US20030158606A1 - Knee arthroplasty prosthesis and method - Google Patents
Knee arthroplasty prosthesis and method Download PDFInfo
- Publication number
- US20030158606A1 US20030158606A1 US10/370,154 US37015403A US2003158606A1 US 20030158606 A1 US20030158606 A1 US 20030158606A1 US 37015403 A US37015403 A US 37015403A US 2003158606 A1 US2003158606 A1 US 2003158606A1
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- US
- United States
- Prior art keywords
- piece
- tibial
- extending
- stem
- component
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
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- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
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- A61F2/30—Joints
- A61F2/30767—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
- A61F2/30771—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves
- A61F2002/30878—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves with non-sharp protrusions, for instance contacting the bone for anchoring, e.g. keels, pegs, pins, posts, shanks, stems, struts
- A61F2002/30884—Fins or wings, e.g. longitudinal wings for preventing rotation within the bone cavity
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/30767—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
- A61F2/30771—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves
- A61F2002/30878—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves with non-sharp protrusions, for instance contacting the bone for anchoring, e.g. keels, pegs, pins, posts, shanks, stems, struts
- A61F2002/30891—Plurality of protrusions
- A61F2002/30892—Plurality of protrusions parallel
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/3094—Designing or manufacturing processes
- A61F2002/30975—Designing or manufacturing processes made of two halves
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/46—Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor
- A61F2002/4631—Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor the prosthesis being specially adapted for being cemented
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/46—Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor
- A61F2/4637—Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor for connecting or disconnecting two parts of a prosthesis
- A61F2002/4638—Tools for performing screwing, e.g. nut or screwdrivers, or particular adaptations therefor
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2220/00—Fixations or connections for prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
- A61F2220/0025—Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2220/00—Fixations or connections for prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
- A61F2220/0025—Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
- A61F2220/0033—Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by longitudinally pushing a protrusion into a complementary-shaped recess, e.g. held by friction fit
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2220/00—Fixations or connections for prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
- A61F2220/0025—Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
- A61F2220/0041—Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements using additional screws, bolts, dowels or rivets, e.g. connecting screws
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2250/00—Special features of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
- A61F2250/0058—Additional features; Implant or prostheses properties not otherwise provided for
- A61F2250/0084—Means for distinguishing between left-sided and right-sided devices; Sets comprising both left-sided and right-sided prosthetic parts
Definitions
- the present invention is directed to a prosthesis for use in knee arthroplasty including total knee arthroplasty which is minimally invasive to the patient and to a method for performing surgery using such prosthesis including the femoral and tibial components thereof.
- the femoral component and, preferably, the tibial component are manufactured in at least two and possibly three or more pieces.
- the tibial component could be a single piece, monoblock construction as well as modular multipiece construction.
- a plastic articular surface insert piece In both the single piece and multipiece construction, there is also provided a plastic articular surface insert piece. The pieces are designed to be assembled together following insertion into the knee.
- the femoral component may have three component pieces for a cruciate retaining design and two component pieces for a cruciate sacrificing design. It may be manufactured as two or three separate pieces or manufactured as a single unitary member which is subsequently cut or otherwise divided into two or three separate pieces.
- the pieces are provided with a locking joint for retaining the pieces together following insertion in distal end of the femur.
- the locking joint for the pieces is placed at the area of low patella/femoral contact, a low stress area of the femur. This corresponds to the anterior chamfer cut of a routine total knee arthroplasty and the area can be easily reinforced to accommodate the additional thickness of the locking joint.
- Various locking mechanisms may be employed for joining the pieces together including screws or a transverse locking pin which may be inserted from the medial side and/or lateral side.
- the locking mechanisms of whatever type lock the component pieces together into a solid assembled prosthesis.
- the prosthesis will be additionally reinforced by the underlying bone and/or cement fixation and will produce a durable construction.
- the patellar flange and the area of any joint between assembled components which may be contacted by the patella should be smoothed and, possibly, recessed to prevent premature wear of the patellar member as it tracks over the joint in the femoral component.
- the tibial component preferably has two pieces, namely, a tibial base and a tibial stem. It is also inserted in pieces from the side. It may also be a monoblock, one-piece tibial component with pegged or short stem fixation.
- the tibial base may have of a flat baseplate with anterior and posterior dovetails and may have a tapered transverse keel.
- the other piece of the tibial component is a modular stem which is inserted from the top after the baseplate is inserted. This design allows the components to be inserted through the minimal incision and still have long term stability.
- the stem is preferably fixed with a reverse Morse taper so that it can be driven through the baseplate like a spike.
- a standard conforming dome configuration patellar component is utilized, with the main difference being its method of insertion. It may be inserted without everting the patella. This is accomplished with the use of special instrumentation.
- FIG. 1 is a perspective view of one embodiment of femoral component showing the medial condyle as a separate piece from the remainder of the femoral component.
- FIG. 2 is a perspective view of a second embodiment of femoral component showing the lateral condyle as a separate piece from the remainder of the femoral component.
- FIG. 2A is a sectional view showing a patellar member engaged to the articulating surface of the patellar femoral flange piece.
- FIG. 3 is a perspective view of another embodiment of femoral component showing both the medial condyle and the lateral condyle as separate pieces from the patellar femoral flange piece of the femoral component.
- FIG. 4 is a perspective view showing the patellar femoral flange piece of FIG. 3 taken from a different angle.
- FIG. 5 is a perspective view of an embodiment of femoral component showing the patellar femoral flange piece as a separate piece from the remainder of the femoral component.
- FIG. 6 is a front view of the embodiment of the femoral component of FIG. 5.
- FIG. 7 is a side view of the embodiment of the femoral component of FIG. 5.
- FIG. 8 is a sectional view taken through line 8 - 8 of FIG. 6.
- FIG. 9 is a sectional view taken through line 9 - 9 of FIG. 6.
- FIGS. 10 and 11 are perspective views of other embodiments of the femoral component showing the patellar femoral flange piece as a separate piece from the remainder of the femoral component.
- FIG. 11A is a view similar to FIG. 9 for the embodiment of FIG. 11.
- FIG. 11B is a sectional view through line 11 B- 11 B of FIG. 11 A.
- FIG. 12 is a perspective view of another embodiment of femoral component showing the patellar femoral flange piece as a separate piece from the remainder of the femoral component and showing one form of design for connecting the patellar femoral flange piece to the remainder of the femoral component.
- FIG. 13 is an enlarged view of the circled portion of FIG. 12.
- FIG. 14 is a perspective view of an embodiment of femoral component showing the lateral condyle as a separate piece from the remainder of the femoral component.
- FIG. 15 is an enlarged view of the circled portion of FIG. 14.
- FIG. 16 is a perspective view of another embodiment of femoral component showing the patellar femoral flange piece as a separate piece from the remainder of the femoral component.
- FIG. 17 is an enlarged view of the circled portion of FIG. 16.
- FIG. 18 is a perspective view of the tibial component showing the stem portion thereof as a separate piece from the base.
- FIG. 18A is a view similar to FIG. 18 with the added feature of a stem extension as part of the tibial component.
- FIG. 19 is a sectional view of another embodiment of tibial component showing the stem portion thereof as a separate piece from the base.
- FIG. 20 is a perspective view of another embodiment of tibial component showing the stem portion thereof as a separate piece from the base.
- FIG. 21 is a side view of the tibial component of FIG. 20 showing its implantation in the proximal end of a prepared tibia.
- the femoral component includes a first piece 12 having a patellar flange portion 14 and an integral, unitary lateral condyle portion 16 extending therefrom.
- a prior art femoral component would also have an integral, unitary medial condyle on the opposite side from the lateral condyle portion 16 .
- a medial condyle piece 18 intended to be assembled to the first piece 12 following implantation of both the first piece 12 and the medial condyle piece 18 in the patient.
- the assembly mechanism or locking joint for securing the medial condyle piece 18 to the first piece 12 will be hereinafter described.
- the medial condyle piece 18 is provided with a recess 15 for receiving bone cement and a pair of fixation pins 17 .
- the first piece 12 may also be provided with one or more recesses and fixation pins. If it is desired to have a prosthesis for implantation without bone cement, the recesses such as the recess 15 can be replaced by one of several types of porous surfaces well known in the art for bone in-growth.
- FIG. 2 there is shown a second embodiment of a femoral component 20 having a first piece 22 with a patellar femoral flange portion 24 and an integral, unitary medial condyle portion 26 .
- the second component of this embodiment is a lateral condyle piece 28 which may be joined with the first piece 22 following implantation of both the first piece 22 and the lateral condyle piece 28 in the femur of the patient.
- FIG. 2A shows a sectional view of patellar member P in contact with the articulating surface of the patellar femoral flange portion 24 .
- FIG. 3 shows yet another embodiment of a three-piece femoral component 30 .
- a patellar femoral flange piece 32 Under this embodiment, there is provided a patellar femoral flange piece 32 , a second piece 34 which is a medial condyle piece and a third piece 36 which is a lateral condyle piece assuming, of course, implantation in the right knee of a patient. If the femoral component 30 were implanted in the left knee of a patient, the second piece 34 would be the lateral condyle piece and the third piece 36 would be the medial condyle piece.
- Each of the second piece 34 and the third piece 36 are joined to the patellar femoral flange piece 32 following insertion in the patient's femur by use of a locking joint to be hereinafter described.
- All three of the pieces of the femoral component may be provided with fixation pins 37 and recesses 35 if intended for use with bone cement or a porous surface if intended for non-cemented implantation.
- FIG. 4 is a perspective view of the patellar femoral flange piece of FIG. 3 taken from a different angle.
- the femoral components 10 , 20 and 30 of FIGS. 1 through 3 could be used for implantation in either knee.
- the foregoing description for each of the femoral components 10 , 20 and 30 is based on the assumption of implantation in the right knee. If they were used for implantation in the left knee, the pieces identified by the numerals 18 and 34 would be lateral condyle pieces, the pieces identified by the numerals 28 and 36 would be medial condyle pieces, the portion identified by the numeral 16 would be a medial condyle portion and the portion identified by the numeral 26 would be a lateral condyle portion.
- FIGS. 5, 6, 7 , 8 and 9 there is shown an embodiment of femoral component 40 having two pieces, namely, a patellar femoral flange piece 41 and a condylar piece 42 .
- the patellar femoral flange piece 41 has a patellar engaging surface 43 shaped to allow anatomical tracking of a natural or prosthetic patella P.
- the patellar femoral flange piece 41 has a superior bone engaging surface 46 and a patellar engaging surface 43 defining a portion of an inferior articulating surface.
- the patellar femoral flange piece 41 extends from an inferior end 45 to a leading end 48 which is contoured to engage the condylar piece 42 .
- the condylar piece 42 includes a first condylar portion 50 and a second condylar portion 52 and extends from an engagement end 54 contoured to receive the leading end 48 of the patellar flange 41 to a posterior end 55 .
- the femoral component 40 could be used for implantation in either a right knee or left knee and the first and second condylar portions will be either lateral or medial facing depending upon the knee in which the femoral component 40 is implanted.
- the condylar piece 42 has a superior bone engaging surface with a series of bone engaging flats 60 , 61 , 62 and 63 disposed at varying angles consistent with cuts made in preparing the distal end of the femur to receive the condylar piece 42 .
- the superior bone engaging surface 46 of the patellar flange piece 41 and the superior bone engaging surfaces 60 , 61 , 62 and 63 of the condylar piece 42 may be formed with recesses for receiving bone cement or porous surfaces for bone ingrowth and may also be provided with fixation pins.
- the condylar piece 42 in the embodiment of FIGS. 5 - 9 is formed as a single unitary piece for implantation.
- the first condylar portion 50 and the second condylar portion 52 are joined together with a posterior cam 56 which may be formed integral with or welded or otherwise joined to the first and second condylar portions 50 , 52 .
- the engagement end 54 of the condylar piece 42 also has the first and second condylar portions 50 , 52 joined together by a laterally extending cross member 57 .
- the use of the posterior cam 56 will result in sacrificing of the posterior cruciate ligament.
- the cross member 57 has a superior bone engaging surface 57 A and a medial surface 57 B approximately midway between the superior bone engaging surface 57 A and the articulating surfaces 51 and 53 of the first condylar portion 50 and second condylar portion 52 , respectively.
- a posterior wall surface 57 C On the posterior side of the cross member 57 is a posterior wall surface 57 C extending between the superior bone engaging surface 57 A and the surface 57 B.
- a fourth surface 57 D Opposite the posterior surface 57 C is a fourth surface 57 D which will engage a corresponding surface to be described of the patellar femoral flange piece 41 .
- the engagement ends 54 for each of the first and second condylar portions 50 , 52 each follows a curved path defined by sidewall engagement surface 54 A as shown in FIGS. 5 and 6.
- Each of the curved engagement wall surfaces 54 A extends to the general area defined by the posterior wall surface 57 C of cross member 57 . (See FIG. 5).
- the positioning of the joint defined by the surfaces 54 A of the condylar piece 42 and the mating surfaces of the patellar femoral flange piece 41 is important and should be in the vicinity of the normal femoral tide mark which is a low stress area of contact by sliding engagement of the patella.
- the prosthesis has great ability to function as desired with no separation of the patellar femoral flange piece 41 from the condylar piece 42 following implantation.
- the normal femoral tide mark corresponds to the area of the inferior chamfer cut of a routine total knee arthroplasty.
- the patellar femoral flange piece leading end 48 has a pair of curved engagement surfaces 64 following a contour for mating engagement with the respective surfaces 54 A of the condylar piece 42 .
- Centrally positioned between the curved engagement surfaces 64 is a central wall surface 65 which, when the patellar femoral flange piece 41 is engaged to the condylar piece 42 , lies in substantially the same plane as the surface 57 C of cross member 57 . (See FIG. 9).
- the central wall surface 65 extends superiorly from the patellar engaging surface 43 to a ledge 66 intended to rest upon the surface 57 B of cross member 57 .
- the ledge 66 extends away from the central wall surface 65 to a central engagement surface 67 which is intended to engage the surface 57 D of cross member 57 .
- a bone engaging surface 68 extends from the central engagement surface 67 toward the anterior end 45 .
- the condylar piece 42 may be secured to the patellar femoral flange piece 41 by means of screws 68 extending through apertures 69 extending through engagement end area 54 of the respective first and second condylar portions 50 and 52 , through the engagement end surfaces 54 A and into aligned threaded apertures 71 extending inwardly from the curved engagement surfaces 64 of the patellar femoral flange piece 41 .
- FIG. 8 there is shown the articulating surface defined by the patellar engaging surface 43 of the patellar femoral flange piece 41 and the articulating surface 59 of the condylar piece 42 in the area of the joint defined by the mating surface 54 A of the condylar piece 42 and surface 64 of the patellar femoral flange piece 41 .
- the respective surfaces 43 and 59 are recessed slightly at such joint to provide a slight dip 73 so that any movement of the patellar member P over such joint will leave a slight gap between the surface of the patellar member P and the surfaces 43 and 59 at the dip 73 .
- the presence of the gap and the dip 73 has a two-fold advantage. It reduces the amount of stress in that area of the joint defined by the mating surfaces 54 A and 64 at the surfaces 43 and 59 . Additionally, if there is a slight mismating of the patellar femoral flange piece 41 relative to the condylar piece 42 such that one of the surfaces 43 or 59 were slightly high or lower than intended for precise fixation, the presence of the dip 73 will serve to prevent the patellar member P from contacting and being subjected to premature wear by a sharp corner of the higher piece.
- FIG. 10 there is shown a further embodiment similar to that of FIGS. 5 through 9 but one in which there is provided a condylar piece 42 A having the first condylar portion 50 A is joined to the second condylar portion 52 A only by a posterior cam 56 A.
- the patellar femoral flange piece 41 A has a central wall surface 65 A centrally positioned between curved engagement surfaces 64 A.
- the central wall surface 65 A extends throughout the thickness of the patellar femoral flange piece 41 A. Therefore, there is no ledge similar to the ledge 66 shown in FIG. 5.
- All other features of the embodiment of FIG. 10 are similar to corresponding features of the embodiment of FIGS. 5, 6, 7 , 8 and 9 .
- FIGS. 11, 11A and 11 B there is shown a further embodiment of femoral component 40 B similar to that of FIGS. 5 through 9 but one in which there is provided a condylar piece 42 B having the first condylar portion 50 B joined to the second condylar portion 52 B only by a cross member 57 B and a modified connector means for fastening the condylar piece 42 B to the patellar femoral flange piece 41 B.
- the cross member 57 B is provided with an extension 130 extending superiorly (i.e., downwardly as viewed in FIGS. 11 and 11A) from the cross member 57 B. Both the cross member 57 B and the extension 130 are provided with a common dovetail slot 132 .
- the extension 130 is an integral unitary part of the cross member 57 B and, in cross section, has a generally semicircular cross sectional configuration with the side facing the patellar femoral flange piece 41 B having a pair of flat faces on opposite sides of the dovetail slot 132 .
- the patellar femoral flange piece 41 B has a configuration similar to that of the patellar femoral flange piece 41 as shown in FIG. 5, including a central wall surface 65 B extending from a patellar engaging surface 43 B, a ledge 66 B and a central engagement surface 67 B.
- a bone engaging surface 68 B extends from the central engagement surface 67 B toward the anterior end 45 B.
- Extending superiorly from the bone engaging surface 68 B is an extension 134 having a dovetail 136 sized to be snugly received in the dovetail slot 132 of the extension 130 with conforming mating surfaces.
- the dovetail 136 and dovetail slot 132 could have other crossectional configurations from that shown in FIGS.
- the dovetail 136 is an integral unitary part of the extension 134 ; however, it extends outwardly from the surface 67 B and upwardly from the surface 68 B to join with surface 66 B.
- an aperture is drilled or otherwise formed in the femur of sufficient size to receive the extensions 130 and 134 .
- the patellar femoral flange piece 41 B is moved therein, the dovetail 136 is aligned with the dovetail slot 132 and the patellar femoral flange piece 41 B is moved toward the prepared femur with the dovetail 136 sliding through the dovetail slot 132 until the surface 66 B of the patellar femoral flange piece 41 B contacts the anterior surface of cross member 57 B.
- bone cement will be positioned in the prepared aperture of the femur to engage the adjoined extensions 130 and 134 .
- FIGS. 12 and 13 there is shown an embodiment of a two-piece femoral component 74 with a first piece 75 of a patellar flange area having a patella engagement surface 76 and a second piece 77 having a medial condyle portion 78 and a lateral condyle portion 79 formed as an integral unitary piece.
- the second piece 77 has a series of flats 96 , 97 , 98 , 99 for engagement with a prepared distal end of a femur.
- the first piece 75 has an abutment wall 81 extending from the patella engagement surface 76 and positioned to engage a corresponding abutment wall 82 of the second piece 77 .
- the line of juncture between the abutment wall 81 of the first piece 75 and the abutment wall 82 of the second piece 77 is in the area of low patella/femoral contact which is a low stress area of the femur.
- the abutment wall 81 extends only partially through the thickness of the first piece 75 .
- the abutment wall 81 joins with a second wall 83 disposed substantially at right angles thereto (See FIG. 13).
- the second wall 83 extends to an end wall 84 .
- a ledge 85 Extending outwardly from the end wall 84 toward the plane defined by the abutment wall 81 is a ledge 85 having an upper surface 86 with a tongue or dovetail 87 projecting upwardly therefrom.
- the tongue 87 and upper surface 86 extend throughout the breadth of the first piece 75 .
- the tongue 87 is provided with a pair of reverse taper surfaces 88 which flare outwardly from one another in a direction away from the upper surface 86 .
- an insert ledge 90 Extending outwardly from the abutment wall 82 of the second piece 77 is an insert ledge 90 having an upper surface for mating engagement with the second wall 83 of the first piece 75 .
- the lower portion of the insert ledge 90 opposite the upper surface has formed therein a dovetail groove 92 extending the full breadth of the second piece 77 and sized to receive the tongue 87 of the first piece 75 .
- a dovetail groove 92 extending the full breadth of the second piece 77 and sized to receive the tongue 87 of the first piece 75 .
- a tapered pin 94 which may be driven into the gap 93 to function as a wedge putting the tongue 87 into compression in the dovetail groove 92 formed in the lower surface of the insert ledge 90 .
- FIGS. 14 and 15 there is provided another embodiment of prosthesis 100 with a first piece 101 having both a patellar flange area 102 and an integral, unitary lateral condyle portion 103 .
- the prosthesis 100 also has a second piece 104 which is a medial condyle piece.
- the first piece 101 has a first abutment wall 105 extending generally laterally and a second abutment wall 106 extending generally longitudinally with a curved wall section 107 joining the first abutment wall 105 and the second abutment wall 106 .
- a projection 110 Protruding outwardly from the second abutment wall 106 is a projection 110 having sidewalls 111 (only one of which is shown) tapering inwardly toward one another as they extend outwardly from the second abutment wall 106 and end walls 112 tapering inwardly toward one another as they extend outwardly from the second abutment wall 106 .
- the tapering sidewalls 111 and end walls 112 are joined by an outer wall 113 substantially parallel with the second abutment wall 106 .
- the projection 110 is integral and unitary with the remainder of the first piece 101 and may be formed by a milling process, for example.
- a threaded aperture 114 extends through the projection 110 from the outer wall 113 and, preferably, extends into the adjacent portion of the first piece 101 .
- the second piece 104 has a first abutment wall 115 positioned to engage the first abutment wall 105 of the first piece 101 , a second abutment wall 116 positioned and sized to engage the second abutment wall 106 of the first piece 101 and a curved wall 117 for engagement with the curved wall 107 of the first piece 101 .
- Formed in the second wall 116 is a recess 118 contoured to snuggly receive the projection 110 of the first piece 101 .
- a laterally extending passageway 108 extends through the second piece 104 in alignment with the threaded aperture 114 of the first piece 101 when the second piece 104 is engaged thereto.
- an elongated screw 120 having a threaded section 121 for mating with the threads of the threaded aperture 114 of the first piece 101 .
- the screw 120 has a cylindrical section 122 of larger diameter than the threaded section 121 and sized to be snugly received in the passageway 108 of the second piece.
- the screw 120 has an enlarged head 123 sized to fit in a countersunk area of the passageway 108 at the outer edge of the second piece 104 .
- a two-piece femoral component 140 including a first piece 141 having both a lateral condyle 142 and a medial condyle 143 formed as part of an integral, unitary piece.
- the second piece 144 defines a patellar flange area of the femoral component 140 .
- the second piece 144 has a contoured abutment wall 145 including a first flat surface 145 A extending inwardly from the lateral side, a second flat surface 145 B extending inwardly from the medial side of the second piece 144 and a recess defined by first and second side walls 145 C and a bottom wall 145 D.
- the sidewalls 145 C taper inwardly toward one another as they extend from their respective flat surfaces 145 A and 145 B to the bottom 145 D.
- the bottom wall 145 D is curved; however, it could be flat.
- the first piece 141 is provided with an abutment wall 146 having a contour to be snuggly engaged to the abutment wall 145 of the second piece 144 .
- the abutment wall 146 includes a tongue 147 contoured to fit snuggly in the groove defined by sidewalls 145 C and bottom wall 145 D of the second piece 144 .
- the tongue 147 is defined by sidewalls 146 C, 146 C and an end wall 146 D contoured to snuggly engaged the wall 145 D forming the bottom of the groove of the second piece 144 .
- the walls 146 C, 146 C taper inwardly toward one another as they extend toward the wall 146 D and snuggly engage the tapered sidewalls 145 C of the second piece 144 .
- the second piece 144 has formed therein a first passageway 148 A which extends inwardly from the lateral edge and is substantially parallel to the first flat surface 145 A and a second passageway 148 B which extends inwardly from the medial edge and is substantially parallel to the second flat surface 145 B.
- a passageway 149 is formed in the tongue 147 in a position to be aligned with the passageways 148 A and 148 B when the first piece 141 is engaged to the second piece 144 , with the tongue 147 fitting in the groove.
- a pin 150 may be inserted through the passageway 148 B, the passageway 149 and the passageway 148 A to secure the first piece 141 to the second piece 144 .
- the pin 150 could be cylindrical and press fit into the respective passageways 148 A, 148 B and 149 assuming the passageways were cylindrical or could be tapered assuming such passageways had the appropriate taper. Additionally, one of the passageways, passageway 148 A, for example, could be threaded, in which case the pin 150 would have a threaded end for engagement therewith.
- the respective lines of juncture between abutting walls of the assembled pieces have been selected to be located generally in the area of the normal femoral tidemark which is a low stress area.
- the tibial component 161 includes a tibial base 162 and a tibial stem 163 .
- the tibial base 162 has an inferior surface 164 intended to engage the prepared proximal end of the tibia of the patient and a superior surface (not shown) to which may be affixed a plastic insert contoured to be engaged by the condylar portions of a femoral component.
- the plastic insert may have one of a number of well known mechanisms for being attached to the tibial base 162 such as a dove tail locking mechanism, for example.
- the plastic insert may be inserted either laterally or proximally depending on the specific design of the tibial base and the condition of the patient as determined by the surgeon.
- Extending distally from the inferior surface 164 is a base extension 165 having a generally cylindrical shape but with a pair of fixation wings or fins 166 extending outwardly from the cylindrical portion of the base extension 165 .
- a platform 167 is raised from the inferior surface 164 and follows a contour encircling the base extension 165 including the wings 166 .
- the wings 166 function as fixation fins for maintaining the tibial base 162 in a fixed rotational position when implanted on the prepared proximal end of the tibia.
- the tibial base 162 is provided with a notch 168 to accommodate the posterior cruciate ligament and a plurality of apertures 169 for receiving screws for engagement to an augmentation block, if one is needed, or for securing the tibial base 162 to the proximal end of a prepared tibia.
- the tibial base 162 has a central passageway 170 extending from the superior surface 164 and through the cylindrical portion of the base extension 165 . That portion of the central passageway 170 in the base extension 165 has wall surface which flares outwardly frusto conically and defines a Morse taper cavity 295 as it approaches the end of the base extension 165 . A recess defining a notch 240 is formed in the end of the base extension 165 . That portion of the passageway adjacent the superior surface has a diameter sized to receive a screw 158 and a countersunk area 297 to receive the enlarged head of such screw 158 .
- the tibial stem 163 is provided with a pair of wings or fixation fins 171 which, when the tibial stem 163 is engaged to the extension 165 , will be aligned with and forming extensions of the respective wings or fins 166 of the tibial base 162 .
- the tibial stem 163 is provided with a Morse taper extension 298 sized to be snugly received in the Morse taper cavity 295 of the tibial base 162 .
- a shoulder 262 extends outwardly from the Morse taper extension 298 .
- a raised tab 242 extends proximally from the shoulder 202 and is sized to fit snugly in the notch 210 and, when so positioned, assures alignment of the fixation fins 171 of the tibial stem 163 with the fins 166 of the tibial base 162 .
- a threaded passageway 172 is formed in the Morse taper extension 298 and is aligned with the central passageway 170 when the tibial stem 163 is engaged to the extension 165 .
- the tibial stem 163 is supported on the tibial base 162 by the screw 158 extending through the central passageway 170 of the tibial base 162 and engaged to the threaded passageway 172 .
- a plug 244 is engaged in the distal end of the tibial stem 163 to prevent blood or other contaminates from entering the threaded passageway 172 .
- the plug 244 may be secured to the tibial stem 163 by means of a threaded extension engaging the threaded passageway 172 .
- FIG. 18A shows an embodiment similar to FIG. 18 but in which there is provided a stem extension 250 but not a plug such as the plug 244 of FIG. 18.
- the stem extension 250 is provided with a Morse taper 252 at its proximal end 253 .
- a threaded recess 254 extends distally from the proximal end and has a size smaller than the threaded passageway 172 .
- a threaded screw 258 sized to engage the threaded recess 254 secures the stem extension 250 and the tibial stem 163 to the tibial base 162 .
- the threaded screw 258 is small enough to pass through the threaded passageway 172 without engaging its threads.
- the distal end of the tibial stem 163 has a cavity 260 tapering outwardly in a distal direction and defining a Morse taper sized to snuggly receive the Morse taper 252 of the stem extension 250 .
- Two grooves 270 are formed in the tibial stem 163 , on opposite sides, distally spaced from the shoulder 262 . The purpose of the grooves 270 is to permit engagement and support for the tibial stem during implantation as will be discussed hereinafter.
- FIG. 19 there is a shown in section a modified embodiment of tibial component 200 .
- a tibial base 202 Under this embodiment there is provided a tibial base 202 , a tibial stem 204 and a plastic insert 206 for engagement with the tibial base 202 .
- the tibial base as shown in FIG. 19, has a raised wall 208 and a flat superior surface 210 .
- the tibial base 202 has an inferior surface 212 intended to engage the prepared proximal end of the tibia of the patient.
- a centrally positioned short extension 213 extends from the inferior surface 212 .
- a passageway 214 Extending through the tibial base 202 including the extension 213 is a passageway 214 . That portion of the passageway 214 adjacent the inferior surface 210 is enlarged from the remainder of the passageway and is provided with inwardly facing threads 215 in the area adjacent the inferior surface 210 . That portion of the passageway 214 extending away from the threads 215 is tapered to define a Morse taper cavity 216 throughout the remainder of the thickness of the tibial base 202 including the stem 213 .
- the tibial stem 204 is provided with an enlarged threaded flange 220 sized to engage the threads 215 of the tibial base 202 .
- Extending from the flange 220 is a Morse taper extension 222 sized and contoured to be snuggly received in the Morse taper cavity 216 .
- Extending inwardly from the inferior surface 210 is a cavity defined by a series of flats 224 which cooperate to define a hexagon or other conveniently shaped cavity for receipt of a tool for engagement therein for threading the threaded flange 220 into the threads 215 .
- Extending from the cavity defined by the flats 224 is a threaded aperture 225 .
- Extending distally from the Morse taper extension 222 is a reduced size cylindrical extension 227 .
- the plastic insert 206 has molded therein a metal insert 230 having an enlarged flange 232 to ensure its firm engagement to the insert 206 .
- the insert 206 is provided with a passageway 234 sized to receive a screw 236 including its enlarged head 238 .
- the metal insert 230 is provided with a passageway 240 sized to receive the threaded portion of the screw 236 but smaller than the enlarged head 238 .
- the proximal end of the tibia is prepared by cutting a flat surface to receive the inferior surface 212 of the tibial base 202 and a cavity is drilled in the intramedullary canal of the tibia to receive. the stem 204 .
- the tibial base 202 is positioned on the prepared flat surface with the extension 213 positioned in the cavity.
- the tibial stem 204 is then positioned in the passageway 214 with the cylindrical extension 227 passing through the Morse taper cavity 216 and into the cavity of the intramedullary canal.
- the stem is threadedly engaged to the threads 215 and the base 202 to cause the Morse taper extension 222 to firmly engage the Morse taper cavity 216 .
- the tibial stem 204 is so contoured relative to the tibial base 202 , that a gap 229 will remain between the distal side of the flange 220 and the surface of the tibial base 202 extending radially outwardly from the Morse taper cavity 216 . This ensures that the Morse taper extension 222 will firmly engage the Morse taper cavity 216 upon threaded engagement of the threaded flange 220 to the threads 215 .
- the tibial component 180 includes a tibial base 181 , a tibial stem 182 and a plastic insert 179 engaged to the tibial base 181 .
- the tibial base 181 has an inferior surface 183 intended to engage the prepared proximal end of the tibia T and a superior surface 184 to which may be affixed a plastic insert 179 contoured to be engaged by a femoral component.
- the tibial base 181 has raised areas 185 along the anterior and posterior edges. Each of the raised areas is provided with an undercut wall surface 186 defining grooves for receiving and retaining the plastic insert 179 .
- the tibial base 181 has a central passageway 188 extending from the superior surface 184 and through the extension 187 .
- the extension 187 and the passageway 188 may be disposed at an angle of up to 100 relative to a line perpendicular to the superior surface 184 in order to accommodate the anatomy of the patient.
- the tibial stem 182 is provided with a recess 190 sized and positioned to become an extension of the passageway 188 of the tibial base 181 .
- the recess 190 may be threaded for engagement by a threaded screw 196 extending through the plastic insert 179 and its articular surface and through the passageway 188 to join the tibial stem 182 to the tibial base 181 .
- the distal end 188 A of the passageway 188 may be tapered to define a Morse taper cavity.
- the tibial stem 182 is also provided, at its proximal end, with a Morse taper extension 197 sized to snugly engage the Morse taper cavity at the distal end 188 A of the passageway 188 .
- the tibial stem 182 is also provided with a plurality of outwardly facing grooves 189 to assist in fixation.
- the proximal end T 1 of the tibia is cut to form substantially a flat surface.
- a cavity T 2 is formed to receive the tibial stem 182 . Since the cavity T 2 may be oversized, the tibial stem 182 is provided with an annular groove 198 sized to receive the tines 195 A of the tool 195 . As can be seen in FIG.
- the tool 195 can support the tibial stem 182 at the proper location relative to the prepared proximal end T 1 of the tibia T until such time as the screw 196 is engaged in the threaded recess 190 to support such tibial stem 182 on the tibial base 181 .
- a tool similar to the tool 195 may be used to engage the grooves 270 to support the stem 163 until it is engaged by the screw 158 or 258 .
- the surface of the tibial base which is to be contacted by a plastic insert be polished to a high degree, on the order of four (4) rms or less, to prevent premature wear on the surface of the plastic insert engaged to the tibial base.
- a medial parapatellar incision is made from the superior pole of the patella to the tibial tuberosity.
- Medial parapatellar arthrotomy is made from the inferior edge of the vastus medial is to the tibial tuberosity.
- a subvastus or mid vastus arthrotomy may be utilized, based upon patient anatomy or surgeon experience.
- the knee is place in extension and the patella excised without eversion, using a patellar clamp inserted into the prepatellar bursa, to prevent damage to the anterior skin.
- An extramedullary tibial alignment guide is placed along the medial or lateral half of the tibia and secured with fixation pins.
- An extrameduallary alignment guide of the type disclosed in application Ser. No. 09/973,584 filed Oct. 9, 2001, assigned to the assignee of the present invention and incorporated herein by reference, is fixed to the femur after performing the extramedullary alignment procedure, and the distal femoral cut is made at the appropriate depth and angle of the implant, nominally 6° valgus and 10-12 mm depth of cut.
- an intramedullar alignment guide system could be used. This cut is taken all the way across both distal femoral condyles, rather than being unicondylar in nature. This cut is made at 90° to the femoral shaft.
- the tibial component is implanted first.
- the fixation surface is coated with cement, and the modular tibial stem is driven through the reverse Morse taper to lock the tibial stem to the bone.
- anterior flange component is then implanted, followed by the lateral then medial condyles. Once all pieces are loosely assembled inside the knee and proper alignment is assured, the locking pin is inserted from the side and rigidly fixes the components together. Final impaction is then accomplished.
- Routine closure is performed, and rapid rehab program initiated.
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Abstract
Description
- This application is based upon and claims priority under U.S. Provisional Application Serial No. 60/358,174 filed Feb. 20, 2002.
- In performing knee arthroplasty with conventional knee prostheses, it has been necessary to form large incisions in order to accommodate the preparation of the femur to receive the prosthesis and to accommodate the reception of a fairly large prosthesis into the incised femur for implantation on the prepared distal end of the femur. As is appreciated by those skilled in the art, it is desirable to minimize the size of any incision as the smaller the incision, the more rapidly the patient may recover. Prior art prostheses formed with a single piece metal component having both left and right condylar portions integral with the patellar flange area require large incisions in order to accommodate implantation in the prepared femur. In contrast, under the present invention, through the use of multiple pieces for the femoral component, it is possible to greatly reduce the size of any such incision, thereby reducing the amount of damage to soft tissue from any such arthroplasty and speeding the time of recovery. Similarly, it is desirable to minimize the size of any incision in the tibia during any implantation of the tibial component.
- The present invention is directed to a prosthesis for use in knee arthroplasty including total knee arthroplasty which is minimally invasive to the patient and to a method for performing surgery using such prosthesis including the femoral and tibial components thereof. Under the invention, the femoral component and, preferably, the tibial component are manufactured in at least two and possibly three or more pieces. However, it is possible that the tibial component could be a single piece, monoblock construction as well as modular multipiece construction. In both the single piece and multipiece construction, there is also provided a plastic articular surface insert piece. The pieces are designed to be assembled together following insertion into the knee. This allows total knee arthroplasty to be performed through very small incisions, as small as three inches, in each of the distal end of the femur and proximal end of the tibia. Following insertion, the pieces of the femoral component implanted at the distal end of the femur are joined together with a locking mechanism to form the modular femoral component and the pieces of the tibial component implanted at the proximal end of the tibia are assembled to form the modular tibial component.
- Femoral Component
- The femoral component may have three component pieces for a cruciate retaining design and two component pieces for a cruciate sacrificing design. It may be manufactured as two or three separate pieces or manufactured as a single unitary member which is subsequently cut or otherwise divided into two or three separate pieces. The pieces are provided with a locking joint for retaining the pieces together following insertion in distal end of the femur. The locking joint for the pieces is placed at the area of low patella/femoral contact, a low stress area of the femur. This corresponds to the anterior chamfer cut of a routine total knee arthroplasty and the area can be easily reinforced to accommodate the additional thickness of the locking joint. Various locking mechanisms may be employed for joining the pieces together including screws or a transverse locking pin which may be inserted from the medial side and/or lateral side. The locking mechanisms of whatever type lock the component pieces together into a solid assembled prosthesis. The prosthesis will be additionally reinforced by the underlying bone and/or cement fixation and will produce a durable construction. The patellar flange and the area of any joint between assembled components which may be contacted by the patella should be smoothed and, possibly, recessed to prevent premature wear of the patellar member as it tracks over the joint in the femoral component.
- Tibial Component
- The tibial component preferably has two pieces, namely, a tibial base and a tibial stem. It is also inserted in pieces from the side. It may also be a monoblock, one-piece tibial component with pegged or short stem fixation. The tibial base may have of a flat baseplate with anterior and posterior dovetails and may have a tapered transverse keel. The other piece of the tibial component is a modular stem which is inserted from the top after the baseplate is inserted. This design allows the components to be inserted through the minimal incision and still have long term stability. The stem is preferably fixed with a reverse Morse taper so that it can be driven through the baseplate like a spike.
- Patellar Component
- A standard conforming dome configuration patellar component is utilized, with the main difference being its method of insertion. It may be inserted without everting the patella. This is accomplished with the use of special instrumentation.
- FIG. 1 is a perspective view of one embodiment of femoral component showing the medial condyle as a separate piece from the remainder of the femoral component.
- FIG. 2 is a perspective view of a second embodiment of femoral component showing the lateral condyle as a separate piece from the remainder of the femoral component.
- FIG. 2A is a sectional view showing a patellar member engaged to the articulating surface of the patellar femoral flange piece.
- FIG. 3 is a perspective view of another embodiment of femoral component showing both the medial condyle and the lateral condyle as separate pieces from the patellar femoral flange piece of the femoral component.
- FIG. 4 is a perspective view showing the patellar femoral flange piece of FIG. 3 taken from a different angle.
- FIG. 5 is a perspective view of an embodiment of femoral component showing the patellar femoral flange piece as a separate piece from the remainder of the femoral component.
- FIG. 6 is a front view of the embodiment of the femoral component of FIG. 5.
- FIG. 7 is a side view of the embodiment of the femoral component of FIG. 5.
- FIG. 8 is a sectional view taken through line8-8 of FIG. 6.
- FIG. 9 is a sectional view taken through line9-9 of FIG. 6.
- FIGS. 10 and 11 are perspective views of other embodiments of the femoral component showing the patellar femoral flange piece as a separate piece from the remainder of the femoral component.
- FIG. 11A is a view similar to FIG. 9 for the embodiment of FIG. 11.
- FIG. 11B is a sectional view through
line 11B-11B of FIG. 11 A. - FIG. 12 is a perspective view of another embodiment of femoral component showing the patellar femoral flange piece as a separate piece from the remainder of the femoral component and showing one form of design for connecting the patellar femoral flange piece to the remainder of the femoral component.
- FIG. 13 is an enlarged view of the circled portion of FIG. 12.
- FIG. 14 is a perspective view of an embodiment of femoral component showing the lateral condyle as a separate piece from the remainder of the femoral component.
- FIG. 15 is an enlarged view of the circled portion of FIG. 14.
- FIG. 16 is a perspective view of another embodiment of femoral component showing the patellar femoral flange piece as a separate piece from the remainder of the femoral component.
- FIG. 17 is an enlarged view of the circled portion of FIG. 16.
- FIG. 18 is a perspective view of the tibial component showing the stem portion thereof as a separate piece from the base.
- FIG. 18A is a view similar to FIG. 18 with the added feature of a stem extension as part of the tibial component.
- FIG. 19 is a sectional view of another embodiment of tibial component showing the stem portion thereof as a separate piece from the base.
- FIG. 20 is a perspective view of another embodiment of tibial component showing the stem portion thereof as a separate piece from the base.
- FIG. 21 is a side view of the tibial component of FIG. 20 showing its implantation in the proximal end of a prepared tibia.
- Referring to FIG. 1, there is shown one embodiment of femoral component generally designated by the numeral10. The femoral component includes a
first piece 12 having apatellar flange portion 14 and an integral, unitarylateral condyle portion 16 extending therefrom. A prior art femoral component would also have an integral, unitary medial condyle on the opposite side from thelateral condyle portion 16. Under the present invention, there is provided, as a separate piece, amedial condyle piece 18 intended to be assembled to thefirst piece 12 following implantation of both thefirst piece 12 and themedial condyle piece 18 in the patient. The assembly mechanism or locking joint for securing themedial condyle piece 18 to thefirst piece 12 will be hereinafter described. - As shown in FIG. 1, the
medial condyle piece 18 is provided with arecess 15 for receiving bone cement and a pair of fixation pins 17. Thefirst piece 12 may also be provided with one or more recesses and fixation pins. If it is desired to have a prosthesis for implantation without bone cement, the recesses such as therecess 15 can be replaced by one of several types of porous surfaces well known in the art for bone in-growth. - Referring to FIG. 2, there is shown a second embodiment of a
femoral component 20 having afirst piece 22 with a patellarfemoral flange portion 24 and an integral, unitarymedial condyle portion 26. The second component of this embodiment is alateral condyle piece 28 which may be joined with thefirst piece 22 following implantation of both thefirst piece 22 and thelateral condyle piece 28 in the femur of the patient. - FIG. 2A shows a sectional view of patellar member P in contact with the articulating surface of the patellar
femoral flange portion 24. - FIG. 3 shows yet another embodiment of a three-piece
femoral component 30. Under this embodiment, there is provided a patellarfemoral flange piece 32, asecond piece 34 which is a medial condyle piece and athird piece 36 which is a lateral condyle piece assuming, of course, implantation in the right knee of a patient. If thefemoral component 30 were implanted in the left knee of a patient, thesecond piece 34 would be the lateral condyle piece and thethird piece 36 would be the medial condyle piece. Each of thesecond piece 34 and thethird piece 36 are joined to the patellarfemoral flange piece 32 following insertion in the patient's femur by use of a locking joint to be hereinafter described. - All three of the pieces of the femoral component may be provided with
fixation pins 37 and recesses 35 if intended for use with bone cement or a porous surface if intended for non-cemented implantation. - FIG. 4 is a perspective view of the patellar femoral flange piece of FIG. 3 taken from a different angle.
- The
femoral components femoral components numerals numerals - Referring to FIGS. 5, 6,7, 8 and 9, there is shown an embodiment of
femoral component 40 having two pieces, namely, a patellarfemoral flange piece 41 and acondylar piece 42. The patellarfemoral flange piece 41 has apatellar engaging surface 43 shaped to allow anatomical tracking of a natural or prosthetic patella P. As shown in FIG. 5, the patellarfemoral flange piece 41 has a superiorbone engaging surface 46 and apatellar engaging surface 43 defining a portion of an inferior articulating surface. The patellarfemoral flange piece 41 extends from aninferior end 45 to aleading end 48 which is contoured to engage thecondylar piece 42. Thecondylar piece 42 includes afirst condylar portion 50 and asecond condylar portion 52 and extends from anengagement end 54 contoured to receive theleading end 48 of thepatellar flange 41 to aposterior end 55. As will be appreciated by those skilled in the art, thefemoral component 40 could be used for implantation in either a right knee or left knee and the first and second condylar portions will be either lateral or medial facing depending upon the knee in which thefemoral component 40 is implanted. - The
condylar piece 42 has a superior bone engaging surface with a series ofbone engaging flats condylar piece 42. If desired, the superiorbone engaging surface 46 of thepatellar flange piece 41 and the superiorbone engaging surfaces condylar piece 42 may be formed with recesses for receiving bone cement or porous surfaces for bone ingrowth and may also be provided with fixation pins. - The
condylar piece 42 in the embodiment of FIGS. 5-9 is formed as a single unitary piece for implantation. As such, thefirst condylar portion 50 and thesecond condylar portion 52 are joined together with aposterior cam 56 which may be formed integral with or welded or otherwise joined to the first and secondcondylar portions engagement end 54 of thecondylar piece 42 also has the first and secondcondylar portions cross member 57. As will be appreciated by those skilled in the art, the use of theposterior cam 56 will result in sacrificing of the posterior cruciate ligament. As will be appreciated, in those cases where it may be necessary to sacrifice the posterior cruciate ligament for other reasons, the feature of having both aposterior cam 56 and across member 57 for joining the first and secondcondylar pieces condylar piece 42. - As can be seen in FIGS. 5, 7 and9, the
cross member 57 has a superiorbone engaging surface 57A and amedial surface 57B approximately midway between the superiorbone engaging surface 57A and the articulatingsurfaces first condylar portion 50 andsecond condylar portion 52, respectively. On the posterior side of thecross member 57 is aposterior wall surface 57C extending between the superiorbone engaging surface 57A and thesurface 57B. Opposite theposterior surface 57C is afourth surface 57D which will engage a corresponding surface to be described of the patellarfemoral flange piece 41. - The engagement ends54 for each of the first and second
condylar portions sidewall engagement surface 54A as shown in FIGS. 5 and 6. Each of the curvedengagement wall surfaces 54A extends to the general area defined by theposterior wall surface 57C ofcross member 57. (See FIG. 5). The positioning of the joint defined by thesurfaces 54A of thecondylar piece 42 and the mating surfaces of the patellarfemoral flange piece 41 is important and should be in the vicinity of the normal femoral tide mark which is a low stress area of contact by sliding engagement of the patella. By providing the joint in this area, the prosthesis has great ability to function as desired with no separation of the patellarfemoral flange piece 41 from thecondylar piece 42 following implantation. The normal femoral tide mark corresponds to the area of the inferior chamfer cut of a routine total knee arthroplasty. - The patellar femoral flange
piece leading end 48 has a pair of curved engagement surfaces 64 following a contour for mating engagement with therespective surfaces 54A of thecondylar piece 42. Centrally positioned between the curved engagement surfaces 64 is acentral wall surface 65 which, when the patellarfemoral flange piece 41 is engaged to thecondylar piece 42, lies in substantially the same plane as thesurface 57C ofcross member 57. (See FIG. 9). Thecentral wall surface 65 extends superiorly from thepatellar engaging surface 43 to aledge 66 intended to rest upon thesurface 57B ofcross member 57. Theledge 66 extends away from thecentral wall surface 65 to acentral engagement surface 67 which is intended to engage thesurface 57D ofcross member 57. Abone engaging surface 68 extends from thecentral engagement surface 67 toward theanterior end 45. - As shown in FIGS. 6, 7 and9, the
condylar piece 42 may be secured to the patellarfemoral flange piece 41 by means ofscrews 68 extending throughapertures 69 extending throughengagement end area 54 of the respective first and secondcondylar portions engagement end surfaces 54A and into aligned threadedapertures 71 extending inwardly from the curved engagement surfaces 64 of the patellarfemoral flange piece 41. - Referring to FIG. 8, there is shown the articulating surface defined by the
patellar engaging surface 43 of the patellarfemoral flange piece 41 and the articulating surface 59 of thecondylar piece 42 in the area of the joint defined by themating surface 54A of thecondylar piece 42 andsurface 64 of the patellarfemoral flange piece 41. As can be seen in FIG. 8, therespective surfaces 43 and 59 are recessed slightly at such joint to provide aslight dip 73 so that any movement of the patellar member P over such joint will leave a slight gap between the surface of the patellar member P and thesurfaces 43 and 59 at thedip 73. - The presence of the gap and the
dip 73 has a two-fold advantage. It reduces the amount of stress in that area of the joint defined by the mating surfaces 54A and 64 at thesurfaces 43 and 59. Additionally, if there is a slight mismating of the patellarfemoral flange piece 41 relative to thecondylar piece 42 such that one of thesurfaces 43 or 59 were slightly high or lower than intended for precise fixation, the presence of thedip 73 will serve to prevent the patellar member P from contacting and being subjected to premature wear by a sharp corner of the higher piece. - Referring to FIG. 10, there is shown a further embodiment similar to that of FIGS. 5 through 9 but one in which there is provided a
condylar piece 42A having thefirst condylar portion 50A is joined to thesecond condylar portion 52A only by aposterior cam 56A. Under this embodiment, the patellarfemoral flange piece 41A has acentral wall surface 65A centrally positioned between curved engagement surfaces 64A. Thecentral wall surface 65A extends throughout the thickness of the patellarfemoral flange piece 41A. Therefore, there is no ledge similar to theledge 66 shown in FIG. 5. All other features of the embodiment of FIG. 10 are similar to corresponding features of the embodiment of FIGS. 5, 6, 7, 8 and 9. - Referring to FIGS. 11, 11A and11B, there is shown a further embodiment of
femoral component 40B similar to that of FIGS. 5 through 9 but one in which there is provided acondylar piece 42B having thefirst condylar portion 50B joined to thesecond condylar portion 52B only by across member 57B and a modified connector means for fastening thecondylar piece 42B to the patellarfemoral flange piece 41B. - The
cross member 57B is provided with anextension 130 extending superiorly (i.e., downwardly as viewed in FIGS. 11 and 11A) from thecross member 57B. Both thecross member 57B and theextension 130 are provided with acommon dovetail slot 132. Theextension 130 is an integral unitary part of thecross member 57B and, in cross section, has a generally semicircular cross sectional configuration with the side facing the patellarfemoral flange piece 41B having a pair of flat faces on opposite sides of thedovetail slot 132. - The patellar
femoral flange piece 41B, has a configuration similar to that of the patellarfemoral flange piece 41 as shown in FIG. 5, including acentral wall surface 65B extending from apatellar engaging surface 43B, aledge 66B and acentral engagement surface 67B. Abone engaging surface 68B extends from thecentral engagement surface 67B toward theanterior end 45B. Extending superiorly from thebone engaging surface 68B is anextension 134 having adovetail 136 sized to be snugly received in thedovetail slot 132 of theextension 130 with conforming mating surfaces. Thedovetail 136 anddovetail slot 132 could have other crossectional configurations from that shown in FIGS. 11, 11A and 11B such as circular or rectangular. As will be appreciated and as can be seen from FIGS. 11A and 11B, thedovetail 136 is an integral unitary part of theextension 134; however, it extends outwardly from thesurface 67B and upwardly from thesurface 68B to join withsurface 66B. - The
respective extensions 130 of thecondylar piece femoral flange piece 41B, when joined together with thedovetail 136 positioned in thedovetail slot 132 will cooperate to define a substantially cylindrical configuration; however, if desired, a different configuration, such as square, rectangular or rounded, could be utilized. - Preparatory to implantation of the
condylar member 42B and patellarfemoral flange piece 41B, an aperture is drilled or otherwise formed in the femur of sufficient size to receive theextensions - Following positioning of the
condylar piece 42B in the prepared femur with itsextension 130 positioned in the prepared bone cavity, the patellarfemoral flange piece 41B is moved therein, thedovetail 136 is aligned with thedovetail slot 132 and the patellarfemoral flange piece 41B is moved toward the prepared femur with thedovetail 136 sliding through thedovetail slot 132 until thesurface 66B of the patellarfemoral flange piece 41B contacts the anterior surface ofcross member 57B. Desirably, bone cement will be positioned in the prepared aperture of the femur to engage the adjoinedextensions - Referring to FIGS. 12 and 13, there is shown an embodiment of a two-piece
femoral component 74 with afirst piece 75 of a patellar flange area having apatella engagement surface 76 and asecond piece 77 having amedial condyle portion 78 and alateral condyle portion 79 formed as an integral unitary piece. Thesecond piece 77 has a series offlats - The
first piece 75 has anabutment wall 81 extending from thepatella engagement surface 76 and positioned to engage acorresponding abutment wall 82 of thesecond piece 77. The line of juncture between theabutment wall 81 of thefirst piece 75 and theabutment wall 82 of thesecond piece 77 is in the area of low patella/femoral contact which is a low stress area of the femur. Theabutment wall 81 extends only partially through the thickness of thefirst piece 75. Theabutment wall 81 joins with asecond wall 83 disposed substantially at right angles thereto (See FIG. 13). Thesecond wall 83 extends to anend wall 84. Extending outwardly from theend wall 84 toward the plane defined by theabutment wall 81 is aledge 85 having anupper surface 86 with a tongue or dovetail 87 projecting upwardly therefrom. Thetongue 87 andupper surface 86 extend throughout the breadth of thefirst piece 75. Thetongue 87 is provided with a pair of reverse taper surfaces 88 which flare outwardly from one another in a direction away from theupper surface 86. - Extending outwardly from the
abutment wall 82 of thesecond piece 77 is aninsert ledge 90 having an upper surface for mating engagement with thesecond wall 83 of thefirst piece 75. The lower portion of theinsert ledge 90 opposite the upper surface has formed therein adovetail groove 92 extending the full breadth of thesecond piece 77 and sized to receive thetongue 87 of thefirst piece 75. As can be seen from FIG. 13, when thefirst piece 75 andsecond piece 77 are joined together, there will remain agap 93 between theend wall 84 of thefirst piece 75 and the end of theinsert ledge 90 of thesecond piece 77. In order to prevent the engagedfirst piece 75 andsecond piece 77 from moving laterally relative to one another, there is provided a taperedpin 94 which may be driven into thegap 93 to function as a wedge putting thetongue 87 into compression in thedovetail groove 92 formed in the lower surface of theinsert ledge 90. - Referring to FIGS. 14 and 15, there is provided another embodiment of
prosthesis 100 with afirst piece 101 having both apatellar flange area 102 and an integral, unitarylateral condyle portion 103. Theprosthesis 100 also has asecond piece 104 which is a medial condyle piece. Thefirst piece 101 has afirst abutment wall 105 extending generally laterally and asecond abutment wall 106 extending generally longitudinally with acurved wall section 107 joining thefirst abutment wall 105 and thesecond abutment wall 106. Protruding outwardly from thesecond abutment wall 106 is aprojection 110 having sidewalls 111 (only one of which is shown) tapering inwardly toward one another as they extend outwardly from thesecond abutment wall 106 and endwalls 112 tapering inwardly toward one another as they extend outwardly from thesecond abutment wall 106. The taperingsidewalls 111 and endwalls 112 are joined by anouter wall 113 substantially parallel with thesecond abutment wall 106. Theprojection 110 is integral and unitary with the remainder of thefirst piece 101 and may be formed by a milling process, for example. A threadedaperture 114 extends through theprojection 110 from theouter wall 113 and, preferably, extends into the adjacent portion of thefirst piece 101. - The
second piece 104 has afirst abutment wall 115 positioned to engage thefirst abutment wall 105 of thefirst piece 101, asecond abutment wall 116 positioned and sized to engage thesecond abutment wall 106 of thefirst piece 101 and a curved wall 117 for engagement with thecurved wall 107 of thefirst piece 101. Formed in thesecond wall 116 is arecess 118 contoured to snuggly receive theprojection 110 of thefirst piece 101. A laterally extendingpassageway 108 extends through thesecond piece 104 in alignment with the threadedaperture 114 of thefirst piece 101 when thesecond piece 104 is engaged thereto. - In order to join the
second piece 104 to thefirst piece 101 there is provided anelongated screw 120 having a threadedsection 121 for mating with the threads of the threadedaperture 114 of thefirst piece 101. Thescrew 120 has acylindrical section 122 of larger diameter than the threadedsection 121 and sized to be snugly received in thepassageway 108 of the second piece. Thescrew 120 has anenlarged head 123 sized to fit in a countersunk area of thepassageway 108 at the outer edge of thesecond piece 104. - Referring to FIGS. 16 and 17, there is shown a two-piece
femoral component 140 including afirst piece 141 having both alateral condyle 142 and amedial condyle 143 formed as part of an integral, unitary piece. Thesecond piece 144 defines a patellar flange area of thefemoral component 140. Thesecond piece 144 has a contouredabutment wall 145 including a firstflat surface 145A extending inwardly from the lateral side, a secondflat surface 145B extending inwardly from the medial side of thesecond piece 144 and a recess defined by first andsecond side walls 145C and abottom wall 145D. The sidewalls 145C taper inwardly toward one another as they extend from their respectiveflat surfaces bottom wall 145D is curved; however, it could be flat. - The
first piece 141 is provided with anabutment wall 146 having a contour to be snuggly engaged to theabutment wall 145 of thesecond piece 144. As such, theabutment wall 146 includes atongue 147 contoured to fit snuggly in the groove defined by sidewalls 145C andbottom wall 145D of thesecond piece 144. Thetongue 147 is defined by sidewalls 146C, 146C and anend wall 146D contoured to snuggly engaged thewall 145D forming the bottom of the groove of thesecond piece 144. Thewalls wall 146D and snuggly engage the taperedsidewalls 145C of thesecond piece 144. - The
second piece 144 has formed therein afirst passageway 148A which extends inwardly from the lateral edge and is substantially parallel to the firstflat surface 145A and asecond passageway 148B which extends inwardly from the medial edge and is substantially parallel to the secondflat surface 145B. Apassageway 149 is formed in thetongue 147 in a position to be aligned with thepassageways first piece 141 is engaged to thesecond piece 144, with thetongue 147 fitting in the groove. Apin 150 may be inserted through thepassageway 148B, thepassageway 149 and thepassageway 148A to secure thefirst piece 141 to thesecond piece 144. Thepin 150 could be cylindrical and press fit into therespective passageways passageway 148A, for example, could be threaded, in which case thepin 150 would have a threaded end for engagement therewith. - In each of the embodiments, the respective lines of juncture between abutting walls of the assembled pieces have been selected to be located generally in the area of the normal femoral tidemark which is a low stress area.
- Referring now to FIG. 18, there is shown a tibial component generally designated by the numeral161. The
tibial component 161 includes atibial base 162 and atibial stem 163. Thetibial base 162 has aninferior surface 164 intended to engage the prepared proximal end of the tibia of the patient and a superior surface (not shown) to which may be affixed a plastic insert contoured to be engaged by the condylar portions of a femoral component. The plastic insert may have one of a number of well known mechanisms for being attached to thetibial base 162 such as a dove tail locking mechanism, for example. The plastic insert may be inserted either laterally or proximally depending on the specific design of the tibial base and the condition of the patient as determined by the surgeon. Extending distally from theinferior surface 164 is abase extension 165 having a generally cylindrical shape but with a pair of fixation wings orfins 166 extending outwardly from the cylindrical portion of thebase extension 165. Aplatform 167 is raised from theinferior surface 164 and follows a contour encircling thebase extension 165 including thewings 166. Thewings 166 function as fixation fins for maintaining thetibial base 162 in a fixed rotational position when implanted on the prepared proximal end of the tibia. Thetibial base 162 is provided with anotch 168 to accommodate the posterior cruciate ligament and a plurality ofapertures 169 for receiving screws for engagement to an augmentation block, if one is needed, or for securing thetibial base 162 to the proximal end of a prepared tibia. - The
tibial base 162 has acentral passageway 170 extending from thesuperior surface 164 and through the cylindrical portion of thebase extension 165. That portion of thecentral passageway 170 in thebase extension 165 has wall surface which flares outwardly frusto conically and defines aMorse taper cavity 295 as it approaches the end of thebase extension 165. A recess defining anotch 240 is formed in the end of thebase extension 165. That portion of the passageway adjacent the superior surface has a diameter sized to receive ascrew 158 and acountersunk area 297 to receive the enlarged head ofsuch screw 158. - The tibial stem163 is provided with a pair of wings or
fixation fins 171 which, when thetibial stem 163 is engaged to theextension 165, will be aligned with and forming extensions of the respective wings orfins 166 of thetibial base 162. Thetibial stem 163 is provided with aMorse taper extension 298 sized to be snugly received in theMorse taper cavity 295 of thetibial base 162. Ashoulder 262 extends outwardly from theMorse taper extension 298. A raisedtab 242 extends proximally from theshoulder 202 and is sized to fit snugly in thenotch 210 and, when so positioned, assures alignment of thefixation fins 171 of thetibial stem 163 with thefins 166 of thetibial base 162. - A threaded
passageway 172 is formed in theMorse taper extension 298 and is aligned with thecentral passageway 170 when thetibial stem 163 is engaged to theextension 165. Thetibial stem 163 is supported on thetibial base 162 by thescrew 158 extending through thecentral passageway 170 of thetibial base 162 and engaged to the threadedpassageway 172. Aplug 244 is engaged in the distal end of thetibial stem 163 to prevent blood or other contaminates from entering the threadedpassageway 172. Theplug 244 may be secured to thetibial stem 163 by means of a threaded extension engaging the threadedpassageway 172. - FIG. 18A shows an embodiment similar to FIG. 18 but in which there is provided a
stem extension 250 but not a plug such as theplug 244 of FIG. 18. Thestem extension 250 is provided with aMorse taper 252 at itsproximal end 253. A threadedrecess 254 extends distally from the proximal end and has a size smaller than the threadedpassageway 172. A threadedscrew 258 sized to engage the threadedrecess 254 secures thestem extension 250 and thetibial stem 163 to thetibial base 162. The threadedscrew 258 is small enough to pass through the threadedpassageway 172 without engaging its threads. - The distal end of the
tibial stem 163 has acavity 260 tapering outwardly in a distal direction and defining a Morse taper sized to snuggly receive theMorse taper 252 of thestem extension 250. Twogrooves 270 are formed in thetibial stem 163, on opposite sides, distally spaced from theshoulder 262. The purpose of thegrooves 270 is to permit engagement and support for the tibial stem during implantation as will be discussed hereinafter. - Referring to FIG. 19, there is a shown in section a modified embodiment of
tibial component 200. Under this embodiment there is provided atibial base 202, atibial stem 204 and aplastic insert 206 for engagement with thetibial base 202. The tibial base, as shown in FIG. 19, has a raisedwall 208 and a flatsuperior surface 210. Thetibial base 202 has aninferior surface 212 intended to engage the prepared proximal end of the tibia of the patient. A centrally positionedshort extension 213 extends from theinferior surface 212. - Extending through the
tibial base 202 including theextension 213 is apassageway 214. That portion of thepassageway 214 adjacent theinferior surface 210 is enlarged from the remainder of the passageway and is provided with inwardly facingthreads 215 in the area adjacent theinferior surface 210. That portion of thepassageway 214 extending away from thethreads 215 is tapered to define aMorse taper cavity 216 throughout the remainder of the thickness of thetibial base 202 including thestem 213. - The tibial stem204 is provided with an enlarged threaded
flange 220 sized to engage thethreads 215 of thetibial base 202. Extending from theflange 220 is aMorse taper extension 222 sized and contoured to be snuggly received in theMorse taper cavity 216. Extending inwardly from theinferior surface 210 is a cavity defined by a series offlats 224 which cooperate to define a hexagon or other conveniently shaped cavity for receipt of a tool for engagement therein for threading the threadedflange 220 into thethreads 215. - Extending from the cavity defined by the
flats 224 is a threadedaperture 225. Extending distally from theMorse taper extension 222 is a reduced sizecylindrical extension 227. - The
plastic insert 206 has molded therein ametal insert 230 having anenlarged flange 232 to ensure its firm engagement to theinsert 206. Theinsert 206 is provided with apassageway 234 sized to receive ascrew 236 including itsenlarged head 238. Themetal insert 230 is provided with apassageway 240 sized to receive the threaded portion of thescrew 236 but smaller than theenlarged head 238. Following engagement of thetibial stem 204 to thetibial base 202, theplastic insert 206 is positioned on theinferior surface 210 within the upwardly extendingwall 208. Thescrew 236 is then engaged to the threadedaperture 225 to secure theplastic insert 206 thereto. - In the surgical procedure for implanting the
tibial component 200, the proximal end of the tibia is prepared by cutting a flat surface to receive theinferior surface 212 of thetibial base 202 and a cavity is drilled in the intramedullary canal of the tibia to receive. thestem 204. Thetibial base 202 is positioned on the prepared flat surface with theextension 213 positioned in the cavity. Thetibial stem 204 is then positioned in thepassageway 214 with thecylindrical extension 227 passing through theMorse taper cavity 216 and into the cavity of the intramedullary canal. Using a tool engaged to theflats 224, the stem is threadedly engaged to thethreads 215 and the base 202 to cause theMorse taper extension 222 to firmly engage theMorse taper cavity 216. As may be seen in FIG. 19, thetibial stem 204 is so contoured relative to thetibial base 202, that agap 229 will remain between the distal side of theflange 220 and the surface of thetibial base 202 extending radially outwardly from theMorse taper cavity 216. This ensures that theMorse taper extension 222 will firmly engage theMorse taper cavity 216 upon threaded engagement of the threadedflange 220 to thethreads 215. - Referring now to FIGS. 20 and 21, there is shown another embodiment of
tibial component 180 along with atool 195 for use in implanting such tibial component in the proximal end of a prepared tibia T. Thetibial component 180 includes atibial base 181, atibial stem 182 and aplastic insert 179 engaged to thetibial base 181. Thetibial base 181 has aninferior surface 183 intended to engage the prepared proximal end of the tibia T and asuperior surface 184 to which may be affixed aplastic insert 179 contoured to be engaged by a femoral component. Thetibial base 181 has raisedareas 185 along the anterior and posterior edges. Each of the raised areas is provided with an undercutwall surface 186 defining grooves for receiving and retaining theplastic insert 179. - Extending distally from the
inferior surface 183 is anextension 187. Thetibial base 181 has acentral passageway 188 extending from thesuperior surface 184 and through theextension 187. Theextension 187 and thepassageway 188 may be disposed at an angle of up to 100 relative to a line perpendicular to thesuperior surface 184 in order to accommodate the anatomy of the patient. - The tibial stem182 is provided with a
recess 190 sized and positioned to become an extension of thepassageway 188 of thetibial base 181. Therecess 190 may be threaded for engagement by a threadedscrew 196 extending through theplastic insert 179 and its articular surface and through thepassageway 188 to join thetibial stem 182 to thetibial base 181. As shown in FIG. 21, thedistal end 188A of thepassageway 188 may be tapered to define a Morse taper cavity. Thetibial stem 182 is also provided, at its proximal end, with aMorse taper extension 197 sized to snugly engage the Morse taper cavity at thedistal end 188A of thepassageway 188. Thetibial stem 182 is also provided with a plurality of outwardly facinggrooves 189 to assist in fixation. - In preparing the proximal end of the tibia T to receive the
tibial component 180, the proximal end T1 of the tibia is cut to form substantially a flat surface. A cavity T2 is formed to receive thetibial stem 182. Since the cavity T2 may be oversized, thetibial stem 182 is provided with anannular groove 198 sized to receive thetines 195A of thetool 195. As can be seen in FIG. 21, with thetines 195A engaged in thegroove 198, thetool 195 can support thetibial stem 182 at the proper location relative to the prepared proximal end T1 of the tibia T until such time as thescrew 196 is engaged in the threadedrecess 190 to support such tibial stem 182 on thetibial base 181. - In implanting the
tibial stem 163 of the embodiment of FIGS. 18 and 18A, a tool similar to thetool 195 may be used to engage thegrooves 270 to support thestem 163 until it is engaged by thescrew - In each of the embodiments of FIGS. 18, 18A,19, 20 and 21, it is preferred that the surface of the tibial base which is to be contacted by a plastic insert be polished to a high degree, on the order of four (4) rms or less, to prevent premature wear on the surface of the plastic insert engaged to the tibial base.
- Description of Surgical Procedure
- A medial parapatellar incision is made from the superior pole of the patella to the tibial tuberosity. Medial parapatellar arthrotomy is made from the inferior edge of the vastus medial is to the tibial tuberosity. A subvastus or mid vastus arthrotomy may be utilized, based upon patient anatomy or surgeon experience.
- The knee is place in extension and the patella excised without eversion, using a patellar clamp inserted into the prepatellar bursa, to prevent damage to the anterior skin.
- An extramedullary tibial alignment guide is placed along the medial or lateral half of the tibia and secured with fixation pins. An extrameduallary alignment guide of the type disclosed in application Ser. No. 09/973,584 filed Oct. 9, 2001, assigned to the assignee of the present invention and incorporated herein by reference, is fixed to the femur after performing the extramedullary alignment procedure, and the distal femoral cut is made at the appropriate depth and angle of the implant, nominally 6° valgus and 10-12 mm depth of cut. As an alternative, an intramedullar alignment guide system could be used. This cut is taken all the way across both distal femoral condyles, rather than being unicondylar in nature. This cut is made at 90° to the femoral shaft.
- The tibial component is implanted first. The fixation surface is coated with cement, and the modular tibial stem is driven through the reverse Morse taper to lock the tibial stem to the bone.
- The anterior flange component is then implanted, followed by the lateral then medial condyles. Once all pieces are loosely assembled inside the knee and proper alignment is assured, the locking pin is inserted from the side and rigidly fixes the components together. Final impaction is then accomplished.
- Lastly, the patella is cemented in place.
- After all cement has hardened and excess is removed, the final poly slides in from the side, and is secured with an AP locking clip or screw, which also helps lock the modular stem in place.
- Routine closure is performed, and rapid rehab program initiated.
- The above detailed description of the present invention is given for explanatory purposes. It will be apparent to those skilled in the art that numerous changes and modifications can be made without departing from the scope of the invention.
Claims (62)
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US11/209,931 US8092545B2 (en) | 2002-02-20 | 2005-08-22 | Knee arthroplasty prosthesis method |
US11/209,930 US8048163B2 (en) | 2002-02-20 | 2005-08-22 | Knee arthroplasty prosthesis |
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US11/209,933 Abandoned US20050283253A1 (en) | 2002-02-20 | 2005-08-22 | Knee arthroplasty prosthesis and method |
US13/311,816 Expired - Fee Related US9072605B2 (en) | 2002-02-20 | 2011-12-06 | Knee arthroplasty prosthesis |
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EP1476097A1 (en) | 2004-11-17 |
EP2359775B1 (en) | 2012-12-26 |
CA2475078C (en) | 2010-05-04 |
JP4193177B2 (en) | 2008-12-10 |
JP2005517491A (en) | 2005-06-16 |
AU2008255226B2 (en) | 2011-07-07 |
US9072605B2 (en) | 2015-07-07 |
ES2399084T3 (en) | 2013-03-25 |
AU2003217551B2 (en) | 2008-10-16 |
US20050283250A1 (en) | 2005-12-22 |
EP2359775A1 (en) | 2011-08-24 |
US20050283252A1 (en) | 2005-12-22 |
US8048163B2 (en) | 2011-11-01 |
US20050283251A1 (en) | 2005-12-22 |
EP1476097A4 (en) | 2010-12-08 |
CA2650862A1 (en) | 2003-08-28 |
US8092545B2 (en) | 2012-01-10 |
AU2008255226A1 (en) | 2009-01-08 |
US20120083893A1 (en) | 2012-04-05 |
WO2003070127A1 (en) | 2003-08-28 |
CA2475078A1 (en) | 2003-08-28 |
AU2003217551A1 (en) | 2003-09-09 |
CA2646389A1 (en) | 2003-08-28 |
US20050283253A1 (en) | 2005-12-22 |
US8092546B2 (en) | 2012-01-10 |
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