RSD, Complex Regional Pain Syndrome – a case report 05/23/2012 — Nancy Sajben MD

RSD, Complex Regional Pain Syndrome – a case report 05/23/2012— Nancy Sajben MD

Severe Pain for Three Years,

 80% better in 10 days

“This has been life altering.”

This is a very bright young woman who was an all state volleyball player until onset of Complex Regional Pain Syndrome three years ago in the right hand and wrist. It began after blood was drawn from the hand for a chemistry study and, one week later, the fingers turned black, lost blood flow, followed by emergency surgery for removal of a blood clot from the back of her hand. She woke after surgery, tearing the sheet off due to intense pain on light touch — that is called allodynia — and then developed severe edema from the hand to the shoulder.

It was four excruciating weeks before the diagnosis of complex regional pain syndrome was made.

CRPS or RSD is a diagnosis that every MD, every surgeon, every ER doctor, every psychiatrist and psychologist, every nurse and therapist should know how to diagnose.

Because she was a minor, they would not do nerve blocks.

She developed contractures of the fingers and hand, was unable to move the fingers.

A major university hospital diagnosed Munchausen Syndrome;

mom was diagnosed with Munchausen’s by proxy.

This happens so often. This is 2012.

If it’s not the doctors,

it’s the insurance companies

creating roadblocks to diagnosis or treatment or both.

Why is pain management not taught at medical schools?

Only 3% of schools today give 30 hours instruction in four years, Yale most recently.

At a major university hospital two hours away, she failed to respond to 14 stellate and brachial plexus blocks. But the wound reopened by itself, the stitch fell out. The psychiatry department evaluated her after she was so drugged with methadone, she does not even recall the interview. They diagnosed Munchausen Syndrome. That changed everything. Relationship went sour. Distrust of MD’s began and was confirmed many times in many places along the northeastern corridor and Texas.

That fall, she became a student at the university of her dreams. The diagnosis of CRPS was confirmed at their university medical center hospital where they wanted to continue the same blocks that had failed. Elsewhere, the chief of a renowned ivy league university pain service wanted to talk to her only about spinal cord stimulators, declined by the family.

In May 2010, she qualified for an NIH study of neurotropin double blind 6 weeks on, 6 weeks placebo. Failed.

She was seen by Dr. Schwartzman in Philadelphia October 2011, and sent from there to NYC to rule out neuroma dorsum right hand, negative.

On Lyrica, she gained 20 lbs, then back to 130 lbs baseline when off of Lyrica. Intolerance to Morphine – hives, Duragesic – total body itching. Ambien – hallucinations, Lunesta – hyper. Benadryl helped somewhat. Detoxing from Nucynta – lips were bright red.

Her weight dropped from 130 to 115. Many medications were trialed and failed. Marinol helps pain slightly and gives the best sleep in years, better appetite. It does cause anxiety, but she had not slept in three years, and it gives 4 to 6 hours of good sleep. She developed sharp bitemporal headaches. I advised headache is a side effect of Pristiq —- now thankfully discontinued and better.

Since August 2011, she has had CRPS pain in the right leg, worse walking, weight bearing.  There is discoloration of the dorsum hand usually, at times along proximal forearm, recently at right foot and leg. She had edema up to the shoulder measuring 30 cm. Nails growth faster at the right hand, possibly less hair growth right hand. Temperature usually cooler on the right hand, at times at night the hand and foot become hotter. No change in sweating noted.

The first year, she had almost total loss of function in the hand with pain and contractures —and forced herself to move the fingers with OT and PT, then home exercise. She still has days when the fingers remain flexed, but 98% of the time there is full movement as she continually tries to use the hand/fingers to write and type. Nose may become ice cold and tingly since CRPS spread to right side of face and right lower limb. At times tingling fingers. She struggles with memory when pain is severe and with lack of sleep.

Pain ranges 7 to 10, average 8. Edema was significant for one year, now comes and goes. Allodynia is present hands and feet, now a different scale than before when she could not even be in the car.

However, with weight bearing and walking, pain of the right lower limb became most intense.  She will be 21 in July, but on a bad day was unable to leave her bedroom to walk downstairs as pain was too severe. She would communicate with family by loudly calling or texting. It was unthinkable to make plans for the next week due to severe pain. She has osteoporosis with atrophy of the right upper limb, and has had color changes and edema of the hand.

She lives in an eastern state inland, two hours away from the mid Atlantic seaboard and major medical center. She failed ketamine infusion at a major university medical center on the east coast. The cost and inconvenience was significant and the family did not know that ketamine may fail to have any effect if taking opioid analgesics. Once mom discovered that, she was able to wean off the opioid medication. Ultimately, after many more interventions, much later, in crisis, she did benefit from IV ketamine infusion, and was able to regain some movement of her fingers on the right hand, but there was no lasting relief. It was a struggle to obtain approval through her insurance.

She has been spending a great deal of time in bed for months. Morning stiffness is widespread for one to two hours. Bending is difficult, feels as if “hit by a bus,” but she does stretching, moving, distraction and Yoga when able.

Much better in 10 days

Day one: pain of the entire right side, face, trunk, limbs, rated 7 to 10 on a scale of 10, average 8. She guards the dominant right hand and the signature is difficult. Atrophy of the right upper limb is present, nails longer on the right hand, dusky dark erythema and long jagged scar over the dorsum right hand, mild erythema of the right upper and right lower limbs.

On the first day, in the office, she tried the first dose of ketamine nasal spray and after a repeat dose, she was puzzled, thinking to herself, then let us know she realized she was able to concentrate. A small dose is not enough to relieve severe pain, but even major depression can vanish at that dose. Two sprays relieved the brain fog of depression; pain was still 8 on a scale of 10. Blood pressure and pulse did not change before and after doses. She felt hopeful.

In the next few days she was able to do the unthinkable: make plans with friends, walk 45 minutes, become active, and remain active in a way that had not been possible. She was far more active with much less pain.  Over the weekend, six days after she arrived, after we had sequentially added several new medications, she found the dosage of nasal and sublingual ketamine that worked for her. She has actually had times when she was pain free. As noted during prior ketamine infusions, she requires a far higher dose than most patients to achieve effect. The plan now is to use higher doses at home when time permits for best effect, and booster sprays of nasal ketamine as needed when away from home. She can carry it in her pocket. There is no need for ICU infusions and the fight to get insurance coverage for those stays.

Of great significance, she has even made plans for the entire summer.

More details of her case will be added, as time permits. For now, this page is here to allow the patient and family and others to send comments. She will continue slow titration of other medications that will take three months before reaching the target dose, before we can assess efficacy. Based on my experience treating chronic intractable neuropathic pain including CRPS, it is possible these medications will be able to stabilize and relieve pain without ketamine.

See other case reports of treatment of CRPS herehere, and here.

You can read some of the science of pain, glia and inflammation. Ketamine is significantly anti-inflammatory. Three of her new medications are glial modulators. Treatment of severe chronic pain usually involves rational polypharmacy, not one medication and not medication alone. It requires a holistic approach to heal: P.T., O.T., massage, cognitive behavioral therapy, guided imagery, visualization, positive thinking, remaining active, and other modalities that depend upon the underlying cause: physical, emotional, spiritual, and financial. The treatment for CRPS is not specific for that condition alone, but the gains can be possible with tremendous discipline, effort, single minded determination and the loving support of friends and family.

Be cautious of spinal cord stimulators. Try everything else first.

They can create pain and scarring or tether the spinal cord.

Be proactive.

Remember that guidelines and strategies for diagnosis and treatment are outdated.

Support RSDSA.org if you can.

They support high quality pain research.

You can go directly to their site or donate to them (not me)

using the link at the top of my site here.

Patients and doctors do not understand that opioids create pain.

A 2006 publication from Vanderbilt shows how much better pain can be to taper off.

The abstract:

Significant pain reduction in chronic pain patients after detoxification from high-dose opioids.

The article:

Significant pain reduction in chronic pain patients after detoxification from high-dose opioids.

.

More on this young woman’s journey coming.

It’s been busy!

Original Article- http://painsandiego.com/2012/05/23/rsd-complex-regional-pain-syndrome-a-case-report-2/

5 thoughts on “RSD, Complex Regional Pain Syndrome – a case report 05/23/2012 — Nancy Sajben MD

  1. I also hv cprs that sounds exactly like the girl in the story. I’ve had it for 12 years & it’s still as painful today as it was the 1st day. Mine is full body, still hv trouble sleeping, thinking, concentrating, tremors and svr chronic pain! I wouldn’t wish this HORRIBLE disease on my worst enemy! No one knows what you are truly going through unless you hv this.
    I was glad to read abt the ketamine nose spray. It seems like Drs. treating us should all know abt the ketamine spray, but very few do….or just don’t want to use it. I know my Dr. Hasn’t offered it to me & he knows how much pain I’ve been in! Why! Why! Why! Still in chronic pain …today until…..?

    Thanks for reading / listening
    Cheri

    Like

  2. NERIDRONATE? WHY do i have to suffer so severely while waiting and waiting for neridronate to be approved by FDA? It’s safely used fot womens osteoporosis? It’s been used safely in Italy for years. I walk on fire every day snd night, screaming in pain, while there’s a drug with an 85% success rate that most PnMgt Drs don’t know about.

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    • Ken,

      The following is from ask the expert archives- Dr. Michael Stanton-Hicks of the Cleveland Clinic. 2014, I believe.

      “jkee: I was a patient of yours in the early 1990s. What are your feelings about intravenous ketamine? Do you know the status of neridronate? Is it FDA approved for reflex sympathetic dystrophy (RSD)?

      Michael_Stanton-Hicks,_MD: Ketamine can be useful for complex regional pain syndrome/reflex sympathetic dystrophy (CRPS/RSD). It may be given over a five-day period with three to four hour infusions. About 50 percent of patients experience relief for six to 12 months. This of course being said, 50 percent of patients will not have a long-lasting results. This treatment can be repeated—particularly when a long duration of improved symptoms result. We do not know whether ketamine or any other treatment of CRPS will prevent the spread to another site. However, ketamine and—for that matter—any other treatment when applied early may prevent CRPS for worsening. And we feel that early treatment may prevent or delay spread.
      I have not used neridronate in my patients. The other biphosphonates may help a little bit with pain at the beginning, but overall they are not very successful drugs to treat RSD.”

      Source: http://my.clevelandclinic.org/health/transcripts/1631_ask-the-expert-complex-regional-pain-syndrome-crps

      Neridronate does currently have orphan status, meaning FDA fast track though it has not yet been FDA approved for current on label or off label use for CRPS.

      http://www.transparencymarketresearch.com/complex-regional-pain-syndrome-therapeutics.html

      Also depending on your type of CRPS, some of these medications are in research and studies for Type 1 only.

      I’m sorry you’re suffering, I know what that feels like. And I hope that relief comes for all of us.

      Sincerely,
      ~Twinkle

      Like

  3. Thx Twinkie. Much appreciated. U know ket infusions cost around a grand per! And 3 are needed minimum. U hear that? What’s it made of? Golden pubic hairs of lost gods? I love pharmacy companies ripping off the sick n needy cuz it’s good business.
    Italian studie proved 85% success Type 1 only. If needed I’ll find link to study. And you’re good for years! Ok ill find thelink.

    Like

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