Abstract: An apparatus for the detection of extravasation is positioned in a manner so that the vicinity of a site is available for palpation and is visible for visual inspection. Another embodiment of the apparatus improves the sensitivity of detection by positioning an energy source and a receiver between a first layer of a high dielectric material and a second lay of a low dielectric material. The apparatus may further include a third layer of a conductive material to shield the apparatus from stray capacitance. In addition, a system for detection of extravasation includes an array of sensors located at, adjacent to and/or remote from an injection site.

Abstract: An adapter includes a syringe carrier adapted to seat at least a portion of the syringe. The syringe carrier includes at least one rearward facing abutment member to abut at least one forward facing surface on a syringe. The syringe carrier includes an opening therein to allow a drive member of an injector to communicate forward force to the plunger through abutment without connective engagement between the drive member and the plunger. The adapter further includes a releasable mounting mechanism positioned to the rear of the syringe carrier to mount the adapter in a desired position relative to the front wall of the injector.

Abstract: Apparatuses for sharing information on syringe configuration between syringes and injector systems comprise a storage system to store encoded information on syringe configuration. The encoded information is readable by a detection circuit in an injector. In one embodiment, the storage system is an electronic storage system in which information relevant to the syringe configuration is encoded. A method comprises the step of conveying syringe configuration information to a detector in an injector for use with the syringe.

Abstract: A method is provided for imaging a vasculature of a patient using an MRI system with an array of local coils. The method includes thestep of providing a housig by which (I) a first plurality of the coils is arrayed along an anterior surface of the patient, (II) a second plurality of the coils is arrayed along a posterior surface of the patient, and (III) the patient is oriented such that portions of the vasculature between and including the renal and feet portions thereof are aligned substantially coplanarly. The method also includes the step of injecting a contrast agent into the patient. The method further involves acquiring images of the vasculature from approximately the renal portion thereof to an including the feet portion thereof so that the images of the portions of the vasculature are acquired successively in timed relation to a progression of the contrast agent therethrough.

Abstract: A syringe includes a body and a plunger disposed therein. The body includes a nozzle formed therein and at least one hub member connected thereto or integrally formed thereon for holding an end of a connector tube. The connector tube includes two ends, each end preferably being connected to a respective hub member to retain the connector tube in contact with the syringe. Preferably, the syringe and the connector tube are packaged in a pre-connected condition for ease of use by the customer. Furthermore, flexible inlet tubing for connection to a syringe for filling the syringe with contrast media, for example, is described. The inlet tubing permits filling of the syringe from either a bag or a bottle and may remain attached to the syringe so that it forms at least a part of the connection to the patient. In addition, an apparatus for facilitating the purge of air from a connector tube that will ultimately be connected between a syringe and a patient is described.

Abstract: A front-loading syringe which comprises a movable plunger for injecting liquid contrast media, is rotatably mountable on a front wall of an injector housing with an interference fit and in sealed relationship with respect thereto, with or without a pressure jacket, by a first-quick release mechanism. At the same time, the plunger is connected to an injector drive mechanism by a second readily releasable mechanism. During the mounting operation, a sensor reads injection information from an indicator device on the syringe and feeds it to an injector control. An audible-and-tactile indicating mechanism also is activated when the syringe is essentially in the desired mounted position. The syringe may include reinforcing ribs, which also function as volumetric gradations, and liquid media presence-or-absence indicating dots which appear circular against a liquid media background and oval-shaped against an air background.

Abstract: An apparatus and method enabling the injection of fluid media into a plurality of patients is provided, including a fluid supply source providing multiple doses, a metering device for measuring the doses, a pressurizing device to effect injection, a contamination prevention device disposed between the fluid source and the patient and, when desired, an electronic control device to integrate operation of the apparatus and process.

Abstract: An adapter for releasably attaching a syringe to an injector includes a first section and a second section connected about a hinge axis that is generally perpendicular to a longitudinal axis of the adapter. The first section and the second section are rotatable about the hinge axis between an open position to allow loading of the syringe into the adapter from a position to the rear of the hinge axis and a closed position to retain the syringe therein. The hinge axis is preferably off-center from the longitudinal axis of the adapter and the adapter further includes a releasable mounting mechanism positioned on a rearward end of the adapter to mount the adapter in a desired position relative to the front wall of the injector.

Abstract: A magnetic resonance imaging receiver/transmitter coil system for providing images for regions of interest includes a first phased array formed of a plurality of electrically conductive members and defining an array volume and a second phased array formed of a second plurality of electrically conductive members and disposed at least partially within the defined array volume. At least one of the first and second phased arrays is adapted to apply a magnetic field to the defined array volume. At least one of the first and second phased arrays is further adapted to receive said applied magnetic field. The first phased array is extendible to define a further array volume and is provided with a switch for electrically coupling and decoupling an extension to effectively extend the length of the first phased array and thereby define the further array volume. In this manner the length of the first phased array is effectively extended to approximately twice its unextended length.

Abstract: An apparatus enables a patient to be positioned optimally for a scanning procedure during which images are to be obtained of the vasculature of the patient. The apparatus includes a lumbar support, a tray, and a leg support. The lumbar support allows the renal portion of the vasculature to be positioned predominately in a single plane. The tray allows the pelvic and femoral portions of the vasculature to be positioned substantially coplanar with each other and with the renal portion of the vasculature. The leg support allows the lower leg and feet portions of the vasculature to be positioned substantially coplanar with each other and with the pelvic and femoral portions of the vasculature. The substantial coplanar alignment of the portions of the vasculature enables the images thereof to be obtained with a smaller field of view and thus at least one of greater resolution and reduced scanning time.

Abstract: A syringe for use with an injector includes a body comprising a distal discharge end, a plunger movably disposed within the body, and an agitation element disposed within the body between the plunger and the distal discharge end. The agitation element is acted on by a magnetic field to agitate the contents of the syringe. The magnetic field is generated by a source operably associated with the syringe or the injector. Preferably, the syringe contains an ultrasound contrast agent that is agitated by the agitation element. An injector system and a method for agitating the contents of a syringe are also provided.

Abstract: A communication system for use in an MRI procedure includes a first communication unit positioned within a shielded housing on an interior side of the isolation barrier. The first communication unit includes a first receiver and a first transmitter. The communication system also includes a second communication unit positioned on an exterior side of the isolation barrier. The second communication unit includes a second receiver and a second transmitter. The first communication unit is in connection via optical cabling with a first light transmitting device positioned on an interior side of the isolation barrier adjacent a viewing window in the isolation barrier. The second communication unit is in connection via optical cabling with a second light transmitting device positioned on the exterior side of the isolation barrier adjacent a viewing window in the isolation barrier.

Abstract: A fluid delivery system for delivery of an injection fluid to a patient generally includes a pump system to pressurize the injection fluid, a patient interface in removable fluid connection with the pump system, and a connector in fluid connection between the pump system and the patient interface. The pump system is connected to an inlet of the connector, and the patient interface is removably connected to an outlet of the connector. The connector includes a sealing member at least partly disposed within a housing of the connector that is biased to close the outlet when the patient interface is removed.

Abstract: The present syringe adapter (100), which permits use of syringes (40) of various types, sizes and configurations to be used with a front-loading injector (10), includes a removable injector face plate (120) having a releasable mounting mechanism (122a, 122b) for attaching the adapter face plate (120) to a front-load injector (10), a reducing sleeve (140) having a recess (190) for receiving the distal flange (44) of syringe (40), locking pivot arms (220, 240) pivotly attached to the reducing sleeve (140) to releasably engage syringe flange (44), and a piston extension (320) provided for extending the injector drive piston (16) for engagement with syringe plunger (46).

Abstract: An injector for use in injecting a fluid in a medical injection procedure includes a drive mechanism to pressurize the fluid; a sensor to measure a variable that is proportional to fluid pressure (that is, a direct or indirect measurement of fluid pressure); and a pressure monitor (for example, including hardwired circuitry and/or software) in communication with the sensor and the drive mechanism to stop the injection procedure when the sensor measures a value of the variable that corresponds to a pressure hazard limit. Preferably, the pressure monitor further limits power input to the drive mechanism to a power limit once the variable reaches a value that corresponds to a power limiting pressure that is below the pressure hazard limit.

Abstract: Embodiments of an injector, syringe, syringe interface, and piston/plunger assembly for an injector (of contrast medium, for example) are described. Preferably, the syringe is adapted to engage a syringe interface mechanism such that the syringe may be connected to an injector without regard to any particular orientation of the syringe to the injector or to the piston/plunger assembly.

Abstract: A fluid injection arrangement, particularly involving a systematic fluid injection programming capability, in the context of patient imaging systems, in which phases of contrast medium infection and flushing medium injection can be freely and selectably ordered so as to make available to the operator and patient a vast array of possible protocols than has hitherto been essentially unattainable. Also contemplated is the use of a “hold” phase, involving an indefinite pause between phases of a protocol, in connection with such imaging systems. Further contemplated is the use of a “pause” phase in which a pause of fixed duration is pre-programmed into the protocols of MRI Injector systems.

Abstract: A syringe system (20) includes an elongated shell (30), a pressure member (80) slidable disposed within the elongated shell (30), and a collapsible cartridge (100). The Collapsible cartridge (100) is inserted within the elongated shell (30), and collapses as the pressure member (30) is advanced within the elongated body (30) to pressurize fluid within the collapsible cartridge (100). The collapsible cartridge (100) preferably further includes a passage (130) through which the fluid passes when pressurized by the pressure member (80).

Abstract: A mounting member for attaching a front-loading syringe to a powered injector is disclosed. The present invention may also include a plunger that has a two-piece molded core portion that is readily attachable to a plunger drive member of a powered injector. The plunger core may also be equipped with an anti-cocking flange to prevent the plunger from being axially misaligned within the syringe body which could result in fluid leakage between the plunger and the syringe body. An alignment flange may also be provided on the plunger to assist with the proper insertion of the plunger into the syringe during the assembly process. A method of manufacturing a syringe plunger is also disclosed. The present invention further includes a sleeve for clampingly engaging a heating blanket to the outer surface of a syringe.

Abstract: A system for dispensing a medium includes at least a first container to hold the medium, a pressurizing device, such as a pump, in fluid connection with the container for pressurizing the medium, and an agitation mechanism or device to maintain the components of the medium in a mixed state. The container and the pressurizing device can be separate units, as in the case of an bag or bottle in fluid connection with a peristaltic or other type of pump. The container and the pump can also be combined in a single unit, as in the case of a syringe, wherein the syringe barrel of the syringe acts to contain the medium and the syringe plunger pressurizes the medium within the syringe barrel. A method of injecting a multi-component medium includes the step of agitating the medium (for example, as described above) before or during an injection procedure to maintain the components of the medium in a mixed state.