Journal Information
Vol. 81. Issue 2.
Pages 133-140 (March - April 2015)
Visits
8622
Vol. 81. Issue 2.
Pages 133-140 (March - April 2015)
Original article
Open Access
Middle ear impedance studies in elderly patients implications on age-related hearing loss
Estudos de impedância da orelha média em pacientes idosos; implicações na perda auditiva relacionada à idade
Visits
8622
Olusola Ayodele Sogebi
Department of Ear Nose and Throat, Olabisi Onabanjo University Teaching Hospital, Sagamu, Nigeria
This item has received

Under a Creative Commons license
Article information
Abstract
Full Text
Bibliography
Download PDF
Statistics
Figures (1)
Tables (4)
Table 1. Socio-demographic characteristics of the patients.
Table 2. Impedance audiometric findings in the patients.
Table 3. Relationship between clinico-audiometric and tympanographic findings.
Table 4. Relationship between clinico-audiometric findings and acoustic reflexes.
Show moreShow less
Abstract
Introduction

Controversies arise with respect to functioning of the middle ear over time.

Objective

To assess changes in middle ear impedance that may be related to aging, and/or if there was an association of these changes with those of the inner ear in the elderly patients.

Methods

Cross-sectional, comparative study of elderly patients managed in ear, nose and throat clinics. A structured questionnaire was administered to obtain clinical information. Pure tone audiometry, tympanometry, and acoustic reflexes were performed. Comparative analyses were performed to detect intergroup differences between clinico-audiometric findings and middle ear measures, viz. tympanograms and acoustic reflexes.

Results

One hundred and three elderly patients participated in the study; 52.4% were male, averagely 70.0±6.3 years old, age-related hearing loss in 59.2%, abnormal tympanograms in 39.3%, absent acoustic reflex in 37.9%. There was no association between age and gender in patients with abnormal tympanograms and absent acoustic reflex. Significantly more patients with different forms and grades of age-related hearing loss had abnormal tympanometry and absent acoustic reflex.

Conclusion

Some abnormalities were observed in the impedance audiometric measures of elderly patients, which were significantly associated with parameters connected to age-related hearing loss.

Keywords:
Acoustic impedance tests
Pure-tone audiometry
Aged
Presbycusis
Acoustic reflex
Resumo
Introdução

Existem controvérsias no que se refere às alterações funcionais da orelha média com o passar dos anos.

Objetivo

Avaliar as mudanças na impedância da orelha média que podem estar relacionadas ao envelhecimento, bem como qualquer associação dessas alterações com as que ocorrem na orelha interna.

Método

Estudo prospectivo comparativo de pacientes idosos atendidos em ambulatórios especializados em otorrinolaringologia e aplicação de questionário estruturado para obtenção de informações clínicas. Foram realizadas audiometria de tons puros, timpanometria e reflexos acústicos e análise comparativa para detectar as diferenças intergrupos entre os achados clínico-audiométricos.

Resultados

Participaram do estudo 103 pacientes idosos: 52,4% do gênero masculino; idade de 70±63 anos; perda auditiva relacionada à idade detectada em 59,2%; timpanograma anormal em 39,3%; e reflexo acústico ausente em 37,9%. Não foi encontrada associação entre idade e gênero em pacientes com timpanograma anormal e reflexo acústico ausente. Um número significantemente maior de pacientes com diferentes graus e configurações de perda auditiva relacionada à idade apresentou timpanometria anormal e reflexo acústico ausente.

Conclusão

Algumas anormalidades foram observadas em medidas de impedância audiométrica em pacientes idosos, que foram significantemente associados com os parâmetros ligados à perda auditiva relacionada à idade.

Palavras-chave:
Impedância elétrica
Audiometria de tons puros
Idoso
Presbiacusia
Reflexos acústicos
Full Text
Introduction

Hearing involves a complex interplay and integration of several mechanisms, including conduction of sound waves from the environment through the external auditory canal, vibrations of the tympanic membrane, stimulation of the transformer mechanism in the middle ear, as well as the sensory hair cells of the cochlea the central neuronal connections with termination at the primary auditory cortex. The functions of some of these mechanisms are affected by aging and tend to manifest as hearing impairment, which is particularly common in the elderly.

A deficit in hearing acuity is the most common sensory disorder that has been associated with aging.1 In fact, studies have shown that approximately one-third of adults aged between 61 and 70 years, and over 80% of those older than 85 years have clinically obvious difficulty understanding speech and following conversations in the presence of background noise.2,3 On the average, hearing threshold increases by approximately 1dB per year for subjects aged 60 years and above, with a tendency to further deterioration with increasing age.4 At audiometry, up to 35% of elderly subjects above 60 years had pure tone average threshold of 25dB HL or more at frequencies between 0.5 and 4kHz, which increased further to 50% in the age group between 70 and 80 years.5 While the reported prevalence of hearing loss among elderly subjects vary in different locations, it is an established fact that it increases with age.6

Traditionally, hearing loss is classified as conductive, sensory, neural, or mixed-type. Age-related changes in the inner ear and its central connections have been well documented among elderly subjects. These include loss of sensory hair cells of the cochlea consequent upon generalized degenerative processes, dysfunction of the stria vascularis (the main blood supply to the organ of Corti), and degeneration of the neurons of the cochlear nerve or its central connections.7 In the external ear, wax impaction in the external auditory meatus has been reported to be disproportionately more common in the elderly patients than in other groups of patients, causing conductive hearing loss.8 This is a consequence of the generalized degeneration of epithelia, including those of the microcilia, affecting the external auditory canal without an accompanying reduction in the rate of wax production. Other causes of conductive hearing loss are often related to the functioning of the middle ear.

Compared with other categories of patients, little attention has been paid to the conductive middle ear components in elderly patients. Controversies arise concerning the functioning of the middle ear as age advances. While some studies concluded that the conducting mechanisms of the middle ear remain normal and functional, or that they may play no serious role in the hearing impairment associated with aging,9,10 others observed some changes in the dynamic characteristics of the middle ear that may be related to aging.11,12 This might have resulted from different types of instruments used for assessing the middle ear functions. As part of the study on the epidemiology of hearing impairment among elderly patients, the author performed both pure-tone and impedance audiometries (tympanometry) to assess the functions of the inner and middle ear, respectively.13 The observation of certain abnormal tympanometric tracings in some patients with normal audiograms and in patients with supposedly purely sensorineural hearing loss (SNHL) stimulated this research.

This study aimed to assess whether there were changes in the middle ear impedance that may be related to aging, and/or whether there were any association of these changes with those of the inner ear in the elderly subjects. This is justifiable because hearing loss impacts the quality of life of elderly subjects.

MethodsStudy design

This was a prospective (cross-sectional), comparative study of elderly patients followed-up at specialized ear, nose, and throat (ENT) clinics for a three-year period.

Setting/study location

This study was conducted at the ENT clinics of a tertiary referral hospital and of a private/missionary hospital. Ethics approval for this study was obtained from the Health Research and Ethics Committee, under approval number OOUTH/DA.326/T/197.

Sampling criteria/technique

The inclusion criteria were elderly patients aged 60 years and above, who had no clinical middle ear disease, attended one of the ENT clinics. Patients were consecutively recruited. The general nature, significance, requirements of the patients, including the fact that declining to participate in the study would not affect treatment, were explained to the patients. Consenting patients were included in the study. The categories of the patients that were excluded were: those who did not consent, history of recurrent ear discharges, and those with tympanic membrane perforations. Patients with wax impaction were treated before the continuation of the study protocols. Patients without complete investigations (both forms of audiometry – pure tone audiometry [PTA] and tympanometry), with asymmetric audiograms, or evidence of conductive or mixed hearing loss in their PTAs were subsequently excluded.

Study period

January of 2010–June of 2013.

Data sources and collection procedure/technique

Data were generated using interviewer-administered questionnaires, divided into three sections. Section A comprised socio-demographic information. Section B consisted of the medical condition including questions on history of perceived hearing loss, duration of hearing impairment, and present or previous ear surgeries, among others.

Section C was documentation of the findings on physical examination, especially the status of the tympanic membranes, and records of the audiometric profiles of the patients, which included the PTA, tympanometry, and acoustic reflexes.

At PTA, air conduction and bone-conduction evaluations were performed in a commercial sound booth, using an Amplivox diagnostic audiometer model 240, with standard earphones enclosed in supra-aural ear cushions, and a standard bone-conduction oscillator and headband to evaluate air-bone gaps. Tympanometry was conducted by broadband middle ear power reflectance and measured using a calibrated, commercially available computer-controlled system (Interacoustics model MT 10.SN 156607) that incorporated a high-quality probe assembly to transduce stimuli and record acoustic responses from the ear canal. The acoustic reflex thresholds were tested with contralateral stapedial reflexes for frequencies of 500, 1000, 2000, and 4000Hz; the thresholds were considered as normal when elicited between 75 and 110dB HL.

Main outcome measure: patients were paired into different categories based on the PTA findings as Normal or Age-related hearing impairment-presbycusis). The tympanograms were classified according to Jerger types A, As, Ad, B, and C;14 with type A considered as normal, and any other tympanographic types as abnormal, while acoustic reflexes were classified as Present or Absent.

Data analysis

Descriptive analysis of the data was done and presented in tabular and graphical forms. Comparative analyses were performed to detect inter-group differences between the clinico-audiometric findings and different middle ear measures, viz. tympanograms and acoustic reflexes, by cross-tabulation with contingency tables. Categorical variables were presented as percentages and proportions and analyzed using Chi-square test, while continuous variables, presented as absolute values and means, were compared using Student's t-test. The level of statistical significance was set at p<0.05. Data analysis was performed using SPSS version 19.0 (Chicago, IL, United States).

Results

One hundred and three (103) elderly patients participated in the study, which comprised 52.4% males, (M:F=1.1:1). The ages of the patients ranged between 61 and 96 years with a mean±SD of 70.0±6.3 years. The socio-demographic characteristics of the patients are shown in Table 1. Over half (59.2%) of the patients had audiometric evidences of ARHL, and the Schuknecht typology is represented in Fig. 1. The impedance audiometry findings based on tympanometric tracings according to Jerger's classification revealed that on average, 60.7% of the participants had normal (type A tympanograms), with a high concordance between the two ears. The acoustic reflexes were present in an average of 62.1% of the patients. The details of the impedance audiometric profile of the patients are shown in Table 2.

Table 1.

Socio-demographic characteristics of the patients.

Variable  n
Age group (years)
61–65  27 (26.2) 
66–70  35 (34.0) 
71–75  25 (24.3) 
76–80  10 (9.7) 
≥81  6 (5.8) 
Mean±SD  70.0±6.3 
Gender
Male  54 (52.4) 
Female  49 (47.6) 
Marital status
Married  83 (80.6) 
Others (divorced/widowed)  20 (19.4) 
Education level
No formal education  3(2.9) 
Primary school  21 (20.4) 
Secondary school  55 (53.4) 
Tertiary  24 (23.3) 
Occupation group
Unskilled  17 (16.5) 
Semi-skilled  44 (42.7) 
Professional  42 (40.7) 
Figure 1.

Distribution of PTA findings of the patients. Schuknecht's typology only for patients with ARHL.

(0.1MB).
Table 2.

Impedance audiometric findings in the patients.

Variable  Right ear (%)  Left ear (%)  Average (%) 
Tympanometry (Jerger's type)
60 (58.3)  65 (63.1)  62.5 (60.1) 
6 (5.8)  7 (6.8)  6.5 (6.3) 
14 (13.6)  9 (8.7)  11.5 (11.2) 
AS  22 (21.4)  21 (20.4)  21.5 (20.9) 
Ad  1 (1.0)  1 (1.0)  1 (1.0) 
Acoustic reflexes
Present  65 (63.1)  63 (61.2)  64 (62.1) 
Absent  38 (36.9)  40 (38.8)  39 (37.9) 

Age, gender, and PTA findings of the patients were comparatively analyzed against the tympanometric findings in Table 3. Based on the age distribution of the patients, they were subdivided into two groups, ≤70 and >70 years. There were no statistically significant differences in the tympanograms regarding age (t=1.498, p=0.137) and gender (χ2=1.837, p=0.175) of the patients. There was a difference when the hearing status (PTA findings) was compared; significantly more patients with age-related hearing loss (ARHL) had abnormal tympanometric findings. These were also obvious when considering the different patterns of audiometric findings that were observed in patients with ARHL. Further analysis of the PTA of patients with ARHL, considering the degrees of hearing losses calculated as pure tone averages (PTAv) in dB HL at the low (0.25, 0.50, 1.0kHz) and the high (2.0, 4.0, and 8.0kHz) frequencies was performed.

Table 3.

Relationship between clinico-audiometric and tympanographic findings.

Clinico-audiometric parameter  Tympanographic findings
  Normal  Abnormal  Statistic  p-value 
Age (mean)  69.2  71.1  1.498a  0.137 
Sex
Male  46.6%  60.0%  1.837  0.175 
Female  53.4%  40.0%  1.837  0.175 
ARHL (all cases)  46.6%  75.6%  8.827  0.003 
Schuknecht's type in ARHL
Type A  19.0%  6.7%  14.252  0.001 
Type B  3.4%  20.0%  13.542  0.001 
Type C  15.5%  28.9%  8.012  0.018 
Type D  8.6%  20.0%  6.641  0.036 
PTAv in best ear
Low frequency (0.25–1.0kHz)  21.6  37.7  5.001a  <0.001 
High frequency (2.0–8.0kHz)  38.2  54.6  3.833a  <0.001 
Low tone accentuation  11.1%  64.7%  17.872  <0.001 
High tone preponderance  53.9%  29.4%  5.482  0.019 
a

Statistic, Student's t-test.

Exploring the PTAv in the better ear at the low (0.25–1.0kHz) frequencies revealed a mean of 28.7dB HL (SD=18.0). Low frequency accentuation of the audiogram was taken as at least 40dB HL for the PTAv (WHO classification for moderate hearing loss) at the low frequencies. At the high (2.0–8.0kHz) frequencies, computation of the PTAv in the better ear, resulted in a mean of 45.4dB HL (SD=23.0). Estimate of the differences in the PTAv between the high tones and low tones in the better ears revealed a mean of 24.1dB HL (SD=10.1), thus a value of ≥25dB HL difference was used as the criterion for a high tone preponderance of the audiogram.

The PTAv at the low and high frequencies in the better ear and other parameters, namely low tone accentuation and high tone preponderance, were compared with the tympanometric findings in patients with ARHL. All parameters presented statistically significantly differences for tympanometric abnormalities, as shown in Table 3.

A similar comparative analysis was performed with the acoustic reflexes as the outcome variable. Similar to tympanometric findings, there were no associations between age of patients that had absent acoustic reflexes (t=0.970, p=0.334), and gender (χ2=0.363, p=0.549) in Table 4. Statistically significant differences were observed for patients with ARHL, those with type B Schuknecht audiometric pattern, the PTAvs, and also in patients with low tone accentuation of their PTAs.

Table 4.

Relationship between clinico-audiometric findings and acoustic reflexes.

Clinico-audiometric parameter  Acoustic reflex
  Normal  Abnormal  Statistic  p-value 
Age in years (Mean)  69.5  70.8  0.970a  0.334 
Sex
Male  54.8%  48.8%  0.363  0.549 
Female  45.2%  51.2%  0.363  0.549 
ARHL (all cases)  50.0%  73.2%  5.487  0.019 
Schuknecht's type
12.9%  14.6%  4.961  0.085 
4.8%  19.5%  10.106  0.006 
17.7%  26.8%  2.937  0.230 
14.5%  12.2%  0.154  0.925 
PTAv in best ear
Low frequency (0.25–1.0kHz)  24.1  35.9  3.326a  0.001 
High frequency (2.0–8.0kHz)  39.3  54.5  3.448a  0.001 
Low tone accentuation  19.4%  63.3%  12.191  <0.001 
High tone preponderance  48.4%  36.7%  0.856  0.355 
a

Statistics, Student's t-test.

Discussion

This study has demonstrated that elderly patients had some functional anomalies in the middle ear impedances and acoustic reflexes. Impedance audiometric abnormalities were significantly higher in elderly patients with various forms and degrees of ARHL, being more pronounced in neural and strial types, and in low frequency accentuation of ARHL. Acoustic stapedial reflexes appeared to be less influenced by ARHL than tympanometry, and it may be a more reliable indicator of abnormal middle ear function.

Researchers assessing hearing and its impairment among elderly patients have focused disproportionately on ARHL relating to the sensorineural aspect of hearing, with apparent neglect of the conductive component. However, the present study revealed that an average of 39.3% of the elderly patients had abnormality in their tympanometric tracings, and average of 37.9% had absent acoustic reflexes. It cannot be conclusively ascertained whether these middle ear abnormalities were due to aging process, or mere coincidental findings. Nondahl et al.15 reported a small degree of middle-ear stiffening occurring over the years among older adults. An animal experiment also found structural changes in the middle ear of mouse that were attributable to aging.16

There was no significant difference between the ages of elderly patients with normal or abnormal tympanograms and between those with and without acoustic reflexes. Gaihede and Koefoed-Nielsen17 compared compliance and middle ear pressure measured by tympanometry between normal elderly subjects (mean age 77 years) and normal younger patients (mean age 29 years); they observed that middle ear compliance was not influenced by variation in age. Similarly, no association was found between the gender of the patients and middle ear mechanics analogous to findings of the Blue Mountains Hearing Study in Australia.18 These are at variance with reports concerning presbycusis, which were reported to be significantly associated with advancing age and also with the male gender.19

The prevalence of anomalies observed in the middle ear mechanisms in this study were comparable to the reported prevalence of ARHL.20,21 This may suggest a simultaneous or concurrent effect in both the inner and the middle ear. The abnormal tympanometric findings of the patients revealed that the Jerger's type As tympanogram was the most common among the patients similar to that found among centenarians in China,20 providing an evidence of increased stiffness (reduced compliance) of the conducting mechanisms.15 This was followed by the type C tympanogram suggestive of eustachian tube dysfunction. Thus, it is hypothesized that common middle ear functional anomalies may be attributable to either of these two pathologies. Sometimes abnormalities occur in the tympanic membrane and in the bony ossicles, resulting in significant middle ear functional impairment.16 There is evidence that, with advancing age, the human tympanic membrane exhibits a loss of vascularization, a reduction in collagen structure, in elasticity, and greater rigidity in the middle fibrous layer.22 These structural changes would be expected to alter the compliance response of the middle ear. One belated investigation of air and bone conduction thresholds has observed middle-ear losses of as much as 12dB in elderly patients.23

The possibility that ARHL either initiates or aggravates abnormalities in the impedance characteristics of the middle ear should also be considered. The audiometric pattern of elderly patients with ARHL observed in the present study showed a preponderance of Schuknecht's type C, such as in other African populations,24 and distinct from the typical sloping pure tone audiogram common among whites.25 The finding that all Schuknecht's audiometric patterns in patients with ARHL were associated with tympanometric abnormalities, suggested a link with the etiopathogenesis of these two entities in elderly patients. It is expected that subjects with abnormal tympanograms should manifest with hearing loss of conductive type. However, the finding of these tympanometric patterns also in patients with normal and sensorineural (ARHL) hearing loss should stimulate further research into middle ear impedance mechanisms.

Using Schuknecht's typology in patients with ARHL, two particular types of audiograms (B and C) theoretically had accentuation at the low frequencies. In this study, these two audiometric types comprised over half (33/61; 54.1%) of the audiometric types in patients with ARHL. Thus, the association of low tone accentuation of audiograms with abnormal tympanograms may derive from the disproportionate distribution of these two audiometric patterns in the ARHL patients. Eustachian tube compliance has been observed to change with aging,26 but whether this change is influenced more by neural or strial types of presbycusis remains to be ascertained. Contrary to reports of Feeney and Sanford,9 the present findings suggest an increase in middle-ear stiffness with specific types of ARHL. Thus, these impedance middle ear changes may be particularly common in the African population, and need further clarification.

It is noteworthy that there were discordant findings in some of the middle ear measures between the ears. These suggest that, despite the ears being exposed to almost the same conditions, the influences and the responses might not be exactly same. The possibility of confounding factors, such as osteoarthritis (which might affect ossicular joints of the ears unequally, producing type As tympanogram), may also be considered. Asymmetrical audiograms have also been reported in patients with ARHL.13,24

Many experts consider 2.0kHz as beginning of high frequency, although the definition varies.4,27,28 PTAv at high frequencies and high tone preponderance HL were associated with abnormalities in tympanometric findings in this study. Wiley et al. 29 reported that, for younger age groups (50–69 years), threshold changes were higher for higher frequencies, while in older age groups (70–89 years), threshold changes were higher for lower frequencies. Interestingly, the age distribution of the present patients is in-between these two divisions. Causes of high-frequency hearing loss have a wide variability,21 and there is a possibility of co-existence of few of these in some of the present patients. Thus, it is possible that not enough patients with pure ARHL were studied. Conversely, low frequency hearing loss is not easy to identify, since it tends to be asymptomatic. In fact, lower frequency sounds do not have as much information as sounds in the higher frequencies.30 One of the few clues to a low-frequency hearing loss is that the person has difficulty hearing in groups or in a noisy place. It was reported that inertia of the middle ear is not an important contribution to the perception of bone conduction sounds for frequencies below 1.5kHz, but appears to contribute at frequencies between 1.5 and 3.5kHz.30 However, this statement may not apply to air-conducted sounds.

The pathway involved in the acoustic reflex is complex and can involve the ossicular chain, cochlea, auditory nerve, brain stem, facial nerve, and other components. The absence of acoustic reflex has been shown to effectively detect hearing losses exceeding 30dB in adult subjects,31 although it may not be conclusive in identifying the source of the problem.32 Like impedance measures, parameters related to ARHL (namely Schnekcht's type B audiogram, PTAv, and low-tone accentuation) were significantly associated with absence of the acoustic reflexes in this study. However, the absence of the acoustic reflex appeared to be less influenced by parameters relating to ARHL, and it may possibly be a more reliable parameter in assessing the effect of ARHL on the functioning of the middle ear.

This study had some limitations. First is the lower sensitivity of the conventional tympanometer in assessing middle ear function compared with sweep frequency middle-ear analyzer. The fact that magnitude of the acoustic reflexes was not ascertained is also a limitation. Furthermore, the hospital-based nature of the study is prone to bias, as patients may not represent a normal population of the elderly. Despite these limitations, the study was able to demonstrate that the middle ear functioning of elderly patients may not be fully normal.

Conclusion

Some abnormalities were observed in impedance audiometric measures of elderly patients, which were significantly associated with parameters related to ARHL. This arouses suspicion of some middle ear changes that may be attributable to aging. It is imperative that elderly patients with hearing impairment have both their inner and middle ear assessed, in order to manage them optimally. Community-based, longitudinal studies are needed to further clarify these findings.

Conflicts of interest

The author declares no conflicts of interest.

References
[1]
E. Van Eyken, G. Van Camp, L. Van Laer.
The complexity of age-related hearing impairment: contributing environmental and genetic factors.
Audiol Neurootol, 12 (2007), pp. 345-358
[2]
A.D. Walling, G.M. Dickson.
Hearing loss in older adults.
Am Fam Physician, 85 (2012), pp. 1150-1156
[3]
H. Glyde, L. Hickson, S. Cameron, H. Dillon.
Problems hearing in noise in older adults: a review of spatial processing disorder.
Trends Amplif, 15 (2011), pp. 116-126
[4]
F.S. Lee, L.J. Matthews, J.R. Dubno, J.H. Mills.
Longitudinal study of pure-tone thresholds in older persons.
Ear Hear, 26 (2005), pp. 1-11
[5]
T.L. Wiley, K.J. Cruickshanks, D.M. Nondahl, T.S. Tweed.
Aging and middle ear resonance.
J Am Acad Audiol, 10 (1999), pp. 173-179
[6]
J.T. Pacala, B. Yueh.
Hearing deficits in the older patient: I didn’t notice anything.
JAMA, 307 (2012), pp. 1185-1194
[7]
E.C. Bielefeld, C. Tanaka, G.D. Chen, D. Henderson.
Age-related hearing loss: is it a preventable condition?.
Hear Res, 264 (2010), pp. 98-107
[8]
O.A. Sogebi.
Profile of ear diseases among elderly patients in Sagamu, south-western Nigeria.
Niger J Med, 22 (2013), pp. 143-147
[9]
M.P. Feeney, C.A. Sanford.
Age effects in the human middle ear: wideband acoustical measures.
J Acoust Soc Am, 116 (2004), pp. 3546-3558
[10]
Y. Uchida, H. Nomura, A. Itoh, T. Nakashima, F. Ando, N. Niino, et al.
The effects of age on hearing and middle ear function.
J Epidemiol, 10 (2000), pp. S26-S32
[11]
H. Wada, T. Koike, T. Kobayashi.
The effect of aging on middle ear dynamic characteristics.
Nippon Jibiinkoka Gakkai Kaiho, 97 (1994), pp. 898-904
[12]
L. Holte.
Aging effects in multifrequency tympanometry.
Ear Hear, 17 (1996), pp. 12-18
[13]
O.A. Sogebi, O.O. Olusoga-Peters.
Clinical and audiometric features of presbycusis in Nigerians.
Afr Health Sci, 13 (2013), pp. 886-892
[14]
E. Onusko.
Tympanometry.
Am Fam Physician, 70 (2004), pp. 1713-1720
[15]
D.M. Nondahl, K.J. Cruickshanks, T.L. Wiley, T.S. Tweed, D.S. Dalton.
16-year change in acoustic admittance measures among older adults: data from a population-based study.
J Speech Lang Hear Res, (2013),
[16]
D.E. Doan, J.S. Erulkar, J.C. Saunders.
Functional changes in the aging mouse middle ear.
Hear Res, 97 (1996), pp. 174-177
[17]
M. Gaihede, B. Koefoed-Nielsen.
Mechanics of the middle ear system: age-related changes in viscoelastic properties.
Audiol Neurootol, 5 (2000), pp. 53-58
[18]
M. Golding, K. Doyle, D. Sindhusake, P. Mitchell, P. Newall, D. Hartley.
Tympanometric and acoustic stapedius reflex measures in older adults: the Blue Mountains Hearing Study.
J Am Acad Audiol, 18 (2007), pp. 391-403
[19]
F. Ma, C.Y. Qu, T. Wang, J. Yin, X.D. Zhang, J. Meng, et al.
Study on hearing impairment among elderly population in the community of Taiyuan city, Shanxi province.
Zhonghua Liu Xing Bing Xue Za Zhi, 30 (2009), pp. 247-251
[20]
Z. Mao, L. Zhao, L. Pu, M. Wang, Q. Zhang, D.Z. He.
How well can centenarians hear?.
[21]
M.S. Cruz, M.C. Lima, J.L. Santos, Y.A. Duarte, M.L. Lebrão, A.T. Ramos-Cerqueira.
Self-reported hearing loss among elderly individuals in the city of São Paulo, Brazil: prevalence and associated factors (SABE Study, 2006).
Cad Saude Publica, 28 (2012), pp. 1479-1492
[22]
C.B. Ruah, P.A. Schachern, D. Zelterman, M.M. Paparella, T.H. Yoon.
Age-related morphologic changes in the human tympanic membrane. A light and electron microscopic study.
Arch Otolaryngol Head Neck Surg, 117 (1991), pp. 627-634
[23]
J.C. Nixon, A. Glorig, W.S. High.
Changes in air and bone conduction thresholds as a function of age.
J Laryngol Otol, 76 (1962), pp. 288-298
[24]
A.O. Ogunleye, A.S. Labaran.
Presbycusis in Nigerians at the University College Hospital, Ibadan.
Afr J Med Med Sci, 34 (2005), pp. 293-296
[25]
S. Arlinger.
Audiometric profile in presbycusis.
Acta Otolaryngol Suppl, 476 (1990), pp. 85-89
[26]
A. Kaneko, Y. Hosoda, T. Doi, N. Tada, T. Iwano, T. Yamashita.
Tubal compliance—changes with age and in tubal malfunction.
Auris Nasus Larynx, 28 (2001), pp. 121-124
[27]
S.T. Frisina, F. Mapes, S.H. Kim, D.R. Frisina, R.D. Frisina.
Characterization of hearing loss in aged type II diabetics.
Hear Res, 211 (2006), pp. 103-113
[28]
J. Mazelova, J. Popelar, J. Syka.
Auditory function in presbycusis: peripheral vs central changes.
Exp Gerontol, 38 (2003), pp. 87-94
[29]
T.L. Wiley, R. Chappell, L. Carmichael, D.M. Nondahl, K.J. Cruickshanks.
Changes in hearing thresholds over 10 years in older adults.
J Am Acad Audiol, 19 (2008), pp. 281-292
[30]
S. Stenfelt.
Middle ear ossicles motion at hearing thresholds with air conduction and bone conduction stimulation.
J Acoust Soc Am, 119 (2006), pp. 2848-2858
[31]
R.H. Margolis.
Detection of hearing impairment with the acoustic stapedius reflex.
Ear Hear, 14 (1993), pp. 3-10
[32]
P. Rudolf, G. Grevers, H. Iro.
Basic otorhinolaryngology: a step-by-step learning guide (second, illustrated, revised ed.).
Thieme, (2006), pp. 185-186

Please cite this article as: Sogebi OA. Middle ear impedance studies in elderly patients: implications on age-related hearing loss. Braz J Otorhinolaryngol. 2015;81:133–40.

Copyright © 2014. Associação Brasileira de Otorrinolaringologia e Cirurgia Cérvico-Facial
Idiomas
Brazilian Journal of Otorhinolaryngology (English Edition)
Article options
Tools
en pt
Announcement Nota importante
Articles submitted as of May 1, 2022, which are accepted for publication will be subject to a fee (Article Publishing Charge, APC) payment by the author or research funder to cover the costs associated with publication. By submitting the manuscript to this journal, the authors agree to these terms. All manuscripts must be submitted in English.. Os artigos submetidos a partir de 1º de maio de 2022, que forem aceitos para publicação estarão sujeitos a uma taxa (Article Publishing Charge, APC) a ser paga pelo autor para cobrir os custos associados à publicação. Ao submeterem o manuscrito a esta revista, os autores concordam com esses termos. Todos os manuscritos devem ser submetidos em inglês.