TOTAL WRIST PROSTHESIS AND RELATED METHODS

Abstract

A tool for locating the insertion point of a radial component of a wrist prosthesis on a human distal radius bone, the guide comprising a handle; a guide face attached to the handle, the guide face being of a shape configured to engage an articular surface of the distal radius bone; the guide face comprising three visual cues respectively adapted to align with a palmar corner of a radio-ulnar joint located on the distal radius, a dorsal corner of a radio-ulnar joint located on the distal radius, and a tip of a radial styloid located on the distal radius; the guide face further comprising an opening designating the insertion point, the opening being at a designated location on the guide face relative to the visual cues; and the opening adapted to facilitate the marking of the insertion point on the articular surface of the distal radius bone.

Description

CLAIM OF PRIORITY

This application is a continuation of U.S. patent application Ser. No. 16/566,160 filed Sep. 10, 2019, now U.S. Pat. No. 11,406,507, which is a continuation of U.S. patent application Ser. No. 15/468,223 filed Mar. 24, 2017, now U.S. Pat. No. 10,413,418, which claims the benefit of U.S. Provisional Patent Application Ser. No. 62/312,869 filed on Mar. 24, 2016. The contents of all of the foregoing are incorporated herein by reference.

FIELD OF INVENTION

The invention relates generally to prosthetic implants and in particular to prosthetic implants for use in a total wrist replacement procedure.

BACKGROUND OF THE INVENTION

As shown in FIG. 1, the human wrist consists of a cluster of 8 small bones, the carpal bones, which flexibly connect the metacarpal bones (15, 16, 17, 18, 19), located in the palm, with the ulna (3) and radius (4) located in the forearm. The carpal bones are generally arranged into distal and proximal rows (5,6). The distal row of carpal bones consists of the trapezium (7), trapezoid (8), capitate (9) and hamate (10) bones. The proximal row of carpal bones consists of the scaphoid (11), lunate (12), triquetrum (13), and pisiform (14) bones. In normal operation of a healthy wrist, the articular surface of the radius (15) provides a concave bearing surface which supports the articulation of the scaphoid (11) and lunate (12) as the wrist goes through its range of motion.

Due to injury, degenerative changes, disease (such as arthritis) or other conditions, a person may experience pain, discomfort, or difficulty when operating the wrist through its range of motion. Known procedures for such wrist conditions are to fuse the scaphoid (11) and lunate (12) bones (and possibly other carpal bones) to themselves in a “four corner” fusion, or, in more extreme cases, total wrist arthrodesis, which fuses the radius, some of the carpal bones and one of the metacarpal bones. While these procedures alleviate pain and discomfort, they greatly restrict the range of motion of the wrist resulting in quality of life issues for the patient by limiting the utility of the wrist. In addition, in certain circumstances, because the bones in question are too deteriorated, or, in the case of fractures, not available, fusion is not possible.

In such circumstances, an available treatment is to replace all or some of the carpal bones with a prosthetic wrist in a procedure commonly referred to as a total wrist replacement. Although previous efforts have been made to develop prosthetic wrists, they have met often with disappointing results. Presently available wrist prostheses provide too limited a range of motion, dislocate too easily, place too much stress on bones resulting in failure or fractures, cause complications such as infections, and wear prematurely requiring additional surgeries during the patient's lifetime, among other flaws. In addition, the methods presently used for implanting such prosthetic wrists often result in poorly aligned joints and poor joint performance.

Accordingly, there is a need in the art for a prosthetic wrist, and associated methods for implanting same, which provides a patient with a range of motion that approximates that of a healthy wrist, is long-lasting, provides adequate support for the remaining hand and forearm bones, and avoids many of the drawbacks of existing prosthetic wrists.

SUMMARY OF THE INVENTION

A wrist prosthesis used in a total wrist replacement is disclosed. The wrist prosthesis of the present invention replaces the proximal row of carpal bones and restores wrist function using three separate components—a carpal component, a lunate component, and a radial component. When assembled, the prosthesis attaches to the radius in the forearm and to the trapezoid (optionally), capitate, hamate (optionally), and third metacarpal bones in the hand. The three components of the prostheses, when assembled provide for a wide range of movement between the radial and carpal components.

The radial component of the wrist prosthesis comprises a stein at its proximal end for insertion into and attachment to the radius, and an approximately semi-spherical concave bearing surface, or “dish”, at its distal end for engaging the lunate component. The carpal component of the wrist prosthesis comprises a stein and an alignment pin at its distal end for attachment to the capitate and third metacarpal bones, and a ball end at its proximal end for engaging the lunate component. Some embodiments of the present invention additionally include holes for attachment of the carpal component to the trapezoidal and/or hamate bones.

Interposed between the radial and carpal components is the lunate component which is comprised, in in its radial-facing side, of a semi-sphere which closely matches the geometry of the dish of the radial component. The carpal-facing side of the lunate component is comprised of a cavity that closely matches the geometry of the ball end of the carpal component and allows the lunate component to “snap” onto the ball end of the carpal component. The center of the ball-shaped cavity in the lunate component is slightly offset proximally relative to the center of the outer spherical surface of the lunate component in order to provide a “self-centering” characteristic to the arrangement of components as discussed in greater detail below.

The lunate component is manufactured from a durable yet resilient material, such as ultra-high-molecular-weight polyethylene (“UHMWPE”). The carpal and radial components are manufactured from a high quality surgical-grade metallic alloy such as Cobalt-Chromium-Molybdenum (“CoCrMo”) well known for biomedical applications such as joint replacements. The use of a polyethylene lunate component in cooperation with the CoCrMo carpal and radial components provides various benefits, including (a) avoidance of any metal-on-metal interfaces between moving parts and known complications thereof; (b) self-lubrication of the internal and external interfaces of the lunate component; (c) dampening and absorption of impact loads on the prosthesis; and (d) exceptional durability.

Also disclosed is a method for performing a total wrist replacement using the wrist prosthesis of the present invention. The method includes making an incision in the dorsal side of the wrist and exposing the carpal bones and the articular surface of the radius. Next, the proximal row of carpal bones, namely the scaphoid, lunate, triquetrum, and pisiform bones, are excised. An insertion hole is next drilled in the articular surface of the radius, optionally using a radial alignment tool, and the stein of the radial component is inserted through the insertion hole into the radius. Optionally, the articular surface of the radius may be prepared using a specialized shaping tool prior to insertion of the radial component.

Two holes are next drilled, optionally using a carpal alignment tool; the first, longitudinally through the capitate bone and into the third metacarpal bone to receive the stein of the carpal component, and the second into the central aspect of the capitate to receive the alignment pin of the carpal component. Optionally, the capitate bone may be resized and prepared using a specialized shaping tool prior to insertion of the stein and alignment pin of the carpal component into the capitate and third metacarpal bones. Optionally, the carpal component may be also attached to the hamate and trapezoidal bones through screws inserted into attachment holes in some embodiments of the carpal component.

The carpal-facing cavity end of the lunate component is next “snapped” onto the ball end of the carpal component and the radial-facing end of the lunate component is buttressed against the dish end of the radial component where it is allowed to “float.” Once all of the components are manipulated into correct alignment to permit a range of motion approximating that of a natural wrist, the incision is closed.

Although the invention is illustrated and described herein as embodied in a wrist prosthesis, it is nevertheless not intended to be limited to only the details shown, since various modifications and structural changes may be made therein without departing from the spirit of the invention and within the scope and range of equivalents of the claims. Moreover, many of the principles and techniques discussed in the following description can be applied to prostheses used in other joints in the human anatomy such as the elbow, shoulder, hip, knee or ankle.

The construction of the invention, together with additional objects and advantages thereof will be best understood from the following description of the specific disclosed embodiments when read in connection with the accompanying drawings.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is an illustration of the bones of the human hand provided for reference only and known in the prior art.

FIG. 2 is an exploded orthographic view of the dorsal aspect of the radial, carpal and lunate components of a wrist prosthesis according to the present invention.

FIG. 3 is an assembled view of the dorsal aspect of the radial, carpal and lunate components of a wrist prosthesis according to the present invention.

FIG. 4 is an orthographic distal end view of the radial component of a wrist prosthesis according to the present invention.

FIG. 5 is a side view of the radial component of a wrist prosthesis according to the present invention.

FIG. 6 is a proximal end view of the radial component of a wrist prosthesis according to the present invention.

FIG. 7 is an orthographic view from the dorsal side of the carpal component of a wrist prosthesis according to the present invention which, optionally, includes two wings and attachment holes for the hamate and trapezoidal bones.

FIG. 8 is an orthographic view from the palmar side of the carpal component of a wrist prosthesis according to the present invention.

FIG. 9 is an orthographic cross-sectional view of the carpal component of a wrist prosthesis of FIG. 8 according to the present invention.

FIG. 10 is an orthographic view of the lunate component of a wrist prosthesis according to the present invention.

FIG. 11 is a top view of the lunate component of a wrist prosthesis according to the present invention.

FIG. 12 is a side view of the lunate component of a wrist prosthesis according to the present invention.

FIG. 13 is a cross-sectional view of the lunate component of a wrist prosthesis according to the present invention.

FIG. 14 is a cross-sectional assembled view of the carpal, lunate, and radial components of a wrist prosthesis according to the present invention.

FIG. 15 is a detail of a cross-sectional view of the assembled lunate and carpal components of a wrist prosthesis according to the present invention.

FIGS. 16A, 16B, and 16C are a sequence of views of the carpal, lunate and radial components illustrating their relative motion through an exemplary range of motion of a wrist prosthesis according to the present invention.

FIG. 17 illustrates an embodiment of the wrist prosthesis of the present invention implanted on a human hand with the surrounding skeletal anatomy, represented as semi-transparent structures, shown for reference only.

FIG. 18 is an orthographic view of a radial drilling guide alignment tool in accordance with the present invention.

FIG. 19 is an orthographic view of a radial dish guide tool in accordance with the present invention.

FIG. 20 is an orthographic view of a radial dish reamer tool in accordance with the present invention.

FIG. 21 is an orthographic view of a keel punch in accordance with the present invention.

FIG. 22 is an orthographic view of a capitate long axis guide in accordance with the present invention.

FIG. 23 is an orthographic view of a stop reamer and planer in accordance with the present invention.

FIG. 24 is an orthographic view of a capitate shaper in accordance with the present invention.

DETAILED DESCRIPTION OF THE INVENTION

FIG. 2 is an exploded orthographic view of the three components of a wrist prosthesis (1) according to the present invention. As shown, the lunate component (300) is interposed between the radial component (100) and the carpal component (200). FIG. 3 shows an assembled view of the three components from the same perspective.

Referring next to FIG. 4, shown is an orthographic representation of a radial component (100) according to the present invention. FIGS. 5 and 6 respectively provide side and proximal end views of the radial component (100) and illustrate all details thereof. As shown in FIG. 4, the radial component (100) is comprised of a proximal end (112) and a distal end (110). Stein (114) is projected in the direction of the proximal end and is adapted for insertion through the articular face of the radius and for penetration into the medullary canal of the radius. The stein of the radial component may optionally include flutes (116) and/or a roughened surface finish, such as titanium plasma spray (“TPS”) coating, to promote post-operative bone growth for more permanent fixation after healing, and to prevent rotation of the component in the bone. The distal end of the radial component provides a distally facing concave dish (118) which is adapted to receive the convex portion (301) (shown in FIGS. 10, 11, 12 and 13) of the lunate component (300) upon assembly of the prosthesis, as described in detail below.

The internal surface (120) of dish (118) is a substantially spherically concave section which closely matches the geometry of the convex portion of the lunate component (300). In some embodiments of the radial component (100), the spherical section defined by the internal surface (120) of dish (118) is less than half of a full sphere. The dish optionally includes one or more lip extensions (122) which provide additional rotational support area for the lunate component (300) which could be beneficial to provide for maximum flexing of the assembled prosthesis without dislocation of the lunate component (300).

To provide optimal alignment between the various components and the surrounding anatomy, stein (112) is arranged with respect to dish (118) so that the longitudinal axis (124) of stein (114) forms an angle (126) of between approximately 60 and 80 degrees with respect to an imaginary line (128) coplanar with the edge (130) of dish (118). In addition, stein (114) is offset laterally with respect to the center of dish (118) so that longitudinal axis (124) of the stein (114) intersects the internal surface (120) of dish (118) approximately tangentially. The external, bone contacting, surface (132) of dish (118) can optionally be spherical or other shape that conforms to the articular face of the radius bone.

An additional optional feature of radial component (100) is keel (134) which buttresses the junction between stein (114) and dish (118). In addition to providing structural support to dish (118), keel (134) minimizes the possibility of radial component (100) rotating about longitudinal axis (124) after insertion into the radius. Furthermore, keel (134) acts as a wedge creating a tighter fit between the radius bone and stein (114). Keel (134) may have a sharp edge to facilitate penetration into the radius bone. Additionally, keel (134) may be of solid construction (as shown) or may be hollow, to provide a dual edge for penetration of the radius bone and allows bone material to become wedged in the inner space of keel (134).

Radial component (100), in one embodiment of the present invention, is manufactured from a high quality surgical-grade metallic alloy, such as CoCrMo well known for biomedical applications such as joint replacements. However, titanium or other metallic or non-metallic materials are also suitable for this component in alternative embodiments.

Referring next to FIG. 7, shown is an orthographic representation of a carpal component (200) according to the present invention. FIG. 8 shows a side view of the carpal component (200) and FIG. 9 shows a cross section of the carpal component (200).

With reference to FIG. 7, the distal end (201) of the carpal component (200) is comprised of a stein (204) which is adapted to penetrate into the third metacarpal bone, preferably into the medullary canal of the third metacarpal bone. The stein of the carpal component may optionally include flutes (206) and/or a roughened surface finish to promote post-operative bone growth for more permanent fixation after healing, and to prevent rotation of the component in the bone. The carpal component also comprises alignment pin (208), in generally parallel alignment with stein (204), which is adapted to penetrate into the central aspect of the capitate bone. The purpose of alignment pin (208) is to minimize the possibility of rotation of carpal component (200) about longitudinal axis (210) of stein (204) after implantation. Carpal component (200) may also, optionally, include one or more wings (212T), (212H) which are positioned for anatomical alignment with the trapezoid (8) and hamate (10) bones and provide additional buttressing support for carpal component (200) against said bones. Wings (212T), (212H) may optionally also include fastener holes (213T), (213H) for securing wings (212T) (212H) to the trapezoid (8) and hamate (10) bones using fasteners ((215) in FIG. 9.

As best observed in FIG. 9, the stein (204) and alignment pin (208) of the carpal component terminate in cap (216) which is a concave structure with respect to distal end (202) of the carpal component. Alignment pin (208) terminates at or near the center (218) of the internal surface (220) of cap (216), while stein (204) is offset dorsally with respect to alignment pin (208) and terminates at the edge of cap (216). The internal surface (220) of cap (216) is adapted to contact, and optionally encapsulate, the capitate bone upon implantation into the patient's hand.

The proximal end (202) of carpal component (200) comprises ball end (222) with a diameter (223) which is connected to cap (216) through neck region (224). Ball end (222) is a semi-complete (between 70% and 97% in the disclosed embodiment but in any event greater than 50% of a sphere) sphere with its center in substantially direct longitudinal alignment with the center of cap (216) and the longitudinal axis (226) of alignment pin (208). The ball end (222) and neck region (224) closely complement the geometry of corresponding features in the lunate component (300) as discussed in more detail below.

Like radial component (100), carpal component (200), in one embodiment of the present invention, is manufactured from a high quality surgical-grade metallic alloy such as “CoCrMo” well known for biomedical applications such as joint replacements. However, titanium or other metallic or non-metallic materials may also be suitable for this component.

Referring next to FIG. 10, shown is an orthographic representation of a lunate component (300) according to the present invention. FIGS. 11 and 12 illustrate, respectively, top and side views of the lunate component (300). FIG. 13 is a cross sectional view, enlarged for clarity, of the lunate component (300) which, as evident from all views, is radially symmetrical.

As shown in FIGS. 10-13, the external surface (301) of lunate component (300), which is adapted to interface with the internal surface (120) of dish (118) of radial component (100) (see FIGS. 4-6), approximately defines a half-sphere. However, alternative embodiments need not necessarily define a half-sphere. Alternative embodiments of lunate component (300) could define an external surface that is greater than half of a sphere, or smaller than half of a sphere, it being understood that the greater the external surface is, the lower the possibility will be of dislocation of the lunate component (300) with respect to radial component (100).

Referring now to FIG. 10 through FIG. 13, lunate component (300) includes a cavity (302) comprised of a spherical region (304) and a shoulder region (306). The spherical region (304) of cavity (302) in all embodiments comprises more than a half-sphere so that the diameter of the “mouth” (308) of the spherical region (304) is narrower than the diameter (310) of the spherical region (304) and also narrower than the diameter (223) of ball end (222) of carpal component (200). Also, the diameter (310) of the spherical region (304) is somewhat larger than the diameter (223) of the ball end (222) of carpal component (200) as to provide sufficient clearance for the ball end of the carpal component to rotate freely within the spherical region (304). The shoulder region (306), in turn, gradually widens away from the spherical region (304) to form a funnel-like toroidal structure atop the lunate component. The spherical and shoulder regions of cavity (302) closely match the geometry of the ball end (222) and neck region (224) of carpal component (200) (See FIGS. 7-9).

Lunate component (300) is manufactured from a durable yet resilient material, such as “UHMWPE”, or other surgical grade resilient material.

Referring next to FIG. 14 and FIG. 15 therein are shown cross-sectional views of the carpal (200), lunate (300) and radial (100) components of the wrist prosthesis (1) of the present invention, upon assembly. As will be noted, since the mouth (308) of spherical region (304) of cavity (302) of the lunate component (300) is narrower than the diameter (223) of the ball end (222) of the carpal component (200), in order to assemble the carpal and lunate components, ball end (222) must be forced into cavity (302) until it snaps into place. That is, the lunate component is briefly deformed but immediately snaps back to its original shape retaining the ball end (222) within its cavity (302). Once in place, however, the lunate component is held securely with respect to the carpal component but the two components freely rotate and swivel with respect to each other.

Shown in FIG. 15 is a detail of the cross sectional view of the assembled lunate component (300) and carpal component (200). As is shown in this view, the center (402) of ball end (222) and the center (400) of the external surface (301) of the lunate component (300) are not coincident. Instead the center (402) of ball end (222) is offset proximally relative to the center (400) of the external surface (301) in the proximal-distal direction by a distance (404) of between 1 and 10 mm. This offset achieves two objectives. First, it minimizes the chance of the lunate and carpal components accidentally separating. By embedding cavity (302) deeper into the lunate component (300), the leverage caused at the limits of flexion will not cause the ball end to be dislodged. Second, the offsets provides the lunate-carpal coupling self-centering characteristics which ensure that through a series of flexions of the prosthesis the lunate component will be urged towards its neutral position, instead of remaining in an extreme position.

The self-centering characteristic of the lunate component is due to the fact that when the center (402) of the ball end (222) is offset proximally with respect to the center (400) of external surface (301) of the lunate component, the moment imparted on the lunate component by the natural normal load forces on the wrist is always greater, and in the center-biased direction, than the moment imparted on the lunate component by rotational frictional forces, which is non-centering. The greater the offset distance (404) between the two centers (400,402), the greater the imbalance between the two moments and the stronger the self-centering tendency.

Referring again to FIG. 14, the lunate component (300), “floats” on top of the dish (118) of the radial component (100) and similarly freely rotates and swivels about the center of the dish (118). The two separate rotational pairings (carpal-lunate and lunate-radial) are independent of each other providing exceptional freedom of movement and flexibility in the prosthesis. Moreover, the interface between the UHMWPE and CoCrMo is naturally self-lubricating and provides exceptional smoothness and comfort in rotational and swiveling motions. It is noted, however, that the frictional torque between the lunate component (300) and the dish (118) of the radial component (100) is greater than the frictional torque between the ball end (222) of the carpal component (200) and the lunate component (300). Therefore, rotation will occur primarily in the carpal-lunate interface. Lunate-radial rotation will generally occur after a limit of rotation has been reached in the carpal-lunate interface, such as when the neck region (224) of the carpal component (200) comes into contact with the shoulder region (306) of the lunate component (300).

Shown in FIGS. 16A, 16B, and 16C is an exemplary sequence of relative movements between the carpal, lunate and radial components. Beginning with FIG. 16A, the carpal (200), lunate (300) and radial (100) components are in a neutral position. As upward force “F” is applied to the carpal component (200), the carpal component begins to rotate in a clockwise direction with respect to the lunate component (300). Because the frictional torque between the carpal and lunate components (200, 300) is less than that between the lunate and radial components (300, 100), there will be very little, if any, relative motion between the lunate (300) and radial (100) components at this phase.

This movement continues until, as shown in FIG. 16B, neck region (224) of the carpal component (200) comes into contact with shoulder region (306) of the lunate component (300). At this point, if upward force F continues to be applied to carpal component (200), the carpal and lunate components will begin to rotate together relative to the radial component (100) in a clockwise direction about the center (400) of the of the external surface (301) of the lunate component (300) as shown in FIG. 16C.

If a downward force is applied at this point to carpal component (200), a similar sequence (not shown) will be repeated in the opposite direction with relative counterclockwise motion first occurring between the carpal and lunate components (200, 300) until a limit of motion is reached and then with the carpal and lunate components (200, 300) moving in tandem in the counterclockwise direction relative to the radial component (100).

Illustrated in FIG. 17 is an embodiment of the disclosed wrist prosthesis (1) shown with the surrounding skeletal anatomy for reference. Shown in dotted contour and transparent for clarity are the bones wherein the wrist prosthesis is implanted: The radius (4), the third metacarpal (17), the trapezoid (8), the lunate (9) and the hamate (10). The proximal row of carpal bones, namely the scaphoid, lunate, triquetrum, and pisiform bones are not shown, having been excised surgically as further explained below.

In addition to the above-disclosed prosthetic wrist, a method for surgically implanting same on a human patient is disclosed. The method includes the following basic sequence of steps:

An incision is made longitudinally on the dorsal side of the affected wrist and skin, muscle and tendons are retracted to expose the carpal bones and the distal end of the radius, including its articular surface.

The proximal row of carpal bones, namely the scaphoid, lunate, triquetrum, and pisiform bones, are excised, exposing the proximal articular surface of the second row of carpal bones, primarily the capitate and hamate bones.

Each of the lunate (300), carpal (200) and radial (100) components are optionally provided in one or more sizes. The proper size of each component is dictated by the patient's anatomy. Optionally, this proper sizing may be accomplished during surgery by selecting and pre-assembling various sizes of equivalent modeling versions (not shown) of each of those components.

An insertion hole is drilled near the center of the articular surface of the distal radius, optionally using a radial sizing/alignment tool for precise location of the hole. The optional radial sizing/alignment tool (500) is shown in FIG. 18. The radial sizing/alignment tool (500) includes visual cues (502, 504, 506) which can be matched- to the palmar and dorsal corners of the radio-ulnar joint, and the tip of the radial styloid, on the articular surface of the distal radius. Once the tool is properly placed, the center of circle (508) marks the spot where the radius should be drilled to insert the stein (114) of the radial component (100). The drilled hole is then reamed to the proper size.

The stein (114) of the radial component (100) is then inserted through the previously drilled hole into the radius until the leading tip of keel (134) contacts the articular surface. The precise orientation of the radial component (100) may be optimized prior to insertion by using an optional radial dish guide tool (550) shown in FIG. 19. The stein (552) of the radial dish guide tool (550) is inserted into the hole drilled into the articular surface of the radius and is then rotated until the outer edge of ring (554) is centered on the articular surface of the radius. A k-wire (not shown) is then inserted through orifice (556) and the radial dish guide tool (550) is removed. The location of the k-wire marks the center of dish (118).

Optionally, the articular surface of the radius may be prepared to receive the radial component (100) by shaping the articular surface of the radius to match the external surface (132) of the dish (118) of the radial component (100). This is accomplished by using the optional radial dish reamer tool (570) shown in FIG. 20. The radial dish reamer tool orifice (572) is inserted over the k-wire placed in the previous step and the articular surface of the radius is then reamed until the cutting flutes (574) of the radial dish reamer tool (570) are flush with the radial edge of the articular surface of the radius. The k-wire can then be removed from the articular surface of the radius.

The radial component (100) is then tapped into the radius with a surgical mallet until external surface (132) of the dish (118) of the radial component (100) makes full contact with the articular surface of the radius, further embedding stein (114) and keel (134) in the radius and locking the radial component in place. The articular surface of the radius may optionally be prepared for insertion of keel (134) by using optional keel punch (580) shown in FIG. 21. This step concludes the placement of the radial component (100).

Next, the long axis of the capitate bone is identified for placement of the carpal component (200). This may optionally be accomplished by using the capitate long axis guide (600) shown in FIG. 22. The guide (600) is placed on the third metacarpal bone and slid distally until ring (602) is flush with the proximate pole of the capitate bone. Next, a k-wire is inserted through orifice (604) of the guide and into the capitate bone. Guide (600) is then removed leaving the k-wire in place. Alignment of the k-wire may be confirmed using fluoroscopy.

As needed, the capitate bone may be shortened by using the optional stop reamer (620) shown in FIG. 23 over the k-wire inserted in the previous step. Next, the capitate bone is optionally prepared to receive the carpal component (200) by shaping the proximal articular surface of the capitate bone to match the internal surface (220) of cap (216) of the carpal component (200). This can be accomplished by using the optional capitate shaper (640) shown in FIG. 24. The orifice (642) of the capitate shaper (640), attached to a drill (not shown), is inserted over the k-wire placed in the previous step. The blades (644) are then used to shape the capitate bone to receive the carpal component (200).

Next, a first hole is drilled into the capitate using the previously inserted k-wire. The first hole is reamed to the appropriate size to accept the alignment pin (208) of the carpal component and the k-wire is removed.

A second hole is next drilled into the third metacarpal bone in longitudinal tangential alignment with the dorsal aspect of the capitate. The offset between the firs and second holes matching the distance between the stein (204) and alignment pin (208) of the carpal component (200).

The alignment pin (208) and stein (204) of the carpal component (200) are then inserted into the first and second holes respectively until stein (204) is in the medullary canal of the third metacarpal bone and cap (216) makes contact with the capitate bone.

The carpal component is then tapped into the capitate bone with a surgical mallet until the capitate bone is fully encapsulated by cap (216). If the carpal component is equipped with optional wings (212H, and/or 212T), the wings should be positioned directly against the hamate and/or trapezoidal bones and can be secured using screws (251) through holes (213H, and/or 213T). Any gap between wings (212H, and/or 212T) and the hamate and/or trapezoidal bones may be filled with bone graft.

The lunate component (300) is next “snapped” onto the ball end (222) of the carpal component (200) through cavity (302) and the surgeon verifies that the carpal and lunate components are securely attached but freely swivel and rotate with respect to each other.

The external surface (301) of the lunate component is then buttressed against the dish (118) of the radial component (100) where it is allowed to “float.” Again, the surgeon verifies that the lunate component (300) is free to rotate and swivel on the dish (118) of the radial component (100).

The surgeon then tests for correct operation of the prosthesis by manipulating and flexing the patient's hand through the range of natural wrist motion and observing proper alignment.

After any remaining alignment issues are corrected and satisfactory range of motion is achieved by the surgeon the incision is closed using standard surgical techniques.

Although described above in connection with a prosthetic wrist, these descriptions are not intended to be limiting, as other prosthetic joints can be made in accordance with the description herein, and applied to different parts of the body such as elbows, shoulders, hips, knees and ankles. As such, although the invention is illustrated and described herein, various modifications and structural changes may be made therein without departing from the spirit of the invention and within the scope and range of equivalents of the claims.

Claims

1. A tool for locating the insertion point of a radial component of a wrist prosthesis on a human distal radius bone, the guide comprising:

a handle;

a guide face attached to the handle, the guide face being of a shape configured to engage an articular surface of the distal radius bone;

the guide face comprising first, second, and third visual cues;

the first visual cue adapted to substantially align with a palmar corner of a radio-ulnar joint located on the distal radius;

the second visual cue adapted to substantially align with a dorsal corner of a radio-ulnar joint located on the distal radius;

the third visual cue adapted to substantially align with a tip of a radial styloid located on the distal radius;

the guide face further comprising an opening designating the insertion point, the opening placed at a location on the guide face relative to the visual cues; and

the opening adapted to facilitate the marking or drilling of the insertion point on the articular surface of the distal radius bone.