Building trust: the workflows around shared data The practice of medicine has a high standard when it comes to clinical evidence. Incomplete or inaccurate data in the patient record could easily lead to confusion and frustration for clinicians. New interoperability solutions provide the means to unify patient data without overwhelming clinical staff in the process. […]
First, they noted that to build an equity-oriented data system, groups should follow best practices from successful multistakeholder efforts, such as engaging key stakeholders early on and building community support. “Engaging with national and state partners is critical to promote buy-in; stakeholders want a path to deliver on REL data improvements that align with other […]
For instance, MercyOne, an accountable care organization (ACO) with over 400 service locations, had several disparate data sources lacking a common standard. “With such enormous stature of the ACO, designing engaged and patient-centric care across the care continuum was challenging along with having multiple practice sites,” VA officials said. Mercy health network partnered with health […]
Building on the progress of the HL7 Clinical Genomics Work Group, including its FHIR Genomics Implementation Guide, CodeX’s GenomeX community will design scalable pilots that use FHIR Genomics for multiple use cases. Proposed use cases are: • FHIR Genomics Data Exchange: Designing and building scalable FHIR Genomics interfaces to support interoperability of genomic data from […]
What Data Applies to the Information Blocking Rule Understanding ONC information blocking rule compliance depends upon a clear understanding of HIPAA-defined terms related to patient health information, according to a HealthITBuzz blog post written by ONC’s Kathryn Marchesini and Michael Lipinski. “EHI is defined as electronic protected health information (ePHI) to the extent that it would be included […]
Stakeholders categorized challenges into six themes that point to the continued need for: Standards development and content for the integration of genomic data into clinical and research systems Support during implementation of genomic standards Flexible infrastructure to support the complexity of genomic data Supporting the utilization of genomic data according to the different needs of […]
Reduce Healthcare Cost By delivering on population health initiatives and supporting care coordination, HIEs can help healthcare organizations cut downstream costs. A 2018 systematic review of studies of health information exchanges found evidence the exchanges reduced the cost of healthcare. The new findings “represent progress in reaching the national goals of better-quality care, improved population […]
Transitions of Care Interoperability Health IT stakeholders are also working to advance interoperability between primary care providers (PCPs) and specialists. Just as a circle has 360 degrees, Holly Miller, MD, MBA, FHIMSS, chief medical officer of MedAllies, says data exchange needs to be a closed-loop process to enable care coordination. That’s what she’s trying to accomplish […]
How can healthcare systems improve data normalization? Refer to the ISA and standardize across your system first There are a handful of interoperability rules that providers and payers must comply with, such as the CMS Interoperability and Patient Access final rule, but outside of these, systems have some freedom with regard to how they code […]
Accelerating the Transition HL7 has formed several accelerators focused on target segments of health care information exchange. The first was the Argonaut Project, established in 2014 to develop the basic building blocks of the FHIR standards. Within each accelerator, developers and users work together to define “use cases” — the contexts in which the proposed information exchange […]