Abstract: A portal access assembly includes an inserter that has a needle, a cap moveable along the length of the needle and an infuser having a cannula through which the needle extends. A safety mechanism inside the cap allows the needle to be moved relative to the cap so long as the shaft of the needle biases against an edge of one of the legs of the mechanism. After the cannula is properly positioned in the implanted port to establish a fluid path between the port and the infuser, the needle is removed by being pulled upwards until it no longer biases the one leg of the mechanism. At which time the safety mechanism fixedly captures the needle inside the cap to prevent the contaminated tip of the needle from being exposed to the environment. At the same time, the cap is detached from the infuser.

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 device for inserting a subcutaneous infusion device into skin of a patient. The device can include a housing, a needle hub including a needle, a sleeve, and a spring engaging the needle hub. The device can also include a cap coupled to the housing, and a retention member configured to maintain the device in a ship state prior to decoupling of the cap from the housing. In one example, the retention member can include a boss coupled to the cap and configured to engage the infusion device to maintain the infusion device in the ship state prior to decoupling of the cap from the housing. In another example, the retention member can include a tab formed by the sleeve, the tab engaging a bead on an internal surface of the cap when the sleeve moves relative to the housing while the device is in the ship state.

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: An infusion device including a site and a set for delivery of a substance to a patient. The site can include a cannula that is introduced into a subcutaneous layer of skin of the patient. The set can be coupled to the site by placing the set over the site and moving the set from an unlocked to a locked position. The set can be oriented at multiple rotational orientations with respect to the site, and can be coupled and uncoupled with the site multiple times. Also included is a device for inserting a subcutaneous infusion device into a subcutaneous layer of skin of a patient. Some devices automatically retract a needle used to introduce the cannula. Upon full introduction of the needle and associated cannula of the subcutaneous infusion device into a subcutaneous layer of skin of a patient, the device can move the needle into a retracted state.

Abstract: A needle protector that protects the tip or distal end of a cannula, a trocar, or a cannula/trocar combination, is provided by an extruded tubing that has at least a section thereof that includes one or a plurality of protrusions or protuberances that are configured in a given fashion so that there is a slight bend created at that section of the tube, when the tube is fitted onto a cannula or trocar with the protrusions coming into contact with the outer diameter surface of the cannula or trocar. This results in friction contact between the protrusions and the cannula or trocar to maintain the tube protector in place relative to the cannula or trocar.

Abstract: A device for inserting a subcutaneous infusion device into skin of a patient. The device can include a housing, a needle hub including a needle, a sleeve, and a spring engaging the needle hub. The device can also include a cap coupled to the housing, and a retention member configured to maintain the device in a ship state prior to decoupling of the cap from the housing. In one example, the retention member can include a boss coupled to the cap and configured to engage the infusion device to maintain the infusion device in the ship state prior to decoupling of the cap from the housing. In another example, the retention member can include a tab formed by the sleeve, the tab engaging a bead on an internal surface of the cap when the sleeve moves relative to the housing while the device is in the ship state.

Abstract: This document discusses, among other things, an apparatus comprising a pump configured to deliver insulin, a wireless communication port, a controller, and a housing to enclose the apparatus. The controller is configured to communicate with a second device via the communication port using an open standard wireless communication protocol. The housing includes a mechanical coupling to slidably engage the second device which includes a second wireless communication port. Slidably engaging the second device positions the first and second communication ports opposite each other to allow communication via the first and second communication ports when slidably engaged.

Abstract: Methods and systems of patient treatment are disclosed. The methods and systems include use of medical device informatics to modify and validate therapies and drugs used in those therapies. In certain embodiments, a medical device, such as a medical infusion pump, interfaces with a server to administer the patient treatments. In one aspect, a method of determining the on-line status of a medical device is disclosed. The method includes expecting communication from the medical device within a predetermined period, and determining whether a message has been received from the medical device within the predetermined period. The method further includes establishing an on-line status for the medical device based on the determining step.

Abstract: Methods and systems of patient treatment are disclosed. The methods and systems include use of medical device informatics to modify and validate therapies and drugs used in those therapies. In certain embodiments, a medical device, such as a medical infusion pump, interfaces with a server to administer the patient treatments. In one aspect, a method of synchronizing clocks between a medical device and a medical device server is disclosed. The method includes maintaining a server time value on a medical device server communicatively connected to a medical device, and transmitting the server time value from the medical device server to the medical device, the medical device maintaining a device time value. The method further includes replacing the device time value with the server time value.

Abstract: Methods and systems of patient treatment are disclosed. The methods and systems include use of medical device informatics to modify and validate therapies and drugs used in those therapies. In certain embodiments, a medical device, such as a medical infusion pump, interfaces with a server to administer the patient treatments. In one aspect, a method of deploying information to a medical device is disclosed. The method includes storing information in a data package on a server, the information intended to be delivered to a medical device. The method also includes receiving a message from the medical device, and in response to receiving the message, indicating to the medical device that information intended for the medical device resides on the server. The method further includes receiving a request for the information, and upon receiving the request, delivering the data package to the medical device.

Abstract: A portal access device that is adapted to provide long term access to a port implanted in a patient has two major components, an infuser assembly and a safety needle insertion device. The infuser assembly has an infuser housing that can be configured into a specific shape, for example a dome. A blunt cannula is attached to and extends downwardly from the underside of the infuser housing. Also connected to the infuser housing, preferably at a side thereof, is a tubing or catheter. The safety needle inserter assembly has a base having a proximal portion that is configured to form fit over the infuser housing. At the distal portion of the base uprights are provided so that a second end of an arm, to which first end a needle or a sharp cannula is connected, may be movably and hingedly connected to the base. The sharp cannula extends from the underside of the proximal end of the arm and passes through the base by way of a bore formed at the proximal portion of the base.

Abstract: Methods and systems of patient treatment are disclosed. The methods and systems include use of medical device informatics to modify and validate therapies and drugs used in those therapies. In certain embodiments, a medical device, such as a medical infusion pump, interfaces with a server to administer the patient treatments. In one aspect, a server is disclosed which includes a memory configured to store identification information regarding a plurality of medical devices at different customer sites, and a programmable circuit operatively connected to the memory. The programmable circuit is configured to execute program instructions to receive data from medical devices at one or more of the different customer sites, store data in the memory associated with the one or more different customer sites, and associate a portion of the data with the medical device that transmitted that portion of data.

Abstract: Methods and systems of patient treatment are disclosed. The methods and systems include use of medical device informatics to modify and validate therapies and drugs used in those therapies. In certain embodiments, a medical device, such as a medical infusion pump, interfaces with a server to administer the patient treatments. In one aspect, a medical device server is disclosed. The medical device server includes a memory configured to store patient status information and command information and a programmable circuit operatively connected to the memory. The programmable circuit is configured to execute program instructions to receive patient status information from a first medical device, the patient status information related to a patient and determine the need for treatment of the patient. The programmable circuit is also configured to execute program instructions to transmit a command to a second medical device configured to provide the treatment.

Abstract: Methods and systems of patient treatment are disclosed. The methods and systems include use of medical device informatics to modify and validate therapies and drugs used in those therapies. In certain embodiments, a medical device, such as a medical infusion pump, interfaces with a server to administer the patient treatments. In one aspect, a method of retrieving medical event log results is disclosed. The method includes receiving at a server event log data generated by a medical device, and storing the event log data in a memory of the server. The method further includes receiving a request for a subset of the event log data, the subset of the event log data defined by at least one characteristic. The method also includes filtering the event log data based on the characteristic.

Abstract: Methods and systems of patient treatment are disclosed. The methods and systems include use of medical device informatics to modify and validate therapies and drugs used in those therapies. In certain embodiments, a medical device, such as a medical infusion pump, interfaces with a server to administer the patient treatments. In one aspect, a software development kit is disclosed. The kit includes medical device installation software containing computer-readable instructions allowing a user to define metadata related to one or more characteristics of a medical device. The kit also includes data package delivery software including computer-readable instructions configured to deliver a data package from a server to a medical device. The kit further includes server software containing computer-readable instructions for execution on a medical device server, the server software configured to control communication from the server to the medical device.

Abstract: Methods and systems of patient treatment are disclosed. The methods and systems include use of medical device informatics to modify and validate therapies and drugs used in those therapies. In certain embodiments, a medical device, such as a medical infusion pump, interfaces with a server to administer the patient treatments. In one aspect, a method of tracking changed parameters in a medical infusion pump is disclosed. The method includes establishing a communication session between a medical infusion pump and a medical device server, and communicating an original parameter value, an updated parameter value, and a final parameter value from the medical infusion pump to the medical device server. The method further includes storing the original parameter value, the updated parameter value, and the final parameter value on the medical device server. Metadata associated with one or more of the parameter values identifies that parameter value to the medical device server and the medical infusion pump.

Abstract: Methods and systems of patient treatment are disclosed. The methods and systems include use of medical device informatics to modify and validate therapies and drugs used in those therapies. In certain embodiments, a medical device, such as a medical infusion pump, interfaces with a server to administer the patient treatments. In one such embodiment, a method for use of metadata on medical devices is disclosed. A method includes associating metadata with one or more medical devices, the metadata corresponding to an attribute of the medical devices. The method also includes storing the metadata on a server, the server configured to communicate with each of the medical devices by using the metadata.

Abstract: Methods and systems of patient treatment are disclosed. The methods and systems include use of medical device informatics to modify and validate therapies and drugs used in those therapies. In certain embodiments, a medical device, such as a medical infusion pump, interfaces with a server to administer the patient treatments. In one aspect, a method of scheduling maintenance of a medical device is disclosed. The method includes storing a medical device maintenance schedule on a computing system remote from the medical device, the medical device maintenance schedule including a reminder to perform maintenance on the medical device. The method further includes transmitting the reminder from the computing system to the medical device.

Abstract: Methods and systems of patient treatment are disclosed. The methods and systems include use of medical device informatics to modify and validate therapies and drugs used in those therapies. In certain embodiments, a medical device, such as a medical infusion pump, interfaces with a server to administer the patient treatments. In one aspect, a medical device network is disclosed which includes a plurality of medical devices dispersed across two or more time zones, and a server operatively connected to the medical devices. The server includes a memory configured to hold event log data and a programmable circuit operatively connected to the memory. The programmable circuit is configured to execute program instructions to receive event log data from the plurality of medical devices, and to modify the time zone information in the event log data. The programmable circuit is also configured to execute program instructions to store the event log data in the memory.