This disclosure relates generally to apparatuses, systems and methods for tracking and providing reminders of predetermined events, or scheduled events, for medical equipment, such as shields for limiting an individual's exposure to ionizing radiation. More specifically, this disclosure relates to a system in which individual identification and reminder apparatuses are associated with the individual pieces of medical equipment that are being tracked. In addition, the present invention relates to methods in which individually tracked medical devices may be inspected, validated, maintained or removed from service.
In a typical healthcare setting, such as a hospital, a clinic or the like, many medical devices are often used. In some settings, and for a variety of reasons, some medical devices may be transported from one location to another. As medical devices are moved, it often becomes difficult to keep track of them. This difficulty is compounded when a number of identical or very similar medical devices are used in the same setting. The difficulty increases even further when medical devices that are difficult to distinguish from one another must be periodically removed from service (e.g., for inspection, validation, maintenance, disposal, etc.), and may become even more complex when the medical devices that are difficult to distinguish from one another should be removed (e.g., are scheduled for removal, etc.) from service at different times.
In various aspects and embodiments, the disclosed subject matter relates to apparatuses, systems and methods for keeping track of the status of various pieces of medical equipment within a particular setting, such as a hospital or another medical facility. The status of each medical device may be monitored in an active manner or a passive manner. In passive monitoring, one or more individuals in a healthcare setting may only be required to take action when provided with notice that a particular piece of medical equipment is due for inspection, validation, maintenance or to be removed from service.
According to one aspect, notice that a particular piece of medical equipment is due to be at least temporarily removed from service, such as for inspection, validation, maintenance or disposal (in which case removal would be permanent, of course), may be provided to an individual by way of a tracking device, or “audit tag,” associated with that piece of medical equipment (e.g., that was previously secured to the medical device, that is integrated into the medical device, etc.). A tracking device may be self-contained or part of a larger system or network.
In embodiments where the tracking device is self-contained, it may include a securing element, a clock, an indicator and a portable power source, among other possible elements. The securing element may be configured to secure the tracking device to a piece of medical equipment, or a medical device. The clock keeps track of, or counts down from, the time that has passed from a first event (e.g., placement of a new medical device into service, placement of a recently inspected, validated or serviced medical device back into service, etc.) to a second event (e.g., a set time (date) on which the medical device is to be at least temporarily removed from service, etc.). The indicator, which may also be referred to as an “alarm,” may provide a user perceivable output, which may comprise a visible output (e.g., a light, a text message, etc.), an audible output (e.g., a beep, buzzer, voice message, etc.) and/or a tactile output (e.g., vibration, etc.). The portable power supply may provide power to the clock and the indicator, enabling them to operate. In some embodiments, a self-contained tracking device may also include a unique identifier, which may be used to enable an individual to manually determine a current status of the piece of medical equipment to which the tracking device has been assigned.
Instead of tracking the amount of time a medical device has been in service since its manufacture, validation, revalidation, or the like, a tracking device may be configured to track use of the medical device. As an example, a tracking device that is configured for use with a shield that attenuates ionizing radiation (e.g., x-rays, gamma radiation, etc.), which may also be referred to herein as a “radio-opaque” shield, may keep track of a cumulative amount of ionizing radiation to which the radio-opaque shield is exposed, a cumulative amount of ionizing radiation attenuated by the radio-opaque shield (e.g., by comparing an amount of ionizing radiation to which a radio-opaque shield is exposed to an amount of ionizing radiation to which an object or body covered by the radio-opaque shield is exposed, etc.) and/or a combination of the foregoing. Such a tracking device may include a securing element, at least one radiation detector and a portable power source, among other possible elements.
In embodiments where the tracking device is part of a larger monitoring system, the tracking device may include a securing element, a processor, a unique identifier, a wireless communication element, an indicator and a power supply. The securing element, the indicator and the power supply may operate as disclosed previously herein. The unique identifier may enable an individual to distinguish the tracking device or its assigned medical device from other pieces of identical medical equipment, it may enable an individual to manually determine the current status of the piece of medical equipment to which the tracking device has been assigned (i.e., attached) or it may enable the monitoring station to distinguish the tracking device from other tracking devices that are part of the same system. The processor may control operation of various elements of the tracking device, including the indicator. The wireless communication element may be configured to enable the processor to communicate with a remote monitoring station, which, in turn, may be configured to communicate with a plurality of tracking devices in a particular healthcare setting. In embodiments where evaluation of the medical device is based on time, a clock of the processing element may keep track of time, while in other embodiments, the time remaining until a particular piece of medical equipment is due for at least temporary removal from service may be kept by the monitoring station. In embodiments where evaluation of the medical device is based upon exposure to ionizing radiation, the radiation detector(s) of the tracking device may keep track of cumulative exposure to ionizing radiation over time, or the monitoring station may maintain a running total of the amount of ionizing radiation to which the tracking device has been exposed (e.g., total exposure, total attenuation, etc.).
According to another aspect, a medical device may include a tracking device, which provides a user with an indication of when the medical device is scheduled to be at least temporarily removed from service, or when the medical device should otherwise be at least temporarily removed from service. The tracking device may be removably secured to the medical device, or it may be integrated into the medical device. Tracking devices that incorporate teachings of this disclosure may be used in connection with a variety of different types of medical devices, including medical devices that are configured to periodic inspection, validation, maintenance or other activities. As indicated previously, in a specific embodiment, the medical device may comprise a radio-opaque shield.
A variety of methods are also disclosed. In some methods, a tracking device may be provided to an individual (e.g., a person using the assigned medical equipment, a person tasked with inventory control responsibilities, a person responsible for ensuring that the medical equipment is in compliance with inspection, compliance and/or validation requirements, etc.) for attachment to an individual piece of medical equipment. Once attached to an assigned piece of medical equipment, the individual may actively or passively monitor the status of that piece of medical equipment. More specifically, the tracking device or a system of which the tracking device is a part, rather than the individual, may keep track and determine when an event (e.g., the arrival of a set time, a parameter of cumulative use of the medical device has reached a predetermined threshold, etc.) at which that piece of medical equipment should be at least temporarily removed from service. As that event approaches, or at the occurrence of that event, the tracking device may provide a user perceptible signal to indicate that it is time to at least temporarily remove the medical device from service. The user perceptible signal may include an electronic message, a visible signal (e.g., a blinking light, etc.), an audible signal or a tactile signal (e.g., vibration, etc.). Once the medical device has been removed from service, it may be inspected, validated, serviced or permanently removed from service (e.g., disposed of, etc.).
Other aspects, as well as various features and advantages of various aspects, of the disclosed subject matter will be apparent to those of ordinary skill in the art though consideration of the ensuing description, the accompanying drawings and the appended claims.
In the drawings:
A tracking device, or audit tag, may enable active of passive monitoring of the status of a medical device. The tracking device may be self contained, or it may be part of a larger tracking system.
In
The securing element 14 is configured to secure the tracking device 10 to a piece of medical equipment, or a medical device, to be tracked. The configuration of the securing element 14 may depend, at least in part, upon the size or configuration of the tracking device 10, and upon the configuration of the medical device. Non-limiting examples of securing elements 14 include fasteners (e.g., cooperating hook and loop, or VELCRO®, type fasteners; snap-fit fasteners; other cooperating fastening systems; etc.), clips, or the like.
Alternatively, a tracking device 10 may lack a securing element, and instead be configured for engagement by a receptacle associated with a medical device to be tracked. Among a wide variety of embodiments, a receptacle may comprise a pocket on the medical device, a holster secured to the medical device, or any other suitable means for securing the tracking device 10 to the medical device.
The monitoring element 20 may comprise a clock or any other element suitable for keeping track of a predetermined duration of time, or counting down from a first time to a second time. In some embodiments, the monitoring element 20 may be configured to keep a running total of the amount of time that has elapsed since the first event. In a specific embodiment, the monitoring element 20 may be set to keep track of a predetermined event, such as a date on which a piece of medical equipment is to be removed from service, when cumulative use of the medical equipment reaches a threshold that corresponds to its removal from service or any other predetermined event.
As an alternative, the monitoring element 20 may comprise one or more radiation detectors. Such a monitoring element 20 may be configured to detect ionizing radiation, and may enable tracking of a cumulative exposure, or dosage, of one or more types of ionizing radiation. The monitoring element 20 may enable tracking of a cumulative amount of ionizing radiation to which the radio-opaque shield is exposed (e.g., with an externally located element, etc.), a cumulative amount of ionizing radiation attenuated by the radio-opaque shield (e.g., with an element located at a shielded side of a medical device, etc.) and/or a combination of the foregoing.
The indicator 22 may be associated with the monitoring element 20 in a way that provides a user with an indication that the time for a predetermined event has come. In some embodiments, the indicator 22 may also be configured to provide an indication that the time for the predetermined event is approaching. In such embodiments, the indicator 22 may generate a perceivable signal that corresponds to an amount of time, exposure or dosage, etc., that remains before the predetermined event.
In various embodiments, the indicator 22 may be configured to provide one or more of a visible signal (e.g., a light, a text message, etc.), an audible signal (e.g., a beep, buzzer, voice message, etc.) and a tactile signal (e.g., vibration, etc.). In embodiments where the indicator 22 provides a visible signal, the indicator 22 may comprise one or more lights (e.g., light-emitting diodes (LEDs), etc.), a display screen, or the like. In embodiments where the indicator 22 provides an audio signal, it may comprise a speaker or any other suitable noise-generating component. Embodiments of indicators 22 that provide tactile signals may comprise one or more components (e.g., eccentric motors, etc.) configured to cause movement (e.g., vibration, etc.) of the tracking device 10.
In addition to, or even as an alternative to, an indicator 22 that provides notifications at the tracking device 10, the tracking device 10 may be configured to wirelessly transmit notifications. In some embodiments, such as that depicted by
In embodiments where a tracking device 10 includes a processor 26, the processor 26 may receive clock signals from the monitoring element 20 and, based on tracking information maintained by the tracking device 10 (e.g., by memory (not shown) associated with the processor 26, etc.), keep track of the time, exposure or dosage, etc., remaining until the predetermined event.
In some such embodiments, the tracking device 10 may also include a location element 30 (e.g., a global positioning system (GPS) receiver, etc.), which may provide information about the location of the tracking device 10 and any medical device with which the tracking device 10 is associated.
When one or both of the monitoring element 20 and the indicator 22 comprises an electronic component, or in embodiments where the tracking device 10 includes other electronic components (e.g., a processor 26, a wireless communication element 28, a location element 30, etc.), the tracking device 10 may include a power supply 24 to enable operation of each electronic component. Without limitation, the power supply 24 may comprise one or more batteries (e.g., disposable batteries, a rechargeable battery, etc.), a solar power cell, or any other type of power supply suitable for use in a portable electronic device.
Referring now to
The processor 26 may comprise a microprocessor or a microcontroller configured to receive signals, process data carried by the signals and output signals. In the context of the tracking device 10′, the processor 26 may receive signals, through the wireless communication element 28, that relate to a predetermined event from a separate monitoring station 50 (
The monitoring station 50, which may comprise a computer, may be configured to store information regarding a plurality of tracked medical devices 40, including, but not limited to, scheduling information pertaining to each of the tracked medical devices 40. As the time for a predetermined event for a particular tracked medical device 40 approaches, the monitoring station 50 may signal the tracking device 10′ associated with that tracked medical device 40 (e.g., by use of a unique identifier, etc.) to provide an indication that the time for the predetermined event is arriving or has arrived. The monitoring station 50 may also be configured to request confirmation that the predetermined event has been completed and, in the event that no confirmation is provided, periodically follow up with subsequent requests for confirmation.
In some embodiments, the monitoring station 50 may also be configured to store information corresponding to a physical (e.g., geographical, etc.) location of each tracked medical device 40. If the time for a predetermined event for a particular tracked medical device 40 arrives, but the monitoring station 50 does not receive confirmation that the predetermined event has occurred, the monitoring station 50 may provide information on the current location of the tracked medical device 40.
Turning now to
In an example of use, an individual (e.g., a person using the assigned medical equipment, a person tasked with inventory control responsibilities, a person responsible for ensuring that the medical equipment is in compliance with inspection, compliance and/or validation requirements, etc.) may optionally secure a tracking device 10, 10′, etc., to a tracked medical device 40.
With the tracking device 10, 10′, etc., in place, it may be activated. In embodiments where the tracking device 10, 10′ is used to identify when a tracked medical device 40 is to be at least temporarily removed from service based on the amount of time the tracked medical device 40 has been in service, activation of the tracking device 10, 10′, etc., may include identification of a first point in time at which the tracked medical device 40 has been calibrated, validated, placed into service, etc. Activation of the tracking device 10, 10′, etc., in such an embodiment may also include setting or scheduling a second point in time at which a reminder is to be provided. The duration of time between the first point in time and the second point in time may be predetermined (e.g., it may correspond to a useful life; a regular, periodic schedule; etc.) or it may be defined during the activation process. Activation of the tracking device 10, 10′ may also include initiating a count down from the first point in time to the second point in time or monitoring an amount of time remaining until the second point in time.
In embodiments where a tracked medical device 40 is removed from service based on its use, activation of a tracking device 10, 10′ may include setting a threshold level of use for the device.
With the tracking device 10, 10′, etc., activated, an individual who is responsible for collecting the tracked medical device 40 and at least temporarily removing the same from operation in accordance with a predetermined event need not actively monitor the location or the status of the tracked medical device 40. Rather, the individual may take a passive approach to his or her responsibilities, waiting for an indication that a predetermined event is approaching or has arrived, then removing the tracked medical device 40 from operation, and performing the predetermined event.
As the predetermined event (i.e., the second point in time, the threshold level of use, etc.) approaches or arrives, the tracking device 10, 10′, etc., may provide (e.g., output, etc.) a user perceivable indication that corresponds to the predetermined event. As that indication is provided, the tracked medical device 40 may be removed from service, the indication provided by the tracking device 10, 10′, etc., may be turned off and optionally removed from the tracked medical device 40, and the tracked medical device 40 may be inspected, validated or maintained. After the tracked medical device 40 has been inspected, validated or maintained, an event tracker, which enables determination of whether or not the predetermined event has occurred (e.g., by cumulating events, such as passage of time, exposure to ionizing radiation, etc.), may be reset.
Although the foregoing description contains many specifics, these should not be construed as limiting the scope of any of the appended claims, but merely as providing information pertinent to some specific embodiments that may fall within the scopes of the appended claims. Other embodiments may also be devised which lie within the scopes of the appended claims. Features from different embodiments may be employed in combination. The scope of the invention is, therefore, indicated and limited only by the appended claims and their legal equivalents. All additions, deletions and modifications to the disclosed embodiments that fall within the meaning and scopes of the appended claims are to be embraced thereby.
A claim for the benefit of priority to the Apr. 26, 2012 filing date of U.S. Provisional Patent Application No. 61/638,845, titled “APPARATUSES, SYSTEMS AND METHODS FOR TRACKING THE STATUS OF MULTIPLE MEDICAL DEVICES” (“the '845 Provisional Application”) is hereby made pursuant to 35 U.S.C. §119(e). The entire disclosure of the '845 Provisional Application is, by this referenced, incorporated herein.
Number | Date | Country | |
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61638845 | Apr 2012 | US |