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Author Topic: Information on Spinal Cord Stimulator (SCS)  (Read 734 times)

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Information on Spinal Cord Stimulator (SCS)
« on: June 25, 2011, 16:30:41 »

This Includes Three Puzzles from Hooshmand's site Be sure to read through them all Please #23, #74 & # 106

http://www.rsdrx.com/rsdpuz4.0/puz_23.htm

RSD PUZZLE # 23
WHY NOT SPINAL CORD STIMULATOR (SCS)? (Revised on 3/29/2002)


Spinal cord stimulator (SCS) has a limited role in treatment of CRPS. As you are well aware, there are two different types of pain, in two different stages of CRPS. In the early stages, in the first few months, the pain is sympathetically maintained pain (SMP) meaning that the pain responds to sympathetic ganglion blocks. However, on the average of almost a year, the nature of the pain changes from sympathetically maintained pain (SMP) to sympathetically independent pain (SIP).

The spinal cord stimulator is effective in the SMP phase of the CRPS, not the SIP. The recent research has shown that the later in the course of the disease spinal cord stimulator (SCS) is started, the less likelihood SCS will relieve the pain.

As a rule of Thumb, if the stellate ganglion nerve blocks have lost their effect, about the same time the SCS loses its effect. This is because both treatments aim at the sympathetic system. With passage of time, as the pain gradually changes to SIP, such treatment cannot be expected to help.

What it boils down to, is the fact that if the stellate ganglion nerve blocks have lost their therapeutic effect, then what is the sense of doing SCS? If the pain has become SIP, what is the sense of doing SCS treatment?

SCS is a digital stimulator utilized for treatment of an analog symptom (the analog pain modality is random and not time locked or digital). It is not a type of treatment that would be successful in every form of chronic pain.

The reason we do not apply SCS is because if the sympathetic ganglion nerve blocks do not work, then epidural nerve blocks which contain Depo- MedrolĀ® applied to the epidural space in the spinal canal are far more effective, and their pain relief lasts longer. On the other hand, even in a patient who suffers from SMP type of pain, after about a year, the successful treatment with SCS will fade away because the SMP has changed to SIP. Then, the patient is left with a foreign body in the spinal canal not providing any decent pain relief. This foreign body causes disturbance of immune system resulting in skin rash, and dermatitis[1] and skin lesions and allergic reaction to SCS [2].

In CRPS/RSD, the immune system is rogue. This is because the immune system is modulated by sympathetic system. The sympathetic system, under pain input, responds by releasing T-cell lymphocytes (in early stages CD4 or helper lymphocytes, and in late stages CD8 or killer T-cell lymphocytes)[3]. So, after the SCS has lost its effect, the sympathetic system considers the foreign body of the spinal stimulator as a source of sympathetic dysfunction. This causes neuroinflammation manifested as skin rash, edema, and infection.

As the condition becomes chronic, the SCS can lead to spread of pain from the original site to other parts of the body[3].

In rare cases, there are other complications noted with SCS application. These complications consist of the following:

1. Epidural abscess or blood clots.

2. In occasional cases, the sensitization of the spinal cord by the spinal cord stimulator causes spinal cord sensitization in the form of myoclonic akinetic seizures [3]. The sensitization is due to prolonged electrical stimulation causing exhaustion of the inhibitory nerve cells. Treatment with KlonopinĀ®, and removal of the stimulator prevents the sensitization.

Such attacks of myoclonic seizures originating from the spinal cord due to the spinal cord sensitization are not limited to the SCS. They are also seen in other spinal procedures[4]. The diagnosis of spinal cord originated myoclonic seizures is quite difficult, and usually these patients are labeled as "functional" or "hysterical." Such patients respond very nicely to treatment with KlonopinĀ®, brand name rather than generic.

The removal of SCS, as well as Multidisciplinary treatments, aiming at desensitizing the spinal cord, help this condition.

Another problem with the SCS is the tendency for electrode movement due to improper anchoring, and the necessity for the surgeon try to correct the position of the stimulator. Every operation is going to be another new source of CRPS pain.

In the rare and severe cases of spinal cord sensitization, the patient may develop myoclonic jerks, and urgency, frequency, and even incontinence of urine, secondary to SCS irritating the urinary bladder and interstitial cystitis.

H. Hooshmand, M.D.

References

1.McKenna KE and McCleane G: Dermatitis induced by spinal cord stimulator implant. Contact Dermatitis.1999; 41: 229.

2. Ochani TD, Almirante J, Siddiqui A, et al: Allergic reaction to spinal cord stimulator. Clin J Pain. 2000; 16; 178-180.

3. Hooshmand H, Hashmi H: Complex regional pain syndrome (CRPS, RSDS) diagnosis and therapy. A review of 824 patients. Pain Digest. 1999; 9: 1-24. (Click on link to view abstract)

4. Rosenblum, JA: Spinal abdominal myoclonus. The Neurologist. 1996; 2: 784-787.

http://www.rsdrx.com/rsdpuz4.0/puz_74.htm


RSD PUZZLE #74
SPINAL CORD STIMULATOR (SCS)
                                                                                                                                                             

Dear Dr. S.,

Many thanks for your letter of 10/7/96. It was very interesting that you had quite a similar experience regarding the spinal cord stimulator treatment for CRPS (RSD).

I have seen 36 patients so far suffering from RSD who have received spinal stimulator for management of the pain. Of the 36 patients, the pain relief lasted an average of six weeks. Relief was as short lasting as a few hours and as long as over four months. Eventually the pain recurred with more severity.

More importantly, the foreign body of the stimulator in a patient who already had disturbance of plasticity due to long standing RSD, resulted in two phenomena:

1. Spread of RSD to the opposite extremity, as well as development of headache, neck pain and dizziness.

2. Reactive spinal cord ischemia resulting in transient paraparesis and incontinence in two cases, and the development of myoclonic type of jerks in the lower extremities in four other cases.

It is about time to differentiate the neuropathic pain of RSD from the somatic pain of failed neck or failed back syndrome.

In the same follow-up study of the patients, we have noted the effective response in control of the somatic type of pain in 32 failed neck and failed back patients with an average duration of relief being 18 months. No such complications of spread of the disease is noted in somatic (non-CRPS) patients.

In regard to your patient, I am glad she is being treated by you, and if I can be of any help, I will be at your service. Even though we have had excellent results (over 70% success) in 96 RSD patients treated with infusion pump, we always like to save the infusion pump treatment as a last resort because of problems of potential of infection (due to the disturbance of immune system secondary to RSD), and the patients intolerant of even the smallest doses of narcotics in the spinal fluid (noted in 11 patients).

H. Hooshmand, M.D.

http://www.rsdrx.com/rsdpuz4.0/puz_106.htm

RSD PUZZLE # 106                           
Complications Of Spinal Cord Stimulator (SCS)                                                                                                               

We have had extensive experience with treating patients who have already undergone spinal cord stimulator (SCS). The SCS is helpful in some patients who suffer from chronic back pain, neck pain, or failed back syndrome. On the other hand, when it is applied to patients suffering from RSD, it may help reduce the pain for anywhere from 7 days to 6-7 months. On average, it helps reduce the pain a little over 2 months. Afterward, SCS will become a new source of pain by stimulating the neuropathic pain sensory fibers in the spinal canal.

Worst of all, the SCS as a foreign body in the spinal canal that instigates a lot of severe pain and inflammation because of the fact that patients with RSD have a tendency to have an abnormal function of sympathetic system, and invariably they suffer from attacks of inflammation in the form of swelling of the extremities, reddish discoloration of the skin, etc. The SCS invariably causes severe inflammatory pain in the spinal canal region. The inflammatory pain is far worse than the original RSD for which the SCS was tried.

The above experience has been the result of treating over 200 patients who already have had SCS treatment. The situation is so bad that when a patient wants to schedule to come to see us for treatment, we first ask the patient to ask the surgeon to remove the SCS before we can give her any effective treatment.

Please ask your doctor to read this letter. At least it will put him on warning that you have more than 95% chance of developing the above mentioned complications.

Another problem with SCS is that it causes disturbance of plasticity and causes rapid acceleration and deterioration of your RSD to later stages of the disease. Another complication of SCS treatment is the fact that it stimulates the sensory neuropathic pain fibers in the spinal canal facilitating the spread of the disease to other extremities.

H. Hooshmand, M.D.


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Re: Information on Spinal Cord Stimulator (SCS)
« Reply #1 on: June 25, 2011, 16:31:04 »

Hi Amanda,

 I have had my scs for almost a yr now and I truly believe that if I didnt have it I would be bed ridden. I had to go thru a trial one first tho to seeif it helped my pain at least 40-50 % and it did for me.I was also scared like you are but I was willing to give it a try anything to get some relief from some pain.
Low pain wishes

Susan
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Re: Information on Spinal Cord Stimulator (SCS)
« Reply #2 on: June 25, 2011, 16:31:40 »

Amanda,

We have several people that have the SCS that think it's wonderful and then we have people that it didn't work for.  So do the trial and see if it works for you if not then nothing gained nothing lost.  I personally chose not to do it for myself as I already had it full body and didn't feel it would be beneficial for me.  I might of made a bad chose but that was the chose I made.  I've often thought about it.  So try the trial see if it works.

Lots of Love,
Patches
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Re: Information on Spinal Cord Stimulator (SCS)
« Reply #3 on: June 25, 2011, 16:32:04 »

Amanda,
I have had my scs for over 2.5 yrs. and as stated above it is great for some and not for others. I would think long and hard about it. think about the trial, it might be what you are looking for.If not you have it taken out in a week and never wonder "what if". I', sorry I cannot remember where your rsd is, mine is upper body so my scs is cervical. Remember that if you do get it there maybe some reprogramming of the remote before the right program for you is found - do not let this discourage you. If you have more indepth questions I would be more than happy to tell you more of my experience.

kb
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Re: Information on Spinal Cord Stimulator (SCS)
« Reply #4 on: June 25, 2011, 16:32:47 »

Hello there :)

Check the video section on our web site later today.  I should have some info there for you that tells you about it.
     
There are other options out there that are less permanent, that I would check into also. You can personal message me anytime or email or call me, I would be glad to talk with you. there are lots of folks here too that would be glad to talk with you.  It is a big decision that is not to be taken lightly.
Learn all that you can about it.  I will do all I can to help with posts about it, research etc.

hang in there.
Dee
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Re: Information on Spinal Cord Stimulator (SCS)
« Reply #5 on: June 25, 2011, 16:33:18 »

Amanda,
I have had my SCS for about 5 monthes or so now. I am glad I have it and it helps but I did not get the pain reducution we had hoped for. The best thing about the SCS is there is a trial for it before you get it permanetly. I would not go on how it works for others because we are all so different. I would recommend the trial & see for yourself whether or not it will help you. Because even though I did not get great pain reduction I would not give up my SCS. The edge it does take off is better than the nothing I had before. But you Really have tomake up your own mind. All I ever heard was not to do it & I was scared. I am so glad I made up my own mind. Good luch hun!

hugs, Denny
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Re: Information on Spinal Cord Stimulator (SCS)
« Reply #6 on: June 25, 2011, 16:33:47 »

Thanks everyone for their advice. I think I am just scared because the Dr told me that basically this is my last chance at helping the pain b/c the SGB never did anygood even though I have had a dozen done. I think that I am more scared of it not working for me and be "out of options" basically. I mean I know that I can continue the rx's and such but I dunno..... I am so DANG CONFUSED!!!!!!!!!

Amanda
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Re: Information on Spinal Cord Stimulator (SCS)
« Reply #7 on: June 25, 2011, 16:34:17 »

Hi. Did your doctor give you the video to watch on scs? I think you can even get it off the manufactor website. I know my pm doctor gave me the one from ans and my mom ordered the one from metronics. I think these are the names.I am not sure if those are on the video library. I know it is a hard decision. Did you discuss the concern of the vibrations with your doctor? He or she may be able to explain more. I wish I had more answers for you but good luck in your decision

Gina
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