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child population
sensorineural hearing loss as birth defect
3/1000 kids
additional 6/1000 acquire by school age
prelingual hearing loss
birth to 3 y.o of age critical speech and language development
newborn hearing screening
UNHS
pass/refer screening protocol
false-negative pass screening, but has hearing loss
refer for complete audiological exam
false-postive fail screening, but pass exam
research supporting UNHS
when hearing loss identified by 6 months or age or younger, the prognosis for good language, speech etc. improves greatly
language similar to the child’s nonverbal cognitive development
low to average language development
pass vs. fail
passes: monitor hearing and language milestones
fail:
audiological assessment
consideration of risk factors
otolaryngological exam
risk factors
family history
low birth weight
low Apgar scores
in utero infection
ototoxic medications
ventilator use for more than five days
carniofacial anomoalies
syndrome
meningitis
hyperbilirubinemia
hearing test
method dependent on child’s age
follow-up testing two to four times per year
audiologist counsels parents about test results
provide opportunity to ask questions
establish follow-up schedule
auditory brainstem response (ABR)
most comprehensive test for identifying infants
birth through five months of age
electrophysiological
elicit brainwave activity
performed on sleeping child
measured in terms of latency
wave correlates to 1500 to 4000
otoacoustic emissions (OAE)
screen for newborns other than audiologist
pass/refer
tests 2000, 3000, 4000, and 5000Hz
record OAEs for hearing better than 30 to 4 dB
visual reinforcement audiometry (VRA)
child from 6 -18 m.o tested in sound booth via an audiometer
child is conditioned to look towards a lit box of moving toy, taking advantage of a child’s natural tendency to look towards sound and to seek positive reinforcement
able to obtain individual ear info
based on operant-conditioned response
conditioned play audiometry (CPA)
audiologist presents sound via an audiometer to a child who is in a sound booth
two or more years of age
“wait and listen” behavior
use familiar toys
can also use for speech testings
onset
prenatal: occurs before birth
perinatal: occurs at birth
postnatal: occurs after birth
non-genetic causes
intrauterine infection
rh-factor complications
pre-maturity
maternal diabetes
parental radiation
toxemia
anoxia
syphilis
genetic causes
half congenital hearing loss
modes
autosomal dominant
autosomal recessive
x-linked
syndromic vs. non-syndromic
configuration of audiogram
bilateral vs. unilateral
progression of hearing loss
affect on vestibular system
mixed conductive hearing losses
mixed
both SNHL and conductive
conductive
anomaly of outer and/or middle ear
most commonly caused by otitis media
also caused by cholesteatoma
questions about impact on academic performance
other disabilities
cognitive delays vision impairment
learning disabilities
attention deficit disorder
autism
counseling
a family centered approach
family system theory: family consists of interdependent individuals, none of whom can be understood in isolation from the family system
parents
siblings
extended family
stages of grief
shock and disbelief
guilt
bargaining
anger
depression or detachment
acceptance