TOTALLY NON-INVASIVE BLOOD SUGAR LEVEL MONITORING APPARATUS INTEGRATED WITH REAL-TIME HEALTH SUPPORT SYSTEM

Abstract

A non-invasive continuous blood sugar level monitoring apparatus integrated with real-time health support system. The blood sugar levels and other vital physiological information of the user can also be tracked wirelessly through the apparatus. The apparatus has an integrated real-time alert and reminder feature for notifying the user during medication and unusual physiological conditions. An automated diet and lifestyle recommendation solution is integrated into the device to help the user maintain healthy blood sugar and blood pressure levels. The low-powered telemetry device is used for communicating the stored physiological information of the user and the computed results between the network of devices.

Claims

1. A multi-spot sensing near-infrared spectrometer apparatus comprising of: a set of tilted near-infrared light source probes arranged on a sensor board with a quantum distance of wavelength number (k) between each of the adjacent light source probes; a tilted near-infrared optical lens system arranged at the signal probe end for constructively interfering and focusing the input radiation on the sensing spot; the set of near-infrared light source probes and optical lens system at the signal probe end tilted at a boundary angle of .sub.B, which is utilized to inject the input signal at the glazing angle; a photodetector end near-infrared optical lens system aligned with signal probe system at an optimal reflective response signal receiving spot, which is utilized for focusing the response signal on the photodetector; and a near-infrared photodetector assembled on a photodetector board at the response receiving spot and aligned with the photodetector end optical lens system.

2. The apparatus of claim 1 further attached to a multi-spot sensing green spectrometer apparatus, which comprises of: a green LED signal probe on the mounting sensor board tilted at a critical angle (c) for injecting green signal at the boundary angle; a green optical lens system tilted at an angle of critical angle (c) at the signal probe end for focusing and injecting the input green signal at the critical angle on the sensing spot; a photodetector end green optical lens placed at an optimal distance from the input signal probe for focusing the reflected response on the photodetector; and a green photodetector assembled on the sensor board and aligned with the photodetector end optical lens system at the optimal response receiving spot.

3. The apparatus of claim 2 further attached to a multi-spot sensing red light spectrometer apparatus, which comprises of: a red LED signal probe with red optical lens system arranged on the central position of the red indicator board; a set of red photodetectors and corresponding red optical lens system assembled on the either side of the LED signal probe at the optimal proximity positions; and a set of red photodetectors and corresponding red optical lens system assembled on the either side of the LED signal probe at the optimal distant positions.

4. The apparatus of claim 3 further attached to a multi-spot sensing infrared spectrometer apparatus, which comprises of: an infrared red LED signal probe with infrared optical lens system arranged on the central position of the infrared indicator board; a set of infrared photodetectors and corresponding infrared optical lens system assembled on the either side of the LED signal probe at the optimal proximity positions; and a set of infrared photodetectors and corresponding infrared optical lens system assembled on the either side of the LED signal probe at the optimal distant positions.

5. A reflective dispersion analyzer apparatus, which comprises of: light source probe set arranged on a sensor board with a quantum distance of wavelength number (k) between the adjacent signal probe; an optical lens system assembled at signal probe end for focusing the input signal on the central photodetector; the light source and the signal probe end optical lens tilted at the boundary angle; a central photodetector set with optical lens system arranged at the optimal central sensing spot; two adjacent non-central photodetectors with corresponding optical lens system assembled on the either side of the central photodetection system at an optimal dispersion response sensing spot; and an instrumental amplifier attached to the central photodetector response line and to the summed response output line of the adjacent non-central photodetectors.

6. The apparatus of claim 1 further comprising of a dual side sensing near-infrared spectrometer configuration, which comprises of: a set of near-infrared light source probes arranged on the sensor board with a quantum distance of wavelength number (k) between each of the adjacent light source probe; a primary near-infrared optical lens system assembled at the signal probe end for focusing the input radiation; a beam splitter assembled at the bottom of the primary lens system for splitting the incoming response into refracted and reflected response; a mirror in the reflected space to invert the phase of the reflected light and focus the input light on the optical lens system of the reflected space; a near-infrared optical lens in the reflected space tilted at the boundary angle (.sub.B1) for injecting the input response at the glazing angle; a near-infrared optical lens in the refracted space tilted at the boundary angle (.sub.B2) for injecting the input response at the glazing angle; a near-infrared photodetector set and a near-infrared optical lens system placed in the reflected space at an optimal response recording spot; a near-infrared photodetector set and a near-infrared optical lens system placed in the refracted space at an optimal response recording spot; and the dual side sensing configuration as the means to elude the errors in the output response due to the varying the physiological parameters and due to the alteration in the stability of the electro-optical components.

7. The apparatus of claim 6 further comprising of a pathlength matched dual side sensing near-infrared spectrometer configuration, which comprises of: a set of near-infrared light source probes arranged on the sensor board with a quantum distance of wavelength number (k) between each of the adjacent light source probe; a primary near-infrared optical lens system assembled at the signal probe end for focusing the input radiation; a beam splitter assembled at the bottom of the primary lens system for splitting the incoming response into refracted and reflected response; a mirror in the reflected space to invert the phase of the reflected light and focus the input light on the optical lens system of the reflected space; a near-infrared optical lens in the reflected space tilted at the boundary angle (.sub.B1) for injecting the input response at the glazing angle; a set two mirrors assembled in the refracted space at optimal orientation and positions for equalizing the wave pathlength and focusing the light on the optical lens system; a near-infrared optical lens in the refracted space tilted at the boundary angle (.sub.B2) for injecting the input response at the glazing angle; a set of near-infrared photodetector and near-infrared optical lens system placed in the reflected space at an optimal response recording spot; and a set of near-infrared photodetector and near-infrared optical lens system placed in the refracted space at an optimal response recording spot.

8. The apparatus of claim 4 further comprising of a low-powered electronic circuit of the telemetry apparatus, which comprises of: near-infrared light sources, green LED, red LED and infrared LED with their corresponding optical lens elements, which are arranged according to their reflective spectrometer configuration; near-infrared photodetector, green photodetector, red photodetectors and infrared photodetectors with their corresponding optical elements, which are arranged according to their reflective spectrometer configuration; a tunable BJT/FET based active amplifier attached to the circuit line of near-infrared light probes, which is utilized to coherently drive the light sources and amplify the output; a main switch set attached to the LED frontend and to the input line of signal probes, which is utilized to reduce the frontend components and power consumption; the LED frontend components of LED driver, LED controller, pulse width modulator and clock controller attached to the microprocessor, which are utilized for variably triggering input signal to the signal probes; a multiple switch set attached between the corresponding red photodetector probes and infrared photodetector probes, which are utilized as the means to alternatively extract the red and infrared response; a darlington pair and small signal DC source attached to near-infrared response diode, which is used as the means to shift and amplify the output infrared response; a darlington pair and small signal source attached to the green photodetector; proximity and distant red-infrared photodetection response lines; a set of darlington pair attached to the red-infrared photodetector response lines; the darlington pair attached to the red-infrared photodetection response line as the means to amplify the low-powered weak output signals; op-amp based adder circuits attached to the distant and proximity infrared-red photodetection line, which is utilized to separately sum the output response; buffer units attached to the distant and proximity infrared-red photodetection line for stabilizing the output response; the stabilized distant and proximity infrared-red photodetection lines attached to a circuit line of ADC IC, ambient noise cancellation IC and DAC IC, which is utilized for curtailing the ambient noise in the response line; an instrumental amplifier attached to the filtered distant infrared-red response line and proximity infrared-red response line, which is utilized for extracting the dispersion information; the red-infrared dispersion analysis circuit line attached to a power notch IC and ADC line connected to the microprocessor, which is used to filter and log dispersion response; a switch set attached to a transimpedance amplifier and to the individual light source output response lines, which is utilized as a low powered means to extract the individual output responses; the transimpedance amplifier attached to a circuit line of power notch filter, ADC IC and ambient noise cancellation IC, which is utilized to filter the noise in the output response; a 9/6-axis accelerometer, which is utilized as the real-time feedback to remove the movement noise in the real-time recording; the MEMs/NEMs accelerometer as the means for operating the telemetry apparatus through gesture interaction and for computing user and device movement signals; a non-contact bio-temperature sensor for extracting the real-time bio-temperature; the non-contact MEMs/NEMs bio-temperature as the means for recording the real-time thermal feedback of the sensors and electronics; an ambient temperature sensor as the means for extracting the environmental temperature; the ambient temperature sensor as the means for computing the real-time thermal feedback of the electronics; wireless antennae set of GPS antenna, Bluetooth antennae and WLAN antenna, which are used for communicating the data between the telemetry apparatus and the external devices; the wireless antennae set also as the means for computing location and movement related data; a microprocessor attached to a memory component, which is utilized for communicating with the electronics frontend, switches, sensors, wireless antenna and other electronics modules; the microprocessor attached to the memory component as the means for internally executing the code and recording the information; a touch display for viewing and accessing the real-time medical signals, health data and other essential information; the touch display also as the means for operating the instrument and device applications; user interaction components of buttons, navigator crown, mic, and speaker, which are utilized to operate the telemetry apparatus and device applications; the navigator crown, which is made of a potentiometer component and a fixed impedance component; the user interaction components as the means to interact with the professional medical and health practitioners; the user interaction components as the means to perceive the recorded and computed information; a programmable fancy led, which is used to represent different operating modes, device status and decorative applications; the fancy led as the means for automatically indicating the patient condition; the navigator attached to the fancy led as the means for adjusting the intensity of the fancy LED; a power supply unit comprising of power management IC, supercapacitor-battery set, supercapacitor set-energy harvester, wireless charging coil, negative voltage converter and USB module; the power management IC for regulating power supply; the super-capacitor attached to a battery unit, as a more stable means to supply and store energy; the negative voltage converter for generating negative reference signal; the charging coil as the wireless means to power the battery and the internal electronics; the USB module attached to the power management unit and microprocessor, which is utilized to power the telemetry apparatus and recharge the battery; the USB module as the wired means to communicate data with external accessorial devices and server; and the supplementary power supply unit of renewable energy harvester and super capacitor, as the auxiliary means to power the battery and the internal electronics.

9. The telemetry apparatus of claim 8 further comprising of GSM module, which is used as the means to: wirelessly communicate the data; and compute location and movement related data.

10. The button set of the apparatus of claim 8 further comprising of button B1, button B2 and button B3, wherein: the long hold of button B1 turns on and off the telemetry apparatus; the short hold of button B1 swaps the device modes to blood sugar monitoring mode, blood pressure monitoring mode, sleep mode, bio-signal tracking mode, stress management mode, work mode and other in-built modes; the long hold of button B2 synchronizes the wireless mobile apparatus and transfers data to other synchronized wireless devices; three short holds of button B2 the turns ON/OFF IOT parallel computation mode; the long hold of button B3 prompts the user to record the calibration values and real-time biometric values; five short holds button B3 caches and records the subjective emotional stress level mark-ups; the combination long hold of button B1 and button B2 silently triggers emergency alert in the wireless life-support network and notifies the life-support network; the combination long hold of button B1 and button B3 triggers alarm and medical emergency alert in the wireless life-support network; and the combination programs and individual programs of button B1, button B2 and button B3 are utilized to operate the telemetry apparatus, in-built applications and other device functionalities.

11. The navigator crown of the apparatus of claim 8, wherein the rotation of the crown: swaps the internal applications in the direction of voltage shift; modifies the intensity of the fancy LED as per the voltage shift; and is utilized to operate the telemetry device and internal applications.

12. A fancy LED apparatus attached to the telemetry apparatus of claim 8, which comprises of: a main optical tube; a set of optical tubes branching from the main optical tubes and further branching from the branching optical tubes; and a multi-coloured LED embedded inside the main optical tube.

13. The system and telemetry apparatus of claim 8 further comprising of an accessorial mobile device, which is wirelessly synchronized to the telemetry apparatus, and utilized for: recording the calibration data of blood sugar levels, blood pressure data and other vital biometric information during the instances of device start-up, fasting glucose, pre-breakfast, pre-lunch, pre-dinner, pre-bedtime, post-sleep, post-breakfast, post-lunch, post-exercise and post-dinner; recording user data of username, height, weight, medical condition, fat %, age, gene info, BMI, user picture and other essential information; recording and processing the contact area picture of the user; recording the meal details, meal quantity, macro-nutrient intake and micro-nutrient intake; accessing and viewing the real-time information on detailed diet intake; recording medication alarms and alerts; accessing and viewing the real-time information of blood sugar data, location data, blood pressure signal, neural parameters, pulse rate, oxygen saturation, bio-temperature and other bio-signal information; accessing and viewing the information on daily health, health progress and present health condition; accessing and viewing the real-time data trends on blood sugar levels, blood pressure signal, neural parameters, pulse rate, oxygen saturation, bio-temperature and other bio-signal information; notifying the user with real-time automated medical alerts and medication alarms; prompting the user with automated health recommendation and guidance data; operating the telemetry apparatus; storing and executing the process code, real-time system, analysis methods and software program; storing and processing the computed results; and accessing the in-built applications of the telemetry apparatus.

14. The real-time telemetry apparatus of claim 8 further comprising of network of computational and storage devices of accessorial wireless mobile devices, server computers and external computers, which are used as the efficient, faster and less complex means to: parallelly and serially execute the real-time system, software programs and computational processes of the telemetry apparatus; and store information, real-time system, process code, user data and computed results.

15. The telemetry apparatus and the network of devices of claim 14 further comprising of real-time blood sugar monitoring and management system, which comprises of process steps: to calibrate blood sugar values during the instances of device start-up, fasting glucose, pre-breakfast, pre-lunch, pre-dinner, pre-bedtime, post-sleep, post-breakfast, post-lunch, post-exercise and post-dinner; to calibrate the device for hypoglycaemic and hyperglycaemic conditions; to calibrate the device in day interval method for recognized conditions of hypoglycaemia, hyperglycaemia and extreme threshold fluctuations; to calibrate the blood sugar values and other vital information during sitting position, relaxing position, standing position and other postures; to re-record and re-calibrate the blood sugar values for recognized hyperglycaemic conditions, hypoglycaemic conditions and unusual blood sugar fluctuations; to re-record and process the contact skin layer numerous times for eluding calibration errors; to calibrate the contact skin layer based on the normalized index value; to alternatively calibrate the color index based on realistic profile picture; to record and calibrate the user data of fat %, gene info, BMI, weight, height and age; to initiate green sensor and measure the green sensor response (G); to remove the oscillatory green values from the recorded green sensor response values using fast-fourier analysis and other processing techniques; to determine the DC green parameter of GDC; to normalize the green parameter DC values; to deduce the green parameter GPAR value from the processed green sensor response values and GDC parameter; to initiate the different modes of near-infrared sensors; to modify the near-infrared response as per temperature stats of the recorded body temperature and ambient temperature; to adjust the processed Near-Infrared response modes as per resonant power loss characteristics; to compute the normalized near-infrared response (NIRT) from the various recorded and processed infrared modes through numerical statistical methods; to derive oscillatory red response mode Rosc from the recorded total red power response Rtot; to adjust the total red power response (Rtot) and oscillatory red response mode (Rosc) from the green parameter GPAR for the skin losses; to extract blood line losses free 1.sup.st order normalized near-infrared sensor value (NIRT1) from the oscillatory red response (Rosc) and normalized near-infrared response (NIRT) using linear and non-linear analysis methods; to extract 2.sup.nd order near-infrared sensor value (NIRT2) from the 1.sup.st order near response value (NIRT1), total infrared response (IRtot) and dispersion infrared response values (IRdis) using linear and non-linear analysis, which is used as the means to compensate for the non-haemoglobin particle and blood particle losses; to derive 3.sup.rd order near-infrared response values (NIRT3) from the red dispersion response values (Rdis) and normalized 2.sup.nd order value of NIRT2 using linear and non-linear methods; to derive 4.sup.th order near-infrared response values (NIRT4) from the green parameter (GPAR) and 3.sup.rd order near-infrared response (NIRT3) utilizing the equation form of either power exponent or linear representation of unknown intercept and unknown coefficient; to modify the processed near-infrared response as per the computed contact layer index using non-linear and linear correlation; to correlate the processed near-infrared values and the recorded real-time blood sugar calibration values utilizing non-linear and linear correlation; to calibrate the correlated near-infrared response and the other sensor values for tracking real-time continuous blood sugar values; and to run re-calculation and re-calibration for the recognized conditions of hypoglycaemia, hyperglycaemia and extreme threshold fluctuations; to run learning methods on the recorded infrared and red response for tracking the real-time blood sugar values, hypoglycaemia, hyperglycaemia and extreme threshold fluctuations from the real-time red and infrared response; to store and display continuous blood sugar level (BSL) and blood sugar fluctuation (BSL); to analyse and evaluate fasting glucose BSL value, post-meal BSL value, normal state BSL value, pre-sleep BSL value, post-sleep value and pre-meal BSL value for predicting prediabetic condition, hyperglycaemia condition, and hypoglycaemia condition; to analyse and evaluate fasting glucose BSL variation (BSL1), post-meal BSL variation (BSL2), normal state BSL variation (BSL3), pre-sleep BSL variation (BSL4), post-sleep variation (BSL5) and pre-meal BSL variation (BSL6) for predicting prediabetic threshold fluctuation, hyperglycaemia threshold fluctuation, and hypoglycaemia threshold fluctuation; to analyse and evaluate BSL fluctuation values (BSL) and real-time BSL values with respect to user location for threshold values; to analyse and evaluate the visible and infrared radiation dispersion values [(RtotR)/Rtot, R/Rtot, Rdiff/Rtot, IRdiff, IRtot, _ _ _ ] for threshold blood sugar conditions and unusual blood sugar fluctuations of hyperglycaemia, hypoglycaemia and prediabetes; to analyse and evaluate the pulse rate with the blood sugar data for threshold blood sugar conditions and other health issues; to inform the user regarding the recognized health condition, present blood sugar levels and current blood sugar fluctuations; to display and verify probable symptoms of the recognized health condition; to automatically generate recommendations from the database on therapy methods, treatment centres, lifestyle practices, diet suggestions, physical activities, mitigation methods and medication advice to treat and manage the recognized blood sugar condition; to automatically suggest the user with the automated recommendations to recover and improve the diagnosed health condition; to automatically notify the user to re-record and re-calibrate the device for the initial diagnosis of threshold conditions; and to automatically alert and notify the life-support network with a warning message and information on user data, user condition, user location, recognized health condition, present blood sugar levels, current blood sugar fluctuation and other essential data; to automatically inform the user with information on location of the medication; and to automatically remind the user to take medication.

16. The real-time system and apparatus of claim 15, further comprising of real-time blood pressure monitoring and management system, which comprises of process steps: to calibrate blood pressure values during the instances of device start-up, fasting glucose, pre-breakfast, pre-lunch, pre-dinner, pre-bedtime, post-sleep, post-breakfast, post-lunch, post-exercise, post-meditation and post-dinner; to calibrate the device for hypertension and hypotension conditions; to calibrate the device in day interval method for recognized conditions of hypotension, hypertension and threshold fluctuations; to calibrate the blood pressure values and other vital information during sitting position, relaxing position, standing position and other postures; to re-record and re-calibrate the blood pressure values for hypertension conditions, hypotension conditions, and unusual blood pressure fluctuations; to modify the total red or infrared signal power response (Rtot) from the derived green signal response parameter (GPAR) utilizing the equation form of logarithmic linear representation of unknown intercept and coefficient [Rtot1=RtotY.ln(GPAR)+C1]; to derive red response signal oscillatory mode (RTosc) from the modified red signal response (Rtot1) utilizing fast fourier analysis and other processing techniques; to obtain total power spectrum response of the red signal (RP) from the modified red signal response (Rtot1) through non-linear processing of the averaged temporal data over peak-peak cycle [RP=.sub.0.sup.tpeak|RTosc|{circumflex over ()}2]; to correlate the processed red power response and the recorded real-time blood pressure calibration values utilizing non-linear and linear correlation [BP=X.RP]; to calibrate the correlated red signal response and the other sensor values for tracking real-time continuous blood pressure values; to verify the threshold conditions for null movement data; to run re-calculation and re-calibration for the recognized conditions of hypotension, hypertension and threshold blood pressure fluctuations; to store and display the real-time blood pressure levels and blood pressure fluctuations; to analyse and evaluate fasting glucose blood pressure values, post-meal blood pressure values, pre-sleep blood pressure values, post-sleep blood pressure values, normal state blood pressure values, and pre-meal blood pressure values for their corresponding hypertension threshold condition, hypotension threshold condition, and pre-hypertension threshold condition; to analyse and evaluate fasting glucose blood pressure variation, post-meal blood pressure variation, pre-sleep blood pressure variation, post-sleep blood pressure variation, normal state blood pressure variation values and pre-meal blood pressure variation for recognizing prehypertension threshold fluctuation, hypertension threshold fluctuation, and hypotension threshold fluctuation; to analyse and evaluate blood pressure fluctuation and real-time blood pressure with respect to user location for threshold values; to inform the user regarding recognized health condition, present blood pressure level and current blood pressure fluctuation; to display and verify probable symptoms of the recognized health condition; to automatically generate recommendations from database on therapy methods, treatment centres, lifestyle practices, diet suggestions, physical activities, mitigation methods and medication advice to treat and manage the recognized blood pressure condition; to automatically suggest the user with the automated recommendations to recover and improve the diagnosed health condition; to automatically notify the user to re-record and recalibrate the device for the initial diagnosis of threshold conditions; and to automatically alert and notify the life-support network with a warning message and information on user data, user condition, user location, recognized health condition, present blood pressure level, current blood pressure fluctuation and other essential data; to automatically inform the user regarding the location of the medication; and to automatically remind the user to take medication.

17. The system and the apparatus of claim 16, further comprising of real-time automated emotional stress recognition system, which comprises of process steps: to analyse and evaluate real-time blood pressure values and blood pressure fluctuation for the emotional stress threshold limits; to measure and cache peak to peak temporal red signal response; to measure and cache summed peak to peak temporal red response (HP3); to measure and incrementally sum cache square power peak to peak temporal red signal response (HP2); to evaluate peak to peak temporal fluctuation for 0.05 s intervals and cache a parameter for positive outcomes (HP1); to assess extracted real-time neural parameters with the resting state and active state neural parameters for evaluating the state of emotional stress and anxiety; to analyse and verify the location of the user to assess the psychological burden and the emotional response category; and to inform the user with information on the current stress and emotional condition; to display and verify probable symptoms; to automatically generate recommendations from database on recovery techniques, meditation methods, therapy methods, treatment centres, lifestyle practices, diet suggestions, physical activities, mitigation methods and health advice to manage the recognized emotional state; to automatically suggest the user with automated recommendations to manage the recognized emotional condition; to automatically alert and notify the life-support network with a warning message and information on user data, user condition, user location, recognized health condition and other essential data; to automatically connect the user with social network based on recognized health condition; and to automatically assist the user with information on guided meditation.

18. The system and apparatus of claim 17, further comprising of real-time automated sleep recognition system, which comprises of process steps: to evaluate and analyse the null movement of the user; to assess the body temperature and bio-signals for realistic range and sleep range; to assess the blood sugar levels and blood pressure data for the state of sleep; to analyse and evaluate the blood sugar levels, blood pressure data and neural parameters (of HP1, HP2 and HP3) with sleep and wake data for recognizing the REM and NREM sleep cycle; to cache the sleep duration, sleep health, REM phase duration and NREM phase duration; to re-evaluate and verify the movement data of actimeter for recognizing sleep health; to assess and verify the state of disturbed sleep; to store and inform the user with information on the computed sleep data and sleep health; to verify and display probable symptoms; to automatically generate recommendations from database on recovery techniques, meditation methods, therapy methods, treatment centres, lifestyle practices, diet suggestions, physical activities, mitigation methods, medications and health advice to manage the recognized sleep health disorder; to automatically suggest the user with the automated recommendations to manage the diagnosed sleep health disorder; to automatically alert and notify the life-support network with a warning message and information on user data, user condition, user location, recognized health condition and other essential data; and to apply learning on the processing method and real-time system for minimizing analysis parameter count, mode switching, complexity and power consumption.

19. The real-time system and apparatus of claim 18 further comprising of a real-time alert and recommendation system, which analyses real-time biological information of the user and: automatically notifies the user with real-time alerts for unusual real-time fluctuations of blood sugar data, blood pressure signal, neural parameters, pulse rate, oxygen saturation, bio-temperature and other bio-signal information; automatically notifies the user with medication reminder for the unusual real-time values of blood sugar data, blood pressure signal, neural parameters, pulse rate, oxygen saturation, bio-temperature and other bio-signal information; automatically notifies the user with real-time values and data trends on the blood sugar levels, blood pressure signal, neural parameters, pulse rate, oxygen saturation, bio-temperature and other bio-signal information; automatically notifies the user with health sense message; automatically notifies the user with information on daily health, health management progress, diet records, nutrition intake and present health condition; automatically suggests information on recovery techniques, meditation methods, therapy methods, treatment centres, lifestyle practices, diet plans, physical activities, mitigation methods and health advice to manage the recognized health condition; automatically informs the user with information on effectiveness of the recommendation; and automatically notifies the user with guided health management and therapeutic methods to alleviate the recognized health condition.

20. The real-time system and apparatus of claim 19 further comprising of a real-time tracking system, which comprises of: an automated interface with real-time information on blood sugar data, user location, blood pressure index, neural parameters, pulse rate, oxygen saturation, bio-temperature and other bio-signal information; an automated interface for recording and accessing meal details, meal quantity, macro-nutrients and micro-nutrients; an automated interface with real-time blood pressure trends; an automated interface with real-time pulse rate and oxygen saturation trends; an automated interface to view real-time blood sugar levels trends; an automated interface with real-time data projection on the neural activity, emotional stress and bio-temperature activity; and an automated interface with health sense information.

21. The real-time system and apparatus of claim 20 further comprising of a life-support system, which comprises of: life-support network of synchronized support devices, near-by-mobile devices, central server machine, SOS network and devices-in-user vicinity; process step to analyse the real-time physiological and psychological information for recognizing the health condition; process step to automatically trigger emergency based on the recognized health condition; process step to recognize the manual emergency trigger of the user's telemetry apparatus; process step to evaluate the status of the internal wireless antennae set; process step to turn on the switched off wireless antennae; process step to cache user location through the wireless antennae set; process step to cache the real-time physiological and psychological information; process step to communicate the recorded bio-signal data, user's health and medical condition, and location data between the life-support network through wireless methods; process step to communicate the data through the medium of central server and through other shorter robust wireless pathways; process step to recognize the alert trigger command and to notify the auxiliary life-support devices through the primary life-support network; data synchronization process step to detect the information transfer and obtain the communication acknowledgement from the life-support client devices and primary device; data synchronization process step to trigger for sequential dataset communication; and data synchronization process step to receive the proceeding dataset from primary apparatus after the acknowledgement and the sequential dataset trigger steps.

22. The telemetry apparatus and network of devices of claim 14 and further comprising of a learning method, wherein: the recorded parameters of color index, age, BMI, fat %, gene Info, sensor intensity, signal response, health condition, health data and calibrated medical data of the user are transferred to the central server; the recorded parameters are processed and matched with the user database for learning and deriving the optimization parameters of color index, sensor calibration data, healthy H.R. index, performance index and health progress index; the derived and learnt parameters are returned to the user devices; and the optimization and learnt parameters are utilized by the user device for processing the real-time biological information, health parameters and essential data.

23. The smart watch embodiment form of the telemetry apparatus of claim 8, which comprises of: a cavity-like structure attached to the contact surface; near-infrared spectrometer apparatus, green spectrometer apparatus, red spectrometer apparatus, infrared spectrometer apparatus and bio-temperature sensor, which are packaged on the contact surface of the device with plurality of sensing probes in contact with user; the plurality of spectrometer apparatuses and bio-sensors arranged inside the cavity-like structure; a foam base placed on the contact surface of the device without impeding the bio-sensors, which is utilized as the mechanical method to reduce movement errors in the measurement; the cavity like structure as the means to evade the background optical interference; an analog and sensor frontend plane packaged on the sub-sequent vertical plane to the sensor plane, which is utilized to reduce tracing efforts and packaging size; a secondary digital and analog plane packed in the successive plane to the analog and sensor frontend plane, which is utilized to reduce tracing efforts and packaging size; a digital and wireless plane digital packaged in the plane next to the secondary digital and analog plane, which is utilized to reduce tracing efforts and packaging size; a power plane packaged between the secondary digital plane and the primary digital plane, which is used as the means to reduce the electronic noise interruptions; a touch screen with mic and micro-speaker packaged on the top surface; a battery packaged inside the device without impeding the wireless antennas and power supply, which is utilized to reduce noise interruption; a micro-USB placed on the side surface of the device; button B1 and button B2 placed on the side surface of the device; navigator crown and button B3 placed on the other side surface of the device; product waterproofing coated on the device; and PCB waterproofing coated on the electrical board and electronic chips of the device.

24. Ear attachment embodiment form of the telemetry apparatus of claim 8, which comprises of: a reflective bio-sensing apparatus affixed on the ear-attachment spot; an ear placement area with plurality sensors embedded on the contact surface; an ear-hook and clip attached to the reflective sensing apparatus; the ear-hook as the means to securely fasten the device; a music ear-bud attached to the earhook, which is utilized as the means for perceiving the device output and holding the device on the sensing spot; a fancy LED apparatus embedded inside the earhook; and waterproof coating.

25. Perpetual Handheld Monitoring embodiment form of the telemetry apparatus of claim 8, which comprises of: a finger placement area; reflective sensing spectrometer and bio-temperature sensing probe embedded inside the finger placement area; a foam cushioning embedded on the contact surface of the finger placement area around the sensing probes, which is utilized as the means to reduce contact vibration and movement errors; button 1 and button 2 placed on the side surface of the device; micro-USB port placed on the side surface; a touch screen embedded on the front surface, which is used as the means for recording the calibration data, diet information, exercise patterns and other essential information; the touch screen as the means for accessing and viewing the real-time biological information and health data; the touch screen as the means for operating the telemetry apparatus, in-built applications and other essential device functionality; a detachable accessorial renewable charging unit attached to the back surface of the apparatus; a fixed mini solar module and an actuatable mini solar module of the renewable charging unit, which are attached to each other through an actuation hinge; an actuator attached to the actuation hinge, which is utilized as the means to automatically extend the actuatable mini solar module for harvesting more energy; a detachable wearable chord with extender chord and chord adjusting element attached to the main device; and the extender chord and the chord adjusting element as the means to modify the length of the wearable chord; and waterproof coating.

Description

BRIEF DESCRIPTION OF THE ARTWORK

[0035] FIG. 1 is the reflective near-infrared optical spectrometer apparatus;

[0036] FIG. 2 is the reflective green optical spectrometer apparatus;

[0037] FIG. 3 is the reflective red optical spectrometer apparatus;

[0038] FIG. 4 is the reflective infrared optical spectrometer apparatus;

[0039] FIG. 5 is the dual-side sensing near-infrared spectrometer apparatus;

[0040] FIG. 6 is the design of pathlength adjusted dual-side sensing near-infrared spectrometer apparatus;

[0041] FIG. 7 is a dispersion analyser apparatus;

[0042] FIG. 8 is the low-powered electronic architecture of the reflective telemetry apparatus;

[0043] Series of FIG. 9 show the method to calibrate the telemetry apparatus;

[0044] Series of FIG. 10 show the processing method for initialization and normalization;

[0045] Series of FIG. 11 is the real-time system for monitoring the continuous blood sugar levels;

[0046] Series of FIG. 12 is the method of blood sugar analysis for recognizing the hypoglycaemia, hyperglycaemia and unusual blood sugar fluctuations;

[0047] FIG. 13 is the real-time system for monitoring continuous blood pressure levels;

[0048] Series of FIG. 14 is the method of blood pressure analysis for recognizing the hypertension, hypotension, and unusual blood pressure fluctuations;

[0049] FIG. 15 is the automated real-time system for monitoring emotional stress levels;

[0050] FIG. 16 is the real-time and automated sleep tracking system;

[0051] FIG. 17 shows a program for operating the telemetry apparatus using the buttons and navigator;

[0052] FIG. 18 is a learning method for estimating processing parameters from the user database;

[0053] FIG. 19 is the design of automated emergency response system;

[0054] FIG. 20 shows the network of devices based parallel computational and storage method;

[0055] FIG. 21 is the design of fancy LED apparatus;

[0056] Series of FIG. 22 show automated interface for recording user information and calibration values;

[0057] FIG. 23 is the automated interface for recording and accessing detailed diet information;

[0058] Series of FIG. 24 show the automated interface for accessing real-time biological information;

[0059] Series of FIG. 25 show the interface of the automated real-time alerting system;

[0060] Series of FIG. 26 show the real-time medication reminders;

[0061] Series of FIG. 27 show the sample interface of the automated recommendation system;

[0062] Series of FIG. 28 is the smart tracker embodiment form of the telemetry apparatus;

[0063] Series of FIG. 29 is the solar powered handheld monitoring embodiment form; and

[0064] FIG. 30 is the ear attachment embodiment form of the telemetry apparatus.

DETAILED DESCRIPTION OF THE INVENTION

[0065] Comprehensively, the disclosure can be utilized and perceived in the form of various applications. The principle of the described invention is not intended to limit to the specific device or instrumentation application. The disclosure can be chiefly classified into live clinical diagnostic instrument, telemetry medical apparatus, mobile wellness management device, automated recommendation system, real-time intelligent medical reminder, software medical device and other forms of health management devices.

[0066] FIG. 1 is the reflective near-infrared spectrometer apparatus. The near-infrared light sources 1 and 2 are embedded on the LD board 3 at a quantum distance of k, which are tilted at a boundary angle of .sub.B (where k is the constructive interference reference number). The light emitted by the 1 and 2 are focused by the near-infrared optical lens system 4 placed on the contact surface and tilted at the boundary angle of .sub.B. The quantum distance of wavelength number is maintained between the LDs and the light source objects to obtain a constructive interference (i.e. the distance can vary depending on the relative angle and path length between the light sources or any coherent sources such as slits). The near-infrared light sources 1-2 and optical lens system 4 are tilted at the angle of .sub.B to inject the input signal at the glazing boundary angle on the sensing spot. Bone generally tends to absorb the near-infrared radiation; hence the glazing critical angle phenomenon is utilized to make the light bounce back from the bone boundary. The photodetector-end near-infrared lens system 5 is placed at an optimal distance from the signal probes of 1-2-4 for eluding the internal reflection noises and for capturing the near-infrared reflected response. The reflected response is focused by the optical lens system 5 on the near-infrared photodetector 6, which records the real-time response.

[0067] FIG. 2 is the design of the reflective green spectrometer. The green LED signal probe 7 and green optical lens 8 placed on the contact surface are tilted at a critical angle of .sub.c. The light is injected at the critical angle of .sub.c, so that light reflects off the skin boundary. A photodetector-end optical lens system 9 is placed an optimal response distance to capture the internal-reflection free reflected response. The light concentrated by the optical lens system 9 is recorded by the green photodetector 10.

[0068] FIG. 3 shows the red indicator apparatus for recording the reflective dispersive signals. The light emitted by the red LED 11 is focused on the sensing spot by the red optical lens system 12. A red photodetector 13 and red optical lens 14 set are placed at an internal-reflection free proximity position from the signal probes 11-12. A red photodetector 15 and red optical lens 16 set are placed on the other side of the signal probes 11-12 at a noise free proximity position. A red photodetector-red optical lens system 17-18 set are placed at the distant position from the signal probes 11-12. The red optical lens-red photodetector 20-19 set are placed on the other side at the optimal distant position. The output response recorded by the set of proximity photodetection probes of 13-14 and 15-16 and the set of distant photodetection probes of 17-18 and 19-20 are analysed to obtain real-time information on the dispersive and non-dispersive signals. The real-time information is utilized to evaluate the medical data, psychological health and dispersion of the red light due to the blood particles.

[0069] FIG. 4 shows the infrared indicator apparatus for recording the reflective dispersive signals. The light emitted by the infrared LED 21 is focused on the sensing spot by the infrared optical lens system 22. An infrared photodetector 23 and infrared optical lens 24 set are placed at an internal-reflection free proximity position from the signal probes 21-22. An infrared photodetector 25 and infrared optical lens 26 set are placed on the other side of the signal probes 21-22 at a noise free proximity position. An infrared photodetector-infrared optical lens system 27-28 set are placed at the distant position from the signal probes 21-22. The infrared optical lens-infrared photodetector 30-29 set are placed on the other side at the optimal distant position. The output response recorded by the set of proximity photodetection probes of 25-26 and 23-24 and the set of distant photodetection probes of 27-28 and 29-30 are analysed to obtain real-time information on the dispersive and non-dispersive signals. The real-time information is utilized to evaluate the medical data, psychological health and dispersion of the infrared light due to the blood particles. Similarly, light sources of different spectrum can be utilized for evaluating the real-time biological information and spectral dispersion data.

[0070] FIG. 5 shows the dual side sensing near-infrared apparatus. The near-infrared light sources of 31 and 32 are placed with k2 distance between them. The radiation emitted by 31-32 is constructively focused by a primary near-infrared optical lens system 33 on the mini beam-splitter 34. The beam splitter 34 splits the incoming radiation into the reflected and refracted space. A mini mirror 35 in the reflected space inverts the phase of the reflected radiation and focuses the light on the secondary near-infrared lens system 36. The secondary near-infrared lens 36 is tilted at an angle of .sub.B1 and placed on the contact surface to inject the light at the glazing angle on the sensing spot. The light refracted by 34 is focused by a secondary near-infrared optical lens system 37, which is placed on the other side of the contact surface. The near-infrared optical lens 37 is tilted at an angle of .sub.B2 for injecting the refracted at the glazing angle. The near-infrared optical lenses of 38 and 39 in the reflected space and refracted space are placed at an optimal noise-free distance for focusing the reflected near-infrared response on their corresponding near-infrared photodetectors of 40 and 41. The dual side configuration is utilized to recognize the uncertainty in the output response due to the changes in optical components with time and varying the physiological parameters.

[0071] FIG. 6 shows the dual side sensing near-infrared apparatus with an additional pathlength adjusting mirror set. The near-infrared light sources of 42 and 43 are placed with la distance between each other. The radiation emitted by 42-43 is constructively focused by a primary near-infrared optical lens system 44 on the mini beam-splitter 45. The beam splitter 45 splits the incoming radiation into the reflected and refracted space. A mini mirror 46 in the reflected space inverts the phase of the reflected radiation and focuses the light on the secondary near-infrared lens system 47. The secondary near-infrared lens 47 is placed on the contact surface and tilted at an angle of .sub.G to inject the light at the glazing angle on the sensing spot. A set of two mirrors 48-49 are placed in optimal orientations and positions in the refracted space to reflect the refracted radiation and focus the radiation on the secondary near-infrared lens 50. The near-infrared optical lens 50 is placed on the other side of the contact surface and tilted at an angle of .sub.G for injecting the refracted at the glazing angle. The near-infrared optical lenses of 51 and 53 in the reflected space and refracted space are placed at an optimal noise-free distance for focusing the reflected near-infrared response on their corresponding near-infrared photodetectors of 52 and 54. The extra set of mirrors are utilized in the refracted space to synchronize the pathlength and response recording.

[0072] FIG. 7 is a dispersion analyser apparatus. The light emitting signal probes of 56-57 on signal board 55 are tilted at an angle of .sub.G1. The light by signal probes 56-57 are interfered and focused by an optical lens system 58 tilted at an angle of .sub.G1. The tilted optical lens 58 focuses the input light on the central photodetector system of optical lens 59 and central photodetector 60. A set of adjacent non-central photodetectors of 62-64 are placed on the either side of the central photodetector 60 at an optimal dispersion recording distance. The dispersive response signals are captured and focused by the set of non-central optical lenses of 61 and 63 on the corresponding non-central photodetectors of 62 and 64. The signal output terminals of the central photodetector's 60 response and summed response of non-central photodetectors 62-64 is attached to an instrumental amplifier 65. The output of the instrumental amplifier 65 is analysed for obtaining the dispersion information.

[0073] FIG. 8 shows the electronic hardware architecture of the reflective telemetry apparatus.

[0074] The set of optical lens system of 66, 67, 68 and 69 tunes and focuses the input radiation of the corresponding light sources of 80-81, 82, 83 and 84. The output response is focused by optical lens system of 70, 71, 72, 73, 74, 75, 76, 77, 78 and 79 on the corresponding photodetector probes of 85, 86, 87, 88, 89, 90, 91, 92, 93 and 94. The input to the near-infrared light sources of 80 and 81 are coherently driven through a resistor line and a tunable FET/RIT based active amplifier circuit 95. The signal input is variably triggered and sent through a LED frontend comprising of LED driver 124, PWM 127, switch set 125, LED controller 126 and clock controller 128. A signal probe end primary switch set 123 is utilized for connecting the LED frontend of 124-125-126-127-128 to the red LED 82, infrared LED 83, green LED 84 and active amplifier circuit 95 attached to the near-infrared LDs 80-81. The primary switch set 123 reduces the overall component use, power consumption and electrical tracing efforts.

[0075] The near-infrared output response recorded by the near-infrared photodetector probe 85 is shifted by small signal source 96 and amplified by the darlington pair 97. The response recorded by the green photodetector probe of 86 is shifted by small signal source 98 and amplified by the darlington pair 99. A set of switches of 100, 101, 102 and 103 are placed between the corresponding set of red photodetector-infrared photodetector of 87-91, 88-92, 89-93 and 90-94. The set of switches of 100, 101, 102 and 103 are utilized to alternatively record output response of the red photodetector probes of 87-88-89-90 and infrared photodetector probes of 91-92-93-94. The output response of proximity red-infrared photodetectors of 87-91 and 88-92 is separately extracted through a proximity response line 106 and summed through an op-amp circuit 108. The output response of the distant red-infrared photodetector set of 89-93 and 90-94 are amplified through darlington circuit of 104 and 105. The response of distant red-infrared photodetectors set is separately extracted through a distant response line 107 and summed through an op-amp circuit 110. The output line of proximity photodetectors and distant photodetectors are stabilized through a buffer circuit of 109 and 111. The summed proximity response line and summed distant response line are filtered and processed using a circuit line of ADC 112, ambient noise cancellation IC 113 and DAC 114. An Instrumental amplifier 115 with gain is attached to the proximity response line and distant response line for extracting the real-time dispersion information. The real-time dispersion is further filtered and recorded through a circuit line of power notch 116 and ADC 117. The processed output response lines of the individual light sources are attached to an op-amp circuit 119 through a photodetector end primary switch set 118. The photodetector-end primary switch set 118 is utilized to reduce the component use and overall power consumption. The output response through op-amp circuit 119 is filtered and processed through a circuit line of power notch 120, ADC 121 and ambient noise cancellation IC 122.

[0076] A MEMs/NEMs non-contact temperature biosensor 129 is attached to the hardware for extracting the real-time body temperature and temperature feedback. An ambient temperature sensor 130 of the hardware is utilized for extracting real-time environment temperature and feedback of the internal electronics. A MEMs/NEMs 9/6-axis accelerometer 131 is attached to the hardware, which is utilized as a real-time motion feedback for the bio-sensor and as a means to compute movement signals. The wireless antennae set of GPS 132, GSM 135, WLAN 133 and BLE 134 of the hardware are used for communicating the information between the telemetry apparatus and external devices. The wireless antenna set of 132-133-134-135 is also utilized to compute the real-time location and movement data of steps taken, speed, phase, etc. A mini touch display 136 is attached to the hardware, which is utilized for viewing and accessing the real-time medical information, real-time medical alerts, automated recommendations, notifications, data trends, daily health check-up data and other essential information. The touch display 136 is also used for operating the telemetry apparatus and its in-built applications. Apart from the display unit 136, the hardware of the telemetry device is attached to a user interaction system of mic 137, speaker 138, button set B1-B2-B3 139-140-141 and potentiometer integrated navigator 142. The navigator crown 142 comprises of a potentiometer and fixed impedance component. The set of interaction components of 136-137-139-140-141 are utilized for operating the telemetry apparatus and accessing the in-built applications. The set of user interaction hardware components of 136-137-138-139-140-141 are utilized as a means for interacting with the professional medical and health practitioners for clinical and health analysis. The speaker 138 is also used as the means to perceive the recorded and computed information. A fancy LED circuit 143 is attached to the hardware, which is utilized for automatically indicating the user condition, displaying decorative applications and representing different operating modes and device status.

[0077] The hardware of the telemetry apparatus is powered by a power supply unit comprising of power management IC 144, supercapacitor 145-battery set 146, supercapacitor 147-renewable energy harvester 148, wireless coil 150, USB module 149 and negative voltage converter 151. The power management IC 144 is used to regulate power supply. The supercapacitor 145-battery 146 is utilized for energy storage and powering the internal electronics. The supercapacitor 147-renewable energy harvester 148 is used as the auxiliary powering unit. The wireless coil 150 is used as the wireless method to charge the battery and power the internal electronics. The negative signal reference is generated by the negative voltage converter 151. The USB module 149 is used for powering the electronic circuit, charging the internal battery and communicating the data with the external devices.

[0078] The microprocessor 152 attached to memory 153, is used for communicating with the internal electronics and operating the internal electronic components. The microprocessor 152 with memory 153 is also utilized for computing and storing the required information.

[0079] FIG. 9A, FIG. 9B and FIG. 9C show the method to calibrate the telemetry device. The user information of age, weight, BMI, fat %, gene info and contact layer's photograph are recorded during the initial device start-up. The recorded contact skin picture is analysed in the RGB hex code and deduced on a scale of 1 to 10. The device prompts the user to re-record the contact picture multiple times and the recorded contact skin picture is analysed to deduce the color of the contact surface. On unavailability of the contact surface picture, the realistic profile picture of the user is recognized, and the profile picture values are altered by an adjusting parameter to extract the contact layer skin color values. The blood sugar levels, blood pressure data and other real-time biological information of the user are recorded during the sitting position, standing position, relaxing position, fasting glucose, post-dinner, post-breakfast, post-lunch, post-morning sleep, post-exercise, pre-dinner, pre-breakfast, pre-lunch, before bed-time, hypoglycaemic state and hyperglycaemic state. The device prompts the user to re-record the blood sugar data, blood pressure levels and other real-time biological information for unusual fluctuations and increasing hyperglycaemic and hypoglycaemic conditions.

[0080] FIG. 10A, FIG. 10B and FIG. 10C show the process chart for sensor initialization and sensor response normalization. The near-infrared LDs, green LED, red LED, infrared LED and biosensors are initialized in a cyclic manner. The near-infrared response of different modes are recorded and normalized with respect to the area (NIRA, NIRB, NIRC, NIRD . . . ). The green response is recorded and normalized with respect to the area (G). The red response values of red Integrated Power Signal (Rtot), red Differential Signal (Rdiff) and Red Power Value (RP) are recorded and normalized with respect to the area. The values of the red signal response are stored with respect to calibrated values in the Rnn Matrix. The infrared response values of IR Integrated Power Signal (IRtot), IR Differential Signal (IRdiff) and IR Power Value (IRP) are recorded and normalized with respect to the area. The values of the infrared signal response are stored with respect to calibrated values in the IRnn Matrix. The system initializes the bio-temperature sensor and ambient temperature sensor for recording the real-time bio-temperature values (Btemp) and ambient temperature values (Atemp). The accelerometer and wireless antennae are initialized for recording the movement data, location data and establishing wireless communication.

[0081] FIG. 11A, FIG. 11B and FIG. 11C is the real-time system for monitoring the continuous blood sugar levels. The recorded green sensor response of G is analyzed to recognize the green sensor DC parameter losses (GDC). The green parameter (GPAR) is deduced from green sensor DC parameter (GPAR=GDC). The recorded near-infrared response values are adjusted as per the temperature stats of the bio-temperature and ambient temperature response and the mean of the adjusted near-infrared modes (NIRT) are deduced (NIRT=(NIRA+NIRB+NIRC . . . +NIRN)/N). The real-time system processes the recorded red signal to deduce oscillatory red signal values (Rosc) and the oscillatory red response values (Rosc) are adjusted for skin losses using the green parameter (GPAR). The blood line losses free 1.sup.st order near-infrared sensor value (NIRT1) is extracted from the oscillatory red response (Rosc) and normalized near-infrared response (NIRT) using linear and non-linear analysis method (|NIRT1|.sub.t=|NIRT|.sub.tX0.|Rosc|.sub.t). The first order near-infrared (NIRT1) is processed with the infrared response (of IRtot and IRdis) for adjusting the near-infrared response for non-haemoglobin particle and other blood particle losses (NIRT2=NIRT1X1IRdisX2.(IRtot+IRP). The 2.sup.nd order near-infrared response (NIRT2) response is further linearly or non-linearly correlated with the red differential value (Rdiff) for extracting the 3.sup.rd order near-infrared response (NIRT3=NIRT2+X3.Rdif). The extracted 3.sup.rd order near-infrared response (NIRT3) is analyzed with green parameter (GPAR) in the equation form of either power exponent or linear representation of unknown intercept and unknown coefficient for extracting the 4.sup.th order near-infrared response (NIRT4=NIRT3X4.ln(GPARX5) (or) NIRT4=NIRT3X4.ln(GPAR)+X5). The processed near-infrared response is adjusted for recorded color index C and real-time blood sugar values using non-linear and linear correlation. The processed near-infrared response is correlated with the recorded blood sugar calibration values utilizing non-linear and linear correlation for computing the real-time continuous blood sugar values. The real-time blood sugar values (BSL) and blood sugar fluctuations (ABSL) are stored and displayed. The calibrated real-time values are further learnt with respect to the calibrated values and red and infrared response for recognizing hypoglycemic and hyperglycemic data and blood sugar levels. The real-time system records additional calibration values for recognized conditions of hypoglycaemia, hyperglycaemia and unusual blood sugar fluctuations.

[0082] FIG. 12A and FIG. 12B show the method of blood sugar analysis for recognizing the hypoglycaemia, hyperglycaemia and unusual blood sugar fluctuations. The values of continuous blood sugar values (BSL) and blood sugar fluctuations (BSL) are analyzed during fasting glucose state, post-meal state, post-sleep condition, regular condition, and pre-meal state for recognizing prediabetic threshold condition, hyperglycaemia threshold condition and hypoglycaemia threshold condition. The real-time system analyses BSL fluctuation values (BSL) and real-time BSL values with respect to user location. The pulse rate and blood sugar data are evaluated for threshold blood sugar conditions and other health issues. The real-time system analyses and evaluates the red signal values, red signal dispersion values, infrared radiation dispersion values and visible signal values [(RtotR)/Rtot, R/Rtot, Rdiff/Rtot, IRdiff, IRtot, _ _ _ ] for learning and recognizing unusual blood sugar fluctuations, hyperglycaemia, hypoglycaemia and prediabetes conditions. The system informs the user with information on the recognized health condition, present blood sugar levels and current blood sugar fluctuations. Subsequently, the system verifies probable symptoms, and automatically generates and displays recommendations from database on therapy methods, treatment centres, lifestyle practices, diet suggestions, physical activities, mitigation methods and medication advice to treat and manage the recognized blood sugar conditions. The real-time system also automatically notifies and alerts the life-support network with a warning message and information on user data, user condition, user location, recognized health condition, present blood sugar levels, current blood sugar fluctuations and other essential data.

[0083] Based on the real-time data and recognized health conditions, the user is automatically presented with real-time medical alert, medication reminder and information on location of the medication.

[0084] FIG. 13 shows the real-time system for monitoring continuous blood pressure levels. Initially, the recorded red signal response is adjusted according to the green signal response (Rtot1=RtotY.ln(GPAR)). Then the oscillatory values of the red signal (RT.sub.osc) are derived from the adjusted red signal values. Then, the peak to peak cycle of the red signal is analysed for a fixed time span for deriving the power of the red oscillatory signal (RP=.sub.0.sup.tpeak|RTosc|*|RTosc|). The linear and non-linear correlation is applied to the red signal power and calibrated blood pressure value to compute the real-time blood pressure (Ex: BP=X.RP). Then, the sensors are calibrated for tracking real-time blood pressure. The computed continuous blood pressure values are stored and displayed.

[0085] FIG. 14A and FIG. 14B show the method to analyse the continuous blood pressure data for recognizing the hypertension, hypotension, and unusual blood pressure fluctuations.

[0086] The values of continuous blood pressure values (BP) and blood pressure fluctuations (BP) are analyzed during fasting glucose state, post-meal state, post-sleep state, post-meditation state, regular condition, and pre-meal state for recognizing hypertension, hypertension stage 2, hypotension, and unusual blood pressure fluctuations. The system further analyses the blood pressure values (BP) and blood pressure fluctuations (BP) for different locations. The system informs the user with information on the recognized health condition, present blood pressure levels and current blood pressure fluctuations. Subsequently, the system verifies probable symptoms, and automatically generates and displays recommendations from database on therapy methods, treatment centres, lifestyle practices, diet suggestions, physical activities, mitigation methods and medication advice to treat and manage the recognized blood pressure condition. Then, the real-time system also automatically notifies and alerts the life-support network with a warning message and information on user data, user condition, user location, recognized health condition, present blood pressure levels, current blood pressure fluctuations and other essential data. Based on the real-time data and recognized health conditions, the user is automatically presented with real-time medical alert, a message to consult the doctor, medication reminder and information on location of the medication.

[0087] FIG. 15 shows the real-time system and automated method for recognizing psychological stress. The real-time system initially evaluates the real-time blood pressure and blood pressure fluctuations for verifying the state of psychological stress. Then, neural parameters of HP1, HP2 and HP3 are derived utilizing temporal analysis. The peak to peak temporal values of red signal response are evaluated for 0.05 s interval difference for deriving HP1. The peak to peak root mean square and mean values are evaluated for deriving HP2 and HP3. The derived parameters of HP1, HP2 and HP3 are compared with the resting values of HP1, HP2 and HP3 for recognizing the state of emotional stress. The system verifies the location data for verifying the state of emotional stress with respect to the relevant location (Ex: stress at work and home is common, else it is chronic stress condition). Then, the real-time system automatically notifies the user regarding the state of emotional stress and generates suggestions to manage the stress through exercise, guided meditation and diet and social networking platform. The real-time system also automatically alerts and notifies the life-support network with a warning message and information on user data, user condition, user location, recognized emotional condition.

[0088] FIG. 16 shows an automated sleep tracking system. The real-time system evaluates the movement data, body temperature, blood sugar levels, blood pressure data and bio-signal data of the user for recognizing the sleep. Then, the system assesses the values of blood pressure data, blood sugar levels and neural parameters (of HP1, HP2 and HP3) with sleep and wake data for recognizing REM sleep cycle and NREM sleep cycle. The REM cycle duration, NREM cycle duration, total sleep duration and sleep health are incremented and cached. The computed results are stored and displayed. The real-time system further analyses the actimeter data and sleep results to automatically recognize the sleep quality and the disturbed sleep condition. Based on the recognized sleep quality, the symptoms are verified, and the system automatically generates recommendations from database on recovery techniques, meditation methods, therapy, treatment centres, lifestyle practices, diet suggestions, physical activities, medications and health advice to manage the recognized sleep disorder. The real-time system also automatically alerts and notifies the life-support network with a warning message and information on user data, user condition, user location and recognized health condition. A learning method is applied on the derived parameters for reducing analysis parameters count, mode switching, complexity and power consumption of the processing method.

[0089] FIG. 17 shows a program for operating the telemetry apparatus using the buttons and navigator input. The long hold of button B1 turns on/off the device and short hold of button B1 swaps the operating modes of the device. The three short holds of the button B2 switches on/off the IOT parallel computational mode and wireless mode of the device. The long hold of button B2 facilitates the wireless synchronization and wireless data transfer between the telemetry apparatus and wireless devices. On recognizing long hold of the button B3, the device prompts the user to record the calibration values and real-time biometric values. The 5 short holds button B3 marks psychological stress levels of the user. Simultaneous long hold of B1/B3 and B2 silently triggers Emergency Alert in the wireless life-support network. Simultaneous long hold of B1 and B3, triggers alarm and medical emergency alert in the wireless life-support network. The rotation of the navigator crown swaps internal applications of the current mode in the direction of voltage shift or adjusts the intensity of the fancy LED.

[0090] FIG. 18 shows a user database based method for estimating calibration and health parameters. The color index, age, BMI, fat %, gene Info, sensor intensity, signal response and real-time calibration values are recorded from the individual user devices and sent to the central server. The values sent from the user device to the central server are analyzed and statically matched with the previously recorded parameters of the database. The optimization parameters of color index, sensor calibration data, healthy H.R. index, performance index and progress index are learnt and derived from the central database. The parameters are returned to user device, which is utilized for processing the real-time biological information and other health parameters.

[0091] FIG. 19 shows the design of the automated emergency response system. The emergency response system comprises of near-by synchronized mobile devices, SOS network, paired life-support devices and devices in the location of user's vicinity. On recognizing emergency trigger, the system checks for the status of the wireless antennae and the system automatically turns on the switched off wireless antennae. The location data and real-time biological information are recorded through the wireless antennae set and the internal sensors. The recorded information is transferred to the central server, SOS network, synchronized life-support device and the devices in the vicinity of user location. The set of life-support devices gets synchronized and receives the dataset. The life-support network triggers the primary network for transferring next dataset to the life-support network. The wireless data transfer occurs through directly via medium of central server and through other wireless methods.

[0092] FIG. 20 shows the network of wireless computational and storage devices. The Telemetry device 154 transfers the information to the server computer 155 and the other accessorial devices 156 thorough wireless methods. The accessorial mobile apparatus 156, server computer 155 and other network devices are utilized for parallelly computing and storing the information. The network of devices based method is used as a faster and efficient means to compute and store the required information. When necessary, the user device 154 retrieves the computed and stored information from the server 155 and accessorial devices network 156.

[0093] FIG. 21 shows the fancy LED apparatus. The fancy LED 157 emits multi-colored light in the line of branching multiple optical tubes 158. The light emitted to represent different device modes, device status and decorative application is perceived through the different branches of the multiple optical tubes 158.

[0094] Series of FIG. 22 show automated user interface of the telemetry apparatus and synchronized accessorial mobile device for recording user information and calibration values.

[0095] FIG. 22A shows the user interface 159 for recording the essential user information. During the device startup, the profile picture 160, user name 161, age 162, basal metabolic index 163, fat % 164, weight 165, height 166 and gene info 167 of the user are recorded through the real-time telemetry or the accessorial mobile apparatus. FIG. 22B shows the interface 168 for recording contact picture. FIG. 22C is the automated interface 169 of the telemetry apparatus and the accessorial mobile apparatus for recording the calibration values of real-time blood sugar levels and blood pressure data during the device startup. FIG. 22D is the interface 170 of the telemetry apparatus and the accessorial mobile apparatus for recording the calibration values of real-time blood sugar levels and blood pressure data during the state of fasting glucose. FIG. 22E is the automated interface 171 of the telemetry apparatus and the accessorial mobile apparatus for recording the post morning sleep calibration values of real-time blood sugar levels and blood pressure data. FIG. 22F is the interface 172 of the telemetry apparatus and the accessorial mobile apparatus for recording the post-breakfast calibration values of real-time blood sugar levels and blood pressure data. FIG. 22G is the interface 173 of the telemetry apparatus and the accessorial mobile apparatus for recording the pre-lunch calibration values of real-time blood sugar levels and blood pressure data. FIG. 22H is the interface 174 of the telemetry apparatus and the accessorial mobile apparatus for recording the post-lunch calibration values of real-time blood sugar levels and blood pressure data. FIG. 22I is the interface 175 of the telemetry apparatus and the accessorial mobile apparatus for recording the post-exercise calibration values of real-time blood sugar levels and blood pressure data. FIG. 22J is the interface 176 of the telemetry apparatus and the accessorial mobile apparatus for recording the pre-dinner calibration values of real-time blood sugar levels and blood pressure data. FIG. 22K is the interface 177 of the telemetry apparatus and the accessorial mobile apparatus for recording the post-dinner calibration values of real-time blood sugar levels and blood pressure data. FIG. 22L is the interface 178 of the telemetry apparatus and the accessorial mobile apparatus for recording the before-bedtime calibration values of real-time blood sugar levels and blood pressure data.

[0096] FIG. 23 shows automated user interface 179 of the telemetry apparatus and synchronized accessorial mobile device for recording and accessing detailed diet information. The device automatically prompts the user to record detailed diet information of the meal name 180, meal quantity 181 and macronutrition and micronutrition 182.

[0097] Series of FIG. 24 show automated user interface of the telemetry apparatus and synchronized accessorial mobile device for accessing detailed real-time biological information. FIG. 24A is the automated interface 183 with real-time information on blood sugar levels, blood pressure data, neural activity, heart rate, oxygen saturation ratio and bio-temperature with health sense message 184. The health sense message 184 shows the current status and progress of the stress management and other health disorder management. FIG. 24B is the automated interface 185, which shows real-time information on current blood sugar levels 186 and past blood sugar trend 187. FIG. 24C is the sample interface 188, which shows real-time information on current blood pressure levels 189 and past blood pressure trend 190. FIG. 24D is the sample interface 191, which shows real-time information on pulse rate 192 and oxygen saturation ratio 193 with real-time signal pattern 194. The automated user interfaces are automatically displayed on the user device in a timely manner.

[0098] Series of FIG. 25 show sample interface of the automated real-time alerting system. FIG. 25A is the sample interface 195 that displays an automated warning 196 based on the real-time data with information on the unusual fluctuation (of the blood sugar levels 197). FIG. 25B is the sample interface 198 that displays an automated warning 199 based on the real-time data with information on the unusual fluctuation (of the blood pressure levels 200).

[0099] Series of FIG. 26 shows the real-time medication reminders that is displayed for unusual real-time biological data fluctuations and unusual physiological state. FIG. 26A is the interface 201 that displays an automated warning 202, unusual fluctuation message 203 and a medication reminder message 205 with information on real-time blood sugar levels 204. FIG. 26B is the interface 206 that displays an automated warning 207, unusual fluctuation message 208 and a medication reminder message 210 with information on real-time blood pressure 209. FIG. 26C is the interface 211 that displays an automated reminder 212, notification on blood sugar abnormality 213 and a medication reminder message 215 with information on real-time blood sugar levels 214. FIG. 26D is the interface 216 that displays an automated reminder 217, notification on blood pressure abnormality 218 and a medication reminder message 220 with information on real-time blood pressure levels 219.

[0100] Series of FIG. 27 show the sample interface of the automated recommendation system. The automated recommendations are displayed on daily basis for specific health management purpose and also based on the real-time biological information. FIG. 27A is the sample interface 221 that displays unusual biological information with location 222, health management method 223 for the recognized health condition, and real-time physiological data 224. FIG. 27B is the sample interface 225 that displays diet management technique 227 for recognized health condition with additional scientific and nutritional information about the recommended diet 226.

[0101] FIG. 28A, FIG. 28B and FIG. 28C show smart tracker embodiment of the telemetry apparatus.

[0102] FIG. 28A is the isometric bottom view of the smart watch embodiment. The set of near-infrared spectrometer apparatus 230, green spectrometer apparatus 231, infrared spectrometer 232, red spectrometer 233 and bio-temperature sensor 234 are embedded at optimal sensing spots on the contact surface 228 and inside a cavity like structure 229. The cavity like structure 229 is utilized as the means to curtail the background noise in the real-time response. A foam like material 235 is placed around the sensor area of the contact surface 228 of the smart tracker, which is used as the means to reduce contact vibration and real-time movement errors.

[0103] FIG. 28B shows the top packaging view of the smart watch. The bottom plane near the contact surface of the device comprises of the sensor plane 236. The sequential plane to the sensor plane 236 is packaged with analog and sensor end plane 237. The plane succeeding to the analog and sensor end plane 237 is packaged with secondary analog and digital plane 238. A power plane 239 is packaged between the secondary analog and digital plane 238 and primary digital and wireless plane 240, which is used as the means to reduce the electronic noise interruptions. The battery 244 of the device is placed on the other rear side end without obstructing the wireless and electronic plane. The aforementioned packaging method is utilized to reduce electronic circuit tracing and electronic noise interruptions. The top surface of the device comprises of mini-touchscreen 243, a micro-speaker 242 and mic 241. The electronic board of the device is covered with PCB waterproof coating 246 and the device is further covered with product water proofing coating 245 for extra protection.

[0104] FIG. 28C shows the isometric side view of the smart tracker embodiment. A micro-USB charging and data transfer port 251, button B1 249 and button B2 250 are placed on the side surface 247 of the device. The other side surface 248 of the device comprises of navigator 253 and button B3 252.

[0105] FIG. 29A shows the front isometric view of the handheld monitoring embodiment form. The micro-USB 255 and a button 256 are embedded on the side surface 254 of the monitor. The mini-touch screen 258 is embedded on the front side of the monitor, which is used to operate the apparatus and its inbuilt applications. The monitoring device is covered with waterproof coating 257. The device further comprises of a detachable wearable chord 259. The detachable chord 259 has a chord adjusting element 260 and an extender chord 261 for altering the size of the chord 259.

[0106] FIG. 29B shows the back-isometric view of the handheld monitor. A button 263 is embedded on the other side surface 262 of the monitor. A set of a detachable auxiliary powering module comprising of solar module 1 266, solar module 2 267, actuator hinge 265 and actuator 264 are attached to the back surface of the device. The actuator 264 extends the solar module 2 267 through the actuator hinge 265 from plane of solar module 1 266 for harvesting more solar energy. The actuation of the solar module 2 267 occurs automatically or through control commands.

[0107] FIG. 29C shows the bottom isometric view of the handheld monitor. The bottom surface 268 of the monitor has a finger placement area 269 embedded with reflective bio-sensing apparatus 271. The area around the bio-sensors of the finger placement area 269 is surrounded by foam base or sponge 270. The foam base or sponge 270 is utilized to enhance the grip and reduce the real-time movement errors.

[0108] FIG. 30 shows the earphone embodiment of the telemetry apparatus. The earphone apparatus comprises of a reflective bio-sensing apparatus 272 with an ear placement area 273. The biosensing apparatus 272 is attached to the music ear-bud 276 through the ear hook clip 274. The fancy LED apparatus 275 is embedded inside the earphone near the ear hook 273. The device is covered with water proof coating 277. The ear-bud 276 and the ear hook 274 are used to securely hold the device on the sensing spot. The music ear-bud 276 is further utilized for perceiving audio output.

[0109] The above described invention disclosure is intended for illustration purposes, and for those skilled in the art may instantly perceive numerous suggestive modifications, variations and equivalents. Therefore, the disclosure is not exhaustive in broader aspects and the invention is not intended to limit to specific details, spectrometer instruments, illustrated hardware designs, described computational methods and embodiment forms. All equivalents and modifications are intended to be included within the scope of disclosure and attached claims. Accordingly, additional changes and modifications may be made without departing from the scope and the spirit of the invention disclosure appended in the document, claims and their equivalents.

INDUSTRIAL APPLICABILITY

[0110] The disclosure presents reflective sensing based low-powered and totally non-invasive continuous glucose monitoring solution. The described intelligent technology can be utilized as telemetry clinical instrumentation, neo-natal medical device, gestational diabetes monitoring apparatus, real-time diagnostic technology, portable medical apparatus, in-vitro and in-vivo biosensing instrument, general wellness management device, smart wearable device, server based real-time clinical diagnosis system, life-support device, health tracking software device, real-time intelligent medical reminder, automated recommendation system and software medical device.

PRIOR ART AND CITATION LIST

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[0117] CN 102217939 A (Shanghai Jiao Tong University) Oct. 19, 2011

[0118] U.S. Pat. No. 8,280,476 B2 (ArKal Medical Inc) Oct. 2, 2012

[0119] CN 103349553 A (Zhao Wei) Oct. 16, 2013

[0120] WO 2014105520 A1 (Omni Medsci, Inc.) Jul 3, 2014