In a method and medical imaging apparatus for determining a feature characterizing intentional breath-holding by an examination object for acquiring medical raw data with breath-holding algorithm, an algorithm, the algorithm being designed to allocate at least one feature characterizing intentional breath-holding to at least one physiological property. The algorithm includes or accesses trained artificial neural network. A physiological property of the examination object is detected during free breathing of the examination object. The feature characterizing intentional breath-holding by the examination object is determined by the computer, by executing the algorithm with the detected physiological property of the examination object, as an input to the algorithm.

A wearable device and respiration sensing module are provided. The wearable device includes a first respiration sensing module and a second respiration sensing module. The first respiration sensing module is configured to sensing respiration of a user to obtain a first respiration information. The second respiration sensing module is configured to sensing respiration of the user to obtain a second respiration information. The second respiration sensing module includes a substrate, a first electrode, a second electrode and a stretchable conductive element. The first electrode and the second electrode are disposed on a first surface of the substrate. The stretchable conductive element is physically and electrically connected between the first electrode and the second electrode. The respiration of the user is judged according to the first respiration information and the second respiration information.

A wearable device and respiration sensing module are provided. The wearable device includes a first respiration sensing module and a second respiration sensing module. The first respiration sensing module is configured to sensing respiration of a user to obtain a first respiration information. The second respiration sensing module is configured to sensing respiration of the user to obtain a second respiration information. The second respiration sensing module includes a substrate, a first electrode, a second electrode and a stretchable conductive element. The first electrode and the second electrode are disposed on a first surface of the substrate. The stretchable conductive element is physically and electrically connected between the first electrode and the second electrode. The respiration of the user is judged according to the first respiration information and the second respiration information.

A system for monitoring medical conditions including pressure ulcers, pressure-induced ischemia and related medical conditions comprises at least one sensor adapted to detect one or more patient characteristic including at least position, orientation, temperature, acceleration, moisture, resistance, stress, heart rate, respiration rate, and blood oxygenation, a host for processing the data received from the sensors together with historical patient data to develop an assessment of patient condition and suggested course of treatment, including either suspending or adjusting turn schedule based on various types of patient movement. The sensor can include bi-axial or tri-axial accelerometers, as well as resistive, inductive, capacitive, magnetic and other sensing devices, depending on whether the sensor is located on the patient or the support surface, and for what purpose.

A method of detecting a vital sign comprising at least one of a heart rate and a respiratory rate of a subject is provided. In one aspect, the method includes transmitting a radio frequency signal towards the subject; and receiving a reflected signal from the subject, wherein the transmitted signal is reflected by the subject and Doppler-shifted due to at least one of the heart rate and the respiratory rate to form the reflected signal. The method also includes mixing the reflected signal with a first reference signal; and providing a vital sign carrying signal based on the mixing to a first input of a phase or frequency comparator. The method further includes generating an adjustable second reference signal and providing the reference signal to a second input of the phase or frequency comparator; and generating an output signal, by the phase or frequency comparator. The method includes varying at least one of a phase and a frequency of the adjustable second reference signal based on the output signal to track a phase or frequency of the vital sign carrying signal.

An implant unit configured for implantation into a body of a subject is provided. The implant unit may include a flexible carrier unit including a central portion and two elongated arms extending from the central portion, an antenna, located on the central portion, configured to receive a signal, at least one pair of electrodes arranged on a first elongated arm of the two elongated arms. The at least one pair of electrodes may be adapted to modulate a first nerve. The elongated arms of the flexible carrier may be configured to form an open ended curvature around a muscle with the nerve to be stimulated within an arc of the curvature.

An implant unit configured for implantation into a body of a subject is provided. The implant unit may include a flexible carrier unit including a central portion and two elongated arms extending from the central portion, an antenna, located on the central portion, configured to receive a signal, at least one pair of electrodes arranged on a first elongated arm of the two elongated arms. The at least one pair of electrodes may be adapted to modulate a first nerve. The elongated arms of the flexible carrier may be configured to form an open ended curvature around a muscle with the nerve to be stimulated within an arc of the curvature.

Radio frequency motion sensors may be configured for operation in a common vicinity so as to reduce interference. In some versions, interference may be reduced by timing and/or frequency synchronization. In some versions, a master radio frequency motion sensor may transmit a first radio frequency (RF) signal. A slave radio frequency motion sensor may determine a second radio frequency signal which minimizes interference with the first RF frequency. In some versions, interference may be reduced with additional transmission adjustments such as pulse width reduction or frequency and/or timing dithering differences. In some versions, apparatus may be configured with multiple sensors in a configuration to emit the radio frequency signals in different directions to mitigate interference between emitted pulses from the radio frequency motion sensors.

Radio frequency motion sensors may be configured for operation in a common vicinity so as to reduce interference. In some versions, interference may be reduced by timing and/or frequency synchronization. In some versions, a master radio frequency motion sensor may transmit a first radio frequency (RF) signal. A slave radio frequency motion sensor may determine a second radio frequency signal which minimizes interference with the first RF frequency. In some versions, interference may be reduced with additional transmission adjustments such as pulse width reduction or frequency and/or timing dithering differences. In some versions, apparatus may be configured with multiple sensors in a configuration to emit the radio frequency signals in different directions to mitigate interference between emitted pulses from the radio frequency motion sensors.

A sensor substrate to detect heart failure decompensation comprises a substrate structure, wherein the substrate structure is configured to have a patient sit, recline, or lie on a surface of the substrate structure, one or more sensors in the substrate structure, wherein the one or more sensors are configured to detect a plurality of parameters of the patient when the patient is in contact with the substrate structure, an interface in the substrate structure to receive an output from the one or more sensors, and a processor, wherein the processor is configured to detect heart failure decompensation in the patient from the plurality of parameters detected by the one or more sensors when the patient is in contact with the substrate structure.