The present disclosure relates to systems, apparatuses, methods, and kits for bone fracture and/or joint repair. Specifically, this disclosure relates to a Jones fracture fixation apparatuses, systems, kits, and methods suitable to accommodate or correct various patient deformities.
Jones fracture is a fracture of the diaphysis of the fifth metatarsal of the foot. The Jones fracture area is weak because of lack of blood flow to that area of the bone. In addition, the bone healing relies upon good circulation; therefore, it is challenging to treat the Jones fracture. The Jones fracture can be either a tiny hairline break that occurs over time (a stress fracture) or a sudden acute break. The Jones fracture is often caused by overuse, repetitive stress, or trauma.
There are two main options for the treatment of a Jones fracture: non-operative and surgical. The non-operative option involves wearing a walking boot for some weeks to let the bone heal on its own. However, as the Peroneus Brevis Muscle constantly puts the bone in tension, natural healing is difficult. Therefore, the surgical option is often used to aid compression at the fracture site to force a union. Surgically, the main options include a bone screw, a bone plate, a bone staple, and external fixators. A bone screw is the most common solution to repair the fracture. Bone screws have threads and a head opposed to the threads that allows the surgeon to apply the screw across a bony fracture. When the fracture is healed, the bone screw may be removed.
Specialized bone screws have been created for fixing Jones fractures. These screws are implanted in the center of the intramedullary canal of the fifth metatarsal. However, implantation is challenging because of the shape of the fifth metatarsal bone. The fifth metatarsal has a lateral bow on the dorsoplanter plane and a dorsal bow on the medolateral plane. In addition, the bone is irregular and shaped like a pyramid in the vertical cross-section. Therefore, screw sizing is very important. Targeting of the distal tip of the screw is also difficult. A misaligned screw could cause high stress concentrations on the inside of the intramedullary canal. In addition, even well-aligned screws have a much higher stiffness than the bone, resulting in elevated stress levels in the bone around the tip of the screw. Therefore, existing systems and procedures for Jones fracture repair may not be as effective as desired.
The present disclosure relates to bone and joint fixation, and instrumentation and methods for preparation and implantation of devices. Bone repair and/or joint fixation may be necessary in cases of fracture, pain and inflammation due to cartilage degeneration, nerve impingement, spinal misalignment, and motion instability. The primary examples described herein illustrate how this concept is applied to repairing a Jones fracture, but this concept applies equally to other fractures and joints. The disclosed bone screw is used for stabilizing a joint or a bone fracture. The bone screw includes a screw head at one end and a slotted tip at the other end. The slotted tip includes a plurality of slots. Further, the bone screw includes a shaft between the head and the tip, with the shaft having a threaded segment at the distal end. The slotted design of the tip partially obviates the need for precision in Jones fracture repair. The slotted tip helps reduce the stiffness differential between the tip of the bone screw and the bone. Further, it reduces stress concentrations imparted to the bone both during insertion and under bending loads. Moreover, the slotted tip conforms to the intramedullary canal of the fifth metatarsal as the bone screw is inserted into the bone to repair a Jones fracture.
According to an embodiment of the present disclosure, the slotted tip of a bone screw has three slots resulting in three arms, a shaft diameter equal to the major diameter of the bone screws, cortical style threads, a non-cannulated solid core, a low profile head, and a hexalobe drive connection. The three arms extend only partially along the length of the threads of the bone screw and have stress relief arcs at the base of each arm.
Those of skill in the art will recognize that the following description is merely illustrative of the principles of the disclosure, which may be applied in various ways to provide many different alternative embodiments and may be applicable outside the fields of surgery or medical devices. While the present disclosure is made in the context of Jones fracture for the purposes of illustrating the concepts of the design, it is contemplated that the present design and/or variations thereof may be suited to other uses, such as to support other joints in the human body and to stabilize bone fractures. Moreover, the implants, instrumentation, and methods set forth herein may be used in open, percutaneous, and/or minimally invasive procedures. All changes that come within the meaning and range of equivalency of the claims are to be embraced within their scope.
Various embodiments of the present disclosure will now be discussed with reference to the appended drawings. It will be appreciated that these drawings depict only typical examples of the present disclosure and are, therefore, not to be considered limiting of its scope.
While certain embodiments are shown and described in detail below by way of illustration only, it will be clear to the person skilled in the art upon reading and understanding this disclosure that changes, modifications, and variations may be made and remain within the scope of the technology described herein. Further, while various features are grouped together in the embodiments for the purpose of streamlining the disclosure, it is appreciated that features from different embodiments may be combined to form additional embodiments that are all contemplated within the scope of the disclosed technology.
Not every feature of each embodiment is labeled in every figure where that embodiment appears, in order to keep the figures clear. Similar reference numbers (for example, those that are identical except for the first numeral) may be used to indicate similar features in different embodiments.
Any of the devices described herein may be fabricated from metals, alloys, polymers, plastics, ceramics, glasses, composite materials, or combinations thereof, including but not limited to: PEEK, titanium, titanium alloys, commercially pure titanium grade 2, ASTM F67, Nitinol, cobalt chrome, stainless steel, UHMWPE, and biodegradable materials, among others. Different materials may be used within a single part. The implants disclosed herein may also encompass a variety of surface treatments or additives to encourage bony attachment, including but not limited to: porous coatings, hydroxyapatite, TCP, anti-microbial additives, analgesics, anti-inflammatories, BMP's, PMA material, bone growth promoting material, PLLA (poly-L-lactide), PGA (polyglycolide), TCP (tricalcium phosphate), demineralized bone, cancellous bone chips, etc. Any implant disclosed herein may include a radiographic marker for imaging purposes. Any implant disclosed herein may be colored, coded, or otherwise marked to make it easier for the surgeon to identify the type and size of the implant.
Further, the diameter of the shaft 106 is equal to the major diameter of the bone screw 100. The bone screw 100 may have fully threaded shaft or a thread configuration with a lag (as shown in the
Referring now to
Referring back to
Further, the bone screw 100 may have a hexalobe drive connection 502 as shown in
Referring now to
At step 904, the surgeon guides a first cannulated drill over the guide wire to drill through the bone (e.g., the fifth metatarsal, when repairing a Jones fracture). The first cannulated drill provides clearance for threaded portion 110 (minor diameter). At step 906, the surgeon employs a second cannulated drill over the guide wire to drill through the bone and provide clearance for the shaft 106 (major diameter) of the bone screw 100. The first cannulated drill and the second cannulated drill may be manually operated or may be operated by, or as, powered devices, Thereafter, at step 908, the surgeon utilizes a cannulated tap to tap the hole drilled by the first cannulated drill and the second cannulated drill. Alternatively, the bone screw 100 may have a self-tapping (or self-threading) feature to tap a drilled hole when the bone screw 100 is inserted into the bone.
Once the implant site is sufficiently prepared to receive the bone screw 100, the surgeon uses the guide wire to orient and insert the bone screw 100 into the bone, at step 910. The surgeon uses the driver 602 to insert the bone screw 100 into the bone, and engages the threaded portion 110 with the bone. Further, the surgeon uses the driver 602 to achieve a required compression between the bones. Once the bone screw 100 is in the proper location, the surgeon can remove the guide wire, the drivers, and any other instrumentation used, and then close the incision site.
The present disclosure further provides a bone screw kit or system, which includes a plurality of bone screws, wherein each bone screw includes a screw head at one end, a slotted tip at the other end and a shaft between the head and tip, the shaft having a threaded segment at the distal end. The slotted tip includes plurality of slots. Moreover, each bone screw in the kit is of a different configuration, wherein the configuration of a bone screw is defined by one or more parameters including a number of slots, a major diameter, a pitch, a length, a lag thread, and a drive connection. In an embodiment, the kit includes screws in 0.5 mm major diameter increments; for example, diameters of bone screws may be 4.5 mm, 5.5 mm, and 6.5 mm. In the same or another embodiment, the length of the bone screws lies in the range of 20-70 mm. The bone screws may be made using titanium alloys in addition to any of the materials mentioned herein. The bone screw kit may further include one or more of a K-wire, one or more drilling tools, one or more tapping tools capable of accommodating all bone screws in the kit, and one or more driving tools.
It should be understood that the present components, systems, kits, apparatuses, and methods are not intended to be limited to the particular forms disclosed. Rather, they are intended to include all modifications, equivalents, and alternatives falling within the scope of the claims. They are further intended to include embodiments which may be formed by combining features from the disclosed embodiments, and variants thereof.
The claims are not to be interpreted as including means-plus- or step-plus-function limitations, unless such a limitation is explicitly recited in a given claim using the phrase(s) “means for” or “step for,” respectively.
The term “coupled” is defined as connected, although not necessarily directly, and not necessarily mechanically.
The use of the word “a” or “an” when used in conjunction with the term “comprising” in the claims and/or the specification may mean “one,” but it is also consistent with the meaning of “one or more” or “at least one.” The term “about” means, in general, the stated value plus or minus 5%. The use of the term “or” in the claims is used to mean “and/or” unless explicitly indicated to refer to alternatives only or the alternative are mutually exclusive, although the disclosure supports a definition that refers to only alternatives and “and/or.”
The terms “comprise” (and any form of comprise, such as “comprises” and “comprising”), “have” (and any form of have, such as “has” and “having”), “include” (and any form of include, such as “includes” and “including”), and “contain” (and any form of contain, such as “contains” and “containing”) are open-ended linking verbs. As a result, a method or device that “comprises,” “has,” “includes,” or “contains,” one or more steps or elements, possesses those one or more steps or elements, but is not limited to possessing only those one or more elements. Likewise, a step of a method or an element of a device that “comprises,” “has,” “includes,” or “contains” one or more features, possesses those one or more features, but is not limited to possessing only those one or more features. Furthermore, a device or structure that is configured in a certain way is configured in at least that way, but may also be configured in ways that are not listed.
The present invention may be embodied in other specific forms without departing from its spirit or essential characteristics. It is appreciated that various features of the above-described examples can be mixed and matched to form a variety of other alternatives. As such, the described embodiments are to be considered in all respects only as illustrative and not restrictive. The scope of the invention is, therefore, indicated by the appended claims rather than by the foregoing description. All changes which come within the meaning and range of equivalency of the claims are to be embraced within their scope.