Spina bifida is a congenital (happening before birth) condition where a part of the baby’s spinal cord develops outside, instead of inside, the bones of the spine. The condition can be found during pregnancy, but some cases may not be discovered until after the baby is born.
There are different types of spina bifida, and treatment will depend on how much of the spinal cord is exposed or has been affected. In some cases, no treatment is required, but some babies will require surgery and lifelong medical care.
Spina bifida is one of the most common birth defects in the world. While no one knows what causes spina bifida, there is proof that women who eat a lot of foods containing folic acid (Vitamin B9) during pregnancy are less likely to deliver a baby with spina bifida.
Spina bifida occurs in the first few weeks of pregnancy when the brain and neurological system are just starting to grow. While no one knows what causes spina bifida, there are factors that may impact its development:
Spina bifida is also seen more often in young mothers, those with a history of miscarriage, and those with a poor diet.
The role of folic acid
Research also shows that women who have had a baby with spina bifida can reduce their chances of having a second baby with the condition by taking more folic acid. Folic acid is found in leafy green vegetables, nuts, beans, citrus fruits, and fortified breakfast cereals. It is also found in prenatal vitamins.
During pregnancy, there are several tests (called prenatal tests) that can help tell if your baby has spina bifida:
Types of Spina Bifida
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The full impact of all of these types of spina bifida is usually not known right after birth, but may be seen as the child grows and develops.
Meningocele. This is a moderate form of spina bifida. A sac of fluid comes through the baby’s back and can been seen outside as a lump or bulge along the spine. The spinal cord and nerves are not in the sac. This type of spina bifida can cause some problems. Timing of the surgery to close the meningocele is determined by neurosurgery.
Spina bifida occulta. This is the mildest form of spina bifida. The spinal cord and nerves are inside the body, but the bones in the lower back do not develop normally, leaving a small gap in the spine. There is no opening you can see or sac on the baby’s back. The baby may have a hairy patch, dimple, or birthmark over this opening. There may be a tethered spinal cord, a condition where the nerves at the end of the spinal cord have limited movement and may not work as they should. This type of spina bifida is not generally found prenatally.
Longer term problems may include:
If a test finds you are carrying a baby with spinal bifida, you will continue to receive care from your doctor. You may also be referred to the Ohio Fetal Medicine Collaborative (OFMC).
Through the OFMC, you will see a doctor who takes care of high-risk patients. You may also meet with a multidisciplinary team including neonatologists (a doctor who specializes in newborn care), neurosurgeons (brain surgeon) and nurses from the Myelomeningocele Program at Nationwide Children’s Hospital to learn more about your baby’s care after birth. Nationwide Children’s has a special Myelomeningocele Clinic to care for children with Myelomeningocele. Nurse coordinators will help answer your questions and concerns, guide you through your pregnancy, and prepare you for what to expect.
Your doctor will watch your pregnancy closely, and will deliver your baby at a hospital that is prepared to care for high-risk babies. Contact your doctor if you ever have any concerns.
At the delivery hospital, a neonatologist will manage the care of your baby. Babies born with more severe forms of spina bifida (meningocele or a myelomeningocele) require care in the Neonatal Intensive Care Unit (NICU) and will need surgery shortly after birth.
Right after delivery:
Your baby may not be able to breastfeed or bottle feed right away. We encourage you to pump and store breast milk for your baby until he or she is ready to start feeding.
The most important goals of treatment are:
Surgical repair for babies with spina bifida after birth:
After surgery, your baby will continue to receive care in the NICU. Your baby may need to be on a ventilator (breathing machine) until fully recovered from surgery. The total length of time your baby will stay in the hospital will vary, depending on whether he or she is born with other health issues.
Besides surgery, postnatal (right after birth) care of babies with spina bifida involves many different teams of doctors, support and therapy services. Additional tests and imaging studies and procedures will be needed as well. Some of these may include:
Preparing for Home:
We will teach you to care for your baby at home. We will show you how to:
Your baby will need regular follow-up appointments to measure growth, development, and nutrition. You will want to find a local doctor who cares for children to take care of the routine checkups, immunizations, and doctor’s visits. The program coordinator can help if needed.
The Spina Bifida Clinic at Nationwide Children’s will also provide follow-up care for your baby’s specialized medical needs. It is a multidisciplinary clinic which meets once a week on Friday mornings from 8 am to noon. During this visit you will see providers from the following specialties: developmental pediatrics, genetics, neuropsychology, nursing, occupational therapy, orthopedics, physical medicine, physical therapy, social work and urology. Visits are scheduled every three months during the first year and every 6-12 months after 1 year of age, or more often, based on your child’s individualized needs.
The Spina Bifida Clinic at Nationwide Children’s will also provide follow-up care for your baby’s medical and surgical needs. This is a multidisciplinary clinic which means you can see the multiple doctors and therapists involved with your baby’s care in one visit.
Some babies may need more surgery in the future to help correct bone problems, such as curving in the back or hip dislocations, or to help with bowel or bladder issues.
Spina Bifida is a lifelong condition that is not curable. Care for children born with spina bifida focuses on preventing problems and maximizing your child’s abilities. With help, children with Spina Bifida can lead full lives. Most do well in school, and many play in sports. Because of today’s medicine, about 90 percent of babies born with Spina Bifida now live to be adults. As type and level of severity differ among people with Spina Bifida, each person with the condition faces different challenges and may require different treatments. The best way to manage Spina Bifida is with a team approach. Members of the team may include developmental pediatrics, neurosurgery, urology, orthopedics, physical medicine, advanced practice nurses, nurse, physical and occupational therapists, orthotists, neuropsychologists and medical social workers. Physical and occupational therapy, early intervention, and approptriate educational interventions through a multidisciplinary approach are important in helping your child. The full extent of Spina Bifida is usually not completely known or understood immediately after birth, but may be revealed as the child grows and develops.
Your doctor may recommend genetic counseling to discuss risks for a future pregnancy. Women who have a child with Spina Bifida should take 400 mcg (4 MG) of folic acid daily for one to 3 months before pregnancy and continue during the first 3 months of pregnancy. Taking folic acid before and during the first three months of pregnancy does not guarantee the baby will not have Spina Bifida, but it can significantly reduce the risk.