the hard bone and so as to provide the shoulders 36 which increase the frictional engagement of the contoured surface with the hard bone.

So that the overall contour of outer surface 22 will be a reasonable approximation of the shape of the inner surface 30 of hard bone 32, or, in other words, so that surfaces 22 and 30 will be in relatively close proximity over a substantial area, it is important to employ a sufficient number of segments 46 so that the outward extent of any shoulder 36 is no greater than approximately 1-2 mm. On the other hand, so that shoulders 36 are effective in increasing the coefficient of friction between the prosthesis and the hard bone, the outward extent of the shoulders should be at least approximately 0.25 mm. Since the outer edges 48 of shoulders 36 are the regions of outer surface 22 which have the highest coefficients of friction, in order to approximate the manner in which fibers of soft bone intersect with hard bone, the spacing between these edges should be on the order of a few millimeters. Ideally, the spacing should be between approximately 1 and 2 millimeters, but in practice it has been found that to keep the depth of shoulders 36 between approximately 0.25 and 2 mm, it is necessary to use longitudinal spacings between edges 48 which vary between approximately 0.5 and 5.0 mm. Referring now to Figures 7-13, these figures illustrate the application of the invention to an artificial knee joint composed of femur component 50, intermediate bearing member 52 and tibia sleeve 38. A detailed discussion of the construction of this joint can be found in U.S. patent application Serial No. 578,437, to Douglas G. Noiles, which is being filed simultaneously herewith and is entitled "Semi-Constrained Artificial Joint." The pertinent portions of that patent application are incorporated herein by reference.

As discussed above, for the artificial knee joint of Figures

7-13, the features of the invention are applied to tibia sleeve 38. Thus this sleeve has a body 20 whose outer surface 22 is contoured to mate with the inner surface of the hard bone at the upper end of the tibia. In addition to being contoured, surface 22 is also textured by means of segments 46 which form spaced shoulders 36. As described in detail above, these shoulders represent regions of increased coefficient of friction between surface 22 and the inside surface of the hard bone. As with the artificial hip embodiment, the combination of a contour which closely matches the shape of the inner surface of the hard bone over a substantial area and the presence of spaced regions having a relatively high coefficient of friction leads to stress transfers between the prosthesis and the hard bone which generally correspond to the stress transfers which occur in natural bone. Implantation of the prostheses of the present invention follows : standard procedures known in the art. Thus, the bone into which the prosthesis is to be inserted is resected as necessary and the core of the bone is reamed of soft bone and marrow. In the region where the contoured surface of the prosthesis and the hard bone will mate, it is desirable to leave some soft bone which can be captured and crushed between the surface and the hard bone as the surface is moved into position. This capturing and crushing process will pulverize some of the soft bone to the point of forming bone chips which can serve as nuclei for regenerative bone growth. The results of the process are illustrated in Figures 6 and 6A where the soft bone is identified by the number 54 and bone chips are identified by the number 56.

In addition to capturing and crushing soft bone between the prosthesis and the hard bone, it is also desirable to further generate bone chips from the hard bone. To this end, it is desirable that edges 48 of shoulders 36 be sharp so that they can scrape away parts of the hard bone as the prosthesis is inserted into the bone, and thus automatically form and deposit the desired bone chips at the prosthesis/hard bone interface. In addition to forming bone chips, the use of sharp edges at the ends of shoulders 36 also serves to shave away any high spots on inner surface 30 of hard bone 32 and thus produces an increased area of engagement between the prosthesis and the hard bone. Although specific embodiments of the invention have been described and illustrated, it is to be understood that modifications can be made without departing from the invention's spirit and scope. For example, surface textures other than those illustrated can be used to enhance the coefficient of friction between the prosthesis and the hard bone. Along these same lines, the contour of the outer surface of the prosthesis need not be formed from discrete segments of the shapes and sizes illustrated, but can be formed from segments having a variety of shapes and sizes or, alternatively, can be formed in a continuous manner without the use of segments with the surface texture being provided separately from contour formation.

Claims

What is claimed is:

1. A prosthesis for implantation in the body comprising:

(a) a first component composed of a titanium-containing material and having an exterior surface at least a portion of which has a porous coating into which bone can grow, said compo¬ nent when implanted being subjected to relatively low levels of applied stress;

(b) a second component composed of a titanium-containing material and having an outer surface which does not include a porous coating into which bone can grow, said component when im¬ planted being subjected to relatively high levels of applied stress; and

(c) means for attaching the second component to the first component.

2. The prosthesis of Claim 1 in the form of the femoral portion of an artificial hip joint wherein the first component includes a collar having a walled aperture passing therethrough, the porous coating being on the outer surface of the collar, and the second component includes an elongated stem, a portion of which is received in the aperture as the prosthesis is assembled.

3. The prosthesis of Claim 2 wherein the means for attaching includes a locking taper on the walls. of the aperture which mates with a complementary taper on a portion of the outer surface of the stem.

4. The prosthesis of Claim 3 wherein the means for attaching further includes pin means associated with the stem which mate with aperture means associated with the collar.

5. The prosthesis of Claim 1 wherein application of the porous coating to the first component involves heating of that component.

6. The prosthesis of Claim 1 wherein the first and second components are each composed of a titanium alloy containing 6% aluminum and 4% vanadium.

7. A method for providing a porous coated, titanium-containing prosthesis for implantation in the body which functionally has high overall strength and flexibility comprising the steps of: (a) forming the prosthesis in two mating portions, one of which when implanted is subjected to relatively low applied stress and the other of which when implanted is subjected to relatively high applied stress; and (b) applying a porous coating to at least a part of the exterior surface of only the portion subjected to relatively low applied stress.

8. The method of Claim 7 wherein the prosthesis is in the form of the femoral component of an artificial hip joint, wherein the portion subjected to relatively low applied stress includes a collar having a walled aperture passing therethrough, wherein the porous coating is applied to the outer surface of the collar, and wherein the portion subjected to relatively high applied stress includes an elongated stem a part of which is received in the aperture as the two porti^'ons are mated.

9. The method of Claim 8 wherein the two portions are mated through complementary, locking tapers on the walls of the aperture and on part of the outer surface of the stem.

10. The method of Claim 9 wherein the two portions are mated through pin means associated with the stem which are received in aperture means associated with the collar.

11. The method of Claim 7 wherein applying the porous coating to the portion subjected to relatively low applied stress involves heating that portion of the prosthesis.

12. The method of Claim 7 wherein the two portions are composed of a titanium alloy containing 6% aluminum and 4% vanadium.