Abstract: A cap assembly universally structured for protectively enclosing differently dimensioned and configured additive ports of an IV container and including a housing, which may include a variably dimensioned interior, structured to receive the additive port therein, in an operative position. A cover is disposed in covering relation to the housing interior and a retaining structure is disposed within the housing in retaining engagement with the additive port. A closure structure is disposed on the housing in an attached orientation, structured to be resistant to detachment, concurrent to the operative position of the additive port within the housing. The operative position further includes the retaining structure disposed in retaining engagement with the additive port on the interior of the housing, concurrent to the attached orientation of said closure structure.

Abstract: A closure assembly for a syringe or other medical administering device includes an outer sleeve having an access opening and a tip cap removably disposed therein. The tip cap includes a flow restrictor structured for removable, flow restricting connection to the syringe. An indicator member is removably connected within the outer sleeve, in interruptive relation to passage of the tip cap through the access opening. A retaining structure is fixedly connected to the flow restrictor and movable therewith relative to the indicator member. The retaining structure and flow restrictor are collectively structured for retaining engagement of the tip cap with the indicator member, as the tip and indicator member are concurrently removed from the outer sleeve and as the tip cap is disconnected from the flow restricting connection with the syringe.

Abstract: A tamper evident seal structure for a vial septum or other cover having a housing including a sidewall terminating in oppositely disposed open and closed ends. A retainer is fixedly disposed within the housing and structured for retaining engagement with a portion of a vial, substantially adjacent the vial cover. The housing also includes a pressure member disposed within an interior thereof in attached, relation to the closed-end. The pressure member and the retainer are cooperatively disposed and structured to respectively exert pressure on the vial cover concurrent to retaining engagement with the vial. Tamper evident capabilities are at least partially defined by a detachment of a removable sidewall section from a remainder of said sidewall.

Abstract: A closure assembly for a medical container having a sleeve with a tip cap disposed therein in an accessible position relative to an access opening. A cover is fixedly secured to one end of said sleeve, opposite to said access opening and a retainer is fixedly secured within the sleeve, adjacent the cover and in a removably retaining engagement with the tip cap. The removably retaining engagement includes the retainer having one or more segments disposed in retaining engagement with an exterior of the tip cap. Upon detachment of the tip cap from the retainer and the removal thereof from the sleeve, the one or more segments are separable from one another and/or a remainder of the retainer, while being maintained in a captured position within the sleeve.

Abstract: A modular connector assembly for a medical container may include a plurality of covers and a plurality of adapters. Each cover is connectable to a cooperatively dimensioned medical container. Each adapter is attachable in fluid sealing engagement with each cover by an interface assembly including a first interface segment formed on each of said plurality of covers and a second interface segment formed on each of said plurality of adapters. The first and second interface segments and corresponding ones of the covers and adapters are initially separable and subsequently connected to define a fluid sealing engagement between connected ones of the cover and adapter. The structural configuration of each of the plurality of adapters is variable to define a different one of a plurality of medical connector types.

Abstract: A closure for a medical container including a base structured to be supported in an operative, upright orientation on a horizontal surface and having an exposed face and a connector disposed thereon and extending outwardly therefrom. A protective cage includes one or more cage members each configured in the form of a helix fixedly connected to the base and extending longitudinally and laterally outward from the connector in at least partially surrounding relation thereto. The base may include self-righting structural features, including an outer surface having a curved, substantially bulbous configuration and a center of gravity disposed between a tipping point of said base and a terminal end thereof.

Abstract: An assembly, for packaging and safely disposing of a needle structure, including a housing having at least one containment structure. The containment structure includes a hinge movably interconnecting a base and a needle retaining segment, between open and closed orientations. The retaining segment includes a compartment removably containing the needle structure therein and the base includes a chamber for reception of the compartment and medical needle therein, when in the closed orientation. The hinge normally biases the retaining segment and compartment outwardly at substantially a predetermined angular orientation relative to said base, in the open orientation, to facilitate access to the medical needle through an access opening in the compartment. A closure is fixedly connected to and movable with both the base and the retaining segment and is structured to removably secure said housing in said closed orientation.

Abstract: A closure structured to adapt a syringe for connection to an incompatible standardized medical connector, including either a male or female ISO 80369 series ENFit® connector. An adapter body has an inlet port and an outlet port disposed in fluid communication with one another. The inlet port is dimensioned and configured to accommodate attachment to a discharge port of the syringe and the outlet port is dimensioned and configured to accommodate attachment to the standardized connector. A tip cap is removably connected to the adapter body in flow sealing relation to the outlet port. The closure may include a tamper evident assembly including a sleeve removably disposed in enclosing relation to the adapter body and tip cap and a retainer structure is disposed in removably retaining relation to the sleeve.

Abstract: A method for detecting a disease state is presented. In accordance with aspects of the present technique, a method for detecting a disease state is presented. The method includes creating a normal standardized data repository, where the normal standardized data repository includes one or more normal reference surface projections, where the normal reference surface projections include anatomical information obtained from one or more groups at different phases corresponding to one or more regions of interest in a normal organ, where each of the one or more groups includes one or more subjects having normal organs, and where the normal standardized data repository may be configured to aid in the detection of a disease state. Systems and computer-readable medium that afford functionality of the type defined by this method are also contemplated in conjunction with the present technique.

Abstract: Method and system for using segmentation and three-dimensional image-processing techniques of a method to create an automatic method to detect coronary artery calcification deposits and identify their location with respect to a major coronary artery. Finally, different scoring algorithms can be applied to generate calcium scores such as Agatston Janovitz, Mass, and Volume. A total score and a more detailed score can be generated based on the major arteries such as right coronary artery, left anterior descending artery, or left circumflex artery to be incorporated into the patient report.

Abstract: A computer-implemented method for quantifying an object in a larger structure using a reconstructed image obtained from an imaging apparatus includes identifying an object boundary in a region of interest of the image and a region of exclusion, and determining a mean value of intensity in a neighborhood of the object to estimate a background value, excluding the region of exclusion. The method further includes determining an interior region, a transition region, and a background region of the object using the object boundary and a transfer function of the imaging apparatus, and determining and displaying a measure of object quantification utilizing intensities of at least one of the determined interior region or the transition region a method for quantifying an object in a larger structure using a reconstructed image obtained from an imaging apparatus.

Abstract: A method for detecting a disease state is presented. In accordance with aspects of the present technique, a method for detecting a disease state is presented. The method includes creating a normal standardized data repository, where the normal standardized data repository includes one or more normal reference surface projections, where the normal reference surface projections include anatomical information obtained from one or more groups at different phases corresponding to one or more regions of interest in a normal organ, where each of the one or more groups includes one or more subjects having normal organs, and where the normal standardized data repository may be configured to aid in the detection of a disease state. Systems and computer-readable medium that afford functionality of the type defined by this method are also contemplated in conjunction with the present technique.

Abstract: Method and system for using segmentation and three-dimensional image-processing techniques of a method to create an automatic method to detect coronary artery calcification deposits and identify their location with respect to a major coronary artery. Finally, different scoring algorithms can be applied to generate calcium scores such as Agatston Janovitz, Mass, and Volume. A total score and a more detailed score can be generated based on the major arteries such as right coronary artery, left anterior descending artery, or left circumflex artery to be incorporated into the patient report.

Abstract: A computer-implemented method for quantifying an object in a larger structure using a reconstructed image obtained from an imaging apparatus includes identifying an object boundary in a region of interest of the image and a region of exclusion, and determining a mean value of intensity in a neighborhood of the object to estimate a background value, excluding the region of exclusion. The method further includes determining an interior region, a transition region, and a background region of the object using the object boundary and a transfer function of the imaging apparatus, and determining and displaying a measure of object quantification utilizing intensities of at least one of the determined interior region or the transition region a method for quantifying an object in a larger structure using a reconstructed image obtained from an imaging apparatus.

Abstract: A method and system for prospectively acquiring data of a region of interest for retrospective re-analysis includes obtaining region of interest data and generating property information of the region of interest data. The method also includes analyzing the property information receptive to generating a measurement of the property information. After storing the property information, the property information is retrievable for further analysis.

Abstract: A system and method are disclosed for event communication on a distributed scanner/workstation platform. In one embodiment, a medical imaging system having at least one host further includes a first application, a second application, and an event name service. The first application is at the at least one host, and is a first event source. The second application is at the at least one host, and is a first event listener capable of receiving a first event provided from the first application. The event name service is in communication with the first and second applications. At least one of the first and second applications is capable of registering with the event name service.