Abstract
A bone joint repair and replacement assembly. A first portion comprising a bone plate is configured to attach to a distal or proximal end of a bone proximate the joint, generally coaxially with an axis defined by the bone. A second portion comprising an articular surface is configured to attach to the first portion, generally normal with respect to the axis, and inserted into the joint. Although versions of the assembly can be configured for use with several different pivotal joints, the invention is particularly suitable for full or partial replacement of an elbow, wherein the articular surface is pivotally attached to the first portion. Another embodiment of the invention is provided to repair a fractured bone head proximate the joint, and still another embodiment of the invention is provided to repair rotator cuff-related shoulder injuries.
Claims
1. A method of partially replacing a portion of a distal humerus in an elbow joint of a patient, comprising: providing a plate portion configured for attachment to a distal end of a humerus, the plate portion having a first mid-longitudinal axis, a first end along the first mid-longitudinal axis, an opposite second end along the first mid-longitudinal axis, a maximum length between the first end and the second end along the first mid-longitudinal axis, a maximum width perpendicular to the maximum length along the first mid-longitudinal axis, a first plate portion extending from the first end toward the second end, and a first lobe portion and a second lobe portion each extending from the first plate portion, the first lobe portion and the second lobe portion being spaced apart to define a yoke portion for receiving an articular portion, the first lobe portion terminating in a first end portion, the second lobe portion terminating in a second end portion, the first end portion and the second end portion being spaced apart at the maximum width of the plate portion; providing the articular portion configured for attachment between the first end portion of the first lobe portion and the second end portion of the second lobe portion, the articular portion including a first end, an opposite second end, a second mid-longitudinal axis extending through the first end and the second end of the articular portion, and an exterior surface approximating at least a portion of a natural articular surface of a distal humerus, the first end of the articular portion being positionable at least adjacent a first interior surface of the first end portion of the first lobe portion, and the second end of the articular portion being positionable at least adjacent a second interior surface of the second end portion of the second lobe portion; attaching the plate portion to a distal end of a humerus of the patient, the plate portion being oriented generally coaxially with a longitudinal axis defined by the patient's humerus; attaching the articular portion between the first end portion of the first lobe portion and the second end portion of the second lobe portion with the second mid-longitudinal axis being generally transverse to the longitudinal axis defined by the patient's humerus; and positioning a portion of the articular portion in a naturally-occurring trochlear notch of a proximal ulna of the patient's elbow joint; wherein portions of the exterior surface of the articular portion include an artificial capitellum sized and shaped to replace a natural capitellum and an artificial trochlea sized and shaped to replace a natural trochlea of the patient's elbow joint, the artificial trochlea being configured to contact portions of the naturally-occurring trochlear notch of the proximal ulna of the patient's elbow joint when the portion of the articular portion is positioned in the naturally-occurring trochlear notch of the patient's elbow joint.
2. The method of claim 1, wherein the articular portion is pivotally attached between the first and second lobe portions of the yoke portion.
3. The method of claim 1, wherein attaching the plate portion to the distal end of the patient's humerus comprises attaching the first portion of the plate portion to the distal end of the patient's humerus.
4. The method of claim 3, wherein the first portion of the plate portion includes a proximal end and an opposite distal end, and each of the first and second lobe portions includes a proximal end and an opposite distal end, the proximal ends of the first and second lobe portions being attached to the distal end of the first portion of the plate portion.
5. The method of claim 4, wherein the first lobe portion includes a first lobe mid-longitudinal axis and the second lobe portion includes a second lobe mid-longitudinal axis, the first and second lobe mid-longitudinal axes being arranged at an acute angle with respect to one another.
6. The method of claim 5, wherein the first end portion of the first lobe portion includes a first aperture therein, the second end portion of the second lobe portion includes a second aperture therein, the first and second apertures being configured to receive at least one fastener inserted therethrough to facilitate attachment of the articular portion between the first end portion of the first lobe portion and the second end portion of the second lobe portion.
7. A partial elbow replacement assembly, comprising: a plate portion having a first mid-longitudinal axis, a first end along the first mid-longitudinal axis, an opposite second end along the first mid-longitudinal axis, a maximum length between the first end and the second end along the first mid-longitudinal axis, a maximum width perpendicular to the maximum length along the first mid-longitudinal axis, a first plate portion extending from the first end toward the second end, and a first lobe portion and a second lobe portion each extending from the first plate portion, the first lobe portion and the second lobe portion being spaced apart to define a yoke portion for receiving an articular portion, the first lobe portion terminating in a first end portion, the second lobe portion terminating in a second end portion, the first end portion and the second end portion being spaced apart at the maximum width of the plate portion; and an articular portion configured for attachment between the first end portion of the first lobe portion and the second end portion of the second lobe portion, the articular portion including a first end, an opposite second end, a second mid-longitudinal axis extending through the first end and the second end of the articular portion, and an exterior surface approximating at least a portion of a natural articular surface of a distal humerus, the first end of the articular portion being positionable at least adjacent a first interior surface of the first end portion of the first lobe portion, and the second end of the articular portion being positionable at least adjacent a second interior surface of the second end portion of the second lobe portion; wherein portions of the exterior surface of the articular portion include portions of an artificial capitellum sized and shaped to replace a natural capitellum and an artificial trochlea sized and shaped to replace a natural trochlea of a patient's elbow joint, the artificial trochlea configured to contact portions of a naturally-occurring trochlear notch of a proximal ulna of the patient's elbow joint when a portion of the articular portion is positioned in the naturally-occurring trochlear notch.
8. The partial elbow replacement assembly of claim 7, wherein the articular portion is pivotally attached to the first end portion of the first lobe portion and the second end portion of the second lobe portion.
9. The partial elbow replacement assembly of claim 8, wherein the first lobe portion of the plate portion includes a first lobe mid-longitudinal axis and the second lobe portion of the plate portion includes a second lobe mid-longitudinal axis, the first and second lobe mid-longitudinal axes being arranged at an acute angle with respect to one another.
10. The partial elbow replacement assembly of claim 9, wherein the first end portion of the first lobe portion includes a first aperture therein, the second end portion of the second lobe portion includes a second aperture therein, the first and second apertures being configured to receive at least one fastener inserted therethrough to facilitate attachment of the articular portion between the first end portion of the first lobe portion and the second end portion of the second lobe portion.
11. A partial elbow replacement assembly, comprising: a plate portion being configured for attachment relative to a humerus, the plate portion having at least a first lobe portion and a second lobe portion extending outwardly from the remainder of the plate portion, each of the first lobe portion and the second lobe portion including a proximal end and an opposite distal end, the first lobe portion terminating in a first end portion at and adjacent the second end thereof, the second lobe portion terminating in a second end portion at and adjacent the second end thereof, the first lobe portion and the second lobe portion being spaced apart to form a yoke portion for receiving an articular portion; and an articular portion configured for attachment between the first end portion of the first lobe portion and the second end portion of the second lobe portion, respectively, the articular portion including a first end, an opposite second end, a first mid-longitudinal axis extending through the first end and the second end of the articular portion, and an exterior surface approximating at least a portion of a natural articular surface at a distal end of the humerus; wherein portions of the exterior surface of the articular portion include portions of an artificial capitellum sized and shaped to replace a natural capitellum and an artificial trochlea sized and shaped to replace a natural trochlea of a patient's elbow joint, the artificial trochlea being configured to contact portions of a naturally-occurring trochlear notch of a proximal ulna of the patient's elbow joint when a portion of the articular portion is positioned in the naturally-occurring trochlear notch.
12. The partial elbow replacement assembly of claim 11, wherein the articular portion is pivotally attached to the first end portion of the first lobe portion and the second end portion of the second lobe portion.
13. The partial elbow replacement assembly of claim 12, wherein the first lobe portion includes a first lobe mid-longitudinal axis and the second lobe portion includes a second lobe mid-longitudinal axis, the first and second lobe mid-longitudinal axes being arranged at an acute angle with respect to one another.
14. The partial elbow replacement assembly of claim 13, wherein the first end portion of the first lobe portion includes a first aperture therein, the second end portion of the second lobe portion includes a second aperture therein, the first and second apertures being configured to receive at least one fastener inserted therethrough to facilitate attachment of the articular portion between the first end portion and the second end portion of the plate portion.
15. The partial elbow replacement assembly of claim 11, wherein, after receipt of the articular portion within the naturally-occurring trochlear notch of the proximal ulna, the articular portion is pivotal with respect to the plate portion.
16. The partial elbow replacement assembly of claim 15, wherein, after receipt of the articular portion within the naturally-occurring trochlear notch of the proximal ulna, portions of the proximal ulna are received between the first lobe portion and the second lobe portion.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1) FIG. 1 is a perspective view of a first component of an elbow replacement assembly in accordance with the present invention;
(2) FIG. 2 is a perspective exploded-parts view of an elbow replacement assembly in accordance with the present invention;
(3) FIG. 3 is a perspective view of a fully-assembled elbow replacement assembly depicted in FIG. 2;
(4) FIG. 4 is a perspective exploded-parts view of a partial elbow replacement assembly in accordance with the present invention;
(5) FIG. 5 is a side view of an assembled partial joint replacement assembly in accordance with the invention pivotally mounted in a trochlear notch of an ulna;
(6) FIG. 6 is a rear perspective view of a bone joint repair implant assembly in accordance with the present invention;
(7) FIG. 7 is a side view of the bone joint repair implant assembly of FIG. 6 mounted in a bone joint;
(8) FIG. 8 is a front perspective view of the bone joint repair implant assembly of FIG. 6;
(9) FIG. 9 is a rear perspective view of another embodiment of a bone joint implant in accordance with the present invention;
(10) FIG. 10 is a front perspective view of the bone joint repair implant assembly of FIG. 9;
(11) FIG. 11 is a side view of the bone joint repair implant assembly of FIG. 9 mounted in a bone joint;
(12) FIG. 12 is a perspective view of a proximal head of a bone, e.g., a radius;
(13) FIG. 13 is a perspective view of a proximal head of a bone, e.g., a radius fractured into a plurality of bone fragments;
(14) FIG. 14 is a perspective view of one embodiment of a bone repair assembly for a fractured head of a bone, e.g., a radius in accordance with the present invention;
(15) FIG. 15 is a side cross-sectional view of the bone repair assembly of FIG. 14;
(16) FIG. 15A is a side cross-section view of another embodiment of a bone repair assembly for a fractured head of a bone, e.g., a radius, in according with the invention;
(17) FIG. 16 is a perspective view of a bone repair assembly in accordance with the present invention installed on a fractured proximal head of a bone, e.g., a radius;
(18) FIG. 17 is a side view broadly depicting heads of a plurality of bones cooperating to define a shoulder joint;
(19) FIG. 18 is a perspective view of a proximal end of a humerus and a humeral head, with a damaged portion on a surface thereof resulting from rotator cuff arthropathy;
(20) FIG. 19 is a perspective view of a shoulder joint rotator cuff repair assembly in accordance with the invention, in contact with the proximal end of the humerus and the humeral head of FIG. 18;
(21) FIG. 20 is a side partial cross-sectional view of the shoulder joint of FIG. 18, with the shoulder joint rotator cuff repair assembly in accordance with the invention attached to the proximal end and humeral head thereof.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
(22) Reference will now be made in detail to the present preferred embodiments of the invention, example of which are illustrated in the accompanying drawings. Wherever possible, the same reference numbers will be used throughout the drawings to refer to the same or like parts.
(23) An exemplary embodiment of an elbow replacement assembly of the present invention is shown in FIGS. 1-3, and designated generally by reference numeral 10. As embodied herein, and referring to FIGS. 1-3, the elbow replacement assembly 10 includes a first component 12. The first component 12 includes a plate portion 14, which is configured with a rear arcuate face 16, and at least one aperture 18, dimensioned for insertion therethrough of appropriate fasteners, for attachment of the plate portion 14 to a distal end of a humerus. First component 12 further includes a generally annular first lobe 20, defining a first aperture 22 therein, and a generally annular second lobe 24, spaced from the first lobe 20, defining a second aperture 26 therein.
(24) Referring to FIGS. 1-3, the elbow replacement assembly 10 further includes a second component 28. Second component 28 includes a generally annular head portion 30, defining a third aperture 32 therein. The head portion 30 inserts between the first and second annular lobes 20 and 24, such that the apertures 22, 32, and 26 substantially align with one another to define a channel. Annular bushings or washers 31 and 33 also may be inserted in the aligned channel. A pivot pin 34 inserts into the channel to define a pivotal hinge. The second component 28 also includes a tapering tip portion 36, projecting away from the head portion 30. The tip portion 36 is configured to be inserted in a medullary cavity of an ulna associated with the elbow. Alternately, rather than including the tip portion 36 for insertion into the medullary cavity of the ulna, the second component could include a plate portion projecting away from the head portion 30. Such a plate portion could be configured for attachment to the exterior of the ulna.
(25) Replacement of an elbow with the elbow replacement assembly of FIGS. 1-3 includes surgically preparing the elbow for implant of the elbow replacement assembly 10; attaching the plate portion 14 to a respective distal end of a humerus substantially coaxially with an axis A-A′ defined by the humerus, with first and second spaced annular lobes 20 and 24 extending proximate the distal end of the humerus; inserting annular head 30 between the first and second lobes 20 and 24; inserting the pivot pin 34 into the channel defined by the aligned apertures 22, 32, and 26 to define a pivotal hinge; and inserting the tip portion 36 in the medullary cavity of the ulna associated with the elbow, thereby defining a complete elbow replacement assembly.
(26) An exemplary embodiment of a partial elbow replacement assembly in accordance with the invention is shown in FIGS. 4-5, and is designated generally by reference numeral 40. A partial elbow replacement also is disclosed in U.S. application Ser. No. 13/282,810, the contents of which are incorporated herein by reference. As broadly embodied in FIGS. 4-5, the partial elbow replacement assembly 40 includes a bone plate 42, configured for attachment to a distal end of a humerus, substantially coaxially with an axis A-A′ defined by the humerus. A distal end of bone plate 42 proximate the elbow joint separates into first and second spaced-apart lobes 43 and 44, defining a yoke portion 46. An artificial prosthetic articular portion 48 is pivotally attachable with a pivot pin (not shown) between the first and second lobes 43 and 44 through an aperture 49 formed in the prosthetic articular portion 48, at an angle α generally transverse to the axis A-A′. Preferably, prosthetic articular portion 48 is made of a relatively strong, corrosion-resistant metal, e.g., titanium, or a suitable strong, corrosion-resistant nickel-alloy.
(27) As broadly embodied in FIGS. 4 and 5, the prosthetic articular portion 48 is configured to replace at least one of a natural capitellum and trochlea associated with the distal end of the humerus in the elbow. The prosthetic portion 48 includes an artificial capitellum portion 49a and an artificial trochlea portion 49b. In addition, as depicted in FIG. 5, the prosthetic articular portion 48 is configured to pivot in a trochlear notch 50 of the ulna, and articulate with respect to a radial head 52 of the radius. In doing so, the prosthetic articular portion 48 serves as a portion of the ulnotrochlear joint and a portion of the radiocapitellar joint.
(28) An exemplary embodiment of a bone joint repair implant assembly in accordance with another aspect of the present invention is depicted in FIGS. 6-8, and designated generally by the reference numeral 60. As broadly embodied in FIGS. 6-8, bone joint repair implant assembly 60 includes a first portion 62 defining a plate portion 64, configured with a plurality of apertures 65 dimensioned to receive fasteners 66 (FIG. 6) therethrough for attachment of the plate portion 64 to a neck of a respective bone proximate either a distal end of the bone, or a proximal end of the bone, depending on the particular joint to which the bone joint repair implant assembly 60 is to be attached. The respective bone defines an axis A-A′, and the plate portion 64 is positioned substantially coaxially with the axis A-A′ proximate the respective joint.
(29) Referring to FIGS. 6-8, the bone joint repair implant assembly 60 further includes a second portion 68 attached to an end portion 67 of the plate portion 64, at an angle α generally normal to the axis A-A′. The second portion 68 is configured to extend into the joint to define an articular surface 70. Articular surface 70 is made of a metal such as titanium, or another suitable bone implant material. As further embodied in FIGS. 6 and 8, in the case of a wrist implant, the articular surface 70 comes into contact with a surface of a volar capsule 75. Preferably, a plurality of openings 73 are defined in the plate portion 64 at the end portion 67. The openings 73 allow for repair of the volar capsule 75 to, for example, bone of a distal end of a radius.
(30) Preferably, bone joint repair implant assembly 60 includes an articular surface support. As broadly embodied in FIGS. 7-8, the articular surface support is defined by a buttress 72 inserted between the first portion 62 and the second portion 68, to provide support to the articular surface 70.
(31) Referring to FIG. 7, because of the need to implant the buttress 72, one of ordinary skill in the art will understand that implantation of bone joint repair assembly 60 requires additional surgical preparation of the end of the respective bone proximate the joint prior to attachment of the implant.
(32) FIGS. 9-11 broadly depict an alternate embodiment 60a of the bone joint repair implant assembly of FIGS. 6-8. In the alternate embodiment 60a of FIGS. 9-11, two buttresses 72a and 72b are provided between the first portion 62 and the second portion 68, supporting articular portion 70 at an angle β with respect to the first portion 62. As broadly depicted in FIG. 11, in the case of a wrist implant, the buttresses 72a and 72b also are configured and positioned to lift the articular portion 70 up to a position spaced away from the end 67 of the first portion 62, so that a volar rim 73 and a dorsal rim 73a do not come in contact with the metal implant. The volar rim 73, and the dorsal rim 73a, therefore, are not covered by the second portion 68, thereby allowing the volar rim 73 and the distal rim 73a to contact soft tissue. One of ordinary skill will understand that use of the alternate embodiment 60a of the bone joint repair implant repair assembly of FIGS. 9-11 will require additional surgical preparation of the respective joint for insertion of the two buttresses 72a and 72b.
(33) The bone joint repair implant assemblies 60 and 60a described above, and broadly depicted in FIGS. 6-11, can be used with several different pivotal joints, including, but not limited to knees, ankles, and wrists. In the case of a knee, the plate portion 64 is configured for attachment to a proximal end of a tibia, and the articular surface 70 is configured as an articular surface for at least one of the plurality of bones defining the knee. In an alternate embodiment, when the joint is an ankle, the plate portion 64 is configured for attachment to a distal end of a tibia, and the articular surface 70 is configured as an articular surface for at least one of a plurality of bones defining the ankle. In yet another alternate embodiment, when the joint is a wrist, the plate portion 64 is configured for attachment to a distal end of a radius, and the articular surface 70 is configured as an articular surface for at least one of a plurality of bones defining the wrist. A bone joint implant replacement assembly similar in function to bone joint replacement implant assemblies 60 and 60a is disclosed in U.S. application Ser. No. 13/663,209, by the same inventor, being filed concurrently herewith, the contents of which are incorporated herein by reference.
(34) In several cases, prior to implanting a repair or replacement of a bone joint, a surgeon must first repair a cracked or fractured head of one of a patient's bones cooperating to define the respective joint. This procedure is particularly essential when a head of a bone is fractured into a plurality of jagged bone fragments, which can become lodged in, and interfere with, the new artificial joint, or can interfere with ligaments and other soft tissue associated with the joint. This issue is particularly problematic in the case of a full or partial joint replacement, or in the case of insertion of a repair implant. FIG. 12 broadly depicts a proximal head 74 and a neck 76 of a proximal end of a radius associated with an elbow. Although the discussion below, and the below disclosure of the preferred embodiment of this aspect of the invention, relates to a proximal head of a radius proximate an elbow, one of ordinary skill will recognize that the bone head, and the bone head fracture assembly discussed below can be modified as necessary to apply to a head of any bone proximate a pivotal bone joint. FIG. 13 broadly depicts the proximal head 74 of the radius fractured into a plurality of jagged bone fracture pieces 78. This fractured radius head will require repair prior to insertion of an elbow replacement or partial replacement assembly, in order to provide a smooth surface to the proximal head 74 of the radius.
(35) Exemplary embodiments of a bone repair assembly for repairing the fractured bone head are shown in FIGS. 14-16, and designated generally by reference numeral 80.
(36) As embodied herein, and referring to FIG. 14, the bone repair assembly 80 for a fractured bone head, e.g., a proximal head of a radius, includes a plate portion 82 configured for attachment to the neck 76 of the bone proximate the fractured head, the bone defining an axis A-A′, and the plate portion disposed generally coaxially with the axis. The plate portion 82 is configured to engage an extramedullary surface of the neck 76 of the radius. The bone repair assembly 80, in accordance with the invention, further includes a generally circular cap (or head) portion 84 projecting generally normal to the plate portion 82, across the fractured head 74 of the bone. As shown in FIG. 16, the cap portion 84 is configured to cover the fractured head 74. The entire bone repair assembly 80 may be made of an absorbable material or other non-metallic material, and the plate portion 82 and the cap portion 84 can be made of different materials. Such materials may include ceramic. Furthermore, the absorbable material may dissolve entirely or partially.
(37) Preferably, the generally circular cap portion 84 can be either solid or hollow, with the particular embodiment chosen depending on the nature of the fracture to bone head 74, and depending on the professional judgment of the respective surgeon.
(38) The generally circular cap portion 84 further includes a peripheral edge 86, and an annular skirt 88 depending from the peripheral edge 86, configured to substantially surround the bone fracture pieces 78. Accordingly, the cap portion 84 can include a cavity C (FIG. 15) for receiving the bone head 74 and/or the fractured bone pieces 78. As broadly depicted in the embodiment of FIG. 16, the peripheral skirt 88 can further be configured for attachment with fasteners 89 to the bone fractured bone pieces 78, in order to fix the fractured bone pieces 78 in place within the confines of the cap 84, so that the fractured bone pieces 78 will be substantially restricted from interfering with repair or replacement of the joint.
(39) Additionally, as shown in FIG. 15A, an alternate embodiment 80a of the bone repair assembly can include an intramedullary extension IE and extension portion EP. The intramedullary extension IE extends downwardly from the cap portion 84, and is configured for receipt in the medullary cavity of the radius. Furthermore, the extension portion (or extramedullary extension) EP extends downwardly from the cap portion 84, and is configured to contact the (in similar fashion to the plate portion 82) an extramedullary surface of the neck 76 of the radius. Fasteners (not shown) can be used to join the plate portion 82, the intramedullary extension IE, the extension portion EP, and/or the neck 76 to one another.
(40) In another aspect of the present invention, FIGS. 19-20 broadly depict an assembly for the repair of injuries to a shoulder joint, particularly rotator cuff injuries, and rotator cuff arthropathy. FIG. 17 broadly depicts a poximal end of a humerus 90 using fasteners (not shown) received through apertures 99 and 100, and a humeral head 92 extending into an (unnumbered) shoulder joint. In addition to heads of various bones, ligaments, muscles, tendons and sockets defining the shoulder, the shoulder is further defined by the rotator cuff (not shown). FIG. 18 also broadly depicts an arthritic damaged surface 94 on a surface of the humerus 90 and the humeral head 92, commonly known as rotator cuff arthropathy, a condition which evolves over time when there is a chronic tear of the rotator cuff. The humeral head 92 subluxes proximally and articulates with an undersurface 93 of an acromion, shown in FIG. 17. Motion of the shoulder in this condition results in painful grinding between arthritic damaged surface 94 and the undersurface 93 of the acromion.
(41) An exemplary embodiment of a rotator cuff repair assembly in accordance with the invention is shown in FIGS. 19-20, and is designated generally by reference numeral 95.
(42) As broadly embodied in FIGS. 19-20, the rotator cuff repair assembly 95 includes a plate portion 96 attachable to a proximal end of the humerus 90 using fasteners (not shown) received through apertures 99 and 100, and a generally circular prosthetic articular portion 97 projecting from a proximal end of the plate portion 95.
(43) Preferably, and as broadly depicted in FIG. 19, the prosthetic articular portion 97 has a diameter δ sufficient to cover the damaged portion 94 of the humeral head 92. In addition, in accordance with the invention, the prosthetic articular portion 97 is configured to act as a gliding surface 98 between the humeral head 92 and the rotator cuff. As further embodied in FIG. 20, an artificial gliding surface portion 101 may be installed on the undersurface 93 of the acromion.
(44) Persons of ordinary skill in the art will recognize that various modifications and variations can be made to the preferred embodiment described above, without departing from the spirit or scope of the invention. The present invention covers any such modifications and variations, provided they fall within the scope of the claims and their legal equivalents.
