US20110213375A1 - Tibial Resurfacing System and Method - Google Patents
Tibial Resurfacing System and Method Download PDFInfo
- Publication number
- US20110213375A1 US20110213375A1 US13/042,382 US201113042382A US2011213375A1 US 20110213375 A1 US20110213375 A1 US 20110213375A1 US 201113042382 A US201113042382 A US 201113042382A US 2011213375 A1 US2011213375 A1 US 2011213375A1
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- Prior art keywords
- excision
- bone
- implant
- passageway
- articular surface
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/14—Surgical saws ; Accessories therefor
- A61B17/15—Guides therefor
- A61B17/154—Guides therefor for preparing bone for knee prosthesis
- A61B17/157—Cutting tibia
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- 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
- A61F2/38—Joints for elbows or knees
- A61F2/389—Tibial components
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/16—Bone cutting, breaking or removal means other than saws, e.g. Osteoclasts; Drills or chisels for bones; Trepans
- A61B17/1637—Hollow drills or saws producing a curved cut, e.g. cylindrical
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/16—Bone cutting, breaking or removal means other than saws, e.g. Osteoclasts; Drills or chisels for bones; Trepans
- A61B17/1662—Bone cutting, breaking or removal means other than saws, e.g. Osteoclasts; Drills or chisels for bones; Trepans for particular parts of the body
- A61B17/1675—Bone cutting, breaking or removal means other than saws, e.g. Osteoclasts; Drills or chisels for bones; Trepans for particular parts of the body for the knee
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/16—Bone cutting, breaking or removal means other than saws, e.g. Osteoclasts; Drills or chisels for bones; Trepans
- A61B17/17—Guides or aligning means for drills, mills, pins or wires
- A61B17/1739—Guides or aligning means for drills, mills, pins or wires specially adapted for particular parts of the body
- A61B17/1764—Guides or aligning means for drills, mills, pins or wires specially adapted for particular parts of the body for the knee
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
- A61B90/06—Measuring instruments not otherwise provided for
- A61B2090/062—Measuring instruments not otherwise provided for penetration depth
Definitions
- This disclosure relates to devices and methods for the repair of defects that occur in articular cartilage on the surface of bones, particularly the knee.
- hyaline cartilage found at the ends of articulating bone in the body, is typically composed of hyaline cartilage, which has many unique properties that allow it to function effectively as a smooth and lubricious load-bearing surface. When injured, however, hyaline cartilage cells are not typically replaced by new hyaline cartilage cells. Healing is dependent upon the occurrence of bleeding from the underlying bone and formation of scar or reparative cartilage called fibrocartilage. While similar, fibrocartilage does not possess the same unique aspects of native hyaline cartilage and tends to be far less durable.
- the implant should have a shape substantially corresponding to the articular cartilage proximate the area where the implant is to be placed in order to maximize the patient's comfort, minimize damage to surrounding areas, and maximize the functional life of the implant.
- FIG. 1 is a schematic diagram illustrating an incision proximate the knee
- FIG. 2 is a perspective view illustrating one embodiment of a drill guide coupled to the tibia consistent with the present disclosure
- FIG. 3 is a perspective view illustrating dowels advanced within the drill guide consistent with the present disclosure
- FIG. 4 is a perspective view illustrating pin advanced within the dowels in the drill guide consistent with the present disclosure
- FIG. 5 is a bottom plan view of one embodiment of a drill guide as generally shown in FIG. 4 consistent with the present disclosure
- FIG. 6 is a perspective view illustrating a drill bit advanced into the drill guide consistent with the present disclosure
- FIG. 7 is a perspective view of one embodiment of a drill bit consistent with the present disclosure.
- FIG. 8 illustrates one embodiment of a first and second excision site formed on the tibial articular surface and a second drill guide coupled thereto consistent with the present disclosure
- FIG. 9 is a perspective view of one embodiment of a third excision site formed on the tibial articular surface using the second drill guide consistent with the present disclosure.
- FIG. 10 is a perspective view of another embodiment of a first, second, and third excision site formed on the tibial articular surface using the first and/or second drill guides consistent with the present disclosure
- FIG. 11 is a perspective bottom view of one embodiment of an implant consistent with the present disclosure.
- FIG. 12 is a cross-sectional side view of another embodiment of an implant consistent with the present disclosure.
- FIG. 13 is a cross-sectional view of yet another embodiment of an implant consistent with the present disclosure.
- one embodiment of the present disclosure may feature a system and method for repairing a portion of the articular surface proximate to a defect. While the present disclosure will be described in terms of a system and method for repairing a portion of the tibial articular surface, it should be understood that the system and method may be used to repair other articular surfaces (such as, but not limited to, femoral articular surfaces and the like).
- the system and method may include securing a one or more guides/jigs defining one or more passageways to a portion of the tibia (e.g., immediately below the tibial articular surface) proximate to the defect.
- the passageways may define a generally cylindrical core pathway for a drill bit (i.e., a coring drill bit).
- a drill bit i.e., a coring drill bit
- the generally cylindrical core pathway may partially intersect/overlap with the articular surface and a portion of the bone beneath the articular surface.
- a first truncated cylindrical excision site may be formed in the articular surface and/or bone beneath the articular surface by advancing the drill along the core pathway.
- the drill may have a diameter large enough to remove a portion of the articular surface as it is advanced through the guide and into the articular surface. Additional truncated cylindrical excision sites may also be formed. One or more of the additional truncated cylindrical excision sites may partially overlap with adjacent truncated cylindrical excision sites.
- the guide and/or the drill may include a depth feature configured to control the depth of the truncated cylindrical excision site formed in the articular surface/bone.
- the depth feature may prevent the drill from being advanced too far, thereby preventing the drill from accidentally damaging any structures proximate to the excision sites (e.g., nerves).
- the system and method may also include an implant having a load bearing surface having a surface contour/geometry based on the surface contour/geometry of the patient's original removed articular surface.
- the surface contour/geometry of the load bearing surface may be based on one or more measurements taken of the patient's original articular surface.
- the implant may also feature a bone facing or distal surface having a surface contour/geometry configured to be received in the truncated cylindrical excision sites.
- the tibial articular surface 12 may include a tibial plateau comprising a plurality of concaved surfaces 14 a, 14 b configured to articulate with the femoral condyles (not shown for clarity). It may be further appreciated that the tibial articular surface 12 may include additional concaved surfaces not shown for the sake of clarity. One or more of the concaved surfaces (e.g., concaved surface 14 a ) may include a defect 13 in the tibial articular surface 12 to be repaired. On the distal side of the tibia 10 , a nerve bundle 16 is located. As described herein, the system and method according to one embodiment of the present disclosure may be configured to avoid damaging the nerve bundle when forming the excision site(s).
- the following will describe a system and method for preparing an implant site comprising three partially overlapping truncated cylindrical excision sites and an implant configured to fit therein.
- the system and method according to the present disclosure may be used to form an implant site having greater than or fewer than three partially overlapping truncated cylindrical excision sites.
- the truncated cylindrical excision sites may be formed by drilling along the anterior-posterior plane (i.e., from an anterior face of the tibia 10 and extending generally towards the posterior face of the tibia 10 ).
- the first guide 20 may include a jig 22 and a spoon 24 .
- the jig 22 may include a body portion 26 defining two excision passageways 28 a, 28 b.
- the excision passageways 28 a, 28 b may each define a generally cylindrical core pathway for a drill bit which may be used to form a first and a second truncated cylindrical excision site on the tibial articular surface 12 .
- first and the second excision passageways 28 a, 28 b may be offset relative to each other (i.e., the first and the second excision passageways 28 a, 28 b may be separated by a distance generally perpendicular to the longitudinal axes of the first and the second excision passageways 28 a, 28 b such that the first and the second truncated cylindrical excision sites formed in the articular surface 12 do not overlap as described herein).
- the position of the jig 22 (and in particular, the excision passageways 28 a, 28 b ) may be set based on, at least in part, the spoon 24 .
- the spoon 24 may include a generally convex base portion 30 having a surface contour substantially corresponding to the curvature of the concaved surface 14 a being repaired (e.g., the concaved surface 14 a which has the defect 13 ).
- the upper portion 32 of the spoon 24 may have a generally concaved surface (e.g., generally corresponding to the curvature of the concaved surface 14 a being repaired).
- the spoon 24 may have a cross-sectional thickness configured to facilitate advancement of the spoon 24 between the tibial articular surface 12 and the femoral condyles (not shown).
- the cross-sectional thickness of the spoon 24 may be selected to provide sufficient rigidity to align the jig 22 relative to the tibial articular surface 12 (and in particular, the defect 13 on the concaved surface 14 a ) while also minimizing the required separation between the tibia 10 and the femur.
- the spoon 24 may be an integral component of the jig 22 (e.g., a unitary or single one-piece structure) or may be configured to be releasably coupled to the jig 22 .
- the spoon 24 may include an arm portion 36 configured to extend generally outwardly from a distal face 38 (e.g., a bone facing surface) of the jig 22 .
- the size and shape of the arm portion 36 may be configured to allow a portion of the distal face 38 to be disposed proximate to the perimeter (e.g., proximate to the meniscus 40 ) when the spoon 24 is disposed on the concaved surface 14 a such that the generally cylindrical core pathways associated with the first and second excision passageways 28 a, 28 b partially overlap with the tibial articular surface 12 .
- the first guide 20 may be positioned relative to the defect 13 on the concaved surface 14 a by advancing the spoon 24 between the tibial articular surface 12 and the femur such that the base portion 30 of the spoon 24 is disposed over at least a portion of the defect 13 on the tibial articular surface 12 .
- the spoon 24 may be advanced until the distal face 38 of the jig 22 generally abuts against a portion of the tibia 10 (e.g., proximate to the meniscus 40 ).
- the size and shape of the base portion 30 as well as the arm portion 36 /distal face 38 may be configured to generally center the spoon 24 within the concaved surface 14 a.
- the spoon 24 and the jig 22 may be secured to the tibia 10 using one or more pins 32 or the like extending through one or more locking passageways 34 in the spoon 24 and/or the jig 22 .
- the spoon 24 may include a spoon locking passageway 34 a extending through a portion of the spoon 24 (e.g., the arm portion 36 ) configured to align a pin 32 a into the tibial bone beneath the tibial articular surface 12 .
- the jig 22 may include a jig locking passageway 34 b extending through a portion of the body 26 configured to align a pin 32 b into the tibial bone beneath the tibial articular surface 12 . While two pins 32 a, 32 b are shown, it should be appreciated that the first guide 20 may be secured using greater than or fewer than two pins 32 a, 32 b.
- the pins 32 a, 32 b may include depth feature 33 a, 33 b configured to control the depth of the pins 32 a, 32 b in the bone 10 (i.e., to prevent the pins 32 a, 32 b from being set too deep or too shallow into the bone 10 ).
- the depth feature 33 a, 33 b may comprise an indicia (e.g., but not limited to, a laser marking, groove, or the like) which may be aligned with the proximal end of the passageways 34 a, 34 b.
- Pin 32 a may extend a smaller distance into the tibia 10 compared to pin 32 b.
- the first guide 20 may optionally be secured to the tibia 10 by advancing one or more dowels or bushings 40 a, 40 b against the bone 10 .
- a first and a second dowel 40 a, 40 b may be advanced through the first and second excision passageways 28 a, 28 b, respectively.
- One or more of the dowels 40 a, 40 b may feature a tapered tip 42 a, 42 b and a longitudinally disposed passageway 44 a, 44 b (a proximal end of the dowels 40 a, 40 b is shown in cross-section to better illustrate the passageway 44 a, 44 b ).
- the dowels 40 a, 40 b may be advanced through the passageways 28 a, 28 b until the tapered tip 42 a, 42 b engages against (e.g., abuts) a portion of the tibia 10 (e.g., proximate to the meniscus 40 ). Once the dowels 40 a, 40 b abut the tibia 10 , the dowels 40 a, 40 b may be locked into position relative to the jig 22 using locking fasteners 46 a, 46 b.
- the locking fasteners 46 a, 46 b may include, but are not limited to, a set screw, biased tab, ratchet mechanism, or the like.
- Alignment pins 48 a, 48 b may be advanced through the passageways 44 a, 44 b in the dowels 40 a, 40 b and into the tibia 10 as generally illustrated in FIG. 4 . Similar to the pins 34 a, 34 b, the alignment pins 48 a, 48 b may include a depth feature 50 a, 50 b configured to control the depth of the alignment pins 48 a, 48 b into the bone 10 (i.e., to prevent the alignment pins 48 a, 48 b from being set too deep or too shallow within the bone 10 ).
- the depth feature 50 a, 50 b may comprise an indicia (e.g., but not limited to, a laser marking, groove, or the like) which may be aligned with the proximal end of the passageway 44 a, 44 b in the dowels 40 a, 40 b.
- an indicia e.g., but not limited to, a laser marking, groove, or the like
- FIG. 5 is a bottom plan view of the first guide 20 generally illustrating one embodiment of the position of the alignment pins 48 a, 48 b as well as pin 32 b relative to the spoon 24 .
- depth features 50 a, 50 b, 33 b are generally aligned with the respective passageways 44 a, 44 b, 34 b such that the distal ends of the pins 48 a, 48 b, 32 b are generally aligned with the distal perimeter of the spoon 24 .
- the distal ends of the pins 48 a, 48 b, 32 b do not extend beyond the tibial bone 10 .
- the position of the distal ends of the pins 48 a, 48 b, 32 b may be disposed shallower (i.e., closer towards the first guide 20 ).
- a first and a second truncated cylindrical excision site may be formed in the tibial articular surface 12 and/or bone 10 .
- the first and second truncated cylindrical excision sites may correspond to a projection of the cylindrical core pathways defined by the excision passageways 28 a, 28 b intersecting with the tibial articular surface 12 and/or bone 10 .
- a dowel 40 a may be removed from the excision passageway 28 a, leaving the pin 48 a remaining as generally illustrated in FIG. 6 .
- a cannulated drill 60 may then be advanced over the pin 48 a and through the excision passageway 28 a to form a first truncated cylindrical excision site. While dowel 40 a is shown removed, the order in which the dowels 40 a , 40 b are removed may be altered.
- the cannulated drill 60 may feature a core drill bit 62 and optionally a shank portion 64 .
- the shank portion 64 may include a multi-faceted proximal end configured to be secured to a drill (e.g., a hand drill, electric drill, pneumatic drill or the like).
- a proximal end of the core drill bit 62 may be directly coupled to the drill.
- the core drill bit 62 may include a cutting surface 66 (for example, comprising a plurality of cutting teeth 67 ) disposed about a distal end of the barrel 63 .
- the cutting surface 66 may be evenly disposed around the generally circular distal end of the barrel 63 .
- the barrel 63 may include an outer diameter substantially corresponding to the inner diameter of the excision passageway 28 a.
- the core drill 62 may have an outer diameter selected from the range of 8-12 mm, for example, 10-11 mm.
- the barrel 63 may define a core cavity 68 configured to receive the removed portion of the tibial articular surface 12 and bone 10 .
- the only portion of the tibial articular surface 12 and bone 10 that is cut by the core drill bit 60 corresponds to the thickness of the cutting surface 66 , which itself is a function of the wall thickness of the barrel 63 . As such, these thicknesses may be selected to remove the least amount of material while also providing the necessary rigidity and/or strength to the core drill bit 60 .
- the core drill bit 62 may optionally feature one or more windows 70 disposed along the length of the barrel 63 .
- the window 70 may allow air, fluid, and cutting chips to exit the barrel 63 .
- the window 70 may also allow the user to align the core drill bit 62 with the first guide 20 and/or pins to control the depth of the excision site (i.e., the length of the excision site as measured across the tibial articular surface 12 ).
- a proximal end of the window 70 may be generally aligned with the opening on the excision passageway 28 a to control the depth of the resulting excision site.
- the core drill bit 62 may also optionally include a centering bearing 72 configured facilitate alignment of the core drill bit 62 as the core drill bit 62 is advanced into the tibial articular surface 12 and bone 10 .
- the centering bearing 72 may be translatably disposed along the longitudinal axis of the core drill bit 62 and may include a passageway 74 configured to receive the pin 48 a.
- the centering bearing 72 may be initially located near the distal end of the barrel 62 .
- the pin 48 a may be received in the passageway 74 and the centering bearing 72 may translate towards the proximal end as the core is received in the passageway 74 .
- the drill bit 60 As the drill bit 60 is advanced through the excision passageway 28 a in the first guide 20 , a portion of the cutting surface 66 may engage the tibial articular surface 12 and/or the bone 10 , thereby forming a truncated cylindrical excision site.
- the second truncated cylindrical excision site may be formed.
- the second dowel 40 b may be removed and a second drill bit 60 may be advanced through the second excision passageway 28 b in a manner similar to that described herein.
- the first and second drill bits 60 may have the same or different outer diameters.
- first and the second excision passageways 28 a, 28 b may be offset relative to each other. Put another way, the first and the second excision passageways 28 a, 28 b may be separated by a distance generally perpendicular to the longitudinal axes of the first and the second excision passageways 28 a, 28 b such that the first and the second truncated cylindrical excision sites do not overlap.
- FIG. 8 generally illustrates one embodiment of the first and the second truncated cylindrical excision sites 80 a, 80 b corresponding to the drill bit 60 and the first and the second excision passageways 28 a, 28 b.
- a center section 81 of articular surface 12 /bone 10 remains separating the first and the second truncated cylindrical excision sites 80 a, 80 b.
- This center section 81 may optionally be removed using second guide/jig 82 .
- the second guide 82 may comprise one or more alignment passageways 83 a, 83 b as well as a third excision passageway 28 c extending through the body portion 85 .
- the third excision passageway 28 c may also define a generally cylindrical core pathway for a drill bit.
- the second guide 82 may feature protrusions 84 a, 84 b configured to be at least partially received in the first and the second truncated cylindrical excision sites 80 a, 80 b to further align and secure the position of the second guide 82 and the third excision passageway 28 c relative to the articular surface 12 /center section 81 .
- the second guide 82 may therefore be advanced along the pins 48 a, 48 b and the protrusions 84 aa , 84 b may be received into the first and the second truncated cylindrical excision sites 80 a, 80 b until at least a portion of the distal face 86 of the second guide 82 generally abuts against the bone 12 and a projection of the third core pathway associated with the third excision passageway 28 c partially intersects with the center section 81 .
- a third drill 60 may be advanced through the third excision passageway 28 c extending through the body 85 to remove the center section 81 and form the third truncated cylindrical excision site 80 c as generally illustrate in FIG. 9 .
- the third excision passageway 28 c may be configured to align the third drill 60 such that the resulting third truncated cylindrical excision site 80 c partially overlaps with the first and the second truncated cylindrical excision sites 80 a, 80 b.
- the third excision passageway 28 c may have a diameter which would partially overlap with the first and the second excision passageways 28 a, 28 b if the three excision passageways 28 a - 28 c were transposed on each other and aligned with the pins 48 a, 48 b.
- the resulting implant site may therefore comprise the first, second, and third truncated cylindrical excision sites 80 a - 80 c wherein the first and the second truncated cylindrical excision sites 80 a, 80 b partially overlap with the third truncated cylindrical excision site 80 c.
- the truncated cylindrical excision sites 80 a - 80 c may be centered/revolved around the pins 48 a, 48 b, 32 b and may extend along the articular surface 12 generally along the anterior-posterior plane.
- the truncated cylindrical excision sites 80 a - 80 c may extend from the anterior face of the tibial articular surface 12 generally towards the posterior face.
- the implant site may therefore include a base portion 90 comprising three overlapping truncated cylindrical extensions or scallops defined by the three excision passageways 28 a - 28 c.
- the resulting implant site therefore may generally eliminate/reduce the occurrence of 90 degree cuts and therefore more evenly distribute loads/forces to the bone 10 compared a traditional 90 degree notch cut.
- the truncated cylindrical excision sites 80 - 80 c have been illustrated extending partially across the tibial articular surface 12 (i.e., one or more of the truncated cylindrical excision sites 80 - 80 c do not extend completely across the articular surface 12 thus leaving a portion 99 of the tibial articular surface 12 and/or bone 10 remaining).
- This embodiment may be particularly beneficial since it further minimizes the potential for accidentally damaging the nerve bundle.
- the system and method according to the present disclosure may also allow for one or more of the truncated cylindrical excision sites 80 a - 80 c to extend completely across the articular surface 12 as generally illustrate in FIG. 10 .
- the system and method according to the present disclosure may be able to accurately enough form the truncated cylindrical excision sites 80 a - 80 c to minimize the potential of damaging the nerve bundle to an acceptable level.
- the system and method may utilize a single guide.
- the first guide 20 may include alignment dowels (not shown) configured to be advanced and/or secured within the first and second excision passageways 28 a, 28 b.
- the alignment dowels may include protrusions 84 a, 84 b configured to engage the first and second truncated excision sites 80 a, 80 b as generally described herein.
- the guide 20 may include a third excision passageway 28 c extending generally along the locking passageway 34 b (which itself may be formed in a removable bushing).
- the alignment dowels may have an outer shape such that the third excision passageway 28 c defines a generally cylindrical core pathway for the drill 60 .
- the implant 100 may comprise a load bearing surface 102 and a bone facing or distal surface 104 .
- the load bearing surface 102 may have a surface contour/geometry substantially corresponding to the contour/geometry of the removed tibial articular surface 12 proximate the defect 13 .
- the contour/geometry of the load bearing surface may be based on a plurality of measurement take of the patient's tibial articular surface 12 , for example, as described in U.S. patent application Ser. No. 10/373,463, filed on Feb. 24, 2003, entitled System and Method for Joint Resurface Repair, which is fully incorporated herein by reference.
- the bone facing surface 104 may have an overall contour/geometry generally corresponding to the contour/geometry of the base portion 90 of the three truncated cylindrical excision sites 80 a - 80 c and the removed bone 10 .
- the bone facing surface 104 may include one or more relief cavities, pockets and/or cross-cuts 106 configured to enhance securing the implant 100 to the bone 10 within the truncated cylindrical excision sites 80 a - 80 c.
- the relief cavities 106 may be configured to allow bone regrowth around a portion of the implant 100 and/or promote cement adhesion.
- the implant 100 may comprise a generally unitary structure (i.e., the implant 100 may be a solid, one-piece component).
- the implant 100 may be made from ultra-high molecular weight polyethylene (UHMWPE).
- Implant 100 b may comprise multiple portions configured to be coupled together, for example, an upper and a lower portion 110 , 112 .
- the upper portion 110 may include a load bearing surface 102 as described herein while the lower portion 112 may comprise a bone facing surface 104 as described herein.
- the upper and lower portions 110 , 112 may be configured to be coupled together.
- the lower portion 112 may be based on the guides 20 , 82 used to form the truncated cylindrical excision sites 80 a - 80 c while the upper portion 110 may be based on the contour/geometry of the patient's removed articular surface 12 .
- the lower portion 112 may be considered “generic” or common in that it is based on the guides 20 , 82 rather than measurements of the patient's articular surface 12 while the upper portion 110 may be selected based specifically on measurements of the patient's articular surface 12 .
- FIG. 13 a cross-sectional view of another implant 100 c is shown generally implanted within the implant site 120 formed by truncated cylindrical excision sites 80 a - 80 c.
- the bone facing surface 104 of the implant 100 c may be generally disposed along the base portion 90 of the truncated cylindrical excision sites 80 a - 80 c while the load bearing surface 102 may be substantially continuous with the surrounding tibial articular surface 12 (i.e., the tibial articular surface 12 adjacent to and abutting the implant 100 c ).
- the implant 100 c may optionally comprise one or more keels, tails, protrusions or the like 122 .
- the keel 122 may extend generally downwardly from the bone facing surface 104 and away from the load bearing surface 102 .
- the keel 122 may be configured to engage a corresponding notch 124 formed in the base portion 90 of the truncated cylindrical excision sites 80 a - 80 c. While the implant 100 c is illustrated having an upper and a lower portion 110 , 112 , the implant 100 as illustrated in FIG. 11 may optionally include one or more keels 122 .
- the keel 122 may be an integral component of the implant 100 or the lower portion 112 or alternatively may be a separate component coupled thereto.
- an implant consistent with at least one embodiment of the present disclosure may have a load bearing surface 102 which is non-planar. While traditional tibial implants have had a generally planar or flat load bearing surface, an implant consistent with at least one embodiment of the present disclosure may have a concaved geometry which may better approximate the geometry of the patient's removed tibial articular surface 12 .
- the implant as shown in FIG. 13 may have a first side (e.g., but not limited to, a medial side) having a height L less than a height H of a second side (e.g., but not limited to, the lateral side).
- FIG. 14 a top view of one embodiments of the implant 100 consistent with the present disclosure is generally illustrated.
- the implant 100 When viewed from the top side (i.e., when viewing the load bearing surface 102 ), the implant 100 may have a generally “D” shape. This “D” shape may correspond to an implant site which extends all the way cross the anterior-posterior plane of the articular surface (e.g., as generally shown in FIG. 10 ).
- the implant 100 may also have a modified or notched “D” shape.
- the implant 100 may include a notched region 130 which may correspond to the area 99 of the tibial articular surface 12 proximate to the posterior face of the tibia 10 which is not removed (e.g., as generally shown in FIG. 9 ). As discussed herein, leaving this portion 99 of the tibial articular surface 12 and/or bone 10 intact may minimize the potential of damaging the nerve bundle 16 ( FIG. 1 ).
- the present disclosure features an implant resection system for preparing an implant site to replace a defect in an articular surface of a first bone.
- the implant resection system includes a guide configured to be coupled generally perpendicular to the first bone proximate to the defect.
- the guide includes a body portion defining a plurality of excision passageways.
- the excision passageways each define a generally cylindrical core pathway configured to extend generally perpendicular to the first bone which partially overlaps with an adjacent generally cylindrical core pathway.
- a projection associated with each of the plurality of the generally cylindrical core pathways defines a truncated cylindrical excision site extending through a portion of the articular surface. Each truncated cylindrical excision site partially overlaps with at least one adjacent truncated cylindrical excision site.
- the present disclosure features a method for preparing an implant site to replace a defect in an articular surface.
- the method includes securing a guide to bone proximate the defect.
- the guide includes a body portion defining a plurality of excision passageways.
- Each excision passageway defines a generally cylindrical core pathway which partially overlaps with an adjacent generally cylindrical core pathway.
- the method further includes advancing at least one drill through the plurality of excision passageways along the generally cylindrical core pathways to form a plurality of partially overlapping truncated cylindrical excision sites extending through the articular surface.
Abstract
An implant resection system for preparing an implant site to replace a defect in an articular surface of a first bone includes a guide configured to be coupled generally perpendicular to the first bone proximate to the defect. The guide includes a body portion defining a plurality of excision passageways. The excision passageways each define a generally cylindrical core pathway configured to extend generally perpendicular to the first bone which partially overlaps with an adjacent generally cylindrical core pathway. A projection associated with each of the plurality of the generally cylindrical core pathways defines a truncated cylindrical excision site extending through a portion of the articular surface. Each truncated cylindrical excision site partially overlaps with at least one adjacent truncated cylindrical excision site.
Description
- This application claims the benefit of U.S. Provisional Patent Application No. 61/310,774, filed Mar. 5, 2010, which is fully incorporated herein by reference. This application is also a continuation-in-part of U.S. patent application Ser. No. 11/779,044, filed Jul. 17, 2007, entitled SYSTEM AND METHOD FOR TISSUE RESECTION, which claims the benefit of U.S. Provisional Patent Application Serial No. 60/807,538, filed Jul. 17, 2006, the entire disclosures of all of which are incorporated fully herein by reference.
- This disclosure relates to devices and methods for the repair of defects that occur in articular cartilage on the surface of bones, particularly the knee.
- Articular cartilage, found at the ends of articulating bone in the body, is typically composed of hyaline cartilage, which has many unique properties that allow it to function effectively as a smooth and lubricious load-bearing surface. When injured, however, hyaline cartilage cells are not typically replaced by new hyaline cartilage cells. Healing is dependent upon the occurrence of bleeding from the underlying bone and formation of scar or reparative cartilage called fibrocartilage. While similar, fibrocartilage does not possess the same unique aspects of native hyaline cartilage and tends to be far less durable.
- In some cases, it may be necessary or desirable to repair the damaged articular cartilage using an implant. While implants may be successfully used, the implant should have a shape substantially corresponding to the articular cartilage proximate the area where the implant is to be placed in order to maximize the patient's comfort, minimize damage to surrounding areas, and maximize the functional life of the implant.
- Features and advantages of the present invention are set forth by description of embodiments consistent with the present invention, which description should be considered in conjunction with the accompanying drawings wherein:
-
FIG. 1 is a schematic diagram illustrating an incision proximate the knee; -
FIG. 2 is a perspective view illustrating one embodiment of a drill guide coupled to the tibia consistent with the present disclosure; -
FIG. 3 is a perspective view illustrating dowels advanced within the drill guide consistent with the present disclosure; -
FIG. 4 is a perspective view illustrating pin advanced within the dowels in the drill guide consistent with the present disclosure; -
FIG. 5 is a bottom plan view of one embodiment of a drill guide as generally shown inFIG. 4 consistent with the present disclosure; -
FIG. 6 is a perspective view illustrating a drill bit advanced into the drill guide consistent with the present disclosure; -
FIG. 7 is a perspective view of one embodiment of a drill bit consistent with the present disclosure; -
FIG. 8 illustrates one embodiment of a first and second excision site formed on the tibial articular surface and a second drill guide coupled thereto consistent with the present disclosure; -
FIG. 9 is a perspective view of one embodiment of a third excision site formed on the tibial articular surface using the second drill guide consistent with the present disclosure; -
FIG. 10 is a perspective view of another embodiment of a first, second, and third excision site formed on the tibial articular surface using the first and/or second drill guides consistent with the present disclosure; -
FIG. 11 is a perspective bottom view of one embodiment of an implant consistent with the present disclosure; -
FIG. 12 is a cross-sectional side view of another embodiment of an implant consistent with the present disclosure; and -
FIG. 13 is a cross-sectional view of yet another embodiment of an implant consistent with the present disclosure. - By way of summary, one embodiment of the present disclosure may feature a system and method for repairing a portion of the articular surface proximate to a defect. While the present disclosure will be described in terms of a system and method for repairing a portion of the tibial articular surface, it should be understood that the system and method may be used to repair other articular surfaces (such as, but not limited to, femoral articular surfaces and the like). The system and method may include securing a one or more guides/jigs defining one or more passageways to a portion of the tibia (e.g., immediately below the tibial articular surface) proximate to the defect. The passageways may define a generally cylindrical core pathway for a drill bit (i.e., a coring drill bit). When the guide is secured to the femur, the generally cylindrical core pathway may partially intersect/overlap with the articular surface and a portion of the bone beneath the articular surface. A first truncated cylindrical excision site may be formed in the articular surface and/or bone beneath the articular surface by advancing the drill along the core pathway. The drill may have a diameter large enough to remove a portion of the articular surface as it is advanced through the guide and into the articular surface. Additional truncated cylindrical excision sites may also be formed. One or more of the additional truncated cylindrical excision sites may partially overlap with adjacent truncated cylindrical excision sites.
- The guide and/or the drill may include a depth feature configured to control the depth of the truncated cylindrical excision site formed in the articular surface/bone. The depth feature may prevent the drill from being advanced too far, thereby preventing the drill from accidentally damaging any structures proximate to the excision sites (e.g., nerves). The system and method may also include an implant having a load bearing surface having a surface contour/geometry based on the surface contour/geometry of the patient's original removed articular surface. For example, the surface contour/geometry of the load bearing surface may be based on one or more measurements taken of the patient's original articular surface. The implant may also feature a bone facing or distal surface having a surface contour/geometry configured to be received in the truncated cylindrical excision sites.
- Turning now to
FIG. 1 , atibia 10 is generally illustrated. As may be appreciated, the tibialarticular surface 12 may include a tibial plateau comprising a plurality ofconcaved surfaces articular surface 12 may include additional concaved surfaces not shown for the sake of clarity. One or more of the concaved surfaces (e.g., concavedsurface 14 a) may include adefect 13 in the tibialarticular surface 12 to be repaired. On the distal side of thetibia 10, anerve bundle 16 is located. As described herein, the system and method according to one embodiment of the present disclosure may be configured to avoid damaging the nerve bundle when forming the excision site(s). - For illustrative purposes, the following will describe a system and method for preparing an implant site comprising three partially overlapping truncated cylindrical excision sites and an implant configured to fit therein. As may be appreciated, the system and method according to the present disclosure may be used to form an implant site having greater than or fewer than three partially overlapping truncated cylindrical excision sites. As will be evident from the following description, the truncated cylindrical excision sites may be formed by drilling along the anterior-posterior plane (i.e., from an anterior face of the
tibia 10 and extending generally towards the posterior face of the tibia 10). - Turning now to
FIG. 2 , one embodiment of afirst guide 20 secured to thetibia 10 is generally illustrated consistent with the present disclosure. Thefirst guide 20 may include ajig 22 and aspoon 24. Thejig 22 may include abody portion 26 defining twoexcision passageways excision passageways articular surface 12. As shown, the first and thesecond excision passageways second excision passageways second excision passageways articular surface 12 do not overlap as described herein). - The position of the jig 22 (and in particular, the
excision passageways spoon 24. In particular, thespoon 24 may include a generallyconvex base portion 30 having a surface contour substantially corresponding to the curvature of theconcaved surface 14 a being repaired (e.g., theconcaved surface 14 a which has the defect 13). Theupper portion 32 of thespoon 24 may have a generally concaved surface (e.g., generally corresponding to the curvature of theconcaved surface 14 a being repaired). Thespoon 24 may have a cross-sectional thickness configured to facilitate advancement of thespoon 24 between the tibialarticular surface 12 and the femoral condyles (not shown). For example, the cross-sectional thickness of thespoon 24 may be selected to provide sufficient rigidity to align thejig 22 relative to the tibial articular surface 12 (and in particular, thedefect 13 on theconcaved surface 14 a) while also minimizing the required separation between thetibia 10 and the femur. - The
spoon 24 may be an integral component of the jig 22 (e.g., a unitary or single one-piece structure) or may be configured to be releasably coupled to thejig 22. For example, thespoon 24 may include anarm portion 36 configured to extend generally outwardly from a distal face 38 (e.g., a bone facing surface) of thejig 22. The size and shape of thearm portion 36 may be configured to allow a portion of thedistal face 38 to be disposed proximate to the perimeter (e.g., proximate to the meniscus 40) when thespoon 24 is disposed on theconcaved surface 14 a such that the generally cylindrical core pathways associated with the first andsecond excision passageways articular surface 12. - In practice, the
first guide 20 may be positioned relative to thedefect 13 on theconcaved surface 14 a by advancing thespoon 24 between the tibialarticular surface 12 and the femur such that thebase portion 30 of thespoon 24 is disposed over at least a portion of thedefect 13 on the tibialarticular surface 12. Thespoon 24 may be advanced until thedistal face 38 of thejig 22 generally abuts against a portion of the tibia 10 (e.g., proximate to the meniscus 40). The size and shape of thebase portion 30 as well as thearm portion 36/distal face 38 may be configured to generally center thespoon 24 within theconcaved surface 14 a. - Once the
spoon 24 is positioned over thedefect 13, thespoon 24 and thejig 22 may be secured to thetibia 10 using one ormore pins 32 or the like extending through one or more locking passageways 34 in thespoon 24 and/or thejig 22. For example, thespoon 24 may include aspoon locking passageway 34 a extending through a portion of the spoon 24 (e.g., the arm portion 36) configured to align apin 32 a into the tibial bone beneath the tibialarticular surface 12. Alternatively (or in addition), thejig 22 may include ajig locking passageway 34 b extending through a portion of thebody 26 configured to align apin 32 b into the tibial bone beneath the tibialarticular surface 12. While twopins first guide 20 may be secured using greater than or fewer than twopins - The
pins pins pins passageways Pin 32 a may extend a smaller distance into thetibia 10 compared to pin 32 b. - Turning now to
FIG. 3 , thefirst guide 20 may optionally be secured to thetibia 10 by advancing one or more dowels orbushings bone 10. For example, a first and asecond dowel dowels tip passageway dowels passageway dowels passageways tip dowels tibia 10, thedowels jig 22 usinglocking fasteners fasteners - Alignment pins 48 a, 48 b may be advanced through the
passageways dowels tibia 10 as generally illustrated inFIG. 4 . Similar to thepins depth feature passageway dowels -
FIG. 5 is a bottom plan view of thefirst guide 20 generally illustrating one embodiment of the position of the alignment pins 48 a, 48 b as well aspin 32 b relative to thespoon 24. As can be seen, depth features 50 a, 50 b, 33 b are generally aligned with therespective passageways pins spoon 24. As such, the distal ends of thepins tibial bone 10. It should be appreciates, however, that the position of the distal ends of thepins - Once the
first guide 20 is secured to thetibia 10, a first and a second truncated cylindrical excision site may be formed in the tibialarticular surface 12 and/orbone 10. The first and second truncated cylindrical excision sites may correspond to a projection of the cylindrical core pathways defined by the excision passageways 28 a, 28 b intersecting with the tibialarticular surface 12 and/orbone 10. For example, adowel 40 a may be removed from theexcision passageway 28 a, leaving thepin 48 a remaining as generally illustrated inFIG. 6 . A cannulateddrill 60 may then be advanced over thepin 48 a and through theexcision passageway 28 a to form a first truncated cylindrical excision site. Whiledowel 40 a is shown removed, the order in which thedowels - One embodiment of a cannulated
drill 60 is generally illustrated inFIG. 7 . The cannulateddrill 60 may feature acore drill bit 62 and optionally ashank portion 64. Theshank portion 64 may include a multi-faceted proximal end configured to be secured to a drill (e.g., a hand drill, electric drill, pneumatic drill or the like). Alternatively, a proximal end of thecore drill bit 62 may be directly coupled to the drill. - The
core drill bit 62 may include a cutting surface 66 (for example, comprising a plurality of cutting teeth 67) disposed about a distal end of thebarrel 63. The cuttingsurface 66 may be evenly disposed around the generally circular distal end of thebarrel 63. Thebarrel 63 may include an outer diameter substantially corresponding to the inner diameter of theexcision passageway 28 a. For example, thecore drill 62 may have an outer diameter selected from the range of 8-12 mm, for example, 10-11 mm. Thebarrel 63 may define acore cavity 68 configured to receive the removed portion of the tibialarticular surface 12 andbone 10. As may be appreciated, the only portion of the tibialarticular surface 12 andbone 10 that is cut by thecore drill bit 60 corresponds to the thickness of the cuttingsurface 66, which itself is a function of the wall thickness of thebarrel 63. As such, these thicknesses may be selected to remove the least amount of material while also providing the necessary rigidity and/or strength to thecore drill bit 60. - The
core drill bit 62 may optionally feature one ormore windows 70 disposed along the length of thebarrel 63. Thewindow 70 may allow air, fluid, and cutting chips to exit thebarrel 63. In addition, thewindow 70 may also allow the user to align thecore drill bit 62 with thefirst guide 20 and/or pins to control the depth of the excision site (i.e., the length of the excision site as measured across the tibial articular surface 12). For example, a proximal end of thewindow 70 may be generally aligned with the opening on theexcision passageway 28 a to control the depth of the resulting excision site. - The
core drill bit 62 may also optionally include a centeringbearing 72 configured facilitate alignment of thecore drill bit 62 as thecore drill bit 62 is advanced into the tibialarticular surface 12 andbone 10. The centeringbearing 72 may be translatably disposed along the longitudinal axis of thecore drill bit 62 and may include apassageway 74 configured to receive thepin 48 a. For example, the centeringbearing 72 may be initially located near the distal end of thebarrel 62. As thecore drill bit 62 is advanced within theexcision passageway 28 a, thepin 48 a may be received in thepassageway 74 and the centeringbearing 72 may translate towards the proximal end as the core is received in thepassageway 74. - As the
drill bit 60 is advanced through theexcision passageway 28 a in thefirst guide 20, a portion of the cuttingsurface 66 may engage the tibialarticular surface 12 and/or thebone 10, thereby forming a truncated cylindrical excision site. Once thedrill bit 60 has been advanced through theexcision passageway 28 a to create the first excision site, the second truncated cylindrical excision site may be formed. For example, thesecond dowel 40 b may be removed and asecond drill bit 60 may be advanced through thesecond excision passageway 28 b in a manner similar to that described herein. The first andsecond drill bits 60 may have the same or different outer diameters. - As discussed herein, the first and the second excision passageways 28 a, 28 b may be offset relative to each other. Put another way, the first and the second excision passageways 28 a, 28 b may be separated by a distance generally perpendicular to the longitudinal axes of the first and the second excision passageways 28 a, 28 b such that the first and the second truncated cylindrical excision sites do not overlap.
-
FIG. 8 generally illustrates one embodiment of the first and the second truncatedcylindrical excision sites drill bit 60 and the first and the second excision passageways 28 a, 28 b. As can be seen, acenter section 81 ofarticular surface 12/bone 10 remains separating the first and the second truncatedcylindrical excision sites center section 81 may optionally be removed using second guide/jig 82. - The
second guide 82 may comprise one ormore alignment passageways third excision passageway 28 c extending through thebody portion 85. Thethird excision passageway 28 c may also define a generally cylindrical core pathway for a drill bit. Once the first and the second truncatedcylindrical excision sites first guide 20 and pins 32 a, 32 b may be removed and pins 48 a, 48 b may remain secured to thebone 10. Thesecond guide 82 may then be advanced over thepins third excision passageway 28 c) relative to thearticular surface 12 and thecenter section 81. Optionally, thesecond guide 82 may featureprotrusions cylindrical excision sites second guide 82 and thethird excision passageway 28 c relative to thearticular surface 12/center section 81. Thesecond guide 82 may therefore be advanced along thepins cylindrical excision sites distal face 86 of thesecond guide 82 generally abuts against thebone 12 and a projection of the third core pathway associated with thethird excision passageway 28 c partially intersects with thecenter section 81. - Once the
second guide 82 is aligned with the first andsecond excision sites pins third drill 60 may be advanced through thethird excision passageway 28 c extending through thebody 85 to remove thecenter section 81 and form the third truncatedcylindrical excision site 80 c as generally illustrate inFIG. 9 . Thethird excision passageway 28 c may be configured to align thethird drill 60 such that the resulting third truncatedcylindrical excision site 80 c partially overlaps with the first and the second truncatedcylindrical excision sites third excision passageway 28 c may have a diameter which would partially overlap with the first and the second excision passageways 28 a, 28 b if the three excision passageways 28 a-28 c were transposed on each other and aligned with thepins - The resulting implant site may therefore comprise the first, second, and third truncated cylindrical excision sites 80 a-80 c wherein the first and the second truncated
cylindrical excision sites cylindrical excision site 80 c. The truncated cylindrical excision sites 80 a-80 c may be centered/revolved around thepins articular surface 12 generally along the anterior-posterior plane. For example, the truncated cylindrical excision sites 80 a-80 c may extend from the anterior face of the tibialarticular surface 12 generally towards the posterior face. The implant site may therefore include abase portion 90 comprising three overlapping truncated cylindrical extensions or scallops defined by the three excision passageways 28 a-28 c. The resulting implant site therefore may generally eliminate/reduce the occurrence of 90 degree cuts and therefore more evenly distribute loads/forces to thebone 10 compared a traditional 90 degree notch cut. - The truncated cylindrical excision sites 80-80 c have been illustrated extending partially across the tibial articular surface 12 (i.e., one or more of the truncated cylindrical excision sites 80-80 c do not extend completely across the
articular surface 12 thus leaving aportion 99 of the tibialarticular surface 12 and/orbone 10 remaining). This embodiment may be particularly beneficial since it further minimizes the potential for accidentally damaging the nerve bundle. However, the system and method according to the present disclosure may also allow for one or more of the truncated cylindrical excision sites 80 a-80 c to extend completely across thearticular surface 12 as generally illustrate inFIG. 10 . In particular, the system and method according to the present disclosure may be able to accurately enough form the truncated cylindrical excision sites 80 a-80 c to minimize the potential of damaging the nerve bundle to an acceptable level. - While the system and method has been described having a first and a
second guide first guide 20 may include alignment dowels (not shown) configured to be advanced and/or secured within the first and second excision passageways 28 a, 28 b. The alignment dowels may includeprotrusions truncated excision sites guide 20 may include athird excision passageway 28 c extending generally along the lockingpassageway 34 b (which itself may be formed in a removable bushing). The alignment dowels may have an outer shape such that thethird excision passageway 28 c defines a generally cylindrical core pathway for thedrill 60. - Turning now to
FIG. 11 , one embodiment of animplant 100 consistent with the present disclosure is generally illustrated. Theimplant 100 may comprise aload bearing surface 102 and a bone facing ordistal surface 104. Theload bearing surface 102 may have a surface contour/geometry substantially corresponding to the contour/geometry of the removed tibialarticular surface 12 proximate thedefect 13. The contour/geometry of the load bearing surface may be based on a plurality of measurement take of the patient's tibialarticular surface 12, for example, as described in U.S. patent application Ser. No. 10/373,463, filed on Feb. 24, 2003, entitled System and Method for Joint Resurface Repair, which is fully incorporated herein by reference. - The
bone facing surface 104 may have an overall contour/geometry generally corresponding to the contour/geometry of thebase portion 90 of the three truncated cylindrical excision sites 80 a-80 c and the removedbone 10. Optionally, thebone facing surface 104 may include one or more relief cavities, pockets and/or cross-cuts 106 configured to enhance securing theimplant 100 to thebone 10 within the truncated cylindrical excision sites 80 a-80 c. Therelief cavities 106 may be configured to allow bone regrowth around a portion of theimplant 100 and/or promote cement adhesion. As shown, theimplant 100 may comprise a generally unitary structure (i.e., theimplant 100 may be a solid, one-piece component). For example, theimplant 100 may be made from ultra-high molecular weight polyethylene (UHMWPE). - Turning now to
FIG. 12 , a cross-sectional view of another embodiment of animplant 100 b consistent with the present disclosure is generally illustrated.Implant 100 b may comprise multiple portions configured to be coupled together, for example, an upper and alower portion upper portion 110 may include aload bearing surface 102 as described herein while thelower portion 112 may comprise abone facing surface 104 as described herein. The upper andlower portions lower portion 112 may be based on theguides upper portion 110 may be based on the contour/geometry of the patient's removedarticular surface 12. Put another way, thelower portion 112 may be considered “generic” or common in that it is based on theguides articular surface 12 while theupper portion 110 may be selected based specifically on measurements of the patient'sarticular surface 12. - Turning now to
FIG. 13 , a cross-sectional view of anotherimplant 100 c is shown generally implanted within theimplant site 120 formed by truncated cylindrical excision sites 80 a-80 c. As shown, thebone facing surface 104 of theimplant 100 c may be generally disposed along thebase portion 90 of the truncated cylindrical excision sites 80 a-80 c while theload bearing surface 102 may be substantially continuous with the surrounding tibial articular surface 12 (i.e., the tibialarticular surface 12 adjacent to and abutting theimplant 100 c). Theimplant 100 c may optionally comprise one or more keels, tails, protrusions or the like 122. Thekeel 122 may extend generally downwardly from thebone facing surface 104 and away from theload bearing surface 102. Thekeel 122 may be configured to engage acorresponding notch 124 formed in thebase portion 90 of the truncated cylindrical excision sites 80 a-80 c. While theimplant 100 c is illustrated having an upper and alower portion implant 100 as illustrated inFIG. 11 may optionally include one or more keels 122. Thekeel 122 may be an integral component of theimplant 100 or thelower portion 112 or alternatively may be a separate component coupled thereto. - As may be appreciated from
FIGS. 11-13 , an implant consistent with at least one embodiment of the present disclosure may have aload bearing surface 102 which is non-planar. While traditional tibial implants have had a generally planar or flat load bearing surface, an implant consistent with at least one embodiment of the present disclosure may have a concaved geometry which may better approximate the geometry of the patient's removed tibialarticular surface 12. For example, the implant as shown inFIG. 13 may have a first side (e.g., but not limited to, a medial side) having a height L less than a height H of a second side (e.g., but not limited to, the lateral side). - Turning now to
FIG. 14 , a top view of one embodiments of theimplant 100 consistent with the present disclosure is generally illustrated. When viewed from the top side (i.e., when viewing the load bearing surface 102), theimplant 100 may have a generally “D” shape. This “D” shape may correspond to an implant site which extends all the way cross the anterior-posterior plane of the articular surface (e.g., as generally shown inFIG. 10 ). As shown inFIG. 15 , theimplant 100 may also have a modified or notched “D” shape. In particular, theimplant 100 may include a notchedregion 130 which may correspond to thearea 99 of the tibialarticular surface 12 proximate to the posterior face of thetibia 10 which is not removed (e.g., as generally shown inFIG. 9 ). As discussed herein, leaving thisportion 99 of the tibialarticular surface 12 and/orbone 10 intact may minimize the potential of damaging the nerve bundle 16 (FIG. 1 ). - According to one aspect, the present disclosure features an implant resection system for preparing an implant site to replace a defect in an articular surface of a first bone. The implant resection system includes a guide configured to be coupled generally perpendicular to the first bone proximate to the defect. The guide includes a body portion defining a plurality of excision passageways. The excision passageways each define a generally cylindrical core pathway configured to extend generally perpendicular to the first bone which partially overlaps with an adjacent generally cylindrical core pathway. A projection associated with each of the plurality of the generally cylindrical core pathways defines a truncated cylindrical excision site extending through a portion of the articular surface. Each truncated cylindrical excision site partially overlaps with at least one adjacent truncated cylindrical excision site.
- According to another aspect, the present disclosure features a method for preparing an implant site to replace a defect in an articular surface. The method includes securing a guide to bone proximate the defect. The guide includes a body portion defining a plurality of excision passageways. Each excision passageway defines a generally cylindrical core pathway which partially overlaps with an adjacent generally cylindrical core pathway. The method further includes advancing at least one drill through the plurality of excision passageways along the generally cylindrical core pathways to form a plurality of partially overlapping truncated cylindrical excision sites extending through the articular surface.
- While the principles of the present disclosure have been described herein, it is to be understood by those skilled in the art that this description is made only by way of example and not as a limitation as to the scope of the invention. The features and aspects described with reference to particular embodiments disclosed herein are susceptible to combination and/or application with various other embodiments described herein. Such combinations and/or applications of such described features and aspects to such other embodiments are contemplated herein. Other embodiments are contemplated within the scope of the present invention in addition to the exemplary embodiments shown and described herein. Modifications and substitutions by one of ordinary skill in the art are considered to be within the scope of the present invention, which is not to be limited except by the following claims.
- All definitions, as defined and used herein, should be understood to control over dictionary definitions, definitions in documents incorporated by reference, and/or ordinary meanings of the defined terms.
- The indefinite articles “a” and “an,” as used herein in the specification and in the claims, unless clearly indicated to the contrary, should be understood to mean “at least one.”
- The phrase “and/or,” as used herein in the specification and in the claims, should be understood to mean “either or both” of the elements so conjoined, i.e., elements that are conjunctively present in some cases and disjunctively present in other cases. Other elements may optionally be present other than the elements specifically identified by the “and/or” clause, whether related or unrelated to those elements specifically identified, unless clearly indicated to the contrary.
- All references, patents and patent applications and publications that are cited or referred to in this application are incorporated in their entirety herein by reference.
- Additional disclosure in the format of claims is set forth below.
Claims (19)
1. An implant resection system for preparing an implant site to replace a defect in an articular surface of a first bone, said implant resection system comprising:
a guide configured to be coupled generally perpendicular to said first bone proximate to said defect, said guide comprising a body portion defining a plurality of excision passageways, said excision passageways each defining a generally cylindrical core pathway configured to extend generally perpendicular to said first bone which partially overlaps with an adjacent generally cylindrical core pathway, wherein a projection associated with each of said plurality of said generally cylindrical core pathways defines a truncated cylindrical excision site extending through a portion of said articular surface, and wherein each truncated cylindrical excision site partially overlaps with at least one adjacent truncated cylindrical excision site.
2. The implant resection system of claim 1 , further comprising:
an arm extending outwardly from a distal face of said body portion of said guide; and
a spoon disposed about a distal end of said arm, said spoon configured to be disposed between said articular surface of said first bone and an articular surface of a cooperating bone.
3. The implant resection system of claim 2 , wherein said spoon further comprises a generally convex base portion configured to abut against said articular surface of said first bone.
4. The implant resection system of claim 3 , wherein said spoon further comprises a generally concaved upper portion configured to abut against said articular surface of said cooperating bone.
5. The implant resection system of claim 2 , further comprising:
a locking passageway extending through a portion of said arm; and
at least one pin configured to be advanced through said locking passageway and into said first bone and to secure said spoon relative to said first bone.
6. The implant resection system of claim 5 , wherein said locking passageway is configured to align said at least one pin such that said at least one pin extends into said first bone proximate to the meniscus.
7. The implant resection system of claim 1 , further comprising:
a locking passageway extending through a portion of said body portion; and
at least one pin configured to be advanced through said locking passageway and into said first bone and to secure said body portion relative to said first bone.
8. The implant resection system of claim 1 , further comprising:
a dowel having a longitudinal passageway, said dowel configured to be advanced through a first of said plurality of excision passageways and to abut against said first bone; and
a pin configured to be advanced through said longitudinal passageway of said dowel and into said first bone;
wherein said dowel and said pin are configured to secure said body portion relative to said first bone.
9. The implant resection system of claim 8 , further comprising a locking feature to secure said dowel within said first excision passageway.
10. The implant resection system of claim 1 , further comprising a core drill configured to advanced through a first one of said plurality of excision passageways along a first of said generally cylindrical core pathways to remove a portion of said bone and said articular surface to define a first of said plurality of partially overlapping truncated cylindrical excision sites.
11. The implant resection system of claim 10 , further comprising:
a pin configured to be advanced through said first excision passageway and into said first bone;
wherein said core drill further comprises a centering bushing disposed within a core cavity of said core drill, said centering bushing configured to be advanced over said pin and to center said core drill along said generally cylindrical core pathway associated with said first excision passageway.
12. The implant resection system of claim 1 , wherein said plurality of excision passageways includes a first, a second, and a third excision passageway, said third excision passageway partially overlapping said first and said second excision passageways;
wherein said guide further comprises a first and a second protrusion configured to extend from said body portion and to be received in a truncated cylindrical excision site associated with said first and said second excision passageway, respectively.
13. The implant resection system of claim 12 , wherein said first and said second protrusions further comprise alignment passageways, each alignment passageway configured to be advanced over an associated pin to secure said guide to said first bone while a core drill is advanced through said third excision passageway to form an excision site associated with said third excision passageway.
14. The implant resection system of claim 1 , further comprising an implant comprising:
a load bearing surface having a contour substantially corresponding to a contour of the articular surface corresponding to said implant site; and
a bone facing surface having a contour substantially corresponding to the contour of said plurality of truncated cylindrical excision sites formed in said first bone.
15. The implant resection system of claim 14 , wherein said bone facing surface further comprises a plurality of relief cavities configured secure said implant to said bone.
16. The implant resection system of claim 14 , further comprising a keel extend generally away from said bone facing surface, said keel configured to engage a corresponding notch formed in one of said plurality of truncated cylindrical excision sites.
17. The implant resection system of claim 14 , wherein said first bone is a tibia, and wherein said implant includes a “D” shaped cross-section.
18. The implant resection system of claim 14 , wherein said implant comprises an upper portion configured to be secured to a lower portion, said upper portion comprising said load bearing surface and said lower portion comprising said bone facing surface.
19. A method for preparing an implant site to replace a defect in an articular surface, said method comprising:
securing a guide to bone proximate said defect, said guide comprising a body portion defining a plurality of excision passageways, each excision passageway defining a generally cylindrical core pathway which partially overlap with an adjacent generally cylindrical core pathway; and
advancing at least one drill through said plurality of excision passageways along said generally cylindrical core pathways to form a plurality of partially overlapping truncated cylindrical excision sites extending through said articular surface.
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US14/133,943 US10624752B2 (en) | 2006-07-17 | 2013-12-19 | Tibial resurfacing system and method |
US16/854,244 US11471289B2 (en) | 2006-07-17 | 2020-04-21 | Tibial resurfacing system and method |
US17/967,427 US20230110492A1 (en) | 2006-07-17 | 2022-10-17 | Tibial Resurfacing System and Method |
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US11/779,044 US20080033443A1 (en) | 2006-07-17 | 2007-07-17 | System and Method for Tissue Resection |
US31077410P | 2010-03-05 | 2010-03-05 | |
US13/042,382 US20110213375A1 (en) | 2006-07-17 | 2011-03-07 | Tibial Resurfacing System and Method |
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US11471289B2 (en) | 2022-10-18 |
EP2542165A4 (en) | 2015-10-07 |
CA2792048A1 (en) | 2011-09-09 |
WO2011109836A1 (en) | 2011-09-09 |
US10624752B2 (en) | 2020-04-21 |
EP2542165A1 (en) | 2013-01-09 |
US20140155902A1 (en) | 2014-06-05 |
US20210038398A1 (en) | 2021-02-11 |
BR112012022482A2 (en) | 2016-07-19 |
AU2011222404A1 (en) | 2012-09-27 |
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