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公开(公告)号：US20250095841A1
公开(公告)日：2025-03-20
申请号：US18970875
申请日：2024-12-05
Applicant: CareFusion 303, Inc.
Inventor： Claire Ellen KNIGHT , Lisa DIGGETT , Michael K. WORKMAN , Evan CHEN
Abstract: A method includes receiving a request to activate a medical device. Response to receiving the request, the method includes generating an automatic programming request (APR) for programming the medical device, receiving a message indicating that the APR failed to activate the medical device, and obtaining historical programming records (HPR)s. The method includes determining that parameters in the APR correspond to historical parameters, identifying a set of HPRs including a historical parameter value corresponding to a requested parameter value included the APR, and generating a deviation metric indicating a degree of difference between a secondary parameter value included in the APR and a corresponding historical parameter value. The method includes, responsive to a determination that a deviation metric meets a criticality threshold, changing a drug library record associated with the respective set of deviations and providing an indication to review the changed drug library record.
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公开(公告)号：US20250166852A1
公开(公告)日：2025-05-22
申请号：US18864504
申请日：2022-05-10
Applicant: CareFusion 303, Inc.
Inventor： Lisa DIGGETT , Michael K. WORKMAN , Claire Ellen KNIGHT , Joshua Jay HARMAN
IPC: G16H70/40 , G06V10/75 , G06V10/94 , G06V10/98 , G06V30/12 , G06V30/19 , G06V30/30 , G16H20/17 , G16H40/63
Abstract: A system for scanning and validating clinical order device configurations is disclosed. A test instance of an infusion device is created based on a request, and an automated programming command is transmitted to the test instance. The automated programming command includes validation information for validating clinical order data, and a programming response is generated by the test instance based on the automated programming command, and provided for storage in a records system. In some implementations, the response includes an image, or reference to the image, of a graphical user interface that would be presented by the infusion device configured according to the validation information.
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公开(公告)号：US20250135110A1
公开(公告)日：2025-05-01
申请号：US18681847
申请日：2022-08-05
Applicant: CareFusion 303, Inc.
Inventor： Michael K. WORKMAN , Reza PAIAM
Abstract: A trigger condition for entering a syringe empty mode is determined. The trigger condition includes adjusting an operational parameter of an infusion device associated with the syringe to complete a fluid delivery performed by the syringe. The fluid delivery is monitored and, responsive to the fluid delivery satisfying the trigger condition, the infusion device is caused to enter the syringe empty mode. While in the empty mode, a flow rate or threshold associated with the fluid delivery is adjusted to facilitate emptying a fluid from the syringe, and an alert is provided when the threshold associated with the fluid delivery has been satisfied.
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公开(公告)号：US20220165411A1
公开(公告)日：2022-05-26
申请号：US17528089
申请日：2021-11-16
Applicant: CareFusion 303, Inc.
Inventor： Lisa DIGGETT , Laura Ann COLLINS , Claire Ellen KNIGHT , Michael K. WORKMAN
Abstract: The disclosed systems and methods manage more notifications between medical devices. A method includes obtaining information corresponding to a clinician and determining whether the information satisfies coordination criteria. The method includes, in accordance with a determination that the clinician is associated with the first medical device and a second medical device, detecting a first and second notification generated by respective medical devices. The method includes identifying, based on detecting the respective notifications, alert information including medical information for a patient receiving medical treatment from the first and second medical device. The method includes determining, based on the identified information, notification priorities between the respective notifications. The method includes adjusting at least one human perceivable manifestation of the respective notifications based on the determined notification priorities, and presenting adjusted human perceivable manifestations of the respective notifications to the user via one of the first medical device or the second medical device.
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公开(公告)号：US20250065032A1
公开(公告)日：2025-02-27
申请号：US18807888
申请日：2024-08-16
Applicant: CareFusion 303, Inc.
Inventor： John LANGAN , Michael K. WORKMAN
Abstract: An infusion pump is secured within a lockbox configured to enclose and prevent access to the infusion pump and a medication receptacle of the infusion pump, the lockbox including a lockbox control interface configured to obtain authorization for access to the lockbox from a pump communication interface of the infusion pump and enclosed within the lockbox. The lockbox control interface is electronically coupled with the pump communication interface. Transmission of a wireless credential is made to the pump communication interface by way of being received at the lockbox control interface or at the pump interface through the lockbox. The lockbox control interface receives the authorization from the pump communication interface for access based on the wireless credential and performs an action according to the received authorization for access. Action includes unlocking the lockbox or the lockbox control interface extending the pump's interface to the authorized user.
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Patent Agency Ranking
公开(公告)号：US20240374811A1
公开(公告)日：2024-11-14
申请号：US18692781
申请日：2022-09-19
Applicant: CareFusion 303, Inc.
Inventor： Michael K. WORKMAN
Abstract: When automated programming data configured to instruct an infusion device regarding an infusion of a medication is received from a server, the disclosed system and method identifies a deviation in the data with respect to stored programming data. Without rejecting the data for the deviation, the infusion device instead sends an acknowledgement of the automated programming data and the deviation, and determines a user interface workflow for correcting the deviation. The infusion device then provides for display one or more user prompts according to the determined user interface workflow to resolve the deviation. If the deviation is resolved by way of user responses, then the infusion is activated. Otherwise, an indication is sent to the server regarding the deviation.
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公开(公告)号：US20210330881A1
公开(公告)日：2021-10-28
申请号：US17240857
申请日：2021-04-26
Applicant: CareFusion 303, Inc.
Inventor： Reza PAIAM , Michael K. WORKMAN
Abstract: A method for detecting an occlusion in a fluidic channel of an infusion device that includes flowing a fluid within the fluidic channel during a first period of time in which a flow rate of the fluid is set to a first flow rate; pausing, the flow rate for a second period of time; measuring, a first pressure at a location along the fluidic channel during the second period of time; increasing, after measuring the first pressure, the flow rate to a second flow rate; pausing, the flow rate for a fourth period of time; measuring, after pausing the flow rate, a second pressure at the location during the fourth period of time; computing, at a processor, a difference between the first and second pressures; and in accordance with a determination that the magnitude of the difference satisfies the threshold, providing an indication, of a presence of the occlusion.
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公开(公告)号：US20250054620A1
公开(公告)日：2025-02-13
申请号：US18929061
申请日：2024-10-28
Applicant: CareFusion 303, Inc.
Inventor： Lisa DIGGETT , Laura Ann COLLINS , Claire Ellen KNIGHT , Michael K. WORKMAN
Abstract: The disclosed systems and methods manage more notifications between medical devices. A method includes obtaining information corresponding to a clinician and determining whether the information satisfies coordination criteria. The method includes, in accordance with a determination that the clinician is associated with the first medical device and a second medical device, detecting a first and second notification generated by respective medical devices. The method includes identifying, based on detecting the respective notifications, alert information including medical information for a patient receiving medical treatment from the first and second medical device. The method includes determining, based on the identified information, notification priorities between the respective notifications. The method includes adjusting at least one human perceivable manifestation of the respective notifications based on the determined notification priorities, and presenting adjusted human perceivable manifestations of the respective notifications to the user via one of the first medical device or the second medical device.
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公开(公告)号：US20240387034A1
公开(公告)日：2024-11-21
申请号：US18787987
申请日：2024-07-29
Applicant: CareFusion 303, Inc.
Inventor： Lisa DIGGETT , Laura Ann COLLINS , Claire Ellen KNIGHT , Michael K. WORKMAN
Abstract: The disclosed systems and methods for reducing alarm strain generated by a medical device. A medical device for reducing generated alarm strain includes a display to present visually perceivable information, an audio output to present audibly perceivable information, processors coupled with the display and the audio output, and memory storing instructions that, when executed by the processors, cause the medical device to perform operations. The instructions, when executed, cause the medical device to receive a notification regarding the medical device. The notification is associated with an audible manifestation and a visual manifestation. The instructions, when executed, also cause the medical device to detect that a user is focused on the medical device, after said detection of the user, determine a volume adjustment to the audio output for presenting the audible manifestation, and adjust the audio output to cause presentation of the audible manifestations according to the volume adjustment.
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公开(公告)号：US20240274257A1
公开(公告)日：2024-08-15
申请号：US18648160
申请日：2024-04-26
Applicant: CareFusion 303, Inc.
Inventor： Evan CHEN , Lisa DIGGETT , Robert M. REGEDANZ , Michael K. WORKMAN
Abstract: The disclosed systems and methods provide patient care unit (PCU) order confirmation. A method may include authorizing a user to operate a medication delivery device. The method may also include retrieving, in response to the authorizing, a user history associated with the user, wherein the user history includes one or more dispensing records for pending medications. The method may also include determining, based on a context that includes the user history, one or more medication order candidates for present administration. The method may also include presenting a user interface for confirming a medication order from the one or more medication order candidates. The method may also include configuring at least one parameter of the medication delivery device based on the confirmed medication order received from the user interface.
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