Literature DB >> 20351857

Evaluation of LOINC for representing constitutional cytogenetic test result reports.

Yan Z Heras1, Joyce A Mitchell, Marc S Williams, Arthur R Brothman, Stanley M Huff.   

Abstract

Genetic testing is becoming increasingly important to medical practice. Integrating genetics and genomics data into electronic medical records is crucial in translating genetic discoveries into improved patient care. Information technology, especially Clinical Decision Support Systems, holds great potential to help clinical professionals take full advantage of genomic advances in their daily medical practice. However, issues relating to standard terminology and information models for exchanging genetic testing results remain relatively unexplored. This study evaluates whether the current LOINC standard is adequate to represent constitutional cytogenetic test result reports using sample result reports from ARUP Laboratories. The results demonstrate that current standard terminology is insufficient to support the needs of coding cytogenetic test results. The terminology infrastructure must be developed before clinical information systems will be able to handle the high volumes of genetic data expected in the near future.

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Year:  2009        PMID: 20351857      PMCID: PMC2815393     

Source DB:  PubMed          Journal:  AMIA Annu Symp Proc        ISSN: 1559-4076


  5 in total

1.  Comparison of targeted and whole genome analysis of postnatal specimens using a commercially available array based comparative genomic hybridisation (aCGH) microarray platform.

Authors:  E Aston; H Whitby; T Maxwell; N Glaus; B Cowley; D Lowry; X L Zhu; B Issa; S T South; A R Brothman
Journal:  J Med Genet       Date:  2008-01-04       Impact factor: 6.318

2.  Clinician perspectives about molecular genetic testing for heritable conditions and development of a clinician-friendly laboratory report.

Authors:  Ira M Lubin; Margaret M McGovern; Zoe Gibson; Susan J Gross; Elaine Lyon; Roberta A Pagon; Victoria M Pratt; Jamila Rashid; Colleen Shaw; Lander Stoddard; Tracy L Trotter; Marc S Williams; Jean Amos Wilson; Kenneth Pass
Journal:  J Mol Diagn       Date:  2009-02-05       Impact factor: 5.568

Review 3.  Delivery of genomic medicine for common chronic adult diseases: a systematic review.

Authors:  Maren T Scheuner; Pauline Sieverding; Paul G Shekelle
Journal:  JAMA       Date:  2008-03-19       Impact factor: 56.272

4.  Providers' knowledge of genetics: A survey of 5915 individuals and families with genetic conditions.

Authors:  Erin K Harvey; Chana E Fogel; Mark Peyrot; Kurt D Christensen; Sharon F Terry; Joseph D McInerney
Journal:  Genet Med       Date:  2007-05       Impact factor: 8.822

5.  Enhanced detection of clinically relevant genomic imbalances using a targeted plus whole genome oligonucleotide microarray.

Authors:  Erin L Baldwin; Ji-Yun Lee; Douglas M Blake; Brian P Bunke; Chad R Alexander; Amy L Kogan; David H Ledbetter; Christa L Martin
Journal:  Genet Med       Date:  2008-06       Impact factor: 8.822

  5 in total
  2 in total

1.  Supporting interoperability of genetic data with LOINC.

Authors:  Jamalynne Deckard; Clement J McDonald; Daniel J Vreeman
Journal:  J Am Med Inform Assoc       Date:  2015-02-05       Impact factor: 4.497

2.  Genetic testing behavior and reporting patterns in electronic medical records for physicians trained in a primary care specialty or subspecialty.

Authors:  Jeremiah Geronimo Ronquillo; Cheng Li; William T Lester
Journal:  J Am Med Inform Assoc       Date:  2012-04-17       Impact factor: 4.497

  2 in total

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