Audiology Flashcards

1
Q

neuroplasticity

A

the ability of a baby’s brain to change with learning

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2
Q

synaptic pruning

A
  • unused or weak connections are eliminated
  • strong connections are strengthened
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3
Q

when do babies with typical hearing start hearing

A

20 weeks

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4
Q

ears function

A
  • transmit and transduce sound to the brain
  • maintain balance
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5
Q

brain

A

true hearing organ

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6
Q

optimal time for auditory neural connections to form

A

first 3 years

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7
Q

babies born with hearing loss

A
  • missed 20 weeks of typical development of the auditory brain before birth pathways before birth
  • missed auditory neural development after birth and that would have happened with hearing aids
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8
Q

0-4 months (hearing milestones)

A
  • startle to loud sounds
  • sensitive to a wide range of sounds
  • quiet to familiar voice
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9
Q

4-6 months (hearing milestones)

A
  • localize sound
  • angry v. friendly voices
  • like sound-making toys
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10
Q

6-12 months (hearing milestones)

A
  • turn to mother’s voice
  • repeat sounds
  • respond to their name, “no-no”, and “bye-bye”
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11
Q

12-18 months (hearing milestones)

A
  • imitate spoken words
  • word approximation (dog = ruff ruff)
  • jabber in response to human voice
  • understand ~50 words
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12
Q

18-24 months (hearing milestones)

A
  • understand simple sentences
  • echo prominent/last words spoken
  • use 10-15 words by 24 months
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13
Q

24-30 months (hearing milestones)

A
  • understand and answer yes/no questions, simple “wh-“ questions
  • listen to simple stories
  • follow simple directions
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14
Q

30-36 months

A
  • understand nearly all sentence types
  • communicate effectively with strangers
  • understood by others
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15
Q

parts of the ear

A
  • outer ear
  • middle ear
  • inner ear
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16
Q

auditory path

A

sound waves travel from the outer ear → auditory canal (causes ear drum or tympanic membrane to vibrate which causes ossicles to move) → oval window → fluid in cochlea and inner ear (vibrations into electrical impulses) → brain

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17
Q

outer ear features

A
  • pinna
  • auditory canal/meatus
  • tympanic membrane (eardrum)
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18
Q

pinna

A
  • cartilage and soft tissue
  • only visible part of the ear (auricle)
  • localization
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19
Q

pinna function

A
  • direct sound into the ear (without it, sound would be lost making it harder to hear)
  • helps overcome pressure difference (air pressure higher in the ear)
  • transition into the auditory canal smoother
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20
Q

auditory canal

A
  • transmit sound from the pinna to the eardrum
  • natural hearing aid (amplifies low sound, compensate for human voice weakness)
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21
Q

tympanic membrane

A
  • sensitive membrane at the end of the auditory canal
  • pressure from sound waves makes the eardrums vibrate
  • marks beginning of middle ear
  • slightly curved to make it difficult to insets to get in
  • earwax
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22
Q

earwax function

A

keeps dust, dirt, and insects out

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23
Q

middle ear features

A
  • ossicles (malleus, incus, and stapes)
  • oval window
  • round window
  • eustachian tube
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24
Q

middle ear function

A

acoustic transformer (amplify sound waves before moving them to the inner ear)

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25
Q

pressure on oval window is ___ higher than the eardrum

A

20x

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26
Q

ossicles

A
  • malleus
  • incus
  • stapes
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27
Q

ossicles form a _____ from the _______ to the _____ ___

A

chain, eardrum, inner ear

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28
Q

oval window

A

a membrane covering the entrance to the cochlea in the inner ear

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29
Q

round window

A
  • vibrates in opposite phase to vibrations entering the inner ear through the oval window
  • allows fluid in the cochlea to move
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30
Q

eustachian tube

A

connects ear to rearmost part of the palate

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31
Q

eustachian tube function

A

equalize the air pressure on both sides of the eardrum ensuring that pressure doesn’t build up

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32
Q

how does eustachian tube pressure equalize

A

tube opens when swallowing allowing pressure to equalize

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33
Q

what happens if ear pressure is not equalized

A

limited vibrations result in a slight hearing reduction

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34
Q

inner ear features

A
  • cochlea
  • semicircular canals
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35
Q

inner ear function

A

hearing and balance

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36
Q

cochlea function

A

responsible for hearing

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37
Q

cochlea

A
  • bony, looks like a snail with fluid and hair cells inside
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38
Q

how ear bone motion turns into understandable sound

A
  • when middle ear bones move, fluid in the inner ear moves which triggers hair cells (different hair cells move for different sounds)
  • hair cells turn movement into electrical signals which go to the brain via the auditory nerve and the brain deciphers the sounds
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39
Q

semicircular canals

A

part of the balance system

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40
Q

ascending auditory pathway

A

the central auditory nervous system

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41
Q

anatomy of the auditory periphery

A

how the basic sound attributes are coded within the auditory periphery

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42
Q

where do fibers from the cochlear nuclei synapse

A

superior olivary complex

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43
Q

central auditory nervous system path

A

Fibers synapse on the cells of the cochlear nuclear complex → superior olivary complex (soc) → lateral lemniscus (some fibers synapse in the lemniscus but most travel through it) → inferior colliculus (ic) → medial geniculate body → auditory cortex

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44
Q

central role of the auditory cortex

A

processing of complex sounds

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45
Q

different neural types are responsible for information about ______ and ________ features of sound

A

spectral, temporal

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46
Q

auditory processing

A

the way our ears communicate with the brain and what the brain does with the information

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47
Q

auditory processing disorder

A

difficulty processing sound and speech with normal hearing

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48
Q

sound is described by _____________ and _____________

A

frequency, intensity

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49
Q

frequency

A
  • the number of vibrations (sound waves)/second
  • measured in Hz
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50
Q

what frequency can healthy young adults hear between

A

20 and 20,000 Hz

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51
Q

does the ability hear high frequencies increase or decrease with age

A

decrease

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52
Q

high frequency example

A

bird chirping

53
Q

low frequency example

A

drum beating

54
Q

intensity

A
  • the amount of energy of a vibration
  • measured in dB
55
Q

intensity extremes can …

A

damage the ear

56
Q

audiogram

A

a sound chart.graph that records a person’s hearing ability

57
Q

thresholds

A

softest sounds/levels

58
Q

tones

59
Q

sounds on the left side of the audiogram are …

sounds on the right side of the audiogram are …

A

low pitch

high pitch

60
Q

the lower you go on the audiogram, the _______ the sound is

61
Q

normal hearing

A

15dB (child) or 20 dB (adult)

62
Q

minimal hearing loss and what they can’t hear

A
  • 16-25 dB
  • can’t differentiate between “f” and “th”
63
Q

mild hearing loss

64
Q

moderate hearing loss and clinical symptom

A
  • 40-55 dB
  • soft speech is inaudible, normal conversation is a whisper
65
Q

moderate to severe hearing loss

A
  • 55-70 dB
  • most (if not all) conversational speech is inaudible
66
Q

severe hearing loss

67
Q

profound hearing loss, what can’t be heard

A
  • > 90 dB
  • conversational and environmental sounds are inaudible
68
Q

treatment options for hearing loss

A
  • surgical intervention
  • amplification/cochlear implants
  • early intervention (for communication and development)
69
Q

possible multidisciplinary team members

A
  • parents
  • audiologist
  • SLTs, OT, ENT
  • teachers
  • psychologists
  • physiotherapist
70
Q

hearing (at home training)

A
  • contrast sound and silence (music on/off)
  • make sounds together (noisy toys and voice)
  • everyday voice
71
Q

awareness (at home training)

A
  • body sounds (cry, cough, sneeze, laugh)
  • verbalize sounds (bad cough, shakey shakey)
  • play with ling 6 voice sounds (mmm…nice, sh….quiet, ssss..snake)
72
Q

attention (at home training)

A
  • focus on something long enough to make sense
  • look and listen, respond consistently to sounds
  • everyday sounds (telephone, dog)
  • tone of voice
73
Q

listening (at home training)

A
  • recognize familiar sounds, words, songs
  • hanen approach (owl: observe, wait, listen)
74
Q

understanding (at home training)

A
  • copy and clarity and add language
  • comment on what is happening
  • follow instructions
  • play
75
Q

turn-taking (at home training)

A
  • take turns using voice
  • translate sound/babble into meaningful words
  • praise and imitate early sounds
76
Q

talking (at home training)

A
  • first words –> expand vocab
  • work on clarity when reading (c-a-t)
  • phonological awareness (e-le-phant)
  • offer choices instead of yes/no questions
  • model please and thank you
77
Q

apd diagnostic steps

A
  • Rule out peripheral auditory involvement with a comprehensive hearing test (with acoustic reflex)
  • Rule out attention deficits, memory, and IQ disorders
  • Rule out language disorder
  • Diagnostic Audiological Assessment battery
    [Comprehensive hearing test (w/ acoustic reflex), Auditory discrimination word list, Degraded speech signals (filtered words, rapid speech, and speech-in-noise), temporal processing (frequency, duration, and gap detection), dichotic/binaural listening (integration/separation)]
78
Q

apd manifests as poor:

A
  • Localization and lateralization
  • Auditory discrimination
  • Auditory pattern recognition
  • Temporal processing
  • Performance with competing or degraded acoustic signals
79
Q

apd treatment

A
  • environmental/classroom modification
  • teacher-directed strategies
  • fm system or low-gain hearing aids
  • strengthen general language skills
  • auditory training
80
Q

signs of hearing loss

A
  • no response to sound at any age
  • infant does not move or jump with loud noise
  • no babbling by 9 months
  • no works spoken by 18-24 months
  • does not follow simple commands by 2 years old
  • visually oriented
81
Q

types of hearing loss causes

A
  • idiopathic
  • congenital (acquired or genetic)
82
Q

idiopathic

A
  • an underlying, unidentifiable cause
  • 70% of all hearing loss
  • most children born with a permanent congential hearing loss are born to normal hearing parents
83
Q

causes of acquired congenital hearing loss

A
  • maternal infections (syphilis, toxoplasmosis, rubella, CMV, herpes)
  • drug/alcohol use during pregnancy
  • maternal diabetes
  • high blood pressure in pregnancy
  • premature birth, low birth weight, birth injury
  • raundice
  • anoxia
84
Q

causes and % of genetic hearing loss

A
  • 50% of hearing loss
  • hearing loss after an environmental infection, trauma, etc.) is influenced by genes
  • sometimes related to a syndrome
  • recessive mutation
85
Q

autosomal dominant

A
  • 50% chance of being affected
  • individual in each generation are affected
86
Q

autosomal recessive inheritance

A
  • 25% chance of being affected
  • 66% chance the unaffected offspring is a carrier
  • one parent is a carrier
87
Q

causes of acquired hearing loss

A
  • infections
  • middle ear problems
  • trauma/aging
  • loud noise exposure
88
Q

conductive hearing loss

A
  • related to disease or deformity
  • normal bone conduction thresholds are <20 dB and an air-bone gap of >15 dB
89
Q

causes of conductive hearing loss

A
  • ear canal obstructions
  • perforations
  • otitis media
  • otoscerlosis
  • cholesteomtoma
  • atresia
  • microtia
90
Q

sensori-neural hearing loss

A

related to disease or deformity of the inner ear/cochlear nerve

91
Q

causes of congenital sensori-neural hearing loss

A
  • genetic
  • nongenetic causes (virus, infection, etc)
92
Q

causes of acquired sensori-neural hearing loss

A
  • genetic (cochlear otosclerosis, syndromic hearing loss)
  • nongenetic (meningitis, ototoxicity, noise induced hearing loss, chronic middle ear problems, etc.)
93
Q

mixed hearing loss

A
  • conductive and sensori-neural hearing loss (conductive overlay)
  • otosclerosis
94
Q

mixed hearing loss causes

A
  • chronic middle ear problems
  • cholesteomtoma
  • otosclerosis
95
Q

unilateral hearing loss

A
  • localization difficulties, turning to one side in order to hear, poor hearing in ambient noise
  • 10x more likely to experience academic failure, 5x more likely to experience academic difficulty
96
Q

causes of unilateral hearing loss

A
  • CMV
  • meningitis
  • mumps
  • auditory neuropathy spectrum disorder
  • sudden sensori-neural hearing loss
  • enlarged bestibular aquect syndrome
  • prematurity
  • trauma
97
Q

auditory neuropathy spectrum disorder

A
  • outer hair cell function in the cochlea is normal but inner hair cell or the auditory nerve function is disrupted
  • affected neural processing of auditory stimuli
  • difficulty understanding speech in noisy settings
  • respond to sound appropriately but decoding speech/language is hindered
  • auditory brainstem response absent or severely hindered at high stimulus levels
  • otoacoustic emissions and or cochlear microphonic present
98
Q

causes of auditory neuropathy spectrum disorder

A
  • history of anoxia, hyperbilirubinemia, mechanical ventilation, hypoxia
  • congenital brain abnormalities
  • extreme premature birth or low birth weight
  • viral disease, high fever
  • seizure/neurological disorders
99
Q

causes of apd

A
  • CNS tumors
  • premature or low birth weight
  • extrinsic brain damage
  • delayed maturity of central auditory pathway
  • metabolic disorder
  • epilepsy
  • auditory deprivation
  • periods of hearing loss
  • glue ear (OME)
100
Q

greater the hearing loss and the earlier it was…

A

the less intelligible the speech

101
Q

hard of hearing children tend to be _______ rather than _________

A

delayed, deviant

102
Q

newborn hearing screen

A
  • automated otoacoustic emission (AOE)
  • automated brainstem test if aoe fails
103
Q

automated otoacoustic emission (AOE)

A
  • shows ear hair cells are reacting in response to a noise
  • can pass with mild hearing loss (looking for moderate to severe hearing loss)
  • 3 out of 5 checks = pass
104
Q

automated brainstem test

A
  • last newborn hearing screening
  • child asleep for 30 minutes
  • specific waveform that moves with sounds (flat line = deaf)
  • normally a sensori-neural hearing loss
105
Q

which children automatically receive AOE and AABR

A

children in NICU > 48 hours

106
Q

management of failed newborn hearing screen

A
  • middle ear fluid testing
  • full auditory brainstem response tests
  • diagnose a permanent hearing loss with degree
107
Q

intervention for newborn who fail the hearing test

A
  • hearing aid (mild to moderate hearing loss)
  • cochlear implant (severe to profound hearing loss)
  • bone anchor implants (conductive hearing loss)
108
Q

when to refer a child for diagnostic hearing assessment

A
  • failed hearing screen
  • delayed speech
  • poor pronunciation or omitting start/end of words
  • poor balance/sensory
  • repeated middle ear infections
  • bad genes
  • parental concerns
109
Q

hearing tests

A
  • tympanometry
  • otoacoustic emissions
  • pure-tone audiometry
  • audiometry
110
Q

newborn hearing test facts

A
  • objective
  • little to no cooperation
111
Q

infant (<2 years old) hearing test facts

A
  • game played
  • no earphones, lots of assuming
112
Q

older child (<2 years old) hearing test facts

A
  • objective
  • earphones used
113
Q

speech discrimination pass

114
Q

types of hearing loss

A
  • permanent minimal and bilateral mild hearing loss
  • unilateral hearing loss
  • moderate to profound sensori-neural hearing loss
  • temporary/fluctuating conductive hearing loss
115
Q

primary cause of permanent minimal and bilateral mild hearing loss

A

otitis media

116
Q

is parental suspicion likely in permanent minimal and bilateral mild hearing loss

A

no, may have subtle language problems, reading difficulty, and behavioral problems instead of extreme hearing difficulty signs

117
Q

permanent minimal and bilateral mild hearing loss

A
  • problem hearing fain/distant speech, subtle conversation, fast conversation, and word distiction (plural and possessive)
  • more obvious in children with additional problems
118
Q

distance hearing

A
  • the distance over which speech sounds are intelligible (not just audible)
  • any hearing loss reduces distance over which speech sounds are intelligible even with amplification
119
Q

passive hearing

A
  • eavesdropping
  • hard of hearing people cannot casually overhear what people are saying
  • learning of social skills is affected
120
Q

hearing loss symptoms on speech and language development

A
  • delayed canonical babbling
  • no auditory feedback loop
  • prelinguistic and early language development stunted
121
Q

_________ and ____________ are vulnerable to omission and substitution with all degrees of hearing loss

A

fricatives, affricatives

122
Q

moderate to profound sensori-neural hearing loss

A
  • incomplete access to speech
  • hearing aids bring much speech into the audible range
  • discriminate between consonants by voicing and manner
  • difficulty identifying syllabic boundaries and speech pattern with hearing loss >95 dB
123
Q

temporary/fluctuating conductive hearing loss

A
  • speech and language difficulties due to developmental period during which the fluctuating hearing loss occurred
  • spatial orientation difficulty
124
Q

chronic otitis media symptoms that last for 8+ weeks consecutively are at risk for ….

A

speech and language problems

125
Q

vocal learning

A

hearing, production of sound, and relating the two together

126
Q

pre-lingual effects of hearing loss in adults

A

impact development of spoken language, reading ability, educational attainment, and vocational potential

127
Q

post-lingual effects of hearing loss in adults

A

cognitive and competency skills are unaffected when the hearing loss occurs slowly

128
Q

why is hearing loss related to dementia

A

greater cognitive resources dedicated to auditory perception processing detrimental to other cognitive processes (memory)