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Dr.Kanwal Fatima
DPT,MS-OMPT
Spina Bifida
Dr.Kanwal Fatima
DPT,MS-OMPT
“Split Spine” caused by incomplete
closure of the neural tube, usually in
the lumbar or sacral region
What is spina bifida?
Types of spina bifida?
Several classifications that vary in
severity depending on location and
extent of opening
1-Spina bifida occulta
2-Spina bifida cystica
 meningocele
myelomenigocele
3-Spina bifida ventralis
1-Spina bifida occulta – “hidden”
The bony vertebra is open, but the spine is within the spinal canal
 The skin may have a lipoma (small benign fatty tumor), some
discoloration (birthmark), or a small tuft of hair overlying the spinal
defect
 Most patients with spina bifida occulta do not know they have it
 There may be tethering of the spinal cord
Spina bifida occulta – tethered spinal cord
Often occurs later in life
 Caused by limitations of movement of the spinal cord within the
spinal column
 Patients often have low back pain, weakness in the legs, and/or
incontinence depending on the site of tethering
2-Spina bifida cystica – meningocele
The bony vertebra is open, part of the meninges is protruding out of
the spinal canal
 Since the spinal cord is not protruding, there is often normal
function
 Some cases of tethering have been reported
Spina bifida cystica – myelomeningocele
The bony vertebra is open, part of the meninges and part or all of
the spinal cord is protruding out of the spinal canal
 Since the spinal cord is protruding, it is often not fully developed
 Involved nerve roots are often not developed resulting in weakness,
pain, and/or paralysis
Spina bifida cystica – myelomeningocele…. (continoue
 Arnold Chiari malformation II is often associated with myelomeningocele and occurs
when the cerebellum is forced downward
 This can result in life-threatening situations because the build-up of cerebrospinal
fluid can cause pressure on the brain
 Patients with Arnold Chiari malformations often require placement of a shunt to drain
the excess fluid
Spina bifida ventralis – anterior opening
 Much less common than other forms of spina bifida
 Meningeal sac will protrude into the retroperitoneal space and impinge on
retroperitoneal organs such as the duodenum, ascending/descending colon, kidneys,
adrenal glands, pancreas, aorta, and inferior vena cava
causes spina bifida
- The exact cause of spina bifida is
unknown
- All research to date has indicated both
a genetic and environmental influence
- The developmental process that results
in spina bifida is well studied
Causes of spina bifida(continoue
• Neural Tube Defect:
– When the neural tube fails to properly close
during the 4th week embryogenesis.
Development of spina bifida in utero
What would prevent the neural tubes from
closing properly?
Folate seems to play a large role in the closing of the neural tube
– but it is unknown exactly how folate works in this process.
Folate influence :The lack of leafy green vegetables caused the
mother to have low levels of folate during conception.
Genetics also play a role in the development of spina bifida.
Mothers with one child with spina bifida have an increased risk
of additional children having spina bifida
Valproic acid (Depakote)
Oral medication used to treat seizures/convulsions,
migraines, and bipolar disorder
 Mechanism of action – thought to increase GABA
levels in the brain
 Pregnant women taking Valproic acid have an
increased risk of having children with spina bifida
Clinical pictures of spina bifida
a-Primary clinical pictures
b-Secondary clinical pictures
a-Primary clinical pictures
1-Abnormal nerve conduction, resulting in:
Somatosensory losses
Motor paralysis, including loss of bowel and bladder
control (all are below level of lesion)
 Changes in muscle tone
Motor level
Lesion Level
Above L3
L4 and below
S1 and below
S3 and below
Spinal-related disability
Complete paraplegia and dermatomal para-
anesthesia, Bladder incontinence, Nonambulatory
Same as for above L3 except preservation of hip
flexors, hip adductors, knee extensors; Ambulatory
with aids, bracing orthopedic surgery
Same as for L4 and below except preservation of feet
dorsiflexors, and partial preservation of hip extensors
and knee flexors; Ambulatory with minimal aids
Normal lower extremity motor function; Saddle
anesthesia; Variable bladder-rectal incontinence
Sensory Levels
T4
T10
L1
L2
L3
L4
L5
S1
S2
S3-S5
2-An enlarged head caused
by:
1- hydrocephalus
(“water on the brain”)
11-Arnolds Chairi
malformation 11
i. Hydrocephalus
VP Shunt done in 85-90% of MMC
(1/3 will require revision at some time)
Most commonly due to obstruction of
Cerebrospinal Fluid (CSF) Flow
ii-Arnold-Chiari Type II Malformation
Arnold-Chiari type II Malformation
Definition: Medulla, Pons, 4th ventricle +/- cerebellar
vermis herniated into the cervical spinal canal
Incidence: 80-90% of those with MMC
Symptomatic: ~20%
Should be managed and treated as an emergency by
(surgical decomperssion operation)
3-Urinary and Bowel symptoms
Urinary symptoms:
• In lumbosacral spina bifida cystica, few children attain urinary
incontinence
• They require urodynamic testing, including cystometrography,
uroflowmetry, and EMG of the urinary sphincter
• Types of lesions
1. “Keepers”- UMN
2. “Leakers”- LMN
According to results and consulting urologist patient may need
intermittent catheterization, pharmacological agents,
implantation of an artificial urinary sphincter or a combination.
Artificial urinary sphincter
Bowel symptoms
A. Constipation
B. Incontinence
Management techniques
-enemas -suppositories
-habit training - digital stimulation
-biofeedback -appendicostomy(ACE)
4-Musculoskeletal deformities (scoliosis)
5-Joint and extremity deformities (joint
contractures, club foot, hip subluxations,
diminished growth of non-weight bearing limbs)
6-Abnormal or damaged nerve tissue which can
lead to loss of extroceptive and prorioceptive
sensation .
Spine Scoliosis
• Plain spine films to measure
scoliosis
b-Secondary clinical pictures
Skin Breakdown
Decubitus ulcers and other types of
skin breakdown
Obesity
Latex Allergy
Osteoporosis .
Management of spina bifida
1-screening and dignosis
2-Treatement
3-followup and observation
4- prevention
1-Screening and Diagnosis
 Prenatal Tests
AFP(alphafeotoprotien)
Ultrasound
Testing of Amniotic fluid(Amniocentesis)
 Evaluation
Analysis of individual medical history
Physical examination
Evaluation of critical body systems
 Imaging Studies
X-rays
Ultrasound
CT scan
MRI
 Gait Analysis
2-Treatment
 No cure
 Regular check ups with
physician
 Surgery (24 hours after
birth)
 Medication
 Physiotherapy
Surgical treatment
Surgery
tethered
untether
 In-utero
Surgery (continue--
Surgery for spina bifida involves a variety of
neurosurgical, orthopedic, and urologic procedures.
 Surgical procedures include the following:
– Closure of the defect over the spinal cord
– Spinal deformity reconstruction
– Lower-extremity deformity correction
Medical treatement
Antibiotics
-preventing infection of the CNS and
urinary tract system
Physical Therapy
Physical therapy helps to direct goals for
patients in each lesion-level group within an
appropriate developmental context from
infancy through adulthood.
Normal achievement of gross motor
milestones.
To establish a baseline of muscle function in
mylomeningocele.
 As the child develops, the physical therapist
monitors joint alignment, muscle imbalances,
contractures, posture, and signs of progressive
neurologic dysfunction.
Provides caregivers with instruction in handling and
positioning techniques and recommends orthotic
positioning devices to prevent soft tissue
contractures.
Provide the infant with sitting opportunities to
facilitate the development of head and trunk
control.
Near the end of the first year of life, provide the
child with an effective means of independent
mobility in conjunction with therapeutic
exercises that promote trunk control and
balance.
 For patients who are not likely to become
ambulatory, place emphasis on developing
proficiency in wheelchair skills
.
For patients who are predicted to ambulate, pregait
training should begin with use of a parapodium or
swivel walker.
Exercise or household-distance ambulation may be
pursued with use of traditional long leg braces (eg,
hip-knee-ankle-foot orthosis, knee-ankle-foot
orthosis) or the reciprocating gait orthosis [RGO]).
Swivel walker and RGO
Example of a Parapodium
• Commonly used for
children with high lesions
(T12-L3)
• Offers support to the
hips, knees, and ankles.
Occupational Therapy
• Children with spina bifida often have
impairment in fine motor skills and
conducting activities of daily living (ADL).
• Initiate training early to compensate for
these deficits and progress along the
developmental sequence as closely as
possible.
Upper-extremity stabilization and dexterous hand use
require adequate postural control of the head and
trunk.
 In the first year of life, encourage development of these
postural mechanisms or substitute passive support, if
necessary, to promote eye-hand coordination and
manipulatory skills.
When adequate fine motor skills have been achieved,
the occupational therapist provides instructions for use
of adaptive equipment and alternative methods for self-
care and other ADL for preschool- and school-aged
children.
Recreational Therapy
• Children with myelomeningocele often
experience restricted play and recreational
opportunities because of limited mobility
and physical limitations.
• This inactivity decreases the potential for
normal development in all spheres and can
exert a negative impact on self-esteem.
For the infant and toddler with
myelomeningocele, recreational therapy
enhances opportunities for environmental
exploration and interaction with other
children.
For the school-aged child, recreational
therapy provides opportunities for
participation in adapted sports and exercise
programs, which can result in long-term
interest in personal fitness and health.
Recreational and physical fitness goals include
socialization, weight control, and improved
fitness (eg, flexibility, strength, aerobic capacity,
cardiovascular fitness, coordination).
Recreational therapy is helpful for promoting
independence with adult living skills and often is
used to assist the patient with shopping for and
purchasing personal items, use of public
transportation, and development of appropriate
leisure activities.
Follow up and careful Observation
 Children with myelomeningocele often have
hydrocephalus (blockage of CSF)
Children may present with paralysis,
blindness, inability to speak, convulsions
Any changes in mental status or behavior
should be quickly brought to the attention of
the child’s physician(s)
Folate intake
Recommended that women of child-bearing
age take 400 micrograms of folate per day
Pregnant women should take 600 micrograms
of folate per day
Women with a previous child with spina
bifida should take 4000 micrograms of folate
per day
 Folate can decrease the risk of spina bifida by
up to 75%
How can spina bifida be prevented?
Social impact
Children born with spina bifida today
require some special treatment :
Multiple surgeries starting as early as 48 hours after birth
Physical therapy
Bowel and/or bladder surgery – helps prevent infection
and social stigmatism
 Latex allergies are often present

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Spinabifida andphysiotherapy

  • 2. “Split Spine” caused by incomplete closure of the neural tube, usually in the lumbar or sacral region What is spina bifida?
  • 3.
  • 4. Types of spina bifida? Several classifications that vary in severity depending on location and extent of opening 1-Spina bifida occulta 2-Spina bifida cystica  meningocele myelomenigocele 3-Spina bifida ventralis
  • 5. 1-Spina bifida occulta – “hidden” The bony vertebra is open, but the spine is within the spinal canal  The skin may have a lipoma (small benign fatty tumor), some discoloration (birthmark), or a small tuft of hair overlying the spinal defect  Most patients with spina bifida occulta do not know they have it  There may be tethering of the spinal cord
  • 6. Spina bifida occulta – tethered spinal cord Often occurs later in life  Caused by limitations of movement of the spinal cord within the spinal column  Patients often have low back pain, weakness in the legs, and/or incontinence depending on the site of tethering
  • 7. 2-Spina bifida cystica – meningocele The bony vertebra is open, part of the meninges is protruding out of the spinal canal  Since the spinal cord is not protruding, there is often normal function  Some cases of tethering have been reported
  • 8. Spina bifida cystica – myelomeningocele The bony vertebra is open, part of the meninges and part or all of the spinal cord is protruding out of the spinal canal  Since the spinal cord is protruding, it is often not fully developed  Involved nerve roots are often not developed resulting in weakness, pain, and/or paralysis
  • 9.
  • 10. Spina bifida cystica – myelomeningocele…. (continoue  Arnold Chiari malformation II is often associated with myelomeningocele and occurs when the cerebellum is forced downward  This can result in life-threatening situations because the build-up of cerebrospinal fluid can cause pressure on the brain  Patients with Arnold Chiari malformations often require placement of a shunt to drain the excess fluid
  • 11. Spina bifida ventralis – anterior opening  Much less common than other forms of spina bifida  Meningeal sac will protrude into the retroperitoneal space and impinge on retroperitoneal organs such as the duodenum, ascending/descending colon, kidneys, adrenal glands, pancreas, aorta, and inferior vena cava
  • 12. causes spina bifida - The exact cause of spina bifida is unknown - All research to date has indicated both a genetic and environmental influence - The developmental process that results in spina bifida is well studied
  • 13. Causes of spina bifida(continoue • Neural Tube Defect: – When the neural tube fails to properly close during the 4th week embryogenesis.
  • 14. Development of spina bifida in utero
  • 15. What would prevent the neural tubes from closing properly? Folate seems to play a large role in the closing of the neural tube – but it is unknown exactly how folate works in this process. Folate influence :The lack of leafy green vegetables caused the mother to have low levels of folate during conception. Genetics also play a role in the development of spina bifida. Mothers with one child with spina bifida have an increased risk of additional children having spina bifida
  • 16. Valproic acid (Depakote) Oral medication used to treat seizures/convulsions, migraines, and bipolar disorder  Mechanism of action – thought to increase GABA levels in the brain  Pregnant women taking Valproic acid have an increased risk of having children with spina bifida
  • 17. Clinical pictures of spina bifida a-Primary clinical pictures b-Secondary clinical pictures
  • 18. a-Primary clinical pictures 1-Abnormal nerve conduction, resulting in: Somatosensory losses Motor paralysis, including loss of bowel and bladder control (all are below level of lesion)  Changes in muscle tone
  • 19. Motor level Lesion Level Above L3 L4 and below S1 and below S3 and below Spinal-related disability Complete paraplegia and dermatomal para- anesthesia, Bladder incontinence, Nonambulatory Same as for above L3 except preservation of hip flexors, hip adductors, knee extensors; Ambulatory with aids, bracing orthopedic surgery Same as for L4 and below except preservation of feet dorsiflexors, and partial preservation of hip extensors and knee flexors; Ambulatory with minimal aids Normal lower extremity motor function; Saddle anesthesia; Variable bladder-rectal incontinence
  • 21. 2-An enlarged head caused by: 1- hydrocephalus (“water on the brain”) 11-Arnolds Chairi malformation 11
  • 22.
  • 23. i. Hydrocephalus VP Shunt done in 85-90% of MMC (1/3 will require revision at some time) Most commonly due to obstruction of Cerebrospinal Fluid (CSF) Flow
  • 24.
  • 25.
  • 26. ii-Arnold-Chiari Type II Malformation
  • 27. Arnold-Chiari type II Malformation Definition: Medulla, Pons, 4th ventricle +/- cerebellar vermis herniated into the cervical spinal canal Incidence: 80-90% of those with MMC Symptomatic: ~20% Should be managed and treated as an emergency by (surgical decomperssion operation)
  • 28. 3-Urinary and Bowel symptoms Urinary symptoms: • In lumbosacral spina bifida cystica, few children attain urinary incontinence • They require urodynamic testing, including cystometrography, uroflowmetry, and EMG of the urinary sphincter • Types of lesions 1. “Keepers”- UMN 2. “Leakers”- LMN According to results and consulting urologist patient may need intermittent catheterization, pharmacological agents, implantation of an artificial urinary sphincter or a combination.
  • 30. Bowel symptoms A. Constipation B. Incontinence Management techniques -enemas -suppositories -habit training - digital stimulation -biofeedback -appendicostomy(ACE)
  • 31. 4-Musculoskeletal deformities (scoliosis) 5-Joint and extremity deformities (joint contractures, club foot, hip subluxations, diminished growth of non-weight bearing limbs) 6-Abnormal or damaged nerve tissue which can lead to loss of extroceptive and prorioceptive sensation .
  • 32. Spine Scoliosis • Plain spine films to measure scoliosis
  • 33. b-Secondary clinical pictures Skin Breakdown Decubitus ulcers and other types of skin breakdown Obesity Latex Allergy Osteoporosis .
  • 34. Management of spina bifida 1-screening and dignosis 2-Treatement 3-followup and observation 4- prevention
  • 35. 1-Screening and Diagnosis  Prenatal Tests AFP(alphafeotoprotien) Ultrasound Testing of Amniotic fluid(Amniocentesis)  Evaluation Analysis of individual medical history Physical examination Evaluation of critical body systems  Imaging Studies X-rays Ultrasound CT scan MRI  Gait Analysis
  • 36. 2-Treatment  No cure  Regular check ups with physician  Surgery (24 hours after birth)  Medication  Physiotherapy
  • 38. Surgery (continue-- Surgery for spina bifida involves a variety of neurosurgical, orthopedic, and urologic procedures.  Surgical procedures include the following: – Closure of the defect over the spinal cord – Spinal deformity reconstruction – Lower-extremity deformity correction
  • 39. Medical treatement Antibiotics -preventing infection of the CNS and urinary tract system
  • 40. Physical Therapy Physical therapy helps to direct goals for patients in each lesion-level group within an appropriate developmental context from infancy through adulthood. Normal achievement of gross motor milestones.
  • 41. To establish a baseline of muscle function in mylomeningocele.  As the child develops, the physical therapist monitors joint alignment, muscle imbalances, contractures, posture, and signs of progressive neurologic dysfunction. Provides caregivers with instruction in handling and positioning techniques and recommends orthotic positioning devices to prevent soft tissue contractures.
  • 42. Provide the infant with sitting opportunities to facilitate the development of head and trunk control. Near the end of the first year of life, provide the child with an effective means of independent mobility in conjunction with therapeutic exercises that promote trunk control and balance.  For patients who are not likely to become ambulatory, place emphasis on developing proficiency in wheelchair skills
  • 43. . For patients who are predicted to ambulate, pregait training should begin with use of a parapodium or swivel walker. Exercise or household-distance ambulation may be pursued with use of traditional long leg braces (eg, hip-knee-ankle-foot orthosis, knee-ankle-foot orthosis) or the reciprocating gait orthosis [RGO]).
  • 45.
  • 46.
  • 47. Example of a Parapodium • Commonly used for children with high lesions (T12-L3) • Offers support to the hips, knees, and ankles.
  • 48. Occupational Therapy • Children with spina bifida often have impairment in fine motor skills and conducting activities of daily living (ADL). • Initiate training early to compensate for these deficits and progress along the developmental sequence as closely as possible.
  • 49. Upper-extremity stabilization and dexterous hand use require adequate postural control of the head and trunk.  In the first year of life, encourage development of these postural mechanisms or substitute passive support, if necessary, to promote eye-hand coordination and manipulatory skills. When adequate fine motor skills have been achieved, the occupational therapist provides instructions for use of adaptive equipment and alternative methods for self- care and other ADL for preschool- and school-aged children.
  • 50. Recreational Therapy • Children with myelomeningocele often experience restricted play and recreational opportunities because of limited mobility and physical limitations. • This inactivity decreases the potential for normal development in all spheres and can exert a negative impact on self-esteem.
  • 51. For the infant and toddler with myelomeningocele, recreational therapy enhances opportunities for environmental exploration and interaction with other children. For the school-aged child, recreational therapy provides opportunities for participation in adapted sports and exercise programs, which can result in long-term interest in personal fitness and health.
  • 52. Recreational and physical fitness goals include socialization, weight control, and improved fitness (eg, flexibility, strength, aerobic capacity, cardiovascular fitness, coordination). Recreational therapy is helpful for promoting independence with adult living skills and often is used to assist the patient with shopping for and purchasing personal items, use of public transportation, and development of appropriate leisure activities.
  • 53. Follow up and careful Observation  Children with myelomeningocele often have hydrocephalus (blockage of CSF) Children may present with paralysis, blindness, inability to speak, convulsions Any changes in mental status or behavior should be quickly brought to the attention of the child’s physician(s)
  • 54. Folate intake Recommended that women of child-bearing age take 400 micrograms of folate per day Pregnant women should take 600 micrograms of folate per day Women with a previous child with spina bifida should take 4000 micrograms of folate per day  Folate can decrease the risk of spina bifida by up to 75% How can spina bifida be prevented?
  • 55. Social impact Children born with spina bifida today require some special treatment : Multiple surgeries starting as early as 48 hours after birth Physical therapy Bowel and/or bladder surgery – helps prevent infection and social stigmatism  Latex allergies are often present