trigeminal neuralgia after wisdom tooth extraction
Answered by
Johns Hopkins Medicine
Baltimore - MD
This forum is for questions and discussions relating to Causes, Clinical Trials, Diagnosis, Family and Friends Issues, Living with
Trigeminal Neuralgia, Pain Management, Research, Risk Factors, Symptoms, Surgery and Treatment of Trigeminal Neuralgia.
Yes I also have a history of trigeminal neuralgia which got started after I went to a dentist for cleaning my teeth. My case was very special since it started @ a age of 18 and i had only mild attacks. My pain stopped within 6 months. I started with 900 mg of carbamazepine daily and today after 10 years i just take 100 mg once in a week. Now I don't have any pain attaks.
I am sorry if I sound disrespectful, but I have suffered from Trigeminal Neuralgia for many years and I over these years I have learned "a little" about it. First, it is NOT something that "has to run it's course" I'm not sure where you are getting this information. It is not at all like Bell's Palsy, and there ARE treatments. Yes it is a horrible thing to have and deal with but everyone is different in both the ONSET (which can occurr after dental procedures, most noted on any website), PROGRESSION, and TREATMENT. I am sorry for what you're going through as well but please be mindful of the information you send to others. Thank you.
Your pain sounds identical to what I experience. My pain is in my lower left jaw area, under the teeth/gumline. When it started I had constant pain in that area and I was able to get that under control with neurontin and vicodin. It went away for about a year and then I recently started having typical trigeminal neuralgia-like attacks. The pain starts in the same area and quickly zaps/burns up my jawline to the area under my left ear. Almost like I feel my parotid (salivary) gland burn and then it doesn't go beyond that. It is usually triggered by eating and when it hurts, I can't move my mouth, talk, or touch that area of my face without making it worse.
I was diagnosed with atypical facial pain about 8 years ago after a great deal of dental restorations that I had to have done due to dry mouth from an underlying medical condition. It IS very common for trigeminal neuralgia to come about after dental work. I think the question, or argument/discussion ongoing in response to your post, is whether or not it would have come about regardless of the dental work, or if the dental work may have expedited the process? Who knows really, and from my experience, you just can't question it or it will make you crazy. As much as it would be nice to find someone to blame for the pain, you can't really hold the physicians that removed your wisdom teeth responsible (believe me, I went through the same battle).
As for your specific questions, atypical facial pain and trigeminal neuragia are different in their symptoms, but can occur at the same time. They aren't always necessarily nerve damage per se (they can be), but can also be that the trigeminal nerve just isn't communicating with the brain properly, which is why antiseizure meds and antidepressants tend to work in some people. They somehow help to rewire the connection and help that nerve to better communicate with the brain. When it is not under control, that nerve is constantly telling the brain to sense pain.
To answer your question, atypical facial pain is a nerve issue. It can go away, sometimes for good. But usually and unfortunately, it does return. Don't freak out. Stress can make it worse (or at least some sources/research supports the idea). Relatively speaking, this can be very manageable. It is just a matter of finding the doctors with experience in treating facial neuropathy that are willing to help find what works best for you. I work with a neurologist, an anesthesiologist, and an oral medicine specialist... and all three doctors communicate regarding my treatment.
And can you explain what you mean when you say neurontin made you ill? I only ask because I was on it at a very high dose for a long time, then went off of it for a while. Now, going back on it is giving me a load of issues. I just can't seem to adjust as quickly as I did before without having really bad side effects... side effects which are preventing me from functioning normally... which never happened before. What I'm getting at though is that if you were having side effects, they can be better dealt with if they increase your dose VERY gradually. If it was making you ill, however, then realize that if you can't take neurontin, there are MANY other antiseizure meds you can try. Some just happen to work better for some people than others. Additionally, there are antidepressants that work for some people (duloxetine and effexor are specifically being used for neuropathic pain). Pain medications work for me for the atypical pain (throbbing, burning, gnawing, ongoing pain), but don't work for preventing typical trigeminal pain (stabbing, shock like, quick to come quick to leave pain and quick to come again pain).
In addition to medication, there are a number of surgical interventions that may help. I have had a number of nerve blocks done (percutaneous glycerol rhyzotomy procedures) which have really helped.
Like you (or at least you sound to be), I was in really poor shape within the first year that I was diagnosed because we didn't have the pain under control... at all. I took numerous trips to the ER because if something wasn't done to help, I was going to lose my mind. Hang in there and realize that it is a matter of finding what works best for you. If you are having pain that is not controlled by anything and that is something that you are unable to handle, just go to the emergency room so that they can help you to get it under control for at least a short period of time. That's actually how I found my anesthesiologist.
Also, if you haven't already, look at the TN association website. I find it to really be helpful. It also has a link to support groups in your area. You can contact these people for information, support, physician referrals, etc.
Good luck.