A therapeutic device for treating an acute medical condition of a patient such as cardiac arrest is provided. The device includes one or more sensors that monitor parameters such as heart rhythm that relate to the patient's medical condition. The device also includes a plurality of medication reservoirs, each reservoir including a conduit, wherein each reservoir holds a predetermined medication that may be used to treat the condition. A manifold is connected with the reservoirs via their respective conduits. A delivery line is connected with the manifold to deliver fluids from the manifold to the patient intravenously. One or more medication pumps are in fluid connection with respective ones of the reservoirs. A processor is connected with the sensors. The processor includes a memory that stores processing instructions to interpret the parameters and to determine a recommended medication to deliver to the patient based on the parameters, the recommended medication being one of the predetermined medications. The processor is operatively connected with the medication pumps. When a recommended medication is determined, the processor actuates the medication pump connected with the reservoir including the recommended medication to deliver the medication to the patient via the manifold and the delivery line.

An infusion system (10) including a radioisotope generator (52) that generates a radioactive eluate via an elution, an activity detector (58) configured to measure an activity of a first radioisotope in the radioactive eluate generated by the radioisotope generator, and a controller (80). The controller can track a cumulative volume of radioactive eluate generated by the radioisotope generator and also track the activity of the first radioisotope in the radioactive eluate generated by the radioisotope generator. The controller can determine a predicted volume of the radioactive eluate generated by the radioisotope generator at which the activity of the first radioisotope in the radioactive eluate will reach a threshold based on the tracked cumulative volume of the radioactive eluate and the tracked activity of the first radioisotope. This information can be useful for proactively removing the radioisotope generator from service and/or replacing the radioisotope generator with a fresh generator.

A method of maintaining an overall flow rate during a sequential delivery of at least two fluids to a patient’s blood vessel includes delivering at least a first fluid into the patient’s blood vessel at a first flow rate, delivering at least a second fluid into the patient’s blood vessel at a second flow rate, and adjusting at least one of a first flow profile of the first flow rate and a second flow profile of the second flow rate to dampen a transient increase in the overall flow rate during a transition between delivering one of the first fluid and the second fluid to delivering the other of the first fluid and the second fluid.

A low dose drug delivery pod comprised of a reciprocating pump, an active valve set, and, in some embodiments, a dispense confirmation sensor. The active valve set can be designed with mechanical interference between them so that both the inlet and outlet valve must close before either one opens, ensuring that at least one of the two valves is closed at all times. The dispense confirmation sensor is a flow-based detection system that provides rapid feedback if an individual dose has or has not been delivered.

Enteral feeding pump systems valves assemblies therefor and related fluid flow control methods. The system includes a disposable fluid delivery set with an integral peristaltic tube section and an enteral feeding pump. The system may also include a pinching mechanism for regulating the flow of nutrient formula or water out of the fluid delivery set. Also disclosed is a flow selector valve assembly for an enteral feeding pump system, the valve assembly including a tube adapter having two input flexible tubing channels and one output tubing channel and being configured to position the flexible tubing channels in relation with a receiver. The receiver has an eccentric bearing that is moveable between a first position in which neither of the input flexible tubing channels is compressed, and a second position in which the eccentric bearing compresses one of the input flexible tubing channels therein to prevent flow therethrough.

An improved anesthetic nerve block and method is disclosed comprising a dispenser including a storage body, a transfer body and a tip for positioning adjacent to the nerve. A local short acting anesthetic is in the storage body. A physiologic carbonate base is in the storage body. The local short acting anesthetic and the physiologic carbonate base are dispensed from the tip of the dispenser where the local short acting anesthetic facilities the penetration of the physiologic carbonate base through the nerve membrane and into the axon. A local long acting anesthetic is in the storage body. The local long acting anesthetic is dispensed from the tip of the dispenser and penetrates through the nerve membrane and into the axon. The local long acting anesthetic and the physiologic carbonate base cause a precipitate and form a crystallization compound for creating a prolonged local nerve block.

An infusion system and method for providing different medical fluids to a patient. The infusion system, which can be used in complex infusion therapies, includes a catheter with a catheter tube and at least one lumen extending longitudinally through the catheter tube between a proximal tube end and a distal tube end. A plurality of pump devices are each connected to the at least one lumen so as to convey fluid. A control device is connected to the pump devices and adapted to control the pump devices so that the different medical fluids can be delivered through the at least one lumen by the pump devices in time division multiplex. The catheter can include the pump devices. Each pump device can be configured as a micropump mounted at the proximal tube end.

In one aspect, a combinatorial drug delivery device is provided for delivering a predetermined selection of drug components. The device includes a plurality of modules, each including: a body having an interior volume; a spike plate movably disposed in the interior volume, the spike plate having a protruding cannula and first and second ports. The device also includes a base tray which includes: a framework defining a plurality of wells, each of the wells formed to insertingly receive one of the modules; for each of the wells, first and second inlet ports formed to interface with the first and second ports of the module being received in the respective well; passageways to connect certain wells with adjacent wells to permit fluid flow therebetween. For each of the wells, the spike plate of the respective module being maintained in a stationary position with the module being inserted into the well.

An infusion system includes a primary delivery device, a secondary delivery device, an ancillary device, and a manifold. The manifold includes a primary connection port fluidly coupled with the primary delivery device. A delivery connection port in fluid communication with the primary connection port is fluidly coupled with the ancillary device. A secondary connection port fluidly coupled with the secondary delivery device is in fluid communication with the primary connection port. The primary connection port is operable to permit bidirectional flow so that fluid flows from the primary delivery device through the primary connection port and through the delivery connection port to the ancillary device, and from the secondary delivery device through the secondary connection port and through the primary connection port to be received by the primary delivery device.

A chemical liquid injector including a driving mechanism which applies a pressure to a chemical liquid in a container and pushes out the chemical liquid, and an injection control unit for setting operating conditions of the driving mechanism. The control unit has a main-injection condition determination section which determines injection conditions for a main injection, and an injection preliminary operation condition determination section which determines injection conditions for an injection preliminary operation, and is configured to execute the injection preliminary operation and the main injection consecutively in this order when injecting chemical liquid.