Page 3 » Donald Corenman MD DC | Spine Surgeon Colorado

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CowboysFan
Member

March 27, 2013 at 1:47 am

Post count: 19

in reply to: 2 Years Post 2 Level ACDF With New Type of Pain #8280

Hello Dr. Corenman,

Just wanted to let you know that I did have a phone consult with Eric (sp?) your physician’s assistant about a week ago. It was very helpful and Eric was an exceptional communicator and highly knowledgable. He asked me to send in a write up of his performance, I hope these comments can serve as that. Simply put, he was outstanding.

As part of another second opinion with a neurosurgeon, I did have a new CT scan performed last week. I met with the neurosurgeon yesterday and the CT scan did show that I have pseudoarthrosis at C5-C6. You can see a horizontal line of non-union at that level as clear as day. However, the plate and screws at that level do look to be in excellent shape.

He also had an X-ray taken of my left shoulder to see if anything is going on. I had that done yesterday and am awaiting his comments. I also had X-rays done on my cervical spine in the flexion, extension and neutral positions.

The neurosurgeon suggested that I try to use a bone stimulator for 3 months to see if a fusion to take place. He is also suggesting that I try Botox injections to see if my very tight trapezius muscles will loosen and to see if my headaches and shoulders stop hurting.

Would you be interested in taking a look at the new CT scan and the X-rays of my left shoulder and cervical spine and giving me further opinions?

CowboysFan
Member

February 9, 2013 at 5:42 am

Post count: 19

in reply to: 2 Years Post 2 Level ACDF With New Type of Pain #7947

Please disregard the question above, Dr. Corenman. I talked with one of your nurses and resolved the issue.

CowboysFan
Member

February 8, 2013 at 11:38 am

Post count: 19

in reply to: 2 Years Post 2 Level ACDF With New Type of Pain #7943

Dr. Corenman, I am getting ready to send all my images to you. Do you require that I fill out the new patient registration and cervical spine history forms and send it with the images?

CowboysFan
Member

February 7, 2013 at 1:52 am

Post count: 19

in reply to: 2 Years Post 2 Level ACDF With New Type of Pain #7931

Thank you, Dr. Corenman. I will be sending the images tomorrow. I look forward to hearing your comments once you have the opportunity to look at them.

CowboysFan
Member

February 6, 2013 at 1:13 am

Post count: 19

in reply to: 2 Years Post 2 Level ACDF With New Type of Pain #7920

Thank you so much for offering to look at my images. I will send them soon and make sure to note my forum screen name in the package that I send so that we can continue the conversation here, if that is appropriate.

If I were to schedule a visit to see you in the future, generally how long are appointments scheduled out? Also, would you do imaging and diagnostic testing at your location or would I do some of that where I am located? I live in Ohio, so I am curious as to how the logistics would work.

Best regards,
Michael

CowboysFan
Member

February 5, 2013 at 3:42 am

Post count: 19

in reply to: 2 Years Post 2 Level ACDF With New Type of Pain #7915

Hello, Dr. Corenman. I cannot thank you enough for the extremely quick response.

Thank you for your thoughts. If you do not mind, I have some more questions:

(1) That is a good point about pseudoarthrosis that I had not considered because my neurosurgeon insisted at the time of the CT that my fusion is rock solid and I took it as the gospel.

The CT that I had was performed 11 months after my ACDF was performed. My neurosurgeon did look at the CT himself and declared the fusion solid. The radiologist’s report does seem ambiguous, as you stated. I did not catch that on my own all this time how the radiologist wrote those comments.

My question is, how likely is it that the fusion was not solid after 11 months? My surgeon used two plastic discs filled with bone material and did not use an autograft or allograft. I did wear an electric bone stimulator for 4 hours a day for 4 months after the surgery.

If the fusion is in doubt and a new CT should be made, do I need to do the CT in conjunction with a myelogram or can it be done without a myelogram?

(2) In regards to the potential facet degenerative changes at C2-3 and C3-4, what would be the diagnostic testing that would be performed on those higher levels to see if that is the problem and what would be the course of treatment if the diagnosis indicated that I have facet degeneration and it is the cause of my pain? I am allergic to all NSAIDs, so if inflammation of those facet joints were the issue, that course of treatment would be a non-starter for me.

(3) Should I try to rule out a shoulder disorder (rotator cuff syndrome) before seeing an experienced spine surgeon and if so, what kind of physician should I see and what kind of imaging would be needed on my shoulder?

(4) Are the upright MRI images worthless because of the weaker magnet that the Fonar machines use? There were some comments in the radiologist’s report that concerned me:

“Spinal canal stenosis is sent at C4-C5 with concentric disc bulge and posterior ligament hypertrophy. The CSF space is erased anteriorly by the bulging disc. Minimal flattening of the cord is also seen at this level”

and

“Spinal canal stenosis at C4-C5 and C5-C6 levels is seen.
Bilateral foraminal stenosis at C3-C4 and C4-C5 levels is seen.”

(The radiologist’s report is contained in my initial post.)

(5) Would you be willing to look at any of imaging that I have had already done and would it be worth it? If so, I would be happy to electronically transfer them to you and if you do not have that capability I could mail/UPS/FedEx them to you.

Please note that I have had two flexion/extension X-rays, one CT scan post-myelogram and 3 MRIs done in 2012. The details of each of the 3 MRIs is in my original post.

Again, thank you so much for your time.

Michael
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Viewing 6 posts - 13 through 18 (of 18 total)

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Donald Corenman, MD, DC

Average rating:

81 reviews

Eric S

Sep 26, 2021

by Eric S on Donald Corenman, MD, DC

Successful pars repair at 46 years old

Back in November of 2018 (at 46 years old) I came from Vancouver BC to have a pars repair done with Dr. Donald Corenman at the Steadman Clinic in Vail Colorado. I'm finally posting this review nearly three years later in late 2021. The reason I waited so long was I wanted to know the final result before I posted my review. Unfortunately in that time Dr. Corenman has retired. Nevertheless, I want to post this review of Dr. Corenman and his staff at the Steadman Clinic in their excellent treatment of my L5 pars interarticularis.

I fractured my pars at age 42 back in 2014 when rolling on the gym floor, and was denied treatment by the Canadian healthcare system, probably due to my age. First my GP told me there was no surgical option for a pars defect, which was quite incorrect! I tried to live with it, but the symptoms worsened (periodic random spine slippage and weeks of resultant pain after just bending over to tie my shoe, so I eventually learned to mostly squat and hardly bend). When I finally consulted with Canadian spine surgeons, I was told they believed my pars defect had been congenital (since birth). This was absurd, considering I had done extreme martial arts (including jiu jitsu) for years prior, as well as 5 years of reinforcing steel full time in my 20s, probably the hardest job on the back you can find. No pars defect like mine would possibly have allowed this--ergo it was impossible that I had had the defect since birth. I did however have an asymptomatic congenital spina bifida occulta that made me more susceptible to a pars fracture. In 2014 in one instant, I went from having the strongest back people I knew said they'd ever seen, to being unable to safely bend over and tie my shoe without a non-negligible risk of my spine slipping randomly (which would lead to weeks of pain after each occurrence). This was due to the unilateral L5 pars defect, otherwise known as spondylolysis. It was when lying in pain on the floor 4 years later after maybe the 6th spine slippage event post injury, that I had had enough, and resolved to have surgery. If Canada's "universal health care" said no, I would make lemonade from lemons, and find the very best surgeon in the world at pars repairs. That was Dr. Donald Corenman. Dr. Corenman back in 2018 ran a website https://neckandback.com/ that dedicated many pages to the science of every aspect of pars repairs, from eligibility (good discs on MRI), to best surgical techniques (minimal open compared to minimally invasive), best imaging to use (i.e., O-Arm with Stealth imaging vs. older fluoroscopy), the ideal amount of BMP to use and why not use too much or too little, and much more, all to do with pars repairs, pages upon pages of his site just on the pars, with scientific references and his own extensive expert opinion. As a health research statistician, I was very impressed with this. It was in stark contrast to the websites of other spine surgeons which barely gave the pars a word or two, focusing almost exclusively on fusions. I had found the best surgeon in the world for pars repairs, and so after Dr. Corenman personally screened my MRI to ensure my discs were healthy, I booked the surgery.

Being 46 years old at the time of surgery in 2018, with a 4-year-old pars fracture from 2014 combined with a congenital SBO meant my pars fragment was somewhat atrophied, but it was "very solid", said Dr. Corenman in the operative report. Nevertheless, it was challenging with two things to fix, the pars and SBO, and OR time was around 4 hours. Recovery over the following months was guided by a very clear "Spine binder" from the Steadman Clinic with strict rules of "no BLT" (no bending, lifting or twisting), and illustrated physiotherapy guidelines. They even warned patients to avoid fish oil supplements, which could excessively dampen inflammation and hence slow bone healing. They answered many questions I had during months of recovery, with responses coming from the very supportive Lori Fugate (then director of Dr. Corenman's practice), and Ehrich Bean (then physician's assistant at the practice), as well as a couple calls with Dr. Corenman himself after two of the CT scans. Ehrich Bean offered great advice for taking the spine binder conservatively due to the nature of pars repairs vs. fusions. The final post-op CT scan I had was a couple weeks ago at 34 months post-op, and Dr. Corenman had retired, but I got a very positive and informative call from Eric Strauch (current PA at the Steadman Clinic under Dr. Corenman's replacement there, and who had also worked with Dr. Corenman previously). The staff at the Steadman Clinic were extremely supportive all the way through the process. I should mention, the local Canadian spine surgeon did offer me very good post-operative support including antibiotics as needed to deal with a mild surface incision-site infection early on, booking numerous x-rays when I felt something was amiss, as well as booking all four of my post-op CT scans. I am very grateful for that support also.

My final result shows plenty of solid bone across the pars and a healed SBO, with my vertebral body now a solid bone ring instead of being broken at two places as it was pre-op. Does my spine hold up in the real world? You bet! I have recently dug and moved several yards of dirt and sand and gravel by myself (shovel and wheelbarrow!) to fix our water main, pulled roots from the yard, moved several "portable" (these are HUGE) air conditioners up several flights of stairs my myself, and lifted weights. I now run 2 miles (3.2 KM) several times weekly with a hard 100 meter dash in the middle. I bend deeply before each run I go on, with no spine slippage. My spine feels amazing. I can bend over to do exercise, or real word tasks, with no risk of spine slippage.

My sincere thanks to God, Dr. Donald Corenman, Lori Fugate, Ehrich Bean, Eric Strauch, and the Steadman Clinic, as well as the Canadian spine surgeon who offered me excellent post-operative care back in Canada. You have all given me a new lease on life.

Sincerely,
Eric S

Robert S

May 11, 2021

by Robert S on Donald Corenman, MD, DC

Back Fusion Surgery

I had my entire lumbar spine fused in November of 2018. I had scoliosis , with pinched nerves that were so painful I could hardly walk - and standing for more than a few minutes was impossible. Even sitting was painful.
The fusion surgery produced immediate relief! And the recovery was much easier than I expected.
To this day I can do all the activities I love from hiking, to standing in a stream fly fishing to riding my bike long distances - or just walking down the street with my wife.
Kudos to Dr. Corenman and his staff, (including the two Erics) for taking such good care of me!

Leslie R

Jul 9, 2020

by Leslie R on Donald Corenman, MD, DC

TLIF

I had my TLIF surgery on 6/24/2020 by Dr. Corenman, I can not say enough good things about the Dr or his staff. I was always treated with respect and explained everything throughly, that made it easy for everyone to understand. I highly recommend Dr. Corenman and the Steadman Clinic.

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