Oral appliance therapy is an effective treatment option for patients who are affected by snoring and/or obstructive sleep apnea. This type of therapy involves having a custom-fitted device inserted in your mouth and designed to use during sleep. An oral appliance is similar to an athletic mouth guard or an orthodontic retainer. The device is fitted, adjusted and monitored by your dentistry sleep specialist.
Oral appliance therapy typically uses one of two types of devices: mandibular repositioning devices and tongue retaining devices. Mandibular repositioning devices pull your lower jaw forward and down so that your airway is not obstructed during sleep. They are the most widely used among oral appliances. Tongue retaining devices hold the tongue in place so it does not block the airway.
According to the American Sleep Association, the average cost of an oral appliance is between $1800 and $5000. This estimate may include the actual device, the visit, adjustments and follow-up appointments. This cost may vary depending on your unique needs. Many health insurers, as well as Medicare, offer coverage for oral appliances that are used for the treatment of sleep apnea.
Once your doctor agrees that oral appliance therapy is a good recommendation for your treatment, he will walk you through all the important details about using these devices. Most patients find the oral appliances are relatively comfortable, portable, convenient for travel, easy to insert and easy to maintain. There are no side effects associated with using these devices. If you experience any discomfort, you should see your dentist for a custom fitting or adjustment.
Role of Oral Appliances in Management of Sleep-disordered Breathing Patient
Oral appliance therapy (OAT) is one of many treatment modalities used to treat sleep-disordered breathing (SDB). Treatment modalities for SDB include a combination of sleep modification, oral appliances (OA), positive airway pressure (PAP), myofunctional therapies, hypoglossal nerve stimulation systems like “Inspire”, and surgery. Behavioral modifications such as weight loss, aerobic exercise, sleep position, sleep hygiene, and alcohol intake modification can assist in the management of OSA.
The American Academy of Sleep Medicine (AASM) guidelines indicate that although OA is not as efficacious as CPAP, OA may be indicated for mild to moderate obstructive sleep apnea (OSA) when patients cannot tolerate CPAP or do not respond to CPAP. Studies on the effectiveness of OA have shown no more than 56% improvement to normal AHI, with compliance as one factor contributing to improved outcomes. An investigation comparing the effect of CPAP to OA on blood pressure (BP) in patients with OSA found that both CPAP and OA were associated with reductions in BP. Approximately 25% of patients receiving an OA may have no improvements and may aggravate the severity of their sleep apnea. PAP pneumatically opens the airway using continuous or on-demand positive air pressure, and is considered the ‘gold standard’ of therapy for OSA.
There are two categories of OAs for OSA: mandibular repositioning devices (MRD), or mandibular advancement devices (MAD), and tongue-retaining devices (TRD). The MRD’s objective is to reposition the mandible forward, enough to enlarge the upper airway and prevent it from collapsing. The TRD’s objective is to maintain the tongue in a forward position, preventing it from falling back and obstructing the airway during sleep. TRDs are poorly tolerated and are not often recommended, but may be considered in TMD patients who cannot tolerate any jaw advancement. For the MRD, the patient’s full range of protrusive movement is measured, and a 75% movement has been shown to be more effective than 50% advancement. However, a systematic review and meta-regression analysis on the effectiveness of different mandibular advancements suggests that it would be prudent to begin therapy at minimum effective advancement, since no significant improvements were found at increased movements. Patient compliance plays an important role in the long-term success of the treatment. The use of an OA concomitant with a PAP machine may reduce the pressure required to treat severe OSA, possibly increasing the acceptability of treatment and patient comfort. Thirty-nine to forty-seven percent of SB patients demonstrate greater reduction of motor activity with mandibular advancement splints than with conventional occlusal splints.
Occlusal changes observed in patients after long-term use of OAs are relatively small and include decreased overbite/overjet, and posterior open-bite in the premolar region. Prosthodontists have an in-depth knowledge of occlusion and TMJ function and are the most qualified to monitor and manage any occlusal changes that can occur with OAs. Occlusal changes will continue as long as an OA is used. Occlusal correction necessitates discontinuation of OA and alternative therapy such as CPAP.
A surgical approach is most effective in children with hypertrophied tonsils and adenoids. Concurrent maxillary expansion and orthodontic/surgical correction of malocclusions will improve OSA in children. Surgical procedures, such as uvulopalatopharyngoplasty (UPPP) in adults, are considered secondary to non-surgical therapy when the patient is non-responsive. There are concerns regarding the predictability and stability of surgery in the adult OSA patient, but when there is a clear maxillomandibular discrepancy, orthognathic surgery is most effective.
Prosthodontists who provide OAs to patients with OSA should have ongoing training in dental sleep medicine (DSM). Understanding the symptoms of SDB, knowing when to refer to a sleep physician, and assessing the TMJ, occlusion, oropharyngeal structures, orofacial pain, and headaches requires additional training and certification, as recommended by the American Academy of Dental Sleep Medicine (AADSM), American Academy of Sleep Medicine (AASM), the Canadian Sleep Society (CSS), and the American Dental Association.
Non-Custom/Over-The-Counter (OTC) Oral Appliance Therapy
A few comments about non-custom/over-the-counter oral appliance therapy. A distinction should be made about two types of non-custom oral appliances, direct-to-consumer and doctor-directed-and-supervised. The composition of the actual devices may not vary between the two subgroups. Often both types of non-custom oral appliances are made up of a thermoplastic resin material that can be heated, molded, and fabricated intraorally. The distinction to be made is not the composition; but rather, the protocol followed by a treating sleep physician and dentist trained in dental sleep medicine versus the patient performing these diagnostic and treatment tasks by him or herself. To the authors knowledge, a majority of the clinical data supporting the effectiveness of oral appliance therapy is based off of custom-made oral appliances and does not include OTC oral appliances.
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