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Sleep Disordered Breathing

Contemporary Management of Sleep-Disordered Breathing

Sleep-disordered breathing (SDB) is a collective term which includes snoring, upper airway resistance syndrome (UARS) and Obstructive Sleep Apnea Syndrome (OSAS). Simply put, the term is descriptive of the effects of an anatomic partial collapse or obstruction of the upper airway during sleep which may cause sleep fragmentation. Surgical management was the first treatment modality available for SDB. Some of the first subjects to undergo surgery for an anatomic narrowing or blockage of the upper airway during sleep were those afflicted with the Pickwickian Syndrome (obesity-hypoventilation syndrome). Tracheotomy was the sole surgical procedure available during this period and since it was life saving in these circumstances, it was also used for other patients with nocturnal upper airway obstruction.1 Morbidity and mortality were not established except for the very severely affected, and the tracheotomy was not well tolerated or accepted by most patients even as a method to improve the quality of life, or even to extend life itself. In the early 70’s the term used to describe nocturnal airway obstruction was hypersomnia with periodic apnea (HPA), later revised to be called obstructive sleep apnea syndrome (OSAS), and now better known collectively as Sleep-Disordered Breathing (SDB).

Over thirty years have passed and our knowledge of sleep disorders has evolved to such an extent that the field of sleep disorders is now a recognized specialty in medicine and should be, in the future, a specialty in surgery. The coupling of medicine and surgery for the definitive management of SDB is necessary due to the fact that upper airway narrowing or blockage during sleep is an anatomic problem and is the surgeon’s domain. In addition, not all patients will accept medical management as the primary first choice, and visa versa, the same holds true for surgical acceptance. Granted, there is surely a central neurologic mediator associated with this syndrome that is not yet identified. However medical management, the present treatment of choice, is now suffering with compliance problems and resistance from the younger subset of patients, who have debilitating daytime somnolence due to Upper Airway Resistance Syndrome (UARS, a mild form of sleep disorder), and do not want to wear a nasal device (CPAP/BiPAP) six to eight hours a night for the next forty or fifty years. Hence, between the two modalities we may offer alternatives as is appropriate.

What we have learned about the obstructive process in sleep disorders through the combined efforts of our surgical and medical colleagues, is that nocturnal narrowing or obstruction may be localized to one or two areas, or may encompass the entire upper airway passages to include the nasal cavity (nose), oropharynx (palate) and hypopharynx (tongue base). Conservative medical therapy is usually recommended first. Treatment centers around sleep hygiene, weight loss, dental splints and nocturnal nasal pressure devices (CPAP/BiPAP). There are also surgical procedures presently available to provide for a logical upper airway reconstruction (UAR) of these regions.2-3 This will usually encompass multiple surgical procedures or sites, in such a manner as to minimize risks and complications, and to subsequently relieve the patient of this problem. Current established surgical procedures offer reconstruction of the airway from the nose and palatal level to the tongue base.

Indications for Treatment (Medically or Surgically)

General indications:

  1. Excessive Daytime Sleepiness ( Altered daytime performance )
  2. RDI >20*
  3. Oxygen saturation < 90%
  4. Arrhythmias ( cardiovascular derangements )
  5. Negative Pes ( esophageal pressure ), more negative than -10 cm H20 during sleep
    1. Treatment for an RDI < 20 acceptable in cases where excessive daytime sleepiness (EDS) causes altered daytime performance (mild OSAS and UARS)

Current Methods of Management:

Medical:

  • CPAP/BIPAP *
  • Weight loss
  • Sleep hygiene
  • Dental splints or tongue retaining devices
  • Nasopharyngeal tubes
    1. This modality has become the mainstay of treatment in most patients with SDB

Surgical:

  • Tracheotomy
  • Nasal
  • Palatal
  • Tongue reduction
  • Genioglossus advancement-Hyoid ( GAHM )
  • Bimaxillary advancement ( MMO )

Rationale for Surgery:

Nearly all patients with documented SDB are candidates for surgical intervention. This mandates that the patients are medically and psychologically stable and wish to undergo a surgical procedure.

Nearly all patients with documented SDB are candidates for surgical intervention. This mandates that the patients are medically and psychologically stable and wish to undergo a surgical procedure. They should be informed of the various medical and surgical treatments, along with current treatment philosophies. Surgical indications should include the two major pathophysiologic parameters of SDB: neurobehavioral and cardiopulmonary derangements caused by nocturnal obstructions during sleep. Patients with the diagnosis of UARS usually present with marked excessive daytime sleepiness (EDS). Since there are numerous other causes of EDS such as narcolepsy, insomnia and sleep deprivation, a nasal CPAP trial, in this group, can be diagnostic and therapeutic thus helping to establish that EDS is secondary to upper airway resistance syndrome and sleep fragmentation (SDB). The cardiopulmonary risks of OSAS have been documented when the respiratory disturbance index is greater than 20 and their lowest oxygen saturation level is below 90%.4 This severity necessitates treatment to lower the risk of cardiopulmonary sequelae and the increased mortality rate.

Specific Indications for Surgery:

Excessive daytime sleepiness (EDS); RDI > 20; Oxygen desaturation > 90%; arrhythmias; negative esophageal pressures (Pes > -10 cmH20); failure of medical management; or desire by the patient to select treatment modality where appropriate. In patients with an RDI < 20 events an hour of sleep and associated excessive daytime somnolence which interferes with daily functioning, surgery is considered appropriate on a case-by-case basis. Our existing Stanford Protocol (Powell-Riley) is predicated on evidence-based medicine for these treatments. Clinical outcomes for all existing surgical procedures are listed below under current surgical techniques and have been validated by other centers in the United States, Europe and Asia.

Pre-surgical evaluation:

As a standard this should include polysomnography, a comprehensive history with head and neck physical examination, fiber-optic nasopharyngoscopy and lateral cephalometric analysis where available. This will give sufficient database information to help in directing surgical therapy and in addressing the possibilities for treatment or clinical outcomes. It is recommended and cautioned that no one test or procedure is to be relied on for such decisions. This systematic medical and surgical review will support the establishment of the following guidelines: determine sleep disorder type, establish parameters of severity, identify co-morbidity factors, identify probable sites of obstruction, decide if treatment is emergent or elective, and assess the risk/benefit ratios.

 

Current Surgical Techniques:

Airway Bypass: Tracheotomy

Rationale: Immediate resolution of obstructive breathing during sleep in most subjects.
Indications: Where an emergent airway is necessary or where there is neither the specialized equipment or surgical expertise to offer an alternative, morbid obesity (BMI > 40 kg/m2), severe hypoxemia (Sa02 < 70%) severe arrhythmia, asystole, PVC’s, uncontrolled hypertension and where surgery to alleviate upper airway obstruction may compromise the airway secondary to edema or drug therapy and CPAP is not available or tolerated by the patient. In reality tracheotomy is usually, but not always, poorly tolerated or accepted. Nasal CPAP has been used so successfully for severe OSAS that tracheotomy has taken a second position in the treatment of OSAS.

Techniques: Temporary or permanent tracheotomy methods may be employed to maintain the airway.

Clinical outcomes: The tracheotomy should be considered a conservative modality of airway protection in severe OSAS and especially in those who are morbidly obese. It is considered a 100% cure in most instances.

Nasal Obstruction: Reconstruction

Rationale: An open nasal airway establishes physiologic breathing and may minimize the use of the open oral airway. It should be remembered that when the mouth is open the lower jaw auto-rotates open and allows the tongue to fall back into the posterior airway space. In some patients improvement of the nasal airway may also improve CPAP tolerance and /or compliance.

Indications: Nasal airway blockage caused by bony, cartilaginous or hypertrophied tissues that interfere with nasal breathing during sleep.

Techniques: Septal and /or bony intranasal reconstruction, alar valve or alar rim reconstruction, turbinectomy.

Clinical outcomes: The ease and high success rate of nasal reconstruction makes this procedure a very valuable technique for those with nasal obstruction and SDB. By itself it is not likely to make a significant impact on moderate or severe SDB such as the improvement seen with palatal or tongue base surgery. However, it is still an essential part of the upper airway that should not be ignored in the overall treatment of SDB. Correction of any defects at this level minimizes oral breathing decreases the possibilities of elevated nasal negative pressure breathing during sleep.5-9

Classification of Obstructive Region by S. Fujita

  • Type l Palate (normal tongue base)
  • Type ll Palate and base of tongue
  • Type lll Base of tongue (normal palate)

Oropharyngeal Obstruction: Reconstruction

Rationale: The palatal and lateral pharyngeal tissues have been found to be the most compliant of the upper airway; documentation of the collapse at this level in SDB is well established.

Indication: A long soft palate, narrow inlet to the nasopharynx, hypertrophic tonsils and redundant lateral pharyngeal mucosa. This level of obstruction is classified as a Fujita Type 1.

Techniques: There are multiple methods to control this region and range from the traditional UPPP first described in the United States by Doctor Fujita (the father of sleep surgery) as well as the many variations of his original procedure. Surgical flaps, lasers, cautery or radiofrequency have also been used.

Clinical outcomes: Individual results vary with the skill of the surgeon and the technique selected. The safe clearance of the tissue blockage at this level is essential to the improvement of SDB and the standard techniques are excellent in accomplishing this goal. The technique has not gained widespread popularity over the years due to the pain and discomfort after surgery and the fact that the cure rate was so varied.10 This was due, in part, to the fact that when UPPP was first introduced there was not an appreciation of the possibility of tongue base obstruction. Many UPPP’s did clear the pharyngeal level of obstruction and were unfairly credited with failure due to the unrecognized tongue base problem (hyopharyngeal). In patients who have been carefully selected for upper airway reconstruction and whose site of primary obstruction is at the oropharyngeal level (Fujita type 1), the cure rate may be 80 to 90 %.11 In unselected patients this rate will fall to a low of 5 to 30%.10

Hypoharyngeal Obstruction: Reconstruction

Rationale: Tongue base obstruction has been documented in SDB by EMG studies, fiber-optic exams, radiographic cephalograms, CT and MRI scans and vidiofluoroscopy. In addition, the basic anatomy and physiology of the skeletal relationships and genioglossus-hyoid complex as it relates to airway size, both awake and asleep, have led to a better understanding of how to surgically approach the base of tongue level.

Indications: Includes the general indications for surgery with additional findings of clinical tongue base obstruction.

Techniques: The obstruction of the hyopharyngeal (base of tongue) region is a very complex problem since there is a large mass of tongue tissue with varied elasticity during sleep, compared to the nasal and palatal levels, coupled with other accessory hypopharyngeal dilators that must be managed in order to successfully open this region during sleep. This region may be bypassed by tracheotomy or approached logically by either making more room for the tongue or reducing the tongue size. There are soft tissue techniques to remove the mid portion of the tongue base using laser midline glossectomy and lingualplasty 12, partial glossectomy 13, or volumetric shrinkage by radiofrequency.14 In addition, there are skeletal advancements that attempt to place tension on the tongue so that during sleep it does not fall as far back into the airway. This procedure is referred to as part of Phase One of the Powell-Riley phased protocol 15 (inferior sagittal mandibular osteotomy and genioglossus advancement, hyoid myotomy and suspension). This is a simple technique that does not move the teeth or jaw and therefore does not interfere with the dental bite. A more aggressive procedure, usually saved for failure of the more conservative surgery above, is the forward movement of the lower jaw and midface (maxillomandibular advancement surgery). This procedure is referred to as Phase Two of the Powell-Riley phased protocol15, and gives the tongue more room, also placing additional tension on the tongue base. There are various new technologies emerging for control of the tongue base which include radiofrequency volume reduction, electrical stimulation of the tongue by a pacing device. All of these new technologies may be used in the future, depending on their respective merits and published clinical outcomes.

Clinical outcomes: A tracheotomy is usually curative in that it bypasses the obstructive region regardless of the site. It is generally used in subjects with refractory (failure of medical and other surgical management) base of tongue obstruction and in those with medical conditions that contraindicate more extensive surgeries. The techniques using soft tissue and skeletal procedures for the hypopharyngeal level have been used by our group in a staged manner so that the most conservative treatment is offered as an entry level procedure. We have named this approach to upper airway reconstruction the Powell-Riley phased surgical protocol, and over the years it has proven to be an effective and safe method for controlling upper airway collapse in sleep-disordered breathing. It has additionally reduced the possibility that unnecessary surgery would be performed. Our published clinical outcomes cure rate for Phase One is 42% to 75% depending on the severity of the disorder.16-18 Similar results have been confirmed by others.19-21 Phase Two has documented cure rates of greater than 90%.10,17,22 Reported studies using bimaxillary surgery for the treatment of SDB give results similar to our work.23-26 Others have used laser midline glossectomy and lingualplasty or partial glossectomy with varied results, depending on the definition they have reported for cure.

Definition of Responder or Cure: (Powell-Riley) Criteria must include 1-4 below or items 4 and 5 are completed.

  • RDI < 20 and /or at least a reduction in the RDI of 50% only if the initial RDI was less than 20 (for example if the RDI is 25 then it must be by definition 12.5 after treatment to call a cure )
  • Sa02 > 90% or a minimal fall below 90%
  • Normalization of sleep architecture
  • Resolution of excessive daytime sleepiness (EDS)
  • Equivalent comparison to nasal CPAP/BiPAP results on a full night titration

Definition of Phase One: ( Powell-Riley ) Three regions of the upper airway are treated as directed by the clinical work-up, using the most conservative surgery for each, but only including treatment at that level if it was considered sufficiently obstructed.

Nasal: Correct nasal obstruction depending on anatomical deformity (septum, turbinates or nasal valve deformities)
Pharyngeal: UPPP or equivalent and tonsillectomy if tonsils present
Hypopharyngeal: Inferior sagittal mandibular osteotomy and genioglossus advancement, hyoid myotomy and suspension, or laser midline glossectomy and lingualplasty, or partial glossectomy.

After Phase One is complete, a period of 4-6 months is allowed for sufficient healing, weight stabilization and neurologic equilibration. Then a repeat polysomnogram accompanied with a sleep assessment and clinical examination is done to assess the clinical outcomes.27 Those patients who are unchanged or incompletely treated are offered either further surgery (Phase two) or medical management (CPAP).

Definition of Phase Two: (Powell-Riley) If our protocol was used previously, the only region that should remain incompletely treated is the hypopharynx (base of tongue). A choice then is made among the remaining methods: maxillomandibular advancement surgery, tracheotomy or nasal CPAP. Other techniques that could be considered to make additional room for the tongue are the laser midline glossectomy and lingualplasty, or partial glossectomy. These procedures are seldom used by our center for Phase Two. Base of tongue reduction using radiofrequency is a new technology that may become an alternative to maxillomandibular surgery in some patients.28

Treatment Philosophy: The successful surgical treatment for sleep-disordered breathing should adhere to a systematic evaluation:

  • Treat to cure
  • Logically direct management
  • Full patient disclosure of options and risks ( medically and surgically)
  • Stage surgical management
  • Follow-up all treatments

Bibliography:

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  • Powell N, Riley R: A Surgical Protocol for Sleep-Disordered Breathing. Oral Maxillofacial Surg Clin North Am 7:345-356, 1995.

  • Sher A, Schechtman K, Piccirillo J: An American Sleep Disorders Association Review: The efficacy of surgical modifications of the upper airway in adults with obstructive sleep apnea syndrome. Sleep 19:156-177, 1996.

  • He J, Kryger M, Zorick T, et al: Mortality and apnea index in obstructive sleep apnea: Experience in 385 male patients. Chest 94:9-14, 1988.

  • Dayal V, Pillipson E: Nasal surgery in the management of sleep apnea. Ann Otol Rhinol Laryngol 94:550-554, 1985.

  • Millman R: Sleep Apnea and nasal patency, Am J Rhinol 2:177-182, 1988.

  • Olsen K, Kern E, Westbrook P, et al: Sleep and breathing disturbance secondary to nasal obstruction. Otolaryngol Head Neck Surg 89:804-810, 1981.

  • Series R, St Pierre S, Carrier G: Effects of surgical correction of nasal obstruction in the treatment of obstructive sleep apnea. Am Rev Respir Dis 46: 1261-1265, 1992.

  • Suratt P, Turner B, Wilhoit S: Effect of intranasal obstruction on breathing during sleep. Chest 90:324-328, 1986.

  • Sher A, Thorpy M, Shprintzen R, et al: Predictive value of Muller maneuver in selection of patients for uvulopalatopharyngoplasty. Laryngoscope 95:1483-1487, 1985.

  • Fujita S, Woodson T, Clark J, et al. Laser midline glossectomy as a treatment for obstructive sleep apnea. Laryngoscope 1991;101:805-09.

  • Mickleson S, Rosenthal L: Midline glossectomy and epiglottidectomy for obstructive sleep apnea syndrome. Laryngoscope 1997; 107:614-19.

  • Powell, N B, Riley, R W, Troell R J, Blumen M B, Guilleminault C. Radiofrequency volumetric reduction of the tongue. A porcine pilot study for the treatment of obstructive sleep apnea syndrome. Chest 111:1348, 1996.

  • Powell NB, Riley RW, Guilleminault C: Rationale and indications for surgical treatment in obstructive sleep apnea syndrome. Operative Techniques Otolaryngol Head Neck Surg 2(2): 87, 1991.

  • Riley R, Powell N, Guilleminault C: Inferior mandibular osteotomy and hyoid myotomy suspension for obstructive sleep apnea: a review of 55 patients. J Oral Maxillofac Surg 47:159, 1989.

  • Riley R, Powell N, Guilleminault C: Obstructive sleep apnea syndrome: a review of 306 consecutively treated surgical patients. Otolaryngol Head Neck Surg 108:117, 1993.

  • Riley R, Powell N, Guilleminault C. Obstructive sleep apnea and the hyoid: a revised surgical procedure. Otolaryngol Head Neck Surg 111: 717, 1994.

  • Ramirez SG, Loube DI: Inferior sagittal osteotomy with hyoid bone suspension for obese patients with sleep apnea. Arch Otolaryngol Head Neck Surg 122: 953, 1996.

  • Johnson, NT, Chinn J: Uvulopalatopharyngoplasty and inferior sagittal mandibular osteotomy with genioglossus advancement for treatment of obstructive sleep apnea. Chest 105: 278, 1994.

  • Lee RN, Givens CD, Wilson J, Robins RB: Staged surgical treatment of obstructive sleep apnea syndrome: A review of 35 patients. J Oral Maxillofac Surg 57:382-385, 1999.

  • Powell, N B, Riley, R W, Guilleminault C: The hypopharynx: upper airway reconstruction in obstructive sleep apnea syndrome. D N F Fairbanks and S Fujita(eds). In Snoring and Obstructive Sleep Apnea, Second Edition. Raven Press, Ltd., New York 1994.

  • Waite PD, Wooten V, Lachner J, et al: Maxillomandibular advancement surgery in 23 patients with obstructive sleep apnea syndrome. J Oral Maxillofac Surg 47: 1256, 1989.

  • Waite P, Shettar S: Maxillomandibular advancement surgery: a cure for obstructive sleep apnea syndrome. In: Waite P (editor). Oral and maxillofacial Surgery Clinics of North America 7(2): 327, 1995.

  • Hochban W, Brandenburg U, Peter JH: Surgical treatment of Obstructive sleep apnea by maxillomandibular advancement. Sleep 17(7):624, 1994.

  • Hochban W, Conradt R, Brandenburg U, et al: Surgical maxillofacial treatment of obstructive sleep apnea. Plastic and Reconstructive Surgery 99 (3): 619, 1995.

  • Guilleminault C, Mondini S: Need for multi-diagnostic approaches before considering treatment in obstructive sleep apnea. Bull Eur Physiopathol Respir 1983;19:583-589 Powell, N B, Riley, R W.

 

 

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