Review



PART 1 Oral cavity, pharynx and esophagus

GI Motility online (2006) doi:10.1038/gimo50
Published 16 May 2006

Medical and rehabilitative therapy of oral, pharyngeal motor disorders

Jeri A. Logemann, Ph.D.

 About the contributor

View article related content

Top

Key Points

  • Effective treatment of motor-based oropharyngeal dysphagia requires accurate diagnosis of the swallow impairment.

  • The effectiveness of many treatments can be evaluated during the diagnostic procedure.

  • The medical diagnosis underlying the dysphagia affects treatment selection.

  • Treatment strategies are generally behavioral in nature such as change in posture, enhancing sensory input, dietary changes, and exercises and swallowing maneuvers.

  • Swallowing maneuvers are voluntary controls applied to specific movements used during swallowing and include tongue holding, supraglottic swallow, effortful swallow, and Mendelsohn maneuver.

  • Intraoral prostheses to lower the hard palate may be useful in selected cases. Other surgical procedures are mainly experimental in nature

Top

Introduction

Dysphagia in the oral cavity and pharynx can result from damage to motor control of various structures or muscles in the region or from damage to sensory nerves or sensory processing from the periphery to the cortex.1, 2, 3 Sensory disorders include reduced awareness of oral or pharyngeal light touch and a delay in triggering the pharyngeal swallow. Swallow apraxia, or difficulty in programming motor actions during swallow, can also have a sensory component. This review focuses on the motor disorders that disrupt the oral and pharyngeal stages of swallow.

A number of types of neurologic damage, structural damage, and muscle damage can cause oral or pharyngeal dysphagia.4, 5, 6, 7, 8, 9, 10, 11, 12 To rehabilitate or treat these motor disorders, the exact nature of the disorder must be identified and its effect on the oropharyngeal mechanism for swallowing must be carefully defined.

A number of oromotor disorders in the oral cavity can cause dysphagia, including reduced strength of labial muscles, and unilateral or bilateral paralysis of labial muscles, which affect the patient's ability to maintain lip closure and may cause drooling and loss of food from the mouth and surgical procedures. There may also be a facial weakness, either unilateral or bilateral, causing pocketing of food into the lateral sulcus or sulci. If the tongue is impaired in range of motion because of weakness, paresis, or paralysis, the individual is not able to manipulate food in the mouth for chewing, organize food into a bolus, hold a bolus, or propel the bolus from the front to the back of the oral cavity. If muscles of the floor of the mouth, including the mylohyoid, geniohyoid, and anterior belly of digastric, are weak or paralyzed, they limit the upward forward movement of the hyoid bone and larynx and thereby restrict the adequacy of the opening of the upper esophageal sphincter. If the muscles that elevate and retract the soft palate to accomplish velopharyngeal closure are damaged, then food can enter the nasal cavity, which is quite uncomfortable and affects the efficiency of the swallow.

In the pharynx, motor disorders can affect the pharyngeal walls, reducing the strength of pharyngeal wall contraction during swallow, or causing a unilateral or bilateral pharyngeal wall paresis or paralysis. The elevation of the larynx during swallow can be damaged by weakness or paralysis of thyrohyoid muscle or the muscles of the floor of the mouth mentioned earlier. These muscles elevate the hyoid and subsequently the larynx during the swallow. Normal laryngeal elevation should be approximately 2 cm in men and 1.5 cm in women, with some reduction of 1 to 3 mm over the age of 80.

The laryngeal closure mechanism begins at the true vocal folds and progresses upward to the laryngeal entrance and finally the epiglottis.13, 14 The most critical level of closure is the laryngeal entrance, where the false cords close and the arytenoids tilt forward to meet the thickening epiglottic base as the larynx elevates. Airway closure may be damaged by weakness, or unilateral or bilateral paralysis affecting all three levels. If the airway fails to close during the swallow, then food or liquid can enter the airway down to and/or below the true vocal folds, causing aspiration. If material enters just the entrance to the airway, this is penetration.1

The opening of the upper esophageal sphincter, a biomechanical sphincter, is dependent on relaxation of the muscular portion of the sphincter, the cricopharyngeus, followed by the upward and forward motion of the larynx, which physically opens the sphincter.15, 16 Weakness in the floor of mouth muscles (geniohyoid, mylohyoid, and anterior belly of digastric) can result in limited opening of the upper esophageal sphincter with food collecting above the sphincter at the pyriform sinus and then overflowing into the airway. Any of the disorders listed above can create aspiration either before the swallow occurs, as in the case of lingual dysfunction in the oral cavity, or after the swallow if leftover material in the pharynx (residue) is inhaled or falls into the airway.17, 18

The tongue base is critical to pressure generation during the pharyngeal stage of swallow. The tongue base begins its backward motion as the tail of the bolus reaches it, causing pressure against the bolus tail to drive the bolus through the pharynx in combination with the contraction of the pharyngeal constrictors. The lowest portion of the superior constrictor, also known as the glossopharyngeus muscle, is responsible for the posterior movement of the tongue base to contact the anteriorly moving pharyngeal wall. Motor impairment of this glossopharyngeus muscle results in reduced movement of the tongue base posteriorly and residue remaining in the valleculae after the swallow. Any disorder causing residue in the pharynx after the swallow can result in aspiration after the swallow as the airway reopens, breathing begins again, and food can fall or be sucked into the airway.

The most significant sensory impairment in the oropharyngeal stages of swallow is a delay in triggering of the pharyngeal swallow.19, 20, 21 This delay can result from a variety of types of damage to the sensory pathways from the periphery to the brainstem. If there is sensory loss in the pharynx or oral cavity itself, an adequate signal may not be sent to the medulla to trigger the pharyngeal stage of swallow, or age or other damage to the medulla may reduce or delay its ability to recognize the incoming sensory stimulus from the periphery. A number of studies have determined that aging slows processing in the central nervous system, resulting in a slight delay in the triggering of the pharyngeal swallow, even in normal subjects over the age of 60. During pharyngeal delay, the bolus is propelled from the oral cavity by the oral tongue. The bolus then falls by gravity through the pharynx and, depending on its consistency, may land in the valleculae, the pyriform sinuses, or the open airway. The airway does not close unless the pharyngeal swallow has been triggered and motor activity for the pharyngeal swallow has been initiated.

Top

Diagnosis

Diagnosis of Oropharyngeal Dysphagia

Accurate diagnosis of the specific oral or pharyngeal motor impairment in each patient is the crucial first step in management of oropharyngeal dysphagia. The patient's external symptoms may include coughing or throat clearing, or obvious increased effort for swallow or repeated swallows on one bolus if there is difficulty generating adequate pressure on the bolus to propel it efficiently through the oral cavity or pharynx. It is important to note, however, that approximately 50% of patients who aspirate do not cough or give any external sign of food or liquid entering the airway. The patient's history, medical diagnosis, and other characteristics can assist the clinician in pointing toward the specific swallow abnormality in the oral cavity or pharynx. Generally, however, an instrumental imaging study of the oral cavity and pharynx, particularly the pharynx, is necessary in order to accurately identify the muscle or muscles that are damaged.

Diagnostic Imaging Studies

Diagnostic imaging procedures for the oral cavity and pharynx should be done to determine the specific types of motor disorders present followed by the introduction of treatment strategies in order to evaluate their effectiveness. There are two primary diagnostic procedures used to assess the oral cavity and pharynx during swallow: videoendoscopy and videofluoroscopy.2, 22, 23, 24, 25 Videoendoscopy has the advantage of providing no x-ray exposure to the patient and being portable. However, there are several disadvantages to this procedure including the inability to visualize the oral aspects of the swallow and the inability to visualize the critical aspects of the pharyngeal stage of swallow including tongue-base motion, laryngeal elevation, and upper esophageal sphincter.23, 24 However, the portable nature of the endoscopic equipment can make it a choice by clinicians for use in nursing homes and intensive care units, where it may not be easy to transport a patient to a radiologic suite in acute care.

In contrast, the use of videofluoroscopy enables the clinician to visualize all aspects of the oral and pharyngeal stages of swallow except vocal fold closure during the pharyngeal swallow.23, 24 However, the oral stage can be examined in detail, as can pharyngeal triggering and the majority of the motor aspects of the pharyngeal stage of swallowing. In either case, the clinician should utilize a consistent protocol as each patient is examined in order to compare one individual to another, normal subjects to dysphagic patients, and a patient to him- or herself over time. The protocol should include a sampling of bolus volumes and viscosities, because both variables can significantly affect the timing and organization of the normal oropharyngeal swallow and the disordered swallow. For example, the volume of the bolus can significantly change bolus transit times, that is, bolus movement through the oral cavity and pharynx as well as the duration and width of upper esophageal sphincter opening and airway closure. The most typical protocol utilized during videofluoroscopy involves presentation of 1, 3, 5, or 10 mL of thin liquids, cup-drinking of thin liquids, straw-drinking of thin liquids, 3 mL of pudding-thick barium, and one quarter of a Lorna Doone cookie coated with barium pudding to be chewed so that mastication can be visualized.2 At least two swallows of each of these bolus types is given in order to gain a clear understanding of motor control of the oral cavity and pharynx for deglutition. If a physiologic or anatomic disorder is observed, the clinician should identify that disorder and, if aspiration results or if there is significant residue after the swallow, the clinician should introduce one or more treatment strategies to examine their immediate effectiveness in improving the patient's swallow. All of the treatment procedures described below except exercise programs can be introduced and evaluated for effectiveness during the radiographic study.1, 3, 26, 27

Top

Treatments

Treatment for Disorders of the Oropharyngeal Swallow

Treatment strategies in the oral cavity and pharynx are generally behavioral in nature, because this is a mechanism that does not respond well to surgical procedures28, 29, 30 and for which no drugs have been identified to improve any or all swallow disorders.1, 31, 32

Postures

Treatment procedures often begin with postural changes, which affect the direction and speed of bolus flow through the mouth and pharynx.3 There are five postural procedures that can impact specific aspects of the swallow as shown in Table 1. The change in posture does not normalize the motor disorder but rather compensates for it, is generally used only temporarily, while spontaneous recovery can take effect, or while sensory stimulation or exercise programs can improve the swallow.


Heightening Sensory Input

A second set of treatment strategies involves heightening sensory input.20, 33 These procedures are generally used for patients with a delay in triggering the pharyngeal swallow, which is a sensory disorder rather than a motor one. Such strategies as changing bolus volume, changing bolus viscosity, or introducing boluses of a strong taste including sour boluses or carbonated boluses can heighten and facilitate faster triggering of the pharyngeal swallow. The more that we understand the way in which normal swallow physiology changes systematically with bolus characteristics, the more we will be able to use this information to understand swallowing disorders and understand the patient with specific oral and pharyngeal swallowing disorders.

Exercise Programs Including Swallow Maneuvers

Another classification or type of rehabilitation technique for the motor disordered dysphagic patient is an exercise program. There are a number of exercises for specific muscles or muscle groups in the oral cavity and pharynx that can be effective in remediating specific swallowing disorders. They may take 2 weeks to 2 months to take effect. For patients with weakness in facial and labial muscles, resistance and range-of-motion exercises can be very helpful. Range-of-motion exercises typically involve moving the target structures to their furthest extension, holding the extended position with effort for 1 second, and then releasing it. Such exercises can be used for the lips and facial muscles as well as lingual muscles. Resistance exercises in which a tongue blade or instrument such as the Iowa Oral Pressure Instrument is pushed against the tongue while the tongue attempts to resist are also known as strengthening exercises. These exercises can be quite effective in improving tongue strength and coordination. Recently, data have been presented illustrating that increasing tongue strength will be applied immediately to the act of swallowing with no transitional therapy.34 These exercises are useful in many patients with generalized lingual weakness and in normal elderly individuals who lose tongue strength from aging. They are not appropriate for patients with motor neuron disease, as they only cause additional fatigue. There have been no exercises defined as consistently effective for improving velopharyngeal closure for swallowing.

Tongue-base exercises are quite different from lingual tongue exercises. Although the lingual tongue is generally elevating during swallow and its contact to the palate is moving posteriorly, the tongue base is retracting on a horizontal plane during swallow. Three exercises have been found to be helpful for the tongue base35: (1) pulling the tongue straight back in the mouth to its maximum position and hold with effort for 1 second, (2) gargling and holding the tongue in its retracted position for 1 second, and (3) yawning and holding the tongue in the most posterior position for 1 second. Clinicians can assess the extent of tongue-base motion with these procedures during videofluoroscopy and identify the one that results in greatest movement. Repeating "ka/ ka/ ka" or "ga/ ga/ ga" is not an exercise for the tongue base, because it results in vertical movement of the back of the tongue rather than horizontal movement of the base of the tongue.

An exercise to improve laryngeal and hyoid upward forward motion to open the upper esophageal sphincter is the Shaker exercise.36, 37, 38 In this exercise, patients lie on their back on a bed or the floor and elevate their head to see their toes while keeping their shoulders against the bed or floor. They then hold the head up for 1 minute, followed by 1 minute of rest. After three repetitions of 1 minute with the head lifted and 1 minute of rest, patients are instructed to lift their head to see their toes and let it down 30 times. This exercise is not appropriate for patients with significant arthritis or damage to their neck.

Swallow Maneuvers

Swallowing maneuvers are generally voluntary controls applied to a specific movement used during swallow.39, 40, 41 There is very little exercise designed to improve pharyngeal wall activity other than the tongue-holding maneuver, which involves holding the tongue tip between the teeth gently but firmly and swallowing with the oral tongue in that position. Holding the tongue in this position pulls the tongue forward, forcing the glossopharyngeal fibers (the lowest fibers) of the superior constrictor to contract more strongly, resulting in a greater bulge at the portion of the posterior pharyngeal wall.42, 43 This is an exercise and cannot be used to eat, because the maneuver makes it more awkward to trigger a pharyngeal swallow with the oral tongue in that position.

Several other swallow maneuvers are helpful in improving specific muscle activities in the pharynx. They can be utilized during swallows and, therefore, during eating. The supraglottic swallow is designed to close the airway voluntarily at the level of the true vocal folds.14, 44 Patients are instructed to hold their breath gently before and during the swallow and to cough when the swallow is completed to clear any residue. The super-supraglottic swallow is designed to close the entrance to the airway before and during the swallow by again holding the breath but this time while bearing down. Bearing down increases muscle effort and closes not only the true vocal folds but also the false vocal folds.44, 45 The arytenoid cartilages are pulled more anteriorly during a super-supraglottic swallow, causing narrowing of the region above the false cords. This procedure is generally used in patients who have undergone laryngeal surgeries such as a supraglottic laryngectomy.

A third swallow maneuver is the effortful swallow. During the effortful swallow, patients are asked to squeeze hard with all of the muscles in their mouth and their throat.46 This increased effort results in greater pressure during swallow and, therefore, better oral tongue and tongue-base movement and less pharyngeal residue. This maneuver can be utilized during eating, though patients may tire more quickly during a meal.

The fourth swallow maneuver is the Mendelsohn maneuver, designed to improve hyolaryngeal elevation and forward movement during the swallow, thereby opening the upper esophageal sphincter more widely and longer to facilitate the clearance of the bolus into the esophagus.47, 48 There are several directions that can achieve the Mendelsohn maneuver. The first is to ask patients to swallow several times and feel with their muscles (not their hand) the degree of lifting in their neck by their voice box. When they can perceive that their voice box does lift during swallow, they are asked to swallow again, and as their voice box elevates, to grab it with muscles—not their hand—and to hold their larynx up for an extra few seconds. The effort of holding the larynx up generally increases the extent and duration of laryngeal elevation, thereby opening the upper esophageal sphincter longer and wider. Although this is generally an exercise, it can be utilized to improve upper esophageal sphincter opening during food swallows.

A second set of directions for this maneuver involves asking patients to feel as they swallow to see if they can perceive that a squeeze occurs during swallow, which is the point at which the tongue base, pharyngeal wall, and larynx all come together. Patients can be instructed to "hold the squeeze" for several seconds. It is at that point that the larynx is most elevated and that elevation can be increased with effort.

Intraoral Prostheses

The development of an intraoral prosthetic to lower the hard palate to meet the tongue that is restrictive in bulk or range of motion can have a major effect on the efficiency or safety or the oropharyngeal swallow.49, 50, 51 These prosthetics are designed individually, usually by the maxillofacial prosthodontist and a speech-language pathologist.

Experimental Treatment Procedures

There have been a number of experimental procedures described recently for improvement of motor control of swallow. None of these procedures has any experimental evidence to support its effectiveness. These procedures include myofascial release, designed to release any scar tissue or connective tissue inhibiting movement of structures in the pharynx; neuromuscular electrical stimulation (NMES), designed to improve the strength of muscle contraction during swallow; and deep pharyngeal neuromuscular stimulation (DPNS), designed to utilize reflexive activity in the pharynx to improve swallow. The rationale for many of these procedures and their effectiveness are unclear. These types of procedures should be utilized with care until efficacy data are clearly identified.

Diet Change

Changing a patient's diet can eliminate some of the effects of dysphagia such as aspiration.

Thickened Liquids

In the past 10 years, thickening liquids to nectar or honey consistencies has become popular to manage aspiration of thin liquids in a wide range of patients, particularly those in nursing homes and other residential facilities.52 Unfortunately, the data to support the efficacy of these procedures is not strong and the use of thickened liquids can reduce the patient's quality of life and hydration. The ongoing clinical trial mentioned earlier, when completed in 2006, should provide us with a great deal more data on the true effectiveness of nectar and honey consistency liquids in contrast to chin-down posture for patients with dementia and/or Parkinson's disease.

Studies have shown that heightening sensory input in the form of strong taste (sour) or carbonation may improve some motor characteristics of the swallow.19, 53 Much more research on the effects of bolus characteristics is needed to understand which motor disorders can be affected by various bolus characteristics.19, 20

Top

The Effect of Diagnosis on Selection of Treatment Strategies and of Needed Treatment

Medical diagnosis as well as the patients' specific swallow disorders often determines which treatment is used, as summarized in Table 2. Patients with motor neuron disease, including amyotrophic lateral sclerosis (ALS), postpolio syndrome, and, in children, Werdnig-Hoffmann disease and spinal muscular atrophy, are generally not candidates for active exercise programs because the exercises will only fatigue involved musculature. Instead, patients can be given postural changes and sensory stimulation, but not swallow maneuvers, which will only increase fatigue. In contrast, patients who have been treated for head and neck cancer, whether by surgery, radiotherapy, or chemoradiation, generally need muscle exercise for recovery. Range of motion exercises, resistance exercises, and swallow maneuvers are all helpful in these patients to strengthen muscles and improve range of motion for swallowing. Similarly, many neurologic patients, especially those who have suffered stroke, head injury, and spinal cord injury, can utilize exercise programs to facilitate their recovery. Some progressive neurologic diseases such as Parkinson's disease will respond well to range of motion exercises. An exercise program known as the Lee Silverman Voice Treatment® (LSVT) program, which focuses on increasing the vocal loudness used by patients, can certainly facilitate swallow by improving tongue function and eliminating the regular tongue pumping seen in these patients.54 The increase in muscular drive to the upper aerodigestive tract, also known as the vocal tract, generated by increasing loudness also improves speech articulation and swallow. This is an example of one exercise program that facilitates a variety of functions in the upper aerodigestive tract. There may be other such specific exercise programs that are appropriate to patients with various diagnoses that have not yet been identified.


Top

Future Considerations

The future of rehabilitation of patients with various motor disorders of oropharyngeal swallow will depend on the care with which new procedures are developed and evaluated. The use of randomized clinical trials is critical to objectively evaluate the effectiveness of treatment strategies. A number of such treatment strategies are currently being evaluated, including the Shaker exercise versus traditional range-of-motion and resistance exercises, the use of thickened liquids to facilitate safe swallow in patients with dementia or Parkinson's disease with or without dementia as compared to chin-down posture, and the use of traditional exercise programs versus posture changes and sensory therapy in patients treated for head and neck cancer who exhibit dysphagia. All of these studies utilize randomized assessment and treatment and should provide us with a great deal more information on therapy programs that are successful for specific types of patients with oropharyngeal dysphagia. There is, however, a great deal more work to be done to understand the effects of various therapy procedures on specific populations. We cannot assume one therapy procedure is best for all patients, but must evaluate each treatment procedure in relation to the patient's diagnosis and other characteristics.

Article related content

Top

References

  1. Logemann JA, ed. Swallowing disorders & rehabilitation. J Head Trauma Rehabil 1989:4; Part 4
  2. Logemann JA. A Manual for the Videofluoroscopic Evaluation of Swallowing, 2nd ed. Austin, TX: Pro-Ed, 1993.
  3. Logemann JA. Evaluation and Treatment of Swallowing Disorders. Austin, TX: Pro-Ed, 1983, 1998.
  4. Bartolome G, Neuman DS. Swallowing therapy in patients with neurological disorders causing cricopharyngeal dysfunction. Dysphagia 1993;8:146–149. | Article | PubMed | ChemPort |
  5. Dworkin JP, Nadal JC. Nonsurgical treatment of drooling in a patient with closed head injury and severe dysarthria. Dysphagia 1991;6:40–49. | PubMed | ChemPort |
  6. Helfrich-Miller KR, Rector KL, Straka JA. Dysphagia: its treatment in the profoundly retarded patient with cerebral palsy. Arch Phys Med Rehabil 1986;67:520–525. | PubMed | ChemPort |
  7. Logemann JA, Pauloski BR, Rademaker AW, Colangelo LA. Speech and swallowing rehabilitation in head and neck cancer patients. Oncology 1997;11(5):651–659.
  8. Logemann JA, et al. Mechanisms of recovery of swallow after supraglottic laryngectomy. J Speech Hear Res 1994;37:965–974. | PubMed | ChemPort |
  9. Neuman S. Swallowing therapy with neurologic patients: results of direct and indirect therapy methods in 66 patients suffering from neurological disorders. Dysphagia 1993;8:150–153. | PubMed |
  10. Rademaker AW, et al. Recovery of postoperative swallowing in patients undergoing partial laryngectomy. Head Neck 1993;15:325–334. | PubMed | ChemPort |
  11. Tippett DC, Palmer J, Linden P. Management of dysphagia in a patient with closed head injury: a case report. Dysphagia 1987;1:221–226. | Article |
  12. Ylvisaker M, Logemann JA. Therapy for feeding and swallowing following head injury. In: Ylvisaker M, ed. Management of Head Injured Patients. San Diego: College Hill, 1986.
  13. Logemann JA, et al. Closure mechanisms of the laryngeal vestibule during swallowing. Am J Physiol 1992;262:G338–G344. | PubMed | ChemPort |
  14. Martin BJW, Logemann JA, Shaker R, Dodds WJ. Normal laryngeal valving patterns during three breath hold maneuvers: a pilot investigation. Dysphagia 1993;8:11–20. | Article | PubMed | ChemPort |
  15. Cook IJ, et al. Opening mechanism of the human upper esophageal sphincter. Am J Physiol 1989;257:G748–759. | PubMed | ChemPort |
  16. Jacob P, Kahrilas PJ, Logemann JA, Shah V, Ha T. Upper esophageal sphincter opening and modulation during swallowing. Gastroenterology 1989;97:1469–1478. | PubMed | ChemPort |
  17. Kahrilas PJ, Lin S, Logemann JA, Ergun GA, Facchini F. Deglutitive tongue action: volume accommodation and bolus propulsion. Gastroenterology 1993;104:152–162. | PubMed | ChemPort |
  18. Kahrilas PJ, Logemann JA, Lin S, Ergun GA. Pharyngeal clearance during swallow. A combined manometric and videofluoroscopic study. Gastroenterology 1992;103:128–136.. | PubMed | ChemPort |
  19. Bisch EM, Logemann JA, Rademaker AW, Kahrilas PJ, Lazarus CL. Pharyngeal effects of bolus volume, viscosity and temperature in patients with dysphagia resulting from neurologic impairment and in normal subjects. J Speech Hear Res 1994;37:1041–1049. | PubMed | ChemPort |
  20. Lazarus CL, et al. Effects of bolus volume, viscosity & repeated swallows in nonstroke subjects and stroke patients. Arch Phys Med Rehabil 1993;74:1066–1070. | Article | PubMed | ChemPort |
  21. Lazzara G, Lazarus C, Logemann JA. Impact of thermal stimulation on the triggering of the swallowing reflex. Dysphagia 1986;1:73–77.
  22. Logemann JA. The dysphagia diagnostic procedure as a treatment efficacy trial. Clin Commun Dis 1993;3(4):1–10.
  23. Logemann JA, Rademaker AW, Pauloski BR, Ohmae Y, Kahrilas PJ. Normal swallowing physiology as viewed by videofluoroscopy and videoendoscopy. Folia Phoniatr Logop 1998;50:311–319. | Article | PubMed | ChemPort |
  24. Logemann JA, Rademaker AW, Pauloski BR, Ohmae Y, Kahrilas PJ. Interobserver agreement on normal swallowing physiology as viewed by videofluoroscopy and videoendoscopy. Folia Phoniatr Logop 1999;51:91–98. | Article | PubMed | ChemPort |
  25. Martin-Harris B, Logemann JA, McMahon S, Schleicher M, Sandidge J. Clinical utility of the modified barium swallow. Dysphagia 2001;15:136–141.
  26. Rasley A, Logemann JA, Kahrilas PJ, Rademaker AW, Pauloski BR, Dodds WJ. Prevention of barium aspiration during videofluoroscopic swallowing studies: value of change in posture. AJR 1993;160:1005–1009. | PubMed | ChemPort |
  27. Shanahan TK, Logemann JA, Rademaker AW, Pauloski BR, Kahrilas PJ. Chin down posture effects on aspiration in dysphagic patients. Arch Phys Med Rehabil 1993;74:736–739. | Article | PubMed | ChemPort |
  28. Berg HM, Jacobs JB, Persky MS, Cohen NL. Cricopharyngeal myotomy: a review of surgical results in patients with cricopharyngeal achalasia of neurogenic origin. Laryngoscope 1985;95(11):1337–1340.
  29. Chodosh PL. Cricopharyngeal myotomy in the treatment of dysphagia. Laryngoscope 1975;85(11 pt 1):1862–1873.
  30. Jacobs J, et al. Failure of cricopharyngeal myotomy to improve dysphagia following head and neck cancer surgery. Arch Otolaryngol Head Neck Surg 1999;125:942–946. | PubMed | ChemPort |
  31. Bryant M. Biofeedback in the treatment of a selected dysphagic patient. Dysphagia 1991;6:140–144. | PubMed | ChemPort |
  32. Kasprisin AT, Clumeck A, Nino-Murcia M. The efficacy of rehabilitative management of dysphagia. Dysphagia 1989;4:48–52. | Article | PubMed | ChemPort |
  33. Fujiu M, Toleikis JR, Logemann JA, Larson CR. Glossopharyngeal evoked potentials in normal subjects following mechanical stimulation of the anterior faucial pillar. Electroencephalogr Clin Neurophysiol 1994;92:183–195. | PubMed | ChemPort |
  34. Robbins JA. Tongue strengthening: dysphagia intervention and prevention. Presentation at Annual Meeting of Dysphagia Research Society, Montreal, Quebec, Canada, October 13, 2004.
  35. Veis S, Logemann JA, Colangelo LA. Effects of three techniques on maximum posterior movement of tongue base. Dysphagia 2000;15:142–145. | PubMed | ChemPort |
  36. Shaker R, et al. Rehabilitation of swallowing by exercise in tube-fed patients with pharyngeal dysphagia secondary to abnormal UES opening. Gastroenterology 2002;122(5):1314–1321.
  37. Shaker R, Kern M, Bardan E, Arndorfer R, Hofmann C. Effect of isotonic/isometric head life exercise on hypopharyngeal intrabolus pressure. Dysphagia 1997;12(2):107.
  38. Shaker R, et al. Augmentation of deglutitive esophageal sphincter opening in the elderly by exercise. Am J Physiol 1997;272:G1518–G1522. | PubMed | ChemPort |
  39. Lazarus C, Logemann JA, Gibbons P. Effects of maneuvers on swallowing function in a dysphagic oral cancer patient. Head Neck 1993;15:419–424. | PubMed | ChemPort |
  40. Kahrilas PJ, Logemann JA, Gibbons MS. Food intake by maneuver; An extreme compensation for impaired swallowing. Dysphagia 1992;7:155–159. | PubMed | ChemPort |
  41. Lazarus CL, Logemann JA, Song CW, Rademaker AW, Kahrilas PJ. Effects of voluntary maneuvers on tongue base function for swallowing. Folia Phoniatr Logop 2002;54(2):171–176.
  42. Fujiu M, Logemann JA. Effect of a tongue holding maneuver on posterior pharyngeal wall movement during deglutition. Am J Speech Lang Pathol 1996;5:23–30.
  43. Fujiu M, Logemann JA, Pauloski BR. Increased postoperative posterior pharyngeal wall movement in patients with anterior oral cancer: preliminary findings and possible implications for treatment. Am J Speech Lang Pathol 1995;4:24–30.
  44. Ohmae Y, Logemann JA, Kaiser P, Hanson DG, Kahrilas PJ. Effects of two breath-holding maneuvers on oropharyngeal swallow. Ann Otol Rhinol Laryngol 1996;105:123–131. | PubMed | ChemPort |
  45. Logemann JA, Pauloski BR, Rademaker AW, Colangelo LA. Super-supraglottic swallow in irradiated head and neck cancer patients. Head Neck 1998;19(6):535–540.
  46. Pouderoux P, Kahrilas PJ. Deglutitive tongue force modulation by volition, volume, and viscosity in humans. Gastroenterology 1995;108(5):1418–1426.
  47. Kahrilas PJ, Logemann JA, Krugler C, Flanagan E. Volitional augmentation of upper esophageal sphincter opening during swallowing. Am J Physiol 1991;260:G450–456. | PubMed | ChemPort |
  48. Logemann JA, Kahrilas PJ. Relearning to swallow post CVA: application of maneuvers and indirect biofeedback: a case study. Neurology 1990;40:1136–1138. | PubMed | ChemPort |
  49. Davis J, Lazarus C, Logemann J, Hurst P. Effect of a maxillary glossectomy prostheses on articulation and swallowing. J Prosthet Dent 1987;57(6):715–719.
  50. Logemann J, Kahrilas P, Hurst P, Davis J, Krugler C. Effects of intraoral prosthetics on swallowing in oral cancer patients. Dysphagia 1989;4:118–120. | Article | PubMed | ChemPort |
  51. Marunick M, Tselios N. The efficacy of palatal augmentation prostheses for speech and swallowing in patients undergoing glossectomy. J Prosthet Dent 2004;91(1):67–74.
  52. Castellanos VH, Butler E, Gluch L, Burke B. Use of thickened liquids in skilled nursing facilities. J Am Diet Assoc 2004;104:1222–1226. | Article | PubMed |
  53. Logemann JA, Pauloski BR, Colangelo L, Lazarus C, Fujiu M. Effects of a sour bolus on oropharyngeal swallowing measures in patients with neurogenic dysphagia. J Speech Hear Res 1995;38(3):556–563.
  54. El Sharkawi A, et al. Swallowing and voice effects of Lee Silverman Voice Treatment (LSVT®): a pilot study. J Neurol Neurosurg Psychiatry 2002;72:31–36. | Article | PubMed |
  55. Horner J, Massey EW, Riski JE, Lathrop D, Chase KN. Aspiration following stroke: Clinical correlates and outcomes. Neurology 1988;38:1359–1362. | PubMed | ChemPort |
  56. Karaho T, Hanyu Y, Murase Y, Kitahara S, Inouye, T. Effect of posture strategies on preventing aspiration. Journal of Otolaryngology (Japan) 1997;100:220–226.
  57. Logemann JA, Rademaker AW, Pauloski BR, Kahrilas PJ. Effects of postural change on aspiration in head and neck surgical patients. Otolaryngol Head Neck Surg 1994;110:222–227. | PubMed | ChemPort |
  58. Welch MV, Logemann JA, Rademaker AW, Kahrilas PJ. Changes in pharyngeal dimensions effected by chin tuck. Arch Phys Med Rehabil 1993;74:178–181. | PubMed | ChemPort |
  59. Ohmae Y, Ogura M, Taraho T, Kitahara S, Inouye T. Effects of head rotation on pharyngeal function during normal swallow. Ann Otol Rhinol Laryngol 1998;107:344–348. | PubMed | ChemPort |
  60. Logemann J, Kahrilas P, Kobara M, Vakil N. The benefit of head rotation on pharyngo-esophageal dysphagia. Arch Phys Med Rehabil 1989;70:767–771. | PubMed | ChemPort |