Computerized system and method for determining whether a consumable may be safely administered to a body site of a patient

• US 20070187477A1
• Filed: 02/10/2006
• Published: 08/16/2007
• Est. Priority Date: 01/29/2004
• Status: Active Grant

• Current Assignee: Cerner Innovation, Inc. (Oracle Corporation)
• Original Assignee: Cerner Innovation, Inc. (Oracle Corporation)
• Inventors: Kline, Kris, Fox, Charles, Durrell, Deborah, Rogers, Stephanie
• Granted Patent: US 7,506,807 B2
• Time in Patent Office: Days
• US Class Current: 235/375
• CPC Class Codes: G06Q 10/06 Resources, workflows, human or project management; Enterprise or organisation planning; Enterprise or organisation modelling
• CPC Class Codes: G16H 10/65 stored on portable record carriers, e.g. on smartcards, RFID tags or CD
• CPC Class Codes: G16H 40/20 for the management or administration of healthcare resources or facilities, e.g. managing hospital staff or surgery rooms
• CPC Class Codes: G16H 50/30 for calculating health indices; for individual health risk assessment

Abstract

A method and system in a computerized health care environment for determining whether a consumable may be safely administered to a body site of a patient is provided. A patient identifier to identify a patient and a consumable identifier identifying a consumable are received. A body site identifier identifying a location on the body of the patient to which the attachment is to be placed is received. The patient identifier, consumable identifier and body site identifier are utilized to determined whether the consumable may be safely administered to the body site of the patient.

Claims

1. A method in a computerized health care environment for determining whether a consumable may be safely administered to a body site of a patient, the method comprising:

receiving a patient identifier to identify a patient;

receiving a consumable identifier identifying a consumable;

receiving a body site identifier identifying a location on the body of the patient to which the attachment is to be placed; and

determining whether the consumable may be safely administered to the body site of the patient.

2. The method of claim 1, wherein the patient identifier is a bar code scanned with a portable information device.

3. The method of claim 1, wherein the consumable identifier is a bar code scanned with a portable information device.

4. The method of claim 1, wherein the body site identifier is a bar code scanned with a portable information device.

5. The method of claim 1, wherein if it is determined that the consumable may be safely administered to the body site of the patient, notifying the caregiver of such.

6. The method of claim 1, wherein if it is determined that the consumable may not be safely administered to the body site of the patient, notifying the caregiver of such.

7. The method of claim 6, wherein the notification is displayed on a portable information device.

8. The method of claim 1, further comprising accessing the patient'"'"'s electronic medical record and data for the consumable and body site to determine whether the consumable may be safely administered to the body site of the patient.

9. The method of claim 1, wherein the consumable is a substance administered to the patient.

10. A computerized system for collecting data from a patient identifier, an attachment identifier, and a body site identifier, the system comprising:

a central information system containing patient data, consumable data and body site data;

a patient identifier linking a patient to patient data in the central information system;

a consumable identifier linking the consumable to the consumable data in the central information system;

a body site identifier linking the site to body site data in the central information system; and

an information device for collecting data from the patient identifier and communicating with the central information system to access the patient data, consumable data and body site data.

11. The system of claim 10, further comprising:

an attachment identifier linking an attachment to attachment data in the central information system.

12. The system of claim 10, wherein the patient identifier, consumable identifier and body site identifier are bar codes scanned with the portable information device.

13. The system of claim 10, wherein the consumable is a substance administered to the patient.

14. The system of claim 11, wherein the patient data, attachment data and body site data from the central information system are utilized to determine whether the attachment may be safely attached to the body site of the patient.

15. A method for retrieving and transmitting patient data in a healthcare computing environment, the method comprising:

retrieving a patient identifier with a portable information device, wherein the patient identifier identifies a patient;

retrieving a consumable identifier with a portable information device, wherein the consumable identifier identifies a consumable to be administered to the patient;

retrieving a body site identifier with a portable information device, wherein the body site identifier identifies a body site of the patient;

communicating the patient identifier, the consumable identifier and the body site identifier to a central information system; and

receiving current patient related information from the central information system at the portable information device.

16. The method of claim 15, wherein the current patient related information from the central information system at the portable information device comprises data identifying whether the consumable may be safely administered to the body site of the patient.

17. The method of claim 15, wherein the patient identifier is a bar code scanned with a portable information device.

18. The method of claim 15, wherein the consumable identifier is a bar code scanned with a portable information device.

19. The method of claim 15, wherein the body site identifier is a bar code scanned with a portable information device.

20. The method of claim 15, wherein the consumable is a substance to be administered to the patient.