Universal content architecture system

• US 10,445,749 B2
• Filed: 06/25/2013
• Issued: 10/15/2019
• Est. Priority Date: 06/25/2013
• Status: Active Grant

• Current Assignee: Cerner Innovation, Inc. (Oracle Corporation)
• Original Assignee: Cerner Innovation, Inc. (Oracle Corporation)
• Inventors: Basey, Wayne Franklin, Ruoff, Chad Barrett
• Primary Examiner(s): Sorey, Robert A
• Assistant Examiner(s): Rapillo, Kristine K
• Application Number:
  US13/926,382
• Publication Number:
  US 20140379359A1
• Time in Patent Office: 2,303 Days
• CPC Class Codes: G06Q 30/02 Marketing; Price estimation or determination; Fundraising
• CPC Class Codes: G16H 10/20 for electronic clinical trials or questionnaires
• CPC Class Codes: G16H 10/60 for patient-specific data, e.g. for electronic patient records
• CPC Class Codes: G16H 30/20 for handling medical images, e.g. DICOM, HL7 or PACS

Abstract

One or more systems, computer-storage media, and methods are described for receiving, storing, and distributing clinical information to clients subscribed to or granted access to the information. Initially, content packages containing clinical information are received and stored. Datasets are extracted from the content packages and stored. The datasets and content packages are made available to clients via an online marketplace which enables one or more clients to edit, update, or request to merge a plurality of datasets.

Claims

1. One or more non-transitory computer-storage media having computer-executable instructions embodied thereon that, when executed by a computing device, cause the computing device to perform a method of generating a regulatory compliant content package the method comprising:

receiving a first content package from a first content provider and a second content package from a second content provider;

performing a structural validation of the first and second content packages that determines the first and second content packages contain a correct number of datasets, and performing a content validation of the first and second content packages that determines the first and second content packages contain a correct type of clinical information, wherein, if the first content package fails the structural validation or the content validation, then a notification that the first content package is deficient is sent to the first content provider and the first content package is not published, and if the second content package fails the structural validation or the content validation, then a notification that the second content package is deficient is sent to the second content provider and the second content package is not published;

based on the first and second content packages passing validation, mining a first dataset from the first content package and a second dataset from the second content package;

associating the first dataset and the second dataset with a computer-usable reference to the first content package and the second content package, respectively, wherein the computer-usable reference links the first dataset to the first content package and the second dataset to the second content package;

extracting identifiers necessary to meet regulatory requirements from the first and second datasets;

merging at least a portion of the first dataset and at least a portion of the second dataset to generate a regulatory compliant content package, the regulatory compliant content package including the identifiers necessary to meet regulatory requirements, wherein merging the portion of the first dataset and the portion of the second dataset includes reformatting the regulatory compliant content package to eliminate duplicate information and replace null field values;

storing the regulatory compliant content package after eliminating the duplicate information and replacing the null field values; and

publishing the regulatory compliant content package in an online marketplace.

2. The one or more computer-storage media of claim 1, further comprising:

receiving a request for clinical information from a client via the online marketplace;

determining that the clinical information is stored in the first content package;

extracting the clinical information from the first content package; and

distributing the clinical information to the client.

3. The one or more computer-storage media of claim 1, further comprising:

receiving a request from a client to subscribe to information stored within the first content package;

receiving updated information associated with the first content package from the first content provider;

storing the updated information in association with the first content package; and

automatically communicating a notification to the client indicating that the updated information has been received.

4. The one or more computer-storage media of claim 3, further comprising:

receiving a request for the updated information from the client; and

distributing the updated information to the client.

5. The one or more computer-storage media of claim 4, further comprising:

replacing at least a portion of the first content package with the updated information, thereby generating a new version of the first content package; and

publishing the new version of the first content package on the online marketplace.

12. The one or more computer-storage media of claim 1, wherein the computing device also performs the step of removing duplicate data from the first content package and the second content package or from the first dataset and the second dataset.

13. The one or more computer-storage media of claim 1, wherein the computing device also performs the step of providing editorial tools to the first content provider, the editorial tools configured to allow the first content provider to edit the first content package or the first dataset.

14. The one or more computer-storage media of claim 1, wherein the first and second content packages are associated with prescription drug information.

15. The one or more computer-storage media of claim 14, wherein the identifiers necessary to meet regulatory requirements are drug identifiers.

19. The one or more computer-storage media of claim 1, wherein the extracted identifiers are drug identifiers, the drug identifiers including at least one of generic drug identifiers, drug synonym identifiers, or produce level identifiers.

20. The one or more computer-storage media of claim 19, further including mapping the drug identifiers to at least one of multiple ingredient generic drug identifiers, single ingredient generic drug identifiers, precise single ingredient generic drug and salt identifiers, or medication brand name identifiers.

6. One or more non-transitory computer-storage media having computer-executable instructions embodied thereon that, when executed by a computing device, cause the computing device to perform a method of generating and distributing a regulatory compliant content package to a client that is subscribed to the information, the method comprising:

determining that the client is subscribed to at least a portion of a regulatory compliant content package;

generating the regulatory compliant content package, wherein generating the regulatory compliant content package comprises;

updating a first content package with updated information associated with the first content package received from a first content provider,

updating a second content package with updated information associated with the second content package received from a second content provider,

performing a structural validation of the updated first content package and the updated second content package, wherein the structural validation determines the updated first and the updated second content packages contain a correct number of datasets,

performing a content validation of the updated first content package and the updated second content package, wherein the content validation determines the updated first and the updated second content packages contain a correct type of clinical information,

merging at least a portion of the updated first content package and at least a portion of the updated second content package to form a derivative content package, wherein merging the portion of the updated first content package and the portion of the updated second content package includes reformatting the derivative content package to eliminate duplicate information and replace null field values,

linking a first dataset to the first content package and linking a second dataset to the second content package with a computer-usable reference,

extracting from the updated first content package and the updated second content package identifiers necessary to meet regulatory requirements, and

mapping the identifiers necessary to meet regulatory requirements onto the derivative content package, resulting in the regulatory compliant content package;

storing the regulatory compliant content package after eliminating the duplicate information and replacing the null field values; and

distributing the regulatory compliant content package to the client.

7. The one or more computer-storage media of claim 6, wherein one or more of the first content package, the second content package, the derivative content package, or the regulatory compliant content package are published in an online marketplace.

8. The one or more computer-storage media of claim 6, wherein the at least the portion of the first content package includes at least one dataset of clinical information associated with the first content package.

16. The one or more computer-storage media of claim 6, wherein the identifiers necessary to meet regulatory requirements comprise one or more of generic drug identifiers, drug synonym identifiers, product-level identifiers, multiple ingredient generic drug identifiers, single ingredient generic drug identifiers, precise single ingredient generic drug and salt identifiers, or medication brand name identifiers.

17. The one or more computer-storage media of claim 6, wherein the computing device also performs the step of receiving a request from a client to subscribe to at least a portion of the regulatory compliant content package.

9. A system for delivering regulatory compliant content from a content provider to a client, the system comprising:

a computing device associated with an application server and a process management server, the application server and the process management server having one or more processors and one or more computer-storage media; and

a data store coupled to the application server, wherein the application server;

receives a request for regulatory compliant clinical information;

determines that the regulatory compliant clinical information is associated with at least a portion of a first content package and at least a portion of a second content package;

performs a structural validation of the first and second content packages that determines the first and second content packages contain a correct number of datasets, and performs a content validation of the first and second content packages that determines the first and second content packages contain a correct type of clinical information;

if the first content package and the second content package are successfully validated based on the structural validation and the content validation, then extract from the first content package and the second content package regulatory compliant identifiers;

maps at least a portion of the first content package and the second content package, including the regulatory identifiers, to a derivative dataset, wherein the derivative dataset comprises the regulatory compliant clinical information requested;

formats the derivative dataset to eliminate duplicate information;

stores the derivative dataset after eliminating the duplicate information;

links the first content package to the derivative dataset and the second content package to the derivative dataset; and

provides to the client the derivative dataset comprising the regulatory compliant clinical information.

10. The system of claim 9, wherein the process management server publishes the first content package in an online marketplace.

11. The system of claim 9, wherein the process management server publishes the regulatory compliant clinical information in an online marketplace.

18. The system of claim 9, wherein the application server further respectively sends a notification of a deficiency to a first content provider associated with the first content package or to a second content provider associated with the second content package if the first content package or the second content package is not successfully validated.