The present invention is directed to a system and method for repairing a ligament and, more particularly, to a system and method of repairing a ligament using anchors.
The hand includes multiple ligaments that attach to the joints of the finger. Injury to these ligaments is commonly due to any hard force on the finger that causes the finger to be bent too far. This force can result in a partial tear or a complete tear of the ligament. A tear to the ligament results in instability of the joint, swelling, pain, bruising, and possible deformity of the finger. Repairing the ligament involves reattaching the torn ligament with internal sutures.
The present disclosure includes one or more of the features recited in the appended claims and/or the following features which, alone or in any combination, may comprise patentable subject matter.
According to a first aspect of the disclosed embodiments, a surgical kit for repairing a damaged ligament includes a first anchor configured to be secured to a first bone during a surgical procedure to repair the damaged ligament. The first anchor includes a first inner bone anchor that is secured in an opening drilled in the first bone. Suture tape is pre-attached to the first anchor prior to the surgical procedure and extends from the first anchor to a free end. The suture tape is configured to extend over the damaged ligament. A second anchor is configured to secure the free end of the suture tape to a second bone adjacent the first bone during the surgical procedure.
In some embodiments of the first aspect, the first inner bone anchor may extend from a top opening in the first anchor to a bottom opening in the first anchor. A press may be configured to engage the first inner bone anchor through the top opening in the first anchor. The press may be configured to push the first inner bone anchor at least partially through the bottom opening in the first anchor. The first inner bone anchor may bend outward into the first bone as the first inner bone anchor is pushed through the bottom opening in the first anchor. The first inner bone anchor may include two first inner bone anchors. The two first inner bone anchors may bend outward in opposite directions into the first bone as the two first inner bone anchors are pushed through the bottom opening in the first anchor. The first inner bone anchor may include a threaded opening and the press may include a threaded screw. The threaded screw of the press is secured within the threaded opening of the first inner bone anchor. The second anchor may include a second inner bone anchor that is secured in an opening drilled in the second bone.
Optionally, in the first aspect, at least one suture may extend from the first anchor. The at least one suture may be configured to suture a first end of the damaged ligament to a second end of the damaged ligament during the surgical procedure. The second anchor may include an opening configured to receive the free end of the suture tape.
According to a second aspect of the disclosed embodiments, a method for repairing a damaged ligament includes drilling an opening into a first bone during a surgical procedure to repair the damaged ligament. The method also includes securing a first anchor to a first bone by securing a first inner bone anchor of the first anchor in the opening drilled in the first bone. The method also includes extending suture tape over the damaged ligament. The suture tape is pre-attached to the first anchor prior to the surgical procedure and extends from the first anchor to a free end. The method also includes securing the free end of the suture tape to a second bone adjacent the first bone during the surgical procedure with a second anchor.
In some embodiments of the second aspect, the method may also include engaging the first inner bone anchor through a top opening in the first anchor with a press. The method may also include pushing the first inner bone anchor at least partially through a bottom opening in the first anchor with the press. The method may also include pushing the first inner bone anchor through the bottom opening in the first anchor so that the first inner bone anchor bends outward into the first bone. The first inner bone anchor may include two first inner bone anchors. The method may also include pushing the two first inner bone anchors through the bottom opening in the first anchor so that the two first inner bone anchors bend outward in opposite directions into the first bone. The method may also include securing a threaded screw of the press within a threaded opening of the first inner bone anchor. The method may also include securing the second anchor to the second bone by securing a second inner bone anchor of second anchor in an opening drilled in the second bone.
Optionally, in the second aspect, the method may also include suturing a first end of the damaged ligament to a second end of the damaged ligament with at least one suture extending from the first anchor during the surgical procedure. The method may also include positioning the free end of the suture tape in an opening of the second anchor.
According to a third aspect of the disclosed embodiments, a surgical anchor for repairing a damaged ligament includes an anchor body having a top and a bottom. The anchor body is positioned on a bone during a surgical procedure to repair the damaged ligament with the bottom of the anchor body positioned against the bone. A top opening is formed in the top of the anchor body. A bottom opening is formed in a bottom of the anchor body. A channel extends from the top opening to the bottom opening. An inner bone anchor extends through the channel. The inner bone anchor is configured to be pushed at least partially through the bottom opening into the bone by a press that engages the inner bone anchor through the top opening.
In some embodiments of the third aspect, the inner bone anchor may bend outward into the bone as the inner bone anchor is pushed through the bottom opening in the anchor body. Suture tape may be pre-attached to the anchor body prior to the surgical procedure and may extend from the anchor body to a free end. The suture tape may be configured to extend over the damaged ligament.
Additional features, which alone or in combination with any other feature(s), such as those listed above and/or those listed in the claims, can comprise patentable subject matter and will become apparent to those skilled in the art upon consideration of the following detailed description of various embodiments exemplifying the best mode of carrying out the embodiments as presently perceived.
The detailed description particularly refers to the accompanying figures in which:
While the concepts of the present disclosure are susceptible to various modifications and alternative forms, specific exemplary embodiments thereof have been shown by way of example in the drawings and will herein be described in detail. It should be understood, however, that there is no intent to limit the concepts of the present disclosure to the particular forms disclosed, but on the contrary, the intention is to cover all modifications, equivalents, and alternatives falling within the spirit and scope of the invention as defined by the appended claims.
Referring now to
At least one suture 30 extends from the primary anchor 12. The at least one suture 30 extends from the base 14 to a free end 32. A needle 34 is secured to the free end 32. In the illustrative embodiment, the primary anchor 12 includes a pair of sutures 30 extending therefrom. It will be appreciated that the primary anchor 12 may include any number of sutures 30. In some embodiments, the at least one suture 30 is utilized to suture two ends of damaged ligament together during the surgical procedure to repair the damaged ligament. It will be appreciated that in some embodiments, the primary anchor 12 does not include the at least one suture 30, and the surgical procedure is performed without suturing the two ends of the damaged ligament together.
Suture tape 40 also extends from the primary anchor 12. The suture tape 40 extends from the base 14 to a free end 42. The suture tape 40 is configured to be positioned over the damaged ligament during the surgical procedure to repair the damaged ligament. The suture tape 40 is configured to increase a suture footprint allowing for increased soft tissue-to-bone contact in soft tissue repairs, e.g. ligament repairs. The suture tape 40 holds the ligament in place post-surgery to allow the ligament to reconnect to the bone. In some embodiments, the suture tape 40 is formed from a biocompatible material that allows the suture tape 40 to be permanently retained in the surgical site. In other embodiments, the suture tape 40 is formed from a material that absorbs into the body after surgery. For example, the suture tape 40 may be biodegradable and/or bio-absorbable. In some embodiments, the suture tape 40 is formed from a biocompatible material that allows tissue ingrowth. The suture tape 40 can be formed in different sizes and shapes to accommodate patient anatomy and pathology.
A secondary anchor 50 incudes a generally rectangular base 52 that extends between a front end 54 and a back end 56. It will be appreciated that, in some embodiments, the secondary anchor 50 may take any suitable shape, for example circular. A secondary anchor tine 60 extends downward from base 52. In the illustrative embodiment, the secondary anchor 50 includes a single secondary anchor tine 60 that extends downward from the base 52 in a cone configuration to a point 62. In other embodiments, the secondary anchor 50 may include any number of secondary anchor tines 60 that extend to points 62. The secondary anchor 50 also includes a top surface 64 that is configured to receive pressure from the pair of pliers 100 during the surgical procedure to repair the damaged ligament. The secondary anchor tine 60 is configured to be pressed into a patient's bone by the pliers 100 during the surgical procedure so that the secondary anchor 50 is secured to the patient's bone.
Referring to
Referring now to
An inner tine 90 extends downward from the top wall 82 toward the bottom wall 84. The inner tine 90 extends partially downward from the top wall 82 toward the bottom wall so that a slot 92 is formed between the inner tine 90 and the bottom wall 84. The inner tine 90 extends to a point 94. The slot 92 is formed between the point 94 and the bottom wall 84. The free end 42 of the suture tape 40 is configured to be inserted into the opening 80 so that the free end 42 of the suture tape 40 slides into the slot 92 under the point 94 of the inner tine 90. When pressure is applied to the secondary suture 50 to secure the secondary suture 50 to the bone, the inner tine 90 is pressed into the free end 42 of the suture tape 40 to secure the suture tape 40 in the secondary suture 50.
Referring to
In one embodiments, the proximal end 202 and the distal end 204 of the ligament 200 are pulled together and sutured with the sutures 30. That is, the needles 34 are utilized to thread the sutures 30 through the proximal end 202 and the distal end 204 of the ligament 200 to secure the proximal end 202 and the distal end 204 of the ligament 200 together. It will be appreciated that in some embodiments, the surgical kit 10 may not include the sutures 30 and the sutures 30 may not be used to secure the proximal end 202 and the distal end 204 of the ligament 200 together. For example, the ligament 200 may only have a partial tear and may not require suturing.
Referring now to
Using the pliers 100, the first arm 102 of the pliers 100 is positioned on the distal bone 212, and the second arm 104 of the pliers 100 is positioned on the top surface 64 of the secondary anchor 50. The arms 102, 104 of the pliers 100 are squeezed together to apply pressure to the secondary anchor 50 so that the secondary anchor tine 60 embeds within the distal bone 212. Concurrently, the inner tine 90 embeds in the free end 42 of the suture tape 40 that has been inserted in the opening 80 to secure the suture tape 40 in the secondary anchor 50. In some embodiments, the top wall 82 collapses toward the bottom wall 84 to collapse the opening 80 so that the inner tine 90 embeds into the suture tape 40.
With the suture tape 40 secure across the damaged ligament 200, the surgical site is closed with the primary anchor 12 and the secondary anchor 50 positioned in the surgical site. In some embodiments, the primary anchor 12 and the secondary anchor 50 are formed from a biocompatible material that allows the primary anchor 12 and the secondary anchor 50 to be permanently retained in the surgical site. In other embodiments, the primary anchor 12 and the secondary anchor 50 are formed from a material that absorbs into the body after surgery. For example, the primary anchor 12 and the secondary anchor 50 may be biodegradable and/or bio-absorbable. In some embodiments, the primary anchor 12 and the secondary anchor 50 are formed from a biocompatible material that allows tissue ingrowth. The primary anchor 12 and the secondary anchor 50 can be formed in different sizes and shapes to accommodate patient anatomy and pathology.
Referring now to
Suture tape 330 is pre-attached to the primary anchor 302 prior to the surgical procedure. The suture tape 330 is attached to the front end 312 of the primary anchor 302 and extends from the primary anchor 302 to a free end 332. During surgery to repair the damaged ligament, the suture tape 330 is configured to extend over the damaged ligament. At least one suture 334 also extends from the primary anchor 302. The at least one suture extends from the front end 312 of the primary anchor 302 to a free end 336. A needle 338 is attached to the free end 336. The at least one suture 334 is configured to suture a first end of the damaged ligament to a second end of the damaged ligament during the surgical procedure.
A pair of flanges 350 extend from each side 316 of the primary anchor 302. The flanges 350 are generally rounded and configured to deform as the primary anchor 302 is secured to the first bone.
The body 310 of the primary anchor 302 includes a top opening 360 formed in the top 318 of the body 310. An opposite bottom opening 362 is formed in the bottom 320 of the body 310. A channel 364 extends through the body 310 from the top opening 360 to the bottom opening 362. A first inner bone anchor 370 extends through the channel 364. The first inner bone anchor 370 has a length 372 that is substantially the same as a length 374 of the body 310. Accordingly, the first inner bone anchor 370 extends from the top opening 360 to a bottom opening 362 so that the first inner bone anchor 370 extends from the top 318 of the body 310 to the bottom 320 of the body 310. The first inner bone anchor 370 is configured to move from a disengaged position within the body 310 to an engaged position, wherein the first inner bone anchor 370 is pushed through the bottom opening 362 and bends outward. A threaded opening 376 is positioned at a top 378 of the first inner bone anchor 370.
In the illustrated embodiment, the first inner bone anchor 370 includes a pair of first inner bone anchors 370. The pair of first inner bone anchors 370 includes a right side inner anchor 380 and a left side inner anchor 382. The right side inner anchor 380 and a left side inner anchor 382 are positioned adjacent to one another in the channel 364. The right side inner anchor 380 and a left side inner anchor 382 are configured to bend outward in opposite directions into the first bone when the first inner bone anchor 370 is moved to the engaged position.
The first inner bone anchor 370 can be made of metal, polymer, plastic, etc. In some embodiments, the first inner bone anchor 370 is a memory anchor that hooks outward via the memory when the primary anchor 302 is secured to the bone. The first inner bone anchor 370 can have dynamic anchoring capabilities that are designed to facilitate bone attachment of ligament and other soft tissues. The first inner bone anchor 370 can come in varying widths, lengths, and sizes, allowing fixation in most procedures. The first inner bone anchor 370 can have sharp ends that assist with anchoring to the inner bone. The first inner bone anchor 370 extends out fully unfolded laterally and medially to anchor to the inner bone.
The secondary anchor 304 is configured to be secured to a second bone during a surgical procedure to repair the damaged ligament. The secondary anchor 304 includes a body 410 having a front end 412 and an opposite back end 414. A pair of sides 416 extend between the front end 412 and the back end 414. The body 410 extends between a top 418 and a bottom 420.
A pair of flanges 450 extend from each side 416 of the secondary anchor 304. The flanges 450 are generally rounded and configured to deform as the secondary anchor 304 is secured to the first bone.
The body 410 of the secondary anchor 304 includes a top opening 460 formed in the top 418 of the body 410. An opposite bottom opening 462 is formed in the bottom 420 of the body 410. A channel 464 extends through the body 410 from the top opening 460 to the bottom opening 462. A second inner bone anchor 470 extends through the channel 464. The second inner bone anchor 470 has a length 472 that is substantially the same as a length 474 of the body 410. Accordingly, the second inner bone anchor 470 extends from the top opening 460 to a bottom opening 462 so that the second inner bone anchor 470 extends from the top 418 of the body 410 to the bottom 420 of the body 410. The second inner bone anchor 470 is configured to move from a disengaged position within the body 410 to an engaged position, wherein the second inner bone anchor 470 is pushed through the bottom opening 462 and bends outward. A threaded opening 476 is positioned at a top 478 of the second inner bone anchor 470.
In the illustrated embodiment, the second inner bone anchor 470 includes a pair of second inner bone anchors 470. The pair of second inner bone anchors 470 includes a right side inner anchor 480 and a left side inner anchor 482. The right side inner anchor 480 and a left side inner anchor 482 are positioned adjacent to one another in the channel 464. The right side inner anchor 480 and a left side inner anchor 482 are configured to bend outward in opposite directions into the second bone when the second inner bone anchor 470 is moved to the engaged position.
The second inner bone anchor 470 can be made of metal, polymer, plastic, etc. In some embodiments, the second inner bone anchor 470 is a memory anchor that hooks outward via the memory when the primary anchor 302 is secured to the bone. The second inner bone anchor 470 can have dynamic anchoring capabilities that are designed to facilitate bone attachment of ligament and other soft tissues. The second inner bone anchor 470 can come in varying widths, lengths, and sizes, allowing fixation in most procedures. The second inner bone anchor 470 can have sharp ends that assist with anchoring to the inner bone. The second inner bone anchor 470 extends out fully unfolded laterally and medially to anchor to the inner bone.
An opening 490 is formed in the front end 412 of the body 410 adjacent the top 418 of the body 410. A cavity 492 extends from the opening 490 into the body 492. The cavity 492 may extend from the front end 412 to the back end 414 of the body 410. During surgery, the front end 312 of the primary anchor 302 is positioned to face the front end 412 of the secondary anchor 304. The cavity 492 is configured to receive the free end 332 of the suture tape 330. In some embodiments, the cavity 490 collapses to secure the suture tape 330 therein.
Referring to
The primary anchor 302 is secured to the first bone 604 by expanding the first inner bone anchor 370 into the opening 620 using the press 500. In particular, as illustrated in
The secondary anchor 304 is secured to the second bone 612 by expanding the second inner bone anchor 470 into the opening 622 using the press 500. In particular, as illustrated in
The first segment 602 of the damaged ligament 600 is sutured to the second segment 610 of the damaged ligament 600 with the at least one suture 334 extending from the primary anchor 302. Next, the suture tape 330 is extended over the damaged ligament 600 and the free end 332 of the suture tape 330 is secured in the cavity 492 of the secondary anchor 304. With the suture tape 330 secure across the damaged ligament 600, the surgical site is closed with the primary anchor 302 and the secondary anchor 304 positioned in the surgical site. In some embodiments, the primary anchor 302 and the secondary anchor 304 are formed from a biocompatible material that allows the primary anchor 302 and the secondary anchor 304 to be permanently retained in the surgical site. In other embodiments, the primary anchor 302 and the secondary anchor 304 are formed from a material that absorbs into the body after surgery. For example, the primary anchor 302 and the secondary anchor 304 may be biodegradable and/or bio-absorbable. In some embodiments, the primary anchor 302 and the secondary anchor 304 are formed from a biocompatible material that allows tissue ingrowth. The primary anchor 302 and the secondary anchor 304 can be formed in different sizes and shapes to accommodate patient anatomy and pathology.
Any theory, mechanism of operation, proof, or finding stated herein is meant to further enhance understanding of principles of the present disclosure and is not intended to make the present disclosure in any way dependent upon such theory, mechanism of operation, illustrative embodiment, proof, or finding. It should be understood that while the use of the word preferable, preferably or preferred in the description above indicates that the feature so described can be more desirable, it nonetheless cannot be necessary and embodiments lacking the same can be contemplated as within the scope of the disclosure, that scope being defined by the claims that follow.
In reading the claims it is intended that when words such as “a,” “an,” “at least one,” “at least a portion” are used there is no intention to limit the claim to only one item unless specifically stated to the contrary in the claim. When the language “at least a portion” and/or “a portion” is used the item can include a portion and/or the entire item unless specifically stated to the contrary.
It should be understood that only selected embodiments have been shown and described and that all possible alternatives, modifications, aspects, combinations, principles, variations, and equivalents that come within the spirit of the disclosure as defined herein or by any of the following claims are desired to be protected. While embodiments of the disclosure have been illustrated and described in detail in the drawings and foregoing description, the same are to be considered as illustrative and not intended to be exhaustive or to limit the disclosure to the precise forms disclosed. Additional alternatives, modifications and variations can be apparent to those skilled in the art. Also, while multiple inventive aspects and principles can have been presented, they need not be utilized in combination, and many combinations of aspects and principles are possible in light of the various embodiments provided above.
This application is a continuation-in-part of U.S. patent application Ser. No. 17/509,410, filed Oct. 25, 2021, and claims priority under 35 U.S.C. § 119(e) to U.S. Provisional Application No. 63/286,212, filed Dec. 6, 2021, both of which are expressly incorporated by reference herein.
Number | Date | Country | |
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63286212 | Dec 2021 | US |
Number | Date | Country | |
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Parent | 17509410 | Oct 2021 | US |
Child | 17676451 | US |