|Publication number||USRE39301 E1|
|Application number||US 08/698,781|
|Publication date||19 Sep 2006|
|Filing date||16 Aug 1996|
|Priority date||3 Apr 1992|
|Also published as||CA2090189A1, CA2090189C, US5258032, US5458645|
|Publication number||08698781, 698781, US RE39301 E1, US RE39301E1, US-E1-RE39301, USRE39301 E1, USRE39301E1|
|Inventors||Kim C. Bertin|
|Original Assignee||Zimmer, Inc.|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (10), Referenced by (131), Classifications (23), Legal Events (3)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This is a division of application Ser. No. 07/862,953 filed Apr. 3, 1992 now abandoned.This application is a reissue of application Ser. No. 08/021,039, now U.S. Pat. No. 5,458,645, which is a divisional of application Ser. No. 07/862,953, filed Apr. 3, 1992, now U.S. Pat. No. 5,258,032.
The present invention relates to a method and apparatus for a knee joint prosthes is and surgical procedure. More particularly concerning the proper fitting of the femoral component of a total knee revision prosthesis, the procedure for performing revision surgery and apparatus used therein.
The present invention relates to a provisional knee prosthesis and resection guide component together with a surgical procedure designed for use as a system in revision surgery of previously performed knee arthroplasties. It may also find utility in an initial knee replacement procedure.
Revision surgery is performed to correct failures of previously implanted knee prostheses. These failures occur for a number of reasons including malposition, loosening of the prosthesis, infection or dislocation. Such categories are not necessarily mutually exclusive since infection may cause a loosening of the prosthesis which, in turn, might cause dislocation.
When a prosthesis must be removed and a revision prosthesis inserted, it is often the case that additional bone must be removed in order to stabilize the new prosthesis. When this occurs, the interior portion of the femoral component of the prosthesis must be augmented to add additional thickness to compensate for the bone that has been removed. In addition, the revision cuts that remove the extra bone must be made correctly relative to the revision prosthesis for accurate positioning in relation to a tibial component and the soft tissues of the knee joint. Such cuts are made with the aid of guides positioned relative to the ends of the femur and tibia.
It is preferable to perform revision in a single surgical procedure. Also, it is desirable to be able to test the fit and operation of the prosthesis relative to the rest of the knee, particularly the patella and the soft tissues, prior to or at the same time as the revision cuts are made in the end of the femur. Indeed, with regard to patellar tracking, it is preferable to ensure a proper fit before the final anterior cuts are made to the distal femur.
The apparatus and method of this invention are intended to be used in conjunction with the revision prosthesis system of applicant's co-pending application which is based around a constant geometry of the anterior flange, the distal prosthesis and the intramedullary stem of the component and uses the intramedullary canal of the femur as a reference point. Accordingly, the present invention is similarly based around the intramedullary canal of the femur as a reference point for all of the bone cuts.
Tibial resection for implantation of the tibial component of an initial knee prosthesis or revision is relatively straight-forward as it essentially only requires surface treatment of the proximal end of the tibia. In such treatments, cutting guides are normally positioned relative to the intramedullary canal of the tibia by attaching the guides to the intramedullary reamer or to an alignment rod placed within the reamed canal. Such devices are shown in U.S. Pat. Nos. 4,952,213 to Bowman, et al., and 5,002,545 to Whiteside, et al.
In contract, however, prior apparatus and methods for performing the comparable resection of the distal femur have included both intramedullary and extramedullary positionable guide means, often both, frequently requiring accurate adjustment for the individual circumstances. The intramedullary positioned guide means have been traditionally used only for the distal and posterior resection of the femur leaving the anterior cuts to be made with extramedullary positioned means.
Such intramedullary positionable distal and posterior cut guide means are represented by U.S. Pat. Nos. 4,703,751 to Pohl and 4,935,023 to Whiteside, et al. The Pohl patent presents a guide means for resection of the distal surface, which guide is positionable on a jig which is removably connected to an intramedullary rod. The jig allows the cutting guide to be angularly pivoted relative to the center line of the femur. Whiteside, et al., present a shaping guide also removably attachable to an intramedullary rod and having an adjustable positioning means together with guides for the shaping of only one condyle in preparation for the implantation of a unicondylar prosthesis.
It is known for anterior surface resection guides to be positionable relative to an intramedullary rod, for example U.S. Pat. No. 4,474,177 to Whiteside presents an apparatus for shaping the distal femoral surface wherein a plurality of shaping instruments or guides are selectively positionable on an intramedullary rod for use in guiding a saw blade during the procedure. However, what the prior art lacks is an apparatus and method whereby all cuts can be made from the common reference point of the intramedullary canal of the femur and whereby the positioning and size of a femoral component may be checked relative to the soft tissues and the track of the patella prior to making the final resection of the anterior surfaces. In the case of Whiteside, the cuts are made first then the guides are removed before any test fittings can be conducted. If the cuts are made in the wrong place or to the wrong degree, then the surfaces must be modified by further resection, bone grafts or bone cement to get a proper fit of the implant.
The present invention provides a provisional component which allows the selected size of a prospective implant to be test fit with respect to the distal and posterior resections of the femur and the soft tissues of the knee joint before making the final resection of the anterior surface of the femur. It also provides a guide means as an integral part of the provisional component for making those final cuts to the anterior surface. Furthermore, it provides a means whereby the relative spacing of the extension and flexion gaps in the knee joint may be tested using the provisional component with prospective augments or trial pieces, when necessary, in place following which the provisional component itself serves as the guide for making the final surface cuts thus ensuring that the resected femur and ultimate permanent prosthesis will result in a properly balanced knee.
The augments, which are modular and therefore independently changeable, allow adjustment of the anterior/posterior box size as well as the distal positioning of the provisional component. Such distal positioning is crucial for obtaining correct soft tissue balance in the knee during trial reduction before final anterior resection and implantation of the permanent prosthesis. Modular augments and pretesting of the knee with the provisional component of the present invention also enable the surgeon to ensure a close contact fit of the prosthesis with the resected bone surface whereby a greater degree of adhesion may be obtained through bone ingrowth or less bone cement need be used.
The provisional component is constructed to emulate the permanent implant while being temporarily placed in the joint space. Such a permanent implant system is described by my copending application Ser. No. 07/862,954 filed Apr. 3, 1992. It includes the anterior and posterior condylar flanges as well as the intermediate distal portion of the joint surface. An intramedullary stem is provided or, alternatively, the provisional may be adapted for attachment to an intramedullary rod or reamer placed in the femoral intramedullary canal. Provision is also made for the provisional component to temporarily accept distal and posterior augments for proper spacing so that the final anterior surface cuts will be accurately made. With regard to those cuts, the provisional component includes bone saw guides positioned through the body of the component relative to the anterior flange for the correct location and angular position of the chamfer and anterior surface cuts necessary to fit a final permanent implant.
It is therefor an object of this invention to provide a combination knee prosthesis provisional apparatus and resection guide for use in knee replacement surgery whereby resection and test fitting of femoral prostheses may be easily and reliably achieved.
It is a further object of this invention to provide a means whereby the spacing of extension and flexion gaps of the knee may be tested and evaluated during the process of replacement surgery prior to final resection and prosthesis implantation.
It is a still further object to provide a means whereby the resection of the distal femur is made on the basis of a reference point common to all resection cuts slid implant sizes.
It is an even further object to provide a combination knee prosthesis provisional apparatus and resection guide which emulates a permanent femoral implant component.
Further objects and advantages will become evident to those of skill in the art from the following drawings and description.
The femoral component revision prosthesis of
For an initial femoral implant, it is generally not as difficult to obtain a correct fit of the proper size component; although the problem can occur where there is a great deal of diseased bone that must be removed before the implant is fitted. Such instances then become similar to those encountered in revision surgery where it is necessary to remove existing bone along with the original implant either due to infection or physical breakdown of the previously prepared distal femur. In these cases the size of the bone supporting the implant is reduced but it is still desired to maintain the size of the original joint in order to obtain proper anatomical characteristics of support and function for the patient. For example, a patient having an anatomical knee size of six may, following resection of the femur, have a distal femoral surface corresponding to that for a size four and a half knee. In order to maintain the proper anatomical characteristics for that knee it is desirable that the implanted component be a size six. However, adapting a larger size implant to a smaller size bone has presented difficulties which, to date, have been solved by the use of custom made implants or multiple augments.
Prior devices and methods have required measuring the size of the bone and then cutting it to fit one specific size of prosthesis. This allows a good fit to be obtained between the prosthesis and the bone but may not provide a good fit with the soft tissues and the patella. In revision surgery, the flexion space of the knee, ie., that space between the posterior edge of the prepared distal femur and the prepared proximal tibia when the knee is fully bent as shown by space B in
The provisional component of this invention, as well as the revision prosthesis of applicant's co-pending application, have a constant relationship between the center line of the stem, or stem fixation point, and the anterior cornea of the femur for all sizes of the component. This relationship provides a constant angle between the stem and the cortex, represented by the inner surface of the anterior flange, as well as a fixed distance therebetween which is the same regardless of the anatomical sizes of the provisional components to be available in a system.
The joint surface 26 is continuous and extends around the outer periphery of the component 20 to include the outer surface 21b of the anterior flange 21 as well as the outer surfaces of the posterior condylar flanges 22 and 23 and the distal femoral joint portion. Similarly, inasmuch as the component emulates the joint surface of a natural distal femur, the condylar surfaces 27 and 28 continue around the periphery of the component as part of the joint surface 26 thereby providing distal, medial and lateral condylar surfaces between which will be located a track area or groove 26a for travel of the patella as the knee joint flexes. Such travel is shown in
It is important that the anterior flange cut be made last, after the posterior and distal cuts and after correct working of the joint and soft tissue balance has been established. Because the system of revision for which the provisional component of this invention is intended uses the intramedullary canal of the femur as a reference point, the angle established between a reamer or intramedullary shaft and the anterior flange of an implant is constant through all sizes of such implants. Therefore, if the anterior flange cut is made before the posterior and distal cuts and before the extension and flexion gaps are stabilized, the constant relationship will be lost once those cuts are made and stabilization of the knee and soft tissue balance will be much more difficult to achieve. Thus, the correct order for the procedure is to first resect the distal and posterior femoral surfaces with the cutting guides therefor positioned relative to the reamer used to prepare the intramedullary canal. Following this, the provisional component is inserted, using either the reamer or a separate intramedullary shaft for positioning, and the fit and balance of the knee are determined before finally making the anterior flange cuts.
To accomplish this, the provisional component 20 is provided with cutting guides 30 and 31. These guides 30 and 31 comprise slots in the body of the provisional component 20 with guide 30 at the correct angle and location for the anterior flange resection cut while guide 31 is at the correct angle and location for the anterior chamfer resection cut. Each guide actually comprises two slots placed on either side of the intramedullary stem fixation point 25 and extending from the edge of the component 20 inward toward the longitudinal center line 35 of the component to a point adjacent the intramedullary stem fixation point 25. The slots further extend completely through the component 20 from the joint surface 26 to the femoral contact surface 24 with the two slots of each guide 30 and 31 being necessarily located on the same relative plane through the component 20. Clearly, cutting guides 30 and 31 do not extend completely across component 20 from edge to edge in order to maintain the component as a complete unit. Also, the cutting is primarily conducted on the condylar surfaces of the femur which will provide a guide for any final dressing of the intervening mid surface.
As shown in
Augments 33 provide buildup for the resected areas of the distal and posterior condyles of the femur 11 in order to maintain the correct anatomical relationships of the knee joint between the joint surface 26 of the provisional component 20 and the corresponding surface of a tibial component 10. The size of the augments 33 is based on the resection cuts made to the femur for the particular size of permanent component to be used. Where such cuts are standardized, there will be an equally standardized set of augments. Alternatively, where the cuts are made on a case by case basis, a wider variety of augment sizes will be available. The augments 33 may be provided with the provisional component 20 or they may be those provided with the permanent component in which case they will be temporarily attachable to the provisional component so that they may be removed and permanently mounted on the permanent component prior to its implantation. As shown in
In the surgical procedure employed with this apparatus the proximal tibia is prepared by incrementally reaming the tibial intramedullary canal out to cortical bone, leaving the reamer in place as a point of reference for a tibial cutter, resecting the proximal tibia and applying provisional components for the tibial portion of the knee joint. Following this, the distal femur is prepared using the above described apparatus. Alternatively, the femur may be prepared first followed by the preparation of the tibia.
For preparation of the distal femur, the femoral intramedullary canal is first reamed incrementally to cortical bone. The canal, as stated, is the constant reference point for the resection of the distal femur. The reamer may be left in place or a provisional stem or similar intramedullary rod may be inserted on which distal and posterior cutters are mounted for resection of the distal and posterior surfaces of the femur. These cuts will be made based on the condition of the bone and on the permanent prosthesis to be implanted but will preferably be made according to a standard established by the prosthesis system being used. The individual condyles of the posterior and distal surfaces may be resected to different levels and brought up to the same level by the use of augments.
Following the posterior and distal resection, the femoral provisional component is put in place to test the positions of the selected prosthesis and the tissues of the knee joint. If the provisional stem was used as the support for the posterior and distal cutters then the provisional component may be substituted for those cutters otherwise it is preferable that the cutter support be removed from the intramedullary canal, the provisional stem attached to the provisional component and that assembly put in place. Augments may be attached as needed to establish the correct joint characteristics or a different size provisional component may be tried. Since all sizes of provisionals have the same stem/anterior flange distance and the same stem/anterior cortex angle, those characteristics and the resulting position of the anterior flange cuts will be the same regardless of the size provisional used. Once all such characteristics have been established, the provisional component and its included anterior resection guides are used for the final anterior chamfer and anterior flange cuts following which the provisional component, stem and augments are removed and the permanent implant component inserted.
The foregoing description sets forth the preferred form of the apparatus of this invention and the method for its use. However, other modifications and variations will become apparent to those having skill in the art from an examination of that description and the accompanying drawings. Therefore, other variations of the present invention may be made which fall within the scope of the appended claims even though such variations were not specifically discussed.
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|US9717510||5 May 2014||1 Aug 2017||Biomet Manufacturing, Llc||Patient-specific numerically controlled instrument|
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|USD691719||22 Jun 2011||15 Oct 2013||Otismed Corporation||Arthroplasty jig blank|
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|U.S. Classification||606/88, 606/86.00R, 623/20.14, 128/898|
|International Classification||A61B17/15, A61F2/00, A61F2/46, A61F2/30, A61F2/38, A61B19/00, A61B17/00|
|Cooperative Classification||A61F2/3859, A61F2220/0025, A61F2002/30797, A61F2002/30672, A61F2002/30736, A61F2002/30405, A61F2002/30594, A61B17/155, A61F2/4684|
|European Classification||A61F2/46T, A61F2/38F, A61B17/15K2|
|24 Mar 2003||AS||Assignment|
Owner name: ZIMMER TECHNOLOGY, INC., ILLINOIS
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:ZIMMER, INC.;REEL/FRAME:013862/0766
Effective date: 20020628
|17 Apr 2007||FPAY||Fee payment|
Year of fee payment: 12
|20 Jul 2009||AS||Assignment|
Owner name: ZIMMER, INC., INDIANA
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:BERTIN, KIM C.;REEL/FRAME:022973/0435
Effective date: 20090426