ENV 13606-1:2000
(Main)Health informatics - Electronic healthcare record communication - Part 1: Extended architecture
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- 23-May-2000
- 27-Feb-2007
- 35.240.80
- CEN/TC 251
Health informatics - Electronic healthcare record communication - Part 1: Extended architecture
The overall goal is to deliver a communication architectural standard for Electronic Healthcare Records. To the healthcare organisation and the clinicians this architecture offers protection for their investment in clinical information against the vagaries of incompatible systems and from the changes arising from the passage of time. To the individual person, in so far as their health and care depends upon the safe communication of clinical information, the architecture offers a more direct benefit both immediately and longer term with respect to continuity of care.
Zdravstvena informatika – Komunikacija z elektronskimi zapisi na področju zdravstva – 1. del: Razširjena arhitektura
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Standards Content (Sample)
SLOVENSKI STANDARD
SIST ENV 13606-1:2003
01-oktober-2003
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Health informatics - Electronic healthcare record communication - Part 1: Extended
architecture
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d) those undertaking independent evaluations/academic reviews of terminological resources;
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This document specifies the business requirements for the structured content of structured or semi-
structured dose instructions for recording dose instructions in the electronic health record (EHR),
supporting clinical decision support, and in exchanging medication orders, as applicable to primary,
secondary and tertiary care.
This document is focused on the dose instructions as will be presented to the individual subject of care
or caregiver. Comprehension of dose instructions by the subject of care or caregiver is an overarching
consideration for subject of care safety and the best outcomes. Related factors are discussed but are not
part of the primary scope.
This document does not define an information model, except to the extent that those information model
concepts are necessary to define business requirements.
Outside the scope of this document are:
— The implementation of dose instructions, i.e. assembling the structured elements into a form
appropriate for the patient or caregiver;
— The content of a medication order (see ISO 17523) beyond content related to dose instructions;
— The content of a record of dispense of a medicinal product (see ISO/TS 19293);
— The functionality of health, clinical and/or pharmacy systems;
— Other kinds of content of health, clinical or pharmacy systems that are needed to support the whole
process of health care providers, such as:
— A drug knowledge database (see ISO/TS 22756);
— A decision support system (see ISO/TS 22756 and ISO/TS 22703);
— A complete medical record (EHR);
— A medicinal product dictionary (see ISO/TS 19256);
— Verification of the medicinal product and dose being administered.
— Some concepts from Identification of Medicinal Products are referenced, but not defined, in this
document. See Clause 4 for discussion of the relationship of this document with IDMP.
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