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Difference between revisions of "RiskEvidenceSynthesis FHIR Resource Proposal"

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* Have the characteristics of high cohesion & low coupling – need to explore whether coupling is good some places, not elsewhere – layers from Bo’s document  
 
* Have the characteristics of high cohesion & low coupling – need to explore whether coupling is good some places, not elsewhere – layers from Bo’s document  
 
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Across the evidence-based medicine community (hundreds of thousands of people communicating the results of healthcare research through systematic reviews and expressing the findings from a body of evidence), the risk estimate synthesized from a body of evidence is the primary method of expressing quantitative results. Standardization is necessary to support interoperability across the evidence-based medicine domain.
  
 
==Expected implementations==
 
==Expected implementations==

Revision as of 13:55, 9 September 2018



riskEvidenceSynthesis

Owning work group name

Clinical_Decision_Support

Committee Approval Date:

June 22, 2018

Contributing or Reviewing Work Groups

  • Clinical Decision Support
  • Clinical Quality Information
  • Biomedical Research and Regulation

FHIR Resource Development Project Insight ID

1422

Scope of coverage

The scope of the riskEvidenceSynthesis resource is to describe the likelihood of an outcome in a population with an exposure where the risk estimate is derived from the combination of research studies. Risk estimates are not effects and do not represent a difference between exposure states.

Expressing risk estimates is done throughout reporting of biomedical research, systematic reviews, and clinical reference across all disciplines.

Risk estimates as a "synthesis" of research studies is a different concept for risk estimation than risk estimates for an individual person.

RIM scope

Resource appropriateness

Across the evidence-based medicine community (hundreds of thousands of people communicating the results of healthcare research through systematic reviews and expressing the findings from a body of evidence), the risk estimate synthesized from a body of evidence is the primary method of expressing quantitative results. Standardization is necessary to support interoperability across the evidence-based medicine domain.

Expected implementations

Content sources

Example Scenarios

Resource Relationships

Resource Boundaries

Timelines

gForge Users

When Resource Proposal Is Complete

When you have completed your proposal, please send an email to FMGcontact@HL7.org

FMG Notes