Spina bifida

 

HydrocephalusSpina bifidaTethered cord

 

Definitions

 

Spina bifida - failure of closure of neural tube (vertebra +/- spinal cord)

 

Spina bifida occulta

- two halves of posterior arches fail to fuse 

- seen in 5-10% of xrays in normal population 

 

Spina bifida cystica

- prolapse of neural elements causing motor and sensory deficit below level of lesion

- meningocele: prolapse of dura only usually with no neurological deficit 

- myelomeningocele: prolapse of cord & dura in defect / associated with neurological deficit

 

Epidemiology

 

1 / 1000 USA / Europe

 

Etiology

 

Multifactorial 

- genetic factors

- low folic acid - folic acid supplementation will prevent 50 - 70% neural tube defects

- maternal obesity 

 

Prenatal Screening

 

Issue

1.  Consider cesarian section and closure of myelomeningocele within 48 hours

2.  Consider pre-natal surgical repair

 

Ultrasound - high sensitive at 20 week ultrasound

 

Prenatal surgical repair of myelomeningocele

 

Laparotomy / hysterotomy / defect repair and closure 

- between 19 and 25 weeks

- evidence that it improves outcomes and preserves neurological levels

 

Adzick et al NEJM 2011

- RCT of prenatal versus postnatal repair in myelomeningocele

- 158 patients followed up for 12 months

- reduced need for shunt and improved motor outcomes in prenatal repair

- prenatal surgery associated with increased preterm delivery and uterine dehiscence

 

Houtrow et al JAMA Pediatr 2021

- follow up of RCT of 150 patients at mean age 7 years

- prenatal surgery increased community ambulation and gait quality

- prenatal surgery less likely to have neurological injury below their anatomic level / preserves neurological level

 

Level of lesion

 

Lowest level at which grade 3 power / antigravity

- Thoracic: no grade 3 strength in lower leg muscles

- L2:      grade 3 hip flexion (psoas)

- L3:      grade 3 knee extension (quadriceps)

- L4:      grade 3 knee flexion (hamstring)

- L5:      grade 3 ankle dorsiflexion (tibialis posterior)

- Sacral: grade 3 ankle plantarflexion (gastrocnemius)

 

Ambulation depends on neurological level / quadriceps strength

 

Thoracic / high lumbar Low lumbar Sacral

Lack quadriceps function

 

Quadriceps and medial hamstring function

 

Lack gluteus medius / maximus function

Quadriceps and gluteus medius function

 

Wheelchair as adult

80% adult community ambulators

Require crutches / AFO

High sacral 

- lack gastrocneumius function / need AFO

 

 

Low sacral 

- have gastrocneumius function / no AFO

 

Schopler et al J Pediatr Orthop 1987

- 109 spina bifida patients

- grade 4 or 5 quadriceps power: 82% community ambulators

- grade 3 quadriceps power: 89% household ambulators

- grade 0,1,2 quadriceps power: 88% non ambulatory

 

Neurosurgical issues

 

Defect closure within 48 hours to prevent bacterial contamination and death from meningitis

 

Hydrocephaus Arnold-Chiari Malformation Syringomelia / Syrinx Tethered cord

85% spina bifida cystica

90% spina bifida cystica 50% spina bifida cystica 100% spina bifida

Disruption of CSF flow

- neural tube defect

- Arnold Chiari malformation

Cerebellar tonsils herniated below foramen magnum

Cord cavitation caused by

- hydrocephalus

- AC malformation

- tethered cord

- pushes CSF into cord

 

Conus medullaris tethered below L2

- attached to myelomenigocele

- prevents normal proximal migration during growth

Hydrocephalus Arnold chiari Cervicomedullary Syrinx 3 Tethered cord

Neurological deterioration

Vision / hearing loss

Symptomatic 30%

- apnea / stridor 

- neurological deterioration

Respiratory compromise

Neurological deterioration

Not always symptomatic

- lower limb progressive weakness

- progressive scoliosis

- cavus foot

Ventriculo-peritoneal shunt

Blocked shunt

- deteriorating neuro function 

- bulging fontanelle

Shunt

Surgical decompression

Shunt hydrocephalus

Treat Arnold-Chiari malformation

Treat tethered cord

Surgical release

 

Examination

 

5 telltale skin defects - tail, skin dimpling, sacral pit, hair tuft, lipoma 

 

Xray

 

Spina bifida occultaSpina bifida occulta

Spina bifida occulta

 

CT

 

Spina bifidaSpina bifida

 

MRI

 

Spina bifidaSpina bifidaSpina bifida

Spina bifida with treated myelomeningocele

 

Tethered cordTethered cord

Spina bifida with tethered cord

 

Cervicomedullary Syrinx 1Cervicomedullary Syrinx 2Cervicomedullary Syrinx 3

Cervicomedullary syrinx

 

Syrinx Thoracic MRI AxialSyrinxSyrinx

Syrinx

 

Management

 

Manage in spina bifida clinic

 

Neurosurgeon / orthopedic surgeon / urologist / physiotherapy / social worker

- monitor neurological levels

- look for deterioration / neurosurgical issues

 

Other clinical issues

- urinary complications - recurrent UTI, hydronephrosis, risk of renal failure

- pressure sores

- latex allergies common

 

Orthopedic issues

 

Hip dislocation

Knee contractures

Foot and ankle deformities

Scoliosis

Fractures / supracondylar femur

 

Hip dislocation

 

Spina bifida hip

 

More likely with higher neurological levels and non ambulators

 

Best treated nonoperatively

- usually not painful

- doesn't affect ability to sit in wheelchair 

- ? treat unilateral hip dislocation in ambulating patients which is a rare scenario

 

Thompson et al J Pediatr Orthop 2019

- 31 adult patients with myelomeningocele

- comparison of bilateral located hips / unilateral dislocation / bilateral dislocation

- when controlled for neurological level, no difference in outcomes with dislocated hips

 

Knee

 

Flexion contracture

 

Issues 

- interferes with walking in ambulatory patient

- interferes with sitting in wheelchair patient

 

Options

- hamstring release / gastrocnemius release / posterior capsulotomy

- extension osteotomy

 

Marshall et al JBJS Br 1996

- surgical release in 45 knee flexion contractures in myelomeningocele

- flexion contractures impeding walking or sitting in wheelchair

- improved from 39 to 13 degrees

 

Spina bifidaSpina bifida kneeSpina bifida knee

 

Extension contracture

 

Typically a congenital anomaly

Serial casting +/- VY quadriceps lengthening

 

Foot & Ankle

 

Issues

 

Nearly all patients will have foot and ankle issues

Multiple deformity types - equinovarus / calcaneus / planovalgus / cavus

Aim for plantigrade / shoeable foot

 

Gunay et al Childs Nerv System 2016

- incidence of of foot deformity in spina bifida by level

- thoracic region 85%

- high-level lumbar-L1-2 region 86%

- lower lumbar regions (L3-4-5) 82%

- sacral region 51%

- 22% clubfoot, 16% pes cavus, 10% pes valgus, 6% isolated equinus, 6% pes calcaneus

 

Equinovarus Calcaneus Cavus Planovalgus

Cast

Posteromedial release aged 1 year

Divide EDL, EHL  anterior ankle capsule 

+/- T Anterior transfer to heel 

Calcaneal osteotomy

Metatarsal osteotomy

Usually not an issue

AFO

Recurrence / triple arthrodesis Recurrence / triple arthrodesis

Triple arthrodesis

Guided growth

Calcaneal osteotomy

Triple arthrodesis

 

Spina bifida Spina bifida

 

Spina bifidaPlanovalgus spina bifida

Spina bifida planovalgus

 

Scoliosis

 

Spina bifida scoliosis

 

Issues

 

Very high incidence / most require surgery

- higher the level, more severe the scoliosis

- interferes with wheelchair seating / respiratory function / PEG feeding / pressure areas

- 10 - 20% congenital spinal anomalies

- 40% spinal dysraphism (syrinx / tethered cord / Arnold Chiari)

- incidence of severe kyphosis

 

Management

 

Brace curves < 40˚

 

Posterior fusion > 40˚

- posterior spinal defects make instrumentation difficult

- congenital anomalies

- spinal dysraphism

- difficult approach due to previous neurosurgical procedures

 

Results

 

Bradko et al CORR 2022

- systematic review of scoliosis surgery in myelomeningocele

- poorer ambulation and increased pressures sores in those patients with scoliosis

- no clear benefit of improved QOL outcomes with surgery