At least the claim is that patients can opt out at any time.  They could
also take a page from VA and only submit lab values along with hashed IDs to
the central system so that the only way to know who the person is would be
to go to the system sending in the data.  VA has centralized databases for
monitoring WBCs weekly for each patient on clozapine, but no one can be
identified by looking at any data in the central database.  The same hash is
generated at each facility (the hash algorithm must be kept secure) so the
same patient's data at different sites can be combined centrally.  Only by
taking the hashed ID at the central system to a local system that sent the
data and has the association between the hash and the patient's ID can the
patient's identity be known.

-----Original Message-----
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Nancy
Anthracite
Sent: Friday, July 15, 2005 7:24 AM
To: hardhats-members@lists.sourceforge.net
Subject: [Hardhats-members] Now this is scary!

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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