This wiki has undergone a migration to Confluence found Here
<meta name="googlebot" content="noindex">

Difference between revisions of "Outline comparison table"

From HL7Wiki
Jump to navigation Jump to search
Line 1: Line 1:
 
This table compares the current GTR section titles to corresponding heading in various recommendations found in the following literature:
 
This table compares the current GTR section titles to corresponding heading in various recommendations found in the following literature:
* '''ACMG''': American College Of Medical Genetics recommendations for standards for interpretation of sequence variations, see at [http://www.acmgfoundation.org/AM/Template.cfm?Section=Content_Area_413&Template=/CM/ContentDisplay.cfm&ContentID=6328]
+
* '''ACMG''': American College Of Medical Genetics recommendations for standards for interpretation of sequence variations, see entry G17 at [http://www.acmgfoundation.org/AM/Template.cfm?Section=Content_Area_413&Template=/CM/ContentDisplay.cfm&ContentID=6328]
 
* '''CAP''': College of American Pathologists - Clinical Laboratory Reports in Molecular Pathology, see at [http://www.archivesofpathology.org/doi/pdf/10.1043/1543-2165%282007%29131%5B852%3ACLRIMP%5D2.0.CO%3B2]
 
* '''CAP''': College of American Pathologists - Clinical Laboratory Reports in Molecular Pathology, see at [http://www.archivesofpathology.org/doi/pdf/10.1043/1543-2165%282007%29131%5B852%3ACLRIMP%5D2.0.CO%3B2]
 
* '''JMD''': Journal of Molecular Diagnostics - Clinician Perspectives about Molecular Genetic Testing for Heritable Conditions and Development of a Clinician-Friendly Laboratory Report, see at [http://moldiag.highwire.org/cgi/reprint/11/2/162]
 
* '''JMD''': Journal of Molecular Diagnostics - Clinician Perspectives about Molecular Genetic Testing for Heritable Conditions and Development of a Clinician-Friendly Laboratory Report, see at [http://moldiag.highwire.org/cgi/reprint/11/2/162]

Revision as of 07:05, 7 November 2011

This table compares the current GTR section titles to corresponding heading in various recommendations found in the following literature:

  • ACMG: American College Of Medical Genetics recommendations for standards for interpretation of sequence variations, see entry G17 at [1]
  • CAP: College of American Pathologists - Clinical Laboratory Reports in Molecular Pathology, see at [2]
  • JMD: Journal of Molecular Diagnostics - Clinician Perspectives about Molecular Genetic Testing for Heritable Conditions and Development of a Clinician-Friendly Laboratory Report, see at [3]

Note that GTR titles in parenthesis represnet parent sections.

GTR ACMG CAP JMD
Findings (Test Details) Genotype and/or haplotype Results Test results and a brief interpretation
Interpretation (Test Details) and Overall Interpretation (Summary) Interpretation including clinical implications Interpretations (optionally distinguish between clinical and analytic) Test results and a brief interpretation (grouped within the report)
Indications (Test Details, Summary) Reason for testing Indications for testing (Demographic information) Indication for testing/specimen sent
Test Performed (Test Details) Test Performed Laboratory procedures performed (Billing information) Test Ordered
Specimen (Test Details, Summary) Specimen type Specimen (within Laboratory/patient/sample identifiers) Specimen type
Background (Test Information) Limitations of the assay (free description under Comments) Ancillary information/information for specialists / supplemental information
Methodology (Test Information) Methodology Procedure (within supplemental information)
References (Test Information) References (Cite peer-reviewed medical literature or reliable Web sites, within Comments) (within supplemental information)
Recommendations (Summary) Recommendations Comment Guidance
FollowUp Genetic Tests (Recommendations / Summary) Follow-up test recommendations N/A Follow-up testing / Additional testing that may be useful for clarifying the test result
Follow Up Visits To Specialists (Recommendations / Summary) N/A N/A N/A
Recommended Actions(Recommendations / Summary) N/A N/A Testing of other family members, Genetic counseling, Resources for additional information