Systems and methods for preparing reinforced graft constructs
11517420 · 2022-12-06
Assignee
Inventors
Cpc classification
A61F2220/0075
HUMAN NECESSITIES
International classification
A61B17/04
HUMAN NECESSITIES
Abstract
Systems and methods for preparing a tissue repair construct for a ligament reconstruction procedure using a reinforced whip-stitching are provided. The described techniques include passing a needle having suture tails attached thereto through a first surface of a graft at an origin point so that a portion of the suture tails exits on a second, opposite surface of the graft while a terminal length of the suture tails is maintained on the first surface of the graft. Multiple suture loops are formed by repeatedly passing the needle with the suture tails around opposite sides of the graft and through the first surface of the graft at subsequent entry points spaced apart along a length of the graft. Each loop is formed so that the construct is reinforced by having a terminal length of each of the suture tails disposed between the first surface of the graft and the loop.
Claims
1. A tissue repair construct, comprising: a graft having first and second ends; and a suture affixed to the graft and extending along a portion of a length of the graft from an origin point remote from the first end of the graft, the suture having a pattern comprising multiple loops of suture spaced apart along the portion of the length of the graft and extending from the origin point to the first end of the graft, each loop overlaying a terminal length of each of two suture tails of the suture such that at least a portion of the terminal length of each suture tail is disposed between a first surface of the graft and a portion of one of the multiple loops.
2. The tissue repair construct of claim 1, wherein the multiple loops of suture encircle opposed sides of the graft.
3. The tissue repair construct of claim 1, wherein the terminal length of each of the two suture tails is disposed along the surface of the graft and extends from the origin point to the first end of the graft.
4. The tissue repair construct of claim 1, wherein the suture penetrates the first surface of the graft at the origin point.
5. A tissue repair construct, comprising: a graft including a first end and a second end opposite the first end; and a suture coupled to the graft and including a first free end, a second free end opposite the first end, and first and second portions extending from the first free end and the second free end respectively, the first free end and the second free end of the suture disposed on a surface of the graft, the first and second portions configured to form multiple loops of suture, each loop being spaced apart along a length of the graft and encircling the graft and the first and second free ends of the suture such that the first and second free ends of the suture are disposed between the surface of the graft and a portion of one of the multiple loops.
6. The tissue repair construct of claim 5, wherein the first free end and the second free end of the suture form a spine when disposed on the surface of the graft.
7. The tissue repair construct of claim 5, wherein the suture penetrates the surface of the graft at an origin point remote from the first end of the graft.
8. A tissue repair construct, comprising: a graft having first and second ends; and a suture affixed to the graft and extending along a portion of a length of the graft from an origin point remote from the first end of the graft, the suture having a pattern comprising multiple loops of suture spaced apart along the portion of the length of the graft and extending from the origin point to a terminal point adjacent to the first end of the graft, each loop overlaying a terminal length of each of two suture tails of the suture such that at least a portion of the terminal length of each suture tail is disposed between a first surface of the graft and a portion of one of the multiple loops, wherein each loop is defined by adjacent portions of the suture tails passing around opposite sides of the graft.
9. The tissue repair construct of claim 8, further comprising: a second suture affixed to the graft and extending along a second portion of the length of the graft from a second origin point remote from the second end of the graft, the second suture having a pattern comprising second multiple loops of suture spaced apart along the second portion of the length of the graft and extending from the second origin point to a second terminal point adjacent to the second end of the graft, each loop overlaying a second terminal length of each of two second suture tails of the second suture such that the second terminal length of each suture tail is disposed between the first surface of the graft and a portion of one of the second multiple loops, wherein each of the second loops is defined by adjacent portions of the second suture tails passing around opposite sides of the graft.
10. The tissue repair construct of claim 8, wherein a needle is positioned at substantially a mid-point of the suture and the first and second suture tails attached to the needle have approximately the same length.
11. The tissue repair construct of claim 8, wherein the suture tails extend beyond the first end of the graft.
12. The tissue repair construct of claim 8, wherein the suture comprises a continuous suture.
13. The tissue repair construct of claim 8, wherein the adjacent portions of the suture tails pass through the first surface of the graft at one entry point to a second surface of the graft, and wherein each of the suture tails passes around opposite sides of the graft to another entry point spaced longitudinally from the origin point.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1) The embodiments described above will be more fully understood from the following detailed description taken in conjunction with the accompanying drawings. The drawings are not intended to be drawn to scale. For purposes of clarity, not every component may be labeled in every drawing. In the drawings:
(2)
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DETAILED DESCRIPTION
(7) Certain exemplary embodiments will now be described to provide an overall understanding of the principles of the systems and methods disclosed herein. One or more examples of these embodiments are illustrated in the accompanying drawings. Those skilled in the art will understand that the systems and methods specifically described herein and illustrated in the accompanying drawings are non-limiting exemplary embodiments and that the scope of the embodiments is defined solely by the claims. Further, the features illustrated or described in connection with one exemplary embodiment may be combined with the features of other embodiments. Such modifications and variations are intended to be included within the scope of the described embodiments.
(8) The embodiments described herein generally relate to systems and methods for preparing ligament grafts for ligament reconstruction, or augmentation, surgeries. A graft is prepared by reinforcing one or both end portions thereof to thus create a tissue repair construct. In some embodiments, a method is provided that includes preparing a tissue repair construct using a whip-stitching technique and reinforcing the graft and the stitching using free ends, or a terminal length, of suture tails of the suture being affixed to the graft. As a needle attached to the suture is passed through a first surface of the graft at a first entry point, the free ends of the suture tails remain positioned on the first surface of the graft so that multiple suture loops subsequently formed around and through the graft encompass the suture tails.
(9) The systems and methods described herein may have a number of advantages over existing techniques for preparing ligament grafts. In particular, a graft is prepared using the described tissue repair construct in a simple and effective manner. Because the tissue repair construct is reinforced using the same suture that is used to form loops, reinforcing the construct does not increase the time required for the construct preparation. Furthermore, the reinforcement improves the overall strength of the tissue repair construct. Thus, the time required to prepare the graft can be reduced, which can reduce the overall time and cost of the surgery and mitigate risk to the patient. Also, the described graft preparation procedure is simplified and is less labor-intensive.
(10) The described techniques can be used in conjunction with a variety of ligament grafts, including hamstring ligament grafts, and in a variety of different surgical contexts regardless of the type of ligament graft being used in a particular surgical procedure. The systems and methods described herein can be utilized in connection with preparing graft ligaments for repairing or replacing ligaments in a variety of joints, but can in some embodiments have particular utility in cruciate ligament reconstruction procedures. For example, the described techniques are used to prepare grafts used in ACL and/or PCL repair procedures.
(11)
(12) The graft 102 can be a tendon or any other type of graft, and it can include one or more graft bundles or strands. The first and second suture tails 106, 108 affixed to the graft 102 have respective free ends 116, 118 that are used to provide structural support for the tissue repair construct 110. As shown in
(13) The suture 104 is passed through the first surface 109 of the graft 202 at the origin point 112 so that it exits from the second surface of the graft 102, opposite to the first surface 109, which is not shown in
(14) In the illustrated embodiment, the suture loops 110 are formed in the direction towards the first end 102a of the graft 102. As shown in
(15) As shown in
(16)
(17) In the prepared tissue repair construct 100, the first and second free ends 116, 118 of the first and second suture tails 106, 108 are positioned on the first surface 109 of the graft 102 so that they are disposed along the sides of the graft 102, as shown in
(18) Regardless of the way in which the first and second free ends 116, 118 are positioned on the surface of the graft 102, the first and second free ends 116, 118 function like a spine extending along the graft 102, thus improving the strength of the construct. In a typical graft preparation technique, at each pass through the surface of the graft 102, the needle 103 pierces the graft 102 approximately in the middle of the graft surface. Thus, the graft fibers can be moved apart by the needle piercing therethrough, which can lead to a certain degree of disintegration of graft fibers, which may ultimately cause weakening of the graft 102. The reinforcement features described herein, such as use of the first and second free ends 116, 118 on the surface of the graft so that they are encircled by the loops, strengthen the tissue repair construct 100 and improve load distribution when a load is applied to the graft 102. In particular, the first and second free ends 116, 118 help to distribute the load from the needle/suture entry points on the graft 102, so that a larger load can be applied without causing damage to tissue of the graft 102. Thus, the first and second free ends 116, 118 act as a “rip-stop” that helps to protect the graft tissue from being excessively deformed or ripped.
(19) As discussed above, the needle 103 having the first and second suture tails 106, 108 of the suture 104 attached thereto is shown in
(20) A length of the first and second free ends 116, 118 reinforcing the tissue repair construct 100 can vary in a number of ways. In the illustrated embodiment, the length of the first and second free ends 116, 118 can be equal or approximately equal to a length of a portion of the graft 102 that has the loops 110 formed thereon. Thus, the first and second free ends 116, 118 can extend from the origin point 112 to the terminal point 128 adjacent to the first end 102a of the graft 102. The first and second free ends 116, 118 can extend beyond the terminal point 128 towards the first end 102a of the graft 102 and they may extend only slightly (e.g., to a distance of less than 1 cm) or not extend at all beyond the first end 102a of the graft 102.
(21) Alternatively, in some embodiments, one or both of the first and second free ends 116, 118 extend beyond the first end 102a of the graft 102 by a distance that is greater than 1 cm. For example, the first and second free ends 116, 118 can extend beyond the first end 102a of the graft 102 so that their length is approximately equal to a length of the free ends of the suture tails 106, 108 that are formed after the suture tails 106, 108 are separated from the needle 103. One skilled in the art will appreciate that the first and second free ends 116, 118 can have any suitable length, as the described embodiments are not limited in this respect.
(22) The suture 104, as well as other sutures that are used in the described graft preparation techniques, can be formed from any suitable materials. In some embodiments, the suture can be from size 0 to size 5, such as Orthocord™ suture commercially available from DePuy Mitek, and Ethibond™ suture available from Ethicon, Inc. Orthocord™ suture is approximately fifty-five to sixty-five percent PDS™ polydioxanone, which is bioabsorbable, and the remaining percent includes ultra high molecular weight polyethylene, while Ethibond™ suture is primarily high strength polyester. In some embodiments, the issue repair construct can be formed from ultra-high-molecular-weight polyethylene (UHMWPE). In some embodiments, the construct can include High-Molecular Weight-polyethylene (HMWPE) sutures or HMWPE sutures with a co-braid (e.g., monofilament polypropylene, nylon or other co-braid). In some embodiments, monofilament sutures such as, for example, Monocryl® available from Ethicon, Inc., may be utilized. As another example, an absorbable suture such as Vycryl® (a copolymer made from 90% glycolide and 10% L-lactide) also available from Ethicon, Inc. may be used. The sutures used herein can have any suitable amount and type of bioabsorbable material, which can depend on a particular surgical procedure and/or surgeon preferences.
(23) It should be appreciated that although the tissue repair construct 100 is shown on one end of the graft 102 in
(24)
(25) In the illustrated embodiment, the suture 204 is attached to the needle 203 so that the needle 203 is positioned approximately in the middle of the suture 204 and the first and second suture tails 206, 208 have approximately the same length. However, it should be appreciated that the first and second suture tails 206, 208 can have any suitable lengths, including different lengths.
(26) As shown in
(27) As also shown in
(28) As shown in
(29) As shown in
(30) The needle 203 with the attached first and second suture tails 206, 208 is passed through the graft 202 from its first surface 209 to the second surface 211, and then extended so that the first and second suture tails 206, 208 are passed through the graft 202 to thereby form the first loop 210A as shown in
(31) In some embodiments, as shown in more detail below with regard to
(32) As shown in
(33) The needle 203 with the attached first and second suture tails 206, 208 is then repeatedly passed through the first surface 209 of the graft 202 at subsequent entry points longitudinally spaced apart from the first and second entry points 212, 214 in the first direction to the second surface 211 to form multiple loops. In this way, a tissue repair construct 200 shown in
(34) As shown in
(35) After the multiple loops are formed, the suture 204 can be cut off to separate the suture tails 206, 208 from the needle 203. As a result, as shown in
(36) In some embodiments, the tissue repair construct 200 is formed so that a length of the free suture ends 216, 218 having at least a portion thereof disposed along a portion of a length of the graft 202 is approximately equal to a length of the free ends of the suture tails 206, 208 shown in
(37) Although not shown in
(38) A person skilled in the art will appreciate that the suture loops, such as suture loops 110 (
(39) A tissue repair construct in accordance with some embodiments can be formed such that the suture reinforcement structure is present on both of the opposite end portions of the graft. For example, in one exemplary embodiment illustrated in
(40) The suture reinforcement regions 401, 401′ of construct 400 can have any suitable configurations. As shown in
(41) One skilled in the art will appreciate that three loops of each of the multiple suture loops 410, 410′ are shown by way of example only, as the suture reinforcement regions 401, 401′ can include any suitable number of loops, including a different number of loops among the regions 401, 401′. For example, in some embodiments, a number of the loops formed in each of the suture reinforcement regions 401, 401′ can range from three to eight. However, other number of loops can be formed. A desired number of loops can depend on characteristics of the graft (e.g., its size, condition, number of bundles used, etc.), a type of the surgery, a nature of the damage at the surgical site, and any other factors.
(42) The suture reinforcement regions 401, 401′ can be formed in any suitable order. For example, the suture reinforcement region 401 can be formed first and then the suture reinforcement region 401′ can be prepared, or vice versa. One or both ends of the graft 402 can be held steady using suitable graft preparation equipment. For example, the DePuy Mitek Graft Preparation System can be utilized.
(43) One skilled in the art will appreciate that the suture reinforcement regions 401, 401′ can vary in any number of ways. For example, different suture reinforcement regions can be formed on opposite ends of the graft. Furthermore, the free suture ends 416, 418, 416′, 418′ are shown in
(44) It should be appreciated that although illustrated embodiments provide techniques for preparing anterior or posterior cruciate ligaments for ligament reconstruction surgery, the techniques can be adapted for preparation of grafts for repair of other ligaments as well. For example, the described method can be used to prepare grafts for proximal or distal biceps repair.
(45) Having thus described some examples of the described embodiments, various alterations, modifications, and improvements will readily occur to those skilled in the art. For example, in some embodiments, as suture loops of a tissue repair construct are formed, free suture ends of the suture can be penetrated through by a needle having tails of the suture attached thereto. Thus,
(46) A needle (not shown) can be attached to the first and second suture tails 506, 508 of the suture 504 in any suitable manner.
(47) After the first and second suture tails 506, 508 are then passed around opposite side surfaces of the graft 502, the needle with the suture tails 506, 508 can pass through the first surface 509 at a second entry point 514. In the illustrated embodiment, as the needle with the suture tails 506, 508 passes through the first surface 509 at the second entry point 514, it also penetrates through one or both of the free suture ends 516, 518. As shown in
(48) One skilled in the art will appreciate that the needle can pass through both or one of the free suture ends 516, 518. Thus, even though in
(49) The free suture ends 516, 518 can have any suitable width. For example, in one embodiment, the width of one or both of the free suture ends 516, 518 can range from about 2 mm to about 4 mm. However, one skilled in the art will appreciate that the free suture ends 516, 518 can have other widths.
(50) The free suture ends 516, 518 can have any suitable configuration. In some embodiments, one or both of the free suture ends 516, 518 can be at least partially flat so that they are easier to penetrate therethrough than a suture with a round or approximately round cross-section. For example, one or both of the free suture ends 516, 518 can be tape-like or ribbon-like or they can be in any other form. The free suture ends 516, 518 can be flattened throughout their entire lengths or at portions thereof. The free suture ends 516, 518 can be formed as at least partially flat in a number of ways. For example, the suture 504 can be flattened (e.g., mechanically and/or by heat, etc.). Additionally or alternatively, the wider portion can be created by braiding, weaving, crocheting, knitting, or otherwise manipulating the suture 504. Furthermore, in some embodiments, the portion of the suture forming the free suture ends 516, 518 can be one or more separate elements that can be attached to the suture tails 506, 508 in a suitable manner.
(51) The above alterations, modifications, and improvements are intended to be within the spirit and scope of the described embodiments. Accordingly, the foregoing description is by way of example only, and not intended to be limiting.