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Difference between revisions of "CDA R3 Right Hand Side of Model Analysis"

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[[Structured Documents WG|SDWG]] page.
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=CDA R3 requirements for right side of model=
 
=CDA R3 requirements for right side of model=
 
* Support for domain models from other committees
 
* Support for domain models from other committees
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* Bob’s Idea:  Take the SDA Approach, build one model that has four choice boxes [one for each backbone class]...
 
* Bob’s Idea:  Take the SDA Approach, build one model that has four choice boxes [one for each backbone class]...
 
* Ensure that use of components is invariant (e.g., C-METS) for some period of time based on review.
 
* Ensure that use of components is invariant (e.g., C-METS) for some period of time based on review.
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* Expressivity
  
  

Revision as of 21:46, 27 October 2009

SDWG page.

CDA R3 requirements for right side of model

  • Support for domain models from other committees
  • Internal consistency across domains
  • Identical XML between HL7 V3 standards
    • May want to consider a different ITS
  • Simplicity for implementers
  • Limited/Fixed set of CDA Schemas for implementers
  • Enter into the architecture at varying degrees of sophistication (levels of CDA)
  • Administrative and Financial Data needs to be addressed
  • Formalization of best practices established over the past five years.
    • Extension mechanisms
    • Creator and Recipient Roles and Responsibilities
    • Adopt existing extensions
  • Extensions need to be “validatable” against schema
    • Support for schema tooling (e.g., binding, API creation, et cetera).
  • Bob’s Idea: Take the SDA Approach, build one model that has four choice boxes [one for each backbone class]...
  • Ensure that use of components is invariant (e.g., C-METS) for some period of time based on review.
  • Expressivity


CDA R2 Design Principles

The goals of the CDA are:

   * Give priority to delivery of patient care.
   * Allow cost effective implementation across as wide a spectrum of systems as possible.
   * Support exchange of human-readable documents between users, including those with different levels of technical sophistication.
   * Promote longevity of all information encoded according to this architecture.
   * Enable a wide range of post-exchange processing applications.
   * Be compatible with a wide range of document creation applications.
   * Promote exchange that is independent of the underlying transfer or storage mechanism.
   * Prepare the design reasonably quickly.
   * Enable policy-makers to control their own information requirements without extension to this specification.

A number of design principles follow from consideration of the above goals:

   * This architecture must be compatible with XML and the HL7 RIM.
   * This architecture must be compatible with representations of clinical information arising from other HL7 committees.
   * Technical barriers to use of the architecture should be minimized.
   * The architecture specifies the representation of instances required for exchange.
   * The architecture should impose minimal constraints or requirements on document structure and content required for exchange.
   * The architecture must be scalable to accommodate fine-grained markup such as highly structured text and coded data.
   * Document specifications based on this architecture should accommodate such constraints and requirements as supplied by appropriate professional, commercial, and regulatory agencies.
   * Document specifications for document creation and processing, if intended for exchange, should map to this exchange architecture.
   * CDA documents must be human readable using widely-available and commonly-deployed XML-aware browsers and print drivers and a generic CDA style sheet written in a standard style sheet language.
   * Use open standards.