US20220202403A1 - Actuated positioning device for arthroplasty and methods of use - Google Patents

Abstract

A joint balancing insert with sensors and an actuated mechanism is disclosed. The joint balancing insert is used to balance a joint during arthroplasty surgery, as the sensors provide force, position and angular data relating to the movement of the joint, while the actuated mechanism allows for highly accurate and dynamic adjustments of the joint based on the data from the sensors. Various configurations of actuated mechanisms and sensors may be implemented in the insert to provide for manual or real time control of the insert, and customized interfaces are provided for visualized feedback of adjustments. Sensor data may also be collected and compared with expected or preferred data sets to provide adjustment recommendations and achieve better outcomes based on historical data.

Description

RELATED APPLICATIONS
• This application is a continuation of U.S. patent application Ser. No. 14/515,375 entitled “ACTUATED POSITIONING DEVICE FOR ARTHROPLASTY SURGERY AND METHODS OF USE,” filed on Oct. 15, 2014, which claims the benefit of U.S. provisional patent application Ser. No. 61/891,397 entitled “ACTUATED POSITIONING DEVICE FOR ARTHROPLASTY SURGERY AND METHODS OF USE,” filed on Oct. 15, 2013, U.S. provisional patent application Ser. No. 61/891,398 entitled “SPRING-ACTUATED POSITIONING DEVICE FOR ARTHROPLASTY SURGERY AND METHODS OF USE,” filed on Oct. 15, 2013, and U.S. provisional patent application Ser. No. 61/990,476 entitled “ACTUATED POSITIONING DEVICE FOR ARTHROPLASTY SURGERY AND METHODS OF USE,” filed on May 8, 2014, which are hereby incorporated by reference in their entirety.
FIELD OF THE INVENTION
• Various embodiments described herein relate generally to devices and methods for balancing a joint during prosthetic arthroplasty, and to an actuated positioning and sensing device for positioning prosthetic components and balancing a joint during arthroplasty surgery.
BACKGROUND
• Arthroplasty involves the repair of a joint by replacing one or more portions of the joint to eliminate pain and improve movement. For example, loss of cartilage or friction between bone surfaces can be treated by inserting an artificial joint, which includes one or more prostheses designed to replace bone surfaces and cartilage while also allowing for a range of movement similar to the original joint.
• Knee arthroplasty typically involves resecting (cutting away) the diseased and damaged surfaces of the lower end of the femur (thigh bone), the upper end of the tibia (shin bone), and the joint surface of the patella (knee cap). These surfaces are then replaced by artificial materials. The femoral component or prosthesis is typically made from a cobalt chrome alloy and is attached to the femur with fixation devices such as pegs, often with the use of bone cement to bond the femoral prosthesis to the underlying bone. The tibial component typically consists of two parts—a metal tray (titanium or cobalt chrome alloy) and a polyethylene insert—that are assembled together during surgery. The metal tray is fixed to bone with screws, pegs, or a stem; while the insert is locked into the metal tray and articulates with the femoral component.
• The technical challenges in knee arthroplasty are: restoration of the natural alignment of the knee with respect to the hip and the ankle; regaining the range of motion of the knee; and inducing the artificially-implanted knee to move in a manner similar to a normal knee. These goals are accomplished by making the bone cuts at precise locations and orientation relative to the rest of the bone, selecting the appropriate size and shape of the prosthetic components, placing the prostheses at the appropriate location on the bones and with respect to each other, and selecting an insert of appropriate thickness such that the knee joint is neither too lose or too tight.
• Despite continuous improvements in the design and manufacture of artificial joints and in surgical instruments, the actual arthroplasty relies primarily on the skill and expertise of the surgeon performing the procedure. Arthroplasty requires that a surgeon not only insert the artificial joint, but also “balance” the joint to ensure that the movement of the artificial joint is as similar as possible to a normal range of motion. Balancing the joint often requires careful measurement and cutting of bone, ligaments and other tissue, as well as load balancing to ensure that the force applied by the bones to the joint is evenly distributed and range of motion testing to determine if the artificial joint is capable of movement in the direction and distance required for normal movement. The balancing process often requires the surgeon to simply physically hold the joint and “feel” whether the movement of the joint and the forces being applied to the joint are correct. As a result, the process of balancing the joint is largely subjective, as it relies upon the experience and knowledge of the surgeon to understand whether the movement of the artificial joint is “about right.” Misalignment of any of these parameters may result in limited range of motion of the joint, continued pain at the joint and early failure of the artificial joint due to excess load distribution or friction.
• To aid in balancing the artificial joint during arthroplasty, measurement devices have been developed which help a surgeon measure some parameters during the balancing of the joint. The most common balancing devices are mechanical in nature: the surgeon manually applies force on the device to distract the bones of the joints and the distance between the bones is visually measured. Some measurement devices incorporate sensors which can be inserted into the artificial joint to provide measurements about load distribution that are useful when attempting to balance the joint. Even with these measurement devices, the surgeon is still required to manually apply an unknown or inaccurate force to the joint in order to determine whether the joint is balanced. If the amount of applied force is inconsistent with the actual force applied to the joint during actual use, the joint may not move appropriately and may wear prematurely, leading to limited movement, pain, and eventual replacement or further surgical repairs.
SUMMARY OF THE DISCLOSURE
• Disclosed herein are devices and methods for balancing a joint during surgical procedures, such as prosthetic arthroplasty. In embodiments, the device is an insert with one or more plates, one or more sensors and at least one actuated mechanism for actuating the device against one or more parts of the joint. The one or more plates are disposed between bone structures which define the joint, such as the femur and the tibia in a knee joint. The one or more sensors provide force, position and angular data about the movement of the joint, which, along with the applied force data derived from the movement of the actuated mechanism, provide for highly accurate and dynamic adjustments of the joint. In one embodiment, at least one actuated mechanism is a spring-actuated mechanism. In another embodiment, at least one actuated mechanism is a pneumatic-actuated mechanism. A pressurizing apparatus is used to pressurize the pneumatic-actuated mechanism. Various types of actuation configurations, such as spring configurations and pneumatic configurations or a combination thereof, and sensors may be implemented in or on the insert to provide for control of the actuated mechanism and measurement of numerous parameters relating to the balancing of the joint. Customized graphical user interfaces (GUIs) are provided for real-time control and visualized feedback of adjustments. Sensor data may also be collected and compared with expected or preferred data sets to provide adjustment recommendations and achieve better outcomes based on historical data. Other features and advantages should become apparent from the following description of the preferred embodiments, taken in conjunction with the accompanying drawings.
BRIEF DESCRIPTION OF THE DRAWINGS
• Various embodiments disclosed herein are described in detail with reference to the following figures. The drawings are provided for purposes of illustration only and merely depict typical or exemplary embodiments. These drawings are provided to facilitate the reader's understanding and shall not be considered limiting of the breadth, scope, or applicability of the embodiments. It should be noted that for clarity and ease of illustration these drawings are not necessarily made to scale.
• FIG. 1 is a functional block diagram of a joint balancing system, according to one embodiment of the invention.
• FIG. 2 is an illustration of an embodiment of the insert ofFIG. 1 disposed in a knee joint.
• FIG. 3 is a perspective view illustration of an embodiment of the insert ofFIG. 1 with displacement sensors.
• FIG. 4 is an illustration of a perspective view of an embodiment of the insert ofFIG. 1 with a pneumatic actuator.
• FIG. 5 is an illustration of an exploded view of the insert ofFIG. 4.
• FIG. 6 is an illustration of a perspective view of the pneumatic actuator ofFIGS. 4 and 5.
• FIG. 7 is a top view of abellows182 ofFIG. 6.
• FIG. 8 is an illustration of a perspective view of the electronics board ofFIGS. 4 and 5.
• FIG. 9 is an exploded view illustration of an embodiment of the insert ofFIG. 1 with a plurality of spring actuators.
• FIG. 10 is an alternate exploded view illustration of the insert ofFIG. 9 without the actuators.
• FIG. 11 is a perspective view illustration of an embodiment of the insert ofFIG. 1 with a unicompartmental configuration.
• FIG. 12 is an illustration of a perspective view of an embodiment of the controller assembly ofFIG. 1 connected to an insert.
• FIG. 13 is an illustration of a perspective view of the controller of the controller assembly ofFIG. 12.
• FIG. 14 is an illustration of an exploded view of the controller ofFIG. 13.
• FIGS. 15 and 16 illustrate an embodiment of a cutting guide assembly connected to the insert that is used to guide cutting bone and tissue during balancing of the joint.
• The various embodiments mentioned above are described in further detail with reference to the aforementioned figured and the following detailed description of exemplary embodiments.
DETAILED DESCRIPTION
• Disclosed herein are systems, devices, and methods for balancing a joint during surgical procedures on joints, such as prosthetic arthroplasty.FIG. 1 is a functional block diagram of ajoint balancing system50, according to one embodiment of the invention.Joint balancing system50 may include a trial insert (“insert”)100, acontroller assembly200, and adisplay system300. Thejoint balancing system50 includes aninsert100 with one or more plates, one or more sensors and at least one actuator/actuated mechanism for actuating the device against one or more parts of the joint as illustrated inFIGS. 2-11. The actuated mechanism may be fluid powered, such as by air, electromechanical, electromagnetic, mechanical, piezoelectric, or a combination thereof. Other actuated mechanisms may also be used. The one or more plates are disposed between bone structures which define the joint, such as the femur and the tibia in a knee joint. The one or more sensors may provide force, position and angular data about the movement of the joint, which, along with the applied force data from the actuation mechanism, provide for highly accurate and dynamic adjustments of the joint. Various configurations of the actuators and sensors may be implemented in or on theinsert100 to provide for control of theinsert100 and measurement of numerous parameters relating to the balancing of the joint. The addition of an actuated mechanism to the inserts provides numerous benefits to the process of balancing a joint during surgical procedures, such as arthroplasty. The surgeon is able to apply a known and controlled amount of force to the joint and correlate the measured load, movement and angular data with the applied force to more precisely determine if adjustments should be made. The actuated mechanism may also be capable of dynamic actuation from a variety of different actuation points on the insert, providing the ability to apply different load amounts, different amounts of movement and different angles of movement to more accurately simulate the movement of the joint and measure the results. The load can be measured across any range of motion to provide significant improvements in load balancing.
• Theinsert100 may include anelectronics board140. Theelectronics board140 may include aboard module141 and aboard communication module143. Theboard module141 may be configured to obtain the data from the sensors and send the data to thecontroller assembly200 via theboard communication module143. Theboard module141 may also be configured to relay a signal from thecontroller assembly200 to the actuators. Theboard module141 may also be configured with a safety override to control the actuator force or the magnitude of distraction or displacement. Theboard module141 may further be configured to communicate a signal when theinsert100 is unbalanced and communicate another signal when the insert is balanced. The signal may cause an alert, such as an auditory alert or a visual alert provided by electronic hardware attached to theelectronics board140 and/or from the display system. The auditory alert may be provided by a sound source, such as a speaker or a piezoelectric sound generator. The visual alert may be provided by a light source, such as a light emitting diode. Theboard module141 may yet further be configured to provide guidance for alignment during surgery to surgical instruments, such as drills and saws. Thecommunications module143 may be configured to send/receive electronic signals to/from the controller assembly over a wired or wireless connection. In some embodiments, thecommunications module143 is configured to communicate with other surgical instruments such as drills and saws.
• Thecontroller assembly200 may be used to manually or remotely control the actuators within theinsert100. In some embodiments, thecontroller assembly200 physically or mechanically controls the actuators which may allow for manual manipulation of the movement of the actuators by a surgeon or medical technician. In other embodiments, thecontroller assembly200 electronically controls the actuators which can be monitored and programmed as a computing device with a processor and memory.
• Controller assembly200 may include acontroller240.Controller240 may include acontroller communication module259. Thecontroller communication module259 is configured to send/receive signals from theinsert100 and from thedisplay system300 over a wired and/or a wireless connection. In some embodiments, thecontroller communication module259 is configured to communicate with other surgical instruments, such as drills and saws. Thecontroller communication module259 may relay the guidance provided by theboard module141 to the surgical instruments.
• Controller assembly200 may be manipulated through one or more input devices, such as a mouse, a keyboard, capacitive buttons, or an interactive display. The interactive display may be part of thedisplay system300 and may display the controls for each actuator along with the relevant values and other measured parameters for easy comparison during joint balancing. Asingle controller240 may be configured to apply the same pressure to all of the actuators. This may simplify the design and ensure that an equal force/pressure is applied at each actuator.
• Display system300 may be a computing device with a processor and memory, such as a computer, tablet, smartphone, or other electronic device that may be used to display the GUI.Display system300 may include adisplay communication module310, adisplay module320, and adisplay330, such as a monitor.Display communication module310 is configured to send/receive wired or wireless communications to/from thecontroller assembly200.
• Display module320 may provide customized graphical user interfaces (GUIs) for viewing ondisplay330. The GUIs may display relevant data for real-time control and visualized feedback of adjustments through visual alignment guides that indicate when all of the measured parameters are within preferred ranges. The GUIs may also present the values for the parameters measured by the various sensors.
• Sensor data may also be collected and compared with expected or preferred data sets to provide adjustment recommendations and achieve better outcomes based on historical data. A GUI may provide visual or audio indications as to whether the joint is balanced by comparing the measured parameters with known accepted ranges of the values. In embodiments, the GUI may provide the force applied to thetop plate110 and thebottom plate150. The force may be determined using the height and pressure measurements provided by the sensors. The force may be determined by thedisplay system300, such as by thedisplay module320, or by another system/module.
• Joint balancing system may also include adata store90. Thedata store90 may be a separate system connected to either thedisplay system300 or thecontroller assembly200, or may be located within either thedisplay system300 or thecontroller assembly200. In embodiments, the data in thedata store90 may be uploaded to a central server for analysis.
• In one embodiment, a visual alignment guide may be presented which graphically illustrates the alignment of the two plates and the movement of the actuators within the joint in real-time. The visual alignment guide may provide guide lines or circular targets that will help the surgeon achieve a desired alignment. The alignment guide may also provide color-coded visual graphics to indicate whether an alignment is good (green) or bad (red).
• In some embodiments, the GUI displays one or more diagrams related to the positioning of theinsert100. The diagrams may display the relative displacement between the top and bottom plates in one or more of the sensor locations. The GUI may also display the tilt between the top and bottom plates. The GUI may include multiple graphs. One graph may display the history of the tilt in the mediolateral (side to side) direction. Another graph may display the tilt in the anteroposterior direction. The GUI may also display the knee flexion angle, pressure, force, and battery voltage. The GUI may also provide buttons to save the data or to generate a screen capture for future reference. This data and information may be archived in thedata store90. A third graph may display the history of the distance between the top and bottom plates. The GUI may also display previously recorded data against which the real time data can be compared.
• In some embodiments, the GUI displays three diagrams. One diagram displays the data collected while the knee is at 0 flexion, another diagram displays the data collected while the knee is at 90 degrees flexion, and the third diagram displays the data in real time.
• In some embodiments, the GUI can be used prior to surgery to set up a custom or patient-specific balance that is unique to the patent and/or theinsert100. The GUI can also contain a list of instructions as to where the problem is within the joint and can provide a recommendation to the surgeon on how to correct the problem. The GUI can also display information from other devices or instruments, such as computer navigation systems, surgical robots, instruments, such as drills and saws, tourniquet sensors, etc.
• FIG. 2 is an illustration of an embodiment of theinsert100 ofFIG. 1 disposed in a knee joint. In the embodiment illustrated, theinsert100 includes atop plate110 and abottom plate150 separated byactuators180 positioned at various points on the interior surfaces of thetop plate110 andbottom plate150. Thetop plate110 is disposed against afemur8, while thebottom plate150 is disposed against a tibia10. Theinsert100 is additionally configured with one or more sensors (shown inFIG. 3) disposed along thetop plate110 and/or thebottom plates150. The sensors are configured to measure and determine various parameters related to the balancing of the joint, as described herein.
• Theinsert100 may be designed as a temporary insert that is positioned into the joint only during a joint balancing procedure, such that it is replaced by a permanent insert of similar shape and size once the joint balancing is complete. In another embodiment, theinsert100 may be permanent, such that it will remain in position between the adjacent bones once the joint has been balanced.
• Theinsert100 may be a standalone device before insertion into the joint. Thetop plate110 andbottom plate150 may vary in shape and size and be aligned in parallel planes. The general shape of thetop plate110 and corresponding bottom plate150 (is designed to fit within the knee joint and provide a large surface area to interface with, such as by contact, the bony surfaces of theadjacent femur8 and tibia10. In the embodiment illustrated, insert100 includes four total actuators180 (three visible) disposed between thetop plate110 and thebottom plate150. Theactuators180 may be evenly spaced and positioned within different quadrants of theinsert100 to provide for actuation from different points within the insert that will allow for dynamic load balancing at each actuator and different angles of actuation of theinsert100. For example, if twoadjacent actuators180 are actuated, the insert may be disposed at an angle which slopes from one side of theinsert100 to the other. The number ofactuators180 may vary and may be as few as one. Theactuators180 may be placed in other configurations, such as triangular, circular, or irregular placements. The actuators may also be tilted or angled to generate shear or rotational forces (torque).
• A method of balancing a joint using theinsert100 in accordance with one embodiment of the invention will now be described. The balance of the joint may be measured at several stages of the surgical procedure. For example: measurements may be taken before making any bone cuts, or after making the tibial bone cut against the uncut femoral surface, or after making the femoral cut against the cut femoral surfaces or against a trial femoral prosthesis, or with trial femoral or tibial prostheses in place, or with the final femoral and tibial prostheses in place. During a first step, the insert is positioned in a gap or opening of a joint between two opposing bone structures, such as an opening between afemur8 and a tibia10 in a knee joint. In some embodiments, insertion/extraction tools are used to insert theinsert100 into the opening. Next, one or more of theactuators180 is activated to apply a load to the bone structures of thefemur8 and tibia10. The sensors measure one or more parameters relating to the joint, such as the movement, pressure, angle, position, range of motion, gap, load applied by each actuator, etc. The measurements may provide an indication as to whether the joint is balanced—i.e. whether pressure is being evenly applied to the insert by the opposing bone structures, whether the joint is able to move within a desired range of motion, the magnitude of the gap between the surfaces of thefemur8 and tibia10 and the change in gap when the knee is flexed or extended, whether the ligaments surrounding the joint are under too much tension, etc. The measurements may also indicate that the bone cuts are not optimum, for example, the tibia10 may have been cut in too much varus or valgus, thefemur8 may have been cut in too much varus or valgus, or in external or internal rotation, or the distal cut of the femur may have been made too deep resulting in a mismatch of the gap between the surfaces of the femur and tibia at different flexion angles. If the measurements and analysis of the measurements indicates that the joint is not properly balanced or the bone cuts are not appropriate, the surgeon will make one or more adjustments to some portion of the joint to improve the balance of the joint. The adjustments may include: re-cutting the bones, releasing or tightening ligaments, adjusting the placement or rotation of the prosthetics or theinsert100; cutting away portions of the bones, ligaments or cartilage; or increasing or decreasing the height of theinsert100 to better fit the gap in the joint. The joint may be tested again by actuating one or more of the actuators and measuring the parameters to determine if improvements have been made. This process may be repeated till the surgeon is satisfied with the measurements. In embodiments including a fluid powered actuator, measuring the distraction while changing the pressure of the fluid powered actuator may be used to characterize the biomechanical properties of the soft tissues and aid in selecting the optimal balance.
• At the point where the measurements fall within certain acceptable ranges, the joint is considered to be balanced. If theinsert100 is designed to function as a permanent prosthetic, it is left in place in the joint opening. If theinsert100 is configured only as a measurement and testing tool, it is removed and then replaced with a permanent prosthesis of identical dimensions. In some embodiments, the data collected by the sensor(s) are used to generate a custom implant on demand.
• Further details of the properties and function of theinsert100 will be described below with regard to the actuators, sensors, shape and configuration of the device, controllers and user interface and additional tools for joint balancing.
Sensors
• Sensors disposed on or within theinsert100 can be configured to measure and be used to determine numerous different parameters related to the balancing of the joint. For example, the sensors can be configured to measure and be used to determine the force, or load, being applied by the actuators and the resulting pressure received on various sections of the top or bottom plates by the adjacent bone. Examples of these sensors are load cells, strain gages, pressure sensors, etc. For spring actuators, the spring force may be calculated indirectly, for example using the known spring stiffness and the measured spring length using displacement sensors. Sensors can also be configured to monitor distance of movement, either total movement between the top and bottom plates or movement of each individual actuator. Examples of these sensors are magnetic sensors, optoelectric sensors, and monitoring the stroke of the actuator mechanism (e.g. screw driven actuators). Sensors may also measure angles of motion, and even angular positions through the use of accelerometers, magnetometer, and gyroscopes.
• Theinserts100 may incorporate a plurality of different sensors in order to measure different types of parameters or to measure the same types of parameters at different places on theinsert100. The sensors communicate via a wired or wireless connection, and may be powered by an external power source or an internal power source within each sensor or a power source located within theinsert100.
• FIG. 3 is a perspective view illustration of an embodiment of theinsert100 ofFIG. 1 withsensors102. Theactuators180 are not shown for clarity.Sensors102 may be used to determine the relationship between thetop plate110 and thebottom plate150, such as the spatial relationship, including the distance and angle between thetop plate110 andbottom plate150, and the pressure between thetop plate110 and thebottom plate150. In the embodiment illustrated,sensors102 are displacement sensors withcorresponding magnets104. Thesensors102 andmagnets104 may be located on opposite interior surfaces of thetop plate110 and thebottom plate150.Insert100 may include any number and configuration ofsensors102 andmagnets104. In the embodiment illustrated, theinsert100 has foursensors102 on an interior surface of thebottom plate150 and fourcorresponding magnets104 configured on an interior surface of thetop plate110 for holding the two plates together. The sensors118 measure displacement between thetop plate110 andbottom plate150 at multiple locations and calculate tilt in two directions. Thesensors102 may be Hall Effect sensors. Thesensors102 andmagnets104 may be aligned between thetop plate110 and thebottom plate150.
• In some embodiments, asingle sensor102 is positioned in a center area of theinsert100, such that thetop plate110 andbottom plate150 pivot around thesensor102 and thecorresponding magnet104. Thesingle sensor102 is therefore able to measure displacement between thetop plate110 and thebottom plate150, as well as rotational movement in three directions. In one embodiment, thesingle sensor102 is a three dimensional magnetometer.
• In some embodiments, thesensor102 is a pressure sensor. In these embodiments, thesensor102 may cover a substantial portion of a surface of thetop plate110 orbottom plate150 and may adjoin that surface. In these embodiments, the pressure sensors may be configured such that a pressure map can be determined and provided by the GUI including the relative position of femoral condyles during the balancing of a knee. In one embodiment, the sensor is positioned above a substantial portion of an interior surface of thebottom plate150. In another embodiment, thesensor102 is positioned on an exterior surface of thebottom plate150. In yet another embodiment, thesensor102 is positioned on an interior surface of thetop plate110. In a further embodiment, thesensor102 is positioned on the articular exterior surface of thetop plate110. Thesensor102 is capable of measuring pressure distribution over the entire surface area of the adjoining surface and may be configured to measure contact pressure between thefemur8 and tibia10.
• Additionally, one or more of thesensors102 may be angle measurement sensors (including accelerometers, magnetometers and gyroscopes) that are configured to measure the angle of the insert relative to the leg, thigh, or any other part of the body, as well as relative to the ground. This information can be used to determine whether there is an imbalance in the joint and to assess if the imbalance is due to ligament imbalance or improper bone cuts.
Pneumatic-Actuated Mechanisms
• In some embodiments, theinsert100 may be actuated by fluid power, such as by pneumatics or hydraulics. Fluids such as air, saline, or more viscous fluids, such as gels, may be used to as the actuating fluid.FIGS. 4-7 illustrate an embodiment of theinsert100, where theinsert100 is a pneumatic insert.FIG. 4 is an illustration of a perspective view of an embodiment of the insert ofFIG. 1 with apneumatic actuator180.
• In the embodiment illustrated,top plate110 includes aplate portion120 and anarticular portion130. Thearticular portion130 attaches to plateportion120 and is configured to interface with, such as by direct or indirect contact, the natural or artificial femur. Thetop plate110 orbottom plate150 may include one ormore grooves138. The grooves may be oval shaped to match the natural shape of the condyles of the adjacent bone. In the embodiment illustrated,grooves138 are located on the outer surface of thetop plate110 with agroove138 on each side of thetop plate110 which would receive corresponding condyles114 (seeFIG. 2) of thefemur8.
• Thegrooves138 may include anarticular contact surface139 that articulates with the articular surface of the natural or artificial femur. In the embodiment illustrated, thegrooves138 andarticular contact surface139 are located on an outer surface of thearticular portion130, located opposite both thetop portion120 and thebottom plate150. Thearticular portion130, including thegrooves138 and the articular contact surfaces139, can be shaped to accommodate any femoral articular size or shape.
• FIG. 5 is an illustration of an exploded view of theinsert100 ofFIG. 4. Theactuator180 is located between thetop plate110 and thebottom plate150. Thetop plate110 and thebottom plate150 may be combined to or may individually match the natural shape of the tibial bone or match the shape of an implant, such as a tibial tray. Apneumatic actuator180 may be formed of one or more bellows. The actuator may include multiple configurations of bellows, such asfirst bellows181 and second bellows182. In the embodiment illustrated, theactuator180 includes four layers of bellows with onefirst bellows181 and threesecond bellows182. In embodiments, thefirst bellows181 and the second bellows182 are stacked between thetop plate110 and thebottom plate150. Theactuator180 is connected and fluidly coupled to afluid supply line70. Thefluid supply line70 allows the fluid, such as air, to be added or removed from the one or more bellows to position thetop plate110 relative to thebottom plate150.
• Plate portion120 may include aplate body121, a board receiving feature124, aconnection feature128, and aconnection hole129.Plate body121 may include a platebody connection end122, a plate body insertion end123, a plate body first side124, and a plate body second side125. Platebody connection end122 may generally have a convex shape. The curvature of the convex shape may be similar to the curvature of the flatter portion of an ellipse. Plate body insertion end123 is opposite platebody connection end122. Plate body insertion end123 may include a concave portion and may generally have the shape of a portion of a Cassini oval that is between an oval and a lemniscate. Plate body first side124 and plate body second side125 may be symmetrical and may each have a circular shape. Platebody connection end122, plate body insertion end123, plate body first side124, and plate body second side125 may form the perimeter ofplate portion120.
• Board receiving feature126 may protrude fromplate body121 towardsarticular portion130 and away frombottom plate150.Board receiving feature126 may generally include a T-shape.Board receiving feature126 may also include a cavity for receivingelectronics board140.Board receiving feature126 may further include one or more electronics receiving features127. Theelectronics receiving features127 may be a protrusion or a recess configured to receiveelectronic hardware142 coupled toelectronics board140.
• Connection feature128 may extend fromplate portion120 at plate body connection end122 generally towardsbottom plate150.Connection feature128 may extend in the opposite direction relative to board receiving feature124.Connection hole129 may extend throughconnection feature128 to provide access toelectronics board140.
• Articular portion130 may include anarticular portion body131, a recess137, and a connection end bevel136 along with thegrooves138 and the articular surfaces138.Articular portion body131 may generally include the same shape about its perimeter asplate body121.Articular portion body131 may include an articular portion body connection end132, an articular portion body insertion end133, an articular portion body first side134, and an articular portion body second side135. Articular portion body connection end132 may generally have a convex shape. The curvature of the convex shape may be similar to the curvature of the flatter portion of an ellipse. Articular portion body insertion end133 is opposite articular portion body connection end132. Articular portion body insertion end133 may include a concave portion and may generally have the shape of a portion of a Cassini oval that is between an oval and a lemniscate. Articular portion body first side134 and articular portion body second side135 may be symmetrical and may each have a circular shape. Articular portion body connection end132, articular portion body insertion end133, articular portion body first side134, and articular portion body second side135 may form the perimeter ofarticular portion130.
• Recess137 may be located oppositegrooves138 andarticular surfaces139. Recess137 may include a T-shape and may be configured to receiveboard receiving feature126. Connection end bevel136 may be located at connection end132 and may be centered in connection end132 between togrooves138.
• Theinsert100 may includeattachment mechanisms112.Attachment mechanisms112 may be fasteners, such as detent posts. Thearticular portion130 may be attached to thetop portion120 using theattachment mechanisms112.Screws113 may extend through and up fromboard receiving feature126.Attachment mechanisms112 may be configured to couple toscrews113 to holdplate portion120 toarticular portion130.
• Thebottom plate150 may include abottom plate body151, one or more magnet recesses156, aconnector recess157, and restraining holes158. Thebottom plate body151 may generally include the same shape about its perimeter asplate portion body121 andarticular body portion131.
• Bottom plate body151 may include bottom plate body connection end152, a bottom plate body insertion end153, a bottom plate body first side134, and a bottom plate body second side155. Bottom plate body connection end152 may generally have a convex shape. The curvature of the convex shape may be similar to the curvature of the flatter portion of an ellipse. Bottom plate body insertion end153 is opposite bottom plate body connection end152. Bottom plate body insertion end153 may include a concave portion and may generally have the shape of a portion of a Cassini oval that is between an oval and a lemniscate. Bottom plate body first side154 and bottom plate body second side155 may be symmetrical and may each have a circular shape. Bottom plate body connection end152, bottom plate body insertion end153, bottom plate body first side154, and bottom plate body second side155 may form the perimeter ofplate portion120.
• Eachmagnet recess156 may extend intobottom plate body151 from an interior surface ofbottom plate body151 and may be configured to hold one ormore magnet104. In the embodiment illustrated, insert100 includes one magnet in eachmagnet recess156. Eachmagnet recess156 may beadjacent actuator180. The embodiment illustrated includes threemagnet recesses156 arranged in a triangular pattern. In other embodiments, different numbers ofmagnetic recesses156 andmagnets104 are used and arranged in different patterns. Eachmagnet recess156 and themagnet104 therein may be aligned with asensor102.
• Connector recess157 may extend intobottom plate body151 from bottom plate body connection end152. In the embodiment illustrated,connector recess157 is a cuboid shaped recess.Connector recess157 is configured so thatbottom plate150 does not interfere withconnector feature128 whenactuator180 is in its narrowest configuration, such as when thebellows182 are empty.
• Restraining holes158 may be used to securebottom plate150 totop plate110. Theinsert100 may include a restraining device115. The restraining device115 is configured to hold thetop plate110 and thebottom plate150 together. The restraining device115 is also configured to prevent thetop plate110 and thebottom plate150 from separating beyond a desired distance and is configured to allow theactuator180 to expand up to a predetermined amount. In the embodiment illustrated, the predetermined amount of expansion is 6 millimeters, which may allow theinsert100 to expand from eight millimeters to fourteen millimeters. In the embodiment illustrated, the restraining device115 is made of medical suture material. In other embodiments, the restraining device115 is integral to each chamber of thepneumatic actuator180. In other embodiments, the restraining device115 is a skirt around the perimeter extending between thetop plate110 and thebottom plate150. Some embodiments may be configured to expand beyond fourteen millimeters. Other embodiments are configured shims are added to thebottom plate150 to increase the distraction. In yet other embodiments, anarticular portion130 with an increased thickness is attached to thetop plate110 to further expand the height of theinsert100 beyond fourteen millimeters.
• In the embodiment illustrated, theinsert100 includes two restraining devices115, one on each side of theinsert100. The restraining device115 may contact the outer surface of thebottom plate150, pass through the restraining holes152 and be affixed to thetop plate110. In the embodiment illustrated, each restraining device115 is affixed to thetop portion120 with retaining fasteners124, such as screws.
• Theinsert100 may also include anelectronics board140. Theelectronics board140 may be housed within thetop plate110 or thebottom plate150. In the embodiment illustrated, theelectronics board140 is located withinboard receiving feature126 and isadjacent actuator180. Anelectronics connector60 may be electronically coupled to theelectronics board140 and may extend from theelectronics board140, throughconnector hole129, and to thecontroller assembly200. Theelectronics connector60 may be an electric wire with an outer casing.Electronic hardware142 may be coupled to and adjacent theelectronics board140. Theelectronic hardware142 may include sensors, sound sources, such as speakers and piezoelectric sound generators, and light sources, such as light emitting diodes.
• FIG. 6 is an illustration of a perspective view of thepneumatic actuator180 ofFIGS. 4 and 5.FIG. 7 is a top view of thefirst bellows181 ofFIGS. 5 and 6. Referring toFIGS. 6 and 7, each bellows is made of an inflatable material that includes one or morepneumatic compartments187 surrounded by acompartment boundary188. The bellows and thevarious compartments187 are manifolded together. In the embodiment illustrated, the bellows have manifolds betweencompartments187 of adjacent bellows as described herein. In other embodiments, a manifold can be used to plumb each bellows separately. In other embodiments, each bellows is plumbed to a separate fluid source and actuated separately. The pneumatic compartments are configured to inflate such that the pneumatic compartments expand and distribute the pneumatic force over different regions of thetop plate110 andbottom plate150. The shape, size, and number of layers of thebellows182 within theactuator180 may be selected based on the desired force at a given pressure. In embodiments, the nominal force is 20 lbf. In some embodiments, the force should not vary by more than 15%. In some embodiments, the force should not vary by more than 3 lbf.
• The shape of thebellows182 may also be configured to maximize the transmission of forces as well as the magnitude of distraction. Changing the shape of thebellows182 may change the surface area which may change the magnitude of the force (for the same pressure). Changing the shape of thebellows182 can also affect the location of the center of application of the force.
• In the embodiment illustrated, thefirst bellows181 and the second bellows182 have the same general dog bone shape. The first bellows181 has fourcompartments187 with eachcompartment187 in one quadrant of the first bellows181. Eachcompartment187 is a quarter of the dog bone shape. In thefirst bellows181 the fourcompartments187 are in direct fluid communication. Thecompartment boundary188 for each compartment is open to theother compartments187 along the neck of the dog bone shape. The first bellows181 may include afluid communication hole184 through the top of eachcompartment187, on the bottom of eachcompartment187, or through both.
• The first bellows181 also has afluid connection tab189 and afluid supply connector183. Thefluid connection tab189 may extend out from the neck of the dog bone shape and be in fluid communication with thefluid supply connector183. Thefluid supply connector183 is configured to fluidly connect thefirst bellows181 to thefluid supply line70.
• The second bellows182 has fourcompartments187 with eachcompartment187 in one quadrant of the second bellows182. Eachcompartment187 is a quarter of the dog bone shape. In the second bellows182 the fourcompartments187 are not in direct fluid communication. Thecompartment boundary188 for each compartment completely encloses the compartment off from the other compartments187. The second bellows182 may include afluid communication hole184 through the top of eachcompartment187, on the bottom of eachcompartment187, or through both.
• Theactuator180 may include multipleannular seals186 andmultiple seals185. In the embodiment illustrated,annular seals186 are adhesive rings and seals185 are adhesive disks. In other embodiment,annular seals186 and seals185 are formed by bonding the bellows to the adjacent structure, such as an adjacent bellows, atop plate110, or abottom plate150. In some embodiments, theannular seals186 and seals185 are formed using RF welding. Anannular seal186 may be located betweenadjacent compartments187 of adjacent bellows, such as thefirst bellows181 and a second bellows182 or twoadjacent bellows182. Theannular seal186 seals theadjacent compartments187 around the adjacent fluid communication holes184 so that theadjacent compartments187 are manifolded together in fluid communication. In embodiments, theannular seals186 and manifold formed by thereby can withstand a vacuum. Theseals185 are located at the outer surface of acompartment187 that is not adjacent to anothercompartment187. Theseals185 may be configured to seal afluid communication hole184 and may attach thefirst bellows181 or the second bellows182 to either thetop plate110 or thebottom plate150.
• FIG. 8 is an illustration of a perspective view of the electronics board ofFIGS. 4 and 5. Theelectronics board140 may include a board surface731 that faces thebottom plate150 with theactuator180 there between (as shown inFIGS. 5 and 6). One ormore sensors102 may be connected to theelectronics board140. The location and number ofsensors102 may correspond to the number and placement of the one ormore magnets104 located at the bottom plate150 (shown inFIG. 7B). Thesensors102 may detect the distance from themagnets104, which may allow the distance and the angle between thetop plate110 and thebottom plate150 to be determined.
Spring-Actuated Mechanisms
• In some embodiments, theinsert100 is configured with one or moremechanical actuators180, such as constant or variable force springs, which apply a load to the plates and the adjoining bone structures of the joint. The number and type ofactuators180 may vary depending on numerous factors, including the intended function of the device and the amount of control needed over the actuation process.
• FIG. 9 is an exploded view illustration of an embodiment of the insert ofFIG. 1 with a plurality of spring actuators. Referring toFIG. 9, theactuators180 are springs. Theactuators180 are not permanently attached with thetop plate110 andbottom plate150 and can therefore be easily removed in order to exchange them with different actuators that have a different stiffness. In addition, theunattached actuators180 also allow for the exchange of thetop plate110 and/orbottom plate150 with plates of different size, shape and thickness in order to best match the needed dimensions of the area where theinsert100 is being positioned. Theunattached actuators180 may then be secured within theinsert100 by providingtop actuator recesses111 intop plate110 and bottom actuator recesses161 inbottom plate150. Thetop plate110 andbottom plate150 may also be connected with each other by a flexible or elastic tether that holds the entire insert assembly together.
• Alternatively, theactuators180 may be attached (either permanently or removably) with thetop plate110 or bottom plate150 (or both) by one or more attachment mechanisms. In one example, the ends of theactuators180 may be bonded to thetop plate110 and thebottom plate150 with various glues such as cyanoacrylate or potted in plate with epoxy, polyurethane, etc. Theactuators180 could also be manufactured with customized ends which snap into a corresponding retaining mechanism on the respectivetop plate110 andbottom plate150 and lock the ends of theactuators180 into place. Theactuators180 could also be manufactured and formed within one or both of thetop plate110 andbottom plate150.
• The shape and dimensions of the spring-actuated mechanism may also vary considerably, but in the embodiments described and illustrated herein, theactuators180 are springs which are cylindrically-shaped with a diameter of approximately 4-8 millimeters (mm) and an expandable height of approximately 6-10 mm. Theactuators180 may be configured to apply a force in the range of 1-50 pounds per actuator, have a force accuracy of approximately 1 percent and a displacement accuracy of approximately 0.2 mm. When a plurality ofactuators180 are used, each actuator180 may be independently controlled and expanded or contracted in order to obtain an angled, or tiltedtop plate110 orbottom plate150, as has been previously described. The number ofactuators180 used may vary between one to four or more, and may depend on the size of theactuator180 and surface areas of thetop plate110 and thebottom plate150 on which they are disposed. Theactuators180 may have varying stroke lengths, shapes, dimensions and force capacities.
• In one embodiment,actuators180 are helical or coil springs that generate force when compressed. In another embodiment,actuators180 are conical or volute springs, in which the coils slide over each other, thus permitting greater travel for the same resting length of the spring. In yet another embodiment,actuators180 are cantilever springs that bend when compressed. The springs could be made of common materials such as metals (steel, titanium, aluminum), polymers, or rubbers. In the embodiment illustrated inFIG. 9, 4 coil springs are located between atop plate110 andbottom plate150. Thebottom plate150 may contain the force, displacement, and angle measurement sensors, a microprocessor powered by a battery, and a radio for wireless communication.
• Different configurations ofactuators180 provide advantages and disadvantages. The choice of a particular configuration ofactuators180 may therefore depend on the specific intended use and desired features for the actuation and measurement, which could vary from one surgeon to another. The use of a mechanical spring as an actuator would allow for the insert to be an entirely wireless device. Wireless sensors coupled with constant force springs provide an insert which would not require any physical connections, and as such could be easily removed and replaced during the balancing process. In addition, a spring-actuated device could be permanently implanted into the joint, whereas other inserts would need to be removed and then replaced with an identically-shaped permanent prosthesis. In a further embodiment, the actuators may be locked into a final position and then disconnected from the external controller and power source.
• FIG. 10 is an alternate exploded view illustration of theinsert100 ofFIG. 9 without the actuators. In the embodiment illustrated,bottom plate150 includes anelectronics recess162 extending from the outer surface of thebottom plate body151, opposite the bottom actuator recesses161. Theelectronics recess162 may house theelectronics board140 and other electronics, such as any sensors, microprocessors, power modules or radios which communicate the sensed data to. Theinsert100 may include a bottom plate cover163 that connects to thebottom plate body151 and covers theelectronics recess162.
Materials, Shapes and Configurations
• Theinsert100 may be made from any combination of biocompatible or medical-grade polymers or metal alloys, as known to one of skill in the art. The biocompatible material may be rated for limited contact. The materials would be required to meet structural and mechanical specifications needed to sustain the pressures, temperatures, fluids and frictions with other components of the insert and any adjoining bone surfaces, cartilage, ligaments and other tissues. The material of thetop plate110 and in particular of the articular contactingsurface139 should be a material that will not damage the articular surface of the femoral bone or component. Theinsert100 should also be made from materials which can be sterilized in order to minimize the risk of infection during surgery. The material requirements will also apply to the actuators and in some aspects to the sensors, particularly with regard to the sterilization and durability requirements. In embodiments, theinsert100 may include radiopaque markers or material for use in fluoroscopic x-ray verification.
• The size of theinsert100 may vary depending on the patient or the type of joint. The insert could conceivably be manufactured in several different sizes for different sized joints, such as a small, medium and large option. In one embodiment, a medium-sized insert would be approximately 70 millimeters (mm) by 45 mm and have an adjustable height of 8-14 mm. The height of the insert may need to be adjusted separately from the actuation mechanism in order to initially fit within the space of the joint between opposing bone structures. This may be accomplished using shims. In some embodiments, shims include a height from 1-6 mm and may be provided in 1 mm increments. In embodiments, thearticular portion130 may be switched out for one with a different height for the initial fit of theinsert100 within the space of the joint. Theactuator180 could then provide additional movement and spacing of at least a maximum height change. In one embodiment, the maximum height change of the insert is of 4-8 mm. In another embodiment, the maximum height change is 5-7 millimeters. In yet another embodiment, the maximum height change is at least 6 mm. The other dimensions of the device may also be adjustable in order to better fit a desired shape and size of the joint and the adjoining bones, ligaments or cartilage. Theinsert100 may also be configured to be stable in shear between thetop plate110 and thebottom plate150 throughout the range of motion of the knee. In some embodiments, the stiffness of the bellows under inflation may be configured to resist shear. In embodiments, the insert can resist a side load of 5 lbf. In some embodiments, the range of dynamic knee flexion angle measurement of theinsert100 may be from 10 degrees of hyperextension to 140 degrees of flexion.
• The shape of the insert may also vary depending on the intended use of the device. Theinsert100 may have a tricompartmental, bicompartmental, or a unicompartmental design. The embodiments illustrated inFIGS. 2 to 10 have a tricompartmental design.FIG. 11 is a perspective view illustration of an embodiment of the insert ofFIG. 1 with a unicompartmental configuration. Theinsert100 with a unicompartmental design may be essentially half of the tricompartmental design bisected down a longitudinal middle of the device. Theinsert100 with a unicompartmental design still includes atop plate110 and abottom plate150 separated by one or more actuators. Aninsert100 with a unicompartmental design may be advantageous for various types of surgical procedures, such as arthroplasty, in particular a partial knee replacement where only one half of the knee joint is replaced. A partial knee replacement arthroplasty preserves some of the ligaments in the knee, and theinsert100 can be placed on only one half of the joint to allow for balancing of the joint with actuation that similarly avoids the need to remove additional ligaments in the knee. The number of actuators in a partial knee replacement may vary according to user preference or the specifications of the joint balancing process when only part of the knee joint is being replaced.
• Multiple inserts100 with a unicompartmental design may also be utilized in a full knee replacement where the central cruciate ligaments are to be preserved by sliding eachinsert100 from lateral sides of the knee joint.
• Thetop plate110 and thebottom plate150 may be modular to allow for easy placement of different types of sensors and actuators. Although the illustrated embodiments of the plates are substantially flat, the plates may take different shapes to accommodate certain types of sensors, actuators and adjoining bone or other tissue. In one embodiment, the plates may have an elastic property to allow them to slightly deform when a load from an adjoining bone is applied (such as that of the femoral condyles). The elastic plates may be made from rubbers, polyurethane, silastic, gel-filled or air-filled containers.
• In some embodiments, the insert may be configured with a rotating bearing disposed in a central portion of the space between the top plate and the bottom plate. The bearing would provide for the top plate to rotate relative to the bottom plate, providing an additional adjustment that can be made to better balance the joint. The bearing may be configured to provide for approximately 5-10 degrees of rotation of the top plate with respect to the bottom plate (or vice versa depending on the configuration of the bearing) or translation from side-to-side and front-to-back.
• The insert may also be configured with only a single plate and a set of actuators which interface with an opposing bone surface, in one embodiment of the invention.
Controller
• FIG. 12 is an illustration of a perspective view of an embodiment of thecontroller assembly200 ofFIG. 1 connected to aninsert100. In the embodiment illustrated, theinsert100 is a pneumatic insert, such as theinsert100 ofFIGS. 4 and 5.Controller assembly200 may include acontroller240, acontroller mount230, and afluid supply device220. Thecontroller mount230 may be a strap or a similar mechanism for mounting thecontroller240 on to the patient's limb, such as the thigh. In embodiments, thecontroller mount230 has a width that is the length ofcontroller240. Thecontroller mount230 may be affixed to the patient's limb using a fastener, such as a hook and loop fastener. Theinsert100 may be connected to thecontroller240 by aninsert connection55. Theinsert connection55 may include thefluid supply line70 and theelectronics connector60 shown inFIGS. 4 to 7.
• Thefluid supply device220 may be an automated source of fluid power, or may be a manually operated source of fluid power, such as a pneumatic syringe as illustrated inFIG. 12. Thefluid supply device220 may be configured to supply fluid, such as a gas, to thecontroller240 and to theinsert100 to actuate the bellows182 (shown inFIGS. 4 to 6) of theinsert100. The gas may be air, such as room air, carbon dioxide, nitrogen, or helium. Thefluid supply device220 may be connected to thecontroller240 by acontroller supply line225. Thecontroller supply line225 may be a tube extending from thecontroller240 to thefluid supply device220. In some embodiments, apressure relief valve226 may be located at the end ofcontroller supply line225adjacent controller240. Thepressure relief valve226 may ensure that thepneumatic actuator180 is not filled above a predetermined maximum pressure, such as 30 psi.
• FIG. 13 is an illustration of a perspective view of thecontroller240 of thecontroller assembly200 ofFIG. 12. Thecontroller240 may include ahousing body241, ahousing side243, and ahousing cover242. Thehousing body241 may include the back and three sides of the housing ofcontroller240.Housing side243 may attach to an end ofhousing body241 forming the fourth side of the housing.Housing cover242 may fasten to thehousing body241 and thehousing side243 to form the enclosure of the housing. Abutton membrane244 may cover a number of buttons251 (shown inFIG. 15) that are accessible throughhousing cover242. Abattery cover249 may attach to an end ofhousing body241,opposite housing side243 and may provide access to a battery248 (shown inFIG. 14).
• FIG. 14 is an illustration of an exploded view of thecontroller240 ofFIG. 13.Housing body241 may be configured with anelectronics chamber253 and anaccumulator chamber252. Abattery248 andcontroller electronics245 may be housed withinelectronics chamber253. In embodiments, thebattery248 has enough power for thecontroller240 to operate for at least an hour.Controller electronics245 may include, inter alia, a controller electronics board250, buttons251, a transmitting radio, and sensors, such as an angle sensor254. Controller electronics board250 is in electronic communication withelectronics board140, such as wireless or wired communication. In embodiments, theelectronics connector60 electronically connects and is coupled to the controller electronics board250 and theelectronics board140. Buttons251 may be affixed to controller electronics board250. The angle sensor254 may provide the angle of the thigh which may indicate the angle of the knee flexion. The angle sensor254 may be an accelerometer, an inclinometer, or a similar device.
• Theaccumulation chamber252 may smooth out pressure fluctuations as the pneumatic actuator(s) of theinsert100 undergo compression and expansion.Housing side243 may form a seal withhousing body241 to prevent leaking fromaccumulation chamber252.
• Controller240 may also include apressure sensor247 for detecting the pressure of the actuating fluid withinaccumulation chamber252, and asensor mount246 configured to holdpressure sensor247 in place. Thesensor mount246 may be sized and shaped to be held withinhousing body241 byhousing side243. In embodiments thecontroller240 also includes a Light emitting diode (LED). The LED may show, inter alia, when thecontroller240 is activated.
• Controller240 may be fastened tocontroller mount230 with a mountingfastener260. In the embodiment illustrated, mounting fastener is a hook and loop fastener. In other embodiments, other types of fasteners may be used.
• In some embodiments, controller functions as a wireless remote and may be configured to transmit the data from theinsert100, including the various sensors and the data from thecontroller240, including thepressure sensor247, to the display system. In other embodiments,controller240 may also serve as a display device when a suitable display screen is included as part of thecontroller240. In further embodiments, thecontroller240 is directly wired to a display device.
• When using thejoint balancing system50, theinsert100 may be placed within the appropriate joint (such as the knee joint in this example). Thecontroller240 may be charged by the surgeon/operator usingfluid supply device220, such as a pneumatic syringe, to pump up the pressure. In embodiments, the pneumatic syringe is a 20 mL syringe. The pressure may be monitored by apressure sensor247. The pressure may be displayed by thedisplay module320 in the graphic user interface on a display screen. In some embodiments, the optimum pressure is between 20 and 30 psi. In some embodiments, the pressure may be modified to exert a defined force. The optimum force may be between 40 and 200 N.Joint balancing system50 may be configured to supply pressures at different ranges, depending on the application. With theinsert100 inflated (i.e. bellows expanded under pressure to actuate the insert100), the knee is flexed (bent) through the full range of available motion. As the knee is flexed, the sensors may measure knee flexion angle, the distance between the top and bottom plates of the insert, and the tilt between the top and bottom plates of the insert. This information may be graphically depicted by wired or wireless transmission to the display.
• The surgeon can make the appropriate changes to the placement of the artificial components, to the cuts made in the bone, or to the ligaments of the knee to generate a distraction gap and tilt that is most desirable for the patient.
• Thejoint balancing system50 may be used to balance the knee during a surgical procedure, such as a total knee arthroplasty or a partial knee arthroplasty. The controller mount1030 may be wrapped around a patient's thigh, such as the lower thigh and tightened firmly. The hook and loop fastener of thecontroller mount230 may be placed anteriorly on the thigh. Thecontroller240 may be aligned with the long axis of the patient's thigh, with thebattery cap249 and thepressure valve226 facing proximally and the insert connection is facing distally.
• Theinsert100 may be positioned in between the tibial and femoral surface. The bottom surface of thebottom plate150 may be flat and may be in direct or indirect contact with the tibial bone cut. The upper surface of thetop plate110 may be curved and may be in direct or indirect contact with the femoral surface. Theinsert100 should fit comfortably and may be centered on the tibial cut surface. The surgeon may verify that the curved upper surfaces articulate with the femoral condyles. If theinsert100 cannot be inserted easily, the surgeon may verify that the gap between the tibial cut surface and the femoral condyles is at least the height of theinsert100, such as 8 mm. If theinsert100 is too big or too small for the knee, the surgeon may select an insert of a different size.
• The actuator may then be pressurized by thefluid supply device220 to a predetermined pressure, such as from 20 psi to 25 psi, and thedisplay module320 may display the current pressure in the GUI. Theinsert100 may be expanded from a first predetermined height, such as 8 mm, where theinsert100 is not inflated up to a second predetermined height, such as 14 mm, where the pneumatic actuator is fully inflated. Shims may be used when the tibiofemoral gap is greater than the second predetermined height. In other embodiments, thearticular portion130 may be interchanged with a thickerarticular portion130 when the tibiofemoral gap is greater than the second predetermined height.
• Once theinsert100 is positioned in the tibiofemoral gap and inflated, thejoint balancing system50 may be calibrated by holding the knee in 0° flexion and selecting a calibration button displayed by the control module on the GUI.
• Thedisplay module320 may also display the net gap between the tibial and femoral surfaces in real time. To check gap in flexion and extension: hold the knee in 0° and read the gap off the display. Then flex the knee to 90° and read the gap off the display. This process can be repeated as many times as needed. If the surgeon desires to recut the bones or reposition the components, theinsert100 can be removed (after deflating the controller). If the surgeon desires to perform soft-tissue releases and there is sufficient access, he or she can perform the soft-tissue releases with the insert in place and monitor the changing gap in real-time on the display.
• Joint balancing system50 may also be used to measure the dynamic knee balance by flexing the knee gently between full extension and full flexion. Thedisplay module320 may display the net gap between the tibial and femoral surfaces in real time in the GUI as well as record the gap and show a plot of the tibiofemoral gap against knee flexion in the GUI.
• The balance of the knee can be changed and monitored in real time by releasing a ligament with theinsert100 in place and monitoring the changes in the tibiofemoral gap and tilt while the release is being performed. The balance of the knee can also be changed and monitored in real time by making suitable changes to the femoral or tibial cuts to realign the components.
• In some embodiments, thejoint balancing system50 may also include a correction module. The correction module may interpret the data received from theinsert100 and thecontroller240 and provide recommendations for a surgical procedure to correct any perceived imbalance. The correction module may receive other inputs including the bone geometry from an imaging modality, such as preoperative CT or MRI scans, the angle between adjacent bony structures, such as the angle between the femoral and tibial bone shafts, and ligament attachments, which may be based on digitizing landmarks using surgical navigation instruments.
• The correction module may calculate the forces across the articular surfaces of the insert210, such as by using rigid bodies to represent the bones and the insert210, and using springs to represent the ligaments. The correction module may refine the ligament attachments, lengths, and stiffnesses to match force displacement data collected or determined by the sensors in thejoint balancing system50. The correction module may also calculate corrections to bone cuts and to the ligaments based on the lengths, stiffnesses, current angle of bone cuts, and the angle of the tibiofemoral shaft.
• If the forces are balanced mediolaterally, but tight in flexion and in extension then the correction module may calculate an amount of bone to be cut from the proximal tibia based on the force-displacement data collected in extension and flexion. If forces are acceptable and balanced mediolaterally in flexion but tight in extension then the correction module may calculate an amount of bone to be cut from the distal femur based on the force versus displacement data collected in extension. The correction module may provide other recommendations, such as modifications to the ligaments based on the measured data.
Cutting Guides and Grinding Surface
• FIGS. 15 and 16 illustrate an embodiment of a cuttingguide assembly400 connected to theinsert100 that is used to guide cutting bone and tissue during balancing of the joint. Cuttingguide assembly400 may be mounted to theinsert100 to provide a surgeon with guides for cutting sections of bone, cartilage or ligaments during the joint balancing.
• In the embodiment illustrated, a cuttingguide assembly400 includes cutting guide mounts402, a cuttingguide406, and mountingfasteners408, such as screws or bolts. Cutting guide mounts402 may be attached to theinsert100 atbottom plate150 ortop plate110.
• The cuttingguide406 is attached to the cutting guide mounts402 using the mountingfasteners408. Cuttingguide406 includes one ormore guiding slots410. In the embodiment illustrated, cuttingguide406 includes twoparallel guiding slots410. The guidingslots410 can be used to align and make cuts to the bone, cartilage, ligaments or other tissues during the process of balancing the joint and positioning the artificial joint prostheses.
• The guidingslots410 have flat surfaces that hold and guide the blades of the cutting devices or saws while the surgeon is cutting the bones. The surgeon inserts the cutting saw into the slot of the cutting guide, which helps maintain the location and angle of the guide. In the embodiment described here, the cutting guides are mounted on the plates of the balancing insert such that the cuts are made with the ligaments appropriately tensioned.
• In some embodiment, a surface of the top plate or bottom plate may be configured as a grinding (or milling or planing) surface or abrasive surface so that it operates to grind against a corresponding bone structure and grind the bone surface into a smoother surface that will fit with the plate more readily.
• Those of skill will appreciate that the various illustrative logical blocks, modules, and algorithm steps described in connection with the embodiments disclosed herein can be implemented as electronic hardware, computer software, or combinations of both. To clearly illustrate this interchangeability of hardware and software, various illustrative components, blocks, modules, and steps have been described above generally in terms of their functionality. Whether such functionality is implemented as hardware or software depends upon the design constraints imposed on the overall system. Skilled persons can implement the described functionality in varying ways for each particular application, but such implementation decisions should not be interpreted as causing a departure from the scope of the invention. In addition, the grouping of functions within a module, block, or step is for ease of description. Specific functions or steps can be moved from one module or block without departing from the invention.
• The various illustrative logical blocks and modules described in connection with the embodiments disclosed herein can be implemented or performed with a general purpose processor, a digital signal processor (DSP), application specific integrated circuit (ASIC), a field programmable gate array (FPGA) or other programmable logic device, discrete gate or transistor logic, discrete hardware components, or any combination thereof designed to perform the functions described herein. A general-purpose processor can be a microprocessor, but in the alternative, the processor can be any processor, controller, microcontroller, or state machine. A processor can also be implemented as a combination of computing devices, for example, a combination of a DSP and a microprocessor, a plurality of microprocessors, one or more microprocessors in conjunction with a DSP core, or any other such configuration.
• The steps of a method or algorithm described in connection with the embodiments disclosed herein can be embodied directly in hardware, in a software module executed by a processor (e.g., of a computer), or in a combination of the two. A software module can reside in RAM memory, flash memory, ROM memory, EPROM memory, EEPROM memory, registers, hard disk, a removable disk, a CD-ROM, or any other form of storage medium. An exemplary storage medium can be coupled to the processor such that the processor can read information from, and write information to, the storage medium. In the alternative, the storage medium can be integral to the processor. The processor and the storage medium can reside in an ASIC.
• While various embodiments have been described above, it should be understood that they have been presented by way of example only, and not of limitation. The breadth and scope should not be limited by any of the above-described exemplary embodiments. Where this document refers to technologies that would be apparent or known to one of ordinary skill in the art, such technologies encompass those apparent or known to the skilled artisan now or at any time in the future. In addition, the described embodiments are not restricted to the illustrated example architectures or configurations, but the desired features can be implemented using a variety of alternative architectures and configurations. As will become apparent to one of ordinary skill in the art after reading this document, the illustrated embodiments and their various alternatives can be implemented without confinement to the illustrated example. One of ordinary skill in the art would also understand how alternative functional, logical or physical partitioning and configurations could be utilized to implement the desired features of the described embodiments. Hence, although the present disclosure, for convenience of explanation, depicts and describes an insert for balancing a knee joint, it will be appreciated that the insert in accordance with this disclosure can be implemented in various other configurations and can be used to balance various other types of joints, such as hip, shoulder, ankle, elbow, and spine joints.
• Furthermore, although items, elements or components may be described or claimed in the singular, the plural is contemplated to be within the scope thereof unless limitation to the singular is explicitly stated. The presence of broadening words and phrases such as “one or more,” “at least,” “but not limited to” or other like phrases in some instances shall not be read to mean that the narrower case is intended or required in instances where such broadening phrases may be absent.

Claims (2)

1.-24. (canceled)

25. An device, comprising:

a first plate configured to interface with a first bone structure of a joint;

a second plate configured to interface with a second bone structure of the joint, wherein the second bone structure is opposite the first bone structure;

at least one actuator disposed between the first plate and the second plate,

wherein the at least one actuator is configured to apply a distraction force to the first plate and the second plate so as to distract the first bone structure from one another, and

wherein the force is configured to balance the joint while the joint is moved through a range of motion including at least one of flexion or extension;

at least one sensor coupled to at least one of the first plate or the second plate, wherein the at least one sensor is configured to capture data indicative of one or more sensors configured to provide data indicative of at least one of a force or a location; and

a processor communicatively coupled to at least one sensor,

wherein the processor is configured (i) to receive the data from the at least one sensor, (ii) to determine data indicative of a balance of the joint, and (iii) to output the data indicative of the balance of the joint to a user.

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