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Spina bifida final

Spina bifida is a birth defect where the spinal cord fails to develop properly, leaving an opening in the vertebrae. There are three main types - spina bifida occulta which has no symptoms, meningocele where only the meninges protrude out, and myelomeningocele where the meninges and spinal cord protrude out. Myelomeningocele is the most severe and can cause paralysis. Diagnosis is usually made prenatally through ultrasound or after birth upon visual inspection. Treatment involves surgery to close the opening soon after birth along with lifelong physical therapy and management of complications which commonly include hydrocephalus, learning disabilities, and bladder/bowel issues.

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Spina Bifida (Spinal dysmorphism) Dpt. Aamir Memon 8/26/2013
Spina Bifida (Spinal dysmorphism) Introduction: → Spina bifida (literally, “cleft spine”) is a congenital neural tube defect in which the vertebral arch fails to close completely over the spinal cord.  This results in a cyst-like protrusion of the meninges alone (meningocele) or of the meninges and the spinal cord (myelomeningocele) out of the vertebral column.  Incomplete closure of the caudal neural tube during development may produce various deformities, ranging from the mild and entirely incidental spina bifida occulta, to the severe, with exposure of neural tissue to the surface (rachischisis).  In the case of a meningocele, neural tissue is unexposed, and thus neural deficits are absent or minor.  With a myelomeningocele, the spinal cord, in a cyst-like protrusion with its nerves, suffers injury, inflammation, and scarring. The result is some loss of neural function, often including paralysis.  A meningocele can occur in any area of the spine; cranial or upper cervical meningoceles are frequently associated with hydrocephalus. A myelomeningocele typically occurs in the lumbar or lumbosacral area.  Another type of spina bifida is one in which minor irregularities in the vertebral arches exist that are not obvious at birth. This is called spina bifida occulta (hidden). → These defects may be associated with abnormal neurological function of the lower limbs, with or without sphincter involvement. Associated tethered cord syndrome may lead to development of neurological problems in later life. Spina bifida may be a teratogenic consequence of drug therapy (e.g., certain antiepileptic drugs). → This defect can be so subtle that it is found only through incidental radiography or MRI, or it can be so severe that the spinal canal is open and the baby may not survive the birth Demographics: → Spina bifida statistics in the United States have recently been declining, but it still occurs about once in every 1,000 live births, or 1,500 to 2,000 times per year. → It clearly has a genetic component, because having this disorder in the family raises the risk of having a child with spina bifida, but about 95% of cases occur in families with no history of the disease. → Hispanics and European whites have a higher incidence of spina bifida than other races. → Women who have spina bifida themselves or who have diabetes or seizure disorders have a higher than normal chance of having a child with this disorder.
Etiology: → Several types of neural tube defects may occur between day 14 and day 28 after conception. → Although the cause of spina bifida is unknown, a genetic predisposition may exist. The main risk factor for is a deficiency of folic acid at conception and in the earliest weeks of fetal development. → Folic acid deficiency is common in women; therefore, it is strongly recommended that all women anticipating pregnancy begin taking folic acid vitamin supplements at least 3 months before conception. → Higher risk factors may include: o Maternal lack of folic acid and vitamins o Previous baby & family history of spina bifida o Maternal obesity o Diabetes during pregnancy o Maternal stress o Woman who has epileptic seizures o Maternal fever in the first trimester o Hispanic background Classification: Detailed classification includes: 1. Open spinal dysraphism (OSD) a. Occult a. Spina bifida occulta b. Cystic a. Spina bifida meningocele b. Spina bifida myelomeningocele c. Rachischisis 2. Closed spinal dysraphism (CSD) a. With spinal mass b. Without spinal mass i. Simple ii. Spina bifida occulta iii. Complex
Spina bifida can be classified as: 1. Spina bifida occulta. → The vertebral arch, usually in a lumbar vertebra, does not completely fuse, but no signs or symptoms are obvious. → Indeed, a person with spina bifida occulta may never be aware of the condition unless a low back radiograph is taken for another reason. → It is difficult to estimate how common it is; some sources suggest that 5 to 10% of the population may be affected. → Some people with spina bifida occulta have a small dimple, birthmark, or tuft of hair on the spine at the location of the abnormality, but they have no dysfunction because of it. → While spina bifida occulta is usually inconsequential, it can be serious. → Two or more vertebrae may be affected, and the person may develop a tethered spinal cord. → This can manifest as problems in the feet (especially pes cavus) and problems with bladder and bowel control. These often arise during puberty, when the child goes through a growth spurt that stretches the spinal cord. 2. Spina bifida meningocele. → This is the rarest type of cystic spina bifida. → Only the dura mater and arachnoid layers of the meninges press through at the site of the vertebral cleft, forming a cyst that is visible at birth. → It is easily reparable with surgery and generally has few or no long-term consequences for the baby. 3. Spina bifida myelomeningocele. → This is the most common and most severe version of cystic spina bifida, accounting for about 94% of cases. → In this case the spinal cord or extensions of the cauda equina protrude along with the meninges through several incompletely formed vertebral arches. → Occasionally the skin doesn’t cover the protrusion, raising a serious risk of CNS infection if no immediate intervention takes place. Clinical Menifestations:  Open spinal dysraphism (OSD)  All OSD are associated with Chiari malformation type II.  Learning disabilities and seizures are more common in children with spina bifida
1) Spina bifida occulta may be asymptomatic or associated with: → Not obvious at birth → May present as: o Patch of hair growth along the spine o Midline dimple, usually in the lumbosacral area → Gait or foot abnormalities → Poor bladder control 2) Cystic spina bifida → Obvious with a sac containing meninges and/or spinal cord material protrudes on the back of the newborn infant. → It usually occurs in the lumbar spine, and the sac is often red and raw looking. → The severity of cystic spina bifida is determined by the location and size of the cyst. The higher the defect, the more paralysis tends to be present. → Fortunately, most cases present in the thoracic or lumbar spine. a) Spinal meningocele may be asymptomatic or associated with: → A sac-like protrusion of meninges (dura and arachnoid only) and CSF from the back → Clubbed foot → Gait disturbance → Bladder incontinence → Seldom neurological consequences b) Spinal myelomeningocele is associated with: → Protrusion of meninges (dura, arachnoid and neural tissue) , CSF, and spinal cord → Evident at birth → Neurologic deficits at and below the site of exposure → Severe disability c) Rachischisis → Exposure of neural tissue to surface → Evident at birth → Severe disability  Closed spinal dysraphism (CSD) = skin-covered 1) With spinal mass: → Lipoma, → Dural defect → Meningocele
2) Without spinal mass: a) Simple: o Tight filum terminale o Intradural lipoma. b) Spina bifida occulta: o Incomplete closure of the vertebral laminae; o May be evident only as dimpling of the skin or a hairy patch over the lumbar spine, or only seen radiologically. o May be asymptomatic or may present with progressive lower limb sensorimotor and sphincter dysfunction in later life due to cord tethering. c) Complex: o Split cord malformation (diastematomyelia) o Caudal regression. Diagnosis: → Spina bifida is detectable prenatally. → Testing begins with a blood sample; it shows elevated levels of a fetal protein called alfa-fetoprotein. → A follow-up ultrasound may diagnose the condition in utero and/or amniocentesis may be scheduled. → Some research indicates that a cesarean section is safer than vaginal birth for a baby with spina bifida; this can be planned. → Furthermore, a few facilities have begun to try in utero corrective surgery. This approach is very new, but early reports suggest a lower risk of hydrocephalus for these children. This procedure carries very high risks, however, to both the mother and the child. Differential Diagnosis: → Severe degrees of dysraphism are unlikely to be mistaken, but the progressive paraparesis of cord tethering has a broad differential, including structural and inflammatory spinal cord disease.
Treatment: → No treatment may be required for spina bifida occulta or meningocele. → Surgical repair of the myelomeningocele, and sometimes the meningocele, is required. → If surgical repair is performed, placement of a shunt to allow for CSF drainage is necessary to prevent hydrocephalus and a subsequent increase in intracranial pressure. → Planned cesarean section before the initiation of labor can be important in reducing the neurologic damage seen in an infant with a spinal cord defect. → Afterward, even tiny babies are supported with rigorous physical therapy and exercises to maintain function in the leg muscles as much as possible. → As children mature and their functional level becomes clear, they may be taught to use crutches, braces, wheelchairs, or other equipment as necessary. → Many spina bifida patients undergo multiple surgeries, not only to reduce the protruding cyst but also to correct a tethered cord, in which the spinal cord doesn’t slide freely within the spinal canal; to deal with the complications of hydrocephalus as discussed earlier; and to address whatever complications may be brought about by severe scoliosis. Complications: → Hydrocephalus, or water on the brain, affects about 85% of children with cystic spina bifida which may occur with a meningocele or myelomeningocele. o The insertion of a shunt that drains cerebrospinal fluid from the brain down the neck and into the abdominal cavity prevents hydrocephalus from damaging the brain. → Many have mild to severe learning disabilities that may make it difficult to function in a mainstream classroom. → Many spina bifida patients develop very severe latex hypersensitivity, possibly from having multiple intrusive surgeries and other medical procedures early in life which may create a dangerous anaphylactic reaction later in life. → Other common complications include: o Decubitus ulcers o Digestive tract problems o Urinary tract problems o Obesity o Severe muscle imbalances that can lead to flaccidity on one side, contractures on the other o Severe scoliosis.