The Experts below are selected from a list of 93522 Experts worldwide ranked by ideXlab platform

James E Tcheng - One of the best experts on this subject based on the ideXlab platform.

  • Constructing the informatics and information technology foundations of a medical Device Evaluation system: a report from the FDA unique Device identifier demonstration
    Journal of the American Medical Informatics Association, 2018
    Co-Authors: Joseph P. Drozda, Thomas Forsyth, Paul Helmering, Benjamin Dummitt, James Roach, James E Tcheng
    Abstract:

    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. 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. 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. 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. © The Author 2017. Published by Oxford University Press on behalf of the American Medical Informatics Association. All rights reserved. For Permissions, please email: journals.permissions@oup.com

  • constructing the informatics and information technology foundations of a medical Device Evaluation system a report from the fda unique Device identifier demonstration
    Journal of the American Medical Informatics Association, 2018
    Co-Authors: Joseph P. Drozda, Thomas Forsyth, Paul Helmering, Benjamin Dummitt, James Roach, James E Tcheng
    Abstract:

    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.

Joseph P. Drozda - One of the best experts on this subject based on the ideXlab platform.

  • Constructing the informatics and information technology foundations of a medical Device Evaluation system: a report from the FDA unique Device identifier demonstration
    Journal of the American Medical Informatics Association, 2018
    Co-Authors: Joseph P. Drozda, Thomas Forsyth, Paul Helmering, Benjamin Dummitt, James Roach, James E Tcheng
    Abstract:

    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. 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. 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. 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. © The Author 2017. Published by Oxford University Press on behalf of the American Medical Informatics Association. All rights reserved. For Permissions, please email: journals.permissions@oup.com

  • constructing the informatics and information technology foundations of a medical Device Evaluation system a report from the fda unique Device identifier demonstration
    Journal of the American Medical Informatics Association, 2018
    Co-Authors: Joseph P. Drozda, Thomas Forsyth, Paul Helmering, Benjamin Dummitt, James Roach, James E Tcheng
    Abstract:

    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.

James Roach - One of the best experts on this subject based on the ideXlab platform.

  • Constructing the informatics and information technology foundations of a medical Device Evaluation system: a report from the FDA unique Device identifier demonstration
    Journal of the American Medical Informatics Association, 2018
    Co-Authors: Joseph P. Drozda, Thomas Forsyth, Paul Helmering, Benjamin Dummitt, James Roach, James E Tcheng
    Abstract:

    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. 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. 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. 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. © The Author 2017. Published by Oxford University Press on behalf of the American Medical Informatics Association. All rights reserved. For Permissions, please email: journals.permissions@oup.com

  • constructing the informatics and information technology foundations of a medical Device Evaluation system a report from the fda unique Device identifier demonstration
    Journal of the American Medical Informatics Association, 2018
    Co-Authors: Joseph P. Drozda, Thomas Forsyth, Paul Helmering, Benjamin Dummitt, James Roach, James E Tcheng
    Abstract:

    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.

Paul Helmering - One of the best experts on this subject based on the ideXlab platform.

  • Constructing the informatics and information technology foundations of a medical Device Evaluation system: a report from the FDA unique Device identifier demonstration
    Journal of the American Medical Informatics Association, 2018
    Co-Authors: Joseph P. Drozda, Thomas Forsyth, Paul Helmering, Benjamin Dummitt, James Roach, James E Tcheng
    Abstract:

    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. 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. 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. 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. © The Author 2017. Published by Oxford University Press on behalf of the American Medical Informatics Association. All rights reserved. For Permissions, please email: journals.permissions@oup.com

  • constructing the informatics and information technology foundations of a medical Device Evaluation system a report from the fda unique Device identifier demonstration
    Journal of the American Medical Informatics Association, 2018
    Co-Authors: Joseph P. Drozda, Thomas Forsyth, Paul Helmering, Benjamin Dummitt, James Roach, James E Tcheng
    Abstract:

    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.

Thomas Forsyth - One of the best experts on this subject based on the ideXlab platform.

  • Constructing the informatics and information technology foundations of a medical Device Evaluation system: a report from the FDA unique Device identifier demonstration
    Journal of the American Medical Informatics Association, 2018
    Co-Authors: Joseph P. Drozda, Thomas Forsyth, Paul Helmering, Benjamin Dummitt, James Roach, James E Tcheng
    Abstract:

    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. 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. 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. 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. © The Author 2017. Published by Oxford University Press on behalf of the American Medical Informatics Association. All rights reserved. For Permissions, please email: journals.permissions@oup.com

  • constructing the informatics and information technology foundations of a medical Device Evaluation system a report from the fda unique Device identifier demonstration
    Journal of the American Medical Informatics Association, 2018
    Co-Authors: Joseph P. Drozda, Thomas Forsyth, Paul Helmering, Benjamin Dummitt, James Roach, James E Tcheng
    Abstract:

    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.