throbber
as) United States
`a2) Patent Application Publication 0) Pub. No.: US 2007/0093786 A1
`(43) Pub. Date: Apr. 26, 2007
`
`Goldsmith et al.
`
`US 20070093786A1
`
`(54)
`
`(75)
`
`WATCH CONTROLLER FOR A MEDICAL
`DEVICE
`
`Inventors: Joel Goldsmith, Studio City, CA (US);
`Andrew C. Hayes, Simi Valley, CA
`(US)
`
`Correspondence Address:
`PILLSBURY WINTHROP SHAW PITTMAN
`LLP
`P.O BOX 10500
`McLean, VA 22102 (US)
`
`Continuation-in-part of application No. 11/204,667,
`filed on Aug. 16, 2005.
`
`Publication Classification
`
`(51)
`
`Int. CL
`AGIK 9/22
`A6IM 37/00
`
`(2006.01)
`(2006.01)
`
`(52) US. CM.
`
`ccsccssscssessseesssessseeesse 604/890.1; 604/131
`
`
`
`(57)
`ABSTRACT
`(73) Assignee: MEDTRONIC MINIMED,_INC.,
`Northridge, CA (US)
`
`(21)
`
`Appl. No.:
`
`11/496,606
`
`(22)
`
`Filed:
`
`Jul. 31, 2006
`
`Related U.S. Application Data
`
`(63)
`
`Continuation-in-part of application No. 11/204,583,
`filed on Aug. 16, 2005.
`
`MEM,
`
`JUL 7-03
`
`An infusion system that includes a watch controller device
`and a communication system to transmit the communica-
`tions from the watch controller device to an infusion device
`
`pump that controls delivery of fluids to the user’s body.
`Moreparticularly, these apparatuses and methods are for
`providing convenient monitoring and control of the infusion
`pump device in determining the appropriate amount of
`insulin to deliver.
`
`29
`
`10
`
`J5
`
`30
`
`40
`
`45b
`
`APPLE 1011
`
`APPLE 1011
`
`1
`
`

`

`Patent Application Publication Apr. 26,2007 Sheet 1 of 10
`
`US 2007/0093786 Al
`
`2
`
`

`

`Patent Application Publication Apr. 26,2007 Sheet 2 of 10
`
`US 2007/0093786 Al
`
`110
`
`130
`
`FIG.
`
`35
`
`3
`
`

`

`Patent Application Publication Apr. 26,2007 Sheet 3 of 10
`
`US 2007/0093786 Al
`
`yO
`
`4
`
`

`

`Patent Application Publication Apr. 26,2007 Sheet 4 of 10
`
`US 2007/0093786 Al
`
`“NAWANOD
`
`WILSAS
`
`34
`
`9S1
`
`(S
`
`TWNOIS
`
`dy
`
`0g!
`
`WSINVHOIN
`
`5
`
`
`

`

`Patent Application Publication Apr. 26,2007 Sheet 5 of 10
`
`US 2007/0093786 Al
`
`210
`
` L__~_=TY= tSSana ghee ee ee eee J
`
`KEYPAD
`
`DISPLAY
`
`6.
`
`° FIG. 6a
`
`
`310
`
`6
`
`

`

`Patent Application Publication Apr. 26,2007 Sheet 6 of 10
`
`US 2007/0093786 Al
`
`400
`
`422
`
`CONNECTOR
`
`
`
`
`
`COMPUTER
`
`
`
`CONTROLLER
`
`410:
`
`
`
`PHYSIOLOGICAL \
`SENSOR -
`MONITOR
`
`450
`
`
`CHARACTERISTIC
`
`492,
`
`BEDSIDE
`
`THERAPY/
`DIAGNOSTIC
`
`DEVICE
`
`CELLULAR
`STATION/
`GPS
`
`488
`
`BG METER
`
`FIG. 7
`
`7
`
`

`

`FIG.
`MAIN BATTERY. 3
`
`=o© a
`
`©—
`
`=©t
`
`cw>O
`
`o
`
`Patent Application Publication Apr. 26,2007 Sheet 7 of 10
`
`US 2007/0093786 Al
`
`—Sa
`
`cte
`
`&
`
`592
`
`o
`id
`
`=S
`
`o
`Qa
`
`8
`
`

`

`Patent Application Publication Apr. 26,2007 Sheet 8 of 10
`
`US 2007/0093786 Al
`
`
`
`9
`
`

`

`Patent Application Publication Apr. 26,2007 Sheet 9 of 10
`
`US 2007/0093786 Al
`
`
`
`440
`
`FIG 16
`
`10
`
`

`

`Patent Application Publication Apr. 26,2007 Sheet 10 of 10
`
`US 2007/0093786 Al
`
`FIG. 10
`
`1022
`
`
`
`
`
`
`
`
` Meter
`
`
`«(
`yy»
`
`- «
`)y) y
`
`1050
`Infusion
`L_pmp
`
`Glucose
`sensing
`device
`1060
`
`buttons
`
`Display
`
`1045
`
`1065
`
`1030
`
`bw www eww we ee ee wm ew eee ee ee eee mee wee me Bee mete mre ee eee ree
`
`11
`
`11
`
`

`

`US 2007/0093786 Al
`
`Apr. 26, 2007
`
`WATCH CONTROLLER FOR A MEDICAL DEVICE
`
`RELATED APPLICATIONS
`
`[0001] This patent application is a continuation-in-part of
`USS. patent application Ser. No. 11/204,583, filed on Aug.
`16, 2005 and a continuation-in-part of U.S. application Ser.
`No. 11/204,667, filed on Aug. 16, 2005, which are herein
`incorporated by reference.
`
`FIELD OF THE INVENTION
`
`[0002] Embodiments of this invention relate generally to
`infusion systems and methods for delivering fluids into an
`individual’s body and monitoring systems and methods for
`monitoring analyte levels in an individual’s body. More
`particularly, embodiments of this invention relate to appa-
`ratuses and methods for providing a convenient way in
`which to monitor and control the fluids delivered to the
`
`individual’s body and to monitor the analyte levels in the
`individual’s body.
`
`DESCRIPTION OF THE RELATED ART
`
`[0003] Patients with Type 1 diabetes and some patients
`with Type 2 diabetes use insulin to control
`their blood
`glucose (BG) level. Diabetics must modify their daily lif-
`estyle to keep their body in balance. To do so, diabetics need
`to keep strict schedules, including ingesting timely nutri-
`tious meals, partaking in exercise, monitoring BG levels
`daily, and-adjusting and administering insulin dosages
`accordingly. Testing of BG levels has been both painful and
`awkward for the patient. Traditionally,
`insulin dependent
`diabetics were required to monitor their BG levels by
`puncturing a finger tip with a needle. Due to the fact that
`many patients must conduct such a test multiple times
`throughoutthe day to regulate their BG levels, the procedure
`can be painful and inconvenient.
`
`[0004] Typically, patients may employ various calcula-
`tions to determine the amount of insulin to inject. For
`example, bolus estimation software is available for calcu-
`lating an insulin bolus. Patients may use these software
`programs on an electronic computing device, such as a
`computer, the Internet, a personal digital assistant (PDA), or
`an insulin delivery device. Insulin delivery devices include
`infusion pumps,
`injection pens, and implantable delivery
`systems. The better bolus estimation software takes into
`account the patient’s present BG level. Presently, a patient
`must measure his/her blood glucose using a BG measure-
`ment device, such as a test strip meter, a continuous glucose
`measurement system, or a hospital hemacue. BG measure-
`ment devices use various methods to measure the BG level
`
`of a patient, such as a sample ofthe patient’s blood, a sensor
`in contact with a bodily fluid, an optical sensor, an enzy-
`matic sensor, or a fluorescent sensor. When the BG mea-
`surement device has generated a BG measurement,
`the
`measurementis displayed on the BG measurement device.
`Then the patient may visually read the BG measurement and
`physically enter the BG measurement into an electronic
`computing device to calculate a bolus estimate. Finally, once
`the bolus estimate is calculated, the patient must inject the
`insulin bolus or program an insulin delivery device to
`deliver the bolusinto their body. Unfortunately, this process
`is also cumbersomeandis subject to transcribing errors—for
`example, the patient may inaccurately enter the BG mea-
`
`surementthat is displayed on the BG measurement device
`into the electronic computing device. Thus,
`if the BG
`measurementis not entered correctly, the bolus estimate is
`not accurate, which may lead to the delivery of an inappro-
`priate insulin dose. In other devices, the measurementis
`transmitted to the electronic computing device.
`
`In infusion systems where a display is included for
`[0005]
`convenient viewing of selected information, such as that
`requested by the user or an instructed act that was under-
`taken by an infusion device or a sensing device, the display
`is generally located on the device. This may be inconvenient
`for the user to view information because infusion devices
`and sensors are typically secured to or near a site on the
`user’s body. Thus, viewing may require the user to move or
`manipulate the infusion device or sensor to view the display
`which may lead to improper reading of the display.
`
`BRIEF SUMMARY OF THE INVENTION
`
`In accordance with embodiments of the invention,
`[0006]
`an infusion system is provided that allows for the control of
`the delivery of a fluid or medication. An embodimentof the
`present invention includes a controller device and a therapy/
`diagnostic device, such as an infusion device. The controller
`device may be a hand-held device, separate from the infu-
`sion device, that allows the user to communicate with the
`infusion device without actually handling the infusion
`device.
`
`[0007] The controller device includes a housing adapted to
`be carried by the user and a communication system con-
`tained in the housing for transmitting a communication or
`command from the user to the infusion device. In alternative
`embodiments, the controller device may receive communi-
`cations sent from the infusion device or other components of
`the infusion system, such as for example, a characteristic
`determining device. Further,
`the controller device may
`include a user input device on the controller device housing,
`such as keys, buttons, or the like, for the user to input data
`or commands.
`
`[0008] The controller device includes on the housing a
`display that may mimic the display on the infusion device.
`In certain embodiments, whatever is shown on the infusion
`device corresponds to that shown and reflected on the
`display of the controller device. The controller device dis-
`play shows information according to communications sent
`to it from the infusion device. The user may more conve-
`niently view what is being processed or acted upon in the
`infusion device without removing or adjusting the infusion
`device to view the display. In further embodiments, the
`controller device may be configuredso that the input devices
`included allow all, or substantially all, viewing and data
`entry to be performed on the controller device without
`moving or referring to the infusion device.
`
`In further embodiments, the controller device may
`[0009]
`control an analyte sensing device such as a continuous
`glucose sensor. The controller device display shows infor-
`mation according to communications sent to it from the
`sensing device.
`In further embodiments,
`the controller
`device may control more than one device, for example, an
`infusion pump and an analyte sensor.
`
`In further embodiments, the controller device may
`[0010]
`include time-telling functions. For example, the controller
`
`12
`
`12
`
`

`

`US 2007/0093786 Al
`
`Apr. 26, 2007
`
`device may be a wrist-worn device, such as a watch. The
`controller device may also be a watch that can be carried on
`other parts of the body or clothing, such as the ankle, neck
`(e.g., on a chain), pocket, or ankle.
`
`[0011] Among other advantages, embodiments of the
`present invention may provide convenience andeaseofuse.
`For example, an embodiment with a user interface and
`display on the controller device may cater to the active
`lifestyles of many insulin dependent diabetics. A large and
`simple display minimizes the potential for error in reading
`and interpreting test data. A small overall size permits
`discretion during self-monitoring and makes it easy to carry.
`In another embodiment, the controller device may be inte-
`grated with a characteristic determining device into one
`housing and feature a large target area for strip insertion to
`make the monitoring procedure fast and accurate. In some
`embodiments, the controller device display may include a
`dedicated backlight to facilitate viewing.
`
`[0012] The controller device also reflects the other func-
`tionsthat the particular infusion device may show, including
`a variety of other displays, for example, when the last bolus
`was administered, when the last alarm occurred, when the
`last finger stick was taken, past
`trends, all alarms that
`occurred in a time period, calibrations, meals, exercise,
`bolus schedules, temporary basal delivery, diagnostic infor-
`mation, and the like. Whenever a bolus is being delivered,
`the infusion device can send a message every time a tenth of
`a unit, or some specified amount, is delivered, to which the
`user may monitor via the controller device display.
`
`In certain embodiments, the infusion device is the
`[0013]
`central hub with peripheral devices being the controller
`device and a characteristic determining device. The charac-
`teristic determining device being adapted to sense and
`determine the concentration of an analyte of a patient and
`directs the infusion device fluid delivery according to the
`measurements. While the term “analyte” is used herein,it is
`possible to determine and use other characteristics as well
`using the same type of system. The control is maintained in
`the central hub andthe infusion device sends out most of the
`commands. The infusion device also sends requests to
`receive specific data from the controller device and the
`characteristic determining device, if one is included.
`
`In particular embodiments, where the controller
`[0014]
`device is integrated with the characteristic determining
`device into one housing, the controller device may auto-
`matically transmit communications
`including the data
`indicative of the determined concentration of the analyte in
`the user to the infusion device. In other particular embodi-
`ments, the controller device further includes a user input
`device for inputting commands, and transmits the commu-
`nications to the infusion device in response to a command
`from the user input device. In additional embodiments, the
`controller device further includes an indicator to indicate a
`status of the communication including the data indicative of
`the determined concentration of the analyte in the user being
`transmitted from the determining device communication
`system to the infusion device communication system. Data
`compression may be employed to speed up communications.
`
`In further embodiments, the infusion device may
`[0015]
`contain all or substantially all of the intelligence. The
`amount of time that the controller communicates with the
`
`infusion device or other components may be limited to save
`
`power in the controller device. For example, radio-fre-
`quency (RF) communications may be minimized, such that
`the marriage between the infusion device and controller
`occurs once until further communication is necessary to
`exchange data. The information regarding the screens dis-
`playedis sent to the controller, and when the infusion device
`needs to display a screen, it sends a screen number to the
`controller. In the case of screen displays, if the data being
`sent is fixed, then the screen can be simply displayed.If the
`data is variable, then the variable data is sent with the screen
`to the infusion device. Exchange IDs, strings to be dis-
`played, and foreign languages are among data that may be
`sent from the controller. Further commandsthat may be sent
`from the infusion device include, among other commands, a
`commandto show a specific screen on the controller device,
`a command for displaying requested information on the
`screen, a command for showing the rules for the input
`devices, a command for showingthe intelligence aboutthat
`screen type (e.g., menus, data entries, etc.), and the like.
`
`[0016] The controller device and the infusion device may
`communicate to one another through wireless or non-wire-
`less methods. Some examples of wireless methods include,
`by no way in limitation, RF,
`infrared (IR), Bluetooth,
`ZigBee, and other 802.15 protocols, 802.11 WiFi, spread
`spectrum communication, and frequency hopping commu-
`nication. Further examples include giving the controller
`device cellular telephone or pager capabilities. In the alter-
`native, the communication may be wired, such as in hospital
`use. In a wired embodiment, there may be a tether physically
`connecting the infusion device to the controller device. In
`yet another alternative, the controlling device and the infu-
`sion device could be both wired and wireless—whenwired,
`the two components communicate by wire, and when dis-
`connected, the two components could operate through wire-
`less communication.
`
`In another wireless example, if the user has access
`[0017]
`to a computer network or phone connection, the user can
`open communication via the internet to obtain communica-
`tions from, and send communications to, a nurse, parent, or
`anyone so desired. A transceiver may be used to facilitate
`data transfer between the PC and the infusion device. Such
`
`a communication mayalso be used bya party, other than the
`user, to control, suspend, and/or clear alarms. This embodi-
`ment could be very useful for a parent
`to monitor the
`infusion system of a child, or for a physician to monitor the
`infusion system of a patient. As a non-limiting example,
`further description of a communication station may be found
`in U.S. Pat. No. 5,376,070, which is herein incorporated by
`reference. The transceiver may allow patients at home or
`clinicians in a hospital setting to communicate with the
`various components of the infusion system via RF telemetry.
`The transceiver may be used to download device informa-
`tion from the infusion device and sent to the PC when the
`
`transceiver is connected in to the serial port of the PC. In
`embodiments, the transceiver may derive its power from the
`PC when the two are connected. In this way, the transceiver
`conveniently does not require a separate power source. In
`another embodiment, a cellular phone may be used as a
`conduit for remote monitoring and programming. In yet
`other embodiments, the controller device may also act as a
`transceiver, which would eliminate an extra component.
`
`In yet further embodiments, the infusion system
`[0018]
`includes an infusion device and/or a sensing device. The
`
`13
`
`13
`
`

`

`US 2007/0093786 Al
`
`Apr. 26, 2007
`
`sensing device includes a sensor and a transmitter in com-
`munication with the infusion device. The transmission may
`occur via wire or wireless methods. The sensing device
`includes a sensor and a transmitter in communication with
`
`the infusion device. The sensing device may sense an
`analyte of a bodily fluid of the user and provide continuous
`monitoring of that analyte. The sensing device may be
`calibrated using data from the infusion device and/or from a
`characteristic determining device. In further embodiments,
`the sensing device senses additional physiological charac-
`teristics. In still further embodiments, the system is set up to
`automatically call for assistance when analytes reach a
`certain level. The system maybeset up to notify others, for
`example, through a cellular network. In such a manner, the
`patient’s cellular telephone may be used to connect
`to
`emergency services. The call may include a global position-
`ing system (GPS)location. GPS functions may be included
`separately from cellular telephone type functions.
`
`[0019] Communications between the system components
`may be performed in a variety of manners. In an embodi-
`ment using RF options, there could be employed a “spread
`spectrum” where a large range of RFs can be usedto relay
`the communication. In another embodiment, changing fre-
`quencies can be used so as to pick up whatever frequencyis
`present. This is known as frequency hopping, where the
`frequency changes periodically or so to take advantage of
`all, or substantially all,
`frequencies available. Another
`embodimentis one that uses adaptive frequency selection, or
`Listen Before Talk (LBT), where the devices select the
`cleanest available channel from thoseallotted priorto trans-
`mitting. In somecases, frequency hopping allowsthe system
`to find frequencies that are not being used by other nearby
`systems and thus avoid interference. In addition, a system
`may operate in a manner where each component-to-compo-
`nent communication is on a different frequency, or where the
`delay for each communication is different. Other types of
`RF, that are not described, may also be used for communi-
`cation, such as, translation frequency.
`BRIEF DESCRIPTION OF THE DRAWINGS
`
`[0020] A detailed description of embodiments of the
`invention will be made with reference to the accompanying
`drawings, wherein like numerals designate corresponding
`parts in the figures.
`
`[0021] FIG. 1 is a front view of a controller device
`according to an embodiment of the invention.
`
`[0022] FIG. 2 is a front view of a blood glucose meter
`integrated into a controller device housing according to an
`embodimentof the invention.
`
`[0023] FIG. 3 is a front view of a blood glucose meter
`integrated into a controller device housing according to
`another embodiment of the invention.
`
`[0024] FIG. 4 is a front view of a blood glucose meter
`integrated into a controller device housing communicating
`with an infusion device according to an embodimentof the
`invention.
`
`[0025] FIG. 5isa block diagram of an RF communication
`system in the infusion device according to an embodimentof
`the invention.
`
`[0026] FIG. 6A is a block diagram of a controller device
`according to an embodiment of the invention.
`
`FIG. 6B is a block diagram of a controller device
`[0027]
`according to an embodiment of the invention.
`
`FIG. 7 is a block diagram of different communi-
`[0028]
`cation paths within the infusion system according to an
`embodimentof the invention.
`
`FIG. 8 is a diagram ofthe electronics architecture
`[0029]
`of a controller device according to an embodiment of the
`invention with a custom integrated circuit.
`
`FIG. 9A is a front view of a combined watch and
`[0030]
`controller device according to an embodimentof the inven-
`tion.
`
`FIG. 9B is a rear view of a combined watch and
`[0031]
`controller device according to an embodimentof the inven-
`tion.
`
`FIG. 10 is a block diagram of a combined watch
`[0032]
`and controller device according to an embodiment of the
`invention.
`
`DETAILED DESCRIPTION OF THE
`INVENTION
`
`In the following description, reference is made to
`[0033]
`the accompanying drawings which form a part hereof and
`whichillustrate several embodiments of the present inven-
`tions.
`It
`is understood that other embodiments may be
`utilized and structural and operational changes may be made
`without departing from the scope of the present inventions.
`
`the controller device is a
`In one embodiment,
`[0034]
`hand-held device separate from the therapy/diagnostic
`device, such as an infusion device, that allows the user to
`communicate with the therapy/diagnostic device without
`actually handling the device. Other examples of therapy/
`diagnostic devices include electronic therapy devices and
`devicesthat receive diagnostic information from cardiac and
`other sensors. Asillustrated in FIG. 1, the controller device
`5 includes a housing 3 adapted to be carried by the user and
`a communication system (not shown) contained in the
`housing 3 for transmitting a communication or command
`from the userto the infusion device. In further embodiments,
`the controller device 5 may receive communications sent
`from the infusion device or other components of the infusion
`system, such as for example, a characteristic determining
`device. Further, the controller device may include one or
`more user input devices 2a and 25 on the controller device
`housing 3, such as keys, buttons, or thelike, for the user to
`input data or commands. The controller device 5 includes a
`display 4 on the controller device housing 3 which simul-
`taneously displays whatever information and/or graph is
`being displayed on the infusion device display at
`that
`moment. The display 4 allows a user to easily monitor and
`control what actions are taking place in, or being performed
`by, the infusion device. In some embodiments,the controller
`device 5 may further include a backlight 1 in the controller
`device display 4 for easier viewing. The backlight may be
`adapted to be in one or more colors, which can be user
`selectable for personalized use. In further embodiments, the
`backlight may be adapted to flash and/or turn to a color such
`as yellow or red when various alerts and alarms take place.
`In additional embodiments,
`the controller device 5 may
`include accessories such as handstraps 6 to provide conve-
`nient handling. In particular embodiments, the controlleris
`sized smaller than 6 inches long by 4 inches wide by 1 inch
`thick.
`
`14
`
`14
`
`

`

`US 2007/0093786 Al
`
`Apr. 26, 2007
`
`In certain embodiments, a characteristic determin-
`[0035]
`ing device that senses and determines the concentration of
`an analyte of a patient, for example blood glucose (“BG”),
`and controls the infusion device according to the measure-
`ments, may be included in an infusion system with the
`controller device and the infusion device. The characteristic
`
`determining device includes a housing, a receptacle coupled
`to the housing for receiving and testing an analyte from the
`user to determine a concentration of the analyte in the user,
`a processor contained in the housing and coupled to the
`receptacle for processing the determined concentration of
`the analyte from the receptacle, and a communication sys-
`tem contained in the housing and coupledto the processor
`for transmitting a communication including data indicative
`of the determined concentration of the analyte in the user. In
`particular embodiments,
`the characteristic determining
`device may also include a lancing device coupled to the
`receptacle for obtaining the analyte from the user.
`
`the infusion device includes a
`In embodiments,
`[0036]
`housing adaptedto be carried by the user, a drive mechanism
`contained in the housing and operatively coupled with a
`reservoir containing the fluid for infusing the fluid into the
`body of the user, a communication system contained in the
`housing for receiving the communication including the data
`indicative of the determined concentration of an analyte in
`the user from a characteristic determining device, and a
`processor contained in the housing and coupled to the
`communication system for processing the data indicative of
`the determined concentration of the analyte in the user and
`controlling the infusion device. In particular embodiments,
`the infusion device is sized smaller than 6 inches long by 4
`inches wide by 1 inch thick.
`
`[0037] The infusion device may further include a bolus
`estimator used in conjunction with the processor for calcu-
`lating an estimated amount of fluid to be infused into the
`body of the user based upon the received data indicative of
`the determined concentration of the analyte in the user and
`a target concentration of the analyte in the user, and an
`indicator to indicate when the estimated amountoffluid to
`
`be infused has been calculated. The system may determine
`the concentration of one of any variety of analyte types
`including, but not limited to, oxygen, blood, temperature,
`lactase, pH,
`implantable, and the like. Additionally,
`the
`infusion device may include a user input device, such as
`keys, buttons, or the like, for inputting an estimate of a
`material to be ingested by the user, and the bolus estimator
`may include the capability to calculate the estimated amount
`of fluid to be infused into the body of the user based upon
`the inputted estimate of the material to be ingested by the
`user. The infusion device may also include a memory for
`storing the data indicative of the determined concentration
`of the analyte in the user received by the infusion device
`communication system from the determining device com-
`munication system.
`
`In still further alternative embodiments, the char-
`[0038]
`acteristic determining device is a BG measurement device
`and may use samples from body fluids other than blood,
`such as interstitial fluid, spinal fluid, saliva, urine, tears,
`sweat, or the like. In yet other alternative embodiments,
`other measurement devices may be utilized to determine the
`concentrations, levels, or quantities of other characteristics,
`analytes, or agents in the user, such as hormones, choles-
`terol, oxygen, pH,lactate, heart rate, respiratory rate, medi-
`
`cation concentrations, viral loads (e.g., HIV), or the like. In
`still other alternative embodiments, other fluids may be
`delivered to the user, such as medication other than insulin
`(e.g., HIV drugs, drugs to treat pulmonary hypertension,iron
`chelation drugs, pain medications, and anti-cancer treat-
`ments), chemicals, enzymes, antigens, hormones, vitamins,
`or the like. Particular embodiments are directed towards the
`use in humans; however, in alternative embodiments, the
`infusion devices may be used in animals. For pain manage-
`ment, a bolus function maybeset up as a Patient Controlled
`Analgesic (PCA) function for customized delivery or the
`user may press a preset bolus button several times.
`[0039]
`In other embodiments, the characteristic determin-
`ing device is a BG meter that determines BG level and the
`infusion device is an insulin infusion pump. The BG meter
`communicates the measurementof BGto the infusion pump
`device to determine the amountof insulin for delivery to the
`user.
`In alternative embodiments,
`the BG measurement
`device may be a continuous glucose measurement system, a
`hospital hemacue, an automated intermittent blood glucose
`measurement system, and the like, and/or the BG measure-
`ment device may use other methods for measuring the user’s
`BG level, such as a sensor in contact with a body fluid, an
`optical sensor, a RF sensor, an enzymatic sensor, a fluores-
`cent sensor, a blood sample placed in a receptacle, or the
`like. The BG measurement device may generally be of the
`type and/or include features disclosed in U.S. patent appli-
`cations Ser. No. 09/377,472 filed Aug. 19, 1999 andentitled
`“Telemetered Characteristic Monitor System and Method of
`Using the Same,” Ser. No. 09/334,996 filed Jun. 17, 1999
`and entitled “Characteristic Monitor with a Characteristic
`
`Meter and Method of Using the Same,” Ser. No. 09/487,423
`filed Jan. 20, 2000 and entitled “Handheld Personal Data
`Assistant (PDA) with a Medical Device and Method of
`Using the Same,” and Ser. No. 09/935,827 filed Aug. 23,
`2001 and entitled “Handheld Personal Data Assistant (PDA)
`with a Medical Device and Method of Using the Same,”
`which are herein incorporated by reference. Such BG mea-
`surement devices may be adapted to be carried by the user,
`for example, in the hand, on the body, in a clothing pocket,
`attached to clothing (e.g., using a clip, strap, adhesive, or
`fastener), and the like. In particular embodiments, the BG
`measurement device is sized smaller than 6 inches long by
`4 inches wide by 1 inch thick.
`[0040]
`In alternative embodiments of the invention, the
`BG meter may be integrated into the controller device
`housing, as shown in FIG. 2, where the controller device
`housing 15 includes a BG meter receptacle 20. The control-
`ler 10 includes a housing 15 adapted to be carried by the
`user, a BG meter receptacle 20 coupled to the housing 15 for
`receiving and testing BG level from the user to determine a
`concentration of the BG in the user. A BGtest strip 25 that
`holds a use blood sample is inserted into the BG meter
`receptacle 20 for the testing by the controller device 10. In
`variations, the controller device 10 may have a cartridge-like
`mechanism whichloads andpresents thestrip for testing and
`then ejects it. The controller device 10 has a display 30 on
`the housing 15 to show information requested by the user or
`an instructed act that was undertaken by the infusion device,
`such as for example, determined concentration of blood
`glucose levels, BG trends or graphs, such as described and
`disclosed in U.S. patent application Ser. No. 10/624,177,
`entitled “System for Monitoring Physiological Characteris-
`tics,” which is herein incorporated by reference. The display
`
`15
`
`15
`
`

`

`US 2007/0093786 Al
`
`Apr. 26, 2007
`
`30 may further include a dedicated backlight 35 to facilitate
`viewing. The backlight 35 may be a user programmable
`multi-color backlight that additionally performsthe function
`of a visual indicator by flashing colors appropriate to the
`level of an alert or alarm. The backlight 35 may also have
`variable intensity (automatic or manual) to preserve the
`battery power and improved viewing. The controller 10
`includes a keypad 40 on which various input devices, such
`as keys, buttons, or the like, are located. The keypad buttons
`45a, 455, 45c, and 45d are used by the user to select options
`and/or input information.
`
`[0041] The powerof the controller device and ofthe other
`various devices discussed herein may be provided from a
`battery. The battery may be a single use or a rechargeable
`battery. Where the battery is rechargeable, there may be a
`connectoror other interface on a device to attach the device
`
`to an electrical outlet, docking station, portable recharger, or
`so forth to recharge the battery while in the device. It is also
`possible that a rechargeable battery may be removable from
`the device for recharging outside of the device, however, in
`some cases, the rechargeable battery may be sealed into the
`housing of the device to create a more water resistant or
`waterproof housing. The devices may be adapted to accom-
`modate various battery types and shapes. In further embodi-
`ments, the devices may be adapted to accommodate more
`than one type of battery. For example, a device may be
`adapted to accommodate a rechargeable battery and, in the
`event of battery failure or other need, also adapted to
`accommodate a readily available battery, such as a AA
`battery, AAA battery, or coin cell battery.
`
`In FIG. 3, another embodiment of a controller
`[0042]
`device is shown. Again, the controller device 110 includes a
`housing 115 adapted to be carried by the user, and a BG
`meter receptacle 120 coupled to the housing 115 for receiv-
`ing and testing BG level from the user to determine a
`concentration of the BG in the user. A BGtest strip 125 that
`holds a user’s blood sample is inserted into the BG meter
`receptacle

This document is available on Docket Alarm but you must sign up to view it.


Or .

Accessing this document will incur an additional charge of $.

After purchase, you can access this document again without charge.

Accept $ Charge
throbber

Still Working On It

This document is taking longer than usual to download. This can happen if we need to contact the court directly to obtain the document and their servers are running slowly.

Give it another minute or two to complete, and then try the refresh button.

throbber

A few More Minutes ... Still Working

It can take up to 5 minutes for us to download a document if the court servers are running slowly.

Thank you for your continued patience.

This document could not be displayed.

We could not find this document within its docket. Please go back to the docket page and check the link. If that does not work, go back to the docket and refresh it to pull the newest information.

Your account does not support viewing this document.

You need a Paid Account to view this document. Click here to change your account type.

Your account does not support viewing this document.

Set your membership status to view this document.

With a Docket Alarm membership, you'll get a whole lot more, including:

  • Up-to-date information for this case.
  • Email alerts whenever there is an update.
  • Full text search for other cases.
  • Get email alerts whenever a new case matches your search.

Become a Member

One Moment Please

The filing “” is large (MB) and is being downloaded.

Please refresh this page in a few minutes to see if the filing has been downloaded. The filing will also be emailed to you when the download completes.

Your document is on its way!

If you do not receive the document in five minutes, contact support at support@docketalarm.com.

Sealed Document

We are unable to display this document, it may be under a court ordered seal.

If you have proper credentials to access the file, you may proceed directly to the court's system using your government issued username and password.


Access Government Site

We are redirecting you
to a mobile optimized page.





Document Unreadable or Corrupt

Refresh this Document
Go to the Docket

We are unable to display this document.

Refresh this Document
Go to the Docket