The pyramidal tract is the direct pathway to the brain in the CNS TRUE
Dysarthria is a neurological condition including having an impaired ability to plan or program motor commands needed for speech FALSE (APRAXIA)
Aspiration is used to describe food or liquid that enters the airway and reaches below the vocal folds TRUE
Difficulty protecting the airway when drinking liquids refers to an impairment to the oral transit phase FALSE (PHARYNGEAL)
Assessing an individual hearing loss only requires determining the decibel threshold FALSE (DECIBELS AND FREQUENCY)
The primary treatment for conductive hearing loss is amplification via hearing aids TRUE
A common cause sof hearing loss in young children is otitis media TRUE
Intact cognitive abilities are necessary for individuals to use an AAC system FALSE
Normal conversation typically occurs around 60 dB
The most common type of dysarthria for an individual with Parkinson's disease is hypokinetic dysarthria (lack of movement)
An individual with dysplasia may require advanced diagnostic imaging such as Videofluoroscopic Swallowing Study (VFSS) and Fiberoptic Endoscopic Evaluation of Swallowing (FEES)
Audiologic assessment that directly stimulated the cochlea BONE CONDUCTION
STRAINED, STRANGLED SOUNDING VOICE is not associated with flaccid dysarthria
The middle ear is TYMPANIC MEMBRANE ANS OSSUCULAR CHAIN
The pharyngeal phase of swallowing is AUTOMATIC
Loud noise can cause conductive hearing loss FALSE
Oral Preparation Phase
Mastication (chewing) and forming bolus
Oral Transit Phase
Bolus moves from the front of the mouth to the back of the mouth
Pharyngeal Phase
Velum raises and covers the nasal cavity
Epiglottis covers airway
Esophageal Phase
Bolus enters the esophagus
Wave-like contractions that help to get the bolus down the esophagus into the stomach
Hearing loss in Children
Profound hearing loss results in no access to speech sounds without amplification
All degrees of hearing loss interfere with ability to do well in school, academically, and socially
~Children with mild hearing loss have more difficulty in challenging listening environments
~Have to rely more on memory and attention abilities
Greater risk for delays in phonological development
Unilateral hearing loss results in difficulty localizing and hearing sound in noise
Children with profound hearing loss do better when the loss is diagnosed and amplified early
Dysarthria
Flaccid Dysarthria
Damage to the cranial or spinal nerves in PNS
Physical characteristics
Weakness or muscle atrophy
Flaccidity (hypotonia)
Fasciculations
Hypoactive gag reflex
Perceptual characteristics
Nasal-sounding speech
Rapid deterioration of performance
Short phrases
Breathy voice
Imprecise AMRs/SMRs
Spastic Dysarthria
Often resulting from damage to the cerebral cortex-pyramidal system, CNS
Increased or hyperactive muscle tone
Physical characteristics
Increased muscle tone (hypertonia)
Hyperactive gag reflex
Perceptual characteristics
Slow speaking rate
Strained or hard vocal quality
Slow but regular AMRs/SMRs
Common causes:
~Cerebral palsy or other conditions where brain damage occurs
~ALS
~Stroke
Ataxic Dysarthria
Damage to cerebellum
Cerebellum = coordination
Physical characteristics
Tremors
Poor coordination in jaw, face, tongue
Perceptual characteristics
Excess and equal stress
Excessive loudness
“Drunk” speech
Irregular AMRs/SMRs
Common causes:
~Lesions to the cerebellum (stroke, tumor, etc.)
~Can be seen in cerebral palsy
Hypokinetic Dysarthria
Damage to the basal ganglia, which controls movement, and extrapyramidal tract
Physical characteristics
Masked facial expression
Resting tremors
Reduced range of motion
Rigidity
Perceptual characteristics
Monopitch
Monoloudness
Short rushes of speech
Reduced loudness
Rapid, “blurred” AMRs/SMRs
Common causes:
Parkinson’s disease
~Chronic, progressive neurological condition that causes problems with voluntary movements
~Decreased dopamine production in the basal ganglia
~Early signs: tremor, stiffness, slow movements
~Later signs: poor balance, speech and swallowing difficulties, slow movements, poor gait, possible dementia
~Second most common degenerative brain condition
Hyperkinetic Dysarthria
Damage to the basal ganglia and extrapyramidal tract
Physical characteristics
Cannot inhibit unwanted movement
Motor tics
Sudden, involuntary jerking
Perceptual characteristics
Excessive loudness
Transient vocal strain and/or breathiness
Inappropriate vocal noises
Fast speaking rate
Sudden changes to pitch
Irregular AMRs/SMRs
Common causes:
Huntington’s disease
~Rare, inherited condition passed down from a parent (50% change)
~Symptoms begin in 30s or 40s most commonly
~Characyerued primarily by movements that can’t be controlled, called chorea → increase in dopamine
~Invoulantary movements affecting all muscles of the body notably the arms, legs, tongue, and face
~Symptoms: muscle contractures, trouble walking and with posture, speech and swallowing difficulties
~Also common to have cognitive and mental health impairments
One of the most common tasks a therapist will ask their patient to do is called diadochokinetic rate:
~Pa-pa-pa-pa-pa
~Ta-ta-ta-ta-ta
~Ka-ka-ka-ka-ka
~Then combined: pataka-pataka-pataka
~All sounds are stop sounds, all sounds require a different part of the mouth to make them
~Alternating motion rate (AMRs) (pa-pa-pa)
~Sequential motion rate (SMRs) (pataka)
Types of AAC
No-tech AAC
Do not involve technology
Use readily available materials
~Paper and pencil for writing
~Alphabet boards
~Picture Exchange Communication System (PECS)
Low tech AAC
Simple to use technology
Limited number of pragmatic functions
Few moving parts or electrical components
~BIGmack
~Quicktalker 1
Mid tech AAC
Have some amount of electrical power
Have speech generation capabilities but limited programming or customization options
~Go Talk 20+
High tech AAC
Most complex and sophisticated electronic devices
Requires training to operate programmatic features
Often uses work prediction software to improve communication efficiency
~iPads
~Tobii Dynavox
Systems will only continue to advance
Audiology
Conductive hearing loss: outer and middle ear
Sensorineural hearing loss: inner ear (cochlea/auditory nerve)
Mixed hearing loss: both conductive and sensorineural loss
Anatomy of the Hearing System
Can be divided into the outer ear, middle ear, inner ear, the vestibulocochlear nerve, the auditory brain stem, and the auditory cortex of the brain
~The first four areas are the peripheral auditory system
~The latter two make up the central auditory system