Abstract:
A hazardous fluid transport container and a hazardous fluid delivery system are disclosed. The hazardous fluid transport container includes a housing enclosing an at least partially shielded enclosure. First and second fluid path elements are disposed within the housing, with the first fluid path element and second fluid path element fluidly coupled together. A pump unit may be provided for dispensing fluid from the first and second fluid path elements optionally into a third fluid path element. Also, methods for priming the hazardous fluid transport container and for mitigating laminar flow injection bolus spreading are disclosed. Additionally, disclosed is a radioactive fluid transport container for a syringe or other container. The radioactive fluid transport container allows the syringe or container to be used in an injection procedure without removal from the container.
Abstract:
A syringe loading/filling device (5) (or "syringe Loader") includes a syringe mounting mechanism (22a, 22b) adapted to cooperate with an attachment mechanism of a syringe (20) to attach the syringe to the syringe loader and a drive member adapted to impart motion to the syringe plunger (40). The syringes for use with the syringe loader include a syringe plunger (40) slidably disposed therein and an attachment mechanism (66a, 66b) for attachment of the syringe (20) to an injector (10). Such injectors include a mounting mechanism adapted to cooperate with the attachment mechanism on the syringe to mount the syringe (20) on the injector.
Abstract:
A system for injecting an injectate into patient includes a first pressurizable container for holding the injectate; a patient interface in fluid connection with the first pressurizable container, the patient interface being adapted to pass the injectate into tissue of the patient; a powered injector in operative connection with the first pressurizable container to pressurize the injectate; a controller system in operative connection with powered injector; and a stereotactic localization frame adapted to be placed in operative connection with the patient interface to assist in controlling localization of the patient interface. A system for processing cells (and/or other injectate components) includes a container and a plunger adapted to be slidably positioned within the container. The system includes at least one inlet port through which a fluid can enter the system and at least one effluent port through which an effluent can exit the system. The plunger section forms a sealing engagement with the inner wall of the container such that rearward motion of the plunger is adapted to draw fluid into the system via the inlet and forward motion of the plunger is adapted to force effluent out of the system via the effluent port.
Abstract:
An injector system includes a source of injection fluid, a pump device, a fluid path set disposed between the source of injection fluid and the pump device, and a fluid control device operatively associated with the fluid path set. The fluid control device is adapted to permit purging of air from the fluid path set and to stop flow of the injection fluid to a patient at substantially any pressure or flow rate generated by the pump device for delivering a sharp bolus of the injection fluid to the patient. The fluid control device is preferably part of the fluid path set between the source of injection fluid and the pump device. In another aspect, an injector system includes a powered injector, a pressurizing chamber in operative connection with the powered injector, a fluid path in fluid connection with the pressurizing chamber, and a manual control in fluid connection with the fluid path. The manual control includes at least one actuator for controlling the injector through application of force by an operator. The actuator provides tactile feedback of pressure in the fluid path to the operator via a fluid connection with the fluid path. A pressure isolation mechanism for use in a medical procedure includes a lumen, an isolation port in fluid connection with the lumen, and a valve having a first state and a second state. The first state occurs when the lumen and the isolation port are connected. The second state occurs when the lumen and the isolation port are disconnected. The lumen remains open for flow of fluid therethrough in the first state and in the second state. The valve is normally in the first state and is switchable to the second state when fluid pressure in the lumen reaches a predetermined pressure level. A pressure transducer can be in fluid connection with the isolation port of the pressure isolation mechanism. A fluid delivery system includes a manually operated syringe and a pressure isolation mechanism as described above.
Abstract:
A tubing set inludes a length of tubing having at least a section thereof that is fabricated to function with an infusion pump. The tubing set further preferably includes a first valve that is removably connected to the length of tubing on a first end thereof. The first valve is preferably in a closed state when disconnected from the length of tubing. The tubing set also preferably includes a second valve on a second end thereof. The second valve is preferably in a closed state until connected to another fluid path component. The tubing set is preferably suitable for use in an MR environment. A method of replacing at least a first infusion pump in connection with a patient with at least a second infusion pump includes the steps: closing a length of patient tubing connected to a patient to prevent blackflow of blood therethrough, the patient tubing being in fluid communication at a first end thereof with a length of administration tubing, the administration tubing being in operative connection with the first infusion pump and being in fluid connection with a source of fluid, the patient tubing being in fluid connection with a patient catheter at a second end thereof; disconnecting the patient tubing from the administration tubing; connnecting an intermediate length of tubing to the administration tubing, the intermediate tubing including at least a section thereof that is fabricated to function with the second infusion pump; placing the second infusion pump in operative connection with the intermediate tubing; removing the first infusion pump from operative connection with the administration tubing; and connecting the intermediate tubing to the patient tubing.
Abstract:
A tubing set inludes a length of tubing having at least a section thereof that is fabricated to function with an infusion pump. The tubing set further preferably includes a first valve that is removably connected to the length of tubing on a first end thereof. The first valve is preferably in a closed state when disconnected from the length of tubing. The tubing set also preferably includes a second valve on a second end thereof. The second valve is preferably in a closed state until connected to another fluid path component. The tubing set is preferably suitable for use in an MR environment. A method of replacing at least a first infusion pump in connection with a patient with at least a second infusion pump includes the steps: closing a length of patient tubing connected to a patient to prevent blackflow of blood therethrough, the patient tubing being in fluid communication at a first end thereof with a length of administration tubing, the administration tubing being in operative connection with the first infusion pump and being in fluid connection with a source of fluid, the patient tubing being in fluid connection with a patient catheter at a second end thereof; disconnecting the patient tubing from the administration tubing; connnecting an intermediate length of tubing to the administration tubing, the intermediate tubing including at least a section thereof that is fabricated to function with the second infusion pump; placing the second infusion pump in operative connection with the intermediate tubing; removing the first infusion pump from operative connection with the administration tubing; and connecting the intermediate tubing to the patient tubing.
Abstract:
A syringe for use in a medical injection procedure in connection with connectors having a tapered fitting includes a syringe tip having a cooperating tapered fitting including a passage therein in fluid communication with an interior of the syringe. The syringe also includes a first connecting member having a radially inward threaded portion on an inner surface thereof adapted to connect to a first type of connector including a tapered fitting having at least one radially outward extending flange adapted to connect to the radially inward threaded portion of the first connecting member. In that regard, the first connecting member allows connection of the syringe to, for example, a standard luer fitting connector. The syringe further includes a second connecting member having at least one attachment member such as a radially outward extending flange adapted to connect to a second type of connector which includes a tapered fitting and a cooperating attachment member to engage the at least one attachment member of the second connecting member. The second connecting member allows connection of the syringe to improved tapered fitting connectors described herein.
Abstract:
A luer connector (10) is provided with a tactile and audible torque indicator. The indicator comprises a detent incorporated between the female cylindrical component (14) of the luer connector and a rotatable collar (32) mounted thereon. As the collar (32) is turned in a clockwise direction, the collar is impeded by the detent formed by opposingly projecting protuberances (34, 38) between the inside of the collar and the outside of the female cylindrical luer component (14). As the threaded luer connection is tightened, requiring additional torque to tighten it further, the additional torque overcomes the resistance of the detent, allowing the collar protuberance to slip past the cylinder protuberance. The female luer component may also be provided with a color patch or pattern (40), to indicate by its rotation, when the detent has been overcome, that the luer connection has been appropriately tightened.