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Review

Ultrasonography for Eating and Swallowing Assessment: A Narrative Review of Integrated Insights for Noninvasive Clinical Practice

1
Nutrition Therapy Support Center, Aichi Medical University Hospital, Nagakute 480-1195, Japan
2
Department of Geriatric Medicine, Hospital, National Center for Geriatrics and Gerontology, Obu 474-8511, Japan
3
Department of Rehabilitation Medicine, Hospital, National Center for Geriatrics and Gerontology, Obu 474-8511, Japan
4
Department of Nursing, Nishinomiya Kyoritsu Neurosurgical Hospital, Nishinomiya 663-8211, Japan
5
Department of Speech Language Pathology and Audiology, Faculty of Rehabilitation, Kawasaki University of Medical Welfare, Okayama 701-0193, Japan
*
Author to whom correspondence should be addressed.
Nutrients 2023, 15(16), 3560; https://doi.org/10.3390/nu15163560
Submission received: 7 June 2023 / Revised: 28 July 2023 / Accepted: 11 August 2023 / Published: 12 August 2023

Abstract

:
Dysphagia is a syndrome of abnormal eating function resulting from a variety of causative diseases, and is associated with malnutrition. To date, the swallowing function has been difficult to examine without the use of invasive and expensive methods, such as the videofluorographic swallowing study or fiberoptic endoscopic evaluation of swallowing. In recent years, progress has been made in the clinical application of ultrasound equipment for the evaluation of body compositions near the body surface, including the assessment of nutritional status. Ultrasound examination is a noninvasive procedure and relatively inexpensive, and the equipment required is highly portable thanks to innovations such as wireless probes and tablet monitoring devices. The process of using ultrasound to visualize the geniohyoid muscle, digastric muscle, mylohyoid muscle, hyoid bone, tongue, masseter muscle, genioglossus muscle, orbicularis oris muscle, temporalis muscle, pharynx, esophagus, and larynx, and the methods used for evaluating these structures, are provided in this study in detail. This study also aims to propose a protocol for the assessment of swallowing-related muscles that can be applied in real-world clinical practice for the diagnosis of sarcopenic dysphagia, which can occur in elderly patients with sarcopenia, and has received much attention in recent years.

1. Introduction

Dysphagia increases the risk of malnutrition, dehydration, aspiration pneumonia, and even death [1,2]. These complications delay functional recovery and reduce the quality of life if the patient is unable to eat or drink [1,2,3]. Previous reviews have highlighted that the videofluorographic swallowing study and fiberoptic endoscopic evaluation of swallowing can accurately identify dysphagia compared with clinical evaluation [1]. The aspiration of oropharyngeal secretions, subclinical aspiration (the absence of coughing response when food or liquid enters the airway), etc., can be observed during these procedures [4]. However, the videofluorographic swallowing study involves exposure to radiation and travelling to the examination room; meanwhile, fiberoptic endoscopic evaluation of swallowing causes pain due to the insertion of a probe into the pharynx through the nasal cavity. The available professional resources that can be used as a guide for performing these examinations are limited. As a result, nonhospital facilities have poor access to the resources required to perform the videofluorographic swallowing study and fiberoptic endoscopic evaluation of swallowing.
Speech–language–hearing therapists (SLHTs) and nurses, etc., who specialize in evaluating the swallowing function perform dysphagia screening tests. The different methods that can be performed at the bedside or in a typical eating scene include tests to identify patients at high risk for developing aspiration and other problems [5]. However, only a limited number of screening methods have been examined as the gold standard tests for assessing the risk of aspiration [6,7]. For example, the water swallowing test [8,9], Toronto bedside swallowing screening test [10], Gugging swallowing screen [11], and the volume–viscosity swallow test [12] are frequently used at the bedside to assess the swallowing function. Although a variety of tests and methods have been developed to assess the swallowing function, no highly accurate, noninvasive method has been established to assess swallowing function that SLHTs and nurses can easily use at the bedside.
In recent years, echography of the swallowing-related muscles has attracted research attention. It is one of the methods used for visualizing the swallowing movement. In general, echography is a widely used examination method in daily practice. It can be utilized to assess the skeletal muscles [13]. Recently, sarcopenia has been associated with dysphagia [14,15,16,17], and measurement of the swallowing-related muscle is clinically important in assessing the swallowing function. Despite its widespread use, promising potential, and over two decades of application in swallowing research, echography has not yet achieved broad recognition as a representative advancement in SLHT literature. This might be attributed to the ongoing debates concerning its efficacy and usage [18,19]. Previous systematic reviews and meta-analyses have evaluated the risk of aspiration and presence of pharyngeal residue associated with echography of the swallowing-related muscles [20]; the majority of these studies targeted specific subsets of swallowing-related muscles. The aim of this research is to extract and synthesize the insights from these specialized studies, providing an overview of how various swallowing-related muscles are visualized and evaluated using echography, and to shed light on the current status, challenges, and future prospects of echography in the assessment of swallowing function. In this regard, we reviewed the current use of echography for measuring muscle mass and assessing swallowing function, after determining the evaluation method suited for each observation site across all vocal and speech organs. This study does not apply specific statistical methods; instead, it is based on an exhaustive review of existing literature. Article searching was conducted in MEDLINE via the PubMed interfaces. Hand searching was also performed. The keywords used during the literature search were “(Ultrasonography OR Ultrasound) AND (swallowing OR dysphagia).” Journal articles written in English published from database inception until October 2021 were searched.
Although the use of ultrasound technology is not universally authorized for all healthcare professionals, in certain regions, a diverse group of healthcare practitioners, including SLHTs and registered dietitians, are permitted to use ultrasound devices in clinical settings. Consequently, this study provides pertinent insights not only for practicing healthcare professionals, but also for students aspiring to become SLHTs and physicians who specialize in evaluating and managing swallowing disorders and using imaging techniques. Therefore, the potential reach of this study extends beyond geographic and professional boundaries. It fosters anticipation for the broader acceptance of these noninvasive assessment techniques in the global healthcare sector. This research serves to collate and enhance the collective knowledge derived from these specialized studies, thereby fortifying the potential for the application and widespread use of echography in routine clinical practice.

2. Geniohyoid Muscle (Figure 1)

The geniohyoid muscle is a short, slender, ribbon-shaped muscle originating from the inferior genial tubercle and inserted into the body of the hyoid bone. The two geniohyoid muscles on either side of the midline are parallel and close to each other [21]. It belongs to the suprahyoid muscle group, elevating the hyoid bone and lifting the oral floor during swallowing; the geniohyoid muscle moves the hyoid bone forward [21]. Decreased cross-sectional area, muscle thickness, and the brightness of the geniohyoid muscle during an ultrasound have been associated with swallowing function [22], sarcopenic dysphagia [23], and jaw opening strength [24]. Ultrasound is also used to determine the effects of swallowing exercises [25,26]. In addition, it is employed to evaluate the geniohyoid muscle movement during swallowing [27,28,29]. Ultrasound measurements of the morphology and movement of the geniohyoid muscle may be useful in assessing the swallowing function and determining the effectiveness of therapeutic interventions.
The method of applying the probe varies depending on the purpose of the measurement (Figure 1). The cross-sectional area of the geniohyoid muscle is measured in the coronal section using a linear probe [24,30]. The probe is placed vertical to the muscle fiber between the chin and hyoid bone [22,23,24,25,27,28,31,32,33]. The probe should be placed vertical to the chin plane. For the cross-sectional area, the geniohyoid muscle is extracted from the area surrounded by the fascia, indicated by the hyperechoic line, and the area excluding the fascia is calculated as the cross-sectional area [23,24,25]. The position of the probe varies from the middle [25] to the posterior one-third [22,28] of the line connecting the mandible and the hyoid bone, and to the posterior one-third [23,24] of the line connecting the parotid gland and hyoid bone. The muscle length changes and the contraction velocity during swallowing are measured on a sagittal section using a convex probe. The probe is placed horizontal to the muscle fibers [29,30,34]. The measurement is usually performed in a sitting position with the head and neck supported [34]; it can also be performed in a natural position [25,27,31] or a 30° reclining position [23,30].
Figure 1. Imaging of the geniohyoid muscle. On the coronal section, the morphology of the geniohyoid muscle changes depending on the position of the probe. The digastric muscle and surficial mylohyoid muscle are appropriate locations to insert the probe. On the sagittal section, the probe should ideally be placed on the midline to visualize the hyoid bone and chin bone in one screen.
Figure 1. Imaging of the geniohyoid muscle. On the coronal section, the morphology of the geniohyoid muscle changes depending on the position of the probe. The digastric muscle and surficial mylohyoid muscle are appropriate locations to insert the probe. On the sagittal section, the probe should ideally be placed on the midline to visualize the hyoid bone and chin bone in one screen.
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3. Digastric Muscle (Figure 2)

The digastric muscle is a spindle-shaped muscle that consists of the anterior and posterior bellies joined by an intermediate tendon. Although it is regarded as one muscle, the anterior and posterior bellies have different embryological origins and roles [21]. The anterior belly arises from the mandible (the digastric fossa near the junction of the mandible), while the posterior belly arises from the temporal bone (the papillary notch); both of these structures terminate at the hyoid bone via the intermediate tendon [21]. During eating, the anterior belly of the digastric muscle opens the lower jaw and brings the hyoid bone forward and upward during swallowing. The posterior digastric muscle assists in the lateral and posterior movement of the lower jaw. It belongs to the suprahyoid muscle group. It depresses the mandible when the hyoid bone is in a fixed position, and elevates the hyoid bone when the mandible is in a fixed position [21,35].
The probe is placed vertical to the fibers of the anterior belly of the digastric muscle, and the thickness is measured on the short axis (Figure 2). A linear probe is used for measurements [26,33,36]. The thickness of the digastric muscle is often measured as the distance from the top to the bottom border of the fascia at the thickest point vertical to the mylohyoid muscle [26,31,32]. The measurement is usually performed in a sitting position [31,32,37].
The thickness of the anterior belly of the digastric muscle is measured by ultrasound, and is used to determine the effects of muscle training, such as head lift exercises and expiratory muscle training, and kinesiology taping [25,31]. Although the ultrasound measurement of the digastric muscle is useful in determining the effects of therapeutic interventions, no study has reported its association with swallowing function; therefore, its relationship with swallowing function should be examined.
Figure 2. Imaging of the digastric muscle. The muscle belly is visualized by applying the probe vertical to the muscle fibers of the digastric muscle. Furthermore, the entire image is observed by sliding the probe from the chin to the top of the hyoid bone.
Figure 2. Imaging of the digastric muscle. The muscle belly is visualized by applying the probe vertical to the muscle fibers of the digastric muscle. Furthermore, the entire image is observed by sliding the probe from the chin to the top of the hyoid bone.
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4. Mylohyoid Muscle (Figure 3)

The mylohyoid muscle is part of the suprahyoid muscle group that shapes the floor of the oral cavity. It works along with the geniohyoid muscle and the anterior belly of the digastric muscle, and aids in swallowing. It is also referred to as the accessory muscle of mastication as it is involved in mouth opening movements [38]. Previous studies have evaluated the therapeutic effects of maximal jaw opening exercises and head lift exercises, as well as tongue strengthening training, as part of dysphagia rehabilitation [26,31,32].
The mylohyoid muscle is measured on the coronal section by placing a probe at the submental region (Figure 3). As the mylohyoid muscles run radially, the probe should be moved from front to back to visualize the largest and most distinct muscle [32,37]. Some previous studies reported that the mylohyoid muscle measurement area is the area directly below the measurement point of the digastric muscle, from the top to the bottom of the fascia [26,31,32]. However, in these studies, the point for visualizing and evaluating the mylohyoid muscle was ambiguous, and the submandibular gland was used as the orientation point when visualizing the mylohyoid muscle. Considering that the submandibular gland is a relatively homogeneous organ, the mylohyoid muscle imaged under the submandibular gland should be measured. The measurements are frequently performed in a sitting position [31,32,36].
Figure 3. Imaging of the mylohyoid muscle. The probe is placed at the submental region and is visualized on a coronal section. When measuring muscle thickness, the probe should be placed in a position that allows the measurement of the thickness of the area where the submandibular gland wraps around the mylohyoid muscle.
Figure 3. Imaging of the mylohyoid muscle. The probe is placed at the submental region and is visualized on a coronal section. When measuring muscle thickness, the probe should be placed in a position that allows the measurement of the thickness of the area where the submandibular gland wraps around the mylohyoid muscle.
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5. Hyoid Bone

The hyoid bone is derived from the branchial arch, with no articulation to other bones. The suprahyoid muscle group (mylohyoid muscle, digastric muscle, stylohyoid muscle, and geniohyoid muscle) and the sublingual muscle group (sternohyoid muscle, omohyoid muscle, sternum thyroid muscle, and thyrohyoid muscle) terminate at the hyoid bone. When the jaw is opened, it is fixed downward by the sublingual muscle group; during swallowing, it is pulled toward the lower jaw by the contraction of the suprahyoid muscle group and moves upward and forward. The hyoid bone can be easily identified on an ultrasound image; ultrasound is useful for evaluating the laryngeal movement during swallowing by measuring the movement of the hyoid bone, travel distance, and duration of hyoid bone movement [37,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53]. In comparison with healthy individuals, the laryngeal elevation distance is decreased in patients with neurologic disease who have dysphagia; moreover, the ratio of the hyoid [48] and laryngeal elevation distance is greater in stroke patients with dysphagia [39]. The ultrasonographic evaluation of hyoid–larynx approximation has good reliability [47]. Cergan et al. reviewed the measurement of the laryngeal structure via ultrasound, and proposed the utility of ultrasound as a safe alternative to endoscopy for evaluating the larynx in patients with coronavirus disease 2019 [54].
In most studies, the hyoid bone was measured by placing the probe vertical to the submental region on the midsagittal plane; in a previous study, the probe was placed on either the left or right side of the thyroid cartilage to avoid interfering with the swallowing movements [41]. The measurements are frequently conducted in a sitting position. When the measurements obtained with the manually operated (handheld) probe were compared with those obtained with the probe fixed in a stabilizer, a significant variability was observed in the measured values [43]. Good intra- and inter-rater reliabilities were also shown when the probe was covered with a self-designed water bag to provide good contact between the skin and probe [44]. During the visualization of the larynx and pharynx, including the hyoid bone, a condom filled with jelly was used for ultrasonography; then, the probe was covered to minimize the inhibition of swallowing and maximize its contact with the skin.

6. Tongue (Figure 4)

The tongue is the largest among the swallowing-related muscles, consisting of a base and body, and is easily visualized via ultrasound. As the muscle fibers run in various directions, are soft, and have well-developed musculature, many studies have measured the muscle mass and movements of the tongue. Some previous studies observed a reduction in tongue movement and tongue muscle mass in older adults and those with sarcopenic dysphagia [23,55], and reported an association between tongue thickness and diadochokinesis [56]. In addition, tongue movement can be captured during swallowing [57]; the assessment of tongue movement is useful for the diagnosis of tongue protrusion [58] and the evaluation of oral function, especially in children [59,60]. By contrast, some studies reported difficulties in determining dysphagia during tongue movement [61].
Figure 4. Imaging of the tongue. On the coronal section (a), the application of the probe to the submandibular surface vertical to the Frankfurt plane allows the visualization of the central part of the tongue. Ideally, the dorsum of the tongue should be visualized on a single screen by adjusting the depth. On the sagittal section (b), the entire tongue is visualized in the deep layer by applying the probe to the midline and visualizing the geniohyoid muscle and genioglossus muscle in one screen.
Figure 4. Imaging of the tongue. On the coronal section (a), the application of the probe to the submandibular surface vertical to the Frankfurt plane allows the visualization of the central part of the tongue. Ideally, the dorsum of the tongue should be visualized on a single screen by adjusting the depth. On the sagittal section (b), the entire tongue is visualized in the deep layer by applying the probe to the midline and visualizing the geniohyoid muscle and genioglossus muscle in one screen.
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The postures and methods of positioning the tongue during ultrasonography differ (Figure 4). With regard to the posture, most of the previous studies used the sitting position [37,50,56,57,59,60,61,62,63], while some used the standing position [55] and supine position [23]. For the evaluation of the central part of the tongue, the probe is often placed vertical to the Frankfurt plane (Figure 5) on the submandibular surface [23,58,59,61]. On the base of the tongue, another method is used that involves applying the probe at a 45° angle to the Frankfurt horizontal plane in line with the second premolars [56]. Convex (3.5 MHz) [50,63] or sector (3.5–5 MHz) [57,58] probes are used when measuring the tongue. By contrast, some studies used the linear type (7.5 MHz) [23,33,37]. However, as the tongue is located in the deep layer, the linear type requires more time for gain and in-depth adjustment, and its imaging accuracy may not be high. Tongue thickness is assessed based on the distance from the mylohyoid muscle to the dorsum of the tongue on the coronal section [33,37,50,63]. During examination, the head and neck are positioned on the midline [60]; however, some studies used a holder [57,61] or headset [59] to secure the neck and jaw to accurately capture the tongue movement.
Figure 5. Frankfurt horizontal plane. The Frankfurt horizontal plane is a straight line connecting the superior margin of the ear canal and the inferior margin of the orbit. As it appears almost horizontal when viewed on a natural position, the plane determined by this line on the left and right portion is called the Frankfurt plane or ear–eye plane, and is used as the standard plane to determine the position and direction of the skull.
Figure 5. Frankfurt horizontal plane. The Frankfurt horizontal plane is a straight line connecting the superior margin of the ear canal and the inferior margin of the orbit. As it appears almost horizontal when viewed on a natural position, the plane determined by this line on the left and right portion is called the Frankfurt plane or ear–eye plane, and is used as the standard plane to determine the position and direction of the skull.
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7. Masseter Muscle (Figure 6)

The masseter muscle is a relatively large swallowing-related muscle; it is located in an area that is not easily affected by the bone, making it suitable for ultrasonography. The association between decreased masseter muscle thickness and decreased masticatory function [64] and the risk of developing dysphagia [65] have been reported. However, the masseter muscle thickness can vary greatly depending on the measurement site [66]. Therefore, appropriate testing protocols should be established to ensure inter- and intra-rater reliability [67].
A linear probe is placed vertical to the muscle fibers of the masseter muscle to measure the thickness of this muscle (Figure 6). The thickest site of the visualized masseter muscle and its thickness are determined [64,66,68,69]. The thickness of the masseter muscle, visualized with a probe placed parallel to the muscle fibers, is easy to measure in the clinical setting [66]. To identify the site of maximal thickness, the entire masseter muscle should be uniformly observed down to the zygomatic bone and lower jaw attachment before determining the measurement site. The changes in the masseter muscle thickness and contractility should be assessed during a relaxed state with the mouth closed and teeth clenched [64,67]. Meanwhile, the trunk, head, and neck can be placed in an upright or natural position during examination [64,67,68].
Figure 6. Imaging of the masseter muscle. To visualize the masseter muscle, the probe can be placed vertical to the muscle fibers or horizontal to the muscle fibers. The entire area, including the bone attachment site, is visualized, and the thickest site is measured. As the purpose of the examination is to evaluate the swallowing function, the examined patient should be placed in a sitting position and looking forward or slightly downward.
Figure 6. Imaging of the masseter muscle. To visualize the masseter muscle, the probe can be placed vertical to the muscle fibers or horizontal to the muscle fibers. The entire area, including the bone attachment site, is visualized, and the thickest site is measured. As the purpose of the examination is to evaluate the swallowing function, the examined patient should be placed in a sitting position and looking forward or slightly downward.
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8. Genioglossus Muscle (Figure 7)

The genioglossus muscle is the major extrinsic tongue muscle that makes up the body of the tongue. It is located at the lingual side of the geniohyoid muscle; it originates from the chin bone and terminates at the dorsum of the tongue and hyoid bone. The genioglossus muscle moves the tongue forward and downward. The genioglossus muscle is a respiratory-related muscle. During inspiration, the genioglossus muscle is displaced downward [70,71]. The genioglossus muscle is reportedly involved in airway obstruction during sleep apnea [72]. Kakudo et al. examined the inter-rater reliability of ultrasound assessment on the genioglossus muscle [73]. They reported that the thickness can be measured from either the upper or lower side of the fascia, depending on the examiner’s judgment, and is less reliable compared with the method used for measuring the geniohyoid muscle.
The sagittal and coronal sections are suitable for ultrasound imaging of the genioglossus muscles (Figure 7). Many studies that examined ultrasound images obtained from the sagittal sections have reported that the evaluations were performed using sector-type or convex-type probes [60,61,70,71,74]. Because the end of the genioglossus muscle reaches the dorsum of the tongue, a probe that allows deep observation may be preferred. On the sagittal section, the probe is placed on the midline of the upper hyoid bone. A linear probe was used in the imaging examination of the coronal section [60]. Therefore, the genioglossus muscle in the shallower layer can be observed. However, if it is viewed in a coronal section, the thickness of the genioglossus muscle and the area visualized vary depending on the position of the probe. A different position was proposed to visualize the global coronal section, with other muscles simultaneously visualized as orientation points. The preferred posture may be similar to that during eating, that is, a sitting position with the head facing forward [60,61,73,74].
Figure 7. Imaging of the genioglossus muscle. The probe is placed vertical to the Frankfurt plane. As the genioglossus muscle partially reaches the dorsum of the tongue, the coronal section, with other muscles as the orientation point, may be a suitable standard evaluation image. 1, Digastric; 2, mylohyoid; 3, geniohyoid; 4, genioglossus; 5, the body of the tongue.
Figure 7. Imaging of the genioglossus muscle. The probe is placed vertical to the Frankfurt plane. As the genioglossus muscle partially reaches the dorsum of the tongue, the coronal section, with other muscles as the orientation point, may be a suitable standard evaluation image. 1, Digastric; 2, mylohyoid; 3, geniohyoid; 4, genioglossus; 5, the body of the tongue.
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9. Orbicularis Oris Muscle (Figure 8)

Because the orbicularis oris muscle is involved in articulation and swallowing, adequate muscle strength and endurance should be maintained. Reduction in the muscle mass of the orbicularis oris muscle causes leakage of food into the mouth during swallowing, and decreases the intraoral pressure during swallowing [75,76]. When the maximal strength and endurance of the orbicularis oris muscle in younger adults were compared with those in older adults, both maximal muscle strength and endurance of the orbicularis oris muscle were significantly lower in older adults [75]. The orbicularis oris muscle has a hierarchical structure with superficial muscles involved in articulation and deep muscles involved in swallowing. Zhang et al. examined the organization of the orbicularis oris muscle in healthy individuals and patients who underwent surgery for the presence of a cleft lip; the orbicularis oris muscle had a hierarchical structure with different superficial and deep muscle fibers [77].
The orbicularis oris muscle is measured by placing the probe on the short axis vertical to the nasal septum, following the curve of the upper lip along the margin, and moving the probe left and right from the midline, or by positioning the probe vertical to the philtrum using the short axis [77,78]. Ultrasonography of the orbicularis oris muscle measures the thickness of the superficial and deep layers after a cleft lip repair, clearly demonstrating the hierarchical structure of the orbicularis oris muscle [77]. Ultrasonography is useful for visualizing the target areas during surgical treatments involving the lips, such as cleft lip and facial paralysis, which are difficult to confirm by inspection alone [78,79]. Facial muscle is a generic term used to describe the cutaneous muscles that are located in the superficial layer of the head and terminate at the skin on one side. Ultrasonography has been used to show the reference values of six facial muscles: frontalis, orbicularis oculi, orbicularis oris, depressor anguli oris, depressor labii inferioris, and mentalis muscles [80]. This study focused on examining the depressor anguli oris, one of the facial muscles surrounding the orbicularis oris muscle. Although there is no clearly defined method for visualizing the depressor anguli oris, visualization can be performed by applying the probe to the muscle fibers on the short axis (Figure 8).
Figure 8. Imaging of the orbicularis oris muscle. The orbicularis oris muscle can be visualized by placing the probe along the margin of the upper lip (a). For the depressor anguli oris muscle, the probe should be placed vertical to the muscle fibers. Since this muscle is located just underneath the surface of the skin, a linear probe should be used (b). 1, Orbicularis oris muscle; 2, alveolar ridge; 3, depressor anguli oris muscle; 4, inferior labial artery.
Figure 8. Imaging of the orbicularis oris muscle. The orbicularis oris muscle can be visualized by placing the probe along the margin of the upper lip (a). For the depressor anguli oris muscle, the probe should be placed vertical to the muscle fibers. Since this muscle is located just underneath the surface of the skin, a linear probe should be used (b). 1, Orbicularis oris muscle; 2, alveolar ridge; 3, depressor anguli oris muscle; 4, inferior labial artery.
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10. Temporalis Muscle (Figure 9)

The temporalis muscle is extensively located in the superficial layer among the swallowing-related muscles, and runs from the left and right temporal bones to the muscular processes of the mandible. The temporalis muscle is among the primary muscles of mastication, while the masseter muscle elevates the mandible and pulls it backward. The masseter muscle thickness and temporalis muscle thickness correlate with age, sex, and body mass index [67]. As the muscle activity of the temporalis muscle decreases to the extent that the dentition can collapse, the muscle activity of people wearing complete dentures is significantly lower than that of people with natural dentition [81]. Following the standardized protocols, ultrasound can be used to assess the superficial and deep masticatory muscle thickness. However, as the target population is limited, patients with clinical conditions such as temporomandibular disorders, malalignment, and dysphagia should be examined.
Temporalis muscle thickness refers to the maximum distance between the lateral and medial fascia. The probe is placed at the superior margin of the zygomatic arch, and the depth is set at 40 mm. Then, the probe is moved gradually toward the head parallel to the short axis of the zygomatic arch and toward the temporal fossa until the temporalis muscle appears on the screen (Figure 9). During measurement, the patient should sit comfortably on a chair with a backrest; the measurement is conducted at the left and right sides when the muscles are relaxed, the teeth are clenched, and the mouth is opened wide. The patient is instructed to clench the teeth as forcefully as possible without inducing pain in the teeth. The patient is then instructed to open the mouth as widely as possible without causing discomfort to the temporomandibular joint [67].
Figure 9. Imaging of the temporalis muscle. The probe is placed horizontally against the superior margin of the zygomatic arch and is moved gradually in a cephalic direction toward the temporal fossa. When evaluating muscle mass, the thickest site should be measured.
Figure 9. Imaging of the temporalis muscle. The probe is placed horizontally against the superior margin of the zygomatic arch and is moved gradually in a cephalic direction toward the temporal fossa. When evaluating muscle mass, the thickest site should be measured.
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11. Pharynx (Figure 10 and Figure 11)

The pharynx is a tubular space extending from the base of the skull behind the nasal cavity to the superior esophageal sphincter. Patients with pharyngeal residue have a 2.8-fold risk of aspiration compared with those without pharyngeal residue [82]. Ultrasonography allows the detection of the residues in the pyriform sinus and epiglottic vallecula (Figure 10 and Figure 11) [82]. Echography was used to evaluate the lateral pharyngeal wall motion during various swallowing maneuvers (supraglottic, super-supraglottic, and Mendelsohn maneuvers) [83].
Figure 10. Imaging of the pharynx. To visualize the epiglottic vallecula, the probe should be placed horizontally at the level of the hyoid bone, so that the base of the tongue and the epiglottis can serve as the orientation points and the epiglottic vallecula can be identified (a). To visualize the left pyriform sinus, the probe should be placed horizontally from the left side at the level of laryngeal prominence (b). The thyroid cartilage and common carotid artery serve as the orientation points.
Figure 10. Imaging of the pharynx. To visualize the epiglottic vallecula, the probe should be placed horizontally at the level of the hyoid bone, so that the base of the tongue and the epiglottis can serve as the orientation points and the epiglottic vallecula can be identified (a). To visualize the left pyriform sinus, the probe should be placed horizontally from the left side at the level of laryngeal prominence (b). The thyroid cartilage and common carotid artery serve as the orientation points.
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Figure 11. Pharynx in a dysphagic patient. A dysphagic patient showing residues in the vallecula (a) and pyriform sinus (b) on the ultrasound image.
Figure 11. Pharynx in a dysphagic patient. A dysphagic patient showing residues in the vallecula (a) and pyriform sinus (b) on the ultrasound image.
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Visualizing the pharynx with echography allows the detection of the residues in the pyriform sinus and epiglottic vallecula [82]. To visualize the left pyriform sinus, the probe is placed horizontally on the left side at the level of the laryngeal prominence, avoiding the midline. The common carotid artery and thyroid cartilage become the orientation points, and the pyriform sinus can be visualized by swinging the probe as necessary. The epiglottic vallecula can be visualized by placing the probe horizontally at the midline at the level of the hyoid bone, establishing the tongue root and epiglottis the orientation points and allowing the epiglottic vallecula to be visualized. Residue can be observed as a hyperechoic area or point (Figure 11). The ideal positioning during examination is the same as that during eating. The head and neck are not fixed to allow the patient to easily swallow at the most comfortable position [82]. Other methods include fixing the head and neck with a head stabilizer [84] and using two probes to evaluate the lateral pharyngeal wall motion [83].

12. Esophagus (Figure 12)

The esophagus is a tubular organ located at the foot of the pharynx, beginning at the level of the inferior margin of the cricoid cartilage; it moves the food mass from the pharynx to the stomach. At the upper end of the esophagus (the border between the pharynx and esophagus) is the superior esophageal sphincter; its incomplete closure causes pharyngeal reflux, aspiration, and pneumonia. The opening capacity of the esophagus increases as the food viscosity increases, suggesting that ultrasonography can be used to evaluate the opening of the esophagus and upper esophageal sphincter [85]. In terms of the water transit time, the front and rear edges of the image displayed during an ultrasound may lack sharpness depending on the food form and swallowing style. In a previous study, due to the slight differences in swallowing styles, the water transit times did not show similar trends among the examined patients [86].
During examination, the patient should be seated vertically so that the Frankfurt horizontal plane is parallel to the floor. The inferior margin of the cricoid cartilage is used as the orientation point; the probe is directed longitudinally from the left toward the esophagus to obtain an image of the opening of the cervical esophagus located 1 cm closer to the foot from the orientation point [85,87]. Tilting the probe in the sagittal and forehead directions allows the visualization of the esophagus opening [84]. The function of the esophagus opening in patients with dysphagia can be evaluated by measuring the opening capacity and the duration of esophagus opening depending on the food consumed [85,86] (Figure 12).
Figure 12. Imaging of the cervical esophagus. The cervical esophagus near the lower end of the cricoid cartilage is visualized by placing the probe longitudinal to the esophagus (a). Visualizing the thyroid gland on the surface of the esophagus provides clear images with less artifacts and noise. In the horizontal section, the esophagus can be visualized deeper than the thyroid gland, on the side of the trachea (b).
Figure 12. Imaging of the cervical esophagus. The cervical esophagus near the lower end of the cricoid cartilage is visualized by placing the probe longitudinal to the esophagus (a). Visualizing the thyroid gland on the surface of the esophagus provides clear images with less artifacts and noise. In the horizontal section, the esophagus can be visualized deeper than the thyroid gland, on the side of the trachea (b).
Nutrients 15 03560 g012

13. Larynx (Figure 13)

The larynx vibrates the vocal cords to produce speech and prevents foreign substances from entering the airways. Foreign body entry into the larynx or aspiration can be observed by performing a videofluorographic swallowing study or swallowing endoscopy. In recent years, foreign bodies were visualized using ultrasound [88,89,90]. By evaluating the risk of aspiration during meals using an echocardiogram, the effect of the compensatory swallowing method and food form adjustment were confirmed to reduce aspiration [88,89,90].
The larynx is mainly visualized at the level of the thyroid cartilage, with the probe placed on a short axis (Figure 13). Many studies have identified the vocal cords by asking the examined patients to speak [89,91,92]. The probe was also placed on the sagittal section against the thyroid cartilage and moved to the back and then to the foot part to visualize the arytenoid cartilage [92]. The position required for ultrasonography varies. Some studies used a comfortable posture (similar to that during eating) without fixing the head and neck to avoid interfering the swallowing movements [88,89]; other studies used supine position with the head and neck extended [91,92,93]. The posture assumed during eating is recommended when undergoing laryngeal examination [89,90].
The aspirated material can be evaluated by placing the probe on the midline of the thyroid cartilage longitudinally to visualize the vocal cords and trachea wall. The structure of the trachea wall must be assessed prior to the examination to determine the presence of aspirated materials. The flow of aspirated material can be observed after swallowing as the movement that differs from the structures, a foggy hyperechoic area above the vocal fold, and a hyperechoic area on a line along the trachea wall in the direction of the trachea area [82,88,89].
Figure 13. Imaging of the larynx. When imaging on a horizontal section, the probe is placed at the level of the thyroid cartilage; the vocal fold and arytenoid cartilage can be visualized when the patient speaks (a). On the sagittal section, the vocal cords, trachea, and trachea wall can be visualized by placing the probe on the midline of the thyroid cartilage (b).
Figure 13. Imaging of the larynx. When imaging on a horizontal section, the probe is placed at the level of the thyroid cartilage; the vocal fold and arytenoid cartilage can be visualized when the patient speaks (a). On the sagittal section, the vocal cords, trachea, and trachea wall can be visualized by placing the probe on the midline of the thyroid cartilage (b).
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14. Swallowing Function Evaluation

Observation of the tongue, pharynx, larynx, esophagus, and hyoid bone is useful when evaluating the swallowing function with an echographic device. By observing the tongue, its movement can be evaluated during swallowing. By observing the pharynx, the residues of the pyriform sinus and epiglottic vallecula can be evaluated. By observing the lateral pharyngeal wall motion, the supraglottic and Mendelsohn maneuvers can be evaluated. The capacity of the esophageal opening can be evaluated by measuring the opening capacity and the duration of opening. Aspiration can be visualized by assessing the larynx. Observing whether aspiration occurs during a meal allows the evaluation of the compensatory swallowing methods and food forms. Measurement of the hyoid bone movement, travel distance, and travel time is useful for evaluating the laryngeal movement during swallowing. They are usually evaluated during visualization procedures, but many studies examine these factors subjectively.
Evaluation of dysphagia associated with sarcopenia requires muscle mass assessment of the swallowing-related muscles [15]. Table 1 shows a practical echographic protocol for evaluating the swallowing-related muscles. During muscle mass evaluation, the static images can be used as objective measurements. The standard values are expected to be reported.

15. Summary

We clarified the latest findings on the method used for conducting an ultrasound assessment of the swallowing function. Several skeletal muscles and organs that are involved in swallowing can be evaluated by echography, both dynamically and statically. Visualization of the pharynx and larynx enables the detection of aspiration and residues. The swallowing function can be evaluated by measuring the travel distance and duration of hyoid bone movement and the opening capacity and the duration of esophagus opening. Many studies have shown the associations between swallowing-related skeletal muscle mass and swallowing function measured by echography; the results indicate that echography is the preferred method for evaluating the swallowing function.
Several issues need to be addressed in the use of echography for the evaluation of the swallowing function. First, standard guidelines on the position and orientation of the probe when measuring a certain site have not yet been established. Depending on the muscle or organ, orientation points should be set for proper visualization. Second, the posture during measurement is not consistent. In most cases, the measurements were obtained in a sitting position; the neck angles varied, from a neutral posture (assumed during eating) to an extended posture. This finding implies that evaluation should be carried out in a position that is the same as that assumed during eating. Another issue is that the probe is not stable due to the swallowing movements; hence, a holder or probe cover is sometimes used to hold the probe in place. Third, only a few studies that conducted food-based assessments were published. In order to effectively apply echography for the evaluation of swallowing function in clinical practice, the methods used for assessing the swallowing movement and function should be standardized.
Echography is expected to be clinically applicable as a noninvasive method for assessing the swallowing function at a patient’s bedside. Muscle mass is an important factor in nutritional evaluation, and an echocardiogram is used as a nutritional evaluation device [94,95,96]. Echocardiography allows the evaluation of the swallowing-related skeletal muscles to identify any disorders, such as sarcopenia dysphagia, which are difficult to visualize using conventional methods. Technological advancements have been made, making the echocardiogram a portable and easy-to-use device. The use of artificial intelligence will enable the accurate identification of sites to be visualized and abnormal findings.

Author Contributions

Conceptualization, methodology, investigation, writing—original draft: all authors; writing—review and editing, K.M.; visualization, M.N.; supervision, K.M.; funding acquisition, K.M. All authors have read and agreed to the published version of the manuscript.

Funding

The study was supported by the Japan Society for the Promotion of Science (grant number: 21H03390 to Maeda) and the Research Funding of Longevity Sciences (grant number: 22-4 to Maeda).

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

We thank the relevant members of the Department of Rehabilitation Medicine, Hospital, National Center for Geriatrics and Gerontology for their assistance and support.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Cohen, D.L.; Roffe, C.; Beavan, J.; Blackett, B.; Fairfield, C.A.; Hamdy, S.; Havard, D.; McFarlane, M.; McLauglin, C.; Randall, M.; et al. Post-stroke dysphagia: A review and design considerations for future trials. Int. J. Stroke 2016, 11, 399–411. [Google Scholar] [CrossRef] [PubMed]
  2. Falsetti, P.; Acciai, C.; Palilla, R.; Bosi, M.; Carpinteri, F.; Zingarelli, A.; Pedace, C.; Lenzi, L. Oropharyngeal dysphagia after stroke: Incidence, diagnosis, and clinical predictors in patients admitted to a neurorehabilitation unit. J. Stroke Cerebrovasc. Dis. 2009, 18, 329–335. [Google Scholar] [CrossRef] [PubMed]
  3. Finestone, H.M.; Greene-Finestone, L.S.; Wilson, E.S.; Teasell, R.W. Malnutrition in stroke patients on the rehabilitation service and at follow-up: Prevalence and predictors. Arch. Phys. Med. Rehabil. 1995, 76, 310–316. [Google Scholar] [CrossRef] [PubMed]
  4. Daly, E.; Miles, A.; Scott, S.; Gillham, M. Finding the red flags: Swallowing difficulties after cardiac surgery in patients with prolonged intubation. J. Crit. Care 2016, 31, 119–124. [Google Scholar] [CrossRef]
  5. Bours, G.J.; Speyer, R.; Lemmens, J.; Limburg, M.; de Wit, R. Bedside screening tests vs. videofluoroscopy or fibreoptic endoscopic evaluation of swallowing to detect dysphagia in patients with neurological disorders: Systematic review. J. Adv. Nurs. 2009, 65, 477–493. [Google Scholar] [CrossRef]
  6. Kertscher, B.; Speyer, R.; Palmieri, M.; Plant, C. Bedside screening to detect oropharyngeal dysphagia in patients with neurological disorders: An updated systematic review. Dysphagia 2014, 29, 204–212. [Google Scholar] [CrossRef]
  7. Daniels, S.K.; Anderson, J.A.; Willson, P.C. Valid items for screening dysphagia risk in patients with stroke: A systematic review. Stroke 2012, 43, 892–897. [Google Scholar] [CrossRef]
  8. Tohara, H.; Saitoh, E.; Mays, K.A.; Kuhlemeier, K.; Palmer, J.B. Three tests for predicting aspiration without videofluorography. Dysphagia 2003, 18, 126–134. [Google Scholar] [CrossRef]
  9. Wu, M.C.; Chang, Y.C.; Wang, T.G.; Lin, L.C. Evaluating swallowing dysfunction using a 100-ml water swallowing test. Dysphagia 2004, 19, 43–47. [Google Scholar] [CrossRef]
  10. Martino, R.; Silver, F.; Teasell, R.; Bayley, M.; Nicholson, G.; Streiner, D.L.; Diamant, N.E. The Toronto Bedside Swallowing Screening Test (TOR-BSST): Development and validation of a dysphagia screening tool for patients with stroke. Stroke 2009, 40, 555–561. [Google Scholar] [CrossRef] [Green Version]
  11. Trapl, M.; Enderle, P.; Nowotny, M.; Teuschl, Y.; Matz, K.; Dachenhausen, A.; Brainin, M. Dysphagia bedside screening for acute-stroke patients: The Gugging Swallowing Screen. Stroke 2007, 38, 2948–2952. [Google Scholar] [CrossRef] [Green Version]
  12. Clave, P.; Arreola, V.; Romea, M.; Medina, L.; Palomera, E.; Serra-Prat, M. Accuracy of the volume-viscosity swallow test for clinical screening of oropharyngeal dysphagia and aspiration. Clin. Nutr. 2008, 27, 806–815. [Google Scholar] [CrossRef] [PubMed]
  13. Casey, P.; Alasmar, M.; McLaughlin, J.; Ang, Y.; McPhee, J.; Heire, P.; Sultan, J. The current use of ultrasound to measure skeletal muscle and its ability to predict clinical outcomes: A systematic review. J. Cachexia Sarcopenia Muscle 2022, 13, 2298–2309. [Google Scholar] [CrossRef] [PubMed]
  14. Hudson, H.M.; Daubert, C.R.; Mills, R.H. The interdependency of protein-energy malnutrition, aging, and dysphagia. Dysphagia 2000, 15, 31–38. [Google Scholar] [CrossRef] [PubMed]
  15. Fujishima, I.; Fujiu-Kurachi, M.; Arai, H.; Hyodo, M.; Kagaya, H.; Maeda, K.; Mori, T.; Nishioka, S.; Oshima, F.; Ogawa, S.; et al. Sarcopenia and dysphagia: Position paper by four professional organizations. Geriatr. Gerontol. Int. 2019, 19, 91–97. [Google Scholar] [CrossRef] [Green Version]
  16. Maeda, K.; Takaki, M.; Akagi, J. Decreased Skeletal Muscle Mass and Risk Factors of Sarcopenic Dysphagia: A Prospective Observational Cohort Study. J. Gerontol. A Biol. Sci. Med. Sci. 2017, 72, 1290–1294. [Google Scholar] [CrossRef]
  17. Maeda, K.; Ishida, Y.; Nonogaki, T.; Shimizu, A.; Yamanaka, Y.; Matsuyama, R.; Kato, R.; Mori, N. Development and Predictors of Sarcopenic Dysphagia during Hospitalization of Older Adults. Nutrients 2019, 12, 70. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  18. Allen, J.E.; Clunie, G.M.; Winiker, K. Ultrasound: An emerging modality for the dysphagia assessment toolkit? Curr. Opin. Otolaryngol. Head. Neck Surg. 2021, 29, 213–218. [Google Scholar] [CrossRef]
  19. Hsiao, M.Y.; Wu, C.H.; Wang, T.G. Emerging Role of Ultrasound in Dysphagia Assessment and Intervention: A Narrative Review. Front. Rehabil. Sci. 2021, 2, 708102. [Google Scholar] [CrossRef]
  20. Miura, Y.; Tamai, N.; Kitamura, A.; Yoshida, M.; Takahashi, T.; Mugita, Y.; Tobita, I.; Arita, M.; Urai, T.; Dai, M.; et al. Diagnostic accuracy of ultrasound examination in detecting aspiration and pharyngeal residue in patients with dysphagia: A systematic review and meta-analysis. Jpn. J. Nurs. Sci. 2021, 18, e12396. [Google Scholar] [CrossRef]
  21. Khan, Y.S.; Bordoni, B. Anatomy, Head and Neck, Suprahyoid Muscle; StatPearls: Treasure Island, FL, USA, 2022. [Google Scholar]
  22. Baba, T.; Goto, T.; Fujimoto, K.; Honda, T.; Yagi, K.; Nagao, K.; Ichikawa, T. Age-related Changes in Geniohyoid Muscle Morphology Predict Reduced Swallowing Function. J. Oral. Health Biosci. 2017, 30, 18–25. [Google Scholar] [CrossRef]
  23. Ogawa, N.; Mori, T.; Fujishima, I.; Wakabayashi, H.; Itoda, M.; Kunieda, K.; Shigematsu, T.; Nishioka, S.; Tohara, H.; Yamada, M.; et al. Ultrasonography to Measure Swallowing Muscle Mass and Quality in Older Patients With Sarcopenic Dysphagia. J. Am. Med. Dir. Assoc. 2018, 19, 516–522. [Google Scholar] [CrossRef]
  24. Miura, Y.; Nakagami, G.; Tohara, H.; Ogawa, N.; Sanada, H. The association between jaw-opening strength, geniohyoid muscle thickness and echo intensity measured by ultrasound. Med. Ultrason. 2020, 22, 299–304. [Google Scholar] [CrossRef] [PubMed]
  25. Pauloski, B.R.; Yahnke, K.M. Using Ultrasound to Document the Effects of Expiratory Muscle Strength Training (EMST) on the Geniohyoid Muscle. Dysphagia 2022, 37, 788–799. [Google Scholar] [CrossRef]
  26. Park, J.S.; Lee, S.H.; Jung, S.H.; Choi, J.B.; Jung, Y.J. Tongue strengthening exercise is effective in improving the oropharyngeal muscles associated with swallowing in community-dwelling older adults in South Korea: A randomized trial. Medicine 2019, 98, e17304. [Google Scholar] [CrossRef]
  27. Cheng, D.T.H.; Lee, K.Y.S.; Ahuja, A.T.; Tong, M.C.F. Sonographic assessment of swallowing in irradiated nasopharyngeal carcinoma patients. Laryngoscope 2018, 128, 2552–2559. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  28. Feng, X.; Cartwright, M.S.; Walker, F.O.; Bargoil, J.H.; Hu, Y.; Butler, S.G. Ultrasonographic evaluation of geniohyoid muscle and hyoid bone during swallowing in young adults. Laryngoscope 2015, 125, 1886–1891. [Google Scholar] [CrossRef] [PubMed]
  29. Yabunaka, K.; Konishi, H.; Nakagami, G.; Sanada, H.; Iizaka, S.; Sanada, S.; Ohue, M. Ultrasonographic evaluation of geniohyoid muscle movement during swallowing: A study on healthy adults of various ages. Radiol. Phys. Technol. 2012, 5, 34–39. [Google Scholar] [CrossRef]
  30. Shimizu, S.; Hanayama, K.; Metani, H.; Sugiyama, T.; Abe, H.; Seki, S.; Hiraoka, T.; Tsubahara, A. Retest reliability of ultrasonic geniohyoid muscle measurement. Jpn. J. Compr. Rehabil. Sci. 2016, 7, 55–60. [Google Scholar] [CrossRef]
  31. Choi, J.B.; Jung, Y.J.; Park, J.S. Comparison of 2 types of therapeutic exercise: Jaw opening exercise and head lift exercise for dysphagic stroke: A pilot study. Medicine 2020, 99, e22136. [Google Scholar] [CrossRef]
  32. Jung, Y.J.; Kim, H.J.; Choi, J.B.; Park, J.S.; Hwang, N.K. Effect of Dysphagia Rehabilitation Using Kinesiology Taping on Oropharyngeal Muscle Hypertrophy in Post-Stroke Patients: A Double Blind Randomized Placebo-Controlled Trial. Healthcare 2020, 8, 411. [Google Scholar] [CrossRef] [PubMed]
  33. van den Engel-Hoek, L.; Erasmus, C.E.; Hendriks, J.C.; Geurts, A.C.; Klein, W.M.; Pillen, S.; Sie, L.T.; de Swart, B.J.; de Groot, I.J. Oral muscles are progressively affected in Duchenne muscular dystrophy: Implications for dysphagia treatment. J. Neurol. 2013, 260, 1295–1303. [Google Scholar] [CrossRef] [PubMed]
  34. Macrae, P.R.; Doeltgen, S.H.; Jones, R.D.; Huckabee, M.L. Intra- and inter-rater reliability for analysis of hyoid displacement measured with sonography. J. Clin. Ultrasound 2012, 40, 74–78. [Google Scholar] [CrossRef]
  35. Tranchito, E.N.; Bordoni, B. Anatomy, Head and Neck, Digastric Muscle; StatPearls: Treasure Island, FL, USA, 2022. [Google Scholar]
  36. Holzapfel, K.; Naumann, M. Ultrasound Detection of Vagus Nerve Atrophy in Bulbar Amyotrophic Lateral Sclerosis. J. Neuroimaging 2020, 30, 762–765. [Google Scholar] [CrossRef]
  37. Winiker, K.; Hammond, R.; Thomas, P.; Dimmock, A.; Huckabee, M.L. Swallowing assessment in patients with dysphagia: Validity and reliability of a pocket-sized ultrasound system. Int. J. Lang. Commun. Disord. 2022, 57, 539–551. [Google Scholar] [CrossRef]
  38. Toth, J.; Lappin, S.L. Anatomy, Head and Neck, Mylohyoid Muscle; StatPearls: Treasure Island, FL, USA, 2022. [Google Scholar]
  39. Feng, S.; Shea, Q.T.; Ng, K.Y.; Tang, C.N.; Kwong, E.; Zheng, Y. Automatic Hyoid Bone Tracking in Real-Time Ultrasound Swallowing Videos Using Deep Learning Based and Correlation Filter Based Trackers. Sensors 2021, 21, 3712. [Google Scholar] [CrossRef]
  40. Winiker, K.; Burnip, E.; Gozdzikowska, K.; Guiu Hernandez, E.; Hammond, R.; Macrae, P.; Huckabee, M.L. Ultrasound: Validity of a Pocket-Sized System in the Assessment of Swallowing. Dysphagia 2021, 36, 1010–1018. [Google Scholar] [CrossRef]
  41. Matsuo, T.; Matsuyama, M. Detection of poststroke oropharyngeal dysphagia with swallowing screening by ultrasonography. PLoS ONE 2021, 16, e0248770. [Google Scholar] [CrossRef]
  42. Costa, B.; Rodrigues, D.S.B.; Magalhaes, D.D.D.; Santos, A.S.; Santos, R.V.; Azevedo, E.H.M.; Almeida, A.A.; Pernambuco, L. Quantitative Ultrasound Assessment of Hyoid Bone Displacement During Swallowing Following Thyroidectomy. Dysphagia 2021, 36, 659–669. [Google Scholar] [CrossRef]
  43. Perry, S.E.; Winkelman, C.J.; Huckabee, M.L. Variability in Ultrasound Measurement of Hyoid Bone Displacement and Submental Muscle Size Using 2 Methods of Data Acquisition. Folia Phoniatr. Logop. 2016, 68, 205–210. [Google Scholar] [CrossRef]
  44. Chen, Y.C.; Hsiao, M.Y.; Wang, Y.C.; Fu, C.P.; Wang, T.G. Reliability of Ultrasonography in Evaluating Hyoid Bone Movement. J. Med. Ultrasound 2017, 25, 90–95. [Google Scholar] [CrossRef]
  45. Rocha, S.G.; Silva, R.G.; Berti, L.C. Qualitative and quantitative ultrasound analysis of oropharyngeal swallowing. Codas 2015, 27, 437–445. [Google Scholar] [CrossRef] [Green Version]
  46. Ahn, S.Y.; Cho, K.H.; Beom, J.; Park, D.J.; Jee, S.; Nam, J.H. Reliability of ultrasound evaluation of hyoid-larynx approximation with positional change. Ultrasound Med. Biol. 2015, 41, 1221–1225. [Google Scholar] [CrossRef] [PubMed]
  47. Huang, Y.L.; Hsieh, S.F.; Chang, Y.C.; Chen, H.C.; Wang, T.G. Ultrasonographic evaluation of hyoid-larynx approximation in dysphagic stroke patients. Ultrasound Med. Biol. 2009, 35, 1103–1108. [Google Scholar] [CrossRef] [Green Version]
  48. Kuhl, V.; Eicke, B.M.; Dieterich, M.; Urban, P.P. Sonographic analysis of laryngeal elevation during swallowing. J. Neurol. 2003, 250, 333–337. [Google Scholar] [CrossRef]
  49. Sonies, B.C.; Wang, C.; Sapper, D.J. Evaluation of normal and abnormal hyoid bone movement during swallowing by use of ultrasound duplex-Doppler imaging. Ultrasound Med. Biol. 1996, 22, 1169–1175. [Google Scholar] [CrossRef] [PubMed]
  50. Hsiao, M.Y.; Chang, Y.C.; Chen, W.S.; Chang, H.Y.; Wang, T.G. Application of ultrasonography in assessing oropharyngeal dysphagia in stroke patients. Ultrasound Med. Biol. 2012, 38, 1522–1528. [Google Scholar] [CrossRef] [PubMed]
  51. Lee, Y.S.; Lee, K.E.; Kang, Y.; Yi, T.I.; Kim, J.S. Usefulness of Submental Ultrasonographic Evaluation for Dysphagia Patients. Ann. Rehabil. Med. 2016, 40, 197–205. [Google Scholar] [CrossRef] [Green Version]
  52. Soder, N.; Miller, N. Using ultrasound to investigate intrapersonal variability in durational aspects of tongue movement during swallowing. Dysphagia 2002, 17, 288–297. [Google Scholar] [CrossRef]
  53. Oh, E.H.; Seo, J.S.; Kang, H.J. Assessment of Oropharyngeal Dysphagia in Patients With Parkinson Disease: Use of Ultrasonography. Ann. Rehabil. Med. 2016, 40, 190–196. [Google Scholar] [CrossRef]
  54. Cergan, R.; Dumitru, M.; Vrinceanu, D.; Neagos, A.; Jeican, I.I.; Ciuluvica, R.C. Ultrasonography of the larynx: Novel use during the SARS-CoV-2 pandemic (Review). Exp. Ther. Med. 2021, 21, 273. [Google Scholar] [CrossRef] [PubMed]
  55. Nienstedt, J.C.; Muller, F.; Rosler, A.; Pflug, C. Presbyphagia Diagnostics Using M-Mode Ultrasound: Changes in the Tongue Movement Pattern. Dysphagia 2020, 35, 696–701. [Google Scholar] [CrossRef]
  56. Chantaramanee, A.; Tohara, H.; Nakagawa, K.; Hara, K.; Nakane, A.; Yamaguchi, K.; Yoshimi, K.; Junichi, F.; Minakuchi, S. Association between echo intensity of the tongue and its thickness and function in elderly subjects. J. Oral. Rehabil. 2019, 46, 634–639. [Google Scholar] [CrossRef] [PubMed]
  57. Peng, C.L.; Jost-Brinkmann, P.G.; Yoshida, N.; Chou, H.H.; Lin, C.T. Comparison of tongue functions between mature and tongue-thrust swallowing--an ultrasound investigation. Am. J. Orthod. Dentofacial Orthop. 2004, 125, 562–570. [Google Scholar] [CrossRef] [PubMed]
  58. Fuhrmann, R.A.; Diedrich, P.R. B-mode ultrasound scanning of the tongue during swallowing. Dentomaxillof. Radiol. 1994, 23, 211–215. [Google Scholar] [CrossRef] [Green Version]
  59. Ohkubo, M.; Scobbie, J.M. Tongue Shape Dynamics in Swallowing Using Sagittal Ultrasound. Dysphagia 2019, 34, 112–118. [Google Scholar] [CrossRef] [Green Version]
  60. Maniere-Ezvan, A.; Duval, J.M.; Darnault, P. Ultrasonic assessment of the anatomy and function of the tongue. Surg. Radiol. Anat. 1993, 15, 55–61. [Google Scholar] [CrossRef]
  61. Galen, S.; Jost-Brinkmann, P.G. B-mode and M-mode Ultrasonography of Tongue Movements during Swallowing. J. Orofac. Orthop. 2010, 71, 125–135. [Google Scholar] [CrossRef]
  62. Umay, E.; Ozturk, E.; Gurcay, E.; Delibas, O.; Celikel, F. Swallowing in Parkinson’s disease: How is it affected? Clin. Neurol. Neurosurg. 2019, 177, 37–41. [Google Scholar] [CrossRef]
  63. Nakamori, M.; Hosomi, N.; Takaki, S.; Oda, M.; Hiraoka, A.; Yoshikawa, M.; Matsushima, H.; Ochi, K.; Tsuga, K.; Maruyama, H.; et al. Tongue thickness evaluation using ultrasonography can predict swallowing function in amyotrophic lateral sclerosis patients. Clin. Neurophysiol. 2016, 127, 1669–1674. [Google Scholar] [CrossRef]
  64. Gaszynska, E.; Godala, M.; Szatko, F.; Gaszynski, T. Masseter muscle tension, chewing ability, and selected parameters of physical fitness in elderly care home residents in Lodz, Poland. Clin. Interv. Aging 2014, 9, 1197–1203. [Google Scholar] [CrossRef] [Green Version]
  65. Sanz-Paris, A.; Gonzalez-Fernandez, M.; Hueso-Del Rio, L.E.; Ferrer-Lahuerta, E.; Monge-Vazquez, A.; Losfablos-Callau, F.; Sanclemente-Hernandez, T.; Sanz-Arque, A.; Arbones-Mainar, J.M. Muscle Thickness and Echogenicity Measured by Ultrasound Could Detect Local Sarcopenia and Malnutrition in Older Patients Hospitalized for Hip Fracture. Nutrients 2021, 13, 2401. [Google Scholar] [CrossRef]
  66. Gawriolek, K.; Klatkiewicz, T.; Przystanska, A.; Maciejewska-Szaniec, Z.; Gedrange, T.; Czajka-Jakubowska, A. Standardization of the ultrasound examination of the masseter muscle with size-independent calculation of records. Adv. Clin. Exp. Med. 2021, 30, 441–447. [Google Scholar] [CrossRef]
  67. Chang, P.H.; Chen, Y.J.; Chang, K.V.; Wu, W.T.; Ozcakar, L. Ultrasound measurements of superficial and deep masticatory muscles in various postures: Reliability and influencers. Sci. Rep. 2020, 10, 14357. [Google Scholar] [CrossRef] [PubMed]
  68. Kiliaridis, S.; Kalebo, P. Masseter muscle thickness measured by ultrasonography and its relation to facial morphology. J. Dent. Res. 1991, 70, 1262–1265. [Google Scholar] [CrossRef] [PubMed]
  69. Tircoveluri, S.; Singh, J.R.; Rayapudi, N.; Karra, A.; Begum, M.; Challa, P. Correlation of masseter muscle thickness and intermolar width—an ultrasonography study. J. Int. Oral. Health 2013, 5, 28–34. [Google Scholar] [PubMed]
  70. Kwan, B.C.; Butler, J.E.; Hudson, A.L.; McKenzie, D.K.; Bilston, L.E.; Gandevia, S.C. A novel ultrasound technique to measure genioglossus movement in vivo. J. Appl. Physiol. 2014, 117, 556–562. [Google Scholar] [CrossRef] [Green Version]
  71. Kwan, B.C.H.; McBain, R.A.; Luu, B.L.; Butler, J.E.; Bilston, L.E.; Gandevia, S.C. Influence of respiratory mechanics and drive on genioglossus movement under ultrasound imaging. PLoS ONE 2018, 13, e0195884. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  72. den Herder, C.; Schmeck, J.; Appelboom, D.J.; de Vries, N. Risks of general anaesthesia in people with obstructive sleep apnoea. BMJ 2004, 329, 955–959. [Google Scholar] [CrossRef] [Green Version]
  73. Kakudo, M.; Matsuo, S.; Maeda, K.; Yasui, Y.; Imai, A.; Tanaka, J.; Tanaka, M. Inter-rater reliability for measurement of tongue movement during chewing and swallowing using ultrasonography. J. Osaka Dent. Univ. 2020, 54, 29–34. [Google Scholar] [CrossRef]
  74. Hanazawa, T.; Araki, K.; Kuroda, M. 3D/4D Ultrasonographic examinations for analyzing swallowing movements: Assessing their ability to delineate tongue and bolus movements. Dent. Radiol. 2019, 58, 79–85. (In Japanese) [Google Scholar] [CrossRef]
  75. Park, H.S.; Kim, J.U.; Park, J.Y.; Oh, D.H.; Kim, H.J. Comparison of orbicularis oris muscle strength and endurance in young and elderly adults. J. Phys. Ther. Sci. 2018, 30, 1477–1478. [Google Scholar] [CrossRef] [Green Version]
  76. Park, H.S.; Park, J.Y.; Kwon, Y.H.; Choi, H.S.; Kim, H.J. Effect of orbicularis oris muscle training on muscle strength and lip closure function in patients with stroke and swallowing disorder. J. Phys. Ther. Sci. 2018, 30, 1355–1356. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  77. Zhang, W.H.; Chen, Y.Y.; Liu, J.J.; Liao, X.H.; Du, Y.C.; Gao, Y. Application of ultrasound imaging of upper lip orbicularis oris muscle. Int. J. Clin. Exp. Med. 2015, 8, 3391–3400. [Google Scholar] [PubMed]
  78. Masuoka, H. The Visualization of the Functional Structure of the Crossing Fibers of the Orbicularis Oris Muscle Using Ultrasound. Plast. Reconstr. Surg. Glob. Open 2017, 5, e1331. [Google Scholar] [CrossRef]
  79. Fujiwara, K.; Yoshida, M.; Nakamichi, N.; Saitoh, S.; Takaichi, M.; Ishizaka, R.; Tomihara, K.; Noguchi, M. Mini-microform cleft lip with complete cleft alveolus and palate: A case report. Congenit Anom 2021, 61, 133–137. [Google Scholar] [CrossRef]
  80. Volk, G.F.; Wystub, N.; Pohlmann, M.; Finkensieper, M.; Chalmers, H.J.; Guntinas-Lichius, O. Quantitative ultrasonography of facial muscles. Muscle Nerve 2013, 47, 878–883. [Google Scholar] [CrossRef]
  81. Gaszynska, E.; Kopacz, K.; Fronczek-Wojciechowska, M.; Padula, G.; Szatko, F. Electromyographic activity of masticatory muscles in elderly women—a pilot study. Clin. Interv. Aging 2017, 12, 111–116. [Google Scholar] [CrossRef] [Green Version]
  82. Miura, Y.; Yabunaka, K.; Karube, M.; Tsutaoka, T.; Yoshida, M.; Matsumoto, M.; Nakagami, G.; Kamakura, Y.; Sugama, J.; Sanada, H. Establishing a Methodology for Ultrasound Evaluation of Pharyngeal Residue in the Pyriform Sinus and Epiglottic Vallecula. Respir. Care 2020, 65, 304–313. [Google Scholar] [CrossRef]
  83. Miller, J.L.; Watkin, K.L. Lateral pharyngeal wall motion during swallowing using real time ultrasound. Dysphagia 1997, 12, 125–132. [Google Scholar] [CrossRef]
  84. Cordeiro, B.A.; Stefani, F.M.; Goldfeder, E.M. Study of the correlation between the linear measurements of the skull and face and palatal wide and length measures. Codas 2015, 27, 472–477. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  85. Moriniere, S.; Hammoudi, K.; Marmouset, F.; Bakhos, D.; Beutter, P.; Patat, F. Ultrasound analysis of the upper esophageal sphincter during swallowing in the healthy subject. Eur. Ann. Otorhinolaryngol. Head Neck Dis. 2013, 130, 321–325. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  86. Watanabe, M.; Hironaka, S.; Utsumi, A.; Murata, N.; Mukai, Y. The standardized method for ultrasound imaging of oropharyngeal on swallowing. J. Jpn. Soc. Disabil. Oral. Health 2011, 32, 19–28. (In Japanese) [Google Scholar]
  87. Manabe, N.; Haruma, K.; Nakato, R.; Kusunoki, H.; Kamada, T.; Hata, J. New ultrasonographic screening method for oropharyngeal dysphagia: Tissue Doppler imaging. Am. J. Physiol. Gastrointest. Liver Physiol. 2018, 314, G32–G38. [Google Scholar] [CrossRef] [Green Version]
  88. Miura, Y.; Nakagami, G.; Yabunaka, K.; Tohara, H.; Hara, K.; Noguchi, H.; Mori, T.; Sanada, H. Detecting pharyngeal post-swallow residue by ultrasound examination: A case series. Med. Ultrason. 2016, 18, 288–293. [Google Scholar] [CrossRef] [Green Version]
  89. Miura, Y.; Nakagami, G.; Yabunaka, K.; Tohara, H.; Murayama, R.; Noguchi, H.; Mori, T.; Sanada, H. Method for detection of aspiration based on B-mode video ultrasonography. Radiol. Phys. Technol. 2014, 7, 290–295. [Google Scholar] [CrossRef]
  90. Miura, Y.; Nakagami, G.; Yabunaka, K.; Tohara, H.; Noguchi, H.; Mori, T.; Sanada, H. A Randomized Controlled Trial to Investigate the Effectiveness of the Prevention of Aspiration Pneumonia Using Recommendations for Swallowing Care Guided by Ultrasound Examination. Healthcare 2018, 6, 15. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  91. de Miguel, M.; Pelaez, E.M.; Caubet, E.; Gonzalez, O.; Velasco, M.; Rigual, L. Accuracy of transcutaneous laryngeal ultrasound for detecting vocal cord paralysis in the immediate postoperative period after total thyroidectomy. Minerva Anestesiol. 2017, 83, 1239–1247. [Google Scholar] [CrossRef] [PubMed]
  92. Fukuhara, T.; Donishi, R.; Matsuda, E.; Koyama, S.; Fujiwara, K.; Takeuchi, H. A Novel Lateral Approach to the Assessment of Vocal Cord Movement by Ultrasonography. World J. Surg. 2018, 42, 130–136. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  93. Carneiro-Pla, D.; Miller, B.S.; Wilhelm, S.M.; Milas, M.; Gauger, P.G.; Cohen, M.S.; Hughes, D.T.; Solorzano, C.C. Feasibility of surgeon-performed transcutaneous vocal cord ultrasonography in identifying vocal cord mobility: A multi-institutional experience. Surgery 2014, 156, 1597–1602; discussion 1602–1594. [Google Scholar] [CrossRef]
  94. Turton, P.; Hay, R.; Welters, I. Assessment of peripheral muscle thickness and architecture in healthy volunteers using hand-held ultrasound devices; A comparison study with standard ultrasound. BMC Med. Imaging 2019, 19, 69. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  95. Lambell, K.J.; Tierney, A.C.; Wang, J.C.; Nanjayya, V.; Forsyth, A.; Goh, G.S.; Vicendese, D.; Ridley, E.J.; Parry, S.M.; Mourtzakis, M.; et al. Comparison of Ultrasound-Derived Muscle Thickness With Computed Tomography Muscle Cross-Sectional Area on Admission to the Intensive Care Unit: A Pilot Cross-Sectional Study. JPEN J. Parenter. Enter. Nutr. 2021, 45, 136–145. [Google Scholar] [CrossRef] [PubMed]
  96. Paris, M.T.; Letofsky, N.; Mourtzakis, M. Site-specific skeletal muscle echo intensity and thickness differences in subcutaneous adipose tissue matched older and younger adults. Clin. Physiol. Funct. Imaging 2021, 41, 156–164. [Google Scholar] [CrossRef] [PubMed]
Table 1. Protocol for evaluating the swallowing muscle mass in clinical practice.
Table 1. Protocol for evaluating the swallowing muscle mass in clinical practice.
MuscleMethods
PostureProbePosition and OrientationEvaluation Method
Geniohyoid cross-sectional area/thicknessSitting positionLinearSagittal sectionIdentify the area surrounded by fascia and calculate the cross-sectional area. Measure the muscle thickness.
Digastric cross-sectional area/thicknessSitting positionLinearVertical to muscle fibersCalculate the cross-sectional area. Measure the muscle thickness.
Mylohyoid thicknessSitting positionLinearCoronal planeMeasure the thickness of the mylohyoid muscle under the submandibular gland.
Tongue thicknessSitting positionConvexCoronal planeMeasure the distance from the mylohyoid muscle to the dorsum of the tongue.
Masseter thicknessSitting positionLinearVertical to muscle fibersMeasure the thickest site.
Depressor anguli orisSitting positionLinearVertical to muscle fibersCalculate the largest area.
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MDPI and ACS Style

Maeda, K.; Nagasaka, M.; Nagano, A.; Nagami, S.; Hashimoto, K.; Kamiya, M.; Masuda, Y.; Ozaki, K.; Kawamura, K. Ultrasonography for Eating and Swallowing Assessment: A Narrative Review of Integrated Insights for Noninvasive Clinical Practice. Nutrients 2023, 15, 3560. https://doi.org/10.3390/nu15163560

AMA Style

Maeda K, Nagasaka M, Nagano A, Nagami S, Hashimoto K, Kamiya M, Masuda Y, Ozaki K, Kawamura K. Ultrasonography for Eating and Swallowing Assessment: A Narrative Review of Integrated Insights for Noninvasive Clinical Practice. Nutrients. 2023; 15(16):3560. https://doi.org/10.3390/nu15163560

Chicago/Turabian Style

Maeda, Keisuke, Motoomi Nagasaka, Ayano Nagano, Shinsuke Nagami, Kakeru Hashimoto, Masaki Kamiya, Yuto Masuda, Kenichi Ozaki, and Koki Kawamura. 2023. "Ultrasonography for Eating and Swallowing Assessment: A Narrative Review of Integrated Insights for Noninvasive Clinical Practice" Nutrients 15, no. 16: 3560. https://doi.org/10.3390/nu15163560

APA Style

Maeda, K., Nagasaka, M., Nagano, A., Nagami, S., Hashimoto, K., Kamiya, M., Masuda, Y., Ozaki, K., & Kawamura, K. (2023). Ultrasonography for Eating and Swallowing Assessment: A Narrative Review of Integrated Insights for Noninvasive Clinical Practice. Nutrients, 15(16), 3560. https://doi.org/10.3390/nu15163560

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