|Publication number||CA2303853 C|
|Application number||CA 2303853|
|Publication date||30 Jan 2007|
|Filing date||24 Sep 1998|
|Priority date||24 Sep 1997|
|Also published as||CA2303853A1, DE69822185D1, DE69822185T2, EP1024763A1, EP1024763A4, EP1024763B1, US6306138, US6780188, US20020058941, WO1999015095A1|
|Publication number||CA 2303853, CA 2303853 C, CA 2303853C, CA-C-2303853, CA2303853 C, CA2303853C, PCT/1998/19931, PCT/US/1998/019931, PCT/US/1998/19931, PCT/US/98/019931, PCT/US/98/19931, PCT/US1998/019931, PCT/US1998/19931, PCT/US1998019931, PCT/US199819931, PCT/US98/019931, PCT/US98/19931, PCT/US98019931, PCT/US9819931|
|Inventors||Ron Clark, Jerry L. Lower, Raymond E. Olsen|
|Applicant||Depuy Orthopaedics, Inc., Ron Clark, Jerry L. Lower, Raymond E. Olsen, Ethicon, Inc.|
|Export Citation||BiBTeX, EndNote, RefMan|
|Referenced by (2), Classifications (17), Legal Events (2)|
|External Links: CIPO, Espacenet|
$ackaround and Summar~~ of the Invention The present invention relates to the anchoring of ligament replacements or soft tissue in bone tunnels, and more particularly to a cross pin and a method of fixing the cross pin which facilitates securing a replacement graft inside a bone and that promotes healing of the graft inside the bone.
When a ligament such as an anterior cruciate ligament (hereinafter "ACL") of a knee is damaged or torn, a replacement ligament is often installed in the 10 knee to reconstruct the natural ACL. During such reconstruction, with the knee bent appropriately, a tunnel is typically drilled through the anterior portion of the tibia upwardly through the tibial plateau and into the distal end of the femur to approximate the natural position ofthe ACL, in accordance with well known surgical techniques. A
bone-ligament-bone graft is then harvested, o$en from the patellar tendon following 15 standard grafting techniques, all well known in the orthopaedic field.
Typically, a wedge-shaped bone-ligament-bone graft is cut and contoured using a graft guide.
Various fixation methods are known in the orthopaedic field for securing a bone-ligament-bone graft within the tibia and femur so that the graft can heal. For example, it is known to use a pin installed transversely to the hone tunnel to 20 secure the replacement ligament within the tunnel such as that shown in U.S. Patent No. 5,397,356 entitled "Pin for Securing a Replacement Ligament to a Bone" to E. Marlowe Goble and Jerry L. Lower. Also, methods for installing such a cross pin are shown in U.S. Patents Nos. 5,139,520 entitled "Method for ACL
to Thomas D. Rosenberg; 5,562,671 entitled "Ligament Replacement Cross Pinning 25 Method" to E. Marlowe Goble and Jerry L. Lower; and 5,350,380 entitled "Method for Securing a Ligament Replacement in a Bone" to E. Marlowe Goble and Jerry L.
These types of pins often operate by holding and forcing the bone block at the end of the replacement ligament against the wall of the tunnel, essentially wedging 34 . the bone block in place. In other known methods, sutures coupled to the graft are anchored to the bone using screws or washers. The replacement ligaments can also be coupled directly to the bone using plates or washers in conjunction with a bone screw.
Alternatively, the replacement ligament can be secured by interference screw fixation, as disclosed in U.S. Pat. No. 4,950,270 entitled "Cannulated Self Tapping Bone Screw" to Jerald A. Bowman and Richard V. Zile.
Other materials which can be used as replacement ligaments include the gracilis tendon, semitendinosus tendon, and small intestine submucosa (hereinafter "SIS). U.5. Patents Nos. 4,902,508 entitled "Tissue Graft Composition" to Stephen F.
Badylak, et al.; 5,281,422 entitled "Graft for Promoting Autogenous Tissue Growth"
to Stephen F. Badylak, et al.; and 5,611,969 entitled "Large Area Submucosal Tissue GraR Constructs" to Umesh H. Patel, et al. describe harvesting and preparation of SIS
While these graft materials perform well, prior art procedures for inserting and securing such material are time consuming. Also, in situations where previous reconstruction has been performed, a new femoral tunnel placed close to the previous tunnel may not allow for fixation methods such as interference screw fixation.
Replacement ligaments can be secured within the femoral tunnel without the use of a bone plug by looping the replacement ligament over a cross pin.
A tendon threader, such as those described in U.S. Patents Nos. 5,266,075 entitled "Tendon Threader for Endosteal Ligament Mounting" to Ron Clark and Raymond E.
Olsen; and 5,601,562 entitled "Forked Insertion Tool and Method of Arthroscopic Surgery Using the Same" to Eugene M. Wolf and Richard D. Grafton, can be used to form a loop in the replacement ligament and to position the replacement ligament within the femoral tunnel so that the loop may be captured by the cross pin.
The devices and methods disclosed in these patents are incorporated herein by reference.
Methods which use a cross pin to secure a looped replacement ligament are effective, especially in situations in which there had been a previous reconstruction.
Unfortunately, existing cross pins were.not designed for this purpose.
Generally, they were designed to wedge a bone block into the medial wall of the bone tunnel.
These pins were not designed to be inserted easily into a graft loop, and they were not designed to hold the graft material in contact with the femoral wall, which would insure better ingrowth.
The graft fixation method and cross pin of the present invention provide advantages over the prior fixation methods and pins. The pin includes two tapered WO 99115095 PC'T/US98/19931 portions, a body, and a threaded portion. In the illustrated embodiment, the first w tapered portion is long, relatively narrow, has a gentle taper, and can be inserted easily through the transversely drilled hole and into the graft insertion tool, where it captures the loop of the replacement ligament more easily than prior pins. The first tapered 5 portion also inserts easily into the medial side of the femur. Because the first tapered portion is relatively narrow, it may eliminate the need for a guidewire during insertion of the pin.
In the illustrated embodiment, the second tapered portion is substantially shorter and has a more severe taper than the first tapered portion. Also, 10 as illustrated, the body portion is cylindrical, but body portions with other shapes may be acceptable. As the cross pin is inserted, the wider second tapered portion compresses the replacement ligament against the wall of the femoral tunnel.
The body of the cross pin then holds the replacement ligament against the wall. Thus, the present invention insures better ingrowth and provides a more secure fixation 1 S technique than previously found. An additional advantage of the current invention is that the second tapered portion provides resistance when it meets the medial wall of the femoral tunnel, thus signaling when the cross pin is fully seated. Another advantage of the current fixation method and pin is that rigid fixation afforded by the cross pin allows the patient immediately to bear weight and start range of motion 20 exercises.
Also in the illustrated embodiment, when the cross pin is fully seated, the threaded portion will be buried in the femur, and the proximal end of the cross pin will be flush with the lateral surface of the femur. However, a cross pin having a head which may protrude from the lateral surface of the femur is also within the scope of 25 this invention. Such a head may aid in installation or may be useful for later removal of the pin.
The present invention also includes a method for installing the cross pin. By using the illustrated method, a surgeon may insert the looped replacement ligament into the femoral tunnel, capture the loop with the cross pin with relative ease, 30 and seat the cross pin at the appropriate depth. The method results in a replacement ligament which is held securely in the femoral tunnel, in such a way as to insure rapid ingrowth.
Additional objects, features, and advantages of the present invention -will become apparent from the following description of a preferred embodiment exemplifying the best mode of carrying out the invention as presently perceived.
Brief Descri~ion of the Drawings Fig. 1 is a cross-sectional view of a femoral tunnel showing a drill pin extending through the femoral tunnel into the medial side of the femoral tunnel;
Fig. 2 is a view similar to Fig. 1 showing the drill pin in a transverse tunnel across the femoral tunnel and into the medial side, and showing a cross pin reamer inserted over the drill pin and extending through the lateral side of the femoral tunnel;
Fig. 3 is a view similar to Fig. 2 after the drill pin and cross pin reamer are withdrawn from the transverse tunnel, a cross pin guidewire is inserted in the lateral side of the transverse tunnel, and a replacement ligament wrapped around a soft tissue tendon passer is inserted into the femoral tunnel;
Fig. 4 is a view similar to Fig. 3 after the tendon passer is removed from the femoral tunnel and showing the cross pin guidewire extending completely through a cross pin (in cross-section), through the femoral tunnel, through the replacement ligament looped over the cross pin, and into the medial side of the femoral tunnel;
Fig. 5 is a view similar to Fig. 4 showing a first tapered portion of the cross pin just being inserted into a medial side of the femoral tunnel;
Fig. 6 shows the cross pin beginning to occupy an increasing portion of the femoral tunnel;
Fig. 7 shows further insertion of the cross pin through the femoral 25 tunnel, such that a second tapered portion has entered the femoral tunnel and the second tapered portion has begun to hold the replacement ligament against the wall of the femoral tunnel;
Fig. 8 shows the cross pin at a position of maximum insertion and tendon compression where the second tapered portion on cross pin is in contact with the medial side of the femoral tunnel, and the body on cross pin compresses the replacement ligament securely against the wall of the femoral tunnel;
Fig. 9 is a side view of the cross pin and the cross pin guidewire in .
accordance with the present invention showing a proximal end of the cross pin having a threaded portion for securing the cross pin within the femur (not shown), two tapered portions, the first tapered portion being positioned at the distal end of the 5 cross pin and proportioned and designed to slide within the tendon passer, through the looped replacement ligament, and into the medial side of the femoral tunnel, the second tapered portion of the cross pin being positioned adjacent to the first tapered portion and proportioned and designed to begin the process of holding the replacement ligament against the wall of the femoral tunnel and to provide resistance when it 10 engages the medial side of the femoral tunnel, and a body proportioned and designed to hold the replacement ligament against the wall of the femoral tunnel for the purpose of ingrowth;
Fig. 10 is a side view of an alternative embodiment of the cross pin showing a head adjacent to the threaded portion;
15 Fig. 11 is a view of a tibia and femur showing a reamer placed within the tibia3 tunnel and femoral tunnel, the reamer extending into the cortex of the femur, a ratcheting cannula positioned through a tunnel locator which is coupled to a cross pin guide, and a drill pin which is placed through the ratcheting cannula;
Fig. 12 is a view similar to Fig. 11 after the reamer has been removed 20 from the femoral tunnel, showing the drill pin through the ratcheting cannula after the drill pin has drilled through the femoral tunnel and into the medial side of the femur, the drill pin intersecting the axis of the femoral tunnel; and Fig. 13 is a view similar to Fig. 12 showing the cross pin over the guide wire as the cross pin is about to be inserted into the femur and also showing the tendon 25 passer holding the replacement Ligament to be inserted through the tibia and into the femoral tunnel.
Detailed Description of the lprawings In accordance with the present invention, a cross pin fixation system is 30 provided for ACL reconstruction. In the method of the present invention, as illustrated, replacement ligaments of semitendinosus tendon, gracilis tendon, or SIS are used to replace the ACL. However, it is understood that other materials may be used as the replacement ligament within the scope of the invention. A looped replacement "
ligament 24 is inserted into the femoral tunnel 10. A cross pin 20 secures the replacement ligament 24 by holding the replacement ligament 24 against the wall 15 of a femoral tunnel 10. See Fig. 10. It will be appreciated that this holding action occurs 5 in the illustrated embodiment by wedging and compressing the replacement ligaments against the wall of the femoral tunnel 10. The improved fixation method also secures the replacement ligament 24 by looping the replacement ligament 24 around the cross pin 20 itself. Thus, the replacement ligament 24 is secured over and around the cross pin 20 which is placed across the femoral tunnel 10 perpendicular to its axis.
While the 10 illustrated embodiment details a cross pin fixation method for ACL
reconstruction, the pin and method of the present invention also may be used for other types of reconstruction. The graft fixation system of the present invention provides accurate and reproducible placement of the cross pin 20 while providing secure rigid fixation of the replacement ligament 24.
15 The fixation system of the present invention briefly includes the following steps and devices:
The present method for replacing the ACL begins with drilling a tunnel 11 through the tibia 34. Before drilling begins, a tibial guide pin (not shown) is inserted from the anteromedial tibia and exits on the tibial plateau. This tibial guide pin 20 is then over-drilled with a reamer. A back cutting burr (not shown) then smooths the tunnel rim (not shown) of debris. The knee is flexed 90 to 110 degrees, and a femoral aimer (not shown) is used to locate a desired position of the femoral tunnel 10. Once the desired position has been secured, a threaded bayonet point pin with eyelet (not shown) is drilled into the femur 36 until it reaches the far cortex 13. Next, the femur 25 36 is drilled using a reamer 32. Ideally, a reamer should be used which is 9 or 10 mm wide, and the drilling should leave a femoral tunnel 10 which is 35 mm deep.
Gradations along the reamer's shaft can be used to indicate the depth of the tunnel.
Although some instruments described herein are not illustrated, all are commonly available and one of ordinary skill in the art will understand their use.
30 Once the femoral tunnel 10 has been drilled, a cross pin guide 38 is attached directly to the reamer 32 and locked into place so that the cross pin guide 38 may rotate freely about the axis 37 of the femoral tunnel 10. As shown in Fig.
11, a _'j_ tunnel locator 40 is mounted on the cross pin guide 38, and a ratcheting cannula 42 is ' inserted into the tunnel locator 40. Ideally, the cross pin guide 38 has graduations which indicate the distance in millimeters from the tip of the reamer in the femoral tunnel. Also ideally, the tunnel locator 40 is placed at the 15 mm mark. .
5 The ratcheting cannula 42 is advanced until it contacts the skin. The cross pin guide 38 is then rotated away and an incision is made down to the bone. The cross pin guide 38 is rotated back into position and the ratcheting cannula 42 is advanced until it contacts the femoral cortex 13. A calibrated drill pin 12 is placed into the ratcheting cannula 42. Preferably, a 2.5 mm drill pin is used. The drill pin 12 also 10 is advanced until it contacts the femoral cortex 13. The drill pin 12 is drilled into the femur 36 until it reaches the reamer 32, which is still located in the femoral tunnel 10.
Calibrated markings on drill pin 12 allow the depth of penetration to be determined.
The overall length of cross pin 20 and depth of the transverse tunnel 14 are determined by adding approximately 30 mm to the depth of penetration (reamer diameter plus 20 15 mm for the cross pin tip). The drill pin is then carefully withdrawn about 5 mm from the reamer.
The cross pin guide 38 (including the tunnel locator 40) and the reamer 32 (along with a reamer pin if it is still in the femoral tunnel) are removed from the femur 36, and the drill pin 12 is gently tapped until it appears in the femoral tunnel 10.
20 The appearance of the drill pin 12 can be seen through the use of an arthroscope which is placed in the femoral tunnel 10. As it is advanced, the drill pin 12 should cross the center of the femoral tunnel 10, so that it intersects with the axis 37 of the femoral tunnel 10. If necessary, the reamer 32 is placed back into the femoral tunnel 10, the cross pin guide 38 is reattached to the reamer 32, and placement of the drill pin 12 is 25 repeated. The drill pin 12 is then advanced into the medial side 25 of the femur 36, at least to the depth as calculated above. Next, a cannulated cross pin reamer 16 is used to enlarge the lateral side 27 of transverse tunnel 14 for insertion of the cross pin 20.
Ideally, a soft tissue protector (not shown) is used in conjunction with the cross pin reamer 16.
30 Once the path has been enlarged, the drill pin 12 is withdrawn and a cross pin guidewire 18 is inserted through the cannulated cross pin reamer 16 and into the medial side 25 of the femur 36. With the guidewire I8 in place, the cross pin -$.
reamer 16 is removed and the cross pin 20 is advanced, distal end first, over the guidewire 18, but not yet through the femoral tunnel I0. See Fig. 13. The guidewire 18 is then withdrawn from the femoral tunnel 10. Finally, the replacement ligament 24 ' is looped onto the tendon passer 22 and inserted through the tlbial tunnel 11 and on into the femoral tunnel 10. A surgical lubricant may be used to ease passage.
Ideally, a tendon passer 22 with a T-handle (not shown) is used, so that when the T-handle is parallel with the cross pin 20, the replacement ligament 24 is aligned such that further insertion of the cross pin 20 will capture the looped replacement ligament 24.
The guidewire 18 is inserted back across the femoral tunnel 10 into the medial side 25 of the femur 36, and the tendon passer 22 is removed. At this point, it is necessary to make sure that the replacement ligament 24 has been captured over the guidewire 18.
This can be done by gently pulling on the ends of the replacement ligament.
The cross pin 20 can now be advanced over the guidewire 18, preferably using a cannulated driver (not shown). As the cross pin 20 is advanced, the body 21 of the cross pin 20 acts to hold the replacement ligament 24 against the wall I 5 of femoral tunnel 10 and, thus, insure better ingrowth. Once fully seated, the body 21 also acts to secure the looped replacement ligament 24 within the femoral tunnel.
When the cross pin 20 can no longer be advanced, the cross pin 20 should be fully seated. This resistance represents the second tapered portion 28 engaging the medial wall 25 of the femoral tunnel 10. The guidewire 18 may then lie removed.
Because of the gradual taper of the first tapered portion 26, the guidewire 18 is not essential, and its use may be omitted. Finally, the replacement ligament Z4 is secured on the tibial side by any of various known fixation methods.
In the illustrated embodiment, the threaded portion 30 of the proximal end 29 of the cross pin 20 will bury into the femur 36 because the length has been custom determined for each patient. However, the cross pin 20 in accordance with the present invention is placed into the femur 36 in such a position that the cross pin 20 may be retrieved from the femur 36 after the replacement ligament 24 has healed into the bone. It is understood that a cross pin 20 with a head 33 adjacent to the threaded portion 30 will operate in the same manner. See Fig. 10. Also, the cross pin 20 used in the fixation system of the present invention provides high graft pull out values.
Finally, the cross pin 20 ei~ectively attaches the replacement graft close to the anatomic origin of the ACL on the femur 36.
Although the invention has been described with reference to several embodiments, variations and modifications exist within the scope and spirit of the 5 invention as described.
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US7867264||29 Mar 2004||11 Jan 2011||Ethicon, Inc.||Apparatus and method for attaching soft tissue to bone|
|US8518091||1 Mar 2011||27 Aug 2013||Depuy Mitek, Llc||System and method for attaching soft tissue to bone|
|International Classification||A61B17/58, A61B19/00, A61B17/17, A61F2/08, A61B17/76, A61B17/04|
|Cooperative Classification||A61B2090/062, A61F2002/0882, A61B17/1714, A61F2/0811, A61F2002/0841, A61F2/0805, A61B17/1764, A61F2002/0852|
|European Classification||A61F2/08D, A61F2/08F, A61B17/17F|
|25 Aug 2003||EEER||Examination request|
|5 Nov 2015||MKLA||Lapsed|
Effective date: 20150924