DETERMINING A RANGE OF MOTION OF AN ARTIFICIAL KNEE JOINT
20210361191 · 2021-11-25
Inventors
- Oliver FLEIG (Baldham, DE)
- Christian BRACK (Neusaess, DE)
- Zohar LEDER (Munich, DE)
- Martin Bauer (Munich, DE)
Cpc classification
A61B2090/397
HUMAN NECESSITIES
A61B2034/104
HUMAN NECESSITIES
A61B34/20
HUMAN NECESSITIES
A61B5/1072
HUMAN NECESSITIES
A61B5/1121
HUMAN NECESSITIES
A61B90/39
HUMAN NECESSITIES
International classification
A61B5/11
HUMAN NECESSITIES
A61B34/10
HUMAN NECESSITIES
A61B34/20
HUMAN NECESSITIES
A61B5/00
HUMAN NECESSITIES
A61B5/107
HUMAN NECESSITIES
Abstract
A data processing method for determining a range of motion of an artificial knee joint which connects a femur and a tibia via a medial ligament and a lateral ligament, wherein at least the femur comprises an implant which forms a medial condyle and a lateral condyle, the method comprising the steps of: acquiring the maximum lengths of the lateral ligament and the medial ligament: for a particular flexion angle of the knee joint; calculating a first virtual position between the femur and the tibia in which the lateral condyle of the femoral implant touches the tibia and the medial ligament is stretched to its maximum length; calculating a maximum valgus angle of the range of motion from the first virtual position; calculating a second virtual position between the femur and the tibia in which the medial condyle of the femoral implant touches the tibia and the lateral ligament is stretched to its maximum length; and calculating a maximum yarns angle of the range, of motion from the second virtual position.
Claims
1-18. (canceled)
19. A data processing method associated with a knee arthroplasty to be performed on a knee joint of a patient, the method implemented by one or more medical navigation computing devices and comprising: subsequent to a cut of a proximal end of a tibia of the patient and an insertion of a spreading device between a femur of the patient and the tibia, determining for one or more flexion angles of the knee joint: a first relative position of the tibia and the femur when the knee joint is under varus stress; and a second relative position of the tibia and the femur when the knee joint is under valgus stress; determining a range of motion from the first and second relative positions; and displaying the range of motion to facilitate selection of one or more parameters associated with the knee arthroplasty.
20. The method of claim 19, wherein the first relative position represents a maximum varus angle and the second relative position represents a maximum valgus angle and wherein the method further comprises determining a relative position between the femur and the tibia for each of the flexion angles.
21. The method of claim 19, further comprising: generating, for each of the flexion angles, a first length of a lateral ligament of the knee joint and a second length of a medial ligament of the knee joint based on the first and second relative positions; generating, for each of the flexion angles, a maximum varus angle and a maximum valgus angle for a femoral implant or a tibial implant based on the first and second lengths; and determining a range of motion envelope.
22. The method of claim 19, further comprising generating one or more transformation matrices representing one or more of the first or second relative positions between the tibia and the femur.
23. The method of claim 21, wherein the insertion of the spreading device fully stretches the medial and lateral ligaments, wherein the resection of the proximal end of the tibia is according to a tibial cutting plane, and wherein the method further comprises measuring the first and second lengths perpendicular to the tibial cutting plane.
24. The method of claim 19, further comprising: receiving at least one position or size parameter for a tibial implant or a femoral implant; and modifying the range of motion based on the position or size parameter.
25. The method of claim 21, further comprising determining the first or second length based on a distance between a point on the femur and the tibial cutting plane.
26. A non-transitory computer readable medium having stored thereon instructions comprising executable code that, when executed by one or more processors, causes the one or more processors to, after an insertion of a spreading device between a femur of a knee joint of a patient and a resected surface of a tibia of the knee joint: determine for one or more flexion angles of the knee joint: a first relative position of the tibia and the femur when the knee joint is under varus stress and a lateral ligament of a knee joint of the patient is stretched to its maximum length; and a second relative position of the tibia and the femur when the knee joint is under valgus stress and a medial ligament of the knee joint is stretched to its maximum length; determine a range of motion based on a difference between the first and second relative positions; and display the range of motion.
27. The non-transitory computer readable medium of claim 26, wherein the second relative position represents a maximum valgus angle, wherein the first relative position represents a maximum varus angle, and wherein the executable code, when executed by the one or more processors, further causes the one or more processors to determine the maximum valgus and varus angles using a surface model of the femur in which the lateral or medial condyle is modelled.
28. The non-transitory computer readable medium of claim 26, wherein the executable code, when executed by the one or more processors, further causes the one or more processors to generate a first length of the lateral ligament or a second length of the medial ligament from one or more transformation matrices.
29. The non-transitory computer readable medium of claim 26, wherein the executable code, when executed by the one or more processors, further causes the one or more processors to: receive input to amend at least one position or size parameter for at least one of a tibial implant or a femoral implant based on the range of motion; and output to a display device a modified range of motion based upon the received input.
30. The non-transitory computer readable medium of claim 26, wherein the executable code, when executed by the one or more processors, further causes the one or more processors to determine the range of motion further based on a position or a size of a femoral implant or a tibial implant.
31. The non-transitory computer readable medium of claim 28, wherein the first and second lengths are further determined in relation to a plane through the resected surface.
32. The non-transitory computer readable medium of claim 28, wherein the insertion of the spreading device stretches the medial and lateral ligaments and wherein the executable code, when executed by the one or more processors, further causes the one or more processors to measure the first and second lengths perpendicular to the tibial cutting plane.
33. A medical navigation device, comprising: a display device; a non-transitory computer-readable data storage medium comprising program instructions stored thereon; and one or more processors connected to the non-transitory computer-readable data storage medium and configured to execute the stored program instructions to: determine for at least one flexion angle of a knee joint of a patient: a first relative position of a tibia of the patient and a femur of the patient when the knee joint is under varus stress and a lateral ligament of the knee joint is stretched to its maximum length; and a second relative position of the tibia and the femur when the knee joint is under valgus stress and a medial ligament of the knee joint is stretched to its maximum length; generate range of motion data based on a difference between the first and second relative positions; and output to the display device the range of motion data.
34. The medical navigation device of claim 33, wherein the first and second relative positions are determined after an insertion of a spreading device between the femur and a resected surface of a cutting plane of the tibia.
35. The medical navigation device of claim 33, wherein the at least one flexion angle comprises a plurality of flexion angles and the range of motion data comprises a range of motion envelope.
36. The medical navigation device of claim 34, wherein the one or more processors are further configured to execute the stored program instructions to determine the first and second maximum lengths of the lateral and medial ligaments, respectively, perpendicular to the tibial cutting plane.
37. The medical navigation device of claim 33, wherein the one or more processors are further configured to execute the stored program instructions to output to the display device an indication of a range of motion over the at least one flexion angle along an axis in order to display the range of motion data.
38. The medical navigation device of claim 35, wherein the range of motion envelope is further based on a position of a femoral implant relative to the femur or another position of a tibial implant relative to the tibia.
39. A method, comprising: generating a cutting plane through a proximal end of a tibia of a knee joint of a patient according to a cutting plane; resecting through the tibial cutting plane; inserting a spreading device between the resected proximal end of the tibia and a femur of the knee joint; applying varus and valgus stress to the knee joint when the knee joint is at one or more flexion angles; determining a first relative position of the tibia and the femur, and a second relative position of the tibia and the femur, during the application of the varus and valgus stress, respectively, for each knee joint flexion angle; determining a range of motion envelope; and outputting to a display device the range of motion envelope.
40. The method of claim 39, wherein the first relative position represents a maximum varus angle and the second relative position represents a maximum valgus angle and wherein the method further comprises determining a relative position between the femur and tibia for each of a plurality of flexion angles of the knee joint.
41. The method of claim 39, further comprising: generating, for each of the flexion angles, a first length of a lateral ligament of the knee joint and a second length of a medial ligament of the knee joint based on the first and second relative positions; generating, for each of the flexion angles, a maximum varus angle and a maximum valgus angle for a femoral implant or a tibial implant based on the first and second lengths; and determining the range of motion envelope from the maximum varus and valgus angles.
42. The method of claim 39, further comprising generating one or more transformation matrices representing one or more of the first or second relative positions between the tibia and the femur.
43. The method of claim 41, further comprising: inserting the spreading device to fully stretch the medial and lateral ligaments; and measuring the first and second lengths perpendicular to the tibial cutting plane.
44. The method of claim 39, further comprising: receiving at least one position or size parameter for a tibial implant or a femoral implant; and modifying the range of motion based on the position or size parameter.
45. The method of claim 41, further comprising determining the first or second length based on a distance between a point on the femur and the tibial cutting plane.
46. The method of claim 41, further comprising: adjusting a position of one or more of a femoral implant or a tibial implant based on the range of motion, wherein the position is defined by a surgical plan generated before the resection; and implanting the femoral or tibial implant according to the adjusted position.
Description
[0030] The invention shall now be explained in more detail with reference to the accompanying figures, which show:
[0031]
[0032]
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[0034]
[0035]
[0036]
[0037]
[0038]
[0039]
[0040]
[0041]
[0042]
[0043]
[0044]
[0045]
[0046]
[0047] A marker device 12 is rigidly attached to the femur 8, and a marker device 13 is rigidly attached to the tibia 9. The femur 8 and tibia 9 are each registered with reference to the corresponding marker device 12 or 13, respectively, for example using a pointer (not shown). The registration data are stored in the memory 4 of the medical navigation system 1. Attaching a marker device to a bone or registering a bone to a marker device is not however part of the present invention.
[0048] In
[0049]
[0050] The range of motion of the knee joint is preferably determined over a range of flexion angles. The envelope describing the range of motion over such a range of flexion angles can be interpolated from the maximum varus and/or valgus angles for the individual flexion angles sampled. For example, a varus stress is applied to the knee and the knee is bent over the range of flexion angles. Over this range, the medical navigation system samples the position of the marker devices 12 and 13 in order to calculate the relative position between these marker devices and therefore also between the femur 8 and the tibia 9. The maximum varus angle can be calculated for each sample, which corresponds to a particular flexion angle. A valgus stress is then correspondingly applied to the knee and the knee is bent over the range of flexion angles. A plurality of maximum valgus angles are calculated, which correspond to the plurality of flexion angles. The maximum varus and valgus angles over the range of flexion angles result in an envelope of the range of motion of the knee joint. An example of such an envelope is shown in
[0051] Due to the shape of the femur and the tibia, even a fully stretched ligament (a ligament stretched to its maximum length) is not completely straight but rather may comprise curved sections. In order to reduce computational complexity, the ligaments 10 and 11 are preferably considered to be straight. In addition, the maximum length of a ligament need not necessarily be defined as the maximum distance between the points at which the ligament is connected to the femur 8 and tibia 9, respectively. In this example embodiment, the length of a ligament is instead defined as the distance between the point F.sub.m or F.sub.l, respectively, and a plane P which defines a tibial cut. The tibial cut can be an actual tibial cut which has been made prior to performing the present invention and which is therefore not part of the present invention, or a planned tibial cut. The ligaments 10 and 11 are considered to be perpendicular to the surface of the tibial cutting plane P. This is shown in
[0052] In
[0053] In this process, a plurality of relative positions between the femur 8 and the tibia 9 are sampled. Each relative position is represented by a transformation matrix wherein 0<i<N is used as an index for identifying the individual samples within the plurality of samples and wherein the matrix is preferably a 4×4 matrix. Since the femur 8 and the tibia 9 are registered to their respective marker devices 12 and 13, the positions of the points F.sub.m and F.sub.l relative to the tibia 9 are also known or can be calculated.
[0054]
[0055]
[0056] The post-operative situation assumes a particular choice for the femoral implant 8c and tibial implant 9a and a particular position of the femoral implant 8c on the femur 8 and the tibial implant 9a on the tibia 9. The purpose of the present invention is to calculate the range of motion of the post-operative artificial knee joint if these assumptions were actually implemented. In. view of the calculated range of motion, it is possible to amend one or more of these assumptions until a desired range of motion results.
[0057] For each sample, the distances D.sub.m,i and D.sub.l,i are calculated using the following equations:
d.sub.m,i=|T.sub.i×F.sub.m,i−P|
d.sub.l,i=|T.sub.i×F.sub.l,i−P|
[0058] The product of the transformation matrix T.sub.i and the position. F.sub.m,i or F.sub.l,i of the feature points F.sub.m and F.sub.l, respectively, transforms the corresponding point into the co-ordinate system of the tibia 9. The length of a ligament is then the shortest signed distance between this transformed point and the plane P of the tibial cut.
[0059]
[0060] The maximum varus and/or valgus angles are calculated for each recorded transformation matrix T.sub.i. This results in a calculated, predicted post-operative envelope for the range of motion, as shown in the screenshot in
[0061] The relative positions shown in
[0062] In the first approach, the condyles of the femoral implant 8c are modelled as ellipses, as shown in
[0063] In this first approach, the two ellipses representing the condyles 8a, 8b are first brought into contact with the surface of the tibia 9. For this purpose, the minimum distances between the two ellipses and the cutting plane P of the tibia (or the surface of the tibia in general) are calculated, as shown in the side view in
[0064] The axis of rotation is defined by a vector r.sub.impl which is calculated as
{right arrow over (r.sub.impl)}={right arrow over (n.sub.sp)}×({right arrow over (t.sub.cut_ant)}×{right arrow over (n.sub.sp)})
where t.sub.cut_ant is a vector pointing in the anterior direction of the tibia 9 and lying in the cutting plane P and n.sub.sp is a vector pointing to the right-hand side of the femur 8. The vector IN, is calculated as
{right arrow over (n.sub.sp)}={right arrow over (f.sub.ant)}×{right arrow over (f.sub.mech)}
where F.sub.ant is a vector pointing in the anterior direction of the femur and f.sub.mech is a vector corresponding to the mechanical axis of the femur. The vector r.sub.impl thus represents the line forming the intersection between the femoral sagittal plane and the tibial cutting plane P.
[0065] The vector
{right arrow over (f.sub.up)}={right arrow over (f.sub.impl_right)}×{right arrow over (r.sub.impl)}
is then used together with the vector
{right arrow over (f.sub.impl_right)}=M.Math.{right arrow over (f.sub.right)}
to calculate the angle by which the femoral implant has to be rotated about the line defined by r.sub.impl as
[0066] The index i has been omitted from the vectors in order to improve the legibility of the formulae. The vector f.sub.impl_right points to the right-hand side of the femoral implant 8c and is calculated from the vector f.sub.right which points to the right-hand side of the femur 8 and the transformation matrix M which represents the position of the femoral implant. 8c relative to the femur 8. The vector n.sub.tibia_cut represents the normal vector to the tibial cutting plane P. A rotation matrix R.sub.i can be defined in terms of β.sub.i and r.sub.impl,i and represents the rotation needed in order to move the femur 8 into a position relative to the tibia 9 in which its condyles 8a and 8b are equally distant from the surface of the tibia 9.
[0067] The distance g by which the femur 8 has to be moved translationally relative to the tibia 9 is given by the shortest distance between the ellipse which represents the condyle and the surface of the tibia 9, as shown in
[0068] As can be seen from the schematic drawing in.
[0069] Alternatively, the condyles are not modelled as ellipses but are rather represented by the actual shape of the femoral implant, as shown in
[0070] In a second general approach, the two condyles of the femur 8 are not initially brought into contact with the tibia 9, as in the first approach. Instead, the feature point F.sub.m or F.sub.l at which a ligament connects to the femur 8 is used as the centre of rotation for the femur 8. The position of the point F.sub.m relative to the tibia 9 as shown in
[0071] It should again be noted that the present invention does not comprise any surgical steps but rather merely relates to simulating the predicted outcome of an arthroplasty performed using the assumed parameters for the implant(s).