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Newborn screening is a routine programme conducted shortly after birth to detect selected medical conditions that may not be apparent at first. Early identification allows timely intervention, treatment, and ongoing care to support a child’s healthy development.

This test checks whether your baby can hear well. It is quick, gentle, and painless. Detecting hearing problems early helps ensure healthy speech and language development.
Universal Newborn Hearing Screening is a screening process conducted for all newborns to detect potential hearing loss within the first few months of life.
It means that your baby should have the hearing screen repeated either before your baby is discharged or at outpatient. This does not mean that your baby has hearing impairment.
Some reasons a baby may need to repeat the hearing screening test include:
Testing is the only way to know if a baby has a hearing loss and the earlier we can detect hearing loss, the better it is for a baby.
If your baby does not pass the repeat screening test, a referral will then be made to the Ear, Nose and Throat (ENT) specialist.
The ENT specialist together with the Audiologist (hearing specialist) will perform detailed hearing tests to get a complete picture of your child's hearing ability.
If they find a problem, there are many things that can be done to help a baby maximize on hearing, speech and language development.
Some babies may have normal hearing at birth. However, hearing impairment may develop gradually during infancy or childhood due to several reasons like recurrent ear infections or genetic factors. Hence, even if your baby has passed the newborn hearing screening tests, it is important to be vigilant and monitor your baby's hearing and language ability. You can track these milestones in your baby's health booklet and in the chart below.

All newborns are screened for hearing impairment after birth under the Universal Newborn Hearing Screening Program. Some are identified to be more vulnerable for hearing impairment if they belong to any one of the categories below:


It means that your baby is at a higher chance for developing hearing impairment that may be present at birth, shortly after birth or may develop later in childhood. It also means that your baby will be screened using 2 screening tools before discharge. If your baby does not pass the newborn hearing screening tests, referral to the ENT will be made for diagnostic tests as early as possible.
Regular outpatient appointments will be scheduled with the Pediatrician to monitor your baby's hearing, speech, and language development, especially in the first 3 years of life. Any concern about your baby's hearing ability or speech should be brought to the attention of the doctor during these clinic visits. For some babies, another hearing evaluation will be scheduled to be done by the ENT specialist during infancy. It is very important for your child to be reviewed regularly to enable early detection of delayed onset or progressive hearing loss.
The ENT doctor will check your baby's ears and an Audiologist (hearing specialist) will conduct comprehensive hearing tests for your baby.
If hearing loss is detected, he/she may need further evaluation to identify the cause, type and severity of hearing loss. Early interventions to optimize speech and language development will also be instituted without delay.
Providing children and families the earliest possible start to intervention is important. Interventions for children may include fitting of hearing aids, cochlear implant surgery and auditory-verbal therapy for the development of speech and language. Children with hearing loss will be taught to listen with their hearing devices. Family members will be taught several strategies to support the child's language growth and provide a language rich environment through daily routines at home. Working together we can help a child achieve the maximum potential in academics and social life.
Universal Newborn Hearing Screening
Ward 53 Central (next to room 22)
Block 5, Level 3, Singapore General Hospital
ENT Centre, Specialist Outpatient Clinics
Block 3, Basement 1, Singapore General Hospital
SGH Baby & Child Clinic
Obstetrics & Gynecology Centre
Block 5, level 1, Singapore General Hospital
To re-schedule, call SGH Central Appointment Desk: 6321 4377 during office hours (Mon - Fri: 8am - 5pm)
Please bring along your baby's health booklet and birth certificate on the day of appointment
This test checks if your baby has a condition that affects how red blood cells work. Babies with G6PD deficiency should avoid certain medicines and foods (like fava beans) that can trigger jaundice or anaemia.
This blood test screens for rare but serious inherited conditions such as:
If any of these are detected early, treatment can help prevent serious complications.
View more about metabolic screening tests.
This simple test measures oxygen levels in your baby’s hands and feet to check for heart problems that may not be seen at birth. It helps detect heart defects early so your baby can receive prompt care.
If the CCHD screen shows low blood oxygen levels (lower than the required 95-100% range), it does not definitively mean the baby has a heart defect. It could be due to other reasons like the baby's heart or lungs still adjusting to life outside the womb. In such cases:
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