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DPOAE measurements in comparison to audiometric measurements in hemodialyzed patients

2015-07-12 09:30:26EvisBendoMargaritaResuliSpirosMetaxasENTDepartmentMotherTerezaUniversityHospitalTiraneAlbaniaEnternalDiseasesDepartmentMotherTerezaUniversityHospitalTiraneAlbaniaENTDepartmentPapageorgiouHospitalThessalonikiGreece
Journal of Acute Disease 2015年3期

Evis Bendo, Margarita Resuli, Spiros MetaxasENT Department, “Mother Tereza” University Hospital, Tirane, AlbaniaEnternal Diseases Department, “Mother Tereza” University Hospital, Tirane, AlbaniaENT Department, ”Papageorgiou” Hospital, Thessaloniki, Greece

DPOAE measurements in comparison to audiometric measurements in hemodialyzed patients

Evis Bendo1*, Margarita Resuli2, Spiros Metaxas3
1ENT Department, “Mother Tereza” University Hospital, Tirane, Albania
2Enternal Diseases Department, “Mother Tereza” University Hospital, Tirane, Albania
3ENT Department, ”Papageorgiou” Hospital, Thessaloniki, Greece

ARTICLE INFO ABSTRACT

Article history:

Received 14 Apr 2015

Received in revised form 15 Apr 2015 Accepted 27 Apr 2015

Available online 8 Jul 2015

Keywords:

Sensorineural hearing loss Hemodialyse

DPOAE

PTA

Objective: To investigate the early detection of the damage of cochlear activity by using distortion product otoacustic emissions (DPOAE) (DP-gram) comparing to the results of the impedance audiometry.

Methods: We examined 53 patients including 43 hemodialyzed patients, and 10 controls. First it was applied a tympanometry, and then in normal results we applied impedance audiometry and DPOAE (DP-gram).

Results: We found sensorineural hearing loss in 67% of audiometric results of the hemodialyzed patients and there was a decrease of the DPOAE amplitude in 77% of hemodialyzed patients. In the control group there was one patient (10%) with neurosensorial in high frequencies hearing loss in both measurements with audiometry and DPOAE.

Conclusions: There is a sensorineural hearing loss observed in most of the patients with chronic renal failure. DPOAE audiogram shows lower amplitudes than impedance audiometry and it can be used for the early detection of cochlear damage.

E-mail: drbendo@gmail.com

1. Introduction

Otoacoustic emissions are tests used to determine the hair cell function of the cochlea. So otoacoustic emission testing can be used as a tool to determine the presence or absence of cochlear function and analysis can be performed for individual cochlear frequency regions[1,2]. Another potential use of distortion product otoacoustic emissions (DPOAE) measurements might be to predict auditory response growth, such as growth of loudness. This application would be of interest clinically because one consequence of cochlear hearing loss may be an abnormal growth of loudness, sometimes referred to as loudness recruitment[3].

DPOAEs are sounds emitted in response to 2 simultaneous tones of different frequencies. Stimuli consist of 2 pure tones at 2 frequencies (f2 > f1) and two intensity levels (L1, L2)[4,5]. The relationship between L1-L2 and f1 / f2 dictates the frequency response. DPOAEs allow great frequency specificity with a great reliability above 1 000 Hz[6].

Hearing losses above 50 dB HL are not quantifiable using DPOAEs and their performance at frequencies below 1 kHz is limited, but their recording time is short[7].

Presence of hearing loss and estimation of type and degree is one of the most common methods used to investigate the effects of renal disease on the auditory system[8]. Degree of hearing loss may give an indication of the extent of damage to auditory function, whereas the type of hearing loss may distinguish between lesions in the outer and middle ear (conductive hearing loss) or the cochlea and the neural pathways (sensorineural hearing loss)[9]. According to these indicators, the reports to be reviewed in the following sections have also described auditory function in CRF with methods such as tympanometry, audiometry and otoacoustic emissions (distortion product OAEs, DPOAEs).

2. Materials and methods

We analyzed 53 patients (106 ears) including 43 subjects of different stages of renal failure disease undergoing hemodialysis treatment and 10 controls.

The criteria for case selection were: age 15-50 years[10], hearing impairment after the occurrence of renal failure, no history of noise exposure, no history of diabetes, no history of renal transplantation.

The criteria for healthy volunteers were: age 15-50 years, normal renal function tests, no history of noise exposure, no history of diabetes, no history of renal transplantation.

Renal failure was diagnosed by elevated level of blood urea and serum creatinine and associated oliguria. We did hearing evaluation by using tympanometry, impedance audiometry and DPOAE. We used a setting of 65 / 55 dB SPL L1 / L2 in DPOAE examination.

3. Results

According to the results of the examinations done to the patients it showed that 29 patients out of 43 under hemodialysis treatment had sensorineural hearing loss in high frequencies in audiometric measurements and 33 of them had decreased DPOAE amplitudes(Figure 1).

In the control group only one patient had pure tone audiometry (PTA) threshold low in high frequencies and DPOAE gram according to the audiogram but lower values in > 4 000 Hz.

It was observed a higher incidence of hearing loss in stages three, four and five of renal failure with lower amplitudes in the DP-gram than PTA thresholds in the same frequencies (Figures 2 and 3).

Figure 1. DPOAE findings in CRF patients.

Figure 2. DPOAE and Audiometric results of one of our patients.

4. Discussion

The survival of chronic renal failure patients is increased with the new hemodialysis treatments[11].

The impact of hearing loss on these patients in the social integration has to be addressed. So both primary prevention and early detection of hearing loss are important for providing management options.

As screening tools, DPOAEs are superior to PTA testing. DPOAE amplitude reduces significantly before behavioral threshold changes are noted at corresponding frequencies in PTA. Decreased emissions in the presence of normal behavioral hearing may indicate an underlying pathologic condition, which if continued might soon result in a significant hearing loss[12]. In this sense, the DP-grams may be predictive, foretelling a substantial threshold shift for a given frequency before a measurable sensitivity loss[13].

Figure 3. DPOAE and Audiometric results, second patient.

Our study demonstrated that DP-grams seem to be a more sensitive test than PTA for determining cochlear dysfunction.

DPOAEs have an extensive dynamic range regarding hearing loss and can be measured over a broader frequency range with more sensitive frequency specific response[14]. With their high sensitivity and excellent reliability, their objectivity makes them ideal for testing patients who cannot cooperate in a traditional examination of behavioral hearing. Their recording is easy for both technician and patient, and can be easily performed at the bedside. DPOAE audiograms provide a tool for a fast automated frequency-specific and quantitative evaluation of a mild or moderate hearing in followup diagnosis[15].

Therefore after a complete audiometric valuation it has to be established to monitor these patients periodically using DP-grams alone causing less inconvenience to these patients who are not feeling well.

Conflict of interest statement

The authors report no conflict of interest.

References

[1] Stamper GC, Johnson TA. Auditory function in normal-hearing, noiseexposed human ears. Ear Hear 2015; 36(2): 172-84.

[2] Reavis KM, McMillan G, Austin D, Gallun F, Fausti SA, Gordon JS, Helt WJ, Konrad-Martin D. Distortion-product otoacoustic emission test performance for ototoxicity monitoring. Ear Hear 2011; 32(1): 61-74.

[3] Thorson MJ, Kopun JG, Neely ST, Tan HY, Gorga MP. Reliability of distortion-product otoacoustic emissions and their relation to loudness. J Acoust Soc Am 2012; 131(2): 1282-95.

[4] Kirby BJ, Kopun JG, Tan H, Neely ST, Gorga MP. Do “optimal”conditions improve distortion product otoacoustic emission test performance? Ear Hear 2011; 32(2): 230-7.

[5] Reuven ML, Neely ST, Kopun JG, Rasetshwane DM, Allen JB, Tan H, et al. Effect of calibration method on distortion-product otoacoustic emission measurements at and around 4 kHz. Ear Hear 2013; 34(6): 779-88.

[6] Shiomi Y, Tsuji J, Naito Y, Fujiki N, Yamamoto N. Characteristics of DPOAE audiogram in tinnitus patients. Hear Res 1997; 108(1-2): 83-8.

[7] Rosner T, Kandzia F, Oswald JA, Janssen T. Hearing threshold estimation using concurrent measurement of distortion product otoacoustic emissions and auditory steady-state responses. J Acoust Soc Am 2011; 129(2): 840-51.

[8] Stavroulaki P, Nikolopoulos TP, Psarommatis I, Apostolopoulos N. Hearing evaluation with distortion-product otoacoustic emissions in young patients undergoing haemodialysis. Clin Otolaryngol Allied Sci 2001; 26(3): 235-42.

[9] Gierek T, Markowski J, Kokot F, Paluch J, Wiecek A, Klimek D. [Electrophysiological examinations (ABR and DPOAE) of hearing organ in hemodialysed patients suffering from chronic renal failure]. Otolaryngol Pol 2002; 56(2): 189-94. Polish.

[10] Lisowska G, Namyslowski G, Orecka B, Misiolek M. Influence of aging on medial olivocochlear system function. Clin Interv Aging 2014; 9: 901-14.

[11] Shi Y, Martin WH. ABR and DPOAE detection of cochlear damage by gentamicin. J Basic Clin Physiol Pharmacol 1997; 8(3): 141-55.

[12] Stavrulaki P, Apostolopulos N, Segas J, Tsakanikos M, Adamopoulos G. Evoked otoacustic emissions-an approach for monitoring cisplatin induced ototoxicity in children. Int J Pediatr Otorhinolaringol 2001; 59(1): 47-57.

[13] Barron SE, Daigneault EA. Effect of cisplatin on hair cell morphology and lateral wall Na, K-ATPase activity. Hear Res 1987; 26(2): 131-7.

[14] Franklin DJ, McCoy MJ, Martin GK, Lonsbury-Martin BL. Test/retest reliability of distortion-product and transiently evoked otoacoustic emissions. Ear Hear 1992; 13(6): 417-29.

[15] Janssen T. A review of the effectiveness of otoacoustic emissions for evaluating hearing status after newborn screening. Otol Neurotol 2013; 34(6): 1058-63.

doi:Medical emergency research 10.1016/j.joad.2015.04.009

*Corresponding author:Evis Bendo, ENT Department, “Mother Tereza” University Hospital, Tirane, Albania.

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