Abstract: A syringe pump including a plunger driver head that selectively urges against a syringe. A drive arm includes an elongate plunger tube. The drive arm is coupled to the plunger driver head and movement of the elongate plunger tube corresponds with movement of the plunger of the syringe along the first central longitudinal axis. A potentiometer generates a signal that is proportional to an insertion distance of the rod inside the elongate plunger tube. The syringe pump records the signal from the potentiometer at the time delivery of infusate from by the syringe pump is paused and again at the time delivery is resumed. The syringe pump detects information about the syringe, accesses an electronic system to determine information about the syringe allowing the syringe pump to calculate the volume of a manual bolus from the syringe while delivery of infusate from the syringe pump was paused.

Abstract: The present disclosure describes dedicated consumable sets for use with syringe pumps. A dedicated consumable set for use with a syringe pump may include a housing configured to receive a flow rate sensor communicatively coupled to the syringe pump and configured to measure flow rate of an infusate, and an optional RFID tag fixedly coupled to the housing and configured to communicate information about the dedicated consumable set to the syringe pump. The flow rate sensor can be further configured to detect the presence of an occlusion and communicate detection of the occlusion to the syringe pump. Advantages of the present disclosure include improvements to syringe pump start-up time, syringe swap time, and syringe pump occlusion detection and resolution times.

Abstract: Dedicated consumable sets with pressure sensors and valves, for use with syringe infusion pumps, are disclosed. A dedicated consumable set for use with a syringe pump may include a housing, a valve positioned between distal and proximal ends of the dedicated consumable set and configured to block or regulate the flow of infusate through tubing from a syringe to a patient, and a pressure sensor for measuring pressure inside the dedicated consumable set, and optionally a flow sensor for measuring flow, the pressure sensor configured to transmit pressure measurements above a predetermined level to the valve. The valve can be further configured to automatically actuate between an open position and a closed position, or to proportionally adjust restriction and modulate contained volume, in response to an external event, which may be receiving a pressure measurement above a predetermined level or detecting the removal of the syringe from the syringe pump.

Abstract: Embodiments of syringes and components thereof described herein provide reduced compliance from flexing or deformation, of not only the syringe barrel but also of the syringe plunger rod and plunger seal. Embodiments of syringes and components thereof described herein also provide improved sealing between the barrel and the syringe plunger rod, and improved resistance to pressure. Embodiments of syringes and components thereof described herein are advantageously suited for use with an infusion pump which may subject syringes to many start/stop operations over a period of hours, sometimes at very low flow rates.

Abstract: Systems and methods for generating dynamic reward workflows based on determined tenant behaviors are described and contemplated herein. The method comprises providing a resident interface configured to receive tenant data. The method further comprises determining a tenant behavior based on the tenant data and generating a reward workflow based on the tenant behavior. A reward can be provided based on a determination that a task associated with the workflow is complete. By incorporating insights based on tenant and property data into reward workflows, embodiments address the need for predictive and customized reward workflows that maximize resource allocation for tenant retention.

Abstract: Airbag cushion chutes and related assemblies comprising airbag cushion chutes for controlling airbag cushion deployment and/or protecting screens or other equipment in a vehicle. In some embodiments, an airbag cushion assembly may comprise a housing and an airbag cushion chute positioned within the housing. An inflatable cushion may be positioned within the airbag cushion chute, which airbag cushion chute may be configured to, upon deployment of the inflatable cushion, extend out of the housing to restrict expansion of the inflatable cushion in a lateral direction, which may allow for protecting, for example, a disassociated screen of a vehicle.

Abstract: Certain aspects of the disclosure are directed toward systems methods and computer readable media containing machine readable programs thereon for managing real estate.

Abstract: Disclosed is a grille assembly, which may comprise a grille plate including airflow cutouts within the grille plate, and may be designed to integrate with, or enhance the décor of a room. In certain embodiments, the grille assembly may further comprise an airflow regulator including a main body configured to insert into an airduct opening within a building structure, and the grille plate is configured to mount to a surface of the building structure over the airduct opening and airflow regulator inserted therein.

Abstract: An airbag includes a first panel and a second panel. A first wing is formed with one of the first panel and the second panel, the first wing being coupled to the other of the first panel and the second panel. At least a second wing is formed with one of the first panel and the second panel, the second wing being coupled to the other of the first panel and the second panel. The airbag includes a first depth that extends from the first panel to the second panel proximate the first wing and the second wing when the airbag is in the deployed position and at least a second depth extending from the first panel to the second panel proximate the first base, wherein the second depth is less than the first depth.

Abstract: An airbag includes first panel and a second panel. A first wing is formed with one of the first panel and the second panel, the first wing being coupled to the other of the first panel and the second panel. At least a second wing is formed with one of the first panel and the second panel, the second wing being coupled to the other of the first panel and the second panel. The airbag includes a first depth that extends from the first panel to the second panel proximate the first wing and the second wing when the airbag is in the deployed position and at least a second depth extending from the first panel to the second panel proximate the first base, wherein the second depth is less than the first depth.

Abstract: An airbag is configured to be coupled to a steering wheel of a motor vehicle. The airbag includes a first panel and a second panel. The first panel is coupled to the second panel to form a split at a bottom area of the airbag forming two or more legs. The two or more legs cooperate to reduce the thickness of the airbag in a lower region upon inflation of the airbag as compared with an upper region of the airbag which interacts with the head and upper torso of an occupant.

Abstract: Airbags and airbag assemblies are disclosed that include passive adaptive venting. The disclosed embodiments include an airbag cushion to define an inflation chamber and that include a set of vents. The set of vents is disposed through a panel of the airbag cushion. The set of vents allow egress of inflation gas from the inflation chamber and to be in an open state when a degree of compression of the airbag cushion is below a threshold level. The set of vents is configured to be in a closed state and/or obstructed by a vehicle surface of a vehicle structure when the degree of compression of the airbag cushion exceeds the threshold level.

Abstract: An insulating construction having a multi-layer synthetic core for use in products such as sleeping bags is provided. A sleeping bag using this construction may include a synthetic core having first and second layers, an inner lining adjacent to the first layer, and an outer shell adjacent to the second layer. The synthetic core may be contained within the inner lining and outer shell. The first layer may be constructed of a first material having a first denier; and the second layer may be constructed of a second material having a second denier larger than the first denier. The inner liner may define an inner space configured to accommodate a human body. Various other products made from this construction, such as jackets, pants, and other garments, are also provided.

Abstract: An insulating construction having a multi-layer synthetic core for use in products such as sleeping bags is provided. A sleeping bag using this construction may include a synthetic core having first and second layers, an inner lining adjacent to the first layer, and an outer shell adjacent to the second layer. The synthetic core may be contained within the inner lining and outer shell. The first layer may be constructed of a first material having a first denier; and the second layer may be constructed of a second material having a second denier larger than the first denier. The inner liner may define an inner space configured to accommodate a human body. Various other products made from this construction, such as jackets, pants, and other garments, are also provided.

Abstract: Methods, particles and kits for determining kinase activity within a sample are provided. An embodiment of a method includes exposing a fluorescent particle to an assay, wherein the fluorescent particle includes a support substrate having one or more fluorescent materials and a peptide substrate coupled to the support substrate via a functional group of the support substrate. The method further includes phosphorylating the peptide substrate during exposure of the fluorescent particle to the assay and processing the fluorescent particle such that the peptide substrate is dephosphorylated and a polarized double bond is generated at a dephosphorylated site. In addition, the method includes coupling a fluorescent reporter having a nucleophilic terminal group to the fluorescent particle via the polarized double bond.

Abstract: The invention relates to methods of characterizing autoimmune diseases by detecting and measuring at least one analyte using multiplexed assay systems. According to one embodiment, a target is detected and measured by different bead sets having different reactants. According to another approach the ratio of self-antigen to autoantibody is measured by exposing a sample suspected of containing self-antigen and autoantibody to a bead set associated with monoclonal antibody specific for the self-antigen and a bead set associated with the self-antigen.

Abstract: A fluid delivery system having a closed-loop control process for delivering a medical fluid to a patient. A fluid infusion system includes a pump for delivering a fluid to a patient via an administration tube. A flow sensor associated with the administration tube provides an indication of the actual flow rate of fluid in the administration tube. Such a flow sensor may comprise a positive displacement flow sensor constructed using micro-fabrication and/or micro-molding techniques. A reader reads the actual flow rate signal and provides an indication to a controller for controlling the pump. The flow rate information can also be used for providing status information, such as the existence of a blockage in the fluid delivery system.

Abstract: Systems and related methods pump fluid through a pump. The pump comprises a pump chamber, which is responsive to applied pressures to convey fluid. The systems and methods place an electrode in electrical conductive contact with fluid in the pump chamber which, in use, is coupled to an electrical source. The electrode generates an electrical field in the pump chamber that varies according volume of fluid in the pump chamber. The systems and methods register variations in the electrical field as fluid is conveyed through the pump chamber.

Abstract: A medical delivery system (10) is provided for delivering a medicament (17) or fluid (17) to a patient. The system comprises a disposable element such as a line set (14) associated with a container (16) containing the fluid (17), an identifier (18) associated with the line set (14) and having identification information associated therewith, and a delivery device (12) configured to engage the line set (14) and deliver the fluid (17) to the patient. The delivery device (12) includes a recognition system (20) that is capable of obtaining the identification information associated with the identifier (18). The identification information may include information regarding the identification of the fluid (17), a type of line set (14), or a type of administration associated with the line set (14). The device (12) can be capable of configuration based on the identification information.

Abstract: An apparatus, system and method of programming a medical therapy in a medical device are provided. Generally, the medical device 10 has a controller 12, a memory 14, a processor 16 and an input device 18. The memory 14 is preloaded with at least one of a plurality of patient profiles and condition profiles. The memory 14 is further preloaded with an associated medication therapy for a plurality of the profiles. The input device 18 receives profile data 90, 91 comprising at least one of a patient profile data and a condition profile data for a specific patient, and the processor 16 processes the received profile data 100 and provides as output one of the preloaded medication therapies based on the processed profile data 102.