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Constructing the informatics and information technology foundations of a medical device evaluation system: a report from the FDA unique device identifier demonstration.

Publication ,  Journal Article
Drozda, JP; Roach, J; Forsyth, T; Helmering, P; Dummitt, B; Tcheng, JE
Published in: J Am Med Inform Assoc
February 1, 2018

OBJECTIVE: The US Food and Drug Administration (FDA) has recognized the need to improve the tracking of medical device safety and performance, with implementation of Unique Device Identifiers (UDIs) in electronic health information as a key strategy. The FDA funded a demonstration by Mercy Health wherein prototype UDIs were incorporated into its electronic information systems. This report describes the demonstration's informatics architecture. METHODS: Prototype UDIs for coronary stents were created and implemented across a series of information systems, resulting in UDI-associated data flow from manufacture through point of use to long-term follow-up, with barcode scanning linking clinical data with UDI-associated device attributes. A reference database containing device attributes and the UDI Research and Surveillance Database (UDIR) containing the linked clinical and device information were created, enabling longitudinal assessment of device performance. The demonstration included many stakeholders: multiple Mercy departments, manufacturers, health system partners, the FDA, professional societies, the National Cardiovascular Data Registry, and information system vendors. RESULTS: The resulting system of systems is described in detail, including entities, functions, linkage between the UDIR and proprietary systems using UDIs as the index key, data flow, roles and responsibilities of actors, and the UDIR data model. CONCLUSION: The demonstration provided proof of concept that UDIs can be incorporated into provider and enterprise electronic information systems and used as the index key to combine device and clinical data in a database useful for device evaluation. Keys to success and challenges to achieving this goal were identified. Fundamental informatics principles were central to accomplishing the system of systems model.

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Published In

J Am Med Inform Assoc

DOI

EISSN

1527-974X

Publication Date

February 1, 2018

Volume

25

Issue

2

Start / End Page

111 / 120

Location

England

Related Subject Headings

  • United States Food and Drug Administration
  • United States
  • Stents
  • Product Surveillance, Postmarketing
  • Product Labeling
  • Medical Informatics
  • Information Technology
  • Information Systems
  • Humans
  • Equipment Safety
 

Citation

APA
Chicago
ICMJE
MLA
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Drozda, J. P., Roach, J., Forsyth, T., Helmering, P., Dummitt, B., & Tcheng, J. E. (2018). Constructing the informatics and information technology foundations of a medical device evaluation system: a report from the FDA unique device identifier demonstration. J Am Med Inform Assoc, 25(2), 111–120. https://doi.org/10.1093/jamia/ocx041
Drozda, Joseph P., James Roach, Thomas Forsyth, Paul Helmering, Benjamin Dummitt, and James E. Tcheng. “Constructing the informatics and information technology foundations of a medical device evaluation system: a report from the FDA unique device identifier demonstration.J Am Med Inform Assoc 25, no. 2 (February 1, 2018): 111–20. https://doi.org/10.1093/jamia/ocx041.
Drozda JP, Roach J, Forsyth T, Helmering P, Dummitt B, Tcheng JE. Constructing the informatics and information technology foundations of a medical device evaluation system: a report from the FDA unique device identifier demonstration. J Am Med Inform Assoc. 2018 Feb 1;25(2):111–20.
Drozda, Joseph P., et al. “Constructing the informatics and information technology foundations of a medical device evaluation system: a report from the FDA unique device identifier demonstration.J Am Med Inform Assoc, vol. 25, no. 2, Feb. 2018, pp. 111–20. Pubmed, doi:10.1093/jamia/ocx041.
Drozda JP, Roach J, Forsyth T, Helmering P, Dummitt B, Tcheng JE. Constructing the informatics and information technology foundations of a medical device evaluation system: a report from the FDA unique device identifier demonstration. J Am Med Inform Assoc. 2018 Feb 1;25(2):111–120.
Journal cover image

Published In

J Am Med Inform Assoc

DOI

EISSN

1527-974X

Publication Date

February 1, 2018

Volume

25

Issue

2

Start / End Page

111 / 120

Location

England

Related Subject Headings

  • United States Food and Drug Administration
  • United States
  • Stents
  • Product Surveillance, Postmarketing
  • Product Labeling
  • Medical Informatics
  • Information Technology
  • Information Systems
  • Humans
  • Equipment Safety