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Cryoablation Protocol Yielding Remarkable Results

Posted: Tue Jun 11, 2024 4:46 am
by jon
Pelvic PT Specialist Stephanie Pendergast posted an interview she did with Dr. John David Prologo of Emory University in Atlanta where he describes a cryoablation protocol that applies cold 3 - 4 times longer than the 'standard" protocol. Results of that treatment almost aways last a few months, at best. That due to the ability of A and C nerve fibers to regrow.

Most doctors apply two cycles of 2 - 3 minutes of hitting the pudendal nerve with a freezing cold gas, which causes a ball of ice to form on the nerve, There's a couple of minutes long pause between applications. Dr. Prologo uses two 8 minutes of cooling with a 4 minute warming period in-between.

He claims everyone he's treated in this manner is still getting the benefit from treatment 4 years later! THAT is incredible!

Hes a link to the interview. I'll include excerpts in case it's ever taken down.

https://pelvicpainrehab.com/blog/cryoth ... neuralgia/

Sara: Is your technique for treating pudendal neuralgia called cryoablation or is it different from cryoablation?

Dr. Prologo: This technique is indeed cryoablation. The unique thing about what we are doing, though – is the implementation of image guidance. We are using our interventional radiology training and evolving image guidance techniques to access nerves that are deep in the body and otherwise inaccessible for injections or ablations, in this case the pudendal canal.

Sara: How is your technique different from pulsed radiofrequency ablation?

Dr. Prologo: Radiofrequency ablation is heat mediated tissue destruction. Cryoablation creates shifts in osmotic gradients and intracellular ice crystals that ultimately results in the shutting off of nerve signals, more like turning down the volume of the stereo vs. blowing it up with a bomb.

Sara: Why do you prefer freezing versus burning?

Dr. Prologo: 1) Cryoablation is great for pain procedures because it is not painful 2) Cryoablation creates an “ice ball” that we can see on CT. Therefore there is no guesswork involved with where we ablated 3) Cryoablation initiates a unique immune response that a) results in longer lasting results and b) stops neuroma formation (vs. radiofrequency ablation or surgery)

Sara: What are the results you are getting?

Dr. Prologo: Our results have been largely durable and positive. That is, the great majority of our patients experience complete relief from their symptoms. That said, pain can be complicated and outcome depends heavily on patient selection.

Sara: Have you followed your patients from four years ago?

Dr. Prologo: I am in touch with most of the patients that were done and they are still doing well.

Sara: What are the side effects?

Dr. Prologo: We have not seen any side effects to date.

Sara: Any long term issues?

Dr. Prologo: Not that we are aware of at this point.

Sara: Is it possible that you are inadvertently treating the posterior femoral cutaneous nerve as well?

Dr. Prologo: No. The ablation zone and CT scanning are both exquisitely precise. This is actually the epicenter of the new therapies and innovation. That is, it isn’t really the cryo that is new, it’s the advanced imaging guidance to treat pain. The techniques are so precise that we can literally treat 2mm nerves in the skull base.

Sara: Who is an appropriate referral?

Dr. Prologo: This is key. Patients who have been diagnosed with pudendal neuralgia are most likely to benefit. That said, many patients come with a wide variety of backgrounds and symptom descriptions. As a result, we can get everyone to the same starting point by performing a diagnostic “test injection.” Again, because we have CT, we can see with 100% certainty where our injection ends up. As a result, there is not guess work. If the patients symptoms improve with the test injection, then they will do well with the cryo. If not, then they don’t have pudendal neuralgia and some other therapy is warranted. That said, interventional radiologists also treat pelvic congestion syndrome, which can be misdiagnosed as pudendal neuralgia.

Re: Cryoablation Protocol Yielding Remarkable Results

Posted: Wed Jun 19, 2024 5:41 am
by April
Thanks, Jon. When I considered doing this with him in 2017, insurance didn't cover it because it wasn't a proven technique. It sounded like he was trying to collect data on the procedure to publish his results. I wonder if he's done that by now. I have had significant questions about the procedure, so I'd be interested in seeing a peer reviewed study of its effectiveness.

April

Re: Cryoablation Protocol Yielding Remarkable Results

Posted: Wed Mar 26, 2025 11:07 pm
by bartland
Has anyone on this forum had this exact procedure with Dr Prologo who can verify results?

Re: Cryoablation Protocol Yielding Remarkable Results

Posted: Tue Apr 01, 2025 10:10 pm
by sadie
Ty for the post and april ty for the peer review question as I am typing on phone with tears in my eyes from a pgad flare and for 15 years I have waited and written and searched for relief. I will go back n put dr prologo name which I am very familiar with in search bar to see what was said way back n I believe there was a woman who saw him in the past n I will contact her to see what happened as it's been a while and I have forgotten. Thank you violet for forum, to the interviewer , and for all who keep this reasech front and center w patient testimonies and asking for peer reviewed paper on his findings...and ty dr P for thinking outside the box. I hope ty these doctors do not give up or see us holding their feet to the fire as disrespectful but I have pgad because of my misguided belief that pudendal nerve blocks would help PN now I am left with something far worse. Hugs n love to all. Sadie All here on this forum are greatful but cautious I hope .

I came back to edit this to add...y we need to be careful .. those of us with you pudendal neuropathy now have more tools than we had in 2006 to 2010 when I was first in the midst of all of this. I did not have a cell phone or internet access to research anything . I had a flip phone and doctors who had no idea what pedental neuropathy and acid like burning in your privates was about.

after 4 years of amitriptyline which kept the acid burning away caused dystonia and I had to slowly titrate from it .. which was hell....had I just switched to different class of antidepressant like I am on now Lexapro I would not have had the pnb w the steriod Depo medrol which formed crystals on the nerve and after both pnb I experienced a brand new sympyom PGAD.... after the second pnb I experienced restless leg which I never had b4 and pgad and a ton of foreign body symptoms stright from hell like ( engorged labia majora . .. feeling like they were as big as base balls) The restless leg left never to return and most if not all foreign bodies symptoms but the pgad never left...

and I believe if I was not with drawing ftom amitriptyline and thrown off the clonazepam I used for sleep to be placed on Valium to stop the dystonia and in a Pharmaceutical spiral I would have been able to research and and merely switched the amitriptyline to Lexapro to stop the burning . I would have never had the two pudendal nerve blocks which both times caused PGAD. So it's an example of how rushing to get help is not always the way to go but those Dr's who are still trying to help need also to be encouraged to continue as they will save lives.