AU5070602A - Methods for anchoring autologous or artificial tendon grafts in bone - Google Patents

Description

1,

AUSTRALIA

Patents Act COMPLETE SPECIFICATION

(ORIGINAL)

Class Int. Class Application Number: Lodged: Complete Specification Lodged: Accepted: Published: Priority Related Art: Name of Applicant: Ethicon, Inc.

Actual Inventor(s): Rickey D Hart Address for Service: PHILLIPS ORMONDE FITZPATRICK Patent and Trade Mark Attorneys 367 Collins Street Melbourne 3000 AUSTRALIA Invention Title: METHODS FOR ANCHORING AUTOLOGOUS OR ARTIFICIAL TENDON GRAFTS IN BONE Our Ref: 672243 POF Code: 348060/455965 The following statement is a full description of this invention, including the best method of performing it known to applicant(s): -1- 6006q -2- METHODS FOR ANCHORING AUTOLOGOUS OR ARTIFICIAL TENDON GRAFTS IN BONE Background of the Invention This invention pertains to methods for attaching autologous or artificial tendon grafts to bone. The invention has applications in, for example, repair or the anterior cruciate ligament (ACL) of the knee. It may also be used, for example, for repair of other ligaments such as of the elbow or ankle.

-3- It is not uncommon for ligaments and other soft tissue to tear or detach from bone. Athletes, for example, often suffer tears or other injuries to the anterior cruciate ligament, one of the ligaments connecting the femur (thigh bone) and the tibia (shin bone) at the center of the knee joint. The ACL, which limits hyperextension of the knee and prevents the backward sliding of the femur on the tibial plateau, may be injured when the knee is twisted beyond the normal range of motion, when the knee is twisted while bending and weaving during skiing and other sports activities. ACL injuries may take the form of total or partial tears.

Reconstruction is the most common form of surgery for injuries to the ACL and involves replacing the ACL with a graft of autologous or artificial tendon. An autologous tendon graft may be "harvested" from the patient's patellar ligament, which is part of the common tendon of the quadriceps femoris, connecting the patella to the tibia. An alternative autologous tendon graft may be harvested from the semitendinosus tendon, a long tendon running posteriorly and medially along the thigh, connecting the upper femur to the tibia. Traditionally, patellar grafts are harvested with attached bone plugs that can be securely fixed at the ends of a bone tunnel drilled through the tibia and femur using metallic interference screws, a metal screw and washer, or buttons.

Drawbacks associated with the use of the patellar tendon, include difficulties in harvesting the tendon and post-operative complications.

More recent success has been found using one or more strands of the triplestranded semitendinosus tendon, which can be harvested with minimal post-operative complications. The strands can be used alone or in combination with the gracilis tendon, which anatomically runs parallel along the thigh to the semitendinosus tendon.

Although semitendinosus tendons are increasingly used in ACL repair, they are difficult to attach to bone, due in part to the absence of associated bone plugs.

The art suggests several techniques for attaching the semitendinosus tendon to bone in ACL repair. One such technique involves suturing the tendon to a button or staple on the exterior of the bone. Drawbacks associated with this method include -4stretching or failure of the suture, which may be subjected to tensile forces ranging from 30-50 pounds.

Another technique involves attaching a tendon graft to bone using metallic interference screws. Although such metal screws demonstrate stable fixation and good tensile strength, drawbacks associated with their use include distortion of post-operative radiological studies, metal sensitivity associated with permanently implanted metal screws, or additional operations for metal removal.

Another technique involves attaching a tendon graft to another anchor affixed within a tunnel drilled in the bone. One anchor intended for this use is the Mitek Ligament Anchor available from Mitek Surgical Products, Inc. That anchor includes prongs that lodge into the bone after the anchor has been pulled into position by a suture. Drawbacks associated with this attachment means includes that the anchor must be fabricated from metal to insure sufficient holding strength. Moreover, it must be lodged in the cortical layer near the surface of the femur and therefore necessitates the use of long tendon segments.

An object of this invention is to provide improved methods for attaching autologous or artificial tendon grafts to bone.

A related object of this invention is to provide methods for attachment of autologous and artificial tendons that minimize drawbacks associated with pullout of tendon grafts in ACL or other reconstructive orthopedic surgery.

The discussion of documents, acts, materials, devices, articles and the like is included in this specification solely for the purpose of providing a context for the present invention. It is not suggested or represented that any or all of these matters formed part of the prior art base or were common general knowledge in the field relevant to the present invention as it existed in Australia before the priority date of each claim of this application.

Summary of the Invention According to the present invention there is provided a method for anchoring soft tissue within bone including: drilling an opening into bone; inserting into said bone a stabilizing element including an elongated sleeve with an axial channel extending therethrough; threading soft tissue through an aperture in an inserting element including an aperture containing stem head proximally located to an elongated stem, said stem having a diameter slightly larger than that of said axial channel of said elongated sleeve; and pulling the distal end of said insertion element into proximal end of said stabilizing element.

The present invention also provides a method for replacing a torn ligament including: obtaining a tendon graft; drilling a hole into bone; looping said tendon graft through an aperture in an insertion element; inserting a stabilizing element comprising a sleeve with a cavity therein into said hole; pulling the insertion element into the stabilizing element including a stem with an aperture containing stem head at the proximal end of said stem and any of an aperture, slot and barb at the distal end of said stem.

Brief Description of the Drawings Embodiments of the invention will now be described by way of example only with reference to the accompanying drawings in which: Figure la depicts a frontal view of the bones of the knee and a partially torn anterior cruciate ligament (ACL); -6- Figure Ib depicts a side view of a method for creating a stepped tunnel through the tibia and partially through the femur for insertion of an anchor assembly; Figure 2 depicts a frontal view of a method for affixing a tendon graft into the tunnel of Figure Ib; Figure 3 depicts a detailed side view of an embedded anchor assembly; Figures 4a-4d depict a detailed view of an anchor assembly; and Figures 5a-5c depict a detailed view of the insertion element of an anchor assembly.

7 Detailed Description of the Invention Figure la depicts a partially torn ligament of the knee, the anterior cruciate ligament (ACL) 1. In the illustration, the ACL is attached to a depression in the anterior intercondylar area (not shown) on the surface of the tibial plateau 5. This tibial attachment lies in front of the anterior intercondylar tubercle and is blended with the anterior extremity of the lateral meniscus (not shown). It passes upward, backward, and laterally to be fixed into the posterior part of the medial surface of the lateral condyle (not shown) of the femur 3. The tibia 2 and the patella 4 are also shown.

Figure lb depicts a method for creating a stepped tunnel 7 through the tibia 2 and partially through the femur 3 for insertion of an anchor assembly of the invention. In the illustration, a drill 7 is used by the surgeon to drill an tunnel beginning at the anterior surface of the tibia 2 and ending within the cancellous region of the femur 3. The drill tunnel 7 preferably will enter the femur 3 at or near the isometric point (not shown) close to the anatomical ACL attachment site in accordance with the prior art. The angle of the drill tunnel is in accord with that practiced in the prior art for semitendinosus-style ACL repair. The stepped hole is formed by use of a stepped drill bit such that the ledge separating the wider and narrower diameter tunnels lies within the cancellous portion of the femur 3, e.g., within at least 10mm to 70 mm within the femur of the posterior part of the medial surface of the lateral condyle and, preferably, approximately 45 mm of that surface.

The drill tunnel 7 may terminate within the cancellous portion of the femur 3, or, in the alternative, the surgeon may elect initially to fully penetrate the femur 3 with a guide wire (not shown), leaving a small exit aperture 9 on the opposing surface of the femur in accordance with the prior art covering ACL reconstructive surgery. It will be appreciated by those skilled in the prior art that the above-described invention is not limited to embedding an anchor assembly in the femur 3 but could also be 8 practiced to embed an anchor in the tibia 2 or in bones comprising other joints, e.g., the ankle or elbow region.

Figure 2 depicts shows a graft anchor assembly 12 of the instant invention embedded in bone, for example in the cancellous layer of the femur 3. A tendon graft 10 is looped through the aperture (see detailed drawing in Figure 3) in a anchor assembly 12 with one or more free ends extending through other bone, for example, through the tibia 2.

to Figure 3 depicts in more detail an anchor assembly 12 in operating position embedded in the stepped bone tunnel. The autologous or artificial tendon graft 10 is looped through aperture 13 in the head of the insertion element 14. The stabilizing element 15 is embedded in the bone tunnel, for example by screwing into the stepped tunnel. The insertion element 14 is held in the stabilizing element 15 for example by compression fit, but could also be held by an attachment that requires twist, e.g., of not more than 1800 (so as to avoid twisting the tendon) or by ratcheting or by other attachment mechanism for holding one element in another without excessive twisting.

Figures 4a-d depict the anchor assembly in detail. Figure 4a depicts the stabilizing element 15 which comprises an elongated sleeve 19 containing external protrusions 16, for example external threads. Stabilizing element 15 has a cavity 17, for example an elongated axial channel 17 extending at least partway from the proximal end of stabilizing element 15. For example, axial channel 17 could extend from the proximal to the distal end of stabilizing element 15. Stabilizing element has a flanged head 18. Stabilizing element 15 is comprised of a biocompatible material, for example implant grade high density polyethylene, low density polyethylene (PE 6010 and PE 2030) and polypropylene (13R9A and 23M2: all made by Rexene, Dallas, Texas) or of a bioabsorbable material, for example poly-l-lactide 9 or such as a lactide-glycolide composition. It may also be comprised of a metal.

such as, surgical implant grade steel.

Figure 4a also depicts insertion element 14. Insertion element 14 has an aperture 13 containing head 21 for retaining a ligament replacement. Stem head 21 has an aperture 13 of a size suitable for receiving multiple strands of autologous and/or artificial tendon, but optimally for receiving two or more strands of semitendinosus tendon. The aperture 13 may have dimensions 0.10 inches 0.35 inches (height) by 0.05 0.30 inches (width), and, preferably approximately 0.220 to inches by 0.160 inches. Insertion element 14 has a stem 20, for example an elongated stem 20. The stem has protrusions 22 extending outwardly. Stem protrusions 22 may be inflexible. The diameter of stem 20 is greater than the diameter of axial channel 17 such that stabilizing element 15 is capable of holding the insertion element 14 by compression fit upon insertion of the insertion element 14 into channel 17 of stabilizing element 15. The insertion element 12 can be tapped into the stabilizing element 15 with an emplacement device (not shown). The insertion element 12 is comprised of a biocompatible material, for example implant grade high density polyethylene, low density polyethylene (PE 6010 and PE 2030) and polypropylene (13R9A and 23M2: all made by Rexene, Dallas, Texas) or of a bioabsorbable material, for example poly-1-lactide or such as a lactide-glycolide composition. It may also be comprised of a metal, such as, surgical implant grade steel.

Figure 4b depicts axial channel 17 which has a non-cylindrical cross-section (not shown), optimally a polygon such as a hexagon. Other non-cylindrical crosssections such as a square or pentagon or even oval configurations are also envisioned.

A non-cylindrical cross-section of the axial channel 17 is designed such that a emplacement device (not shown) such as a driver (not shown) with a corresponding non-cylindrical diameter can be inserted into a axial channel and turned such that the external threads 16 of the stabilizing element 15 are screwed into and grip the bone.

One such driver is, an Allen wrench.

Figure 4c depicts insertion of the distal end of an insertion element 12 into the axial channel 17 at the proximal end of a stabilizing element 15. The diameter of elongated stem 20 is slightly greater that the diameter of the non-cylindrical axial channel 17 of the stabilizing element. As a result as depicted in Figure 4d, an elongated stem 20 of the insertion element 12 is held tightly in stabilizing element for example by compression fit into stabilizing element 15 embedded in a stepped bone hole.

Figure 5a depicts an insertion element 10 that can be pulled into the stabilizing element 15 (Figure As above, the insertion element 10 has an aperture 12 containing a head for retaining a ligament replacement and a stem 14 with outwardly expanding protrusions. The diameter of stem is greater than the diameter of axial channel such that stabilizing element 15 is capable of holding the insertion element by compression fit upon insertion of the insertion element into the channel of the stabilizing element. Additionally, the insertion element 10 contains a structure, e.g., aperture 16, suitable for receiving a suture, a wire or other device that can be used to pull the element 10 into the stabilizing element 15 instead of, or in addition to, its being tapped into that element The aperture 16 or other such structure can be located at any point on the insertion element 10 but is preferably located at the distal end of the insertion element. Thus, for example, in an embodiment in which the stem of the insertion element is approximately 0.75 inches long with a diameter of 0.16 inches, the aperture is located 0.05 0.20 inches from the end of the insertion element and preferably 0.12 inches from the distal end.

11 The aperture 16 (or other such structure) is sized sufficiently to accomodate a suture, wire or other pulling device. Those of ordinary skill in the art will of course appreciate that in lieu of an aperture, a slot, barb, hook (as shown in Figures 5b and or any other structure by which the insertion element can be pulled, can be utilized.

An anchor assembly incorporating an insertion element 10 of Figure 5a is generally implanted as described above. In ACL reconstructive surgery, for example, atunnel is drilled at the anterior surface of the tibia and ending within the cancellous region of the femur. The drill tunnel preferably enters the femur at or near the isometric point close to the anatomical ACL attachment site in accordance with the prior art. The angle of the drill tunnel is in accord with that practiced in the prior art for semitendinosus-style ACL repair. A stepped hole is formed by use of a stepped drill bit such that the ledge separating the wider and narrower diameter tunnels lies within the cancellous portion of the femur, within at least 10 mm to 70 mm within the femur of the posterior part of the medical surface of the lateral condyle and, preferably, approximately 45 mm of that surface.

Although the drill tunnel may terminate within the cancellous portion of the femur, a guide wire or K-wire is preferably used to fully penetrate the femur, leaving a small exit aperture on the opposing surface on the femur. The stabilizing element is then embedded in the drilled bone tunnel, for example, by screwing it into the stepped tunnel. At this point, the K-wire (which is preferably equipped with an eyelet at its end) is used to thread a suture through the skin, bone and through the channel of the stabilizing element. The suture is then looped through the aperture, hook, barb, or slot, or other such structure in the insertion element. The insertion element is then pulled into the stabilizing element using that suture. Those skilled in the art will appreciate that a wire, hook or other such apparatus can be used in place of the aforementioned suture.

-12- Described above are methods meeting the preferred objects set forth above.

Those skilled in the art will appreciate that the illustrated embodiments are shown and described by way of example only, and that other methods incorporation modifications therein fall within the scope of the invention. For example, in addition to ACL reconstruction, the invention can be beneficially applied in connection with other soft tissue-to-bone attachments using bone tunnels, such as (by way of non-limiting example) repair of ligaments and tendons in other joints such as the elbow and ankle.

Claims (11)

1. A method for anchoring soft tissue within bone including: drilling an opening into bone; inserting into said bone a stabilizing element including an elongated sleeve with an axial channel extending therethrough; threading soft tissue through an aperture in an insertion element including an aperture containing stem head proximally located to an elongated stem, said stem having a diameter slightly larger than that of said axial channel of said elongated sleeve; and pulling the distal end of said insertion element into proximal end of said stabilizing element.

2. A method according to claim 1, wherein said soft tissue is a tendon graft.

3. A method according to claim 1 or claim 2, wherein the method of drilling said opening includes creating a stepped opening.

4. A method according to claim 3, wherein the stepped opening has at least two different diameters, one less than the diameter of the stabilizing element, and one greater than the diameter of the stem head.

A method according to claim 4, wherein said elongated sleeve of said stabilizing element is screwed into said bone opening at the diameter where said stepped bone opening is slightly smaller than that of said elongated sleeve.

6. A method according to claim 5, wherein said stabilizing element is screwed into said stepped bone opening by use of an emplacement device fitted into said axial channel of said stabilizing element. -14-

7. A method according to claim 5, wherein said insertion element retaining said tendon graft is inserted forcibly into said stabilizing element screwed into said stepped bone hole.

8. A method for replacing a torn ligament including: obtaining a tendon graft; drilling a hole into bone; looping said tendon graft through an aperture in an insertion element; inserting a stabilizing element comprising a sleeve with a cavity therein into said hole; pulling the insertion element into the stabilizing element including a stem with an aperture containing stem head at the proximal end of said stem and any of an aperture, slot and barb at the distal end of said stem.

9. A method according to claim 8, wherein said ligament is an anterior cruciate ligament and said bone aperture is in either a femur or tibia.

A method according to claim 8 wherein said stabilizing element is affixed into bone by interference fit.

11. A method substantially as hereinbefore described with reference to the accompanying drawings. DATED: 28 June2002 PHILLIPS ORMONDE FITZPATRICK Attorneys for: ETHICON, INC.