US 4,908,034 AGrant
Endoprosthetic Bone Joint Components
Issue Date:1990-03-13
•5 Claims
•1 Drawing Sheets
Abstract
An endoprosthetic bone component is produced from parts respectively having a projection and cavity engaged in a mutual clearance fit, and a third part of plastics material located in the space of such fit, the space and third part being dimensioned to inhibit ejection of the latter and to lock the two parts against mutual articulation during post-operative use. Normally the space and third part will be of generally uniform thickness overall which is small compared to that of the projection. Also the projection and cavity are preferably of uniform cross-sectional shape over at least major portions thereof. Typically the two parts will be of different materials, such as ceramic and metal, suited respectively to articulation and bone fixation roles.
Metadata
Assignee
- National Research Development Corporation
Inventors
- Barry O. Weightman
- Robert A. Wordsworth
Application Information
Application Number:US 314285&
Filing Date:1989-02-23
Priority Date:1983-12-01
Art Unit:332
Classifications
IPC:
A61F 230A61F 236
Field of Search:
62322;23;18;19;20;16;66
Patent Drawings (1 sheets)
Description
While the above discussion of the present invention is thought to be adequate, it may be useful to clarify the same further by way of example with reference to the drawings, in which:
FIG. 1 partially illustrates in schematic cross-sectional view a femoral head replacement component according to the invention, and
FIG. 2 shows in transverse cross-sectional views (a) to (d) four respectively different modifications of FIG. 1 at I--I.
The component of FIG. 1 comprises an assembly of first, second and third parts respectively denoted 10, 20 and 30.
The first part 10 is of one-piece metal construction including an elongate tapered stem 11 of which only the wider end is shown, and from which end projects generally axially a spigot 12 of circular cylindrical shape terminating at its free end in a hemisphere. The spigot 12 is formed with a very narrow passageway 13 extending axially therethrough from its free end to emerge radially adjacent the wider end of the stem 11.
The second part 20 is a spherical ball of ceramic material and formed with a cavity 21 of stopped bore form of similar shape to, but sightly larger size than the spigot which is freely receivable therein.
Lastly in respect of the ball, the outer spherical surface is ground and polished to a suitable finish for the purpose of mutual articulation with an acetabular cup whereas the surface of the cavity is as-fired.
The third part 30 is of plastics material, such as RCH 1000, preformed to an axially symmetrical cup shape to serve as a push fit intermediary between the spigot and cavity when assembled as illustrated. This part also has a narrow passageway 31 axially through its base which passageway forms a continuation of passageway 13 and serves therewith for escape of air during assembly.
Also it may be appropriate to plug the passageway 13 as a final step in assembly.
The benefits of this component are evident from the earlier discussion above, namely: there is no direct wedging interference fit between the spigot and ball cavity and so no frozen stresses; the cavity is not ground and so the ball is of significantly reduced cost; and loads on the ball at its cavity are distributed over the whole of the cavity surface by the intimate contact adopted by the plastics cup, this effect being enhanced by post-operative use. Also, it is to be noted that any tendency for escape of the plastics material is reduced by the relatively small wall thickness of this material, and any alternative possibility of plastics material escape through the passageway 13 is also reduced by its narrow width.
A component according to FIG. 1 with a ball head of 32 mm diameter, a spigot of 15 mm diameter, and a plastics material thickness of 0.5 mm, is currently undergoing in vitro testing in Ringers solution at body temperature. In impact testing the minimum fracture strength is found to be double that of an equivalent tapered interference-fitted head. No tendency to significant escape of plastics material has arisen during extensive cyclic loading. More specifically, this second test has involved a load variation between 2 and 27 times body weight, compared to a normal variation between 0 and a maximum of about 4 times body weight when ascending stairs, over 10 million cycles which generally equates with 10 years usage. Also, in a third test, the torque required to effect mutual rotary articulation in such a component is found to exceed by a large factor any torque which naturally occurs in normal usage.
The illustrated component is, of course, only one of many variations possible within the invention as discussed more generally above. For example the plastics material can be formed in situ and the transverse cross-sectional form of the interconnection geometry can be non-circular to provide prismatic, ribbed or other shapes acting against mutual rotation, such as shown in FIG. 2.
Also while reference has been made to ceramic/metal and metal/metal material combinations for the first two parts, yet other material combinations may be advantageously deployed by use of the present invention. This possibility is especially relevant to a situation where one of the materials of a combination thought to be useful is not suited to economical and/or conventional interconnection techniques. This may be the case, for example with carbon fibre reinforced carbon or other carbon-based materials which appear to make available desirable properties, such as porosity and bone-like modulus of elasticity, for the purposes of fixation in bone but are possibly not readily connectable with different materials better suited to articulation.
Lastly, while the invention has been described with particular reference to femoral components for hip prostheses, application to other components having articulatory parts of ball or different form is clearly possible.
Claims
We claim:
1. A method of producing an endoprosthetic bone component, comprising: providing three parts, two such parts being of material non-deformable under patient body load, and the third such part being of plastics material deformable under such load; forming one of said two parts with a cavity and the other of said two parts with a projection, said cavity and projection being configured to be engageable in a mutual a non-wedging clearance fit to define therebetween a space of cup shape having uniform wall thickness; forming said third part to said cup shape; assembling said component by engaging said cavity and projection to form said space, and locating said third part therebetween in said space in direct engagement with said cavity and projection; and subjecting said assembled component to said load to engage said cavity and projection further to force said third part plastics material by deformation towards complete accommodation with the surfaces of said cavity and projection thereby to lock by a non-wedging interference fit, absent any other action on, by and between, said two parts, against mutual articulation; said wall thickness being sufficiently small to inhibit ejection of said plastics material by creep under said load.
2. A method according to claim 1 wherein said third part is preformed relative to assembly of said component.
3. A method according to claim 1 wherein said cup shape is circular cylindrical.
4. A method according to claim 1 wherein said one part is formed with a surface area of polished finish quality to replace a natural articulation surface in a bone joint, but said cavity and projection surfaces are formed to a lesser quality finish.
5. A method according to claim 1 wherein said one part is made of ceramic produced by a firing process and said cavity surface is retained in as-fired condition.