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Blogposium -- April 18 - 21 2006 The Blogposium will be a multi-day collaboration among a circle of health-IT bloggers to show the world that together, we
can do
real and practical work. To make this first-ever, cross-blog cooperative experiment a success, we'll keep the work and the
objective
relatively simple: to continue fleshing out
The Clinical Informatics Wiki with a dozen or more new entries, so
that this wikipedia-like resource will become more useful for all. (Ed. Everyone is encouraged to participate as either a
writer or
reviewer.)
CalRHIO Data Standards Recommendations CalRHIO’s data standards roadmap provides a guide for health care organizations as they purchase new or upgrade current health
information technology. It is also intended to assist health IT vendors in upgrading and developing products. The roadmap
illustrates the
current data standard in use and the standard expected to be in use by 2010 and beyond. Nine areas are addressed: administration
and finance,
allergies, clinical documentation, imaging, immunization, laboratory, medication, services, and vocabulary.
Arizona Health-e Connection Steering Committee delivers its Roadmap for the future of electronic health records The Roadmap outlines a path for Arizona’s health care community to securely exchange medical information statewide with the
goal of reducing costs and improving the quality of patient care in Arizona. The Roadmap also sets the stage for the advent
of electronic
medical records in the future. The Roadmap was developed with participation from over 200 Arizonans representing health care
providers,
payers and patients with strong representation from rural constituencies.
Taking the Least of You -- The Tissue-Industrial Complex This is a fascinating article about how various healthcare organizations and researchers have abused patients' generousity.
For
example, in 1999 the
RAND Corporation published a report with what it called a
"conservative estimate" that more than 307 million tissue samples from more than 178 million people were stored in the United
States. This number, the report said, was increasing by more than 20 million samples each year. These samples come from routine
medical
tests, operations, clinical trials and research donations. (Ed. And we are concerned with the "personal information" stored
in
various clinical information systems? I think our worries are misplaced!)
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