During both invasive and non-invasive treatments and therapies, health professionals need to accurately locate areas of interest. Inaccuracies may mean that not all the area is treated, or the treatment is incomplete. Electro-magnetic and RFID (Radio-Frequency Identification) markers have been developed, but these are bulky and prone to failure. For example, any inaccuracy may result in an incomplete resection or removal of the lesion, requiring additional treatments.

A magnetic field probe 100, 101 is provided for determining an angular disposition 180, 190 of an implantable magnetic marker 200, the probe comprising: a first magnetic sensor 110 close to the distal end 160, and a second magnetic sensor 120, closer to a proximal end 165, configured to determine two or more magnetic field vectors of the marker 200; the probe being further configured: to define two or more marker detection zones 170, 171, 172, 173, 174, extending from the distal end 160; to determine the angular disposition 180, 190 to the implantable marker 200; and to determine whether the angular disposition 180, 190 substantially coincides with one of the two or more marker detection zones 170, 171, 172, 173, 174, thereby determining that the marker falls within the one marker detection zones.

By defining two or more marker detection zones, and configuring the probe to determine whether the magnetic marker appears to be within the one marker detection zone, a simplified and intuitive decision algorithm is provided for indicating the disposition of the marker relative to the probe.

A body electrode unit includes a body electrode and a release sheet to which the body electrode is attached. The body electrode includes a first electrode configured to stimulate a muscle of a body, a second electrode, and a third electrode. The second electrode and the third electrode are configured to detect a physiological signal from the muscle that is stimulated by the first electrode. The body electrode also includes a first connection portion arranged between the first electrode and the second electrode, and a second connection portion arranged between the third electrode and one of the first electrode and the second electrode. The first connection portion has at least one first direction changing part configured to change a direction in which the first connection portion extends, such that at least one of a distance and an angle between the first electrode and the second electrode is adjustable.

A measurement chamber that is essentially dome shaped and has a base area with a membrane and has at least two connection points fora fluid flow. The measurement chamber has two outer webs opposite each other, one of the webs engaging a clamping edge of a coupling element.

Provided according to embodiments of the invention are methods of monitoring the direction of blood flow that include processing with a computer photoplethysmography (PPG) signal streams from a sensor array on a body site of the individual to determine the direction and/or velocity of the blood flow at the body site of the individual. In some embodiments, direction of the blood flow at the body site is determined by the phase difference between at least three PPG signal streams from the sensor array, wherein the at least three PPG signal streams are generated from emissions of the at least three emitters.

Embodiments are directed to an electronic device configured to measure temperature from within an ear canal having a first bend, a second bend, and a tympanic membrane. The device comprises an enclosure comprising an in-canal section dimensioned for deployment in the ear canal. The in-canal section comprises a trough extending axially along at least a portion of the in-canal section and arranged to be positioned between the first bend and the tympanic membrane when the in-canal section is fully deployed in the ear canal. A temperature sensor is disposed in the trough. The temperature sensor comprises a flexible circuit board, a distal temperature sensor disposed on the flexible circuit board, and a proximal temperature sensor disposed on the flexible circuit board and situated proximal of, and spaced apart from, the distal temperature sensor in an outer ear direction.

An esophageal monitoring device includes a camera and, optionally, one or more lights to enable visualization of an interior of a subject's esophagus. Visualization of the interior of the subject's esophagus before and after a left atrial ablation procedure may enable a healthcare provider to determine whether or not the left atrial ablation procedure has damaged the subject's esophagus before the subject experiences any symptoms of such damage. An esophageal monitoring device may also include sensors and/or markers that enable a determination of its location within a subject's esophagus. Such an esophageal monitoring device may be configured for three-dimensional mapping, and enable the generation of an accurate three-dimensional map of the physical relationship between a subject's esophagus and the left atrium of his or her heart. Methods of monitoring a subject's esophagus while a left atrial ablation procedure is being conducted on the subject's heart are also disclosed.

Embodiments related to methods and wearable medical detecting systems for detecting disease states and/or treatment states of a subject are described. In one embodiment, a wearable structure may include one or more radiation detectors use to detect a time varying radiation signal emitted from a labeled compound within a body portion of interest. The radiation signal may be analyzed to determine one or more signal characteristics that may be compared to one or more predetermined standard characteristics associated with known disease and/or treatment states to determine a current disease and/or treatment state of a subject.

Electrode array for monitoring of physiological parameters and devices including or utilizing same, the electrode array including an active electrode configured to provide an electrical signal and at least two inactive electrodes configured to collect the electrical signal transferred from the active electrode, wherein each of the at least two inactive electrodes are positioned at a different predetermined distance from the active electrode.

This application relates to a pressure sensor array for urodynamic testing capable of simultaneously measuring bladder pressure, prostate pressure, and urethral pressure, and to a test apparatus including the pressure sensor array. In one aspect, the pressure sensor array for urodynamic testing is installed in a catheter and includes a base substrate having flexibility.

The pressure sensor array may also include a bladder pressure sensor formed on a portion of the base substrate to be positioned in bladder and measuring bladder pressure. The pressure sensor array may further include a prostate pressure sensor formed on a portion of the base substrate to be positioned in prostate and measuring prostate pressure. The pressure sensor array may further include a urethral pressure sensor formed on a portion of the base substrate to be positioned in urethra and measuring urethral pressure.

A device comprising a piece of planar substrate embedded with two sensors and two emitters. The substrate has a generally planar surface for application onto the wearer's body part. The emitters and sensors are shown to be arranged in such a way that no subset of any two emitters and one sensor, or subset of any two emitters and one sensor, forms a straight line, which prevents the two sensors from detecting the same noise caused by the same wearer movements.