Abstract: A method and medical pump to perform a flushing procedure are provided. The medical pump is configured to execute the flushing procedure subsequent to an infusion procedure, the flushing procedure and infusion procedure lacking a specified relationship between each other until after performance of the infusion procedure. The method comprises performing an infusion procedure of a medicament with the medical pump and automatically querying in human detectable form whether to execute a flushing procedure in response to conclusion of the infusion procedure.

Abstract: An apparatus and method for indicating a change in operation of a medical infusion pump includes a memory configured to store an original pump parameter and a current pump parameter. The apparatus further includes a programmable circuit in electrical communication with the memory, the programmable circuit programmed to display the original pump parameter and the current pump parameter.

Abstract: A pump module is provided for use in a medical fluid dispensing system that includes a pump body made of a non-compliant material and first and second pump chambers formed in the body. Each of the chambers has a first, open end and an opposite, closed end. The pump module further includes first and second pistons in the first and second pump chambers, respectively. At least one fluid inlet and a fluid outlet are selectively in fluid communication with the first and second pump chambers. Each of the pistons extends through the open end of a respective one of the pump chambers, with each of the pistons being operably translatable within the pump chamber toward and away from the closed end of the chamber. The pistons are translatable independently of one another.

Abstract: This document discusses, among other things, an apparatus comprising a pump configured to deliver insulin, a processor, and a user interface including a bistable display. A display element of the bistable display is placed in one of two stable orientations upon application of a biasing voltage and stays in the stable orientation when the biasing voltage is removed. The processor includes a display module configured to display a non-blank reversion display screen on the bistable display when no input is received at the user interface after a specified time duration, and to recurrently change the reversion display screen until input is received at the user interface.

Abstract: A wireless network having an architecture that resembles a peer-to-peer network has two types of nodes, a first sender type node and a second receiver/relay type node. The network may be used in a medical instrumentation environment whereby the first type node may be wireless devices that could monitor physical parameters of a patient such as for example wireless oximeters. The second type node are mobile wireless communicators that are adapted to receive the data from the wireless devices if they are within the transmission range of the wireless devices. After an aggregation process involving the received data, each of the node communicators broadcasts or disseminates its most up to date data onto the network. Any other relay communicator node in the network that is within the broadcast range of a broadcasting communicator node would receive the up to date data.

Abstract: A breathing circuit includes inspiratory and expiratory limbs, each having a respective electrically energizable heating circuit. The heating circuits are independently and selectively electrically energized through separate power circuits such as to control the temperature in each limb in a desired fashion so as to reduce rainout in the breathing circuit and particularly in the expiratory limb.

Abstract: A computing system of an answering service answers an incoming call from a calling party on behalf of a called party, and allows an agent to converse with the calling party relating to a purpose of the incoming call from the calling party. At a triggering point, a signal is received from the agent while the incoming call from the calling party is still in progress. The triggering point occurs when the agent determines that the calling party is calling regarding a predetermined urgent matter. Contact with the called party is commenced upon receiving the signal and communication between the calling party and the called party is effectuated while the incoming call from the calling party is still in progress.

Abstract: A computing system of an answering service answers an incoming call from a calling party on behalf of a called party, and allows an agent to converse with the calling party. Contact with the called party is established while the incoming call from the calling party is still in progress, and a signal is received from the called party for the called party to monitor the incoming call without joining in. Upon detecting a disconnection of the monitored incoming call between the agent and the calling party, the called party is notified that the incoming call has ended and the agent and the called party are allowed to converse with each other over the called party call regarding the incoming call from the calling party.

Abstract: A device such as for example a electronic medical device has a memory that has prestored therein a number of programs or routines for performing various functions. Some of those functions are optional functions that were not enabled when the equipment was put into service. If the user of the equipment desires thereafter to activate any one of those optional functions, an options card that has a number of memory blocks each specifically configured to enable one of the prestored optional functions is sent to the user. The user can then insert the options card into a receptacle integrated into the device and, upon power up of the device, elect a menu for enabling the desired optional function(s) prestored in the device. The options card may be configured to have a count number that indicates the number of devices the card may be used for enabling a particular optional function.

Abstract: An implantable portal includes a septum that has embedded therein an indicia adapted to identify at least one characteristic of the portal. The indicia may be formed as an impression at a base layer of the septum, and is filled with a radiopaque material. The septum base layer is covered by liquid silicone, which bonds with the septum base layer when solidified, so that an integral one-piece septum, with the identifier indicia embedded therein, is effected. The indicia embedded septum is fitted to the reservoir housing of the portal for providing identification information for that portal. The septum embedded indicia is viewable visually and also by x-ray or computer tomography imaging.

Abstract: A catheter assembly includes a catheter hub defining an interior cavity and a catheter tube extending distally thereof. A rigid actuator extends proximally in the interior cavity and supports a seal member thereon. The seal member includes a central membrane, a distal portion, and a proximal portion. An hourglass shaped actuator cavity is formed in the distal portion and receives a barbed end of the actuator. The outer surface of the seal member is in partial circumferential engagement with the catheter hub to define an air path that allows fluid communication between areas of the interior cavity distal and proximal of the seal member. A punch tool is provided to form a tri-slit in the membrane of the seal member. The seal member may be configured for multi-use and include a biasing member that moves the seal member to force the membrane back over the actuator to close the membrane.

Abstract: A catheter assembly includes a catheter hub defining an interior cavity and a catheter tube extending distally thereof. A rigid actuator extends proximally in the interior cavity and supports a seal member thereon. The seal member includes a central membrane, a distal portion, and a proximal portion. An hourglass shaped actuator cavity is formed in the distal portion and receives a barbed end of the actuator. The outer surface of the seal member is in partial circumferential engagement with the catheter hub to define an air path that allows fluid communication between areas of the interior cavity distal and proximal of the seal member. A punch tool is provided to form a tri-slit in the membrane of the seal member.

Abstract: A safety catheter includes a catheter hub, a catheter tube, a needle hub, a needle cannula having a tip, and a tip protector. The tip protector includes an outer member having a flexible tab configured to releasably engage with the catheter hub and release therefrom upon inward flexing of the tab. An inner member is positioned entirely within the outer member and has a portion that impedes inward flexing of the tab when disposed adjacent the tab. The inner member is axially shiftable relative to the outer member between a first position wherein the needle tip is distal of the tip protector and the inner member portion is disposed adjacent the tab to impede release from the catheter hub, and a second position wherein the tip is within the outer member and the inner member portion is no longer adjacent the tab and no longer impedes release from the catheter hub.

Abstract: An antimicrobial lubricant combines an antimicrobial agent, preferably silver based, with a silicone lubricant. This is achieved by first formulating a lubricant solution that has a non-volatile silicone lubricant and a volatile solvent carrier. An antimicrobial agent is added to the lubricant solution. The solution is then subjected to ultrasonic energy so that the antimicrobial agent is uniformly mixed with the lubricant in the solution. The solution containing the antimicrobial lubricant may be sprayed onto a medical device, for example the outer surface of the catheter of a peripheral IV catheter. After the solvent flashes off, a coat of uniform antimicrobial lubricant is formed on the catheter surface. The antimicrobial lubricant coating facilitates the insertion of the catheter to a patient, and at the same time prevents the growth of microorganisms from the device and infection to the patient.

Abstract: The present invention safety device is a one-piece needle assembly that has a base and a housing pivotally connected to the base. The base has a distal portion to which a needle is fitted. At the base there is formed longitudinally along its distal portion a catch mechanism that may be in the form of an anchor projection. At the back wall of the housing there is extended another catch mechanism that may be configured in the form of two clasping fingers. Also providing in the housing is an integral hook. As the housing and the base are pivoted relative to each other, and as the needle makes contact with the hook, the respective catch mechanisms at the base and the housing also make contact with each other, resulting in the coupling of the catch mechanisms and the coupling of the needle to the hook. As a result, the catch mechanisms are interlocked and the needle is fixedly retained by the hook within the housing.

Abstract: A heated breathing circuit detection system verifies the proper set up and connection of a breathing circuit to a heater unit of a humidification system. The detection system automatically detects that the breathing circuit is connected to the heater unit, and the nature of the heating circuit(s) thereof. In one embodiment, the resistance of the heating circuit(s) is determined and compared to an expected resistance or range of acceptable resistances to determine if the heater circuit(s) is properly or actually attached and properly operating. The humidification system also has the ability to determine the delivery mode of the breathing circuit, i.e., whether a single inspiratory limb, or both inspiratory and expiratory limbs, is connected to the heater unit.

Abstract: A fixed needle syringe has a syringe barrel with its distal portion modified to accept a needle protective housing. In particular, the distal portion is formed with the a groove dimensioned to accept a collar that is attached to the housing. The inside surface of the collar is provided with a number of flanges that fit within the groove formed at the distal portion of the syringe barrel of the fixed needle syringe. Protrusions are provided at the inside surface of the collar to frictionally act against the syringe barrel, so that the needle protective housing does not freely rotate, but is rotatable relative to the syringe barrel by the application of a predetermined torque to either the collar or the housing attached thereto. An internal hook is provided in the housing to grasp the needle of the syringe, when the housing is pivoted to cover the needle extending from the needle hub of the syringe.

Abstract: A temperature probe, such as for a respiratory system in which breathable gases are supplied to a patient, includes a housing having a cavity sized to snugly receive therein a generally cylindrical container within which is secured a thermistor, with the container adapted to provide a barrier to moisture. The probe provides a quick temperature response but minimizes migration of moisture to the thermistor notwithstanding the high temperature and heat levels encountered in normal operation of the respiratory system.

Abstract: Each leg of a U tube blanket is configured to have at least one row of holes extending substantially along the length thereof. The size of the holes is incrementally increased from the proximal portion that is closest to the air inlet cross section of the blanket where heated air is input to the blanket for inflating the same to the distal portion of the legs of the blanket. For an embodiment of the inventive blanket, the plurality of vent holes along each leg of the blanket are grouped into a number of sections, for illustration purposes three, with the vent holes in each section having the same dimension. With the size of the holes being incrementally larger along the leg away from the heat source, a greater amount of warm air is output at the distal portion of the blanket to compensate for the distance the warm air needs to travel before it is vented from the blanket.