Spinal Cord Stimulators for Chronic Radiculopathy, FBSS, and CRPS

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DigableCat

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In my experience(albeit limited), I've been less than impressed with their outcomes. Although patients do tend to complain of "less pain", and have successful trials prior to implantation, I've seen no improvements per se in
1. Return to work.
2. Decrease in opioid medication consumption.

I've seen some improvement in ADLs. But given what insurance companies see as justification for reimbursement on procedures, I don't necessarily see them seeing this as a valuable end point. So, I sometimes wonder if it's nothing more than a $15,000 implantable TENS unit.

Anyone care to elaborate on their experiences with SCS.

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#1 reason they don't work is poor patient selection.

Right patient, right procedure, right time = highly effective treatment.

The trick is to put the patient ahead of the payments and be strict regarding criteria for implantation. Trial everybody with the right ICD-9 if you want, just don't pop a computer in their body and act like you cured them.
 
I have seen improvements with stims. We had a pt with CRPS who ADL's were significantly diminshed. After the stim placement we weaned her off her pain meds and eventually she went back to work. Later, she lost about 45 lbs and is looking pretty hot. I would count her as a success with stims. However, the truth is more often than not they only partially alleviate the pain and then around 4-5 years they just dont work anymore. I agree with lobelsteve. You must have the proper patient selection.
 
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I don't think there has ever been an disagreement with "patient selection" being a key element in the success before implantation. Even those that "pass" their psychometric evaluation, have questionable outcomes despite their testing.

But if you have to reach for success cases anectodally instead of it being more the norm, than I think that maybe some people in this field are being rather cavalier with their implantation practices.

If you want to use "evidence based" decision making in your practice(and I think we should), there was a Cochrane Review by Mailis-Gagnon et al. in 2004 which found only 2 studies that were useful enough to be included. Two RCTs, with only 81 patients in total. One was judged as being of high quality and the other of low quality. With follow-up periods between 6 to 12 months.

I am surprised that, despite the lack of quality long term outcomes published, physicians consider this venue for pain managment. Especially in the private practice sector.
 
Your comments are cavalier and clearly inflammatory.

Read these first, or wait for Slipman's text to come out and read the Chapter on SCS for FBSS. I'm thinking the literature is convincing that they do work.

References
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2. Alo K, Yland M, Radko R, et al 1999 Lumbar and sacral nerve root stimulation (NRS) in the treatment of chronic pain: A novel anatomical approach and neuro stimulation technique. Neuromodulation 2(1):23-31

3. Alo K, Ziddan A 2000 Selective nerve root stimulation in the treatment of end-stage, diabetic, peripheral neuropathy: A case report. Neuromodulation 3(4):201-208

4. Alo K, McKay E 2001 Selective Nerve Root Stimulation (SNRS) for the Treatment of Intractable Pelvic Pain and Motor Dysfunction: A Case Report. Neuromodulation 4(1):19-24

5. Alo K, Redko V, Charnov J 2002 Four year follow up of dual electrode spinal cord stimulation for chronic pain. Neuromodulation 5(2):79-88

6. Augustinsson L E, Carlsson C A, Holm J et al 1985 Epidural electrical stimulation in severe limb ischemia. Pain relief, increased blood flow, and a possible limb-saving effect. Annals of Surgery 202(1):104-110

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Are we to assume that the Cochrane Reviews are without merit. I don't have anything against spinal cord stimulation. As a matter of fact, I've got to give a presentation(assigned to me) to the orthopaedics department at my program. Which was one of the reasons why my question was posed, that and to promote more discussion on this board.

Could you cite your bibliography reference please?

BTW, just how many of these do you do per month...or should I ask per week?
 
I've been doing about 1 per month, but that number will increase shortly.

PM me for a sneak peak of the textbook chapter.
I do not own the rights to it and could not publish it here.

The Cochrane reviews are with some merit. But they are held in much to high esteem to be clinically useful.

Look at the reviews for LBP. They report that ESI is ineffective, but so were opioids and all other meds except NSAIDs. I defy you to rupture a disc and just tough it out on some Motrin. The advice based on EBM is weak at best- and this exists because RCT's are too costly or do not make much sense for painful conditions that are "ill-defined".
 
My experience, CRPS patients s/p implant, most want to be off their opiods, even in the trial phase. Most of the patient that I have implanted continue to work full/part time, even the fail back patients. In fact, that is one of my criteria before I implant them. If they are not working, I discuss goals of returning to work with them or send them to a vocational counselor before trial.

May I ask what your patient population is like?
 
Our criteria include: 1. Cannot get into a position that completely alleviates pain-pain is constant and unrelenting but may have exacerbations 2. Primarily burning dysesthetic pain treated rather than mechanical pain 3. At least 75% or greater improvement in overall pain before implantation 4. Trial for 1-3 weeks on everyone before implantation 5. No psych red flags
 
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