Abstract: Methods and systems are provided for obtaining cleaned sequences showing trajectories of movement of a center of gravity and for estimating a biometric information pattern or value of a target. One of the methods includes removing noises from initial sequences showing trajectories of movement of a center of gravity to obtain the cleaned sequences. Another one of the methods includes reading cleaned sequences of the target into a memory, extracting features from the cleaned sequences, and estimating a biometric information pattern or value of the target from the extracted features, using a classification or regression model of biometric information patterns or values. The biometric information pattern may be a pattern derived from respiratory or circulatory organs of a target.

Abstract: An infant sleep device may include a platform for supporting an infant, a base upon which the platform is supported, and one or more weight sensors positioned to measure weight of an infant positioned on the platform.

Abstract: A method for aesthetic soft tissue treatment includes placing at least one applicator in contact with the patient's body. The applicator has at least one electrode. Electrotherapy and radio frequency therapy are provided to the soft tissue, optionally with overlay or sequentially. A handheld applicator may be used, with the applicator moving during the therapy, which may provide muscle stimulation in the patient, or provide an analgesic effect during the treatment. A spacing object may be positioned between the skin of the patient and the applicator.

Abstract: Systems, methods and apparatus are disclosed for properly using and locating object retention wands via the use of at least one sensor located on or in the wand body for determining when the wand is capable of properly scanning a target area. In one form, a proximity sensor is used. In another form a motion sensor is used. In still other forms, both a proximity sensor and motion sensor are used. In some forms, the wand system further includes an indicator for indicating whether the wand is within proper read range, speed and/or orientation of a target area so as to confirm proper use of the wand to locate retained objects before concluding a procedure. In other forms one or more of a user interface, scanner and network interface may also be used with the system. Further systems, methods and apparatus are also disclosed herein.

Abstract: A configurable electrosurgical generator front panel. The configurable electrosurgical generator front panel has a front panel frame, a display screen or tablet computing device, and a plurality of connectors for connecting accessories to the front panel frame. The front panel in the front panel assembly provides a novel structure for inserting a screen or tablet device into the front panel frame and securing it in place.

Abstract: Systems, methods, and devices for automatic generation of a stimulation therapy that mimics electrographic activity in the brain at natural seizure termination define a stimulation therapy to be generated by an implanted component of a medical device system and delivered to a subject through identifying data characterizing a patient's seizures, especially at termination. A machine learning model identifies the seizures or seizure types from which to establish a canonical seizure or seizure type, and an algorithm translates the canonical seizure or seizure type into data that can be used to characterize a stimulation therapy. The systems, methods, and devices, include those configured to deliver the stimulation therapy that emulates the canonical seizure or seizure type when the seizure is detected, with the aim of terminating the seizure sooner than it would terminate without intervention.

Abstract: In one embodiment, a method of implanting a stimulation lead to stimulate a dorsal root ganglion (DRG) of a patient, comprises: placing a distal portion of the stimulation lead within an implant tool; accessing the epidural space of the patient with the distal end of the implant tool; contacting a surface of a pedicle of the patient with a distal tip of the Implant tool above a foramen leading to a target DRG; after contacting the surface of the pedicle with the distal tip, advancing the stimulation lead from a side port of the implant tool, wherein the side port is located proximal to the distal tip of the implant tool; advancing the stimulation lead through the foramen to position one or more electrodes of the stimulation lead adjacent to the target DRG; and providing electrical stimulation to the target DRG to stimulate the target DRG using one or more electrodes of the stimulation lead.

Abstract: A rapid chest pain risk assessment system includes an assessor, a computed tomography (CT) scanner, an electrocardiogram device for providing electrocardiogram related data, and an enzyme analyzer for analyzing the patient's blood. A computer enabled risk calculator categorizes the patients into low, intermediate, and high risk categories. The computer enabled risk calculator, using data from electrocardiogram, blood analyzer and patient's age, other risk factors and history, automatically generates orders for patients in low and intermediate risk categories to undergo a CT scan. A CAC analyzer using the computer file for analyzing the CT scan results then provides a CAC score based on those CT scan results. A risk score based on electrocardiogram, blood analyzer and patient's age, other risk factors and history of symptoms plus the CAC score is generated.

Abstract: Devices and systems for treating based on light therapy are disclosed. One example device includes an eyewear configured for placement in front of an eye to allow light to reach the eye, and one or more filters having transmission spectra within a range that approximately spans 450 to 570 nm associated with blue or green light. The one or more filters is configured to block light spectra outside of said range and to allow the blue or green light to reach the eye for administering light therapy to a subject exhibiting pain.

Abstract: Methods, systems, devices, assemblies and apparatuses for treatment of hypertension in a patient using renal denervation. The therapeutic assembly includes an energy delivery element. The energy delivery element is configured to provide renal denervation energy to a nerve within a blood vessel of a patient. The therapeutic assembly includes a controller. The controller is coupled to the energy delivery element. The controller is configured to determine that the hypertension in the patient is orthostatic. The controller is configured to apply renal denervation energy to the patient using the energy delivery element.

Abstract: A system, apparatus, and method for physiological data collection, providing targeted content, and facilitating remote diagnostics. In one embodiment, a kiosk contains physiological data collection devices, electronic computing devices, and targeted-content display devices to automatically collect physiological data regarding a patient and display targeted content specifically tailored to that patient based on the collected data.

Abstract: Various implementations include a device for locating a position in a body. The device includes a first body portion. The first body portion has a first longitudinal axis. The device includes a second body portion. The second body portion is slidably coupled to the first body portion. The second body portion has a second longitudinal axis. The device includes a first set of markers disposed on the first body portion for measuring along the first longitudinal axis. The first set of markers includes at least two radiopaque markers. The device also includes a second set of markers disposed on the second body portion for measuring along the second longitudinal axis. The second set of markers includes at least two radiopaque markers. The first body portion is slidable along the second longitudinal axis. The second body portion is slidable along the first longitudinal axis.

Abstract: There is provided a nerve activity monitoring method that includes receiving an input signal indicative of activity in a nerve of a subject; receiving physiological data indicative of physiological activity in the subject; establishing a relationship between the physiological data and the input signal; identifying a plurality of periodic portions in the input signal based on the relationship between the physiological data and the input signal; and outputting the periodic portions identified.

Abstract: Systems and methods are described for functional brain mapping using neuronavigational equipment and additional features. For example, some implementations described combine novel cortical stimulator tools with stereotactic navigation for three-dimensional position tracking of the cortical stimulator tools. In some implementations, the systems and methods described herein can be used on an awake patient. In some implementations, the systems and methods described herein can be used on a patient that is asleep, via motor evoked potentials (MEPs), phase reversal, or electromyography (EMG) monitoring. Accordingly, in some cases sensory and language regions of the brain can be identified in addition to motor regions.

Abstract: The present disclosure relates generally to systems, methods, and devices for interpreting neural signals to determine a desired movement of a target, transmitting electrical signals to the target, and dynamically monitoring subsequent neural signals or movement of the target to change the signal being delivered if necessary, so that the desired movement is achieved. In particular, the neural signals are decoded using a feature extractor, decoder(s) and a body state observer to determine the electrical signals that should be sent.

Abstract: Methods for detecting tubing in a pump assembly of a pump system are provided. For example, a method comprises connecting a power supply to each of a plurality of pump motors of the pump system. Each pump motor of the plurality of pump motors has a power supply cable configured to connect to the power supply and drives a pump head of a plurality of pump heads of the pump system. The method also comprises sensing a motor current from each of the power supply cables, determining whether tubing is loaded in each pump head, and, if tubing is not loaded in a pump head, then disconnecting from the power supply the power supply cable of the pump motor associated with the pump head in which tubing is not loaded. Systems for detecting the presence of tubing within a pump head of a plurality of pump heads also are provided.

Abstract: A smart tourniquet for self-administering a medication is provided. When a patient needs to inject themselves with a medication, intravenously, called an “infusion,” the patient wears the smart tourniquet around their arm and tightens the device. While the patient is using the smart tourniquet, the device automatically records the date and time of the infusion, called a “timestamp”. The patient can also use the device to record the dosage or “number of units” taken at the time of the infusion. The smart tourniquet can store the timestamp as well as other related information as a record. At a later time, the patient can recall prior records on the smart tourniquet itself. The smart tourniquet can also be synchronized with an application and the records can be downloaded for review by the patient, nurse or doctor to render accurate and timely care.

Abstract: A method, apparatus and computer program, the method comprising: receiving a first biopotential signal obtained by a first capacitive sensor; receiving a second biopotential signal obtained by a second capacitive sensor, the first capacitive sensor and the second capacitive sensor being positioned at different locations on a subject; synchronising biopotential signals obtained by the first capacitive sensor and the second capacitive sensor by applying a time adjustment to biopotential signals obtained by at least one of the first capacitive sensor or the second capacitive sensor; wherein features in at least one of the first biopotential signal and the second biopotential signal are used to synchronise the biopotential signals obtained by the first capacitive sensor and the second capacitive sensor.

Abstract: A heart treatment system is disclosed capable of diagnosing one or more critical regions of interest for a biological rhythm disorder by sensing signals from biological tissue. If a critical region is not present at the current location of sensed signals, the system is capable of indicating a guidance direction in which to navigate to reach one or more critical regions. Ablation energy is delivered to treat said region of interest. Signals are again sensed and analyzed to assess the impact of treatment. This process is repeated until all critical regions of interest are treated. In some embodiments, all functionality is provided by a single sensing and treating catheter with display device and analytical software.

Abstract: Disclosed systems include an electrocardiogram sensor configured to sense electrocardiograms of a subject and a processing device operatively coupled to the electrocardiogram sensor. The processing device receives an electrocardiogram from the electrocardiogram sensor. The electrocardiogram is input into a machine learning model, the machine learning model to generate an output based on the received electrocardiogram. The processing device determines based on the electrocardiogram, that the output does not match an expected range of outputs for the target subject and generates an alert indicating a possible change in a status of the subject in response to the output not matching the expected range of outputs for the target subject.