Courtesy of U.S. Dept. of Energy
Human Genome Program
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| Advances
in genetics are transforming the medical framework.
Now, in addition to the physiological, practitioners
will look at health issues in terms of cells, chromosomes
and DNA. |
Imagine a day in the not-so-distant future when,
in addition to taking temperatures, checking blood pressures
and noting oxygen saturation levels, you scan your patients'
genetic information from a computer microchip.
This information, interpreted by a superfast computer,
tells you if your new cancer patient metabolizes certain
medicines quickly, normally or slowly. It tells what
medication works best for her high blood pressure. It
indicates whether her breast cancer will best respond
to standard treatment or to a new drug on the market,
and whether she is in a high-risk category for other
cancers triggered by certain environmental factors like
cigarette smoke or air pollution.
You work with a pharmacist and physicians to administer
doses of medication based on genetic information that
shows how your patient responds to them. Your cancer
patient slowly metabolizes the cancer drug shown to
work best for her. She will start off with low doses
to reduce the side effects of toxic drugs lingering
in her system. But she metabolizes pain medications
quickly and may need more frequent doses of painkillers
to stay comfortable.
You explain to her children why their mother is
receiving a lower dose of the cancer drug than an aunt
on the same medication. You explain why this therapy
has a better chance of working, based on their mother's
individual genetic profile, than a different drug they
read about on the Internet.
You work with the patient and her family to draw
up a health plan based on certain environmental indicators
shown by her genetic information. For instance, she
seems to be susceptible to stress and should take care
to avoid situations that might exacerbate her illness
or increase chances of a recurrence. You recommend testing
for family members to see whether they also have indicators
that should be watched-or even blocked with early intervention
medications based on their own genetic information.
The children wonder if they should share this information
with other relatives. They also are concerned about
how this might affect their own health insurance-would
it be considered a pre-existing condition? You explain
the privacy laws that cover genetic information and
discuss ways they could alert other family members without
unduly alarming them.
Thanks to your explanations, the patient and her
family feel much more relieved about the new therapy.
Some details of this marvelous medical scenario-the
microchip containing detailed genetic information, for
instance-are still at least 10 years and perhaps many
more years away, those who work in genetics say. Others,
such as genetic information that helps determine what
blood pressure medicine to take, may arrive within a
few years. Some are happening as you read this: Patients
across the country are receiving medicines targeted
to their illnesses and genetic makeup.
In the world of medical therapies, one size no longer
necessarily fits all.
What does this mean for nurses? Nurses already are
involved as researchers for genetically targeted tests,
drugs and procedures, and the demand probably will rise
as the need for more research and clinical trials increases,
those who work with pharmaceutical companies say. Nurses
already may be dealing with patients' questions about
genetically targeted therapies and tests in clinical
trials or already on the market.
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