The present disclosure invention relates to data processing apparatus, data processing methods and methods for use in knee replacement surgical procedures.
Knee replacement surgery or knee arthroplasty is a generally well known surgical procedure in which one compartment (unicompartmental knee arthroplasty or partial knee replacement) or the whole of the knee (total knee replacement) is replaced by prosthetic implants typically including a femoral component and a tibial component. The femoral component is attached to the distal end of the femur and generally replaces the femoral condyles. The tibial component is attached to the proximal end of the tibia and generally replaces the tibial plateau.
An important feature of knee arthroplasty generally is the size, position and orientation of the prosthetic components. This generally involves determining the positions and orientations of the various cuts made to resect the distal femur and the proximal tibia and is generally known in the art.
A further important feature of knee arthroplasty is management of the soft tissues that surround the knee and which can be an important aspect the surgical outcome for the patient. During some knee procedures, some of the native soft tissue structures may be sacrificed as part of the surgical procedure, such as the anterior cruciate ligament or posterior cruciate ligament. In some instances, surgeons may perform soft tissue release to reduce the tension in the soft tissues so as to improve the overall performance of the knee joint. Additionally or alternatively, surgeons may adjust bone cut positions to take up some of the laxity that would otherwise be present in the soft tissue structures.
However, the knee joint is not purely a simple pivot about a constant axis of rotation and involves quite a complex relative movement between the articulating surfaces of the femur and tibia and which there is a complex interaction of the various forces exerted on the knee by the various soft tissue structures.
Hence, apparatus and methods which help take into account the soft tissue structures of the knee during replacement knee surgery would be beneficial.
A first aspect of the disclosure provides a data processing method carried out by a data processing apparatus and comprising: storing measured medial knee gap data items and first measured resulting force data items and measured lateral knee gap data items and second measured resulting force data items for a plurality of knee flexion angles; determining a lateral force-distance characteristic for each of the plurality of knee flexion angles; determining a medial force-distance characteristic for each of the plurality of knee flexion angles; using the lateral force-distance characteristic to determine a lateral knee gap distance corresponding to a target force for at least one of the plurality of knee flexion angles; using the medial force-displacement characteristic to determine a medial knee gap distance corresponding to a target force for at least one of the plurality of knee flexion angles; and outputting the lateral knee gap distance corresponding to the target force and the medial knee gap distance corresponding to the target force as a function of knee flexion angle.
Outputting may comprise outputting in a visual form and in particular in a graphical form, for example by displaying one or more graphs.
The target force may be a pre-selected value. For example, the target force may be in the range of 50 Newtons to 150 Newtons or more preferably in the range of 80 Newtons to 120 Newtons.
The target force may be determined from the lateral force-distance characteristic and/or from the medial force-distance characteristic.
The target force may be based on a crossover force at which the force-distance characteristics changes from a first behaviour to a second behaviour. The target force may be the cross over force or may be at least 110% of the cross over force or may be less than 90% of the cross over force. The target force may lie with the second behaviour of the force-distance characteristic.
The data processing method may further comprise: using the lateral force-distance characteristic to determine a variation in lateral knee gap distance corresponding to a variation in the target force for at least one of the plurality of knee flexion angles; using the medial force-displacement characteristic to determine a variation in medial knee gap distance corresponding to a variation in the target force for at least one of the plurality of knee flexion angles; and outputting the variation in lateral knee gap distance with the lateral knee gap distance and/or the variation in medial knee gap distance with the medial knee gap distance.
The data processing method may further comprise: receiving a thickness of a planned tibial component; determining the planned lateral knee gap and the planned medial knee gap arising from the thickness of the planned tibial component as a function of knee flexion angle; using the lateral force-distance characteristic to determine a predicted lateral force corresponding to the planned lateral knee gap as a function of knee flexion angle; using the medial force-distance characteristic to determine a predicted medial force corresponding to the planned medial knee gap as a function of knee flexion angle; and outputting the predicted lateral force and the predicted medial force as a function of knee flexion angle.
The predicted lateral force as a function of knee angle and/or the predicted medial force as a function of knee flexion angle may be output together with the output of the lateral knee gap distance corresponding to the target force and the medial knee gap distance corresponding to the target force as a function of knee flexion angle.
The data processing method may further comprise receiving a further thickness of the planned tibial implant, and repeating the method steps using the further thickness.
The data processing method may further comprise: receiving a modified plan for a femoral component and/or tibial component; and repeating the method using the modified plan for the femoral component and/or tibial component.
The data processing method may further comprise compensating the lateral knee gap distance to correspond to a lateral knee gap distance for a knee having tension in the medial ligaments and the lateral ligaments and/or compensating the medial knee gap distance to correspond to a medial knee gap distance for a knee having tension in the medial ligaments and the lateral ligaments.
The measured medial knee gap data items and/or the measured lateral knee gap data items may be derived from tracking data received from a tracking system.
The first measured resulting force data items and/or the second measured resulting force data items may be derived from measurements received from a knee tensioner.
The first measured resulting force data items and/or the second measured resulting force data items may be derived from measurements received from an electronic force senor.
In some embodiments, using the lateral force-distance characteristic to determine the lateral knee gap distance corresponding to a target force for at least one of the plurality of knee flexion angles may include:
In some embodiments, using the medial force-distance characteristic to determine the medial knee gap distance corresponding to a target force for at least one of the plurality of knee flexion angles may include:
A second aspect of the disclosure provides a non-transitory computer readable medium storing instructions executable by a data processor to carry out the data processing method of the first aspect.
A third aspect of the disclosure provides a data processing apparatus comprising: a processor; and the non-transitory computer readable medium of the second aspect.
A fourth aspect of the disclosure provides a computer assisted surgery system including the data processing apparatus of the third aspect.
The computer assisted surgery system may further comprise: a tracking system; and/or a surgical robot; and/or a knee force sensor.
A fifth aspect of the disclosure provides a method comprising measuring a lateral force-distance characteristic and a medial force-distance characteristic of a knee of a patient at a plurality of knee flexion angles; determining a lateral knee gap corresponding to a lateral target force as a function of knee flexion angle from the lateral force-distance characteristics; determining a medial knee gap corresponding to a medial target force as a function of knee flexion angle from the medial force-distance characteristics; and using the medial knee gap and the lateral knee gap as a function of knee flexion angle to assess a knee gap arising from a planned knee replacement procedure to be carried out on the knee of the patient.
The lateral target force and/or the medial target force may be a pre-selected target force.
The lateral target force may be determined from the lateral force-distance characteristic and/or the medial target force may be determined from the medial force-distance characteristic.
The lateral target force may be based on a lateral cross over force corresponding to a change of the lateral force-distance characteristic of the knee from a first behaviour to a second behaviour and/or the medial target force may be based on a medial cross over force corresponding to a change of the medial force-distance characteristic of the knee from a first behaviour to a second behaviour.
The lateral target force may be the lateral cross over force and/or the medial target force may be the medial cross over force.
The lateral target force may be greater than the lateral cross over force and/or the medial target force may be greater than the medial cross over force.
The lateral target force may be a predetermined percentage of the lateral cross over force and/or the medial target force may be a predetermined percentage of the medial cross over force. For example, the predetermined percentage may be 80%, 90%, 110%, 120% or 130%. The predetermined percentage may be at least 110%. The predetermined percentage may be less than 90%.
The plurality of knee flexion angles may include at least three, five, seven or nine different knee flexion angles. The plurality of knee flexion angles may include at least a flexion angle, an extension angle and an angle between flexion and extension.
The plurality of knee flexion angles may fall within the range of at least −10 to 120 degrees or at least −10 to 90 degrees or at least 0 to 90 degrees.
The method may further comprise inserting a tension meter into the knee of the patient between the proximal tibia and a one of the medial and the lateral condyles; using the tension meter to vary the tension in at least a collateral ligament of the knee adjacent the tensioner; and measuring the distance between the femur and the tibia and the force applied to at least the collateral ligament of the knee as the tension is varied.
The method may further comprise: inserting an electronic force sensor into the knee of the patient between the proximal tibia and a one of the medial and the lateral condyles; moving the tibia in a one of the medial and the lateral direction in the coronal plane to vary the tension in the other of the medial and the lateral ligaments of the knee; and measuring the other of the medial and the lateral distance between the femur and the tibia and the force detected by the electronic force sensor as the tension is varied.
The method may further comprise: tracking the position of the femur and the position of the tibia of the patient; determining the knee flexion angle from the tracked position of the femur and the tracked position of the tibia; and/or determining the lateral distance between the distal femur and the proximal tibia from the tracked position of the femur and the tracked position of the tibia; and/or determining the medial distance between the distal femur and the proximal tibia from the tracked position of the femur and the tracked position of the tibia.
The method may further comprise: displaying the medial knee gap and the lateral knee gap as a function of knee flexion angle.
The method may further comprise: using the lateral force-distance characteristic to determine a variation in lateral knee gap corresponding to a variation in the target force for a plurality of knee flexion angles; using the medial force-displacement characteristic to determine a variation in medial knee gap corresponding to a variation in the target force for a plurality of knee flexion angles; and displaying the variation in lateral knee gap with the lateral knee gap and/or the variation in medial knee gap with the medial knee gap.
The variation may be a pre-selected percentage of the target force. The size of the variation may be 10% or 20%. The variation may be 105% and 95% of the target force or 110% and 90% of the target force.
The method may further comprise: inputting a planned tibial component thickness; using the lateral force-distance characteristic to determine a predicted lateral force corresponding to the planned tibial component thickness as a function of knee angle; using the medial force-distance characteristic to determine a predicted medial force corresponding to the planned tibial component thickness as a function of knee angle; and displaying the predicted lateral force and the predicted medial force as a function of knee angle.
The method may be carried out using a computer assisted surgery system. The computer assisted surgery system may be used to carry out the planned knee replacement procedure on the patient.
The method may include:
The method may include:
The computer assisted surgery system may include a surgical robot. The surgical robot may be used to carry out at least some of the planned knee replacement procedure on the patient.
Embodiments will now be described in greater detail, and by way of example only, and with reference to the accompanying drawings, in which:
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In the Figures of drawings, the same reference numerals are used to refer to like items unless indicated otherwise.
With reference to
In the illustrated embodiment, the tracking system 102 is provided in the form of an infrared optical tracking system including one or more sources of infrared radiation 112, a pair of mutually spaced infrared cameras, 114, 116, mounted on a support 118. However, other wired and wireless tracking systems are also generally known in the art and may utilise, for example, acoustic, magnetic, light or other radiation based tracking technologies. However, simply for the sake of clarity of explanation, an infrared wireless tracking system will be described. The tracking system 102 is in communication with the data processing system 104 which may also implement some of the functionality of the tracking system.
The data processing system 104 includes substantially conventional data processing apparatus, including one or more data processors, memory and storage devices together with various communication buses, power supplies, communication interfaces and user input/output interfaces and devices. The data processing apparatus is configured by suitable software stored in memory to carry out various operations as described in greater detail below. As schematically illustrated in
The data processing system 104 illustrated in
Data processing system 104 includes software 122 which may include one or more software modules as schematically illustrated in
A planning software module 126 may also be provided by which the user may plan various aspects of the surgical procedure. For example, for an orthopaedic surgical procedure, this may include planning the type of implant to be used, the size of the implant, a position and/or orientation of the implant and the position and/or orientation of various cuts to be made to the bones of the patient in order to implement the surgical plan. In other instances, planning may be carried out on a separate application and the planning data imported to the CAS system over a network connection or similar.
The software 122 may also include a registration software module 128 which receives tracking data from the tracking system in order to register the position of the patient's bones within the reference frame of the tracking system. Registration is generally known in the art and is not described in the greater detail herein.
As also illustrated in
As also illustrated in
At 206 the femur and the tibia are registered within the reference frame of the tracking system. For example, the surgeon may use the trackable pointer to register the position of various anatomical points of the femur relative to the femoral marker 150 and various anatomical points of the tibia relative to the tibial marker 152. For example, the positions of the centre of the distal femur and the position of the femoral head may be registered and used to define the femoral mechanical axis. The anterior of the femur, the most distal points of the medial and lateral condyles and the most posterior points of the medial and lateral condyles may also all be registered. For the tibia, the centre of the proximal tibia and the tibial malleoli may be registered and used to define the tibial mechanical axis.
Also, the anterior-posterior axis of the tibia can be registered by positioning the trackable pointer stationary and pointed in a direction parallel to the anterior-posterior axis of the tibia so as to define the anterior posterior axis. The sagittal plane is then defined by having the mechanical axis of the tibia lying on it and also being parallel to the registered anterior-posterior axis of the tibia. This sagittal plane of the tibia allows the system to distinguish between pure flexion-extension angles and varus-valgus angles in which the mechanical axis of the tibia is tilted out of the sagittal plane.
Also, the most distal point on the medial and lateral tibial condyles and the direction of the tibial anterior/posterior axis may all be registered.
In other embodiments, in which a detailed 3D image of the knee is available, e.g. from a CT scan, then the CT scan images can be used instead and the knee registration may be carried out by registering the CT scan to the patients knee bones in a manner generally known to a person of ordinary skill in this art.
Then at 208, the planning software module 126 may then be used to plan an initial tibial cut. The initial tibial cut plan is known relative to the position of the tibial array and hence the planned position can be determined as the tibia is moved by tracking the tibial array. For example, the tibial cut plan may define the planned initial tibial cut as being perpendicular to the tibial mechanical axis in the coronal view, a three degree posterior slope in the sagittal view and a 9 mm resection level from the most proximal condyle.
Then at 210, the planning software module 126 may be used to plan a first femoral implant position. The first femoral implant plan is known relative to the position of the femoral array and hence the planned position of the femoral component can be determined as the femur is moved by tracking the femoral array. For example, the first femoral implant plan may define the femoral implant being positioned perpendicular to the femoral mechanical axis, 3 degrees of external rotation relative to the posterior condyle points, an implant size and anterior-posterior position to restore the medial condyle and minimise overhand and/or notching anteriorly, and a 9 mm resection from the most prominent distal condyle.
Then at 212 the tibial resection is performed. In particular the tibia is resected according to the tibial plan created previously. This may include navigation of instruments such as a tibial cutting block. Additionally or alternatively, this may include controlling the robotic arm 132 to position and use a saw, burr or some other end effector to resect the tibia.
At 214, an electronic force sensor 154 is inserted into the gap and secured to the resected tibia. Ideally the force sensor has a thickness equivalent to the thickness of tibial bone that has been removed/ Hence, the force sensor acts as a spacer and essentially recreates the native tibia. In other embodiments, in which a film force sensor is used, the tibial does not need to be resected first, and the film force sensor may simply be inserted in the knee between the femur and tibia and secured to the native surface of the tibia.
The electronic force sensor 154 can measure the force applied to it and transmit force data via a wired or wireless connection to the data processing system 104. As described in greater detail below, the electronic force sensor 154 is used to measure medial and lateral forces as a function of medial and lateral gap distances over a range of flexion angles of the knee joint.
At 216, the patient leg is placed in a first flexion angle corresponding to full extension (i.e. 0° flexion). Then, at 218, the surgeon applies an increasing varus moment to the knee joint in full extension by tilting the tibia medially relative to the femur within the coronal plane. This is illustrated by arrows 160, 162, in
Then, at 220, the preceding step is repeated but while applying an increasing valgus moment to the knee joint, by moving the tibia in a lateral direction relative to the femur within the coronal plane. Similarly to 218, the force output by the sensor and the position of the femoral and tibial markers are tracked to provide force, tibial position and femoral position data as a function of time.
At 222, a next knee flexion angle is selected. For example, with full extension corresponding to 0° flexion, then the knee angle may be increased by, for example, 15°, to provide a 15° flexion knee angle. For this new knee angle, as illustrated by process flow line 224, the method returns and for the new knee flexion angle, further sets of force-position data values are recorded by applying varus and valgus moments respectively within the coronal plane of the tibia. The method then repeats at increasing knee flexion angle values until a maximal flexion angle is arrived at, for example, sets of data may be recorded for flexion angles of 0°, 15°, 30°, 60°, 90° and 120°.
After the force-position data has been measured for the patient's knee as a function of knee flexion angle, and captured by the data processing system 104, the data processing system 104 can carry out various data processing operations, described in greater detail below. Graphical representations of the results of the data processing can then be output via the display device 120 for viewing by the surgeon. In particular, as described in greater detail below, the data processing system 104 may display one or more graphical indications of the medial and lateral knee gap value as a function of knee angle for a predetermined medial force and lateral force. This force-gap data may be used by the surgeon to assess or review and/or modify one or more planned properties of the surgical plan in order to arrive at an acceptable knee gap as illustrated by step 226 in
With reference to
For example, and with reference to
In other embodiments, if the resected surface of the tibia has been registered, then the minimum distance perpendicular to the resected tibial surface and the lateral condyle of the first planned femoral position may be determined instead.
For example,
As illustrated in
Depending on the knee flexion angle various different soft tissue structures of the knee will be involved in resisting the varus and valgus loads. For example in extension, the force-distance function 330 will represent the properties of the posterior capsule, and at some flexion angles, the anterior cruciate ligament (ACL) and/or posteriori cruciate ligament (PCL) may also affect the force-distance function. Hence, depending on the knee flexion angles, the force-distance function will be the result of various soft tissue structures of the knee and/or the result of aggregates of multiple soft tissue structures, including, but not limited to, the collateral ligaments.
Further, when multiple soft tissue structures are involved, the force-distance characteristic may not have the same shape or form as the “ideal” one illustrated in
Although
In a similar way, the minimum perpendicular distance, d, between the planned tibial cut and the medial condyle for the first planned femoral implant position is determined for each recorded force value to provide a medial force-distance function.
This is then repeated for each of the knee flexion angles, to provide a medial force-distance function and also a lateral force-distance function for each of the different knee flexion angles.
After the force-distance function for each knee flexion angle, for both the medial and lateral sides, has been determined at 304, at 306, those functions are used to determine the medial and lateral gaps arising for a particular force value for each of the knee flexion angles. The particular force value may be based on some characteristic of the force-distance function for at least one knee flexion angle, or otherwise related to the measured force-distance characteristic, and hence may be patient specific.
For example, with reference to
As a patient specific force example,
Optionally, distances corresponding to small changes in the target force FT may also be calculated and used in a sensitivity assessment as described in greater detail below. For example, as illustrated in
Similarly,
These calculations may be carried out using the respective force-distance functions for the lateral and the medial sides of the knee and potentially for each of the knee flexion angles as illustrated by processes 306 and 308 in
However, as discussed above, the force-distance characteristic may not have the ideal form shown in
Hence, at 306, for several knee angles, the medial gap and the lateral gap for the knee corresponding to target medial and lateral force values have been determined.
Optionally, as illustrated by box 308 of
At 310, the medial and lateral distance values calculated previously may be compensated, using a compensation value or function or look up table data or similar, to take into account the differences in the knee geometry during the force measuring process and the knee during normal operation.
For example
Similarly,
The compensation factors may be determined empirically. For example an anatomic study may be carried out to generate a database capturing the relationship between La and Lc and Ma and Mc at different knee flexions angle and that can be interpolated to provide correction factors for any particular values of Lc and Mc. Another example would be to relate the correction factor to the epicondylar width, as the amount of correction increases with the width of the femur. For example a simple geometric formula or equation may be used to determine the correction factor to apply to correct Lc to La and Mc to Ma using the width femur and/or separation between the epicondyles of the femur.
Using a correction factor will improve the accuracy of the method but is not essential. As an example only, a typical value for the correction factor for an average adult knee may be about 20%. That is, La maybe approximately 20% greater than Lc, e.g., La is 120% of Lc.
Use of a correction factor in the range of about 10% to 30% can improve the accuracy but is not essential. Without the correction factor, the medial-lateral balance will still be correct, but the actual size estimates for the medial and lateral gaps will be undersized (by up to about 20%). This should be reasonably constant though and a consequence may be simply that a slightly thicker insert (20% thicker) than planned may be used in order to fill up the extra 20% of space in order to arrive at the target force.
Hence after step 310, the system has stored corrected values of the medial and lateral distance between the resected tibial surface and the femoral condyles for the planned femoral implant position for a target force FT, and +/−5% values, over a range of knee flexion angles. This data may then be output, for example in a visual form, for the user and/or for use by other software processes.
For example at 312, a graphical representation of the data may be output to the user as illustrated in
As can also be seen in the example illustrated by
The plots 404, 406 and 412, 414 of sensitivity of the medial and lateral forces to medial and lateral distance also help the surgeon to understand that the sensitivity of the force in the ligaments to gap size is higher at lower flexion angles (0°) but lower at higher flexion angles (90°). Hence, setting the gap size on the lateral and medial sides at lower flexion angles may be preferable, for the specific example illustrated in
In some embodiments, the process described above may be streamlined as follows.
Some structures, for instance medial or extension structures, may be relatively stiff. In such structures, the distraction forces described herein may have relatively little effect on the resulting distance measurement. An example of this is shown in
In the example shown in
The stiffness of the ligaments may be associated with a given range of knee flexion angles. For instance, the apparent stiffness of the ligaments may be higher within a certain range of knee flexion angles, but less pronounced at other knee flexion angles. Nevertheless, it is anticipated that stiff ligaments may generally lead to a relatively steep second generally linear part 332 across a range of knee flexion angles.
The stiffness of the ligaments would generally be evident to a surgeon taking the force/distance measurements described herein and would also be detected by the tracking system 102 of a CAS system 100 of the kind described herein.
For knee flexion angles at which the relatively high stiffness of the ligaments results in a steep second generally linear part 332, the process described herein in relation to
On the other hand, if the aforementioned threshold, which may also be referred to as a stiffness threshold, is not met or exceeded at any given knee flexion angle, then the normal methodology described herein in relation to
It is envisaged that the approach described above, involving setting the target distance to the nominal value may be applied to lateral as well as medial force versus distance measurement results.
The use of the nominal value for the target distance for knee flexion angles having relatively steep second generally linear parts 332 may simplify the methodology shown in
It is envisaged that in some examples, this simplification may be applied to some or even all of the knee flexion angles (for the medial and/or lateral structures) involved in the overall procedure, namely any knee flexion angles in which the aforementioned stiffness threshold is met or exceeded.
It is noted setting the target distance to a nominal value that is slightly less (e.g. by an amount in the range 0.5 mm-1.0 mm) than the maximum gap can avoid over tensioning in the ligaments.
The tibial insert will result in a fixed medial and lateral distance between the tibial cut and the articulating surface of the currently planned femoral implant position though the range of flexion angles of the knee. For example, a particular thickness of tibial insert, providing the tibial articulating surface, may result in an actual medial and lateral distance, Ma and La of 10 mm. The medial and lateral forces likely to result from that distance may be calculated and output to the user.
The distance from the resected tibia to the femoral articulation surface is the thickness of the overall tibial component. Depending on the implant system that may be the thickness of a tibial tray and the thickness of the insert or in the case of an all polyethylene tibial component it is just the thickness of the polyethylene component. Also, some implant systems use a nomenclature where the insert thickness actually describes the thickness of the overall tibial construct (i.e. insert and tibial tray), whereas other implant system, use a nomenclature in which the insert thickness is the actual thickness of the insert alone. In that case the overall tibial construct has a thickness larger than this. So, for example, a tibial tray may have a thickness of 4 mm, in which case, for an insert thickness of 5 mm, the overall thickness of the tibial construct, would be 9 mm.
In the following description, the value of 6 mm represents a 6 mm thick insert, and so the actual thickness of the overall tibial construct (insert +4 mm tibial tray) and hence the distance between the resected tibia and femoral articulation surface, La/Ma, is 10 mm.
So, in some instances, for convenience for the surgeon, the distance between the resected tibia and femoral articulation surface, La/Ma, may be calculated, but may be plotted as a distance that takes into account a fixed tray thickness, e.g. 4 mm, so that the numbers correspond to the number that the surgeon is interested in for the implant system being used, e.g. the insert thickness to use.
As illustrated in
For example,
As illustrated in
At 320, the user may determine whether current plan is acceptable or not and if not then at 322 the user may modify the plan. As illustrated in
Additionally or alternatively at 322, the user may modify the planned position of the femoral component in particular. Some modification of the tibial component plan may be possible at this stage even though the tibia has already been resected. For example recuts are possible and relatively easy to achieve particularly in embodiments using surgical robot 106. Hence, recuts may be made, for example to make changes to the angle of the resected tibia. When bone is removed a larger insert may be used to compensate for the removed bone so as to achieve a better balanced joint.
For example, in the specific situation illustrated in
As the tibial insert results in a constant distance throughout the flexion range, it is desirable to have a planned femoral implant position that results in a medial and lateral distances corresponding to the target forces, that are reasonably constant throughout much of the range of knee flexion and which also have similar medial and lateral values. Therefore, at step 322, the user may modify the planned position of the femoral component as described above. As the position of the femoral component is defied relative to the anatomy of the femur and the position of that is known as the tracked femoral marker or array 150 is attached to the femur 142, the planned position of the femoral implant may also be determined relative to the position of the tracked femoral marker. Hence, processing returns 326 and a modified femoral plan may be used and steps 304 onward may be repeated using the modified planned position of the femoral implant and hence giving rise to different initial force-implant gap functions for each knee angle. There is no need to repeat the measurement of the force data as the physical native femur has not changed, simply the planned position of the femoral implant relative to the native femur.
Hence, steps 304 onward of the method 300 may be repeated one or more times until the user is happy with the planned femoral position and resulting knee gap distance for a selected tibial insert thickness.
Hence, plot 510 corresponds to measured force as a function of knee flexion angle (for a particular knee distance) plot 512 corresponds to a measured force-distance characteristic (for a particular knee flexion angle) and hence is similar to
The surgical procedure may then continue in a generally conventional manner and using the panned femoral implant position and tibial insert thickness arrived at after step 320. Hence, once the surgeon is happy with the planned implant positions at 226 of
A second embodiment will now be described which is similar to the first embodiment in many respects and differs largely in that the minimal perpendicular distance between the tibia and the lateral native femoral epicondyle and the medial native femoral epicondyle are used instead of the medial and lateral condyles. This can avoid using compensation factors as described above and illustrated in
Hence many of the steps of method 200 and process 300 are either generally the same or need only minor modification, as will be apparent to a person of ordinary skill in the art, form the further description herein. Indeed, method 200 is substantially the same in terms of how the force data and data from the tracking markers 150, 152 is generated and stored by the CAS system.
However, at step 304, the distance calculated for the force-implant distance function is the minimal perpendicular distance from either the resected surface of the tibia, or the planned tibial resection surface, and the lateral epicondyle of the planned femoral implant position or the medial epicondyle of the planned femoral implant position, as illustrated in
Again, if the actual tibial cut has been made and registered then the minimal perpendicular distance from the actual tibial cut to each of the medial and lateral epicondyles may be calculated and used instead. Also, if a film sensor on the native surface of the tibia is used then there is no need to make the tibial cut during method 200 and then the minimal perpendicular distance from the native tibia to each of the medial and lateral epicondyles may be calculated and used instead. Alternatively, it may be more computationally convenient to use the planned tibial cut position, if the tibial cut has not been made, so that a flat plane is used rather than the more complex 3D surface of then native tibia. Hence, below, the tibial plane will generally be used to mean the actual plane of the resected tibia or the plane of the planned tibial resection. Hence, even if a film force sensor is used on the native tibia, then the calculations may be based on the planned position of the tibial cut. A benefit of this is that more options are retained for changing the tibial cut, as the tibia has not yet been cut and therefore the compromises associated with a recut may be avoided.
Processing then proceeds at steps 306 and 308 in which the medial and lateral force-distance functions for each knee flexion angle determined at 304 are used to determined medial and lateral distances corresponding to medial and lateral target force values and target force values +/−5% over the range of knee flexion angles.
Then, instead of the compensation step 310, a femoral position modelling step is carried out. In particular, the position of the native femur having the previously calculated medial and lateral distances corresponding to the target force values for each knee flexion angle is determined. For example,
The method then resumes as illustrated in
Again, based on the output data the user can determine whether the planned tibial insert thickness and/or planned femoral implant position is acceptable or not at 320 and the insert thickness may be changed and/or the planned femoral implant position. However, in this second embodiment, there is no need to repeat the modelling of the femur position at different knee flexion angles. All that needs to be done is to re-calculate the perpendicular lateral distance, La, and medial distance, Ma, from the tibial cut to the modified position of the lateral condyle and medial condyle of the femoral implant at its new position relative to the native femur. The positional relationships between the tibial and femoral tracking markers, the femoral epicondyles and the forces are already known.
Again, initially the knee joint is accessed at 202 and navigation markers attached to the tibia and femur at 204. At 206, the native femur and the native tibial are registered using the trackable pointer 156. At 208 and 210 the femoral plan and the tibial plan are created and at 212 the tibia is resected using the planned tibial cut, for example using a navigated tibial cutting block. Then at 242, the tension meter 190 is inserted in the knee gap between the resected tibial plateau and a one of the lateral or medial condyles. For example, as illustrated in
Once the medial measurements have been carried out, then at 250, the tension meter is moved to the lateral side and again used to apply an increasing load to the lateral condyle to tension the lateral ligament and the femoral marker and tibial marker positions are tracked and measured for a current knee flexion angle. Again, at 252 the knee is placed in a new knee flexion angle and the measurements repeated as illustrated by line 254.
Alternatively, a medial value and a lateral value could be measured at each angle, rather than doing all medial measurements and then all lateral measurements.
At 226, the force-distance data generated by data processing system 104 may be used by the surgeon to assess and/or review and/or modify the planned implant positions as illustrated by process flow line 228.
The data processing operations carried out by the data processing system are substantially the same as those described previously, but the manner in which the force-distance data is collected as a function of knee flexion angle is different.
A number of devices such as distractors or pivoting tensioners are known in the art, which may be used in the approach shown in
In a first stage, shown in
In a next stage, shown in
In a next stage, shown in
In a next stage, shown in
As will be described below, the pivoting tensioner may include electrical/mechanical sensors or other means of determining the forces operating between the superior plate 604 and the inferior plate 602. This may include one or more pressure sensors which are configured to electrically output force values, and/or a mechanical indicator, which may be visually read off by the surgeon.
The use of the force sensors 610, 612 in combination with the reference arrays 150, 152 allow force and distance data to be collected in a synchronised manner, while the superior plate 604 is moved in the manner described above in relation to
As described in relation to
perpendicular to tensions Tmed and Tlat.
Resolving the forces vertically in
a. Fdistraction=TMed+TLat
Here it may be assumed that the sum of moments around the hinge point 606 is zero. Hence:
a. TMed×dMed=TLat×dLat
and thus
a. TMed=Fdistraction−TLat
i. =Fdistraction−(TMed×dMed)/dLat
ii. =(Fdistraction×dLat)/(dLat+dMed)
and
a. TLat=Fdistraction−TMed
i. =Fdistraction−(TLat×dLat)/dMed
ii. =(Fdistraction×dMed)/(dMed+dLat).
Accordingly, the tension in the medial collateral ligament (see
In this specification, example embodiments have been presented in terms of a selected set of details. However, a person of ordinary skill in the art would understand that many other example embodiments may be practiced which include a different selected set of these details. It is intended that the following claims cover all possible example embodiments.
Any instructions and/or flowchart steps can be executed in any order, unless a specific order is explicitly stated. Also, those skilled in the art will recognize that while one example set of instructions/method has been discussed, the material in this specification can be combined in a variety of ways to yield other examples as well, and are to be understood within a context provided by this detailed description.
While the disclosure is amenable to various modifications and alternative forms, specifics thereof have been shown by way of example in the drawings and described in detail. It should be understood, however, that other embodiments, beyond the particular embodiments described, are possible as well. All modifications, equivalents, and alternative embodiments falling within the scope of the appended claims are covered as well.
Number | Date | Country | Kind |
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2002918.7 | Feb 2020 | GB | national |
The present application claims priority to PCT/EP2021/054474, filed on Feb. 23, 2021, which claims priority to UK Patent Application No. 2002918.7, filed on Feb. 28, 2020, both of which are incorporated in their entireties by reference herein.
Filing Document | Filing Date | Country | Kind |
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PCT/EP2021/054474 | 2/23/2021 | WO |