by corasharma | March 15, 2012
A few years ago my daughter began developing asthma-like symptoms brought on by reactions to pollen, cat dander, and other triggers. I can still remember the panic I felt in my chest the first time she ran to me wheezing and crying that she couldn’t breathe. Thankfully, her wheezing episodes
by ndrao | February 20, 2012
(Note: This is the second of a two-part post.) Keeping it Local This is most representative of the status quo and the most realistic path forward for the vast majority of payers who typically operate at the local level. In this scenario, one or more health plans in a regional
by John Moore | February 13, 2012
Chilmark Research tends to shy away from the thorny, nearly intractable issues of privacy and security of Personal Health Information (PHI) (we'll leave that to the lawyers and policy wonks to figure out). However one thing is very clear: As we continue to conduct more and more of our daily
by John Moore | January 31, 2012
Since its start in 2007, Chilmark Research has kept a fairly low profile as analyst firms go, focusing on a few discrete domains of healthcare IT (HIT). First there was patient and consumer engagement that led to the publication of our first report on Personal Health Records (PHRs). That first
by corasharma | October 07, 2010
I recently had the opportunity to speak with Henry J. Feldman, M.D., instructor of medicine at Harvard Medical School at the Beth Israel Deaconess Medical Center (BIDMC). Dr. Feldman also serves as Chief Information Architect in addition to practicing as a hospitalist at BIDMC. Dr. Feldman discussed BIDMC’s platform-agnostic mobile
by John Moore | July 15, 2010
Everyone seems to have an opinion, or at least has written something, about the final Meaningful Use (MU) Rules that were released on July 13th. Of the multitude of posts and articles out there on the net, there the top three to get you started are: 1) ONC Chief, David
by John Moore | March 26, 2010
One of the thornier issues regarding the establishment of public Health Information Exchanges (HIEs) is how to manage consumer consent of personal health information (PHI) sharing. Today, there is no single standard approach across the US. Some states have an opt-in process, others an opt-out. Granularity of data shared, use
by John Moore | January 06, 2010
On Saturday, Jan. 10th, I'll be moderating a panel at the Consumer Electronics Show's (CES) Digital Health Summit. The distinguished panel that includes executives from Dossia, Kaiser-Permenante, Microsoft and Walgreens will address the topic: Who Will you Trust with Your Health Data? In preparation, I have been doing some research
