US20150257689A1 - Physiological monitor calibration system - Google Patents

Abstract

A calibration system is disclosed for calibrating a first physiological monitoring device using a second physiological monitoring device. The first physiological monitor measures a first indication of a physiological parameter. The second physiological monitor measures a second indication of the physiological parameter. The first and second indications are used to calibrate the first physiological monitoring device.

Description

RELATED APPLICATIONS
• This application is a continuation of U.S. application Ser. No. 13/274,306, filed Oct. 15, 2011, titled “Physiological Monitor Calibration System,” the disclosure of which is hereby incorporated by reference in its entirety and which claims priority under 35 U.S.C. §119(e) as a nonprovisional of U.S. Provisional Application No. 61/393,551, filed Oct. 15, 2010, titled “Physiological Monitor Calibration System,” the disclosure of which is hereby incorporated by reference in its entirety. U.S. application Ser. No. 13/274,306 also claims priority under 35 U.S.C. §120 as a continuation-in-part of U.S. application Ser. No. 11/746,451, filed May 9, 2007, titled “Systems and Methods for Calibrating Minimally Invasive and Non-Invasive Physiological Sensor Devices,” the disclosure of which is hereby incorporated by reference in its entirety and which claims priority under 35 U.S.C. §119(e) as a nonprovisional of U.S. Provisional Application No. 60/800,512, filed May 15, 2006, titled “Systems and Methods for Calibrating Minimally Invasive and Non-Invasive Physiological Sensor Devices,” the disclosure of which is hereby incorporated by reference in its entirety.
BACKGROUND
• Diabetes is a common cause of kidney disease, blindness among adults under the age of 65, and limb amputation. The effects of diabetes can be greatly reduced, if not eliminated all together, with proper monitoring of blood glucose. Many glucose monitors in use today require that a person be pricked with a sharp object in order to draw a small amount of blood to test for glucose levels. This process of measuring blood is often painful and uncomfortable. Although minimally and non-invasive blood glucose systems are being developed, they generally suffer from signal processing challenges affecting accuracy. One common challenge of minimally invasive glucose monitoring systems is referred to as drift. Drift generally occurs during the first few hours or days that a minimally invasive monitor's probe is inserted in the body and may cause inaccuracies.
SUMMARY
• Aspects of the present disclosure include systems and methods for calibrating minimally invasive and non-invasive physiological sensor devices. The calibration is used to improve accuracy. In some embodiments, when the system begins taking measurements, the system may experience drift.FIG. 1 illustrates agraph100 ofglucose levels101 in a patient vs. measuredglucose103 measured by a minimally invasive glucose monitor affected by drift. As illustrated, for a period of time, referred to herein as the calibration period, the measured glucose is less accurate due to, for example, drift. In minimally invasive systems, drift may be caused by protein buildup on the implanted device. In other systems, drift or other inaccuracies may be caused by any number of other issues known to an artisan from the disclosure herein. As with all patient monitors, more accurate and more reliable systems are preferred.
• In an embodiment, a minimally invasive glucose monitor is described. The minimally invasive glucose monitor includes a probe which is inserted into a patient. The probe nearly continuously measures the patient's glucose levels and reports glucose information to the minimally invasive glucose monitor. The minimally invasive glucose monitor also includes a calibration input for receiving glucose information about the patient derived from a reliable glucose monitor. The glucose information received from the reliable glucose monitor is used to calibrate the minimally invasive glucose monitor. The minimally invasive glucose monitor may also include one or more outputs for outputting glucose and calibration related information. The inputs and outputs can be wired or wireless.
• Although described with respect to glucose monitoring, a person of skill in the art will recognize that the present calibration system can be used to monitor and calibrate other physiological parameters, such as, for example, blood oxygen levels, blood carbon monoxide levels, blood pH levels, methemoglobin levels, pulse rates, trend or physiological traces, or any other physiological parameter. In addition, although described with respect to a minimally invasive patient monitor, the present disclosure is also applicable to the calibration of both invasive and non-invasive patient monitors.
• In an embodiment, a method of calibrating a glucose measurement device is disclosed. The method includes acquiring a first indication of a glucose measurement from a first device, acquiring a second indication of a glucose measurement from a second device, and calibrating the second device using the first indication from the first device and the second indication from the second device. In an embodiment, the first and second devices comprise patient monitors. In an embodiment, the first and second devices are operably connected to the same patient. In an embodiment, the first and second indications are obtained at substantially the same time. In an embodiment, calibration comprises one or more of modeling, scaling, transforming, finding a best fit, finding a linear fit, filtering, adaptive correlation, and cross correlation. In an embodiment, the first device comprises an invasive physiological measurement device. In an embodiment, the second device comprises a minimally invasive physiological measurement device. In an embodiment, the second device comprises a non invasive physiological measurement device.
• In an embodiment, a method of calibrating a physiological measurement device is disclosed. The method includes acquiring a first indication of one or more physiological measurements from a first device, acquiring a second indication of the one or more physiological measurements from a second device, and calibrating the second device using the first indication from the first device and the second indication from the second device. In an embodiment, the first and second devices comprise patient monitors. In an embodiment, the first and second devices are operably connected to the same patient. In an embodiment, the first and second indications are obtained at substantially the same time. In an embodiment, calibration comprises one or more of modeling, scaling, transforming, finding a best fit, finding a linear fit, filtering, adaptive correlation, and cross correlation. In an embodiment, the one or more physiological parameters comprise one or more of glucose, blood oxygen, pH, blood carbon monoxide levels, and methemoglobin. In an embodiment, the first device comprises an invasive physiological measurement device. In an embodiment, the second device comprises a minimally invasive physiological measurement device. In an embodiment, the second device comprises a non invasive physiological measurement device.
• In an embodiment, a calibration system for calibrating a physiological measurement monitor is disclosed. The calibration system includes a first physiological monitor, a calibration module including a first input for inputting measured physiological data and a second input for inputting reliable data indicative of one or more physiological parameters. The calibration module is configured to calibrate the first physiological monitor using the information inputted over the first and second inputs. In an embodiment, the calibration system also includes a second physiological monitor for measuring the reliable data indicative of one or more physiological parameters. In an embodiment, the second physiological monitor comprises an invasive physiological measurement device. In an embodiment, the first physiological monitor comprises a minimally invasive physiological measurement device. In an embodiment, the first physiological monitor comprises a non invasive physiological measurement device. In an embodiment, the calibration system also includes one or more signal outputs. In an embodiment, the one or more signal outputs comprise a display output. In an embodiment, the one or more signal outputs comprise a trend output. In an embodiment, the one or more signal outputs comprise a waveform output. In an embodiment, the waveform output comprises a synthesized waveform. In an embodiment, the waveform output comprises a scaled waveform. In an embodiment, the one or more signal outputs comprise an error output.
• In an embodiment, a method of calibrating a physiological measurement device is disclosed. The method of calibrating a physiological measurement includes acquiring a first indication of a glucose measurement from a first device, acquiring a second indication of a glucose measurement from a second device, and comparing the first indication and the second indication. Based on the comparison of the first indication and the second indication, if the first and second indications are not the same or close, the method also includes calibrating the second device using the first indication from the first device and the second indication from the second device, waiting an amount of time and requiring the first and second indications, comparing the reacquired first and second indications, and based on the comparison of the reacquired first and second indications, recalibrating the second device using the reacquired first and second indications.
• In an embodiment, the amount of time comprises a predetermined amount of time. In an embodiment, the amount of time comprises about 5 minutes or less to about 12 hours or more. In an embodiment, the predetermined amount of time comprises about 5 minutes to about 10 minutes. In an embodiment, the predetermined amount of time comprises about 1 hour to about 2 hours. In an embodiment, the method also includes dynamically determining the amount of time. In an embodiment, dynamically determining comprises determining an amount of time based on the comparison of the first and second indications. In an embodiment, dynamically determining comprises determining an amount of time based on the comparison of the reacquired first and second indications.
BRIEF DESCRIPTION OF THE DRAWINGS
• The drawings and the associated descriptions are provided to illustrate embodiments of the disclosure and not to limit the scope of the claims.
• FIG. 1 illustrates a graph of actual glucose v. measured glucose for a glucose monitor experiencing drift.
• FIG. 2 illustrates a calibration system.
• FIG. 3 illustrates a minimally invasive glucose monitor.
• FIG. 4 illustrates a glucose calibration system.
• FIG. 4A illustrates another embodiment of a glucose calibration system.
• FIG. 4B illustrates yet another embodiment of a glucose calibration system.
• FIG. 5 illustrates a flow chart of an embodiment of a calibration system.
• FIG. 6 illustrates a flow chart of another embodiment of a calibration system.
• FIG. 7 illustrates another embodiment of a calibration system.
• FIG. 8 illustrates a flow chart of an embodiment of a calibration process.
• FIGS. 9 through 11 illustrate embodiments of physiological monitor displays.
DETAILED DESCRIPTION
• Embodiments of the present disclosure include systems and methods for calibrating a physiological monitoring device. A reliable, often invasive, method of measuring a physiological parameter is used to calibrate measurements of a minimally invasive or non-invasive physiological measurement device. In an embodiment, the reliable monitor and the minimally invasive or non-invasive monitor measure the same physiological parameter from the same patient within a time period deemed appropriate. In an embodiment, a patient can be set up with a long term, minimally invasive physiological measurement device with minimized discomfort during the initialization period. In an embodiment, a patient can use a minimally invasive physiological measurement device to continuously measure a physiological parameter, using an invasive measurement device periodically to calibrate the minimally invasive physiological measurement device. In an embodiment, the physiological parameter is one or more of glucose, blood oxygen, pH, blood carbon monoxide levels, and methemoglobin.
• FIG. 2 illustrates acalibration system200. The calibration system includes aparameter calculator201. The parameter calculator includes one ormore inputs203 for reliable data indicative of one or more parameters and one ormore inputs205 for measurement data. The reliable data indicative of one or more parameters is communicated from a reliable, often invasive, patient monitor. The measurement data is communicated from a physiological sensor.
• Theparameter calculator201 uses the reliable data indicative of one or more parameters to calibrate, if necessary, the measurement data or information derived from the measurement data. Calibration may include modeling, scaling, transforming, finding a best fit, finding a linear fit, filtering, adaptive correlation, cross correlation, or any other calibration steps known to a skilled artisan from the disclosure herein.
• Theparameter calculator201 can calculate one or more physiological parameters and output information indicative of that parameter. Theparameter calculator201 may also advantageously calculate trend data and synthesize or scale waveform data. Theparameter calculator201 includes one or more outputs, such as, for example,parameter data output207,trend data output209, synthesized, scaled, oractual waveform output211, orcalibration data output213. Theparameter data output207 communicates data indicative of one or more physiological measurements. Thetrend data output209 communicates data indicative of trend information for the one or more physiological measurements. The synthesized, scaled, or actualwaveform data output211 communications waveform data which has been synthesized, scaled, or unaltered. Thecalibration data output213 communicates information related to calibrations performed by theparameter calculator201. Theoutputs207,209,211,213 can communicate withdisplay215, a separate patient monitoring device, or other device configured to receiving physiological parameter information.
• In an embodiment, theparameter calculator201 is included within a single device. In an embodiment, theparameter calculator201 is included within several separate devices. In an embodiment, theparameter calculator201 comprises a processor, processor board, or OEM board. In an embodiment, theparameter calculator201 is portable. In an embodiment, theparameter calculator201 comprises a desktop parameter calculator. Data communicated between the various components of the calibration system can be communicated through cables or wirelessly. A skilled artisan will also understand from the disclosure herein, that other inputs and/or outputs can be included with the system of the present disclosure. For example, an error data output can be used to communicate the error calculated between the measured data and the reliable data.
• FIG. 3 illustrates an embodiment of a minimally invasive glucose monitor. As illustrated, a minimally invasive glucose monitor301 is attached to apatient300. The minimally invasive glucose monitor301 includes aprobe303 which is inserted into the body, often just beneath the skin. Theprobe303 measures glucose levels in thepatient300. Theprobe303 communicates the measurements to the minimallyinvasive glucose monitor301. In an embodiment, theprobe303 is attached to themonitor301. In an embodiment, the probe is separate from themonitor301. In an embodiment, theprobe303 communicates through a cable connection with themonitor301. In an embodiment, theprobe303 communicates wirelessly withmonitor301. In an embodiment, themonitor301 is attached to thepatient300 byattachment piece309. In an embodiment, themonitor301 includes adisplay305. In an embodiment, the monitor includes one ormore buttons307.
• In operation, the minimally invasive glucose monitor301 continuously, nearly continuously, or intermittently (periodically or otherwise) measures bloodglucose using probe303. The probe detects glucose levels present in the body and communicates the glucose levels to the minimallyinvasive glucose monitor301. The minimally invasive glucose monitor301 calculates the patient's glucose level based upon information acquired from probe105. Examples of a minimally invasive glucose monitor and probe are described in U.S. Pat. No. 6,613,379, entitled “Implantable Analyte Sensor,” issued to Ward et al., and U.S. Pat. No. 6,695,860, entitled “Transcutaneous Sensor Insertion Device,” also issued to Ward et al, the entire contents of both of which are herein incorporated by reference.
• FIG. 4 illustrates an embodiment of a glucose calibration system. For example, the glucose level of apatient300 is measured by a minimallyinvasive glucose monitor301. As described above, the minimally invasive glucose monitor301 includes aprobe303 inserted into thepatient300 for measuring glucose levels. The glucose level ofpatient300 is also measured by areliable glucose monitor401. The reliable glucose monitor401 communicates data indicative of glucose levels inpatent300 to the minimallyinvasive glucose monitor201. The minimally invasive glucose monitor301 uses the communicated reliable data indicative of glucose levels inpatent300 to calibrate glucose information communicated byprobe303.
• In an embodiment, the reliable glucose monitor401 communicates with the minimally invasive glucose monitor301 through a cable or a wireless connection. In an embodiment, thereliable glucose monitor401 and the minimally invasive glucose monitor301 communicate with a separate calibration unit either through a cable or wirelessly. In an embodiment, the minimally invasive glucose monitor301 communicates with thereliable glucose monitor401. In an embodiment, the minimally invasive glucose monitor301 communicates a command to take a measurement to thereliable glucose monitor401.
• In an embodiment, the reliable glucose monitor401 is operably connected to anIV line409. TheIV line409 is operably connected to acatheter411 which is inserted into a vein of thepatient300. The reliable glucose monitor401 is also operably connected to anIV line405 which is operably connected to anfluid bag407. In operation, the reliable glucose monitor401 intermittently draws blood frompatient300 throughcatheter411 andIV line409 and tests the blood for glucose levels. When the reliable glucose monitor401 is not drawing blood from thepatient300, it supplies fluid to the patient300 fromfluid bag407 andIV line405 throughIV line409 andcatheter411. In an embodiment, the reliable glucose monitor401 uses glucose test strips to measure glucose levels in the blood. In an embodiment, the reliable glucose monitor401 uses chemicals analyses to test the glucose levels.
• In an embodiment, the reliable glucose monitor401 is programmed to take measurements at predetermined intervals. In an embodiment, the measurements are taken in intervals of about 5 minutes to about 12 hours. In an embodiment, the measurements are taken in intervals of about 5 minutes to about 10 minutes. In an embodiment, the measurements are taken in intervals of about 1 to about 2 hours. In an embodiment, the measurement intervals are dynamically determined based on calibration feedback as described below. In an embodiment, the minimally invasive glucose monitor301, or another intermediary device communicate a take measurement command to the reliable glucose monitor. In an embodiment, the minimally invasive or intermediary device communicate a take measurement command in predetermined or dynamically determined intervals as described above.
• FIG. 4A illustrates another embodiment of a glucose calibration system in which glucose test strips and a glucose test meter are used to measure glucose levels. A user uses the glucose test strips and glucose test meter to measure glucose levels. Once measured, the glucose test meter communicates the glucose levels to the minimally invasive glucose meter for calibration.
• FIG. 4B illustrates yet another embodiment of a glucose calibration system. In this embodiment, a glucose test meter is incorporated into the minimally invasive glucose monitor. A user uses the glucose test strips in conjunction with the minimally invasive glucose monitor to calibrate the minimally invasive glucose measurements. In an embodiment, the minimally invasive glucose monitor alerts a user that a reliable glucose measurement should be taken for calibration purposes.
• FIG. 5 illustrates a flow chart of an embodiment of a calibration system. The system begins by nearly continuously acquiring minimally invasive glucose measurements atblock501. The system then moves on to block503 where the system acquires reliable glucose data. The system then moves on to block505, where a calibration module compares the invasive blood glucose measurement to the acquired minimally invasive glucose measurement.
• Once the measurements are compared, the system moves on to decision block507, where the system looks to see if the measurements are the same or similar. Similar being defined herein as within a predetermined threshold. If the acquired minimally invasive measurement is the same or similar to the acquired reliable glucose data, then the system moves on to block511 where the glucose reading is outputted, either to a display, a patient monitor, or to another device. If the minimally invasive measurement is not similar, or within a predetermined threshold, then the system moves on to block509 where the minimally invasive measurements are calibrated. Once calibration is complete, the system moves on to block511 where the glucose reading is outputted. The system then moves to block513, where the system decides whether or not the calibration period is complete. If the calibration period is not complete, the system moves to block515 where it waits a predetermined period of time. After the period of time is complete, the system returns to block503 and repeats the calibration process. If atblock513, the calibration period is completed, then the system moves to block517 where the system communicates a calibration complete signal.
• In an embodiment, the determination of whether the calibration period is complete is based on an averaging of calibration periods required by other minimally invasive monitors. In an embodiment, the determination of whether the calibration period is compete is based on one or more comparisons of the reliable data and the minimally invasive measurement information. In one embodiment, the determination of whether the calibration period is complete is based on an averaging of calibration periods required by other minimally invasive monitors and one or more comparisons of the reliable data and the minimally invasive measurement information.
• FIG. 6 illustrates a flow chart of another embodiment of a calibration system. The system begins by nearly continuously acquiring minimally invasive glucose measurements atblock601. The system then moves on to block603 where the system acquires reliable glucose data. The system then moves on to block605, where a calibration module compares the invasive blood glucose measurement to the acquired minimally invasive glucose measurement.
• Once the measurements are compared, the system moves on to decision block607, where the system looks to see if the measurements are similar. If the acquired minimally invasive measurement is the same or similar to the acquired reliable glucose data, then the system moves on to block611 where the predetermined wait period ofblock617 is recalculated. The recalculation can be based on the number of accurate readings made by the minimally invasive device and/or the accuracy level of the readings made by the minimally invasive device and/or any other parameter which is useful for determining the duration between calibration cycles. The system then moves on to block613 where the glucose readings are outputted.
• If the minimally invasive measurement is not similar, or within a predetermined threshold, then the system moves on to block609 where the minimally invasive measurements are calibrated. The system then moves on to block613 where the glucose readings are outputted. Once calibration is complete, the system moves on to block615, where the system decides whether or not the calibration period is complete. If the calibration period is not complete, the system moves to block617 where it waits the predetermined period of time, either as initially set or as dynamically recalculated atblock611. After the period of time is complete, the system returns to block503 and repeats the calibration process. If atblock615, the calibration period is completed, then the system moves to block619 where the system communicates a calibration complete signal.
Another Example Calibration System
• FIG. 7 illustrates another embodiment of acalibration system700. Thecalibration system700 can implement any of the features described above with respect toFIGS. 1 through 6. In addition, thecalibration system700 can implement additional features that can advantageously enable a clinician to compare noninvasive physiological parameter measurements with alternative measurements. Thecalibration system700 can enable field calibrations of physiological parameters that can supplement any factory calibration provided during manufacture of thecalibration system700.
• Thecalibration system700 includes ameasurement module710 and acalibration module712. Each of thesemodules710,712 can be implemented in hardware and/or software. Themeasurement module710 can acquire, receive, or otherwise obtain signals reflecting physiological information from one ormore sensors720. The one ormore sensors720 can be any of the sensors described above or any other physiological sensor(s), including, for example, optical sensors, glucose sensors, pulse oximetry sensors, hemoglobin sensors, dishemoglobin sensors, acoustic sensors, ECG sensors, EEG sensors, and the like.
• Themeasurement module710 can analyze the physiological information to measure one or more physiological parameters, analytes, or concentrations thereof, including, but not limited to, oxygen saturation (SpO₂), total hemoglobin (SpHb), glucose, respiratory rate, and the like. Themeasurement module710 can output parameter data, trend data, and/or synthesized, scaled, or actual waveforms, to a display730 (seeFIGS. 9 and 10).
• Thecalibration module712 receives, acquires, or otherwise obtains analternative measurement722. In one embodiment, the alternative measurement is a calibration measurement that enables thecalibration module712 to calibrate one or more of the measurements made by themeasurement module710. Thealternative measurement722 can be an invasive measurement, such as a measurement made in a hospital lab, a minimally-invasive measurement, or the like. As used herein, the term “invasive,” in addition to having its ordinary meaning, can also mean minimally-invasive. Thealternative measurement722 can be related to a parameter measured by themeasurement module710. For instance, if themeasurement module710 noninvasively measures hemoglobin of a patient, thealternative measurement722 can be an invasive measurement for the same patient. Thealternative measurement722 can also be a noninvasive measurement from another noninvasive sensor, or even a different type of noninvasive sensor. Multiplealternative measurements722 can be input into thecalibration module712.
• In one embodiment, the alternative measurement(s)722 is input into thecalibration module712 by a clinician. Thecalibration module712 can expose a user interface for presentation to the clinician (or other user), for example, on thedisplay730. The user interface can include one or more user interface controls, such as context menus, buttons, or the like that enable the clinician to input thealternative measurement722. Thealternative measurement722 can also be received from another device, for example, over a network (such as a hospital network, a LAN, a WAN, the Internet, or a combination of the same). Thealternative measurement722 can also be received from a second sensor coupled with a patient.
• Thecalibration module712 can output thealternative measurement722 in conjunction with or separate from the measurement(s) obtained by themeasurement module710. In one embodiment, thecalibration module712 outputs a value that reflects thealternative measurement722 next to, alongside, above, below, or in relation to the measurement obtained by themeasurement module710. Thecalibration module712 can output thealternative measurement722 instead of the noninvasive measurement obtained by themeasurement module710. Thecalibration module712 can also average or otherwise combine the noninvasive measurement and thealternative measurement722. Thecalibration module712 can also use thealternative measurement722 or measurements to adjust a calibration curve corresponding to the noninvasive measurement.
• In another embodiment, thecalibration module722 outputs the difference between thealternative measurement722 and the measurements obtained by themeasurement module710. Further, thealternative measurement722 can be a value that represents a difference between a noninvasive measurement and a second (e.g., invasive) measurement. Thus, this difference can be input (e.g., by a clinician) into theparameter calculator701 instead of the actualalternative measurement722 itself.
• Thecalibration module722 can output a trend graph, line, or trend data points that reflect differences between thealternative measurement722 and the noninvasive measurements over time. This trend graph can be output or overlaid on the same trend graph display output by themeasurement module710. Thus, in certain embodiments, the trend graph or graphs shown on thedisplay730 can include a trend line (or set of data points) reflecting the noninvasive measurement values together with a trend line (or set of data points) reflecting an offset. The offset can be the difference between the noninvasive measurement values and thealternative measurement value722. Examples of such offsets are shown inFIGS. 9 and 10 (described below).
• FIG. 8 illustrates a flow chart of an embodiment of acalibration process800. Thecalibration process800 can be implemented by any of the systems or parameter calculators described herein, including theparameter calculator700. Thecalibration process800 enables a physiological monitor to be calibrated, in certain embodiments, by receiving an alternative measurement and displaying the alternative measurement (or an offset derived from that measurement) together with one or more noninvasive measurements.
• Atblock802, noninvasive physiological parameter measurements are acquired. These measurements can be acquired by themeasurement module710 from a sensor coupled with a patient. Atblock804, an alternative physiological parameter measurement is received. This measurement can be received with thecalibration module720, as described above.
• Atblock806, a trend graph of the noninvasive physiological parameter measurements is output. A second trend graph is output atblock808. This second trend graph reflects a difference between the noninvasive physiological parameter measurements and the alternative physiological parameter measurement. If desired (e.g., by a clinician), theprocess800 can be repeated to acquire multiple alternative measurements and to display these alternative measurements as trends together with a trend of the noninvasive measurements.
• FIGS. 9 and 10 illustrate embodiments ofphysiological monitors900,1000 havingparameter displays910,1010. Thedisplays910,1010 include several features in the depicted embodiment, includingparameter values920,trend graphs930,1030, and ameasurement input button940. Themeasurement input940 is an example of a user interface control that provides functionality for a clinician or other user to input one or more alternative measurements.Additional buttons950 located on thephysiological monitor900 can control a variety of other tasks. The features shown inFIGS. 9 and 10 can be implemented by thecalibration module712 described above.
• Referring specifically toFIG. 9, thetrend graph930 includes ameasurement waveform932 and an offsetwaveform934. Themeasurement waveform932 is an example trend graph for a noninvasive physiological parameter, representing values of that parameter for a given patient over time. The offsetwaveform934 is an example trend graph that is offset or biased from thetrend graph932. The offsetwaveform934 can represent the difference between noninvasive physiological measurements and an alternative physiological measurement. In one embodiment, the offsetwaveform934 is displayed on thetrend graph930 in response to an alternative measurement being entered using thebutton940. In the depicted embodiment, themeasurement waveform932 represents SpHb, or hemoglobin, values, and the offsetwaveform934 represents values derived from a invasive or minimally invasive hemoglobin. The offsetwaveform934 is termed CHb, or calibrated hemoglobin, in thedisplay910.
• In one embodiment, the calibration provided by the offsetwaveform934 is terminated when a probe or sensor is taken off of the patient. The calibration can therefore be reset in certain embodiments. However, the offsetwaveform934 instead may not be terminated when the probe is taken off.
• Referring toFIG. 10, thetrend graph1030 includes ameasurement waveform1032 as before and an offsetwaveform1034, also as before. However, a second offsetwaveform1036 is also shown, which represents an offset or bias obtained from a second alternative measurement. Thus, multiple alternative measurements can be taken and displayed as offsets or biases from the noninvasively-measured parameter values. In one embodiment, an initial alternative measurement is taken at an initial time, such as shortly before, shortly after, or at about the time that the noninvasive measurements commence. Thereafter, a second alternative measurement is taken partway through a monitoring session (such as a hospital stay).
• Instead of displaying both offsets from the first and second alternative measurements, the offset from the second alternative measurement can be displayed in place of the first offset once the second alternative measurement is received by thephysiological monitor1000. In another implementation, the offsets from the first and second alternative measurements can be combined, for example, by averaging. In still other embodiments, the first and second alternative measurements can be used to adjust a calibration curve specific to the individual being measured.
• Further, the alternative measurement data from many patients can be used to improve factory calibration settings of the physiological monitor. The alternative measurements and/or their offsets can be averaged, for instance, to determine an average offset to be applied to the factory calibration setting. The measurements can be averaged based on type of patient, type of patient condition, age, gender, and so forth.
• InFIG. 11, another embodiment of apatient monitor1100 is shown that includes auser interface1100. Theuser interface1100 can be generated at least in part by thecalibration module712. Theexample user interface1100 shown outputs parameter values instead of waveforms, including an SpO₂value1112, aheart rate value1114, arespiratory rate value1116, and a noninvasivetotal hemoglobin value1118. The parameter values shown in this example are merely examples, and fewer or more parameters can be shown in other implementations.
• An offsetvalue1120 is also shown next to thehemoglobin value1118. The offsetvalue1120 can represent a difference between the noninvasivetotal hemoglobin measurement1118 and an alternative measurement, such as an invasive or minimally-invasive measurement (or optionally another noninvasive sensor). This offsetvalue1120 can be used in place of the offset waveforms described above. Of course, in some embodiments, the offsetvalue1120 can be depicted on a user interface together with an offset waveform. The value of the offset1120 is “+1.0” in the depicted embodiment. In some embodiments, the offsetvalue1120 is represented as a positive or negative deviation from thehemoglobin value1118.
• In some embodiments, a clinician or user directly enters the offsetvalue1120 into thepatient monitor1100. Various types of user interface controls can be used by the clinician or user to input the offsetvalue1120. As an example,buttons1130 are shown on thepatient monitor1100 belowmenu options1142,1144 on theuser interface1100. Selection of theappropriate buttons1130 can cause the offsetvalue1120 to increase or decrease in value. For purposes of illustration, step values of +0.1 and −0.1 are shown asmenu options1142,1144. Thus, for example, selection of the +0.1 value via acorresponding button1130 can cause the offsetvalue1120 shown to increase by 0.1. The step values shown are merely examples and can vary in different implementations. Further, the step values can be represented as percentages, such as percentage differences from the alternative measurement, in some embodiments.
• In other embodiments, the offsetvalue1120 is communicated to thepatient monitor1100 over a network, for example, from a lab that generates an invasive value or from another computing device. A lab technician or other individual can input the invasive value into a computing system, which then transmits the invasive value to thepatient monitor1100. The patient monitor1100 can then calculate the difference between a current noninvasive measurement and the invasive value and output this difference as the offsetvalue1120. In another embodiment, the invasive value received from the lab (or other computing device) has a time stamp associated with it. The patient monitor1100 may then calculate the offsetvalue1120 by comparing the invasive value with the noninvasive value that occurred at the same time or a close time to the timestamp of the invasive value.
• In other embodiments, the actual alternative measurement is shown in place of or in addition to an offsetvalue1120. Further, the clinician or user can enter the actual invasive measurement instead of an offsetvalue1120 in some embodiments. In addition, user interface controls other than buttons, such as touch screen inputs, can be employed to add offset values or alternative measurements.
• Other features that may be employed by thepatient monitor1100 can include a feature that displays an indication of the age of the offsetvalue1120. This feature can include a timestamp of when the value was either obtained (e.g., at the lab) or when the value was input into thepatient monitor1100. The patient monitor1100 can include further user interface controls that enable a clinician or other user to input the timestamp, or the timestamp can be obtained directly from the lab or other computing device over a network. In another embodiment, the appearance of the offsetvalue1120 can change to reflect the aging of the offsetvalue1120. Any of the following display features can equally apply to the parameter value itself (e.g., the hemoglobin value1118). For instance, the offset value1120 (or parameter value1118) can be one color when first entered (such as green) but change to another color (such as red) as the offsetvalue1120 ages. In another embodiment, the offset value1120 (or parameter value1118) blinks with a frequency that depends on the age of the offsetvalue1120. In another embodiment, the offsetvalue1120 begins blinking when the age of the offsetvalue1120 reaches a certain threshold. In yet another embodiment, the offsetvalue1120 can be reset to a value 0 when a threshold time has passed. Showing the age of the offsetvalue1120 in any of these ways or using other techniques can assist a clinician in determining the relevancy of the offsetvalue1120. Age-related techniques may also be implemented using the trend graph user interfaces described above with respect toFIGS. 9 and 10, including blinking, changing color, showing timestamps, and the like.
CONCLUSION
• Although the foregoing inventions have been described in terms of certain preferred embodiments, other configurations are possible. For example, an invasive blood pressure monitor can be used to calibrate a non-invasive blood pressure monitor. In addition, various types of physiological monitors can be used to calibrate various other types of physiological monitors. For example, a minimally invasive physiological monitor can be used to calibrate a non-invasive physiological monitor.
• The modules described herein of certain embodiments may be implemented as software modules, hardware modules, or a combination thereof. In general, the word “module,” as used herein, can refer to logic embodied in hardware or firmware or to a collection of software instructions executable on a processor. Additionally, the modules or components thereof may be implemented in analog circuitry in some embodiments.
• Conditional language used herein, such as, among others, “can,” “could,” “might,” “may,” “e.g.,” and the like, unless specifically stated otherwise, or otherwise understood within the context as used, is generally intended to convey that certain embodiments include, while other embodiments do not include, certain features, elements and/or states. Thus, such conditional language is not generally intended to imply that features, elements and/or states are in any way required for one or more embodiments or that one or more embodiments necessarily include logic for deciding, with or without author input or prompting, whether these features, elements and/or states are included or are to be performed in any particular embodiment.
• Depending on the embodiment, certain acts, events, or functions of any of the methods described herein can be performed in a different sequence, can be added, merged, or left out all together (e.g., not all described acts or events are necessary for the practice of the method). Moreover, in certain embodiments, acts or events can be performed concurrently, e.g., through multi-threaded processing, interrupt processing, or multiple processors or processor cores, rather than sequentially.
• The various illustrative logical blocks, modules, circuits, and algorithm steps described in connection with the embodiments disclosed herein can be implemented as electronic hardware, computer software, or combinations of both. To clearly illustrate this interchangeability of hardware and software, various illustrative components, blocks, modules, circuits, and steps have been described above generally in terms of their functionality. Whether such functionality is implemented as hardware or software depends upon the particular application and design constraints imposed on the overall system. The described functionality can be implemented in varying ways for each particular application, but such implementation decisions should not be interpreted as causing a departure from the scope of the disclosure.
• The various illustrative logical blocks, modules, and circuits described in connection with the embodiments disclosed herein can be implemented or performed with a general purpose processor, a digital signal processor (DSP), an application specific integrated circuit (ASIC), a field programmable gate array (FPGA) or other programmable logic device, discrete gate or transistor logic, discrete hardware components, or any combination thereof designed to perform the functions described herein. A general purpose processor can be a microprocessor, but in the alternative, the processor can be any conventional processor, controller, microcontroller, or state machine. A processor can also be implemented as a combination of computing devices, e.g., a combination of a DSP and a microprocessor, a plurality of microprocessors, one or more microprocessors in conjunction with a DSP core, or any other such configuration.
• The blocks of the methods and algorithms described in connection with the embodiments disclosed herein can be embodied directly in hardware, in a software module executed by a processor, or in a combination of the two. A software module can reside in RAM memory, flash memory, ROM memory, EPROM memory, EEPROM memory, registers, a hard disk, a removable disk, a CD-ROM, or any other form of computer-readable storage medium known in the art. An exemplary storage medium is coupled to a processor such that the processor can read information from, and write information to, the storage medium. In the alternative, the storage medium can be integral to the processor. The processor and the storage medium can reside in an ASIC. The ASIC can reside in a user terminal. In the alternative, the processor and the storage medium can reside as discrete components in a user terminal.
• While the above detailed description has shown, described, and pointed out novel features as applied to various embodiments, it will be understood that various omissions, substitutions, and changes in the form and details of the devices or algorithms illustrated can be made without departing from the spirit of the disclosure. As will be recognized, certain embodiments of the inventions described herein can be embodied within a form that does not provide all of the features and benefits set forth herein, as some features can be used or practiced separately from others. The scope of certain inventions disclosed herein is indicated by the appended claims rather than by the foregoing description. All changes which come within the meaning and range of equivalency of the claims are to be embraced within their scope.

Claims (20)

1. (canceled)

2. A measurement device comprising:

a measurement module that obtains a noninvasive physiological parameter measurement from a sensor coupled to a patient; and

a calibration module, implemented in a hardware processor, that:

receives an alternative physiological parameter measurement;

determines an offset value based at least in part on a difference between the noninvasive physiological parameter measurement and the alternative physiological parameter measurement;

calibrates the measurement module based at least in part on the offset value;

tracks an age of the offset value over time;

outputs the offset value for presentation on a display; and

provides an indication to a user of the age of the offset value.

3. The measurement device ofclaim 2, wherein the noninvasive physiological parameter measurement comprises a set of measurements.

4. The measurement device ofclaim 2, wherein the alternative physiological parameter measurement comprises a set of measurements.

5. The measurement device ofclaim 2, wherein the calibration module further provides a user interface control enabling a user to provide an additional offset value.

6. The measurement device ofclaim 2, wherein the presentation of the offset value on the display is modified over time to reflect the age of the offset value over time.

7. The measurement device ofclaim 2, wherein the calibration module further provides a user interface control enabling a user to input the alternative physiological parameter measurement into the measurement device.

8. The measurement device ofclaim 2, wherein the sensor measures a hemoglobin parameter.

9. A system for calibrating a measurement device, the system comprising:

a measurement module configured to:

receive a signal from a physiological sensor;

obtain a noninvasive measurement value of a physiological parameter responsive to the signal; and

a calibration module comprising a hardware processor, the calibration module configured to:

receive an input reflecting an invasive measurement value for the physiological parameter;

calculate a calibration value based at least in part on a difference between the noninvasive measurement value and the invasive measurement value;

calibrate the measurement device using the calibration value; and

output an age of the calibration value for display to a user.

10. The system ofclaim 9, wherein the calibration module is further configured to receive the input reflecting the invasive measurement value at the user interface from the user.

11. The system ofclaim 9, wherein the calibration module is further configured to receive input reflecting the invasive measurement value over a network.

12. The system ofclaim 9, wherein the calibration module is further configured to receive a modification value to the calibration value via the user interface.

13. The system ofclaim 12, wherein the modification value comprises an incremental adjustment.

14. The measurement device ofclaim 9, wherein the user interface modifies a depiction of the calibration value output for display based on the age of the offset value.

15. A method of calibrating a measurement device, the method comprising:

by a noninvasive measurement device,

acquiring, from a sensor coupled to a patient, noninvasive physiological parameter measurements;

receiving an alternative physiological parameter measurement at the noninvasive measurement device;

determining an offset value based at least in part on a difference between the noninvasive physiological parameter measurements and the alternative physiological parameter measurement;

calibrating the noninvasive measurement device based at least in part on the offset value;

tracking an age of the offset value over time; and

displaying a representation of the offset value on a user interface of the noninvasive measurement device, wherein the representation of the offset value is based at least in part on the age of the offset value.

16. The method ofclaim 15, further comprising providing a user interface on the noninvasive measurement device, the user interface configured to provide functionality for a user to input the alternative physiological parameter measurement.

17. The method ofclaim 15, further comprising providing a user interface on the noninvasive measurement device, the user interface configured to provide functionality for a user to modify the offset value.

18. The method ofclaim 15, further comprising providing a user interface on the noninvasive measurement device, the user interface configured to provide functionality for a user to provide an additional offset value

19. The method ofclaim 15, wherein the noninvasive physiological parameter is hemoglobin.

20. The method ofclaim 15, wherein the noninvasive physiological parameter is glucose.

Images