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Difference between revisions of "EffectEvidenceSynthesis FHIR Resource Proposal"

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Current version: https://confluence.hl7.org/display/FHIR/EffectEvidenceSynthesis+FHIR+Resource+Proposal<div style="float: left;">[[Image:OpenHotTopic.GIF|35px| ]]</div>
 
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This page documents a [[:category:Pending FHIR Resource Proposal|Pending]] [[:category:FHIR Resource Proposal|FHIR Resource Proposal]]
 
This page documents a [[:category:Pending FHIR Resource Proposal|Pending]] [[:category:FHIR Resource Proposal|FHIR Resource Proposal]]
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=effectEvidenceSynthesis=
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=EffectEvidenceSynthesis=
  
 
<!-- Resource names should meet the following characteristics:
 
<!-- Resource names should meet the following characteristics:
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<!-- The name of the committee that is proposed to have responsibility for developing and maintaining the resources. -->
 
<!-- The name of the committee that is proposed to have responsibility for developing and maintaining the resources. -->
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[[YourWorkGroupName]]
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[[Clinical_Decision_Support]]
  
 
==Committee Approval Date:==
 
==Committee Approval Date:==
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<i>Please enter the date that the committee approved this Resource proposal</i>
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*Initial PSS: June 22, 2018
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*CDS WG: September 12, 2018
  
 
==Contributing or Reviewing Work Groups==
 
==Contributing or Reviewing Work Groups==
  
 
<!-- Additional work groups that may have an interest in contributing to, or reviewing  the content of the resource (optional) -->
 
<!-- Additional work groups that may have an interest in contributing to, or reviewing  the content of the resource (optional) -->
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* Work Group Name
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*Clinical Decision Support
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* or link
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*Clinical Quality Information
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* or "None"
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*Biomedical Research and Regulation
  
 
==FHIR Resource Development Project Insight ID==
 
==FHIR Resource Development Project Insight ID==
  
 
<!-- Please specify the id of your work group’s PSS for doing FHIR work.  (If submitted but not yet approved, just write “pending”.) The link to the PSS template can be found here: http://gforge.hl7.org/gf/download/docmanfileversion/6832/9398/HL7FHIR_DSTUballotPSS-20120529.doc -->
 
<!-- Please specify the id of your work group’s PSS for doing FHIR work.  (If submitted but not yet approved, just write “pending”.) The link to the PSS template can be found here: http://gforge.hl7.org/gf/download/docmanfileversion/6832/9398/HL7FHIR_DSTUballotPSS-20120529.doc -->
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1422
  
 
==Scope of coverage==
 
==Scope of coverage==
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As a rule, resources should encompass all of these aspects.
 
As a rule, resources should encompass all of these aspects.
 
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The scope of the EffectEvidenceSynthesis resource is to describe the estimates of an effect of an exposure on an outcome where the effect estimates are derived from the combination of research studies.  Effect estimates are a measure of difference between the exposure state and an alternative exposure state (often called the control or comparator state)
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Expressing effect estimates is done throughout reporting of biomedical research, systematic reviews, and clinical reference across all disciplines.
  
 
==RIM scope==
 
==RIM scope==
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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 effect 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==
  
 
<!--Key resources are justified by CCDA, for resources not deemed "key", what interest is there by implementers in using this particular resource. Provide named implementations if possible - ideally provide multiple independent implementations. -->
 
<!--Key resources are justified by CCDA, for resources not deemed "key", what interest is there by implementers in using this particular resource. Provide named implementations if possible - ideally provide multiple independent implementations. -->
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Many knowledge producers who express the biomedical research community knowledge will be the implementers using this resources. Examples of these knowledge producers include Agency for Healthcare Research and Quality (AHRQ), Centers for Disease Control and Prevention (CDC), Cochrane, Duodecim Medical Publications Ltd (from the Finnish Medical Society), EBSCO Health, MAGIC (stands for Making GRADE the Irresistible Choice), and numerous guideline development organizations.
  
 
==Content sources==
 
==Content sources==
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Are there any source specifications that you wish to consult but are concerned about access to or expertise to consider? -->
 
Are there any source specifications that you wish to consult but are concerned about access to or expertise to consider? -->
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None expected beyond the standard source specifications.  However, the method for expressing citations (eg referring to a publication) is not yet defined and may require additional source specifications.
  
 
==Example Scenarios==
 
==Example Scenarios==
  
 
<!-- Provide a listing of the types of scenarios to be represented in the examples produced for this resource.  They should demonstrate the full scope of the resource and allow exercising of the resources capabilities (full element coverage, inclusion & omission of optional elements, repeating and singleton repeating elements, etc.) -->
 
<!-- Provide a listing of the types of scenarios to be represented in the examples produced for this resource.  They should demonstrate the full scope of the resource and allow exercising of the resources capabilities (full element coverage, inclusion & omission of optional elements, repeating and singleton repeating elements, etc.) -->
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A systematic review and meta-analysis combines 17 trials comparing Superdrug against Placebo in 12,356 study participants with Stressitis and finds that Superdrug reduces the Stressiness Score by a mean of 4.6 points but increases headache by 50% (ie 4% of people taking Placebo and 6% of people taking Superdrug had a headache).
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The effect estimates that may be reported from this example include:
 +
 +
*Mean reduction of 4.6 points in a score
 +
*Relative risk increase of 50% (or risk ratio 1.5) for the risk of headache
 +
*Absolute risk increase of 2% (or risk difference 0.02) for the risk of headache
 +
 +
The EffectEvidenceSynthesis resource describes:
 +
 +
*the point estimate for this effect estimate
 +
*classification of the estimate type (relative risk, odds ratio, absolute risk difference, etc)
 +
*a precision estimate (such as 95% confidence intervals)
 +
*rating of certainty of the effect estimate
 +
*descriptions of the population (eg Stressitis), exposure (eg Superdrug), alternative exposure (eg Placebo), and outcome (eg. Stressiness Score, or risk of headache) that the effect estimate is about
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*descriptions of the source of the effect estimate (eg author, citation, type of research, sample size)
  
 
==Resource Relationships==
 
==Resource Relationships==
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Reference to resources is really only relevant at the "same or higher level" (Bo – fix this wording)
 
Reference to resources is really only relevant at the "same or higher level" (Bo – fix this wording)
 
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  -->
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The EffectEvidenceSynthesis resource will reference:
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*RiskEvidenceSynthesis
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*PicoElementDefinition
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*PicDefinition
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*citation (an expected resource for future proposal)
  
 
==Resource Boundaries==
 
==Resource Boundaries==
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Are we confident existing implementations will be able to make the distinction? -->
 
Are we confident existing implementations will be able to make the distinction? -->
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To be determined if implementers have questions that need explanations to support distinction and clarification.
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EffectEvidenceSynthesis is about the difference (or "effect") between an exposure and alternative exposure state on an outcome in a population.  RiskEvidenceSynthesis is about the "risk" of an outcome with an exposure state in a population.  RiskEvidenceSytnhesis does not include an alternative exposure state of difference between states.
  
 
==Timelines==
 
==Timelines==
  
 
<!-- Indicate the target date for having the resource complete from a committee perspective and ready for vetting and voting -->
 
<!-- Indicate the target date for having the resource complete from a committee perspective and ready for vetting and voting -->
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First STU Ballot 2019 May
  
 
==gForge Users==
 
==gForge Users==
  
 
<!-- Identify the userids who will require commit access to gForge to maintain the resource.  (Ensure all users have registered for gForge.) -->
 
<!-- Identify the userids who will require commit access to gForge to maintain the resource.  (Ensure all users have registered for gForge.) -->
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brynrhodes (github user)
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KhalidShahin-EBSCO (github user)
  
 
==When Resource Proposal Is Complete==
 
==When Resource Proposal Is Complete==

Latest revision as of 15:07, 31 October 2019

Current version: https://confluence.hl7.org/display/FHIR/EffectEvidenceSynthesis+FHIR+Resource+Proposal
OpenHotTopic.GIF

This page documents a Pending FHIR Resource Proposal



EffectEvidenceSynthesis

Owning work group name

Clinical_Decision_Support

Committee Approval Date:

  • Initial PSS: June 22, 2018
  • CDS WG: September 12, 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 EffectEvidenceSynthesis resource is to describe the estimates of an effect of an exposure on an outcome where the effect estimates are derived from the combination of research studies. Effect estimates are a measure of difference between the exposure state and an alternative exposure state (often called the control or comparator state)

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

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 effect 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

Many knowledge producers who express the biomedical research community knowledge will be the implementers using this resources. Examples of these knowledge producers include Agency for Healthcare Research and Quality (AHRQ), Centers for Disease Control and Prevention (CDC), Cochrane, Duodecim Medical Publications Ltd (from the Finnish Medical Society), EBSCO Health, MAGIC (stands for Making GRADE the Irresistible Choice), and numerous guideline development organizations.

Content sources

None expected beyond the standard source specifications. However, the method for expressing citations (eg referring to a publication) is not yet defined and may require additional source specifications.

Example Scenarios

A systematic review and meta-analysis combines 17 trials comparing Superdrug against Placebo in 12,356 study participants with Stressitis and finds that Superdrug reduces the Stressiness Score by a mean of 4.6 points but increases headache by 50% (ie 4% of people taking Placebo and 6% of people taking Superdrug had a headache).


The effect estimates that may be reported from this example include:

  • Mean reduction of 4.6 points in a score
  • Relative risk increase of 50% (or risk ratio 1.5) for the risk of headache
  • Absolute risk increase of 2% (or risk difference 0.02) for the risk of headache

The EffectEvidenceSynthesis resource describes:

  • the point estimate for this effect estimate
  • classification of the estimate type (relative risk, odds ratio, absolute risk difference, etc)
  • a precision estimate (such as 95% confidence intervals)
  • rating of certainty of the effect estimate
  • descriptions of the population (eg Stressitis), exposure (eg Superdrug), alternative exposure (eg Placebo), and outcome (eg. Stressiness Score, or risk of headache) that the effect estimate is about
  • descriptions of the source of the effect estimate (eg author, citation, type of research, sample size)

Resource Relationships

The EffectEvidenceSynthesis resource will reference:

  • RiskEvidenceSynthesis
  • PicoElementDefinition
  • PicDefinition
  • citation (an expected resource for future proposal)

Resource Boundaries

To be determined if implementers have questions that need explanations to support distinction and clarification.

EffectEvidenceSynthesis is about the difference (or "effect") between an exposure and alternative exposure state on an outcome in a population. RiskEvidenceSynthesis is about the "risk" of an outcome with an exposure state in a population. RiskEvidenceSytnhesis does not include an alternative exposure state of difference between states.

Timelines

First STU Ballot 2019 May

gForge Users

brynrhodes (github user) KhalidShahin-EBSCO (github user)

When Resource Proposal Is Complete

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

FMG Notes

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