Citizens will be notified that their data legally can
be exchanged with others. But under the federal rule,
they won't be guaranteed the right to stop the flow of
data for purposes related to treatment, electronic
claims processing, and healthcare operations - this last
term being so broad that it includes marketing.
How did this federal rule come about? Who was behind
it? What can Americans do to protect their medical
privacy?
Until now, medical privacy was primarily regulated by
the states. Most states have laws requiring patients'
consent before their information is shared with others.
However, abiding by many different state privacy laws
has proved difficult for the industries that want to
create a national health-information system. National
leaders of the medical, hospital, health-insurance, and
other industries have been working for more than a
decade to nationalize standards for sharing patients'
health data.
In 1993, President Clinton's Health Security Plan
included a provision titled "Administrative
Simplification." It called for a national
health-information infrastructure and required that
unique identifiers be assigned to four groups for
processing health claims electronically. These included
healthcare providers, health plans, employers, and
individuals. The plan also called for creating uniform
national codes for medical claims and for establishing
federal privacy rules.
Congress and the American people vehemently rejected
the Clinton plan to nationalize healthcare. However
Administrative Simplification was tucked away in the
Health Insurance Portability and Accountability Act of
1996 (HIPAA), which was signed into law in 1996. Many
remember HIPAA as the legislation that was supposed to
make health insurance portable and affordable. (It never
met those purported goals.) Under HIPAA the same four
groups mentioned above would be required to have unique
identifiers for processing claims electronically.
Thanks to Rep. Ron Paul (R) of Texas federal funding
for a health-identifier system has been put on hold over
the past few years. But unless that provision of HIPAA
is repealed, all Americans may soon be assigned a number
for tracking their personal health information from
cradle to grave.
Aware of the American people's concerns with creating
and transferring personal health data electronically,
Congress included a provision in HIPAA requiring that if
a medical-privacy law was not passed by Aug. 21, 1999,
the secretary of Health and Human Services (HHS) would
have to generate such a rule to cover the new electronic
medical-records system.
Congress missed its own deadline and so the authority
shifted to the Clinton administration. In November 1999,
that administration proposed regulations that would have
prohibited doctors, hospitals, and others from obtaining
patients' consent before releasing their medical
information. The public objected.
A final rule was published in December 2000, just
before Mr. Clinton's departure. It did require
healthcare providers and organizations to obtain
patients' consent before releasing their medical records
for treatment, payment, or broadly defined "healthcare
operations." However, many others did not need patients'
consent before obtaining their records, including
law-enforcement officials, certain researchers, and
public-health officials, among many others.
The medical and insurance industries strongly opposed
the consent provision and lobbied the incoming Bush
administration to eliminate it. Not surprisingly, the
Bush administration modified the rule so that healthcare
insurers, providers, institutions, and others could
transfer medical information electronically to pay
claims, treat patients, and do other tasks - without
patients' consent.
In essence, the federal government is giving the
medical industry regulatory authority to decide whether
personal health information can be obtained by others
without patients' permission. What's more, some powerful
industry groups strongly support having the federal rule
preempt state medical-privacy laws. Given their lobbying
success, it is likely that in the near future these
groups will attempt to accomplish this.
That is why citizens and state legislators should
make sure that their stronger medical-privacy laws
requiring patient consent are protected against
preemption by the new federal rule.
• Sue A. Blevins is president of the Institute for
Health Freedom.