Abstract: A differential pressure based flow sensor assembly and method of using the same to determine the rate of fluid flow in a fluid system. The sensor assembly comprises a disposable portion, and a reusable portion. A flow restricting element is positioned along a fluid flow passage between an inlet and an outlet. The disposable portion further has an upstream fluid pressure membrane and a downstream fluid pressure membrane. The reusable portion has an upstream fluid pressure sensor and a downstream fluid pressure sensor. The upstream fluid pressure sensor senses the upstream fluid pressure at a location within the fluid flow passage between the inlet and the flow restricting element. The downstream fluid pressure sensor senses the downstream fluid pressure at a location within the fluid flow passage between the flow restricting element and the outlet. The process utilizes output of the sensors to calculate the flow rate of the fluid.

Abstract: A method of monitoring pressure inside a fluid line and a system for implementing the method. The method is applicable to syringe pump systems. The method includes the steps of measuring a force value caused by a pressure inside the fluid line; collecting the measured force values during at least two consecutive moving time windows; calculating a slope of a best-fit line within each time window; calculating a slope difference of the slopes of the best-fit lines; comparing the slope difference with a pre-determined threshold gradient value; defining a baseline force as the detected force value when the slope difference is equal to the threshold gradient value; determining a relative force value by subtracting the baseline force from the detected force value; and, triggering an alarm if the relative force is greater than a pre-defined threshold force.

Abstract: A system for maintaining drug information and communicating with medication delivery devices includes software designed for use in a hospital, pharmacy or biomedical technical service environments. The software may be provided on a computer readable medium. The software allows a facility to customize a drug library with both hard and soft drug limits and other parameters for use with an infuser having a plug and play module removably inserted into a slot within a housing, or for use with an infuser having a connectivity engine enclosed within the housing. The system supports data transfer to one or more infusers connected to one or more computers. The connection between the computer and the pump can be hard wired or wireless.

Abstract: A method and pump that accurately senses air in a fluid delivery line pulses or activates and deactivates the air sensor(s) multiple times during the pumping phase of the fluid delivery cycle and can generate alarms based upon a single indication or a cumulative indication of air in the line. The pump can include multiple air sensors spaced along the delivery line so that the method can use the multiple signals therefrom to distinguish real moving air bubbles from false positives and/or air bubbles adhered to the inner wall of the line.

Abstract: A method and formulation for preparing spray dried vancomycin. In various embodiment, the formulation includes vancomycin HCl (10-20%) and one or more of the following PEG (0-5%), mannitol (0-5%), ethanol (0-10%), and a citrate buffer. Spray dried vancomycin has favorable reconstitution times and water content.

Abstract: A fluid delivery device such as a cassette removably disposed in a medical pump to control fluid flow in the medical pump. The fluid delivery device has an elongated main body including an inlet, an outlet, and a fluid passage extending from the inlet to the outlet. A flow stop is pivotally mounted to the main body for selectively allowing and stopping fluid flow from the fluid passage to the outlet. The fluid delivery device can have various features including the flow stop having grooved sections, a T-shaped collar on the main body inlet or a flange on the main body to prevent inadvertent engagement of the flow stop during removal of the fluid delivery device from the medical pump.

Abstract: A system and method for intermixing the contents of two containers. The system includes a first container, a second container, and a connector for providing fluid communication between the first and second containers. The connector includes at least one resilient retention member for securing the first container to the connector. In addition, the connector accommodates standard vials containing, for example, medicaments, and prevents the unwanted discharge of the contents of the vial into the environment.

Abstract: The presently disclosed subject matter relates to pharmaceutical compositions comprising dexmedetomidine or a pharmaceutically acceptable salt thereof wherein the composition is formulated as a liquid for parenteral administration to a subject, and wherein the composition is disposed within a sealed container as a premixture. The pharmaceutical compositions can be used, for example, in perioperative care of a patient or for sedation.

Abstract: A system and method to configure a rule set used in connection with a medical monitoring system for monitoring patients and patient care equipment, especially medication delivery pumps, based on a variety of conditions and parameters associated with monitored biometric information and equipment information and for providing user-defined responses to those conditions and parameters.

Abstract: The presently disclosed subject matter relates to methods of administering an effective amount of dexmedetomidine to a pediatric patient in order to reduce the incidence of neurological damage. More particularly, the presently disclosed subject matter relates to methods of providing sedation or analgesia to a pediatric patient by administering a dexmedetomidine infusion and optionally a loading dose. The dexmedetomidine can be administered before, during, or after surgery.

Abstract: A medical pump system includes an input device for entering a command or a value of a pump programming parameter and a memory for storing a programming code. A processor is in communication with the memory and the input device in order to generate a display signal for an output device to generate one of a plurality of screens, such as near view and far view screens. The programming code is operable to display on a far view screen a plurality of medical therapy buttons that can be used to navigate directly to a near view programming screen. The far view screen can also concurrently display quick titration buttons that are associated with the medical therapy buttons and can be used to navigate directly to a quick titration screen without having to go to a general near view delivery screen or near view programming screen.

Abstract: A method of monitoring performance of a fluid testing system is provided. The method draws a fluid sample to the testing system using a pump. A voltage output of a sensor, such as an optical sensor, is generated. The voltage output of the optical sensor during the drawing is compared to an upper fluid volume drawn based voltage limit and a lower fluid volume drawn based voltage limit stored within a memory. The system is flushed with a flushing fluid using the pump to flush the flushing fluid from the testing system. The voltage output of the optical sensor during the flushing is compared to an upper fluid volume flushed based voltage limit and a lower fluid volume flushed based voltage limit stored within the memory. An alert generates if at least one of the voltage output during the drawing of the fluid sample is outside of voltage limits.

Abstract: A medical pump with a closed loop stroke feedback system and method, for use with a pumping chamber, for example in a cassette, is disclosed. The pump includes a pumping element that intermittently pressurizes a pumping chamber during a pumping cycle. A pressure sensor detects the pressure exerted by the pumping element on the pumping chamber. A position sensor detects the position of the pumping element. A processing unit processes pressure data from the pressure sensor and position data from the position sensor to determine a calculated stroke volume of the pump for a pump cycle, and to adjust a stroke frequency of the pump to compensate for variation in the stroke volume.

Abstract: A system and method to configure a rule set used in connection with a medical monitoring system for monitoring patients and patient care equipment, especially medication delivery pumps, based on a variety of conditions and parameters associated with monitored biometric information and equipment information and for providing user-defined responses to those conditions and parameters.

Abstract: A first portable medical device is adapted for use in an interlocking system for interlocking the first medical device to a second medical device. The first device includes a housing having opposite sides, a selective element, a blocking element, and a clamp mechanism. At least one of the opposite sides includes a matable element to detachably attach a second medical device. The selective element restricts the attachment of the second device to only one side of the first device. The blocking element prevents a third medical device from attaching to the first and second devices once the first and second devices are attached. The clamp restricts the attachment of the second device to only one side of the first device when the clamp is attached to a support member. The clamp permits slide ratcheting axial movement of a clamp shaft.

Abstract: The presently disclosed subject matter relates to pharmaceutical compositions comprising dexmedetomidine or a pharmaceutically acceptable salt thereof wherein the composition is formulated as a liquid for parenteral administration to a subject, and wherein the composition is disposed within a sealed container as a premixture. The pharmaceutical compositions can be used, for example, in perioperative care of a patient or for sedation.

Abstract: A system for mixing or reconstituting a drug contained in a first container with a diluent or fluid contained in a second container. The second container has a port docking assembly for engaging the first container. The first container is rotatable and axially slidable within the port docking assembly. The port docking assembly has an actuator to urge a stopper fluidly sealing the first container into the interior of the first container. The port docking assembly further includes a movable plug constructed to fluidly seal the second container in a first, docked position and to provide access to the interior of the second container in a second, activated position, whereby fluid communication between the first and second containers is provided when the first and second containers are in the second, activated position.

Abstract: An ultrasonic monitoring device includes a substrate, a plurality of ultrasonic transducer elements, a computer readable memory medium, a microprocessor, and a power source. The ultrasonic transducer elements are coupled to the substrate. Each ultrasonic transducer element is separately configured to transmit a signal to a target area of a mammal and to receive an echo return signal from the target area. The computer readable memory medium includes program instructions. The microprocessor is coupled to the ultrasonic transducer elements and to the computer readable memory medium for executing the program instructions to determine a physiological parameter of the mammal based on a combined analysis of the echo return signals received by the ultrasonic transducer elements. The power source is coupled to at least one of the ultrasonic transducer elements, the computer readable memory medium, or the microprocessor for supplying electrical energy.

Abstract: A system, method, and computer program for controlling at least one infusion pump wherein the system comprises a first channel for delivering a first fluid, a second channel for delivering a second fluid, a first input for receiving channel sequence data wherein the channel sequence data identifies the sequence for delivering the first fluid from the first channel and the second fluid from the second channel, a second input for receiving first delivery data for the first channel and the second delivery data for the second channel, and a processor for controlling delivery of the first fluid from the first channel and the second fluid from the second channel according to the channel sequence data, the first delivery data, and the second delivery data.

Abstract: A system for mixing or reconstituting a drug contained in a first container with a diluent or fluid contained in a second container. The second container has a port docking assembly for engaging the first container. The first container is rotatable and axially slidable within the port docking assembly. The port docking assembly has an actuator to urge a stopper fluidly sealing the first container into the interior of the first container. The port docking assembly further includes a movable plug constructed to fluidly seal the second container in a first, docked position and to provide access to the interior of the second container in a second, activated position, whereby fluid communication between the first and second containers is provided when the first and second containers are in the second, activated position.