Mrs.
J.
Mrs.
J is a 47 year old female who presented to our clinic in 2001
with a two year history or intractable headaches. She states
that she suffered a rear end collision in 1999 leading to a
whiplash injury and a concussion. She states that she did not
lose consciousness at the time of the accident but was "dazed"
for several hours. For several weeks following the accident
she suffered sensitivity to light as well as some minor antegrade
amnesia.
At
the time of presentation to Georgia Pain Physicians, her dominant
complaint was daily, severe headaches. She stated that she had
already seen three neurologists, had three brain MRI's, two
EEG's, and had been on a myriad of medications for migraines,
none of which helped. She had also been to another pain clinic
where she had been treated with cervical epidural cortisone
injections, facet joint injections, trigger point injections
and physical therapy.
When she presented to our clinic, X-rays were obtained which
demonstrated minor (nonsurgical) instability in the upper cervical
spine and pain to palpation at the point where the greater occipital
nerve crossed the nuchal ridge. This nerve was blocked with
local anesthetic during the initial visit which gave her 70%
pain relief for the first time since the accident in 1999. She
returned to clinic in one week reporting that the pain relief
had lasted for 2 days at which point it returned. This injection
was repeated upon at the first follow up visit with local anesthetic
and cortisone. This time the pain relief lasted one week but
returned to its previous baseline. Upon return to clinic, a
TENS unit was prescribed which was well tolerated but failed
to relive her pain. As a result, a subcutaneous spinal cord
stimulator was pursued.
Spinal
cord stimulation (SCS) is in the United States is usually used
for chronic lumbar radiculopathy or complex regional pain syndrome
(CRPS, RSD). It has only recently been used for the treatment
of occipital headaches responsive to occipital nerve blocks.
To perform this technique, an epidural needle is placed in the
soft tissues extending from the midline towards the mastoid
process and a spinal cord stimulating lead is placed in the
needle. Care is taken to thread the needle superficial to the
greater occipital nerve so that when the needle is removed and
the lead is left in place it lies superficial to the nerve.
The nerves may then be stimulated which places paresthesia in
the occipital region. This treatment method is performed as
a temporary test to evaluate its effectiveness at blocking the
transmission of pain signals to the brain and then is implanted
as a permanent device if the test proves successful.
Mrs.
J underwent an 8 day test in May, 2001 and received 90% reduction
in pain. She was permanently implanted bilaterally in June,
2001. As of the time of this writing, she has been followed
every three months for 2 ½ years. She has maintained 80% reduction
in pain and continues to use her device daily. She is working
full time and is taking no habit forming medication. She is
extremely pleased with her implant.