NYC Department of Health is asking to mandate that all of the city's labs 
report A1C Hemoglobin values into a patient registry of Diabetics in New 
York. 

This is one of the things that concerns me about all of this enthusiasm for a 
Health Data Repositories.  You may be told your information is private, but 
then once it is stored like this, you can loose control of it for the "public 
good".  This article does not suggest this is data they want is scrubbed of 
personal identifiers.  This is far too "Big Brother" for me, and this doesn't 
even involve a HDR yet.

I feel things are a little safer if the nationwide network were a database to 
where patient information might be found if the patient wants it to be found.

http://govhealthit.com/article89548-07-13-05-Web
-- 
Nancy Anthracite


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