An Integrated Workflow For Secondary Use of Patient Data for Clinical Research

被引：10

作者：

Bouzille, Guillaume ^{[1
,2
,3
]}

Sylvestre, Emmanuelle ^{[1
,2
,3
]}

Campillo-Gimenez, Boris ^{[1
,2
]}

Renault, Eric ^{[1
,2
]}

Ledieu, Thibault ^{[1
,2
]}

Delamarre, Denis ^{[1
,2
]}

Cuggia, Marc ^{[1
,2
,3
]}

机构：

[1] INSERM, U1099, F-35000 Rennes, France

[2] Univ Rennes 1, LTSI, F-35000 Rennes, France

[3] CHU Rennes, CIC INSERM 1414, F-35000 Rennes, France

来源：

MEDINFO 2015: EHEALTH-ENABLED HEALTH | 2015年 / 216卷

关键词：

Biomedical research; Secondary use of data; Confidentiality;

D O I：

10.3233/978-1-61499-564-7-913

中图分类号：

TP39 [计算机的应用];

学科分类号：

081203 ; 0835 ;

摘要：

This work proposes an integrated workflow for secondary use of medical data to serve feasibility studies, and the prescreening and monitoring of research studies. All research issues are initially addressed by the Clinical Research Office through a research portal and subsequently redirected to relevant experts in the determined field of concentration. For secondary use of data, the workflow is then based on the clinical data warehouse of the hospital. A datamart with potentially eligible research candidates is constructed. Datamarts can either produce aggregated data, de-identified data, or identified data, according to the kind of study being treated. In conclusion, integrating the secondary use of data process into a general research workflow allows visibility of information technologies and improves the accessability of clinical data.

引用

页码：913 / 913

页数：1