Spinal Stimulator removal after nine years concerned about potential p

I'm scheduled for an appointment in March to see about having my Medtronics SCS removed after 5.5 years. It worked fine for about 3.5 years, then just stopped. Had the battery replaced with a NEVRO HFX unit. They kept the Medtronics paddle and leads, but had ot use an adapter to connect the NEVRO to the Medtroniccs lead. Did nothing for the pain. The adapter means that I can't have an MRI. With by back and butt going south, I really need an MRI to see wht's going on. I am hoping that the neurosurgeon can get the paddle and leads taken out after 5 years. My prayers are with you, my friend. This back pain stuff is no joke.

I had the Boston Scientific removed about 3 years ago. Don't think the removal caused any problems.

Did they remove the lead and electrode/paddle? How long did you have it in?
Thanks.

They removed everything. I only had it in for 2 months.

I had a Medtronics SCS removed after about 4 years of use. There’s were no problems removing the actual device. However, the paddles and leads are still in me, meaning no MRI’s ever. So far my docs have been able to use other diagnostics to get the info they need. No one seems to want to take them out. It’s been over 10 years now.

Have you had previous back surgeries? I am just wondering because sometimes MRI’s when you have a lot of scar tissue are less diagnostic.
When I did the trial of the Boston Scientific SCS in October I did have pain on one side after removal of the leads. The doc said it likely fired up my nerves and that would get better. It lasted about 3 days so I iced the area often in the meantime. It did completely go away.
I know this does not answer your question as you have had the implant so long. Hopefully someone with more experience can answer.
Best to you and your health 🙏

Thanks for your reply. Appreciate it. Glad things worked out for you. Happy New Year!

What other types of diagnostices, besides x-rays, have they used?

I’ve had several CT’s with and without contrast, including nuclear meds. I’ve also had ultrasound depending on the body part.
I’ve asked if I needed to have them removed and been told there are other types of diagnostics available. I go to Stanford in California.

I had a trial for the Nevro and it seems like the pain is worse now after they took the trial out. I'm beginning to have a strong dislike for pain management doctors and the reps for these companies who tell you it's all pie in the sky.