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Confused

Spine Health | Last Active: Jan 16, 2023 | Replies (6)

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@jenniferhunter

@dadcue I know seeking an answer can be tough when your doctors don't really have enough information on how to prevent heterotopic ossification. I have been looking for research papers trying to find information that could help. Here are some of my thoughts, and perhaps it may lead to asking specific questions of your medical providers. I am not a trained medical professional, but I have knowledge because of a background in biology, having worked in scientific research, and what I have learned as a patient from my experiences with surgeries and physical therapy. I will list some links at the end where you can read about research involving HO.

Generally, I've learned that there is an inflammatory process that happens during the formation of extra bone as you've also said, but a few other things also caught my attention. Bone formation happens as a sequence of changes that first create cartilage that is later replaced by bone, and inflammation is part of that process to set the stage for creating new bone.

Sometimes surgeons are using bone morphogenic proteins as a kind of "cement" during surgery and that can be linked to a higher risk for heterotopic ossification (HO) and this is used in some spine surgery.

Spine surgeons also speak about excess pressure causing bone remodeling in the spine, and if I were to take a guess, I would think that scar tissue that forms in the fascial layers because of surgery and the surgical path, could also increase pressure in those tissues and may perhaps increase the risk of HO because the scar tissue may connect directly to the spine via the surgical path. This is why surgeons want knee replacement patients to begin walking right away to prevent formation of restrictive scar tissue. Some papers mention that over aggressive manipulation of limbs after joint replacement could be involved in causing additional trauma to the limbs, that could initiate HO as it heals and forms scar tissue.

I do therapy involving the fascia called myofascial release. This is a gentle way to stretch fascia and allow it to remodel and you have to hold a gentle shearing pressure and wait. The fascia undergoes a change from a semi solid to a liquid like consistency and the facial fibers unwind and and become more mobile. If you are too aggressive in stretching fascia, it will tear and form scar tissue that just adds to the problem causing further restriction. With gentle facial stretching and patience, a patient can restore better body movement by removing tight restrictions that run through the body. My PT has worked on and stretched my surgical scars to help release this tightness. If you keep the fascia moving and sliding on itself, it keeps fluids circulating, and proper electrical conduction in the fascia itself as well as releasing any stored waste products. Some of the literature stated that HO was common among spinal cord injury and head trauma patients and the hypothesis was that HO can form when electrical signaling is lost to the tissues resulting from nerve damage. Restricted fascia is dehydrated and may no longer conduct electric signals. Some doctors embrace myofascial release therapy and others haven't heard of it. In medical school , they study dead tissues in cadavers that have lost all the properties of living fascia, so perhaps they don't think about it.

This video demonstrates how living fascia unwinds and reorganizes.
"Strolling Under the Skin" by Dr. Jean-Claude Guimberteau


So I wonder if myofascial release could help prevent HO? Some other considerations of course are how much movement is allowed post op after a spine procedure. I had a fusion with only a bone graft and no hardware, and had to stay immobile in a hard collar until the fusion process started which was 3 months. My PT was not allowed to do any MFR during that time, but after when I began rehab for weakened neck muscles because of immobilization, we also did MFR and it helped relieve pain by removing pressure. I had also done MFR before surgery so my tissues would be more pliable and easier to retract, making the surgeon's job a bit easier.

Here is our MFR discussion with lots of links to information:

Myofascial Release Therapy (MFR) for treating compression and pain: https://connect.mayoclinic.org/discussion/myofascial-release-therapy-mfr-for-treating-compression-and-pain/

There is a provider search at http://mfrtherapists.com/

Here are links to some literature that I found about heterotopic ossification:

Medical Hypotheses
Volume 68, Issue 1, 2007, Pages 67-73
"The function of proprioceptors in bone organization: A possible explanation for neurogenic heterotopic ossification in patients with neurological damage"
https://www.sciencedirect.com/science/article/abs/pii/S0306987706004932
J Musculoskelet Neuronal Interact 2012; 12(4):230-240
Heterotopic ossification following traumatic brain injury
and spinal cord injury: insight into the etiology and
pathophysiology
https://ismni.org/jmni/pdf/50/06SAKELLARIOU.pdf
The Journal of Bone and Joint Surgery. British volumeVol. 90-B, No. 12
"Heterotopic ossification after the use of commercially available recombinant human bone morphogenetic proteins in four patients"
https://online.boneandjoint.org.uk/doi/full/10.1302/0301-620X.90B12.20975
So my question is this.... if you did myofascial release with a therapist to prepare yourself for spine surgery ahead of time, and also after surgery when appropriate, could you prevent the HO from happening? This may be something to discuss with your surgeon.

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Replies to "@dadcue I know seeking an answer can be tough when your doctors don't really have enough..."

Thank-you very much for all of the information. I will need to study it more. I can relate to much of it. I don't understand everything except to acknowledge how complicated it is.

I have a nursing background in neurology/neurosurgery. I never fully appreciated how integrated the nervous system is with every other system in the body. I never imagined becoming a neurosurgery patient.

My rheumatologist sometimes says I have "systemic inflammation" and other times says that I have a "full range" of rheumatology problems. As a patient, I try to avoid the neurology/neurosurgery aspects of medicine although that is becoming harder to do. I have diffuse peripheral neuropathy which is enough all by itself.

The pain of trigeminal neuralgia was over the top. The facial electricity was mercifully stopped after microvascular decompression (MVD) surgery. Unfortunately the neurosurgeon couldn't completely separate a large vein "traversing through" my trigeminal nerve. The amount of dissection that was needed left the left side of my face numb and tingling including my eye. Now my ophthalmologist is worried about neurotrophic keratitis.

Radicular leg pain was comparable to trigeminal neuralgia. The acute neurological changes of foot drop and leg weakness sent me right back to the neurosurgeon who did the MVD surgery. I would have consented to leg amputation except that prednisone stopped the pain. That same neurosurgeon couldn't believe I only took prednisone for trigeminal neuralgia. That neurosurgeon referred me to God when I asked how a large vein got tangled up with my trigeminal nerve.

The HO was discovered by my rheumatologist when she pressed on a small spot on my knee. She wasn't sure if I needed to be seen by neurology or the orthopedic surgeon because of having knee replacements. She described that spot as "exquisitely painful" which was the first time I ever heard of pain being described that way. Apparently there is some bone that shouldn't be where it is and it is pressing on a nerve. The best recommendation they could give me was that I shouldn't touch that spot!

I'm thinking more and more that I shouldn't do the lumbar fusion. Seems like there are way too many nerves and bones to mess around with. There seems to be too many unknowns about all the connective tissue that is involved too. I have already had an idiopathic tendon rupture. I have only been diagnosed with reactive arthritis, uveitis, PMR and possible arachnoiditis. I'm thinking maybe some mixed connective tissue disease (MCTD) too.

All in all, I'm doing well and I feel better than I have in years. I read somewhere that prednisone only controls the inflammatory pain but doesn't prevent the damage caused by chronic inflammation. I'm thinking that might be true in my case. I don't know exactly what my biologic is doing but I think it may have actually stopped the inflammation . Maybe the problem is solved and my spine won't get any worse.

I truly appreciate your response ... thank-you again. I have read some of your other responses to other people and I think they are fantastic!