What are the different type of special audiometry test and what are their indications
"audiometry" AND "hearing tests"
special audiometry tests indications SISI ABLB Bekesy impedance audiometry
| Test | Principle / typical result | Main indication |
|---|---|---|
| SISI test (Short Increment Sensitivity Index) | Ability to detect repeated 1 dB increments in a continuous tone, usually 20 dB above threshold. A high score suggests cochlear recruitment. | Suspected cochlear lesion, especially to demonstrate recruitment in Ménière disease or cochlear SNHL. |
| ABLB test (Alternate Binaural Loudness Balance, Fowler test) | Compares loudness growth between ears. Rapid loudness growth in the affected ear indicates recruitment. | Unilateral/asymmetrical SNHL with a normal or near-normal opposite ear; helps distinguish cochlear from eighth-nerve pathology. |
| Tone-decay test (Carhart test) | Measures inability to sustain perception of a continuous tone just above threshold. Marked decay is classically associated with auditory-nerve involvement. | Suspected retrocochlear lesion, such as vestibular schwannoma. |
| Békésy audiometry | Patient traces thresholds for continuous and interrupted tones. Type II pattern favors cochlear pathology; Types III/IV may suggest retrocochlear disease. | Site-of-lesion assessment in SNHL and assessment of test reliability. |
| Loudness discomfort level / UCL | Determines the intensity at which sound becomes uncomfortably loud. | Demonstration of recruitment, hyperacusis assessment, and setting safe hearing-aid output. |
| Speech discrimination and rollover test | Measures word recognition at increasing intensities. Disproportionately poor discrimination or rollover raises concern for retrocochlear involvement. | Speech-understanding complaints, hearing-aid evaluation, and suspected retrocochlear pathology. Poor speech discrimination despite relatively preserved pure-tone thresholds warrants further work-up. |
| Component | Main indication |
|---|---|
| Tympanometry | Assesses tympanic-membrane mobility and middle-ear pressure. Used for otitis media with effusion, Eustachian-tube dysfunction, tympanic-membrane perforation, ossicular problems, and otosclerosis. A flat trace supports middle-ear effusion. |
| Acoustic stapedius reflex | Helps assess the middle ear, cochlea, auditory nerve, and facial nerve reflex arc. Useful in suspected otosclerosis, facial palsy, and retrocochlear pathology. |
| Reflex decay | Decay of an acoustic reflex during sustained stimulation may suggest retrocochlear involvement. |
| Test | Main indication |
|---|---|
| BERA / ABR (Brainstem Evoked Response Audiometry) | Estimation of hearing threshold in infants, young children, sedated/uncooperative patients, suspected auditory neuropathy, and suspected retrocochlear lesion. Also used in newborn hearing screening pathways. |
| ASSR (Auditory Steady-State Response) | Frequency-specific objective threshold estimation, particularly in infants and patients with severe or profound hearing loss; useful when fitting hearing aids or considering cochlear implantation. |
| OAE (Otoacoustic emissions) | Tests outer hair-cell function. Used for newborn hearing screening, monitoring ototoxicity/noise-related cochlear injury, and distinguishing normal cochlear outer-hair-cell function from many cochlear losses. OAEs can be present in auditory neuropathy. |
| Electrocochleography (EcochG) | Records cochlear/auditory-nerve potentials. Used as an adjunct in suspected Ménière disease/endolymphatic hydrops, auditory neuropathy, and selected intraoperative assessments. |
| Test | Indication |
|---|---|
| Stenger test | Best test for suspected unilateral or asymmetrical non-organic hearing loss. A positive Stenger result supports functional exaggeration of unilateral loss. |
| Lombard test | Detects non-organic hearing loss by observing involuntary increase in voice intensity when masking noise is introduced. |
| Doerfler-Stewart test | Speech-based test for suspected functional unilateral hearing loss. |
| Objective tests: OAE and ABR | Used to confirm cochlear/neural function when behavioural audiometry is unreliable or inconsistent. |