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4 Redening Outcome Measures
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31. Fujita S, Conway W, Zorick F, Roth T. Surgical correction of anatomic azbnormalities in obstructive sleep apnea syndrome: uvulopalatopharyngoplasty. Otolaryngol Head Neck Surg. 1981;89(6):923–34.
32. He J, Kryger MH, Zorick FJ, Conway W, Roth T.Mortality and apnea index in obstructive sleep apnea. Experience in 385 male patients. Chest. 1988;94(1):9–14.
33. Sher AE, Schechtman KB, Piccirillo JF. The efcacy of surgical modications of the upper airway in adults with obstructive sleep apnea syndrome. Sleep. 1996;19(2):156–77.
34. Elshaug AG, Moss JR, Southcott AM, Hiller JE.Redening success in airway surgery for obstructive sleep apnea: a meta analysis and synthesis of the evidence. Sleep. 2007;30(4): 461–7.
35. Ravesloot MJ, de Vries N.Reliable calculation of the efcacy of non-surgical and surgical treatment of obstructive sleep apnea revisited. Sleep. 2011;34(1):105–10.
36. Weaver TE, Grunstein RR.Adherence to continuous positive airway pressure therapy: the challenge to effective treatment. Proc Am Thorac Soc. 2008;5(2):173–8.
37. Kribbs NB, Pack AI, Kline LR, Smith PL, Schwartz AR, Schubert NM, etal. Objective mea­surement of patterns of nasal CPAP use by patients with obstructive sleep apnea. Am Rev Respir Dis. 1993;147(4):887–95.
38. Weaver TE, Maislin G, Dinges DF, Bloxham T, George CF, Greenberg H, etal. Relationship between hours of CPAP use and achieving normal levels of sleepiness and daily functioning. Sleep. 2007;30(6):711–9.
39. Wozniak DR, Lasserson TJ, Smith I.Educational, supportive and behavioural interventions to improve usage of continuous positive airway pressure machines in adults with obstructive sleep apnoea. Cochrane Database Syst Rev. 2014;1:CD007736.
40. Vanderveken OM, Dieltjens M, Wouters K, De Backer WA, Van de Heyning PH, Braem MJ.Objective measurement of compliance during oral appliance therapy for sleep-disordered breathing. Thorax. 2013;68(1):91–6.
41. Ravesloot MJ, de Vries N, Stuck BA.Treatment adherence should be taken into account when reporting treatment outcomes in obstructive sleep apnea. Laryngoscope. 2014;124(1):344–5.
42. Boyd SB, Walters AS. Effectiveness of treatment apnea-hypopnea index: a mathemati­cal estimate of the true apnea-hypopnea index in the home setting. J Oral Maxillofac Surg. 2013;71(2):351–7.
43. Ryan CF, Lowe AA, Li D, Fleetham JA.Magnetic resonance imaging of the upper airway in obstructive sleep apnea before and after chronic nasal continuous positive airway pressure therapy. Am Rev Respir Dis. 1991;144(4):939–44.
44. Holty J-EC, Guilleminault C.Maxillomandibular advancement for the treatment of obstruc­tive sleep apnea: a systematic review and meta-analysis. Sleep Med Rev. 2010;14(5):287–97.
45. Stuck BA, Leitzbach S, Maurer JT.Effects of continuous positive airway pressure on apnea– hypopnea index in obstructive sleep apnea based on long-term compliance. Sleep Breath. 2012;16(2):467–71.
46. Ribeiro de Almeida F. Complexity and efcacy of mandibular advancement splints: under­standing their mode of action. J Clin Sleep Med. 2011;7(5):447–8.
47. Bianchi MT, Alameddine Y, Mojica J.Apnea burden: efcacy versus effectiveness in patients using positive airway pressure. Sleep Med. 2014;15(12):1579–81.
48. Vonk P, Rotteveel P, Ravesloot M, den Haan C, De Vries N. The inuence of position­dependency on surgical success in sleep apnea surgery—a systematic review. Sleep Breath. 2020;24(2):433–42.
49. Katsantonis GP, Miyazaki S, Walsh JK.Effects of uvulopalatopharyngoplasty on sleep archi­tecture and patterns of obstructed breathing. Laryngoscope. 1990;100(10):1068–72.
50. Lee CH, Kim S-W, Han K, Shin J-M, Hong S-L, Lee J-E, etal. Effect of uvulopalatopharyn­goplasty on positional dependency in obstructive sleep apnea. Arch Otolaryngol Head Neck Surg. 2011;137(7):675–9.
51. Van Maanen J, Ravesloot M, Witte B, Grijseels M, De Vries N.Exploration of the relation­ship between sleep position and isolated tongue base or multilevel surgery in obstructive sleep apnea. Eur Arch Otorhinolaryngol. 2012;269(9):2129–36.
57
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https://t.me/medicina_free
52. Lee YC, Eun YG, Shin SY, Kim SW.Change in position dependency in non-responders after multilevel surgery for obstructive sleep apnea: analysis of polysomnographic parameters. Eur Arch Otorhinolaryngol. 2014;271(5):1081–5.
53. Li H-Y, Cheng W-N, Chuang L-P, Fang T-J, Hsin L-J, Kang C-J, etal. Positional dependency and surgical success of relocation pharyngoplasty among patients with severe obstructive sleep apnea. Otolaryngol Head Neck Surg. 2013;149(3):506–12.
54. van Maanen J, Witte B, de Vries N.Theoretical approach towards increasing effectiveness of palatal surgery in obstructive sleep apnea: role for concomitant positional therapy? Sleep Breath. 2014;18(2):341–9.
55. Kastoer C, Benoist L, Dieltjens M, Torensma B, de Vries L, Vonk P, etal. Comparison of upper airway collapse patterns and its clinical signicance: drug-induced sleep endoscopy in patients without obstructive sleep apnea, positional and non-positional obstructive sleep apnea. Sleep Breath. 2018;22(4):939–48.
56. Benoist LB, de Ruiter MH, de Lange J, de Vries N.Residual POSA after maxillomandibular advancement in patients with severe OSA.In: Positional therapy in obstructive sleep apnea. Cham: Springer; 2015. p.321–9.
57. Vonk PE, Rotteveel PJ, Ravesloot MJ, Ho J-PT, de Lange J, de Vries N.The inuence of position dependency on surgical success in patients with obstructive sleep apnea undergoing maxillomandibular advancement. J Clin Sleep Med. 2020;16(1):73–80.
58. Benoist L, Verhagen M, Torensma B, van Maanen J, De Vries N.Positional therapy in patients with residual positional obstructive sleep apnea after upper airway surgery. Sleep Breath. 2017;21(2):279–88.
59. MacKay S, Carney AS, Catcheside PG, Chai-Coetzer CL, Chia M, Cistulli PA, et al. Effect of multilevel upper airway surgery vs medical management on the apnea-hypopnea index and patient-reported daytime sleepiness among patients with moderate or severe obstructive sleep apnea: the SAMS randomized clinical trial. JAMA. 2020;324(12):1168–79.
60. Steffen A, Hartmann JT, König IR, Ravesloot MJ, Hofauer B, Heiser C.Evaluation of body position in upper airway stimulation for obstructive sleep apnea—is continuous voltage suf­cient enough? Sleep Breath. 2018;22(4):1207–12.
61. Lee CH, Shin H-W, Han DH, Mo J-H, Yoon I-Y, Chung S, etal. The implication of sleep posi­tion in the evaluation of surgical outcomes in obstructive sleep apnea. Otolaryngol Head Neck Surg. 2009;140(4):531–5.
62. Beyers J, Vanderveken OM, Kastoer C, Boudewyns A, De Volder I, Van Gastel A, Verbraecken JA, De Backer WA, Braem MJ, Van De Heyning PH, Dieltjens M. Treatment of sleep-disordered breathing with positional therapy: long-term results. Sleep and Breathing. 2019;23:1141–9.
63. Sutherland K, Phillips CL, Cistulli PA. Efcacy versus effectiveness in the treatment of obstructive sleep apnea: CPAP and oral appliances. J Dent Sleep Med. 2015;2(4):175–81.
64. Dieltjens M, Braem MJ, Van de Heyning PH, Wouters K, Vanderveken OM.Prevalence and clinical signicance of supine-dependent obstructive sleep apnea in patients using oral appli­ance therapy. J Clin Sleep Med. 2014;10(9):959–64.
65. Marklund M, Persson M, Franklin KA.Treatment success with a mandibular advancement device is related to supine-dependent sleep apnea. Chest. 1998;114(6):1630–5.
66. Lee CH, Jung HJ, Lee WH, Rhee CS, Yoon IY, Yun PY, etal. The effect of positional depen­dency on outcomes of treatment with a mandibular advancement device. Arch Otolaryngol Head Neck Surg. 2012;138(5):479–83.
67. Chung JW, Enciso R, Levendowski DJ, Morgan TD, Westbrook PR, Clark GT.Treatment out­comes of mandibular advancement devices in positional and nonpositional OSA patients. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2010;109(5):724–31.
M. J. L. Ravesloot
Part II
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Diagnosis of Epiglottis Collapse
Relevant Anatomy andPhysiology
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oftheEpiglottis
MatejDelakorda
5.1 Introduction
The nutritional and respiratory paths are joined in the upper aerodigestive tract that serves multiple functions. Due to the complex relationship between the skeletal frame and soft tissues, accurate neurological coordination is essential for maintain­ing adequate patency during breathing and for exerting effective constrictions dur­ing swallowing. A comprehensive knowledge of the anatomy of this region is fundamental for understanding pathophysiologic processes as well as performing safe and successful surgery.
The larynx is a cartilaginous segment of the respiratory tract, which is located in the anterior aspect of the neck. Phylogenetically, its primary function was to prevent ingested food and liquids from entering the trachea; the function of phonation developed with further evolution. Complete glottic closure is necessary for effective lung cleaning (coughing, sneezing) and for generating a positive intrathoracic pres­sure required for defecation, lifting heavy objects, body stabilization, and child­birth. The larynx also plays an important role in breathing and is actively involved in the regulation of respiration by a complex of sensory feedback loops. The epi­glottis is a part of the supraglottic larynx and has an important function, especially in breastfeeding newborns and infants. It is exposed to many possible diseases, developmental anomalies, infections, and neoplasms. The role of epiglottis in obstructive sleep apnea (OSA) has only recently been observed and elucidated.
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M. Delakorda (*) General Hospital Celje, Celje, Slovenia
© The Author(s), under exclusive license to Springer Nature Switzerland AG 2023 M. Delakorda, N. de Vries (eds.), The Role of Epiglottis in Obstructive Sleep Apnea, https://doi.org/10.1007/978-3-031-34992-8_5
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5.2 Embryology
The larynx begins to form during the third and fourth weeks of embryologic devel­opment as a morphogenetic component of the respiratory system, and by the 41st day, its cartilage and the intrinsic muscles are already observable. Its formation starts as a longitudinal ridge from the foregut caudal to the fourth pharyngeal pouch. Its lower portion grows inferiorly as a diverticulum to form the trachea and lungs, while the cephalic part forms a primitive laryngeal aditus covered by an endoderm lining—future epithelium. As it extends toward the caudal part of the embryo, it becomes invested by mesenchyme that gives rise to the cartilaginous and muscular structures. Antero-superior to this ridge is a hypobranchial eminence, a midline pro­liferation of mesenchyme anterior to third and fourth branchial arches visible as a swelling of the oor of the primitive hypopharynx. The epiglottis will develop from this structure and the ventral parts of the third and fourth arches. The latter will also give rise to the aryepiglottic folds and cuneiform cartilages. The arytenoids and corniculate cartilages are derived from the arytenoid swellings of the sixth branchial arches (Fig.5.1).
The lesser cornu and the upper body of the hyoid are formed by the second pha­ryngeal arch, while the greater cornu and the lower portion of the body derive from the third pharyngeal arch. The process of hyoid chondrication begins in the fth fetal week and is completed in the third and fourth months. Ossication in the greater cornu begins toward the end of the intrauterine life, in the hyoid body shortly before or after birth, and in the lesser cornu around puberty. The thyroid cartilage is
Fig. 5.1 The ventral part of the pharynx in the fourth week (I) and fth month (II) of fetal life. A lateral lingual swellings, B medial lingual swelling, C1 hypobranchial eminence, C2 epiglottal swelling, D arytenoid swellings, and * foramen cecum
5 Relevant Anatomy andPhysiology oftheEpiglottis
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derived from the fourth pharyngeal arch. The future thyroid cartilage and hyoid are connected ventrally at the hypobranchial eminence and dorsally by a cartilaginous bar—the hypothyroid cartilage. At the third month of fetal development, the hyoid bone and thyroid cartilage separate, sometimes leaving a remnant of this connection in the form of a small oval-shaped hyaline cartilage called triticeal cartilage [1].
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5.3 Developmental Anomalies
The incidence of congenital anomalies of the larynx and trachea is fairly low, reported at 1in 10,000 to 50,000 live births, either as isolated occurrences or as synchronous lesions, frequently seen as part of syndromes such as short rib poly­dactyly, or tricho-rhino-phalangeal and lacrimo–auriculo-dental-digital syndromes [2]. The identication of such anomalies soon after birth, or prenatally, is often vital for the survival and growth of the infant. Laryngeal anomalies are commonly related to symptoms of aspiration and/or stridor, which can also be caused by dynamic conditions such as laryngomalacia (see Chap. 11).
Interruption before or during the embryological period during which the larynx is formed can result in aplasia, hypoplasia, and bid epiglottis. The absence of the epiglottis can also be accompanied by severe glottic stenosis [3]. Patients with bid epiglottis commonly experience symptoms of respiratory compromise caused by one or both of the cartilaginous halves being drawn into the glottic inlet with inspiration.
5.4 Maturation: Laryngeal Descent
The anatomy and position of the larynx in infants and children differ from that in adults [3]. From fetal to adult life, the epiglottis undergoes a considerable gradual descent in relation to the vertebral column as well as some morphologic changes [4,
5]. These anatomic changes of the upper respiratory tract probably evolved mainly
to facilitate speech by enabling better articulation. An elevated laryngeal position enables contact between the epiglottis and soft palate, thus supporting nutrition by allowing breathing while sucking. It not only prevents aspiration but also makes newborns obligatory nasal breathers. Laryngeal descent is believed to be the ana­tomic basis predisposing humans to OSA as a developmental extension of the tongue backward and downward creates a compliant oropharynx prone to col­lapse [68].
At birth, the inferior margin of the cricoid cartilage is located at the level of the upper border of the C-4 vertebra, while the tip of the epiglottis is at the level of the C-1 vertebra. Usually, it can be visualized over the dorsum of the tongue in most infants. From birth, the larynx starts to descend with the most obvious changes tak­ing place during puberty when the larynx lengthens rapidly. The cricoid cartilage descends to the level of the C-7 vertebra in men and the C-6 vertebra in women, and the tip of the epiglottis is opposite the C-3 vertebra.
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The infant larynx has softer cartilage and laxer supporting ligaments. Epiglottis is omega- or tubular-shaped, and hence, it is more susceptible to collapse due to negative pressure during inspiration [9]. During maturation, the epiglottis becomes increasingly at with the aryepiglottic folds in a more lateral position; but in most adults, it retains its curved shape. Additionally, an angle of the thyroid cartilage’s laminae narrows from 110–120 to 90° in men after puberty but does not change signicantly in women.
M. Delakorda
5.5 Skeletal Framework
An adult larynx is superiorly limited by the free end of the epiglottis and inferiorly by the lower edge of the cricoid cartilage. Its cartilaginous skeleton consists of mul­tiple cartilage types: hyaline cartilage—specically, thyroid, cricoid, arytenoid, and triticeal; elastic epiglottis; and broelastic corniculate (Santorini) and cuneiform (Wrisberg) cartilage. Together with the hyoid bone, they form a complex skeletal framework interconnected by numerous ligaments, brous membranes, and syno­vial joints that are moved by muscles in different directions.
The thyroid cartilage is the largest cartilage of the larynx. It is formed by two quadrangular alae that unite anteriorly and form a thyroid notch superiorly with the laryngeal prominence (Adam’s apple) just below it, most obvious in males. On the lateral surface, there is an oblique line to which the sternothyroid, thyrohyoid, and inferior pharyngeal constrictor muscles attach [9]. Posteriorly, each ala has a supe­rior and inferior horn. The inferior horn articulates with a facet on the cricoid carti­lage to form the synovial cricothyroid joint that allows rotation of the cricoid cartilage. The superior horn attaches to the greater cornu of the hyoid bone with the lateral thyrohyoid ligament. In about one-third of the general adult population, this ligament contains small triticeal cartilages, which can cause symptoms such as dys­phagia and odynophagia or can be mistaken for a foreign body when calcied [10
14]. The corniculate cartilages are housed on the apex of the arytenoids. The
cuneiform cartilages, when present, are lateral to the corniculate cartilages embed­ded in the aryepiglottic fold. Although some feel that these cartilages are vestigial, they do appear to add rigidity to the aryepiglottic folds.
The epiglottis is a thin lamella of yellow cartilage, shaped like a leaf. It projects obliquely and vertically behind the base of the tongue and ventrally to the entrance of the larynx. Its broad and round free end, which is occasionally notched in the midline, is directed upward and sometimes bent anteriorly. Its lower part, called petioles, is like a stalk, long, and narrow and connected to the back of the thyroid cartilage. On the posterior surface of its lower half, there is a projecting part called the tubercle that, when prominent, can obscure the view of the anterior part of the vocal cords. The epiglottis is higher and wider in males with no signicant changes observed with aging [15]. It can be divided into a suprahyoid and an infrahyoid por­tion. The suprahyoid portion protrudes into the laryngeal lumen, without any attach­ments, whereas on the infrahyoid part, only the posterior-laryngeal surface is exposed. Split lines in the epiglottic cartilage reect the arrangement of its collagen
5 Relevant Anatomy andPhysiology oftheEpiglottis
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bundles. On the posterior aspect, they run primarily in a horizontal direction throughout the upper one to two-thirds above the epiglottic tubercle and are most pronounced between the attachments of the lateral and median hyoepiglottic liga­ment. This area, approximately one-third of the way from the superior margin of the epiglottis, also referred to as the epiglottic folding plane, is important for the mecha­nism of epiglottic downfolding during swallowing [16]. The lower third, including the petiolus of the epiglottis, demonstrates a vertically directed orientation of split lines. The anterior aspect of each epiglottis shows a different, more complex orien­tation of split lines surrounding the holes and recesses formed by the mucous glands. The cartilage is also perforated by the branches of the internal laryngeal nerve.
It was traditionally believed that only structures composed of hyaline cartilage can undergo calcication (thyroid, cricoid, and arytenoid cartilages) [14, 17]. Enchondral calcication of these cartilages begins with skeletal maturity and pro­gresses thereafter with aging. Based on macroscopic observations, the epiglottis had been considered a permanent elastic cartilage that does not undergo ossication [18]. However, a more detailed analysis of age-related changes in calcium deposi­tion has shown that calcication increases with age and is more pronounced in males [15, 19, 20]. Laryngeal cartilage calcication may affect some mechanical properties and while it could theoretically add to its stability, it can also be a cause of different swallowing problems, such as dysphagia, foreign body sensations, or aspirations [21].
The hyoid bone is the central movable anatomical structure of the neck and func­tional part of the larynx. This U-shaped bone is located in the anterior midline and serves as an attachment for various muscles of the oor of the mouth, tongue, and pharynx. It is unique because in humans, unlike in other mammals, it does not artic­ulate with any other bone or cartilage. Instead, it is suspended from the styloid processes by the bilateral stylohyoid ligaments, brous cords extending from the tip of the styloid processes to the lesser cornus of the hyoid bone. The hyoid position is determined by this suspension apparatus and the activity of muscles attached to it. Due to these connections, the hyoid position is closely related to pharyngeal airway dimensions and associated with critical closing pressure in OSA patients [22]. During inspiration, contraction of pharyngeal dilators causes anterior movement of the hyoid and increases the anteroposterior dimension of the retrolingual airway, contributing to upper airway (UA) patency. In resting state, it is positioned in the neck roughly parallel with the lower border of the mandible, and, when viewed in lateral projection, the tip of the greater cornue partially overlaps with the cervical spine [23].
The epiglottis has two anterior attachments. Inferiorly, at the petiolus, the epi­glottis is attached to the inner surface of the laryngeal prominence of the thyroid cartilage, just above the level of the anterior commissure and below the thyroid notch, by the elastic thyroepiglottic ligament. At this point, bilateral vestibular liga­ments and vocal ligaments are also attached, forming the Broyles’ ligament that contains blood vessels and lymphatics [24, 25]. Superiorly, the epiglottis is attached to the hyoid bone by the paired lateral hyoepiglottic ligaments and a single medial hyoepiglottic ligament. The lateral hyoepiglottic ligaments are attached to the
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M. Delakorda
lateral edges of the upper portion of the epiglottis, running laterally to the tip of the greater horns of the hyoid bone forming the pharyngoepiglottic folds (lateral glos­soepiglottic folds) [16]. The medial ligament is a brous fan-shaped band of tissue running in the midline from the upper border of the hyoid bone to the anterior sur­face of the epiglottis, forming the medial glossoepiglottic fold. The upper limit of its epiglottic attachment is at the level of the lower borders of the greater cornu of the hyoid bone and its lower attachment blends with the attachment of the thyroepi­glottic ligament [26]. It had been traditionally believed that anteriorly the medial hyoepiglottic ligament attaches only to the hyoid bone, but a more recent anatomi­cal study revealed that the hyoepiglottic ligament also extends to one of the intrinsic lingual muscles, most probably the genioglossus muscle [27, 28] (Fig. 5.2). Accordingly, two parts can be distinguished in the medial hyoepiglottic ligament: the lingual and the hyoid part. A signicantly decreased number of elastic and col­lagen bers has been found in these ligaments in elderly persons, which may put them at an increased risk of epiglottic instability [29, 30]. Taking into account the progressive attening of epiglottis with aging, it is possible that this ligament main­tains its anterior convexity.
The thyrohyoid membrane is a broad broelastic layer attached to the upper border and superior horn of the thyroid cartilage, the upper margin of the posterior surface of the body, and the greater horns of the hyoid bone. It thus ascends behind the concave posterior surface of the hyoid and is separated from its body by a bursa that facilitates the ascent of the larynx during speech and deglutition. The thickened portion of this membrane in the midline constitutes the thyrohyoid ligament. The aryepiglottic folds are paired structures arising from the apex and corniculate tuber­cle of the arytenoids and merging with the lateral margins of the epiglottis. Together with the laryngeal surface of the epiglottis, they enclose the space referred to as the laryngeal vestibule. The body of each aryepiglottic fold is composed of the
Fig. 5.2 Attachments of hyoepiglottic ligament. 1 hyoepiglottic ligament (a lingual part and b hyoid part), E epiglottis, H hyoid bone, and T thyroid cartilage
5 Relevant Anatomy andPhysiology oftheEpiglottis
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aryepiglottic muscle and quadrangular membrane, with its inferior margin terminat­ing as a thickened ligamentous tissue, forming the ventricular ligament.
Behind, the thyrohyoid membrane lies a preepiglottic space (PES), which takes the shape of a triangular pyramid with an inferior apex and is divided into left and right sides by a thin sagittal membrane (septum) [31]. It is bounded by the medial hyoepiglottic ligament and valleculae superiorly; the hyoid bone, thyrohyoid mem­brane, and thyroid cartilage anteriorly; and the thyroepiglottic ligament and anterior surface of the epiglottic cartilage posteroinferiorly. The PES is continuous with the paraglottic space (PGS) that is laterally and posteriorly surrounded by the thyroid lamina and by the mucosa of the hypopharynx (piriform sinus), respectively. At the supraglottic level, it lies postero-inferiorly to the PES and medial to the lamina of the thyroid cartilage. The PES and PGS are composed of adipose tissue and loose elastic and collagen bers [32]. Preepiglottic adipose tissue, sometimes referred to as “laryngeal fat body,” plays an important role in the process of swallowing. PES also contains one or two lymph nodes, while the PGS is a space for the main laryn­geal arteries and allows interrupted blood ow within it [33].
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5.6 Muscles
There is a large number of skeletal muscles that have to act in a coordinated way to enable important physiological processes taking place in the larynx and pharynx (breathing, deglutition, phonation, and articulation). Many of them inuence the UA patency and are sometimes referred to as accessory respiratory muscles. They can dilate and open or stiffen the airway to make it less prone to collapse by the negative inspiratory pressure. Describing all muscles involved in pharyngeal and laryngeal functions is beyond the scope of this work. Their characteristics and func­tions are presented in Table5.1. Pharyngeal dilators and muscles that affect the distance between the thyroid cartilage and the hyoid bone, as well as their orienta­tion, can also affect the position and shape of the epiglottis. That is why we believe these muscles are the most relevant for the development of obstructive respiratory events at the level of the tongue base and epiglottis.
Although many anatomic studies have evaluated the function of pharyngeal mus­cles during swallowing, a complete understanding of their role in sleep-disordered breathing still needs to be established. The pharyngeal muscles are anatomically and functionally connected and do not act as simple individual structures but rather move and function together in a very coordinated way. It is important to realize that a particular pharyngeal muscle can have different mechanical effects on the UA depending on the size and shape of the airway at the time of muscle activation, muscle ber orientation, simultaneous activation of other muscles, and the timing of activation relative to the phase of respiration. This may help explain how pharyn­geal muscles can play a role in such disparate functions as respiration, deglutition, and phonation [34].
The pharynx is a tube-like muscular structure that comprises three external cir­cular muscles (the superior, middle, and inferior constrictor muscles) and three