4159 results about "Pressure sense" patented technology

A convective warmer to which blankets of different dimensions may be connected is capable of providing air to the various blankets at flow rates that optimally inflate those blankets to achieve the optimal clinical result for the patients covered by those blankets. The blanket connected to the warmer may range from a full size adult warming blanket to a pediatric warming blanket. The convection warmer may have multiple fixed air flow rates each selectable by a user, via switch(es) either electronically or mechanically. For the electronic selection of a given flow rate, a motor adaptable to rotate a different speeds is used. To vary the flow rate mechanically, a valve is controlled to vary the amount of air that may pass to the blanket. Instead of different fixed flow rates, variable air flow rates, selectable by the user, may be used. Also, a feedback circuit that maintains the pressure sensed at the outlet of the warmer to a preset pressure may be used to eliminate the need for user intervention.

A control panel for controlling a device in response to user indications, the control panel comprising, a position sensing element (60) having a sensing surface, and a position interface circuit (76). The position interface circuit (76) is operable to determine a position of an object (100) on the sensing surface, when the object (100) is applied to the sensing surface of the position sensing element (60). At least one pressure sensing device (54, 66) and the sensing surface of the position sensing element (60) are arranged with the effect that a displacement of the sensing surface with respect to the pressure sensing device in response to the pressure applied by the object is detectable by the pressure sensing device. As such, in one example, the position interface circuit (76) is operable to identify one or more of a plurality of user indicated signals by correlating the position of the object on the sensing surface with a pressure detected by the pressure sensing device. The sensing surface may include pre-designated and pre-determined locations representing virtual buttons so that by determining whether the object is at one of a plurality of pre-determined locations on the sensing surface of the position sensing element, the position interface circuit (76) can identify the user indicated signal by correlating the position of the object at one of the predetermined locations with the detected pressure, each of the pre-determined location corresponding to one of the plurality of user indicated signals.

A telemetry method and apparatus using pressure sensing elements remotely located from associated pick-up, and processing units for the sensing and monitoring of pressure within an environment. This includes remote pressure sensing apparatus incorporating a magnetically-driven resonator being hermetically-sealed within an encapsulating shell or diaphragm and associated new method of sensing pressure. The resonant structure of the magnetically-driven resonator is suitable for measuring quantities convertible to changes in mechanical stress or mass. The resonant structure can be integrated into pressure sensors, adsorbed mass sensors, strain sensors, and the like. The apparatus and method provide information by utilizing, or listening for, the residence frequency of the oscillating resonator. The resonant structure listening frequencies of greatest interest are those at the mechanical structure's fundamental or harmonic resonant frequency. The apparatus is operable within a wide range of environments for remote one-time, random, periodic, or continuous / on-going monitoring of a particular fluid environment. Applications include biomedical applications such as measuring intraocular pressure, blood pressure, and intracranial pressure sensing.

A system and method for detecting perforations in a body cavity. In accordance with the method of the invention, a fluid (liquid or gas) is delivered into a body cavity to slightly pressurize the cavity. A pressure sensing system monitors the pressure within the cavity for a predetermined test period. If cavity pressure is not substantially sustained during the test period, the physician is alerted to further assess the cavity for perforations before initiating treatment within the cavity. In a preferred form of the system, a medical treatment system such as an RF ablation system is provided with perforation detection functionality. The system preferably includes a pre-test and post-test lockout system. The lockout system prevents RF power delivery unless, during a predetermined test period, the pressure sensing system determines that no perforation exists, or unless a previously performed perforation detection procedure determined a perforation was present but the lockout system was subsequently overridden by the physician.

There is provided a display unit including a touch panel disposed on a display screen of a display panel to detect a touch position of a pointing device, operation being conducted by touching a touch operation member displayed on the screen. The display unit includes a sensor for sensing a pushing pressure caused when touching the touch operation member, and a control section for conducting first processing concerning the touch operation member pushed by the pointing device when the pressure sensed by the sensing unit satisfies a first predetermined pressure condition, and conducting second processing concerning the touch operation member, when the pushing pressure has changed from the first condition to a second one. Upon the change from the first condition to the second one, a function of moving the screen in a direction of pushing pressure caused by the pointer is executed by the second processing.

The invention discloses a system and a method for instant hydrogen production and power generation. The system comprises a hydrogen production subsystem, an air pressure adjusting subsystem and a power generation subsystem, wherein the hydrogen production subsystem is used for preparing hydrogen from methanol water and transmitting the prepared hydrogen to the power generation subsystem in real time through a transmission pipeline; the transmission pipeline is provided with the air pressure adjusting subsystem for adjusting air pressure inside the transmission pipeline; the power generation subsystem is used for generating power by virtue of hydrogen prepared by the hydrogen production subsystem; the air pressure adjusting subsystem comprises a microprocessor, an air pressure sensor, a valve controller and an air outlet valve; the air pressure sensor is arranged in the transmission pipeline, and is used for sensing data of the air pressure inside the transmission pipeline and sending the data of the air pressure to the microprocessor; the microprocessor is used for controlling the on and off of the air outlet valve according to the data of the air pressure sensed by the air pressure sensor. Power can be generated by instantly prepared hydrogen, a hydrogen buffer tank is not required, and thus the portability and mobility of the hydrogen production and power generation system can be improved.

A system and method for verifying that a particular fluid supply is connected to an infusion pump or pump channel. An upstream pressure sensor coupled to a fluid conduit associated with the fluid supply is used to provide pressure signals in response to pressure sensed in the conduit to a processor. In a connection verification mode, the processor is configured to receive the pressure signals and delay the flow control device of the infusion pump from moving fluid through the conduit until the processor detects a pressure change in the conduit indicated by the pressure signals to thereby verify that the particular fluid supply is connected to the infusion pump.

In one embodiment, a pressure sensing system is described which transmits data to a patient management system external to a patient. The pressure sensing system can rigidly couple to an implantable port or flexibly couple to an implantable port. In some embodiments, the pressure sensing system communicates with a hydraulic actuating system. In some embodiments, the pressure sensing system is implantable and comprises a circuit capable of wireless transmission through the skin of a patient to an external receiver which is part of a patient management system. A patient management system is described which receives up to date as well as historical data from the pressure sensing system and manages the these data in the context of a patient database. In some embodiments, an extragastric balloon is described in which the balloon is contoured to fit a portion of the stomach but not circumscribe the stomach. In some embodiments, electroactive polymers or nitinol structures are utilized to create restriction on the stomach in response to food boluses entering the stomach. In some embodiments, a nasogastric connector is described with two expandable structures translateable toward and away from one another so as to create pressure between two organ lumens when brought toward each other and fixed with respect to one another.

A biopsy guidance device is enclosed based on a tactile imaging probe adapted to accept a biopsy gun. The tactile imaging probe includes a pressure sensing surface providing real-time 2-D images of the underlying tissue structures allowing to detect a lesion. A cannula is provided supported at a center point by a ball and socket joint. The joint is equipped with linear and angular sensors and supports the cannula with the ability to rotate thereof about the center point. The position, linear and angular displacement and direction of the needle tip of a biopsy needle placed inside the cannula is therefore known at all times and provided as a feedback signal to a physician. Also provided to a physician is a position of the target site at a lesion, as well as a linear and angular deviation of the needle tip away from the target site. Such audio, light, or visual feedback allows the physician to correct the insertion angle and depth to confidently reach the target site to perform a biopsy. Method is also disclosed to guide the biopsy procedure.

In one embodiment, a pressure sensing system is described which transmits data to a patient management system external to a patient. The pressure sensing system can rigidly couple to an implantable port or flexibly couple to an implantable port. In some embodiments, the pressure sensing system communicates with a hydraulic actuating system. In some embodiments, the pressure sensing system is implantable and comprises a circuit capable of wireless transmission through the skin of a patient to an external receiver which is part of a patient management system. A patient management system is described which receives up to date as well as historical data from the pressure sensing system and manages the these data in the context of a patient database. In some embodiments, an extragastric balloon is described in which the balloon is contoured to fit a portion of the stomach but not circumscribe the stomach. In some embodiments, electroactive polymers or nitinol structures are utilized to create restriction on the stomach in response to food boluses entering the stomach. In some embodiments, a nasogastric connector is described with two expandable structures translateable toward and away from one another so as to create pressure between two organ lumens when brought toward each other and fixed with respect to one another.

A display device is disclosed which includes: a display panel; a lighting unit to illuminate the display panel and having a state in response to a lighting control signal; a pressure sensing unit generating a first sensor output signal according to a touch on the display panel; a light sensing unit receiving light from the lighting unit and ambient light and generating a second sensor output signal according to the touch on the display panel; a sensor scanning driver outputting sensor scanning signals to the pressure sensing unit and the light sensing unit in response to a sensor scanning control signal; and a sensing controller generating the lighting control signal and the sensor scanning control signal based on the first and the second sensor output signals and outputting the lighting control signal to the lighting unit and the sensor scanning control signal and the sensor scanning driver.

In one embodiment, a pressure sensing system is described which transmits data to a patient management system external to a patient. The pressure sensing system can rigidly couple to an implantable port or flexibly couple to an implantable port. In some embodiments, the pressure sensing system communicates with a hydraulic actuating system. In some embodiments, the pressure sensing system is implantable and comprises a circuit capable of wireless transmission through the skin of a patient to an external receiver which is part of a patient management system. A patient management system is described which receives up to date as well as historical data from the pressure sensing system and manages the these data in the context of a patient database. In some embodiments, an extragastric balloon is described in which the balloon is contoured to −..it..i poi.jLυπo± the stomach nur not circumscribe the stomach. In some embodiments, electroactive polymers or nitinol structures are utilized to create restriction on the stomach in response to food boluses entering the stomach. In some embodiments, a nasogastric connector is described with two expandable structures translateable toward and away from one another so as to create pressure between two organ lumens when brought toward each other and fixed with respect to one another.

A small sensor surface designed to control a smart phone or Mobile Internet Device (MID). The sensor surface may be mounted on the side of the proposed device in a position where a user's thumb or finger naturally falls when holding the device in his / her hand. The sensor surface is simultaneously convex and concave, providing both visual and physical cues for the use of the sensor surface. The sensor may include capacitive sensing, optical sensing and pressure sensing capabilities to interpret thumb gestures into device control.

The present disclosure provides one or more structures, techniques, components and / or methods for avoiding or positively resolving failure modes for an implanted medical device coupled to one or more sensors. A common fault scenario involves unintended stimulation during therapy delivery. A pacing stimulus can couple to exposed conductive portion(s) of a medical electrical lead (e.g., a tip portion) that includes a sensor to cause the stimulation. Stimulation also occurs due to insulation breaches of a lead. Stimulation can also result from a breach in insulation surrounding a conductive set screw that couples the lead to active circuitry. Stimulation also results when high energy therapy energy shunts to sensor circuitry (e.g., sensor bus) via insulation breach of the sensor lead and / or the circuitry. Such unintended stimulation is avoided by disconnecting the pressure sensing lead and sensor: during therapy delivery, when impedance measurement or current measurement to the sensor indicate unintended stimulation.

A system and method for verifying that a particular fluid supply is connected to an infusion pump or pump channel. An upstream pressure sensor coupled to a fluid conduit associated with the fluid supply is used to provide pressure signals in response to pressure sensed in the conduit to a processor. In a connection verification mode, the processor is configured to receive the pressure signals and delay the flow control device of the infusion pump from moving fluid through the conduit until the processor detects a pressure change in the conduit indicated by the pressure signals to thereby verify that the particular fluid supply is connected to the infusion pump.

A pressure sensing apparatus for operative arrangement within an environment, having: a sensor comprising a hermetically-sealed receptacle, at least one side of which has an flexible membrane to which a magnetically hard element is attached. Enclosed within the receptacle is a magnetostrictive element that vibrates in response to a time-varying magnetic field. Also included is a receiver to measure a plurality of successive values for magneto-elastic emission intensity of the sensor taken over an operating range of successive interrogation frequencies to identify a resonant frequency value for the sensor. Additional features include: (a) the magnetically hard element may be adhered to an inner or outer side of, or embedded within, the membrane; (b) the magnetostrictive element can include one or more of a variety of different pre-formed, hardened regions; (c) the magneto-elastic emission may be a primarily acoustic or electromagnetic emission; and (d) in the event the time-varying magnetic field is emitted as a single pulse or series of pulses, the receiver unit can detect a transitory time-response of the emission intensity of each pulse (detected after a threshold amplitude value for the transitory time-response is observed). A Fourier transform of the time-response can yield results in the frequency domain. Also, an associated method of sensing pressure of an environment is included that uses a sensor having a magnetostrictive element to identify a magneto-elastic resonant frequency value therefore. Using the magneto-elastic resonant frequency value identified, a value for the pressure of the environment can be identified.

A hybrid touch system that utilizes a combination of a capacitive touch system for position sensing and an optical touch system for pressure sensing is disclosed. The optical touch system includes a transparent sheet having a surface, at least one light source and at least one detector which are operably arranged relative to the transparent sheet to transmit light through the sheet and to detect the transmitted light. Performing position sensing using the capacitive touch system simplifies the pressure-sensing optical touch system.

A food intake restriction device for forming a restriction in a patient's gastro-intestinal tract and non-invasively communicating pressure data regarding the restriction to an external monitor. The device includes a food intake restriction device implanted substantially about a patient's gastro-intestinal tract to form a restricted opening in the tract. A port is connected to the restriction device. The port contains a working fluid for affecting the size of the restricted opening. A pressure sensing system communicates with the working fluid to measure the pressure of the working fluid. A transmitter communicates the measured fluid pressure to the external monitor.

A display apparatus may include touch detection circuitry including a light sensing circuit and a physical parameter sensing circuit (e.g., a pressure sensing circuit). The display apparatus may further include processing circuitry implementing a power-saving mode and a normal mode, and configured to generate touch information. An display driver may include a photo sensing circuit and a pressure sensing circuit. An embodiment of the display driver may include: an amplifying unit amplifying a photo sensing signal and a pressure sensing signal; a parallel-to-serial converting unit converting the amplified photo sensing signal and the amplified pressure sensing signal into serial sensing signals; and an analog-to-digital converter converting the serial sensing signals into digital sensing signals, wherein the amplifying unit, the parallel-to-serial converting unit, and the analog-to-digital converter operate in one of a normal mode and a power saving mode according to the pressure sensing signal.

A pressure sensing catheter having a pressure sensor and an antenna that is coupled to the pressure sensor, e.g., by a connector, are provided. The pressure sensor can be adapted to measure a pressure surrounding the catheter, and the antenna can be adapted to telemetrically communicate the measured pressure to an external device. In an exemplary embodiment, the antenna, pressure sensor, and / or connector are hermetically sealed, e.g., by the catheter and / or a coating, to prevent the antenna, pressure sensor, and connector from coming into contact with fluid, thereby allowing the catheter to be permanently implanted or otherwise used for long term use. Exemplary methods for manufacturing and using pressure sensing catheters are also provided.

An input system for a TV remote control or other system has a single touch surface with a deformable haptic assembly below the touch surface such that a user placing a finger on the touch surface can feel deformation of the haptic assembly. A pressure sensing assembly is below the haptic assembly and sensing motion of a finger on the touch surface, with a processor receiving input from the pressure sensing assembly and providing output to the haptic assembly in response. Also, a display receives input sent by the processor in response to input from the pressure sensing assembly to cause the display to present a changing image of a keypad as a user moves a finger on the touch surface.

An infusion device with a disposable administration set which is inexpensive to manufacture. In the preferred embodiment of the present invention the disposable administration set has a plurality of elongated cam followers connected to a plate assembly, wherein the cam followers are displaced in a predetermined sequence and forced against a delivery tube by cam means driven by rotary drive means. The disposable administration set is injection molded as a single integral piece. The disposable administration set includes adjustment spacers disposed between the plate assembly and the cam followers which adjust the distance between them to keep the device accurate. In the preferred embodiment of the present invention the cam assembly is configured to provide fluid delivery at a consistent and uniform rate. The device may also incude a pressure sensing pin positioned on the cam assembly which contacts the tubing during the pumping cycle. The drive current is sampled and processed at predetermined phases during the cam rotation cycle to detect the presence of an occlusion in the tubing.

A pressure sensing system for a seeding machine such as a planter to measure the down force on a planter row unit uses a wireless pressure sensor embedded in a load carrying wheel of the row unit. In a preferred embodiment, the pressure sensor is a passive piezoelectric pressure sensor that is a transmitter only, transmitting both pressure and RFID the information that identifies the particular sensor. Multiple sensors may be employed in each wheel and sensors may be employed in more than one wheel of the row unit, such as the gauge wheels on opposite sides of the trench opening disks. The sensors may be made of a PVDF, a known piezoelectric material. A wireless receiver is located on the planter frame or could be located elsewhere to receive the signals from the pressure sensor. A controller determines from the signal, any change in down force and commands the change to a down force generator on the row unit.

A device for creating a surgical perforation with a functional distal tip for creating a controlled perforation. The functional tip may comprise at least one active electrode for creating the perforation through the application of Radio Frequency (RF) energy. The device is curved in order to decrease the likelihood of injury to structures of a patient such as inadvertent cardiac perforation when used in transseptal perforation procedures. The device is introduced into the right atrium, and the functional tip is then positioned against the atrial septum. Energy is applied to create the perforation. The tip is advanced toward the left atrium to create the perforation and as it advances into the left atrium, the device takes on its curved shape to direct the tip away from cardiac structures. The position of the tip of the device can be determined in response to pressure sensed at the tip and determined by a monitor.

In one embodiment, a pressure sensing system is described which transmits data to a patient management system external to a patient. The pressure sensing system can rigidly couple to an implantable port or flexibly couple to an implantable port. In some embodiments, the pressure sensing system communicates with a hydraulic actuating system. In some embodiments, the pressure sensing system is implantable and comprises a circuit capable of wireless transmission through the skin of a patient to an external receiver which is part of a patient management system. A patient management system is described which receives up to date as well as historical data from the pressure sensing system and manages the these data in the context of a patient database.

The present invention relates to a pressure sensor module for use in catheters having a pressure sensor operable to provide a signal representative of pressure. The pressure sensor includes a sensing side and a pressure reference side. At least one signal transmission media is coupled to the sensor for transmitting the signal representative of pressure. A convex-shaped carrier is provided having a slot formed to expose the sensing side of the sensor. The convex-shaped carrier is adapted for receiving the sensor such that the sensing side of the sensor is adjacent the slot. A bonding material is provided for mounting the sensor to the carrier. The pressure sensing module provides ease of installation and manufacture because the module may easily be bonded and installed within a catheter.

An interactive display system comprising a touch sensitive display surface for sensing pressure applied thereto and in response generating control signals indicating locations of the applied pressure, a personal computer for receiving the control signals and in response generating graphic images, and an LCD panel in combination with an overhead projector for receiving and projecting the graphic images onto the touch sensitive display surface at the indicated locations. The LCD panel and overhead projector may be provided an integral unit.

An absolute pressure sensor includes a sense die with a reference chamber on a top side thereof. The reference chamber comprises a precisely fabricated beam that limits the travel of a diaphragm. The beam can be positioned in a cap or cover member of the sense die, thereby allowing the sense die diaphragm to move freely for a particular distance. Over this distance, the sense die will have one sensitivity. When the sense die is pressurized to a certain point, the diaphragm moves until it contacts the beam member in the cap or cover. When the diaphragm hits the beam, the sensitivity of the sense die changes, thereby allowing a smaller voltage out for the greater pressure in. Such an arrangement permits the sensor to provide a function that accurately measures low pressure and measures a higher pressure without utilizing a linear scale.