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Most babies born with Spina Bifida require early medical and surgical treatment. The hospital stay is usually three - four weeks.

Once you are ready to go home with your baby, you will continue to see the Spina Bifida service as an outpatient (someone who is not staying at the hospital). During the initial hospital stay, we will ensure new parents understand the needs of their own child.

The Spina Bifida service team includes:

• paediatrician
• neurosurgeon
• orthopaedic surgeon
• spinal surgeon
• urologist
• clinical nurse consultant
• social worker
• physiotherapist
• orthotist
• occupational therapist.

The medical coordinator (usually a paediatric rehabilitation specialist) takes overall care of your baby and talks with all the members of the team.

If necessary, closure of the Spina Bifida lesion is performed within the first two or three days of life. This operation involves:

• protecting and preserving function of the spinal cord
• bringing the skin together to cover the lesion.

Hydrocephalus (a build-up of fluid on the brain) may not be apparent while the Spina Bifida lesion remains open as the fluid is able to escape. Hydrocephalus may develop after the back is closed. Additional surgery may be needed to insert a shunt which will redirect the fluid from the brain. 

The physiotherapist will assess your baby to review lower limb function and musculoskeletal alignment. They will decide what treatment is required based on your child’s individual needs.

Some treatment options include:

• casting
• splinting
• stretches
• stimulation of weak muscle groups
• stimulation of normal development.

During your baby’s first few weeks in hospital, an initial assessment is made of kidney health and bladder function. These tests include:

• ultrasound of the kidneys and bladder
• sometimes a micturating cysto-urethrogram (checks for reflux of urine back into the kidneys).

These tests help to determine whether intervention is needed for bladder management and catheters may be used to ensure the bladder is emptying completely.

Follow up varies based on the individual needs of each child. The first medical follow up is usually six weeks after discharge from hospital. Babies grow rapidly and pass through many developmental stages in the first two years of life. Regular reviews are usually needed about every three months to six months or as required.

Physiotherapy and Occupational Therapy may be required. Sometimes it is possible to organise therapy closer to home, but most families return to the children’s hospital for their therapy.

Every family will have different needs for support, especially during the early years. Each hospital has its own suggestions and ways to provide you with the support that you may need. Make sure you ask your Spina Bifida service or social worker for assistance. The Spina Bifida Resource ÐÇ¿ÕÌåÓý explaining what Spina Bifida is.