Early Identification of HL Flashcards

1
Q

Why is HL an “important health problem” that warrants screening?

A
  • Unrecognized HL in young children compromises the development of speech and language
  • Could consider impaired hearing as a primary health condition (cochlea= primary sense organ)
  • HL is a causal or mediator variable that along with other factors can have a strong influence on long-term language outcomes
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2
Q

What is the prevalence of congenital HL in developed countries and high-risk populations?

A
  • Congenital HL: 1-3/1000 (.2-.3%) in developed countries

- 1-2% in “high risk” populations (~10x that of the general newborn population)

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3
Q

Describe OAEs as a screening test.

A
  • Some variation in OAE detectability

- Vulnerable to minor CHL

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4
Q

Describe ABRs as a screening test.

A
  • Strong relationship between detectability of ABR and audibility of transient sound
    - Unlike OAE, can be used to directly estimate thresholds. However, process can be time consuming
    - Not as susceptible to minor middle ear disorders but is affected by disorders that reduce or abolish temporal synchrony of the stimulus-evoked action potential
    - In screening context, specific stimulus and recording parameters are applied to yield a binary decision regarding ABR presence or absence
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5
Q

What are some limitations of OAE & ABR as screening tests?

A
  • Don’t have intrinsic validity
    - Responses may be observed consistently in absence of behavioral response to sound and behavioral responses may be observed in the absence of response
  • Errors due to environmental noise, physiological noise, natural biological variations in response amplitude (inaccuracy)
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6
Q

What is sensitivity?

A

-the probability of a positive test when the disorder is truly present

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7
Q

What is specificity?

A

-the probability of a negative test when the disorder is truly absent

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8
Q

Describe OAE & ABR screening sensitivity.

A
  • Sensitivities of DPOAE, TEOAE, and ABR are ~0.6-0.65 (not really that acceptable)
  • Could be influenced by:
    - Difference in ABR stimuli
    - Screening stimulus level (nHL vs. HL)
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9
Q

Describe OAE & ABR screening specificity.

A
  • Very well understood
  • Must information available re: specificity because population prevalence of HL is low
  • The vast majority of babies who fail the initial screen will not have HL
  • Overall proportion of babies who fail is generally an accurate estimate of the screen false positive rate given a substantial sample size that is relatively easy to obtain
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10
Q

What could possibly cause false positives in OAE & ABR screening?

A
  • Random algorithmic error
  • High environmental noise (AOAEs)
  • High electromyogenic noise (AABR)
  • Partially blocked probe/insert
  • Naturally small OAEs/ABRs
  • Minor middle ear conditions (AOAEs)
  • Substantial transient conductive loss (AABR)
  • Suboptimal test methods
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11
Q

What is “case definition” in hearing screening programs?

A

-Most current programs target permanent HL of 30-40 dB or greater

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12
Q

Describe the protocols and equipment in screening programs.

A
  • Most manufacturers target HL of 40 dB HL or greater
  • Automated ABR and OAEs are the primary test methods used in NBHS
  • OAEs may be preferred for hospitals with dedicated personnel who can become proficient at probe placement
  • Costs make ABR prohibitive
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13
Q

Describe follow-up procedures after screening.

A
  • 1, 3, 6 benchmarks
  • Knowing method used to screen is important so that outpatient re-screen is the same
  • Must have a mechanism in place for communicating with parents and PCPs as well as prompt referral to EI
  • Familiarization of funding sources for amplification
  • Employ EBP
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14
Q

What did Yoshinago-Itano et al. (1998) state about NBHS?

A

-Provided evidence that children whose HL was identified early and received early intervention before 6 months of age had better language outcomes

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15
Q

What did Norton et al. (2000) find about NBHS?

A

-TEOAEs, DPOAEs, and ABR have similar abilities to identify HL of 30 dB or greater as assessed by subsequent VRA at 8-12 months corrected age

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