System and method for managing a patient with chronic disease

• US 7,716,071 B2
• Filed: 10/04/2005
• Issued: 05/11/2010
• Est. Priority Date: 10/04/2004
• Status: Active Grant

• Current Assignee: Liana Gold
• Original Assignee: Liana Gold
• Inventors: Gold, Liana
• Primary Examiner(s): O'Connor; Gerald J.
• Assistant Examiner(s): Najarian; Lena
• Application Number:
  US11/243,254
• Publication Number:
  US 20060085225A1
• Time in Patent Office: 1,680 Days
• Field of Search: 705/2, 705/3, 600/300
• US Class Current: 705/3
• CPC Class Codes: G06Q 10/10 Office automation; Time management
• CPC Class Codes: G16H 10/20 for electronic clinical trials or questionnaires
• CPC Class Codes: G16H 10/40 for data related to laboratory analysis, e.g. patient specimen analysis
• CPC Class Codes: G16H 10/65 stored on portable record carriers, e.g. on smartcards, RFID tags or CD
• CPC Class Codes: G16H 20/10 relating to drugs or medications, e.g. for ensuring correct administration to patients

Abstract

A system, method and apparatus for managing a patient affected with a disease. In one aspect, the invention is directed to an apparatus for managing a patient, the apparatus comprising a system that provides: A) a means for enrolling a patient into a system including storing general information about the patient into the system'"'"'s database; B) a means for storing a schedule for the patient; C) a means for reminding the patient to execute the patient care activities; D) a means for retrieving patient information comprising responses to side effects questionnaires and laboratory results; E) a means for storing the patient information into the system; F) a means for analyzing the patient information and generating a recommendation; G) a means for submitting the recommendation to a provider for approval; and H) a means for receiving approval or a modified recommendation and sending the recommendation or modified recommendation to the patient.

Claims

1. A computer program product, tangibly embodied in a computer readable storage medium, the computer program product being operable to cause a data processing apparatus, in a network of interconnected computers to:

A) enroll a patient into a system by storing general information about the patient comprising medical history, reaction to drugs, symptoms and side effects, test results, contact information and family history into the system'"'"'s database;

B) prompt a provider to specify a preferred method of external communication;

C) develop a schedule of patient care activities that is specific to the patient comprising routine laboratory work, side effects questionnaires and regular injections and appointments wherein the side effects questionnaires comprise asking the patient questions related to the patient'"'"'s symptoms and side effects;

D) repeatedly inquire whether information including laboratory results and responses to the side effects questionnaires are available for processing;

E) optionally remind an entity of scheduled patient care activities;

F) retrieve and store patient information comprising the responses to the side effects questionnaires and the laboratory results;

G) analyze the patient information by applying a set of algorithms to the patient information;

H) generate a recommendation based on the analysis in step G) comprising a dosage adjustment, instructions on an administration of a treatment, advising for more tests and an intervention instruction wherein the intervention instruction is an adjusted treatment instruction aimed at ameliorating side effects and detecting and preventing potential adverse outcomes from an administered therapy;

I) submit the recommendation to the patient directly and/or to the provider for an approval or a modified recommendation; and

J) receive the approval of the recommendation or the modified recommendation from the provider and send the recommendation or the modified recommendation to the patient.

2. The computer program product of claim 1, wherein in step H) the recommendation is marked as critical status and the patient information is sent to the provider in real-time using the provider'"'"'s preferred method of external communication.

3. The computer program product of claim 1, wherein laboratory information including whether a laboratory facility has an electronic interface to communicate with the system is stored in the system'"'"'s database.

4. The computer program product of claim 1, wherein a frequency at which the side effects questionnaires are scheduled depends upon the patient'"'"'s needs.

5. The computer program product of claim 1, wherein the side effects questionnaires ask questions specific to the patient'"'"'s disease and to the patient'"'"'s symptoms.

6. The computer program product of claim 1, which is further able to receive a question from the patient, match the question with a stored answer when the stored answer exists and forward the question to an appropriate medical staff member when the stored answer does not exist.

7. The computer program product of claim 1, wherein the entity is selected from the group consisting of the patient, the provider and a third-party.

8. The computer program product of claim 1, which is accessible via a network.

9. The computer program product of claim 8, wherein the network is the internet.

17. The computer program of claim 1, wherein the side effects questionnaires are modeled after questions asked by the provider during routine follow-up visits.

18. The computer program of claim 1, wherein the system determines whether the patient needs a medication refill and if so, generates and sends a refill request directly to a pharmacy.

19. The computer program of claim 6, which is further able to receive an answer to the patient'"'"'s question from the medical staff member, stored the answer to the patient'"'"'s question on the system, and provide the patient access to the answer.

21. The computer program product of claim 5, wherein the provider can modify, add or delete questions asked in the side effects questionnaires.

22. The computer program product of claim 1, wherein a question asked in the side effects questionnaires is dependent upon a response to a previous question.

23. The computer program product of claim 1, wherein step A) further includes storing information about the provider, a medical staff, a laboratory facility and a pharmacy in the database.

10. An apparatus for managing a patient, the apparatus comprising a system that provides:

A) a means for enrolling a patient by storing general information about the patient comprising medical history, reaction to drugs, symptoms and side effects, test results, contact information and family history into a database;

B) a means for developing and storing a schedule for the patient, wherein the schedule determines an execution date for a plurality of patient care activities comprising routine laboratory work, symptoms and side effects questionnaires and regular injections and appointments;

C) a means for reminding an entity to execute the patient care activities;

D) a means for retrieving patient information comprising responses to the symptoms and side effects questionnaires and laboratory results;

E) a means for storing the patient information into the system;

F) a means for analyzing the patient information by applying a set of algorithms to the patient information;

G) a means for generating a recommendation on an output from the analyzing means wherein the recommendation comprises a dosage adjustment, instructions on an administration of a treatment, advising for more tests and an intervention instruction;

H) a means for submitting the recommendation directly to the patient and/or to a provider for an approval;

I) a means for receiving the approval of the recommendation or a modified recommendation from the provider; and

J) a means for sending the approval or the modified recommendation to the patient.

11. The apparatus of claim 10, wherein the recommendation is marked as critical status and the patient information is sent to the provider in real-time.

12. The apparatus of claim 10, further comprising a means for determining whether a laboratory facility has an electronic interface to communicate with the system.

13. The apparatus of claim 10, which further provides a means to receive a question from the patient and match the question with a stored answer when the stored answer exists and forward the question to the provider when the stored answer does not exist.

14. The apparatus of claim 10, wherein the entity is selected from the group consisting of the patient, the provider and a third-party.

15. The apparatus of claim 10, which includes a network.

16. The apparatus of claim 10, wherein the network is the internet.

20. A computer program product, tangibly embodied in a computer readable storage medium, the computer program product being operable to cause a data processing apparatus, in a network of interconnected computers to:

A) enroll a patient into a system by storing general information about the patient comprising medical history, reaction to drugs, symptoms and side effects, test results, contact information and family history into a database;

B) prompt a provider to specify a preferred method of external communication;

C) develop a schedule of patient care activities comprising routine laboratory work, side effects questionnaires, regular injections and appointments;

D) retrieve and store the patient'"'"'s laboratory results;

E) analyze the laboratory results by applying a first set of algorithms to the laboratory results;

F) generate a first recommendation for a first dosage adjustment or a first intervention instruction based on the analysis in step E);

G) submit the first recommendation to the provider for approval or a first modified recommendation;

H) receive the approval of the first recommendation or the first modified recommendation from the provider and send the first recommendation or the first modified recommendation to the database;

I) contact the patient with questions from the side effects questionnaires;

J) retrieve and store responses to the side effects questionnaires;

K) analyze the responses to the side effects questionnaires by applying a second set of algorithms to the responses to the side effects questionnaires;

L) generate a second recommendation for a second dosage adjustment or a second intervention instruction based on the analysis in step K);

M) submit the second recommendation directly to the patient;

N) submit the second recommendation to the provider for approval or a second modified recommendation;

O) receive the approval of the second recommendation or the second modified recommendation from the provider; and

P) reconcile the first recommendation or the first modified recommendation with the second recommendation or the second modified recommendation to derive a coordinated recommendation and submit the coordinated recommendation to the system and to the patient.