SYSTEM AND APPARATUS FOR PROVIDING DIAGNOSIS AND PERSONALIZED ABNORMALITIES ALERTS AND FOR PROVIDING ADAPTIVE RESPONSES IN CLINICAL TRIALS

• US 20140221858A1
• Filed: 04/10/2014
• Published: 08/07/2014
• Est. Priority Date: 11/10/2009
• Status: Active Grant

• Current Assignee: Makor Issues & Rights Ltd.
• Original Assignee: Makor Issues & Rights Ltd.
• Inventors: MYR, David
• Granted Patent: US 9,131,843 B2
• Time in Patent Office: Days
• US Class Current: 600/513
• CPC Class Codes: A61B 5/0006 ECG or EEG signals
• CPC Class Codes: A61B 5/0205 Simultaneously evaluating both cardiovascular conditions and different types of body conditions, e.g. heart and respiratory condition
• CPC Class Codes: A61B 5/021 Measuring pressure in heart or blood vessels A61B5/0205 takes precedence
• CPC Class Codes: A61B 5/022 by applying pressure to close blood vessels, e.g. against the skin; Ophthalmodynamometers
• CPC Class Codes: A61B 5/318 Heart-related electrical modalities, e.g. electrocardiography [ECG]
• CPC Class Codes: A61B 5/681 Wristwatch-type devices
• CPC Class Codes: A61N 2005/0626 Monitoring, verifying, controlling systems and methods

Abstract

A personalized real-time automated cardiovascular monitoring system monitors abnormalities in a patient'"'"'s cardiovascular activity data through the use of individually adjusted electrocardiogram Holter apparatus (Holter/ECG device) that provides an automatic medical diagnosis of cardiac abnormalities and generates abnormality alert signals representative of certain abnormalities in patient'"'"'s cardiac activities. The signals are transmitted using a wireless network through a bi-directional wireless protocol. Individual parameters indicative of patient'"'"'s cardio activities are personalized to allow for adjustments of chronic patients. A base Holter/ECG unit, includes the wireless/electric electrodes and their respective wireless/electric connections, and a Holter/ECG recording unit affixed to the base unit. Data is collected and subjected to statistical analysis.

Claims

1. A method for automatic detection of adverse effects and risks of adverse effects resulting from use of at least one medication or medical treatment, based on automatic cardiac abnormality alert detection from Holter/ECG data, and for providing automatic real-time medical response in clinical trials, said method comprising the steps of:

a) identifying the at least one medication or medical treatment for the clinical trial;

b) identifying a safe use profile for the at least one medication or medical treatment;

c) identifying a group of clinical trial participants that use the at least one medication or medical treatment and creating a database of the clinical trial participants;

d) identifying parameters of the safe use profile for the at least one medication or medical treatment used by the group of clinical trial participants;

e) supplying each clinical trial participant with a Holter/ECG-type device which generates said Holter/ECG data, said Holter/ECG-type device including a wireless device that is part of a wireless phone network each Holter/ECG-type device having respective buttons including a Medicine button for pressing when the patient has taken any particular medicine, a Sports button for pressing when the patient will be engaged in a sporting activity;

a Meal button for pressing when the patient will have a meal and;

a Sleep button for pressing when the patient will start/finish his sleep;

f) automatically and in real-time monitoring the group of clinical trial participants and the respective buttons and obtaining abnormality alerts data from the Holter/ECG-type devices;

g) determining whether the abnormality alerts data is within the parameters of the safe use profile for each of the participants;

h) providing an emergency medical alert if the abnormality alerts data constitutes an adverse effect risk; and

i) collecting the alerts data for the group of participants and performing statistical analysis on the group of participants.

2. The method of claim 1, further comprising the step of:

j) transmitting wirelessly to the participant a clinical trial medical order to change a dosage of said medication or medical treatment.

3. The method of claim 1, further comprising the step of:

j) transmitting wirelessly to the participant a clinical trial medical order to stop taking said medication or medical treatment.

4. The method of claim 1, further comprising the step of:

j) transmitting wirelessly to the participant a clinical trial medical order to start taking another medication or medical treatment.

5. The method of claim 1, further comprising the step of:

j) pulling the participant out of the clinical trial based at least in part on the abnormality alerts data.

6. The method of claim 1, further comprising the step of:

j) stopping the clinical trial based at least in part on the abnormality alerts data.

7. The method of claim 1, wherein the wireless device further includes a blood pressure apparatus, and further comprising the step of:

j) transferring a blood pressure measurement taken with the blood pressure apparatus wirelessly to the medical emergency center after the generation of the medical abnormality alert.

8. The method of claim 7, wherein the blood pressure apparatus comprises:

an inflatable cuff chamber operable to be inflated during an inflation interval and deflated during a deflation interval;

a sensor coupled to said inflatable cuff chamber and configured to measure a blood pressure; and

a control electronic module configured for controlling the operation of said inflatable cuff chamber and said sensor.

9. The method of claim 7, further comprising the step of:

k) taking a permanent continuous blood pressure measurement in predetermined time-intervals.

10. The method of claim 9, further comprising the step of:

l) transmitting wirelessly a personalized abnormality blood pressure alert to the medical emergency center based on personalized blood pressure measurements thresholds.

11. The method of claim 10, further comprising the steps of:

m) obtaining as an input from the centralized database initial patient personalized blood pressure emergency alerts thresholds;

n) obtaining as an input real-time cardiological data of the patient from the continuous blood pressure measurement, including the initial patient personalized blood pressure emergency alerts thresholds;

o) updating said initial patient personalized blood pressure emergency alerts thresholds with the real-time cardiological data.