ASTM E2538 - 06(2011)

    Standard Practice for Defining and Implementing Pharmacotherapy Information Services within the Electronic Health Record (EHR) Environment and Networked Architectures

    Active Standard ASTM E2538 | Developed by Subcommittee: E31.25

    Book of Standards Volume: 14.01

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    Significance and Use

    Health information networks (HINs) have arisen in recent years as a way to share common information within organizational arrangements among those healthcare facilities that have been formed into large, more comprehensive integrated delivery systems (IDS) and managed care organizations (MCO) offering a full range of healthcare services, both inpatient and ambulatory.

    The specific organizational structures to which the MCO term was originally applied most probably have evolved into something quite different. Furthermore, IDS organizations are contracting with other organizations that have a market larger than a single IDS itself and are buying such services for themselves rather than offering them internally.

    These organizations will need a frame of reference for the global information needed to provide all of the services required during patient care. For a global Concept Model consult ADA Specification 1000.01000.18 and TR 1039.

    Pharmacotherapy will require a number of these services, including those of the clinical laboratory for therapeutic drug monitoring as well as pharmacy services of both resident and nonresident care organizations and stand-alone pharmacies to ensure freedom from medication errors and conduct ongoing investigations of both the outcomes of care and the management of resources related to pharmacotherapy.

    Pharmacotherapy functions include prescribing (clinical orders), dispensing, administering, and monitoring, which support pharmaceutical care defined as provision of drug therapy to achieve desired therapeutic outcomes that improve a patients quality of life. These functions address patients needs that require information support as noted in Table 1.

    Another aspect of the monitoring function is the development of instrumentation for testing at point of care (POCT) for high-value immediate-benefit services that support pharmacotherapy. POCT, however, needs supervision and training from skilled laboratorians for the actual performers, whether that supervision comes from within the IDS or outside of it. This range of operation is only achievable by distributed HIN structures that shall have the same quality of clinical and data services as offered by laboratories close at hand. Data management of POCT is documented separately (see CLSI POCT1, ASTP2), but such data management for support of pharmacotherapy shall be placed into the broader context of this practice and linked to CLSI LIS-9A. Thus, this practice should be used to first organize the global domain and then the interconnected subdomains.

    1. Scope

    1.1 This practice applies to the process of defining and documenting the capabilities, logical data sources, and pathways of data exchange regarding pharmacotherapy information services within a given network architecture serving a set of healthcare constituents.

    1.2 This practice is not a technical implementation standard but, rather, describes how the implementation methods and techniques can be used to coordinate pharmacotherapy services logically within an electronic health record (EHR) systems environment involving participating organizations and sites connected by a networked communication system.

    1.3 This practice covers the content of the nodes and arcs of the resulting logical network involving EHR, pharmacy, and clinical laboratory-capable sites. This practice also considers the various purposes and organizational arrangements for coordinating pharmacotherapy services within the network boundaries and the considerations for connections among external networks.

    1.4 This practice refers to other standards for conventions within various data domains, such as pharmacy systems, clinical laboratory information management systems (CLIMS), and EHR systems, and for messaging conventions.

    1.5 This practice is intended to outline how integration of pharmacy, CLIMS, and EHR information systems can be undertaken to result in a transparent pharmacotherapy clinical decision support environment, regardless of the underlying implementation architecture, by describing the logical interoperability of information domains as facilitated by information and communications technology (ICT).

    1.6 This practice is directed at pharmacists, clinical pharmacologists, clinical laboratorians, information system managers, and information systems vendors for use in planning and implementing coordinated pharmacotherapy services through effective dialog.

    1.7 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 limitations prior to use.

    2. Referenced Documents (purchase separately) The documents listed below are referenced within the subject standard but are not provided as part of the standard.

    ASTM Standards

    E1239 Practice for Description of Reservation/Registration-Admission, Discharge, Transfer (R-ADT) Systems for Electronic Health Record (EHR) Systems

    E1340 Guide for Rapid Prototyping of Information Systems

    E1384 Practice for Content and Structure of the Electronic Health Record

    E1578 Guide for Laboratory Informatics

    E1633 Specification for Coded Values Used in the Electronic Health Record

    E1714 Guide for Properties of a Universal Healthcare Identifier (UHID)

    E1715 Practice for An Object-Oriented Model for Registration, Admitting, Discharge, and Transfer (RADT) Functions in Computer-Based Patient Record Systems

    E1744 Practice for View of Emergency Medical Care in the Electronic Health Record

    E1762 Guide for Electronic Authentication of Health Care Information

    E1869 Guide for Confidentiality, Privacy, Access, and Data Security Principles for Health Information Including Electronic Health Records

    E1985 Guide for User Authentication and Authorization

    E1986 Guide for Information Access Privileges to Health Information

    E1987 Guide for Individual Rights Regarding Health Information

    E1988 Guide for Training of Persons who have Access to Health Information

    E2017 Guide for Amendments to Health Information

    E2066 Guide for Validation of Laboratory Information Management Systems

    E2084 Specification for Authentication of Healthcare Information Using Digital Signatures

    E2085 Guide on Security Framework for Healthcare Information

    E2086 Guide for Internet and Intranet Healthcare Security

    E2145 Practice for Information Modeling

    E2147 Specification for Audit and Disclosure Logs for Use in Health Information Systems

    E2171 Practice for Rating-Scale Measures Relevant to the Electronic Health Record

    E2457 Terminology for Healthcare Informatics

    E2473 Practice for the Occupational/Environmental Health View of the Electronic Health Record

    P110 Proposed Guide to Assist in the Defining, Procuring, Installing, and Implementing of a Computerized Hospital Pharmacy System Withdrawn 1988.

    ICS Code

    ICS Number Code 35.240.80 (IT applications in health care technology)

    Referencing This Standard
    Link Here
    Link to Active (This link will always route to the current Active version of the standard.)

    DOI: 10.1520/E2538-06R11

    Citation Format

    ASTM E2538-06(2011), Standard Practice for Defining and Implementing Pharmacotherapy Information Services within the Electronic Health Record (EHR) Environment and Networked Architectures, ASTM International, West Conshohocken, PA, 2011,

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