Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-23 Thread Mike Lieman
On 2/23/06, Chris Farley <[EMAIL PROTECTED]> wrote:
> Dude...Special Olympics??  That was tasteless and uncalled for.  You should
> be ashamed of yourself.

Less for the joke than forgetting that fully 50% of email is misinterperted.

If I offended anyone, I apologize.

While I'm at it, I apologize for any possible infringement on either
the Special Olympics or Olympics intellectual property.

A question though.  The sentiment is valid.  Even the "winner" of an
internet argument is a fool among fools.  How would you rephrase it?

Forget I asked.  Me not reply to thread no more.


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RE: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-23 Thread Chris Farley
Dude...Special Olympics??  That was tasteless and uncalled for.  You should
be ashamed of yourself.

Chris Farley


-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Mike
Lieman
Sent: Thursday, February 23, 2006 10:00 AM
To: hardhats-members@lists.sourceforge.net
Subject: Re: [Hardhats-members] A Pill, a Scalpel, a Database

On 2/23/06, Kevin Toppenberg <[EMAIL PROTECTED]> wrote:
> Hey guys, can we agree to disagree, or move any ensuing flame war to
> another venue?
>
> Kevin

Agreed.  This thread is dead.

Arguing in a mailing list is like competing in the Special
Olympics  Even if you win, ...


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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-23 Thread Mike Lieman
On 2/23/06, Kevin Toppenberg <[EMAIL PROTECTED]> wrote:
> Hey guys, can we agree to disagree, or move any ensuing flame war to
> another venue?
>
> Kevin

Agreed.  This thread is dead.

Arguing in a mailing list is like competing in the Special
Olympics  Even if you win, ...


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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-23 Thread Kevin Toppenberg
Hey guys, can we agree to disagree, or move any ensuing flame war to
another venue?

Kevin




On 2/23/06, Mike Lieman <[EMAIL PROTECTED]> wrote:
> On 2/23/06, Ruben Safir <[EMAIL PROTECTED]> wrote:
> > > >
> > >
> > > I dunno,
> >
> > Well that would be obvious
> >
> > > your duty to The State in obeying it's regulations about
> > > privacy and your duty to your customers seems pretty clear cut.
> >
> > Not so clear cut.  First I don't have any customers.  Maybe you have
> > customers, but as a Pharmacist I have patients, which is why they call
> > me Doctor.
> >
> > >   I
> > > don't exactly know where you figure unlawfully disclosing HIPPA
> > > protected info to unauthorized people sets in, but if that's your idea
> > > of the RIGHT THING, I don't want you counting MY pills.
> > >
> >
> > That is fine.  HIPPA doesn't override my professional responsibilities.
>
> Of course, those are your professional responsibilities as YOU see them.
>
> The will of The People which you AGREED to obey when you begged for a
> license from the state is very clear cut in what your responsibilites
> are.  You obey the regulations, or you don't deserve a license.
>
> That's to protect The People.  Your Patients.  From cases where your
> judgement of your professional responsibilities don't agree with what
> the rest of society has deemed them to be.
>
> Don't want to obey The State's regulations in all their glory?  Give
> up your license.   Don't say you're being moral when you PROMISED to
> obey the regulations, then BREAK YOUR PROMISE when convenient.
>
>
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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-23 Thread Mike Lieman
On 2/23/06, Ruben Safir <[EMAIL PROTECTED]> wrote:
> > >
> >
> > I dunno,
>
> Well that would be obvious
>
> > your duty to The State in obeying it's regulations about
> > privacy and your duty to your customers seems pretty clear cut.
>
> Not so clear cut.  First I don't have any customers.  Maybe you have
> customers, but as a Pharmacist I have patients, which is why they call
> me Doctor.
>
> >   I
> > don't exactly know where you figure unlawfully disclosing HIPPA
> > protected info to unauthorized people sets in, but if that's your idea
> > of the RIGHT THING, I don't want you counting MY pills.
> >
>
> That is fine.  HIPPA doesn't override my professional responsibilities.

Of course, those are your professional responsibilities as YOU see them.

The will of The People which you AGREED to obey when you begged for a
license from the state is very clear cut in what your responsibilites
are.  You obey the regulations, or you don't deserve a license.

That's to protect The People.  Your Patients.  From cases where your
judgement of your professional responsibilities don't agree with what
the rest of society has deemed them to be.

Don't want to obey The State's regulations in all their glory?  Give
up your license.   Don't say you're being moral when you PROMISED to
obey the regulations, then BREAK YOUR PROMISE when convenient.


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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-23 Thread Ruben Safir
> >
> 
> I dunno, 

Well that would be obvious

> your duty to The State in obeying it's regulations about
> privacy and your duty to your customers seems pretty clear cut.

Not so clear cut.  First I don't have any customers.  Maybe you have
customers, but as a Pharmacist I have patients, which is why they call
me Doctor.

>   I
> don't exactly know where you figure unlawfully disclosing HIPPA
> protected info to unauthorized people sets in, but if that's your idea
> of the RIGHT THING, I don't want you counting MY pills.
> 

That is fine.  HIPPA doesn't override my professional responsibilities. 
I will not let people die because of HIPPA, or any OTHER regulation. 
See, as a medical professional, we have a responsibility that goes well
beyond the letter of the law.  We are actually called upon to do what it
right.

As for counting pills, I have no IDEA what your talking about.  I have
no pills in my pharmacy, unless you mean the birth control tablets,
which are not pills either.  Nor do have I counted any tablets in about
10 years.  There is a big machine and a few non-professional techs
running around to do that.  Its time for you to put your bigoted ideas
away and upgrade your perspective of what a Pharmacist does and is. 
More often then not they are saying some more patients neck.

   
> You might decide the RIGHT THING is to swap my BP meds for something
> different, or short me cause you believe the doc prescribed too many.

Well, on the first case, I might very well indeed do that.  Better me
than the pharmacist working for your insurance company.  But if I did,
and it was in a outpatient situation, I would confer with the
physician.  If it was an inpatient situation, I would need to know the
protocols for institution.  In some places I would indeed just change
it.  In others I'd write the problem in the chart.

I would CERTAINLY never authorize the dispensing of anything I found
which I deemed not in your interest, and potentially harmful to your
health,
 
>  
> Maybe the RIGHT THING is to not fill a "morning after" script.
> 

Maybe, but that would be a different issue which has zero to do with
this thread.  And some dentists refuse to work with HIV patients, and
many physicians refuse to perform abortions.  And then you have
physician assisted suicide and the recent questions about the use of
injections for executions in the criminal system.  Your welcome to break
each of these issues out to different threads, but I no interest in
participating in those discussions at this time. 

> Perhaps you don't want to admit violating the law, your oath, and
> professional cannons in something archived forever by Google, too.
> 
> 

You are obviously clueless what my professional responsibilities are
anyway.  By all means, google away!

Ruben




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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-22 Thread Mike Lieman
On 2/22/06, Ruben Safir <[EMAIL PROTECTED]> wrote:
> On Wed, 2006-02-22 at 11:35, Mike Lieman wrote:
> > On 2/21/06, Ruben Safir <[EMAIL PROTECTED]> wrote:
> > > On Mon, 2006-02-20 at 08:02, Mike Lieman wrote:
> > > > On 2/16/06, Ruben Safir <[EMAIL PROTECTED]> wrote:
> > > >
> > > > >
> > > > > Open my records!  Please open my records.
> > > > >
> > > > > Is that clear enough?
> > > > >
> > > >
> > > > How do you think your patients feel about that?
> > >
> > > I don't really care how they feel about it any more than I care how they
> > > feel about any other professional decision.
> >
> > Great.  I know what kind of physician you are now.
> >
> > There's no need to continue this.
> >
> >
> I'm a Pharmacist.  The kind that does the ***RIGHT THING*** when faced
> with a dilemma and not swayed by personal considerations, corruption, or
> profit when faced with healthcare concerns.
>
> Ruben
>

I dunno, your duty to The State in obeying it's regulations about
privacy and your duty to your customers seems pretty clear cut.  I
don't exactly know where you figure unlawfully disclosing HIPPA
protected info to unauthorized people sets in, but if that's your idea
of the RIGHT THING, I don't want you counting MY pills.

You might decide the RIGHT THING is to swap my BP meds for something
different, or short me cause you believe the doc prescribed too many. 
Maybe the RIGHT THING is to not fill a "morning after" script.

Perhaps you don't want to admit violating the law, your oath, and
professional cannons in something archived forever by Google, too.


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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-22 Thread Ruben Safir
On Wed, 2006-02-22 at 11:35, Mike Lieman wrote:
> On 2/21/06, Ruben Safir <[EMAIL PROTECTED]> wrote:
> > On Mon, 2006-02-20 at 08:02, Mike Lieman wrote:
> > > On 2/16/06, Ruben Safir <[EMAIL PROTECTED]> wrote:
> > >
> > > >
> > > > Open my records!  Please open my records.
> > > >
> > > > Is that clear enough?
> > > >
> > >
> > > How do you think your patients feel about that?
> >
> > I don't really care how they feel about it any more than I care how they
> > feel about any other professional decision.
> 
> Great.  I know what kind of physician you are now.
> 
> There's no need to continue this.
> 
> 
I'm a Pharmacist.  The kind that does the ***RIGHT THING*** when faced
with a dilemma and not swayed by personal considerations, corruption, or
profit when faced with healthcare concerns.

Ruben

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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-22 Thread Kevin Toppenberg
Ruben is not a physician, as far as I know.  I believe he is a pharmacist.

Kevin


On 2/22/06, Mike Lieman <[EMAIL PROTECTED]> wrote:
> On 2/21/06, Ruben Safir <[EMAIL PROTECTED]> wrote:
> > On Mon, 2006-02-20 at 08:02, Mike Lieman wrote:
> > > On 2/16/06, Ruben Safir <[EMAIL PROTECTED]> wrote:
> > >
> > > >
> > > > Open my records!  Please open my records.
> > > >
> > > > Is that clear enough?
> > > >
> > >
> > > How do you think your patients feel about that?
> >
> > I don't really care how they feel about it any more than I care how they
> > feel about any other professional decision.
>
> Great.  I know what kind of physician you are now.
>
> There's no need to continue this.
>
>
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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-22 Thread Mike Lieman
On 2/21/06, Ruben Safir <[EMAIL PROTECTED]> wrote:
> On Mon, 2006-02-20 at 08:02, Mike Lieman wrote:
> > On 2/16/06, Ruben Safir <[EMAIL PROTECTED]> wrote:
> >
> > >
> > > Open my records!  Please open my records.
> > >
> > > Is that clear enough?
> > >
> >
> > How do you think your patients feel about that?
>
> I don't really care how they feel about it any more than I care how they
> feel about any other professional decision.

Great.  I know what kind of physician you are now.

There's no need to continue this.


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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-21 Thread Greg Woodhouse
--- Ruben Safir <[EMAIL PROTECTED]> wrote:

> Or do you care more how
> your
> patient "feels" about it then saving the life of your patients wife
> when
> you tell her that her husband has AID's.  What kind of professional
> ethics are you displaying?
> 
> 
> Ruben

I think Ruben raises some valid points here. When we say that there is
no need, from a public health perspective, to track progress of a
disease at the individual level, is that a conclusion based on science
or policy? I'm not saying policy is unimportant, of course, but we
often fail to distinguish between the two. I don't pretend to know the
answers, but it does at least seem that these are valid questions. I am
inclined to agree that legal protections are all the more important
with technologies such as electronic health records being introduced,
and the last thing I want to do is suggest that I don't think privacy
is very important, but I cringe when I think of a repeat of 1918, too.

===
Gregory Woodhouse  <[EMAIL PROTECTED]>
"All truth passes through three stages: First, it is ridiculed.
Second, it is violently opposed. Third, it is accepted as
being self-evident."
--Arthur Schopenhauer


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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-21 Thread Ruben Safir
On Mon, 2006-02-20 at 08:02, Mike Lieman wrote:
> On 2/16/06, Ruben Safir <[EMAIL PROTECTED]> wrote:
> 
> >
> > Open my records!  Please open my records.
> >
> > Is that clear enough?
> >
> 
> How do you think your patients feel about that?

I don't really care how they feel about it any more than I care how they
feel about any other professional decision.  

Isn't that a stupid question on your part?  Or do you care more how your
patient "feels" about it then saving the life of your patients wife when
you tell her that her husband has AID's.  What kind of professional
ethics are you displaying?


Ruben




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RE: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-21 Thread Ruben Safir
I believe local governments has a carve out.  In fact, governments and
law enforcement in general have a carve out.


On Mon, 2006-02-20 at 08:06, Mike Ginsburg wrote:
> I assume that while we still have HIPAA, that the City of New York meets all
> HIPAA requirements and that all the appropriate paper work has been taken
> care of. Otherwise, would participating labs be liable for fines?
> 
> -Original Message-
> From: [EMAIL PROTECTED]
> [mailto:[EMAIL PROTECTED] On Behalf Of Mike
> Lieman
> Sent: Monday, February 20, 2006 8:00 AM
> To: hardhats-members@lists.sourceforge.net
> Subject: Re: [Hardhats-members] A Pill, a Scalpel, a Database
> 
> On 2/16/06, Ruben Safir <[EMAIL PROTECTED]> wrote:
> 
> > The health department, as far as I'm concerned, can ask for any 
> > information it wants.  Unless your showing me that this information is 
> > being miss used, or used legally, I'm ABSOLUTELY not interested.
> >
> > In fact, they need to flush HIPPA which is just stupid.
> >
> > Ruben
> 
> Privacy v. Responsibility.  Geez, what a hot button topic.  Let me confine
> my comments to this:
> 
> If we return responsibility for ensuring the privacy of medical records to
> the individual, how would you handle a patient who hands you a "Personal
> Copyright and License" which ONLY permits YOU to use and store the
> information needed for treatment but not to disclose it without written
> permission?
> 
> 
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RE: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-20 Thread Mike Ginsburg
I assume that while we still have HIPAA, that the City of New York meets all
HIPAA requirements and that all the appropriate paper work has been taken
care of. Otherwise, would participating labs be liable for fines?

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Mike
Lieman
Sent: Monday, February 20, 2006 8:00 AM
To: hardhats-members@lists.sourceforge.net
Subject: Re: [Hardhats-members] A Pill, a Scalpel, a Database

On 2/16/06, Ruben Safir <[EMAIL PROTECTED]> wrote:

> The health department, as far as I'm concerned, can ask for any 
> information it wants.  Unless your showing me that this information is 
> being miss used, or used legally, I'm ABSOLUTELY not interested.
>
> In fact, they need to flush HIPPA which is just stupid.
>
> Ruben

Privacy v. Responsibility.  Geez, what a hot button topic.  Let me confine
my comments to this:

If we return responsibility for ensuring the privacy of medical records to
the individual, how would you handle a patient who hands you a "Personal
Copyright and License" which ONLY permits YOU to use and store the
information needed for treatment but not to disclose it without written
permission?


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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-20 Thread Mike Lieman
>
> Blaming the CEO isn't fair.  They have every right to be compensated at
> ridiculous levels, being that they are in charge of such large
> organizations.  All CEOs are ridiculously compensated.
>

Sure, but I'm struck by the thought that if the LAW was a corporate
office could have only the healthcare plan offered to the janitory, we
wouldn't be having a lot of these arguements.


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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-20 Thread Mike Lieman
On 2/16/06, Ruben Safir <[EMAIL PROTECTED]> wrote:

>
> Open my records!  Please open my records.
>
> Is that clear enough?
>

How do you think your patients feel about that?


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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-20 Thread Mike Lieman
On 2/16/06, Ruben Safir <[EMAIL PROTECTED]> wrote:

> The health department, as far as I'm concerned, can ask for any
> information it wants.  Unless your showing me that this information is
> being miss used, or used legally, I'm ABSOLUTELY not interested.
>
> In fact, they need to flush HIPPA which is just stupid.
>
> Ruben

Privacy v. Responsibility.  Geez, what a hot button topic.  Let me
confine my comments to this:

If we return responsibility for ensuring the privacy of medical
records to the individual, how would you handle a patient who hands
you a "Personal Copyright and License" which ONLY permits YOU to use
and store the information needed for treatment but not to disclose it
without written permission?


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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-17 Thread JohnLeoZimmer

Mike Schrom wrote:


CBF: This should definitely be legal.  Why should the employer be saddled
with the cost of your lowered productivity due to illness?

MS: That sounds great, unless you are the one whose children can't have 
food or clothes or go to college because you can't get a job because 
EVERY potential employer can find out your A1C or how often you've 
filled your asthma inhaler prescription.


As I understand "insurance", the concept is that a large pool of folks 
<> risk so that all the members suffer less from life's 
uncertainties.


As I understand insurance as it applies to the unfortunate citizens of 
the United States, we have evolved a large industry dedicated to profit 
by <> providing health care.


That is the situation on the ground where I see patients.
This discussion is about some other planet.

Regards to all,
jlzimmer



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RE: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread Chris Farley


Chris Farley
Independent Consultant
540-722-2143

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Mike
Schrom
Sent: Thursday, February 16, 2006 4:33 PM
To: Hardhats-members@lists.sourceforge.net
Subject: RE: [Hardhats-members] A Pill, a Scalpel, a Database

(Snip)

CBF: This should definitely be legal.  Why should the employer be saddled
with the cost of your lowered productivity due to illness?

MS: That sounds great, unless you are the one whose children can't have 
food or clothes or go to college because you can't get a job because 
EVERY potential employer can find out your A1C or how often you've 
filled your asthma inhaler prescription.

CBF: I am confident that laws can and will be passed that will prevent
employers from using medical information against candidates.  Laws already
exist in the form of the ADA that can be applied.

(Snip)

That is the
idea of co-pays today, just a little hurtle to make sure you really are sick
- though that doesn't seem to be working very well.

MS: Not true! The copay is a way of shifting the costs away from the 
insurance plan which has converted to a 'for profit' and needs to pay an 
increasing percentage of your ever rising premium dollars to their 
millionaire CEO and stockholders. I have patients who have a $30 copay 
for a $45 visit, which costs the Insurer $7 after the copay and the $8 
risk withhold (which I may never see)!

CBF: I'd call that a poor plan.  I have a ten dollar co-pay, regardless of
the visit cost.  

Blaming the CEO isn't fair.  They have every right to be compensated at
ridiculous levels, being that they are in charge of such large
organizations.  All CEOs are ridiculously compensated.


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RE: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread Chris Farley


Chris Farley
Independent Consultant
540-722-2143

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Stephen
Hay
Sent: Thursday, February 16, 2006 4:32 PM
To: hardhats-members@lists.sourceforge.net
Subject: Re: [Hardhats-members] A Pill, a Scalpel, a Database

Likewise:

Chris Farley wrote:
> Comments are inserted below:
> 
> Chris Farley
> 
> -Original Message-
> From: [EMAIL PROTECTED]
> [mailto:[EMAIL PROTECTED] On Behalf Of Stephen
> Hay
> Sent: Thursday, February 16, 2006 3:31 PM
> To: hardhats-members@lists.sourceforge.net
> Subject: Re: [Hardhats-members] A Pill, a Scalpel, a Database
> 
> (SNIP)
> 
> And people who make policy tend not to be subject to that 
> policy - at least, where I live that's the case... Likewise, 
> the people who demand the information be made public are 
> usually in a position, I say usually, that doesn't require 
> that their own records are open to public display... or 
> they're currently in a situation in which it doesn't matter. 
> Funny how the onset of disease affects people's perspective 
> on things like this...
> 
> CBF: Ultimately, no one is exempt.  If you abuse the power the people give
> you, you won't be in a position to make policy very long.

True. But the policies remain. It's rare that these things 
are reversed.

CBF: I agree.  The policies are also very slow moving and this is something
to guard against.  We the people, so to speak, need to keep our politicians
in line.

> 
> (SNIP)
> 
> There is also the possibility to profile and apply user-pays 
> to those who have a non-contagious disease which treatment 
> costs a lot. So suddenly if you're sick, you're financially 
> responsible for that too. So much for *public* health.
> 
> CBF: I don't see an issue with this.  Why shouldn't sick people pay for
> care?  When I was a child, I hardly ever went to the doctor.  My mother
> didn't want to pay for it.  I only went when I was very ill.  That is the
> idea of co-pays today, just a little hurtle to make sure you really are
sick
> - though that doesn't seem to be working very well.
> 
> But there's insurance. For a start, the life insurance 
> companies would be VERY interested because they'd have a way 
> of checking the truth or not of insurance applications. In 
> fact, you wouldn't even need to fill in the application. 
> They could just send you a bill based on your life expectancy.
> 
> CBF: This is a perfect way to handle life insurance.  The idea of life
> insurance is to help the survivors should you be taken before you have a
> chance to plan for it.  Those who are going to die early, should live life
> in that manner and plan appropriately - and pay more for life insurance.
If
> my life expectancy is 80, I don't want to pay more because someone with a
> shorter life expectancy wanted to lie to the insurer so they could live
high
> off the hog.

It's one way of looking at it. Up to now, life insurance 
premiums spread the risk across all policy holders. Basing 
it on individual circumstances reduces the need to spread 
the risk. And places it all on the individual carrying the 
condition. How do you deal with congenital illness in this 
case? Is the individual to be financially penalised for 
carrying a condition he didn't "choose"?

CBF: Yes, the individual is to be penalized.  I understand that there are
moral differences in this regard.  However, I don't feel that I should be
forced to pay for another person's illness.  I may choose to do so,
philanthropically, but I don't want to be forced.

> Employers would be interested because they'd be able to pick 
> and choose employees based on health factors as well as 
> competence. Meaning, if you had the choice between two 
> candidates and one suffered from a condition that might 
> affect their work, which would you choose? Is that legal? 
> Maybe not now, but just wait until the next downturn...
> 
> CBF: This should definitely be legal.  Why should the employer be saddled
> with the cost of your lowered productivity due to illness?
 >
> So the sick become the unemployed, who can't afford the 
> insurance for the treatment they need. No problem, you say. 
> That's what happens now...
> 
> And it goes on.
> 
> You'll be able to check whether or not people are carrying 
> the gene that makes them pre-disposed to a certain disease. 
> You could even sterilise them so that they don't propagate 
> the gene, in the interest of the common good, of course.
> 
> CBF: The points you made in the previous paragraphs closely align with the
> eugenics debates of the 1920s.  The same debates

Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread Stephen Hay

Sometimes a picture is worth, well, you know... ;-)

http://www.claybennett.com/pages/10_29_01.html

Kevin Toppenberg wrote:

This sounds like a discussion from an ethics course, where we have a
discordance between conflicting principles.

As physicians, we are trained to be patient advocates.  We don't
usually step back and look at the big picture--at least those in
private practice.  It takes researches in the CDC etc to address group
concerns etc.  So I see this as a public health policy issue. 
"Rights" can be seen as universal (the "right" to life, liberty, and

the pursuit of happiness), or perhaps granted--the "rights" of those
in China differ from our "rights".  It often seems to come down to
"might is right".  The government has the might, and thus dictates the
rights.

But I think that many want to do the correct/right thing for the
majority of people.  Does the "right" of privacy outweigh the need for
others to be safe?  I think not.  Thus I would understand manditory
reporting of HIV (and especially not that it is not seen so much like
'leprosy' from the bible, and more like cancer.)  But I agree with
Nancy that collecting HgbA1c's is an unreasonable breach of privacy.

But to be honest, I think that privacy is nebulus concept that is
rapidly being stripped away.  We carry cell phones--> our movement can
be tracked.  We watch TiVo TV--> our watching habits can be tracked. 
Even our searches on Google are being tracked.  I read in Wired

Magazine about thermal imaging techniques were people outside one's
home can thermally image those inside.  I can anticipate times where
we all have to acknowledge that it becomes nigh unto impossible to
keep secrets.

Kevin

On 2/16/06, Ruben Safir <[EMAIL PROTECTED]> wrote:

On Thu, 2006-02-16 at 15:49 -0400, Joseph Conn wrote:

I'm with you, Nancy.  The road to Hell is paved with good intentions and
I'm surprised I haven't heard the ACLU filing an injunction against NYC
on this program.  Since diabetes is not contagious, I don't think that
because the city may end up paying the cost of care for some of its
citizens gives it the right to snoop on all of its citizens.


What is this?  Your making a bald faced lie here.  You know as well as
anyone on this list that the costs here is not just a few dollars, but
money that runs into the BILLIONS not to mention the real morbitiy and
mortality.

But what do you care?  Your not a minority poor from Brownsville, or a
tax payer of the city of New York so its no sweat off your back.

Disguesting


 This
program isn't a slippery slope in my book, it's a toboggan run.

Joseph Conn
Staff writer
Modern Healthcare
Modern Physician
Heatlh IT Strategist
312-649-5395
[EMAIL PROTECTED]

Check out the NEW ModernPhysician.com, and register now for Modern
Physician Stat and Modern Physician Alert


[EMAIL PROTECTED] 2/16/2006 1:27 PM >>>

Most if not all health departments require that contacts be notified.
They
just don't allow the contact to be told who had the positive HIV test
without
permission.

I don't think anyone who has a positive HIV test is a priori a
murderer.

If someone in NYC hears the Health Department is collecting this data
and does
not want a Health Department envelope arriving in his mailbox, he has
no way
to stop that at the moment.  He cannot contact the Health Department
until
they contact him by mail.  If he wishes to keep the fact he has
diabetes to
himself, that makes it very difficult if someone else uses the same
mailbox.

And collecting every A1C that has been done does not even invade the
privacy
of just the diabetics.  I am sure it is much easier just to grab all of
the
data than it is to write the programs to sort out all the A1Cs above 7,
so
they took the easy out.  This represents a little more sliding down
that
slippery slope and the program is just getting started!


On Thursday 16 February 2006 13:29, Ruben Safir wrote:
On Thu, 2006-02-16 at 12:07, Nancy Anthracite wrote:

I have been working with the CDC with an eye to include in VistA the

option

to report deidentified data to the Biosense project to help with the

early

detection of disease such outbreaks, etc.  Privacy does not have to

be

violated in order to achieve most of what you are concerned about.

Yeah, actually it does.

In order to intervene with specific patient about their diabetes, the
individual patient must be contacted.  In order to prevent potential
sex
partners from getting AIDs and dieing, the diseased patients identity,
and their current and recent sex partners need to be identified AND
contacts.

in the later case you have to decide if your for or against murder.

Ruben



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RE: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread Mike Schrom

(Snip)

CBF: This should definitely be legal.  Why should the employer be saddled
with the cost of your lowered productivity due to illness?

MS: That sounds great, unless you are the one whose children can't have 
food or clothes or go to college because you can't get a job because 
EVERY potential employer can find out your A1C or how often you've 
filled your asthma inhaler prescription.


(Snip)

That is the
idea of co-pays today, just a little hurtle to make sure you really are sick
- though that doesn't seem to be working very well.

MS: Not true! The copay is a way of shifting the costs away from the 
insurance plan which has converted to a 'for profit' and needs to pay an 
increasing percentage of your ever rising premium dollars to their 
millionaire CEO and stockholders. I have patients who have a $30 copay 
for a $45 visit, which costs the Insurer $7 after the copay and the $8 
risk withhold (which I may never see)!



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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread Stephen Hay

Likewise:

Chris Farley wrote:

Comments are inserted below:

Chris Farley

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Stephen
Hay
Sent: Thursday, February 16, 2006 3:31 PM
To: hardhats-members@lists.sourceforge.net
Subject: Re: [Hardhats-members] A Pill, a Scalpel, a Database

(SNIP)

And people who make policy tend not to be subject to that 
policy - at least, where I live that's the case... Likewise, 
the people who demand the information be made public are 
usually in a position, I say usually, that doesn't require 
that their own records are open to public display... or 
they're currently in a situation in which it doesn't matter. 
Funny how the onset of disease affects people's perspective 
on things like this...


CBF: Ultimately, no one is exempt.  If you abuse the power the people give
you, you won't be in a position to make policy very long.


True. But the policies remain. It's rare that these things 
are reversed.


(SNIP)

There is also the possibility to profile and apply user-pays 
to those who have a non-contagious disease which treatment 
costs a lot. So suddenly if you're sick, you're financially 
responsible for that too. So much for *public* health.


CBF: I don't see an issue with this.  Why shouldn't sick people pay for
care?  When I was a child, I hardly ever went to the doctor.  My mother
didn't want to pay for it.  I only went when I was very ill.  That is the
idea of co-pays today, just a little hurtle to make sure you really are sick
- though that doesn't seem to be working very well.

But there's insurance. For a start, the life insurance 
companies would be VERY interested because they'd have a way 
of checking the truth or not of insurance applications. In 
fact, you wouldn't even need to fill in the application. 
They could just send you a bill based on your life expectancy.


CBF: This is a perfect way to handle life insurance.  The idea of life
insurance is to help the survivors should you be taken before you have a
chance to plan for it.  Those who are going to die early, should live life
in that manner and plan appropriately - and pay more for life insurance.  If
my life expectancy is 80, I don't want to pay more because someone with a
shorter life expectancy wanted to lie to the insurer so they could live high
off the hog.


It's one way of looking at it. Up to now, life insurance 
premiums spread the risk across all policy holders. Basing 
it on individual circumstances reduces the need to spread 
the risk. And places it all on the individual carrying the 
condition. How do you deal with congenital illness in this 
case? Is the individual to be financially penalised for 
carrying a condition he didn't "choose"?


Employers would be interested because they'd be able to pick 
and choose employees based on health factors as well as 
competence. Meaning, if you had the choice between two 
candidates and one suffered from a condition that might 
affect their work, which would you choose? Is that legal? 
Maybe not now, but just wait until the next downturn...


CBF: This should definitely be legal.  Why should the employer be saddled
with the cost of your lowered productivity due to illness?

>
So the sick become the unemployed, who can't afford the 
insurance for the treatment they need. No problem, you say. 
That's what happens now...


And it goes on.

You'll be able to check whether or not people are carrying 
the gene that makes them pre-disposed to a certain disease. 
You could even sterilise them so that they don't propagate 
the gene, in the interest of the common good, of course.


CBF: The points you made in the previous paragraphs closely align with the
eugenics debates of the 1920s.  The same debates that Hitler used to justify
his final solution.  While history does tend to repeat itself, I think we
can all clearly see that sterilization and selective abortion is wrong - and
we have Hitler as a prime example of just how wrong it is..  Plus, the
Republicans would never let this happen, so most of that part of your
argument is too fantastic.


It was said "tongue-in-cheek" - difficult to see on a 
mailing list, I realise...


Whether or not the Republicans would or wouldn't let 
something happen is out of my domain. I don't live "there".


But, fantastic or not, you can, incidentally, achieve the 
same results by neglect. You just have to know which parts 
of the population you wish to neglect.


The advantage of this approach is, of course, no-one can 
point the finger later. Because there's nothing to point at...




The typhoid/AIDS argument is valid as an example of the 
contagious disease-type policy. It's a valid public health 
argument. For *after* the disease makes itself known...


CBF: Why would we wait until after an epidemic starts?

Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread Kevin Toppenberg
This sounds like a discussion from an ethics course, where we have a
discordance between conflicting principles.

As physicians, we are trained to be patient advocates.  We don't
usually step back and look at the big picture--at least those in
private practice.  It takes researches in the CDC etc to address group
concerns etc.  So I see this as a public health policy issue. 
"Rights" can be seen as universal (the "right" to life, liberty, and
the pursuit of happiness), or perhaps granted--the "rights" of those
in China differ from our "rights".  It often seems to come down to
"might is right".  The government has the might, and thus dictates the
rights.

But I think that many want to do the correct/right thing for the
majority of people.  Does the "right" of privacy outweigh the need for
others to be safe?  I think not.  Thus I would understand manditory
reporting of HIV (and especially not that it is not seen so much like
'leprosy' from the bible, and more like cancer.)  But I agree with
Nancy that collecting HgbA1c's is an unreasonable breach of privacy.

But to be honest, I think that privacy is nebulus concept that is
rapidly being stripped away.  We carry cell phones--> our movement can
be tracked.  We watch TiVo TV--> our watching habits can be tracked. 
Even our searches on Google are being tracked.  I read in Wired
Magazine about thermal imaging techniques were people outside one's
home can thermally image those inside.  I can anticipate times where
we all have to acknowledge that it becomes nigh unto impossible to
keep secrets.

Kevin

On 2/16/06, Ruben Safir <[EMAIL PROTECTED]> wrote:
> On Thu, 2006-02-16 at 15:49 -0400, Joseph Conn wrote:
> > I'm with you, Nancy.  The road to Hell is paved with good intentions and
> > I'm surprised I haven't heard the ACLU filing an injunction against NYC
> > on this program.  Since diabetes is not contagious, I don't think that
> > because the city may end up paying the cost of care for some of its
> > citizens gives it the right to snoop on all of its citizens.
>
>
> What is this?  Your making a bald faced lie here.  You know as well as
> anyone on this list that the costs here is not just a few dollars, but
> money that runs into the BILLIONS not to mention the real morbitiy and
> mortality.
>
> But what do you care?  Your not a minority poor from Brownsville, or a
> tax payer of the city of New York so its no sweat off your back.
>
> Disguesting
>
> >  This
> > program isn't a slippery slope in my book, it's a toboggan run.
> >
> > Joseph Conn
> > Staff writer
> > Modern Healthcare
> > Modern Physician
> > Heatlh IT Strategist
> > 312-649-5395
> > [EMAIL PROTECTED]
> >
> > Check out the NEW ModernPhysician.com, and register now for Modern
> > Physician Stat and Modern Physician Alert
> >
> > >>> [EMAIL PROTECTED] 2/16/2006 1:27 PM >>>
> > Most if not all health departments require that contacts be notified.
> > They
> > just don't allow the contact to be told who had the positive HIV test
> > without
> > permission.
> >
> > I don't think anyone who has a positive HIV test is a priori a
> > murderer.
> >
> > If someone in NYC hears the Health Department is collecting this data
> > and does
> > not want a Health Department envelope arriving in his mailbox, he has
> > no way
> > to stop that at the moment.  He cannot contact the Health Department
> > until
> > they contact him by mail.  If he wishes to keep the fact he has
> > diabetes to
> > himself, that makes it very difficult if someone else uses the same
> > mailbox.
> >
> > And collecting every A1C that has been done does not even invade the
> > privacy
> > of just the diabetics.  I am sure it is much easier just to grab all of
> > the
> > data than it is to write the programs to sort out all the A1Cs above 7,
> > so
> > they took the easy out.  This represents a little more sliding down
> > that
> > slippery slope and the program is just getting started!
> >
> >
> > On Thursday 16 February 2006 13:29, Ruben Safir wrote:
> > On Thu, 2006-02-16 at 12:07, Nancy Anthracite wrote:
> > > I have been working with the CDC with an eye to include in VistA the
> > option
> > > to report deidentified data to the Biosense project to help with the
> > early
> > > detection of disease such outbreaks, etc.  Privacy does not have to
> > be
> > > violated in order to achieve most of what you are concerned about.
> >
> > Yeah, actually it does.
> >
> > In order to intervene with specific patient about their diabetes, the
> > individual patient must be contacted.  In order to prevent potential
> > sex
> > partners from getting AIDs and dieing, the diseased patients identity,
> > and their current and recent sex partners need to be identified AND
> > contacts.
> >
> > in the later case you have to decide if your for or against murder.
> >
> > Ruben
> >
> >
> >
> > ---
> > This SF.net email is sponsored by: Splunk Inc. Do you grep through log
> > files
> > for problems? 

RE: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread Chris Farley
Comments are inserted below:

Chris Farley

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Stephen
Hay
Sent: Thursday, February 16, 2006 3:31 PM
To: hardhats-members@lists.sourceforge.net
Subject: Re: [Hardhats-members] A Pill, a Scalpel, a Database

(SNIP)

And people who make policy tend not to be subject to that 
policy - at least, where I live that's the case... Likewise, 
the people who demand the information be made public are 
usually in a position, I say usually, that doesn't require 
that their own records are open to public display... or 
they're currently in a situation in which it doesn't matter. 
Funny how the onset of disease affects people's perspective 
on things like this...

CBF: Ultimately, no one is exempt.  If you abuse the power the people give
you, you won't be in a position to make policy very long.

(SNIP)

There is also the possibility to profile and apply user-pays 
to those who have a non-contagious disease which treatment 
costs a lot. So suddenly if you're sick, you're financially 
responsible for that too. So much for *public* health.

CBF: I don't see an issue with this.  Why shouldn't sick people pay for
care?  When I was a child, I hardly ever went to the doctor.  My mother
didn't want to pay for it.  I only went when I was very ill.  That is the
idea of co-pays today, just a little hurtle to make sure you really are sick
- though that doesn't seem to be working very well.

But there's insurance. For a start, the life insurance 
companies would be VERY interested because they'd have a way 
of checking the truth or not of insurance applications. In 
fact, you wouldn't even need to fill in the application. 
They could just send you a bill based on your life expectancy.

CBF: This is a perfect way to handle life insurance.  The idea of life
insurance is to help the survivors should you be taken before you have a
chance to plan for it.  Those who are going to die early, should live life
in that manner and plan appropriately - and pay more for life insurance.  If
my life expectancy is 80, I don't want to pay more because someone with a
shorter life expectancy wanted to lie to the insurer so they could live high
off the hog.

Employers would be interested because they'd be able to pick 
and choose employees based on health factors as well as 
competence. Meaning, if you had the choice between two 
candidates and one suffered from a condition that might 
affect their work, which would you choose? Is that legal? 
Maybe not now, but just wait until the next downturn...

CBF: This should definitely be legal.  Why should the employer be saddled
with the cost of your lowered productivity due to illness?

So the sick become the unemployed, who can't afford the 
insurance for the treatment they need. No problem, you say. 
That's what happens now...

And it goes on.

You'll be able to check whether or not people are carrying 
the gene that makes them pre-disposed to a certain disease. 
You could even sterilise them so that they don't propagate 
the gene, in the interest of the common good, of course.

CBF: The points you made in the previous paragraphs closely align with the
eugenics debates of the 1920s.  The same debates that Hitler used to justify
his final solution.  While history does tend to repeat itself, I think we
can all clearly see that sterilization and selective abortion is wrong - and
we have Hitler as a prime example of just how wrong it is..  Plus, the
Republicans would never let this happen, so most of that part of your
argument is too fantastic.

The typhoid/AIDS argument is valid as an example of the 
contagious disease-type policy. It's a valid public health 
argument. For *after* the disease makes itself known...

CBF: Why would we wait until after an epidemic starts?  Isn't that the
ultimate failure of the government's response to AIDS - they waited to act.
"After" is too late.  The disease made itself known by either killing
someone or making them very ill.

The diabetes argument is largely a financial one, I think 
billions was mentioned. And no, I don't live in Brooklyn. 
But we do have a huge diabetes problem...

CBF: You state this as if the financial considerations just don't matter.
But, they certainly matter.  Unless you are an economist and fully
understand the full implications, you probably shouldn't brush the costs off
so quickly.

I think one of the issues in all this is the potential for 
the misuse of this information in making *predictions*. If 
you moved to a town in which 40% of the population didn't 
live to 60, would you feel obliged to die?

CBF:  I don't really understand this point.  Can you clarify it's meaning
for me a little?





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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread Ruben Safir
On Fri, Feb 17, 2006 at 09:36:02AM +1300, Stephen Hay wrote:
> Loud and clear...!
> 
> Shame I'm not a policy maker... ;-)
> 


We're all responsible for policy although I apreciate the attempt at humor.

Ruben


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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread Stephen Hay

Loud and clear...!

Shame I'm not a policy maker... ;-)

Ruben Safir wrote:
And people who make policy tend not to be subject to that 
policy - at least, where I live that's the case... Likewise, 
the people who demand the information be made public are 
usually in a position, I say usually, that doesn't require 
that their own records are open to public display... or 
they're currently in a situation in which it doesn't matter. 
Funny how the onset of disease affects people's perspective 
on things like this...





Open my records!  Please open my records.

Is that clear enough?





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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread Ruben Safir
> 
> And people who make policy tend not to be subject to that 
> policy - at least, where I live that's the case... Likewise, 
> the people who demand the information be made public are 
> usually in a position, I say usually, that doesn't require 
> that their own records are open to public display... or 
> they're currently in a situation in which it doesn't matter. 
> Funny how the onset of disease affects people's perspective 
> on things like this...
> 


Open my records!  Please open my records.

Is that clear enough?


-- 
__
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that Brooklyn, like Atlantis, reaches mythological 
proportions in the mind of the world  - RI Safir 1998

DRM is THEFT - We are the STAKEHOLDERS - RI Safir 2002
http://fairuse.nylxs.com

"Yeah - I write Free Software...so SUE ME"

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http://www.nylxs.com - Leadership Development in Free Software
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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread Stephen Hay

Consider this.

A database/patient management system exists full of rich 
patient data.


What's being debated in this thread is policy, which 
translates into business rules, the data's the same, 
regardless. If the business rules are set up to reflect 
policy, they can be changed as policy changes.


And people who make policy tend not to be subject to that 
policy - at least, where I live that's the case... Likewise, 
the people who demand the information be made public are 
usually in a position, I say usually, that doesn't require 
that their own records are open to public display... or 
they're currently in a situation in which it doesn't matter. 
Funny how the onset of disease affects people's perspective 
on things like this...


Unfortunately, once the decisions of this magnitude have 
been made, there is little chance of them being reversed. So 
before making such decisions, the potential policy changes 
need to be considered, which is why decisions like this take 
so long...


So what happens if everything is public?

There is the possibility of rich data-mining to profile and 
prevent epidemics. That's a positive for public health.


There is also the possibility to profile and apply user-pays 
to those who have a non-contagious disease which treatment 
costs a lot. So suddenly if you're sick, you're financially 
responsible for that too. So much for *public* health.


But there's insurance. For a start, the life insurance 
companies would be VERY interested because they'd have a way 
of checking the truth or not of insurance applications. In 
fact, you wouldn't even need to fill in the application. 
They could just send you a bill based on your life expectancy.


Employers would be interested because they'd be able to pick 
and choose employees based on health factors as well as 
competence. Meaning, if you had the choice between two 
candidates and one suffered from a condition that might 
affect their work, which would you choose? Is that legal? 
Maybe not now, but just wait until the next downturn...


So the sick become the unemployed, who can't afford the 
insurance for the treatment they need. No problem, you say. 
That's what happens now...


And it goes on.

You'll be able to check whether or not people are carrying 
the gene that makes them pre-disposed to a certain disease. 
You could even sterilise them so that they don't propagate 
the gene, in the interest of the common good, of course.


The typhoid/AIDS argument is valid as an example of the 
contagious disease-type policy. It's a valid public health 
argument. For *after* the disease makes itself known...


The diabetes argument is largely a financial one, I think 
billions was mentioned. And no, I don't live in Brooklyn. 
But we do have a huge diabetes problem...


I think one of the issues in all this is the potential for 
the misuse of this information in making *predictions*. If 
you moved to a town in which 40% of the population didn't 
live to 60, would you feel obliged to die?


Stephen

Greg Woodhouse wrote:

--- James Gray <[EMAIL PROTECTED]> wrote:


We may be wasting bandwidth, but I do agree.

Jim Gray



It's not an either/or situation, or at least it shouldn't be. You've
both discussed valid functional requirements, and the question should
be how you are to accomodate both.


===
Gregory Woodhouse  <[EMAIL PROTECTED]>
"All truth passes through three stages: First, it is ridiculed.
Second, it is violently opposed. Third, it is accepted as
being self-evident."
--Arthur Schopenhauer


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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread Ruben Safir
On Thu, Feb 16, 2006 at 03:06:04PM -0500, Nancy Anthracite wrote:
> >From the NYC Health Department web site 
> http://www.nyc.gov/html/doh/html/ah/ahn1.shtml
> 
> New York State began implementation of this law on June 1, 2000. ...
> 
> 1 .What is this new law about, and what will it do?
> The new law requires doctors and laboratories to tell the Health Department 
> about new cases of HIV infection and HIV illness, along with AIDS cases as 
> they do now. It also requires doctors to discuss with their HIV infected 
> patients those whom they may have exposed to HIV infection through sex or 
> needle sharing. The Health Department or physicians can then notify people 
> who are at risk about where to get counseling, testing, and treatment if they 
> are infected. ...


Not good enough.  Hospitals and healthcare providers are still getting sued and
prosecuted for disclosing HIV status to the family.  There is still a gag order.

-- 
__
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So many immigrant groups have swept through our town 
that Brooklyn, like Atlantis, reaches mythological 
proportions in the mind of the world  - RI Safir 1998

DRM is THEFT - We are the STAKEHOLDERS - RI Safir 2002
http://fairuse.nylxs.com

"Yeah - I write Free Software...so SUE ME"

http://www.mrbrklyn.com - Consulting
http://www.inns.net <-- Happy Clients
http://www.nylxs.com - Leadership Development in Free Software
http://www2.mrbrklyn.com/resources - Unpublished Archive or stories and 
articles from around the net
http://www2.mrbrklyn.com/downtown.html - See the New Downtown Brooklyn



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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread Ruben Safir
On Thu, 2006-02-16 at 15:49 -0400, Joseph Conn wrote:
> I'm with you, Nancy.  The road to Hell is paved with good intentions and
> I'm surprised I haven't heard the ACLU filing an injunction against NYC
> on this program.  Since diabetes is not contagious, I don't think that
> because the city may end up paying the cost of care for some of its
> citizens gives it the right to snoop on all of its citizens.


What is this?  Your making a bald faced lie here.  You know as well as
anyone on this list that the costs here is not just a few dollars, but
money that runs into the BILLIONS not to mention the real morbitiy and
mortality.

But what do you care?  Your not a minority poor from Brownsville, or a
tax payer of the city of New York so its no sweat off your back.

Disguesting

>  This
> program isn't a slippery slope in my book, it's a toboggan run.
> 
> Joseph Conn
> Staff writer
> Modern Healthcare 
> Modern Physician
> Heatlh IT Strategist
> 312-649-5395
> [EMAIL PROTECTED]
> 
> Check out the NEW ModernPhysician.com, and register now for Modern
> Physician Stat and Modern Physician Alert
> 
> >>> [EMAIL PROTECTED] 2/16/2006 1:27 PM >>>
> Most if not all health departments require that contacts be notified. 
> They 
> just don't allow the contact to be told who had the positive HIV test
> without 
> permission.  
> 
> I don't think anyone who has a positive HIV test is a priori a
> murderer.
> 
> If someone in NYC hears the Health Department is collecting this data
> and does 
> not want a Health Department envelope arriving in his mailbox, he has
> no way 
> to stop that at the moment.  He cannot contact the Health Department
> until 
> they contact him by mail.  If he wishes to keep the fact he has
> diabetes to 
> himself, that makes it very difficult if someone else uses the same
> mailbox.
> 
> And collecting every A1C that has been done does not even invade the
> privacy 
> of just the diabetics.  I am sure it is much easier just to grab all of
> the 
> data than it is to write the programs to sort out all the A1Cs above 7,
> so 
> they took the easy out.  This represents a little more sliding down
> that 
> slippery slope and the program is just getting started!
> 
> 
> On Thursday 16 February 2006 13:29, Ruben Safir wrote:
> On Thu, 2006-02-16 at 12:07, Nancy Anthracite wrote:
> > I have been working with the CDC with an eye to include in VistA the
> option
> > to report deidentified data to the Biosense project to help with the
> early
> > detection of disease such outbreaks, etc.  Privacy does not have to
> be
> > violated in order to achieve most of what you are concerned about.
> 
> Yeah, actually it does.
> 
> In order to intervene with specific patient about their diabetes, the
> individual patient must be contacted.  In order to prevent potential
> sex
> partners from getting AIDs and dieing, the diseased patients identity,
> and their current and recent sex partners need to be identified AND
> contacts.
> 
> in the later case you have to decide if your for or against murder.
> 
> Ruben
> 
> 
> 
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> -- 
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> 
> 
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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread Nancy Anthracite
From the NYC Health Department web site 
http://www.nyc.gov/html/doh/html/ah/ahn1.shtml

New York State began implementation of this law on June 1, 2000. ...

1 .What is this new law about, and what will it do?
The new law requires doctors and laboratories to tell the Health Department 
about new cases of HIV infection and HIV illness, along with AIDS cases as 
they do now. It also requires doctors to discuss with their HIV infected 
patients those whom they may have exposed to HIV infection through sex or 
needle sharing. The Health Department or physicians can then notify people 
who are at risk about where to get counseling, testing, and treatment if they 
are infected. ...

On Thursday 16 February 2006 14:54, Ruben Safir wrote:
On Thu, 2006-02-16 at 14:27 -0500, Nancy Anthracite wrote:
> Most if not all health departments require that contacts be notified.  They
> just don't allow the contact to be told who had the positive HIV test
> without permission.
>
> I don't think anyone who has a positive HIV test is a priori a murderer.

SOcial workers were prevented from telling partners that they sex
partners were HIV positive.

That was/is and continues to be MURDER.

I've seen enough of it and I'm fed up with the excuses.

Public health information in the specific and the general is a priority
1 public safety need.  Everything else to my ears is utter nonsense and
in fact dangerous.

The health department, as far as I'm concerned, can ask for any
information it wants.  Unless your showing me that this information is
being miss used, or used legally, I'm ABSOLUTELY not interested.

In fact, they need to flush HIPPA which is just stupid.

Ruben



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-- 
Nancy Anthracite


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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread Ruben Safir
On Thu, 2006-02-16 at 15:49 -0400, Joseph Conn wrote:
> I'm with you, Nancy.  The road to Hell is paved with good intentions and
> I'm surprised I haven't heard the ACLU filing an injunction against NYC
> on this program.  Since diabetes is not contagious, I don't think that
> because the city may end up paying the cost of care for some of its
> citizens gives it the right to snoop on all of its citizens. This
> program isn't a slippery slope in my book, it's a toboggan run.
> 

Oh yeah, you ever read about Tyhpoid Mary?  And how about the HELL that
the family of the young 14 year old girl who slowly died of AIDs in 1992
at Woodhul hospital after her boyfriend put the squash on informing her
that he had AIDs.

She died, her baby died, the boyfried was already dead and her FAMILY
went through a living HELL

Your position turns my stomach.

And I just want to let your know that it is an OUTRAGE.




> Joseph Conn
> Staff writer
> Modern Healthcare 
> Modern Physician
> Heatlh IT Strategist
> 312-649-5395
> [EMAIL PROTECTED]
> 
> Check out the NEW ModernPhysician.com, and register now for Modern
> Physician Stat and Modern Physician Alert
> 
> >>> [EMAIL PROTECTED] 2/16/2006 1:27 PM >>>
> Most if not all health departments require that contacts be notified. 
> They 
> just don't allow the contact to be told who had the positive HIV test
> without 
> permission.  
> 
> I don't think anyone who has a positive HIV test is a priori a
> murderer.
> 
> If someone in NYC hears the Health Department is collecting this data
> and does 
> not want a Health Department envelope arriving in his mailbox, he has
> no way 
> to stop that at the moment.  He cannot contact the Health Department
> until 
> they contact him by mail.  If he wishes to keep the fact he has
> diabetes to 
> himself, that makes it very difficult if someone else uses the same
> mailbox.
> 
> And collecting every A1C that has been done does not even invade the
> privacy 
> of just the diabetics.  I am sure it is much easier just to grab all of
> the 
> data than it is to write the programs to sort out all the A1Cs above 7,
> so 
> they took the easy out.  This represents a little more sliding down
> that 
> slippery slope and the program is just getting started!
> 
> 
> On Thursday 16 February 2006 13:29, Ruben Safir wrote:
> On Thu, 2006-02-16 at 12:07, Nancy Anthracite wrote:
> > I have been working with the CDC with an eye to include in VistA the
> option
> > to report deidentified data to the Biosense project to help with the
> early
> > detection of disease such outbreaks, etc.  Privacy does not have to
> be
> > violated in order to achieve most of what you are concerned about.
> 
> Yeah, actually it does.
> 
> In order to intervene with specific patient about their diabetes, the
> individual patient must be contacted.  In order to prevent potential
> sex
> partners from getting AIDs and dieing, the diseased patients identity,
> and their current and recent sex partners need to be identified AND
> contacts.
> 
> in the later case you have to decide if your for or against murder.
> 
> Ruben
> 
> 
> 
> ---
> This SF.net email is sponsored by: Splunk Inc. Do you grep through log
> files
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> https://lists.sourceforge.net/lists/listinfo/hardhats-members 
> 
> -- 
> Nancy Anthracite
> 
> 
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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread Ruben Safir
On Thu, 2006-02-16 at 14:27 -0500, Nancy Anthracite wrote:
> Most if not all health departments require that contacts be notified.  They 
> just don't allow the contact to be told who had the positive HIV test without 
> permission.  
> 
> I don't think anyone who has a positive HIV test is a priori a murderer.
> 

SOcial workers were prevented from telling partners that they sex
partners were HIV positive.

That was/is and continues to be MURDER.

I've seen enough of it and I'm fed up with the excuses.

Public health information in the specific and the general is a priority
1 public safety need.  Everything else to my ears is utter nonsense and
in fact dangerous.

The health department, as far as I'm concerned, can ask for any
information it wants.  Unless your showing me that this information is
being miss used, or used legally, I'm ABSOLUTELY not interested.

In fact, they need to flush HIPPA which is just stupid.

Ruben



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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread Joseph Conn
I'm with you, Nancy.  The road to Hell is paved with good intentions and
I'm surprised I haven't heard the ACLU filing an injunction against NYC
on this program.  Since diabetes is not contagious, I don't think that
because the city may end up paying the cost of care for some of its
citizens gives it the right to snoop on all of its citizens. This
program isn't a slippery slope in my book, it's a toboggan run.

Joseph Conn
Staff writer
Modern Healthcare 
Modern Physician
Heatlh IT Strategist
312-649-5395
[EMAIL PROTECTED]

Check out the NEW ModernPhysician.com, and register now for Modern
Physician Stat and Modern Physician Alert

>>> [EMAIL PROTECTED] 2/16/2006 1:27 PM >>>
Most if not all health departments require that contacts be notified. 
They 
just don't allow the contact to be told who had the positive HIV test
without 
permission.  

I don't think anyone who has a positive HIV test is a priori a
murderer.

If someone in NYC hears the Health Department is collecting this data
and does 
not want a Health Department envelope arriving in his mailbox, he has
no way 
to stop that at the moment.  He cannot contact the Health Department
until 
they contact him by mail.  If he wishes to keep the fact he has
diabetes to 
himself, that makes it very difficult if someone else uses the same
mailbox.

And collecting every A1C that has been done does not even invade the
privacy 
of just the diabetics.  I am sure it is much easier just to grab all of
the 
data than it is to write the programs to sort out all the A1Cs above 7,
so 
they took the easy out.  This represents a little more sliding down
that 
slippery slope and the program is just getting started!


On Thursday 16 February 2006 13:29, Ruben Safir wrote:
On Thu, 2006-02-16 at 12:07, Nancy Anthracite wrote:
> I have been working with the CDC with an eye to include in VistA the
option
> to report deidentified data to the Biosense project to help with the
early
> detection of disease such outbreaks, etc.  Privacy does not have to
be
> violated in order to achieve most of what you are concerned about.

Yeah, actually it does.

In order to intervene with specific patient about their diabetes, the
individual patient must be contacted.  In order to prevent potential
sex
partners from getting AIDs and dieing, the diseased patients identity,
and their current and recent sex partners need to be identified AND
contacts.

in the later case you have to decide if your for or against murder.

Ruben



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-- 
Nancy Anthracite


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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread Nancy Anthracite
Most if not all health departments require that contacts be notified.  They 
just don't allow the contact to be told who had the positive HIV test without 
permission.  

I don't think anyone who has a positive HIV test is a priori a murderer.

If someone in NYC hears the Health Department is collecting this data and does 
not want a Health Department envelope arriving in his mailbox, he has no way 
to stop that at the moment.  He cannot contact the Health Department until 
they contact him by mail.  If he wishes to keep the fact he has diabetes to 
himself, that makes it very difficult if someone else uses the same mailbox.

And collecting every A1C that has been done does not even invade the privacy 
of just the diabetics.  I am sure it is much easier just to grab all of the 
data than it is to write the programs to sort out all the A1Cs above 7, so 
they took the easy out.  This represents a little more sliding down that 
slippery slope and the program is just getting started!


On Thursday 16 February 2006 13:29, Ruben Safir wrote:
On Thu, 2006-02-16 at 12:07, Nancy Anthracite wrote:
> I have been working with the CDC with an eye to include in VistA the option
> to report deidentified data to the Biosense project to help with the early
> detection of disease such outbreaks, etc.  Privacy does not have to be
> violated in order to achieve most of what you are concerned about.

Yeah, actually it does.

In order to intervene with specific patient about their diabetes, the
individual patient must be contacted.  In order to prevent potential sex
partners from getting AIDs and dieing, the diseased patients identity,
and their current and recent sex partners need to be identified AND
contacts.

in the later case you have to decide if your for or against murder.

Ruben



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-- 
Nancy Anthracite


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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread Greg Woodhouse
--- James Gray <[EMAIL PROTECTED]> wrote:

> We may be wasting bandwidth, but I do agree.
> 
> Jim Gray
> 

It's not an either/or situation, or at least it shouldn't be. You've
both discussed valid functional requirements, and the question should
be how you are to accomodate both.


===
Gregory Woodhouse  <[EMAIL PROTECTED]>
"All truth passes through three stages: First, it is ridiculed.
Second, it is violently opposed. Third, it is accepted as
being self-evident."
--Arthur Schopenhauer


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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread James Gray

We may be wasting bandwidth, but I do agree.

Jim Gray

- Original Message - 
From: "Ruben Safir" <[EMAIL PROTECTED]>

To: 
Sent: Thursday, February 16, 2006 11:32 AM
Subject: Re: [Hardhats-members] A Pill, a Scalpel, a Database



Why do I have to fill Lipitor prescriptions without knowing the patients
liver enzyme test results?


Is that nuts or what



Ruben

On Thu, 2006-02-16 at 11:59, James Gray wrote:
- Original Message - 
From: "Nancy Anthracite" <[EMAIL PROTECTED]>

>
> Where is patient control of their information?
>
Yes.  Why can't I get the medical lab to send me a copy of my lab 
results?

Why do I have to make special request to the lab each time to get them to
send my primary care provider the results along with the specialist who
ordered the results?  Why can't I give the lab a list of my specialists 
once
and get them to send each one a copy of my results each time I have a 
test

done?

Jim Gray



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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread Ruben Safir
Why do I have to fill Lipitor prescriptions without knowing the patients
liver enzyme test results?


Is that nuts or what



Ruben

On Thu, 2006-02-16 at 11:59, James Gray wrote:
> - Original Message - 
> From: "Nancy Anthracite" <[EMAIL PROTECTED]>
> >
> > Where is patient control of their information?
> >
> Yes.  Why can't I get the medical lab to send me a copy of my lab results? 
> Why do I have to make special request to the lab each time to get them to 
> send my primary care provider the results along with the specialist who 
> ordered the results?  Why can't I give the lab a list of my specialists once 
> and get them to send each one a copy of my results each time I have a test 
> done?
> 
> Jim Gray 
> 
> 
> 
> ---
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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread Ruben Safir
On Thu, 2006-02-16 at 12:07, Nancy Anthracite wrote:
> I have been working with the CDC with an eye to include in VistA the option 
> to 
> report deidentified data to the Biosense project to help with the early 
> detection of disease such outbreaks, etc.  Privacy does not have to be 
> violated in order to achieve most of what you are concerned about.
> 

Yeah, actually it does.

In order to intervene with specific patient about their diabetes, the
individual patient must be contacted.  In order to prevent potential sex
partners from getting AIDs and dieing, the diseased patients identity,
and their current and recent sex partners need to be identified AND
contacts.  

in the later case you have to decide if your for or against murder.

Ruben



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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread Nancy Anthracite
I have been working with the CDC with an eye to include in VistA the option to 
report deidentified data to the Biosense project to help with the early 
detection of disease such outbreaks, etc.  Privacy does not have to be 
violated in order to achieve most of what you are concerned about.

On Thursday 16 February 2006 12:09, Ruben Safir wrote:
On Thu, 2006-02-16 at 11:17, Nancy Anthracite wrote:
> Yes indeed.  You all know I believe in VistA and what it can do, but I have
> ever increasing anxiety about what this is going to do to privacy and thus
> what impact it will have on the physician patient relationship.
>
> New York City Department of Health is getting the results of ALL A1C tests
> in the city and patients are not allowed to opt out of having the data sent
> and cannot even opt out of receiving mailings from the city until AFTER
> they receive the first one.
>
> How can we protect the databases with our patients information if this sort
> of thing is allowed?  If the labs were not so much more convenient to tap
> into than the physicians' records, this would probably have been demanded
> from them, and when physicians become more widely computerized, they we,
> patients and physicians, will all be at great risk.
>
> Where is patient control of their information?

I think I've already said that I disagree that health records should be
private.


I STRONGLY disagree.  The issue of privacy of health records has caused
MURDER, especially with regard to AIDs and other infectious disease.

And if someone is having a gun shot wound pulled out of their buttocks,
I sure as hell want to know how it got in there,

It's irresponsible, in my opinion, to be an advocate for increased
privacy with medical records as this nation is teetering on the brink of
so many lethal epidemics.  And this is not limited to just infectious
disease.  This the billions of dollars this city spends on diabetes, I
absolutely want the government to identify and monitor diabetics as
early as possible, This saves lives and reduces to the future
expenditures on the publics money.

You can't have it both ways.  You can't go running around like chicken
little about healthcare privacy and then expect healthcare to be an
interest of the public domain and then expect privacy from the
government.  Obviously we all depend on the government to maintain
healthcare, to pay for healthcare, the be the insurer of last resort for
healthcare, to subsidize healthcare, to mandate healthcare standards and
to directly intervene into the healthcare concerns of every individual
in this nation. There is not a single person in this nation that has not
had the government directly intervene for the sake of their health and
safety.

The sharing and responsible use of healthcare information is critical to
saving lives and maintaining the publics safety.

PERIOD.

> I am finding this more and more outrageous, but apparently I am trumped by
> by everyone figuring the good is outweighed by the bad.  This is such a
> steep slippery slope. Having someone listen in on telephone conversations
> is causing outrage in the congress, but not a PEEP from them about this.
>
> On Thursday 16 February 2006 10:24, Mike Schrom wrote:
> As long as it's quality medical information FOR patients, not quality
> medical information ABOUT patients, that is not specifically authorized.
>
> Kevin Toppenberg wrote:
> > If HIS were standardized, I could anticipate a "Google" of the future
> > coming up with fantastic ways of enhancing patient care by optimal
> > presentation of patient data, i.e. scanning, filtering etc..  Already
> > Google makes it very easy to look up quality medical information for
> > patients on the internet.
> >
> > Kevin
> >
> > On 2/15/06, Gregory Woodhouse <[EMAIL PROTECTED]> wrote:
> >>A Pill, a Scalpel, a Database
> >> InformationWeek (02/13/06)No. 1076, P. 38; McGee, Marianne Kolbasuk
> >>
> >>Information technology is making strides in three critical areas of
> >>medicine: The filtering and delivery of information to the patient's
> >>bedside, allowing for personalized care; formatting existing data to
> >> obtain a richer, more helpful picture of the patient's condition; and
> >> the use of analytics to integrate data that yields new insights. IBM
> >> Healthcare and Life Sciences' Brett Davis says the interim between the
> >> discovery of new medical breakthroughs and their standard
> >> application--which can take as long as 17 years--is decreasing thanks to
> >> the use of IT and other new tools for research and collaboration. In
> >> addition to helping enable more customized patient treatments,
> >> health-care IT can cut the time and cost of testing new drugs and
> >> improve the development of safer, more targeted drugs via data mining
> >> and analysis. Analytic, pattern-recognition, and decision-support
> >> software can examine data from countless sources, and they could emerge
> >> as some of the most critical health-care tools. But delivering m

Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread James Gray


- Original Message - 
From: "Nancy Anthracite" <[EMAIL PROTECTED]>


Where is patient control of their information?

Yes.  Why can't I get the medical lab to send me a copy of my lab results? 
Why do I have to make special request to the lab each time to get them to 
send my primary care provider the results along with the specialist who 
ordered the results?  Why can't I give the lab a list of my specialists once 
and get them to send each one a copy of my results each time I have a test 
done?


Jim Gray 




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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread Ruben Safir
On Thu, 2006-02-16 at 11:17, Nancy Anthracite wrote:
> Yes indeed.  You all know I believe in VistA and what it can do, but I have 
> ever increasing anxiety about what this is going to do to privacy and thus 
> what impact it will have on the physician patient relationship.
> 
> New York City Department of Health is getting the results of ALL A1C tests in 
> the city and patients are not allowed to opt out of having the data sent and 
> cannot even opt out of receiving mailings from the city until AFTER they 
> receive the first one.  
> 
> How can we protect the databases with our patients information if this sort 
> of 
> thing is allowed?  If the labs were not so much more convenient to tap into 
> than the physicians' records, this would probably have been demanded from 
> them, and when physicians become more widely computerized, they we, patients 
> and physicians, will all be at great risk. 
> 
> Where is patient control of their information?

I think I've already said that I disagree that health records should be
private.


I STRONGLY disagree.  The issue of privacy of health records has caused
MURDER, especially with regard to AIDs and other infectious disease.

And if someone is having a gun shot wound pulled out of their buttocks,
I sure as hell want to know how it got in there,

It's irresponsible, in my opinion, to be an advocate for increased
privacy with medical records as this nation is teetering on the brink of
so many lethal epidemics.  And this is not limited to just infectious
disease.  This the billions of dollars this city spends on diabetes, I
absolutely want the government to identify and monitor diabetics as
early as possible, This saves lives and reduces to the future
expenditures on the publics money.

You can't have it both ways.  You can't go running around like chicken
little about healthcare privacy and then expect healthcare to be an
interest of the public domain and then expect privacy from the
government.  Obviously we all depend on the government to maintain
healthcare, to pay for healthcare, the be the insurer of last resort for
healthcare, to subsidize healthcare, to mandate healthcare standards and
to directly intervene into the healthcare concerns of every individual
in this nation. There is not a single person in this nation that has not
had the government directly intervene for the sake of their health and
safety.

The sharing and responsible use of healthcare information is critical to
saving lives and maintaining the publics safety.

PERIOD.
 

> 
> I am finding this more and more outrageous, but apparently I am trumped by by 
> everyone figuring the good is outweighed by the bad.  This is such a steep 
> slippery slope. Having someone listen in on telephone conversations is 
> causing outrage in the congress, but not a PEEP from them about this.
> 
> On Thursday 16 February 2006 10:24, Mike Schrom wrote:
> As long as it's quality medical information FOR patients, not quality
> medical information ABOUT patients, that is not specifically authorized.
> 
> Kevin Toppenberg wrote:
> > If HIS were standardized, I could anticipate a "Google" of the future
> > coming up with fantastic ways of enhancing patient care by optimal
> > presentation of patient data, i.e. scanning, filtering etc..  Already
> > Google makes it very easy to look up quality medical information for
> > patients on the internet.
> >
> > Kevin
> >
> > On 2/15/06, Gregory Woodhouse <[EMAIL PROTECTED]> wrote:
> >>A Pill, a Scalpel, a Database
> >> InformationWeek (02/13/06)No. 1076, P. 38; McGee, Marianne Kolbasuk
> >>
> >>Information technology is making strides in three critical areas of
> >>medicine: The filtering and delivery of information to the patient's
> >>bedside, allowing for personalized care; formatting existing data to obtain
> >>a richer, more helpful picture of the patient's condition; and the use of
> >>analytics to integrate data that yields new insights. IBM Healthcare and
> >>Life Sciences' Brett Davis says the interim between the discovery of new
> >>medical breakthroughs and their standard application--which can take as
> >> long as 17 years--is decreasing thanks to the use of IT and other new
> >> tools for research and collaboration. In addition to helping enable more
> >> customized patient treatments, health-care IT can cut the time and cost of
> >> testing new drugs and improve the development of safer, more targeted
> >> drugs via data mining and analysis. Analytic, pattern-recognition, and
> >> decision-support software can examine data from countless sources, and
> >> they could emerge as some of the most critical health-care tools. But
> >> delivering more timely and customized bedside care requires a national
> >> infrastructure for electronic health data that facilitates the exchange of
> >> standardized medical records, which President Bush flagged as a national
> >> goal to be realized by 2014. "The key tipping point will be in getting the
> >> national health IT inf

Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread Nancy Anthracite
Yes indeed.  You all know I believe in VistA and what it can do, but I have 
ever increasing anxiety about what this is going to do to privacy and thus 
what impact it will have on the physician patient relationship.

New York City Department of Health is getting the results of ALL A1C tests in 
the city and patients are not allowed to opt out of having the data sent and 
cannot even opt out of receiving mailings from the city until AFTER they 
receive the first one.  

How can we protect the databases with our patients information if this sort of 
thing is allowed?  If the labs were not so much more convenient to tap into 
than the physicians' records, this would probably have been demanded from 
them, and when physicians become more widely computerized, they we, patients 
and physicians, will all be at great risk. 

Where is patient control of their information?

I am finding this more and more outrageous, but apparently I am trumped by by 
everyone figuring the good is outweighed by the bad.  This is such a steep 
slippery slope. Having someone listen in on telephone conversations is 
causing outrage in the congress, but not a PEEP from them about this.

On Thursday 16 February 2006 10:24, Mike Schrom wrote:
As long as it's quality medical information FOR patients, not quality
medical information ABOUT patients, that is not specifically authorized.

Kevin Toppenberg wrote:
> If HIS were standardized, I could anticipate a "Google" of the future
> coming up with fantastic ways of enhancing patient care by optimal
> presentation of patient data, i.e. scanning, filtering etc..  Already
> Google makes it very easy to look up quality medical information for
> patients on the internet.
>
> Kevin
>
> On 2/15/06, Gregory Woodhouse <[EMAIL PROTECTED]> wrote:
>>A Pill, a Scalpel, a Database
>> InformationWeek (02/13/06)No. 1076, P. 38; McGee, Marianne Kolbasuk
>>
>>Information technology is making strides in three critical areas of
>>medicine: The filtering and delivery of information to the patient's
>>bedside, allowing for personalized care; formatting existing data to obtain
>>a richer, more helpful picture of the patient's condition; and the use of
>>analytics to integrate data that yields new insights. IBM Healthcare and
>>Life Sciences' Brett Davis says the interim between the discovery of new
>>medical breakthroughs and their standard application--which can take as
>> long as 17 years--is decreasing thanks to the use of IT and other new
>> tools for research and collaboration. In addition to helping enable more
>> customized patient treatments, health-care IT can cut the time and cost of
>> testing new drugs and improve the development of safer, more targeted
>> drugs via data mining and analysis. Analytic, pattern-recognition, and
>> decision-support software can examine data from countless sources, and
>> they could emerge as some of the most critical health-care tools. But
>> delivering more timely and customized bedside care requires a national
>> infrastructure for electronic health data that facilitates the exchange of
>> standardized medical records, which President Bush flagged as a national
>> goal to be realized by 2014. "The key tipping point will be in getting the
>> national health IT infrastructure in place," notes Davis. Other challenges
>> include the increasingly pressing issues of security, privacy, and ethical
>> data usage as more and more health-care information becomes electronically
>> accessible. Progress can also be hindered by hesitancy among some
>> researchers to share information. Click Here to View Full Article
>>
>>==
>>Gregory Woodhouse
>>[EMAIL PROTECTED]
>>
>>"If you give someone Fortran, he has Fortran.
>>If you give someone Lisp, he has any language he pleases."
>>--Guy L. Steele, Jr.
>
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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread Mike Schrom
As long as it's quality medical information FOR patients, not quality 
medical information ABOUT patients, that is not specifically authorized.


Kevin Toppenberg wrote:


If HIS were standardized, I could anticipate a "Google" of the future
coming up with fantastic ways of enhancing patient care by optimal
presentation of patient data, i.e. scanning, filtering etc..  Already
Google makes it very easy to look up quality medical information for
patients on the internet.

Kevin

On 2/15/06, Gregory Woodhouse <[EMAIL PROTECTED]> wrote:



A Pill, a Scalpel, a Database
InformationWeek (02/13/06)No. 1076, P. 38; McGee, Marianne Kolbasuk

Information technology is making strides in three critical areas of
medicine: The filtering and delivery of information to the patient's
bedside, allowing for personalized care; formatting existing data to obtain
a richer, more helpful picture of the patient's condition; and the use of
analytics to integrate data that yields new insights. IBM Healthcare and
Life Sciences' Brett Davis says the interim between the discovery of new
medical breakthroughs and their standard application--which can take as long
as 17 years--is decreasing thanks to the use of IT and other new tools for
research and collaboration. In addition to helping enable more customized
patient treatments, health-care IT can cut the time and cost of testing new
drugs and improve the development of safer, more targeted drugs via data
mining and analysis. Analytic, pattern-recognition, and decision-support
software can examine data from countless sources, and they could emerge as
some of the most critical health-care tools. But delivering more timely and
customized bedside care requires a national infrastructure for electronic
health data that facilitates the exchange of standardized medical records,
which President Bush flagged as a national goal to be realized by 2014. "The
key tipping point will be in getting the national health IT infrastructure
in place," notes Davis. Other challenges include the increasingly pressing
issues of security, privacy, and ethical data usage as more and more
health-care information becomes electronically accessible. Progress can also
be hindered by hesitancy among some researchers to share information.
Click Here to View Full Article

==
Gregory Woodhouse
[EMAIL PROTECTED]

"If you give someone Fortran, he has Fortran.
If you give someone Lisp, he has any language he pleases."
--Guy L. Steele, Jr.









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Re: [Hardhats-members] A Pill, a Scalpel, a Database

2006-02-16 Thread Kevin Toppenberg
If HIS were standardized, I could anticipate a "Google" of the future
coming up with fantastic ways of enhancing patient care by optimal
presentation of patient data, i.e. scanning, filtering etc..  Already
Google makes it very easy to look up quality medical information for
patients on the internet.

Kevin

On 2/15/06, Gregory Woodhouse <[EMAIL PROTECTED]> wrote:
>
>
> A Pill, a Scalpel, a Database
>  InformationWeek (02/13/06)No. 1076, P. 38; McGee, Marianne Kolbasuk
>
> Information technology is making strides in three critical areas of
> medicine: The filtering and delivery of information to the patient's
> bedside, allowing for personalized care; formatting existing data to obtain
> a richer, more helpful picture of the patient's condition; and the use of
> analytics to integrate data that yields new insights. IBM Healthcare and
> Life Sciences' Brett Davis says the interim between the discovery of new
> medical breakthroughs and their standard application--which can take as long
> as 17 years--is decreasing thanks to the use of IT and other new tools for
> research and collaboration. In addition to helping enable more customized
> patient treatments, health-care IT can cut the time and cost of testing new
> drugs and improve the development of safer, more targeted drugs via data
> mining and analysis. Analytic, pattern-recognition, and decision-support
> software can examine data from countless sources, and they could emerge as
> some of the most critical health-care tools. But delivering more timely and
> customized bedside care requires a national infrastructure for electronic
> health data that facilitates the exchange of standardized medical records,
> which President Bush flagged as a national goal to be realized by 2014. "The
> key tipping point will be in getting the national health IT infrastructure
> in place," notes Davis. Other challenges include the increasingly pressing
> issues of security, privacy, and ethical data usage as more and more
> health-care information becomes electronically accessible. Progress can also
> be hindered by hesitancy among some researchers to share information.
> Click Here to View Full Article
>
> ==
> Gregory Woodhouse
> [EMAIL PROTECTED]
>
> "If you give someone Fortran, he has Fortran.
> If you give someone Lisp, he has any language he pleases."
> --Guy L. Steele, Jr.
>
>
>
>
>


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