Implementation of an anonymisation tool for clinical trials using a clinical trial processor integrated with an existing trial patient data information system

被引:8
作者
Aryanto, Kadek Y. E. [1 ]
Broekema, Andre [1 ]
Oudkerk, Matthijs [1 ]
van Ooijen, Peter M. A. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Radiol, NL-9700 RB Groningen, Netherlands
关键词
Anonymisation tool; Clinical trial processor; Privacy; Clinical trials; Software; Patient data;
D O I
10.1007/s00330-011-2235-y
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
To present an adapted Clinical Trial Processor (CTP) test set-up for receiving, anonymising and saving Digital Imaging and Communications in Medicine (DICOM) data using external input from the original database of an existing clinical study information system to guide the anonymisation process. Two methods are presented for an adapted CTP test set-up. In the first method, images are pushed from the Picture Archiving and Communication System (PACS) using the DICOM protocol through a local network. In the second method, images are transferred through the internet using the HTTPS protocol. In total 25,000 images from 50 patients were moved from the PACS, anonymised and stored within roughly 2 h using the first method. In the second method, an average of 10 images per minute were transferred and processed over a residential connection. In both methods, no duplicated images were stored when previous images were retransferred. The anonymised images are stored in appropriate directories. The CTP can transfer and process DICOM images correctly in a very easy set-up providing a fast, secure and stable environment. The adapted CTP allows easy integration into an environment in which patient data are already included in an existing information system. Store DICOM images correctly in a very easy set-up in a fast, secure and stable environment Allows adaptation of the software to perform a certain task based on specific needs Allows easy integration into an existing environment Reduce the possibility of inappropriate anonymisation.
引用
收藏
页码:144 / 151
页数:8
相关论文
共 50 条
  • [31] Validation of the UVA Simulation Replay Methodology Using Clinical Data: Reproducing a Randomized Clinical Trial
    Villa-Tamayo, Maria F.
    Colmegna, Patricio
    Breton, Marc
    DIABETES TECHNOLOGY & THERAPEUTICS, 2024, 26 (10) : 720 - 727
  • [32] Practices and trends in clinical trial registration in the Pan African Clinical Trials Registry (PACTR): a descriptive analysis of registration data
    Ndwandwe, Duduzile Edith
    Runeyi, Sinazo
    Pienaar, Elizabeth
    Mathebula, Lindi
    Hohlfeld, Ameer
    Wiysonge, Charles Shey
    BMJ OPEN, 2022, 12 (01):
  • [33] Wireless Clinical Trial of Data Capture using a Personal Digital Assistant
    Park, Sook-Kyoung
    Park, Soo-Heon
    Kang, Min-Goo
    Chae, Young Moon
    Kim, Sukil
    Choy, Soon
    Choi, Inyoung
    HEALTHCARE INFORMATICS RESEARCH, 2009, 15 (02) : 235 - 244
  • [34] Eliciting remote data entry system requirements for the collection of cancer clinical trial data
    Meadows, BJ
    CIN-COMPUTERS INFORMATICS NURSING, 2003, 21 (05) : 234 - 240
  • [35] Open Access Platforms in Spinal Cord Injury: Existing Clinical Trial Data to Predict and Improve Outcomes
    Kramer, John L. K.
    Geisler, Fred
    Ramer, Leanne
    Plunet, Ward
    Cragg, Jacquelyn J.
    NEUROREHABILITATION AND NEURAL REPAIR, 2017, 31 (05) : 399 - 401
  • [36] Increasing the efficiency of clinical trials in neurodegenerative disorders using group sequential trial designs
    van Eijk, Ruben P. A.
    Nikolakopoulos, Stavros
    Ferguson, Toby A.
    Liu, Dawei
    Eijkemans, Marinus J. C.
    van den Berg, Leonard H.
    JOURNAL OF CLINICAL EPIDEMIOLOGY, 2018, 98 : 80 - 88
  • [37] Rare use of patient-reported outcomes in childhood cancer clinical trials-a systematic review of clinical trial registries
    Riedl, David
    Rothmund, Maria
    Darlington, Anne-Sophie
    Sodergren, Samantha
    Crazzolara, Roman
    de Rojas, Teresa
    EUROPEAN JOURNAL OF CANCER, 2021, 152 : 90 - 99
  • [38] Incorporation of genuine prior information in cost- effectiveness analysis of clinical trial data
    Stevens, JW
    O'Hagan, A
    INTERNATIONAL JOURNAL OF TECHNOLOGY ASSESSMENT IN HEALTH CARE, 2002, 18 (04) : 782 - 790
  • [39] EliIE: An open-source information extraction system for clinical trial eligibility criteria
    Kang, Tian
    Zhang, Shaodian
    Tang, Youlan
    Hruby, Gregory W.
    Rusanov, Alexander
    Elhadad, Noemie
    Weng, Chunhua
    JOURNAL OF THE AMERICAN MEDICAL INFORMATICS ASSOCIATION, 2017, 24 (06) : 1062 - 1071
  • [40] How a Psychopharmacology Clinical Trial Site in the Seattle Area Managed Clinical Trials and Patient Care During the COVID-19 Pandemic
    Schilling, Shirin
    Mohanarajah, Sinthuja
    Mengstu, Abraham
    Khan, Arif
    Brown, Walter A.
    AMERICAN JOURNAL OF GERIATRIC PSYCHIATRY, 2020, 28 (09) : 999 - 1003