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Saliva and the Control of Its Secretion 47
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Feeding and Respiration
https://t.me/med1917
Olle Ekberg, Anna I. Ha˚rdemark Cedborg, Katarina Bode´n, Hanne Witt Hedstro¨m, Richard Kuylenstierna, Lars I. Eriksson, and Eva Sundman
Contents
1 Introduction.............................................................. 49
2 Feeding Respiratory Pattern .................................. 50
References.......................................................................... 53
O. Ekberg (&) Department of Diagnostic Radiology, Skåne University Hospital, 205 02 Malmö, Sweden e-mail: olle.ekberg@med.lu.se
A. I. Hårdemark Cedborg L. I. Eriksson E. Sundman Department of Anaesthesiology and Intensive Care Medicine, Karolinska University Hospital and Karolinska Institute, Stockholm, Sweden
K. Bodén Department of Diagnostic Radiology, Karolinska University Hospital and Karolinska Institute, Stockholm, Sweden
H. W. Hedström Department of Neuroradiology, Karolinska University Hospital and Karolinska Institute, Stockholm, Sweden
R. Kuylenstierna Department of Otorhinolaryngology, Karolinska University Hospital and Karolinska Institute, Stockholm, Sweden
Abstract
Coordination of breathing and swallowing is essential for normal bolus transportation through the pharynx and for protection of the airways. During passage of the bolus through the pharynx, respiration is interrupted. Normal swallowing occurs during the expiratory phase of breathing. Incoordination of the feeding respiratory pattern may lead to penetration of the bolus into the airways. This may cause choking, death, aspiration pneumonia, or chronic laryngitis.
1 Introduction
Swallowing and breathing are closely controlled by specialized neuronal groups colocalized to the brain­stem. Interaction occurs between neuronal groups controlling breathing and those controlling swallow­ing (Dick et al. 1993; Saito et al. 2002; Ertekin and Aydogdu 2003). Such central neuronal control, toge­ther with local anatomic conditions and sensory input from the larynx and pharynx, allows safe and direct passage of air, liquids, and solids. Moreover, factors primarily thought to influence breathing (e.g., arterial partial pressure of CO et al. 1998; Sai et al. 2004), and other factors con­trolling pharyngeal function affect breathing pattern (Nilsson et al. 1997; Hadjikoutis et al. 2000; Butler et al. 2007; Terzi et al. 2007). Posture and positioning are such factors.
Miller (1999), in his neurophysiological investi­gations of swallowing, concluded that brainstem neuronal control is involved in the central inhibition
) affect swallowing (Nishino
2
O. Ekberg (ed.), Dysphagia, Medical Radiology. Diagnostic Imaging, DOI: 10.1007/174_2012_587, Ó Springer-Verlag Berlin Heidelberg 2012
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Fig. 1 Registrations of pharyngeal manometry, nasal air
pressure, and oral and nasal respiratory airflow by the bidirectional gas flow discriminator, diaphragmatic and abdom­inal EMG, and spirometry. Recordings of two swallows at normocapnia (a) and one swallow at hypercapnia (b). The swallows presented show the respiratory phase pattern E–E (inspiration–expiration–swallow–expiration). The start of pha­ryngeal swallowing was defined as the start of pressure rise at the tongue base (TB-start) and the end was defined as the point in time when the upper esophageal sphincter started to contract
of respiration during swallowing. Therefore, swal­lowing apnea is not an effect of closure of the vocal folds even though, together with laryngeal closure, it often occurs at the same time as apnea.
Swallowing apnea has also been registered in patients after laryngectomy (Hiss et al. 2003). The presence of swallowing apnea also remains 10 years after laryngectomy. Therefore, swallowing apnea is a central phenomenon and not the result of obstructive forces of closed airways during swallowing. On the other hand, closure of the laryngeal vestibule, including vocal folds, is an important part of the protective mechanism that hinders the bolus from reaching the airways. Swallowing apnea may start long before vocal fold closure; however, it ends when the vocal folds begin to reopen.
(UES-start). The duration of pharyngeal swallowing is marked with a horizontal bar (swallow). Swallowing apnea was detected by the respiratory airflow discriminator as an oscillat­ing signal, representing zero airflow. Diaphragmatic activity during swallowing apnea is marked with arrows. Pharyngeal manometry was recorded at the tongue base (TB), upper/lower level of the pharynx (Pharynx Up./Pharynx Low.) and upper esophageal sphincter (UES). I inspiration, E expiration. (Rep­rinted from Hårdemark Cedborg et al. 2009)
2 Feeding Respiratory Pattern
In a recent study, Hårdemark Cedborg et al. (2009) explored breathing during spontaneous swallowing using a bidirectional gas flow discriminator. They used a complex experimental setting in volunteers including manometry for registration of pressure at the level of the tongue base, midpharynx, and upper esophageal sphincter and including nasal and oral airflow. A diaphragmatic and abdominal EMG was used as well. Spirometry was used for quantitative registration of airflow in liters per minute. They studied spontaneous swallowing during normocapnia and hypercapnia. The latter was achieved by subjects breathing air with the addition of 5% CO
. The term
2
Feeding and Respiration 51
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Fig. 2 A swallow preceded and followed by expiration (E–E
pattern) and the diaphragmatic activity during swallowing apnea. The time from the onset of diaphragmatic activity during swallowing apnea to the onset of pharyngeal swallowing was measured and is marked in the figure. The start of pharyngeal
‘‘spontaneous swallowing’’ refers to the fact that the subjects were allowed to swallow saliva spontane­ously and were not given any instruction for how to swallow. Hypercapnia was used to evaluate how an increased respiratory drive and higher breathing fre­quency interfered with spontaneous swallowing (Fig. 1).
Hårdemark Cedborg et al. (2009) found that all swallows occur during expiration. The normal sequence is that expiration is interrupted by a period of apnea, during which time the bolus passes through the pharynx. Then the expiration is resumed. The expiration before swallowing may be as short as 30 ms. Expiration before swallowing lasts about 1.3 s and expiration after swallowing lasts about 1.5 s. The preswallowing expiration time could be very short but could always be discerned. They speculated that swallowing is in fact controlled by the respiratory
swallowing is defined as the start of the pressure rise at the tongue base (TB-start) and the end of pharyngeal swallowing is defined as the start of the pressure rise at the upper esophageal sphincter (UES-start). (Reprinted from Hårdemark Cedborg et al. 2009)
neurons, in that sense that swallowing was only allowed to occur during an expiratory phase. By studying the EMG pattern, they confirmed the phrenic nerve activity described by Saito et al. (2002). This EMG pattern is distinctly different from that of an inspiration and was not followed by airflow. They called this ‘‘active breath holding.’’ This central control of breathing ensures that respiration is stopped before pharyngeal swallowing and that a significant proportion (approximately 200 ml) of the tidal vol­ume is ‘‘put on hold’’ by the activated diaphragm, only to be expired at the end of swallowing apnea. Expiratory airflow after swallowing clears the lar­yngeal inlet from misdirected bolus material, and thereby aspiration is prevented (Fig. 2).
In an experimental prospective study, Gross et al. (2003) showed that during a standardized pudding­like consistency swallow at three randomized lung
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Fig. 3 Temporal
coordination of swallowing and respiratory events in a the upright and left decubitus positions with normocapnia and b the left decubitus position with normocapnia and with hypercapnia. All values are in milliseconds and are mean values ± the 95% confidence interval. TB tongue base, UES upper esophageal sphincter, PhCM middle pharyngeal constrictor, PhCL lower pharyngeal constrictor. (Reprinted from Bodén et al.
2009)
Feeding and Respiration 53
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volumes (total lung capacity, functional residual capacity, and residual volume), the pharyngeal activity duration of deglutition for swallows produced at residual volume was significantly longer than that for swallows occurring at total lung capacity or at functional residual capacity. No significant differ­ences were found for the bolus transit time or intra­muscular electromyography of the superior constrictor. This supports the hypothesis that the respiratory system may have a regulatory function related to swallowing and that positive subglottic air pressure may be important for swallowing integrity.
Hårdemark Cedborg et al. (2009) also studied the length of preswallowing and postswallowing apnea. The duration of swallowing apnea decreased consid­erably at hypercapnia. Interestingly, they found that the duration of preswallowing apnea shortened, whereas the duration of postswallowing apnea did not change during hypercapnia. Hence, the temporal positioning of pharyngeal swallowing is asymmetri­cal, occurring in the late part of swallowing apnea at normocapnia but not at hypercapnia. This means that when breathing at a high frequency the preswallowing apnea period shortens considerably and that may put the patient at risk of misdirected swallowing. This may be a considerable problem in patients with chronic obstructive pulmonary disease who have a high respiration frequency (Martin et al. 1994; Martin-Harris et al. 2003, 2005). Chronic aspiration may then aggravate the patient’s pulmonary condi­tion, introducing a vicious cycle (Gross et al. 2009).
Respiration and swallowing coordination is not affected by changes in body position, bolus types, and respiratory drive (Hårdemark Cedborg et al. 2010). However, during water swallows, the duration of preswallowing apnea is significantly longer than that of spontaneous saliva swallow (Hårdemark Cedborg et al. 2010). During water swallow, the duration of the postswallowing apnea is also very constant.
Elderly adults have been shown to have a longer swallowing apnea duration than young and middle­aged adults (Hiss et al. 2001). That study also showed that women have a longer swallowing apnea duration than men and that the swallowing apnea duration increases as the bolus volume increases.
Martin-Harris et al. (2005) showed a higher occurrence of inhalation with swallowing apnea, with increased occurrence in individuals older than 65 years. Although it was not shown, the hypothesis
is that this predisposes the elderly to aspiration pneumonia. However, they also found that the elderly have a prolonged swallowing apnea duration. Partic­ularly, the onset of apnea could occur rather early compared with the onset in young individuals.
The coordination of respiration and swallow rhythms has also been studied in preterm and term infants (Gewolb and Vice 2006). The initial feeding efforts at 32–34 weeks (postmenstrual age) are char­acterized by periods of apneic suckle-feeding that alternate with tidal respiration. With further devel­opment, respiration is interposed into spaces parti­tioned by the swallows and the breathing efforts are integrated into an oral suck–swallow–breathing rhythm.
It has also been shown that an increase in respi­ratory drive by inhalation of 7% CO
in preterm
2
infants is accompanied by a decrease in the rate of both sucking and swallowing during nutritive feeding. Increased ventilatory drive may directly inhibit nutritive feeding behavior in premature infants. Also, this speaks in favor of respiratory neurons in the brainstem that have superior control of swallowing and not vice versa (Timms et al. 1993).
Temporal coordination of swallowing and respi­ratory events has also been studied in a more global perspective (Bodén et al. 2009; Fig. 3). This confirms several of the studies forming the basis for the con­cept of a fixed pattern generator that controls muscular activity in the swallowing apparatus (Miller 1999).
References
Bodén K, Hårdemark Cedborg AI, Eriksson LI, Witt Hedström
H, Kuylenstierna R, Sundman E, Ekberg O (2009) Swal-
lowing and respiratory pattern in young healthy individuals
recorded with high temporal resolution. Neurogastroenterol
Motil 21:1163–e101 Butler SG, Stuart A, Pressman H, Poage G, Roche WJ (2007)
Preliminary investigation of swallowing apnea duration and
swallow/respiratory phase relationships in individuals with
cerebral vascular accident. Dysphagia 22:215–224 Dick TE, Oku Y, Romaniuk JR, Cherniack NS (1993)
Interaction between central pattern generators for breathing
and swallowing in the cat. J Physiol 465:34–44 Ertekin C, Aydogdu I (2003) Neurophysiology of swallowing.
Clin Neurophysiol 114:2226–2244 Gewolb IH, Vice FL (2006) Maturational changes in the
rhythms, patterning, and coordination of respiration and
54 O. Ekberg et al.
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swallow during feeding in preterm and term infants. Develop Med Child Neurol 48:589–594
Gross RD, Atwood CW Jr, Grayhack JP, Shaiman S (2003)
Lung volume effects on pharyngeal swallowing physiology. J Appl Physiol 95:2211–2217
Gross RD, Atwood CW Jr, Ross SB, Olszewski JW, Eichhorn
KA (2009) The coordination of breathing and swallowing in chronic obstructive pulmonary disease. Am J Respir Crit Care Med 179:559–565
Hadjikoutis S, Pickersgill TP, Dawson K, Wiles CM (2000)
Abnormal patterns of breathing during swallowing in neurological disorders. Brain 123:1863–1873
Hiss SG, Treole K, Stuart A (2001) Effects of age, gender,
bolus volume, and trial on swallowing apnea duration and swallow/respiratory phase relationships of normal adults. Dysphagia 16:128–135
Hiss SG, Strauss M, Treole K, Stuart A, Boutilier S (2003)
Swallowing apnea as a function of airway closure. Dyspha­gia 18:293–300
Hårdemark Cedborg AI, Sundman E, Bodén K, Witt Hedström
H, Kuylenstierna R, Ekberg O, Eriksson LI (2009) Co­ordination of spontaneous swallowing with respiratory airflow and diaphragmatic and abdominal muscle activity in healthy adult humans. Exp Physiol 94:459–468
Hårdemark Cedborg AI, Bodén K, Witt Hedström H, Kuylen-
stierna R, Ekberg O, Eriksson LI, Sundman E (2010) Breathing and swallowing in normal man––effects of changes in body position, bolus types, and respiratory drive. Neurogastroenterol Motil 22:1201–e316
Martin BJ, Logemann JA, Shaker R, Dodds WJ (1994)
Coordination between respiration and swallowing: respira­tory phase relationships and temporal integration. J Appl Physiol 76:714–723
Martin-Harris B, Brodsky MB, Michel Y, Ford CL, Walters B,
Heffner J (2005) Breathing and swallowing dynamics across
the adult lifespan. Arch Otolaryngol Head Neck Surg
131:762–770 Martin-Harris B, Brodsky MB, Price CC, Michel Y, Walters B
(2003) Temporal coordination of pharyngeal and laryngeal
dynamics with breathing during swallowing: single liquid
swallows. J Appl Physiol 94:1735–1743 Miller AJ (1999) The neuroscientific principles of swallowing
and dysphagia. Singular Publishing Group, San Diego,
pp 73–92 Nilsson H, Ekberg O, Bülow M, Hindfelt B (1997) Assessment
of respiration during video fluoroscopy of dysphagic
patients. Acad Radiol 4:503–507 Nishino T, Hasegawa R, Ide T, Isono S (1998) Hypercapnia
enhances the development of coughing during continuous
infusion of water into the pharynx. Am J Respir Crit Care
Med 157:815–821 Sai T, Isono S, Nishino T (2004) Effects of withdrawal of
phasic lung inflation during normocapnia and hypercapnia
on the swallowing reflex in humans. J Anesth 18:82–88 Saito Y, Ezure K, Tanaka I (2002) Swallowing-related
activities of respiratory and non-respiratory neurons in the
nucleus of solitary tract in the rat. J Physiol 540:1047–1060 Terzi N, Orlikowski D, Aegerter P, Lejaille M, Ruquet M,
Zalcman G, Fermanian C, Raphael JC, Lofaso F (2007)
Breathing–swallowing interaction in neuromuscular
patients: a physiological evaluation. Am J Respir Crit Care
Med 175:269–276 Timms BJM, DiFiore JM, Martin RJ, Miller MJ (1993)
Increased respiratory drive as an inhibitor of oral feeding
of preterm infants. J Pediatr 123:127–131
Oral and Pharyngeal Function
https://t.me/med1917
and Dysfunction
Olle Ekberg
Contents
1 Introduction.............................................................. 55
2 The Normal Swallow ............................................... 56
2.1 The Oral Stage........................................................... 56
2.2 The Pharyngeal Stage................................................ 57
2.3 The Pharyngoesophageal Segment ........................... 58
2.4 The Esophageal Stage ............................................... 59
3 The Abnormal Swallow .......................................... 59
3.1 The Oral Stage........................................................... 59
3.2 The Pharyngeal Stage................................................ 59
4 Dysfunction of the Pharyngoesophageal
Segment..................................................................... 63
5 Radiologic Evaluation in Specific Disease
Entities ...................................................................... 64
5.1 Cerebrovascular Diseases .......................................... 65
6 The Role of the Radiologist in the Design
of Therapy ................................................................ 66
References.......................................................................... 67
O. Ekberg (&) Diagnostic Centre of Imaging and Functional Medicine, Skåne University Hospital, 205 02 Malmö, Sweden e-mail: olle.ekberg@med.lu.se
Abstract
Normal pharyngeal swallow is coordinated in a
precise and exact manner. It is controlled from a
swallowing centre in the brain stem. Normal
swallowing is adjusted to bolus volume tempera-
ture and viscosity. Abnormal pharyngeal swallow
may lead to misdirected swallowing that chal-
lenges the airways. Inefficient transportation into
the esophagus, stomach and bowel may lead to
dehydration and malnutrition.
1 Introduction
Normal pharyngeal swallow is precisely scheduled and symmetric. It is finely tuned and coordinated in a precise and exact manner to establish a safe swallow (Miller 1986; Dodds 1989). The swallowing process is regulated by a command center in the brainstem, a central program generator which receives input from the cerebral cortex and peripheral muscle and directs the sequence of swallowing. This process is both voluntary and involuntary and incorporates motor activity from the oral cavity, pharynx, and esophagus. It involves both motor and sensory activity. There is an evolving amount of knowledge concerning normal and abnormal swallowing (Jones and Donner 1991; Ekberg and Wahlgren 1985; Hannig and Hannig
1987; Brühlmann 1985; Pokieser et al. 1995; Dodds
1989).
O. Ekberg (ed.), Dysphagia, Medical Radiology. Diagnostic Imaging, DOI: 10.1007/174_2011_391, Ó Springer-Verlag Berlin Heidelberg 2012
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56 O. Ekberg
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Fig. 1 The oral, pharyngeal, and pharyngoesophageal segment
(PES) stages are readily appreciated radiographically. This is a sequence of a barium swallow (ah) in lateral projection. The bolus is gathered in the oral cavity (ac) and is propelled into the pharynx by an upward and backward movement of the back of the tongue (d)(arrow). The tilting down to a horizontal position of the epiglottis is seen in d. The airways are closed
2 The Normal Swallow
2.1 The Oral Stage
The oral, pharyngeal, pharyngoesophageal segment (PES), and esophageal stages of swallowing are readily appreciated radiographically (Fig. 1). The oral stage of swallowing is bolus-specific, i.e., the patient handles different boluses differently,i.e., a strawberryis handled differently from a cup of tea. Therefore, the oral stage is notoriously more difficult to evaluate radiologically
and none of the barium reaches into the laryngeal vestibule or trachea. The PES opens. The upward and forward movements of the larynx including the hyoid superiorly and the PES inferiorly are extremely important for the normal execution of pharyngeal transit. There are no, or only minimal, remnants of barium in the pharynx after swallowing
than the rest of the swallowing apparatus. However, the oral stage should be included in the radiologic evalua­tion. The recording should start with the ingestion. During oral processingthere is superior and inferior and some anterior–posterior movement of the hyoid bone. However, liquid barium should not be processed or modified in the oral cavity. Therefore, oral preparation for swallowing is tested with a solid or semisolid bolus. When the ingested material is ready to be swallowed, the material is brought onto the back of the tongue, which obtains the shape of a groove (Hamlet et al.
1988). This is the preparatory position for swallowing.
Oral and Pharyngeal Function and Dysfunction 57
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No part of the bolus is allowed to leak anteriorly from the mouth through the lips. Even more important radiologically is to observe if posterior leak occurs. The patient should be able to control the sealing of the tongue base to the soft palate and posterior pharyngeal wall.
2.2 The Pharyngeal Stage
The pharyngeal swallow is initiated voluntarily and the material to be swallowed is usually called a bolus from this point. Initiation of the pharyngeal swallow coincides with the beginning of the anterior move­ment of the hyoid bone from an elevated position. Pharyngeal constriction is probably cued by the bolus interfering with sensory innervation at the faucial isthmus. Radiologically it is convenient to use the beginning of the anterior hyoid movement as the starting point of pharyngeal swallow. The tongue then propels the bolus posteriorly into the pharynx and further down into the PES and cervical esophagus. If the pharyngeal constrictor wall has normal com­pliance, only minor dilatation of the pharynx occurs (Fig. 2).
The palatopharyngeal isthmus is closedby elevation of the muscular palate and constrictor convergence, which is most medial of the lateral walls. Normally, no regurgitation of barium into the nasopharynx occurs.
In a patient with severe oral impairment, the pha­ryngeal phase may be elicited by injecting a small barium bolus directly into the pharynx through a soft tube. Thismay beplaced intothe pharynx via either the mouth or the nose. Such techniques, however, are used only for examination and not for feeding. Patients with uncoordinated, weak, or jerky tongue movements commonly cannot correctly position the bolus on the tongue. Accordingly, the tongue cannot displace the bolus posteriorly. There is a strong correlation between an abnormal anterior movement of the hyoid bone and overall abnormal oral and pharyngeal function, as well as defective opening of the PES.
Protection of the airways occurs at four separable anatomically and functionally different sites, i.e., the vocal folds, the supraglottic portion of the laryngeal vestibule, the subepiglottic portion of the laryngeal vestibule, and the epiglottis (Curtis and Hudson 1983; Curtis and Sepulveda 1983; Ekberg 1982). The most crucial of these levels is the supraglottic portion of the
Fig. 2 An 80-year-old man with cerebrovascular disease.
There is paresis in the right side of the pharynx. This is not seen in lateral projection (b) and is only seen in frontal projection (a). There is pooling of contrast medium in the right piriform sinus (broad arrow). Small amounts of barium are also seen coating the inside of the laryngeal vestibule down to the false vocal cords
laryngeal vestibule. Barium in the vestibule com­monly extends into the trachea, as the vocal folds offer poor protection of the lower airway (Ekberg and Hilderfors 1985). Radiographic observation of barium penetration into the larynx and trachea is strategic in dysphagia evaluation. Bedside evaluation for aspira­tion has a low sensitivity. This is partly because many of these patients have sensory impairment in the lar­ynx and/or trachea and fail to cough (Splaingard et al.
1988).
Of even more fundamental importance, and
basically a prerequisite for airway closure and con­strictor activity, is the elevation of the pharynx and larynx. The airways are also protected by a move­ment of the thyroid cartilage toward the hyoid, and by closure of the laryngeal vestibule. Additional protection is offered by the epiglottis and the vocal folds. Closure of the larynx starts at the vocal folds and progresses in a superior direction in a peristaltic­like manner.
The constrictors have a minor role in the con-
veyance of a bolus through the pharynx. The tongue base pressure does not differ significantly between those individuals with and those individuals without retention (Olsson et al. 1997). This finding is important because many research groups advocate normal tongue-base and constrictor activity as a prerequisite for a successful outcome of cricopha­ryngeal myotomy (Buchholz 1995). Tongue-base