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pure tone test
not measuring hearing, recording a set of behavioral responses to a set of acoustic signals that we interpret as representing hearing
threshold of audibility
defined as a set of minimum effect sound pressure level of an acoustic signal producing an auditory sensation in a specified fraction of trials—50% of the time
air conduction testing
involves a response following the normal route of hearing, ear canal—middle ear—cochlea
issues along the route to the cochlea
outer and middle—impacted cerumen—collapsed ear canal—issue in the middle ear—result in a conductive loss
bone conduction
direct stimulation of the cochlea via a bone oscillator place behind the ear via vibration of the temporal bone
bone conduction relationship to air conduction
it should never be worse since we are directly stimulating the cochlea, the response will always be better than or equal to the air conduction scores
hearing test results
tells us nothing about the impact or the patient’s individual issues
conductive hearing loss
result from issues in the outer and middle ear, the signal is not delivered to the inner ear because of issues in the OE and ME
sensorineural hearing loss
involve the cochlea, typically damage to the outer and or inner hair cells—retrocochlear involve issues—auditory nerve—to auditory cortex
mixed hearing loss
due to both issues in the OE and/or ME and issues in the cochlea
pure tone average
average of the thresholds at 500, 1000 and 2000 Hz
Issues involving the use of PTA
only used for the lay person, does not reflect frequencies above 2000 Hz, dB scale is logarithmic
speech reception threshold
lowest intensity in dB an individual can repeat or identify 2 syllable phonetically balanced words
speech detection threshold
lowest intensity in dB that an individual can tell the presence of speech—does not have to identify or repeat just detect the presence of sound
relationship between SRT, SDT, and pure tone thresholds
should be consistent with thresholds at 500, 1000, and 2000 Hz
dynamic range
difference in dB between threshold—speech or pure tones—and the point at which sounds become uncomfortable—UCL uncomfortable loudness level
dynamic range normal hearing vs hearing loss
normal hearing is large range as much as 100 to 110 dB. range narrows with hearing loss, recruitment—an abnormal growth in loudness—small increases in intensity very quickly become uncomfortable
word discrimination testing
repetition of one syllable—phonetically balance words—at a prescribed level above SRT in a sound treated room—no real relationship to the real world but it does give us an idea of the ability of that individual to understand speech
importance of speech testing
gives us a clue as to the impact of a hearing loss—also indicative of central processing
Intramural attenuation an air conductive signal and bone conducted signal (cross hearing)
approx 40 dB for an air conducted signal and 0 dB for a bone conducted signal
signal to noise ratio SNR
dB level of signal is what we want to hear, we always want a positive ratio—the level of the signal we want to listen to to the level of the background noise
difference between behavioral and objective tests
objective tests do not need any interpretation on the part of the patient
otoacoustic emissions—DPOAES—distortion product otoacoustic emissions
originate in the outer hair cells of the cochlea, an actual signal generated by distortion of the basilar membrane as sound travels up the basilar membrane, reflective of the sound we send into the cochlea, signal travels through ME into the ear canal, detected by a very sensitive microphone in the probe inserted in the ear canal
OAEs are not detected when
ME issues—fluid—negative pressure—holes in the TM, hearing losses greater than 30 dB (damage to outer hair cells)
OAEs tell us
if present, the outer hair cells are functional, but can be absent in individuals with normal hearing, typically used as a screening tool, can also be used to monitor cochlear function in individuals undergoing chemotherapy
can we use OAEs to estimate pure tone thresholds
no, a screening tool cannot be used for threshold
auditory evoked potentials
far field recording of the electrical activity of the neurological activity from the cochlea to the brainstem—takes approximately .5 msecs fir a signal generated in the cochlea to reach the brainstem—looking at brainwave activity before and after sound is introduced—can be used to determine threshold in an infant who failed an OAE screening—also can be used to detect tumors/growths on the auditory nerve—signal continues on to the auditory cortex, therefore could apply to auditory processing
time of onset of HL
congenital or acquired
time course of HL
acute, chronic, sudden, temporary, permanent, progressive, fluctuating
conductive hearing loss
involves issues in the outer and middle ear, generally are medically treatable, not usually longterm in most cases, compare AC to BC, remediation—generally responds well to amplification, degree is reflective of mass and stiffness
disorders—structural/malformations of the outer ear
embryologic development crania facial anomalies, congenital auricular malformations, microtia congenital fissure (low set ears, pits, or tags/atresia), TM perforations impacted cerumen Otitis Externa—swimmers ear, carcinomas
disorders of the middle ear
ET dysfunction, OM with and without effusion, conductive loss, upper respiratory, inflammation, treatment consists of abx, PE tubes, radical mastoid… otosclerosis, physical trauma, barotrauma, tympanosclerosis
otosclerosis
make things louder
sensorineural hearing loss
outer vs inner hair cells, malformations or trauma, X or Y linked hearing disorder, progressive loss in children during early childhood, common causes such as congenital, CMV, HIV, Rubella, Syphillis, mumps, serous labyrinthitis, herpes, ototoxicity, ahminoglycosides, heavy duty abx, cancer meds, aspirin, diuretics, industrial solvents… as we age, presbycusis… others, autoimmune, idiopathic sudden, acoustic trauma, physical trauma, radio necrosis
central nervous system
retrocochlear, effects on speech understanding, effects on sensitivity, brainstem disorders, infarcts blood flow interruption, gliomas—tumors, MS, temporal lobe, CVAs, receptive language