阅读说明：本技术 平台骨折固定植入物 (Platform fracture fixation implant ) 是由 C·P·罗奇 D·库格尔 K·A·埃戈 G·S·阿思瓦尔 J·桑切斯-索特罗 于 2018-03-12 设计创作，主要内容包括：一种用于修复肱骨近端的多部分骨折的植入物的近侧部分包括：非对称体,所述非对称体具有近端、远端、内侧、外侧、前边缘、和后边缘；内侧表面,所述内侧表面沿着所述内侧的至少一部分延伸并且具有近端和远端；形成所述非对称体的所述外侧的突起,所述突起沿向前方向偏移,并且当所述近侧部分被植入所述肱骨时指向所述肱骨的二头肌沟；前支撑表面,所述前支撑表面被配置成支撑小结节；后支撑表面,所述后支撑表面被配置成支撑大结节；成角表面,所述成角表面具有由所述内侧表面限定的第一侧、由所述前支撑表面限定的第二侧、以及由所述后支撑表面限定的第三侧；以及锚定点。(A proximal portion of an implant for repairing a multi-part fracture of a proximal humerus comprising: a non-symmetric body having a proximal end, a distal end, a medial side, a lateral side, a leading edge, and a trailing edge; an inner side surface extending along at least a portion of the inner side and having a proximal end and a distal end; a protuberance forming the lateral side of the asymmetric body, the protuberance offset in an anterior direction and directed toward a biceps groove of the humerus when the proximal portion is implanted in the humerus; an anterior support surface configured to support a nodule; a rear support surface configured to support a large nodule; an angled surface having a first side defined by the medial side surface, a second side defined by the anterior support surface, and a third side defined by the posterior support surface; and an anchor point.)

1. A proximal portion of an implant for repairing a multi-part fracture of a proximal humerus of a human, the proximal portion comprising:

a non-symmetric body having a proximal end, a distal end opposite the proximal end, a medial side, a lateral side opposite the medial side, a leading edge, and a trailing edge opposite the leading edge;

an inner side surface extending along at least a portion of the inner side, the inner side surface having a proximal end and a distal end;

a protuberance forming the lateral side of the asymmetric body, the protuberance offset in an anterior direction, the protuberance extending in a direction to point toward a biceps groove of the humerus when the proximal portion is implanted in the humerus;

an anterior support surface defined by an anterior side of the protuberance and extending to an anterior edge of the non-symmetric body, the anterior support surface configured to support a tuberosity of the proximal humerus;

a posterior support surface defined by a posterior side of the protuberance and extending to a posterior edge of the asymmetric body, the posterior support surface configured to support a greater tuberosity of the proximal humerus;

a generally triangular angled surface having a first side defined by a proximal end of the medial side surface, a second side defined by a proximal end of the anterior support surface, and a third side defined by a proximal end of the posterior support surface; and

at least one anchor point formed in the asymmetric body, the at least one anchor point configured to engage an anchoring device, thereby anchoring the proximal portion to a portion of the humerus.

2. The proximal portion of claim 1, further comprising an engagement mechanism positioned at a distal end of the asymmetric body and configured to engage a distal portion of the implant.

3. The proximal portion of claim 2, wherein the engagement mechanism is a cone.

4. The proximal portion of claim 1, wherein the proximal portion is integrally formed with a distal portion of the implant.

5. The proximal portion of claim 1, wherein the protrusion comprises a fin.

6. The proximal portion of claim 1, wherein the at least one anchor point comprises at least one threaded hole configured to receive at least one screw.

7. The proximal portion of claim 1, further comprising a plurality of suture holes.

8. The proximal portion of claim 1, wherein at least a portion of an outer surface of the proximal portion is porous.

9. The proximal portion of claim 1, further comprising a humeral head support abutment configured to engage a humeral head support.

10. The proximal portion of claim 9, wherein the angled surface forms the junction.

11. The proximal portion of claim 1, wherein at least one of the anterior support surface and the posterior support surface is concave.

12. A kit for repairing a multi-part fracture of a proximal humerus of a human, the kit comprising:

a plurality of proximal portions, each of the plurality of proximal portions comprising:

a non-symmetric body having a proximal end, a distal end opposite the proximal end, a medial side, a lateral side opposite the medial side, a leading edge, and a trailing edge opposite the leading edge;

an inner side surface extending along at least a portion of the inner side, the inner side surface having a proximal end and a distal end;

a protuberance forming the lateral side of the asymmetric body, the protuberance offset in an anterior direction, the protuberance extending in a direction to point toward a biceps groove of the humerus when the proximal portion is implanted in the humerus;

an anterior support surface defined by an anterior side of the protuberance and extending to an anterior edge of the non-symmetric body, the anterior support surface configured to support a tuberosity of the proximal humerus;

a posterior support surface defined by a posterior side of the protuberance and extending to a posterior edge of the asymmetric body, the posterior support surface configured to support a greater tuberosity of the proximal humerus;

a generally triangular angled surface having a first side defined by a proximal end of the medial side surface, a second side defined by a proximal end of the anterior support surface, and a third side defined by a proximal end of the posterior support surface;

at least one anchor point formed in the asymmetric body, the at least one anchor point configured to engage an anchoring device, thereby anchoring the proximal portion to a portion of the humerus; and

an engagement mechanism positioned at a distal end of the asymmetric body and configured to engage a distal portion of the implant,

wherein each of the proximal portions within the kit is a different size than all other proximal portions within the kit;

a plurality of distal portions, each of the distal portions having a distal end and a proximal end, the distal end of the distal portion configured to be placed within a medullary cavity of the humerus and the proximal end of the distal portion configured to engage with the engagement mechanism of a selected one of the plurality of proximal portions, wherein each of the plurality of distal portions within the kit is a different size than all other proximal portions within the kit; and

at least one humeral head support configured for attachment to a selected one of the plurality of proximal portions, each of the at least one humeral head support comprises a medial surface, a lateral surface opposite the medial surface of the humeral head support, a proximal end, a distal end opposite the proximal end of the humeral head support, and at least one anchor point configured to engage an anchoring device, wherein when the lateral surface of the humeral head support is positioned adjacent to a surface of the proximal portion of the implant, the proximal end of each of the at least one humeral head supports has a profile that is complementary to the angled surface of a selected one of the proximal portions, and wherein a lateral surface of the humeral head support is configured to support a humeral head of the humerus during repair of the four-part fracture of the humerus.

13. The kit of claim 12, wherein each of the plurality of proximal portions has a different dimension in the proximal-distal direction.

14. The kit of claim 12, wherein each of the plurality of proximal portions has a different dimension in the anterior-posterior direction.

15. The kit of claim 12, wherein each of the plurality of distal portions has a different length or a different diameter than all other distal portions within the kit.

16. The kit of claim 12, wherein the engagement mechanism of the plurality of proximal portions comprises a taper.

17. The kit of claim 12, the at least one anchor point of each of the proximal portions comprising at least one threaded hole configured to receive at least one screw.

18. The kit of claim 12, wherein at least one of the anterior and posterior support surfaces of at least one of the proximal portions is concave.

19. A humeral head support for use in an implant for repairing a multi-part fracture of the proximal humerus of a human, the humeral head support comprising:

a base configured for attachment to a proximal end of the implant; and

a support portion configured to support a humeral head of the humerus during repair of a four-part fracture of the humerus.

20. The humeral head support of claim 19,

wherein the humeral head support has an inside surface, an outside surface opposite the inside surface of the humeral head support, a proximal end, a distal end opposite the proximal end of the humeral head support, and at least one anchor point configured to engage an anchor, and

wherein the base configured for attachment to the proximal end of the implant comprises the proximal end of the humeral head support having a profile that is complementary to a surface of a proximal portion of the implant when a lateral side surface of the humeral head support is positioned adjacent to a surface of the proximal portion of the implant.

21. The humeral head support of claim 19, further comprising at least one anchor point.

22. The humeral head support of claim 21, wherein the at least one anchor point comprises at least one threaded bore configured to receive at least one screw.

Technical Field

Background

The open reconstruction of long bone fractures presents multiple challenges to orthopaedic and trauma surgeons, affecting their ability to reliably treat traumatic injuries. In particular, changes in patient anatomy, fracture pattern, patient health quality, and patient complications all affect the quality of fracture reconstruction, and also affect the rate and probability of fracture healing over time. Because of these numerous variables, a variety of implant options are contemplated for open reduction and internal fixation of long bone fractures, including: intramedullary nails, locking plates, wires, and screws (all provided in a kit of various sizes and materials). Each implant type is associated with its own features and advantages and their inherent complication rates for use in different fracture modes and different bones.

Despite the geographic and ethnic consistency of fracture types, there is no clear consensus on the treatment method, as this is related to the implant type. The selection of a particular implant for a given fracture type varies and depends on a variety of factors, including implant design characteristics, range, instrumentation, and the inherent mechanical integrity provided by the device for a particular fracture type and bone quality.

Disclosure of Invention

Exemplary embodiments relate to a trauma system that provides a number of different fracture reconstruction solutions.

In one embodiment, there is provided a proximal portion of an implant for repairing a multi-part fracture of a proximal humerus of a human, the proximal portion comprising: a non-symmetric body having a proximal end, a distal end opposite the proximal end, a medial side, a lateral side opposite the medial side, a leading edge, and a trailing edge opposite the leading edge; an inner side surface extending along at least a portion of the inner side, the inner side surface having a proximal end and a distal end; a protuberance forming the lateral side of the asymmetric body, the protuberance offset in an anterior direction, the protuberance extending in a direction to point toward a biceps groove of the humerus when the proximal portion is implanted in the humerus; an anterior support surface defined by an anterior side of the protuberance and extending to an anterior edge of the non-symmetric body, the anterior support surface configured to support a lesser tuberosity (user tuberosity) of the proximal humerus; a posterior support surface defined by a posterior side of the protuberance and extending to a posterior edge of the asymmetric body, the posterior support surface configured to support a greater tuberosity of the proximal humerus (great tuberosity); a generally triangular angled surface having a first side defined by a proximal end of the medial side surface, a second side defined by a proximal end of the anterior support surface, and a third side defined by a proximal end of the posterior support surface; and at least one anchor point formed in the asymmetric body, the at least one anchor point configured to engage an anchoring device, thereby anchoring the proximal portion to a portion of the humerus.

In one embodiment, the proximal portion further comprises: an engagement mechanism positioned at a distal end of the asymmetric body and configured to engage a distal portion of the implant. In one embodiment, the engagement mechanism is a cone. In one embodiment, the proximal portion is integrally formed with the distal portion of the implant.

In one embodiment, the protrusions comprise fins.

In one embodiment, the at least one anchor point comprises at least one threaded hole configured to receive at least one screw. In one embodiment, the proximal portion further comprises a plurality of suture holes.

In one embodiment, at least a portion of the outer surface of the proximal portion is porous.

In one embodiment, the proximal portion further comprises: a humeral head support junction configured to engage a humeral head support. In one embodiment, the angled surfaces form the junction. In one embodiment, at least one of the front support surface and the rear support surface is concave.

In one embodiment, a kit for repairing a multi-part fracture of a proximal humerus in a human comprises: a plurality of proximal portions, each of the plurality of proximal portions comprising: a non-symmetric body having a proximal end, a distal end opposite the proximal end, a medial side, a lateral side opposite the medial side, a leading edge, and a trailing edge opposite the leading edge; an inner side surface extending along at least a portion of the inner side, the inner side surface having a proximal end and a distal end; a protuberance forming the lateral side of the asymmetric body, the protuberance offset in an anterior direction, the protuberance extending in a direction to point toward a biceps groove of the humerus when the proximal portion is implanted in the humerus; an anterior support surface defined by an anterior side of the protuberance and extending to an anterior edge of the non-symmetric body, the anterior support surface configured to support a tuberosity of the proximal humerus; a posterior support surface defined by a posterior side of the protuberance and extending to a posterior edge of the asymmetric body, the posterior support surface configured to support a greater tuberosity of the proximal humerus; a generally triangular angled surface having a first side defined by a proximal end of the medial side surface, a second side defined by a proximal end of the anterior support surface, and a third side defined by a proximal end of the posterior support surface; at least one anchor point formed in the asymmetric body, the at least one anchor point configured to engage an anchoring device, thereby anchoring the proximal portion to a portion of the humerus; and an engagement mechanism positioned at a distal end of the asymmetric body and configured to engage a distal portion of the implant, wherein each of the proximal portions within the kit is a different size than all other proximal portions within the kit; the kit further comprises a plurality of distal portions, each of the distal portions having a distal end configured for placement within the medullary cavity of the humerus and a proximal end configured for engagement with the engagement mechanism of a selected one of the plurality of proximal portions, wherein each of the plurality of distal portions within the kit is a different size than all other proximal portions within the kit; and the kit further comprises at least one humeral head support configured for attachment to a selected one of the plurality of proximal portions, each of the at least one humeral head support comprises a medial surface, a lateral surface opposite the medial surface of the humeral head support, a proximal end, a distal end opposite the proximal end of the humeral head support, and at least one anchor point configured to engage an anchoring device, wherein when the lateral surface of the humeral head support is positioned adjacent to a surface of the proximal portion of the implant, the proximal end of each of the at least one humeral head supports has a profile that is complementary to the angled surface of a selected one of the proximal portions, and wherein a lateral surface of the humeral head support is configured to support a humeral head of the humerus during repair of the four-part fracture of the humerus.

In one embodiment, each of the plurality of proximal portions has a different dimension in the proximal-distal direction. In one embodiment, each of the plurality of proximal portions has a different dimension in the anterior-posterior direction. In one embodiment, each of the plurality of distal portions has a different length or a different diameter than all other distal portions within the kit.

In one embodiment, the engagement mechanism of the plurality of proximal portions comprises a taper. In one embodiment, the at least one anchor point of each of the proximal portions comprises at least one threaded hole configured to receive at least one screw. In one embodiment, at least one of the anterior and posterior support surfaces of at least one of the proximal portions is concave.

In one embodiment, there is provided a humeral head support for use in an implant for repairing a multi-part fracture of the proximal humerus of a human, the humeral head support comprising: a base configured for attachment to a proximal end of the implant; and a support portion configured to support a humeral head of the humerus during repair of the four-part fracture of the humerus.

In one embodiment, the humeral head support has an inside surface, an outside surface opposite the inside surface of the humeral head support, a proximal end, a distal end opposite the proximal end of the humeral head support, and at least one anchor point configured to engage an anchor, and the base configured for attachment to the proximal end of the implant comprises the proximal end of the humeral head support having a profile complementary to a surface of the proximal portion of the implant when the outside surface of the humeral head support is positioned adjacent a surface of the proximal portion of the implant.

In one embodiment, the humeral head support further comprises at least one anchor point. In one embodiment, the at least one anchor point comprises at least one threaded hole configured to receive at least one screw.

Drawings

Some embodiments of the present invention are described herein, by way of example only, with reference to the accompanying drawings. Referring now in detail to the drawings in particular, it should be emphasized that the details are shown by way of example and for purposes of illustrative discussion of embodiments of the invention. In this regard, the description taken with the drawings make apparent to those skilled in the art the manner in which the embodiments of the invention may be practiced.

Fig. 1 shows a fracture line of a proximal four-part fracture of the humerus.

Fig. 2 shows a first embodiment of a platform fracture fixation implant, including a first embodiment of a proximal portion of the platform fracture fixation implant, in which the fracture line of a four-part fracture of the proximal humerus is shown for reference.

Fig. 3 shows a detailed view of the proximal portion of fig. 2.

Fig. 4 shows detailed views of embodiments of various sizes of the distal portion of the platform fracture fixation implant of fig. 2.

Fig. 5 shows a further view of the platform fracture fixation implant of fig. 2.

Fig. 6 shows a further view of the flat fracture fixation implant of fig. 2 in combination with a supplemental humeral head support.

Fig. 7 illustrates embodiments of various dimensions of a second embodiment of a platform fracture fixation implant (including a second embodiment of a proximal portion of a platform fracture fixation implant).

Fig. 8 shows a detailed view of various sized embodiments of the proximal portion of fig. 7.

Fig. 9 illustrates various sized embodiments of a third embodiment of a platform fracture fixation implant (including a third embodiment of a proximal portion of a platform fracture fixation implant).

Fig. 10 shows a detailed view of various sized embodiments of the proximal portion of fig. 9.

Fig. 11 shows various views of a fourth embodiment of a platform fracture fixation implant (including a fourth embodiment of a proximal portion of a platform fracture fixation implant).

Fig. 12 shows a detailed view of the proximal portion of fig. 11.

Fig. 13 illustrates various views of a fifth embodiment of a platform fracture fixation implant (including a fifth embodiment of the proximal portion of the platform fracture fixation implant), with the fracture line of a four-part fracture of the proximal humerus shown for reference.

Fig. 14 shows a detailed view of the proximal portion of fig. 13.

Fig. 15 shows various views of a sixth embodiment of a platform fracture fixation implant (including a fifth embodiment of the proximal portion of the fracture fixation implant) and a locking plate, with the fracture line of a four-part fracture of the proximal humerus shown for reference.

Fig. 16 shows various views of a seventh embodiment of a platform fracture fixation implant (including a seventh embodiment of the proximal portion of the fracture fixation implant) and an embodiment of a locking plate, with the fracture line of a four-part fracture of the proximal humerus shown for reference.

Fig. 17 shows a detailed view of the proximal portion of fig. 16 and the locking plate.

Fig. 18 shows various views of an eighth embodiment of a platform fracture fixation implant (including an eighth embodiment of a proximal portion of a platform fracture fixation implant).

Fig. 19 shows a detailed view of embodiments of various sizes and configurations of the proximal portion of fig. 18.

Fig. 20 shows various sized embodiments of a ninth embodiment of a platform fracture fixation implant (including a proximal portion as an adapter suitable for revision in arthroplasty).

Fig. 21 shows a tenth embodiment of a platform fracture fixation implant configured for repairing a femoral neck fracture.

Fig. 22 shows an eleventh embodiment of a flat fracture fixation implant (an eleventh embodiment comprising a proximal portion of the flat fracture fixation implant) and a humeral head support.

Fig. 23 shows a twelfth embodiment of a flat fracture fixation implant (a twelfth embodiment including a proximal portion of the flat fracture fixation implant) and a humeral head support.

Detailed Description

Among those benefits and improvements that have been disclosed, other objects and advantages of this invention will become apparent from the following description taken in conjunction with the accompanying drawings. Detailed embodiments of the present invention are disclosed herein; however, it is to be understood that the disclosed embodiments are merely illustrative of the invention that may be embodied in various forms. In addition, each of the examples given in connection with the various embodiments of the invention are intended to be illustrative, and not restrictive.

Throughout the specification and claims, the following terms take the meanings explicitly associated herein, unless the context clearly dictates otherwise. The phrases "in one embodiment" and "in an embodiment" as used herein do not necessarily refer to the same embodiment, although they may. Furthermore, the phrases "in another embodiment" and "in some other embodiments" as used herein do not necessarily refer to a different embodiment, although they may. Thus, as described below, the embodiments of the present invention can be easily combined without departing from the scope or spirit of the present invention.

In addition, as used herein, the term "based on" is not exclusive and allows for being based on other factors not described, unless the context clearly dictates otherwise. In addition, throughout the specification, the meaning of "a", "an", and "the" includes plural references. The meaning of "in … …" includes "in … …" and "on … …".

Exemplary embodiments relate to a platform fracture fixation implant (alternatively referred to herein for brevity as an "implant") and kits including such implants that facilitate reconstruction of long bone fractures using treatments of a variety of different sizes and methods in a simpler and more inventively efficient manner. Exemplary embodiments may be suitable for cost-sensitive but anatomically diverse markets served by multiple orthopedic surgeons that may have been trained using various techniques, as exemplary embodiments may provide many different sizes and options for implant fixation methods. In some embodiments, the exemplary implants and kits including the exemplary implants may be suitable for addressing fracture reconstruction of long bones (more particularly humerus). More specifically, the exemplary embodiments shown in the figures are shown for reconstructing a proximal humeral head and/or a mid-humerus. In other embodiments, the implants may be adapted to address fracture reconstruction of other long bones, such as the proximal and distal sections of the femur and tibia, fibula, radius, ulna, clavicle, and the like.

When an orthopaedic surgeon or trauma doctor attempts to reconstruct a fracture of one or both parts of the proximal humerus, the shoulder joint can be cut through as small an opening as possible to protect the rotator cuff and other surrounding musculature from any further damage. However, when an orthopaedic surgeon or trauma doctor attempts to reconstruct a three or four part fracture of the proximal humerus, the shoulder joint is opened to substantially reconstruct all of the bone fragments. Thus, surgeons may attempt to reconstruct these differently classified proximal humeral fractures by different methods. In some embodiments, the flat fracture fixation implant is modular such that it can be preassembled on a "back table" as a single unit of appropriate size for a particular patient anatomy or fracture mode (i.e., such that it can be configured as an intramedullary rod that can be inserted through a small incision for a one-part or two-part fracture), or can be assembled in situ by positioning a distal portion with the fracture line (or aligned at the surgical humeral neck height (level)) and then positioning a proximal portion shaped as a scaffold (scaffold) through which the implant can be used to reconstruct multiple bone fragments (such as a three-part fracture or a four-part fracture) around the proximal portion. Fig. 1 shows the four proximal humeral fracture lines, a first line extending horizontally along the surgical neck (hypertrophic neutral), a second line extending upwardly through the biceps sulcus (periodomy), and a third line extending along the plane of the humeral head at the level of the anatomical neck of the humerus. The four-part fracture is called because these three fracture lines create four parts: (1) humeral head, (2) lesser tuberosity, (3) greater tuberosity, and (4) humeral shaft.

In some embodiments, the platform/scaffold is used to attach or augment (co-opt) bone fragments as traditionally done with hemiarthroplasty, and is used in conjunction with modular nails. In some embodiments, the proximal portion is non-cylindrical and asymmetric in design such that it is provided on the left and right sides to conform to the different shapes and sizes of the lesser and greater tuberosities of the proximal humerus. Referring now to fig. 2-6, a first embodiment of a platform fracture fixation implant 200 (for brevity, "implant 200") is shown. Fig. 2 shows a first embodiment of a flat fracture fixation implant 200 from a side perspective view and a top perspective view, with the four-part fracture of the proximal humerus shown from the upper right and lower right for reference.

In one embodiment, implant 200 includes an asymmetric proximal portion 210 for improved tuberosity reconstruction. In some embodiments, the asymmetric proximal portion 210 includes at least one anchor point 262 (e.g., a threaded hole) configured to receive a screw or other anchoring element to anchor the portion of the humerus to the asymmetric proximal portion 210. In one embodiment, as shown in the upper left and lower left of fig. 2, implant 200 does not include a humeral head support. In one embodiment, as shown in the top center and bottom center of fig. 2, the implant includes a humeral head support 270. In some embodiments, modular humeral head support 270 can be attached to proximal portion 210 to provide additional humeral head support.

In some embodiments, additional humeral head support can help avoid varus collapse in clinical scenarios where a medial osteophyte (medial calcar) is affected/destroyed by trauma. In some embodiments, a screw or other anchoring device may be secured (secured) through or directly to the humeral head support 270 to act as a buttress and reinforce the construct. In one embodiment, the proximal portion 210 provides less space for small nodules and more space for large nodules. In one embodiment, the protrusions 240 (e.g., fins) are oriented toward the biceps sulcus to assist the surgeon in reconstructing the fracture components in the patient's native humeral head posterior slope.

In some embodiments, implant 200 includes a distal portion 290 that is substantially cylindrical. In some embodiments, distal portion 290 is configured as a hollow intramedullary nail (see fig. 4). In some embodiments, distal portion 290 is configured as a modular (e.g., glued or press-fit) humeral stem (humeral stem). In some embodiments, distal portion 290 includes supplemental fixation features along the length of the implant. In some embodiments, distal portion 290 does not include supplemental fixation features along the length of the implant.

Fig. 3 shows a detailed view of a first embodiment of a proximal portion 210 of the implant for use in the implant 200 of fig. 2. Fig. 3 includes dimensional measurements of various portions of the proximal portion 210 shown therein, but it will be apparent to those skilled in the art that these are merely exemplary dimensions and that the proximal portion 210 of fig. 3 may be provided in a variety of sizes. In some embodiments, proximal portion 210 includes a proximal end 212, a distal end 214, a medial side 216, a lateral side 218, a leading edge 220, and a trailing edge 222. In some embodiments, proximal portion 210 includes a medial surface 230 having a proximal end 230 and a distal end 232.

In one embodiment, the proximal portion 210 includes an asymmetric body to facilitate tuberosity reconstruction. In one embodiment, an anterior support surface 250 is provided for the small nodes, a posterior support surface 254 is provided for the large nodes, and the protrusion 240 separates the anterior support surface 250 from the posterior support surface 254. In some embodiments, anterior support surface 250 has a proximal end 252 and posterior support surface 254 has a proximal end 256. In such embodiments, the proximal end 210 is thus provided on the left and right sides (shown as the left proximal end 210 in fig. 2, 3, 5, and 6). In one embodiment, suture holes 264 are included to aid in bone reattachment (bonereattachment). In one embodiment, the asymmetric proximal portion 210 is provided in multiple heights to better support the nodule size of patients of greater or lesser height or bone size. In one embodiment, the height of the proximal portion 210 is 35 mm. In one embodiment, the height of the proximal portion 210 is in the range of 20mm to 50 mm. In one embodiment, the asymmetric proximal portion 210 is provided in a variety of widths. In one embodiment, the width of the proximal portion 210 is 15 mm. In one embodiment, the width of the proximal portion 210 is in the range of 10mm to 40 mm. In one embodiment, the asymmetric proximal portion 210 is provided in a plurality of thicknesses. In one embodiment, the thickness of the proximal portion 210 is 12 mm. In one embodiment, the thickness of the proximal portion 210 is in the range of 5mm to 50 mm. In one embodiment, the radius, location, and orientation of the protrusions 240 may be variously configured within any of the aforementioned size ranges. In some embodiments, the radius, location, and orientation of the protrusion 240 may be configured to accommodate (accmod ate) the small nodule, which is typically 50% to 80% of the size of the large nodule, and such that the protrusion 240 points to the biceps sulcus. In some embodiments, the kit can include various embodiments of an asymmetric proximal portion 210 having a height, width, and depth that vary in proportion to one another to accommodate anatomical variations of different patients. In some embodiments, the distal end 214 of the proximal portion 210 is provided with a male taper 266 (i.e., engagement mechanism). In some embodiments, the male taper 266 has a diameter of 10 mm. In some embodiments, the male taper 266 has a diameter in the range of 7mm to 14 mm. In some embodiments, the size of the distal end 214 of the distal portion 210 may vary based on the size of the proximal portion 210 and/or the size of the entire implant 200. In some embodiments, the distal end 214 of the proximal portion 210 may be provided with another suitable type of engagement mechanism for engaging the distal portion 290.

In one embodiment, the asymmetric proximal portion 210 may include a humeral head support 270 (see fig. 2, top center and bottom center). In some embodiments, the humeral head support 270 includes a proximal end 272, a distal end 274, a medial surface 276, a lateral surface 278, an anterior side 280, and a posterior side 282. In one embodiment, the humeral head support 270 can be provided in a variety of lengths. In one embodiment, the humeral head support 270 has a length of 40 mm. In one embodiment, the humeral head support 270 has a length in the range of 10mm to 60 mm. In one embodiment, the humeral head support 270 is provided in a variety of widths. In one embodiment, the humeral head support 270 has a width of 11 mm. In one embodiment, the humeral head support 270 has a width in the range of 5mm to 35 mm. Fig. 3 includes dimensional measurement embodiments for various portions of various dimensions of the humeral head support 270, but it will be apparent to those skilled in the art that these are merely exemplary dimensions and that the humeral head support 270 of fig. 3 can be provided in various sizes or shapes and also connected to proximal portions of various sizes or shapes of humeral nails. For example, the humeral head support can be adapted to connect to a proximal portion of a conventional cylindrical nail. In some embodiments, the proximal portion 210 includes a substantially triangular angled surface 260 configured to engage a humeral head support. In some embodiments, angled surface 260 extends from proximal end 232 of medial surface 230 and is defined by proximal end 232 of medial surface 230, proximal end 252 of anterior concave surface 250, and proximal end 256 of posterior concave surface 254. In some embodiments, a portion of the humeral head support 270 adjacent its proximal end 272 has a profile that is complementary to a profile of the angled surface 260 of the proximal portion 210.

Fig. 4 shows a detailed view of a first embodiment of a distal portion 290 of implant 200 for use in implant 200 of fig. 2. Fig. 4 includes dimensional measurement embodiments of various portions of various dimensions of the distal portion 290 shown therein, but it will be apparent to those skilled in the art that these are merely exemplary dimensions and that the distal portion 290 of fig. 4 may be provided in various dimensions.

In some embodiments, distal portion 290 includes locking jaws 292 (i.e., an auxiliary fixation feature) for distal fixation without the need for diaphyseal locking screws. In some embodiments, distal portion 290 is a rod (e.g., hemiarthroplasty). In some embodiments, distal portion 290 is a cylindrical or other shaped (i.e., cross-sectional shaped) shaft (e.g., an intramedullary nail). In some embodiments, the diameter of distal portion 290 is in the range of 7.5mm to 9 mm. In some embodiments, the diameter of distal portion 290 is in the range of 7.5mm to 20 mm. In some embodiments, distal portion 290 is 80mm in length. In some embodiments, the length of distal portion 290 is in the range of 40mm to 260 mm. In some embodiments, the proximal end 294 of the distal portion 290 is provided with a female taper 296 configured to engage the male taper 266 of the proximal portion 210. In some embodiments, female taper 296 has a diameter of 10 mm. In some embodiments, the female taper 296 has a diameter in the range of 7mm to 14 mm. In some embodiments, the size of proximal end 294 of distal portion 290 may vary based on the size of distal portion 290 and/or the size of the entire implant 200. In some embodiments, proximal end 294 of distal portion 290 may be provided with another suitable type of engagement mechanism for engaging proximal portion 210.

Fig. 5 shows an additional view of the implant of fig. 2. Fig. 5 includes dimensional measurements of various portions of the implant shown therein, but it will be apparent to those skilled in the art that these are merely exemplary dimensions and that the implant of fig. 5 may be provided in a variety of sizes. In some embodiments, the implant includes an asymmetric proximal portion for improving tuberosity reconstruction.

In some embodiments, as shown in fig. 5, the implant 200 does not include a supplemental humeral head support 270. Fig. 6 shows an additional view of the implant 200 of fig. 2. Fig. 6 includes dimensional measurements of various portions of the implant 200 shown therein, but it will be apparent to those skilled in the art that these are merely exemplary dimensions and that the implant 200 of fig. 6 may be provided in a variety of sizes. In some embodiments, implant 200 includes an asymmetric proximal portion for improved tuberosity reconstruction. In some embodiments, as shown in fig. 5, the implant includes a supplemental humeral head support 270.

In some embodiments, as shown in fig. 2-6, implant 200 includes a proximal portion 210 that provides a smaller surface/space for the lesser tuberosity (e.g., anterior support surface 250) and a larger surface/space for the greater tuberosity (e.g., posterior support surface 254). In some embodiments, the surgeon will need to reconstruct the bone fragments in a manner that complies with the original anatomy of the patient. In some embodiments, to accomplish this, the surgeon will orient the humeral head fracture according to the patient's humeral head retroversion. In some embodiments, to assist in such orientation when performed in situ, the protrusion 240 separating the lesser tuberosity bed from the greater tuberosity bed is oriented toward the biceps sulcus (this is an anatomical landmark commonly utilized/referenced in the general fracture location and reconstruction involved in fracture classification to recreate the retroversion of the patient's anatomical humeral head).

In some embodiments, the platform fracture fixation implant, the proximal portion of the platform fracture fixation implant, and the distal portion of the platform fracture fixation implant may be provided in different lengths, widths, thicknesses, and different aspect ratios in order to best fill the proximal humeral defect and act as a scaffold to reconstruct the surrounding components. Those skilled in the art will appreciate that the proximal humeral anatomy is highly variable. Thus, in some embodiments, the implant is provided in different sizes such that its proximal portion is provided in a patient size specific manner, which will better configure the location of the screws for a patient's fracture.

In some embodiments, a modular platform fracture fixation implant kit may include different embodiments of the proximal portion and/or the distal portion. Fig. 7 shows a second embodiment of a platform fracture fixation implant 700. In the embodiment of fig. 7, the implant 700 comprises an intramedullary nail that utilizes multiple locking screws in different sized proximal segments 710, 712, 714 to ensure anatomically correct screw positions through the bone fragments for various sizes of humeral anatomy. In some embodiments, the intramedullary nail of fig. 7 may also be adapted to receive the humeral head support 270 depicted in fig. 2, 3, and 6. Fig. 8 illustrates various sized embodiments of a second embodiment of a proximal portion (e.g., small size 710, medium size 712, and large size 714) that may form the proximal portion of the implant of fig. 7. Fig. 8 includes dimensional measurements of various portions of various dimensional embodiments of the proximal portion shown therein, but it will be apparent to those skilled in the art that these are merely exemplary dimensions and that the proximal portion of fig. 8 may be provided in various sizes. In some embodiments, implant 700 of fig. 7 includes the proximal portion of fig. 8, facilitating in situ reconstruction of a proximal humeral fracture and providing improved tuberosity reconstruction while accounting for various humeral head sizes and anatomical variations.

In some embodiments, multiple sizes of cephalad medullary (cephalad) style proximal portions are utilized in order to center (or some other desired location) the larger lag screw in the humeral head despite significant anatomical variations in humeral head size, humeral head diameter, and medial/lateral and anterior/posterior humeral head offset relative to the intramedullary canal. Fig. 9 shows a third embodiment of a platform fracture fixation implant 900 that includes proximal portions 910, 912, 914 in a cephalad marrow pattern. More specifically, fig. 9 shows multiple views of a third embodiment of a flat fracture fixation implant showing proximal portions of various sizes of straight nails (e.g., small size 910, medium size 912, large size 914) having lag screws for insertion into the center of a humeral head (taking into account various humeral head sizes) when reconstructing a proximal humeral fracture. Fig. 10 shows various sized embodiments of a third embodiment of proximal portions 910, 912, 914 that may form the proximal portion of the implant 900 of fig. 9. Fig. 10 includes dimensional measurements of various portions of various dimensional embodiments of the proximal portion shown therein, but it will be apparent to those skilled in the art that these are merely exemplary dimensions and that the proximal portion of fig. 10 may be provided in various sizes. In some embodiments, the proximal portion of fig. 10 provides implants 900 of various sizes that are straight nails with lag screws to facilitate insertion of the lag screws into the center of the humeral head (taking into account various humeral head sizes) in reconstructing a proximal humeral fracture.

Fig. 11 shows a fourth embodiment of a platform fracture fixation implant 1100 that includes a cephalad-medullary-style proximal portion 1110. More specifically, fig. 11 shows a number of views of a third embodiment of a platform fracture fixation implant, showing a number of views of the proximal portion that is asymmetric in shape to provide a reconstruction that is more rotationally stable than a conventional cylinder. In the embodiment of fig. 11, the extension of the proximal portion in both the direction of the lesser and greater tuberosities provides better distribution of the screw within the fractured bone to prevent stress concentrations and provide more compression of the fragment. Fig. 12 shows various views of a fourth embodiment of a proximal portion 1110 that may form the proximal portion of the implant of fig. 11. In some embodiments, proximal portion 1110 includes a proximal end 1112, a distal end 1114, a medial side 1116, a lateral side 1118, a front end 1120, and a rear end 1122. Fig. 12 includes dimensional measurements of various portions of the proximal portion 1110 shown therein, but it will be apparent to those skilled in the art that these are merely exemplary dimensions and that the proximal portion 1110 of fig. 12 may be provided in a variety of sizes. As described above, the medullary proximal portion 1110 of fig. 12 is asymmetric and therefore more rotationally stable than a cylinder to improve tuberosity reconstruction.

In the embodiment of fig. 12, locations 1162 for attachment screws are distributed across the proximal portion 1110 and suture holes 1164 are provided to aid in bone reattachment. In the embodiment of fig. 12, the proximal portion 1110 has a height of 25mm and a width of 27 mm. In some embodiments, the proximal portion 1110 has a height in the range of 5mm to 45mm and a width in the range of 7mm to 47 mm. In some embodiments, differently sized proximal portions 1110 correspond to differently sized humeral heads of a patient, as described above for a cephalad medullary design, thereby ensuring that the central lag screw is positioned in the center of the humeral head regardless of the patient's humeral head size (i.e., diameter and/or thickness) or the patient's humeral head offset (i.e., medial/lateral or anterior/posterior) relative to the intramedullary axis.

Fig. 13 shows a fifth embodiment of a platform fracture fixation implant 1300 that includes a head-marrow style proximal portion 1310. More specifically, fig. 13 shows a number of views of a third embodiment of a platform fracture fixation implant 1300, showing a number of dimensions of a proximal portion 1310 that is asymmetric in shape to provide a reconstruction that is more rotationally stable than a conventional cylinder. In the embodiment of fig. 13, medial support 1370 is integrated into the proximal portion to provide improved humeral head support in the event of a medial osteophyte fracture. Similar to the embodiment of fig. 11 and 12, in the embodiment of fig. 13, the locations 1362 for screw attachment are deployed from the central axis to better distribute the screws through the fractured tuberosity into the humeral head while maintaining a larger central lag screw. The upper left corner shows a four-part fracture of the proximal humerus for reference.

Fig. 14 shows various views of a fifth embodiment of a proximal portion 1362 that may form the proximal portion of the implant of fig. 13. In some embodiments, proximal portion 1310 includes a proximal end 1312, a distal end 1314, a medial side 1316, a lateral side 1318, a forward end 1320, and a rearward end 1322. As described above, the medullary proximal portion of fig. 14 is asymmetric and therefore more rotationally stable than a cylinder to improve tuberosity reconstruction. Locations for attachment screws 1362 are distributed through the proximal portion and suture holes 1364 are provided to aid in bone reattachment. Proximal portion 1310 of fig. 14 includes medial strut 1370 to provide improved humeral head support in the event of a medial osteophyte fracture.

In some embodiments, the proximal humeral nail and the locking plate are used in conjunction with one another. Such embodiments may be suitable for repairing severe and multi-part comminuted fractures. In some embodiments of the modular platform fracture fixation implant, this combination may be achieved by providing proximal nail portions of various sizes having any of the foregoing configurations, while ensuring that the central lag screw is centered in the humeral head, with the plate positioned on the lateral humerus in a desired manner, and achieving adequate distribution of the screws into the fractured bone. Fig. 15 shows various views of a sixth embodiment of a flat fracture fixation implant 1500 having a proximal portion 1510 in combination with a locking plate 1511. A four-part fracture of the proximal humerus is shown on the right for reference. In the embodiment of fig. 15, the locations for screw attachment are spread out from the central axis in order to better distribute the screws into the humeral head through the tuberosity of the fracture, while maintaining a larger central lag screw and positioning the plate on the lateral proximal humerus bone increases the stability of the multi-part fracture. In some embodiments, the screws that attach the locking plate may also lock into the intramedullary nail to increase construct stiffness.

In some embodiments, the distal end of the locking plate is configured to include modular connections to the proximal ends of the distal staples for constructing a hybrid staple plate (with or without proximal staple components). Fig. 16 shows various views of a seventh embodiment of a platform fracture fixation implant 1600 having a taper connection between a locking plate 1610 and a distal nail 1690. The four-part fracture of the proximal humerus is shown on the left for reference. In the embodiment of fig. 16, the locations for screw attachment are deployed from the central axis in order to better distribute the screws through the fractured tuberosity into the humeral head, while maintaining a distal plateau segment to increase rotational stability and resistance to bending. In the embodiment of fig. 16, a central lag screw is included.

Fig. 17 shows various views of an embodiment of a locking plate 1610, which forms a portion of the implant of fig. 16 and may be referred to as a seventh embodiment of a proximal portion of a platform fracture fixation implant 1600. In the embodiment of fig. 17, lateral locking plate 1610 includes a modular connector for securing to a distal portion of a platform fracture fixation implant 1600. In the embodiment of fig. 17, a central lag screw (not shown) may be included or may be omitted. In some embodiments, the cone connector is modularly connected to the locking plate to improve manufacturability and can be used without a cone if needed as a stand-alone locking plate.

For a mid-shaft fracture or a partial or two-part fracture of the proximal humerus, the surgeon may wish to insert a nail through a small incision in the upper humeral head (superior humeral head). Fig. 18 shows various views of an eighth embodiment of a platform fracture fixation implant 1800, which may be adapted for use with such techniques. Fig. 18 includes dimensions of various portions of the platform fracture fixation implant 1800 shown therein, but those skilled in the art will appreciate that these dimensions are exemplary only, and that the platform fracture fixation implant of fig. 18 may be provided in a variety of sizes. In the embodiment of fig. 18, the flat fracture fixation implant is in the form of a curved nail. In some embodiments, the implant is pre-assembled in the background. In some embodiments, a suitably sized proximal portion is selected from the kit and has a bend adapted to facilitate insertion while minimizing damage to the rotator cuff or surrounding musculature of the patient.

Fig. 19 shows various sized embodiments of an eighth embodiment of a proximal portion (e.g., small size 1810, medium size 1902, large size 1904, and high angle large size 1906) that may form a proximal portion of implant 1800 of fig. 18. Fig. 19 includes dimensional measurements of various portions of various dimensional embodiments of the proximal portion shown therein, but it will be apparent to those skilled in the art that these are merely exemplary dimensions and that the proximal portion of fig. 19 may be provided in various sizes. In some embodiments, the angled bend of the proximal portion of fig. 19 can be varied to account for various humeral size and anatomical variations. In the embodiment shown in fig. 19, the angled bend may range from an angle of 6 ° to an angle of 12 °. In some embodiments, the angled bend may range from an angle of 0 ° to an angle of 20 °.

In some embodiments, the kit provides a correction scenario. Arthroplasty is commonly used for revision cases where a fracture fails to heal. Fig. 20 illustrates an adapter that provides the ability to convert a failed fracture reconstruction to a shoulder arthroplasty 2000 (e.g., a hemi-arthroplasty, a total shoulder arthroplasty, or a reverse total shoulder arthroplasty) using a taper and screw connection, or other similar connection device. More specifically, fig. 20 shows modular tapered adapters (illustrated as left-side split adapters) of various sizes (e.g., small size 2002, medium size 2004, and large size 2006) that may enable conversion of a flat fracture fixation implant into a hemiarthroplasty, a total shoulder arthroplasty, or a reverse total shoulder arthroplasty, all of which may be secured to a proximal portion of the adapter of fig. 20. In FIG. 20, the adapter is shown connected to various sized prostheses sold under the trademark EQUINOXE by Exactech corporation of Gernesville, Florida.

In some embodiments, the various modular proximal and distal portions of the above-described flat fracture fixation implants may be arranged in different shape variations than described herein. In some embodiments, the claw-like fixation units may be used to obtain bone capture (bony purchase) of fragments or backbones of long bones. In some embodiments, bone screws may be used. In some embodiments, the modular segments (i.e., the respective proximal and distal portions) of the platform fracture fixation implant may be attached or keyed to one another by various methods, including taper locking, threaded segments, or sliding and cross-pinning to allow for various rotational orientations. In some embodiments, the screw connection may be a threaded or a slide fit, as appropriate. In some embodiments, any of the concepts embodied by the modular proximal and distal portions of the above-described plateau fracture fixation implants may be applied to other long bones (e.g., proximal and distal segments of the femur, tibia, fibula, radius, ulna, clavicle, etc.). Fig. 21 shows only one such variation, where an implant 2100 comprising a proximal portion 2110 and a distal portion 2190 is adapted to be positioned proximal to the femur in order to reconstruct a femoral neck fracture.

Fig. 22 illustrates various views of an eleventh exemplary embodiment of a platform fracture fixation implant 2200. In some embodiments, the platform fracture fixation implant 2200 includes a proximal portion 2210 and a distal portion 2290. In some embodiments, the proximal portion 2210 includes at least one anchor point 2262 (e.g., a threaded hole) configured to receive a screw or other anchoring element to anchor the portion of the humerus to the asymmetric proximal portion 2210. In some embodiments, the proximal portion 2210 includes a protrusion 2240 configured to extend toward the biceps sulcus when the implant 2200 is implanted in a patient's humerus. In some embodiments, the proximal portion 2210 includes a proximal end 2212, a distal end 2214, an inner side 2216, an outer side 2218, a front end 2220, and a rear end 2222. In some embodiments, the proximal portion 2210 includes a humeral head support abutment 2260 at the proximal end 2212. In some embodiments, the humeral head support joint 2260 is substantially cylindrical. In some embodiments, implant 2200 comprises a humeral head support 2270. In some embodiments, the humeral head support 2270 is configured to mount to a humeral head support engagement point 2260 of the proximal portion 2210.

Fig. 23 illustrates various views of a twelfth exemplary embodiment of a platform fracture fixation implant 2300. In some embodiments, the platform fracture fixation implant 2300 includes a proximal portion 2310 and a distal portion 2390. In some embodiments, the proximal portion 2310 includes at least one anchor point 2362 (e.g., a threaded hole) configured to receive a screw or other anchoring element to anchor the portion of the humerus to the asymmetric proximal portion 2310. In some embodiments, proximal portion 2310 includes a proximal end 2312 and a distal end 2314. In some embodiments, the proximal portion 2310 includes a humeral head support abutment 2360 at the proximal end 2312. In some embodiments, the humeral head support abutment 2360 is substantially cylindrical. In some embodiments, implant 2300 includes a humeral head support 2370. In some embodiments, the humeral head support 2370 is configured to mount to a humeral head support engagement point 2360 of the proximal portion 2310. In some embodiments, humeral head support abutment 2360 comprises a cylindrical portion with internal threads, and implant 2300 comprises a screw 2384 configured to mount humeral head support 2370 to humeral head support abutment 2360.

In some embodiments, the various modular proximal and distal portions of the above-described platform fracture fixation implants may be fabricated from a variety of different biocompatible materials, including, but not limited to, cobalt chrome, stainless steel, titanium alloys, carbon fiber reinforced polymers, ceramics, polymethylmethacrylate ("PMMA") bone cement, pyrolytic carbon, bone graft, and/or any other suitable biocompatible material. In some embodiments, the various modular proximal and distal portions of the above-described flat fracture fixation implants may be manufactured by conventional computer-aided manufacturing processes, by using additive manufacturing or similar processes, or by any other suitable manufacturing process. In some embodiments, the modular proximal and distal portions of the above-described flat fracture fixation implants may be surface coated or treated with various processes to facilitate fixation to soft tissue, muscle, and/or bone. In some embodiments, each of the modular proximal and distal portions of the above-described flat fracture fixation implant may be porous on some or all of its surfaces to promote bone ingrowth therein, thereby promoting bone fixation.

While a number of embodiments of the present invention have been described, it is to be understood that these embodiments are illustrative only and not limiting, and that many modifications will be apparent to those of ordinary skill in the art. For example, all dimensions discussed herein are provided by way of example only and are intended to be illustrative and not limiting. Further, any desired number and shape of screw holes, suture holes, etc. may be utilized (and may be placed at any desired location on the prosthesis). Still further, while the term "fin" is used in this application and may be considered to mean a separate independent feature, it is to be understood that the present invention may, of course, utilize one or more surfaces having a substantially continuous structure in addition to (or instead of) the "fin".