Intraocular pressure sensing devices and methods of use. The intraocular pressure sensing devices may include one or more calibration sensors that are adapted to sense fibrotic growth over the implant post-implantation. Methods can take into account the amount of fibrosis over the implant, and its effect on IOP, when calculating the subject's IOP. Additionally, methods herein can calculate IOP while factoring in blink-induced variation in IOP.

An appliance (1) for enteral nutrition by means of a probe of the type comprising a tubular element of elongated shape and substantially flexible which defines a feeding channel open at the extremities for the introduction of nutritional substances in the stomach of a patient and which comprises at least a first inflatable balloon for detecting the pressure inside the oesophagus of a patient, the tubular element comprising at least a first inlet/outlet mouth for the air in/from the first balloon, the appliance (1) further comprising: at least a pneumatic circuit (3) having pumping means (4) associable at least with the first inlet/outlet mouth for inflating/deflating the first balloon; processing means (8) comprising: detection means which can be connected to the first balloon to detect the patient's oesophageal pressure (p.sub.es); reading means of the pressure of the respiratory tract (p.sub.aw) which can be connected to an external detection device; calculation means operatively connected to the detection means and to the reading means and able to calculate at least the transpulmonary pressure (p.sub.tp); graphic display means (10) operatively connected to the processing means (8) and able to display at least one of the oesophageal pressure (p.sub.es), the pressure of the respiratory tract (p.sub.aw) and the transpulmonary pressure (p.sub.tp).

A system for detecting disease progression can include an injection device configured to deliver medicament to a patient, one or more load sensors, one or more motion sensors, and a processor configured to read data from one or more of the load sensors and motion sensors and produce an output for display to a user.

A system for detecting disease progression can include an injection device configured to deliver medicament to a patient, one or more load sensors, one or more motion sensors, and a processor configured to read data from one or more of the load sensors and motion sensors and produce an output for display to a user.

The present invention makes it possible to, even when a stainless steel is adopted in a diaphragm: prevent the diaphragm and a strain sensor from exfoliating from each other; be hardly susceptible to the influence of temperature in an operating environment; not allow the sensitivity of a pressure sensor to be dominated only by the mechanical characteristic of a material constituting the diaphragm; and increase the degree of freedom in design of members constituting the pressure sensor. A pressure sensor according to the present invention is, in order to solve the above problems, characterized in that: the pressure sensor has a diaphragm deforming by the pressure of a fluid, an elastic body covering the whole surface of the diaphragm and joining to the diaphragm on one side, and a strain sensor being arranged by joining on the other side of the elastic body and on an end side apart from a position corresponding to the center of the diaphragm and detecting the deformation of the elastic body working together with the deformation of the diaphragm as a strain; and the elastic body is formed of a material having a linear expansion coefficient close to the linear expansion coefficient of a material constituting the strain sensor.

Hat, helmet, and other headgear apparatus includes dry electrophysiological electrodes and, optionally, other physiological and/or environmental sensors to measure signals such as ECG from the head of a subject. Methods of use of such apparatus to provide fitness, health, or other measured or derived, estimated, or predicted metrics are also disclosed.

A system for automated adjustment of a pressure set by a ventilation device, in particular a positive and-expiratory pressure and/or a maximum airway pressure, the system comprising a pressure detection arrangement for detecting a transpulmonary pressure at the end of an expiration phase and/or for detecting a transpulmonary pressure at the end of an inspiration phase, and a device for automated adjustment of the pressure set by the ventilation device on the basis of the transpulmonary pressure detected at the end of the expiration phase and/or the transpulmonary pressure detected at the end of the inspiration phase.

A biodegradable pressure sensor for measuring vital physiological pressures and for preventing the buildup of dangerous internal forces in impaired organs. The pressure sensor is constructed by depositing Mg or Mo on both sides of a PLLA film. This layered configuration (Mg/PLLA/Mg) or (Mo/PLLA/Mo) may then be encapsulated by layers of high molecular weight PLA. These materials are biodegradable such that after implantation, the sensor does not require invasive removal surgery that can damage directly interfaced tissues.

A biodegradable pressure sensor for measuring vital physiological pressures and for preventing the buildup of dangerous internal forces in impaired organs. The pressure sensor is constructed by depositing Mg or Mo on both sides of a PLLA film. This layered configuration (Mg/PLLA/Mg) or (Mo/PLLA/Mo) may then be encapsulated by layers of high molecular weight PLA. These materials are biodegradable such that after implantation, the sensor does not require invasive removal surgery that can damage directly interfaced tissues.

Provided is a pressure gauge capable of being effectively used for internal pressure measurement of a balloon catheter and capable of providing easy monitoring of a pressure value even when measuring internal pressure of an extracorporeal circulation circuit. The pressure gauge measures internal pressure of a balloon catheter used for treatment and diagnosis or pressure of a body lumen of a living body and includes a coil-shaped tube 2 to elastically deform. One end of the tube 2 is set as an open fixed end and the other end is set as a sealed free end and pressure introduced from the open fixed end can be measured based on a displacement position of the tube 2 due to the pressure.