A method for diagnosis of temporomandibular disorders (TMD) and related systems and apparatuses are disclosed. In the method, a visual evaluation of the patient in a standing position is first conducted. Condyle position in ear canals of the patient is palpated during jaw movement. A hip level of the patient is evaluated when back teeth of the patient are closed. If hips are unlevel, a first spacer is inserted between front teeth of the patient. The condyle position felt in the ear canals of the patient are re-palpated during jaw movements with the first spacer in place. The patient then raises and lowers his or her body by going up on their toes, and dropping to their heels. A reevaluation of the hip level of the patient is conducted and a positive or negative TMD diagnosis is indicated based on the reevaluation of the hip level of the patient.

Systems and methods are disclosed for measuring a femoral alignment of a femur of a patient via a surgically implanted measurement device. An exemplary method may include: receiving, via at least one processor, first data from the measurement device, wherein: a housing of the measurement device is coupled to a musculoskeletal system of a patient; and the first data includes a plurality of measurements from each of an accelerometer and a gyroscope included with an inertial measurement unit disposed within the housing; determining the femoral alignment based on the first data; and causing a display to output the determined femoral alignment.

A system is disclosed herein for providing a kinetic assessment and preparation of a prosthetic joint comprising one or more prosthetic components. The system comprises a prosthetic component including sensors and circuitry configured to measure load, position of load, and joint alignment. The system further includes a remote system for receiving, processing, and displaying quantitative measurements from the sensors. The kinetic assessment measures joint alignment under loading that will be similar to that of a final joint installation. The kinetic assessment can use trial or permanent prosthetic components. Furthermore, adjustments can be made to the applied load magnitude, position of load, and joint alignment by various means to fine-tune an installation. The kinetic assessment increases both performance and reliability of the installed joint by reducing error that is introduced by elements that load or modify the joint dynamics not taken into account by prior assessment methods.

Disclosed are methods and systems to provided planning tools for surgery, particularly for THA. Images of musculoskeletal structure of a patient (e.g. associated with respective planes and in a same or different functional position) may be displayed together and via co-registration and spatial transformations, 3D implants or other objects may be rendered and overlaid in a same position correctly with respect to each image. Measures may be represented with respect to various planes associated with the respective image and/or with respect to an existing implant. A safe zone (graphical element) may be rendered and overlaid with respect to each displayed image to indicate a clinically accepted safe range of positions for the 3D implant. Different instances of implants having respective characteristics affecting range of motion may be available for use during a procedure. For a set of available implants minimal and maximal safe zones may be presented for planning assistance.

Methods and apparatus for performing joint laxity measurement are disclosed. A retractor includes a plurality of spacers, such as plates, that are capable of being moved from a central portion of the retractor by a carriage mechanism. In some cases, the carriage mechanism may press against ramps connected to internal sides of the plates, thereby causing the plates to be displaced outwardly. In other cases, the carriage mechanism may include blades that rotate and press against the internal sides of the plates, thereby causing the plates to be displaced outwardly. The retractor is mounted on a surgical device configured to actuate the carriage mechanism. When the retractor is placed in a joint and the carriage mechanism is actuated, a measurement of the joint laxity may be determined based upon characteristics of the retractor and/or the surgical device.

The present disclosure includes systems and methods for deriving certain characteristics of the patient's body related to motion from captured motion data. The characteristics may be used to compare the characteristics of the supposed injury to the characteristics of a normally functioning body part as well as the functions of an injured body part. The present disclosure provides a reliable and reproducible way to determine whether a supposed injury is a feigned or exaggerated injury or an actual injury.

A method includes collecting reference motion data in a device from a motion sensor worn by a user for a movement having a predetermined classification. The motion sensor is attached to a limb having a joint. A user library entry is generated in the device based on the reference motion data and the predetermined classification. Additional motion data is collected in the device from the motion sensor. User motions in the additional motion data corresponding to the user library entry are classified in the device. Range of motion data associated with the user motions is generated in the device. A report is generated in the device including the user motions and the associated range of motion data.

Disclosed herein is a joint implant including a first implant coupled to a first bone of a joint, and a second implant coupled to a second bone of the joint and contacting the first implant. The second implant can include a plurality of sensors configured to measure data and a processor operatively coupled to the plurality of sensors and adapted to receive the data from the sensors. The first implant can be a femoral implant coupled to a femur. The second implant can be a patellar implant coupled to a patella. Sensor data from the patellar implant can indicate movement between the femoral implant and the patellar implant and identify patella condition such as a patellar rotation, patellar tilt and patellar tendonitis.

Systems and methods are described to determine joint center of rotation during a procedure. Joint center measurements may be useful to determine other clinically relevant measurements and/or to assist with replacement surgery.

A data processing method performed by a computer for judging implant orientation data representing an orientation of a first implant part relative to a first bone, the first implant part being part of an implant pair which further comprises a second implant part for a second bone, the implant pair being envisaged to be implanted in a patient, range of comprising the steps of: —acquiring the implant orientation motion volume data, —acquiring second implant orientation data representing the orientation of the second implant part relative to the second bone, —acquiring implant shape data representing the shapes of the first and second implant parts, —acquiring activity data representing at least one desired activity of the patient to be possible after implanting the implant, wherein Flexion extension each desired activity has an associated range of motion between the first bone and the second bone, —calculating a range of motion volume, which represents possible orientations between the first bone and the second bone over three rotational axes, from the implant orientation data, the second implant orientation data and the implant shape data, and—judging the implant orientation data to be feasible if the ranges of motion of all desired activities lie within the range of motion volume.