Anyone had an Abbott SCS put in? BurstDR strength setting?
I'm curious to know what strength setting your spinal cord stimulator is set at for anyone implanted with an Abbott device that uses BurstDR technology.
I had a good trial and significant pain reduction after my permanent implant, but feel like the device has become less effective over time. I'm now 6 months post-op and feel like the device is no longer providing much relief at all.
I have a follow up appointment with my surgeon and the device rep in two weeks but want to experiment with different settings between now and then. However, I know it's possible to overstimulate the nerves and create irritation and pain at settings that are too high. My initial strength setting was at 7, then I increased to 8 a couple of weeks post-op. I briefly increased to 9 after a muscle spasm flare up and then returned back to 8.
I felt a little more confident experimenting with settings on my Medtronic device with tonic stimulation, but the Abbott BurstDR technology is more difficult to determine the delayed impact of adjustments due to the lack of paresthesia.
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It does nothing for my pain.
The generator has fallen about 2 inches almost down into my buttock from my flank
I get no follow up from my doctor because they referred me to Abbott
Cannot even reach the Abbott representative anymore
Have no phone number for him because apparently that phone number belongs to some person now
I’m having an emergency at this moment, and I cannot turn the device off, and I cannot get a hold of a representative or a doctor, and I cannot get a hold of Abbott.
I am in an emergency situation here and it is the weekend.
My advice is do not do this.
I have never heard anybody say that it has helped them.
Everyone I know says they want it removed and I want mine removed ASAP, especially after the ordeal. I’ve been through this weekend and unable to have a life-saving procedure and cannot get a hold of anybody to help me.
@adteague - call Abbott Neurostimulation Customer Support at 1-800-727-7846
I was one of the first patients in the US to have the Abbott Eterna implanted. In general, I am satisfied with the results and the patient support from the network of device reps covering my area. Programming for BurstDR stimulation is difficult, and it can be challenging to determine the best strength setting where you are neither under stimulated nor over stimulated. I use my system in tonic mode now and have had much better results even though I need to recharge more frequently (once every three to four weeks).
These systems aren't a magic cure, and they don't work for everyone. The clinical endpoint for a successful outcome is generally considered to be a 50% reduction in pain, which is achieved by anywhere from 50% to 80% of patients depending on which study results to review. But you may still need pain meds. And you should still maintain some type of exercise program for your back and/or neck. It's important to find the right doctor and have the best device for you implanted after a successful treatment.
@adteague if you are having device connectivity issues with your controller you may need to update your patient controller app to version 2.0
May I ask how you were able to keep your nerves in check while in the MRI machine for 45 minutes? I had an MRI for the spine in 2023 and due to the Abbott SCS, the tube is more narrow, more deliberate, became uncomfortable and hot. I stopped the test after 25 minutes. I will not repeat an MRI while the SCS is present, as the experience was not a good one. I have had plenty in the past, but will not schedule one unless I am under an anesthetic.
I am so sorry to hear your frustration. To be close to Christmas, and not have the support from the Abbott staff to be there, after spending countless hours with the stimulator in your spine, and not performing at what we understand to be the magic to counter the pain is over the top.
I hope the phone number a person gave you will help. Please continue to keep this site updated on your condition.
I have had the Abbott WaveWriter since August 2023 for chronic L5 nerve damage. It has helped until just recently and now I may need another surgery. I had L4-5 fusion in 2020.
My Abbott rep responds within hours and helps me as needed. I've never had an issue with response time. I would tell the surgeon who placed your SCS that the rep isn't replying to you, they will get it handled. It's big bucks for the surgeon with minimal work. Unfortunately this is not the best time of year to get anything done.
I am waiting to find an MRI machine that can do me, otherwise I may see if we can't just do a CT. I had an arthrogram (CT with direct joint injection) of my shoulder vs an MRI prior to that surgery. I may ask if that can be done on my back vs a MRI.
I wish you luck. Pain is a problem.
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1 Reaction@vikkitennis I have had several MRIs since having my first SCS implanted in 2017. I tend to be cold blooded, so was never too warm in the MRI tube. But this is a potential issue with any SCS and perhaps some other medical devices. During my last MRI they refused to give me a blanket due to a policy change at the imaging center. Apparently, they had some patients get too warm due to metal medical devices, even if non-ferrous, and would no longer allow blankets for imaging patients with an implanted medical device.
I haven't heard of anyone having an MRI under anesthesia, but I know it's common for doctors to prescribe a Valium tablet for patients who experience anxiety in the MRI tube. Or perhaps imaging in an open MRI system would make the experience better for you.
I talked with imaging at the Center in Phoenix, and she mentioned about MRI's in a hospital setting and placing a patient under anesthetic. I inquired about an open MRI, but that isn't possible for SCS patients. Yes, I have heard about the medication a Valium, for relaxation. As I mentioned in the past before the SCS, I have had many MRI's, and sailed through them. I believe it was due to the narrow "tube" that freaked me out after 25 minutes. I was told a CT scan is close to what the medical staff can analyze. I am to see the neurosurgeon today who implanted the SCS and discuss removing it. He is very personal, I like him, and respect him.
My friend has to anesthesia for an MRI. She has lots of sensory issues.