This application claims priority under 35 U.S.C. § 119 to Japanese Patent Application No. JP2005-336379 filed Nov. 21, 2005, the entire content of which is hereby incorporated by reference.
1. Field of the Invention
The present invention relates to a medical simulation system used for supporting examination of diabetes or the like, and to a computer program product thereof.
2. Description of the Related Arts
For treatment of disease, generally, a variety of tests are carried out on a patient in addition to interview made by a physician. Under existing circumstances, a physician selects therapeutic strategy based on test results and clinical presentation by the seat-of-the-pants approach.
Therefore, if information which is useful for examination is provided by a computer, examination by a physician would be effected more appropriately. As a system that supports examination, there are known systems that predict blood glucose level as described in U.S. Pat. Nos. 6,421,633 and 5,971,922. These systems support examination by predicting change in blood glucose level of a patient and providing a physician with a predicted blood glucose level.
For selecting an appropriate therapeutic method, it is desired for a physician to properly grasp the factors constituting causes of various conditions of disease. Properly grasping factors and conducting therapy for improving the factors would realize more appropriate therapy. However, the data that is available to a physician for grasping factors is no more than test values obtainable by testing of the patient. Although a physician can grasp factors only from test results for some diseases, it may significantly difficult to properly grasp factors from test values for some diseases.
For example, in the case of diabetes, “blood glucose level” is used as an index representing the degree of the disease. However, the “blood glucose level” is merely a result, and it is difficult to accurately grasp the causative pathogenic conditions such as insufficient insulin secretion, peripheral insulin resistance, hepatic glucose incorporation deterioration, and increase in hepatic glucose release resulting therefrom based on the clinical representation as described above.
Therefore, it is still difficult to accurately determine a pathologic condition of a patient only by provision of predicted value of blood glucose level as described in U.S. Pat. Nos. 6,421,633 and 5,971,922. In diabetes, cardiac diseases and the like, a specialty physician usually determines a pathologic condition of a patient with the use of test results of, e.g., oral glucose tolerance test, electrocardiogram, measurements of blood pressure and pulse rate, and blood test. However, it is difficult for a physician of other specialty to accurately determine the pathogenic condition from such test results because abundant experience is required for such determination. In view of this, there is a need for a system useful for training inexperienced physicians and physicians of other specialty so that they can accurately determine a pathologic condition from test results.
The scope of the present invention is defined solely by the appended claims, and is not affected to any degree by the statements within this summary.
The first aspect of the present invention relates to a medical simulation system comprising: biological response inputting means for receiving input of biological response information indicating biological response of a biological body; biological model generating means for generating a biological model which generates a simulated response simulating the biological response; pathologic condition characteristics acquiring means for acquiring pathologic condition characteristics information indicating pathologic condition characteristics of the biological body based on the generated biological model; and outputting means for outputting the biological response information and the pathologic condition characteristics information.
The second aspect of the present invention relates to a medical simulation system comprising: pathologic condition characteristics inputting means for receiving input of pathologic condition characteristics information indicating characteristics of pathologic condition of a biological body; simulated response acquiring means for generating a biological model reflecting the inputted characteristics of pathologic condition and acquiring simulated response information based on the biological model; and outputting means for outputting the pathologic condition characteristics information and the simulated response information.
The third aspect of the present invention relates to a computer program product comprising: a computer readable medium, and software instructions, on the computer readable medium, for enabling a computer to perform predetermined operations comprising: receiving input of biological response information indicating biological response of a biological body by an input device; generating a biological model for reproduction of a simulated response simulating the biological response; acquiring pathologic condition characteristics information indicating characteristics of pathological condition of the biological body based on the biological model; and displaying the biological response information and the pathologic condition characteristics information in a display.
The fourth aspect of the present invention relates to a computer program product comprising: a computer readable medium, and software instructions, on the computer readable medium, for enabling a computer to perform predetermined operations comprising: receiving input of pathologic condition characteristics information indicating characteristics of pathological condition of a biological body by an input device; generating a biological model reflecting the inputted characteristics of pathologic condition; acquiring simulated response information based on the biological model; and displaying the pathologic condition characteristics information and the simulated response information in the display.
Embodiments of a medical simulation system is described hereinafter with reference to drawings.
[System Overall Construction]
The system SS includes a server S having a function of a Web server S1, and a client terminal C connected to the server S via network. The client terminal C is used by a user such as physician. The client terminal C has a Web browser C1. The Web browser C1 functions as a user interface of the system SS, and a user is allowed to make input or required operation on the Web browser C1. Further, to the Web browser C1, a screen generated in the server S and transmitted is outputted.
The server S has a function of the Web server S1 that receives access from the Web browser C1 of the client terminal C. Further, in the server S, a user interface program S2 for generating a user interface screen displayed in the Web browser C1 is mounted in a computer-executable manner. The user interface program S2 has a function of generating a screen to be displayed in the Web browser C1 and transmitting it to the client terminal C, and receiving information inputted on the Web browser C1 from the client terminal C. In the client terminal C, Java (™) applet or the like program for realizing the function of generating a part or the whole of the screen to be displayed in the Web browser C1 may be downloaded from the server S, and a part or the whole of the screen is generated and displayed in the screen of the Web browser C1.
Further, in the server S, a pathogenic condition simulator program S3 is mounted in a computer-executable manner. The pathogenic condition simulator program S3 is provided for conducting simulation concerning disease based on the biological model as will be describe later. Further, the server S is provided with a database S4 having various data such as test results of a patient. Data inputted to the system SS, data generated in the system, and other data is stored in this database S4.
As described-above, the server S has a function of Web server, an interface (screen) generating function, and a function of pathologic condition simulator. In
The CPU S110a is capable of executing a computer program recorded in the ROM S110b and a computer program loaded in the RAM S110c. And the CPU S110a executes an application program 140a such as the above programs S2, S3 to realize each function block as described later, thereby the computer functions as the system SS.
The ROM S110b comprises mask ROM, PROM, EPROM, EEPROM, etc., and is recoded with computer programs executed by the CPU S110a and data used for the programs.
The RAM S110c comprises SRAM, DRAM, etc. The RAM S110c is used to read out computer programs recorded in the ROM S110b and the hard disk S110d. And the RAM S110c is used as a work area of the CPU S110a when these computer programs are executed.
The hard disk S110d is installed with an operating system, an application program, etc., various computer programs to be executed by the CPU S110a, and data used for executing the computer programs. The programs S2, S3 are also installed in this hard disk S110d.
The readout device S110e which comprises a flexible disk drive, a CD-ROM drive or DVD-ROM drive is capable of reading out a computer program or data recorded in a portable recording media S140. And the portable recording media S140 stores the application program S140a (S2, S3) to function as a system of the present invention. The computer reads out the application program S140a related to the present invention from the portable recording media S140 and is capable of installing the application program S140a in the hard disk S110d.
In addition to that said application program S140a is provided by the portable recording media S140, said application program S140a may be provided through an electric communication line (wired or wireless) from outside devices which are communicably connected to the computer via said electric communication line. For example, said application program S140a is stored in a hard disk in an application program providing server computer on the Internet to which the computer accesses and said application program S140a may be downloaded and installed in the hard disk S110d.
The hard disk S110d is installed with an operating system which provides a graphical user interface environment, e.g. Windows® manufactured by US Microsoft Corp. In the explanation hereinafter, the application program S140a (S2, S3) related to this embodiment shall operate on said operating system.
The input/output interface S110f comprises a serial interface, e.g. USB, IEEE1394, RS-232C, etc.; a parallel interface, e.g. SCSI, IDE, IEEE1284, etc.; and an analog interface, e.g. D/A converter, A/D converter, etc. The input/output interface S110f is connected to the input device 130 comprising a keyboard and a mouse and users can input data into the computer using the input data device 130.
The image output interface S110h is connected to the display S120 comprising LCD, CRT or the like so that picture signals corresponding to image data provided from the CPU S110a are output to the display S120. The display S120 displays a picture (screen) based on input picture signals.
The hardware construction of the client terminal C is substantially equal to the hardware construction of the server S.
[Biological Model in Simulation System]
Each block 1, 2, 3, 4 has input and output. As to the pancreas block 1, a blood glucose level 6 is set as input and an insulin secretion rate 7 is set as output to other blocks. As to the hepatic block 2, a glucose absorption 5 from digestive tract, a blood glucose level 6 and an insulin secretion rate 7 are set as input and net glucose release 8 and post liver insulin 9 are set as output to other blocks. As to the insulin kinetics block 3, post liver insulin 9 is set as input and peripheral tissue insulin concentration 10 is set as output to other blocks. As to the peripheral tissue block 4, a net glucose release 8, and insulin concentration 10 in the peripheral tissue are set as input and a blood glucose level 6 is set as output to other blocks.
Glucose absorption 5 is data provided from outside of the biological model. In the present embodiment, as to data concerning glucose absorption, predetermined values are stored in advance depending on the kind of the inputted test data to be inputted (biological response). Further, the function blocks 1 to 4 are each realized by the CPU in the server 2 executing the simulator program.
Next, the above-mentioned blocks each are described in detail. FGB expresses a fasting blood glucose level (FGB=BG (0)), and Ws expresses an assumed weight. DVg and DVi respectively express a distribution capacity volume against glucose and a distribution capacity volume against insulin.
[Pancreas Block of Biological Model]
Relationship between input and output of the pancreas block 1 may be expressed using the following differential equation (1). A block diagram as in
Variables:
BG(t): blood glucose level
X(t): total amount of insulin capable of secretion from pancreas
Y(t): supply rate of insulin newly supplied for glucose stimulation
SR(t): pancreas insulin secretion rate
Parameters:
h: threshold of glucose concentration capable of stimulating insulin supply
α: following performance to glucose stimulation
β: sensitivity to glucose stimulation
M: secretion rate per unit concentration
where a blood glucose level 6 which is input to the pancreas block in
In a block diagram in
[Hepatic Block of Biological Model]
Relationship between input and output of the hepatic block 2 may be described using the following differential equation (2). A block diagram as in
Variables:
BG(t): blood glucose level
SR(t): pancreas insulin secretion rate
SRpost(t): post hepatic insulin
RG(t): glucose absorption from digestive tract
HGP(t): hapatic [sic] glucose release
HGU (t): hepatic glucose uptake
SGO (t): net glucose from liver
I4(t): hepatic insulin concentration
Parameter:
Kh: hepatic glucose uptake rate per unit insulin and unit glucose
A7: insulin uptake rate in liver
Goff: glucose release rate to basal metabolism
b2: adjustment term for hepatic glucose release suppression rate
r: insulin-dependent hepatic glucose uptake distribution rate
α2: transmission efficiency to insulin stimulation
I4off: insulin concentration threshold of hepatic glucose release suppression
Function:
Goff (FBG): glucose release rate to basal metabolism
Func1(FBG): hepatic glucose uptake rate to stimulation of glucose from digestive tract
Func2 (FBG): hepatic glucose release-suppression rate to insulin stimulation
f1 to f9: constants used to express the above-mentioned three elements
b1(I4(t)): adjustment item for hepatic glucose incorporation rate
where the glucose absorption 5 from digestive tract which is input to the hepatic block in
In a block diagram in
[Insulin Kinetics Block of Biological Model]
Relationship between input and output of the insulin kinetics secretion may be described using the following differential equation (3). A block diagram as in
Differential equation (3):
dI1(t)/dt=−A3I1(t)+A5I2(t)+A4I3(t)+SRpost(t)
dI2(t)/dt=A6I1(t)−A5I2(t)
dI3(t)/dt=A2I1(t)−A1I3(t)
Variables:
SRpost(t): post hepatic insulin
I1(t): blood insulin concentration
I2(t): insulin concentration in insulin-independent tissues
I3(t): insulin concentration in peripheral tissues
Parameters:
A1: insulin disappearance rate in peripheral tissues
A2: insulin distribution rate to peripheral tissues
A3: post hepatic insulin distribution rate
A4: post peripheral tissue insulin flow out rate
A5: insulin disappearance rate in insulin-independent tissues
A6: insulin distribution rate to insulin-independent tissues
where the post liver insulin 9 which is input to the insulin kinetics block in
In a block diagram in
[Peripheral Tissue Block of Biological Model]
Relationship between input and output of the peripheral tissue block 4 may be described using the following differential equation (4). A block diagram as in
Variables:
BG′(t): blood glucose level (BG[mg/dl], BG′[mg/kg])
SGO(t): net glucose from liver
I3(t): insulin concentration in peripheral tissues
FBG′: fasting blood glucose (provided that FBG′=BG(0))
Parameters:
Kb: insulin-independent glucose consumption rate in peripheral tissues
Kp: insulin-dependent glucose consumption rate in peripheral tissues per unit insulin and per unit glucose
u: ratio of insulin-independent glucose consumption to basal metabolism in glucose release rate to basal metabolism
Functions:
Goff(FGB): glucose release rate to basal metabolism
f1 to f3: constant used to express Goff
where the peripheral tissue insulin concentration 10 which is input to the peripheral tissue block in
In a block diagram in
As shown in
With regard to calculation of the differential equations of the present system, e.g. E-Cell (software disclosed by Keio University) and MatLab (manufactured by The MathWorks, Inc.) may be employed. Or other calculation system may be employed.
[Biological Model Generating Section]
To simulate individual patient biological organs using the above-mentioned biological models as shown in FIGS. 3 to 7, it is required to generate a biological model having characteristics suited for individual patients. To be more specific, it is required to determine parameters and initial values of variables of biological model according to the individual patient, and apply the determined parameters and initial values to the biological model, thereby generating a biological model suited for the individual patient. (Unless otherwise specified, an initial value of variable is also included in parameters to be generated.)
In order to realize the function of the biological model generating section, the server 2 of the system SS also has a function of determining an internal parameter set which is a set of internal parameters of biological model (hereinafter, also simply referred to as “parameter set”), and generating a biological model to which the determined parameter set is applied. This function is realized by the pathogenic condition simulator program S3.
By giving the parameter set generated by the biological model generating section to the biological model, the biological model calculating section is enabled to conduct simulation of a function of biological organ and output a simulated response simulating the actual biological response (test result).
[Parameter Set Generating Section]
In the following, description will be made for a parameter set generating section for forming a biological model that simulates a biological organ of a patient based on an actual test result (biological response) of the patient (biological body).
[OGTT Time-Series Data Input: Step S1-1]
OGTT time-series data are a result of OGTT (given amount of glucose solution is orally loaded to measure the time-series of blood glucose level and blood insulin concentration) from the actual examination of patients simulated by a biological model. The present system receives input as an actual biological response (actual examination values) from the client terminal 3. Here, two data of and OGTT glucose data (blood glucose change data) and OGTT insulin (blood insulin concentration change data) are input as OGTT time-series data.
In
In
[Template Matching: Step S1-2]
Next, the present system SS matches the input OGTT time-series data to the template of template database DB1. The template database DB1 is one of database included in the database 24 of the server S.
As shown in
The system SS computes similarity between each reference time-series datum of the above-mentioned template database DB1 and OGTT time-series data. The similarity is obtained by obtaining error summation. The error summation is obtained by the following formula.
where
BG: input data blood glucose level [mg/dl]
PI: input data blood insulin concentration [μU/ml]
BGt: template blood glucose level [mg/dl]
PIt: template blood insulin concentration [μU/ml]
t: time[minute]
Here, α and β are coefficient used for normalization
α=1/Average {ΣBG(t)}
β=1/Average {ΣPI(t)}
The average of the formula shows average level to all templates stored in the template database DB1.
Based on
Σ¦BG(t)−BGt(t)¦=29
Σ¦PI(t)−PIt(t)¦=20
where, provided α=0.00035, β=0.00105
Thus, CPU 100a obtains an error summation to each template in the template database DB1, and determines the template having the minimum error summation (similarity). Thus, CPU 100a determines the template which is the most approximate to OGTT time-series data (Step S1-2).
[Acquisition of Parameter Set: Step 1-3]
Further, in a step S1-3, the system SS obtains from template database DB1 a parameter set corresponding to the template which has been determined in the step S1-2 and has been judged to be similar in the step S1-3. That means, a parameter set PS#01 corresponding to the template T1 is obtained (Refer to
The table below exemplifies the specific numeral values of the parameter values included in the parameter set PS#01 obtained by the above-mentioned way.
[Simulated Response Acquiring Section (Biological Model Calculating Section)]
When the above-mentioned parameter set PS#01 is given to the biological model, the system SS makes calculation based on the biological model, and outputs simulated response information which simulates the input OGTT time-series data (time courses in blood glucose level and insulin concentration) (functions as a simulated response acquiring section of the system SS (biological model calculating section)).
That is, the system SS is capable of simulating a biological organ of a patient based on the generated biological model. This function is realized by a pathogenic condition simulator program S3.
The generated parameter set is also used for acquiring pathologic condition characteristics information, and this point will be described later. [User Interface (Input/Output Part)]
The screen in
The operating section 100 has a data input part 101 for input and registration of various data, a registered content revising part 102 for revise of registered data, an examination ending part 103 at which examination ending operation is made, and a logout part 104 at which logging out is made.
[Data Input Part 101]
The data input part 101 has a “Register test result” button 101a for registration of results of basic tests (test results of test items shown in the test data display part 120 in
[Basic Test Result Input 101a]
When the “Register test result” button 101a is clicked, an input screen of test result (not shown) is displayed, and a test result can be inputted for each basic test item displayed in the test data display part 120 of
When the “Register prescription” button 101b is clicked, an input screen for prescription for the patient is displayed in the input screen, and is ready for registration of input prescription in the database S4. Upon input and registration of prescription, the fact that prescription is registered is indicated by the mark “?” together with the registered date (examination date) in the test history display part 110.
The input screen for prescription will be described later.
[OGTT Input (Biological Response Input Part) 101c]
When the “Register OGTT data” button 101c is clicked, OGTT data input screen (window) W1 is open and displayed as shown in
The screen W1 includes an input box column W1a for test time, an input box column W1b for blood glucose level, and an input box column W1c for insulin concentration (IRI), and as OGTT data which is an actual test result, time courses of blood glucose level and insulin concentration may be inputted.
When the register button W1R on the screen W1 is clicked after inputting values of blood glucose level and insulin concentration, the contents thereof are registered in the database S4.
Upon registration of the OGTT data, the fact that OGTT data is registered is indicated by the mark “?” together with the registered date (examination date) in the test history display part 110.
Here, the data inputted in the screen W1 functions as original data in drawing the graph showing time courses in blood glucose level and insulin concentration shown in
When the “Register analysis of pathologic condition” button 101d is clicked, the pathogenic condition simulator program S3 makes simulation using OGTT data, executes analysis of pathologic condition, and acquires the pathologic condition characteristics information indicating characteristics of pathogenic condition. The acquired pathologic condition characteristics information is registered in the database S4 in relation with the OGTT data. The details of the analysis of pathologic condition will be described later.
[Test History Display Part 110]
The test history display part 110 displays presence/absence of registrations of (general) test, OGTT, prescription for each examination date. The absence of registration is indicated by the mark “x”.
The test history display part 110 also functions as a display changeover operation part for switching display in the test data display part 120 and the prescription data display part 140, and display contents in the screen of
[Test Data Display Part 120]
The test data display part 120 is provided for display of a basic test result or OGTT result of a patient.
When a basic test result is displayed in the test data display part 120, “Display OGTT result” button 121 is displayed (see
[Pathologic Condition Analysis Result Display Part (of Outputting Section of Biological Response Information and Pathologic Condition Characteristics Information) 130]
As shown in
In a graph 131, time course of blood glucose level 131a in the actual OGTT test result, as well as time course 131b of insulin concentration in the actual OGTT test result are displayed.
[Pathologic Condition Simulation Analysis (Acquiring of Pathologic Condition Characteristics and Acquiring of Simulated Response)]
As shown in
In simulation, a parameter set constituting a biological model capable of outputting a reproduced value (simulated response information) simulating an actual OGTT test result (biological response information) is determined by calculation. Then the system SS determines a reproduced value of OGTT test result (simulated response information) as an output value of biological model to which the parameter set is applied (simulated response acquiring function of system SS).
As shown in
A user such as a physician compares the actual test result (biological response information) and the reproduced value (simulated response information) produced by simulator in the graph display 131 to check whether the both values are close and the biological model by the simulator properly simulates an actual biological organ of a patient. According to the graph display 131 in
[Pathologic Condition Characteristics Acquiring Section]
The system SS determines pathologic condition characteristics information indicating characteristics of pathogenic condition of a patient based on (parameter set of) the generated biological model (pathologic condition characteristics information acquiring function of system SS).
As shown in
As such indexes those clearly indicating characteristics of pathologic condition are employed, and in particular, biological functions that can be improved by some therapy are employed.
Here, the fasting blood glucose 132a is calculated from blood glucose level BG (t=0) which is a variable of biological model. The basic secretion 132b is calculated from fasting insulin I1(t=0) which is a variable of biological model. The additional secretion is calculated from an integration value of I1(t=). The secretion sensitivity 132d is calculated from sensitivity β against glucose stimulation which is a parameter of biological model. The hepatic gluconeogenesis prevention 132e is calculated from hepatic glucose release HGTP (t) which is a variable of biological model. The glucose processing ability 132f is calculated from net glucose from liver SGO (t) and blood glucose level BG (t) which are variables of biological model. The processing sensitivity 132g is calculated from insulin-dependent glucose consumption rate Kp in peripheral tissues per unit insulin and unit glucose that are parameters of biological model.
As described above, since the biological model is made up of a mathematical model having parameters (including variables) indicating characteristics of biological organs, parameter values of the biological model show values related with pathologic condition. Therefore, pathologic condition characteristics information indicating characteristics of pathologic condition can be calculated based on these parameters can be compared.
Here, in the radar chart 132 of
In the radar chart 132 of
In addition, since the actual OGTT test result 131a, 131b and the pathologic condition characteristics information 132 are displayed in the same screen, the physician can compare these and study the relationship between the graph shape of the OGTT test result and the pathologic condition. Therefore, an effective study for grasping the pathogenic condition from the OGTT test result is expected by gaining practical experience using this system SS.
Further, any desired value rather than actual test result (biological response information) may be inputted to the input screen of OGTT test result (biological response). And outputs of test result reproduced value (simulated response information) and pathologic condition characteristics information can be obtained for the any desired value. Therefore, the physician inputs any desired test result value (biological response information) and know the pathologic condition that will be expected in that case. Therefore, even when there is no data of actual patient, one can use the present system for training purpose by inputting a certain appropriate test result.
In other words, the system SS may be used for training physicians of other specialty and inexperienced physicians.
Since there is provided a pathologic condition analysis result display part 130 in
Further, in the pathologic condition analysis result display part 130, after completion of the pathologic condition analyzing process, pathologic condition describing text is displayed in the pathologic condition description display part 133. The pathologic condition describing text is registered in advance in the database S4, and pathologic condition describing text corresponding to (parameter of) the generated biological model is selected by the system, and the selected text is displayed in the pathologic condition description display part 133. When the “Display details of pathologic condition” button 134 is clicked, more detailed describing text will be displayed in another window.
By displaying the pathologic condition describing text in the manner as described above, the pathologic condition characteristics information displayed in the radar chart 132 can be readily understood, and a physician can grasp the pathologic condition more properly.
When the physician grasps the pathologic condition in the manner as described above, and determines therapeutic strategy and prescription, the prescription may be registered in the system SS. To be more specific, when the “Register prescription” button 101b is clicked, the “prescription register screen” W2 shown in
[Pathologic Condition Characteristics Inputting Section and Simulated Response Acquiring Section]
When values of indexes in the radar chart are changed, the simulated response acquiring section (biological model calculating section) calculates reproduced values of blood glucose level and insulin concentration, and reproduced values 131e, 131f in the changed pathologic condition are displayed.
That is, when the pathologic condition characteristics information is inputted, the system SS changes parameters of the biological model in correspondence with the inputted pathologic condition characteristics information and generates a new biological model. Then based on the biological model in which the inputted pathologic condition characteristics is reflected to parameters of the biological model, the simulated response acquiring section (biological model calculating section) makes calculation to determine reproduced values 131e, 131f which are simulated response.
As described above, since the system SS has a pathologic condition characteristics information input function, and an OGTT reproduced value output function based on the inputted pathologic condition characteristics information, one can ascertain beforehand an OGTT test result which is expected when the current pathologic condition is improved by therapy. Therefore, the physician can readily predict the therapeutic effect. By variously changing the pathologic condition characteristics information, one can ascertain which pathologic condition index should be improved to realize effective therapy, which is advantageous for establishment of appropriate therapeutic strategy.
In the present embodiment, input of the pathologic condition characteristics information is made on the radar chart, however, the manner of input is not particularly limited, and input may be made by numerical input.
[Modified Example of Output of Pathologic Condition Characteristics Information]
The present invention is not limited to the above embodiment, and various modifications are available. For example, the biological response information and the pathologic condition characteristics information, and other information may be outputted to media such as paper as well as to the screen display. Regarding the biological response information and the pathologic condition characteristics information, and other information, the input format and the output format may not be necessarily the same. For example, input of the biological response information (OGTT test result) in the above embodiment is achieved in a numerical input format, and output thereof is achieved in a graph output format. In this manner, formats of input and output may differ in the same information.
The foregoing detailed description and accompanying drawings have been provided by way of explanation and illustration, and are not intended to limit the scope of the appended claims. Many variations in the presently preferred embodiments illustrated herein will be obvious to one of ordinary skill in the art, and remain within the scope of the appended claims and their equivalents.
Number | Date | Country | Kind |
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2005-336379 | Nov 2005 | JP | national |