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Feasibility of implementing a universal neonatal
hearing screening programme using distortion product otoacoustic
emission detection at a university hospital in Hong Kong
PK Ng, Y Hui, BCC Lam, WHS
Goh, CY Yeung
Childrens Habilitation Institute, The Duchess of Kent Childrens
Hospital at Sandy Bay, 12 Sandy Bay Road, Pokfulam, Hong Kong
OBJECTIVE. To assess the feasibility of implementing
a universal neonatal hearing screening programme using distortion
product otoacoustic emission detection at a major teaching hospital
in Hong Kong.
DESIGN. Descriptive study and questionnaire.
SETTING. Teaching hospital, Hong Kong.
METHODS. A total of 1064 infants, together with
their mothers, were successfully recruited for the study. The participation
rate was 99.3%. A three-stage hearing screening protocol using distortion
product otoacoustic emission detection was
adopted. Each of the participating infants was screened on three
separate occasions (day 1-4, day 5-14, and day 21-30 after birth),
irrespective of the test results. A questionnaire was administered
to 364 randomly selected mothers to determine whether as consumers
of the hearing screening service, mothers would find screening desirable.
RESULTS. Results of the screening demonstrated an
incidence of permanent bilateral hearing loss (�40 dB in the better
ear) of 0.28%. The results also showed that 3.5% of the screened
infants were referred for subsequent diagnostic audiological assessment,
including those suspected with unilateral as well as bilateral hearing
loss. Data obtained were comparable to other reported results obtained
using multi-stage screening protocols. Taking b oth the false positive
rate and the default rate into consideration, the most appropriate
time for screening in this hospital setting appeared to be around
day 5 to 14 when infants returned to the hospitals day centre
as out-patients for routine medical follow-up. Since this day centre
service is not generally provided by all maternity hospitals in
Hong Kong, an alternative time for screening would be around day
21 to 30 when infants could return as out-patients solely for the
hearing test. The results of the questionnaire suggested that most
mothers thought a neonatal hearing screening would be desirable
(91.35%). The majority (81.70%) indicated a preference for screening
either within a few days of birth at the maternity ward prior to
discharge from the hospital, or between 5 and 30 days when returning
to the hospital as an outpatient.
CONCLUSION. It was concluded that a universal neonatal
hearing screening programme could be readily implemented in a maternity
hospital setting in Hong Kong.
Hong Kong Med J 2004;10:6-13
Key words: Feasibility studies; Hearing tests; Infant,
newborn; Neonatal screening
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