Patent application number | Description | Published |
20090143726 | MEANS FOR USING SINGLE FORCE SENSOR TO SUPPLY ALL NECESSARY INFORMATION FOR DETERMINATION OF STATUS OF MEDICAL PUMP - A medical pump, for use with a cassette having a pumping chamber, includes a pumping element with a piston slider assembly which intermittently pressurizes the pumping chamber during a pumping cycle and has a piston head connected to a main body with a single pressure sensor positioned there between. A camshaft is associated with the pumping element, an inlet control element, and an outlet control element for closing the pumping chamber to flow when the pumping chamber is pressurized. A processing unit receives pressure and position data from the pressure sensor and a position sensor associated with the pumping element, and processes this data to determine the operating condition of the pump. The operating conditions determined include: blocked fluid flow, no fluid in the line, no cassette associated with the pump, proper pump priming, or proper valve sealing. | 06-04-2009 |
20090143727 | MEANS FOR USING SINGLE FORCE SENSOR TO SUPPLY ALL NECESSARY INFORMATION FOR DETERMINATION OF STATUS OF MEDICAL PUMP - A medical pump, for use with a cassette having a pumping chamber, includes a pumping element with a piston slider assembly which intermittently pressurizes the pumping chamber during a pumping cycle and has a piston head connected to a main body with a single pressure sensor positioned there between. A camshaft is associated with the pumping element, an inlet control element, and an outlet control element for closing the pumping chamber to flow when the pumping chamber is pressurized. A processing unit receives pressure and position data from the pressure sensor and a position sensor associated with the pumping element, and processes this data to determine the operating condition of the pump. The operating conditions determined include: blocked fluid flow, no fluid in the line, no cassette associated with the pump, proper pump priming, or proper valve sealing. | 06-04-2009 |
20090144025 | METHOD FOR DISCRIMINATING BETWEEN OPERATING CONDITIONS IN MEDICAL PUMP - A method is disclosed for determining the operating condition of a medical pump based on data derived from a pressure sensor and a position sensor. The pressure sensor generates pressure data by sensing the force on the pumping element. The position sensor generates position data by tracking the pumping cycle and determining the position of the pumping element. The pump pressure data and pump position data are processed and the calculated results compared with a pre-determined threshold value to determine the operating condition of the pump. The three main types of operating conditions of concern are the following: normal condition, where liquid is present and no leaks exist in pumping chamber; leak condition, where liquid is present but a leak exists in the pumping chamber; and air stroke condition, where the chamber contains some air. | 06-04-2009 |
20090144026 | METHOD FOR DISCRIMINATING BETWEEN OPERATING CONDITIONS IN MEDICAL PUMP - A method is disclosed for determining the operating condition of a medical pump based on data derived from a pressure sensor and a position sensor. The pressure sensor generates pressure data by sensing the force on the pumping element. The position sensor generates position data by tracking the pumping cycle and determining the position of the pumping element. The pump pressure data and pump position data are processed and the calculated results compared with a pre-determined threshold value to determine the operating condition of the pump. The three main types of operating conditions of concern are the following: normal condition, where liquid is present and no leaks exist in pumping chamber; leak condition, where liquid is present but a leak exists in the pumping chamber; and air stroke condition, where the chamber contains some air. | 06-04-2009 |
20100216563 | SYSTEM FOR DETERMINING PERFORMANCE CHARACTERISTICS OF A GOLF SWING - An instrumented golf club system and methods are disclosed. A variety of golf swing parameters are measured by the instrumented golf club and wirelessly transmitted to a portable computer device. The portable computer device generates a user interface that displays the golf swing parameters against preferred golf swing parameters. The instrumented golf club system allows a golfer to receive feedback in real time while playing golf. | 08-26-2010 |
20100216564 | SYSTEM FOR DETERMINING PERFORMANCE CHARACTERISTICS OF A GOLF SWING - An instrumented golf club system and methods are disclosed. A variety of golf swing parameters are measured by the instrumented golf club and wirelessly transmitted to a portable computer device. The portable computer device generates a user interface that displays the golf swing parameters against preferred golf swing parameters. The instrumented golf club system allows a golfer to receive feedback in real time while playing golf. | 08-26-2010 |
20100216565 | SYSTEM FOR DETERMINING PERFORMANCE CHARACTERISTICS OF A GOLF SWING - An instrumented golf club system and methods are disclosed. A variety of golf swing parameters are measured by the instrumented golf club and wirelessly transmitted to a portable computer device. The portable computer device generates a user interface that displays the golf swing parameters against preferred golf swing parameters. The instrumented golf club system allows a golfer to receive feedback in real time while playing golf | 08-26-2010 |
20120074330 | Device and Method for Determining Activity of Radiopharmaceutical Material - A detector system measures radioactive material. A fluid path receives at least one aliquot of radiopharmaceutical. The fluid path locates the aliquot within a positioner formed with a concave configuration. A detector is located at an axial distance from the concave surface and determines the level of radioactivity of the aliquot. Alternatively, the fluid path may be less concave and a variable attenuator may be placed between the fluid path and detector. The variable attenuator may have a concavity that is based on the concavity of the fluid path so that the detector's ability to read the radioactivity is optimized. A method for forming an aliquot of radiopharmaceutical in a concave fluid passage. Positioning a detector located a distance from the concave surface to optimize reading spectral energy of the aliquot and activity is determining activity regardless of the position of the aliquot in the passage. | 03-29-2012 |
Patent application number | Description | Published |
20090082646 | ACCESS DISCONNECT DETECTION SYSTEM - An access site disconnection system and method are disclosed. Radio frequency transmitters and receivers are placed near an access site. When a patient receives dialysis treatment, wetness may arise from blood if the access needle becomes disconnected from the access site. Radio-frequency transmitters are mounted on or near gauze or other absorbent material placed adjacent the access site, as are radio-frequency receivers. After the sensors are placed, the dialysis machine and radio-frequency control circuit may be initialized or baselined, and dialysis treatment, such as hemodialysis, begun. If blood leaks from the access site, such as if the access needle is dislodged, the blood attenuates the radio frequency transmissions, which are detected by the receivers. A signal is sent to a controller or to an output device to raise an alert or sound an alarm. | 03-26-2009 |
20090088612 | ACCESS DISCONNECT DETECTION - Techniques are disclosed for monitoring the flow of blood returning to a patient from an extracorporeal therapy machine, such as a hemodialysis machine or an apheresis machine. Blood returning from such a machine is pumped, typically by a peristaltic pump, which returns the blood in pulsed flow or pulses. This flow can be sensed by Doppler flow sensors or accelerometers as it returns to the patient. If the flow is interrupted by dislodgement of the venous access needle, or by leaking of blood from the needle, these sensors will detect significantly different flow or vibrations. A controller can then cease therapy, alert a caregiver, or sound an alarm. | 04-02-2009 |
20120259284 | ACCESS DISCONNECT DETECTION SYSTEM - An access site disconnection system and method are disclosed. Radio frequency transmitters and receivers are placed near an access site. When a patient receives dialysis treatment, wetness may arise from blood if the access needle becomes disconnected from the access site. Radio-frequency transmitters are mounted on or near gauze or other absorbent material placed adjacent the access site, as are radio-frequency receivers. After the sensors are placed, the dialysis machine and radio-frequency control circuit may be initialized or baselined, and dialysis treatment, such as hemodialysis, begun. If blood leaks from the access site, such as if the access needle is dislodged, the blood attenuates the radio frequency transmissions, which are detected by the receivers. A signal is sent to a controller or to an output device to raise an alert or sound an alarm. | 10-11-2012 |
20130015361 | RADIOPHARMACEUTICAL CZT SENSOR AND APPARATUS - A gamma ray detector includes a gamma ray detecting rod elongated along a longitudinal axis, wherein gamma ray detection is enhanced along the longitudinal axis, and a gamma ray shield encapsulating the rod, the shield having an aperture at an end of the detecting rod along the longitudinal axis to admit gamma rays substantially parallel to the longitudinal axis of the elongated detecting rod, wherein gamma ray detection is enhanced along the longitudinal axis and aperture to substantially collimate the sensitivity of the gamma ray detector along the combined aperture and longitudinal axis of the detecting rod. | 01-17-2013 |
20130022525 | METHODS AND COMPOSITIONS FOR DRYING IN THE PREPARATION OF RADIOPHARMACEUTICALS - A method of drying a radioisotope solution having radioisotopes includes passing the radioisotope solution through a solid phase extraction column containing an anion exchange group, thereby trapping the radioisotopes in the column. The method also includes passing an eluent through the column, thereby removing the radioisotopes from the column. The eluent includes a cation trapping agent/salt complex, less than 4% water, and the remainder is a solvent. A method of producing the eluent includes reacting a cation trapping agent with a salt in the presence of less than 4% water and a solvent to form solubilized cation trapping agent/salt complex, wherein one of the cation trapping agent and the salt is present in en excess of a stoichiometric amount and ending the reaction when a predetermined amount of solubilized cation trapping agent/salt complex has been formed. | 01-24-2013 |
20130102772 | SYSTEMS, METHODS AND DEVICES FOR PRODUCING, MANUFACTURING AND CONTROL OF RADIOPHARMACEUTICALS-FULL - Systems, methods, and devices for generating radionuclides for use in production of radiopharmaceuticals; synthesizing the radionuclides generated and removing any unwanted products; measuring the quantity and activity level of the synthesized radionuclides; distributively delivering the radionuclides in appropriate quantities to modular cassette synthesis units in a modular cassette subsystem for contemporaneous/parallel production of radiopharmaceutical output and that allow reuse and/or quick, safe, and disposable replacement of portions of the subsystem; delivering non-radionuclide components to the modular cassette synthesis units as part of production of radiopharmaceutical output; measuring the quantity and activity level of each stream of radiopharmaceutical output; purifying the radiopharmaceutical output; dispensing individual doses in sterile vial(s); automatically producing labeling and dose related information; performing automated quality control on extracted samples of produced radiopharmaceutical output; and providing software and hardware controls for overall and sub-portion operation for optional remote data collection, communication, and/or control. | 04-25-2013 |
20130124103 | Radiopharmaceutical Concentration Measurement System and Method - The system for measuring the radioactive concentration of a radiopharmaceutical includes a container, an interrogation region, a radiation detector, a signal capture device and microprocessor system. The interrogation region associated with the container. The radiation detector to focus detecting radiation emitted from the interrogation region. The signal capture device capable of obtaining a radiation measurement of the interrogation region. The microprocessor system in data communication with the signal capture device. The microprocessor system is capable of calculating a radioactive concentration of a radiopharmaceutical emitting radiation contained in the interrogation region from the signal capture device. | 05-16-2013 |
20130274599 | SYSTEMS FOR DETECTING FLUID CHANGES AND SENSOR DEVICES THEREFOR - A sensor device for detecting a change in fluid level within body tissue comprising a housing with bridge segments connecting at intersections arranged to circumscribe an opening. Further, antenna elements are partially seated within the housing at intersections of bridge segments, comprise a generally planar antenna mounted to a substrate material at a base of the planar antenna, and an electrical shield surrounding the substrate. Also, an outer surface of the planar antenna faces away from the substrate. The antenna elements comprise at least first and second antenna element pairs having transmitting and receiving antenna elements and a bridging segment. A high sensitivity zone is formed between the transmitting antenna and receiving antenna. The antenna element pairs are spaced to create an area of reduced sensitivity between the high sensitivity zones, and the space is set so that the sensor is insensitive to fluid changes of a predetermined volume. | 10-17-2013 |
20140371588 | DISTRIBUTED EXTRAVASATION DETECTON SYSTEM - A system and method enhance clinical effectiveness for monitoring for a change in a level of fluid in tissue by using a device attached to a body portion that wirelessly reports to a remote apparatus or receiver a current received power level for indications of extravasation or infiltration. Adjusting an activation rate of fluid detection, reporting or both extends service life of the device. | 12-18-2014 |
20150011876 | WIRELESS AND POWER-SOURCE-FREE EXTRAVASATION AND INFILTRATION DETECTION SENSOR - A system detects extravasation or infiltration by segregating active components that drive a passive sensor for economical single use. A receiving antenna of the passive sensor receives antenna for receiving a transmitted signal comprising RF electromagnetic power. A first circuit transmits a first portion of the received signal through a body portion. A sensor detects a resultant signal from the body portion. A second circuit combines a reference signal comprising a second portion of the received signal with the resultant signal so as to define an output signal. A transmit antenna transmits the output signal to a receiver. | 01-08-2015 |