The present disclosure relates generally to a method for repairing soft tissue and/or bone defects, and more particularly to a method for repairing cartilage and/or bone defects in a knee joint.
This section provides background information related to the present disclosure which is not necessarily prior art.
Articular cartilage enables bones to move smoothly relative to one another, as is known in the art. Damage to articular cartilage, such as in a knee joint, can be caused by injury, such as tearing, by excessive wear, or by a lifetime of use. Such damage to the articular cartilage can also cause damage to the underlying bone. The damaged articular cartilage can lead to, in certain circumstances, pain and reduced mobility. Various surgical procedures have been developed to repair damaged articular cartilage, such as microfracture, OATS, mosaicplasty or a unicondylar or partial knee replacement.
While these surgical procedures are effective for their intended purpose, there remains a need for improvement in the relevant art for treating focal defects in articular cartilage in a minimally invasive manner.
This section provides a general summary of the disclosure, and is not a comprehensive disclosure of its full scope or all of its features.
In one form, a method for repairing a soft tissue or bone defect is provided according to the teachings of the present disclosure. The method can include selecting one of a plurality of sizing guides having a base perimeter size corresponding to a size of the defect, where each base has a different perimeter size and a plurality of apertures spaced apart a predetermined distance from each other, with the predetermined distance being the same for each of the plurality of sizing guides. The base of the selected one of the sizing guides can be positioned against a distal end of the femur relative to the defect. A plurality of guide wires can be positioned through the plurality of apertures in the base of the selected one of the sizing guides and the plurality of guide wires can be fixed to the distal end of the femur such that the plurality of guide wires are parallel to each other. A first guide can be positioned over the plurality of guide wires and against the distal end of the femur to guide a first cutting member relative to the femur.
In another form, a method for repairing a soft tissue or bone defect is provided according to the teachings of the present disclosure. The method can include forming a reference pocket in a distal end of a femur relative to the soft tissue or bone defect, where the reference pocket is configured to receive a femoral implant. A first cutting member can be guided relative to the reference pocket to form a bore through the femur in a first direction relative to the femur. The method can further include maintaining the first cutting member in the femur and using the bore formed in the femur to guide the first cutting member in a second direction opposite the first direction to form a pocket in a tibia.
In yet another form, a method for repairing a soft tissue or bone defect is provided according to the teachings of the present disclosure. The method can include locating a first guide relative to a distal end of a femur and guiding a first cutting member with the first guide to form a bore through the femur in a first direction relative to the femur. The method can further include removing the first guide from the femur and maintaining the first cutting member in the femur and using the bore formed in the femur to guide the first cutting member in a second direction opposite the first direction to form a pocket in a tibia.
Further areas of applicability will become apparent from the description provided herein. The description and specific examples in this summary are intended for purposes of illustration only and are not intended to limit the scope of the present disclosure.
The present teachings will become more fully understood from the detailed description, the appended claims and the following drawings. The drawings are for illustrative purposes only of selected embodiments and not all possible limitations, and are not intended to limit the scope of the present disclosure.
The following description is merely exemplary in nature and is not intended to limit the present disclosure, its application, or uses. It should be understood that throughout the drawings, corresponding reference numerals indicate like or corresponding parts and features. Although the following description is related generally to methods and systems for repairing a cartilage defect in a knee joint, it should be appreciated that the methods and systems discussed herein can be applicable to other bones and/or joints of the anatomy.
Exemplary embodiments are provided so that this disclosure will be thorough, and will fully convey the scope to those who are skilled in the art. Numerous specific details are set forth such as examples of specific components, devices, systems and/or methods, to provide a thorough understanding of exemplary embodiments of the present disclosure. It will be apparent to those skilled in the art that specific details need not be employed, that exemplary embodiments may be embodied in many different forms and that neither should be construed to limit the scope of the disclosure. In some exemplary embodiments, well-known processes, well-known device structures, and well-known technologies are not described in detail.
Turning now to
With particular reference to
A pair of cannulated outer shafts 50 and an inner or central cannulated shaft 54 can extend from the base 42 and can define the opposite end 38. Shafts 50 and 54 can align with corresponding through bores 58 and 62, respectively, formed in base 42, as shown in
Once an appropriate sizing guide 22 has been selected that has a base 42 corresponding to the size of the defect or that best matches with the size of the defect, the base 42 can be positioned over the defect such that the inner shaft 54 is aligned at an angle α of about 30 to 40 degrees below or posterior to a longitudinal axis 66 of femur 14, as shown in
Referring to
As will be discussed in greater detail below, the implanted guide pins 70 can serve as a guidance system for other instruments and/or procedures to be performed in connection with repairing the cartilage defect in accordance with the teachings of the present disclosure. Once the guide pins 70 have been implanted as discussed above, the sizing guide 22 can be removed by sliding the guide 22 away from femur 14 about guide pins 70. In one exemplary configuration, the sizing guide 22 can be reusable and formed of a biocompatible material, such as stainless steel, titanium, or the like, consistent with such purpose.
With particular reference to
End 112 of base 104 can include a pair of apertures 128 positioned on opposite sides of shaft 116 so as to correspond with the spacing of outer guide pins 70 implanted in femur 14. As briefly discussed above and shown in
As will be discussed in greater detail below, by cutting the outline 126 in the cartilage, any tearing of cartilage outside the cut perimeter as a result of subsequent drilling in femur 14 can be substantially mitigated or eliminated. In this regard, in one exemplary configuration, only the outline 126 can be cut in the cartilage with cartilage cutter 100 such that cartilage is not removed by the cutting technique discussed above. However, it should be appreciated that cartilage within the perimeter outline cut into the cartilage could be removed in connection with cutting the perimeter outline into the femoral cartilage.
In one exemplary configuration, cartilage cutter 100 can be formed as a two-piece component where shaft 116 is removably engaged to base 104 via a threaded connection or the like. In this configuration, shaft 116 can be reusable and base 104 can be disposable.
With continuing reference to
Drill bit 154 can include a first or bone engaging end 186 and an opposite second or driver engaging end 190, as shown for example in
In use, drill bit 154 can be separately positioned about each of the outer guide pins 70 such that the pins are received in the throughbore 206 of drill bit 154. An outer diameter 214 of the bone engaging end 186 can be sized to cooperate with an inner diameter 218 of outer drill stop apertures 174, as shown in
With continuing reference to
In the exemplary configuration illustrated, projections 268 can be in the form of semicircles having a radius substantially corresponding to a radius of outer bores 226. With the inner drill stop 248 in place as shown in
Referring additionally to
Drill guide 290 can include a base 302 having a first or bone engaging side 306 and a second opposite side 310. A handle 314 can extend from the second side of base 302 and perpendicular thereto, as shown in
With additional reference to
As can be seen in
As briefly discussed above, first end 338 is configured to receive a quick-release driver 382 about first hexagon portion 354 for coupling drill bit 322 to a driving member to drill a bore 386 in the femur, as shown in
Once bore 386 has been formed in femur 14 as discussed above, quick-release driver 382 can be removed from drill bit 322 and drill guide 290 can then be removed from femur 14 by sliding drill guide about drill bit 322. In this regard, angled portion 328 can facilitate sliding the lower projection 326 out of bore 226 along the forty-five degree angle of drill bit 322 relative to the longitudinal axes of bores 226, 272. Drill bit 322 can then be slidably advanced to a position where first end 338 is proximate the joint space 390 between femur 14 and tibia 18, as shown in
Once stop collar 412 has been positioned on drill bit 322 as discussed above, a drive collar 438 can be positioned over second end 342 of drill bit 322, as shown in
A cutter 472 can be threadably received on threaded portion 350 of bit 322 for use in cutting a pocket in tibia 18, as shown in
Cutter 472 can include a body 512 having a first or proximal end 516 and an opposite second bone engaging end 520, as shown in
Once spacer 484 is positioned on drill bit 322 as discussed above, one side of spacer 484 can be brought into contact with proximal end 416 and stop collar 412 can be brought into contact with an opposite side of spacer 484, as shown in
Pocket 550 can be formed to remove a corresponding lesion or defect in tibia 18. In this regard, cutter 472 can be provided in various sizes, such as various diameters, to account for varying sizes of the tibial defect. Tibial bearing 554 can similarly be provided in various diameter sizes corresponding to the various sizes of cutter 472.
Once pocket 550 has been formed in tibia 18, a trial tibial bearing 562 (
On the other hand, if it is determined that pocket 550 has been formed too deep into tibia 18 and/or the sub-cortical bone is too soft, a tibial adjustment screw 570 can be implanted into pocket 550, as generally shown in
Before tibial adjustment screw 570 is coupled to drill bit 322 and implanted into pocket 550, an optional tibial adjustment screw tap 600 (
A screw and tap guide ring 632 can be used to guide both the tap 600 and/or the screw 570, as discussed below and shown in
With screw tap 600 coupled to drill bit 322 in the manner discussed above, tibia 18 can be tapped in a central location of pocket 550 using optional guide ring 632 as a guide. The tap 600 can be threaded into tibia 18 until a proximal end of the threads is flush with a bottom of pocket 550. In one exemplary aspect, drive collar 438 can be used to rotate drill bit 322 instead of the drive member to perform the tapping and implanting operation associated with screw 570. The tap 600 can then be removed from drill bit 322 and tibial screw 570 can be coupled to bit 322 in the manner discussed above. Tibial screw 570 can be threaded into the tapped threads in tibia 18 using drive collar 438. The guide ring 632 can be optionally removed before implanting screw 570, as discussed above. Screw 570 can be provided in various sizes, such as various lengths and diameters. Tap 600 can therefore also be provided in various sizes corresponding to the various sizes of screw 570. The guide ring 632 can also be provided with various through bore sizes.
First end 338 of drill bit 322 can then be slidably removed from screw 570 and the trial bearing 562 can again be positioned in pocket 550 to check the fit of the trial bearing 562. If it is determined that the trial bearing 562 needs to be raised toward the articular surface of the tibia 18 (i.e., toward femur 14), then first end 338 can be inserted through a central throughbore 644 of the trial bearing 562 and into engagement with screw 570. Drill bit 322 can then be rotated in an appropriate direction to raise the trial bearing 562 to an appropriate position. In this regard, it should be appreciated that the diameter of through bore 644 is large enough to allow drill bit 322 to pass through, but smaller in diameter than screw 570 so that the trial bearing 562 can be raised or lowered when screw 570 is turned. Once screw 570 is adjusted to place the trial bearing 562 in the appropriate position, drill bit 322 can be removed from femur 14 along with the associated stop collar 412, drive collar 438 and drill stop member 400.
Before implanting the femoral and tibial implants 30, 554, a femoral trial (not shown) can be positioned in the femoral pocket 280 and the trial bearing 562 can remain removably positioned in tibia 18. The femoral trial can be substantially similar to femoral implant 30 shown in
The femoral and tibial trials can then be removed and the femoral and tibial pockets 280, 550 can be prepared for receipt of respective implants 30, 554. In one exemplary aspect, bone cement can be used to secure the implants 30, 554 to the respective pockets 280, 550. In this aspect, bone cement can be applied to one or both of the bottom of pocket 550 and the bottom of tibial bearing 554. Instrument 568 can then be used to position tibial bearing 554 into pocket 550, as shown in
As can be seen in
With additional reference to
In the exemplary aspect where bone cement can be used as a securing method, bone cement can similarly be applied to the pocket engaging side 692 of femoral implant 30 and a bottom of bores 226, 272 of pocket 280. Implant 30 can then be positioned in femoral pocket 280 such that outer projections 234 are received in outer bores 226 and inner projection 276 is received in inner bore 272, as shown in
With additional reference to
Bullet 766 can be threadably advanced until it engages femur 14 to secure bullet 766 and guide relative to femur 14, as also shown in
With particular reference to
While one or more specific examples have been described and illustrated, it will be understood by those skilled in the art that various changes may be made and equivalence may be substituted for elements thereof without departing from the scope of the present teachings as defined in the claims. Furthermore, the mixing and matching of features, elements and/or functions between various examples may be expressly contemplated herein so that one skilled in the art would appreciate from the present teachings that features, elements and/or functions of one example may be incorporated into another example as appropriate, unless described otherwise above. Moreover, many modifications may be made to adapt a particular situation or material to the present teachings without departing from the essential scope thereof.
This application is a divisional of U.S. patent application Ser. No. 13/169,074 filed on Jun. 27, 2011. The entire disclosure of the above application is incorporated herein by reference.
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Number | Date | Country | |
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Child | 14524473 | US |