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Neonatal Murine Cochlear Explant Technique as an In Vitro Screening Tool in Hearing Research
Published on: June 8, 2017
Cochlear microphonics in sensorineural hearing loss: lesson from newborn hearing screening
Ansar Ahmmed1, Christopher Brockbank, June Adshead
1Lancashire Teaching Hospitals NHS Foundation Trust, Preston, United Kingdom. dipu@ahmmed.freeserve.co.uk
Abstract:
The diagnostic dilemma surrounding the presence of cochlear microphonics (CM) coupled with significantly elevated auditory brainstem response (ABR) thresholds in babies failing the newborn hearing screening is highlighted. A case report is presented where initial electo-diagnostic assessment could not help in differentiating between Auditory Neuropathy/Auditory Dys-synchrony (AN/AD) and sensorineural hearing loss (SNHL). In line with the protocol and guidelines provided by the national Newborn Hearing Screening Programme in the UK (NHSP) AN/AD was suspected in a baby due to the presence of CM at 85 dBnHL along with click evoked ABR thresholds of 95 dBnHL in one ear and 100 dBnHL in the other ear. Significantly elevated thresholds for 0.5 and 1kHz tone pip ABR fulfilled the audiological diagnostic criteria for AN/AD. However, the possibility of a SNHL could not be ruled out as the 85 dBnHL stimuli presented through inserts for the CM would have been significantly enhanced in the ear canals of the young baby to exceed the threshold level of the ABR that was carried out using headphones. SNHL was eventually diagnosed through clinical and family history, physical examination and imaging that showed enlarged vestibular aqueducts. Presence of CM in the presence of very high click ABR thresholds only suggests a pattern of test results and in such cases measuring thresholds for 0.5 and 1 kHz tone pip ABR may not be adequate to differentiate between SNHL and other conditions associated with AN/AD. There is a need for reviewing the existing AN/AD protocol from NHSP in the UK and new research to establish parameters for CM to assist in the differential diagnosis. A holistic audiological and medical approach is essential to manage babies who fail the newborn hearing screening.
Insights
Diagnosing hearing loss in babies is challenging. Cochlear microphonics (CM) with elevated auditory brainstem response (ABR) thresholds may not always distinguish auditory neuropathy/dys-synchrony (AN/AD) from sensorineural hearing loss (SNHL).
Area of Science:
- Audiology
- Pediatric Medicine
- Genetics
Background:
- Newborn hearing screening aims for early detection of hearing loss.
- Distinguishing Auditory Neuropathy/Auditory Dys-synchrony (AN/AD) from Sensorineural Hearing Loss (SNHL) in infants presents diagnostic challenges.
- Cochlear microphonics (CM) and Auditory Brainstem Response (ABR) are key electro-diagnostic tools.
Observation:
- A case is presented where initial electro-diagnostic assessments were inconclusive in differentiating AN/AD from SNHL in a baby failing newborn hearing screening.
- The presence of CM at 85 dBnHL with elevated click-evoked ABR thresholds (95-100 dBnHL) initially suggested AN/AD according to UK National Newborn Hearing Screening Programme (NHSP) guidelines.
- Elevated tone pip ABR thresholds at 0.5 and 1kHz further supported the AN/AD diagnosis, but SNHL could not be excluded due to potential sound amplification effects.
Findings:
- Sensorineural hearing loss (SNHL) was ultimately diagnosed through clinical history, family history, physical examination, and imaging revealing enlarged vestibular aqueducts.
- The study highlights that CM with very high click ABR thresholds alone is insufficient for definitive diagnosis.
- Measuring only 0.5 and 1kHz tone pip ABR thresholds may not adequately differentiate SNHL from AN/AD.
Implications:
- The findings suggest a need to review the current AN/AD diagnostic protocol within the UK's NHSP.
- Further research is required to establish reliable parameters for CM in differential diagnosis.
- A comprehensive audiological and medical approach is crucial for managing infants who fail newborn hearing screening.
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