Dysphagia Unplugged



Dysphagia Unplugged


MICHAEL E. GROHER and JO PUNTIL-SHELTMAN




WHAT IS DYSPHAGIA?


Dysphagia takes its name from the Greek root phagein, meaning to ingest or engulf. Combined with the prefix dys-, it connotes a disorder of or difficulty with swallowing. It is correctly pronounced with a long or short “a.” The final syllable, “ja,” requires a hard pronunciation rather than the soft “dja” to avoid confusion with the communicative language disorder, dysphasia.


Taber’s Cyclopedic Medical Dictionary1 defines five subcategories of dysphagia:



In clinical practice, only oropharyngeal dysphagia from this list is used with any frequency.



Interestingly, medical students learn that dysphagia is a swallowing problem primarily associated with disease of the esophagus. However, when used properly the term should refer to a swallowing disorder that involves any one of the three stages of swallowing: oral, pharyngeal, or esophageal. It is not a primary medical diagnosis but rather a symptom of underlying disease and therefore is described most often by its clinical characteristics (signs). Complaints such as coughing and choking during or after a meal, food sticking, regurgitation, odynophagia, drooling, unexplained weight loss, and nutritional deficiencies all may be associated with dysphagia. Because dysphagia is a symptom of underlying disease that is not necessarily specific to the swallowing tract, it can be associated with varied diagnoses. These diagnoses are summarized in Box 1-1. Throughout this text, most of these diagnoses will receive individualized attention. See Chapter 7 for a full discussion of symptoms and signs associated with dysphagia.



Dictionary-based definitions of dysphagia imply that it is the result of a physiologic change in the muscles needed for swallowing. Physiologic change often leads to the two hallmarks of dysphagia: delay in the propulsion of a bolus as it transits from the mouth to the stomach and/or misdirection of a bolus. Misdirection can be defined as bolus material entering the upper airway and/or lungs or material that enters the mouth, pharynx, or esophagus during swallowing attempts but fails to reach the stomach. In these circumstances, classification of dysphagia by either clinical or instrumental examination seems warranted and straightforward.



However, not all patients with physiologic abnormalities of the swallowing mechanism show obvious delay in bolus flow or misdirection of bolus flow. The question that may arise for the clinician (and often for the researcher who has selected a cohort of patients with dysphagia) is the degree of severity of physiologic changes in the swallowing musculature needed before a patient is classified as having dysphagia. For instance, physiologic changes in the swallowing musculature have been described in older persons2—such as reduction in tongue strength or esophageal motility—both of which may delay the delivery of food or liquid to the stomach. However, only when such changes result in perceptible changes in eating habits or associated medical complications such as undernutrition or aspiration pneumonia is a person classified as truly having dysphagia. Because swallowing is a dynamic process, persons may not exhibit signs and symptoms of dysphagia with every swallow and every bolus type. In these cases, they may be considered to be at risk for dysphagia or, alternatively, operationally defined as dysphagic. It is also possible that the swallowing musculature is normal but the patient is not alert enough to use that musculature because of his or her decompensated medical condition. In such cases it is assumed that attempts to swallow would result in dysphagic complications. In these cases, the patient may be classified as at risk for dysphagia. Patients may demonstrate abnormalities of behavior that interfere with the normal swallowing process; these may cause dysphagic signs and symptoms or put the patient at risk for dysphagia. Therefore dysphagia is defined not only by abnormalities of the mechanics of the swallowing musculature, but also by the consequences of failure, or potential failure, of that musculature owing to factors not always specifically related to swallow mechanics. For this reason the authors prefer the definition of dysphagia offered by Tanner3: “Dysphagia: [an] impairment of emotional, cognitive, sensory, and/or motor acts involved with transferring a substance from the mouth to stomach, resulting in failure to maintain hydration and nutrition, and posing a risk of choking and aspiration” (p. 152).




A swallowing disorder should be distinguished from a feeding disorder. A feeding disorder is impairment in the process of food transport outside the alimentary system. A feeding disorder usually is the result of weakness or incoordination in the hand or arm used to move the food from the plate to the mouth. In the United Kingdom and the United States a feeding disorder, particularly in the context of infants and children, may be the same as a swallowing disorder. Persons with feeding disorders (motor transfer problems) also may be dysphagic, such as those with cerebral palsy whose neurologic disability affects both feeding (motoric transfer) and swallowing. It is not known whether a feeding disorder that might require assistance with food transport also affects the subsequent act of swallowing, perhaps by interfering with timing of swallowing events.


A swallowing disorder also is to be distinguished from an eating disorder such as anorexia or bulimia nervosa. Whereas patients with dysphagia, bulimia, and anorexia may have difficulty with poor appetite, changes in dietary selections, and problems with the oral preparation of the bolus, patients with bulimia and anorexia rarely have demonstrable changes in or complaints of swallowing difficulty.4



INCIDENCE AND PREVALENCE


The incidence of a disorder is the reported frequency of new occurrences of that disorder over a long time (usually at least 1 year) in relation to the population in which it occurs. The prevalence of a disorder is the number of cases in a population during a shorter, prescribed period, usually in a specific setting. Exact measures of the incidence and prevalence of swallowing disorders in large and various populations are impossible because of differences in accepted definitions of dysphagia, the setting in which it is measured (acute, rehabilitation, chronic), and differences in the measurement tools across studies to detect it.5 For instance, asking a patient if she or he has a swallowing disorder to determine the prevalence is a very different method of detection compared with the use of an instrumental examination such as videofluoroscopy. Most demographic data that are reported relating to swallowing disorders are prevalence data. The importance of knowing the prevalence of a disorder can help guide clinicians in the detection of that disorder and therefore helps plan how resources might be devoted to that disorder. For instance, if an examiner knew that a certain abnormality was found in less than 1% of that population, the examiner may not spend time looking for that abnormality because its expected frequency of occurrence would be low. If, however, a particular abnormality was found in more than 50% of the persons with a particular disorder, the examiner would be alerted to expect the occurrence of deficits associated with that disorder. Therefore if the data suggested that 50% of patients who have had an acute stroke could have dysphagia, and that 20% of that group might have silent aspiration, an examiner would expect that half of the patients with acute stroke would have swallowing impairment and about half of those are at high risk for silent aspiration. Furthermore, pneumonia develops in 37% of acute stroke patients with aspiration.6 Knowledge of these prevalence data provides valuable assistance to medical personnel who initially screen for and manage the medical complications after acute stroke (see Chapter 4).



The American Speech-Language-Hearing Association (ASHA) estimates that 6 to 10 million Americans show some degree of dysphagia, although it is not known how these estimates were made.7 Kuhlemeier8 reported that the incidence of reported dysphagia in the state of Maryland rose from 3 in 1000 in 1979 to 10 in 1000, probably as a result of better reporting methods. Using these estimates, approximately 25,000 persons in Maryland in 1989 had dysphagia as either a primary or secondary diagnosis.



Prevalence by Setting


Estimates of prevalence of dysphagia vary by setting because certain age groups (older adults and newborns) and diagnoses (neurogenic) are more likely to demonstrate dysphagia. For instance, patients entering a rehabilitation setting may not have as many accompanying medical problems and dysphagia as those entering a nursing home. Conversely, infants born prematurely may have many medical problems that may secondarily result in dysphagia. In a survey of the entire population of an acute general hospital, fewer patients with dysphagia would be found in the general population compared with a survey of a special section of that hospital, such as the stroke unit.



Community


Estimates of the prevalence of dysphagia among older persons living in the community range from 16% to 22%.9,10 One study reported on the prevalence of dysphagia in a younger cohort (14- to 30-year-olds) living in the community who had been referred for complaints of dysphagia.11 In this selected group, 70% had demonstrable pathologic conditions that accompanied their symptoms.



Acute and Chronic Geriatric Care


Of the 211 patients admitted to an acute geriatric unit in Singapore, the prevalence of dysphagia was 29% on admission and 28% at discharge.12 In a nursing home in Maryland (chronic care), as many as 60% of residents had a combination of swallowing and/or feeding difficulty.13 One study found that when feeding and swallowing difficulty were combined, as many as 87% of the residents in a home for the aged were at risk for inadequate oral intake.14 Follow-up data of nursing home residents with oropharyngeal dysphagia indicate a mortality rate of 45% at 1 year.15



Acute General Hospitals


Using the Fleming Index of Dysphagia, a tool to identify dysphagia, Layne et al.16 found that nearly one third of their patients had a diagnosis consistent with dysphagia. These findings were nearly 18% higher than those provided by Groher and Bukatman,17 who reported a 13% prevalence rate in similar settings. The discrepancy in prevalence was explained by the fact that patients who were dehydrated in the study by Layne et al. were classified as dysphagic, whereas this was not a marker for dysphagia used in the collection of the Groher and Bukatman data.



Acute Rehabilitation Unit


Of 307 consecutive admissions to an acute rehabilitation facility, one third of patients were dysphagic.18 Of this group, half had dysphagia as a result of a stroke, followed by traumatic brain injury (20%), spinal cord injury and brain tumor (7%), and progressive neurologic disease (5%). On admission, the patients with the most severe dysphagia were those with traumatic brain injury, followed by stroke. The least severe dysphagia occurred in those with brain tumors.



Special Populations


Some primary medical diagnoses are more likely to precipitate dysphagic symptomatology, such as diseases that affect the central and peripheral nervous system and disorders affecting the structures of the alimentary tract, such as cancer. An estimated 300,000 to 600,000 persons in the United States each year are affected by dysphagia from neurologic disorders alone; most cases occur after a stroke.5 If these data are reliable, dysphagia is a common symptom after a stroke.



Stroke

Prevalence reports of dysphagia after stroke depend on when in the course of recovery the detection of a swallowing impairment was made. For instance, in acute stroke (less than 5 days after onset) the prevalence of dysphagia may be as high as 50%, whereas 2 weeks after stroke only 10% to 28% of patients may be dysphagic. Recognizing these discrepancies, Smithard et al.19 provided follow-up of 121 (untreated) acute stroke patients for 6 months using a clinical dysphagia examination and videofluoroscopy to detect swallowing deficits. Immediately after stroke, 51% were believed to be at risk for aspiration. After 7 days, only 27% were still considered to be at risk. At 6 months, 3% of the survivors had persistent difficulty, whereas 3% who previously were not dysphagic were now considered at risk. These results suggest that early detection is important in preventing dysphagic complications and that a significant number of patients will improve without intervention specific to their dysphagia. Similarly, comparable prevalence figures for dysphagia on admission (43% to 51%) were found by Gordon et al.20 and Mann et al.,21 although the latter group noted a higher prevalence of dysphagic symptoms at 6 months (50%) than other studies with prevalence rates that ranged from 3% to 9%.19,21 Daniels et al.22 found that 36 (65%) of 55 patients with acute stroke had dysphagia. Of these 36, more than half aspirated. Of these, two thirds did so silently, suggesting that events of aspiration could be detected only by videofluoroscopy, not the bedside examination. In long-term follow-up, 94% of these patients returned to oral intake. Interestingly, the presence or absence of silent aspiration did not discriminate between patients who returned to successful oral feeding.



Head/Neck Cancer

Surprisingly, there have been no large studies of the prevalence or incidence of swallowing disorders in unselected patients after treatment for head/neck cancer, although it is well known that dysphagia is a frequent complication. Dysphagia can be result from the removal of tissue, with subsequent sensory and motor loss, and the effects of radiation therapy and chemotherapy. Before patients in their study received treatment, Pauloski et al.23 found that 59% had symptoms consistent with dysphagia. In a large multicenter treatment trial of patients with laryngectomies who were treated with either surgery and radiation or radiation and chemotherapy, approximately 33% had some type of swallowing-related difficulty at 2-year follow-up.24 In a series of 46 patients treated by supraglottic laryngectomy, 60% had dysphagia after their hospital stay.25 Evidence suggests that patients with pharyngeal tumor resections and those with tumors involving the tongue base are more likely to have dysphagia.26



Head Injury

Dysphagia is common after severe head injury. Data report that the incidence of dysphagia ranges from 4.5% (9 of 199) of consecutive admissions in an acute care setting27 to an incidence of 78% (31 of 40) in a similar setting.28 Discrepancies in reporting may be attributable to the initial severity of the injury and the method used to detect and define dysphagia. Incidence data are available for patients who survive head injury and enter a rehabilitation setting; the incidence ranges from 27% to 30%27,29 to 42% (218 of 524).30 In a mixed group (type of injury and time after onset), Lazarus and Logemann31 found that approximately half of the patients they examined with videofluoroscopy showed evidence of dysphagia. Among patients with head injuries entering a rehabilitation setting, Winstein29 found that 27% were dysphagic on admission to rehabilitation and that only 6% were dysphagic after 5 months of rehabilitation. Of 62 consecutive patients receiving outpatient rehabilitation, Yorkston et al.28 reported that 13% remained dysphagic. In general, the more severe the initial injury, the higher the incidence of dysphagia. Some patients remain comatose and are unable to eat, whereas others require extensive neurosurgical procedures with prolonged intubation and mental status changes, all of which may preclude attempts at oral ingestion. However, once patients enter the rehabilitation setting, their chances of returning to oral feeding are good.



Progressive Neurologic Disease

Progressive neurologic diseases that frequently result in dysphagia include Parkinson’s disease and its variants, amyotrophic lateral sclerosis, multiple sclerosis, myasthenia gravis, and diseases of systemic rheumatic origin, such as dermatomyositis, polymyositis, rheumatoid arthritis, scleroderma, and Sjögren’s syndrome. Systemic rheumatic disorders are far rarer than Parkinson’s disease or multiple sclerosis but merit consideration in a discussion of dysphagia and neurologic disease. Because of the progressive nature of these disease processes, the point in disease progression at which dysphagic symptoms occur is never certain. For instance, some patients report dysphagia as the initial symptom of the disease, whereas others may never mention dysphagia. In general, however, as disease severity increases, so does dysphagia. Complications from dysphagia, particularly those that threaten pulmonary function, may lead to aspiration pneumonia and death.



Parkinson’s Disease

Although dysphagia secondary to Parkinson’s disease appears to be common, accurate measurements are restricted by subject selection bias and dysphagia detection methods. However, most authors agree that dysphagia occurs in at least 50% of patients with Parkinson’s disease.3234 In 72 patients with Parkinson’s disease of varying severity, Leopold and Kagel35 found that as many as 82% reported swallowing difficulty. The prevalence of dysphagia may be higher in patients with Parkinson’s disease who also have significant dementia.36



Amyotropic Lateral Sclerosis

When amyotrophic lateral sclerosis (ALS) affects the bulbar musculature, dysphagia may be one of the first symptoms of the disease. In studies of patients with ALS at first diagnosis, 25% to 30% have evidence of bulbar symptomatology.37,38 It can be assumed that at least one third of patients with a diagnosis of ALS will have some difficulty swallowing, particularly as the disease progresses. Known characteristics of disease progression that affect the bulbar musculature result in progressively severe dysphagia symptomatology.39

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Aug 27, 2016 | Posted by in GASTROENTEROLOGY | Comments Off on Dysphagia Unplugged

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