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Patients with Parkinson's disease understand that over time, their
medications won't work as well to control symptoms causing their quality
of life
to deteriorate.
So what can help some of these patients
adding an electronic version of medication to the mix.
This is Parkinson's patient Carroll Phillips singing in the church choir at
this point she had Parkinson's for nine years. Notice how she can stay still that
uncontrollable movement is a side effect from her medication and progression of
her disease. It impacted everything. When I tried to feed myself,
I would bring my
fork up
or spoon
and I might hit my eye, or
I might hit my nose. Carol dropped from about 130 pounds
to just 94 pounds. Friends offered to help.
They'd say, "Let me feed you." and I said, "No, no, I want my dignity for as long as I can get it."
Carol relied on a cane or walker to get around.
Even then, more side effects. i would be walking, and I would just freeze.
I couldn't go anywhere.
The good news, Carol didn't have any other serious illnesses, so that made her
a good candidate for an electronic version of her medicine, deep brain
stimulation or DBS.
Deep brain stimulation is a method by which high frequency electrical
stimulation
through a very small electrode placed strategically in the brain
can actually control the abnormal circuit in the
brain and bring the patients' symptoms such as stiffness or tremor
back into control for that person.
the DBS system is made up of an electrode and a device that looks like a
pacemaker.
Patients may need one or to implants depending on whether symptoms on one
side of the body or both
this brain surgery is a delicate procedure with small but potentially
serious risks
everything from stroke
paralysis to even death.
Every week people make a decision that
taking that small risk is worth it because the symptoms they have
for their disease are so disabling or so painful
or affect their life so severely
that they find it valuable.
Despite the risks Carol knew DBS was her only hope for a more normal life.
This may sound like a lie, but
I was never
scared of anything.
Because of the potential for life threatening risks each DBS candidate
must first have a thorough physical and neurological assessment.
During a monthly conference, staff ranging from neurologists, neurosurgeons
electrophysiology to physical therapist discuss each patient's case weighing DBS risks
versus benefits for each patient. Patient selection is one of the most
important aspects of deep brain stimulation.
The more people who can lay eyes on the patient preoperatively, the more likely
we are to have a good outcome.
They should be satisfied and have a
better quality of life.
Most hospitals map the DBS surgery and implant electrodes over a very long day.
Vanderbilt specialists say that's difficult on patients, so they've
modified it so DBS is done in four stages. It's more accurate that way.
Plus, it's much easier on patients.
In Stage One sedated patients have four small markers implanted which will
secure the frame for the delicate brain surgery.
Vanderbilt neurosurgeons no longer rely on the large metal stereotactic halo
used by many hospitals. Instead four years ago, they were the first to use a
unique stereotactic system. It's a much smaller and lighter frame tailor made
for each patient.
What this means for the patient is improved patient comfort because the surgery time
is cut by at least two to three hours.
It retains all the accuracy and,I feel
in our research that we've published,that it's actually more accurate than the stereotactic frame.
Patients also undergo a CT brain scan and an MRI scan.
Research proves groups of faulty cells develop in specific areas deep in the brain
causing debilitating symptoms like tremors. Neurosurgeons can't see those cells
or targets in the scans,
so they turn to a one-of-a-kind computer program developed at Vanderbilt.
The computer can help us find that target faster and more accurately.
That computer program combines standard brain maps, scans from previous DBS
success cases, plus the patient's own scans to make a prediction of the
specific area where electrodes must be place to control symptoms.
A week later Stage Two: surgery to place electrodes in the brain. Using local
anesthesia the frames attach so the electrodes can be guided to the target.
As for the patient with no pain sensors in the brain they feel nothing.
We may give them a little bit of sedation, but we need most of our
patients awake because we want to see
where the therapy is most effective and controlling their stiffness or their tremor.
Right now I'm advancing an electrode down there.
The electrophysiology listens for this
the faulty brain activity, the predicted target, the first target a bullseye,
the second almost dead center. That's how accurate that
computer prediction process is for us. It's amazing.
Next, a test simulation. A small electrical current is set to the target.
Too much stimulation can cause side effects like tingling. The neurologist and patient
help the neurosurgeon determine if the electrodes are truly in the best spot
to relieve symptoms.
The electrodes are then permanently implanted.
The following week. Stage Three: the pacemaker-like device is surgically
implanted under the skin and connected to the electrode.
After healing about a month later, Stage Four a Vanderbilt neurologist programs
the DBS system
With this wireless device, he can send electricity to any of four contact
points on the electrode in the patient's brain.
tYou can make the shape of the
electrical field less like a ball
and more like a football. This custom programming plus adjusting the patient's
medications will be what helps keep symptoms under control.
This system makes a difference. When off, see how the tremors return?
When on the tremors go away.
So, for your left hand you have 1.9 volts and for your right hand 2.5 volts.
The neurologist also sets parameters, so patients can safely adjust their
electronic medication at home as needed.
As for Carol...
I have had people who don't even recognize me from the back because I'm not
jerking and tremoring so much.
She's back to doing the things she loves: gardening
exercising,
and reading. Look how steady her hands are.
And she's back to a healthier weight because she can now feed herself again.
As for her walker, it now houses are quilt.
Carol is the typical DBS patient success story. She's got her Parkinson's
pills from 37 a day to just 3.
it took about six months of adjusting her medications and the DBS system
to optimize the control of her symptoms.
My dignity is there.
Everything about my life is
100s of times better.
Although the potential benefits are great there are rare times where a patient may need
additional DBS surgery.
An electrode like this it may have to be repositioned if it shifts,
breaks or
if an infection develops around it.
Vanderbilt specialists say it's important patients understand that as they
consider this treatment.
Coming up, could DBS actually the first treatment to ever slow the progression of
Parkinson's?