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ashley
Member

May 11, 2013 at 12:29 am

Post count: 25

in reply to: medication after fusion #8630

Thanks. That’s good to know. The reason I had asked that is because the other morning I woke up with a sore neck. It’s been 3 days now and it’s still bothering me.

I went on a vacation with my husband when I was 7 months post fusion (beginning of Feb) and when getting off the trolley cart lost my footing and fell. Face first. Damn flip flops. Anyway, not sure if that would cause any damage to my fusion so long after it was done?

At the time I fell I was fine, no neck symptoms. And I have a plate and screws for fixation.

Maybe I am just having a flare up of some sort. I have done nothing to reinjure myself since that time.

How would one know the difference between a flare and re herniation?

I have pain and stiffness at the base of my neck. Where the big bone is at the base of my neck if that makes any sense.

But it’s not severe excrutiating pain like when I herniated it. It is annoying pain. And there is no radiculopathy extending to my hand either. More like a soreness or stiffness when I turn my head from side to side. I notice that when I turn my head to the right there is a small grinding or clicking noise.

Thank you again for all your time and knowledge Dr Corenman.

ashley
Member

May 8, 2013 at 7:43 pm

Post count: 25

in reply to: medication after fusion #8610

I notice this hasn’t been answered. Do I have it in the right category?

I have asked my own gp this question and she doesn’t know the effect of spironolactone on bone growth/loss and my neurosurgeon has me refer to my gp at this point.

Thank you.

ashley
Member

November 7, 2012 at 10:04 pm

Post count: 25

in reply to: extruded disc #7358

Thanks for explaining all that to me. You are a huge help. Have a great day Dr.

ashley
Member

November 7, 2012 at 3:26 am

Post count: 25

in reply to: extruded disc #7352

Hi Dr Corenman,

I had my acdf in July and have been doing well. Aa you may or may not remember before my surgery my patellar reflexes were abnormal when checked. Left knee absent right knee hyper. No clonus. It was 10 months ago when they were abnormal.

Every reflex check since then has been normal. Also yesterday I had my reflexes checked again and they were both normal. As well as a normal neurological exam. Checked my legs for weakness and numbness and tingling. All normal this time.

I still haven’t had my lumbar mri as it takes a year to get one here in Canada.

I am somewhat concerned now that my reflexes are normal? And my dr said that if after I get my lumbar mri and that nothing abnormal is found then they will have to investigate further.

What other causes could that have been to cause abnormal reflexes? I have had a cervical mri just before my acdf and that was fine other than the extruded c6/c7.

I know that MS is something that causes abnormal reflexes but I have no other symptoms of that.

Just thought Id geyt your opinion as I still have 2 months to wait for my lumbar mri.

Thanks for your help.

ashley
Member

August 20, 2012 at 10:36 pm

Post count: 25

in reply to: back from acdf #6805

Thanks so much Dr.

At 5 weeks out my dr cleared me to drive,light activities and physical relations. I have been fine with all of this.

However Friday night I slept wrong and kinked my neck. I have had to take 8mg dilaudid just to take the edge off the pain coming from the back of my neck. No radiculopathy.

Is this flare up something common or could I have done something more serious? I do have a plate and screws.

Thanks.

ashley
Member

August 14, 2012 at 1:15 am

Post count: 25

in reply to: back from acdf #6750

Good to know thank you.

I was given limited aftercare instructions after my acdf with internal fixation when released from hospital. Nowhere did it mention not to take ibuprofen in my aftercare booklet.

For the first 2 weeks after my acdf I took 400 mg of ibuprofen 4 times a day.

I have noticed looking at other after care instructions that this is not advised because they say it can lead to a nonunion.

Will this ibuprofen that I took have an affect on my fusion?

And I also have robaxacet. Is this safe to take after fusion?

Thank you.
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Viewing 6 posts - 7 through 12 (of 19 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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ashley

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