The subject invention relates to implants including a tibial tuberosity advancement implant.
The veterinary surgical procedure known as tibial tuberosity advancement is used to correct a rupture of the CrCL in the knee of a dog. “See Tibial Tuberosity Advancement” by Dr. Jeff Mayo incorporated herein by this reference. Typically, a tibial tuberosity advancement includes a selection of cages, tension band plates, and forks. A jig is used to place the holes in the tibial tuberosity at the proper angle and spacing, a fork inserter is used to insert the forks to secure the tension band plate into the bone, a T-handle with spreaders is used to bend the plates and to hold the osteotomy open for testing of the cage size and insertion of the cage implant. Pins are used to lock the jig in place and a plate bender is used to bend the plates and the ears of the cage.
The fork is inserted through the plate into drilled holes and the osteotomy is advanced. The amount of advancement is predetermined and the proper cage is selected and installed. The selected cage is placed approximately 4-6 mm below the joint surface and secured medially. The osteotomy is then closed over the cage and the distal most holes in the tension band plate are secured using screws. Once the two distal screws are placed in the plate, the resulting void is filled in with a graft.
Presently, the procedure is complex and expensive due to the need for the implanted cage, the tension plate, the fork, the jig, the fork inserter, the T-handle with spreaders, and the plate bender.
It is therefore an object of this invention to provide a new tibial tuberosity advancement implant.
It is a further object of this invention to provide such an implant which has fewer components.
It is a further object of this invention to provide such an implant which is easier to install.
It is a further object of this invention to provide such an implant which is strong.
It is a further object of this invention to provide such an implant which enables bone growth.
It is a further object of this invention to provide such an implant which is biocompatible and light weight.
It is a further object of this invention to provide such an implant which reduces the surgery time and the chance of infection.
It is a further object of this invention to provide such an implant which does not require numerous specialized pieces of instrumentation.
It is a further object of this invention to provide such an implant that allows increased flexibility in the amount of advancement.
It is a further object of this invention to provide such an implant that allows 2-17 mm of advancement at 1 mm increments.
It is a further object of this invention to provide such an implant with “locking wings” to mechanically fixate the osteotomy.
It is a further object of this invention to provide such an implant that contacts the inner cortical walls of the osteotomy and tibia once installed.
The subject invention results from the realization, in part, that a better tibial tuberosity advancement implant includes first and second arms in a V configuration and made of an open frame-like structure with anchor apertures extending inwardly from one arm across the other arm to maintain the spacing between the arms during the tibial tuberosity advancement procedure.
The subject invention features a tibial tuberosity advancement implant comprising first and second arms pivotally joined at an apex, tabs including anchor apertures extending from each arm for attachment of the arms in a transverse osteotomyized tibia and a selection of various with keys each insertable between the arms for setting the distance between the arms and the width between the osteotomyized tibia.
In one example, select tabs extend inwardly form one arm across the other arm to maintain the spacing between the arms. Typically, each arm includes multiple spaced channels for a key for varying the distance between the arms. One preferred key includes opposing convex members receivable in the channels. There is also typically a compression element extending between the opposing convex members.
In one embodiment, the arms taper in width from a narrow portion proximate the apex to a widest portion at the distal end of the arm. Also, each arm may include a framework construction to promote bone ingrowth about the implant. Preferably, the anchor apertures are chamfered.
One implant in accordance with the subject invention includes first and second arms pivotally jointed at an apex each including a plurality of spaced channels, anchor apertures extending from each arm for attachment of the arms, and at least one key insertable between the arms in the channels for setting the distance between the arms. In one example, there are a selection of varying width keys.
An implant kit in accordance with the subject invention features a plurality of different size implants each including first and second arms pivotally joined at an apex, each arm including a plurality of spaced channels, and anchor apertures for each arm for attachment of the arms. A plurality of different size keys are each insertable between the arms in the channels for setting the distance between the arms. The distance between the arms is then defined by the size of the implant, the size of the key, and the position of the key channels selected.
The subject invention, however, in other embodiments, need not achieve all these objectives and the claims hereof should not be limited to structures or methods capable of achieving these objectives.
Other objects, features and advantages will occur to those skilled in the art from the following description of a preferred embodiment and the accompanying drawings, in which:
Aside from the preferred embodiment or embodiments disclosed below, this invention is capable of other embodiments and of being practiced or being carried out in various ways. Thus, it is to be understood that the invention is not limited in its application to the details of construction and the arrangements of components set forth in the following description or illustrated in the drawings. If only one embodiment is described herein, the claims hereof are not to be limited to that embodiment. Moreover, the claims hereof are not to be read restrictively unless there is clear and convincing evidence manifesting a certain exclusion, restriction, or disclaimer.
A key such as key 20a,
Each key 20a,
As shown in
The result, in the preferred embodiment is a new tibial tuberosity advancement implant with fewer components. In any embodiment, the implant of the subject invention is easier to install, is strong, and preferably enables bone growth due to its overall construction. The preferred tibial tuberosity implant is also biocompatible and lightweight, typically made of titanium. One benefit of the subject invention is that the surgery time is reduced and thus the chance of infection is also reduced.
Typically, additional specialized instrumentation are not needed other than a tool used to insert the key between the V-arms. The implant of the subject invention has increased flexibility in the amount of arm displacement. In one example, the implant of the subject invention allows for 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 15, 16 and 17 mm spacings with fewer parts. Cross tabs 16b and 16e,
Thus, although specific features of the invention are shown in some drawings and not in others, however, this is for convenience only as each feature may be combined with any or all of the other features in accordance with the invention. The implant described herein may also find uses for other medical procedures such as spinal spacing. The words “including”, “comprising”, “having”, and “with” as used herein are to be interpreted broadly and comprehensively and are not limited to any physical interconnection. Moreover, any embodiments disclosed in the subject application are not to be taken as the only possible embodiments.
In addition, any amendment presented during the prosecution of the patent application for this patent is not a disclaimer of any claim element presented in the application as filed: those skilled in the art cannot reasonably be expected to draft a claim that would literally encompass all possible equivalents, many equivalents will be unforeseeable at the time of the amendment and are beyond a fair interpretation of what is to be surrendered (if anything), the rationale underlying the amendment may bear no more than a tangential relation to many equivalents, and/or there are many other reasons the applicant can not be expected to describe certain insubstantial substitutes for any claim element amended.
Other embodiments will occur to those skilled in the art and are within the following claims.