Wilunda et al 1 address an important concern in this issue of Paediatric and Perinatal Epidemiology: Is tobacco exposure prenatally or via passive exposure during early childhood associated with childhood hearing loss? Studies on the association between tobacco smoke and childhood hearing loss are limited, although the potential impact of passive smoking on otitis media (OM, both acute and chronic middle ear infections) has been examined extensively. Associations have been reported but it remains unclear how sizeable the likely effect of passive smoking is on the burden of childhood OM. 2 OM leads to conductive hearing loss (vs sensorineural) and is unquestionably a principal risk factor for childhood hearing loss; recent studies have also demonstrated associations with adult sensorineural hearing loss. 3 To gain perspective and appreciation for the aetiology of childhood hearing loss, a fuller examination of established factors may be useful. 4,5 Rapid advances in mobilisation of hearing health care screening for neonates and infants based on state-wide implementation of programmes to identify, refer for diagnosis, and provide early intervention-have led to impressive results in the United States and abroad. 6 Universal newborn hearing screening programmes can identify infants with hearing loss across the frequency range for speech understanding (500-4000 Hz) equal to or exceeding 30-40 decibels hearing level (dB HL, decibels in terms of the "hearing level" scale of measurement, which is calibrated relative to the quietest sounds a young healthy adult is able to hear). As many as 6000 infants are born each year in the United States with this degree of hearing loss yielding an estimated prevalence of 1-2 per 1000 live births. The mean age at identification has been reduced from greater than 2 years before implementation of state-wide universal newborn hearing screening programmes to approximately 3 months of age following implementation. 7 Many of these infants receive rehabilitation services, including fitting with hearing aids or insertion of cochlear implants before reaching their first birthday.
Yoshinago-Itano et al 8 have demonstrated the benefit for language development if children's hearing impairment is identified before 6 months of age and they receive intervention services quickly thereafter. Korver et al 9 classified the aetiology of permanent childhood hearing impairment (PCHI) as due to (a) hereditary/genetic causes; (b) acquired causes (prenatal congenital infections such as CMV and rubella; perinatal risk factors including birth asphyxia, preterm delivery, low birthweight, ototoxic drugs, hyperbilirubinemia with exchange transfusion; postnatal conditions such as meningitis, cholesteatoma, etc.); (c) miscellaneous conditions (eg, cleft palate and other birth defects); or (d) unknown origin. Based on this 2003-05 Dutch national study (DECIBEL), 185 children with PCHI were classified by cause as: hereditary, 38.9%; acquired, 29.7%; miscellaneous, 7.1%, and unknown, 24.3%. 9 These children were identi...