Computerized system and method for documenting patient vital signs during blood product administration and transfusion

• US 8,032,306 B2
• Filed: 12/29/2004
• Issued: 10/04/2011
• Est. Priority Date: 12/29/2004
• Status: Active Grant

• Current Assignee: Cerner Innovation, Inc. (Oracle Corporation)
• Original Assignee: Cerner Innovation, Inc. (Oracle Corporation)
• Inventors: Fry, Jeffrey D., Hauck, Arthur J., Cross, Lori N.
• Primary Examiner(s): Clow; Lori A
• Application Number:
  US11/025,096
• Publication Number:
  US 20060149588A1
• Time in Patent Office: 2,470 Days
• Field of Search: None
• US Class Current: 702/19
• CPC Class Codes: A61B 5/02055 Simultaneously evaluating both cardiovascular condition and temperature
• CPC Class Codes: A61M 1/02 Blood transfusion apparatus blood infusion by syringes A61M5/14
• CPC Class Codes: A61M 2205/6009 for matching patient with his treatment, e.g. to improve transfusion security
• CPC Class Codes: A61M 2205/6072 Bar codes
• CPC Class Codes: A61M 5/1723 using feedback of body parameters, e.g. blood-sugar, pressure measurement of body parameters A61B5/00
• CPC Class Codes: G16H 10/40 for data related to laboratory analysis, e.g. patient specimen analysis
• CPC Class Codes: G16H 10/60 for patient-specific data, e.g. for electronic patient records
• CPC Class Codes: G16H 20/30 relating to physical therapies or activities, e.g. physiotherapy, acupressure or exercising
• CPC Class Codes: G16H 40/67 for remote operation

Abstract

A computerized system and method for processing patient vital signs during blood product administration in a computerized healthcare environment is provided. A blood product to be administered to a patient is identified. The patient is identified. Vital signs for the patient are received during blood product administration by a healthcare provider and automatically, without user intervention, the vital signs for the patient are documented in a database.

Claims

1. One or more computer-storage media having computer-executable instructions for performing a method for processing patient vital signs during blood product administration in a computerized healthcare environment, the method comprising:

identifying a blood product to be administered to a patient by receiving, at a remote computer at the patient'"'"'s bedside, a blood product identifier identifying the blood product to be administered to the patient;

identifying the patient by receiving, at the remote computer at the patient'"'"'s bedside, a patient identifier identifying the patient;

communicating the blood product identifier and the patient identifier to a blood bank database to maintain a record of the blood product administration;

communicating a start time of the blood product administration to the blood bank database;

receiving vital signs, at the remote computer at the patient'"'"'s beside, at a first time instance for the patient identified at the patient'"'"'s bedside during administration of the blood product identified at the patient'"'"'s bedside by a healthcare provider;

determining whether the vital signs at the first time instance for the patient during the blood product administration are within an acceptable range by comparing the vital signs received at the remote computer at the patient'"'"'s beside with an acceptable range of vital signs during blood product administration;

upon determining that the vital signs at the first time instance for the patient during the blood product administration are within the acceptable range, determining whether the blood product administration is complete;

upon determining that the blood product administration is not complete, notifying the blood bank database that the blood product administration is not complete such that the blood bank database includes accurate information regarding blood product administration status and receiving, at the remote computer at the patient'"'"'s beside, vital signs at a second time instance for the patient during the blood product administration;

determining whether the vital signs at the second time instance for the patient obtained during the blood product administration are within the acceptable range by comparing the vital signs at the second time instance received from the remote computer at the patient'"'"'s beside with the acceptable range of vital signs during blood product administration;

upon a determination that the vital signs at the second time instance are not within the acceptable range, displaying a notification at the bedside of the patient to the healthcare provider currently administering the blood product to the patient; and

automatically, without user intervention, documenting in a patient database the vital signs for the patient and whether the vital signs for the patient are within the acceptable range.

2. The media of claim 1, wherein the patient database is the patient'"'"'s electronic medical record.

3. The media of claim 1, further comprising:

receiving and documenting identification of a healthcare provider taking the patient vital signs.

4. The media of claim 1, further comprising:

receiving and documenting identification of a healthcare provider administering the blood product.

5. The media of claim 1, further comprising:

receiving and documenting patient vital signs before blood product administration.

6. The media of claim 5, further comprising:

receiving and documenting identification of the healthcare provider taking the patient vital signs before the blood product administration.

7. The media of claim 1, further comprising:

receiving the time and date when the patient vital signs were taken.

8. The media of claim 1, further comprising:

receiving and documenting the identification of the healthcare provider completing the blood product administration.

9. The media of claim 1, wherein the patient vital signs are input using a remote computing device.

10. The media of claim 1, wherein the patient vital signs are received directly from a healthcare device.

11. The media of claim 1, wherein the patient is identified by a patient identification number.

12. The media of claim 11, wherein the patient identification number is received by scanning a bar code on a patient identification bracelet.

13. The media of claim 1, wherein the blood product is identified by a blood product identification number assigned by the blood product supplier.

14. A computing device for processing patient vital signs during blood product administration, the computing device comprising:

a first identifying component for identifying a blood product to be administered to a patient;

a second identifying component for identifying the patient;

a first communicating component for communicating an identifier identifying the identified blood product to be administered to the patient, a patient identifier identifying the patient, and a start time of a blood product administration of the identified blood product to the identified patient;

a receiving component for receiving vital signs for the patient during the blood product administration by a healthcare provider;

a first determining component for determining whether the vital signs for the patient obtained during the blood product administration are within an acceptable range;

a second determining component for determining whether the blood product administration is complete based upon a determination that vital signs for the patient obtained during the blood product administration are within the acceptable range;

a second communicating component for communicating an indication that the blood product administration is not complete to the blood bank database;

a displaying component for notifying the healthcare provider currently administering the blood product that the vital signs for the patient are not within an acceptable range; and

a documenting component for automatically, without user intervention, documenting in a database the vital signs for the patient and whether the vital signs for the patient are within the acceptable range.

15. The computing device of claim 14, wherein the database is the patient'"'"'s electronic medical record.

16. The computing device of claim 14, wherein the receiving component receives the patient vital signs for the patient from a remote computing device.

17. The computing device of claim 14, wherein the receiving component receives the patient vital signs directly from a healthcare device.

18. The computing device of claim 14, wherein the second identifying component identifies the patient by a patient identification number.

19. The computing device of claim 14, wherein the first identifying component identifies the blood product by a blood product identification number assigned by the blood product supplier.