The REUSE project: EHR as single datasource for biomedical research

被引:14
作者
El Fadly, AbdenNaji [1 ,2 ]
Lucas, Noel [3 ]
Rance, Bastien [3 ]
Verplancke, Philippe [5 ]
Lastic, Pierre-Yves [4 ]
Daniel, Christel [1 ,2 ,3 ]
机构
[1] INSERM, UMR S 872, Eq 20, F-75006 Paris, France
[2] Univ Paris 05, F-75006 Paris, France
[3] Hop George Pompidou, AP HP, Dept Informat Hosp, F-75015 Paris, France
[4] Sanofi Aventis R&D, F-92220 Bagneux, France
[5] XClin GmbH, Munich, Germany
来源
MEDINFO 2010, PTS I AND II | 2010年 / 160卷
关键词
HL7; CDISC; ODM; IHE profile; RFD; Electronic health record; Clinical data management system; Biomedical research; Clinical trial; Cardiovascular; Single source; ELECTRONIC MEDICAL-RECORDS; CLINICAL-RESEARCH;
D O I
10.3233/978-1-60750-588-4-1324
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Integrating biomedical research and patient care is a challenging issue requiring interoperability solutions. During a clinical trial, clinical data are captured twice, first in the Electronic Health Record (EHR) and then in the Clinical trials Data Management System (CDMS). The aim of REUSE (Retrieving EHR Useful data for Secondary Exploitation) project is to provide a single source solution for electronic data capture to the investigators of a university hospitals involved in a multi-centric clinical trial. We first investigated the differences between the workflows of patient care and biomedical research to specify the use of EHR for clinical trials. Then we defined a semantic interoperability framework in order to enable the reuse of EHR clinical data and implemented a mediator that transforms CDISC Operational Data Model (ODM) XML into proprietary XML document templates of different EHR solutions and vice-versa. Implementing electronic data capture for biomedical research within EHR eliminates redundant data entry, thus improving data quality and processing speed. Moreover, unlike other initiatives such as IHE integration profile "Retrieve Form for Data Capture" (RFD), the REUSE approach ensures that all clinical data is kept in the EHR whatever the context of data capture is.
引用
收藏
页码:1324 / 1328
页数:5
相关论文
共 13 条
[1]  
[Anonymous], 2008, CRD S
[2]  
[Anonymous], 2006, FUT VIS EL HLTHR EC
[3]  
[Anonymous], 2006, RFD S
[4]  
Dolin R H., 2007, Enabling Joint Commission Medication Reconciliation Objectives with the HL7/ASTM Continuity of Care Document Standard, P186
[5]   The BRIDG project: A technical report [J].
Fridsma, Douglas B. ;
Evans, Julie ;
Hastak, Smita ;
Mead, Charles N. .
JOURNAL OF THE AMERICAN MEDICAL INFORMATICS ASSOCIATION, 2008, 15 (02) :130-137
[6]   Configuration challenges: Implementing translational research policies in electronic medical records [J].
Kahn, Michael G. ;
Kaplan, David ;
Sokol, Ronald J. ;
DiLaura, Robert P. .
ACADEMIC MEDICINE, 2007, 82 (07) :661-669
[7]   Experiences with an interoperable data acquisition platform for multi-centric research networks based on HL7 CDA [J].
Klein, A. ;
Prokosch, H.-U. ;
Mueller, M. ;
Ganslandt, T. .
METHODS OF INFORMATION IN MEDICINE, 2007, 46 (05) :580-585
[8]  
Murphy EC, 2007, NATL I HLTH, V48, P4383
[9]  
Pakhomov S, 2007, AM J MANAG CARE, V13, P281
[10]  
Picard S, 2006, Sante Publique, V18, P107