1. The Field of the Invention
The present invention relates to generally to the attachment of tendon to bone, and more particularly, to systems and methods for implantable bridge anchors for tendon attachment to bone.
2. The Relevant Technology
One of the most difficult aspects of a tendon attachment procedure is providing a consistency and superior fixation to the bone. While this challenge exists in the re-attachment of to any tendon to the corresponding bone, it represents a particular problem for biceps tendon re-attachment (biceps tenodesis). In some cases the biceps tendon is not fixed to the bone but is simply cut allowing the muscle to retract distally. Although this approach can be effective it creates a “Popeye” deformity. In one method of biceps tenodesis the biceps stump is secured to the rotator cuff. Since this is a soft tissue fixation it is inherently weak.
Other techniques include the “Key-Hole” technique in which the tendon is rolled into a ball and secured inside a key-hole shaped cavity in the bicipital groove. This procedure requires deltoid split and surgical exposure. Furthermore the key-hole requires a large hole in the bone and it is difficult to secure the tendon in the hole.
Yet another technique is referred to as the tunnel technique where the tendon is cut from the superior labral attachment and secured to the proximal humerus via sutures passing through two holes that are drilled into the humerus. This method requires a mini-open incision in the axilla and risks regional nerve damage.
Yet another technique uses a suture anchor to secure the tendon to the humerus. Primary drawbacks of this technique include the anchor dislodging from the driver, anchor pullout, suture cutting through the degenerative tendon, and difficult arthroscopic visualization.
Yet another technique, known as the interference screw technique, requires a large hole to be drilled into the bone. A screw is secured to the tendon and then the screw is secured into the bone over the top of the tendon. However, this technique creates a large socket and may result in development of a cyst. Furthermore, this technique requires extra-corporeal extraction of the tendon, i.e., the drawing of the tendon out of the body. This adds to the time required for surgery, and to the probability of damage or infection to the surrounding tissues.
As the above described techniques illustrate, the existing systems and procedures for attaching a tendon to a bone may not be as effective as desired or may lead to further reconstructive surgeries.
Various embodiments of the present invention will now be discussed with reference to the appended drawings. It is appreciated that these drawings depict only typical embodiments of the invention and are therefore not to be considered limiting of its scope.
The present invention relates to systems and methods for fastener assemblies for securing a tendon. Those of skill in the art will recognize that the following description is merely illustrative of the principles of the invention, which may be applied in various ways to provide many different alternative embodiments. This description is made for the purpose of illustrating the general principles of this invention and is not meant to limit the inventive concepts in the appended claims.
One embodiment of the present invention includes a suture, a first fastener with a sharpened end and a capture body with an at-least partially spherical shaped head, an impactor, a second fastener with a sharpened end and an at-least spherical shaped head, which may be a bone screw, and a screw driver. A method of securing a tendon to a bone consists of securing a suture to a tendon proximately to a fixation site on the bone and passing a suture through a first aperture site on the first fastener. This suture through the first aperture acts as a guide for the fastener toward the fixation site on the bone. The first fastener penetrates the bone compressing the tendon against the fixation site and the suture is secured to the first fastener. The second fastener penetrates the bone piercing the first fastener hole and first fastener channel, potentially piercing the tendon as well, adding further securement of the tendon to the bone as well as further securement of the suture to the first fastener.
Referring to
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A first fastener proximal hole 118 extends through the capture body 108 and may be an engagement feature for a second fastener 120. The gap between the first sharpened leg 106 and the second sharpened leg 114 forms a channel 116 sized to receive at least a portion of a tendon. Each aperture 110, 112 is sized to slidably receive one suture working portion 103, 105. An alternate embodiment may have one aperture on one side or both sides of the first fastener 100 sized to slidably receive two working portions 103,105, or alternatively, one or any other number of working portions.
Alternatively the first fastener 100 capture body 108 may have alternate shapes such as square, rectangular, hexagonal or other common shapes known or used in the art, with the rim 132 of the capture body 108 configured to engage the second fastener 120. The apertures 110, 112 are configured in a similar manner to the circular embodiment of the first fastener 100 in that they may be positioned on one side of the capture body 108 or on both sides of the capture body, the second aperture set opposite the first aperture set. Furthermore, the apertures 110, 112 may be positioned around the entire rim 132 equidistant to each other.
Referring to
As the first fastener 100 is guided toward the fixation site, the tendon 131 is captured in the channel 116 between the sharpened legs 106, 114. The first sharpened leg 106 is driven into the bone 158 at the fixation site to a point where the capture surface 109 compresses the tendon 131 to the bone 158. The second sharpened leg 114 is driven into the bone 158 further compressing the tendon 131 to the bone 158.
The first fastener proximal hole 118 is sized to receive the second fastener 120. The second fastener 120 may be a bone screw, a nail, or other possible fasteners well known in the art. The proximal end of the second fastener 120 comprises a head 124 and the distal portion 126 comprises a sharpened point 122, a threaded portion 128, and may have a cannulation running longitudinal through the center of the second fastener 120. The threaded portion 128 may extend the entire length of the distal portion 126 of the second fastener. The head 124 includes a screw driver engagement portion which may be hexagonal, square, star-shaped or have any other shape known in the art for engaging a screw driver with the same engagement feature.
The second fastener 120 is secured by sliding the distal portion 126 through the first fastener proximal hole 118 into the channel 116 using a screwdriver 150 or other method well known in the art, thus joining the first fastener 100 and second fastener 120 while driving the second fastener 120 into the bone 158. The sharpened point 122 and threaded portion 128 may pierce the captured tendon 131 and further secure it to the bone 158. Alternatively, the threaded portion 128 need not pierce the captured tendon 131, but may instead pass alongside it. Further advancement of the sharpened distal end 126 of the second fastener 120 urges the first fastener 100 toward the bone 158.
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Alternative embodiments for securing the second fastener to the first fastener may include a taper, a snap fit, a cam lock, a separate lock out fastener secured to the fastener assembly, a threaded head portion of the second fastener or any other feature known in the art.
The fastener assembly 119 may be comprised of any materials commonly surgically implanted including but not limited to stainless steels, titanium and its alloys, cobalt-chrome and its alloys, superelastic alloys, shape memory alloys, ceramics, natural or artificial bones, porous coatings, porous materials, porous substrates, bioactive materials such as hydroxylapatite, polyesther, silk, bioabsorbable materials, and polymers such as polyethylene, polyetheretherketone (PEEK), polyaryletherketone (PAEK), polylactic acid (PLA), and acetal copolymer.
It is important to note that the system of attaching the tendon 131 to the bone 158 with the first fastener 100 can operate with or without the second fastener 120.
The threadable engagement feature 148 is threaded into the threads 133 encircling the proximal hole 118 of the first fastener 100. The suture 102 may be secured to a tendon 131 using a Mehalik Hitch, or other method known in the art, thus providing two suture working portions 103, 105. The suture working portions 103, 105 pass through the first and second apertures 110, 112 of the proximal end 108 of the first fastener 100 and may further pass through the suture grooves 138 on the impactor 136. The suture working portions 103, 105 provide a guide for the first fastener 100 and the impactor 136 to a fixation point on the bone 158. The impactor 136 is used to drive the first fastener 100 into the bone. A K-wire may pass through the center of the impactor 136 K-wire aperture 144 and may pass through the center of the first fastener 100 proximal hole 118. The K-wire may be driven into the bone 158 at the fixation point. The impactor 136 may be disengaged from the first fastener 100 by unthreading the threadable engagement feature 146 from the proximal hole 118 of the first fastener and then withdrawn over the K-wire, leaving the K-wire extending from the bone 158 through the first fastener 100. The suture 102 may be secured to the first fastener 100.
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An alternative embodiment of the second fastener may be a nail (not shown), which may comprise a sharpened distal portion, a proximal head portion and a K-wire hole passing longitudinally through the nail. The nail may further comprise an engagement feature designed to engage a nail impactor. The nail impactor may comprise a body, a K-wire hole passing longitudinally through the nail impactor body and an engagement feature designed to engage the nail.
One method for attaching the second fastener nail to the bone may involve sliding the nail and nail impactor over the K-wire so it is encircling the K-wire. The second fastener nail passes slidably through the proximal hole of the first fastener piercing the tendon channel. The nail impactor may drive the nail, which may pierce the tendon, into the bone further securing the first fastener and the suture. The nail impactor may be disengaged from the proximal head portion and the nail impactor may be withdrawn from encircling the K-wire.
Alternative embodiments of a fastener known in the art that may be used in place of the second fastener described above to provide further securability of the tendon to the bone, further securability of the suture to the first fastener and/or further securability of the second fastener to the first fastener.
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The features of the
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The features of the
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Similar to the preferred embodiment the lateral barbs 416 provide further securability of the first fastener 400 to the bone 158. The medial barbs 418 add even further securability of the first fastener 400 when the second fastener 120 drives the first fastener 400 further into the bone, which may cause the first and second sharpened distal legs 404, 414 to wedge, further engaging the medial barbs 418 adding greater first fastener 400 and tendon security.
Another possible embodiment of the first fastener may be similar to
A further embodiment of the first fastener may be a first fastener (not shown) comprising a proximal end capture body and a distal end first sharpened leg extending from the capture body. The first sharpened leg may comprise a backward facing hook or barb extending from the distal end of the first sharpened leg providing added securability of the first fastener to the bone. A second sharpened leg may extend from the capture body opposite the first sharpened leg and may also comprise a backward facing hook or barb extending from the distal end of the second sharpened leg. Each sharpened leg may be separate and independently insertable into the bone. The sharpened legs can be connected by a flexible member that permits independent insertion of screws.
Fastener assemblies 200, 300, and 400, as well as other embodiments, may be assembled and implanted similarly to the method described for first fastener assembly 100. In all assemblies the suture is secured to the tendon with the sutures then being passed through the suture apertures in the first fastener. The sutures serve as a guide to the fixation point for the first fastener. The first fastener is driven into the bone with an impactor which is engaged to the first fastener. The K-wire is driven into the bone through the impactor. The impactor is disengaged and the suture is secured to the first fastener.
The second fastener and screwdriver are guided with the K-wire to the first fastener and fixation site. The second fastener pierces the first fastener hole and is driven into the bone with the screwdriver, piercing the tendon. The second fastener further secures the first fastener and the tendon to the bone. The second fastener further secures the suture to the first fastener as the second fastener engages the rim of the first fastener. The system of attaching a tendon to a bone with a first fastener can operate with or without a second fastener.
The present invention may be embodied in other specific forms without departing from its spirit or essential characteristics. For example, above are described various alternative examples of fasteners for providing tendon attachment. It is appreciated that various features of the above-described examples can be mixed and matched to form a variety of other combinations and alternatives. It is also appreciated that this system should not be limited to a single tendon and bone. This fastener system may be used to attach any tendon to its appropriate bone. 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.
This application claims the benefit of the following, which is incorporated herein by reference: Pending prior U.S. Provisional Patent Application No. 60/963,081, filed 2 Aug. 2007, which carries Applicants' docket no. RED-3 PROV, and is entitled Surgical Implant and Technique.
Number | Date | Country | |
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60963081 | Aug 2007 | US |