A mucosal impedance measuring apparatus detects and measures a condition of mucosa. The mucosal impedance measuring apparatus includes a catheter comprising a tube, impedance sensing electrodes on an exterior surface of the catheter, a balloon mounted on the tube in which the balloon is capable of inflation and deflation, and an impedance measuring system. The impedance measuring system is adapted to measure a pressure-regulated impedance measurement of the mucosa that is indicative of the condition of the mucosa when the balloon is inflated and the impedance sensing electrodes direct an electric current through mucosa while the balloon is pressed against the mucosa.

Disclosed is an implant and method of making an implant. The implant having a housing that defines a cavity. The housing includes a sensor comprising a base attached to a diaphragm wherein said base may be positioned within said cavity. The sensor may be a capacitive pressure sensor. The diaphragm may be connected to the housing to hermetically seal said housing. The sensor may include electrical contacts positioned on the diaphragm. The attachment between the base and the diaphragm may define a capacitive gap and at least one discontinuity configured to enhance at least one performance parameter of said implant.

The present technology relates to intracardiac pressure monitoring devices, and associated systems and methods. In some embodiments, the present technology includes a device for monitoring pressure within a patient's heart. The device can include a pressure sensor configured to reside within a first chamber of a heart of a patient, and a pressure transmission element configured to extend from the first chamber through a septal wall to a second chamber of the heart of the patient. When the device is implanted in the patient's heart, the pressure transmission element is configured to transmit pressure from the second chamber to the pressure sensor residing within the first chamber.

A wearable blood pressure meter includes a semi-conformable bladder, serving as a reservoir for an incompressible fluid, and a pressure sensor. The semi-conformable bladder includes a rigid housing defining a cavity within which the incompressible fluid is rigidly constrained and an elastic membrane for elastically constraining the incompressible fluid. The elastic membrane extends across an aperture into the cavity through the rigid housing. The elastic membrane conforms to a body part at the aperture when pressed against the body part. The pressure sensor mechanically couples to the incompressible fluid to measure pressure signals emanating from an artery within the body part and which propagate through the conformable membrane and the incompressible fluid to the pressure sensor.

An electronic device is provided. The electronic device includes a housing including at least one electronic component, and a pad structure coupled with the housing, and attached to a user body. The pad structure includes a first adhesive material having an adhesive strength at which the electronic device holds attachment in response to lack of existing water or humidity, and a second adhesive material abutting the first adhesive material and having an adhesive strength at which the electronic device holds the attachment in response to existing water or humidity.

According to an aspect of the invention there is provided a system for use in monitoring one or more physiological states of a user, the system comprising one or more processors configured to: receive a pressure signal representing pressure within a cushioning layer supporting at least a portion of a user and an acoustic signal representing acoustic vibrations within the cushioning layer; and determine, based on the pressure signal and acoustic signal, the one or more physiological states of the user.

There is provided a method of forming a thin film-based microfluidic electronic device. The method includes: providing a first elastomeric thin film layer on a substrate; depositing a first elastomer on the first elastomeric thin film by direct ink writing to form an elastomeric structure configured to define a microfluidic channel on the first elastomeric thin film layer; providing a second elastomeric thin film layer over the elastomeric structure to cover the microfluidic channel; providing a sacrificial layer on the second elastomeric thin film; depositing liquid metal into the microfluidic channel to form a conductor in the microfluidic channel; and electrically connecting the conductor to an electronic component. The thin film-based microfluidic electronic device is a tissue or skin adhesive sensor including a skin adhesive acoustic device.

The invention relates to physiological sensor for measurement of carbon dioxide and a method of securing a carbon dioxide permeable membrane of the physiological sensor. The physiological sensor comprising a closed chamber containing a sensor liquid and being bounded, at least partially, by a carbon dioxide permeable membrane (12), at least two electrodes (10) provided within the chamber in contact with the sensor liquid, a support structure (23) for supporting the membrane (12); and at least one filament 28) wound around the support structure (23) and on top of the membrane (12) for securing the gas-permeable membrane (12) to the support structure (23).

A method for measuring cardiac pressure includes positioning a fluid-filled catheter and a pressure wire sensor at a cardiac pressure calibration location. A first pressure measurement is acquired from the fluid-filled catheter and a second pressure measurement is acquired from the pressure wire sensor. A set of equalization parameters is identified to apply to the first pressure measurement to reduce an error between the first pressure measurement and the second pressure measurement. The equalization parameters include a frequency correction parameter and a damping correction parameter to correct for frequency and damping of oscillations in the first pressure measurement. A third pressure measurement is acquired from the fluid-filled catheter. The set of equalization parameters is applied to equalize the third pressure measurement.

A system for detecting pressure sores includes an artificial skin configured to be coupled to a patient's skin. The artificial skin includes a substrate and a strain sensor configured to detect deformation of the substrate. A transmitter is configured to transmit signals indicative of the deformation of the substrate. A control system is configured to receive the signals from the transmitter. The control system includes a timer to track a period of time that the substrate is deformed.