Literature DB >> 27343161

The Mercy unique device identifier demonstration project: Implementing point of use product identification in the cardiac catheterization laboratories of a regional health system.

Joseph P Drozda1, Curtis Dudley1, Paul Helmering1, James Roach1, Lisa Hutchison1.   

Abstract

Mercy, a 4 state health system, conducted an FDA-sponsored demonstration whereby prototype unique device identifiers (UDIs) of coronary stents were implemented in its electronic information systems for safety surveillance and research. To accomplish this, a multi-disciplinary team implemented a point of use barcode scanning inventory management system in all 5 Mercy cardiac catheterization laboratories. The system's potential for improving inventory management and tracking Cath Lab supplies was felt to be sufficiently compelling for system deployment outside of the context of the demonstration. Further, it was felt to be useful for all Cath Lab renewable supplies and not just coronary stents. Benefits included preventing procedure delays, lowering costs, and increasing revenue. Finally, the system is extensible to all implanted medical devices and generalizable to most hospitals.
Copyright © 2015 Elsevier Inc. All rights reserved.

Keywords:  Device identification; Process improvement; Safety surveillance

Mesh:

Year:  2015        PMID: 27343161     DOI: 10.1016/j.hjdsi.2015.07.002

Source DB:  PubMed          Journal:  Healthc (Amst)        ISSN: 2213-0764


  6 in total

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

Authors:  Joseph P Drozda; James Roach; Thomas Forsyth; Paul Helmering; Benjamin Dummitt; James E Tcheng
Journal:  J Am Med Inform Assoc       Date:  2018-02-01       Impact factor: 4.497

2.  Multi-institutional distributed data networks for real-world evidence about medical devices: building unique device identifiers into longitudinal data (BUILD).

Authors:  Joseph P Drozda; Jove Graham; Joseph B Muhlestein; James E Tcheng; James Roach; Tom Forsyth; Stacey Knight; Andrew McKinnon; Heidi May; Natalia A Wilson; Jesse A Berlin; Edgar P Simard
Journal:  JAMIA Open       Date:  2022-05-25

3.  Preliminary feasibility assessment of CDM-based active surveillance using current status of medical device data in medical records and OMOP-CDM.

Authors:  Sooin Choi; Soo Jeong Choi; Jin Kuk Kim; Ki Chang Nam; Suehyun Lee; Ju Han Kim; You Kyoung Lee
Journal:  Sci Rep       Date:  2021-12-15       Impact factor: 4.379

4.  Advancing Patient Safety Surrounding Medical Devices: A Health System Roadmap to Implement Unique Device Identification at the Point of Care.

Authors:  Natalia A Wilson; James E Tcheng; Jove Graham; Joseph P Drozda
Journal:  Med Devices (Auckl)       Date:  2021-11-30

5.  Advancing Patient Safety Surrounding Medical Devices: Barriers, Strategies, and Next Steps in Health System Implementation of Unique Device Identifiers.

Authors:  Natalia A Wilson; James E Tcheng; Jove Graham; Joseph P Drozda
Journal:  Med Devices (Auckl)       Date:  2022-06-21

6.  How real-world evidence can really deliver: a case study of data source development and use.

Authors:  Joseph Drozda; Angelique Zeringue; Benjamin Dummitt; Byron Yount; Frederic Resnic
Journal:  BMJ Surg Interv Health Technol       Date:  2020-03-24
  6 in total

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