Abstract: A physiological detection system including an array sensor and a processing unit is provided. The array sensor is configured to output array PPG signals. The processing unit is configured to construct a 3D energy distribution according to the array PPG signals to accordingly identify different microcirculation states.

Abstract: A blood pressure meter includes a pump and a first fluid path provided inside a main body. The first fluid path feeds a fluid from the pump to a fluid bladder or discharges the fluid from the fluid bladder. A pressure sensor is mounted on a first substrate disposed inside the main body. A second fluid path that introduces the fluid from the fluid bladder to the pressure sensor is provided. The second fluid path includes an inlet pipe that is integrally formed with a sensor package that incorporates the pressure sensor, and extends straight between the fluid bladder and the pressure sensor. A second substrate on which a blood pressure measurement element is mounted is disposed in a space that is located between the first substrate and the fluid bladder in a thickness direction and is adjacent to the second fluid path in a planar direction.

Abstract: A biopsy device is configured wherein a first retraction of a charge handle moves a cannula slide and a sampling slide in unison to charge a sampling spring, to latch the sampling slide to retain the sampling spring in a charged state, and to charge a vacuum system. A second retraction of the charge handle occurs, and a return of the charge handle to the home position moves the cannula slide in a distal direction away from the sampling slide to charge the cannula retract spring and to latch the cannula slide to retain the cannula retract spring in a charged state. A third retraction of the charge handle moves the carriage assembly as a whole in the proximal direction to charge the prime pierce spring and to latch the carriage latch cover member to retain the prime pierce spring in a charged state.

Abstract: A device for capturing and concentrating volatile organic compounds (VOCs) in a sample of breath air. The device includes an intake for accepting an air sample; a disposable mouth piece; a sensor array for measuring physical parameters of the air sample; an exhaled air sampler for capturing a pre-determined volume of air; a concentrator for concentrating VOCs in the air sample; and an ionic liquid collector, the latter of which may be removed from the device. The ionic liquid collector, which may have one compartment or multiple compartments, includes at least one ionic liquid. Analysis of VOCs in the ionic liquid or liquids may identify biomarkers that can provide a medical diagnosis for a human patient based on a sample of breath air.

Abstract: An instrument (1) for use in measuring blood flow in the femoral head after a femoral neck fracture comprises a sleeve (2) and a rod (3) which is displaceably mounted in the sleeve. The sleeve (2) is configured for insertion into a bore (4) in the femoral neck (5) and femoral head (6) and provided with at least one aperture (8) at a front portion (2a) thereof. The aperture (8) in the front portion (2a) of the sleeve (2) is intended for location in the femoral head (6) distally of the fracture (7) after the sleeve has been inserted into said bore (4). The rod (3) is configured for closing the aperture (8) in the sleeve (2) during insertion of the sleeve into the bore (4) in the femoral neck (5) and femoral head (6) and for exposing said aperture after said insertion. Thereby, blood leaking into the bore (4) at the front portion (2a) of the sleeve (2) can be collected by the sleeve through the aperture (8) therein for subsequent measuring of the volume of the collected blood.

Abstract: An EEG monitor with sensors placed to detect signals and analyze the signals to determine if a frequency below 12 Hz, and more particularly between 3 Hz and 8 Hz, called theta waves, are present. Theta waves are generated when the brain is entering a drowsy or sleep mode. The sensors detect brain wave signals and transmit the signals to a microprocessor which analyzes the signals and determines the brain waves being detected. The brain waves are continuously monitored and the data is continuously transmitted to a microprocessor. If brain waves are detected in the predetermined range of between 3 Hz and 8 Hz the microprocessor activates a stimulus, to wake up the person wearing the device. The stimulus may be visual, auditory or tactile, such as an actuator, a phone call or any other stimulus.

Abstract: Systems and method may be used for interfacing with a patient. Systems may include a plurality of electrodes in electrical communication with a processor. The processor may determine a relative impedance difference between a first electrode and a second electrode, and apply a sub-therapeutic stimulation pulse to one of the first and second electrodes to adjust the relative impedance difference therebetween. Systems may include a processor capable of one or both of providing therapeutic stimulation to a patient via at least one electrode, and receiving electrical signals indicative of the patient's physiological activity. In some examples, the processor may simultaneously provide therapeutic stimulation to a patient and receive electrical signals from the patient indicative of the patient's physiological activity.

Abstract: Introduced here are diabetes management platforms able to guide people with diabetes toward a glycemic target. Rather than state the absolute amount of glucose within the blood, the diabetes management platform can instead produce personalized glycemic goals based on the physiological data associated with an individual. For example, if the diabetes management platform determines that the time spent within a first glycemic range exceeds a specified threshold, then the diabetes management platform may recommend that the individual attempt to keep their blood glucose level within a second glycemic range. Generally, the second glycemic range is closer than the first glycemic range to a target glycemic range corresponding to a healthy glycemic state.

Abstract: A breath testing apparatus is provided with a mouthpiece, a collection chamber, and a discharge chute. A breath sample is captured within the collection chamber and transferred to an evacuated container through the discharge chute by a sample transfer assembly.

Abstract: Disclosed is a mobile device (15) for analyzing breath samples, comprising:—at least one mouthpiece (16) provided with at least one inlet opening (17) and at least one outlet opening (21) for allowing a person to respectively inhale and exhale via the mouthpiece,—at least one air filter (20) connected to the mouthpiece for filtering ambient air to be inhaled by the person,—at least one analysis compartment (19) connecting to the outlet opening of the mouthpiece and provided with at least one chemical trace detector (1), wherein the chemical trace detector comprises: at least one semi-conducting sensor (2); at least one heating element (4) for heating the semi-conducting sensor; at least one processor (6) for controlling the heating element; and a detection circuit (7) for detecting the change in resistance of the semi-conducting sensor which is at least partially determined by the presence of at least one chemical trace which reacts in the presence of the semi-conducting sensor.

Abstract: The present invention relates to method and a system for detecting sleep phenomena, the phenomena including at least one of sleep cycles and sleep disorders such as sleep apnea and hypopnea. Ballistocardiologic signals are detected from a subject person, which provide simultaneous information on heart rate variability (HVV) and stroke volume (SV) of the subject. Values of parameters reflecting measured characteristics of currently occurring cardiologic and respiration related sleep phenomena are obtained by processing at least said ballistocardiologic signals. Obtained parameters are used for making decisions on detection of said sleep phenomena, and a monitoring result is output in response to detection of a currently occurring sleep phenomenon.

Abstract: A carrier assembly includes a sub-assembly including a pump, at least one solenoid valve, and a check valve. The pump, the at least one solenoid valve, and the check valve are in fluid communication with each other and with at least one pressure transducer via a manifold. Also, the carrier assembly is configured to be mounted to a medical device's main assembly board.

Abstract: A gatekeeper electronic signal can be generated by a patient sensor and/or in an intermediate device, such as an electrical cable, that is separate from a patient's physiological information electronic signal. The gatekeeper signal can be generated to indicate to a computer monitor that the sensor and/or cable is of the type that is compatible with, and/or usable with, such computer monitor, and/or that the sensor and/or cable is properly attached to the computer monitor. The gatekeeper signal can be created by an ambient temperature sensor on, or in electrical communication with, the patient monitor, and/or the gatekeeper signal can be created by a gatekeeper electronic signal generator to simulate an ambient temperature value. The gatekeeper signal can be separate from an electronic signal or plurality of signals that include patient physiological information, and the gatekeeper signal may not include any patient physiological information.

Abstract: A profile of optical reflectance relative to a depth within a depth range from an epidermis to an upper layer of a dermis is created based on a coherence signal obtained by optical coherence tomography, an evaluation index is determined by calculating a difference between reflectance at a local minimum point and reflectance at a second local maximum point from the created profile, and skin conditions are evaluated based on the evaluation index.

Abstract: A system for monitoring blood pressure includes a blood pressure cuff, a blood pressure measurement device removably connected to the blood pressure cuff, and a cuff verification module. The cuff verification module is executable on a processor to receive medical record information from a patient, determine an expected cuff size for the patient based on the medical record information, receive a detected cuff size for the blood pressure cuff, and verify that the detected cuff size is consistent with the expected cuff size.

Abstract: In an arrangement for detecting acne, particularly in its earliest stages before any humanly visible or palpable manifestations thereof have emerged, a green fluorescence image of skin illuminated with blue light is captured and processed to detect the presence of microcomedones. After correcting the green fluorescence image for the non-uniform distribution of excitation light on the skin, fluorescent spots are detected therein. The subset of fluorescent spots having an intensity lower than an intensity threshold and an area smaller than an area threshold are selected as representing candidate microcomedones. The subset can be further refined by eliminating fluorescent spots having irregular shapes, are associated with inflammation, or exhibit comedone features. Additional filtering can be applied by selecting those spots whose locations correspond to pore locations.

Abstract: Methods and systems are disclosed herein for a system configured to determine a position of a brain monitoring user device, and a brain state of a user. Based on the determined position and the determined brain state, the system provides access to a set of media guidance application operations corresponding to the determined brain state and to brain regions corresponding to the determined position of the brain monitoring user device.

Abstract: A device for extracting physiological information indicative of at least one vital sign of a subject from detected electromagnetic radiation transmitted through or reflected from a subject comprises an input interface for receiving a data stream of detection data derived from detected electromagnetic radiation transmitted through or reflected from a skin region of a subject. The detection data comprises wavelength-dependent reflection or transmission information in at least two signal channels representative of respective wavelength portions. A signal mixer dynamically mixes the at least two signal channels into at least one mixed signal. A processor derives physiological information indicative of at least one vital sign from the at least one mixed signal, and a controller controls the signal mixer to limit the relative contributions of the at least two signal channels mixed into at least one mixed signal and/or the rate-of-change at which said relative contributions are allowed to dynamically change.

Abstract: A stand-on physiological sensor (e.g. floormat) measures vital signs and various hemodynamic parameters, including blood pressure and ECG waveforms. The sensor is similar in configuration to a common bathroom scale and includes electrodes that take electrical measurements from a patient's feet to generate bioimpedance waveforms, which are analyzed digitally to extract various other parameters, as well as a cuff-type blood pressure system that takes physical blood pressure measurements at one of the patient's feet. Blood pressure can also be calculated/derived from the bioimpedance waveforms. Measured parameters are transmitted wirelessly to facilitate remote monitoring of the patient for heart failure, chronic heart failure, end-stage renal disease, cardiac arrhythmias, and other degenerative diseases.

Abstract: A wearable breathing sensor, such as a piezoelectric chest belt system, generates a breathing signal that is analyzed by a classifier to identify apnea patterns indicating that the subject has swallowed during breathing. These breathing signals are computer-analyzed to extract inferences regarding the subject's eating and drinking patterns and thereby provide useful data for monitoring food or beverage intake for remote health monitoring.