The present invention relates generally to the field of orthopaedics, and, more particularly, to an apparatus and method for sizing a distal femur.
Total joint arthroplasty (“joint replacement”) is the surgical replacement of a joint with a prosthesis. A typical knee prosthesis has three main components: a femoral implant, a tibial implant, and a tibio-femoral insert. In general, the femoral implant is designed to replace the distal femoral condyles. The femoral implant is typically made from metal. It typically includes a generally concave, facetted (i.e., piecewise planar) inwardly facing surface defining a cavity for receiving a resected distal femur and typically further includes a generally convex outwardly facing surface with medial and lateral rounded portions for emulating the medial and lateral condyles, respectively, and with a valley or depression between the rounded portions for emulating the patella sulcus/trochlear region of the distal femur. In general, the tibial implant is designed to support and align the tibio-femoral insert. The tibial implant is also typically made from metal. It typically includes a substantially planar tray or plate portion (“tibial plate”) for supporting the insert, and an elongated stem extending away from the tibial plate for anchoring the tibial implant in the intramedullary canal of the proximal tibia. In general, the tibio-femoral insert is designed to replace the tibial plateau and the meniscus of the knee. It is typically somewhat disk-shaped, and typically includes one or more substantially planar surfaces for bearing on the tibial plate and one or more generally concave surfaces for bearing against the femoral implant. The insert is typically made of a strong, smooth, low-wearing plastic.
In a conventional knee replacement operation, the surgeon makes an anterior incision spanning the distal femur, the knee, and the proximal tibia; everts (i.e., flips aside) the patella; separates the distal femur and the proximal tibia from surrounding tissues; and then hyperflexes, distally extends, and/or otherwise distracts the proximal tibia from the distal femur to enlarge the operating space. Next, the surgeon secures a resection guide to the proximal tibia. A resection guide is a jig or template configured to provide a desired cutting angle for a saw blade or other resection tool. Conventional resection guides are used somewhat similarly to the manner in which a carpenter uses a miter box to achieve a desired angle for cutting wood. The surgeon uses the resection guide to position to a saw blade or other suitable resection tool and cuts off the tibial plateau. This prepares the proximal tibia to receive the tibial implant. Then, the surgeon aligns one or more additional resection guides for cutting and shaping the distal femur as required to fit the femoral implant. Resection of the distal femur typically includes removing anterior portions of the medial and lateral condyles. The position of the corresponding anterior cut is typically referenced or measured-off from posterior surfaces of the condyles. The distance from the posterior surfaces to the plane of the anterior cut typically corresponds to an anterior-posterior size for the receiving cavity of the femoral implant. Femoral implants are typically available only in a limited number of predetermined sizes. Accordingly, the surgeon typically attempts to limit the bone removed to that which must be disposed of due to deterioration plus the minimum additional amount required to accommodate the closest standard sized implant. After completing the necessary resections, the surgeon may apply cement to the distal femur and/or to the proximal tibia to ultimately help hold the femoral implant and/or tibial implant, respectively, in place. Alternatively, cementless implants may be used. Finally, the surgeon secures the respective implants to the distal femur and proximal tibia, secures the cushion to the top of the tibial implant, and closes the incision. If the operation is successful, the artificial knee properly mimics the operation of a healthy natural knee.
Complications may result if either the distal femur or the proximal tibia is not resected properly. Such complications can include accelerated wear of the prosthesis; bending, cracking or fracture of the remaining parts of the proximal tibia and/or distal femur; dislocation of the prosthesis, excessive rotation or loss of motion of the prosthesis; and/or angular deformity of the prosthetic joint.
Some devices have included features for positioning anterior cuts to the distal femur. Other devices have included features for indicating corresponding anterior-posterior femoral implant sizes. However, maintaining accurate correlations between separate mechanisms for positioning the cuts and indicating the implant sizes has been challenging. Preventing undesirable slippage in such mechanisms during operations has also been challenging.
Moreover, minimally invasive surgical techniques are becoming increasingly popular. Minimally invasive surgeries generally involve, among other things, considerably smaller incisions and tighter working spaces than historical techniques in efforts to reduce patient traumas and accelerate post-operative recoveries. Some devices for positioning anterior cuts to the distal femur and/or for indicating corresponding anterior-posterior femoral implant sizes are not well suited for operation in the tight spaces of minimally invasive surgeries.
The present invention provides an apparatus for sizing a distal femur having a distal surface located in a first plane and a posterior surface located in a second plane angularly disposed from the first plane by about 90 degrees. The apparatus includes a base configured to concurrently abut the distal surface and the posterior surface, and further includes an axial distance scale. The scale includes a first sleeve axially fixedly coupled to the base and further includes a second sleeve spirally movably coupled to the first sleeve.
The present invention provides an apparatus for sizing a distal femur having a distal surface located in a first plane and a posterior surface located in a second plane angularly disposed from the first plane by about 90 degrees. The apparatus includes means for concurrently abutting the distal surface and the posterior surface, and further includes means, coupled to the abutting means, for measuring a distance relative to the abutting means.
The present invention provides a method for sizing a distal femur having a distal surface located in a first plane and a posterior surface located in a second plane angularly disposed from the first plane by about 90 degrees. The method includes concurrently abutting a base against the distal surface and the posterior surface, and further includes measuring a distance relative to the base. The measuring step includes spirally moving a first sleeve relative to a second sleeve.
The above-noted features and advantages of the present invention, as well as additional features and advantages, will be readily apparent to those skilled in the art upon reference to the following detailed description and the accompanying drawings, which include a disclosure of the best mode of making and using the invention presently contemplated.
Like reference numerals refer to like parts throughout the following description and the accompanying drawings. Additionally, unless otherwise stated all parts are made from one or more rigid sterilizable surgical materials such as stainless steel.
Further, as used herein the terms “medial,” “medially,” and the like mean pertaining to the middle, in or toward the middle, and/or nearer to the middle of the body when standing upright. Conversely, the terms “lateral,” “laterally,” and the like are used herein as opposed to medial. For example, the medial side of the knee is the side closest to the other knee and the closest sides of the knees are medially facing, whereas the lateral side of the knee is the outside of the knee and is laterally facing. Further, as used herein the term “superior” means closer to the top of the head and/or farther from the bottom of the feet when standing upright. Conversely, the term “inferior” is used herein as opposed to superior. For example, the heart is superior to the stomach and the superior surface of the tongue rests against the palate, whereas the stomach is inferior to the heart and the palate faces inferiorly toward the tongue. Also, as used herein the terms “anterior,” “anteriorly,” and the like mean nearer the front or facing away from the front of the body when standing upright, as opposed to “posterior,” “posteriorly,” and the like, which mean nearer the back or facing away from the back of the body.
Apparatus 100 further includes a rod 240 (
Apparatus 100 further includes a peg 260 configured to, among other things, help couple rod 240 to base 140.
Apparatus 100 further includes an axial distance scale 280 configured to, among other things, selectively axially expand or contract and to indicate a corresponding distal femoral size as discussed further below.
Apparatus 100 further includes an anterior contact sub-assembly 300 configured to, among other things, selectively rotate about scale 280 as indicated by directional lines 310 and to abut a desired anterior surface 320 (see
Base 140 also includes a tab 540 extending roughly orthogonally from portion 380 and a tab 560 extending roughly orthogonally from portion 400. Tab 540 defines a through-hole 544 and includes a substantially planar surface 580 surrounding through-hole 544. Surface 580 is angularly disposed from surface 520 by an angle 600. Tab 560 defines a through-hole 564 and includes a substantially planar surface 620 surrounding through-hole 564. Surface 620 is angularly disposed from surface 520 by an angle 640. In the exemplary embodiment, angle 600 is about 90 degrees and angle 640 is about 90 degrees. Additionally, surface 580 and surface 620 are coplanar along a line 660.
Base 140 also includes a generally cylindrical post 680 extending from portion 380 about an axis 700. Axis 700 is parallel to surface 520, and is angularly disposed from line 660 by a rotation angle 720 for positioning a cut slot 740 (see
As further discernable in
In the exemplary embodiment, flat 850 has a longitudinal span 860 that is about 60 percent of span 840. Meanwhile, end 800 defines a generally cylindrical socket 880 (see
End 820 defines a generally cylindrical internally partially screw-threaded socket 950 (see also
As further discernable in
When apparatus 100 is fully assembled, sleeve 980 is coaxially and movably spirally coupled into sub-assembly 960. Sleeve 980 also includes an annular wall 1060 and an annular wall 1080 that are axially spaced apart by an annular surface 1100. Wall 1060, wall 1080, and surface 1100 define an annular channel 1120.
As further discernable in
Clamp 1140 also includes a generally cylindrical knob 1300 abutting handle 1200, a screw-threaded member 1320 (see
In the exemplary embodiment angle 1480 is about 110 degrees. When apparatus 100 is fully assembled, member 1160 of clamp 1140 is positioned in channel 1120 (of sleeve 980) such that clamp 1140 removably and selectively rotatively couples sub-assembly 300 to sleeve 980 (and, thus, removably and selectively rotatively couples sub-assembly 300 to scale 280) and line 1400 is roughly perpendicular to axis 700.
Sub-assembly 1540 also includes a peg 1740. Peg 1740 includes a generally cylindrical screw-threaded portion 1760 and a cylindrical screw-threaded portion 1780. Portion 1780 is inserted through through-channel 1720 (of bearing 1680) and welded into through-channel 1660 (of member 1620) (see also
Sleeve 1800 includes an annular knob 1820 defining a generally cylindrical through-channel 1840 (see also
Sidewall 1880 defines a plurality of elongated apertures 1900 and includes an outer surface 1920 with a plurality of femoral implant size graduations 1940 thereon. For full assembly of sub-assembly 960, sub-assembly 1540 is coupled to sleeve 1800 by inserting sub-assembly 1540 into through-channel 1840 (of sleeve 1800), by positioning bearing 1680 such that through-channels 1860 are aligned roughly tangentially with race 1700, by inserting pegs 1790 through the respective through-channels 1860, and by press-fitting and/or welding pegs 1790 in place.
As further discernable in
Here, it is noted that in assembly of apparatus 100, sleeve 980 is first separated from sub-assembly 960. Next, end 800 of rod 240 is inserted into through-channel 1000 (of sleeve 980). Next, end 820 of rod 240 is inserted into through-channel 1840 (of sleeve 1800 of sub-assembly 960), and peg 1740 is screwed tightly into socket 950 (of end 820) by torquing an Allen wrench or any other suitable tool in socket 1580.
Thus, sleeve 1800 is axially fixed yet rotatively movably coupled to end 820 of rod 240. Next, sleeve 980 is spiraled into sleeve 1800 of sub-assembly 960 until end 800 of rod 240 protrudes from sleeve 980 and through-hole 900 is exposed. Thus, sleeve 980 is spirally movably coupled to sleeve 1800. Next, post 680 (of base 140) is press-fitted into socket 880 (of rod 240).
Next, peg 260 is inserted through through-hole 940 (of rod 240), through through-hole 760 (of post 680), and into through-hole 900 (of rod 240), where peg 260 is press-fitted and/or welded in place. Lastly, member 1160 of clamp 1140 is positioned in channel 1120 (of sleeve 980) such that clamp 1140 removably and selectively rotatively couples sub-assembly 300 to sleeve 980 (and, thus, removably and selectively rotatively couples sub-assembly 300 to scale 280) and line 1400 is roughly perpendicular to axis 700.
Next, the user abuts surface 520 (see
Next, the user turns knob 1300 as indicated by directional line 332 (see also
However, it is noted that surface 320 may correspond to any other suitable location on distal femur 120.
After preliminarily rotationally positioning tip 1500, the user axially expands scale 280 by rotating knob 1820 as indicated by directional line 328 (see
After finally rotationally positioning tip 1500, the user turns knob 1300 as indicated by directional line 336 (see also
After rotatively fixing sub-assembly 300 about sleeve 980, the user resumes and/or continues the axially expansion of scale 280 until tip 1500 desirably firmly abuts surface 320. This provides a final setting for scale 280. The resulting axial position of portion 1960 of sleeve 980 relative to graduations 1940 of sleeve 1800 indicates a corresponding anterior-posterior dimension or femoral implant size. Accordingly, the user visually observes portion 1960 through one or more of apertures 1900 (see also
Guide 5020 defines cut slot 5040 roughly orthogonal to surface 520 and extends generally away from sleeve 980 and rod 240 along a line 5060 that is roughly perpendicular to axis 700. Guide 5020 also defines a plurality of through-channels 5080. Guide 5020 also includes a hook-like arm 5100 removably positioned on sleeve 980 in channel 1120. Guide 5020 also defines a pin slot 5120 and a pin slot 5140. Slot 5120 and slot 5140 are each roughly orthogonal to surface 520.
The foregoing description of the invention is illustrative only, and is not intended to limit the scope of the invention to the precise terms set forth. Further, although the invention has been described in detail with reference to certain illustrative embodiments, variations and modifications exist within the scope and spirit of the invention as described and defined in the following claims.
This application claims the benefit of U.S. Provisional Patent Application Ser. No. 60/540,616, filed Jan. 29, 2004, entitled “APPARATUSES AND METHODS FOR ARTHROPLASTIC. SURGERY.”
Number | Date | Country | |
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60540616 | Jan 2004 | US |