Table 5. Strength of Evidence for Universal Newborn Hearing Screeninga
|
Key Question |
Evidence Codeb |
Quality of Evidence |
|
1a. Can UNHS accurately diagnose moderate-to-profound
sensorineural hearing impairment?
OAE and ABR are highly accurate screening tests for
congenital PHL (sensitivity 84%, specificity 90%).
|
II-1, II-2 |
Good: One controlled trial measured the predictive value of a positive test result (6.7%), and a good quality cohort study measured sensitivity and specificity against an independent gold standard. |
|
1b. In UNHS programs, how many children are identified
and treated before 6 months?
UNHS increases the chance that diagnosis and treatment
will occur before 6 months of age. UNHS increases
early identification between 19% and 42% over selective
screening in high-risk children.
|
II-1, II-2 |
Good: One controlled study in the United Kingdom and 1 cohort study in the United States reported the frequency of treatment before 10 and 6 months, respectively. Other studies did not provide sufficient information, and none included patients who, although screened, were diagnosed and treated late because of loss to followup. However, no controlled trials of UNHS versus selective screening have been done. |
|
2. Does identification and treatment prior to 6 months improve
language and communication in infants who would not be
diagnosed that early in a selective, high-risk screening
program?
Evidence is inconclusive.
|
II-2, II-3 |
Fair/Poor: Studies have selection bias and baseline differences between compared groups. These studies did not specifically describe outcomes in the subgroup of children who would be identified by UNHS but not by selective screening. |
|
3. What are the potential adverse effects of screening and
early treatment?
Evidence is inconclusive.
|
III |
Poor: Most postulated adverse effects have not been evaluated in studies. |
a ABR indicates automated brainstem response; OAE, otoacoustic emissions; PHL, permanent hearing loss; UNHS, universal newborn hearing screening.
bEvidence codes: I: Randomized controlled trial; II-1: Controlled trial without randomization; II-2: Cohort or case-control analytic study;
II-3: Multiple time series, dramatic uncontrolled experiments; III: Opinions of respected authorities.
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