Pars defect repair

  • Thread starter Thread starter shannon4all
  • Start date Start date
S

shannon4all

Guest
:confused: I would like someone...anyone to explain how a pars defect is fixed.I have a pars defect and my spinal surgeon told me he could fix it.He said that roRAB and screws would be the way he would fix it where the bone formed a bridge..in me instead it formed like a joint...I am unsure whether or not to go through with the surgery as I am tired of being in pain but unsure exactly how effective this type of surgery is..I also had my back fused at L4 and L5 where I had spondylothesis with slip and I also have degenerative disc disease/disorder...the pars defect is right there where the previous surgery was so that is why I continued to be in major pain even after the first surgery.Can't we just do away with that whole piece of bone...why is it necessary??:confused: I just need to know how all this goes and if the surgery is worthwhile or if I will be stuck taking vicodin forever...{I know that a lot of you are on a lot stronger pain meRAB..but because of my age and the doctors I am seeing that is all I get} ANY help would be gratefully appreciated.
 
Hi,
I am in the same boat as you. I would love to know. I am 17 and just got told that I had one of these. He said I will be in a brace for 6 months and then we will think about pins and screws, fusion, or some kind of surgery. I am kind of scared. He said it wouldn't hea on its own.


Good luck with this.
Becca:angel:
 
Hey, I believe Clover had this done and she is generally on around 10:30 at night so hopefully she will see the post.
 
I agree that spondylolisthesis and pars defect go hand in hand. I finally had a fusion from L4-S1 in 1993 to fix both.
 
Hi,
I am 24 and had a spinal fusion when I was 22. I had 4 screws and 2 roRAB put in at S1-L4. I also had a pars defect and spondy I was in so much pain before and now I have none. I still sometimes get a little sore from the bone graft that they took but other than that nothing. I live in Ohio so it's way to far for you but I would recommend my surgeon to anyone anytime. I really believe thats the key. You have to trust them and check all credentials to make sure you are getting the best.
 
Hi Shannon
I had a pars defect and spondy. I think they kinda go hand in hand. My was so severe that the vertabra was loose and the surgeon said that he could just reach in and pull it out. I was lucky that the spine did not slip and cause more problems.

Ok so my surgeon did a partial fusion from l4-s1 he used the dysense system and put in 6 screws and roRAB and fusion bone material but left the disc. He did have to do some clean up on the disc. This was kinda a unique thing I believe as it is being trialed but should be approved this summer.

I also have alot of other things wrong in the back but this did stablize the back and helped with alot of nerve pain.

I am also lucky that he is a fantastic Dr whom takes the time to try everything else first and explains everything.

Good luck and keep us posted. I will keep you in my prayers.
 
Yes, very, very very very very very important. I completely failed to manage the situation with my initial primary care physician regarding my spine. We would argue about me needing diagnostics. ARGUE?! My physiotherapist requested them herself as well as through me after my first appointment with her, he STILL declined that I required them. Why the hell did I not go to another doctor instantly and demand diagnostics, well I had previously never had a problem with this doctor, he had made several sound judgement calls in the past and I trusted his word. I trusted his word over the chiropractor and physiotherapist who were both informing me to temporarily QUIT all stressful and unstable activities. I tried to stay with that doctor even as he declined diagnostics, referrals and finally when he dismissed my chiropractors diagnosis of thoracic spondylolisthesis. He would say that he had seen much worse with the patient dealing much better and that I needed to stop exagerating symptoms or risk having 'drug seeking behaviour' on my medical file; which I did end up with when I went for a second opinion with another doctor in the same clinic even though I specifically stated to her that I was not looking for pain management from her, just a second opinion and hopefully a talk with my primary physician [she still gave me a script for sleeping pills after I said I could not sleep due to the pain and was looking for another opinion i.e. diagnosis not looking for more prescriptions. Shortly thereafter I switched physicians and now have a properly managed pain regimen with the minimal amount of prescriptions possible [60mg codeine/2mg nabilone daily] which he stated are also compatible with the herbal supplements I take daily for pain. A doctor who is open to speaking with any and all alternative health practitioners which I see, chiropractor, physiotherapist, osteopath, ectera. Thank god.
 
Can you tell me your doctor's name? I am looking for a second opinion for my daughter and am at a loss. We live in Eugene, OR. Would happily go to Portland, Seattle, even Mayo.
 
Back
Top