Issue StoriesWhen to Use Oral Appliances for OSA Treatmentby John Basile, BS, RRT Some patients are pushing for oral appliance therapy, but it is not the right treatment for all cases.
Obstructive sleep apnea (OSA) has a long list of associated pathologies. The scientific evidence associating sleep apnea to cardiovascular disease, stroke, diabetes, and neurocognitive defects is exhaustive.1 The viable treatment options for this serious problem consist of a much shorter list. Once the diagnosis of OSA is definitively made, the treatment options are usually arranged based on the severity of the disorder. The treatments include weight reduction, positive airway pressure (PAP) devices, surgery, and oral appliances to stabilize the airway. Whatever therapy is selected, health care professionals must carefully consider the patients severity of OSA, potential for adherence to treatment, and the subsequent effectiveness of that therapy. In examining the treatment options, weight reduction frequently decreases the pressure required for airway stabilization in OSA but often does not eliminate the problem with airway occlusion. Surgical procedures are most frequently successful in mild cases of OSA and in pediatric cases where tonsillectomy is effective.2 And while PAP therapy should work for all cases of OSA, it is sometimes poorly tolerated, medically contraindicated, or impossible to utilize due to logistics or lack of an electrical power source where the patient normally sleeps. It has been our experience at Swedish Medical Centers Sleep Medicine Institute in Seattle that a patients initial introduction to the options for treatment is accompanied by his or her personal views. Some newly diagnosed OSA patients have already been influenced by negative public perceptions of PAP therapy and are predisposed against it. The insurance industry has, in some cases, made this worse by putting certain restrictions on coverage of oral appliances that make patients think that they have to first intentionally fail with PAP therapy before they can get what they think is the more desirable alternative: oral appliance therapy. For example, coverage for an oral appliance is typically withheld until a patient fails PAP therapy, and the result is that patients sometimes state that they are preselecting oral appliance therapy and first need to fail on PAP. These same patients come to do business with a durable medical equipment (DME) provider expecting to fail using PAP therapy because they mistakenly believe oral appliances are an equally effective treatment for OSA. However, the scientific evidence is not present to support that belief.2-5 Sleep medicine providers need to present the scientific evidence regarding long-term efficacy of oral appliances so that patients can make informed decisions regarding their next steps in therapy. Recent scientific articles identifying cardiovascular risk in patients with apnea-hypopnea indices (AHIs) as low as 14 per hour call into question the use of an oral appliance in a moderate to severe case of OSA where, potentially, the AHI may be lowered to only 14 per hour.1 The careful education and re-education of patients will help them understand which mode of therapy will sufficiently lower their risks of associated diseases. Patients typically are concerned with the encumbrance of PAP machines and the potential for social embarrassment. In this era of seemingly limitless media and information resources, patients have their opinions colored by news stories, advertisements, and friends and family members experiences with PAP therapy. As the percentage of patients diagnosed and treated in our general population for OSA increases, these patient-to-patient communications will increase as well. It is important that the DME industry help improve the adherence/compliance rates and the general impression of PAP therapy in our health care community and in the lay population. The interventions that work to improve adherence and compliance with patients acclimating to PAP therapy are a combination of good education and close support. The respiratory care practitioners at Swedish Sleep Therapy Supply make a contracted contact with new PAP therapy patients within the first 4 to 7 days of therapy. They then follow up at 3 weeks and 3 months into therapy. The need for more support is balanced by information from the patient reports and objective usage data from the patients compliance-recording PAP machines. When patients believe they need to entertain other options in the face of failure with PAP therapy, oral appliances will certainly be a first-line option. Oral appliances, in particular mandibular repositioning (advancement) devices or MRDs, have proved to be a potentially effective option in mild to moderate cases of OSA for some patients. The MRD is the most often used oral appliance for OSA. In some published studies, the effectiveness of these appliances was reported to be 50% to 70%. It should be noted that the groups of patients in these studies had AHIs of less than 10 to 15 per hour.1-4 In patients with mild to moderate OSA, an MRD should be considered over no treatment at all.4 The American Sleep Disorders Association (ASDA, now the American Academy of Sleep Medicine) practice parameters state that oral appliances are indicated for snoring and mild OSA as a primary device and in moderate sleep apnea only when PAP therapy has failed. Long-term adherence for patients using MRDs has been reported to be 60%.6-9 Many Device Options Contraindications for oral appliances include insufficient teeth to support the oral appliance, periodontal problems, active temporomandibular joint (TMJ), disorder, and maximum mandibular protrusion distance of less than 6 mm. In a study of 100 unselected polysomnography subjects examined by maxillofacial surgeons, 31% had an insufficient number of teeth, 16% had periodontal abnormalities that would require prior treatment, and 2% had a significant TMJ disorder. Side effects of MRDs include increased salivation, dental pain, and TMJ pain. Other long-term side effects may include tooth movement and changes in the patients ability to bite properly.3.4,6 To guard against these potential problems, it is suggested that patients with oral appliances should make periodic visits to a dentist. In addition, concurrent follow-up with a sleep physician is recommended to monitor adherence to therapy and symptom control. Most patients discontinuing use of their oral appliance do so due to discomfort.4 In a recently published case presentation, a woman utilized an MRD oral appliance successfully after failing CPAP therapy and uvulopalatopharyngoplasty (UPPP) surgery. The UPPP surgery was deemed ineffective after 5 months postoperative.3 While MRDs should be considered in patients with mild to moderate OSA who are intolerant of PAP therapy, oral appliances may be useful for patients who have a lifestyle that may make daily use of PAP therapy impossible. In working with the sleep apneic population on PAP therapy, I have found that some patients enjoy bike rides or backpacking trips that make use of an electrically powered PAP device nearly impossible. In these situations, an oral appliance will decrease snoring and obstructive events enough to allow them to comfortably enjoy their various outdoor interests. I am careful to make the point with the patient that the oral appliance ordered by their sleep provider is a temporary treatment and will most likely not lower their AHI to safe levels. In addition, the experimental use of an oral appliance in conjunction with CPAP has been documented.7,8 Theoretically, the use of an oral appliance may decrease the pressure required for airway stabilization in OSA and thereby increase PAP treatment adherence and compliance. In a case study published in 2002, a patient utilized both an oral appliance and nasal CPAP successfully at night. The patient was able to decrease his positive airway pressure setting from 16 to 5.8 cm H2O and gain improved quality of life over using a single mode of therapy. Concerns over the presence of something in the mouth and the ability to maintain a tight seal are valid. However, it was noted in the study that the presence of an oral appliance created a more patent airway, and, therefore, lower nasal CPAP pressures were needed to reduce the AHI adequately. More work needs to be done in this area in order for us to potentially help the small population of OSA patients who would benefit from combined therapy. In the meantime, we can consider an oral appliance as a viable and effective alternative for some OSA patients, provided they are carefully selected, professionally fitted, well educated about the use of the device, and receive diligent, thorough follow-up care. John Basile, BS, RRT, is manager of Swedish Sleep Therapy Supply (SSTS), which works in conjunction with the Swedish Sleep Medicine Institute, Seattle. SSTS is a hospital-based DME provider specializing in PAP therapy for sleep-disordered breathing patients. Basile is a committee chair of the American Association for Respiratory Cares Sleep Section. References
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