Devices, systems and methods for treating various disorders and medical conditions through noninvasive stimulation of a nerve. A system comprises a stimulator including an electrode configured to contact an outer skin surface of a patient and an energy source coupled to the housing, The energy source generates an electrical impulse and the stimulator transmits the electrical impulse from the electrode transcutaneously through an outer skin surface of the patient to a selected nerve within the patient. The system further includes an application on a mobile device that receives data from a remote source. The mobile device couples to the stimulator and the application causes the mobile device to transmit the data to the stimulator.

The present invention relates to methods for tuning treatment parameters in movement disorder therapy systems. The present invention further relates to a system for screening patients to determine viability as candidates for certain therapy modalities, such as deep brain stimulation (DBS). The present invention still further provides methods of quantifying movement disorders for the treatment of patients who exhibit symptoms of such movement disorders including, but not limited to, Parkinson's disease and Parkinsonism, Dystonia, Chorea, and Huntington's disease, Ataxia, Tremor and Essential Tremor, Tourette syndrome, stroke, and the like. The present invention yet further relates to methods of tuning a therapy device using objective quantified movement disorder symptom data acquired by a movement disorder diagnostic device to determine the therapy setting or parameters to be provided to the subject via his or her therapy device. The present invention also provides treatment and tuning remotely, allowing for home monitoring of subjects.

Physiological monitoring can be provided through a wearable monitor that includes a flexible extended wear electrode patch and a removable reusable monitor recorder. A pair of flexile wires is interlaced or sewn into a flexible backing, serving as electrode signal pickup and electrode circuit traces. The wearable monitor sits centrally on the patient's chest along the sternum, which significantly improves the ability to sense cutaneously cardiac electric signals, particularly those generated by the atrium. The electrode patch is shaped to fit comfortably and conformal to the contours of the chest approximately centered on the sternal midline. To counter the dislodgment due to compressional and torsional forces, non-irritating adhesive is provided on the underside, or contact, surface of the electrode patch, but only on the distal and proximal ends. Interlacing the flexile wires into the flexile backing also provides structural support and malleability against compressional, tensile and torsional forces.

Disclosed herein are spirometers that can be used for assessment of pulmonary lung function. The disclosed systems, computer readable mediums and methods can be directed towards use in a variety of settings by health care professionals, clinical trial specialists, and individual users.

The apparatus includes a source of treatment radiation which is arranged to generate radiation at one of a plurality of radiation parameters (such as power levels), a control unit and a base unit. The control unit is arranged to removably dock with the base unit and includes a sensor which can sense one of a plurality of skin parameters, and an actuator for enabling a user to interface with the control unit. The control unit operates in a sensing mode, in which the control unit is undocked from the base unit to sense a parameter of skin to be treated (such as skin tone), and a control mode in which the control unit is docked to the docking unit and is arranged to select the power level of the radiation generated by the source.

A plaque detecting device including a light emitting unit which irradiates light toward a tooth, and first and second light receiving units which receive radiated light from the tooth. The first light receiving unit extracts the spectral component of a first wavelength region containing fluorescent light specific to plaque and obtains a first output value corresponding to intensity of that spectral component. The second light receiving unit extracts the spectral component of a second wavelength region containing fluorescent light specific to enamel and obtains a second output value corresponding to the intensity of this spectral component. Determination of the relative magnitude of the ratio between the first output value and the second output value as compared to a first threshold value is performed. Determination of the relative magnitude of the difference between the first output value and the second output value as compared to a second threshold value is performed.

Provided is an electronic device including a housing; a battery; a user interface; a photoplethysmogram (PPG) sensor including a light receiving module exposed through a portion of the housing, at least one light emitting diode (LED), and at least one photodiode; a processor operatively connected to the battery, the user interface, and the PPG sensor; and a memory. According to an embodiment, the memory stores instructions that, when executed, cause the processor to determine whether the PPG sensor is facing a surface of an external object having a reference color, determine whether to perform a test of the PPG sensor based on whether the PPG sensor is facing the surface, receive data from the PPG sensor by operating the PPG sensor in response to determining to perform the test, and perform calibration of the PPG sensor based on at least a portion of the received data. Other embodiments are possible.

A connector includes a connector array of magnets having a first magnetic polarity pattern. A port includes a port array of magnets having a second magnetic polarity pattern that is complementary to the first magnetic polarity pattern. The connector is guided and aligned toward a mounted position in which the connector is retained on the port. The guiding and the aligning is through both (i) attraction when the connector is properly aligned to the port and (ii) repulsion when the connector is improperly aligned to the port. The port further includes a securing magnet configured to be activated when the connector reaches the mounted position, to magnetically secure the connector to the port.

A multi-parameter patient monitoring device rack can dock a plurality of patient monitor modules and can communicate with a separate display unit. A signal processing unit can be incorporated into the device rack. A graphics processing unit can be attached to the display unit. The device rack and the graphic display unit can have improved heat dissipation and drip-proof features. The multi-parameter patient monitoring device rack can provide interchangeability and versatility to a multi-parameter patient monitoring system by allowing use of different display units and monitoring of different combinations of parameters. A dual-use patient monitor module can have its own display unit configured for displaying one or more parameters when used as a stand-alone device, and can be docked into the device rack when a handle on the module is folded down.

A distributed ultrasound system includes a portable ultrasound system comprising: one or more transmitters configured to transmit ultrasound waves into a subject region; one or more receivers configured to receive ultrasound waves from the subject region in response to the ultrasound waves transmitted into the subject region; and a portable ultrasound processing unit configured to perform ultrasound image processing for generating one or more ultrasound images of the subject region using, at least in part, the ultrasound waves received from the subject region by the one or more receivers, wherein the portable ultrasound system is handheld and capable of being moved over a patient's body to an area proximate to the subject region; and an external ultrasound docking unit configured to receive and electrically couple with the portable ultrasound system and offload at least a portion of the ultrasound image processing from the portable ultrasound system when the portable ultrasound system is coupled to the external ultrasound docking unit, wherein the portable ultrasound system determines whether to offload the at least a portion of the ultrasound image processing based at least one of a temperature or a battery level of portable ultrasound system.