Newborn Hearing Screening with Combined Otoacoustic Emissions and Auditory Brainstem Responses

414
*Department of Communicative Disorders, College of Public Health and Health Professions, University of Florida, Gainesville,
Florida; †Physicians Hearing & Balance Center and NeuroAudiology/Vestibular Laboratory, Drs. Kitchens, Chapman, & Anderson,
P.A., Montgomery, Alabama; **Department of Otolaryngology, Washington University, St. Louis, Missouri; ††Everest Biomedical
Instruments, Chesterfield, Missouri
Reprint requests: James W. Hall III, Ph.D., Department of Communicative Disorders, University of Florida, P.O. Box 100174, 101
S. Newell Drive, Room 2150A, Gainesville, FL 32610-0174; Phone: 352-273-6168; Fax: 352-273-6545; E-mail: jhall@phhp.ufl.edu
Supported in part by NIH grant R 42 DC03614.
Newborn Hearing Screening with
Combined Otoacoustic Emissions and
Auditory Brainstem Responses
James W. Hall III*
Steven D. Smith†
Gerald R. Popelka* ** ††
Abstract
Accurate assessment of neonatal hearing screening performance is impossible
without knowledge of the true status of hearing, a prohibitive requirement
that necessitates a complete diagnostic evaluation on all babies screened.
The purpose of this study was to circumvent this limitation by integrating two
types of screening measures obtained near simultaneously on every baby.
Peripheral auditory function was defined by otoacoustic emission results. A
complete diagnostic evaluation was performed on every baby who received
a “Refer” outcome for auditory brainstem response screening. The integrated
results for auditory brainstem response screening in an unselected group of
300 newborns estimated sensitivity at 100%, specificity at 99.7%, overall referral
rate at 2.0%, and a positive predictive value of 83.3%. Conductive loss
associated with amniotic fluid in the middle ear can persist several weeks after
birth; conductive loss can produce a “Refer” outcome for auditory brainstem
response screening; and auditory neuropathy can be detected with screening
measures. Prevalence results were consistent with the published literature.
The implications of this study are that otoacoustic emissions and auditory
brainstem measures provide much more information than either alone and
that both are needed for a comprehensive hearing screening program.
Key Words: Auditory brainstem response, distortion-product otoacoustic emission,
neonate, sensitivity, specificity, universal hearing screening
Abbreviations: ABR = auditory brainstem responses; OAE = otoacoustic
emissions; PPV = positive predictive value; NIH = National Institutes of Health
Sumario
La evaluación precisa del desempeño en el tamizaje auditivo neonatal es
imposible sin conocer el verdadero estado de la audición, un requisito prohibitivo
que exige una evaluación diagnóstica completa de todos los bebés
evaluados. El propósito de este estudio fue superar esta limitación integrando
dos tipos de medidas obtenidas casi simultáneamente en cada bebé. La función
auditiva periférica fue definida por los resultados de las emisiones
otoacústicas. Se realizó una evaluación diagnóstica completa en cada bebé
que obtuvo un resultado de “refer” en el tamizaje por respuestas auditivas de
tallo cerebral. Los resultados integrados para el tamizaje por respuestas auditivas
de tallo cerebral, en un grupo no seleccionado de 300 recién nacidos,
estimaron una sensibilidad de 100%, una especificidad de 99.7%, una tasa
global de referencia de 2.0%, y un valor predictivo positivo de 83.3%. Una
pérdida conductiva asociada con líquido amniótico en el oído medio puede
persistir semanas después del nacimiento; una pérdida conductiva puede
generar como resultado un “refer” para tamizaje por respuestas auditivas de
tallo cerebral; una neuropatía auditiva puede ser detectada con medidas de
tamizaje. Los resultados de prevalencia fueron consistentes con los publica-
J Am Acad Audiol 15:414–425 (2004)
For over a quarter of a century,
accumulated clinical experience with
millions of babies has supported the
value of auditory brainstem responses (ABR)
in newborn hearing screening (Hecox and
Galambos, 1974; Schulman-Galambos and
Galambos, 1975). Initially, hearing screening
was limited to babies meeting selected criteria
placing them at risk for hearing loss (AAP,
1982; Mauk et al, 1991). The development of
automated ABR technology was a major factor
contributing to the emergence of universal
newborn hearing screening (Hall et al, 1987;
Stewart et al, 2000). Similarly, beginning
with the earliest published reports over 20
years ago, transient evoked otoacoustic
emissions (OAE) (Bray and Kemp, 1987;
Johnsen et al, 1988; Vohr et al, 1998; Norton,
Gorga, Widen, Vohr et al, 2000), and then
distortion product OAEs (Lafreniere et al,
1991; Bonfils et al, 1992; Smurzynski et al,
1993; Gorga et al, 2000; Hall, 2000), have
assumed an important role in newborn
hearing screening. Subsequently, several
papers also described the combined use of
ABRs and OAEs in newborn hearing
screening (Norton et al, 2000; Stewart et al,
2000; Gorga et al, 2001), although not always
with automated devices. A variety of
automated OAE devices are now available
commercially. Despite recommendations for
a two-step or two-stage screening approach
(Norton, Gorga, Widen, Folsom et al, 2000;
Gorga et al, 2001), there are among the
dozens of studies documenting the usefulness
of ABR or OAE techniques in newborn
hearing screening no published papers
describing the application of both
technologies, in combination, and with a
single, automated commercially available
device.
Determining true sensitivity and
specificity for any neonatal hearing-screening
program is virtually impossible for two
reasons. First, all babies would have to have
complete diagnostic evaluations at the time
of the screening to fulfill the basic
requirements of such determinations. Second,
a very large number of babies would have to
be screened to have sufficient numbers of
hearing-impaired babies because of the rather
low incidence of hearing impairment in the
general population (<1%). Therefore, to
calculate true sensitivity and specificity, and
to document accurately the false negative
rate, many tens of thousands of babies would
have to be screened, and all of them would
have to receive complete diagnostic
evaluations often done under light sedative.
This approach is prohibitive because of the
amount of effort required and the financial
cost. Sedating so many normal-hearing babies
may also be a dubious practice on an ethical
basis as well. However, with the use of
combined OAE and ABR screening, one type
of testing can be used to evaluate or
crosscheck the other type of testing. Though
this reasoning is circular, combining OAE
and ABR technologies offers a viable approach
to establishing reasonably accurate sensitivity
and specificity values. This approach is a
substantial improvement over all previous
approaches that have not used an
independent hearing measure on all babies.
Further, the strategy offers an advantage
over the approach taken in the large-scale
multicenter, multiyear National Institutes
of Health (NIH) study (Norton, Gorga, Widen,
Folsom et al, 2000), namely, the two measures
can be made essentially concurrently
compared to the many months separating
the screening measures and the behavioral
measures of hearing. This last point should
be stressed. In a population with a high
incidence of transient conductive problems,
comparison of test results separated by even
a few minutes may complicate interpretation
of the data.
Newborn Hearing Screening/Hall et al
415
dos en la literatura. Las implicaciones de este estudio establecen que las emisiones
otoacústicas y las medidas de potenciales auditivos del tallo cerebral
aportan juntas más información que cada prueba por separado, y que ambas
se necesitan en un programa integral de tamizaje auditivo.
Palabras Clave: Respuestas auditivas del tallo cerebral, emisiones otoacústicas
por productos de distorsión, neonatos, sensibilidad, especificidad, tamizaje
auditivo universal
Abreviaturas: ABR = Respuestas auditivas del tallo cerebral; OAE = emisiones
otoacústicas; PPV = valor predictivo positivo; NIH = Institutos Nacionales
de Salud
Combined automated OAE and ABR
screening offers a variety of other potential
advantages. Integrated OAE and ABR
technology allows for an individual patient's
in-ear calibration of signal levels for ABR, as
well as for OAE test signals. Screening
efficiency is enhanced by a combined OAE and
ABR screening capability that allows
immediate application of many different
protocols that account for differences in
hearing loss prevalence and etiology (Gorga
et al, 2001). For example, a protocol may be
selected for a well-baby nursery whereby a
baby initially is screened rapidly with an
automated OAE and then screened with an
automated ABR in the case of an OAE “Refer.”
A different protocol may be selected for a
neonatal intensive care nursery with a higher
prevalence of hearing loss and fewer
restrictions associated with longer hospital
stays. For example, a baby initially may be
screened with an automated ABR and then
immediately screened with an automated
OAE in the case of an ABR “Refer.”
With the combination of automated OAE
and automated ABR technologies, universal
newborn hearing screening can yield a refer
rate of <2% and a false-positive rate of <2.0%
(Stewart et al, 2000; Gorga et al, 2001).
Parental anxiety can be minimized by
reducing the period between an initial
newborn screening in the hospital and the
secondary screening scheduled later, or the
diagnostic assessment scheduled after
hospital discharge. Follow-up rates for infants
who do not pass hearing screening are often
far below the 95% target set by the American
Academy of Pediatrics (Erenberg et al, 1999).
With low refer rates, the number of babies
that must return for diagnostic audiologic
assessment is lower, and therefore, it is likely
that fewer hearing-impaired infants will be
lost to follow-up. Also, the low refer rates
characteristic of combined OAE/ABR
screening result in the need for fewer
diagnostic follow-up assessments and
markedly lower costs associated with the
identification of each hearing-impaired child.
The combined use of OAEs and ABRs in
newborn hearing screening permits, before
hospital discharge, the initial differentiation
of conductive versus sensory versus neural
auditory dysfunction. For example, the
combination of an OAE “Refer” with an
automated ABR “Pass” suggests a peripheral
conductive etiology such as vernix caseosa in
the external ear canal or subtle middle ear
dysfunction. This possibility can then be
confirmed with other procedures, for example,
tympanometry. Immediate differentiation
among major types of auditory dysfunction,
in turn, can result in quicker and more
appropriate management. Finally, the
combined application of OAE and ABR in
newborn hearing screening leads to early
identification of auditory neuropathy in the
well-baby population, as well as in the
intensive care nursery. A “Pass” outcome for
OAE screening, coupled with a “Refer”
automated ABR outcome, raises the question
of auditory neuropathy and certainly
warrants follow-up diagnostic audiometry.
Many universal neonatal hearing
screening programs use only the ABR as an
indicator of the status of the baby's hearing.
Though all screening ABR devices
automatically determine the presence or
absence of the ABR, measurement procedures
differ substantially across devices and are not
standardized. One automatic ABR screening
device determines the presence of an ABR by
matching the measurement to a template
representing a normal response. An
increasing number of other ABR screening
devices determine the presence of the
response by ascertaining if the measured
variance ratio, an ABR signal-to-noise ratio,
exceeds a criterion.
The most common ABR variance ratio is
based on the magnitude of the response in the
averaged ABR waveform (the signal) divided
by the magnitude of the noise. In babies who
have an ABR, the measured response is larger
than the noise, and the signal-to-noise ratio
is a value greater than 1.0. In babies who do
not have an ABR, the measured response is
approximately the same as the noise, and
the signal-to-noise ratio is approximately
1.0. Originally this signal-to-noise ratio was
labeled Fsp (Don et al, 1984) because the
response was evaluated with the F statistic
using the variance of the value at a single
point in the ABR waveform to measure the
magnitude of the noise. Though the signalto-
noise ratio values in all modern devices are
based on multiple points for calculating the
noise variance rather than a single point,
the older Fsp label is still commonly used and
also will be used in this paper. The
effectiveness of Fsp values for neonatal
hearing screening in combination with the use
of concurrent OAE measures in assessing
416
Journal of the American Academy of Audiology/Volume 15, Number 6, 2004
screening performance is the focus of this
paper.
The magnitude of an ABR is quite stable
in an individual for stimuli at a fixed level.
Conversely, the magnitude of the noise varies
greatly depending on patient-related factors
(unrelated brain activity, muscle movements,
etc.), environmental factors (stray electrical
activity from lights, other electronic
equipment, etc.), and most importantly,
measurement parameters. Signal averaging
reduces the noise allowing the ABR to be
detected. In general, the more the response
is averaged, the more the noise is lowered,
which in turn increases the Fsp value.
In the large NIH-sponsored multicenter
study of over 7,000 newborns (Norton, Gorga,
Widen, Folsom et al, 2000), the authors
specifically used Fsp as the parameter for
ABR measures. Further, they demonstrated
that a criterion Fsp value of 3.1 effectively
separates normal-hearing babies (“Pass”)
from those who require a full diagnostic
evaluation (“Refer”).
Desktop systems that employ a personal
computer and various related amplifiers and
components generally have sufficient
capability to both adequately measure and
store ABRs and perform the complex data
processing necessary to calculate Fsp values.
However, desktop devices are not optimized
for screening because of their complexity,
their size, and the fact that they require an
AC outlet, an arrangement that usually
results in transporting the babies to the
device. Even those systems that use a batteryoperated
laptop computer are not optimized
for screening because the AC line is still
required for the other components. On the
other hand, a self-contained battery-operated,
handheld device is better suited for neonatal
screening because it allows the measurements
to easily be made wherever the baby is
located, including the mother's room.
PURPOSE
The purpose of the present study was to
estimate sensitivity and specificity values
using ABR measures alone and when
combined with OAE measures obtained
nearly simultaneously in a well-baby
population. A secondary purpose was to
determine if a recommended criterion Fsp
value (3.1) was valid for ABR measures. The
intent was to determine the validity of a new
hearing screening approach and to evaluate
the recommendations from a large NIH study.
METHOD
Subjects
A series of 300 neonates in a well-baby
nursery were measured using convenience
sampling. There were no exclusion criteria.
Both OAEs and ABRs were measured
concurrently in both ears 13 to 42 hours after
birth. The number of females (161) was
slightly more than the number of males (139).
Institutional Review Board approval was
obtained for this study.
Screening Instrumentation and
Procedures
A self-contained battery-operated
handheld hearing screener (Audioscreener,
developed by Everest Biomedical Instruments
and licensed to Grason-Stadler Instruments)
was used for all screening OAE and ABR
measures. This device is about the size of a
paperback book with a single probe and three
electrode wires. The same probe is used for
both OAE and ABR measures and allows the
two types of measures to be obtained within
seconds of each other.
Distortion product OAEs at 2f1-f2 were
evoked with two tones (f1 and f2) at each of
four f2 frequencies (2000, 3000, 4000, and
5000 Hz), with an f1 level (L1) set at 65 dB
SPL and an f2 level (L2) set at 55 dB SPL (L2
- L1 = -10 dB) as measured in the external ear
canal. Signals were presented, and DPOAEs
detected, with a probe assembly that
contained a microphone and two miniature
loudspeakers. For each subject, a complete
probe fit was determined and signal levels
were verified and adjusted with real ear
measures immediately before data collection.
Signal calibration tolerance was within ±2 dB.
The f2/f1 ratio was 1.2. DP amplitudes (Ldp),
and noise floor levels (Lnf) were calculated for
each test frequency. A “Pass” outcome for
DPOAE screening was defined as a minimum
signal-to-noise level difference (Ldp - Lnf) of
6 dB, and minimum Ldp values of -7 dB SPL
for 2000 Hz, -8 dB SPL for 3000 Hz, -5 dB SPL
for 4000 Hz, and -7 dB SPL for 5000 Hz
(Gorga et al, 1997) at a minimum of three of
the four test frequency regions.
Newborn Hearing Screening/Hall et al
417
The ABRs were recorded from the scalp
using disposable electrodes placed at Fz
(noninverting) and the ipsilateral mastoid
process (Mi, with the contralateral mastoid
process used as ground) in response to click
signals (100 μsec) presented through the
same probe assembly that was used for
DPOAE measurements. The device was
configured to present rarefaction clicks at
35 dB nHL at a rate of 37.1/sec. A unique
feature of this device is that the adequacy of
the probe fit and the level of the ABR stimulus
is verified and adjusted in the actual ear
being measured instead of relying on a
coupler calibration as is typically done. The
level of the real-ear ABR stimulus was
determined automatically using the
microphone built into the probe, similar to the
procedure used for OAE. The ABR was
collected with a high-pass filter setting of
100 Hz and a low-pass filter setting of 3000
Hz. Electrode impedance was ≤12 kohms,
while the maximum electrode impedance
mismatch between electrodes was ≤5 kohms.
The device stores “Pass” or “Refer” results,
OAE levels in dB SPL, Fsp values, and the
averaged ABR waveform for each ear in a
single record for each baby. These data can
then be downloaded through a wireless
infrared port and stored in an external
software application (Audiotrac) on an external
computer and then exported into conventional
statistical and other software applications for
further, more detailed analyses.
The presence or absence of an ABR was
determined with the Fsp statistic described
earlier. The Fsp value for each auditory
brainstem response was based on a fixed
number of 3000 sweeps to allow direct
comparison of Fsp values across subjects.
Screening Data Analyses
The OAE results were used to determine
if peripheral auditory function was normal.
Specifically, an ear that had OAEs that
exceeded the “Pass” criteria was assumed to
have normal-hearing sensitivity and no
significant conductive abnormality. In the
analysis of the ABR screening data, OAEs
provided an independent indication of
peripheral auditory status.
The criterion for an ABR “Pass” outcome
was an Fsp value ≥3.2, the closest setting to
the recommended value of 3.1 from the large
NIH multicenter study. All of the ears that
received an ABR “Pass” result had normal
peripheral auditory status as determined by
an OAE “Pass” result obtained nearly
simultaneously. No further testing was
performed on these ears.
Each ear that obtained an ABR Fsp value
of less than 3.2 received a “Refer” result
regardless of the OAE outcome. All babies
who received an ABR “Refer” result in one or
both ears received a full diagnostic evaluation
on an outpatient basis after the initial
screening. These diagnostic evaluations
employed auditory threshold searches using
a diagnostic ABR desktop system and a full
complement of other diagnostic measures,
for example, aural immittance measures,
diagnostic OAEs, behavioral audiometry, and
so forth.
Diagnostic Instrumentation and
Procedures
Acomprehensive diagnostic evaluation was
performed within four to six weeks of the initial
hospital referral for every neonate with an ABR
“Refer” screening outcome. Prior to the diagnostic
audiologic assessment, each infant underwent
a medical evaluation by an otolaryngologist.
Repeat ABR and OAE screenings first were
performed with the screening device at the time
of the diagnostic evaluation.
A comprehensive ABR and OAE
assessment was conducted within our medical
practice or in an audiology clinic under
natural sleep or at one of the outpatient
surgical centers under light sedation (chloral
hydrate or Versed) with anesthesiology
support. Afull diagnostic ABR was performed
with a commercially available auditory
evoked response system (Bio-Logic Traveler
SE EP system or Bio-Logic Navigator Pro
EP System). Air-conduction clicks and toneburst
signals were delivered monaurally at
rates of 27.1 to 37.1/sec via insert earphones
(ER-3A). Stimulus polarity was either
rarefaction or condensation. Clicks were 100
μsec, and tone-burst signals were centered at
500, 1000, 2000, and/or 4000 Hz with
Blackman ramping and duration of two cycles
of rise/fall time, and 0 cycle plateau. Stimulus
level was referenced to normal-hearing levels
for adults (dB nHL). Bone-conduction
stimulation was utilized, as appropriate,
based on otologic findings or the pattern of
air-conduction ABR findings. Diagnostic ABRs
were recorded with scalp electrodes located
Journal of the American Academy of Audiology/Volume 15, Number 6, 2004
418
in the high forehead location (noninverting)
and the ipsilateral mastoid process or earlobe
(inverting), and with a ground electrode
located on the low forehead. Filter settings
were 30 to either 1500 or 3000 Hz. The gain
was typically 100,000. The analysis window
was set to either 15 or 20 msec (for 500 Hz
tone burst signals). For each ear of all infants,
the diagnostic ABR was performed for
neurodiagnosis (i.e., analysis of interwave
latency values in msec) and threshold
estimation (i.e., latency/intensity functions in
dB nHL). Aural immittance measurement
was not performed due to unavailability of a
high-frequency probe tone option required
for infants under the age of six months. In
some cases sound-field behavioral observation
audiometry was conducted with frequencymodulated
tones or narrow-band noise signals
centered at standard audiometric frequencies
with the infant in either an infant carrier or
in the parent’s lap while located between two
ear level sound-field speakers.
RESULTS
Afrequency distribution of the Fsp values
for all ears is shown in Figure 1. The bin
width was selected so that bins labeled 3
and lower represent Fsp values ≤3.1, the
criterion for separating “Pass” from “Refer”
recommended by the large NIH study. The
distribution is symmetrical and appears to be
normally distributed. The distribution clearly
identifies the ten ears that required a full
diagnostic evaluation. The performance of
the ABR screening using traditional methods
for evaluating sensitivity, specificity, and
positive predictive value (PPV) (called
Baysian analysis) analyzed separately by
ear is shown in Table 1. Of the 600 ears that
were screened, 590 yielded an ABR “Pass”
(Fsp ≥3.2). All of these 590 ears also received
a “Pass” result for the OAE measure at the
time of the ABR screening providing
substantial evidence that there were no
hearing-impaired cases in this group. The
remaining ten ears each received an ABR
“Refer” outcome defined as an Fsp value <3.2.
The actual hearing sensitivity of these
ears was determined at the time of the
diagnostic evaluation. The sensitivity of the
ABR screening test (the percentage of ears
Newborn Hearing Screening/Hall et al
419
0 1 2 3 4 5 6 7 8 9 10 11 12
Variance Ratio (Fsp)
0
25
50
75
100
125
Frequency (Number of Ears)
Figure 1. Frequency distribution of the auditory
brainstem responses for clicks (37.1/sec at 35 dB
nHL) and measured as a variance ratio (Fsp, 3000
frames) for 600 ears of 300 neonates in a well-baby
nursery. The bin widths were selected so that the bins
labeled 3 and lower represent Fsp values <3.2.
Table 1. Summary of the Test Performance for an Auditory Brainstem Response Hearing
Screening Technique in a Series of 300 Newborns
Screening Outcome
Diagnostic Outcome Pass Refer Number of Ears
Normal 590 2 592
Hearing Impaired 0 8 8
Number of Ears 590 10 600
Sensitivity 100.0%
Specificity 99.7%
Refer Rate 1.7%
Positive Predictive Value (PPV) 80.0%
Note: The “Pass” criterion was an Fsp value of ≥3.2. The results are separated by individual ears.
with actual hearing impairment that received
a “Refer” outcome) was 100%. The specificity
of the ABR screening test (the percentage of
normal-hearing ears that received a “Pass”
outcome) was 99.7%. The overall referral
rate (the percentage of ears referred for a
full diagnostic evaluation) was 1.7%. The
positive predictive value (the probability that
an ear that received an ABR screening “Refer”
result was in fact hearing impaired) was
80.0%.
Though analyses of the data by individual
ear is instructive, analyses by individual
neonate would represent the actual clinical
situation. Performance of the ABR screening
using traditional methods for evaluating
sensitivity, specificity, and positive predictive
value analyzed separately by neonate is
shown in Table 2. Of the 300 neonates who
were screened, 294 yielded an ABR “Pass”
(Fsp ≥3.2) in both ears. All of these 294
neonates also received a “Pass” result in both
ears for the OAE measure at the time of the
ABR screening providing substantial evidence
that there were no hearing-impaired neonates
in this group. The remaining six neonates
each received an ABR “Refer” outcome defined
as an Fsp value <3.2 in at least one ear. The
actual hearing sensitivity of these neonates
was determined at the time of the diagnostic
evaluation. The sensitivity of the ABR
screening test (the percentage of neonates
with actual hearing impairment who received
a “Refer” outcome) was 100%. The specificity
of the ABR screening test (the percentage of
normal-hearing neonates who received a
“Pass” outcome) was 99.7%. The overall
referral rate (the percentage of neonates
referred for a full diagnostic evaluation) was
2.0%. The positive predictive value (the
probability that a neonate received an ABR
screening “Refer” result was in fact hearing
impaired) was 83.3%.
Findings for the full diagnostic
evaluations for these six neonates are
summarized in Table 3. These results were
used to estimate prevalence of hearing
impairment by type though caution must be
used in interpretation because of the small
numbers.
Journal of the American Academy of Audiology/Volume 15, Number 6, 2004
420
Table 2. Summary of the Screening Test Performance for a Combined Otoacoustic Emissions
and Auditory Brainstem Response Hearing Screening Technique in a Series of 300 Newborns
Screening Outcome
Diagnostic Outcome Pass Refer Number of Neonates
Normal 294 1 295
Hearing Impaired 0 5 5
Number of Neonates 294 6 300
Sensitivity 100.0%
Specificity 99.7%
Refer Rate 2.0%
Positive Predictive Value (PPV) 83.3%
Table 3. Summary of Diagnostic Evaluations Following a “Refer” Outcome with Combined
Otoacoustic Emissions and Auditory Brainstem Response Hearing Screening for 300
Neonates in a Well-Baby Nursery
Prevalence
Diagnostic Outcome Number % Per 1000
Conductive 2 0.67% 6.7/1000
Sensorineural (Cochlear) 2 0.67% 6.7/1000
Sensorineural (Auditory Neuropathy) 1 0.33% 3.3/1000
Normal 1 N/A N/A
Note: The results also were used to calculate prevalence of hearing impairment.
Case Reports
The audiologic results for each baby who
received a complete diagnostic evaluation
will be given in greater detail. This approach
will shed more light on the screening process
and allow a more direct comparison to the
screening results.
Case 1. This infant initially yielded a “Refer”
outcome bilaterally for both the ABR and
OAE hearing screenings. The first diagnostic
evaluation showed no detectable OAE.
Diagnostic ABR findings, however, were
consistent with a bilateral conductive hearing
loss. That is, absolute latencies for ABR waves
I, III, and V were proportionally prolonged in
comparison to the age-appropriate normative
data provided graphically with the auditory
evoked response system. Analysis of the
latency/intensity function for click signals
confirmed the presence of a repeatable wave
V down to a level of 40 dB nHL for the right
ear and down to 35 dB nHL for the left ear.
Neurodiagnostic ABR findings (interwave
latency values) were normal with respect to
the age of infant. Bone-conduction ABR
threshold estimations were within normal
limits. Taken together, these results were
consistent with a conductive component
bilaterally.
Otolaryngology examination showed
bilateral clear middle ear fluid with slight
vernix impaction upon the tympanic
membrane. Vernix was removed and the
infant was followed up audiologically in three
weeks. Upon return, subsequent screening
with OAEs and ABR produced a “Pass”
outcome bilaterally. A full ABR
latency/intensity function was repeated
showing the presence of a clear and
repeatable wave V down to an intensity of 15
dB nHL bilaterally. Otologic examination
yielded normal findings, consistent with
resolution of middle ear pathology. There is
substantial evidence that this case had a
bilaterally conductive hearing loss at the
time of the screening and even after hospital
discharge. It also demonstrates that ABR
screening is not always insensitive to
conductive conditions as is commonly
believed.
Case 2. For this infant, the initial screening
yielded a “Refer” outcome bilaterally for both
ABRs and OAEs. A secondary screening
yielded a “Pass” outcome bilaterally for ABR
and OAEs. A later diagnostic ABR also
showed normal wave I, III, and V latency
values (in comparison to the age-appropriate
normative database) and a normal
latency/intensity function with a reliable
wave V down to a level of 15 dB nHL for
each ear.
Otologic examination confirmed normal
appearing tympanic membranes with no
obvious debris in the external ear canal or
middle ear fluid. The child passed bilaterally
a subsequent OAE screening five months
later. This case demonstrates a true screening
false positive result, although it is possible
that bilateral middle ear fluid resolved
spontaneously during the interval between
the screening and follow-up diagnostic
assessment.
Case 3. This infant was referred for
diagnostic follow-up after screening in the
well-baby nursery yielded bilateral “Refer”
outcomes for the ABR and OAE techniques.
Diagnostic audiologic evaluation yielded no
measurable OAEs. In addition, there were no
observable behavioral responses in the sound
field to pure-tone, warble-tone, or narrow
band noise signals. There was no reliable
ABR for air-conduction clicks or tone bursts,
or bone-conduction clicks at the intensity
limits of the evoked response system for each
signal.
Otologic examination findings were
reported as normal with no observed external
or middle ear pathology. The infant was
referred to a regional Children's Hospital
and subsequently followed there by audiology
and pediatric otolaryngology. The infant
initially was provided with amplification at
5 months of age and then, when amplification
was not successful, underwent a cochlear
implantation at 12 months of age. This case
demonstrates a true correct referral.
Case 4. At the initial screening in the wellbaby
nursery, this infant yielded a “Refer”
outcome only for the right ear with the ABR
technique. The infant passed OAE screening
bilaterally and the ABR screening for the
left ear. Subsequent diagnostic audiologic
evaluation produced normal OAE findings
bilaterally. The diagnostic ABR assessment
indicated the presence of waves I, III, and V
at normal age-corrected latencies for the left
ear, and the latency/intensity function showed
Newborn Hearing Screening/Hall et al
421
a clear wave V down to an intensity level of
15 dB nHL for click stimuli. ABR thresholds
were also obtained at normal levels for toneburst
signals of 500 Hz, 1000 Hz, 2000 Hz,
and 4000 Hz. For right ear stimulation, there
was no detectable ABR at the limits of the
evoked response system (95 dB nHL) for click
signals, and for tone-burst signals at 500 Hz,
1000 Hz, 2000 Hz, and 4000 Hz. However,
during ABR assessment the presence of a
cochlear microphonic provided evidence of
some cochlear function, presumably due to
outer hair cell integrity further indicating
this may not be a sensory hearing loss.
Otologic examination indicated normal
findings with no external or middle ear
abnormalities noted. Due to the presence of
repeatable OAEs and the subsequent
abnormal right ear ABR, the infant was
referred to Children's Hospital for further
testing. Radiographic imaging yielded no
abnormalities within the cochlea or
brainstem, such as a retrocochlear lesion.
Auditory neuropathy cannot be ruled out
and presently is the current diagnosis. This
case demonstrates clearly that the
combination of OAE and ABR testing can
detect correctly all auditory disorders up to
the level of the brainstem.
Case 5. This infant yielded a “Refer” outcome
bilaterally for ABR and OAE hearing
screening in the well-baby nursery. On
diagnostic audiologic evaluation, OAEs were
not observed for the right and left ears. An
ABR assessment revealed a wave V for a
stimulus level of 95 dB nHL bilaterally, and
down to 60 dB nHL for the right ear and
down to 85 dB nHL for the left ear. An ABR
for tone-burst stimulation was observed for
the right ear at stimulus levels down to 65 dB
nHL for 2000 Hz and 4000 Hz. No response
was obtained for tone-burst signals of 500 or
1000 Hz, and no response was observed
bilaterally for air-conduction or boneconduction
signals. For the left ear, there
was no detectable ABR for tone-burst or boneconduction
stimulation. In addition, the child
showed no observable behavioral response
to sound-field auditory stimulation.
Findings for the otologic evaluation were
reported as normal. Audiology recommended
a hearing aid consultation and assessment,
and the infant was referred back to the
pediatrician for approval of hearing aid
fitting. This child was then placed into the
Children's Rehabilitative Services for early
intervention. This case demonstrates that
the current screening pass criteria are
adequate for detecting even moderate
sensorineural hearing losses.
Case 6. This infant was scheduled for followup
audiologic assessment due to a “Refer”
outcome on ABR and OAE hearing screening.
A secondary screening resulted in a “Pass”
outcome for the left ear on both ABR and
OAE, and a “Refer” outcome on both the ABR
and the OAE for the right ear. Follow-up
diagnostic ABR and OAE assessment yielded
absent OAEs. Diagnostic ABR showed normal
waveforms for the left ear, and the presence
of a wave V down to a level of 10 dB nHL. ABR
latencies were analyzed with respect to ageappropriate
normative data. With tone-burst
stimulation at 2000 and 4000 Hz of the left
ear, there was a reliable wave V down to 20
dB nHL. The infant awoke before an ABR
could be evoked for tone-burst stimulation of
the left ear at 500 or 1000 Hz.
With right ear stimulation, ABR waves
I, III, and V were observed for a click signal
presented at 80 dB nHL. Latencies were
slightly delayed, consistent with a possible
conductive loss. A latency/intensity function
indicated the presence of a wave V down to
an intensity level of 40 dB nHL. With tone
bursts of 1000 and 4000 Hz, there was an
ABR wave V at 40 and 45 dB nHL,
respectively. An ABR recording for 500 Hz
tone-burst signals could not be completed
due to high activity level from the infant.
Bone-conduction ABRs were recorded for
levels better than 20 dB nHL, suggesting
the presence of a conductive component,
rather than a sensory loss.
Otologic examination indicated
significant right ear middle ear fluid upon
microscopic evaluation. No other
abnormalities were noted for the external or
middle ear.
Follow up diagnostic audiologic
assessment four weeks later yielded normal
OAEs for both the right and left ears. Another
screening ABR produced a “Pass” outcome for
both the right and left ears. A repeat
diagnostic ABR assessment further indicated
the presence of wave V down to a level of 15
dB nHL for both ears. This case demonstrates
that unilateral hearing loss also can be
detected accurately in a neonatal hearing
screening program.
Journal of the American Academy of Audiology/Volume 15, Number 6, 2004
422
DISCUSSION AND CONCLUSIONS
Neonatal hearing screening performance
can be assessed accurately by
integrating two types of screening measures
to circumvent the requirement that all babies
receive a complete diagnostic evaluation.
Peripheral auditory function can be
accurately defined by otoacoustic emission
results. The approach has the added
advantage that the measure used to estimate
cochlear function, an OAE measure, is
obtained within seconds of the measure that
is used to quantify neural function, the ABR
screening. The use of a combined approach
improves the overall effectiveness of a hearing
screening program compared to the use of
either measure alone.
ABRs can be measured accurately with
a battery-operated handheld device. The
results obtained in a typical hospital nursery
are comparable to those obtained in the wellcontrolled
large multicenter NIH study. In
addition, Fsp values computed in a batteryoperated
handheld device are equivalent to
those obtained with large, desktop computer
systems in the NIH multicenter study.
Middle ear fluid can occur at birth and
persist even several weeks later. Published
estimates of the prevalence in the newborn
period of middle ear fluid vary widely (de
Sa, 1973; Eavey, 1993; Roberts et al, 1995).
Although there is some agreement that
middle ear disorders are more common among
infants with extended stays in the intensive
care nursery, consensus is lacking on the
likelihood of these disorders in the well-baby
population (Eavey, 1993; Roberts et al, 1995;
Priner et al, 2003). With reliance on a single
newborn hearing screening technology,
detection of auditory dysfunction secondary
to middle ear disorders is rarely possible.
That is, a “Refer” outcome for OAE screening
may be due to auditory dysfunction in
multiple sites, such as the external ear canal
(vernix), middle ear, and/or the cochlea. Yet
a “Pass” outcome with ABR does not
necessarily rule out middle ear disorder. The
combination of a “Refer” finding for an OAE
screening and a “Pass” outcome for ABR
screening raises the distinct possibility of
either external or middle ear disorder. This
possibility can be confirmed with diagnostic
ABR techniques, including bone-conduction
stimulation, along with tympanometry and
otoscopic examination.
We also present evidence, however, that
conductive hearing loss associated with
neonatal middle ear disorder can produce an
ABR screening “Refer” outcome. Although
data are generally lacking, the conventional
opinion expressed in the literature is that the
ABR will be detected in infants with modest
degrees of conductive hearing loss (Hall,
1992). To be sure, if the ABR wave I latency
were calculated in these cases, the analysis
would reveal the delay associated with a
conductive hearing loss component. Decisions
on screening outcome, however, are invariably
based not on ABR latency values but, rather,
on some statistical measure of the simple
presence of a wave V component. It is clear
that ABR screening can be affected by
neonatal conductive problems.
Consistent with previous citations in the
literature (Feinmesser and Tell, 1976;
Feinmesser et al, 1982; NIH, 1993; Cone-
Wesson et al, 2000), we report in this modest
sized sample of newborn infants that the
prevalence of bilateral deafness (profound
hearing impairment) is 0.33%, or about
3/1000, and the prevalence of bilateral severe
or greater sensorineural hearing impairment
is 0.67%, or about 6/1000.
Finally, the longitudinal diagnostic
findings for one infant in the present study
show that unilateral auditory neuropathy
can occur, as reported in the literature
(Sininger et al, 2000; Sininger and Starr,
2001). The case (number 4) reported in this
paper would have been missed with OAE
screening alone or with a policy of unilateral
hearing screening as followed in some
hospitals. The question of auditory
neuropathy is often raised in discussions of
newborn hearing screening strategy. Clearly,
with total reliance on OAEs as a screening
technique, auditory neuropathy will go
undetected. That is, the rare infants with
auditory neuropathy will yield a “Pass”
outcome along with the large numbers of
infants with normal (cochlear and
retrocochlear) auditory function. A logical
approach for minimizing the number of babies
with auditory neuropathy who are missed
during hearing screening is to perform
ABR screenings in populations likely
to include these infants, for example,
infants with neurologic risk factors (e.g.,
hyperbilirubinemia, asphyxia, degenerative
neurologic disease) or, conservatively, all
infants in the intensive care nursery. This
Newborn Hearing Screening/Hall et al
423
approach, however, does not immediately
differentiate babies with auditory neuropathy
from those with sensory or serious conductive
hearing loss, as all will yield a “Refer” ABR
screening outcome. The use of neurologic
risk factors as a factor in the detection of
auditory neuropathy, and the decision about
when to use the ABR versus OAE screening
technique, also is of very limited value in
the identification of auditory neuropathy in
the well-baby population. Although the
prevalence of auditory neuropathy in
apparently healthy children is not known, it
will no doubt be exceedingly low. Nonetheless,
auditory neuropathy has been reported in
well-baby screening populations. We
demonstrate herein that the surest and most
feasible strategy for early detection of
auditory neuropathy is to utilize a combined
OAE and ABR screening technique for all
infants. Acombination OAE/ABR device offers
the clinician multiple options for newborn
hearing screening, depending on
characteristics of the infant population, the
availability of other diagnostic
instrumentation, and the overall objective
of the screening program
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Newborn Hearing Screening/Hall et al
425


ULASAN JURNAL DI ATAS VERSI BAHASA MELAYU 

Tajuk : Bayi yang baru lahir memerlukan alat  Otoacoustic Emissions(OAE)

Dan Audiometry Brainstem Response (ABR) untuk ujian pendengaran.

Abstrak :

Jurnal ini adalah satu kajian yang dijalankan untuk mengetahui tahap pendengaran seseorang bayi dengan menggunakan penilaian Diagnostik. Fungsi pendengaran memainkan peranan yang penting dan ujian diagnostik adalah salah satu penilaian yang digunakan untuk menghasilkan pendengaran brainstem dalam pemeriksaan yang memberi tindakbalas.

Menurut kajian, kehilangan konduksian cecair amnion dalam telinga tengah boleh menghasilkan satu pendegaran brainstem pemeriksaan respon. Manakala pendengaran neuropathy pula boleh dikesan dengan langkah-langkah pemeriksaan.

Pengenalan :

Banyak pusat-pusat kesihatan dan klinikal memggunakan (ABR) iaitu pendengaran brainstem untuk pemeriksaan bayi yang baru lahir. Pada permulaan, bayi-bayi yang menjalankan pemeriksaan ini adalah bayi yang  berisiko untuk hilang pendengaran. ABR adalah salah satu alat pemeriksaan tahap pertuturan dan kefahaman. Selepas 20 tahun yang lampau OAE pula diperkenalkan iaitu Otoacoustic Emissions. Kedua-dua alat ini adalah untuk menentukan tahap kepekaan bayi terhadap bunyi dan tahap kebolehan mereka untuk berinteraksi.

Dalam menentukan tahap kepekakan dan ketentuan dalam berinteraksi, bayi perlulah mempunyai penilaian diagnostik yang lengkap untuk memenuhi syarat-syarat dalam pemeriksaan tahap kepekakan. ABR dan OAE mempunyai kelebihan tertentu dan saling berkaitan antara satu sama lain. ABR adalah untuk menentukan tahap isyarat manakala OAE pula adalah untuk menguji isyarat-isyarat tersebut. Alatan ini digunakan untuk

menapis dan menentukan samaada seseorang bayi itu mempuyai pendengaran ataupun tidak

Isi- isi penting :

Mengikut kajian, hasil gabungan OAE dan ABR yang menggunakan teknologi, pemeriksaan tahap kebolehan pendengaran seseorang bayi yang baru lahir boleh menghasilkan satu rujukan kadar <2% dan satu positif yang palsu <2.0%. Oleh yang demikian, kebimbangan ibubapa boleh dikurangkan dengan cara bayi yang baru lahir perlulah melanjutkan pemeriksaan pada satu tempoh masa yang ditetapkan. Bayi yang tidak melepasi tahap 95% aras sasaran yang di tentukan oleh Amerika Akademi Pediatrik maka ia perlulah membuat tindakan susulan yang selanjutnya. Pemeriksaan yang dijalankan ini bertujuan untuk memastikan tahap pendengaran bayi berfungsi dan dapat berinteraksi dengan alam semujadi dengan berkesan.

Penggunaan gabungan OAE dan ABR kepada bayi yang baru lahir ia bergantung kepada awal konduksi dimana pengunaan deria pendengaran dengan saraf otak. Sebagai contoh yang dapat kita perhatikan ialah kedudukan OAE dan ABR dalam saluran telinga luar haruslah berfungsi dengan baik. Dengan ini, alat ini dapat menghubungkan kesaluran pendengaran ke otak.

Banyak program-program yang dijalankan dengan menggunakan ABR sebagai petunjuk kepada tahap perkembangan bayi untuk mendengar. ABR adalah ukuran bagi magnitud dalam bentuk gelombang iaitu ABR (isyarat) yang dibahagikan kepada bunyi bising. Bayi yang menggunakan ABR, ransangan yang diterima adalah lebih besar berbanding bunyi bising. Keadaan bunyi bising berbeza-beza dan ia bergantung kepada keadaan pesakit. Walaupun demikian keadaan ini juga berpunca daripada factor-faktor persekitaran dan lain-lain.

v     Audiometry Brainstem Response (ABR)

Tujuan ujian ini dijalankan adalah untuk menilai integriti sistem auditori pada batang otak (brainstem) terhadap bunyi yang mempunyai frekeunsi yang tinggi sahaja. Ujian ini tidak memerlukan kerjasama dari kanak-kanak kerana mereka perlu ditidurkan semasa ujian ini dilakukan. Ubat pelali hanya akan diberikan ketika perlu sahaja di bawah penguasaan doktor.

Semasa tidur klien dipakaikan dengan penyalur elektrik di atas kepala. Alat ini berfungsi untuk mengukur tindakbalas rangsangan bunyi ke telinga, saraf pendengaran, keseimbangan saraf dan batang otak. Klien juga memakai earphone yang digunakan untuk menyalurkan bunyi kepada kedua-dua belah telinga. Audiologi akan mengawal dan mengubah keamatan bunyi tersebut manakala gelombang otak pula akan direkodkan menggunakan komputer.  Gelombang ini akan dianalisa untuk mengenalpasti sama ada telinga dapat mengesan bunyi atau tidak. Ujian ini dijalankan selama satu jam setengah.

Sebelum ujian dijalankan klien boleh makan atau minum tetapi dilarang untuk mengambil makanan yang mengandungi kafein, coklat dan minuman coca-cola 12 jam sebelum ujian dilakukan. Ujian ABR ini sesuai dijalankan bagi bayi yang baru lahir hinggalah peringkat dewasa.

v     Otoacoustic Emissions(OAE)

Tujuan otoacaustic Emissions adalah untuk menentukan fungsi koklea samaada normal atau tidak. Biasa ia digunakan dalan Saringan Pendengaran Bunyi Bayi (UNHS). Ujian Otoacoutic Emissions (OAE) juga merupan ujian yang boleh digunakan untuk kanak-kanak yang baru lahir. Tujuan ujian ini ialah untuk menentukan fungsi koklea samaada normal atau tidak. Biasanya digunakan dalam Saringan Pendengaran bayi. Ujian ini merupakan ujian yang mudah, ringkas dan cepat.

Tujuan kajian

Kajian ini adalah untuk menentukan tahap kepekaan dan ketentuan nilai-nilai dalam menggunakan langkah-langkah ABR dan OAE apabila digabungkan dan memberi impak yang positif kepada deria pendegaran. Oleh yang demikian pemeriksaan dan penilaian diagnostik adalah amat perlu dalam memastikan objektif kajian tercapai. Kajian ini di jalankan kepada kanak-kanak yang baru lahir dan seandainya penilaian dibuat dan dapat pastikan bayi mengahadapi masalah pendengaran alatan ABR dan OAE adalah digunakan untuk mengujinya.

Kaedah kajian

Banyak kaedah yang digunakan untuk menentukan tahap kepekaan dan ketentuan dengan menggunakan ABR dan OAE. Antara kaedah yang digunakan adalah kaedah pensampelan. Dalam kaedah ini tiada sebarang pengecualian. OAE dan ABR digunakan secara serentak kepada kedua-dua belah telinga bayi selama 42 jam selepas kelahiran.

Produk herotan OAEs di 2f1 f2 adalah salah satu cara yang digunakan untuk  menyembunyikan dua nada-nada (f1 dan f2) pada setiap empat f2 frekuensi-frekuensi (2000, 3000, 4000, Dan 5000 Hz), dengan satu f1 paras (L1) dikunci pada 65 dBSPL dan satu f2 paras (L2) dikunci pada 55 dB SPL (L2 - L1 = -10 dB) seperti yang diukur dalam saluran telinga luar. Isyarat-isyarat telah dibentangkan, dan DPOAEs dikesan, dengan satu penyiasatan yang mengandungi sebuah mikrofon dan dua pembesar suara miniatur. setiap seorang yang layak, penyiasatan lengkap akan disahkan dan menyesuaikan dengan  langkah-langkah telinga dengan serta-merta sebelum pengumpulan data dibuat. Toleransi yang di perolehi adalah dalam lingkungan 2 dB.F2 / f1 nisbah adalah 1.2.

Walaupun begitu, kaedah yang digunakan ini banyak kepada membuat kajian keatas bayi-bayi. Daripada kajian yang diperolehi ini, banyak symbol-simbol yang diperolehi dan ia menekankan kepada kaedah dan cara penggunaan OAE dan ABR.

Peralatan Diagnostik Dan Tatacara

Peralatan Diagnostik adalah satu alat untuk pesakit yang mengalami masalah pendengaran dan ujian diagnostik telah pun dijalankan. Diagnostik Acomprehensive adalah satu penilaian yang di gunakan dalam tempoh empat hingga enam minggu bagi pesakit awal untuk setiap neonat dengan satu ABR. Sebelum penilaian diagnostic audiologi di lakukan, setiap bayi akan dinilai melalui satu penilaian perubatan. Penggunaan ABR dan OAE digunakan dalam penilaian perubatan ini.

Kesimpulan

Secara keseluruhannya, hasil daripada pemeriksaan yang dilakukan, semua bayi perlulah melakukan ujian diagnostic yang lengkap untuk menguji tahap pendengaran mereka. Dalam ujian ini, peralatan yang digunakan alatan ABR dan OAE untuk mengukur tahap pendengaran kanak-kanak. ABR dan OAE adalah satu alatan yang berguna dalam menjalani ujian diagnostik.