Patent Application
20100256758
This disclosure relates to orthopedic implants and in particular to orthopedic implants for repair of focal articular cartilage and osteochondral defects.
As the population of an active society ages, medical advancements are developed to improve the health of individuals. One of the most active and successful medical treatments is joint reconstruction, also known as arthroplasty, to resolve activity limiting pain caused by arthritis. Current technology supports various forms of arthroplasty, including hemi-arthroplasty, partial joint arthroplasty and total joint arthroplasty. These successful procedures reconstruct a new continuous, low friction articular surface for pain free function of the skeletal joint. A remaining challenge in arthroplasty deals with resolving activity limiting pain in patients with smaller focal cartilage lesions. These lesions represent earlier stages of arthritis and if left untreated potentially progress to later stages of arthritis requiring a more invasive procedure such as partial or total joint replacement. The current challenge in treating arthritis lies in developing a more versatile implant for focal, regional or global resurfacing that successfully interacts with mating articular cartilage, surrounding articular cartilage and the underlying bone bed.
Diarthrodial joints in the human skeleton provide the nearly frictionless pain free movement supporting locomotion, spatial positioning relative to the environment and active manipulation of the surroundings. These skeletal joints have a strong fibrous capsule enclosing bone ends encapsulated by smooth continuous cartilage surfaces to accomplish this function. This biologic configuration represents the majority of skeletal joints in the human body.
The encapsulating surface on the ends of moving bones is known as hyaline cartilage, a hydrated soft tissue comprised of collagen, trapped proteoglycans, other proteins and chondrocytes. This tissue is more commonly known as articular cartilage or native articular cartilage. This ordered tissue provides a resilient, continuous layer of protective tissue on the bone ends. In addition to protecting the bone ends, it also helps develop an extraordinarily low coefficient of friction during joint movement, by interacting with the synovial fluid.
The resiliency of articular cartilage is supported by a dense bone layer, called the subchondral plate, which provides foundational strength for the articular cartilage. The bone side of the subchondral plate is supported by cancellous bone. Cancellous bone is a highly porous structure with a stiffness 1/10th that of the subchondral plate. The cancellous bone acts to distribute loads across the joint in the metaphyseal region of bone ends.
Skeletal joints are subject to wear and tear though use, trauma and aging. These factors eventually cause biologic changes to the articular cartilage resulting in arthritis, a group of progressive conditions ultimately resulting in irreversible damage to the articular cartilage in skeletal joints.
As damage to the affected articular cartilage surfaces progress, the smooth continuous layer of protective tissue becomes torn and discontinuous. Unlike other tissues, the body is unable to regenerate this well ordered hyaline cartilage and substitutes a less durable, rougher form of cartilage known as fibrocartilage. This less protective fibrocartilage increases the coefficient of friction in the joint and results in a greater volume of microfracturing in the cancellous bone. In reaction to this structural breakdown, the body reacts by thickening the subchondral plate to assist in distributing the load across the bone end. Researchers have sighted this stiffening of the subchondral bone as a possible mechanism for the initiation of cartilage damage. This may be why untreated cartilage lesions cause arthritis to progress and affect larger areas of articular cartilage in a joint over time, leading to activity limiting pain and decreased joint function.
Osteoarthritis (OA) or Degenerative Joint Disease (DJD) is the most common form of arthritis and presents the patient with debilitating pain during daily activities. It is the leading cause of chronic disability in the United States in the middle-aged population, but affects people of all ages. It is estimated that 21 million people have a form of arthritis in the US, accounting for 25% of visits to primary care physicians and half of all NSAID (Non-Steroidal Anti-Inflammatory Drugs) prescriptions.
OA commonly affects the joints at the hips, knees, shoulder, elbow and spine, and small joints such as those found in the hands and feet. As a result, various methods have been developed to treat and repair damaged or destroyed articular cartilage.
For smaller defects, usually identified early in the onset of arthritis during diagnostic workups, arthroscopic debridement, abrasion arthroplasty or abrasion chondralplasty procedures are conducted. The principle behind these procedures is to stimulate bleeding of the subchondral bone bed by abrading it with a burr or shaver to stimulate the fibrocartilage healing response. Although this procedure has been widely used over the past two decades, with good short term results out to three years, the resulting fibrocartilage developed in the healed area does not always support longer term low friction weight bearing function.
Another procedure referred to as “microfracture” incorporates the concept of fibrocartilage healing by removing the damaged cartilage layer and using a surgical awl to perforate the subchondral bone. This technique creates a replacement surface similar in type and outcome to the one created from the abrasion chondralplasty technique.
Transplantation of previously harvested hyaline cartilage cells, known as cell-based therapy, has been utilized in recent years. This technique uses autologous chondrocytes obtained from a specimen of articular cartilage obtained from an uninvolved area of the injured joint. The cartilage cells are isolated, cultured and implanted in the defect area under a periosteal flap. Compared to the previously discussed abrasion techniques, this procedure requires a lengthy post-operative non-weight bearing course and is still viewed somewhat as experimental because of the technical challenges involved in the procedure producing variations in patient outcomes.
Cartilage transplant, referred to as Mosaicplasty or Osteoarticular Transfer System (OATS) is a technique utilizing articular tissue grafts in the form of plugs. These plugs consist of articular cartilage, subchondral bone and cancellous bone to assure they heal to the bone and surrounding articular cartilage in the surgically prepared defect region.
Two different types of donor plugs are harvested for this procedure. The first is taken from a matched articular location in a cadaver bone (allograft). The second type is taken directly from the patient (autograft) in boundary or non-weight bearing locations in the joint being reconstructed.
In either case, the technique for utilizing articular cartilage grafts is challenging. Success of the technique requires accurate harvesting and positioning of single or multiple plugs to reconstruct the articular surface of the subject joint. The plug must be harvested perpendicular to the articular surface, then positioned perpendicular and flush with the retained articular cartilage surrounding the defect area. If the grafts are placed too far below the level of the surrounding articular surface, no benefit from the procedure will be gained and cartilage damage can progress beyond the perimeter of the original defect. If the grafts are placed proud to the surrounding articular surface, detrimental effects can be seen on the mating articular surface over time in the joint. This is important to consider since arthritis often affects one side of an articular joint first before progressing to the mating surface.
The result of positioning these plugs in a mosaic-like fashion establishes a new hyaline cartilage surface. The result is a hyaline-like surface interposed with a fibrocartilage healing response between each graft.
In addition to the many challenges discussed surrounding this procedure, a lengthy post-operative non-weight bearing course is required to improve the patient's chance for success in restoring functional articular cartilage in the skeletal joint.
Other clinical challenges exist beyond the technique issues previously discussed. In the case of allograft plugs graft availability, potential disease transmission and tissue quality are all concerns. In the case of autograft plugs, the quantity and articular shape of available tissue create limitations in the defect size to be treated.
Advances in tissue engineering are beginning to provide treatments to repair focal cartilage lesions in skeletal joints by implanting collagen based scaffold devices, with and without impregnated autologous chondrocytes (cartilage cells). This reconstructive technique, referred to as scaffold guided regeneration, establishes a generic tissue foundation which is converted over time by the body into hyaline cartilage. Initial results using this reconstructive technique show promise, but are currently used in non-weight bearing applications which limit their use in reconstructive procedures presently favoring more traditional devices made from implantable metals, ultra high molecular weight polyethylene(UHMWPE) and ceramics.
One type of joint replacement technique using more traditional devices is called hemi-arthroplasty. This reconstructive procedure replaces one bone end of the two or more bone ends comprising a skeletal joint. The procedure leaves the healthy part or parts of the joint unaltered. The challenge is for the artificial implant to articulate with the native cartilage surfaces over time without recreating painful arthritis as the healthy cartilage tissue becomes arthritic. Clinical experience in using hemi-arthroplasty implants with metal articular surfaces in younger more active patients has shown undesirable thinning and damage of the mating native articular cartilage in early term follow-up. For this reason, this class of procedure is most commonly performed in older patients following a hip fracture. During hemi-arthroplasty of the hip, the surgeon removes the damaged bone and cartilage from the hip joint, usually the femoral head. The healthy mating surface in the acetabulum or pelvis is left intact. One such implant in accordance with the prior art is shown in
When arthritis progresses to all aspects of an articular joint a total joint arthroplasty is performed to reconstruct the cartilage on all bone ends making up the skeletal joint. This comprehensive procedure is required to effectively resolve the activity limiting pain caused by the arthritis. In a total knee, for example, a highly polished metal implant is placed onto the distal femur. A modular metal tray is implanted in the proximal tibia and a UHMWPE bearing joined to it to articulate with the highly polished femoral component. A UHMWPE patellar implant is placed to resurface the patella and articulate against the anterior flange of highly polished femoral implant. This completely resurfaces the femoral-tibial and patella-femoral articular surfaces in the total knee replacement.
The risks involved in joint arthroplasty described previously include mal-position of the components, skeletal loosening, instability/dislocation, loss of range of motion and recurring activity limiting pain.
One long term risk is loosening of the components, because the bond between the bone and the components or the cement may break down or fatigue. Various approaches in the prior art attempt to address the loosening risk. For example, U.S. Pat. No. 6,685,987 describes a porous coating comprised of metallic particles applied over a cobalt chromium molybdenum alloy implant.
Generally joint replacement bearing surfaces are made of cobalt chromium; however other materials have been used or proposed including titanium and titanium alloys. U.S. Patent Application Publication No. 2005/0107888 to Khandkar et al. describes a metal-ceramic composite for joint replacement materials. U.S. Pat. No. 6,398,815 to Pope et al. describes a prosthetic joint with diamond like surfaces.
As described above, the replacement with prosthetic joints is currently the preferred option for serious degeneration of joint function involving loss of articular cartilage. Other techniques include U.S. Pat. No. 7,029,479 to Tallarida et al. that discloses a method for joint resurface repair which involves mapping and measuring the articular surface, U.S. Pat. No. 5,782,835 to Hart et al. that discloses an apparatus and method for repair of articular cartilage including a bone plug removal tool, and a bone plug emplacement tool, U.S. Pat. No. 6,679,917 to Ek that discloses an implant for installation into a portion of an articular surface including a protrusion configured to cover an un-excised portion of the articular surface proximate to the implant, U.S. Pat. No. 5,413,608 to Keller that discloses a knee joint endoprosthesis for replacing the articular surfaces of the tibia comprising a bearing part that is anchored on the bone having an upper bearing surface and a rotatable plateau secured on the bearing surface and forming a part of the articular surface to be replaced, U.S. Pat. No. 5,632,745 to Schwartz that describes a method of surgically implanting into a site a bio-absorbable cartilage repair assembly, U.S. Pat. No. 5,683,466 to Vitale that discloses an articular joint surface replacement system having two opposing components, U.S. Pat. No. 5,702,401 to Shaffer that discloses an intra-articular measuring device including a hollow handle defining a first passageway and a hollow tube having a second passageway extending from the handle, and U.S. Pat. No. 5,771,310 to Vannah that describes a method of mapping the three-dimensional topography of the surface of an object by generating digital data points at a plurality of sample points on said surface. Another implant is described in U.S. Publication No. 2003/0074081 to Ayers that describes a method for production of tissue implants and prosthetics. U.S. Publication No. 2007/0113951 to Huang describes an osteochondral composite scaffold for articular cartilage repair.
Another orthopedic procedure involves fusing bones together and is clearly distinct from joint replacement. One such application is for spinal fusion. For example U.S. Patent Application Publication No. 2005/0049706 and U.S. Pat. No. 6,790,233 to Brodke et al. describe radio lucent spinal fusion cages, one of which is shown in
The reconstructive prior art methods for articular cartilage repair previously discussed have disadvantages and drawbacks related to treating early stage arthritis to prevent progression to a more final stage requiring total joint replacement.
What is needed is a more versatile articular orthopedic implant to function in a collaborative environment with native tissue. Also needed is a non-resorbable implant to support loads imposed by an opposing joint end. In particular what is needed is an implant that will facilitate surgical repair of focal, regional and global articular cartilage and osteochondral defects on a bone end of a skeletal joint to prevent or delay the global progression of arthritis to the entire joint. The embodiments of the present disclosure answer these and other needs.
In a first embodiment disclosed herein, a monolithic orthopedic implant includes a porous region having a form of interconnected porosity similar to cancellous bone to promote skeletal fixation by bone ingrowth, a transition region adjacent to and integrally joined to the porous region, the transition region having a form of interconnected porosity similar to subchondral bone, a substantially dense region integrally joined to the transition region and having a perimeter, and a surface on the substantially dense region, the surface having a finish adapted for articulation against native articular cartilage.
In another embodiment disclosed herein, an orthopedic implant comprises a porous region having a form of interconnected porosity similar to cancellous bone to promote skeletal fixation by bone ingrowth, and a transition region adjacent to and integrally joined to the porous region, the transition region having a form of porosity similar to subchondral bone, wherein the transition region is adapted to promote regeneration of articular cartilage, and wherein the porous region and the transition region are non-resorbable.
In another embodiment disclosed herein, a dental implant comprises a porous region having a form of interconnected porosity similar to cancellous bone to promote skeletal fixation by bone ingrowth, and a substantially dense region integrally joined to the porous region, the substantially dense region having a top surface and a perimeter, wherein the top surface and the perimeter are adapted to be compatible with oral gum tissue, and wherein the porous region and the substantially dense region are non-resorbable.
In another embodiment disclosed herein, a method of forming a monolithic orthopedic implant includes forming a porous region having a form of interconnected porosity similar to cancellous bone to promote skeletal fixation by bone ingrowth, forming a transition region adjacent to and integrally joined to the porous region, the transition region having a form of interconnected porosity similar to subchondral bone, forming a substantially dense region integrally joined to the transition region and having a perimeter, and forming a surface on the substantially dense region, the surface having a finish adapted for articulation against native articular cartilage, wherein the porous region has a porosity gradient that increases as a distance from the substantially dense region increases, and wherein the porous region, the transition region and the substantially dense region are non-resorbable.
In yet another embodiment disclosed herein, a method for orthopedic surgery includes removing a portion of the articular cartilage at an implant site, forming a socket in bone underlying the articular cartilage to a depth placing the surface of the substantially dense region of the monolithic implant approximately flush to the articular cartilage at the implant site, and implanting a monolithic orthopedic implant into the socket, the monolithic orthopedic implant comprising a porous region having a form of interconnected porosity similar to cancellous bone to promote skeletal fixation by bone ingrowth, a transition region adjacent to and integrally joined to the porous region, the transition region having a form of interconnected porosity similar to subchondral bone, a substantially dense region integrally joined to the transition region, and a surface on the substantially dense region, the surface having a finish adapted for articulation against native articular cartilage, wherein the porous region, the transition region, the substantially dense region, and the surface are non-resorbable.
In yet another embodiment disclosed herein, an orthopedic implant comprises a three dimensional framework of structural members with interstitial interconnected passages there between, wherein the structural members comprise non-resorbable ceramic, and wherein each structural member is similar in size to a trabecula in bone.
These and other features and advantages will become further apparent from the detailed description and accompanying figures that follow. In the figures and description, numerals indicate the various features, like numerals referring to like features throughout both the drawings and the description.
In the following description, numerous specific details are set forth to clearly describe various specific embodiments disclosed herein. One skilled in the art, however, will understand that the presently claimed invention may be practiced without all of the specific details discussed below. In other instances, well known features have not been described so as not to obscure the invention.
Referring now to
In another embodiment a transition region 58 may be between a porous region 56, which as shown in
The substantially dense region 54 has relatively little or no porosity compared to the porous region 56 and the transition region 58. The following discusses porosity as it relates to present invention.
The bulk porosity (Pb) of a material is inversely proportional to the bulk density (Db) of the material, which can be calculated by dividing the total mass (Mtot) by the total volume (Vtot), where the mass and volume of a solid portion of the material and a porous portion of the material are designated by (Ms, Vs) and (Mp, Vp), respectively:
Db=(Mtot)/(Vtot)=(Ms+Mp)/(Vs+Vp), (1)
and because the mass of porous portion of a material can be considered to be zero, equation 1 can be rewritten as:
Db=(Mtot)/(Vtot)=(Ms)/(Vs+Vp). (2)
Thus, the bulk porosity (Pb) of a material is therefore:
Pb˜1/Db=(Vs+Vp)/Ms. (3)
The porosity that may be most deleterious to a surface having a finish adapted for articulation against native articular cartilage, such as surface 60, is porosity with pores connected to the material surface. A material with substantial porosity is generally not appropriate for surface 60, because there can be material breakage under and at the edges of pores of such a material. It is also more difficult to polish porous materials, because coarser abrasive particles from early stages of grinding and polishing can become trapped in the pores, and then the particles can escape during polishing and finishing, which causes unwanted scratches and surface damage.
On the other hand, open and interconnected pores are preferable for promoting bone ingrowth.
The monolithic orthopedic implant of the present disclosure solves this contradiction in desired properties by providing the porous region 56 with a form of interconnected porosity of a form similar to cancellous bone, the transition region 58 with a form of interconnected porosity similar to subchondral bone, and the substantially dense region 54 with relatively little if any porosity, which are all integrally joined to form the monolithic orthopedic implant 50. In one embodiment the substantially dense region 54 may have a bulk porosity of 4% or less, and in another embodiment the bulk porosity of the substantially dense region 54 may be 0.1% or less. The porous region 56 may have a bulk porosity of 50% or greater. The transition region 58 has an interconnected porosity that is relatively lower than the porous region 56 to provide strength while supporting capillary movement of fluid between the cancellous bone and articular cartilage. The result is an orthopedic implant 50 that provides a scaffold for bone ingrowth and fluid communication between the cancellous bone and cartilage, while providing strength and a surface that can be finished for articulation against native articular cartilage.
In the following the porous region is referred to as porous region 56, although it should be understood that in the following reference to a porous region may also refer to the porous region 52, which includes the porous region 56 and the transition region 58.
The monolithic orthopedic implant 50 is preferably non-resorbable. Thus, the porous region 56, the transition region 58, and the substantially dense region 54 are not resorbed or converted into a specific tissue type by the body and do not lose any substance over time when implanted in a skeletal joint location. This avoids a disadvantage of many prior art implants, because in some of those implants the biologic timing of this resorption or conversion happens relatively quickly causing cyst formation and a loss of structural support for the articular cartilage, a clearly undesirable phenomenon.
The dividing line between the porous region 56 and the transition region 58, shown in
The porous region 56, and also the transition region 58 may have porosity gradients that increase as a distance from the substantially dense region 54 increases. In general the porous region 56 may be described as having a three dimensional framework with interconnected structural members with interstitial interconnected passages between the structural members. Each structural member may be similar in size to a trabecula in bone. This structure allows fluid to flow through the porous region 56 which provides for cell transfer that encourages and sustains bone ingrowth. As discussed above, the structure of the transition region 58 is adapted to have a form of porosity similar to subchondral bone, which facilitates capillary movement of fluid between the cancellous bone and articular cartilage.
In one embodiment the porous region 56 has interconnected pore passageways each with a dimension less than 1000 micrometers to promote bone ingrowth. In another embodiment the porous region 56 has interconnected pore passageways each with a dimension between 200 micrometers and 600 micrometers to promote bone ingrowth.
The porous region 56 may be further adapted to promote bone ingrowth for bone fixation. In one embodiment the porous region 56 has a roughness, characterized by a frictional coefficient similar to cancellous bone, which is generally greater than 0.5. The frictional coefficient is a biomechanical characterization of friction between cancellous bone and cortical bone. The frictional coefficient of the porous region 56 helps prevent the formation of a fibrous layer, which can retard bone ingrowth. The roughness may be on the outside of the porous region 56 and also on the inside of the porous region 56. The porous region 56 is preferably a three dimensional framework of interconnected structural members with interstitial interconnected passages there between and the roughness may be on the structural members, which provides a microstructure to promote bone ingrowth and fixation by facilitating cell adhesion. Each structural member may be similar in size to a trabecula in bone.
In another embodiment the porous region 56 has a hydrophilic or a charged surface that can influence a cell population to enhance bone ingrowth for bone fixation. These surface modifications have been shown to attract a cell population and/or influence the organization of cells to enhance healing of the surrounding native articular cartilage.
In yet another embodiment the porous region 56 may include a bioactive mineral coating, which may be hydroxyapatite, bioglass, or a form of calcium phosphate, nonlimiting examples of which are tri-calcium phosphate (TCP), alpha TCP, or beta TCP, or any combination thereof to promote bone ingrowth for bone fixation.
In still another embodiment the porous region 56 may include a bioengineered coating to promote bone ingrowth for bone fixation. The bioengineered coating may consist of one or more proteins, a peptide, or any combination thereof. An example of a peptide is a synthetic peptide analogue of collagen designed to create biomimetic cell binding habitats. Examples of proteins that can be used include the family of bone morphogenetic proteins, known as BMP's.
The surface 60 on the substantially dense region 54 may be finished to a surface roughness of 6 micrometers Ra or less for articulation with articular cartilage on an opposing joint. The 6 micrometers Ra or less surface roughness provides a smooth surface for opposing articulating cartilage in a joint to ride or bear upon, which avoids the wear and eventual tearing of the articulating cartilage that would occur if the surface roughness were high, especially if the surface had open pores. In one embodiment, the surface roughness is less than 0.025 micrometers Ra.
The porous region 56, the transition region 58, and the substantially dense region 54 may have the same material composition. For example, in one embodiment the monolithic orthopedic implant 50 may be entirely made of ceramic. Partially stabilized zirconia is a preferred material for the entire monolithic orthopedic implant 50. In another embodiment the porous region 56, the transition region 58, and the substantially dense region 54 are composed of different material compositions, and in this embodiment the transition region 58 may have a composition that is a mix of the composition of the porous region 56 and the composition of the substantially dense region 54.
A cross section of another embodiment of the monolithic orthopedic implant is shown in
The thermal processing may also form a thin layer 322 on the porous region 314 and the transition region 312; however, this thin layer 322 preferably does not close the pores on or in the porous region 314 and the transition region 312, so that the pores remain open.
The articular surface 320 may be formed by depositing material. For example, pyrolytic carbon or diamond-like carbon may be deposited on the substantially dense region. Yet another method to form the articular surface 320 is coating the substantially dense region with, for example, ceramic or ceramic like material.
Throughout the following description, the embodiments are generally described with reference to the embodiment of
The porous region 56, the transition region 58, the substantially dense region 54 and the surface 60 may have a Vickers hardness of 500 MPa or greater, a nickel content of less than 4%, and a chrome content of less than 10%. Alternatively, the monolithic orthopedic implant 50 may have a substantially dense region 54, which is formed from materials with a Vickers hardness of 1000 MPa or greater and with a bulk porosity of 4% or less. In another embodiment the monolithic orthopedic implant 50 may have a substantially dense region 54, which is formed from materials with a Vickers hardness of 1200 MPa or greater and with a bulk porosity of 0.1% or less.
The substantially dense region 54 may have a composition of materials chosen from the group consisting of oxides, nitrides, carbides or borides, which are all ceramics or any combination thereof. Alternatively, the substantially dense region 54 may include a coated metal selected from oxidized, nitrided-, carburized- or boronized-titanium, zirconium, hafnium, tantalum or molybdenum or any combination thereof. For example, oxidized zirconium forms a coating of zirconia on the outside of the zirconium. One coating that can be used is a thin diamond like coating, which can be polished to the desired very low surface roughness. In another embodiment the substantially dense region 54 may be of a material chosen from the group consisting of partially stabilized zirconia, alumina, silicon nitride or SiAlON or any combination thereof. As discussed above a preferred material for the substantially dense region 54 is partially stabilized zirconia.
The transition region 58 and the porous region 56 may be formed from materials from the group consisting of oxides, carbides, nitrides, or borides or any combination thereof. Alternatively, the transition region 58 and the porous region 56 may be a coated metal comprising oxidized-, nitrided-, carburized- or boronized-titanium, zirconium, hafnium, tantalum or molybdenum. The coated metal is configured for bone ingrowth and is porous. In another embodiment the porous region 56 and the transition region 58 may be formed of materials chosen from the group consisting of partially stabilized zirconia, alumina, silica, silicon nitride, SiAlON, tantalum, titanium, or zirconium or any combination thereof. As discussed above a preferred material for the porous region 56 and the transition region 58 is partially stabilized zirconia.
Another material that may be used for the monolithic orthopedic implant is pyrolytic carbon, a biocompatible material with desirable articular surface properties.
The monolithic orthopedic implant 50 may be used in many joint locations and can be used for a femoral knee prosthesis, a tibial knee prosthesis, a patellar knee prosthesis, a femoral head hip prosthesis, an acetabular hip prosthesis, a finger or thumb prosthesis, a shoulder prosthesis, a toe prosthesis, a spine prosthesis, a wrist or ankle prosthesis, or an elbow prosthesis, among others.
To further promote bone ingrowth into the porous region 56, the porous region 56 may have two or more projections, such as shown in
In another embodiment shown in
In another embodiment shown in
As discussed above, the dimples and bumps 69 serve as examples, and do not limit other protrusion and/or indentation features that can exist on the perimeter of the substantially dense region 54 to help facilitate the desired hydrostasis. For example, other protrusion or indentation features may include radial or angled bumps and radial or angled grooves, respectively.
In
In one embodiment the perimeter 66 has a roughness, which may be 6 micrometers Ra or less, to promote healing of surrounding articular cartilage. In another embodiment the perimeter roughness may be greater than 6 micrometers Ra.
In another embodiment the perimeter 66 has a hydrophilic surface or a charged surface that influences a cell population to enhance healing of surrounding native articular cartilage. These surface modifications can attract a cell population and/or influence the organization of cells to enhance healing of the surrounding native articular cartilage.
In yet another embodiment the perimeter 66 may include a bioactive mineral coating, which may be hydroxyapatite, bioglass, or a form of calcium phosphate, nonlimiting examples of which are tri-calcium phosphate (TCP), alpha TCP, or beta TCP, or any combination thereof to promote healing of surrounding articular cartilage.
In still another embodiment the perimeter 66 may include a bioengineered coating to promote healing of surrounding articulate cartilage. The bioengineered coating may consist of a blood derived product, such as fibrin glue or fibrin clot, one or more proteins, a peptide, collagen, impregnated autologous chondrocytes, which are cartilage cells, a pharmaceutical agent, or any combination thereof.
The adaptation of the perimeter 66 discussed above in reference to
In yet another embodiment the top surface 71 may include a bioactive mineral coating, which may be hydroxyapatite, bioglass, or a form of calcium phosphate, nonlimiting examples of which are tri-calcium phosphate (TCP), alpha TCP, or beta TCP, or any combination thereof to promote healing of surrounding articular cartilage.
In still another embodiment the top surface 71 may include a bioengineered coating to promote healing of surrounding articulate cartilage. The bioengineered coating may consist of a blood derived product, such as fibrin glue or fibrin clot, one or more proteins, a peptide, collagen, impregnated autologous chondrocytes (cartilage cells), a pharmaceutical agent, or any combination thereof.
To match the curvature of a joint, the surface of the substantially dense region may have the following embodiments. Note that the following surface curvatures may be applied to many implant configurations, including those with substantially dense regions smaller or larger than the porous region and those with beveled or reverse beveled perimeters.
The monolithic orthopedic implant 50 can be fabricated as shown in
The articular surface on the substantially dense region may be formed by thermally processing the substantially dense region or the entire monolithic orthopedic implant as shown in step 212 of
The porosity of the porous region 56 and the transition region 58 may be formed by oxidizing a fugitive material, dissolving a fugitive material, using a lost foam process, using a solid freeform fabrication process, or using a foaming process, which are processes well known in the art.
The orthopedic implant 50 may be formed into a desired geometrical form by milling, turning or other machining processes. Preferably these processes are adjusted to account for any shrinkage that may occur during milling, turning or other machining processes. Such shrinkage can be 10% or greater.
In an orthopedic surgery method to implant the monolithic orthopedic implant 50, a portion of articular cartilage at an implant site may be removed, as shown in
In one embodiment the method for implanting includes implanting a plurality of monolithic orthopedic implants adjacent to one another to create a nearly continuous articular surface, which can have a varying contour to match the curvature of a joint, as shown in
In one embodiment removing a portion of the articular cartilage at the implant site includes preparing the implant site by excising the portion of the articular cartilage to form a predetermined geometrical lesion and forming at the implant site a socket in the bone conforming geometrically to a form of the orthopedic implant. The dimensions of the socket preferably allow for a compressive or interference fit between the bone and the orthopedic implant 50. Also two or more sockets may be formed at the implant site if the orthopedic implant 50 has multiple projections, as shown in
In another embodiment, shown in
A scaffold 166 adapted to promote regeneration of the surrounding articular cartilage may be coupled to the transition region 164, and
The transition region 164 may be further adapted to promote regeneration of articular cartilage. In one embodiment the transition region has a roughness, which may be on the outside of the transition region 164 and also on the inside of the transition region 164. Preferably the transition region includes a three dimensional framework of interconnected structural members with interstitial interconnected passages there between and the roughness may be on the structural members.
In another embodiment the transition region 164 has a hydrophilic surface or a charged surface that can influence a cell population to enhance healing of surrounding native articular cartilage. These surface modifications can attract a cell population and/or influence the organization of cells to enhance healing of the surrounding native articular cartilage.
In yet another embodiment the transition region 164 may include a bioactive mineral coating, which may be hydroxyapatite, bioglass, or a form of calcium phosphate, nonlimiting examples of which are tri-calcium phosphate (TCP), alpha TCP, or beta TCP, or any combination thereof to promote healing of surrounding articular cartilage.
In still another embodiment the transition region 164 may include a bioengineered coating to promote healing of the articulate cartilage. The bioengineered coating may consist of a blood derived product, such as fibrin glue or fibrin clot, one or more proteins, a peptide, collagen, impregnated autologous chondrocytes (cartilage cells), or any combination thereof.
The porous region 162 also may be further adapted to promote bone ingrowth for bone fixation. In one embodiment the porous region 162 has a roughness, characterized by a frictional coefficient similar to cancellous bone, which is generally greater than 0.5. The frictional coefficient is a biomechanical characterization of friction between cancellous bone and cortical bone. The frictional coefficient of the porous region 162 helps prevent the formation of a fibrous layer, which can retard bone ingrowth. The roughness may be on the outside of the porous region 162 and also on the inside of the porous region 162. The porous region 162 is preferably a three dimensional framework of interconnected structural members with interstitial interconnected passages there between and the roughness may be on the structural members, which provides a microstructure to promote bone ingrowth and fixation by facilitating cell adhesion.
In another embodiment the porous region 162 may also have a hydrophilic or a charged surface that can influence a cell population to enhance healing of surrounding native articular cartilage. The described surface modifications can attract a cell population or influence the organization of cells to enhance healing of the surrounding native articular cartilage.
In yet another embodiment the porous region 162 may include a bioactive mineral coating, which may be hydroxyapatite, bioglass, or a form of calcium phosphate, nonlimiting examples of which are tri-calcium phosphate (TCP), alpha TCP or beta TCP, or any combination thereof to promote bone ingrowth for bone fixation.
In still another embodiment the porous region 162 may include a bioengineered coating to promote bone ingrowth for bone fixation. The bioengineered coating may consist of one or more proteins, a peptide, or any combination thereof.
As shown in
The porous implants 180 and 182 have a three dimensional framework of structural members with interstitial interconnected passages between the structural members. The material of the framework is preferably non-resorbable ceramic, and each structural member may be similar in size to a trabecula in bone.
The interconnected pore passageways may each have a dimension less than 1000 micrometers or each have a dimension between 200 and 600 micrometers. The framework may have a bulk porosity of 50% or greater.
The porous implants 180 and 182 of
To promote bone ingrowth, each structural member may have a roughness. In another embodiment to promote bone ingrowth, the framework may have a hydrophilic coating or a charged coating, which as discussed above can attract a cell population and/or influence the organization of cells to enhance healing of the surrounding native articular cartilage.
In another embodiment, the framework may have a bioactive mineral coating, which can be hydroxyapatite, bioglass, or a form of calcium phosphate or any combination thereof. In another embodiment the framework has a bioengineered coating one or more proteins or a peptide or any combination thereof.
The implants 180 and 182 may be formed from materials from the group consisting of oxides, carbides, nitrides, or borides or any combination thereof. Alternatively, the implants may be formed of coated metal consisting of oxidized-, nitrided-, carburized- or boronized-titanium, zirconium, hafnium, tantalum, or molybdenum or any combination thereof. The framework may also be formed of materials chosen from the group consisting of partially stabilized zirconia, alumina, silica, silicon nitride, SiAlON, tantalum, titanium, or zirconium or any combination thereof.
Having now described the invention in accordance with the requirements of the patent statutes, those skilled in this art will understand how to make changes and modifications to the present invention to meet their specific requirements or conditions. Such changes and modifications may be made without departing from the scope and spirit of the invention as disclosed herein.
The foregoing Detailed Description of exemplary and preferred embodiments is presented for purposes of illustration and disclosure in accordance with the requirements of the law. It is not intended to be exhaustive nor to limit the invention to the precise form(s) described, but only to enable others skilled in the art to understand how the invention may be suited for a particular use or implementation. The possibility of modifications and variations will be apparent to practitioners skilled in the art. No limitation is intended by the description of exemplary embodiments which may have included tolerances, feature dimensions, specific operating conditions, engineering specifications, or the like, and which may vary between implementations or with changes to the state of the art, and no limitation should be implied therefrom. Applicant has made this disclosure with respect to the current state of the art, but also contemplates advancements and that adaptations in the future may take into consideration of those advancements, namely in accordance with the then current state of the art. It is intended that the scope of the invention be defined by the claims as written and equivalents as applicable. Reference to a claim element in the singular is not intended to mean “one and only one” unless explicitly so stated. Moreover, no element, component, nor method or process step in this disclosure is intended to be dedicated to the public regardless of whether the element, component, or step is explicitly recited in the Claims. No claim element herein is to be construed under the provisions of 35 U.S.C. Sec. 112, sixth paragraph, unless the element is expressly recited using the phrase “means for . . . ” and no method or process step herein is to be construed under those provisions unless the step, or steps, are expressly recited using the phrase “comprising the step(s) of . . . ”
