A medical sensing system (100) includes an elongate interventional device (101) and an adjustable capacitance circuit (102). The elongate interventional device (101) includes a sensor (103) having a capacitance (C.sub.ss). The elongate interventional device (101) also includes a first electrical conductor (104) and a second electrical conductor (105). The first electrical conductor (104) and the second electrical conductor (105) are in electrical contact with the sensor (103) and extend along the elongate interventional device (101). The elongate interventional device (101) also includes i) an electrically conductive shield (106) that overlaps the electrical conductors (104, 105) and/or ii) an electrically conductive shaft (107). The adjustable capacitance circuit (102) provides an adjustable capacitance (C.sub.Adj1, C.sub.Adj2) between at least one of the electrical conductors (104, 105) and i) the electrically conductive shield (106) that overlaps the electrical conductors (104, 105) and/or ii) the electrically conductive shaft (107).

An aspect of the disclosure pertains to a wrist-worn device that may be characterized by the following features: an external surface that is not in contact with the user when the wrist-worn device is worn; a force sensor; a PPG sensor disposed on the wrist-worn device; and control logic configured to: (i) generate one or more sensor data samples, each sensor data sample including data that links force data generated by the force sensor when a user presses a against the external surface at a given time with heart rate data obtained from the PPG sensor at the given time; and (ii) calculate an estimate of blood pressure from the one or more sensor data samples. As examples, the force sensor may be a force sensitive touch screen or film, a strain gauge integrating into the device, or a calibrated spring element configured to be pressed by the user.

A method for determining stenosis of the carotid artery in a human patient consisting of a first step of placing a sensing device comprising an array and three sensing elements onto the patient, wherein a first sensing element is placed near the heart and the two remaining sensing elements are placed adjacent to the carotid arteries; the sensing elements then measure sounds from each of the three sensing elements, resulting in sound from three channels. The sound is measured in analog and modified to digital format and then each of the three channels are analyzed before a power spectral density analysis is performed. The power spectral density graph reveals peaks that are not due to noise that are then analyzed to provide for a calculation of percent stenosis or complete occlusion of the carotid artery.

Methods and apparatuses, including devices and systems, for remote and detection and/or diagnosis of acute myocardial infarction (AMI). In particular, described herein are handheld and adhesive devices having an electrode configuration capable of recording three orthogonal ECG lead signals in an orientation-specific manner, and transmitting these signals to a processor. The processor may be remote or local, and it may automatically or semi-automatically detect AMI, atrial fibrillation or other heart disorders based on the analyses of the deviation of the recorded 3 cardiac signals with respect to previously stored baseline recordings.

The present invention relates to a method to be performed by a computing device part of or coupled to an ECG device for applying a marker element in a process of determining positions of a set of ECG electrodes as placed on a human torso relative to a 3D model of a body, preferably a torso model of the torso of the human body. The method includes receiving an imaging information recording relating to the human body from an optical imaging device, preferably a 3D imaging device. The optical imaging information includes imaging information of the exterior of the body, such as imaging information of the exterior of the torso, and imaging information of the marker element. The method also includes performing an image recognition on the imaging information for obtaining a presence determination, preferably a positive or negative determination, of the marker element in the imaging information.

Systems and methods for positioning one or more sensors on a user. The system has user sensors, apparatus sensors, and treatment sensors. A processing device, executing computer readable instructions stored in a memory, cause the processing device to: generate an enhanced environment representative of an environment; receive apparatus data representative of a location of the apparatus in the environment; generate an apparatus avatar in the enhanced environment; receive user data representative of a location of the user in the environment; generate a user avatar in the enhanced environment; receive treatment data representative of one or more locations of the treatment sensors in the environment; generate, treatment sensor avatars in the enhanced environment; calculate a treatment location for each treatment sensor, wherein the treatment location is associated with an anatomical structure of a user; and generate instruction data representing an instruction for positioning the treatment sensors at the treatment location.

A system for EIT imaging comprises an electrode array for positioning on a patient and measuring an impedance distribution, a data entry unit and a calculation unit. The electrode array contains a visual aid coupled to the electrode array for visually indicating the position of at least one electrode, the data entry module accepts an entry of data describing the position of the visual aid, and the calculation unit calculates the position of the individual electrodes relative to the patient's body and provides correction for the image creation algorithm. A sensor device for EIT imaging may comprise the electrode array, which is connectable to an EIT imaging system comprising a data entry unit and a calculation unit. An EIT imaging method may employ the system or sensor device.

The present embodiments provide systems and methods for, among others, tracking sensor insertion locations in a continuous analyte monitoring system. Data gathered from sensor sessions can be used in different ways, such as providing a user with a suggested rotation of insertion locations, correlating data from a given sensor session with sensor accuracy and/or sensor session length, and providing a user with a suggested next insertion location based upon past sensor accuracy and/or sensor session length at that location.

A method for measuring a myocardial physiologic parameter according to an embodiment includes placing an at least partially convex portion of a spectral sensor against an intercostal space of a human over a heart of the human and measuring the physiologic parameter of a myocardium of the heart with the spectral sensor over time during an emergency medical event. The spectral sensor may be configured to determine and visually display a suggested position adjustment for directing the spectral radiation more directly toward the tissue of interest (e.g. the myocardium), and/or for placing the operative elements of the spectral sensor closer to the tissue of interest (e.g. the myocardium).

One variation of a method for testing contact quality of electrical-biosignal electrodes includes: outputting a drive signal through a driven electrode, the drive signal comprising an alternating-current component oscillating at a reference frequency and a direct-current component; reading a set of sense signals from a set of sense electrodes at a first time; calculating a first combination of the set of sense signals; calculating a first direct-current value comprising a combination of the first combination and the direct-current component of the drive signal at approximately the first time; and at a second time succeeding the first time, shifting the direct-current component of the drive signal output by the driven electrode to the first direct-current value.