Abstract: The present disclosure relates to noninvasive methods, devices, and systems for measuring various blood constituents or analytes, such as glucose. In an embodiment, a light source comprises LEDs and super-luminescent LEDs. The light source emits light at at least wavelengths of about 1610 nm, about 1640 nm, and about 1665 nm. In an embodiment, the detector comprises a plurality of photodetectors arranged in a special geometry comprising one of a substantially linear substantially equal spaced geometry, a substantially linear substantially non-equal spaced geometry, and a substantially grid geometry.

Abstract: Systems and methods of in vivo hydroxyl radical protein foot-printing are presented. These teachings may be used to, for example, study three-dimensional protein structure or bio-kinetics. Radical Dosimetry including an optional intrinsic standard is used on isolated intact cells. Real-time feedback based on an internal standard provides comparability between different experiments and in vivo analysis results in data that is representative of actual biological conditions.

Abstract: A monitoring system includes a surgical implant configured for implantation in vivo and having at least one sensing fiber configured to measure a preselected physiological parameter, and a receiving unit in wireless communication with the at least one sensing fiber and configured to receive measurements of the preselected physiological parameter. A surgical system includes an end effector having a plurality of fasteners, and a surgical implant securable to tissue via the plurality of fasteners. The surgical implant includes at least one sensing fiber configured to measure a preselected physiological parameter.

Abstract: A physiological characteristic sensor system includes a physiological characteristic sensor. The physiological characteristic sensor includes a housing having a first housing portion coupled to a second housing portion, and an antenna coupled to the first housing portion. The physiological characteristic sensor system includes a sensor inserter configured to be coupled to the physiological characteristic sensor. The sensor inserter includes a sensor retainer, and the sensor retainer is configured to couple to the second housing portion in a second state to couple the physiological characteristic sensor to the sensor inserter.

Abstract: A method of calculating at least one physiological parameter using a reticulocyte production index (RPI) value can include: measuring a plurality of first glucose levels over a first time period; measuring a first glycated hemoglobin (HbA1c) level corresponding to an end of the first time period; measuring the RPI value; calculating a red blood cell elimination constant (kage) based on the RPI value; and calculating the at least one physiological parameter selected from the group consisting of: a red blood cell glycation rate constant (kgly), a red blood cell generation rate constant (kgen), and an apparent glycation constant (K), based on (1) the plurality of first glucose levels, (2) the first HbA1c level, and (3) the kage. Further, one or more related analyses (e.g., personalized-target glucose range, personalized-target average glucose, cHbA1c, and the like) can be estimated and/or adjusted based on the at least one physiological parameter.

Abstract: Systems, methods, apparatuses, and medical devices for harmonizing data from a plurality of non-invasive sensors are described. A physiological parameter can be determined by harmonizing data between two or more different types of non-invasive physiological sensors interrogating the same or proximate measurement sites. Data from one or more first non-invasive sensors can be utilized to identify one or more variables that are useful in one or more calculations associated with data from one or more second non-invasive sensors. Data from one or more first non-invasive sensors can be utilized to calibrate one or more second non-invasive sensors. Non-invasive sensors can include, but are not limited to, an optical coherence tomography (OCT) sensor, a bio-impedance sensor, a tissue dielectric constant sensor, a plethysmograph sensor, or a Raman spectrometer.

Abstract: Glucose measurement and glucose-impacting event prediction using a stack of machine learning models is described. A CGM platform includes stacked machine learning models, such that an output generated by one of the machine learning models can be provided as input to another one of the machine learning models. The multiple machine learning models include at least one model trained to generate a glucose measurement prediction and another model trained to generate an event prediction, for an upcoming time interval. Each of the stacked machine learning models is configured to generate its respective output when provided as input at least one of glucose measurements provided by a CGM system worn by the user or additional data describing user behavior or other aspects that impact a person's glucose in the future. Predictions may then be output, such as via communication and/or display of a notification about the corresponding prediction.

Abstract: Provided are methods and apparatus for receiving sensor data from an analyte sensor of a sensor monitoring system, processing the received sensor data with time corresponding calibration data, outputting the processed sensor data, detecting one or more adverse conditions associated with the sensor monitoring system, disabling the output of the sensor data during the adverse condition time period, determining that the one or more detected adverse conditions is no longer present in the sensor monitoring system, retrieving the sensor data during the adverse condition time period, processing the retrieved sensor data during the adverse condition time period, and outputting the processed retrieved sensor data.

Abstract: The invention relates to a functional wound dressing being able to detect and indicate the state of the wound, in particular with regard to an infection which is reported to be frequently associated with poorly healing wounds, such as chronic wounds. The present wound dressing can be used in moist wound healing and contains a substance being able to absorb wound exudate from the wound and to provide moisture to the wound.

Abstract: Embodiments of the present disclosure provide a hypersaturation index for measuring a patient's absorption of oxygen in the blood stream after a patient has reached 100% oxygen saturation. This hypersaturation index provides an indication of the partial pressure of oxygen of a patient. In an embodiment of the present invention, a hypersaturation index is calculated based on the absorption ratio of two different wavelengths of energy at a measuring site. In an embodiment of the invention, a maximum hypersaturation index threshold is determined such that an alarm is triggered when the hypersaturation index reaches or exceeds the threshold. In another embodiment, an alarm is triggered when the hypersaturation index reaches or falls below its starting point when it was first calculated.

Abstract: A blood separation device that allows high quality plasma to be generated using a single power source. The device includes a housing with an inlet port adapted to receive the blood sample, a first chamber having a first chamber flow channel in fluid communication with the inlet port, a second chamber having a second chamber flow channel, a separation member disposed between the first chamber and the second chamber. In some embodiments, the blood separation device detects or tests for the presence of a substance, such as an antigen or an antibody.

Abstract: Devices and processing systems are configured to enable physiological event prediction based on blepharometric data analysis. For example, some embodiments provide methods and associated technology that enable retrospective analysis of blepharometric data driving subsequent hardware/software configuration, thereby to provide for personalized and/or generalized biomarker identification.

Abstract: The present disclosure provides a cuboid magnetometer with high fluorescence collection efficiency, used for cardiac magnetic field measurement, and based on nitrogen-vacancy (NV) centers in diamond, and a cardiac magnetic field measurement system. The cardiac magnetic field measurement system includes a magnetic shielding chamber, a non-magnetic bed, an array probe for cardiac magnetic field measurement, a three-axis displacement platform, a high-speed data collection card, a fiber laser source, a microwave source, and a computer. The array probe for cardiac magnetic field measurement includes a non-magnetic shell, a stepping motor, a porous rotary fiber coupling apparatus, a fiber bundle set, a special photodetector (PD) set, a filter set, a ring-shaped antenna, and special diamond.

Abstract: Head-mountable apparatus for measuring magnetic brain response to auditory stimuli is disclosed. The apparatus comprises a first case adapted to be mounted on the head on the right auditory cortex, wherein the first case houses a first set of optically pumped magnetometers for measuring magnetic brain response to auditory stimuli. The apparatus also comprises a second case adapted to be mounted on the head on the left auditory cortex, wherein the second case houses a second set of optically pumped magnetometers for measuring magnetic brain response to auditory stimuli. Finally, the apparatus comprises at least one output interface for transmitting measurement data from the apparatus.

Abstract: A computing device may include (1) biosignal-acquiring circuitry that captures a biosignal from a user's body and (2) one or more composite bioelectrodes electrically coupled to the biosignal-acquiring circuitry. The one or more composite bioelectrodes may include (1) a circuitry-interfacing side with a mechanical or electrical property having a first predetermined configuration and (2) a user-interfacing side with the mechanical or electrical property having a second predetermined configuration. Various other composite bioelectrodes, systems, and methods are also disclosed.

Abstract: An example sensor apparatus includes two inductors with a first elastomer material between and at least one capacitor coupled to the two inductors. The at least one capacitor is configured, while in use, to at least partially wrap a circumference of an object and to exhibit a change in impedance in response to a pressure-manifestation change associated with the object, the change in impedance is to cause a change in the resonant frequency of the two inductors.

Abstract: A catheter has excellent in torque transmission properties to easily process a distal end portion of a catheter shaft to form a side hole, thereby protecting a lead wire that is inserted in a side hole. The catheter includes a shaft, ring-shaped electrodes that are mounted at an outer peripheral surface of a distal end portion of the shaft, and electrode lead wires. The shaft is made up of a braid that is embedded in a tube wall over an entire length of the shaft, side holes are formed in a tube wall of the distal end portion of the shaft, a distal end portion of each lead wire is joined to an inner peripheral surface of each electrode, the lead wires are inserted into the side holes and thus pass through meshes of the braid and enter a lumen of the shaft, and the side holes in which the lead wires are inserted are filled with a resin material.

Abstract: Devices, systems and techniques are provided to facilitate chronic monitoring of biological signals. An implant device can include a set of branch portions. Each branch portion can include multiple electrodes disposed on a bottom surface and can have vias that connect the electrode to a trace on the top of the branch portion. Each branch portion can include a hole through which a connector (e.g., suture) can be pulled. The connector can also be threaded through a hole in a curved arm of an implantation tool, To implant the implant device, the implantation tool can be inserted through an incision, moved to a target location and stabilized. An end of the connector can then be pulled, which can cause the implant device to move to the target location. The implant device can then be stabilized and the implantation tool explanted.

Abstract: Subdermal electroencephalogram (EEG) electrodes are coated to minimize pain and bleeding, and to improve electrical signal transmission.

Abstract: A method and apparatus for the quantitative determination of an individual's risk for sudden cardiac death (SCD) is described. Risk stratification is accomplished (and may have a sensitivity and specificity of greater than about 90%) by determining the presence in any individual being tested for SCD risk of sequences identified herein to correlate quantitatively with SCD risk. Both the number of such sequences present and their alignment scores (similarity) with the SCD risk sequence ensemble are used to calculate quantitative SCD risk.

Abstract: Disclosed relates to a method and an apparatus for analyzing an ECG signal, an electrophysiological signal recorder, a three-dimensional mapping system, and a computer device. The method includes: acquiring (S202) N first intracardiac electrical signals in a region of interest or at a reference point/in a reference region; generating (S204) a first comparison signal spectrogram according to the N first intracardiac waveforms; acquiring (S206) M second intracardiac electrical signals at the point of interest to acquire M second intracardiac waveforms; generating (S208) a second comparison signal spectrogram according to the M second intracardiac waveforms; performing (S210) a comparative analysis on the first comparison signal spectrogram and the second comparison signal spectrogram and generating a comparative analysis result; and outputting (S212) prompt information indicating whether the point of interest is a focal point according to the comparative analysis result.

Abstract: A heartbeat detection device includes a heartbeat time calculation unit configured to calculate a heartbeat time from a sampling data string of an electrocardiographic waveform, a heart rate calculation unit configured to calculate, for each heartbeat time, a heart rate from the heartbeat time calculated by the heartbeat time calculation unit, and a skip period calculation unit configured to calculate, based on the heart rate calculated by the heart rate calculation unit, a length of a skip period every time the heartbeat time is calculated. If a time difference between a latest time calculated from the sampling data string and an immediately preceding heartbeat time is not longer than the length of the skip period calculated from the immediately preceding heartbeat time, the heartbeat time calculation unit does not adopt, as a heartbeat time, the latest time calculated from the sampling data string.

Abstract: Systems, devices, and techniques are disclosed for automatically detecting arrhythmia locations. The systems, devices, and techniques include a plurality of body surface electrodes configured to sense electrocardiogram (ECG) data. The systems, devices, and techniques include a processor including a neural network configured to receive a plurality of historical ECG data and corresponding arrhythmia locations determined based on each of the plurality of historical ECG data, train a learning system based on the plurality of historical ECG data and corresponding arrhythmia locations, generate a model based on the learning system. New ECG data may be received from the plurality of body surface electrodes and the processor may provide a new arrhythmia location based on the new ECG data. Additionally, a new coherent mapping adjustment may be provided based on a model that is trained using historical coherent mapping adjustments.

Abstract: A brain wave monitoring system includes an electronic device and at least one electroencephalograph connected to the electronic device, each electroencephalograph includes 8 channels respectively connected to a corresponding electrode for receiving a brain wave signal. The electronic device scans a number of the at least one electroencephalograph and sequentially displays multiple channels of the at least one electroencephalograph according to an identifier of each of the at least one electroencephalograph. The brain wave monitoring system can automatically detect the number of electroencephalographs connected to the electronic device, and display the brain wave signals of all channels of all electroencephalographs according to the number of electroencephalographs and 8 channels of each electroencephalograph. The brain wave monitoring system can also prompt a guide message according to a channel impedance value and a signal quality index to assist a user improving a quality of the brain wave.

Abstract: A neural analysis and treatment system includes a computing device with a memory for storing an application that is executable on a processor to receive amplitude-integrated electroencephalography (aEEG) and range-EEG (rEEG) measurements associated with a patient. The systems determine a spectral edge frequency (SEF) measurement from the received EEG measurements, and determine one or more neural characteristics of the patient according to the determined SEF, aEEG, and rEEG measurements. These neural characteristics may then be used to identify and implement an appropriate therapeutic treatment.

Abstract: A system for assessing stroke conditions includes a wearable stimulator and a sensor device configured to obtain physiological data from a patient. The sensor device can include electrodes configured to detect electrical signals corresponding to brain activity. A computing device communicatively coupled to the wearable stimulator and the sensor device is configured to receive the physiological data and analyze the physiological data to provide a patient stroke assessment.

Abstract: A method for monitoring a subject, includes: capturing high-bandwidth data pertaining to the subject; cyclically storing a recent portion of the high-bandwidth data in a first memory; monitoring one or more physiological signals of the subject; analyzing the monitored physiological signals to allow detection of one or more target events; upon detection of a target event: copying a then recent portion of the high-bandwidth data from the first memory to a second memory; and storing high-bandwidth captured in a predetermined period subsequent to the detection in the second memory. The one or more physiological signals include EEG. The one or more target events include epileptic seizures. A computer program product and a system may use the method.

Abstract: An oral tool is provided that includes a body and a measurement unit. The measurement unit is disposed in a movable configuration with respect to the body, and includes a sensor unit at an end opposite to an end where the body is disposed. The sensor unit is constructed to be inserted into a mouth. The end of the measurement unit opposite to the end where the sensor unit is disposed is disposed inside the body. The oral tool includes a stress reliever disposed between the measurement unit and the body at a portion where the measurement unit changes a distance from the body while moving.

Abstract: Wearable fetal health monitoring device for determining a heath condition of a fetus based on biosignals of an expecting mother and the fetus is provided. The device includes a MEMS accelerometer that converts an acoustic wave sensed in an abdominal region into an abdominal acoustic signal. The device also includes a pulse oximeter generates a maternal photoplethysmogram (mPPG) value from a pulse sensed in the abdominal region. The device further includes a microcontroller configured to: generate a maternal phonocardiogram (mPCG) value from the abdominal acoustic signal; calculate a first maternal heart rate (mHR) value from the mPCG value; calculate a second mHR value from the mPPG value; compare the first mHR value with the second mHR value to identify a noise correction value; and apply the identified noise correction value to the mPCG value to extract a fetal phonocardiogram (fPCG) value.

Abstract: A Skin Tanning Measuring Device is provided to determine tanning level and skin penetration to various wavelengths, comprising of a device capable to inject light into the skin and monitor the light level emerging out from the skin tissue at a different location. By measuring the amount of emerging light, an individual tanning level could be deducted based on at least one additional measurement performed at an untanned location. The measurements will be used to compare between those levels and the saturated tanning levels, and will issue out a warning when the tanning is too high and additional exposure may be hazardous. Moreover, the offered system will measure skin penetration to UV hazardous radiation with and without sunscreen protection. The device will also provide information regarding melanin absorption as a function of UV exposure, and monitor those values over time and issue out a warning to users.

Abstract: Provided is a non-invasive system and method for determining a fuel value for a target muscle and potentially at least one indicator muscle. The method includes receiving an ultrasound scan of a target muscle; evaluating at least a portion of the ultrasound scan to determine fuel value within the target muscle; recording the determined fuel value for the muscle as an element of a data set for the muscle; evaluating the fuel data set to determine a value range; and in response to the range being at least above a pre-determined threshold, establishing a target score for the muscle as based on an upper portion of the value range. The method may be repeated to identify ranges for a plurality of muscles, the muscle with the greatest range being identified as an indicator muscle. Based on these findings the muscles estimated fuel level, fuel rating and energy status may be determined. An associated system is also disclosed.

Abstract: Disclosed herein is a joint evaluation device and corresponding systems and methods for evaluating ligaments and other soft tissue connections between, for example, a tibia and a femur at a knee joint. The joint evaluation device being arranged and configured to induce and measure forces while positions of the tibia and femur are monitored. Some embodiments use a computer assisted surgery device to track positions of the tibia and the femur, and may include a computing device configured to evaluate the forces measured between a first engagement portion and a second engagement portion of the joint evaluation device to output information related to the status of the ligament and other soft tissue connections prior to any bone resections being made to the tibia or the femur.

Abstract: A fluid replacement method including: determining the amount of urine expelled by a patient; infusing via a pump fluid from a first fluid source into a patient; determining an amount of fluid infused into the patient from the first fluid source; adjusting the operating of the pump based on the determined amount of urine expelled and the amount of fluid infused into the patient; setting a desired fluid balance for the patient; setting an amount of at least one additional fluid delivered to the patient, wherein the at least one additional fluid is not pumped into the patient; calculating an actual fluid balance based on the determined urine output, the determined amount of fluid infused into the patient from the first fluid source, and the set amount of said at least one additional fluid delivered to the patient; and automatically controlling the pump based on the actual fluid balance and the set desired fluid balance so the actual fluid balance conforms to the desired fluid balance.

Abstract: In an example, a method of detecting cyanide exposure of an individual comprises measuring a thiocyanate level of the individual, and comparing the measured thiocyanate level to a preset thiocyanate threshold to determine whether the measured thiocyanate level is above the preset thiocyanate threshold indicating a level of acute cyanide poisoning for which medical treatment is recommended to treat health effects of the exposure.

Abstract: A method of analysing a target bodily tissue of a subject. The method involves manipulating image data from the target bodily tissue and a background bodily tissue after dosing the subject with a contrast agent. The relative intensities of the light emitted from selected areas of the target bodily tissue and background bodily tissue at different time points after dosing are compared to determine whether 1) the intensity of light emitted from the target bodily tissue is lower than the intensity of light emitted from the background bodily tissue during the first part of the time period; and/or 2) the intensity of light emitted from the target bodily tissue is higher than the intensity of light emitted from the background bodily tissue during the second part of the time period; to assist in the determination of whether the target bodily tissue is benign or malignant.

Abstract: A liner associated with an adhesive skin patch of a physiological characteristic sensor deployed with a sensor inserter having a housing with a removable cover includes a surface to couple to the adhesive skin patch. The liner includes a removal portion to couple the liner to the removable cover of the sensor inserter such that a separation of the removable cover from the housing removes the liner from the adhesive skin patch.

Abstract: A venous catheter assembly includes a hub with opposing suture wings, an extension leg coupled to the hub, and an elongate catheter tube designed for insertion into a blood vessel of a patient. The elongate catheter tube is coupled to the hub and includes at least one fluid-carrying lumen within the outer wall extending between a proximal end and a distal end of the elongate catheter tube. The fluid-carrying lumen is in fluid communication with the extension leg and an opening in the outer wall at the distal end of the elongate catheter tube. The elongate catheter tube also includes at least one terminating lumen within the outer wall extending to a closed termination point.

Abstract: In one embodiment, a catheter manufacturing method includes forming flexible circuit strips with respective different symbols marked thereon, each strip including at least one respective electrode, attaching one end of each of the flexible circuit strips to a catheter coupler with the flexible circuit strips being ordered around a circumference of the catheter coupler responsively to the respective symbols of respective ones of the flexible circuit strips, and forming a distal end assembly of a catheter, the distal end assembly comprising the flexible circuit strips attached to the catheter coupler.

Abstract: An intravascular device for placement within an animal vessel, the intravascular device being adapted to at least one of sense and stimulate activity of neural tissue located outside the vessel proximate the intravascular device.

Abstract: A liner associated with an adhesive skin patch of a physiological characteristic sensor includes a first end opposite a second end. The liner includes a first side opposite a second side. The liner includes a surface to couple to the adhesive skin patch, at least a portion of which extends from the first end to the second end. The liner includes at least one graspable member defined between the first side and the second side that extends beyond the first end or the second end to initiate a peel of the liner from the adhesive patch at a center of the liner.

Abstract: A system and method include a memory storing processor executable code for a denoised autoencoder, and one or more processors coupled to the memory to execute the processor executable code to receive raw signal data comprising signal noise, encode, by the denoised autoencoder, the raw signal data by performing a denoising autoencoder operation to produce a latent representation, and decode, by the denoised autoencoder, the latent representation to produce clean signal data reconstructed without the signal noise. A first filter is applied to a signal to emphasize activity within the signal and to produce a first modified signal, a rectifier and a second filter are applied to the first modified signal to smooth areas of the first modified signal with clinical importance and to produce a second modified signal, and high frequency energy zones of the second modified signal are automatically detected using an energy threshold to produce a weights vector.

Abstract: A method of filtering a signal in a continuous analyte monitoring (CAM) system includes applying time-varying filtering to the signal using a time-varying filter to generate a filtered continuous analyte monitoring signal during an analyte monitoring period. Other methods, apparatus, continuous analyte monitoring devices, and continuous glucose monitoring devices are also disclosed.

Abstract: A method of filtering a signal in a continuous analyte monitoring system (CAM) includes applying adaptive filtering to the signal using an adaptive filter to generate a filtered continuous analyte monitoring signal during an analyte monitoring period, and increasing the adaptive filtering applied to the signal as a function of increasing noise on the signal. Other methods, apparatus, continuous analyte monitoring devices, and continuous glucose monitoring devices are also disclosed.

Abstract: Systems and methods to determine a risk factor related to dehydration and thermal stress of a subject are disclosed. Exemplary implementations may: generate output signals, by one or more sensors worn on a body of a subject, conveying information related to one or more of location of the subject, motion of the subject, temperature of the subject, cardiovascular parameters of the subject; store information related to the subject; obtain the output signals; determine in an ongoing manner, from the output signals, values of a water loss metric that correlates with estimated percentage of bodyweight of the subject lost in water; obtain heat index information for a contextual environment surrounding the subject; determine in an ongoing manner, from the output signals, values of an exertion metric that correlates with exertion of the subject due to work; and determine in an ongoing manner values for an aggregated risk factor of the subject.

Abstract: Improved graphical user and digital interfaces for analyte monitoring systems are provided. For example, disclosed herein are various embodiments of GUIs including Time-in-Ranges, Analyte Level/Trend Alert, and sensor usage interfaces. In addition, various embodiments of digital interfaces are described, including methods for data backfilling, expired or failed sensor transmissions, merging data from multiple devices in an analyte monitoring system, transitioning a previously activated analyte sensor to a new reader device, and autonomous sensor system alarms, among other embodiments.

Abstract: A blood pressure estimating apparatus includes a sensor configured to obtain a bio-signal of an object; and a processor configured to extract a first cardiovascular feature and a second cardiovascular feature based on the bio-signal, and estimate blood pressure based on a first changing tendency of the first cardiovascular feature from a first reference level and a second changing tendency of the second cardiovascular feature from a second reference level, the first changing tendency and the second changing tendency being independent from each other.

Abstract: The disclosure relates to techniques for triggering magnetic resonance data acquisition. The techniques include detecting a respiration direction of a respiration signal of an acquisition subject, predicting in real time an amplitude peak value of an expiration signal in the current respiration period according to the real-time respiration signal of the acquisition subject, multiplying the amplitude peak value by a preset coefficient, and using the product as a trigger point threshold of the current respiration period. When it is determined that an expiration stage of the current respiration period is starting, the techniques also include calculating in real time or periodically the absolute value of the difference between the amplitude of the current expiration signal and the trigger point threshold currently calculated, and if the absolute value of the difference is less than a preset difference threshold, then triggering MR data acquisition.

Abstract: Methods and apparatus including determining a rate of occurrence of a glycemic excursion event, determining a frequency of an alarm activation associated with the glycemic excursion event, determining an analyte level associated with the alarm activation, and setting an alarm parameter based on one or more of the determined rate of occurrence of the glycemic excursion event, the frequency of the alarm activation associated with the glycemic excursion event or the determined analyte level are provided.

Abstract: A weightbearing simulation assembly includes a substrate comprising a mounting surface extending in a first direction a subject support disposed on a first region of the mounting surface and a pedal assembly disposed on a second region of the mounting surface. The pedal assembly includes a spring assembly including a contact plate facing the subject support, a compression plate, and a first spring disposed between the contact plate and the compression plate. A subject applies a compressive force to the contact plate in a compression direction to simulate a load-bearing condition by compressing the first spring. An orientation of the pedal assembly may be adjusted to change a relative angle between the compression direction and the first direction to alter an imaging angle.

Abstract: An example scanner positioning control system includes: a display; a processor; and a computer readable storage medium comprising computer readable instructions which, when executed, cause the processor to: output, via the display, a first visual representation of an arrangement of a radiation source, a radiation detector, and a workpiece positioner; identify a change to be made to the arrangement of at least one of the radiation source, the radiation detector, or the workpiece positioner; output, via the display, a second visual representation of the arrangement of the radiation source, the radiation detector, and the workpiece positioner based on the change to be made to the arrangement; and control a scanner positioning system to physically move the at least one of the radiation source, the radiation detector, and the workpiece positioner based on the change.