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Re: Bob Gellman and me
On Tue, 21 Nov 1995, James Love wrote:
> My response:
>
> The following language is what we want added to S. 1360, Sec.
> 202.
>
> Sec. 202 (e) Disclosure for Payment. -- A health
> information trustee that receives protected health care
> information for purposes of authorization of payment
> may only use information for this purpose, and may not
> redisseminate the information to any third parties,
> including persons who seek information under sections
> 204, 205, 206, 207, 208, 209, 210, 211 or 212 of this
> act. Protected information received for purposes of
> payment authorization shall be removed or destroyed at
> the earliest opportunity once payment has been
> authorized.
Under this proposal, a patient cannot consent to the use of their
medical information for other purposes. This is the FIRST time that
anyone has proposed restricting how an individual can use or authorize
the use of their own records.
Destroying information once payment is authorized will prevent
investigations of fraud. It will also mean that it will be harder or
impossible to compile information for health oversight, including
identifying substandard doctors and hospitals.
>
> Mr response:
> An alternative is for patients and doctors to decide, without
> the coercion of insurance payments, if they want to enter the
> records in databases. Doctors and patients may decide that they
> want to give Equifax, Travelers, or whoever the records, to
> handle all these requests for data (gee, it sounds like there is
> such a huge demand for records), but why not give them the
> choice, instead of the insurer. Are you afraid that people will
> just say no?
People can say what they want. But the use of records for cost
containment, fraud control, and research benefits everyone. Some of this
work is done through databases. Now let's guess who will refuse to make
their records available. Those who are committing fraud or those who are
not? If there are proper restrictions as proposed in the Bennett/Condit
bills, then we can have privacy and meet the other goals.
> Bob, this is a low blow, and you know it. Why are indentifed
> records necessary for cost containment? And for fraud,
> investigators will surely be allowed to investigate, but do they
> need to know if a woman had an abortion 15 years ago, if I was
> ever treated for VD, or what I told a mental health professional
> about my family life. Why is it so important to have these
> massive cradle to grave databases, without any omissions except
> for those who pay out of pocket?
Why don't you learn something about how cost containment is done before
you ask these questions. And the legislation will stop fraud
investigators from obtaining old, irrelevant records. See section
201(a)(2) which says:
Every disclosure of protected health information by a health
information trustee shall be limited to the minimum amount of
information necessary to accomplish the purpose for which the
information is disclosed.
That cuts of irrelevant disclosures and fishing expeditions. There is
nothing like that in current law or practice. It is a MAJOR advance.
> > So who should be prohibited from maintaining computerized
> > records? Doctors, labs, pharamcists, hospitals?
>
> My response:
> No one. Anyone can put their records on computers. What are
> "their" records? If an insurance company gets notes from my
> sessions with my doctor, which I have paid for with insurance
> that I have also paid for, does the record "belong" to the
> insurance company? If a hospital has a record of my visit, is it
> theirs to sell or redisseminate? This is about who has the right
> to release and redisseminate information that is or should be
> private.
Okay. This is what the legislation is designed to accomplish. But what
does private mean to you. Like it or not, there are lots of lawful
institutions that use these records for purposes beyond treatment and
payment. Medical records are not actually less private than your bank
records, school records, and criminal history records. You don't have to
like this. I don't. But you can't pass legislation that prevents cost
containment and research. And some or much of it requires identifiable
records. You can have privacy or cost containment, but you may not be
able to have both. I am sorry about that. I don't like it any more than
you do. But a bill that gets a multi-billion dollar price tag cannot pass.
>
> Robert Gellman:
> > Can everyone
> > have their own computer and print out information to pass on to
> > the next person who then re keys it? Do you want to ban
> > computerized patient records?
>
> My Response:
> I guess exaggeration seems like an effective polemic, Bob, but
> its not really becoming someone as sophisticated as you. Saying
> the insurance company can't get my records without non-coercive
> consent won't bring the world back to the stone ages, or
> eliminate the use of computers. But will give people more power
> to control the redissemination of their records. Don't be so
> silly or alarmist.
That is quite a statement coming from someone who keeps talking about dog
catchers getting access to medical records. Now there's a non-silly,
non-alarmist point.
>
> My response.
> Ok. The Medical Records Confidentially Act does in fact contain
> some modest, if cosmetic measures toward privacy. Fraud
> investigators can get records without consent and without notice,
> but they can only use them against you if you committed fraud.
>
That's better protection than you get today.
> Mr Response:
> Wow, what an improvement. Law enforcement officals get access to
> everything, on computer, without consent, but they need a warrant
> from a judge -- any judge in America will do of course. I feel
> much better.
>
What is the matter with having judges rule on warrants and subpoenas?
You have another proposal? Judges make life and death rulings every
day. I can live with this as a control.
Bob
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