Medical emergency alert system and method

• US 20090322513A1
• Filed: 06/11/2009
• Published: 12/31/2009
• Est. Priority Date: 06/27/2008
• Status: Abandoned Application

• Current Assignee: Ching Ching Huang, Franklin Dun-Jen Hwang
• Original Assignee: Ching Ching Huang, Franklin Dun-Jen Hwang
• Inventors: Hwang, Franklin Dun-Jen, Huang, Ching Ching
• Application Number:
  US12/456,057
• Publication Number:
  US 20090322513A1
• Time in Patent Office: Days
• US Class Current: 340/539.12
• CPC Class Codes: A61B 2560/0456 Apparatus provided with a docking unit
• CPC Class Codes: A61B 5/0022 Monitoring a patient using a global network, e.g. telephone networks, internet
• CPC Class Codes: A61B 5/02055 Simultaneously evaluating both cardiovascular condition and temperature
• CPC Class Codes: A61B 5/1112 Global tracking of patients, e.g. by using GPS
• CPC Class Codes: A61B 5/1117 Fall detection
• CPC Class Codes: A61B 5/681 Wristwatch-type devices
• CPC Class Codes: G08B 25/001 Alarm cancelling procedures or alarm forwarding decisions, e.g. based on absence of alarm confirmation
• CPC Class Codes: G08B 25/016 Personal emergency signalling and security systems emergency non-personal manually actuated alarm activators G08B25/12
• CPC Class Codes: G16H 40/67 for remote operation
• CPC Class Codes: H04W 4/90 Services for handling of emergency or hazardous situations, e.g. earthquake and tsunami warning systems [ETWS]

Abstract

A medical emergency reporting system and methodology that utilize a wearable monitoring device to continuously monitor key physiological parameters of a person, and when measurements exceed programmed threshold levels, it will automatically issue a medical emergency alert along with location information to a remote monitoring center via a wireless network and the Internet for immediate local response. This system will also provide manual emergency alert activation, continuous updates with key physiological measurements to the emergency response personnel along with the medical history of the subject as well as redundancy in emergency alert reporting and malfunction diagnosis to assure ultimate accuracy, immediacy and reliability for the person that requires medical assistance.

Claims

1. A transparent and automated personal medical emergency alert system consists of:

(1) a wearable monitoring device contains data processing and controlling as well as radio frequency transceiver/antenna circuitries which are integrated with sensors within a single or multiple enclosures to measure, on a periodic basis, a person'"'"'s physiological parameters, such as pulse rate, heart rate, EKG, blood pressure, blood oxygen level, breathing rate and/or body temperature. It will compare the measurements against the threshold levels stored or pre-programmed in its memory to determine whether abnormality or severe abnormality has occurred and will wirelessly transmit via radio frequency (RF) signals corresponding to medical emergency alert, abnormal readings or normal measurements along with its unique identification code. Each monitoring device (consequently each person wearing this device) will be assigned a unique identification code, and it will not process or react to any incoming RF signals without its unique identification code as part of signals. This wearable monitoring mean is also integrated with an impact sensor for detecting a severe fall as well as a microphone to detect loud scream to issue an emergency alert for assistance. Also included in this wearable monitoring mean is a simple keypad for manually issuing emergency alert, temporarily suspending measurements and for manually entering ranges of blood glucose measurement (high, normal or low) after being prompted (by built-in vibration and/or audio component) periodically to conduct the measurement with a blood glucose meter.

(2) a battery charger that can rapidly charge up the built-in battery of the wearable monitoring device, a spare battery or a spare wearable monitoring device with same identification code to allow un-interrupted monitoring.

(3) a network of distributed wireless RF relay transceivers which will receive the signals from the wearable monitoring devices, determine the strength of each received signal and retransmit the signal along with its own unique identification code and signal strength data (thus providing the location data to the remote monitoring center) at a different frequency and power level (maybe utilizing a separate antenna tuned and oriented for long distance transmission) to another relaying transceiver for furthering distance of transmission or an Internet gateway directly.

(4) an Internet gateway which will convert the received RF signals from the distributed relay transceivers into proper protocol (such as TCP/IP) and transmit the data to a remote monitoring center via the Internet or an intranet.

(5) a remote monitoring center will process and archive the data received from various gateways according to the following software routines;

(i) if an emergency alert is received, it will flash in a prominent alarm color (such as red) the person'"'"'s identification, calculated location (derived from the signal strength, position of the reporting relays and historical movement track of the subject, or from the Global Positioning Satellite receiver incorporated within a wearable monitoring device), type of medical emergency and the information corresponding local emergency response team on the monitoring screen for the monitoring personnel to react immediately. The remote monitoring center will also continuously forward the physiological measurement data and medical history of the person in need of assistance to the local response team;

(ii) if abnormalities in physiological measurements are received, it will flash in a less alarming color (such as amber) the person'"'"'s identification, calculated location, type of medical abnormalities and the corresponding local resident response personnel information on the monitoring screen for the monitoring personnel to respond immediately;

(iii) if normal measurements are received, it will simply calculate location and archive the data without cautionary display on the monitoring screen.

(6) a local emergency response team which consists of at least one contracted ambulatory firm and a resident response personnel (a nurse, nurse-aid or a medical technologist). This team will respond to the direction of the remote monitoring center to render immediate assistance to the person in need.

2. The automated emergency alert threshold as described in claim 1 can be pre-programmed into a wearable monitoring device based on the physical conditions (such as age, gender, ethnicity, weight and special medical conditions) of the subject being monitored, or it can be derived from a general set of criteria based on subjects of similar age, gender, ethnicity, weight and normal medical conditions while adjusted automatically by the software residing in the remote monitoring center based on the average of measurements after a period (such as a few days) of continuous monitoring or after a history of measurements can be established. The threshold levels can also be manually adjusted by the subject or his/her physician (through either keypad of the wearable sensor device or through the Internet access) to accommodate prescription of new medication, treatment or new circumstances.

3. The automated emergency alert threshold as described in claim 1 can be further adjusted corresponding to typical activity levels of the subject throughout a day.

4. The automated emergency alert threshold as described in claim 1 can also be temporarily suspended by the subject under monitoring using the keypad on the monitoring device through a sequence of key strokes prior to exercises or extraneous activities. The key stroke sequence can also be used to cancel an alarm.

5. The system described in claim 1 can further utilize radio frequencies designated by the U.S. Federal Communication Commission for short distance communication without special licensing, such as 2.4 GHz, 315 MHz, etc.

6. The system described in claim 1 can further have its relaying transceivers distributed to provide redundancy in coverage area to allow each reporting signal from a wearable monitoring device to be received by at least two or more relaying transceivers to ascertain that each reporting signal will be properly relayed to the monitoring center. Each relaying transceiver will be powered by a combination of a rechargeable battery and a switching AC/DC power source to assure its functionality at all time.

7. To avoid mis-identification of subject and his/her medical status, the relaying transceivers described in claim 1 can further employ a hand-shaking method of having the monitoring device first transmit its identification code for a period of a few seconds at a specific frequency rate (such as once every second) when reporting until one or more relay transceivers responds by a “

O.K. send report”

signal in conjunction with this monitoring device ID code. The monitoring device will then transmit its data string repeatedly in burst mode (such as 10-50 microsecond burst) until all responding relaying transceivers each sends a “

received”

signal back (again including the ID code of the monitoring device). This hand-shaking method assures that each reporting signal strings are received properly by one or more relaying transceiver, matched with monitoring device ID code and forwarded to the remote monitoring center accurately.

8. The medical emergency alert system described in claim 1 can further have multiple tiers of relaying transceiving devices. Each relaying transceiver will have two separate antenna tuned to transmit and receive at two different frequencies. Whereas the first tier devices will be tune to receive signals from wearable monitoring devices (such as at 2.4 GHz) and to transmit at a different frequency (such as 315 MHz) to a second tier relaying transceiver, which, in turn, is tuned to receive at this frequency (e.g. 315 MHz) and transmit at another frequency.

9. The relaying transceiver described in claim 1 can further have a unique identification code assigned to each, and it will employ the following hand-shaking method to assure accurate signal transmission and avoid interference from other transmitting devices:

it will first transmit its identification code for a period of a few seconds at a specific frequency rate (such as once every second) when relaying a set of signals received from one or more monitoring devices until a next tier relay transceivers responded with a “

O.K. send report”

signal in conjunction with the ID code of this first tier relaying transceiver. Then, it will transmits its data strings repeatedly in burst mode (such as 10-50 microsecond burst) till the responding next tier relay transceivers sends a “

received”

signal back (again including the ID code of the relaying transceiver device). This hand-shake method will be repeated from one tier to the next in relaying the data received from the monitoring device on either direction of communication.

10. The wearable monitoring device described in claim 1 can be in the form of wrist band, integrated with a watch module to form a wrist watch, an arm band, a leg band, a head band or a torso belt. Its sensors, processing and transceiving circuitry along with display, keypad and rechargeable battery will be enclosed in a waterproof structure. Furthermore, its can have an inscription of the name of the subject along with key medical information and contact phone numbers on its exterior.

11. The wearable monitoring device described in claim 1 can further include a battery level monitoring circuitry along with audio, video and/or vibration prompts to alert the person wearing the device to recharge the battery as well as transmitting a code for the remote monitoring center to remind the subject of this impending malfunction.

12. The wearable monitoring device described in claim 1 can further be connected (wirelessly or wired) to separate sensor pads (in addition to the sensors integrated within), such as transducers for recording electrocardiogram (EKG), for measuring breathing rate and/or blood pressure sensor. The measurements received will be transmitted periodical in conjunction with those derived from the integrated sensors. These separated sensor pads can be in disposable format or equipped with a rechargeable battery for reuse.

13. The wearable monitoring device described in claim 1 can also be programmed to periodically remind (such as by audio, video and/or vibration prompts) a diabetic subject to perform a manual blood glucose measurement with a glucose meter and enter the data on the keypad of the wearable device for transmission. The prompts will be repeated until a data entry act has been done.

14. The wearable monitoring device described in claim 1 can further include a speaker in conjunction with a built-in microphone to achieve two way verbal communications with the remote monitoring center and/or the emergency response personnel. The verbal communications will be digitized into a signal string and incorporate the unique identification code of a monitoring device (thus, the subject). The wearable monitoring device will only decode any incoming signals incorporated with its unique identification code, thus achieving exclusivity in two way verbal or text communications.

15. The wearable monitoring device described in claim 1 can further include a GPS receiver to determine its location and provide redundant position data for the remote monitoring center.

16. The method in determining the location of a subject issuing emergency alert as described in claim 1 can also be a combination of using signal strength received by the overlapping relaying transceivers at fixed locations (the intersection of two or more circles of different radii from each relaying transceiver, which signify different signal strengths) and movement track of the subject from his/her immediate past periodic reports.

17. The critical malfunctions for the system described in claim 1 can be diagnosed by determining whether there are periodic reporting signals from a specific wearable monitoring device or the reporting signal provides no physiological measurement data. In the event of no signal, the software resided at the remote monitoring center will examine the past reports from the device in question to see whether it is due to battery drain (continuous decline in signal strength or receiving battery drain signal from the monitoring device), moving out of the coverage area (movement track of the subject) or device failure (sudden cease of signal). In the case of no physiological measurement data, again the prior reports will indicate whether it is due to sudden device failure or simply the subject no longer wearing the monitoring device. The remote monitoring center will notify the local resident emergency response personnel about the type of malfunction and to contact the subject to resolve the problem, which can be simply replacing the wearable monitoring device with a spare device having the same identification code or change the battery.

18. The remote monitoring center described in claim 1 can further include software and/or resident physicians to provide likely medical diagnosis based on received physiological measurements to assist the local emergency response team in giving timely and proper treatment.

19. A relaying transceiver described in claim 1 can be in the form of an integrated component within a cellular phone to relay the physiological measurements and emergency alert signals to the remote monitoring center via cell phone networks. This relaying transceiver can be activated automatically by a special signal code, which the perimeter relaying transceivers of a coverage area transmits continuously, so when a subject is departing the coverage area, his/her physiological measurement and emergency alert signals can be received by the remote monitoring center without interruption. Furthermore, the cellular network will be able to provide location information (by triangulation) as part of the alert information package in addition to the GPS location data transmitted by the wearable monitoring device. This approach will further expand the coverage area of the system (thus freedom of movement of the subjects under monitoring) described in claim 1 to wherever cell phone signals can be received.

20. The employment of the system described in claim 1, as a paid service, can be subscribed by individuals, a community or by an entity such as a recreation and entertainment facility to provide medical emergency alert and security coverage.

21. The employment of the system described in claim 1 as an integral part of service for a retirement community, a mental hospital and/or nursing care facility to permit its residents or patients freedom of movement while providing continuous medical monitoring and emergency alert response.

22. The system described in claim 1 can also be linked to a home security and/or fire alarm monitoring system to provide a comprehensive safety monitoring for an individual/family.

23. Utilizing pre-arranged security codes (such as passwords), relatives, police, or legal guardians of a person suffering Alzheimer'"'"'s or dementia can use the system described in claim 1 to monitor, locate and track the movement of the subject via the Internet.

24. Utilizing pre-arranged security codes (such as passwords), personal physicians of a subject person under monitoring by the system described in claim 1 can access the archived physiological measurements via the Internet to track the wellness of the person, particularly after new medication or treatment is instituted.