Literature DB >> 17938783

Experiences with an interoperable data acquisition platform for multi-centric research networks based on HL7 CDA.

A Klein1, H-U Prokosch, M Müller, T Ganslandt.   

Abstract

OBJECTIVES: Today's increasing specialization of medicine necessitates the integration of telematic platforms for cross-institutional cooperation. In order to leverage the strengths of each cooperating institution a centralized unified storage using shared electronic patient records (EPRs) as well as secured remote data entry capabilities for supporting collaborative clinical research and care is essential. The objective of this project was to develop and introduce into routine use such a shared remote data entry (RDE) platform for the German multicentric Epidermolysis Bullosa (EB) network.
METHODS: An existing telematic application was extended by a remote data entry (RDE) module enabling the storage of structured data and pedigrees. HL7 Clinical Document Architecture (CDA) was chosen as a suitable standardized storage format that provides flexibility and future interoperability. Flexible data entry forms adaptable to distinct medical domains were implemented using XML-based technologies.
RESULTS: A flexible and comprehensive EPR/RDE platform was successfully implemented in the German EB network. A set of specific data entry forms was created to fully cover the network's documentation needs. The platform has been in productive use since 2005.
CONCLUSIONS: Standardized documentation by using HL7 CDA to store the medical research data as an EPR can contribute to high interoperability and an easier integration of heterogeneous health care information systems. Existing XML technologies offer a high degree of flexibility and adaptability to distinct medical domains. The ongoing development of standards (e.g. HL7 CDA R2) and interfaces (CDA/CDISC bridge) could further improve semantic and syntactic interoperability.

Entities:  

Mesh:

Year:  2007        PMID: 17938783     DOI: 10.1160/me9060

Source DB:  PubMed          Journal:  Methods Inf Med        ISSN: 0026-1270            Impact factor:   2.176


  6 in total

1.  [Current legal framework conditions for running and utilization of biobanks. Part 2: data protection and informed consent].

Authors:  J Haier
Journal:  Chirurg       Date:  2013-10       Impact factor: 0.955

2.  Assessing the prognoses on Health care in the information society 2013--thirteen years after.

Authors:  Petra Knaup; Elske Ammenwerth; Carl Dujat; Andrew Grant; Arie Hasman; Andreas Hein; Achim Hochlehnert; Casimir Kulikowski; John Mantas; Victor Maojo; Michael Marschollek; Lincoln Moura; Maik Plischke; Rainer Röhrig; Jürgen Stausberg; Katsuhiko Takabayashi; Frank Uckert; Alfred Winter; Klaus-Hendrik Wolf; Reinhold Haux
Journal:  J Med Syst       Date:  2014-07       Impact factor: 4.460

3.  Unlocking Data for Clinical Research - The German i2b2 Experience.

Authors:  T Ganslandt; S Mate; K Helbing; U Sax; H U Prokosch
Journal:  Appl Clin Inform       Date:  2011-03-30       Impact factor: 2.342

4.  Benefits of a clinical data warehouse with data mining tools to collect data for a radiotherapy trial.

Authors:  Erik Roelofs; Lucas Persoon; Sebastiaan Nijsten; Wolfgang Wiessler; André Dekker; Philippe Lambin
Journal:  Radiother Oncol       Date:  2013-02-05       Impact factor: 6.280

5.  EsPRit: ethics committee proposals for Long Term Medical Data Registries in rapidly evolving research fields - a future-proof best practice approach.

Authors:  S Oberbichler; W O Hackl; A Hörbst
Journal:  BMC Med Inform Decis Mak       Date:  2017-10-18       Impact factor: 2.796

Review 6.  Paperless clinical trials: Myth or reality?

Authors:  Sandeep K Gupta
Journal:  Indian J Pharmacol       Date:  2015 Jul-Aug       Impact factor: 1.200

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.