1931 results about "Fluid administration" patented technology

An infusion medium delivery system, device and method for delivering an infusion medium to a patient-user, includes a needle inserter device and method for inserting a needle and/or cannula into a patient-user to convey the infusion medium to the patient-user. The needle inserter device and method operate to insert a needle and cannula into a patient-user's skin and automatically withdraw the needle from the patient-user, leaving the cannula in place and in fluid flow communication with a reservoir. The delivery device may include a base portion and a durable portion connectable to the base portion, and wherein the base portion can be separated from the durable portion and disposed of after one or more specified number of uses. The base portion supports the reservoir and the needle inserter device, while the durable portion supports a drive device for selectively driving the infusion medium out of the reservoir and into the needle and/or cannula.

A pharmacodynamic (PD), pharmacokinetic (PK), or both and PK guided infusion device, system and method optimizes the safety and efficacy of various forms of treatment or therapy (e.g., drug and/or fluid) in a variety of health-care and other settings.

An infusion set having an infusion part for insertion into a patient and a connector for connecting the infusion part with a medical device through a tube is provided. The connector is axially displaceable relative to the infusion part. The infusion part includes an adhesive support, a base part with a first set of guiding means and at least two retention devices for locking the connector to the infusion part, a cannula extending from the base part and being in fluid communication with a cavity. The cavity is further adapted to receive a second cannula extending from the connector where the second cannula is in fluid communication with the tube. The infusion set further includes a second set of guiding means that are adapted to fit with the first set of guiding means and at least two arms. The retention devices extend from an upper surface of a main surface of the base part and the arms include means corresponding to the retention members.

A system and user interface according to invention principles supports concurrently managing and maintaining multiple medical devices (e.g., infusion pumps) and processing and displaying the data produced by the medical devices within a Healthcare enterprise. An information system supports a plurality of network connected infusion pumps. The system includes an acquisition processor for acquiring fluid infusion related data from a plurality of concurrently operating infusion pumps. A data processor processes the acquired fluid infusion related data to provide data suitable for presentation in a single display image identifying the plurality of concurrently operating infusion pumps together with status information identifying status of individual pumps of the plurality of concurrently operating infusion pumps.

Tilting of a drip chamber from its vertical axis during fluid administration can have negative effects upon the accuracy of systems configured for drop counting and/or for volumetric measurement of individual drops passing through the drip chamber. To address these negative effects, in accordance with one embodiment of the present disclosure, a fluid delivery system engages in a fluid control process that comprises determining an error parameter, based at least in part on a tilt signal, generating an error condition, and either holding the fluid flow at the present rate or stopping the flow.

Tilting of a drip chamber from its vertical axis during fluid administration can have negative effects upon the accuracy of systems configured for drop counting and/or for volumetric measurement of individual drops passing through the drip chamber. To address these negative effects, in accordance with one embodiment of the present disclosure, a fluid delivery system that measures the flow volume of a fluid delivery system is disclosed, which includes an imaging apparatus that captures a first image of a drip chamber while a drop is falling therein and a second image of the drip chamber with no drop. Portions of each image that are in substantially the same position in each image are subtracted.

A valve connector for medical infusion lines including an external tubular body with an inlet end and an outlet end, an internal hollow spike and an intermediate sealing member including a head with pre-slit and an elastic hollow element formed with fluid-tight members in contact with the hollow spike and with an elastic thrust means, which tends to maintain the elastic head in a closed condition. The elastic thrust means comprises a base part joined to the elastic hollow element of the sealing member through a generally transverse annular wall, which, during axial displacement of the elastic head from the closed condition to the open condition, bends within an annular chamber defined between the base part and a portion with conical surface of the hollow spike.

A patient hydration system with a patient urine output measurement device, a hydration fluid administration subsystem, and a controller, responsive to the patient urine output measurement device. The controller is configured to control the hydration fluid administration subsystem to administer hydration fluid to the patient to prevent dehydration of the patient. A hydration sensor is also included to detect at least one patient parameter indicative of the patient's hydration state.

A catheter system and method is provided for overcoming various problems commonly associated with the application of regional anesthesia. Disclosed herein are several embodiments for providing continuous regional anesthesia. In general, the catheter system includes an epidural catheter, an epidural needle, tubing for optional fluid administration, an attached conductive wire (for connection to a nerve stimulator) and a catheter introducer, which is integrated within the proximal hub of the insulated needle. The embodiments may differ in several ways.

A patient hydration system with a first infusion subsystem for infusing a patient with fluid from a first source and a second infusion subsystem for infusing a patient with fluid from a second source. A urine output measurement subsystem determines the amount of urine output by the patient. A controller is responsive to the first infusion subsystem, the second infusion subsystem, and the urine output measurement subsystem and is configured to control the first infusion subsystem based on the amount of urine output by the patient and/or the amount of infused fluid measured by the second infusion subsystem.

The present invention concerns a housing for supporting the proximal inlet ports of at least two isolated lumens, for use in a patient fluid administration system, wherein each of the lumens further comprises a distal outlet for connecting to at least one patient fluid administration member, and wherein the housing further comprises an integral unit, wherein the unit comprises a distal frame layer, a female connector layer, for connecting to at least one of the fluid peripheral elements and at least one intermediate gasket layer for providing sealing between each of the isolated lumens.

A system extrapolates and interpolates patient fluid intake or output parameter values and associated cumulative values over variable time intervals from a reduced set of stored fluid parameter values affecting fluid cumulative volume computation or rate of fluid intake or output computation. The extrapolation and interpolation function accomodates drip (continuing) fluid volumes as well as supplemental (non-continuing e.g., bolus) fluid volumes. A patient medical parameter data processing system provides patient medical parameter data for trend indicative display covering a time period comprising user selectable patient parameter acquisition time intervals. The system includes an acquisition processor for receiving data identifying, for a continuing infusion, rate of volume of fluid infusion into a patient, a fluid type identifier and a start time and start date of said continuing infusion. The received data also identifies for a non-continuing infusion, a total volume of fluid infusion, a fluid type identifier and a time and date of the non-continuing infusion. A data processor determines, from the received data, a cumulative total volume infusion of a particular fluid into a particular patient for a particular user selectable patient parameter acquisition time interval.

Systems, devices and methods for sensing physiologic data and draining and analyzing bodily fluids are described which are capable of sensing physiologic data based on sensors incorporated into a catheter adapted to reside in any of a urinary tract, gastrointestinal tract, rectal location, pre-peritoneal, pleural space or other body cavity. The devices aid emptying of the bladder, measure urine output and various urine parameters such as oxygen tension, urine conductance and urine specific gravity, monitor renal function, analyze urine parameters, including urine content, including the presence of infection, and track and/or control fluid administration.

A handpiece assembly is provided that is adapted for use with a medication infusion system that applies pressure to the handpiece assembly for delivering medication to a body. The handpiece assembly includes a cartridge holder that is configured for disposal of a medication cartridge. A tubing is provided having a first end, which is sealed with the cartridge holder such that the cartridge holder facilitates communication between the tubing and the medication cartridge. A handpiece is sealed with a needle and the second end of the tubing so that the tubing and the needle are in communication. One of the cartridge holder, the tubing, the needle or the handpiece is configured for a selective structural failure at a predetermined pressure threshold applied to the handpiece assembly from the medication infusion system. The cartridge holder may be designed to facilitate aspiration.

An elastomeric bladder stored energy type infusion apparatus that can be filled with a medicinal fluid and, after being filled, can efficiently delivery the medicinal fluid to the patient at a selected rate. The apparatus includes a delivery component for delivering medicinal fluid to the patient and a fill component that can expeditiously be used to fill the fluid reservoir of the delivery component in the field.

An automatic stop valve formed in a container of a medical fluid administration system includes an electrical field that attracts the float and valve seat together to shut off flow from the exit port of the container when the fluid within the container is reduced to a predetermined level. One or both of the float and valve seat creates an electric field that attracts the other, which is made of a non-magnetic dielectric, into engagement. In one embodiment, the valve seat is formed of an electret that creates the electric field attracting the float to it to stop flow. In another embodiment, the float comprises an electret that attracts the float to the dielectric valve seat. In yet another embodiment, both the float and valve seat include electrets of opposite polarity that attract each other into engagement. The lack of magnetic and metallic materials makes the shut off valve suitable for use in an MRI environment.

The invention relates to a micro-needle array chip, a transdermal delivery device, a transdermal delivery patch and a preparation method thereof, wherein a micro-needle is obliquely fixed on a substrate at a set angle, the upper surface of the needle is an elliptic plane parallel to the substrate or obliquely provided with an acute angle, the needle is further treated to have more edge angles, a metal wire bar or tube penetrates a non-metallic material substrate such as polymer and the like along a certain angle, and then a nick of the metal wire bar or tube on the substrate is grinded and polished; and photosensitive resist patterns are formed nearby the nick at one end by adopting photoetching and etching technology, then the metal wire bar or tube is subjected to chemical or electrochemical corrosion to form a needle point and the photosensitive resist is removed, the surface of the manufactured solid micro-needle array chip can be covered with drugs, and the manufactured solid micro-needle array chip can deliver liquid medicine or extract body fluid. The method avoids the skin plugging a transfusion hole, is easy to adjust and control the maximum penetrating depth of the micro-needle, and is suitable for percutaneous transportation of biological macromolecular drugs and cosmetics and skincare and new percutaneous preparation of the prior drugs.