dysphagia Flashcards
except for voluntary manipulation and preparation of food, swallowing is primary ____
involuntary (pg.364)
______ is difficulty or abnormality in moving food from the mouth to the stomach
dysphagia (pg.364)
what muscle composes the upper esophageal sphincter?
cricopharyngeal muscles (pg. 364)
the ______ contains the epiglottis, valleculae, pyriform sinuses and laryngeal aditus
laryngeopharynx (pg.364)
a. trigeminal V
b. facial VII
c. glossopharyngeal (IX)
d. vagus (X)
e. spinal accessory (XI)
f. hypoglossal (XII)
- sensation in anterior 2/3 of tongue (hot, cold, oral pain)
- sensation to teeth, gums, and oral mucosa
- salivary flow to major and minor glands
- motor control of mouth opening, mandible motion and mastication
- motor innervation to floor of mouth muscles to elevate larynx and hyoid
a. trigeminal V (pg.364)
a. trigeminal V
b. facial VII
c. glossopharyngeal (IX)
d. vagus (X)
e. spinal accessory (XI)
f. hypoglossal (XII)
- taste in anterior 2/3 of the tongue
- sensation to soft palate
- salivation from all salivary glands except parotid glad
- motor control of lip motion and bilabial seal
- motor control for the facial muscles, FOM muscles and cheeks
- assists in elevation of hyoid and larynx to protect airway
b facial VII (pg.364)
a. trigeminal V
b. facial VII
c. glossopharyngeal (IX)
d. vagus (X)
e. spinal accessory (XI)
f. hypoglossal (XII)
- taste in posterior 1/3 of tongue
- sensation to faucial pillars and soft palate
- salivation from the parotid gland
- sensation to the pharynx and larynx
- motor velopharyngeal closure
- motor control of the upper pharyngeal constrictor muscles
c. glossopharyngeal IX (pg.365 )
a. trigeminal V
b. facial VII
c. glossopharyngeal (IX)
d. vagus (X)
e. spinal accessory (XI)
f. hypoglossal (XII)
- controls sensory information for pharyngeal and esophageal phases
- motor innervation to the base of the tongue and all pharyngeal muscles
- major innervation to the larynx, diaphragm and lungs
- pharyngeal contraction and esophageal peristalsis
d. vagus X (pg. 365)
a. trigeminal V
b. facial VII
c. glossopharyngeal (IX)
d. vagus (X)
e. spinal accessory (XI)
f. hypoglossal (XII)
- partial innervation of soft palate and uvula
- partial innervation of muscles of upper pharynx
- primary function is to provide stability of shoulder and neck muscles during swallowing and allow rotation of head and neck
e. spinal accessory XI (pg.365)
a. trigeminal V
b. facial VII
c. glossopharyngeal (IX)
d. vagus (X)
e. spinal accessory (XI)
f. hypoglossal (XII)
- primary motor for all tongue muscles
- motor innervation of the pharynx (aids in hyolaryngeal elevation and airway protection
f. hypoglossal XII (pg. 366)
the swallowing center is located in the ____ and _____
medulla and pons (pg. 366)
a. oral prep
b. oral phase
c. pharyngeal phase
d. esophageal phase
- entirely voluntary
- manipulate bolus to swallow-ready state
a. oral prep (pg.366)
what are the main muscles in the oral prep stage?
- orbicularis oris
- buccinator
- tongue
- masseter
- medial and lateral pterygoids
(pg. 366)
what cranial nerves are involved in the oral prep stage?
- CN V
- CN VII
- CN IX
- CN XII
(pg. 366)
a. oral prep
b. oral phase
c. pharyngeal phase
d. esophageal phase
- partially voluntary, because it requires some cortical control
- bolus is transferred to pharynx
b. oral phase (pg.366)
what muscles are involved in the oral phase?
- orbicularis oris
- masseter
- temporalis
- pterygoids
- mylohyoid
- geniohyoid
- digastric
- levator veli palatini
- palatoglossus
- palatopharyngeous
(pg. 366)
what cranial nerves are involved the oral preparatory phases?
- CN V
- CN VII
- CN IX
- CN X
- CN XI
- CN XII
(pg. 366)
a. oral prep
b. oral phase
c. pharyngeal phase
d. esophageal phase
- the bolus flows vertically through the pharynx to the esophagus while the airway is protected from bolus entry
- this stage is involuntary
c. pharyngeal phase (pg. 367)
how long does the pharyngeal phase last?
1.5 seconds (pg.367)
a. oral prep
b. oral phase
c. pharyngeal phase
d. esophageal phase
- totally involuntary
- lasting 8-10 seconds
- the bolus is moved into the stomach
d. esophageal phase (pg.367)
what cranial nerve innervates the esophagus?
CN X (pg.367)
what are common effects of aging on swallowing?
- increased duration of swallow, delayed hyoid elevation, longer opening of UES, decline in pressure reserves, decreased lingual pressure and strength
(pg. 367)
what is sarcopenia?
muscle wasting (pg.367)
affects tongue muscle and swallow function in older people
what is a tastant?
- any substance capable of eliciting gustatory excitation (pg.371)
what are the most common neurological conditions that result in dysphasia?
- stroke
- parkinson’s disease
(pg. 371)
what are the signs and symptoms of oropharyngeal dysphagia?
- feelings that something is stuck in his throat
- excessive coughing during eating
- excessive drooling
- wet gurgling vocal quality after eating
- poor lung sounds
- dysphonia
- pocketing of food in the mouth
- pills stuck in throat
- shortness of breath after eating
- unexplained weight loss
- fever
- pneumonia of unknown origin
- voice changes
- heartburn
(pg. 372)
true/false: bilateral damage to the pons and medulla may cause total dysphagia with poor prognosis
true (pg. 372)
true/false: subcortical stokes will have mild symptoms including mild oral and pharyngeal transit delays
true (pg.372)
a. right
b. left
______ hemisphere damage is more susceptible to pharyngeal problems such as delayed pharyngeal stripping wave motion
- mild oral delays, longer pharyngeal delays
- aspiration before or during swallow due to incomplete laryngeal elevation
a. right (pg.373)
a. right
b. left
____ hemisphere damage results in the oral phase of the swallow being impaired
- may have difficulty initiating a swallow
- mild delay in triggering pharyngeal phase which may result in aspiration or laryngeal penetration before the swallow is triggered
- better recovery of swallow function
b. left (pg.373)
a. parkinsons
b. progressive supra nuclear palsy
c. amyotrophic lateral sclerosis
d. myasthenia gravis
- dysphasia is found in 50% of patients
- a movement disorder caused by dopamine depletion in the substantia nigra in the subcortical region
- symptoms include resting tremor, rigidity, impaired postural reflexes and paucity of movement
a. parkinsons (pg. 373)
a. parkinsons
b. progressive supra nuclear palsy
c. amyotrophic lateral sclerosis
d. myasthenia gravis
- a severe and rapid progressive degeneration of UMN and LMN tracts, causing severe motor dysfunction, dysarthria and dysphagia affecting all stages of swallow
- cognition is not impaired
c. ALS (pg. 373)
a. parkinsons
b. progressive supra nuclear palsy
c. amyotrophic lateral sclerosis
d. myasthenia gravis
- a degenerative disorder of the CNs, caused by widespread neuronal degeneration in multiple systems in the brain stem and basal ganglia
- resembles parkinsons, but differed due to disturbed ocular motility and earlier signs and cognitive loss
- minimally responsive to dopamine
b. progressive supra nuclear palsy (pg.373)
a. parkinsons
b. progressive supra nuclear palsy
c. amyotrophic lateral sclerosis
d. myasthenia gravis
- a LMN disorder in which conduction is impaired at the myoneural junction, due to a defect of acetylcholine release
- weakness that exacerbates with repeated effort is the primary symptom
- dysphasia occurs due to fatigue of the muscles of mastication
d. myasthenia gravis (pg.373)
treatment
a. parkinsons
b. progressive supra nuclear palsy
c. amyotrophic lateral sclerosis
d. myasthenia gravis
- focuses on sensory awareness and control of the oral swallow
- expiratory muscle strength training
- lee silverman voice treatment
a. parkinsons (pg.373)
treatment
a. parkinsons
b. progressive supra nuclear palsy
c. amyotrophic lateral sclerosis
d. myasthenia gravis
- there is no cure
- dysphagia treatment is temporary and minimally successful
- family and patient counseling is essential in early stages
c. ALS (pg.373)
treatment
a. parkinsons
b. progressive supra nuclear palsy
c. amyotrophic lateral sclerosis
d. myasthenia gravis
- medical treatments include removal of the thymus glad and use medication to help facilitate muscle movement
- behavioral treatment includes energy conversation
- small meals, increased frequency
- modify texture so less chewing effort needed for oral preparation
d.myashenia gravis (pg.373)
a. multiple sclerosis
b. huntington’s disease
c. postpolio syndrome
d. guillain-barre syndrome
- an immune-mediated demyelination of nerve fibers in the brain and spinal cord
- dysphagia occurs if corticobulbar tracts or brain stem pathways affected
a. multiple sclerosis (pg.374)
a. multiple sclerosis
b. huntington’s disease
c. postpolio syndrome
d. guillain-barre syndrome
- an autosomal-dominant, neurodegenerative disease that can be detected with blood tests
- progressive psychiatric disturbance
- choreatic movements
- oropharyngeal dysphagia
b. huntington’s disease (pg. 374)
a. multiple sclerosis
b. huntington’s disease
c. postpolio syndrome
d. guillain-barre syndrome
- viral induced degeneration of the LMN and brain stem
- degeneration decades after polio exposure
- dysphagia occurs in almost all cases and is found in all phases of the swallow
c. postpolio syndrome (pg.374)
a. multiple sclerosis
b. huntington’s disease
c. postpolio syndrome
d. guillain-barre syndrome
- autoimmune disorder affecting the peripheral nervous system, resulting in demyelination of cranial nerves
- causes weakness and sensory loss of the oral cavity, pharynx and larynx during the acute phase of the disease
d. guillain-barre syndrome (pg. 374)
treatment
a. multiple sclerosis
b. huntington’s disease
c. postpolio syndrome
d. guillain-barre syndrome
-medical treatment by high-dose intravenous corticosteroids and beta-interferon has been proven effective
a. multiple sclerosis (pg.374)
treatment
a. multiple sclerosis
b. huntington’s disease
c. postpolio syndrome
d. guillain-barre syndrome
-treatment involves feeding them in an uncluttered space, with seating that provides head and trunk support
b. huntington’s disease (pg.374)
treatment
a. multiple sclerosis
b. huntington’s disease
c. postpolio syndrome
d. guillain-barre syndrome
-oral exercises are minimally effective, while postural and dietary treatments appear helpful
c. postpolio syndrome (pg.374)
treatment
a. multiple sclerosis
b. huntington’s disease
c. postpolio syndrome
d. guillain-barre syndrome
-plasmapheresis or intravenous immunoglobulin are highly effective cures
d. guillain-barre syndrome (pg.374)
a. dystonia
b. dermatomyositis
c. TBI
d. dementia
-difficulty coordinating respiration and swallowing
-different types
neck=delayed swallow initiation and vallecular residue
laryngeal/spasmodic= swallwoing presrved
oromandibular=premature spillage of bolus into pharynx with vallecualr reside, difficulty in oral preparation stage
lingual= biting tongue, expel food from mouth
a. dystonia (pg. 374)
a. dystonia
b. dermatomyositis
c. TBI
d. dementia
- an immune system disorder, which may appear in childhood
- a serious condition in children, appears as sun sensitivity
- rash on upper eyelid
- weakness, stiffness and pain in muscles in abdominal area
b. dermatomyositis (pg.374)
a. dystonia
b. dermatomyositis
c. TBI
d. dementia
- the leading cause of death and disability in the US for persons 40 and under
- usually causes memory and other cognitive impairments
c. TBI (pg.374)
a. dystonia
b. dermatomyositis
c. TBI
d. dementia
- a cognitive impairment where dysphagia is not typical
- if there is dysphagia it will appear in volitional eating, transporting food to the mouth, lack of awareness of food placed in the oral cavity and an inability to determine when to swallow
d. dementia (pg. 375)
treatment
a. dystonia
b. dermatomyositis
c. TBI
d. dementia
-treatment may include Botox injections or lesion surgery but effects remain inconclusive
a. dystonia (pg.374)
treatment
a. dystonia
b. dermatomyositis
c. TBI
d. dementia
- dysphagia may appear and can be treated with medication such as steroids
- prednisone or corticosteroid treatment results in improvement in a majority of patients
b. dermatomyositis (pg. 374)
treatment
a. dystonia
b. dermatomyositis
c. TBI
d. dementia
- directed feeding and individual assistance during meals is often required
- as cognition become more impaired, treatment may no longer be beneficial for swallowing or feeding
c. dementia (pg. 375)
in regards to tumor size, T1=_____ and T2=_______
smallest, largest (pg.376)
when there is surgical removal of a tumor when should treatment for dysphagia begin?
-after major healing (pg.376)
treatment for tongue tumors and glossectomy include…
-thermal tactile stimulation, lingual exercises, poster bolus placement, and backward head movement if the main problem targeted is oral transfer to pharynx (pg. 376)