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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I have an Abbott scs that I've had for 4 years now. It helps me alot. Had to turn it off for an mri and after 45 minutes of laying on my back I came out in extreme pain after. Turned it back on and it took awhile to calm things down. I had taken it for granted that it was working and it has helped me alot. Recently had some problems with break through sciatica and met with an Abbott rep who turned up the amplitude and now back to working well. Mine is for lumbar pain & sciatica. Yes i think insurance requires a 5 or 7 day trial to make sure it's right for you. Best of luck to you.
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1 Reaction@smithki 3 lower lumbar back surgeries with rods & pins being the last one on 5/27/25. The pain that I went to the ortho about originally was for an excruciating "cold" pain & numbness in my right outer thigh, from my hip to my knee that had been going on & intensifying for approximately 2 years. The ortho was convinced that the nerve was compressed & PLIF surgery would fix it. Now a year later & absolutely no relief in my hip, but added numbness in the pad of my foot, my ortho surgeon has said there is nothing else he can do & was sent to a Pain Specialist. I feel like I am being "pushed" to do a trial with an Abbott SCS.
I have asked my ortho surgeon on numerous occasions to do a mri to see what is wrong. They do an x-ray of my spine every time I go that shows the surgery hardware is doing exactly what it was intended to do. BUT!!! It has YET to fix my pain!
I went to the pain specialist yesterday, & he just kept saying that this is what will help. That he has talked with my surgeon & this is what he is recommending. . . I "argued" with the specialist for probably 30 minutes (lol!), but I want to KNOW how this is going to help the pain that no one seems to care about! He DID say that he would order an mri if I just REALLY wanted one, but he was confident that it wouldn't show anything. (and I began to worry that if I insisted on an mri that they would word it so that my insurance wouldn't pay for it!) Plus they say that regardless of what is causing my pain, the SCS will help. So, I finally agreed that I would at least do the psych evaluation & talk to the Abbott rep.
I got home & started researching the Abbott device & found that there are several lawsuits against these companies INCLUDING Abbott models Proclaim & Eterna, alleging that the company "failed to warn patients about device malfunctions that cause severe electric shocks, burns, nerve damage, and lead migration that forced victims to undergo painful revision or removal surgeries." (Drugwatch.com) THEN goes on to cite "High-profile cases - such as Furia v. Abbott Laboratories and Tuttle v. Abbott - allege that defective Eterna and Proclaim models caused severe complications like bladder incontinence, paralysis, and excruciating pain."
So I asked the rep about lawsuits, & at first she said that it was ONLY OTHER companies, not Abbott. So, I sent her a link to the article. . . HOURS later (& she had been responding within a couple of minutes!) she replies with "With anything in healthcare, I'm not surprised to see individual lawsuits, but there have been no class action lawsuits brought to my attention regarding these generators."
So, I'm even MORE skeptical!!! Any help would be appreciated!
@phxratt1 Question for anyone that was helped during the trial but not after the permanent one was implanted.
Do you know if they used the same model in the trial & permanent placement?
@linda6101 "You have nothing to lose."
But don't we? The trial is not FREE and you have at LEAST 5-7 days of not being able to do what you want. (like getting in the pool or go out on a boat, and I work in the school system. . .)
So, that alone is a LOT to loose IMO.
@stevenla313 wow, that is a great question. I assumed the permanent one was the same one used in the trial, but I'm not 100% sure. I will have to check with my Abbott rep.
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1 Reaction@stevenla313 honest I had the Abbott put in originally they had it set too high and it burned burn me in my pelvic area,After seeing a urologist who told me it was the Abbott unit causing it. So meeting with the rep she discovered they set it way high after the implant. I now have it turned down very low and to tell you the truth I am not sure it has helped or my last surgery after much healing was successful.
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1 Reaction@stevenla313
They should use the exact same one, no?
@bajjerfan yes I would THINK so. But it just seems odd to me that there are a LOT of people who say that their pain was relieved in the trial but not with the permanent one. š¤·š»āāļø
@phxratt1 please let me know what they say.
@stevenla313
I had an MIS PLIF in May of 2025, too. Like you, my pain has continued. Doctor decided it was coming from my SI joints so those were fused in November of 2025 and March of 2026. I was diagnosed with lymphedema in both legs in August of 2026 (the swelling and pain began 10 days post op). A new internist believes it is RSD! I had an SI joint surgery post op appointment (via telehealth) a week ago. The PA was surprised Iām still having burning pain in my buttocks running to the thighs and feet. Iāve asked for a new MRI and CT scan and have heard crickets!
A SCS trial was done in February. It caused the most severe pain I have ever had in my life! They took it out on day3 (on a Friday) and then I developed a migraine Friday night! They couldnāt do a blood patch until Monday!! It was a horrible trial.
All this to say that I am still being told the only option I have is to go with a SCS, in this case the Boston Scientific Wavewriter (not rechargeable one). Iām a 4ā11ā, 98 lb 62 year old female who is the size of a 10 year old child. I think the gauge of wire is what caused my severe pain in the trial. I was told thatās the only size they use. Iām scared to death of them now! I canāt believe this is the only treatment, other than narcotics! Iāve lost my job. Iāve lost my social life. Iāve lost my intimacy with my husband of 42 years, and Iāve lost my independence- I cannot drive. I cannot clean my house, do yard work or gardening. Worse yet, I can no longer drive my 2000 Harley Davidson Fatboy!
My prayers go out to all of us who are on the struggle bus, as well as those who have found pain relief. Any advice is appreciated.
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