New? Free Sign Up
Then check our Welcome Center to a Community Caring about Sleep Apnea diagnosis and Sleep Apnea treatment:
CPAP machines, Sleep Apnea surgery and dental appliances.
Tags:
Some of the oral appliances for treating OSA are very similar to the oral devices used for bruxism (teeth-grinding), except that they move the bottom jaw forward a fixed amount to expand the back of the throat to lessen sleep-breathing problems. Other oral appliances for OSA are very different, much more complicated, and very adjustable.
It would have been nice if your device for bruxism could have been the type that can be made to take your sleep apnea into account. That way it would move your jaw forward a bit while preventing the teeth-grinding at the same time. In fact, I would be pretty mad at a dentist who made me an anti-bruxism device without considering my sleep-breathing problem, if he knew about it, myself.
-jeff
Vickie Reynolds said:I have a question...are we talking a dental device that is used to stop grinding my teeth at night? I hesitated to even get this device due to the fact that I am a CPAP user....I will be picking up my dental device on 7/6/2010 - can I used this and CPAP or is this device totally different than the one we are talking about. This device took about an hour for all the measuring/fitting/molds to be done - sorry, but I'm confused...
Hallo from an industry insider and someone who has specialised in making oral appliances for sleep
Hallo from an industry insider and someone who has specialised in making oral appliances for sleep disordered breathing for over 15 years. My name is obviously not John Doe but in order not to be perceived as advertising for a particular company and to protect my identity I have used this as a pseudonym. I would like to HELP and INFORM where I can.
Let's begin!
May I suggest we work on some terminology? Dental Appliances is one name but this is incredibly broad ranging and could include dentures and childrens orthodontic appliances. In the industry there are several acronyms but one that is CURRENTLY favoured is MRD - meaning "mandibular repositioning device". (mandible being the lower jaw).
Some designs of MRD's may be used for patients that present with both jaw pain that may be from temporo-mandibular joint dysfunction (TMD) and sleep disordered breathing when a specialist expert dental professional has assessed the patient and a thorough baseline is established before commencing treatment. I have to say that (in my personal opinion) TMD treatment consists of certain factions or schools of thought and there is a great deal of VooDoo and somewhat sketchy clinical data substantiating the claims made for each factions views. I think we are best to confine ourselves to treatment of sleep disordered breathing which is what this forum is about.
With regard to efficacy of MRDs the facts are (in my opinion) that CPAP remains the best treatment for significant OSA. HOWEVER.... you will note that I have used an ambiguous word "significant" and this is quite deliberate. Significant is an undefined quantity. That's because each individual is unique and may respond better or less well to an MRD. I believe its fair to say that CPAP is an arduous therapy AND SO ARE MRDs!
Why then are MRDs confined to less significant OSA? Well without compliance data (evidence that the device has been used) it could be potentially dangerous to rely on an MRD as a treatment for say an airline pilot or lorry driver. Its also doesnt end there... with a CPAP (simplistically) regardless of how 'significant' the OSA is we can pretty much just dial up the pressure until it overcomes the apnea. With an MRD we don't know yet whether someone will respond to its use before they BUY one and if so whether the improvement will really be adequate. You can think of MRDs as allowing you to breath for yourself (passive) whereas a CPAP is actively pushing air into you.
OK thats enough for now. Please keep up the good work on Sleep Guide and I hope that I have been of some help and can continue to do so.
I use a mandibular advancement device for UARS. I actually felt worse on CPAP. Upon awakening the first morning after using the MAD, I woke up and did not want to get out of bed, not because I felt unrested, but because I was so relaxed...my limbs felt both heavy and heavenly because I had not struggled all night to breathe. I had completely forgotten what that feels like...it has been years! I use my MAD every night and my sleep deprivation symptoms have gone away. It has been over a year now, and I would never choose to go to sleep without it.
Interestingly, my husband was diagnosed with UARS one year later. He has been using the CPAP religiously for a year now and feels no better. My dental device was approved through insurance without problem while 6 months later, my husband's prior authorization request to the same insurance company for the very same device and for the very same diagnosis was denied...after 4 appeal letters, it is being covered...he is anxiously awaiting the final fitting. So, the insurance piece, at least for UARS, clearly can be tricky.
Some sources have indicated that patients with UARS are less tolerant to CPAP use due to an increased sensitivity in the nervous system...I understand that UARS is placed on a continuum with OAS, and it is treated the same as OAS; however, there are some differences that I think need to be taken into consideration.
Was there special wording included by your doctor to get the insurance payment for UARS? So far, my insurance has denied CPAP and has not given any alternate treatment. I've been using the CPAP (purchased on my own) for over 1 year and still have fatigue and memory, sleep deprivation issues.
SaraLynn said:I use a mandibular advancement device for UARS. I actually felt worse on CPAP. Upon awakening the first morning after using the MAD, I woke up and did not want to get out of bed, not because I felt unrested, but because I was so relaxed...my limbs felt both heavy and heavenly because I had not struggled all night to breathe. I had completely forgotten what that feels like...it has been years! I use my MAD every night and my sleep deprivation symptoms have gone away. It has been over a year now, and I would never choose to go to sleep without it.
Interestingly, my husband was diagnosed with UARS one year later. He has been using the CPAP religiously for a year now and feels no better. My dental device was approved through insurance without problem while 6 months later, my husband's prior authorization request to the same insurance company for the very same device and for the very same diagnosis was denied...after 4 appeal letters, it is being covered...he is anxiously awaiting the final fitting. So, the insurance piece, at least for UARS, clearly can be tricky.
Some sources have indicated that patients with UARS are less tolerant to CPAP use due to an increased sensitivity in the nervous system...I understand that UARS is placed on a continuum with OAS, and it is treated the same as OAS; however, there are some differences that I think need to be taken into consideration.
© 2025 Created by The SleepGuide Crew.
Powered by