ANDREA MITCHELL, MSW, LCSW
Social Work at Clermont St, Denver, CO
License number
Colorado 09923354
Category
Social Work
Type
Clinical
Address
Address
1055 Clermont St, Denver, CO 80220
Phone
(303) 294-5623
(303) 296-2798 (Fax)
(303) 296-2798 (Fax)
Professional information
Andrea Mitchell
Location:
Greater Denver Area
Industry:
Information Technology and Services
Skills:
Healthcare IT, Clinical Data Management, Business Analysis, EHR, Healthcare Information Technology
Consultant At Mckesson
Position:
Consultant at McKesson
Location:
Greater Denver Area
Industry:
Information Technology and Services
Work:
McKesson
-
Consultant
System, Method And Computer Program Product For Performing Automatic Surveillance And Tracking Of Adverse Events
US Patent:
2009021, Aug 27, 2009
Filed:
Feb 22, 2008
Appl. No.:
12/035478
Inventors:
Andrea Claire Mitchell - Denver CO, US
Deborah J. Bulger - Millbury MA, US
Anne Coultas - Aurora CO, US
Kathleen C. Aller - Gaithersburg MD, US
Patricia Elder - Florence MA, US
Alice M. Gasowski - Boulder CO, US
Timothy Yeager - Baltimore MD, US
Deborah J. Bulger - Millbury MA, US
Anne Coultas - Aurora CO, US
Kathleen C. Aller - Gaithersburg MD, US
Patricia Elder - Florence MA, US
Alice M. Gasowski - Boulder CO, US
Timothy Yeager - Baltimore MD, US
International Classification:
G06Q 10/00
US Classification:
705 3
Abstract:
A system, method and computer program product are provided for automatically detecting and tracking adverse events. The system may include one or more data sources configured to provide a combination of clinical, operational and financial data associated with each of a plurality of patients. The system may further include a network entity configured to receive at least part of the combination of data and to apply one or more trigger rules to the combinations of data to identify one or more suspected adverse events. The network entity may further be configured to receive an indication of one or more confirmed adverse events from among the suspected adverse events, and to automatically compile at least part of the combination of data associated with respective patients in association with which the confirmed adverse events occurred. The system may further include a user device configured to enable performance of a root cause analysis of the compiled data.