Fauled Pudendal Block

Nerve blocks using many techniques, and medications - options discussed in detail
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Alfredo
Posts: 6
Joined: Thu Aug 23, 2018 12:33 pm

Fauled Pudendal Block

Post by Alfredo »

During a CT guided nerve Block the nerve on the left side was spiked and i felt a strong electrical pain weich led me
react and move against the needle. Thais happens 5 month ago
and since then the pain was stronger and I can not sit on my
special cushions as I was able before the infiltration.
Anyone having had the same experience?

I have the feeling the nerve on left side could be damaged.

Regards Alfredo
Andrew1985
Posts: 1
Joined: Thu May 04, 2023 10:44 pm

Re: Fauled Pudendal Block

Post by Andrew1985 »

Sorry to respond to this so late, as I'm just seeing it. Did your pain from the pudendal block ever get better? It can be extra discouraging when a procedure that's meant to help ends up making things worse for a bit. I'm looking at getting a pudendal nerve block done, but I hesitate when I read stories like yours. I would be less worried if I knew that the increased pain eventually abated.

I genuinely hope you're feeling some relief.
April
Posts: 615
Joined: Fri Jun 19, 2015 9:59 am

Re: Fauled Pudendal Block

Post by April »

Hi Andrew and Alfredo,

Although blocks (with both a numbing agent and a steroid) do seem to very often give people flares (they did me), I don't think long-term problems are common at all. In fact, I can't remember reading about that on here. I think my block-related flares usually lasted a few days. If it will just be diagnostic block, Andrew, you could ask them to skip the steroid. I've often wondered if that would reduce the likelihood of a flare.

April
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Violet M
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Re: Fauled Pudendal Block

Post by Violet M »

I have known of several people who got worse long-term from nerve blocks but like April said it’s not common. I see nerve blocks as useful for diagnostic purposes but I don’t know of many people who had long term relief from them.
PNE since 2002. Started from weightlifting. PNE surgery from Dr. Bautrant, Oct 2004. Pain now is usually a 0 and I can sit for hours on certain chairs. No longer take medication for PNE. Can work full time and do "The Firm" exercise program. 99% cured from PGAD. PNE surgery was right for me but it might not be for you. Do your research.
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