Authors

  • G.Khaydarova
    Researcher, Tashkent Medical Academy, Uzbekistan

DOI:

https://doi.org/10.37547/ijmscr/Volume03Issue10-03

Keywords:

Auditory neuropathy otoacoustic emissions short-latency auditory evoked potentials

Abstract

The article presents the results of dynamic observation of indicators of objective methods of hearing testing in 36 children with auditory neuropathy. Based on the data obtained, a comparative analysis of the indicators of SAEP and TEOAE in dynamics was carried out.


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Volume 03 Issue 10-2023

13


International Journal of Medical Sciences And Clinical Research
(ISSN

2771-2265)

VOLUME

03

ISSUE

10

P

AGES

:

13-17

SJIF

I

MPACT

FACTOR

(2021:

5.

694

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5.

893

)

(2023:

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184

)

OCLC

1121105677















































Publisher:

Oscar Publishing Services

Servi

ABSTRACT

The article presents the results of dynamic observation of indicators of objective methods of hearing testing in 36

children with auditory neuropathy. Based on the data obtained, a comparative analysis of the indicators of SAEP and

TEOAE in dynamics was carried out.

KEYWORDS

Auditory neuropathy, otoacoustic emissions, short-latency auditory evoked potentials.

INTRODUCTION

Today, thanks to the widespread introduction into the

practice of audiologists of objective methods for

studying auditory function, a new type of hearing

impairment has been identified - auditory neuropathy

(AN) [1, 2, 3]. According to G. Rance[4] and T. Picton[5],

approximately 10% of children diagnosed as having

sensorineural hearing loss may actually have HF. This

figure reaches 15-20% in children with severe hearing

loss [6].

It is already known that in HF, unlike sensorineural

hearing loss, the outer hair cells are not damaged; the

Research Article

INDICATORS OF OTOACOUSTIC EMISSIONS AND SHORT-LATENCY
EVOKED POTENTIALS IN CHILDREN WITH AUDITORY NEUROPATHY

Submission Date:

October 01, 2023,

Accepted Date:

October 06, 2023,

Published Date:

October 11, 2023

Crossref doi:

https://doi.org/10.37547/ijmscr/Volume03Issue10-03


G.Khaydarova

Researcher, Tashkent Medical Academy, Uzbekistan

Journal

Website:

https://theusajournals.
com/index.php/ijmscr

Copyright:

Original

content from this work
may be used under the
terms of the creative
commons

attributes

4.0 licence.


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Volume 03 Issue 10-2023

14


International Journal of Medical Sciences And Clinical Research
(ISSN

2771-2265)

VOLUME

03

ISSUE

10

P

AGES

:

13-17

SJIF

I

MPACT

FACTOR

(2021:

5.

694

)

(2022:

5.

893

)

(2023:

6.

184

)

OCLC

1121105677















































Publisher:

Oscar Publishing Services

Servi

complexity of diagnosis and the diversity of the clinical

picture of this disorder complicates the choice of

rehabilitation method.

Various symptoms of HF are explained by functional

disorders or pathological changes in the peripheral

part of the auditory analyzer. However, in HF, the main

clinical manifestation is sensorineural hearing loss of

varying degrees with preserved outer hair cell

function. Patients have otoacoustic emissions (OAE)

but no short-latency auditory evoked potentials

(SLEPs).

Studies have examined that in patients with HF,

conventional rehabilitation tactics that help patients

with sensorineural hearing loss are not always

effective [7]. However, most studies studying the

characteristics of HF were carried out on small groups

of patients, and there is inconsistency in the results

obtained by different authors.

AIM OF THE RESEARCH

To study the indicators of SAEP and TEOAE in auditory

neuropathy over time.

PATIENTS AND RESEARCH METHODS

180 children with hearing impairment were examined.

Of these, 36 children with auditory neuropathy (AN)

were selected. This represented 20% of all patients.

Among those examined, 20 were boys (56%), 16 were

girls (44%).

In the majority of patients (29 people), the diagnosis of

HF was established before the age of 5 years. In 5

patients, HF was detected at the age of 1-3 years. In one

patient, HF was diagnosed in adolescence.

As objective methods for assessing hearing, we used

the method of recording otoacoustic emissions (OAE)

and short-latency auditory evoked potentials of the

brain (SAEP). The study was carried out at initial

treatment and over time after 3 months.

The study was carried out using the Neuro-Audio

apparatus. To register the UAE, they used a probe

containing two phones and a microphone. One tone is

continuously transmitted through one telephone, and

a second tone is continuously transmitted through the

other. The microphone provides registration of OAE

and control of the level of test tones. To isolate OAEs,

it is also necessary to reduce the level of input noise as

much as possible. Therefore, the examination was

carried out in a quiet room, and the probe was

hermetically installed in the external auditory canal.

The stimuli were broadband acoustic clicks presented

at a repetition rate of 20

50/s. The response signal

picked up by the microphone is amplified with a

bandwidth of 500 to 5000 Hz and sent to the computer

through an analog-to-digital converter.

The source of sound stimuli for recording SAEP was in-

ear telephones with an earmold pre-selected to size.

Silver chloride cup electrodes were used to record


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Volume 03 Issue 10-2023

15


International Journal of Medical Sciences And Clinical Research
(ISSN

2771-2265)

VOLUME

03

ISSUE

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SJIF

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MPACT

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(2021:

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(2022:

5.

893

)

(2023:

6.

184

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OCLC

1121105677















































Publisher:

Oscar Publishing Services

Servi

brain responses. Electrodes were fixed to the area at

the border of the scalp (reference electrode) and in the

area of the mastoid processes on the right and left

(active electrodes). During the studies, the

interelectrode resistance did not exceed 5 kOhm,

which was achieved by pre-treatment of the patient's

skin and the use of special conductive gels. When

conducting SAEP, various types of stimuli were used -

an acoustic click lasting 100 ms, tones with a frequency

of 1000, 4000, 2000 and 500 Hz

RESULTS AND DISCUSSION

Analysis of the results showed that in all patients with

HF we examined during the initial examination, OAE

was registered in the right and left ear. The exception

was one patient in whom OAE was recorded in only

one ear.

The acoustic reflex was not recorded in 55% of children

with HF. In 29% of children, the acoustic reflex was

recorded at frequencies of 500 Hz and 1000 Hz. The

reflex registration threshold in these cases was 120 dB.

When registering SAEP, we obtained the following

results: in 95% of children, SAEP was not registered

during the initial and repeated examinations. In 2 (5%)

children, SAEP was recorded to sound stimuli at a level

of 95-103 dB nHL.

HF refers to disorders of sound perception and differs

from other hearing pathologies in terms of damage to

the structures of the inner ear and auditory nerve [3,7].

In HF, the outer hair cells are preserved, which is why

OAE and OAEPI are recorded. The presence of OAE in

the absence of SAEP or recording of SAEP only at

maximum stimulus levels is a generally accepted sign

specific to CH.

However, our data indicate that in some patients with

HF, TEOAE may disappear over time. According to our

data, this was observed in 22% of patients. Similar cases

were reported in the study by J. Attias [8] (Table 1).

Table 1 shows the results of a dynamic study of OAE in

children with heart failure 3 months after the initial

examination.

Table 1

Comparative analysis of the results of registration of UAE in patients

with auditory neuropathy (N=36)

OAE was recorded during the initial

examination

OAE was registered after 3 months

Quantity in percentage

92%

76%


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Volume 03 Issue 10-2023

16


International Journal of Medical Sciences And Clinical Research
(ISSN

2771-2265)

VOLUME

03

ISSUE

10

P

AGES

:

13-17

SJIF

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MPACT

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(2021:

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(2022:

5.

893

)

(2023:

6.

184

)

OCLC

1121105677















































Publisher:

Oscar Publishing Services

Servi

Significant changes in patients with HF were also

detected when registering SAEP. In 95% of patients

with auditory neuropathy, SAEP were not recorded

during stimulation of either the right or left ear. In only

2 out of 36 patients, SAEP were recorded to sound

stimuli at a level of 95-103 dB nHL.

Repeated examination of patients with auditory

neuropathy did not reveal any changes in SAEP.

Dynamic observation was carried out to analyze the

variability of the registration parameters of SAEP and

TEOAE in children with HF (Table 2).

Table 2

Dynamics of changes in the registration indicators of

SAEP

and TEOAE

during repeated examinations

Number

of children

Frequency of occurrence (%)

Raising

thresholds

Lowering

thresholds

Threshold stability

SAEP

OAE

SAEP

OAE

SAEP

OAE

36

-

-

-

-

100

100

The data obtained indicate that a single study of

auditory function in children is not enough and requires

dynamic observation.

Based on the above, electrophysiological criteria for

diagnosing hearing loss are quite specific and do not

allow for discrepancies. At the same time, the results

of instrumental studies of patients with auditory

neuropathy are not always clear and require a deep

understanding of the complexity of the mechanisms of

sound perception.

Timely identification of the peculiarities of the nature

of the pathology in the sound perception system is of

great clinical importance due to the difference in

treatment tactics and rehabilitation of such patients.

This, in turn, makes it possible to carry out full

rehabilitation of such patients.

CONCLUSION

Features of auditory function in patients with auditory

neuropathy (AN) indicate differences in the

mechanisms underlying hearing impairment in these


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Volume 03 Issue 10-2023

17


International Journal of Medical Sciences And Clinical Research
(ISSN

2771-2265)

VOLUME

03

ISSUE

10

P

AGES

:

13-17

SJIF

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MPACT

FACTOR

(2021:

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(2022:

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)

(2023:

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184

)

OCLC

1121105677















































Publisher:

Oscar Publishing Services

Servi

groups of patients. Differences in the structure of risk

factors in patients with AN from other hearing

pathologies indicate the etiological heterogeneity of

these forms. This gives grounds for their isolation into

independent nosological units.

The results obtained showed that children with AN, on

the one hand, have disturbances in the transmission of

acoustic signals to the central auditory system, and, on

the other hand, there are disturbances in the

maturation of the auditory pathways and centers.

REFERENCES

1.

Kaga K., Nakamura M., Shinogami M., Tsuzuku T.,

Yamada K., Shindo M. Auditory nerve disease of

both ears revealed by auditory brain- stem

responses, electrocochleography and otoacoustic

emissions. Scand Audiol 1996; N25: P.233-238.

2.

Starr A., Picton T.W., Sininger Y.S., Hood L.J., Berlin

C.I. Auditory neuropathy. Brain 1996; N119: P.741-

753.

3.

Deltenre P., Mansbach A., Bozet C., Clercx A.,

Hecox K. (1997). Auditory neuropathy: A report on

three cases with early onsets and major neonatal

illnesses. Electroencephalography and Clinical

Neurophysiology, 104, P.17-22.

4.

Rance G. Auditory neuropathy/dys-synchrony and

its perceptual consequences. Trends Amplif 2005;

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5.

Picton T.W. Auditory neuropathy

when time is

broke. In: Human Auditory-Evoked Potentials.

Plural Publishing Inc 2011; P.648.

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Hood L.J., Morlet T. Current issues in auditory

neuropathy spectrum disorder. In: K.E. Tremblay,

R.F. Burkard. Eds. Translational Perspectives in

Auditory Neuroscience. Plural Publishing 2012;

P.577.

7.

Madden C., Rutter M., Hilbert L., J.H.Greinwald.,

D.I.Choo (2002). Clinical and audiological features

in auditory neuropathy. Arch Otolaryngol Head

Neck Surg 128, P.1026-1030.

8.

Attias J., Raveh E. (2007). Transient deafness in

young candidates for cochlear implants. Audiol

Neuro Otol 12 (5), P.325-333.

References

Kaga K., Nakamura M., Shinogami M., Tsuzuku T., Yamada K., Shindo M. Auditory nerve disease of both ears revealed by auditory brain- stem responses, electrocochleography and otoacoustic emissions. Scand Audiol 1996; N25: P.233-238.

Starr A., Picton T.W., Sininger Y.S., Hood L.J., Berlin C.I. Auditory neuropathy. Brain 1996; N119: P.741-753.

Deltenre P., Mansbach A., Bozet C., Clercx A., Hecox K. (1997). Auditory neuropathy: A report on three cases with early onsets and major neonatal illnesses. Electroencephalography and Clinical Neurophysiology, 104, P.17-22.

Rance G. Auditory neuropathy/dys-synchrony and its perceptual consequences. Trends Amplif 2005; N9: P.1-43

Picton T.W. Auditory neuropathy—when time is broke. In: Human Auditory-Evoked Potentials. Plural Publishing Inc 2011; P.648.

Hood L.J., Morlet T. Current issues in auditory neuropathy spectrum disorder. In: K.E. Tremblay, R.F. Burkard. Eds. Translational Perspectives in Auditory Neuroscience. Plural Publishing 2012; P.577.

Madden C., Rutter M., Hilbert L., J.H.Greinwald., D.I.Choo (2002). Clinical and audiological features in auditory neuropathy. Arch Otolaryngol Head Neck Surg 128, P.1026-1030.

Attias J., Raveh E. (2007). Transient deafness in young candidates for cochlear implants. Audiol Neuro Otol 12 (5), P.325-333.