Standardized cardiovascular data for clinical research, registries, and patient care: A report from the data standards workgroup of the national cardiovascular research infrastructure project

Relatively little attention has been focused on standardization of data exchange in clinical research studies and patient care activities. Both are usually managed locally using separate and generally incompatible data systems at individual hospitals or clinics. In the past decade there have been nascent efforts to create data standards for clinical research and patient care data, and to some extent these are helpful in providing a degree of uniformity. Nonetheless, these data standards generally have not been converted into accepted computer-based language structures that could permit reliable data exchange across computer networks. The National Cardiovascular Research Infrastructure (NCRI) project was initiated with a major objective of creating a model framework for standard data exchange in all clinical research, clinical registry, and patient care environments, including all electronic health records. The goal is complete syntactic and semantic interoperability. A Data Standards Workgroup was established to create or identify and then harmonize clinical definitions for a base set of standardized cardiovascular data elements that could be used in this network infrastructure. Recognizing the need for continuity with prior efforts, the Workgroup examined existing data standards sources. A basic set of 353 elements was selected. The NCRI staff then collaborated with the 2 major technical standards organizations in health care, the Clinical Data Interchange Standards Consortium and Health Level Seven International, as well as with staff from the National Cancer Institute Enterprise Vocabulary Services. Modeling and mapping were performed to represent (instantiate) the data elements in appropriate technical computer language structures for endorsement as an accepted data standard for public access and use. Fully implemented, these elements will facilitate clinical research, registry reporting, administrative reporting and regulatory compliance, and patient care. © 2013 American College of Cardiology Foundation.

Contributors

Anderson, H. V. Weintraub, W. S. Radford, M. J. Kremers, M. S. Roe, M. T. Shaw, R. E. Pinchotti, D. M. Tcheng, J. E.

Publication

Journal: Journal of the American College of Cardiology
Volume: 61
Issue: 18
Pages: 1835 - 1846
Year: 2013
DOI: 10.1016/j.jacc.2012.12.047

Further Study Information

Current Stage: Not Applicable
Date: March 2011 - October 2011
Funding source(s): This work was supported by National Cardiovascular Research Infrastructure grant no. 1RC2HL101512-01. This paper is a collaboration of the Duke Clinical Research Institute and the American College of Cardiology-National Cardiovascular Data Registry.


Health Area

Disease Category: Heart & circulation

Disease Name: Cardiovascular Disease

Target Population

Age Range: Unknown

Sex: Either

Nature of Intervention: Not specified

Stakeholders Involved

- Clinical experts
- Researchers
- Statisticians
- Other

Study Type

- COS for clinical trials or clinical research
- COS for practice

Method(s)

- Literature review
- Other
- Semi structured discussion

Other: telephone conference, email exchanges
Semi structured discussion: meeting

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