Electronic Data Capture and DICOM Data Management in Multi-Center Clinical Trials

被引:1
作者
Haak, Daniel [1 ]
Page, Charles-E. [1 ]
Deserno, Thomas M. [1 ]
机构
[1] Rhein Westfal TH Aachen, Dept Med Informat, Pauwelsstr 30, D-52057 Aachen, Germany
来源
MEDICAL IMAGING 2016: PACS AND IMAGING INFORMATICS: NEXT GENERATION AND INNOVATIONS | 2016年 / 9789卷
关键词
Workflow; clinical trials; integration; DICOM; PACS; open source;
D O I
10.1117/12.2218257
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Providing eligibility, efficacy and security evaluation by quantitative and qualitative disease findings, medical imaging has become increasingly important in clinical trials. Here, subject's data is today captured in electronic case reports forms (eCRFs), which are offered by electronic data capture (EDC) systems. However, integration of subject's medical image data into eCRFs is insufficiently supported. Neither integration of subject's digital imaging and communications in medicine (DICOM) data, nor communication with picture archiving and communication systems (PACS), is possible. This aggravates the workflow of the study personnel, in special regarding studies with distributed data capture in multiple sites. Hence, in this work, a system architecture is presented, which connects an EDC system, a PACS and a DICOM viewer via the web access to DICOM objects (WADO) protocol. The architecture is implemented using the open source tools OpenClinica, DCM4CHEE and Weasis. The eCRF forms the primary endpoint for the study personnel, where subject's image data is stored and retrieved. Background communication with the PACS is completely hidden for the users. Data privacy and consistency is ensured by automatic de-identification and re-labelling of DICOM data with context information (e.g. study and subject identifiers), respectively. The system is exemplarily demonstrated in a clinical trial, where computer tomography (CT) data is de-centrally captured from the subjects and centrally read by a chief radiologists to decide on inclusion of the subjects in the trial. Errors, latency and costs in the EDC workflow are reduced, while, a research database is implicitly built up in the background.
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页数:6
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