An infusion device includes a safety metric sensor. The infusion device is configured to operate in a default safety mode, where operating in the default safety mode includes monitoring, via the safety metric sensor, an infusion therapy for compliance with a safety metric indicating a property of a fluid path between a fluid container and a fluid administration site. The infusion device is also configured to connect, while operating in the default safety mode, with an external safety device that is configured to monitor the safety metric. Additionally, the infusion device is configured to determine, based on the connection with the external safety device, that the external safety device is monitoring the safety metric. Further, the infusion device is configured to switch, responsive to determining that the external safety device is monitoring the safety metric, from operating in the default safety mode to operating in an adjusted safety mode.
A system for reducing twisting of medical tubing includes a spinning component and a tubing connector. The spinning component includes a first fluid channel and a protrusion, and the tubing connector includes a second fluid channel, male mating portion, and a sheath. Accordingly, the spinning component is configured to couple to the tubing connector such that the first fluid channel and the second fluid channel together form a unified fluid channel, the first fluid channel encompasses the male mating portion, the protrusion is positioned within a recess of the sheath, and the spinning component is rotatable relative to and independently of the tubing connector.
An intelligent control device provides an option to select a medical procedure and receives a selection of the medical procedure. The intelligent control device also operates an infusion device to administer a medication at a first rate. Further, the intelligent control device identifies a set of events associated with the selected medical procedure, including a procedural event expected to cause a physiological change for which an administration of the medication is prescribed. Moreover, the intelligent control device determines that the procedural event is about to occur based on the infusion information, the physiological information, or the selected medical procedure. After determining that the procedural event is about to occur, and before the procedural event occurs, the intelligent control device prompts an operator to cause an adjustment of the infusion device to administer the medication at a second rate; or the intelligent control device causes the adjustment of the infusion device.
G16H 20/17 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered via infusion or injection
G16H 20/40 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to mechanical, radiation or invasive therapies, e.g. surgery, laser therapy, dialysis or acupuncture
G16H 40/63 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for local operation
A61B 5/00 - Measuring for diagnostic purposes ; Identification of persons
4.
PIVC-INTEGRATED HEMOLYSIS-REDUCTION ACCESSORIES FOR DIRECT BLOOD DRAW ON MULTIPLE NEEDLE GAUGES
A fluid connector device for a blood collection system is disclosed. In order to be safely used with different gauges, the fluid connector device can regulate blood flow therethrough based upon the catheter gauge. For example, when 18-to-22-gauge catheters are used, the fluid connector device regulates the blood flow by positioning a slider assembly (within the fluid connector device) to a setting that allows a single channel to transmit blood through the fluid connector device into a fluid inlet and out of a fluid outlet of the fluid connector device. Alternatively, in another example, when 24-gauge (or greater) catheters are used, the slider assembly can be actuated to a new position, which allows multiple channels to transmit blood into the fluid inlet and out of the fluid outlet. By regulating blood flow, the fluid connector device can limit or prevent hemolysis, while being universally used with different catheters.
A61B 5/153 - Devices for taking samples of blood specially adapted for taking samples of venous or arterial blood, e.g. by syringes
A61B 5/154 - Devices for taking samples of blood specially adapted for taking samples of venous or arterial blood, e.g. by syringes using pre-evacuated means
A flow restriction device includes a proximal housing configured to couple to a fluid collection device, a distal housing configured to couple to a catheter assembly, an intermediate housing interposed between the proximal housing and the distal housing and an internal fluid channel extending transversely therethrough. The flow restriction device also includes a fluid shield assembly having an enclosure coupled to an end of the distal housing and a split septum coupled to an end of the enclosure, the split septum comprising a flexible material with a centrally disposed slit. The fluid shield assembly provides for connection of a female connector to a male connector of the distal housing through the slit of the split septum, and to contain fluid within the enclosure and split septum upon disconnection and withdrawal of the female connector from the male connector. Blood collection systems and fluid shield assemblies are also provided.
A61B 5/153 - Devices for taking samples of blood specially adapted for taking samples of venous or arterial blood, e.g. by syringes
A61B 5/154 - Devices for taking samples of blood specially adapted for taking samples of venous or arterial blood, e.g. by syringes using pre-evacuated means
A61M 39/06 - Haemostasis valves, i.e. gaskets sealing around a needle, catheter or the like, closing on removal thereof
A61M 39/26 - Valves closing automatically on disconnecting the line and opening on reconnection thereof
6.
INTRAVENOUS SET WITH PUMP INTERFACE FOR RAPID INFUSION VIA REUSABLE DRIVER
An IV infusion set includes at least one infusion component, a first IV tube coupled to the infusion component, a second IV tube and a disposable pump head that. The pump head includes an inlet port coupled to the first IV tube, an outlet port coupled to the second IV tube and a drive interface configured to be coupled to a first end of a drive shaft. The drive interface is configured to be rotated by rotation of the drive shaft having a second end coupled to a driver to increase a fluid flow rate through the IV infusion set. IV set assemblies and methods of use are also provided.
Fluid connector systems including first and second connector portions couplable together to form a fluid pathway therethrough, and can resist fluid flow through the connector when the connector portions are separated from each other. A connector portion can include a connector housing, a luer portion, and a deformable valve member. The deformable valve member is disposed within the connector housing and includes a spherical portion extending partially through a valve opening of the connector housing. The spherical portion defines a slit, and the deformable valve member is configured to selectively prevent fluid flow from the housing volume through the valve opening and to deform to expand the slit and permit fluid flow from the housing volume through the valve opening.
Activatable medicament delivery containers and assemblies are disclosed that can be activated to direct a medicament from the container using an expandable material that causes an expansion chamber to displace the medicament from the container, where the medicament can be directed from the container at a predetermined or use-specific rate, and for a predetermined period of time, and the container being couplable with a dock to form an activatable medicament delivery assembly, where the container can be removably coupled or replace with the dock, and where the dock can be coupled directly to an intravenous fluid delivery device.
Pump assemblies for use with an IV set are described herein. A pump assembly includes a rotatable crank, a piston rod, and a diaphragm assembly. The crank includes a crank profile defining a plurality of lobes. The piston rod includes a first follower and a second follower spaced apart from the first follower. The rotation of the crank relative to the piston rod causes the piston rod to reciprocate relative to the crank. The diaphragm assembly includes a housing and a diaphragm member. The diaphragm member is coupled to the housing and cooperatively defines a volume in fluid communication with the IV set. The diaphragm member is movable between an extended position configured to draw in fluid from the IV set and a contracted position configured to expel fluid into the IV set. The diaphragm member is coupled to the piston rod to reciprocate the diaphragm member.
A single use disposable elapsed time indicator and methods for using same include an indicator that can have a flexible chamber for holding an aqueous medium and a slot with a viewing window and a longitudinal axis. The slot is connected to the chamber via a passage having a breakable seal therein. An absorbable material is located within and at a first end of the slot that swells upon exposure to the aqueous medium. A graded scale is also included along the longitudinal axis of the slot to indicate periods of elapsed time. The absorbable material is configured to expand from the first end of the slot toward an opposing end of the slot along the longitudinal axis and thereby mark elapsed time on the graded scale.
G04F 1/00 - Apparatus which can be set and started to measure-off predetermined or adjustably-fixed time intervals without driving mechanisms, e.g. egg timers
G04F 13/06 - Apparatus for measuring unknown time intervals by means not provided for in groups using fluidic means
A fluid-fitting tool is disclosed that can align with and rotationally couple with a fluid fitting where the fluid-fitting tool can include a passage and an engagement feature for engaging against the fluid fitting such that when the fluid-fitting tool is spaced apart from the fluid fitting, the fluid-fitting tool can move in a longitudinal direction toward and away from the fluid fitting, and can rotate relative to the fluid fitting around a longitudinal axis of the passage, and when a portion of the fluid-fitting tool and the fluid fitting are rotationally aligned and longitudinally overlap, the fluid-fitting tool can move longitudinally relative to the fluid fitting, and the fluid fitting is rotated when the fluid-fitting tool is rotated around a longitudinal axis of the passage.
A first venous rhythm of a patient is detected above a venous insertion site when a venous catheter connected to an infusion set is inserted into the venous insertion site and, concurrently with the first venous rhythm, a second venous rhythm is detected at a location remote from the venous insertion site. An irregularity between the first and second venous rhythms is identified, and a failure of the venous catheter is determined based on the identified irregularity satisfying a irregularity threshold. An alarm may be provided on detecting the irregularity or the failure of the venous catheter.
A61M 5/168 - Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters
A61M 5/172 - Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters electrical or electronic
A61M 5/46 - Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm rests having means for controlling depth of insertion
Needleless connectors are described herein. A needleless connector includes a housing and a flexible valve element. The housing includes a cavity, a proximal fluid port in fluid communication with the cavity, and a distal fluid port in fluid communication with the cavity. The flexible valve element is disposed within the cavity. The flexible valve element can selectively permit flow between the proximal fluid port and the distal fluid port.
A single use disposable elapsed time indicator and methods for using same can include an indicator having a chamber and a longitudinal channel for receiving a volatile fluid. A sponge is located and seated in the longitudinal channel and configured to allow evaporation of volatile fluid from within the longitudinal channel to an exterior of the longitudinal channel. A spring is included in the longitudinal channel which presses against an end of the chamber and against a plunger that is seated and moveable in the longitudinal channel along a longitudinal axis thereof. The spring is configured to exert force on and move the plunger from a first end of the chamber toward a second end of the chamber along the longitudinal axis in the longitudinal channel as volatile fluid in the longitudinal channel evaporates through the sponge. The movement of the plunger thereby marks elapsed time along a graded scale.
G04F 1/02 - Apparatus which can be set and started to measure-off predetermined or adjustably-fixed time intervals without driving mechanisms, e.g. egg timers by consuming prefixed quantities of materials, e.g. by burning candle
G04F 13/06 - Apparatus for measuring unknown time intervals by means not provided for in groups using fluidic means
15.
HEMOLYSIS-REDUCTION EXTENSION SET FOR DIRECT BLOOD DRAW
A flow restriction device may include a male luer connector portion, a female luer connector portion, and a flexible tube. The male luer connector portion defies a first lumen. The female luer connector portion defines a second lumen. The flexible tube defines a third lumen. The third lumen is in fluid communication with the first lumen and the second lumen. The third lumen has a diameter of about 0.02 inches.
A stable flow regulator assembly includes a body having a tube slot adjacent a perimeter of the body and having an opening at the perimeter to slidingly receive a portion of an intravenous (IV) tube, and a spiral slide groove extending into the body from the tube slot, wherein a width of the spiral slide groove narrows as the groove extends further into the body. A tube arm is rotatingly coupled to the body, the tube arm having a slot open to the perimeter of the body and configured to slidingly receive the IV tube when the slot is aligned with the tube slot of the body and to regulate a flow rate through the IV tube based on the compression of the IV tube due to a position of the IV tube within the spiral slide groove. Methods of operating a stable flow regulator assembly are also provided.
The disclosed device, system and method manages medication delivery failures. An effective therapeutic range of a patient physiological property is determined based on a pharmacokinetic profile of a medication. During an administration of the medication to the patient, an expected trend in the measured physiological property is determined based on sensor data, the pharmacokinetic profile of the medication, a dose of the medication provided to the patient, and the at least one physical property of the patient, and an infusion device is caused to adjust the dose of the medication to cause the physiological property to follow the expected trend. Responsive to determining that a current trend in the physiological property has deviated from the expected trend, and will fall outside the effective therapeutic range within a predetermined time period, a delivery failure is determined and an alarm is provided.
A dual chamber single-hand pump is described that includes a pump chamber with four fluid pathways. Two pathways are configured to conduct fluid to the chamber and to stop flow therethrough from the chamber, and two pathways are configured to conduct fluid from the chamber and to stop flow therethrough to the chamber. A piston positioned and moveable within the chamber separates two of the pathways from the other two pathways within the chamber. The pump can be held in a single hand by having finger grips for stabilizing the pump and a palm grip for advancing the piston. A return spring can return the piston to the original position when the palm is relaxed to allow expansion of the spring.
An infusion device control system intercepts a first command provided to a first infusion pump by a closed-loop control algorithm, the first command configured to adjust delivery of a first fluid by the first infusion pump according to sensor measurements provided to the closed-loop control algorithm. The control system receives a therapy target control parameter for modifying the delivery of the first fluid based on a real time parameter for delivering a second fluid by a second infusion pump, receives real time operating parameters and infusion status information associated with the first and second infusion pumps, and modifies the intercepted first command based on the real time operating parameters and infusion status information and the therapy target control parameter to control an effect of the deliveries of the first and second fluids, without providing input for modifying the intercepted first command to the closed-loop control algorithm.
G16H 20/17 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered via infusion or injection
G16H 40/63 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for local operation
G16H 40/67 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for remote operation
Fluid connector systems that can include first and second connectors that are couplable together to form a fluid pathway through the fluid connector system when the first and second connectors are coupled together, and can resist fluid flow through each of the first and second connectors when the first and second connectors are separated from each other, where the first and second connectors can include a valve within a channel and configured resist fluid flow through the respective first or second connector in an closed position and to reduce the resistance to fluid flow through the first or second connector in an open position, and the first and second connectors including one or more arm configured to engage each other to form a snap fitting feature that can resist separation therebetween.
A fluid flow disconnect sensor and alarm system includes first and second sensor units configured to be removably coupled to a first and second portions of a fluid connector assembly, respectively. The first sensor unit comprises a sensor configured to sense when the second sensor unit is within a threshold distance of the first sensor unit, and comprises a transmitter configured to transmit, to a device remote from the first and second sensor units, an indication regarding whether the first and second portions of the fluid connector assembly are coupled together responsive to the sensing. A computing device receiving the indication determines when the first and second portions of the fluid connector assembly are coupled together, and when the assembly becomes disconnected, and may generate an alarm when the first and second portions become disconnected.
A method for medical device resource management includes monitoring a plurality of medical devices for adjustments to the medical devices during a period of time; identifying, based on the monitoring, the adjustments to the plurality of medical devices during the period of time; building a therapy profile associated with a patient and the medical devices based on the identified adjustments; identifying an adverse event pertaining the patient or a respective medical device of the plurality of medical devices; and after identifying the adverse event: generating, based on the therapy profile, a plurality of consecutive control signals to correct the adverse event, each being associated with a different one of the medical devices or a different user.
G16H 20/17 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered via infusion or injection
G16H 40/40 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the management of medical equipment or devices, e.g. scheduling maintenance or upgrades
G16H 40/67 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for remote operation
G16H 50/20 - ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for computer-aided diagnosis, e.g. based on medical expert systems
A61B 5/00 - Measuring for diagnostic purposes ; Identification of persons
A coupling device that is removably couplable with a mating connector is disclosed where the coupling device can include a housing and another structure that is movable relative to the housing such as an inner body or a cuff, and in a first configuration, the coupling device resists separation between the coupling device and a mating connector, in a second configuration, the resistance to separation between the mating connector and the coupling device is reduced relative to the first configuration such that the coupling device can permit separation between the coupling device and the mating connector when any of the inner body or the cuff is moved, biased, and/or flexed, and where the coupling device can be re-coupled with a mating connector after separation between the coupling device and the mating connector.
A syringe pump includes a receptacle for receiving a syringe and a drive head for advancing the plunger of the syringe within the syringe's barrel. The syringe pump also includes a processor. The processor is configured to receive a programmed flow rate. The processor is also configured to detect an extension of the syringe, the extension including a distance between a starting position of the plunger within the barrel and a current position of the plunger within the barrel. Additionally, the processor is configured to estimate an amount of friction between the plunger and the barrel based on the programmed flow rate and the detected extension. Further, based on the estimated amount of friction, the processor is configured to adjust an occlusion-detection operation of the syringe pump or adjust an operating speed of the drive head.
A method may include receiving a selection of an order associated with a patient. A scannable token, such as a barcode, may be generated for interacting with one or more medical devices involved in a patient encounter to fulfill the order. In some cases, the same scannable token may be further associated with one or more additional patient encounters associated with the same patient or different patients and conducted by a same clinician or different clinicians. The scannable token may be sent to a client device. In response to the scannable token being scanned at the one or more medical devices, at least a portion of information associated with the order may be sent to the one or more medical devices. Related methods and articles of manufacture are also disclosed.
G16H 20/13 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered from dispensers
G16H 20/17 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered via infusion or injection
G16H 40/20 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the management or administration of healthcare resources or facilities, e.g. managing hospital staff or surgery rooms
G16H 40/63 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for local operation
A method for managing patient hydration is provided. The method includes receiving a fluid delivery request that includes a first programmed amount of a first fluid to be provided by a first medical device. Additionally, the method includes identifying a second programmed amount of a second fluid provided by or to be provided by a second medical device. Further, the method includes determining that a medical device operation should be adjusted based on the first and second programmed amounts. Finally, the method includes adjusting the medical device operation responsive to the determination and based on the fluid delivery request and the first and second programmed amounts.
G16H 20/10 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients
G16H 20/13 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered from dispensers
G16H 20/17 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered via infusion or injection
Medical tubing can have a chromic material such that the medical tubing is configured to transition from a first state of color to a different, second state of color by application of a stimulus to the medical tubing.
Methods, devices, and systems for determining soon to expire items. Historical item data are received. A soon to expire analysis model is trained using the training data to generate a trained soon to expire analysis model configured to receive item data associated with the item and to generate soon to expire prediction for one or more items associated with the item data. The bar includes a platform at a distal edge of the bar. The platform is configured to come in contact with an item deposited in the housing. A sensor is configured to generate a signal indicative of a fill level of the housing based on the platform coming in contact with the item deposited in the housing. Actions are performed to prevent the item from remaining unused past the target date.
Fluid flow devices including a fluid passage for regulating movement of a fluid therethrough, including flow restriction devices having first and second passages that can regulate a fluid flow in a first direction through the device and can regulate a fluid flow in a second direction through the device, and fluid flow restriction devices that can include a first connector having an internal surface defining an inner lumen, a second connector coupled to an end of the first connector, a cannula mounted in the inner lumen extending into the second connector, a lumen of the cannula may define a first flowpath along which a fluid flows into a fluid collection device, and an annulus may be defined between an outer surface of the cannula and the internal surface of the first connector, the annulus may define a second flowpath along which a fluid flows into a catheter assembly.
A61B 5/153 - Devices for taking samples of blood specially adapted for taking samples of venous or arterial blood, e.g. by syringes
A61B 5/154 - Devices for taking samples of blood specially adapted for taking samples of venous or arterial blood, e.g. by syringes using pre-evacuated means
A pressure detection system includes a body having an internal chamber with input and output ports and a flexible membrane fluidically sealed to an exposed opening of the chamber to prevent a fluid passing through the chamber from passing through the exposed opening. The membrane is configured to change shape responsive to an increase in pressure caused by the fluid within the chamber satisfying a predetermined threshold. In some implementations, the membrane includes or is part of an identification mechanism which moves outwards, away from the chamber, as the pressure increases to indicate the pressure increase. In some implementations, the identification mechanism includes markings on the surface of the membrane, and an image sensing device reads the markings, and provides an indication of a current pressure associated with the fluid in the chamber based on a variation in the markings from a default state.
A fluid container is encompassed by a custom fluid container pressure sleeve, which is configured to wrap around, connect and form to the malleable fluid container such that, when the fluid container pressure sleeve is inflated with a gas, the fluid container pressure sleeve applies an inward directional pressure to the malleable fluid container from an exterior of the malleable fluid container to compress the malleable fluid container. A pump connected to the fluid container pressure sleeve is activated to provide the gas to the fluid container pressure sleeve to compress the malleable fluid container and direct a fluid (e.g., the blood product) within the malleable fluid container toward and through a connected infusion tubing.
A system for scanning and validating clinical order device configurations is disclosed. A test instance of an infusion device is created based on a request, and an automated programming command is transmitted to the test instance. The automated programming command includes validation information for validating clinical order data, and a programming response is generated by the test instance based on the automated programming command, and provided for storage in a records system. In some implementations, the response includes an image, or reference to the image, of a graphical user interface that would be presented by the infusion device configured according to the validation information.
G16H 20/17 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered via infusion or injection
G16H 40/67 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for remote operation
33.
HEMOLYSIS-REDUCTION ACCESSORIES FOR DIRECT BLOOD DRAW
A flow restriction device including a housing forming a fluid flow path with a resilient valve positioned between first and second segments of the fluid path, where a segment of the fluid path includes a spiral or involute shape, and where the resilient valve is responsive to a change in pressure along the fluid path such that the resilient valve can move or bias toward the fluid path to restrict a fluid flow through the fluid path, thereby reducing a flow rate and pressure of the fluid, and where the fluid is blood, reducing the hemolysis index of the blood, and in some instances the resilient valve stopping the fluid flow through the fluid flow path responsive to exceeding a pressure along the fluid path to reduce the hemolysis index of the blood.
An infusion line gas removal device and process for its fabrication and use is disclosed herein. The gas removal device includes a gas permeable tubing coupled between first and second couplers, and an impermeable tubing shield encasing the gas permeable tubing between the first and second couplers. The impermeable tubing shield is larger in diameter than the gas permeable tubing and comprises at least one vent and a plurality of supports, the plurality of supports being between the tubing shield and the gas permeable tubing and configured to support the gas permeable tubing within the impermeable tubing shield in a fixed position between the first and second couplers and facilitate passage of gas from the gas permeable tubing to the at least one vent.
A61M 5/36 - Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm rests with means for eliminating or preventing injection or infusion of air into body
A61M 39/08 - Tubes; Storage means specially adapted therefor
A method for adjusting a medical device within the medical facility to conserve usage of the medication is provided. The method may include receiving, from a medication inventory system, medication inventory data comprising an ordered quantity of a medication ordered to supply a medical facility and a received quantity of the medication delivered to the medical facility. The method may also include generating, based on the medication inventory data, a medication inventory metric, which indicates a likelihood of an interruption in supply of the medication to the medical facility. The method may also include adjusting, based on the medication inventory metric, a medical device within the medical facility to conserve usage of the medication. Related methods and articles of manufacture are also disclosed.
Fluid connector systems that can include first and second valve assemblies that are couplable together to form a fluid pathway through the fluid connector system when the first and second valve assemblies are coupled together, and can resist fluid flow through each of the first and second valve assemblies when the first and second valve assemblies are separated from each other, where the first and second valve assemblies can include a compressible element or post positioned within a channel and configured resist fluid flow through the respective first or second valve assembly in a first position and to reduce the resistance to fluid flow through the first or second valve assembly in a second position, and the first and second valve assemblies including a sleeve and one or more arm configured to engage each other to form a snap fitting feature that can resist separation therebetween.
An infusion device determines, using a pressure sensor, a pressure decay inside an infusion line associated with an infusion of a fluid to a patient by an infusion device, whereby the pressure decay does not satisfy a default pressure threshold for triggering an occlusion alarm. The infusion device further detects, using an air sensor, air inside the infusion line in an amount that does not satisfy a default air-in-line threshold for triggering an air-in-line alarm. Then, before the pressure decay satisfies the default pressure threshold, the infusion device triggers the occlusion alarm based on the determined pressure decay and the detected amount of air.
A61M 5/168 - Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters
A61M 5/36 - Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm rests with means for eliminating or preventing injection or infusion of air into body
38.
OVERMOLDED HEMOLYSIS-REDUCTION ACCESSORIES FOR DIRECT BLOOD DRAW
A flow restriction device may include a male luer connector portion, a female luer connector portion, a tube, and an overmolded body portion. The male luer connector portion defies a first lumen. The female luer connector portion defines a second lumen. The tube defines a third lumen. The third lumen is in fluid communication with the first lumen and the second lumen. The third lumen has a diameter less than 0.025 inches. The overmolded body portion is formed around the tube.
A flow restriction device may include a male luer connector portion and a female luer connector portion. The male luer connector portion can define a cavity and a first lumen in fluid-flow continuity with the cavity. The female luer connector portion defines a second lumen and an extension in fluid-flow continuity with the second lumen. The extension includes a first end, a second end, an outer surface, and a channel. The channel is defined on the outer surface. The channel is helically disposed around the outer surface of the extension and extends between the first and second ends. The extension is configured to be at least partially disposed within the cavity. The channel and the inner surface of the cavity define a fluid passage in fluid-flow continuity with the first lumen and the second lumen.
A flow restriction device may include a housing and an insert body. The housing defines a first lumen, a second lumen, and a cavity disposed between the first lumen and the second lumen. The insert body can be disposed within the cavity. The insert body includes a first end, a second end, a longitudinal axis extending through the first and second ends, an outer surface, and a channel. The channel is defined on the outer surface. The channel extends between the first and second ends. The channel includes a first portion that extends in a first direction away from the longitudinal axis and a second portion that extends in a second direction toward the longitudinal axis. The channel and an inner surface of the cavity define a fluid passage in fluid communication with the first lumen and the second lumen.
A61B 5/153 - Devices for taking samples of blood specially adapted for taking samples of venous or arterial blood, e.g. by syringes
A61B 5/154 - Devices for taking samples of blood specially adapted for taking samples of venous or arterial blood, e.g. by syringes using pre-evacuated means
Fluid clamps are described herein. A fluid clamp includes a clamp body and a rotating body. The clamp body includes a first and second valve element. Each valve element includes a valve extension portion and a valve end portion extending from the valve extension portion. The first and second valve elements are disposed opposite to each other to allow a tubing to pass between the first and second valve elements. The rotating body is rotatably coupled to the clamp body. The rotation of the rotating body moves the valve end portion of at least one of the first and second valve elements to adjust a flow rate through the tubing.
A tubing junction assembly may include a body, and a collar coupled to the body. The body may include a head portion, a base portion, and an intermediate portion. At least a portion of an outer surface of the body at the intermediate portion may define a cross-sectional width that tapers from the head portion to the base portion. The collar may have an inner surface defining a passage. A tubing may be stretched over the outer surface of the body with a proximal end portion of the tubing stretched over at least a portion of the outer surface of the body at the intermediate portion. The inner surface of the collar may be sleeved over a portion of the outer surface of the tubing and coupled to the collar such that the proximal end portion of the tubing is sandwiched and compressed between the body and the collar.
F16L 33/22 - Arrangements for connecting hoses to rigid members; Rigid hose-connectors, i.e. single members engaging both hoses with means not mentioned in the preceding groups for gripping the hose between inner and outer parts
F16L 33/00 - Arrangements for connecting hoses to rigid members; Rigid hose-connectors, i.e. single members engaging both hoses
43.
DEVICE, METHOD, AND SYSTEM FOR ACCURATE DELIVERY OF FLUSH INFUSION
A syringe pump determines, upon receiving a new syringe, that at least a first portion of a predetermined amount of a first fluid was previously delivered by the syringe pump according to a first fluid delivery order before the new syringe was loaded into the syringe pump, and determines a second portion of the first fluid remaining to be delivered to complete the predetermined amount of the first fluid for the first fluid delivery order. A delivery of a second fluid is initiated by the syringe pump and, when an amount of the second fluid delivered from the new syringe satisfies the second portion of the first fluid remaining to be delivered, the pump automatically, without user intervention, indicates the first fluid delivery order as being complete, de-associates the first fluid delivery order from the syringe pump, and associates the syringe pump with the second fluid delivery order.
G16H 20/17 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered via infusion or injection
G16H 40/63 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for local operation
A61M 5/145 - Pressure infusion, e.g. using pumps using pressurised reservoirs, e.g. by means of pistons
A61M 5/168 - Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters
A precision roller clamp assembly for adjusting the fluid flow rate in a tube of an infusion set is provided. The roller clamp assembly includes a housing to receive the tube and a roller wheel moveably engaged with the housing. The housing includes a tube groove disposed in a guide wall, the tube groove dimensions configured to provide a precise fluid flow adjustment over a majority of the travel path of the roller wheel. A method of operating a precision roller clamp assembly is also provided.
A dispensing device monitors a plurality of containers for a change event, including at least one of: a fill order or a dispense of an item unit stored within the container, an opening or closing of the container, sensing a user within a predetermined proximity of the container, or a predetermined time. Based on an occurrence of the change event, the device causes an emission of a non-radio based transmission of one or more waves to an internal space of the container. A sensor with the container measures the one or more waves, and a supply level of an item unit within the container is determined based on the measurement and training data pertaining to measurements associated with past supply levels for the container. A notification is generated when the supply level satisfies a predetermined threshold.
G06Q 10/087 - Inventory or stock management, e.g. order filling, procurement or balancing against orders
G16H 20/13 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered from dispensers
Medical fluid extension set systems are disclosed that can include a tubing anchor (1100) coupled to tubing (16) and a fluid coupling device (2100), and can be anchored to a patient to resist unintended separation of the tubing anchor or a catheter (18) coupled to the tubing, from a patient, and to permit separation or disconnection of a fluid pathway between the tubing and another device coupled to thereto upon exceeding a pulling force on the fluid coupling device, and where disconnection includes separation of first and second valve assemblies such that a fluid pathway of the first and second valve assemblies is obstructed upon disconnection of the fluid coupling device.
A method may include receiving, from a safety system coupled to an infusion system, repair data associated with a repair event, during which a user accesses the infusion system. The method may also include detecting, based on the repair data, the repair event is unauthorized. The method may also include causing, based on the detecting, at least one safety adjustment to operation of the infusion system. Related methods and articles of manufacture, including apparatuses and computer program products, are also disclosed.
A61M 5/14 - Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
G16H 40/40 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the management of medical equipment or devices, e.g. scheduling maintenance or upgrades
G05B 21/00 - Systems involving sampling of the variable controlled
An intravenous IV pressure assembly includes a body, an outlet port disposed on the body and a connector coupled to the outlet port, the connector being configured to couple with a fluid reservoir and the IV pressure assembly configured as a pressurized container. IV sets with an IV pressure assembly and methods of operating an IV pressure assembly are also provided.
A universal flow limiter assembly includes a body configured to receive a portion of an IV tube, where the body includes two opposing side beams, a hinge portion disposed at a first end of the body, a control portion disposed at a second end of the body, a groove defined between the side beams and disposed between the hinge portion and the control portion and a control knob. The universal flow limiter assembly is configured to regulate a flow rate of fluid flowing through the IV tube based on rotation of the control knob. IV sets with universal flow limiter assemblies and methods of operating universal flow limiter assemblies are also provided.
An IV set hand pump includes a body having an egg-shape, a grip portion extending radially outward from the body, an inlet port disposed at a first end of the body and an outlet port disposed at a second end of the body. The IV set hand pump is configured, when squeezed, to increase a fluid flow rate of an IV set downstream of the IV set hand pump beyond a maximum gravity based fluid flow rate of the IV set. IV sets with IV set hand pumps and methods of operating IV set hand pumps are also provided.
An external infusion control device operably connects to an infusion device and one or more sensors, and is configured to control the infusion device based on sensor data provided by the sensors and user input provided at the control device. The control device provides a user interface to a display and, on receiving a therapy selected by a user, confirms the sensors for the therapy are operably connected to the control device and that the control device is operably connected to an infusion device that may be controlled by the sensor data. One or more algorithms are obtained, for example by way of being downloaded from a server, to control the infusion device based on the sensor data, and performance of the selected therapy is facilitated by the control device based on sensor data received from the one or more sensor devices.
G16H 20/17 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered via infusion or injection
G16H 40/63 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for local operation
G16H 40/67 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for remote operation
G16H 50/20 - ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for computer-aided diagnosis, e.g. based on medical expert systems
52.
HEMOLYSIS-REDUCTION ACCESSORIES FOR DIRECT BLOOD DRAW
A flow restriction device may include a housing with first and second end portions forming respective first and second openings, and a cavity configured to receive an insert body defining a fluid passage that extends from a first opening of the housing at the first end portion to a second opening of the housing at the second end portion, where the fluid passage extends in more than one direction along a path between the first and second end portions of the housing to induce a resistance to a fluid flow moving through the device, thereby reducing a flow rate and pressure of the fluid, and where the fluid is blood, reduce the hemolysis index of the blood.
An infusion pump determines whether a pressure change is due to backpressure associated with a patient infusion line set associated with the intravenous infusion line or due to static pressure associated with a fluid container providing a fluid to the intravenous infusion line, determines that the pressure change did not result from an occlusion event based on the pressure change occurring over the first threshold period of time and, after determining that the pressure increase did not result from an occlusion event, the pump provides an indication that the pressure change is associated with the medical container or patient infusion line set and adjusts a motor speed of the pump or an amount of compression provided to the intravenous infusion line.
An infusion pump may include one or more pressure sensors. A controller associated with the infusion pump may determine, based on pressure signals from the pressure sensors, a current pressure profile for the infusion pump. The controller may further determined a first metric representative of the current pressure profile of the infusion pump. The controller may detect, based at least on a difference between the first metric and a second metric representative of a reference pressure profile of the infusion pump, one or more anomalous conditions of the infusion pump such as a valve failure. The controller may perform a corrective action in response to detecting the anomalous conditions. For example, the controller may prevent the infusion pump from performing an infusion and/or generate a notification identifying the anomalous conditions. Related systems, methods, and computer program products are also provided.
A method for improving a performance of scanning data tags in a medication station is provided. The method may include receiving, from a scanner of a medication station, scan data associated with a scan of a plurality of data tags positioned within the medication station. The method may also include generating, based on the scan data, a performance metric indicating a performance of the plurality of data tags. The method may further include adjusting, based on the performance metric, a scan parameter of the scan of the plurality of data tags and/or transmitting, based on the performance metric, an indication associated with the performance of the plurality of data tags. Related methods and articles of manufacture are also disclosed.
G06Q 10/087 - Inventory or stock management, e.g. order filling, procurement or balancing against orders
G06K 7/00 - Methods or arrangements for sensing record carriers
G16H 20/13 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered from dispensers
An IV set corkscrew hand pump includes a body, a corkscrew member disposed in the body, an inlet port disposed on a first end of the body, an outlet port disposed on a second end of the body and a drive mechanism coupled to the corkscrew member. The drive mechanism is configured to cause the corkscrew mechanism to turn within the body to increase fluid flow downstream in an IV set. IV sets with IV set corkscrew hand pumps and methods of operating IV set corkscrew hand pumps are also provided.
An IV disposable time indication device includes one of a tube and a slot containing a volume of gel, wherein the gel is configured to evaporate at a determined rate of time upon activation by exposure to ambient air. A seal is configured to prevent contact of the gel with ambient air. One or more time indicators are disposed on the device, wherein evaporation of the gel is configured to provide a visual indication of a passage of time after activation. Methods of operating an IV disposable time indication device are also provided.
An IV blood set foot pump includes a base plate, a squeezing plate movably coupled to the base plate by a pivot member and a biasing member coupled to the base plate and the squeezing plate. The biasing member is configured to exert a biasing force against the squeezing plate when the biasing member is in a compressed state. One of the base plate and the squeezing plate comprises a cavity configured to receive an IV pump bulb. IV sets with IV blood set foot pumps and methods of operating IV blood set foot pumps are also provided.
An IV set includes an IV component and a duration monitor device coupled to the IV component. The duration monitor device may include an indicator portion configured to change color after a determined amount of time upon activation of the indicator portion, or an RFID tag configured to be detected by an RFID reader. The duration monitor is configured to provide an indication of passage of a useful-life time period for the IV set or the IV component. Methods of operating a duration monitor device are also provided.
A61M 5/14 - Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
A61M 5/50 - Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm rests having means for preventing re-use, or for indicating if defective, used, tampered with or unsterile
G01N 31/22 - Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroups; Apparatus specially adapted for such methods using chemical indicators
A circular roller clamp assembly includes a semi-circular housing configured to receive a portion of an IV tube, a motor and a motor arm coupled to the motor. A roller is coupled to the roller arm, the roller movably received by a guide groove disposed in the semi-circular housing. A flow rate of fluid flowing through the IV tube is regulated based on roller impingement of the IV tube against a tube channel in the guide groove via circumferential movement of the roller along the guide groove. IV sets with circular roller clamp assemblies and methods of operating circular roller clamp assemblies are also provided.
Syringes are described herein. In certain embodiments, a syringe includes a syringe body, a movable plunger, and a biasing member. The syringe body defines a cavity and a port in fluid communication with the cavity. The movable plunger is disposed within the cavity. The plunger and cavity define a volume. The port is in fluid communication with the volume. The biasing member is coupled to the plunger. The biasing member is configured to urge the plunger toward the port to dispense a fluid stored within the volume at a desired rate.
A61M 5/315 - Pistons; Piston-rods; Guiding, blocking or restricting the movement of the rod; Appliances on the rod for facilitating dosing
A61M 5/48 - Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm rests having means for varying, regulating, indicating or limiting injection pressure
A mini peristaltic pump is provided that includes a base plate, first and second gears disposed on a first side of the base plate, first and second roller wheels disposed on a second side of the base plate and coupled to the first and second gears, respectively, and one or more rollers coupled to each of the first and second roller wheels. A motor is coupled to the first gear, the motor configured to rotate the first gear and the first roller wheel to move the one or more rollers coupled to the first roller wheel in a first orbital path to peristaltically engage and compress a hand pump disposed between the first and second roller wheels. A profile feature on the base may be provided instead of the second gear and roller wheel. Systems and methods are also provided.
An IV bag wringer includes a frame defining a frame opening and multiple roller assemblies disposed within the frame opening. Each roller assembly includes a shaft coupled to the frame and a roller coupled to the shaft. Two opposing rollers are positioned to receive an IV fluid bag in a gap between the rollers such that the IV bag wringer hangs on the IV fluid bag. The weight of the IV bag wringer moves it downward along the IV fluid bag so that the opposing rollers squeeze fluid out of the IV fluid bag at a rate greater than a gravity flow rate from the IV fluid bag alone. Hand cranked IV bag wringers, motor actuated IV bag wringers and methods of operating IV bag wringers are also provided.
Medical tubing has at least one layer having a composition prepared from a melt blend of (i) a thermoplastic material, (ii) a filler and (iii) a heat reactive coupling agent. The medical tubing can have a kink resistance no worse than a medical tube composed of polyvinyl chloride with the same tubing wall dimensions. The medical tubing can be multilayer and can include single lumen and multi-lumen tubing.
A sensor assembly for an infusion system is provided. The sensor assembly includes a body, a pressure diaphragm, a fluid passageway formed between the body and pressure diaphragm, and a sensor. The pressure diaphragm includes a diaphragm interface. The sensor includes a sensor interface that is coupled to the diaphragm interface in an interlocked connection. The interlocked connection is configured to transfer a load from the pressure diaphragm to the sensor. The load may indicate a fluid pressure of the fluid passing through the fluid passageway.
The subject technology provides for automatic selection of a disposable medication container during an infusion. A user interface configured to display a selectable list of disposables and configured for receiving a selection of a disposable from the selectable list for use in providing a therapy to a patient by the medical device. When an indication of a selected disposable is received, a first sensor or a motor associated with the medical device is adjusted to provide the therapy to the patient, according to a characterization of the selected disposable. Automated programming data configured to instruct an infusion device regarding an infusion of a medication is received from a server, and includes disposable information, including a selection of the disposable. The selectable list of disposables is then bypassed and not displayed when the automated programming data is received and selects the selected disposable.
G16H 20/17 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered via infusion or injection
G16H 10/60 - ICT specially adapted for the handling or processing of patient-related medical or healthcare data for patient-specific data, e.g. for electronic patient records
G16H 40/63 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for local operation
G16H 40/67 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for remote operation
An infusion pump is placed in a default mode in which a lower occluder valve is activated to compress a tubing loaded within the pump. While in the default mode, a downstream pressure sensor of the infusion device monitors for a lower force spike while the lower occluder valve is activated, and determines whether the spike is detected before the pump receives an indication to start an infusion of a fluid through the tubing. When the spike is detected, the pump is automatically configured to start the infusion. Otherwise, a warning is provided without starting the infusion.
A method for transfusing blood using a syringe pump is disclosed. The method includes connecting a blood supply line to an upstream connection of a check valve, an intravenous transfusion line to a downstream connection of the check valve, and a syringe pump to a second upstream connection of the check valve, and activating the syringe pump to automatically retract and drive a plunger of the syringe pump, repeatedly, according to a pump rate programmed into the syringe pump according to the automatic retracting and driving of the plunger. By this mechanism, a blood product is automatically withdrawn from the blood supply line, through the check valve, and into a chamber of a syringe loaded into the syringe pump during each cycle of the automatic retracting of the plunger, and provided through the intravenous transfusion line from the chamber during each cycle of the automatic driving of the plunger.
An identification system identifies a new infusion device that moved into a predetermined area associated with an active infusion device currently performing an ongoing infusion of a medication to a patient and, responsive to that identifying, determines that an orientation of the new infusion device is indicative of the new infusion device arriving to replace or supplement the active infusion device. Responsive to determining the orientation, the system automatically programs the new infusion device with settings currently being used by the active infusion device in the ongoing infusion of the medication to the patient, without user input of the settings, and the new infusion device is activated to initiate a new infusion or to continue the ongoing infusion of the medication based on the automatically programmed settings.
G16H 20/17 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered via infusion or injection
When automated programming data configured to instruct an infusion device regarding an infusion of a medication is received from a server, the disclosed system and method identifies a deviation in the data with respect to stored programming data. Without rejecting the data for the deviation, the infusion device instead sends an acknowledgement of the automated programming data and the deviation, and determines a user interface workflow for correcting the deviation. The infusion device then provides for display one or more user prompts according to the determined user interface workflow to resolve the deviation. If the deviation is resolved by way of user responses, then the infusion is activated. Otherwise, an indication is sent to the server regarding the deviation.
G16H 20/17 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered via infusion or injection
G16H 40/63 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for local operation
G16H 40/67 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for remote operation
A61M 5/14 - Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
An apparatus, method, and system for detecting a leaking occluder valve is disclosed. At least one measurement instrument is connected to a fluid within a fluid tubing upstream or downstream of a pump element of an infusion device. The pump element is configured to periodically cause a compression of the fluid tubing and to isolate a downstream portion of the fluid tubing from an upstream portion of the fluid tubing when the pump element is operating under a normal operating condition. A response of the fluid is measured when the pump element is caused to compress the fluid tubing and a determination is made, based on the response whether the compression has fluidically isolated the downstream portion from the upstream portion. One or more shims may be inserted into the occluder valve to move the platen away from the pump element during the test to determine a degree of fault.
A male luer connector is provided that includes a luer slip having a first material, the luer slip sized and shaped to mate with a female connector. A collar is disposed on an outer surface of the luer slip, the collar having a second material and a plurality of first grip features disposed on an outer surface of the collar. A grip is coupled to the luer slip, the grip having a third material and a plurality of second grip features disposed on an outer surface of the grip, wherein one of the plurality of first and second grip features are configured to provide a slip resistant grip surface. Infusion sets and infusion set luer connector assemblies are also provided.
A needle-free connector assembly is provided that includes a main housing coupled to an indicator housing. A plunger is coupled to a bellows disposed in the main housing. An inlet port is disposed at an upstream end of the indicator housing and an outlet port is disposed at a downstream end of the main housing, with a valve disposed within the indicator housing and adjacent the inlet port. A switch member is slidingly disposed in the main housing, wherein the needle-free connector assembly provides both flow regulation and pressure indication when the switch member is in a downstream position and only pressure indication when the switch member is in an upstream position. Infusion sets and methods of operating a needle-free connector are also provided.
A61M 5/48 - Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm rests having means for varying, regulating, indicating or limiting injection pressure
A flow restriction device may include a distal end configured to couple to a catheter assembly, a proximal end configured to couple to a fluid collection device, and a body extending from the proximal end to the distal end. The body may include an outer surface and an inner surface defining a lumen of the body. The flow restriction device may further include a fluid pathway disposed between the distal end and the proximal end when the outer surface is coupled within a mating luer. The fluid pathway may include a non-linear portion on at least a portion of the outer surface along which a fluid flows from the distal end into the fluid collection device.
A medical device includes a body configured to receive and secure an IV tube that is configured to allow for the transportation of a fluid. The medical device includes a pump mechanism including a first element positioned along a first axis and configured to move in a first direction along the first axis to compress the IV tube. The pump mechanism includes a second element positioned along a second axis perpendicular to the first axis and configured to move in a second direction along the second axis and perpendicular to the first direction to provide a force against a side of the IV tube. The pump mechanism includes a third element positioned along the second axis opposite the second element and configured to move in a third direction along the second axis opposite the second direction to provide a force against another side of the IV tube.
A flow restriction device may include a male luer connector portion, a female luer connector portion disposed proximally to the male luer connector portion, and a body portion extending between the male and female luer portions, and integrally formed with the male and female luer portions to form a single monolithic piece. The male luer connector portion may have an internal surface defining a lumen thereof, and the female luer connector portion may have an internal surface defining a lumen fluidly connected to the lumen of the male luer connector portion. The body portion may have a recess extending longitudinally therethrough and fluidly communicated with the lumens of the male luer portion and the female luer portion. The recess may define a micro-channel along which fluid flows from the male luer connector portion into the fluid collection device via the female luer connector portion.
A coupling device that can removably couple medical tubing with a mating connector is disclosed and can include a housing and an inner body movable to different orientations, where an orientation is configured to resist separation of the coupling device and mating connector, and another orientation is configured such that resistance to separation from the mating connector is reduced, where any of the housing and the inner body can be moved relative to each other, and where the coupling device can permit separation of the coupling device and mating connector when a portion of the coupling device is moved, biased, and/or flexed when the coupling device and the mating connector are moved in directions away from each other, and where the coupling device can be re-coupled with a mating connector after separation of the coupling device and the mating connector.
A flow restriction device may include a proximal housing including an internal fluid channel, a distal housing including an internal fluid channel, and an intermediate housing interposed between the proximal and distal housings. The intermediate housing may include an internal chamber, and a slider reciprocally disposed in the internal chamber. The slider may include an internal fluid channel and a seal overlaying an outer surface of slider excluding the fluid channel, and may be reciprocally movable between (i) a first position where the internal fluid channel of the slider is axially aligned with the internal fluid channels of the proximal and distal housings to allow a fluid to flow therethrough, and (ii) a second position where the internal fluid channel of the slider is not aligned with the internal fluid channels of the proximal and distal housings and the seal blocks fluid connection between the proximal and distal housings.
A61B 5/154 - Devices for taking samples of blood specially adapted for taking samples of venous or arterial blood, e.g. by syringes using pre-evacuated means
Check valves are described herein. A check valve includes an inlet body, an outlet body, a valve body, a valve member, and a wiping extension. The inlet body defines an inlet portion. The outlet body defines an outlet portion. The valve body is coupled between the inlet bod and the outlet body. The valve body defines a valve cavity. The valve cavity is in fluid communication with the inlet portion and the outlet portion. The valve member is disposed within the valve cavity. The valve member is configured to permit flow from the inlet portion to the outlet portion and prevent flow from the outlet portion to the inlet portion. The wiping extension extends from the valve body toward the valve member. The wiping extension is movable relative to the valve member to dislodge particulate from the valve member.
A trigger condition for entering a syringe empty mode is determined. The trigger condition includes adjusting an operational parameter of an infusion device associated with the syringe to complete a fluid delivery performed by the syringe. The fluid delivery is monitored and, responsive to the fluid delivery satisfying the trigger condition, the infusion device is caused to enter the syringe empty mode. While in the empty mode, a flow rate or threshold associated with the fluid delivery is adjusted to facilitate emptying a fluid from the syringe, and an alert is provided when the threshold associated with the fluid delivery has been satisfied.
A levered flow regulation clamp assembly for adjusting the fluid flow rate in a connector tube of an infusion set is provided. The levered flow regulation clamp assembly includes a housing to receive the connector tube and a slider rotatably engaged within the housing and configured to compress the connector tube to provide a fluid flow adjustment. Infusion sets and methods of adjusting fluid flow rates are also provided.
Robotic automated dispensing systems that include a dispensing cabinet, a location tracking device configured to transmit information identifying a current location of the dispensing cabinet, a drive unit, and one or more movement elements in dynamic connection with the drive unit. In a first mode, at least one of the one or more movement elements is engaged to move via a first force provided by the drive unit. In a second mode, at least one of the one or more movement elements is disengaged from the drive unit to move via a second force. Mobile automated dispensing systems and robotic delivery devices are also provided.
A system for controlled delivery of a medical fluid may include an elastomeric pump, a valve member fluidly coupled to the elastomeric pump at one side and a catheter at an opposite side for delivering the medical fluid to a patient, and tubing fluidly coupling the elastomeric pump and the valve member. The elastomeric pump may include an elastomeric membrane and a shell surrounding the elastomeric membrane. The pressure of the medical fluid may be greater than a pressure of the vein to keep the vein open. The valve member may be movable between an initial closed position, a fully open position where the medical fluid is delivered to the vein of the patient at a predetermined fluid flow rate, and at least one intermediate open flow position where the medical fluid is delivered to the vein of the patient at a flow rate below the predetermined fluid flow rate.
Tubing anchors (100) are disclosed that can include an anchor body (102) configured to couple with a length of tubing (16) and to be coupled with a patient to resist unintended separation of the tubing from the patient, where the tubing anchor can include any of a sidewall (106, 108), a top surface, and a bottom surface configured to define a surface area to engage against any of a tape and adhesive to resist unintended separation of the anchor body from the patient.
Fluid connector systems including first and second valve assemblies couplable together to form a fluid pathway therethrough, and can resist fluid flow through the connector system when the valve assemblies are separated from each other, the first valve assembly including a compressible valve within a cavity and configured to surround a post forming a fluid passage, the compressible valve can resist fluid flow through the post in a first position and to reduce the resistance to fluid flow through the post in a second position, and the second valve assembly including a valve plug positioned within a bore and configured to obstruct a fluid passage, such that when the valve assemblies are coupled together the compressible valve is moved toward the second position and the post extends through the compressible valve and the valve plug to form the fluid pathway through the connector system.
A method for managing trips from a pharmacy may include receiving a plurality of transaction records that, as received, represent an independent transaction of a plurality of transactions at an ADC. The plurality of transaction records may include: time information between respective transactions and an elapsed time for a portion of the plurality of transactions. The method may include identifying, based at least in part on: (i) a comparison of the time information between respective transactions and a threshold inter-transaction trip time; and (ii) a comparison of the elapsed time for the portion and a threshold elapsed trip time, a sequence of the portion as a unique trip from a pharmacy. The method may include annotating, with an identifier for the unique trip, a portion of the plurality of transaction records representing the portion of the plurality of transactions. Related methods and articles of manufacture are also disclosed.
G06Q 10/06 - Resources, workflows, human or project management; Enterprise or organisation planning; Enterprise or organisation modelling
G06Q 10/08 - Logistics, e.g. warehousing, loading or distribution; Inventory or stock management
G16H 20/13 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered from dispensers
G16H 40/20 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the management or administration of healthcare resources or facilities, e.g. managing hospital staff or surgery rooms
A flow regulation clamp assembly for adjusting the fluid flow rate in a connector tube of an infusion set is provided. The flow regulation clamp assembly includes a housing to receive the connector tube, a slider slideably engaged within the housing and configured to compress the connector tube to provide a fluid flow adjustment, and a rotator knob moveable engaged with the housing and configured to move the slider. Infusion sets and methods of adjusting fluid flow rates are also provided.
Drip chamber inserts including an elongate body portion for coupling to a drip chamber and including an outlet orifice of the drip chamber insert. The drip chamber inserts may further include first and second chambers, the first chamber may be disposed in the elongate body portion and fluidly coupled to an inlet orifice and to the outlet orifice. An anti-run-dry membrane may extend over the inlet orifice. The second chamber may be disposed in the elongate body portion, and a low flowrate orifice may extend from a base of the second chamber into a base portion for fluidly coupling the second chamber with the outlet orifice.
Unattended robotic pharmacy systems are provided that include an enclosure defining a controlled access space and a prescription filling unit disposed within the controlled access space, the prescription filling unit configured to package and label a patient prescription of medication obtained from medication storage within the prescription filling unit. A finished prescription unit is disposed within the controlled access space and coupled to the prescription filling unit, the finished prescription unit configured to store the packaged and labeled patient prescription obtained from the prescription filling unit. An interface kiosk is coupled to the enclosure and disposed adjacent the finished prescription unit, the interface kiosk configured to receive input from a user and to dispense a finished prescription obtained from the finished prescription unit to the user.
G16H 20/13 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered from dispensers
A61J 1/00 - Containers specially adapted for medical or pharmaceutical purposes
A61J 7/00 - Devices for administering medicines orally, e.g. spoons; Pill counting devices; Arrangements for time indication or reminder for taking medicine
B65B 5/10 - Filling containers or receptacles progressively or in stages by introducing successive articles, or layers of articles
B65C 9/00 - LABELLING OR TAGGING MACHINES, APPARATUS, OR PROCESSES - Details of labelling machines or apparatus
G06Q 10/08 - Logistics, e.g. warehousing, loading or distribution; Inventory or stock management
G07F 17/00 - Coin-freed apparatus for hiring articles; Coin-freed facilities or services
IV stand assemblies are provided that include a base, a stand, a platform and a motorized pole assembly having a housing, a pole and a drive. The drive moves the pole to extend and retract the pole relative to the housing. A weight measurement assembly measures weight of a fluid within a fluid container hanging from the IV stand assembly. IV stand assemblies with a pulley/belt assembly and methods of operating IV assemblies are also provided.
Bonding dissimilar materials of medical device components can be carried out by applying an adhesive on at least one surface of two components which are composed of dissimilar materials and contacting the surfaces and exposing the contacted surfaces to heat and/or irradiate the adhesive to cure the adhesive and bond the surfaces. One medical component, e.g., medical tubing, can be composed of a non-polar, polyvinyl chloride free thermoplastic polymeric material and the other medical component, e.g., a medical connector, can be composed of polyacrylate, polyacrylonitrile, acrylonitrile-butadiene-styrene (ABS), methyl methacrylate-acrylonitrile-butadiene-styrene (mABS), polyester, and/or a polycarbonate material. The adhesive formulation can include: (a) a polyolefin oligomer having reactive acrylate groups and alkenyl groups, (b) an initiator, and optionally (c) a solvent.
C09J 5/06 - Adhesive processes in general; Adhesive processes not provided for elsewhere, e.g. relating to primers involving heating of the applied adhesive
C09J 5/00 - Adhesive processes in general; Adhesive processes not provided for elsewhere, e.g. relating to primers
C09J 123/00 - Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers
92.
NEEDLELESS CONNECTOR WITH COMPRESSIBLE AND DEFLECTABLE VALVE
A needleless connector may include a housing having a proximal end, a distal end, and an inner surface defining an internal cavity extending between the proximal and distal ends. A compressible valve may be disposed within the internal cavity. The compressible valve may include a head portion, a flange portion for securing the compressible valve in the housing, and a body portion extending between the head portion and the flange portion. The body portion may include a cylindrical outer surface having an external notch extending along a portion of a circumference of the cylindrical outer surface and recessed radially-inward from the cylindrical outer surface. The body portion may further include a planar face extending distally from the external notch and disposed between the external notch and the flange portion. The planar face may be recessed radially inward relative to at least a portion of the cylindrical outer surface.
Tubing systems are described herein. A tubing system can include a tubing assembly, a tubing system component, and a coupling portion. The tubing assembly includes a tubing and a tubing assembly connector coupled to the tubing. The tubing assembly connector defines a connector lumen in fluid communication with the tubing lumen. The tubing assembly connector has a tubing assembly connector elastic modulus greater than the tubing elastic modulus. The tubing system component has a component connector abutted against the tubing assembly connector. The component connector has a component connector elastic modulus greater than the tubing elastic modulus. The coupling portion is overmolded over the tubing assembly connector and the component connector to couple the tubing to the tubing system component.
A needleless connector may include a housing comprising a central longitudinal axis, a body portion, and a base portion. The body portion may include an inner surface forming an internal cavity, and a first port forming a first fluid passage to the internal cavity. The base portion may include a top section including a valve seal support, and a bottom section including a second port forming a second fluid passage to the internal cavity. The needleless connector may further include an asymmetrically-shaped valve disposed in the internal cavity. The asymmetrically-shaped valve may include a head portion, a valve body portion extending distally from the head portion, and a wall having an inner surface forming a valve cavity. The valve may be coupled with the housing such that the inner surface of the valve at the valve body portion is seated and radially supported on the valve seal support.
A access control system includes a catch configured to be affixed to an inner portion of an enclosure, a latch configured to engage the catch when the catch is attached to the enclosure and an access door of the enclosure is in a closed position. The access control system is configured to detect, using one or more sensors, when the latch is within a predetermined proximity of the catch, and responsive to detecting that the latch is not within the predetermined proximity of the catch, determine whether an authorized credential was received via a communication interface to open the latch, and when the authorized credential was received, register an authorized opening of the latch in a memory device, and when the authorized credential was not received, register an the unauthorized opening of the latch in the memory device and enter an alert state.
A biometric sensor may include a scanner configured to capture a biometric data and an adjustment mechanism configured to respond to a force applied to the biometric sensor by shifting the biometric sensor from a neutral position to an adjusted position. The adjustment mechanism may be configured to respond to the removal of the force by returning the biometric sensor to the neutral position. While the biometric sensor is in the neutral position, the scanner may be capable of capturing a biometric data of a majority of users interacting with the apparatus. Accordingly, the biometric sensor may be able to operate with minimal adjustments. The biometric sensor may be part of a dispensing cabinet such that the biometric data captured by the biometric sensor may be used to control access to the dispensing cabinet. Related methods are also disclosed.
A camera assembly may include a camera and one or more heat sinks configured to dissipate heat generated by the camera. The heat sinks being in thermal contact with a printed circuit board including the camera. A housing of the camera assembly may be configured to maintain the camera in a fixed position while the camera assembly is mounted on a medical device such as a dispensing cabinet. The camera in the fixed position may have a deterministic field of view that includes a first area in which interactions with the medical device and adjacent medical devices occurs or is expected to occur. The deterministic field of view of the camera may further exclude a second area where surveillance is unsuitable, prohibited, and/or unnecessary. Images captured by the camera may be analyzed to detect anomalous behavior such as diversion, medical error, hazardous behavior, and protocol noncompliance.
H04N 7/18 - Closed-circuit television [CCTV] systems, i.e. systems in which the video signal is not broadcast
G03B 17/55 - APPARATUS OR ARRANGEMENTS FOR TAKING PHOTOGRAPHS OR FOR PROJECTING OR VIEWING THEM; APPARATUS OR ARRANGEMENTS EMPLOYING ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ACCESSORIES THEREFOR - Details of cameras or camera bodies; Accessories therefor with provision for heating or cooling, e.g. in aircraft
An infusion device determines, based on a medication loaded by the device, a number of digit fields for inputting a parameter associated with the medication, obtains first and second limits pertaining to the medication, determines which of the digit fields are selectable based on the first limit, displays, on a display screen, a plurality of selectable character input fields corresponding to the number of digit fields, visually identifies a first of the input fields as an adjustable field, displays one or more controls for incrementing or decrementing a value of the identified adjustable field, visually identifies, responsive to receiving the selection of a second character input field, the second character input field as the adjustable field and, in response to determining that an adjusted value exceeded the second limit, displays an alert proximate to the adjusted value of the second selectable character input field.
G16H 40/63 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for local operation
99.
NEEDLELESS CONNECTOR DISINFECTION DEVICES AND METHODS
Needleless connector disinfecting devices are provided that include a body having a top surface and a bottom surface, a cavity in the body, the cavity configured to receive a needleless connector, an activation arm disposed on the body, a cartridge housing disposed on the activation arm, a swab cartridge disposed in the cartridge housing, and a disposal chamber disposed in the body, the disposal chamber configured to receive used cleaning swabs. The activation arm is configured to slidably move the cartridge housing on the top surface of the body between a non-biased position in which a bottommost cleaning swab in the swab cartridge is in contact with an end portion of a needleless connector and a biased position in which the cartridge housing is disposed over the disposal chamber. Additional needleless connector disinfecting devices and methods of using needleless connector disinfecting devices are also provided.
A61M 5/00 - Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm rests
A61M 39/18 - Methods or apparatus for making the connection under sterile conditions, i.e. sterile docking
A61M 39/16 - Tube connectors or tube couplings having provision for disinfection or sterilisation
IV filters are described herein. An IV filter includes a filter housing, a filter media, a filter channel, a priming channel, and a disk valve. The filter housing defines an inlet and an outlet. The filter media is disposed within the filter housing. The filter channel is disposed within the filter housing. The filter channel is in fluid communication with the inlet and the filter media, and the filter media permits flow from the filter channel to the outlet and captures particulate from the flow. The priming channel is disposed within the filter housing. The priming channel is in fluid communication with the inlet and the outlet. The disk valve is coupled to the filter housing. The disk valve is moveable to direct flow from the inlet to the priming channel in a first position and to direct flow from the inlet to the filter channel in a second position.
A61M 5/14 - Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
A61M 5/168 - Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters
A61M 5/36 - Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm rests with means for eliminating or preventing injection or infusion of air into body
patents
