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  • ASTM E 1239 : 2004 : R2010

    Withdrawn A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
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    Standard Practice for Description of Reservation/Registration-Admission, Discharge, Transfer (R-ADT) Systems for Electronic Health Record (EHR) Systems (Withdrawn 2017)

    Available format(s):  Hardcopy, PDF

    Withdrawn date:  17-04-2017

    Language(s):  English

    Published date:  01-03-2010

    Publisher:  American Society for Testing and Materials

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    Abstract - (Show below) - (Hide below)

    CONTAINED IN VOL. 14.01, 2015 Specifies the minimum information capabilities needed by an ambulatory care system or a resident facility R-ADT system.

    Scope - (Show below) - (Hide below)

    1.1 This practice identifies the minimum information capabilities needed by an ambulatory care system or a resident facility R-ADT system. This practice is intended to depict the processes of: patient registration, inpatient admission into health care institutions and the use of registration data in establishing and using the demographic segments of the electronic health record. It also identifies a common core of informational elements needed in this R-ADT process and outlines those organizational elements that may use these segments. Furthermore, this guide identifies the minimum general requirements for R-ADT and helps identify many of the additional specific requirements for such systems. The data elements described may not all be needed but, if used, they must be used in the way specified so that each record segment has comparable data. This practice will help answer questions faced by designers of R-ADT capabilities by providing a clear description of the consensus of health care professionals regarding a uniform set of minimum data elements used by R-ADT functions in each component of the larger system. It will also help educate health care professionals in the general principles of patient care information management as well as the details of the constituent specialty areas.

    1.2 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory requirements prior to use.

    General Product Information - (Show below) - (Hide below)

    Committee E 31
    Document Type Standard Practice
    Product Note Reconfirmed 2010
    Publisher American Society for Testing and Materials
    Status Withdrawn
    Supersedes

    Standards Referenced By This Book - (Show below) - (Hide below)

    ASTM E 2473 : 2005 : R2011 Standard Practice for the Occupational/Environmental Health View of the Electronic Health Record (Withdrawn 2020)
    ASTM E 2522 : 2007 : R2013 Standard Guide for Quality Indicators for Health Classifications (Withdrawn 2022)
    ASTM E 2457 : 2007 : R2013 Standard Terminology for Healthcare Informatics (Withdrawn 2022)
    ASTM E 2538 : 2006 : R2011 Standard Practice for Defining and Implementing Pharmacotherapy Information Services within the Electronic Health Record (EHR) Environment and Networked Architectures (Withdrawn 2020)

    Standards Referencing This Book - (Show below) - (Hide below)

    ISO 639:1988 Code for the representation of names of languages
    CLSI LIS5 A : 1ED 2003 SPECIFICATION FOR TRANSFERRING CLINICAL OBSERVATIONS BETWEEN INDEPENDENT COMPUTER SYSTEMS
    CLSI LIS9 A : 1ED 2003 GUIDE FOR COORDINATION OF CLINICAL LABORATORY SERVICES WITHIN THE ELECTRONIC HEALTH RECORD ENVIRONMENT AND NETWORKED ARCHITECTURES
    CLSI LIS8 A : 1ED 2003 GUIDE FOR FUNCTIONAL REQUIREMENTS OF CLINICAL LABORATORY INFORMATION MANAGEMENT SYSTEMS
    ISO/IEC 5218:2004 Information technology Codes for the representation of human sexes
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