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Sailormoon
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November 3, 2020 at 9:38 am

Post count: 29

in reply to: Numbness after microdiscectomy #33340

Hi Dr Corenman,

My MRI showing advancement of infection in nerve root and there is large abscess on invertebrae.

My doctor suggest me to have an operation again to clean the pus and abscess and then continued with fusion.

I still feel advancement on nerve deterioration because pin and needle getting stronger, deterioration sensory skin keep happening. Saddle anaesthesia on my right getting worst.

What do you think, Doc to have another surgery 3 times in a row?
Could fusion been done exactly together with draining the pus and abscess?

What is the worst scenario that could happen after surgery? Any other things that i should put attention on?

Sailormoon
Participant

November 1, 2020 at 6:26 am

Post count: 29

in reply to: Numbness after microdiscectomy #33328

Dr Corenman,

Scarring should be grow slowly, right?

I feel worry much regarding nerve deterioration. Almost area of L5-S1 now had deterioration on skin sensory. And pin and needles at my soles becomes stronger.

Looking at blood check result that showing better result, should be the nerve deterioration at least not progressing.

Other than discitis, what else causing gradual on set of cauda equina? MRI would be done next Tuesday, i feel so nervous until then.

Sailormoon
Participant

October 31, 2020 at 2:39 am

Post count: 29

in reply to: Numbness after microdiscectomy #33322

Hi Dr Corenman,

Just like you told before, my blood culture came out negative.
After additional 7days antibiotics IV here is the result compared to a week ago:

ESR decrease from 54 to 38
CRP decrease from 9.3 to 4.9

It means the ceftriaxone works for me. But ESR still high, what does it means?
Next tuesday i will req for MRI. Regarding pain, until now i still took anti inflammatory so i cant tell.

Regarding nerve deterioration, could it possibly because of scarring due to infection?

Sailormoon
Participant

October 30, 2020 at 12:43 am

Post count: 29

in reply to: Numbness after microdiscectomy #33284

Hi dr,

Thank you for keep answering me ????.
I dont feel bloated or sick. Overall im fine. I took anti inlammatory once a day though, so dont feel much pain.
I can walk but feel stiff at my back and cramp at my leg all the time. But its tolerable.

Im still on antibiotics IV 2gr ceftriaxone injected every night together with oral antibiotics once a day.

My concern always nerve deterioration. It keep progressing day by day. The antibiotics IV so far didnt prevent it progressing. Maybe its the wrong antibiotics , i dont know.

I have another blood check today and waiting for the result. My blood culture no result until now.

I want to req for MRI but do you think its too soon?
My MRI that shows spondylodiscitis did on October 7.
On Oct 10 i have 5 days antibiotics IV, continue with 5 days oral.
On Oct 23, i have another antibiotics IV, and now on day 7 and still continue.
So now is 20 days after MRI showing discitis.

If the blood result shows that ESR and CRP increasing, do you think its better for me to have surgery soon to clean up the infection? What kind of surgery need to be performed considering the infection involving my nerve root? Can clean up the infection on nerve root performed from anterior?

Or waiting until antibiotics works with risk more damage to my nerve root?

Btw, this spondylodiscitis means pus on my spine, right?

Thank you, doctor

Sailormoon
Participant

October 28, 2020 at 2:43 am

Post count: 29

in reply to: Numbness after microdiscectomy #33274

Hi Dr,

Eventhough on antibiotics i still have continuos nerve deterioration, does it means i have abscess on my nerve root and need surgery?

What is complication of the surgery? It involving my nerve root, does the surgery will result permanent nerve damage?

Which doctor usually perform the surgery? Orthopedi spine or neurosurgeon spine? In my country there is no infection surgeon.

Sailormoon
Participant

October 25, 2020 at 9:29 pm

Post count: 29

in reply to: Numbness after microdiscectomy #33267

Hi Dr Corenman,

I still feel deterioration on my nerve, it progressed day by day. My pin and needles is back like i have after surgery. Im afraid i will have complete CES.

I dont know what to do to stop it. Id already on antibiotics and still going on.

I read some people which had spondylodiscitis triggered by surgery, the infection will be resolved at least 18 months, waiting for the vertebrae fused naturally. Is that true?

If that the case then my nerve root will have permanent damage? And i will have foot drop and bowel/bladder damage? I cant just lay down here only to wait until that day came. Its awful
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Viewing 6 posts - 13 through 18 (of 28 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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Sailormoon

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