US20090135196A1 - Medication management system - Google Patents

Abstract

A method for dynamically adjusting the screen brightness of a pump screen display. The method includes providing a medical pump including an internal clock and a screen display having a first screen brightness and a second screen brightness. The method further includes providing a medication management unit operatively connected to the medical pump and transmitting configuration instructions from the medication management unit to the medical pump. The configuration instructions include instructions to display the first screen brightness during the daytime hours and instructions to display the second screen brightness during the nighttime hours. The method also includes determining a time of day using the internal clock of the pump and displaying the first or second screen brightness according to the time of day determined by the internal clock of the pump.

Description

CROSS REFERENCE TO RELATED APPLICATIONS
• This application claims priority based upon U.S. Provisional Application Ser. No. 60/509,404 filed Oct. 7, 2003 and U.S. Provisional Application Ser. No. 60/527,583 filed Dec. 5, 2003, which are expressly incorporated herein by reference in their entirety.
BACKGROUND OF THE INVENTION
• The present invention relates to the field of delivering medication to patients, more particularly to an integrated system for maximizing patient safety and caregiver productivity for medication delivery.
• Modern medical care often involves the use of medical pump devices to deliver fluids and/or fluid medicine to patients. Medical pumps permit the controlled delivery of fluids to a patient, and such pumps have largely replaced gravity flow systems, primarily due to the pump's much greater accuracy in delivery rates and dosages, and due to the possibility for flexible yet controlled delivery schedules. However, modern medical devices, including medical pumps, can be complicated and time-consuming for caregivers to program. Medical facilities struggle to provide appropriate caregiver staffing levels and training while holding down the cost of medical care. Human errors in pump programming and other medication errors can have adverse or even deadly consequences for the patient.
• Therefore, a principal object of this invention is to provide an integrated medication management system that reduces the risks of medication error and improves patient safety.
• A further object of the invention is to provide a medication management system that improves caregiver productivity.
• Another object of the invention is to provide a medication management system that improves the accuracy of the medication delivery process by eliminating labor-intensive tasks that can lead to human errors.
• A still further object of the invention is to provide a medication management system that relies on an electronically-transmitted medication order and machine readable indicia on the drug container, patient, and medication delivery device to insure the “five rights” of medication management, i.e., that the right medication is delivered to the right patient through the right route in the right dosage at the right time.
• Another object of the invention is to provide the caregiver with a pass code or machine-readable indicia to insure that only an authorized individual caregiver can initiate a medication order and that an authorized caregiver must confirm the medication order prior to its administration to the patient.
• A still further object of the invention is to provide a medication management system wherein the medical device receives delivery information electronically only through a medication management unit.
• Another object of the invention is to provide medication management system wherein the medical device is preprogrammed and executes the medication order only after a user has validated delivery data.
• A still further object of the invention is to provide a medication management system wherein the physical location of a medical device can be determined and pinpointed based on the last access node used by the medical device.
• Another object of the invention is to provide a medication management system for adjusting a patient-specific rule set based on new patient conditions and/or recent lab results.
• A still further object of the invention is to provide a medication management system for determining drug-drug incompatibility between two medication orders for concurrent delivery (to the same patient at the same time) and/or in an unacceptably close time sequence.
• Another object of the invention is to provide a medication management system for remotely sending an order or information to the medical device to modulate a planned or ongoing medication order and delivery thereof to the patient.
• A still further object of the invention is to provide a medication management system for automatically associating a medical device with a patient based on wireless transmission of a patient ID to the medical device, thereby establishing a patient area network.
• Another object of the invention is to provide a medication management system for caching an updated drug library at the medical device to replace an existing drug library, during execution of a medication order.
• A still further object of the invention is to provide a medication management system for displaying a picture of the patient on a device within the system, such as at the medical device, for a caregiver to perform a visual validation of the right patient.
• Another object of the invention is to provide a medication management system for evaluating the performance of multiple medical devices based on information from the multiple medical devices.
• A still further object of the invention is to provide a medication management system for evaluating the performance of one or more caregivers based on information from multiple medical devices.
• Another object of the invention is to provide a medication management system for adjusting medical device output conveyed to a caregiver based on multiple factors.
• These and other objects will be apparent to those skilled in the art.
SUMMARY OF THE INVENTION
• A medication management system includes a medication management unit (MMU) associated with a medical device for performing a prescribed medication order. The MMU compares medication order information from a first input means to machine readable delivery information from a second input means and downloads a medication order to the medical device only if the information from the first input means matches the information from the second input means. The medical device receives medication order information electronically only through the medication management unit (i.e., does not receive delivery information directly from the second input means). The MMU permits the medical device to perform the order only after a user has validated delivery data at the medical device.
• The MMU determines the general physical location of a medical device based on the last access node used by the wireless connectivity capability in the medical device and an audible alarm can be activated to allow a user to pinpoint the physical location of the medical device more precisely.
• Using expert clinical support decision rules, the MMU also determines drug-drug incompatibility between two medication orders for concurrent delivery (to the same patient at the same time) and/or in an unacceptably close time sequence through the same output IV line. Further, the MMU also adjusts patient-specific rule sets based on newly measured or observed patient conditions and/or recent lab results. Advantageously, warnings, alarms or alerts based on violations of these rules are provided as close as possible to the actual delivery time so that they are more meaningful, ripe for corrective action, and less likely to be ignored due to incomplete information.
• Based on laboratory data or other newly received patient information, the MMU can modulate the medication order planned or currently being delivered. The MMU sends an order from the MMU to the medical device to modulate performance of the medication order. The patient and the medical device automatically associate with each other to form a patient area network based on wireless transmission of ID information. During execution of a medication order, the medical device caches an updated drug library in a cache memory and, upon occurrence of a triggering event, replaces an existing drug library in the primary memory of the device with the updated library. A picture of the patient is displayed at a device within the system, such as the medical device, for a caregiver to perform a visual validation of the right patient. The MMU evaluates the performance of multiple medical devices and one or more caregivers based on information communicated from the medical devices. The MMU adjusts medical device output conveyed to a caregiver based on multiple factors.
DESCRIPTION OF THE DRAWINGS
• FIG. 1 is a schematic diagram of the medication management system including a medication management unit and a medical device, integrated with an information system, according to the present invention;
• FIG. 1A is an alternative schematic diagram of the medication management system including a medication management unit and a medical device, integrated with an information system, according to the present invention;
• FIG. 2 is a schematic diagram of the medication management unit according to the invention;
• FIG. 3 is a schematic diagram illustrating some of the major functions performed by the medication management unit according to the invention;
• FIG. 4 is a pictorial schematic diagram of the medication management system and its interaction with medical devices and an information system in a hospital environment;
• FIG. 4A is a schematic diagram of the medical device according to the invention;
• FIG. 5 is a partial flow chart of the medication management system processing a drug order through the medication management unit and medical device, and integrated with an information system according to the invention;
• FIG. 5A is a continuation of the flow chart ofFIG. 5;
• FIG. 6, is an alternative flow chart of the medication management system processing a drug order through the medication management unit and medical device, and integrated with an information system according to the invention;
• FIG. 6A is a continuation of the flow chart ofFIG. 6;
• FIG. 7 is a screen shot of a delivery information input device for entry of a caregiver specific pass code;
• FIG. 8 is a screen shot of a delivery information input device for pulling up a scan patient option;
• FIG. 9 is a screen shot of a delivery information input device for entry of patient-specific information;
• FIG. 10 is a screen shot of a delivery information input device displaying a task list;
• FIG. 11 is a screen shot of a delivery information input device displaying a medication order prescribed for a patient;
• FIG. 12 is a front view of a medical device displaying a start up screen;
• FIG. 13 is a front view of a medical device with a display and user interface means for selecting a clinical care area of a medical facility;
• FIG. 14 is a front view of a medical device with a display and user interface means for selecting a desired input channel of the medical device;
• FIG. 15 is a front view of a medical device with a display and user interface means for confirming correct delivery programming code data at the medical device;
• FIG. 16 is a screen shot of a delivery information input device for confirming correct delivery programming code data;
• FIG. 17 is a schematic diagram of the medication management system including a medication management unit and one or more medical devices, showing the medication management unit communicates with a medical device to locate the device;
• FIG. 18 is a flow chart of the medication management system locating a medical device;
• FIG. 19 is a flow chart of the medical device retrieving/receiving an updated drug library from the medication management unit;
• FIG. 20 is a flow chart of the medication management system updating a delivery program code executed on the medical device based on new information from a lab system, HIS and/or monitoring device;
• FIG. 21 is an alternative pictorial schematic diagram of the medication management system and its interaction with medical devices and the information system; and
• FIG. 22 is a flow chart of the medication management system generating an operation evaluation report of a caregiver or medical device.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
• With reference toFIGS. 1 and 1A, the medication management system (MMS)10 of the present invention includes a medication management unit (MMU)12 and amedical device14, typically operating in conjunction with one or more information systems or components of ahospital environment16. The term hospital environment should be construed broadly herein to mean any medical care facility, including but not limited to a hospital, treatment center, clinic, doctor's office, day surgery center, hospice, nursing home, and any of the above associated with a home care environment. As discussed below, there can be a variety of information systems in a hospital environment. As shown inFIG. 1, theMMU12 communicates to a hospital information system (HIS)18 via acaching mechanism20 that is part of thehospital environment16.
• It will be understood by those of skill in art that thecaching mechanism20 is primarily a pass through device for facilitating communication with the HIS18 and its functions can be eliminated or incorporated into the MMU12 (FIG. 1A) and/or themedical device14 and/or the HIS18 and/or other information systems or components within thehospital environment16. TheCaching Mechanism20 provides temporary storage of hospital information data separate from theHIS18, the medication administration record system (MAR)22, pharmacy information system (PhIS)24, physician order entry (POE)26, and/orLab System28. TheCaching Mechanism20 provides information storage accessible to theMedication Management System10 to support scenarios where direct access to data within thehospital environment16 is not available or not desired. For example, thecaching mechanism20 provides continued flow of information in and out of theMMU12 in instances where the HIS18 down or the connectivity between theMMU12 and the electronic network (not shown) is down. Thecaching mechanism20 also provides improved response time to queries from theMMU12 to theHIS18, as direct queries to theHIS18 are not consistently processed at the same speed and often require a longer period of time for the HIS18 to process.
• The HIS18 communicates with a medication administration record system (MAR)22 for maintaining medication records and a pharmacy information system (PhIS)24 for delivering drug orders to the HIS. A physician/provider order entry (POE)device26 permits a healthcare provider to deliver a medication order prescribed for a patient to the hospital information system directly or indirectly via thePhIS24. One skilled in the art will also appreciate that a medication order can be sent to theMMU12 directly from thePhIS24 orPOE device26. As used herein the term medication order is defined as an order to administer something that has a physiological impact on a person or animal, including but not limited to liquid or gaseous fluids, drugs or medicines, liquid nutritional products and combinations thereof.
• Lab system28 andmonitoring device30 also communicate with theMMU12 to deliver updated patient-specific information to theMMU12. For example, thelab system28 sends lab results of blood work on a specific patient to theMMU12, while themonitoring device30 sends current and/or logged monitoring information such as heart rate to theMMU12. As shown, theMMU12 communicates directly to thelab system28 andmonitoring device30. However, it will be understood to those of skill in art that theMMU12 can communicate to thelab system28 andmonitoring device30 indirectly via theHIS18, thecaching mechanism20, themedical device14 or some other intermediary device or system. This real-time or near delivery time patient-specific information is useful in adapting patient therapy because it may not have been available at the time the medication order was prescribed. As used herein, the term real-time denotes a response time with a latency of less than 3 seconds. The real-time digital communications between theMMU12 and other interconnected devices and networks prevents errors in patient care before administration of medications to the patient, especially in the critical seconds just prior to the start of medication delivery.
• Deliveryinformation input device32 also communicates with theMMU12 to assist in processing drug orders for delivery through theMMU12. The deliveryinformation input device32 can be any sort of data input means, including those adapted to read machine readable indicia such as barcode labels; for example a personal digital assistant (PDA) with a barcode scanner. Hereinafter the deliveryinformation input device32 will be referred to asinput device32. Alternatively, the machine readable indicia may be in other known forms, such as radio frequency identification (RFID) tag, two-dimensional bar code, ID matrix, transmitted radio ID code, human biometric data such as fingerprints, etc. and theinput device32 adapted to “read” or recognize such indicia. Theinput device32 is shown as a separate device from themedical device14; alternatively, theinput device32 communicates directly with themedical device14 or may be integrated wholly or in part with the medical device.
• With reference toFIG. 2, themedication management unit12 includes anetwork interface34 for connecting theMMU12 to multiple components of ahospital environment16, themedical device14, and any other desired device or network. Aprocessing unit36 is included inMMU12 and performs various operations described in greater detail below. A display/input device38 communicates with theprocessing unit36 and allows the user to receive output from processingunit36 and/or input information into theprocessing unit36. Those of ordinary skill in the art will appreciate that display/input device38 may be provided as a separate display device and a separate input device.
• Anelectronic storage medium40 communicates with theprocessing unit36 and stores programming code and data necessary for theprocessing unit36 to perform the functions of theMMU12. More specifically, thestorage medium40 stores multiple programs formed in accordance with the present invention for various functions of theMMU12 including but not limited to the following programs: MaintainDrug Library42;Download Drug Library44;Process Drug Order46; Maintain ExpertClinical Rules48; Apply ExpertClinical Rules50; Monitor Pumps52;Monitor Lines54; GenerateReports56;View Data58; Configure theMMS60; and Monitor theMMS62. The MaintainDrug Library42 program creates, updates, and deletes drug entries and establishes a current active drug library. TheDownload Drug Library44 program updatesmedical devices14 with the current drug library. TheProcess Drug Order46 program processes the medication order for a patient, verifying that the point of care (POC) medication and delivery parameters match those ordered. The Maintain ExpertClinical Rules48 program creates, updates, and deletes the rules that describe the hospital's therapy and protocol regimens. The Apply ExpertClinical Rules50 program performs logic processing to ensure safety and considers other infusions or medication orders, patient demographics, and current patient conditions that include blood chemistry values such as insulin/glucose, monitored data such as pulse and respiration, and clinician assessments such as pain or responsiveness. The Monitor Pumps52 program acquires ongoing updates of status, events, and alarms transmitted both real-time and in batch mode, as well as tracking the location, current assignment, and software versions such as the drug library version residing onmedical device14. TheMonitor Lines54 program acquires ongoing updates of status, events and alarms for each channel or line for amedical device14 that supports multiple drug delivery channels or lines. The Generate Reports56 program provides a mechanism that allows the user to generate various reports of the data held in theMMU storage medium40. TheView Data58 program provides a mechanism that supports various display or view capabilities for users of theMMU12. The Notifications59 program provides a mechanism for scheduling and delivery of events to external systems and users. The Configure theMMS60 program provides a mechanism for system administrators to install and configure theMMS10. The Monitor theMMS62 program enables information technology operations staff capabilities to see the current status ofMMS10 components and processing, and other aspects of day-to-day operations such as system start up, shut down, backup and restore.
• With reference toFIG. 3, the various functional programs42-62 of theMMU12, each including separate features and rules, are partitioned (at a higher level than shown inFIG. 2) and logically organized into interrelated managing units of theMMU12. As shown, theMMU12 includes anasset manager64, analarm manager66, a drug library manager (such as, for example, ABBOTT MEDNET™)68, acaregiver manager70, atherapy manager72, and/or a clinical data manager73. However, one of ordinary skill in the art will appreciate that additional or alternative hospital system managing units can be provided without departing from the present invention. Additionally, theMMU12 includes amaster adjudicator74 between the separate interrelated hospital system managing units64-73 of theMMU12, to regulate the interaction between the separate management units.
• Further, while theMMU12 as described herein appears as a single device, there may be more than oneMMU12 operating harmoniously and sharing the same database. For example theMMU12 can consist of a collection of MMU specific applications running on distinct servers in order to avoid a single point of failure, address availability requirements, and handle a high volume of requests. In this example, each individual server portion of theMMU12 operates in conjunction with other server portions of theMMU12 to redirect service requests to another server portion of theMMU12. Additionally, themaster adjudicator74 assigns redirected service requests to another server portion of theMMU12, prioritizing each request and also ensuring that each request is processed.
• With reference toFIGS. 2 and 3, the managing units64-72 each include separate features and rules to govern their operation. For example theasset manager64 governs the execution of the Monitor Pumps52 andMonitor Lines54 programs; thedrug library manager68 governs the execution of theDrug Library42 and DownloadDrug Library44 programs; thetherapy manager72 governs the execution of theProcess Drug Order46, Maintain ExpertClinical Rules48, and Apply ExpertClinical Rules50 programs; and the clinical data manager73 governs the execution of the GenerateReports56 andView Data58 programs. Other distribution of the functional MMU programs42-62 among the hospital system managing units64-73 can be made in accordance with the present invention.
• With reference toFIG. 4, anelectronic network76 connects theMMU12,medical device14, HIS18, andinput device32 for electronic communication. Theelectronic network76 can be a completely wireless network, a completely hard wired network, or some combination thereof. Themedical device14 andinput device32 are located in a treatment location77. As shown, themedical device14 andinput device32 are equipped withantennas78 and80, respectively. Theantennae78 and80 provide for wireless communication to theelectronic network76 via anantenna82 ofaccess node84 connected to theelectronic network76. Further details on theantenna78 can be found in commonly assigned co-pending application entitled SYSTEM FOR MAINTAINING DRUG INFORMATION AND COMMUNICATING WITH MEDICATION DELIVERY DEVICES filed on Feb. 20, 2004, which is expressly incorporated herein in its entirety.
• In the context of the present invention, the term “medical device” includes without limitation a device that acts upon a cassette, reservoir, vial, syringe, or tubing to convey medication or fluid to or from a patient (for example, an enteral pump, infusion pump, a patient controlled analgesia (PCA) or pain management medication pump, or a suction pump), a monitor for monitoring patient vital signs or other parameters, or a diagnostic device.
• For the purpose of exemplary illustration only, themedical device14 ofFIG. 4 is disclosed as a cassette type infusion pump. The pump stylemedical device14 includes a user interface means86,display88,first channel90, and first channel machinereadable indicator92. Afirst IV line98 has a conventional cassette99A (not shown) that is inserted into thefirst channel90, and includes amedication bag100 with a machinereadable indicator102. Asecond IV line101 is connected to an input port of the cassette99A, and includes amedication bag106 with a machinereadable indicator108. A singleoutput IV line98 is connected to an outlet port of the cassette99A and connected to apatient110 who has a machinereadable indicator112 on a wristband, ankle band, badge or similar article that includes patient-specific and or identifying information, including but not limited to patient ID, and demographics.
• In an alternative embodiment illustrated by dashed lines inFIG. 4, themedical device14 is a multi-channel pump having afirst channel90 with first channel machinereadable indicator92 and at least a second channel94 with a second channel machinereadable indicator96. Theline101 from themedication bag106 is eliminated and replaced byline104 with a cassette99B (not shown) inserted into the second channel94 and anoutput line104 extends from the cassette to the patient. The same type of cassette99 (not shown) is inserted in thefirst channel90. Additional details on such a multi-channel pump and cassette99A can be found in commonly owned U.S. patent application Ser. No. 10/696,830 entitled MEDICAL DEVICE SYSTEM, which is incorporated by reference herein in its entirety.
• Within a patient area network113 (hereinafter, PAN113), a caregiver114 (if present) has a machinereadable indicator116 on a wristband, badge, or similar article and operates theinput device32. Theinput device32 includes an input means118 for reading the machinereadable indicators92,96,102,108,112, and116. An input/output device120 is included on theinput device32. The input/output device120 allows the user to receive output from theinput device32 and/or input into theinput device32. Those of ordinary skill in the art will appreciate that display/input device120 may be provided as a separate display device and a separate input device.
• With reference toFIG. 4A, the pump stylemedical device14 includes anetwork interface122 for connecting themedical device14 to theelectronic network76. Thenetwork interface122 operates theantenna78 for wireless connection to theelectronic network76. Aprocessor124 is included in themedical device14 and performs various operations described in greater detail below. The input/output device87 (display88 and user interface means86) allows the user to receive output from themedical device14 and/or input information into themedical device14. Those of ordinary skill in the art will appreciate that input/output device87 may be provided as a separate display device and a separate input device (as shown inFIG. 4,display88 and user interface means86) or combined into a touch screen for both input and output. Amemory126 communicates with theprocessor124 and stores code and data necessary for theprocessor124 to perform the functions of themedical device14. More specifically, thememory126 stores multiple programs formed in accordance with the present invention for various functions of themedical device14 as is relates to theMMU12 including the following programs:Process Drug Order128,Monitor Pump130, and DownloadDrug Library132.
• With reference toFIGS. 5 and 5A, the functional steps of theProcess Drug Order46 and Apply ExpertClinical Rules50 programs of theMMU12 and theProcess Drug Order128 program of themedical device14 are shown in operation with theHIS18, thecaching mechanism20 and theinput device32.
• With reference toFIGS. 4,5 and7, to begin to process a drug order, theinput device32 displays a default screen (not shown) on input/output device120 which the caregiver uses to accesspassword screen133B (FIG. 7). Thepassword screen133B prompts thecaregiver114 to enter caregiver specific identification information (caregiver ID). Thecaregiver114 enters caregiver ID such as a username and/or password or pass code, or the machinereadable indicator116. Theinput device32 enters this caregiver ID atstep134.
• With reference toFIGS. 4,5 and8-9, theinput device32 then displays ascan patient screen135A (FIG. 8) which prompts thecaregiver114 to enter patient-specific identification information (patient ID). Thecaregiver114 enters the patient ID such as the machinereadable indicator112. Theinput device32 enters this patient ID and atstep136, and displays a confirmedscan patient screen135B (FIG. 9) indicating that the patient ID was successfully entered into theinput device32.
• With reference toFIG. 5, theinput device32 then transmits the patient ID to thecaching mechanism20 atstep138. Thecaching mechanism20 transmits the patient ID to the HIS18 atstep140. The HIS18 retrieves a patient-specific task list and patient-specific order information based on the patient ID and transmits both to thecaching mechanism20 atstep142. The order information includes but is not limited to an order detail for a medication order, patient demographic information, and other hospital information systems data such as lab results data. Thecaching mechanism20 transmits the task list to theinput device32 atstep143.
• With reference toFIGS. 4,5 and10-11, theinput device32 then displays atask list screen143A (FIG. 10) which prompts thecaregiver114 to accesses the task list on theinput device32. Theinput device32 prompts thecaregiver114 to enter drug specific identification information (dispense ID). Thecaregiver114 enters a dispense ID such as the drug container specific machinereadable indicator102. Theinput device32 enters this dispense ID atstep144. Theinput device32 processes the dispense ID to select the correct task from the task list, then displays atask screen143B (FIG. 11), and transmits a dispense ID to thecaching mechanism20 requesting an order ID atstep146. Thecaching mechanism20 transmits a dispense ID to the HIS18 requesting an order ID atstep148. The HIS18 transmits an order ID to thecaching mechanism20 atstep150. Thecaching mechanism20 forwards this order ID to theinput device32 atstep152.
• Alternatively, the three entered IDs (patient ID, dispense ID, and channel ID) are entered in a different specific order or without regard to order. Where the IDs are entered without regard to order, the IDs would be maintained within theMMS10 and/orcaching mechanism20 as they are entered, so that the IDs can be recalled when needed to complete the medication delivery workflow.
• Theinput device32 matches the order ID with an item in the task list to ensure a Five Rights check atstep154. The “Five Rights” in this section refer to the “Five Rights of Medical Administration”. Alternatively, the Five Rights check is done at theMMU12 once theMMU12 receives the order information as well as the patient, dispense, and channel IDs. A description of these “rights” follows. Right patient, is the drug being administered to the correct patient. Right drug, is the correct drug being administered to the patient. Right dose, is the correct dosage of the drug being administered to the patient. Right time, is the drug being administered to the patient at the correct time. Right route, is the drug being administered into the patient by the correct route, in this case intravenously through an IV. Once the order ID and item in the task list are reconciled, theinput device32 sends an order confirmed message to thecaching mechanism20 atstep156. In response, thecaching mechanism20 sends the order detail (medication order prescribed for a patient) of the order information to theinput device32 atstep158.
• With reference toFIGS. 4,5,11, theinput device32 then displays a scan device/channel screen143B (FIG. 11) which prompts thecaregiver114 to enter channel identification information (channel ID) regarding which channels of themedical device14 are to be used for the delivery. Thecaregiver114 enters a channel ID such as the machinereadable indicator92. Theinput device32 enters this channel ID atstep160, and displays a confirmed scan device screen159B (FIG. 11B) indicating that the channel ID was successfully entered into theinput device32. It will be appreciated that thechannel ID indicator92 can include information also identifying the medical device14 (medical device ID). Alternatively, it is contemplated that an additional machine readable indicator (not shown) may be provided for the medical device itself separate from the channel ID machinereadable indicator92. If themedical device14 has a single channel, a single indicator will clearly suffice. If themedical device14 is a multi-channel device, the channel indicators can also carry information that uniquely identifies the device the channel is on. At any rate, it should be apparent that a second entry of a combined device/channel ID may be redundant and could be eliminated. Theinput device32 then transmits the delivery information including caregiver ID, patient ID, medical device ID and/or channel ID, dispense ID, and order ID to theMMU12 atstep162.
• With reference toFIGS. 4,5 and12-14, when themedical device14 is turned on atstep164 themedical device14 displays a start upscreen163A (FIG. 12) on thedisplay88 of themedical device14. Themedical device14 then displays a clinical carearea selection screen163B (FIG. 13) which prompts thecaregiver114 to select the clinical care area (CCA) that themedical device14 is being assigned to. Thecaregiver114 enters or selects the CCA atstep166 using scroll and select/enter keys on the user interface means86. Themedical device14 then displays achannel selection screen163C (FIG. 14) that prompts thecaregiver114 to select the desired channel (90 or94) or bag source (100 or106) usingsoft keys163D-G, more particularly163E,163F respectively. Themedical device14 enters this channel ID atstep168. The CCA information is transmitted to theMMU12 by themedical device14 atstep170. Alternatively, where the CCA is known and available to theHIS18, the CCA can be automatically generated for themedical device14, and sent from the HIS18 to theMMU12
• With reference toFIGS. 2 and 5, theMMU12 executes theProcess Drug Order46 program and sends an active order request based on the delivery information from theinput device32 to thecaching mechanism20 atstep172. Thecaching mechanism20 responds by sending the corresponding patient-specific order information to theMMU12 atstep174. Thecaching mechanism20 may send to theMMU12 order information regarding all information associated with the particular patient, including but not limited to order detail for a medication order, patient demographic information, and other hospital information systems data such as lab results data or monitoring data.
• Referring toFIG. 5A, theMMU12 then executes the Apply ExpertClinical Rules50 program to process the CCA information from themedical device14 and the delivery information from theinput device32, atstep178. The Apply ExpertClinical Rules50 program compares the delivery information with an expert rule set to determines expert rule set violations based on correlating treatment based protocols, disease based protocols, drug-drug incompatibility, patient data (age, height, weight, etc), vital signs, fluid in/out, blood chemistry, and status assessments (such as pain and cognition). As used herein, the term drug-drug incompatibility includes but is not limited to determinations of drug-drug interactions and/or drug-drug compatibility between two or more medication orders for concurrent delivery (to the same patient at the same time) and/or in a time sequence for the same patient (i.e. through a common output IV line). In cases where the Apply ExpertClinical Rules50 program finds an expert rule set violation (such as a drug-drug incompatibility), the Apply ExpertClinical Rules50 program generates an alarm and/or requires a time delay in execution for one of the two separate delivery information submissions.
• The Apply ExpertClinical Rules50 program also establishes a patient-specific rule algorithm. The patient-specific rule algorithm is primarily based on the expert rule set described above applied to a specific order detail. The patient-specific rule algorithm generates a patient-specific rule set (discussed in greater detail below, at the description ofFIG. 20) according to patient-specific order information including but not limited to patient demographic information, and other hospital information systems data such as lab results data or monitoring data. The patient-specific rule set includes hard and soft dosage limits for each drug being administered. The patient-specific rule set is included in the delivery programming code sent to themedical device14 atstep182.
• Any alarms generated by theProcess Drug Order46 or Apply ExpertClinical Rules50 programs are delivered to themedical device14, HIS18, and/orinput device32, computer254 (FIG. 17) atstep180.Computer254 can be located in a remote nurse station or a biomedical technician area. If no alarms are generated, theMMU12 transmits a delivery program code to themedical device14, atstep182. The delivery program code sent fromMMU12 to themedical device14 includes a patient-specific rule set generated from any rule based adjudication at theMMU12, including hard and soft dosage limits for each drug being administered. Themedical device14 caches the patient-specific rule set contained in the delivery program code. Alternatively, theMMU12 can generate an alarm at themedical device14 or another location and not download the delivery program code.
• With reference toFIGS. 5,5A and15, themedical device14 displays an orderdose confirmation screen187A (FIG. 15) which prompts thecaregiver114 to confirm the delivery data. As shown, thecaregiver114 selects the “yes” soft key187B on themedical device14 to confirm the delivery data and the “no” soft key187C to cancel the delivery. Thecaregiver114 confirms the delivery data at themedical device14 atstep188. Once thecaregiver114 confirms the delivery data at themedical device14, themedical device14 then executes the delivery program code and begins infusion atstep198. As part of the program code, the infusion may be delayed for a predetermined period of time.
• Alternatively, confirmation from the caregiver can be made at theinput device32 or required from both theinput device32 andmedical device14. As shown, a redundant additional confirmation performed by thecaregiver114 at theinput device32 after the medical device has received the delivery program code. Specifically, themedical device14 transmits a canonical representation of the delivery programming code data (delivery data) to theMMU12 detailing the infusion to be performed by themedical device14, atstep184. TheMMU12 then transmits the same delivery data that was originally transmitted to themedical device14 to theinput device32 atstep186. Alternatively, the delivery data can be passed to another remote computer (254 inFIG. 17) including but not limited to a computer at a nurse station, for confirmation.
• With reference toFIGS. 5A and 16, theinput device32 displays an orderdose confirmation screen191A (FIG. 16) that prompts thecaregiver114 to confirm the delivery data. As shown, thecaregiver114 selects thecomplete button191B on theinput device32 to confirm the delivery data and the cancelbutton191C to cancel the delivery. Thecaregiver114 confirms the delivery data at theinput device32 atstep192, and the confirmation is used for documentation by theHIS18, or other systems within thehospital environment16.
• With reference toFIGS. 4A and 5A, during infusion, themedical device14 executes itsProcess Drug Order128 program. TheProcess Drug Order128 program sends infusion change events and infusion time events in a deliveryevent log message200 to theMMU12. TheMMU12 forwards these delivery event log messages to theinput device32 or other system within thehospital environment16 atstep202. Thecaregiver114 acknowledges these delivery event log messages on theinput device32, atstep204. Theinput device32 then sends an acknowledged deliveryevent log message206 to thecaching mechanism20, detailing the delivery event, the caregiver ID, and the caregiver acknowledgment. The caching mechanism passes the delivery event message to the HIS18 atstep208.
• Once infusion has ended atstep210, themedical device14 sends an infusion endedmessage212 to theMMU12. TheMMU12 then aggregates all thedelivery event messages200 sent during the infusion atstep214. TheMMU12 sends the aggregateddelivery events216 to theinput device32. Thecaregiver114 enters a completedtask218 on theinput device32, and sends the aggregated delivery events to the caching mechanism atstep220, which in turn passes the delivery event log messages to the HIS18 atstep222.
• With reference toFIGS. 6 and 6A, an alternative flow chart of theMMS10 processing a drug order through theMMU12 andmedical device14 is shown. With reference toFIGS. 4,6 and6A, thecaregiver114 enters the patient ID, which then is stored in thecaching mechanism20. Thecaching mechanism20 transmits the patient ID to the HIS18 and retrieves a patient-specific task list for that patient ID. Thecaregiver114 then enters the dispense ID, which subsequently is stored in thecaching mechanism20. Thecaching mechanism20 transmits the dispense ID to theHIS18, and retrieves a patient-specific order information, including but not limited to an order detail, patient demographic information, and other hospital information systems data such as lab results data. Thecaregiver114 then enters the channel ID, which is stored in theMMU12.
• Alternatively, the three entered IDs (patient ID, dispense ID, and channel ID) are entered in a different specific order or without regard to order. Where the IDs are entered without regard to order, the IDs would be maintained within theMMS10 and orcaching mechanism20 as they are entered, so that the IDs can be recalled when needed to complete the medication delivery workflow.
• Upon receipt of the channel ID, theMMU12 requests the order information (order detail, patient demographic information, and other hospital information systems data) and retrieves it from thecaching mechanism20. This order information is stored within theMMU12 and utilized for subsequent rule processing such as “Five Rights” checking and other rule set algorithms. TheProcess Drug Order46 program processes the delivery information from the input device32 (including caregiver ID, patient ID, medical device/channel ID, and dispense ID) and compares this delivery information with the corresponding order detail portion of the order information from thecaching mechanism20, atstep176. Where the order information and delivery information do not match, the device program code downloaded to themedical device14 atstep182 includes an alarm message indicating that the five rights check was not met. Additionally, the alarm message can include a description of which particular right(s) did not match. Alternatively, theNMU12 can generate an alarm at themedical device14 or another location and not download the program code for delivery of the medication order.
• Alternatively, theMMU12 can accept a Five Rights check from another device, such as a HIS18 or aninput device32. This check can be accepted either by a direct data element being sent to theMMU12 indicating a Five Rights check, or implied through the workflow provided by theHIS18 orinput device32.
• The other steps shown inFIGS. 6 and 6A are similar to corresponding steps inFIGS. 5 and 5A. Accordingly, these steps will not be described with any further detail here. One skilled in the art will appreciate that the vertical lines inFIGS. 5,5A,6,6A do not necessarily represent a firm time sequence. Some steps may be done sooner than shown (for example, turning on the medical device) or later than shown (for example, aggregate delivery events).
• With reference toFIGS. 2,4A,5,5A and20, in one embodiment, theProcess Drug Order46 program of theMMU12 and the correspondingProcess Drug Order128 program of themedical device14 permit theMMU12 to remotely control themedical device14 to modulate performance of a medication order. For example, theMMU12 can remotely start and/or stop themedical device14. Once the delivery program code is received by themedical device14 atstep184, theProcess Drug Order46 ofMMU12 remotely starts execution of the infusion by sending astart order224, which triggers the medical device to begin infusion atstep225. Likewise, when the infusion is to end atstep228, theProcess Drug Order46 program can remotely stop the infusion by sending astop order226 to themedical device14, which triggers the medical device to end infusion atstep228. In most cases, theMMU12 requires the caregiver to confirm the start or stop of execution. This confirmation by the caregiver may take place at theinput device32 or themedical device14. However, one skilled in the art will appreciate that there may be emergency situations where an order could and should be stopped without human confirmation.
• With reference toFIGS. 2,5,5A and20, in one embodiment, the Apply ExpertClinical Rules50 program of theMMU12 permits theMMU12 to adjust a previously fixed patient-specific rule set based on new patient conditions and/or recent lab results, and notify the caregiver that adjustment is recommended by theMMU12. As discussed above in regard toFIGS. 5 and 5A, the Apply ExpertClinical Rules50 program establishes a patient-specific rule algorithm. The patient-specific rule algorithm is primarily based on the expert rule set described above applied to a specific order detail. The patient-specific rule algorithm generates a patient-specific rule set according to patient-specific order information including but not limited to patient demographic information, and other hospital information systems data such as lab results data or monitoring data. The patient-specific rule set includes hard and soft dosage limits for each drug being administered, and these hard and soft dosage limits likewise are adjusted when the patient-specific rule set is adjusted.
• For example, during or even before an infusion, theMMU12 may receive updated patient information that can impact an ongoing or impending infusion. As shown inFIG. 20, thelab28 sends updated patient-specific lab results to theMMU12 atstep230. Likewise, themonitoring device30 sends updated patient-specific monitoring information to theMMU12 atstep232. Additionally theMMU12 queries the HIS18 for patient information including: Patient Allergies, Patient Diet, and Current Patient Medical Orders. Patient Allergies are used to check for drug-allergy interactions, atstep231. Patient Diet information is used to check for drug-food interactions. Current Patient Medical Orders are used to check for drug-drug incompatibility. Like the patient information gathered from theLab28 and themonitoring device30, the patient information from HIS18 is also used by theMMU12 to update the delivery program order.
• As shown inFIGS. 5 and 5A, in cases where theMMU12 is processing a drug order for themedical device14, theMMU12 executes the Apply ExpertClinical Rules50 program atstep178 to establish a patient-specific rule set based on updated patient information received or retrieved from thelab28, themonitoring device30, and or the HIS18 (FIG. 20). This real-time or near delivery time updated patient-specific information is useful in adapting patient therapy because it may not have been available at the time the medication order was prescribed.
• As shown inFIG. 20, TheMMU12 also modifies the existing patient-specific rule set in the existing delivery program code atstep234 based on updated patient information received or retrieved from thelab28, themonitoring device30, and or theHIS18. TheMMU12 optionally alerts theinput device32 and/or themedical device14 of changes to the patient-specific rule set.MMU12 also optionally generates an alert message if the delivery programming code violates any parameter of the adjusted hard and soft dosage limits. Additionally, theMMU12 optionally requests confirmation by the caregiver prior to instituting the new patient-specific rule set. TheMMU12 then delivers an updated delivery program code to themedical device14 for execution atstep236. Themedical device14 then executes this updated delivery program code asstep238. The updated delivery program code sent fromMMU12 to themedical device14 includes an updated patient-specific rule set generated from any rule based adjudication at theMMU12, including hard and soft dosage limits for each drug being administered. Themedical device14 caches the updated patient-specific rule set contained in the delivery program code. Additionally, theMMU12 collects, stores, and reports the changes to the patient-specific rule set, changes to the hard and soft limits, as well as the history of each medication order.
• An example of how theMMU12 updates the patient-specific rule set based on lab results or monitored patient conditions is provided below with respect to the drug Heparin, which is a blood thinner. The medication order entered by the physician might be:
• • Giveheparin 1000 units/hour. If the activated partial thromboplastin time (APTT)>75 seconds then decrease heparin to 800 units/hour.
    If themedical device14 has started the infusion at 1000 units/hour and theMMU12 subsequently receives an updated APTT value of 100 seconds from thelab28 on the patient, the MMU automatically commands themedical device14 to decrease the infusion rate to 800 units/hour. Alternatively, when the MMU is notified bylab28, an alarm will be generated to thePDA32 and/or themedical device14 to notify the caregiver of the need to change the infusion rate. The MMU can preprogram the pump for the caregiver to confirm the recommended change.
• In further embodiment or method, the hospital may establish expert rules or clinical decision support rules in theMMU12 that will be applied automatically to incoming prescribed orders, such that the physician may simply write an order for 1000 or 1200 units/hour. The hospital best practices formulated by the appropriate medical personnel are established in theMMU12 and can dictate that all heparin orders are to be conditioned on the APTT lab result and such an expert rule or clinical decision support rule will be used by theMMU12 to govern the operation of themedical device14. TheMMU12 also can check the most recent patient data and provide an alarm and/or temporarily modify the delivery order prior to the start of the infusion if the prescribed order is no longer appropriate given the expert rules or clinical decision support rules and the latest lab results or monitored patient conditions. It should be apparent that this kind of intervention by theMMU12 during or immediately prior to an infusion is particularly useful in preventing adverse consequences for the patient and the hospital.
• Where theMMU12 adjusts a previously fixed patient-specific rule set based on new patient conditions and/or recent lab results, as described above, theMMU12 provides dynamic advanced reports of real-time rule set changes in relation to changes in the condition of the patient (an “information cascade”). These advanced reports detail the history of both hard and soft upper and lower limits, as well as the activation of overrides and confirmations based on these limits for eachmedical device14 managed by theMMU12. Further details on this feature can be found in commonly owned co-pending application entitled SYSTEM FOR MAINTAINING DRUG INFORMATION AND COMMUNICATING WITH MEDICATION DELIVERY DEVICES filed on Feb. 20, 2004, which is expressly incorporated herein in its entirety.
• With reference toFIGS. 2,4A and19, theDownload Drug Library44 program in theMMU12 and the correspondingDownload Drug Library132 program in themedical device14 operate to send a drug library to themedical device14 from theMMU12. The drug library includes drug and device related information, which may include but is not limited to drug name, drug class, drug concentration, drug amount, drug units, diluent amount, diluent units, dosing units, delivery dose or rate, medication parameters or limits, device/infuser settings and/or modes, CCA designations and constraints, and library version. TheDownload Drug Library132 program is designed to cache in acache memory126A a new database or drug library atmedical device14 while maintaining an existing older version database or drug library in itsprimary memory126. This allows the medical device to operate or deliver an infusion based on the older version of the drug library without disruption until a trigger event occurs, at which time the new drug library replaces the older version in theprimary memory126. It is contemplated that themedical device14 can be equipped with an initial drug library at the factory.
• TheDownload Drug Library132 program in themedical device14 begins at ablock240 and at block242 a determination is made that a drug library update needed event has occurred. For instance the drug library update needed event could be a completed infusion, a stopped infusion, elapsed time, a specific date and time, creation of the new drug library, themedical device14 being or entering into a particular configurable mode such as stop, “sleep” or “wakeup”, connection of themedical device14 to anaccess node84 in a new CCA, a download of a new or modified drug library to the medication management unit, or a determination that the existing drug library at the medical device needs updating. The configurable mode could be any number of device modes including a power-on sleeping mode and a power-off mode. The determination that a drug library update needed event has occurred can be made by (at) theMMU12, themedical device14 or by a combination of the two.
• Based on the specific drug library update needed event, theDownload Drug Library132 proceeds to block244 where it retrieves or receives a new drug library. Once retrieved or received, theDownload Drug Library132 proceeds to block246 where it stores the new drug library in thecache memory126A of themedical device14. While amedical device14 is operating on a patient or in an otherwise nonconfigurable mode, information such as a new drug library or database is stored in acache memory126A of themedical device14 as the information is received from a wired or wireless link through thenetwork interface122. TheDownload Drug Library132 proceeds to block248 where it determines if a specific trigger event has occurred. For instance, the trigger event could be a completed infusion, a stopped infusion, a determination that the device is in a configurable mode, elapsed time, a specific date and time, creation of the new drug library, a download of a new or modified drug library to the medication management unit, and a determination that the existing drug library at the medical device needs updating. The configurable mode could be any number of device modes including a power-on sleeping mode and a power-off mode. The determination that a trigger event has occurred can be made by (at) theMMU12, themedical device14 or by a combination of the two.
• TheDownload Drug Library132 then proceeds to block250 where it deletes the existing drug library inprimary memory126 and installs the new drug library, and the new drug library fromcache memory126A will replace the older information in thememory126 of themedical device14. TheDownload Drug Library132 process is then complete and ends inblock252.
• Additional related features of theDownload Drug Library44 program in theMMU12 and the correspondingDownload Drug Library132 program include recording the history of the download, verify the correct download, notification to the caregiver of a change of library, and a preliminary note on themedical device14 display stating that the drug library will be changed after any current infusion (i.e., before the next infusion).
• Additionally, partial updates of the drug database within themedical device14 are also made possible by the present invention. TheMMU12 is supplied with a drug database that allows a user to update a single data item (row, column, or cell) in the database without re-writing the entire database. This provides faster processing and downloading times when modifying the drug database.
• Further, theDownload Drug Library44 program in theMMU12 is designed to modify a medication library from theHIS18 in such a way that only a single configuration of a single drug library is necessary to provide download information to multiple separate and differentmedical devices14 where each device has unique parameters (different models, processors, computer architecture, software, binary format, or manufacturers, for example). In this embodiment, the configured drug library is designed so that only a subset of the configured drug library is specific for each unique type ofmedical device14, and only the specific information is selected for transfer to eachmedical device14. Additionally, pre-validation of the configured drug library is done through use of a rule set editor prior to sending from theMMU12 to themedical device14, and post-validation occurs where themedical device14 confirms receipt of an acceptable drug library back to theMMU12. Further details on these additional related features can be found in commonly owned co-pending application entitled SYSTEM FOR MAINTAINING DRUG INFORMATION AND COMMUNICATING WITH MEDICATION DELIVERY DEVICES filed on Feb. 20, 2004, which is expressly incorporated herein in its entirety.
• With reference toFIGS. 2,3, and4A, theMonitor Pump44 program in theMMU12 and thecorresponding Monitor Pump130 program in themedical device14 operate to map the approximate or general physical location of eachmedical device14 within the hospital environment and to enable a user to trigger a locator alarm to locate a particularmedical device14. Additionally, the programming enabling the medical device locator would be located in anasset manager64 portion of theMMU12.
• With reference toFIG. 17, theMMU12 communicates with one or more (more preferably a plurality of)medical devices14A,14B, and14C through theelectronic network76. The medical device ordevices14A,14B, and14C connect to theelectronic network76 through one or more (more preferably a plurality of)access nodes84A,84B, and84C distributed in one or more (more preferably a plurality of)CCAs253A and253B. More than onemedical device14 can operate from anindividual access node84 and be associated with a particular patient. Typically, there is one access node per room (101,103, and301), but it also is possible to have more than one access node per room and more than one room or CCA per access node. Additionally, as discussed above with regard toFIG. 4, the connection between themedical devices14A,14B, and14C and theaccess nodes84A,84B, and84C can be wireless. A user access device such as acomputer system254 is remotely located from theMMU12 and themedical device14 and communicates with theMMU12 to permit auser256 to activate theMonitor Pump44 program in theMMU12 and remotely activate thecorresponding Monitor Pump130 program in themedical device14. Thecomputer254 can be located in a variety of locations, including but not limited to a nurse station or a biomemdical technician area.
• With reference toFIG. 18, the functional steps of theMonitor Pump52 program in theMMU12 and thecorresponding Monitor Pump130 program in themedical device14A are shown in operation with thecomputer254. To begin to request a physical location for amedical device14, the user256 (not shown) enters a query for the location of amedical device14A. Thecomputer254 sends arequest device location258 message to theMMU12. TheMMU12 in turn sends a request last usedaccess node260 message to themedical device14A. It is also contemplated that theMonitor Pump Program130 can be operated with theinput device32.
• Themedical device14A determines thelast access node84A-84C used to connect with theelectronic network76 atstep262. A report of the last usedaccess node264 is sent from themedical device14 to theMMU12. TheMMU12 processes the report of the last usedaccess node264 to determine the general physical location of the device atstep266. Once the physical location of themedical device14A is determined by theMMU12, a reportphysical location268 message is sent from theMMU12 to thecomputer254. Additionally, theMMU12 tracks “change of infuser access node” events, when amedical device14 begins to communicate through a differentnetwork access node84. TheMMU12 communicates the physical locations ofmedical devices14 to theHIS18.
• If theuser256 requires additional assistance in locating the particularmedical device14A, theuser256 can instruct thecomputer254 to send a requestaudio location alarm270 message to theMMU12. TheMMU12 in turn sends an orderaudio locator alarm272 message to themedical device14A. Themedical device14A then activates an audio alarm atstep274 to assist theuser256 in locating themedical device14A. The audio alarm activation can be delayed by a predetermined time to allow the user time to travel to the area of the last used access node. The audio alarm feature is useful in allowing the user to more precisely pinpoint the location of themedical device14. The audio alarm feature is particularly useful if themedical device14 is very close to other medical devices or has been moved to a storage closet or other location where it is not readily apparent visually.
• Alternatively, the functional steps of theMonitor Pump44 program in theMMU12 and the corresponding theMonitor Pump130 program shown inFIG. 18 can be performed as a series of “push” steps instead of a series of “pull” steps (as shown inFIG. 18). In a “push” embodiment themedical device14A periodically determines the last used access node and periodically reports the last used access node to theMMU12 as a “here I am” signal. Likewise, theMMU12 periodically determines the physical location of themedical device14A based on thelast access node84A used by themedical device14, and periodically reports the physical location of themedical device14A to theuser access device254. Alternatively, theMMU12 programming allows it to determine which ofaccess nodes84 was the last access node used by the device14 (step259 indicated by a dashed line) and the MMU can report the general physical location of themedical device14 to thecomputer254 without requesting a report from themedical device14.
• In one embodiment described above, the association betweenmedical devices14,patient110,drug100, and caregiver114 (if present), is accomplished by swiping machine readable indicators on each of these elements of the PAN113 (SeeFIG. 4). This association is made in software residing theMMU12. Alternatively, the association is made in software residing in themedical device14. With reference toFIG. 21, in another embodiment, the association betweenmedical devices14A,patient110,drug100, andcaregiver114, is accomplished by “auto-association”. Auto-association is desirable in situations where the patient's wrist is not readily accessible (e.g. during surgery, or a neonate in an incubator).
• In the auto-association embodiment, theMMU12 andmedical device14A are designed to establish the patient as the focus of theMMS10. In this embodiment, thepatient110 is equipped with a machinereadable indicator112A on a wristband, toe tag, badge or similar article. The machinereadable indicator112A contains transmitter/receiver chip278, capable of short-range transmission. The transmitter/receiver chip278 is a low power RF Bluetooth™, a dedicated RF transmitter working with a PIC processor, or any other suitable transmitter/receiver. Thepatient110 is fitted with the machinereadable indicator112A at the time of admission. The unique ID number of the particular machinereadable indicator112A is stored with an electronic patient record at theHIS18 and henceMMU12. TheMMU12 is thereby notified of the particular machinereadable indicator112A associated with theparticular patient110. Additionally, it is contemplated, that any other machine readable indicator used with the present invention, may also contains transmitter/receiver chip capable of short-range transmission. For instance, the caregiver machinereadable indicator116 and medication machinereadable indicator102 may also be equipped with a transmitter/receiver chip.
• Eachmedical device14A is also equipped with a transmitter/receiver chip280A. Upon placing amedical device14 at thepatient110 bedside, within thePAN113, the transmitter/receiver chip280A of themedical device14A “pings” by sending out a “request for patient” command to any transmitter/receiver chip278 that is in the area. Each transmitter/receiver chip278, which is in the area (usually about 0-10 meters, more preferably about 0-3 meters), replies to the ping by sending the transmitter/receiver chip280 of themedical device14A the unique ID number of the particular machinereadable indicator112A. Upon receipt of a signal from the machinereadable indicator112A, themedical device14A places the ID number of the machinereadable indicator112A in memory126 (SeeFIG. 4A) and also transmits the same to theMMU12. Alternatively, the unique ID of theindicator112A can be transmitted directly to anMMU12 located in the area or indirectly through another route, including but not limited to themedical device14. With reference toFIGS. 5,5A,6 and6A, theMMU12Process Drug Order46 program then checks the patient ID entered atstep162 and the device/channel ID entered atstep160 to ensure the correct match. TheMMU12 associates themedical device14A only to the identified patient based on the patient ID number sent to theMMU12. Dissociating themedical device14A from the patient is done based on a command from a user, or other method.
• It should be noted, that the machinereadable indicator112A (as well as the machine readable indicator112), can include equipment for monitoring the wearer, and transmitting this monitored information to themedical device14 and/or theMMU12.
• With reference back toFIG. 21, placing a secondmedical device14B within thePAN113 leads to a repeat of the same process. In this case the firstmedical device14A “pings” any transmitter/receiver chip that is in the area. The transmitter/receiver chip280B of the secondmedical device14B replies to the ping by sending the transmitter/receiver chip280A of the firstmedical device14A the unique ID number of the particular machinereadable indicator92B. Upon receipt of a signal from the machinereadable indicator92B, the firstmedical device14A places the ID number of the machinereadable indicator92B in memory126 (SeeFIG. 4A) and also transmits the same to theMMU12. The patient ID number is then sent from the firstmedical device14A to the secondmedical device14B.
• An additional or alternative validation of the “right patient” can be accomplished by caregiver visual confirmation of the patient following the auto-association procedure described above in relation toFIG. 21, and is also applicable to the five-rights procedures described above with respect toFIGS. 5,5A,6 and6A. In this process, thepatient110 is photographed with a digital camera (not shown) at the time of admission and the digital photo is stored with the electronic patient record at theHIS18. When a medication order is requested for a specific patient, the digital photo is sent to theMMU12 and upon completion of the association process, the digital photo is transmitted fromMMU12 to themedical device14 at thepatient110 bedside. The image of thepatient110 is sent to thedisplay88 of themedical device14, which is preferably a high resolution touch screen at least approximately 12 cm by 12 cm. The image of thepatient110 is then placed on thedisplay88 and thecaregiver114 is prompted by thedisplay88 to “Confirm Patient”. Thecaregiver114 confirms a patient match upon visual comparison of thepatient110 with the image on thedisplay88.
• Alternatively, the digital photo information alternatively can be stored on theindicator112 or112A and transmitted by the transmitter/receiver178 thereof. The digital photo is transmitted to themedical device14 when themedical device14 has been associated with thepatient110.
• With reference toFIG. 22, another portion of the functional steps of theMonitor Pump52 program in theMMU12 and thecorresponding Monitor Pump130 program in themedical device14 are shown in operation with thecomputer254. To begin to request a specific evaluation for the operation of a specificmedical device14, or group ofmedical devices14, the user256 (not shown) enters a query for the operation evaluation of amedical device14. Thecomputer254 sends anoperation evaluation request282 message to theMMU12. TheMMU12 in turn sends arequest operation data284 message to themedical device14. Themedical device14 sends areport operation data286 message (including but not limited to event logs, settings, CCA and utilization information) back to theMMU12 atstep286. TheMMU12 processes thereport operation data286 to generate an operational evaluation atstep288. Once the operational evaluation of themedical device14 is determined by theMMU12, a reportoperational evaluation290 message is sent from theMMU12 to thecomputer254.
• Alternatively, the functional steps of theMonitor Pump44 program in theMMU12 and the corresponding theMonitor Pump130 program shown inFIG. 22 can be performed as a series of “push” steps instead of a series of “pull” steps (as shown inFIG. 22). In a “push” embodiment themedical device14 periodically reports the operation data to theMMU12. Likewise, theMMU12 periodically processes thereport operation data286 to generate an operational evaluation atstep288, and periodically reports the operational evaluation of themedical device14 to theuser access device254 atstep290.
• The automated operational evaluation described above, provides a method of evaluatingmedical device14 while in operation; thus eliminating the need to postpone evaluation until themedical device14 is taken out of use. The real-time data collection capabilities of theMMU12 andMonitor Pump52 program allow theMMU12 to determinemedical device14 performance including advanced statistical operations in order to provide quality control data sorting algorithms and aggregation of data and control for a PAN113 (not shown). For example, consider aMMS10 where multiple discreet single or multiple channel medical devices14 (or channels) are connected to a single patient110 (not shown). TheMonitor Pump52 program collects allmedical device14 information in real-time and then comparesmedical device14 statistics to one another. Likewise, infuser channels can be compared to other infuser channels within the same multiple channel medical device or in other devices.Monitor Pump52 program therefore can detect a “bad actor” if any one of themedical devices14 or channels is operating at a level statistically lower or higher than the othermedical devices14 or channels. This statistical determination can be made by collecting and comparing the mean and standard deviation of appropriate data elements. This statistical determination can be performed selectably on any of the data that is routinely collected by themedical device14 event log and any that may be acquired from the instrumentation of themedical device14. For example, statistical determinations could be performed based on air alarm events, occlusion alarm events, battery usage data, screen response time, etc.MMU12 then sends the operational evaluation message (including any relevant quality control alert) to an appropriate area (including but not limited to the computer254) in a form that is appropriate for the particular alert (usually including but not limited to graphically or audibly). Additionally, operational evaluation message (including any relevant quality control alert) can be sent to any number of individuals including but not limited to the caregiver, a biomedical engineer, caregiver supervisor, and a doctor.
• With reference toFIG. 17, themedical device14 is designed as a multi-processor, where many features are not hardwired, but instead can be uniquely configured based on rules, the location of themedical device14, etc. For example, themedical device14 is designed to allow a customized display based on the Clinical Care Area (CCA)253A or253B themedical device14 is located in and/or assigned too. An example of this would be theMMU12 instructing themedical device14 to have a display of a particular color or warning tones/volumes based on the location of themedical device14 in the hospital, time of day, caregiver information, patient information, or the type of medication being supplied. For example, the patient information could include a patient diagnosis and/or a disease state. For example, alarm volumes and display brightness can be set lower in the pediatric clinical care area or at night than in the emergency room clinical care area or during the daytime.
• With reference toFIG. 4, similarly, themedical device14 is designed to allow a customized display based on user information supplied to the medical device14 (from theMMU12 for example). Such user based customized display could include changes in language preference, limited access depending on the security level of thecaregiver114, customizing the displayed information based on the training level of the individual or recent interactions therewith, and/or customizing an automated help function based on training level of the user or recent interactions therewith. TheMMU12 presents a user with a default view based on the user's role. TheMMU12 permits a default view for each role to be configurable in terms of the data detail presented. TheMMU12 allows a user with the appropriate privilege to set a particular presented view as the preferred or default starting view for that user following login. TheMMU12 allows a user to access databases and details based on role and privilege. TheMMU12 allows a user to access other views based on role and privilege. Each presented view includes: a common means of navigating among views, both summary and detail, access to privacy, security, and other policy statements, access to online help, and a logoff capability. Additionally, an emergency bypass (such as a pass-code) would be provided to bypass security restrictions in case of an emergency.
• With reference toFIG. 22, another portion of the functional steps of theMonitor Pump52 program in theMMU12 and thecorresponding Monitor Pump130 program in themedical device14 are shown in operation with thecomputer254. TheMMU12 tracks and records actions taken by thecaregiver114 based on operational data reported from one or moremedical devices14. Just as theMMU12 is capable of generating an operational evaluation of eachmedical device14, theMMU12 can likewise generating an operational evaluation of each caregiver114 (not shown) atstep288. This operational evaluation of eachcaregiver114 includes records of each caregiver's114 actions (or, in some cases, inactions), sorting of these actions based on given criteria, and tracking of any trends in these actions. In general, these records of actions include any task lists, medication administration records, treatments, and other actions associated with the caregiver's114 responsibilities. Such records of actions may combine medications administered, treatments, and other actions for multiple patients under the care of an individual caregiver.MMU12 then sends the operational evaluation message (including any relevant quality control alert) to an appropriate area (e.g. to thecomputer254 or caregiver supervisor's computer (not shown)) in a form that is appropriate for the particular alert (usually including but not limited to graphically or audibly). Additionally, operational evaluation message (including any relevant quality control alert) can be sent to any number of individuals including but not limited to the caregiver, a biomedical engineer, caregiver supervisor, and a doctor.
• Additionally, theMMU12 can instruct themedical device14 to customizeddisplay88 based on the operational evaluation message. Thus, thedisplay88 is adjusted by theMMU12 based a determination that thecaregiver114 requires additional or different information displayed to improvecaregiver114 interaction with themedical device14. For example, detailed step by step instructions can be placed ondisplay88, where theMMU12 recognizes acaregiver114 who is not familiar with a particular therapy, using thedisplay88 as the instruction means. Likewise, where theMMU12 recognizes that acaregiver114 has limited experience programming the medical device14 (caregiver experience) or in previous interactions had made errors programming a particular function (caregiver error rate) or was a statistically longer than the norm at programming a particular function (caregiver response time), theMMU12 instructs themedical device14 to display pertinent training information.
• In another embodiment best understood with reference toFIG. 4A, themedical device14 is designed to act as a web server for theinput device32 or other similar devices within proximity to themedical device14. In this embodiment,medical device14 is equipped to supply theinput device32 web browser with medical device related information as well as non-medical device related information such as task lists, etc. Additionally, themedical device14 displays a dual function screen having both a pump monitor screen portion and a web browser screen portion. Further, supplying themedical device14 as a web server permits a remote web browser to associate with themedical device14 to configure themedical device14 or run diagnostics on themedical device14.
• With reference toFIGS. 2 and 4A, another portion of theMonitor Pump52 program in theMMU12 and thecorresponding Monitor Pump130 program in themedical device14 is directed to cloning betweenmedical devices14. Themedical devices14 are designed to have wireless data sharing between eachmedical device14 sufficient to permit cloning of all patient information between eachmedical device14, and/or the multi-sequencing of a set ofmedical devices14 without a hardwired connection. TheMMU12 adjudicates this cloning and/or multi-sequencing.
• Whereas the invention has been shown and described in connection with the embodiments thereof, it will be understood that many modifications, substitutions, and additions may be made which are within the intended broad scope of the following claims. From the foregoing, it can be seen that the present invention accomplishes at least all of the stated objectives.

Claims (3)

1-30. (canceled)

31. A method for dynamically adjusting the screen brightness of a pump screen display, comprising the steps of:

providing a medical pump comprising a screen display and an internal clock, the screen display having a first screen brightness and a second screen brightness;

providing a medication management unit operatively connected to said medical pump, said medication management unit configured to transmit configuration instructions to said medical pump, said configuration instructions comprising instructions to display said first screen brightness during daytime hours and instructions to display said second screen brightness during nighttime hours;

determining a current time of day using said internal clock;

displaying said first screen brightness or said second screen brightness based upon the determined time of day.

32. The method ofclaim 31, wherein said first screen brightness is brighter than said second screen brightness.

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