Dysphagia
BASICS
BASICS

BASICS
Subjective sensation of difficulty or abnormality of swallowing
DESCRIPTION
DESCRIPTION
DESCRIPTION
- Oropharyngeal: difficulty transferring food bolus from oropharynx to proximal esophagus
- Esophageal: difficulty moving food bolus through the body of the esophagus to the pylorus
EPIDEMIOLOGY
EPIDEMIOLOGY
EPIDEMIOLOGY
5–8% of the general population >50 years of age
Incidence
Incidence
Incidence
- Esophageal food impaction 25 per 100,000 persons per year
- Males to female (1.5:1)
Prevalence
Prevalence
Prevalence
- 14–33% among community-dwelling individuals ≥65 years old
- Up to 40% in hospital settings
- 29–32% of patients in nursing homes
- 44% in patients in geriatrics acute care
- 60% in older patients that are institutionalized
ETIOLOGY AND PATHOPHYSIOLOGY
ETIOLOGY AND PATHOPHYSIOLOGY
ETIOLOGY AND PATHOPHYSIOLOGY
- Oropharyngeal (transfer dysphagia):
- Functional motor disorder in the oropharynx
- Mechanical: pharyngeal and laryngeal cancer, acute epiglottitis, carotid body tumor, pharyngitis, tonsillitis, strep throat, lymphoid hyperplasia of lingual tonsil, lateral pharyngeal pouch, hypopharyngeal diverticulum
- Neuromyogenic: stroke, head trauma, Parkinson disease, amyotrophic lateral sclerosis (ALS), myasthenia, polymyositis, dermatomyositis, muscular dystrophies, thyrotoxicosis, hypothyroidism, amyloidosis, Cushing syndrome
- Esophageal:
- Mechanical: carcinomas, diverticula, webs, Schatzki ring, structures (peptic, chemical, trauma, radiation), foreign body; eosinophilic esophagitis
- Extrinsic mechanical: peritonsillar abscess, thyroid disorders, tumors, vascular compression (enlarged left atrium, aberrant subclavius, aortic aneurysm), adenopathy, duplication cyst
- Neuromuscular: achalasia, spasm, hypertonic sphincter, scleroderma, CVA, Alzheimer disease, Huntington chorea, Parkinson disease, multiple sclerosis, polymyositis, dermatomyositis, neuromuscular junction disease (myasthenia gravis, Lambert-Eaton syndrome, botulism), hyperthyroidism and hypothyroidism, Guillain-Barré syndrome, SLE, ALL, amyloidosis, diabetic neuropathy, brainstem tumors, Chagas disease
- Infections: diphtheria, meningitis, tertiary syphilis, Lyme disease, rabies, poliomyelitis, CMV, esophagitis (Candida, herpetic)
RISK FACTORS
RISK FACTORS
RISK FACTORS
- Children: hereditary and/or congenital malformations
- Adults: age >50 years; elderly: GERD, stroke, COPD, chronic pain
- Medications: quinine, potassium chloride, vitamin C, tetracycline, trimethoprim (Bactrim), clindamycin, NSAIDs, procainamide, anticholinergics, bisphosphates, seizure meds: phenobarbital, carbamazepine, and phenytoin; antihistaminics, TCA’s: amitriptyline, imipramine, anti-psychotics: haloperidol, phenothiazine, butyrophenone, thioxanthene; oxybutynin; opiates; rizatriptan; ACE, ARB, calcium channel blockers, β-blockers, α2-agonist; HCTZ and chlorothiazide; cytotoxic, (antineoplastics; interferon-α, ribavirin); sibutramine; β2-agonist bronchodilators, muscle relaxants
- Xerostomia: ACE inhibitors, antiarrhythmics, antiemetics, diuretics, SSRI, sunitinib everolimus
- Neurologic: CVA, myasthenia gravis, multiple sclerosis, Parkinson disease, ALS, Huntington chorea, dementia; HIV patients with CD4 cell count <100 cells/mm3
- Trauma or irradiation of head, neck, and chest; mechanical lesions; extrinsic mechanical lesions: lung, thyroid tumors, lymphoma, metastasis; iron deficiency
- Smoking, excess alcohol intake, obesity
GENERAL PREVENTION
GENERAL PREVENTION
GENERAL PREVENTION
Liquid and soft food diet as appropriate
COMMONLY ASSOCIATED CONDITIONS
COMMONLY ASSOCIATED CONDITIONS
COMMONLY ASSOCIATED CONDITIONS
Peptic structure, esophageal webs and rings, carcinoma, history of stroke, dementia, pneumonia
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