Carpometacarpal (CMC) joint arthroplasty implants and related jigs

Abstract

Thumb carpometacarpal (CMC) joint implants include a trapezium implant defining an articulating surface and a cooperating first metacarpal implant with a base portion of the first metacarpal defining an articulating surface. The first metacarpal base articulating-surface is configured to articulate against the trapezium implant articulating surface.

Claims

1. A thumb Carpo-MetaCarpal (CMC) joint implant, comprising: a thumb trapezium implant defining an articulating surface, wherein the trapezium implant comprises at least one keel that has a flat segment that merges into a second segment with a substantially circular cross-sectional shape, wherein the flat segment of each respective at least one keel has parallel, straight outer short sides and a width that is greater than a length of the short sides, and wherein the substantially circular shape has a cross-sectional size that is greater than a cross-sectional size of the flat segment, and wherein the at least one keel is configured to reside in a correspondingly shaped channel formed in a target trapezium; and a cooperating thumb first metacarpal implant with a base of the first metacarpal implant defining an articulating surface, wherein the base of the first metacarpal implant is configured to articulate against the trapezium implant articulating surface, wherein the trapezium implant and the first metacarpal implant articulating surfaces have shapes similar to natural articular surfaces of a CMC joint, wherein at least one of the articulating surfaces has a saddle shaped configuration, and wherein the at least one keel is sized and configured to slidably snugly enter a bone channel with substantially parallel closely spaced trapezium bone sidewalls in a target trapezium from a volar radial surgical approach, wherein the trapezium implant keel is sized and configured to snugly reside in a trapezium bone channel that has parallel vertically extending sidewalls that merge into a lowermost semi-circular portion, and wherein the flat segment of each respective at least one trapezium keel extends in a vertical orientation with a width that is greater than a length thereof, with the length being between about 0.1-0.25 inches.

2. A thumb Carpo-MetaCarpal (CMC) joint implant, comprising: a thumb trapezium implant defining an articulating surface, wherein the trapezium implant comprises at least one keel that has a flat segment that merges into a second segment with a substantially circular cross-sectional shape, wherein the flat segment of each respective at least one keel has parallel, straight outer short sides and a width that is greater than a length of the short sides, and wherein the substantially circular shape has a cross-sectional size that is greater than a cross-sectional size of the flat segment, and wherein the at least one keel is configured to reside in a correspondingly shaped channel formed in a target trapezium; and a cooperating thumb first metacarpal implant with a base of the first metacarpal implant defining an articulating surface, wherein the base of the first metacarpal implant is configured to articulate against the trapezium implant articulating surface, wherein the trapezium implant and the first metacarpal implant articulating surfaces have shapes similar to natural articular surfaces of a CMC joint, wherein at least one of the articulating surfaces has a saddle shaped configuration, and wherein the at least one keel is sized and configured to slidably snugly enter a bone channel with substantially parallel closely spaced trapezium bone sidewalls in a target trapezium from a volar radial surgical approach, the implant in combination with a plurality of trapezium implant trials, wherein the trials have a substantially planar bottom surface devoid of any downwardly projecting anchoring member.

3. A thumb Carpo-MetaCarpal (CMC) joint implant, comprising: a thumb trapezium implant defining an articulating surface, wherein the trapezium implant comprises at least one keel that has a flat segment that merges into a second segment with a substantially circular cross-sectional shape, wherein the flat segment of each respective at least one keel has parallel, straight outer short sides and a width that is greater than a length of the short sides, and wherein the substantially circular shape has a cross-sectional size that is greater than a cross-sectional size of the flat segment, and wherein the at least one keel is configured to reside in a correspondingly shaped channel formed in a target trapezium; and a cooperating thumb first metacarpal implant with a base of the first metacarpal implant defining an articulating surface, wherein the base of the first metacarpal implant is configured to articulate against the trapezium implant articulating surface, wherein the trapezium implant and the first metacarpal implant articulating surfaces have shapes similar to natural articular surfaces of a CMC joint, wherein at least one of the articulating surfaces has a saddle shaped configuration, and wherein the at least one keel is sized and configured to slidably snugly enter a bone channel with substantially parallel closely spaced trapezium bone sidewalls in a target trapezium from a volar radial surgical approach, the implant in combination with a plurality of trapezium implant trials, wherein the trials have a substantially planar bottom surface with at least one downwardly extending anti-rotational post, wherein the at least one post has a different configuration than the implant at least one keel wherein the at least one post is flat with parallel, straight outer short sides and a width that is greater than a length of the short sides that slidably enters the bone channel.

4. A thumb Carpo-MetaCarpal (CMC) joint implant, comprising: a thumb trapezium implant defining an articulating surface, wherein the trapezium implant comprises at least one keel that has a flat segment that merges into a second segment with a substantially circular cross-sectional shape, wherein the flat segment of each respective at least one keel has parallel, straight outer short sides and a width that is greater than a length of the short sides, and wherein the substantially circular shape has a cross-sectional size that is greater than a cross-sectional size of the flat segment, and wherein the at least one keel is configured to reside in a correspondingly shaped channel formed in a target trapezium; and a cooperating thumb first metacarpal implant with a base of the first metacarpal implant defining an articulating surface, wherein the base of the first metacarpal implant is configured to articulate against the trapezium implant articulating surface, wherein the trapezium implant and the first metacarpal implant articulating surfaces have shapes similar to natural articular surfaces of a CMC joint, wherein at least one of the articulating surfaces has a saddle shaped configuration, and wherein the at least one keel is sized and configured to slidably snugly enter a bone channel with substantially parallel closely spaced trapezium bone sidewalls in a target trapezium from a volar radial surgical approach, the implant in combination with trapezium implant trials, wherein the trials have a planar fin with a length that is shorter than a length of the keel of the trapezium implant and has a flat configuration with parallel, straight outer short sides and a width that is greater than a length of the short sides that is sized and configured to slidably enter the bone channel that is sized and configured to slidably enter the bone channel.

5. A thumb Carpo-MetaCarpal (CMC) joint implant, comprising: a thumb trapezium implant defining an articulating surface, wherein the trapezium implant comprises at least one keel that has a flat segment that merges into a second segment with a substantially circular cross-sectional shape, wherein the flat segment of each respective at least one keel has parallel, straight outer short sides and a width that is greater than a length of the short sides, and wherein the substantially circular shape has a cross-sectional size that is greater than a cross-sectional size of the flat segment, and wherein the at least one keel is configured to reside in a correspondingly shaped channel formed in a target trapezium; and a cooperating thumb first metacarpal implant with a base of the first metacarpal implant defining an articulating surface, wherein the base of the first metacarpal implant is configured to articulate against the trapezium implant articulating surface, wherein the trapezium implant and the first metacarpal implant articulating surfaces have shapes similar to natural articular surfaces of a CMC joint, wherein at least one of the articulating surfaces has a saddle shaped configuration, and wherein the at least one keel is sized and configured to slidably snugly enter a bone channel with substantially parallel closely spaced trapezium bone sidewalls in a target trapezium from a volar radial surgical approach, the implant in combination with at least one trapezium implant jig with at least one downwardly extending flat slot with parallel straight sides configured to define a bone preparation guide or template for preparing at least one slot in a target trapezium from a Wagner surgical approach.

6. The implant of claim 5, wherein the trapezium implant jig comprises a plurality of apertures for accepting members to secure the jig in position during formation of the slot in the target trapezium.

7. The implant of claim 6, wherein the at least one downwardly extending slot of the trapezium implant jig merges into a keyhole on a medial to lower portion thereof.

8. The implant of claim 5, wherein the jig comprises a top portion that merges into a downwardly extending side portion, with the side portion being substantially orthogonal to the top portion, and wherein the jig at least one downwardly extending slot is configured to continuously extend from the downwardly extending portion upward and across the top portion to define a substantially horizontal slot extending through a top surface of the jig.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 is an anatomical drawing of the palmar aspect of the carpal and metacarpal bones illustrating the 1st metacarpal, the CMC joint and the trapezium.

(2) FIG. 2 is an axial view illustrating motions of the thumb.

(3) FIGS. 3A and 3B are schematic illustrations of the bones of the trapezio-metacarpal joint (the upper bones associated with the trapezium and the lower bones associated with the metacarpal).

(4) FIG. 3C is an enlarged schematic illustration of the corresponding articular surfaces of the metacarpophalangeal joint (the trapezium and the first metacarpal base).

(5) FIG. 4A is a side perspective view of a 1st metacarpal implant with a cooperating trapezium implant according to embodiments of the present invention.

(6) FIG. 4B is an end view of the 1st metacarpal implant shown in FIG. 4A.

(7) FIG. 4C is an exemplary end view of the trapezium implant shown in FIG. 4A according to some embodiment of the present invention.

(8) FIG. 4D is a top perspective view of an alternate configuration of the distal end member (the shape being similar to the natural articular surface of the CMC joint) according to some embodiments of the invention.

(9) FIG. 5A is an enlarged side view of the trapezium implant shown in FIG. 4A.

(10) FIG. 5B is an enlarged side view of an alternate configuration of the trapezium implant shown in FIG. 4A.

(11) FIG. 5C is an enlarged end view of the trapezium implant shown in FIG. 5A or 5B.

(12) FIG. 5D is an enlarged end view of an alternative configuration of the trapezium implant shown in FIG. 5A or 5B according to some embodiments of the invention.

(13) FIG. 6 is a schematic illustration of a thumb with a region of the trapezium removed to define a prepared distal surface suitable for the trapezium implant according to embodiments of the present invention.

(14) FIG. 7A is a side View of an intramedullary implant portion of a 1st metacarpal implant configured to matably attach to a selected distal end member (facing the trapezium).

(15) FIG. 7B is an opposing side view of the distal end member shown in FIG. 7A.

(16) FIG. 7C is a side view of an articulating base member for a saddle configuration of the 1st metacarpal with the intramedullary portion of the implant in position and the distal end member attached thereto and extending beyond the bounds of the metacarpal to define an articular surface according to some embodiments of the present invention.

(17) FIG. 7D is a side view of an alternate attachment configuration for the intramedullary member and the distal end member according to other embodiments of the invention.

(18) FIG. 8 is an exploded view of an alternate configuration of the trapezium implant and the cooperating 1st metacarpal implant according to yet other embodiments of the invention.

(19) FIGS. 9A and 9B are schematic illustrations of a trapezial jig according to embodiments of the invention.

(20) FIG. 10 is a schematic illustration of a drill that extends through the jig shown in FIGS. 9A and 9B to define an anchoring tunnel, aperture or hole for the trapezial implant according to some embodiments of the invention.

(21) FIG. 11A is a schematic illustration of a saw that extends through the jig shown in FIGS. 9A and 9B to connect the anchoring holes with a distal cut surface of the trapezium according to embodiments of the invention.

(22) FIG. 11B is a schematic illustration of a surgically prepared trapezium according to embodiments of the invention.

(23) FIG. 12 is a schematic illustration of a broach that can be used to size the 1st metacarpal implant. A trial can be inserted to determine the appropriate implant size.

(24) FIG. 13A is a schematic illustration of a medical set or kit of different sized trapezium trials according to embodiments of the present invention.

(25) FIGS. 13B and 13C are alternate end views of other trapezium trials according to embodiments of the present invention.

(26) FIG. 14 is a schematic illustration of a medical set or kit of different components for a CMC total joint replacement procedure according to embodiments of the invention.

(27) FIG. 15 is a flow chart of exemplary operations that can be used to carry out embodiments of the invention.

(28) FIGS. 16-23 illustrate exemplary steps that can be used to surgically implant a total TCMA prosthesis according to embodiments of the present invention.

DESCRIPTION OF EMBODIMENTS OF THE INVENTION

(29) The present invention will now be described more fully hereinafter with reference to the accompanying figures, in which embodiments of the invention are shown. This invention may, however, be embodied in many different forms and should not be construed as limited to the embodiments set forth herein. Like numbers refer to like elements throughout. In the figures, certain layers, components or features may be exaggerated for clarity, and broken lines illustrate optional features or operations unless specified otherwise. In addition, the sequence of operations (or steps) is not limited to the order presented in the figures and/or claims unless specifically indicated otherwise. In the drawings, the thickness of lines, layers, features, components and/or regions may be exaggerated for clarity and broken lines illustrate optional features or operations, unless specified otherwise.

(30) It will be understood that when a feature, such as a layer, region or substrate, is referred to as being on another feature or element, it can be directly on the other feature or element or intervening features and/or elements may also be present. In contrast, when an element is referred to as being directly on another feature or element, there are no intervening elements present. It will also be understood that, when a feature or element is referred to as being connected, attached or coupled to another feature or element, it can be directly connected, attached or coupled to the other element or intervening elements may be present. In contrast, when a feature or element is referred to as being directly connected, directly attached or directly coupled to another element, there are no intervening elements present. Although described or shown with respect to one embodiment, the features so described or shown can apply to other embodiments.

(31) Unless otherwise defined, all terms (including technical and scientific terms) used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. It will be further understood that terms, such as those defined in commonly used dictionaries, should be interpreted as having a meaning that is consistent with their meaning in the context of the relevant art and should not be interpreted in an idealized or overly formal sense unless expressly so defined herein. The term polymer includes copolymers and derivatives and/or combinations thereof.

(32) The implant can be a total joint replacement implant that allows articulation of the bones. The term total joint replacement means that both the base of the first metacarpal and the opposing articular surface of the trapezium are replaced with cooperating implant surfaces, resulting in a total thumb carpo-metacarpal arthroplasty (TCMA), thereby providing complete joint replacement as in total hip arthroplasty (THA) or total knee arthroplasty (TKA).

(33) As shown in FIG. 4A, embodiments of the invention provide an intramedullary first metacarpal implant 40 that cooperates with a trapezium implant 60. The first metacarpal implant 40 includes a base portion 45 that defines a base of the CMC joint. As shown, the base portion 45 has a socket 46 (FIG. 4B) that matably receives the projecting portion 61 of the trapezium implant 60, allowing articulation between the two implants 40, 60 such that the corresponding articulating surfaces 40s, 60s articulate against each other. In the embodiment shown in FIG. 4A, the first metacarpal implant 40 has a substantially concave articulating surface 40s substantially matched to a convex articulating surface 60s of the trapezium implant 60. The first metacarpal implant 40 can be a single unitary member or can include a matable base member that defines the articulating surface 40s. For example, if the implants 40, 60 comprise pyrocarbon or a similarly lubricious and/or strong composite or polymer, the two surfaces 40s, 60s can articulate against each other without requiring an intermediary material or component. Alternatively, if the first metacarpal implant 40 and trapezium implant 60 are made out of stainless steel or titanium or other suitable biomedical metal, then a base member (typically attached to the first implant 40) can be used to define one of the articulating surfaces, formed of a suitable biocompatible material, such as, for example, polyethylene (so that there is no metal on metal contact for the articulating surfaces 40s, 60s).

(34) In other embodiments, the first metacarpal implant 40 can include a base portion 45 that is shaped as a substantially anatomically equivalent of a natural metacarpal base (FIGS. 3B and 3C) and, similarly, the trapezium implant 60 can have a corresponding substantially natural anatomic distal articular surface that can cooperate with the first metacarpal implant 40. Examples of implants 45, 60 with alternative articulating surfaces 40s, 60s having more natural surface contours are shown in FIG. 4D. The implants 40, 60 can thus define a natural anatomical contour of the CMC joint to act as a resurfacing implant system.

(35) FIG. 4B is an end view of the base portion 45 of the first metacarpal implant 40 shown in FIG. 4A that can define a receiving socket 46 with the articulating surface 40s forming part of the CMC replacement joint. The socket 46 can have a width W.sub.1 with an overall width of the base portion 45 can have a width W.sub.2. The implant 40 can be provided in different sizes with different widths, recognizing that the anatomical constraints and needs will likely vary by patient (age, gender, bone structure and the like). In some embodiments, the socket 46 has a concave hemispherical shape with an arc radius R.sub.1.

(36) FIG. 4C illustrates an end view of the trapezium implant 60 shown in FIG. 4A. As shown, the implant 60 includes at least one anchoring member 63, shown as two keels 63.sub.1, 63.sub.2. More or fewer anchoring members 63 can be used and different anchoring member configurations may also be used. FIG. 4A illustrates that the anchoring member 63 can be oriented to extend transversely across at least a major portion of the width of the implant 60.

(37) The keels 63.sub.1, 63.sub.2 are typically rigid and reside in a bone tunnel or channel formed in the trapezium, but may be flexible and/or otherwise configured to promote and/or allow for local tissue ingrowth. The implant 60 can have a substantially planar bottom mounting surface 62 and the at least one anchoring member 63 can extend below the bottom surface 62. As shown, the anchoring member 63 can extend downwardly substantially orthogonal to the mounting surface 62, but the anchoring member 63 may be oriented at different angles.

(38) The thickness T.sub.1 of the projecting portion of the trapezium implant 60 can vary to allow a clinician to select the size that substantially fills the target CMC cavity. Sets of the implant 60 can be provided with different thickness T.sub.1 to allow a clinician to select an appropriate one for the patient, as, again, the desired thickness may vary due to target anatomical considerations, age, gender and the like. The downwardly extending length of the anchoring member 63 (e.g., keels 63.sub.1, 63.sub.2), is typically between about 0.1 inch to about 0.25 inches, defining an overall thickness T.sub.2. In some embodiments, the projecting portion (e.g., dome) 61 can have a convexity with a radius R.sub.2 that may, in some particular embodiments, be between about inch to about inches, which is typically slightly less than that of the socket radius R.sub.1, thereby allowing for an articulating snug fit to inhibit misalignment or separation during articulation.

(39) FIG. 5A is an enlarged side view of the trapezium implant 60. As shown, the at least one anchoring member 63 can reside inside the bounds of the bottom surface 62 and terminate prior to the outer portions thereof. FIG. 5B illustrates that the at least one anchoring member 63 can extend closer to one outer side edge of the implant than the opposing side edge. FIG. 5C illustrates that the at least one anchoring member 63 can have a larger and/or differently configured lower portion 64. As shown, the at least one anchoring member 63 can have a substantially thin planar body that merges into a substantially circular (cross-section) lower portion 64. As will be discussed further below, the lower portion can reside in a correspondingly shaped tunnel or channel in local bone to help retain the implant in a desired position. Alternatively, or in combination with the anchoring member(s) 63, bone cement or other anchoring mechanisms may be used. FIG. 5D illustrates an alternative anchoring member configuration, located substantially medially on the implant body 60. The lower portion 63 may be flexible and able to be press fit into a holding bone channel or tunnel. Combinations of the above anchoring configurations or other configurations may also be used.

(40) To prepare the surgical site for the implants 40, 60, the base of the 1.sup.st metacarpal can be planarized and/or flattened and the intramedullary implant 42 can be inserted into the proximal portion of the 1.sup.st metacarpal 20. Similarly, as shown in FIG. 6, the distal articulating portion 10r of the anatomic trapezium can be removed to flatten and planarize the implant support surface and the implant 60 can be attached to the remaining trapezium. The first metacarpal intramedullary component 42 can be selected to fill and match the contour of the target endosteal (inside) surface of the proximal aspect of the first metacarpal 20. FIG. 7A illustrates that the implant 40 can include a base portion 45 that is matably attachable to the intramedullary portion 42 (e.g., stem). The intramedullary portion 42 of the implant 40 can be provided in various sizes to allow for correct patient sizing. Similarly, the base portion 45 can be provided in different sizes and/or configurations to allow a clinician to select the appropriate size for a patient.

(41) In some embodiments, the implants 40, 60 can be provided in S, M, L and XL sizes, such as in the exemplary sizes provided below. The size of the trapezium implant 60 will determine the desired size of the first metacarpal implant 40, making the size of the trapezium implant 60 determinate thereof.

(42) TABLE-US-00001 Size Trapezium Radius 1st MC base member Small 3-4 mm (typically about matching inch (3.18 mm)) Medium 5-7 mm (typically about matching inch (6.35 mm)) Large 8-10 mm (typically about matching inch (9.52 mm))

(43) The intramedullary surface 42s of the implant 42 can be roughened (cintered, pitted, scraped, filed, contoured, etc.) to promote bone ingrowth. The intramedullary implant 42 can be press fit into position, but also or alternatively can be cemented in with suitable biocompatible cement, such as, for example, polymethylmerthacolate. The intramedullary implant 42 can be manufactured out of various substantially rigid biocompatible materials, such as metals, rigidized polymers, ceramics, and/or carbon. As shown in FIG. 7A, the intramedullary implant 42 can include a locking member 44 to mate to the base portion 45 which defines the articular component. FIG. 7A shows that the locking member 44 can be a trunnion or post and FIG. 7B illustrates that the base portion 45 can include an aperture or channel 49 sized and configured to matably receive the locking member 44. FIG. 7C illustrates that the base portion 45 with the 1.sup.st MC articulating component can have a saddle (natural) configuration and may be snap-fitted and/or locked onto the proximal portion of the 1.sup.st MC intramedullary component 42. FIG. 7D illustrates that the base portion 45 can include the locking member 44 while the intramedullary implant 42 can include the corresponding locking aperture 49. In other embodiments, the first metacarpal implant 40 can be pre-formed at an OEM or offsite location or defined by a single member (not shown).

(44) In some embodiments, the intramedullary implant 42 and the trapezium implant 60 are metallic while the base portion 45 can comprise a polymer that provides the articulating surface 40s with the desired sliding frictional and/or lubricity property. The base portion 45 can be formed of a unitary member and material, similar to a spacer. In some embodiments, the base portion 45 comprises polyethylene. It can be provided in varying thicknesses as discussed herein in order to substantially fill the articulating cavity of the CMC joint. As also noted above, the articulating surface 40s can be substantially concave in shape but also can be fashioned more like an anatomic 1.sup.st MC articular surface (e.g., saddle shaped), as noted above (see, e.g., FIGS. 4D, 7C).

(45) The trapezial implant 60 has an articulating surface 60s that can be generally and/or substantially convex but also can be saddle shaped. The convex shape can reduce the stresses on the component at the bone implant interface.

(46) FIG. 8 also shows that the trapezium implant 60 can define a socket that has a substantially concave articulating surface 60s while the base portion 45 of the first metacarpal implant 40 can be substantially convex. The concave shape may reduce the stresses on the component at the bone implant interface.

(47) The anchoring member 63 of the trapezium implant 60 can be configured to be resistance-fitted. The keel(s) and/or anchoring portion of the implant 60 can be forced into position by hammering, pushing and/or forcibly sliding the implant 60 into place. The placement can be done by overcoming the friction of the trapezial bone against the implant 60. A jig or series of jigs can be employed to prepare the implant bone site to facilitate the implantation (see, for example, an exemplary surgical procedure described below). The lower bone contact surface of the implant 60 and/or anchoring member(s) 63 can be roughened to promote bone ingrowth. The trapezium implant 60 can be configured to withstand loosening forces. The implant system can allow early motion, obviating the need for a cast post-operatively.

(48) Surgical Procedure

(49) It is contemplated that the implantation procedure should be able to be completed in less than about 1.5 hours. It may be performed under intravenous block anesthesia, but axillary block or general anesthesia are additional options. During the surgical procedure, the hand is typically in the palm up or semi-supinated position. A Wagner approach can be used, taking down the thenar muscles to expose the CMC capsule. A suitable needle, such as an 18-gauge needle, can be inserted into the CMC joint, identifying the joint. The CMC capsule can be incised axially, in line with the joint surface, taking care to preserve the capsular attachments to the trapezium and the base of the first metacarpal. The capsular cut can be made closer to the trapezium since the capsular attachment to the base of the 1.sup.st MC is tenuous. As shown in FIG. 6, a wafer of bone comprising the articular surface is cut from the distal aspect of the trapezium with a suitable cutting member, such as, for example, a microsagital saw. This cut can be flat and made parallel to the scapho-trapezial joint, that is, perpendicular to the long axis of the trapezium. A thin wafer of articular surface can also be cut from the proximal aspect of the base of the first metacarpal (1.sup.st MC).

(50) Next, as shown in FIG. 9A, a trapezial jig 80 is applied to the trapezium 10 with its flat top surface 81 placed against the distal cut surface of the trapezium. The jig 80 can be rigid and may be metallic. The jig 80 has a top segment 80s that merges into a downwardly-extending side segment 80s. The jig 80 can include cutting and drilling guide channels 83 and holding apertures 81a that allow pins, staples, nails, screws, wires and/or sutures to hold the jig 80 in position. The drilling and cutting guide channels 83 can be slots that extend across the top segment 80s down through at least a major portion of the side segment 80s. Although shown with two channels 83, the jig 80 can include one channel or more than two channels, typically corresponding to the number of anchoring members 63 (FIG. 5C). Also as shown, the channels 83 can end at a keyhole 84 that is sized and configured to correspond to a shape that can receive the lower portion of the anchoring member 63. As shown, the shape is circular, and may be sized to be the same or slightly less than the size of the lower portion of the anchoring member 64 for frictional fit thereof.

(51) As shown in FIG. 9B, in some embodiments, a plurality of holding members 82, such as 0.35 or 45 kirschner wires, can be used to secure the jig 80 to the trapezium 10. FIG. 10 illustrates a suitably sized drill bit 85 (e.g., a 3/32 drill bit) with a stop feature can be used to drill the lower anchoring holes 164 (FIG. 11B) for the trapezial implant 60. Referring to FIGS. 11A and 11B, a cutting member 86, such as a microsagital saw, can be used to form bone tunnels or channels 163 that connect the anchoring holes 164 with the distal cut surface 10s of the trapezium to form a prepared implant site 10p as shown in FIG. 11B. The cutting may be done with a knife rather than a saw. Also, the cutting may be done before or after the drilling.

(52) The trapezial jig 80 can be removed and the thumb ray can be extended and adducted to expose the base of the 1.sup.st MC for intramedullary sizing. As shown in FIG. 12, broaches 90 can be inserted to size the 1.sup.st MC. Intramedullary trials 190 (FIG. 22) can be used to select an intramedullary implant 40 or 42 of the desired size. Trapezial trials 100 can also be inserted to establish a suitable trapezium implant 60 size/configuration. As shown in FIG. 13A, the trapezium trials 100a, 100b, 100c (corresponding to different sizes) can be provided as a kit 100. In FIG. 13A, the trials 100a-c do not include the anchoring member(s) 63. However, as shown in FIGS. 13B and 13C, the trials 100a (only one trial is shown) can include at least one relatively thin fin 101 that can fit into the anchoring member channel and act as a post that can inhibit rotation during the trailing (but do not bind or lock into position). The thumb ray is distracted and the space created is sized. A 1.sup.st MC trial 190 (typically without the 1.sup.st MC articulating surface) can be attached to the 1.sup.st MC intramedullary trial. Range of motion is tested. The final implants 42, 45, 60 can be inserted in the following order: 1.sup.st MC intramedullary implant 42, trapezial articulating implant 60, and 1.sup.st MC articulating implant 45. Once positioned, the surgeon can proceed with capsular, muscle and skin closure and can optionally reinforce the capsule with a GRAFT JACKET reinforcement (Wright Medical Technologies). A removable thumb spica splint can be used for support and range of motion can begin early.

(53) FIG. 14 illustrates an exemplary medical kit 125 that can include trial base implants 145, trial trapezium implants 100a, 100b, a selection of different size actual implants 42, 45, 60 (or these may be provided separately in individual sterilized sealed packages) and optionally broaches 90 and/or intramedullary trials 190 (not shown), all in a sterile package or packages. The kit 125 may also include the jig(s) 80, saw 86 and/or drill bit 85 (with or without drill).

(54) FIG. 15 is a flow chart of exemplary operations that can be used to carry out embodiments of the invention. As shown, a trapezium implant can be implanted in a target (prepared) trapezium so that the trapezium defines an articulating surface of a CMC joint in a patient (block 200).

(55) In some particular embodiments, the target trapezium can be prepared for receiving the trapezium implant by planarizing the natural articular surface of the target trapezium (removing a thin wafer), then forming at least one channel in the target trapezium (block 202). Different size trapezium trials can be positioned in the CMC joint to determine a proper size trapezium implant for the patient (block 204).

(56) In some embodiments, before the step of implanting the trapezium implant, a jig with a drilling and cutting channel guide can be temporarily affixed to the trapezium, and at least one channel can be drilled and/or cut into the target trapezium using the jig drilling and cutting channel guide (block 206).

(57) The first metacarpal implant can include an elongate intramedullary stem and an attachable base member with a socket, and before the step of implanting the first metacarpal implant, the method may include trying different size base members to select a base member that substantially fills the CMC cavity (block 208).

(58) FIGS. 16-23 schematically illustrate the steps in an exemplary surgical procedure. FIG. 16 illustrates that a Wagner incision is made. FIG. 17 illustrates that a capsular incision (do not section abductor to thumb). FIG. 18 illustrates the 1st metacarpal articular resection 300 (variable according to space needed) and a minimal trapezium resection 400 to preserve bone for the trapezium implant 60. FIG. 19 illustrates the jig 80 in position (pinned in place) and a drill 85 used to create the anchoring hole 164 for the keel 63. As shown, the drill bit 85 can include a stop collar to inhibit forward movement of the drill into the trapezium at a certain distance. FIG. 20 illustrates the saw 86 for creating the keel shaft 163 in the bone. FIG. 21 shows the thumb adducted and extended for the first metacarpal base exposure and a broach 93 used to (rasp, broach and/or prepare) an intramedullary space for the first metacarpal implant 40. FIG. 22 illustrates the placement of the trapezium trial 100a (with anti-rotational fin 101) and first metacarpal trial 190. A clinician can measure or size the distance or size D of the gap 350 created between the first metacarpal base and the trapezial implant 60, then select the appropriate articulating thickness. As shown, where a separate base member 45 is used, this member 45 can define the articulating thickness. In other embodiments, the entire implant 40 can be selected from a kit to provide the desired thickness.

(59) The foregoing is illustrative of the present invention and is not to be construed as limiting thereof. Although a few exemplary embodiments of this invention have been described, those skilled in the art will readily appreciate that many modifications are possible in the exemplary embodiments without materially departing from the novel teachings and advantages of this invention. Accordingly, all such modifications are intended to be included within the scope of this invention as defined in the claims. In the claims, means-plus-function clauses, if used, are intended to cover the structures described herein as performing the recited function and not only structural equivalents but also equivalent structures. Therefore, it is to be understood that the foregoing is illustrative of the present invention and is not to be construed as limited to the specific embodiments disclosed, and that modifications to the disclosed embodiments, as well as other embodiments, are intended to be included within the scope of the appended claims. The invention is defined by the following claims, with equivalents of the claims to be included therein.