Interoperability
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Exchange of Blood Product Information: An Initiative to Develop an HL7 FHIR® Standard
Lantana is initiating and looking for supporting partners to develop a standard for exchange of blood banking genotyping and phenotyping information.
Read MoreIncreasing Voluntary Public Health Reporting to the NHSN Antimicrobial Use Option
A Year of Stories
Interoperability Standards Enabling Cross-border Patient Summary Exchange
FHIR CDA Position Statement and Roadmap
This position statement addresses the relationship between HL7’s Clinical Document Architecture (CDA) product line and the Fast Health Interoperability Resource (FHIR) product line. It was prepared jointly by Lantana Consulting…
Read MoreDevelopment, implementation, and initial evaluation of a foundational open interoperability standard for oncology treatment planning and summarization, JAMIA January 2015
Authors: Jeremy L. Warner, Suzanne E. Maddux, Kevin S. Hughes, John C. Krauss, Peter Paul Yu, Lawrence N. Shulman, Deborah K. Mayer, Mike Hogarth , Mark Shafarman , Allison Stover Fiscalini,…
Read MoreAre Meaningful Use Stage 2 certified EHRs ready for interoperability? Findings from the SMART C-CDA Collaborative
Upgrades to electronic health record (EHR) systems scheduled to be introduced in the USA in 2014 will advance document interoperability between care providers. Specifically, the second stage of the federal…
Read MoreSMARTPlatforms.org: “C-CDA Endoscopy, or Improving Clinical Document Exchange” by David Kreda and Joshua Mandel
In 2014, the industry will see wide-scale production and exchange of Consolidated CDA documents among healthcare providers. Indeed, live production of C-CDAs is already underway for anyone using a Meaningful…
Read MoreMt. Washington Revisited
This paper examines changes in the health care industry since a contrarian proposal was submitted to CMS in January 2005. That proposal focused on CMS exercising its commercial power as…
Read MoreAPIC Announces New CDC Approach to HAI Reporting using CDA
The Centers for Disease Control and Prevention (CDC)…is developing a standards-based solution for transmission of health care-associated infection (HAI) data from existing commercial software systems to the agency’s National Healthcare…
Read MoreQuality Reporting Document Architecture (QRDA) Initiative Phase I Final Report
The Quality Reporting Document Architecture (QRDA) initiative results from a private collaboration sponsored by the Alliance for Pediatric Quality (Alliance), a joint effort of the American Academy of Pediatrics, The…
Read MoreImplementing Single Source: The STARBRITE Proof-of-Concept Study
The “Single Source” concept applies the write-once, use-many principle to data gathering for clinical trials using CDA as the key to interoperability in this case study. The article reports on…
Read MoreHealthcare Informatics: “Guidelines Will Standardize Dictated Documents” by Brian Albright
“Dictated medical notes and other types of transcribed patient records are usually available in electronic form, but have traditionally not been very useful in the context of an electronic medical…
Read MoreModernHealthcare.com: “HL7’s first ballot in expected series under way” by Joe Conn
“Implementation guides for documents containing ‘history and physical reports’ were submitted Monday to Ann Arbor, Mich.-based HL7. It is the first ballot in what is expected to be a series…
Read MoreHL7 Clinical Document Architecture, Release 2, JAMIA Paper
Release 2 (CDA R2) became an ANSI-approved HL7 Standard in May 2005 and is the subject of this article, where the focus is primarily on how the standard has evolved…
Read MoreMt. Washington Vision: A Response to ONCHIT’s Request for Information
The Mt. Washington Vision was created in response to the ONCHIT RFI.
Read MoreThe Clinical Document Architecture (CDA), Release 1.0, JAMIA Paper
This was our debut to the informatics community in 2000.
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