From: Universal newborn hearing screening in the Lazio region, Italy
Audiological risk factor — JCIH | |
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Family history of hereditary childhood sensorineural hearing loss | |
In-utero infection (e.g., rubella, cytomegalovirus, syphilis, toxoplasmosis, herpes) Craniofacial anomalies | |
Low birth weight (b1500 g or 3.3 lb) | |
Hyperbilirubinemia at levels requiring exchange transfusion | |
Bacterial meningitis | |
Exposure to ototoxic medications | |
Mechanical ventilation lasting 5 days or longer | |
Stigmata or other findings associated with a syndrome known to include a sensorineural and/or conductive hearing loss | |
Apgar scores of 0–4 at 1 min or 0–6 at 5 min | |
Admission to the Neonatal Intensive Care Unit (NICU) | |
Parent/caregiver concern regarding hearing, speech, language, and/or developmental delay | |
Head trauma associated with loss of consciousness or skull fracture | |
Recurrent or persistent otitis media with effusion lasting for at least 3 months |