Kinematic Alignment and Novel Femoral and Tibial Prosthetics
A tibial component placement guide for use in a knee arthroplasty procedure involving a knee joint comprising a tibia, a patella, and a femur, the tibial component placement guide comprising an overlay configured to be overlaid a resected tibia that typifies at least one of a shape and an outline of the resected tibia, the overlay including at least one of an indicia and an opening indicative of at least one of an orientation and a position of a presurgical kinematic axis of at least one of the femur and the patella.
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The present application is a continuation of U.S. Nonprovisional patent application Ser. No. 15/627,844, titled “KINEMATIC ALIGNMENT OF FEMORAL AND TIBIAL COMPONENTS,” filed Jun. 20, 2017, now U.S. Pat. No. 11,045,330, which is a continuation of U.S. Nonprovisional patent application Ser. No. 14/686,685, titled “KINEMATIC ALIGNMENT OF FEMORAL AND TIBIAL COMPONENTS,” filed Apr. 14, 2015, now U.S. Pat. No. 9,901,463, which claims the benefit of U.S. Provisional Patent Application Ser. No. 61/979,034, titled “KINEMATIC ALIGNMENT OF FEMORAL AND TIBIAL COMPONENTS,” filed Apr. 14, 2014, and U.S. Provisional Patent Application Ser. No. 62/013,198, titled “KINEMATIC ALIGNMENT OF FEMORAL AND TIBIAL COMPONENTS,” filed Jun. 17, 2014, and U.S. Provisional Patent Application Ser. No. 62/022,894, titled “KINEMATIC ALIGNMENT OF FEMORAL AND TIBIAL COMPONENTS,” filed Jul. 10, 2014, the disclosure of each of which is incorporated herein by reference.
INTRODUCTION TO THE INVENTIONThe present disclosure is directed to knee kinematics as well as techniques, surgical guides, and orthopedic prosthetics to enhance knee arthroplasty.
Knee arthritis causes debilitating pain affecting activities of daily living. When pain is not well controlled by non-operative treatments and the failure in managing disease' symptoms (pain, stiffness, swelling, and/or bony spurs), Total Knee Arthroplasty (TKA) is recommended if the patient is medically fit for the surgery and has no active infection.
One common objective in TKA is to restore normal kinematics. However, what are normal kinematics? Is it the relationship between ligaments menisci and articular surfaces of femur, tibia and patella or the distribution of contact stresses across the articulating joint as symmetrically as possible, avoiding overloading of the one compartment? Although trying to achieve the same goal, these two philosophies require different surgical techniques—one to provide a restoration to normal anatomy (in the case of osteoarthritis), second is to correct defective anatomy (i.e. varus/valgus).
The former philosophy is a measured resection technique where bone and cartilage are replaced by implants that are of generally the same thickness. The latter philosophy is a balanced flexion gap technique that may require altering the patient's pre-arthritic anatomy. The major assumption underlying this philosophy is many patients who develop medial compartment arthritis of the knee are bowlegged, or walk with a varus thrust, since childhood. Therefore, restoring the condition of the pre-arthritic alignment would result in greater varus component position than is generally considered acceptable for knee arthroplasty.
However, whether using measured resection or flexion gap surgical technique, the predominant method of alignment is the mechanically aligned (mechanical neutral) TKA. In this method, the surgeon cuts the distal femur and the proximal tibia perpendicular to the mechanical axes (Appendix A). The second alignment method, which is gaining more acceptance, is the kinematically aligned TKA. The goal of this latter method is to restore the natural difference in symmetry and varus-valgus laxity between 0 degrees of extension and 90 degrees of the normal knee (Appendix B).
Prosthetic placement in TKA is a complex problem related to the complex shapes of the femur and tibia, out of plane geometrical relationships of the articular surfaces and bones, and the additive factor of ligamentous changes, anatomical variation and deformity resulting from chronic disease. The relationship between axial and rotational alignment is not well documented. It is known that decreased femoral anteversion in Caucasians patients and decreased tibia torsion in Asian patients can be associated with osteoarthritis. In one study, genu varum has been associated with external tibial torsion. It is likely that both deformations coexist in a typical three-dimensional deformity. For example, an externally rotated leg with the knee flexed will appear as a varus deformity. A logical conclusion is that detrimental joint overloads can result from combined rotational and axial malalignment.
The instant disclosure involved analyzing both alignment methods and coming to the conclusion that the current implant designs (femur, tibia and instruments) are not well suited for the kinematic aligned TKA.
Surgical techniques in TKA have relied on recreating primarily the two dimensional mechanical axis alignment in the coronal plane (see
In addition, the cuts that are made to the femur and tibia during TKA may change the angle and the level of natural joint line causing abnormal tightening or slackening of the collateral, retinacular, and posterior cruciate ligaments and abnormal kinematics. The undesirable consequences of the abnormal kinematics are instability, motion loss, accelerated component wear and component loosening from uneven load-sharing between compartments.
In order to better understand what the term natural kinematics means several studies have been performed and published by various authors. One gold standard method requires analysis of digital fluoroscopic images, taken during a series of activities. For each activity the pose of the femur relative to the tibia is tracked throughout—allowing for the capture of the entire kinematic profile for each subject during activity (this process is well described in the document—and is easily referenced to existing literature if space saving is desired). Both contact maps, tracking the closest point between the two surfaces, and the instantaneous axis of rotation (helical axis) suggest that the knee pivots clearly about the medial side, and rolls back on the lateral side. In fact, during deep knee bend, the medial side may experience slight anterior translation—a motion sometimes referred to as paradoxical motion. Interestingly, this helical axis very closely follows the sagittal kinematic plane during all activity. This is shown in
Another clue as to how the normal knee behaves is uncovered with investigation of the ligament lengths during flexion. Looking at the MCL and LCL during flexion shows, as with the contact analysis, that the MCL length changes very little during flexion compared to the LCL length—and has significantly less translation than the LCL. This would suggest a medial side which is considerable tighter throughout flexion than the lateral. Further, the LCL is longest at full extension—suggesting a rigid joint at extension and a fairly lax lateral side in extension, but still fairly tight medially. Finally, when examining the PCL/ACL, we again see significant length changes, but in a way that relates the PCL length inversely to the ACL length, suggesting an “exchange” of load during flexion. It is worth mentioning that the posterior translation of the lateral side is not a linear one, but happens rapidly as the lateral curvature of the femur transitions from the relatively flat surface in early flexion and extension to the more curved posterior surface in deeper flexion. The soft tissue profiles of the normal knee during activity are totally counterintuitive to mechanical alignment and balanced gaps. In fact, this helps to explain why mechanically aligned knees cannot achieve normal kinematics—the joint balance and joint lines have been altered significantly. Thus a method is required which can align the implant in a way to restore, or maintain, natural loading of the knee (not equal medial/lateral loads) and normal kinematics.
As part of the instant disclosure, X-ray fluoroscopy may be utilized to generate two dimensional (2D) fluoroscopy images of components of a joint across a range of motion of the joint. Thereafter, three dimensional models of the patient's anatomy, having already been constructed from static images (e.g., MM, CT, X-ray, etc.) taken of the patient anatomy, need to be registered to the 2D fluoroscopy images. In the instance circumstance, 2D fluoroscopy images are taken of a human knee joint at distinct points along its range of motion, as well as construction of a 3D component model of the human knee joint. In exemplary form, perspective images of the 3D joint model (comprising the femur, tibia and the patella (with the fibula)) are overlaid onto the 2D fluoroscopy images, across the range of motion, taking into account the position of the X-ray source and to the image intensifier. When the 3D joint model is correctly registered (i.e., overlaid) with the 2D fluoroscopy images, the relative pose of the components of the 3D joint model is the same as the pose of those components at the time the fluoroscopy images were created. Registering the joint model to the 2D fluoroscopy images across selected frames of the range of motion is utilized to calculate the relative pose between the three bones over the entire range of motion.
The pose of a rigid body {A} with respect to another coordinate system {B} can be represented by a six element vector ABx=(BxAorg,ByAorg,BzAorg,α,β,γ)T, where BpAorg=(BxAorg,ByAorg,BzAorg,α,β,γ)T is the origin of frame {A} in frame {B}, and (□□□□□) are the angles of rotation of {A} about the (z, y, x) axes of {B}. An alternative representation of orientation is to use three elements of a quaternion; the conversion between Euler angles and quaternions is straightforward.
Equivalently, pose can be represented by a 4×4 homogeneous transformation matrix:
where ABR is the 3×3 rotation matrix corresponding to the angles (□□□□□). The letter H designates the equivalent 4×4 homogeneous transformation matrix.
Homogeneous transformations are a convenient and elegant representation. Given a homogeneous point Ap=(AxP,AyP,AzP,1)T, represented in coordinate system {A}, it may be transformed to coordinate system {B} with a simple matrix multiplication Bp=ABHAp. The homogeneous matrix representing the pose of frame {B} with respect to frame {A} is just the inverse of the pose of {A} with respect to {B}; i.e., BAH=ABH−1. Finally, if one knows the pose of {A} with respect to {B}, and the pose of {B} with respect to {C}, then the pose of {A} with respect to {C} is easily given by the matrix multiplication ACH=BCHABH.
The pose of each bone in the joint model is represented by a 4×4 homogeneous transformation matrix TibFemH that is comprised of rotation matrix and translation vector. The rotation matrix fluoroModelRxyz(γ,β,α) is given by:
where γ, β, and α are the model's angles of rotations about x, y, and z axes, and the translation vector is Modelpfluoro(Modelxfluoro,Modelyfluoro,Modelzfluoro)T, respectively. Therefore, the relative pose of the femur with respect to the tibia is then calculated using the equation TibFemH=FluoroTibHFemFluoroH (similarly FemPatH=FluoroFembHPatFluoroH).
In accordance with the instant disclosure, three methods were utilized for analyzing the relative motion of the femur and tibia across a range of motion of a knee joint. The first method was the method of screw axis decomposition, also called the helical axis of motion method. In this method, the axis in space about which the moving body rotates is determined. Simply put, the motion of a rigid body from one time instant to another can be decomposed as a rotation about an axis, plus a translation along that axis. The axis is represented as a point on the axis (C0), along with a unit vector K specifying the direction of the axis. The point C0 and the vector K are represented in the coordinate system of the body at the first time instant. An initial computation uses the rotation matrix R to compute the rotation axis and angle:
θ=arccos((R11+R22+R33−1)/2)
K=[R32−R23 R13−R31 R21−R12]T/(2 sin(θ))
Thereafter, the components of translation parallel and perpendicular to the rotation axis is computed:
Tpara=(T·K)K
Tperp=T−Tpara
Then, the vector C0 is computed to the screw axis:
M=I3×3−R
C0=(MTM)−1MTTperp
where I3×3 is the 3×3 identity matrix. Note that the matrix M is singular.
The point C0 is an arbitrary point on the axis, which may be far away. Sometimes it is useful to choose a specific point on the axis. In the instant application, it is useful to find the point on the axis that is the intersection of the axis with the XY plane of the body:
s=C0z−Kz
P=C0+sK
where C0z and Kz are the z components of the vectors C0 and K, respectively. Here, s is the distance from C0 to the XY plane, along the vector K. The point P is in the XY plane of the body at the first position.
The location and orientation of the helical axis of motion may be defined with respect to the coordinate system of the tibia. If the knee was a simple hinge joint, with pure rotation about the medial axis, then the helical axis of motion would be a stationary line perpendicular to the sagittal plane. However, the motion of the knee joint is more complex than a simple hinge joint, and can include translation as well as rotation about other axes. As a result, the helical axis of motion is not exactly perpendicular to the sagittal plane, and is not fixed in space.
A second method used to analyze the relative motion of the knee joint pursuant to the instant disclosure involved tracking the contact paths of the femur on the tibia during a range of motion of the knee joint as evidenced by fluoroscopic images. The minimum point on the surface of the medial and lateral condyles for each respective flexion angle was calculated automatically as the closest points to the tibia and projected down onto the tibial plateau (see
As part of this second method, all anterior-posterior (AP) measurements were made with respect to a plane (frontal) that is located at the geometric center of the tibia (see
As part of this second method, fluoroscopic images of a patients' knee joints with normal structure and kinematics were obtained that included in the range of motion a deep knee bend. Patient's performing this deep knee bend experienced posterior femoral translation of their lateral condyle and minimal change in the position of the medial condyle (see
As evidenced from the fluoroscopic images of patients with normal knee structure and kinematics, patients' knees experienced a normal axial rotation pattern during a deep knee bend (tibia internally rotating with increased knee flexion), because the posterior translation of femorotibial contact laterally was greater than that observed medially (see
The helical axis of motion is an imaginary line in space, around which the femur rotates. Because of the out of plane motion of the knee (6 degrees of freedom), this axis is almost never perpendicular to the sagittal plane (see
A third method utilized to analyze the relative motion of the knee joint pursuant to the instant disclosure included tracking the paths of specific contact areas on the distal and posterior anatomy of the femur on the tibia (see
Using the 3D-to-2D registration method described previously with respect to the first method, the 3D patient bone models were overlaid onto the fluoroscopic images. Relative rotations of the femur to the tibia were calculated at every 20 degrees of flexion using the 3D motion captured. In addition, at least one of computed tomography (CT) scans and magnetic resonance imaging (MRI) scans were obtained for each knee joint having been the subject of the fluoroscopic images. From the CT and/or MIR scans, the origin and insertion points were marked on the femur, fibula, and tibia models for the Anterior Cruciate Ligament (ACL), Posterior Cruciate Ligament (PCL), Medial Collateral Ligament (MCL) and Lateral Collateral Ligament (LCL). Using the rotational matrices methods previously described in paragraphs [0013]-[0018], the origin and insertion points were calculated and tracked during the motion (see
As evidenced in
After including the soft tissues (ACL/PCL, MCL/LCL) and morphology of the knee, it was observed that the motion of lateral femoral condyle does not just continuously rollback. In order to understand this motion, the four contact areas A1, A2, A3 and A4 depicted in
Referring to
No currently available TKA consistently reproduces the kinematic pattern observed in the normal knee. Along with the inability to provide native kinematics, most patients having TKA fail to achieve full function when compared with a sex and age matched group. More importantly, weight bearing knee flexion is significantly reduced compared with passive flexion and only a small subset of patients undergoing TKA obtain more than 120 degrees flexion in weight bearing deep knee bend. Part of the reasons of the failure of the current implants to reproduce normal kinematic patterns is the absence of evaluating: (1) the relationships between underlying joint deformity and preoperative alignment in vivo joint kinematics, and (2) the relationships between rotational deformity and the subsequent effect on the in vivo joint. Furthermore, there is an absence of evaluating the effect of standard surgical techniques (e.g., gap balance) on joint kinematics. Thus, there is a need in the art for surgical solutions as part of TKA to consistently approach the kinematics of a natural knee.
It is a first aspect of the present invention to provide a tibial component placement guide for use in a knee arthroplasty procedure involving a knee joint comprising a tibia, a patella, and a femur, the guide comprising an overlay configured to be overlaid a resected tibia, the overlay including at least one of an indicia and an opening indicative of at least one of an orientation and a position of at least one of a first axis of the femur, a second axis of the femur, and a first axis of the patella.
In a more detailed embodiment of the first aspect, the overlay includes an opening indicative of the orientation of the first axis of the femur and the second axis of the femur. In yet another more detailed embodiment, the opening comprises a through hole. In a further detailed embodiment, the through hole outlines a T-shape, a horizontal aspect of the T-shape is indicative of orientation of the first axis of the femur, and a vertical aspect of the T-shape is indicative of orientation of the second axis of the femur. In still a further detailed embodiment, the through hole outlines a + shape, a horizontal aspect of the + shape is indicative of orientation of the first axis of the femur, and a vertical aspect of the + shape is indicative of orientation of the second axis of the femur. In a more detailed embodiment, the opening comprises a first through hole and a second through hole, the first through hole is indicative of the first axis of the femur, and the second through hole is indicative of orientation of the second axis of the femur. In a more detailed embodiment, the opening comprises a first cutout and a second cutout, the first cutout is indicative of the first axis of the femur, and the second cutout is indicative of orientation of the second axis of the femur. In another more detailed embodiment, the first axis of the femur comprises the posterior condylar axis of the femur. In yet another more detailed embodiment, the second axis of the femur comprises the helical axis of the femur. In still another more detailed embodiment, the overlay has a contour outline that is aligned with the resected tibia.
In yet another more detailed embodiment of the first aspect, the contour outline is patient-specific. In yet another more detailed embodiment, the tibial component placement guide further includes at least one of an indicia and an opening indicative of at least two of a medial guide, a lateral guide, a size of the guide, and a particular patient. In a further detailed embodiment, the guide is fabricated from at least one of titanium, a titanium alloy, stainless steel, and a stainless steel alloy. In still a further detailed embodiment, the guide includes a through aperture configured to align a through fastener mounted to the resected tibia. In a more detailed embodiment, the through fastener comprises a pin. In a more detailed embodiment, the through aperture comprises a plurality of through apertures, and each of the plurality of apertures is configured to receive a pin. In another more detailed embodiment, the overlay comprises a base plate. In yet another more detailed embodiment, the base plate includes a flange along a periphery of the base plate. In still another more detailed embodiment, the tibial component placement guide further includes at least one of an indicia and an opening indicative of the orientation of a third axis of the femur, the third axis being parallel to the first axis.
It is a second aspect of the present invention to provide a method of using a tibial component placement guide for use in a knee arthroplasty procedure involving a knee joint comprising a tibia, a patella, and a femur, the method comprising: (a) applying an overlay to a resected tibia, the overlay including at least one of an indicia and an opening indicative of at least one of an orientation and a position of at least one of a first axis of the femur, a second axis of the femur, and a first axis of the patella; (b) marking the resected tibia with at least one mark using the overlay to denote at least one of an orientation and a position of at least one of a first axis of the femur, a second axis of the femur, and a first axis of the patella; and, (c) orienting and attaching at least one of an orthopedic tibial tray trial and an orthopedic tibial tray to the resected tibia using the mark.
In a more detailed embodiment of the second aspect, the step of applying the overlay includes aligning a peripheral shape of the overlay with a peripheral shape of the resected tibia and placing the overlay on top of the resected tibia. In yet another more detailed embodiment, the overlay includes an opening indicative of the orientation of the first axis of the femur and the second axis of the femur. In a further detailed embodiment, the opening comprises a through hole. In still a further detailed embodiment, the through hole outlines a T-shape, a horizontal aspect of the T-shape is indicative of orientation of the first axis of the femur, and a vertical aspect of the T-shape is indicative of orientation of the second axis of the femur. In a more detailed embodiment, the through hole outlines a + shape, a horizontal aspect of the + shape is indicative of orientation of the first axis of the femur, and a vertical aspect of the + shape is indicative of orientation of the second axis of the femur. In a more detailed embodiment, the opening comprises a first through hole and a second through hole, the first through hole is indicative of the first axis of the femur, and the second through hole is indicative of orientation of the second axis of the femur. In another more detailed embodiment, the opening comprises a first cutout and a second cutout, the first cutout is indicative of the first axis of the femur, and the second cutout is indicative of orientation of the second axis of the femur. In yet another more detailed embodiment, the first axis of the femur comprises the posterior condylar axis of the femur. In still another more detailed embodiment, the second axis of the femur comprises the helical axis of the femur.
In yet another more detailed embodiment of the second aspect, the overlay has a contour outline that is aligned with the resected tibia. In yet another more detailed embodiment, the contour outline is patient-specific. In a further detailed embodiment, the overlay further includes at least one of an indicia and an opening indicative of at least two of a medial guide, a lateral guide, a size of the guide, and a particular patient. In still a further detailed embodiment, the guide is fabricated from at least one of titanium, a titanium alloy, stainless steel, and a stainless steel alloy. In a more detailed embodiment, the guide includes a through aperture configured to align a through fastener mounted to the resected tibia. In a more detailed embodiment, the through fastener comprises a pin. In another more detailed embodiment, the through aperture comprises a plurality of through apertures, and each of the plurality of apertures is configured to receive a pin. In yet another more detailed embodiment, the overlay comprises a base plate. In still another more detailed embodiment, the base plate includes a flange along a periphery of the base plate.
In a more detailed embodiment of the second aspect, the overlay further comprises at least one of an indicia and an opening indicative of the orientation of a third axis of the femur, the third axis being parallel to the first axis. In yet another more detailed embodiment, the at least one mark comprises a pin, and the step of marking the resected tibia includes fastening the at least one pin to the resected tibia. In a further detailed embodiment, the at least one mark comprises an indentation formed into the resected tibia, and the step of marking the resected tibia includes using a punch to form the indentation into the resected tibia. In still a further detailed embodiment, the at least one mark comprises a representation formed into the resected tibia, and the step of marking the resected tibia includes writing the representation onto the resected tibia. In a more detailed embodiment, the orienting and attaching step includes orienting and attaching an orthopedic tibial tray to the resected tibia using the mark. In a more detailed embodiment, the method further includes removing the overlay prior to orienting and attaching at least one of the orthopedic tibial tray trial and the orthopedic tibial tray to the resected tibia using the mark. In another more detailed embodiment, the overlay includes an opening indicative of the orientation of the first axis of the patella. In yet another more detailed embodiment, the opening comprises a through hole.
It is a third aspect of the present invention to provide a method of fabricating a tibial component placement guide for use in a knee arthroplasty procedure involving a knee joint comprising a tibia, a patella, and a femur, the method comprising generating a tibial component placement guide that typifies at least one of a shape and an outline of a resected tibia, along with at least one identifier representative of at least one of a position and an orientation of a kinematic axis of at least one of the femur and the patella.
In a more detailed embodiment of the third aspect, the tibial component guide typifies at least one of the shape of the resected tibia, and the tibial component guide is mass-customized. In yet another more detailed embodiment, the tibial component guide typifies at least one of the outline of the resected tibia, and the tibial component guide is mass-customized. In a further detailed embodiment, the tibial component guide typifies at least one of the shape of the resected tibia, and the tibial component guide is patient-specific. In still a further detailed embodiment, the tibial component guide typifies at least one of the outline of the resected tibia, and the tibial component guide is patient-specific. In a more detailed embodiment, the at least one identifier is representative of an orientation of the kinematic axis of the femur, and the kinematic axis comprises a femoral post condylar axis. In a more detailed embodiment, the at least one identifier is oriented parallel to the femoral post condylar axis. In another more detailed embodiment, the at least one identifier is representative of a position of the kinematic axis of the femur, and the kinematic axis comprises a femoral helical axis. In yet another more detailed embodiment, the position of the at least one identifier is representative of a projected position of the femoral helical axis onto the resected tibia. In still another more detailed embodiment, the at least one identifier is representative of the position of the kinematic axis of the patella, and the kinematic axis comprises a patella transverse axis.
In yet another more detailed embodiment of the third aspect, the at least one identifier is representative of the orientation of the kinematic axis of the patella, and the kinematic axis comprises a patella transverse axis. In yet another more detailed embodiment, the at least one identifier is representative of a position of the kinematic axis of the femur, and the kinematic axis of the femur is parallel to the sagittal kinematic plane of the femur. In a further detailed embodiment, the position of the at least one identifier is representative of a projected position of the sagittal kinematic plane onto the resected tibia. In still a further detailed embodiment, the method further includes establishing at least one of the shape and the outline of the resected tibia. In a more detailed embodiment, the step of establishing at least one of the shape and the outline of the resected tibia includes performing a virtual resection upon a tibial bone model to generate a virtual resected tibia. In a more detailed embodiment, the virtual resected tibia is analyzed to generate a two dimensional shape of a virtual resected surface, and the two dimensional shape of the virtual resected surface typifies the shape of the resected tibia. In another more detailed embodiment, the virtual resected tibia is analyzed to generate a two dimensional outline of a virtual resected surface, and the two dimensional outline of the virtual resected surface typifies the outline of the resected tibia. In yet another more detailed embodiment, the method further includes establishing at least one of the position and the orientation of the kinematic axis of at least one of the femur and the patella when superimposed onto the tibia. In still another more detailed embodiment, the kinematic axis comprises at least one of a femoral helical axis, a femoral post condylar axis, a patella transverse axis, a femoral sagittal kinematic plane, and a patella sagittal kinematic plane.
In a more detailed embodiment of the third aspect, the step of establishing at least one of the position and the orientation of the kinematic axis when superimposed onto the tibia includes at least one of establishing a femoral helical axis with respect to the femur, establishing a femoral post condylar axis with respect to the femur, establishing a patella transverse axis with respect to the patella, establishing a femoral sagittal kinematic plane with respect to the femur, and establishing a patella sagittal kinematic plane with respect to the patella. In yet another more detailed embodiment, the step of establishing at least one of the position and the orientation of the kinematic axis when superimposed onto the tibia includes establishing the femoral helical axis with respect to the femur, and the step of establishing the femoral helical axis with respect to the femur comprises analyzing the relative motion of the femur with respect to the tibia. In a further detailed embodiment, the step of analyzing the relative motion of the femur with respect to the tibia includes analyzing tracked contact points between the tibia and the femur using fluoroscopy. In still a further detailed embodiment, the step of analyzing the relative motion of the femur with respect to the tibia includes analyzing tracked contact paths of the femur with respect to the tibia using fluoroscopy. In a more detailed embodiment, the step of establishing at least one of the position and the orientation of the kinematic axis when superimposed onto the tibia includes establishing the femoral post condylar axis with respect to the femur, and the step of establishing the femoral post condylar axis with respect to the femur comprises analyzing the relative motion of the femur with respect to the tibia. In a more detailed embodiment, the step of analyzing the relative motion of the femur with respect to the tibia includes analyzing tracked contact points between the tibia and the femur using fluoroscopy. In another more detailed embodiment, the step of analyzing the relative motion of the femur with respect to the tibia includes analyzing tracked contact paths of the femur with respect to the tibia using fluoroscopy.
In a more detailed embodiment of the third aspect, the step of establishing at least one of the position and the orientation of the kinematic axis when superimposed onto the tibia includes establishing the femoral sagittal kinematic plane with respect to the femur, and the step of establishing the femoral sagittal kinematic plane with respect to the femur comprises analyzing the relative motion of the femur with respect to the tibia. In yet another more detailed embodiment, the step of analyzing the relative motion of the femur with respect to the tibia includes analyzing tracked contact points between the tibia and the femur using fluoroscopy. In a further detailed embodiment, the step of analyzing the relative motion of the femur with respect to the tibia includes analyzing tracked contact paths of the femur with respect to the tibia using fluoroscopy. In still a further detailed embodiment, the step of establishing at least one of the position and the orientation of the kinematic axis when superimposed onto the tibia includes establishing the patella transverse axis with respect to the patella, and the step of establishing the patella transverse axis with respect to the patella comprises analyzing the relative motion of the patella with respect to the femur. In a more detailed embodiment, the step of analyzing the relative motion of the patella with respect to the femur includes analyzing tracked contact points between the patella and the femur using fluoroscopy. In a more detailed embodiment, the step of analyzing the relative motion of the patella with respect to the femur includes analyzing tracked contact paths of the patella with respect to the femur using fluoroscopy. In another more detailed embodiment, the step of establishing at least one of the position and the orientation of the kinematic axis when superimposed onto the tibia includes establishing the patella sagittal kinematic plane with respect to the patella, and the step of establishing the patella sagittal kinematic plane with respect to the patella comprises analyzing the relative motion of the patella with respect to the femur.
In yet another more detailed embodiment of the third aspect, the step of analyzing the relative motion of the patella with respect to the femur includes analyzing tracked contact points between the patella and the femur using fluoroscopy. In yet another more detailed embodiment, the step of analyzing the relative motion of the patella with respect to the femur includes analyzing tracked contact paths of the patella with respect to the femur using fluoroscopy. In a further detailed embodiment, the tibial component placement guide includes an opening indicative of the orientation of the first axis of the femur and the second axis of the femur. In still a further detailed embodiment, the opening comprises a through hole. In a more detailed embodiment, the through hole outlines a T-shape, a horizontal aspect of the T-shape is indicative of orientation of the first axis of the femur, and a vertical aspect of the T-shape is indicative of orientation of the second axis of the femur. In a more detailed embodiment, the through hole outlines a + shape, a horizontal aspect of the + shape is indicative of orientation of the first axis of the femur, and a vertical aspect of the + shape is indicative of orientation of the second axis of the femur. In another more detailed embodiment, the opening comprises a first through hole and a second through hole, the first through hole is indicative of the first axis of the femur, and the second through hole is indicative of orientation of the second axis of the femur. In yet another more detailed embodiment, the opening comprises a first cutout and a second cutout, the first cutout is indicative of the first axis of the femur, and the second cutout is indicative of orientation of the second axis of the femur. In still another more detailed embodiment, the first axis of the femur comprises the posterior condylar axis of the femur.
In a more detailed embodiment of the third aspect, the second axis of the femur comprises the helical axis of the femur. In yet another more detailed embodiment, the tibial component placement guide has a contour outline that is aligned with the resected tibia. In a further detailed embodiment, the contour outline is patient-specific. In still a further detailed embodiment, the guide further includes at least one of an indicia and an opening indicative of at least two of a medial guide, a lateral guide, a size of the guide, and a particular patient. In a more detailed embodiment, the guide is fabricated from at least one of titanium, a titanium alloy, stainless steel, and a stainless steel alloy. In a more detailed embodiment, the guide includes a through aperture configured to align a through fastener mounted to the resected tibia. In another more detailed embodiment, the through fastener comprises a pin.
In a more detailed embodiment of the third aspect, the through aperture comprises a plurality of through apertures, and each of the plurality of apertures is configured to receive a pin. In yet another more detailed embodiment, the tibial component placement guide comprises a base plate. In a further detailed embodiment, the base plate includes a flange along a periphery of the base plate. In still a further detailed embodiment, the tibial component placement guide further comprises at least one of an indicia and an opening indicative of the orientation of a third axis of the femur, the third axis being parallel to the first axis. In a more detailed embodiment, the at least one mark comprises a pin, and the step of marking the resected tibia includes fastening the at least one pin to the resected tibia. In a more detailed embodiment, the at least one mark comprises an indentation formed into the resected tibia, and the step of marking the resected tibia includes using a punch to form the indentation into the resected tibia.
In a more detailed embodiment of the third aspect, the at least one mark comprises a representation formed into the resected tibia, and the step of marking the resected tibia includes writing the representation onto the resected tibia. In yet another more detailed embodiment, the orienting and attaching step includes orienting and attaching an orthopedic tibial tray to the resected tibia using the mark. In a further detailed embodiment, the method further includes removing the tibial component placement guide prior to orienting and attaching at least one of the orthopedic tibial tray trial and the orthopedic tibial tray to the resected tibia using the mark.
It is a fourth aspect of the present invention to provide a kinematic femoral component for use in a knee arthroplasty procedure involving a knee joint comprising a tibia, a patella, and a femur, the kinematic femoral component comprising a femoral component replicating a natural trochlear groove angle of a femur that is parallel to a sagittal femoral kinematic plane.
In a more detailed embodiment of the fourth aspect, a lateral aspect of an anterior flange extends proximally, the respect to a femur, between 10 to 45 millimeters beyond a femoral knee center of the femur. In yet another more detailed embodiment, a lateral aspect of an anterior flange extends proximally, the respect to a femur, between 10 to 25 millimeters beyond a femoral knee center of the femur.
The exemplary embodiments of the present disclosure are described and illustrated below to encompass devices, methods, and techniques relating to knee arthroplasty. Of course, it will be apparent to those of ordinary skill in the art that the embodiments discussed below are exemplary in nature and may be reconfigured without departing from the scope and spirit of the present disclosure. It is also to be understood that variations of the exemplary embodiments contemplated by one of ordinary skill in the art shall concurrently comprise part of the instant disclosure. However, for clarity and precision, the exemplary embodiments as discussed below may include optional steps, methods, and features that one of ordinary skill should recognize as not being a requisite to fall within the scope of the present disclosure.
Referring to
Referencing
Referring back to
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The instant disclosure relates to guides and trials for use with total or partial knee replacement surgeries as well as femoral and tibial orthopedic implants. As will be discussed in more detail hereafter, the exemplary embodiments of the instant disclosure include tibial and femoral placement guides to facilitate placement of the tibial and femoral implant components, as well as methods of fabricating these placement guides, in addition to method of using the placement guides, as well as methods of fabricating and placing novel prosthetic apparatuses that more closely approximate the natural kinematics of the knee in comparison to present day knee prosthetic components.
As discussed previously, present day placement of prosthetic knee components is premised solely upon mechanical alignment. In particular, the center of the femoral head and center of the ankle (see
Kinematic alignment of the knee is based on the normal kinematics of the knee. Kinematics in this context refers to the relative relationship of the femur, patella and tibia at any angle of flexion without load bearing force applied to the knee. The knee joint surface, menisci, and ligament structures determine the normal kinematic relationship among the femur, patella, and tibia. The following is a discussion of populating a statistical atlas that will be described in more detail hereafter as part of generating mass-customized guides and orthopedic implants in accordance with the instant disclosure.
A premise supporting kinematic alignment of the knee is accounting for and replicating three axes that govern the movement of the patella and tibia with respect to the femur. The primary axis of these three axes is a first transverse axis (i.e., helical axis) in the femur about which the tibia flexes and extends. In order to determine this first transverse axis of a knee joint, the instant disclosure makes use of X-ray fluoroscopy to image the knee joint. More specifically, a knee joint is imaged at distinct points throughout its range of motion (e.g., between full extension and 160 degrees flexion). These fluoroscopic images are registered to 3D models of the knee joint, as discussed previously, which are specific to that knee joint (i.e., patient and knee side specific). After registering the 3D model to the fluoroscopic images, a first transverse axis fitting process is conducted.
The first transverse axis fitting process involves fitting a sphere or cylinder to each joint condyle and, using this shape fitting information, calculating the transverse axis. Specifically, a circular or cylindrical shape is fit to the articular surfaces of the femoral and tibial condyles ranging between 10 to 160 degrees of flexion (see
An ancillary axis to the first transverse axis for kinematic alignment is the PCA. The PCA is approximately parallel to the transverse axis and may be used in aligning the femur (see
There is a second transverse axis, which is a second of the three kinematic axes, in the femur about which the patella flexes and extends (see
In order to determine the second transverse axis about which the patella flexes or extends, the center of mass of the patella (Loci) is tracked with respect to the femur using X-Ray fluoroscopy (see
This second transverse axis fitting process involves determining the position of the patella loci (i.e., centroid) for each fluoroscopic image. In exemplary form, a software package determines the loci for each fluoroscopic image with respect to the femur. Each loci is then plotted as a point with respect to the 3D femur model, which creates a series of points—one for each fluoroscopy image—in 3D space with respect to the femur 3D model. The software then conducts a planar regression on the loci points to establish a best fit plane, which is either parallel or almost parallel with the sagittal kinematic plane extending through the femur. Likewise, the fitting process involves fitting a sphere or cylinder to each patella loci and, using this shape fitting information, calculating the second transverse axis. Specifically, a circular or cylindrical shape is fit to the loci across a knee range of motion, for example, between 10 to 160 degrees of flexion. It should be note that the loci points in 3D space essentially replicate a curve, and it is this curve that is fit to the curvature of the sphere or cylinder. The hypothesis behind using the spherical or cylindrical axes is to approximate the true axis of rotation of the patella about the femur. In sum, the software best fits either a sphere or cylinder with known dimensions to the loci points, after which the second transverse axis extending through the sphere/cylinder is calculated by the software program to be perpendicular to the sagittal kinematic plane. In contrast to this kinematic alignment approach, conventional orthopedic implants the patella groove angle is not parallel to or closely approximates a parallel orientation with respect to the sagittal plane. Moreover, quadriceps length is not restored by current implant designs (see
The third of the three axes is a longitudinal axis in the tibia about which the tibia internally and externally rotates on the femur. This longitudinal axis is perpendicular to each of the first and second transverse axes in the femur. This longitudinal axis is parallel to the sagittal kinematic plane, which is perpendicular to the posterior PCA of the femur (see
As part of the instant technique, the Projected Plane Normal to PCA (PPNP) (i.e., sagittal kinematic plane) was compared to traditional landmarks (see
However, as part of the instant technique, a large angular rotation was observed between the PPNP and the ⅓ Tubercle-PCL of approximately 14 degrees (see
Referring to
The process flow diagram is carried out electronically as part of a software package that automatically calculates position of a given orthopedic implant with respect to a template bone model or a patient specific bone model. For purposes of explanation, it is presumed that the example refers to a patient specific case. Nevertheless, those skilled in the art will readily understand the applicability of the exemplary process flow in cases involving non-patient specific implants and bone models (e.g., mass customized orthopedic implants and template bone models).
As an initial matter, the patient's bone 3D bone model is virtually cut in accordance with protocols from the manufacturer of the orthopedic implant in question. Using this virtual bone cut (VBC), an initial placement of a virtual model of the intended orthopedic implant (VM) is positioned in accordance with the anterior-posterior axis (see
If the answer is “yes,” the pose information is visually made available via a user graphical interface to allow for human intervention and further error minimization. Presuming the human operator is satisfied with the pose (see
Referring to
Turning to
In view of the foregoing explanation, the following is an explanation of the process for generating a tibial, mass customized kinematic alignment guide. As depicted in
The exemplary statistical atlas comprises a compilation of data from multiple subjects that involves the knee joint. By way of example, the statistical atlas may include various images and associated data derived from human knees such as, without limitation, X-ray images, CT images, MRI images, or other imaging technology. In the case of MRI images, the statistical atlas may include images of the soft tissue (e.g., cartilage) of the knee joint. By way of further example, it is presumed that the exemplary statistical atlas has been created from 100 MRI images and 66 CT images. These 166 images were then segmented to create 166 virtual joint models, which are also part of the statistical atlas.
Referring to
Post resection, the contour (i.e., outline shape) of each resected tibia is determined to identify the outermost bounds. After the outermost bounds (i.e., outline shape) of the resected tibia have been determined, a number of calculations are undertaken with respect to these bounds to measure various aspect of the resected tibia. By way of example, and not limitation, the following eight measurements were computed for each resection: (1) M_ML, width of medial plateau; (2) M_AP, height of medial plateau; (3) L_ML, width of lateral plateau; (4) L_AP, height of lateral plateau; (5) BB_AP, overall anterior-posterior height; (6) BB_ML, overall medial-lateral width; (7) LLMLR, ratio of widths between the lateral and medial plateaus; and, (8) MLAPR, ratio of heights between the lateral and medial plateaus. In other words, each resected tibia included shape/outline data, as well as eight sets of measurement data. Referencing
Referring to
In addition to utilizing the shape outline of the resected tibias from the statistical atlas, the statistical atlas is also utilized to calculate the kinematic axes for each joint model. These kinematic axes, as discussed previously, are transformed into data that accompanies each tibial bone model and the resulting bone model having been resected. The kinematic axes data for each resected bone model within a given size population are averaged and superimposed onto the shape outline of the average tibia for each size group. In particular, the sagittal kinematic axis of the femur from anterior to posterior is superimposed onto the tibial outline, in addition to the first transverse axis of the femur. Other axes may likewise be superimposed on to the average tibial shape outline for each size group. This superimposition is eventually utilized to form structural signs informing the surgeon as to the position of certain kinematic axes with respect to the kinematic guide that, when positioned correctly to align its outline with that of the actual resected tibia during TKA, indicates the position of certain kinematic axes with respect to the actual resected tibia.
Using the shape outline data and the superimposition data, a tibial guide may be constructed. A first exemplary mass customized kinematic guide for a tibial implant is shown in
This first exemplary mass customized kinematic guide also includes a contour on the posterior side to account for retention of the posterior cruciate ligament (PCL). In addition, the posterior portion of the guide includes a series of projections that lie on opposing sides of the PCL contour. These projections represent the location of the tibial PCA, which should be aligned with the most posterior points of the medial and lateral condyles. The surgeon may utilize these projections to ensure the guide is properly positioned with respect to the tibia.
As shown in
Referring to
In addition to the openings formed through this second exemplary mass customized kinematic guide, the guide also includes various indicia. In particular, the face of the guide opposite the resected tibia includes a “MED” indicia indicating to a surgeon that this side of the guide should be aligned with the medial portion of the tibia. In order for the surgeon to quickly know whether the guide is for the right tibia or the left tibia, the face includes a “R” indicia indicating that this guide is for use with the right tibia. In cases where the guide is fabricated to correspond to the left tibia, this “R” would be replaced with an “L.” Finally, the face of the guide also includes a size indicia, in this case a “4” indicating to the surgeon that this guide is a size four. Should the initial selection of the guide be too large or small, the surgeon can quickly request a smaller or larger size guide and operating room assistants can quickly discern the size of the guide using this size reference indicia. And similar to the first exemplary mass customized kinematic guide, this second exemplary mass customized kinematic guide also includes a contour on the posterior side to account for retention of the posterior cruciate ligament (PCL).
Referring to
Similar to the first and second exemplary mass customized kinematic guides, this third exemplary mass customized kinematic guide also includes a contour on the posterior side to account for retention of the posterior cruciate ligament (PCL). A fourth set of cutouts is formed on opposing sides of this posterior contour. These fourth cutouts extend in the medial and lateral directions, terminating in circular openings. The circular openings are sized and configured to receive pins or other fasteners that are mounted to the resected tibia and retained after the guide is removed from the resected tibia. The dominant length of these fourth cutouts are delineated by parallel walls that cooperate to establish an axis that is parallel with the femoral PCA.
In addition to the openings formed through this third exemplary mass customized kinematic guide, the guide also includes various indicia. In particular, the face of the guide opposite the resected tibia includes a “MED” indicia indicating to a surgeon that this side of the guide should be aligned with the medial portion of the tibia. In order for the surgeon to quickly know whether the guide is for the right tibia or the left tibia, the face includes a “R” indicia indicating that this guide is for use with the right tibia. In cases where the guide is fabricated to correspond to the left tibia, this “R” would be replaced with an “L.” Finally, the face of the guide also includes a size indicia, in this case a “4” indicating to the surgeon that this guide is a size four. Should the initial selection of the guide be too large or small, the surgeon can quickly request a smaller or larger size guide and operating room assistants can quickly discern the size of the guide using this size reference indicia.
While the foregoing explanation has been directed to processes and generation of mass customized tibial kinematic guides, it should be noted that patient-specific guides can be fabricated in accordance with the instant disclosure. Consequently, the following is an exemplary explanation of the process and resulting fabrication of a patient specific tibial kinematic guide.
Referring to
The tibia from the patient-specific virtual joint model is subjected to a resection process using a software resection algorithm. As part of this resection process, the tibia has a plane applied thereto that simulates the bone cut a surgeon would make during a total knee arthroplasty (TKA) procedure to remove the proximal end of the tibia, thereby leaving a planar tibial end. As those skilled in the art are aware, the tibial bone cut carried out during a TKA is preferably made perpendicular to the sagittal plane. But absolute precision is not always possible, leading to tibial bone cuts that may be angled ±5 degrees from proximal to distal and ±5 degrees from medial to lateral, as well as having different heights ±1 millimeter from proximal to distal along the longitudinal length. Consequently, the resection process is carried out upon the tibia model taking into account a perfect bone cut (±0 degrees from proximal to distal, and ±0 degrees from medial to lateral) in order to make a resection cut, within 1 degree increments, for each combination between the ±5 degree deviation.
Post resection, the contour (i.e., outline shape) of the resected tibia is determined to identify the outermost bounds using a software contour algorithm. After the outermost bounds (i.e., outline shape) of the resected tibia have been determined, a number of calculations are undertaken with respect to these bounds to measure various aspect of the resected tibia. By way of example, and not limitation, the following eight measurements were computed for each resection: (1) M_ML, width of medial plateau; (2) M_AP, height of medial plateau; (3) L_ML, width of lateral plateau; (4) L_AP, height of lateral plateau; (5) BB_AP, overall anterior-posterior height; (6) BB_ML, overall medial-lateral width; (7) LLMLR, ratio of widths between the lateral and medial plateaus; and, (8) MLAPR, ratio of heights between the lateral and medial plateaus. In other words, each resected tibia includes shape/outline data, as well as eight sets of measurement data. Using this shape/outline data and the measurement data, the size and outline of the resected tibia is computed and utilized to form the shape outline of the patient-specific tibial kinematic guide.
It should be noted that this shape outline may be further refined by using data from the patient-specific images to account for ligament retention. By way of example, where the posterior cruciate ligament is retained, the orthopedic tibial implant should not impinge or obstruct the ligament. In order to account for one or more retained ligaments, the patient-specific virtual model of the knee joint includes one or more ligaments with respect to the bones of the knee joint. By knowing the attachment locations on the bones of the knee joint where ligaments attach, the shape outline of the patient-specific tibial kinematic guide can be altered to ensure the outline does not overlap or otherwise impinge upon one or more locations where a ligament will be retained as part of a TKA. The most common of these alterations is a sweeping curved notch cut into the shape outline to allow for retention of the posterior cruciate ligament.
In addition to generating the shape and size of the patient-specific kinematic guide, the computer program also calculates the kinematic axes for the patient-specific joint model using one or more axis/axes algorithms. These calculated kinematic axes, as discussed previously, are transformed into data that accompanies the tibial bone model and the resulting tibial bone model post resection. The kinematic axes data for the resected tibial bone model is superimposed onto the shape outline of the bone model. In particular, the sagittal kinematic axis of the femur from anterior to posterior is superimposed onto the shape outline, in addition to the first transverse axis of the femur. Other axes may likewise be superimposed onto the tibial shape outline for. This superimposition is eventually utilized to form structural signs informing the surgeon as to the position of certain kinematic axes with respect to the kinematic guide that, when positioned correctly to align its outline with that of the actual resected tibia during TKA, indicates the position of certain kinematic axes with respect to the actual resected tibia.
Using the shape outline data and the superimposition data, a patient-specific tibial guide may be constructed. A first exemplary patient-specific kinematic guide for a tibial implant is shown in
This first exemplary patient-specific kinematic guide also includes a contour on the posterior side to account for retention of the posterior cruciate ligament (PCL). In addition, the posterior portion of the guide includes a series of projections that lie on opposing sides of the PCL contour. These projections represent the location of the tibial PCA, which should be aligned with the most posterior points of the medial and lateral condyles. The surgeon may utilize these projections to ensure the guide is properly positioned with respect to the tibia.
As shown in
Referring to
In addition to the openings formed through this second exemplary patient-specific kinematic guide, the guide also includes various indicia. In particular, the face of the guide opposite the resected tibia includes a “MED” indicia indicating to a surgeon that this side of the guide should be aligned with the medial portion of the tibia. In order for the surgeon to quickly know whether the guide is for the right tibia or the left tibia, the face includes a “R” indicia indicating that this guide is for use with the right tibia. In cases where the guide is fabricated to correspond to the left tibia, this “R” would be replaced with an “L.” Finally, the face of the guide also includes a size indicia, in this case a “4” indicating to the surgeon that this guide is a size four. Should the initial selection of the guide be too large or small, the surgeon can quickly request a smaller or larger size guide and operating room assistants can quickly discern the size of the guide using this size reference indicia. And similar to the first exemplary patient-specific kinematic guide, this second exemplary patient-specific kinematic guide also includes a contour on the posterior side to account for retention of the posterior cruciate ligament (PCL).
Referring to
Similar to the first and second exemplary patient-specific kinematic guides, this third exemplary patient-specific kinematic guide also includes a contour on the posterior side to account for retention of the posterior cruciate ligament (PCL). A fourth set of cutouts is formed on opposing sides of this posterior contour. These fourth cutouts extend in the medial and lateral directions, terminating in circular openings. The circular openings are sized and configured to receive pins or other fasteners that are mounted to the resected tibia and retained after the guide is removed from the resected tibia. The dominant length of these fourth cutouts are delineated by parallel walls that cooperate to establish an axis that is parallel with the femoral PCA.
In addition to the openings formed through this third exemplary patient-specific kinematic guide, the guide also includes various indicia. In particular, the face of the guide opposite the resected tibia includes a “MED” indicia indicating to a surgeon that this side of the guide should be aligned with the medial portion of the tibia. In order for the surgeon to quickly know whether the guide is for the right tibia or the left tibia, the face includes a “R” indicia indicating that this guide is for use with the right tibia. In cases where the guide is fabricated to correspond to the left tibia, this “R” would be replaced with an “L.” Finally, the face of the guide also includes a patient indicia, in this case a last name or abbreviated name indicating to the surgeon that this guide is for a particular patient in order to distinguish one patient-specific guide from another patient-specific guide.
In addition to tibial guides, the present disclosure also provides for tibial orthopedic trials that are mass customized and patient-specific.
An exemplary sequence will now be described for use of the exemplary tibial guides and trials. In particular, those skilled in the art are familiar with total knee arthroplasty. Accordingly, a detailed discussion of all procedures performed is unnecessary and certain procedures have been omitted in furtherance of brevity. In order to prepare the tibia for implantation of an orthopedic component, the surgeon resects the tibia to remove the proximal end of the tibia to leave a relatively planar surface to which the eventual tibial tray implant will sit. After the tibia has been resected, the surgeon obtains a medial or lateral guide and places the guide on the resected surface. In the case of a mass-customized guide, the surgeon will choose a guide size and orient the guide so that the outer periphery of the guide best matches or aligns with the outline of the resected tibia. While this positioning is not as precise as a patient specific approach, it nonetheless provides greater accuracy to replicate natural kinematics that using mechanical alignment techniques. In the context of a patient-specific guide, the surgeon will orient the guide to precisely overlay and align the guide so that the outer contours of the guide match or align themselves with the same contours of the resected tibia.
In either instance, after positioning the guide on top of the resected tibia and aligning the guide, the surgeon can than make a mark, indicia, or other visual representation onto the surface of the resected tibia by using one of the openings of the guide. By way of example, one of the through openings in the guide may be oriented in parallel to the femoral post condylar axis. If the surgeon wishes to align the tibial tray component with respect to this reference axis, the surgeon may use a punch and drive it through the opening in the guide in order to make an indentation into the surface of the resected femur. In addition or alternatively, the surgeon may use a biologically acceptable marker and draw the reference axis onto the resected tibia using the guide to orient the mark.
As discussed previously, the guides in accordance with the instant disclosure may provide openings that allow for one or more reference axes or planes to be carried over to the resected tibia from the femur. The surgeon, depending upon his preference, may use one or more of these openings to make marks or other visually perceptible notations upon the resected tibia that will remain as one or more points of reference. After making one or more marks, the guide may be removed from the tibia.
In an instance where the guide doubles as a trial tibial tray, post markings, the surgeon may retain the guide/trial on top of the resected tibia and mount to it one or more tibial tray insert trials that allow the surgeon to test the size and orientation of the ultimate tibial tray and tray insert. When using the guide that doubles as a trial, the surgeon may nonetheless make any markings desired onto the resected tibia and thereafter remove the tibia guide/trial to carry out further procedures to prepare the resected tibia to receive the final tibial tray implant. But it should be note that, for example, it is within the scope of the disclosure for the guide/trial to include a large enough opening to accommodate through put of a broach or other reaming instrument while retaining the guide/trial in position on top of the resected tibia.
In addition to tibial guides, the present disclosure also provides for tibial tray orthopedic implants that are mass customized and patient-specific. The orthopedic components may be fabricated precisely as discussed above with respect to the guides and trials in terms of the shape of the tibial tray and, in addition, include a tibial stem adapter on the underside of the plate that receives a tibial tray stem. Accordingly, a detailed description that is redundant process of creating one or more bone models, calculating relevant landmarks for the bones of the model, performing a virtual tibia resection along with accounting for expected cut deviations, creation of plate contours that account for soft tissue and thereafter aligning various axes and planes with respect to the resected tibia, and in the case of a mass customize implant, extracting the contour features and clustering the contour features to establish one or more shapes and sizes that account for soft tissue retention (e.g., the posterior cruciate ligament), with respect to the creation of tibial tray plates has been omitted in furtherance of brevity. Nevertheless, to the extent necessary for basis in claiming a mass customized or patient-specific tibial tray orthopedic implant, the prior disclosure directed to fabricating guides and trials is incorporated herein by reference.
While the foregoing disclosure has been directed to the tibial side of a knee arthroplasty procedure, many of the foregoing processes and techniques are applicable to the femur and alignment of the femoral orthopedic implant component. By way of introduction, when the knee is in significant flexion, a large component of quadriceps force compresses the patella against the femur (see
The adult human knee is thus a complex interaction product of its habitual motion pattern as produced by the interactions of condylar form and ligamentous restraint, dictated by positional information, and cartilage/fibrous tissue modeling throughout ontogeny. As a consequence, when both processes ceased development at adulthood, the myriad fiber lengths within its restraint systems have remained congruent with the joint's condylar surface geometry, and in the adult will continue to work together, maintaining a normal stereotyped motion pattern such that the velocity vectors of the two rigid bodies are uniformly tangent to their points of contact throughout the joint's normal range of motion (See
Such modeling provides an explanation for a unique feature of the human knee, its medial condylar boss (see
As mentioned previously, the combination of cartilage modeling and the habitual contact of the distal femoral surface with the anterior portion of the medial and lateral menisci leaves small corresponding grooves on the dry femur, the medial and lateral meniscal grooves. A line connecting these grooves, the meniscal axis (see
As seen in
Previous systems must strike a balance between performance in flexion and performance in extension.
Using the meniscal axis in
The tibial footprint of existing systems also can benefit from optimization for kinematic alignment.
Following from the above description and invention summaries, it should be apparent to those of ordinary skill in the art that, while the methods and apparatuses herein described constitute exemplary embodiments of the present invention, it is to be understood that the inventions contained herein are not limited to the above precise embodiment and that changes may be made without departing from the scope of the invention as defined by the following proposed points of novelty. Likewise, it is to be understood that it is not necessary to meet any or all of the identified advantages or objects of the invention disclosed herein in order to fall within the scope of the invention, since inherent and/or unforeseen advantages of the present invention may exist even though they may not have been explicitly discussed herein.
Claims
1. A tibial component placement guide for use in a knee arthroplasty procedure involving a knee joint comprising a tibia, a patella, and a femur, the tibial component placement guide comprising:
- an overlay configured to be overlaid a resected tibia that typifies at least one of a shape and an outline of the resected tibia, the overlay including at least one of an indicia and an opening indicative of at least one of an orientation and a position of a presurgical kinematic axis of at least one of the femur and the patella.
2. The tibial component placement guide of claim 1, wherein the overlay includes an opening indicative of an orientation of a first presurgical axis of the femur and the second presurgical kinematic axis of the femur.
3. The tibial component placement guide of claim 2, wherein the opening comprises a through hole.
4. The tibial component placement guide of claim 3, wherein:
- the through hole outlines a T-shape;
- a horizontal aspect of the T-shape is indicative of the orientation of the first presurgical axis of the femur; and,
- a vertical aspect of the T-shape is indicative of the orientation of the second presurgical axis of the femur.
5. The tibial component placement guide of claim 3, wherein:
- the through hole outlines a + shape;
- a horizontal aspect of the + shape is indicative of the orientation of the first presurgical axis of the femur; and,
- a vertical aspect of the + shape is indicative of the orientation of the second presurgical axis of the femur.
6. The tibial component placement guide of claim 2, wherein:
- the opening comprises a first through hole and a second through hole;
- the first through hole is indicative of the orientation of the first presurgical axis of the femur; and,
- the second through hole is indicative of the orientation of the second presurgical axis of the femur.
7. The tibial component placement guide of claim 2, wherein:
- the opening comprises a first cutout and a second cutout;
- the first cutout is indicative of the position of the first presurgical axis of the femur; and,
- the second cutout is indicative of the position of the second presurgical axis of the femur.
8. The tibial component placement guide of claim 1, wherein the presurgical kinematic axis of the femur comprises a posterior condylar axis of the femur.
9. The tibial component placement guide of claim 1, wherein the presurgical kinematic axis of the femur comprises a helical axis of the femur.
10. The tibial component placement guide of claim 1, wherein the overlay includes the outline of the resected tibia.
11. The tibial component placement guide of claim 10, wherein the outline is patient-specific.
12. The tibial component placement guide of claim 1, further comprising at least one of an indicia and an opening indicative of at least two of a medial guide, a lateral guide, a size of the tibial component placement guide, and a particular patient.
13. The tibial component placement guide of claim 1, wherein the tibial component placement guide is fabricated from at least one of titanium, a titanium alloy, stainless steel, and a stainless steel alloy.
14. The tibial component placement guide of any of the foregoing claims, wherein the tibial component placement guide includes a through aperture configured to align a through fastener mounted to the resected tibia.
15. The tibial component placement guide of claim 14, wherein the through fastener comprises a pin.
16. The tibial component placement guide of claim 15, wherein:
- the through aperture comprises a plurality of through apertures; and,
- each of the plurality of apertures is configured to receive a pin.
17. The tibial component placement guide of any of the foregoing claims, wherein the overlay comprises a base plate.
18. The tibial component placement guide of claim 17, wherein the base plate includes a flange along a periphery of the base plate.
19. The tibial component placement guide of any of the foregoing claims, further comprising at least one of an indicia and an opening indicative of the orientation of a third axis of the femur, the third axis being parallel to the first axis.
20. The tibial component placement guide of claim 1, wherein the overlay includes an opening indicative of the orientation of the first presurgical axis of the patella.
21. The tibial component placement guide of claim 20, wherein the opening comprises a through hole.
22. A kinematic femoral component for use in a knee arthroplasty procedure involving a knee joint comprising a tibia, a patella, and a femur, the kinematic femoral component comprising:
- a femoral component replicating a presurgical trochlear groove angle of a femur that is parallel to a sagittal femoral kinematic plane.
23. The kinematic femoral component of claim 22, wherein a lateral aspect of the kinematic femoral component includes an anterior flange extending proximally, with the respect to a femur, between 10 to 45 millimeters beyond a femoral knee center of the femur.
24. The kinematic femoral component of claim 22, wherein a medial aspect of the kinematic femoral component includes an anterior flange extending proximally, the respect to a femur, between 10 to 25 millimeters beyond a femoral knee center of the femur.
Type: Application
Filed: Apr 26, 2021
Publication Date: Sep 14, 2023
Applicant: TechMah Medical, LLC (Knoxville, TN)
Inventor: Mohamed R. Mahfouz (Knoxville, TN)
Application Number: 17/240,495