2. Definition
Scoliosis-Greek word meaning “crooked”.
It is defined as lateral deviation of the normal vertical
line of the spine, which when measured on the
radiographs, is greater than 10 degree, with
associated rotation of vertebrae.
It is three dimensional deformity of spine-sagittal,
frontal and coronal.
3. Incidence and Etiology
2 percent of children effect at same stage of their life.
Girls are effected more than boys.
Multifactorial in etiology, 80 percent idiopathic.
Mostly patients have positive family history -11
percent risk in first degree relative.
Related to hormonal, brainstem and proprioception
disorder.
4. Clinical Features
Deformity is usually the Presenting Complaint
Pain
Rib hump due to asymmtry of trunk rotation (ATR
Headache
Neck pain
Lower back pain
Shoulder Elevation
6. Classification
Structural: Radiographic Cobb angle greater than 25 degree
on ipsilateral bending radiographic views.
Further classified into infantile, Juvenile, congenital and
adolescent(Age group), traumatic,Neuromuscular and
degenerative
Non structural: Compensatory and postural i. e
Postural scoliosis, hysterical scoliosis, contracture around hip
joint etc
7. Lenke classification
Six curve types
3 lumbar
3 thoracic sagittal
Helps to determine fusion levels during surgery
Structural curves:
Largest curve, fails to bend to less than 25 degree
Lumbar Modifier:
Based on position of CSVL in relation to apical vertebra of thorocolumbar
curve
8. Type A:
CSWL is between the pedicles of the apical vertebra
Type B:
CSWL touches between the concave pedicle and lateral
body
Type C:
CSWL falls outside of apical vertebral body
9.
10. Congenital Scoliosis
It is progressive three dimensional deformity of the spine, caused by
congenital anomalies of the vertebrae, results in imbalance in
longitudinal growth.
Developmental defect during 5th-8th week of gestation.
High incidence of associated anomalies
Intraspinal-20 to 40 percent, syringomyelia, thetered cord
Cardaic-12 to26 percent,
Genitourinary-20 percent, renal agensis, ectopic kidney
3 basic types of defects-failure of segmentation, failure of formation
and mixed
VACTERL association(vertebral defects,Anal atresia, Cardaic
anomalies, Tracheo-esophageal fistula, renal defects,limb defect
11.
12. Neuromuscular Scoliosis
Second most common form
Associated with disorders of nerves and muscular system
Neuropathic:
Lower motor neuron (Polio)
UMN(cerebral palsy)
Myopathetic
progressive (muscular dystrophy)
Static(Amyotonia congenita)
others(Friedreich’s ataxia)
13. Idiopathic Scoliosis
Most common tyoe
No etiological factor
Divided into three categories on the basis of chronological
age.
Infantile:birth to 3 years
Juvenile:3 years to 10 years
Adolescent:10 years to 18 years
14. Infantile Scoliosis
Male predominant
Left sided thoracic curve patterm is present.
Plegiocephaly often present.
Congeintal defects may also be present.
2 types - resolving, progressing; depends upon RVAD”position of medial
rib relative to apical vertebra.
Phase 1:no overlap
RVAD less than 20 percent:80 percent chance of no progression
RVAD greater than 20 percent:80 percent chance of progression(Mehta
classification)
Phase 2: rib overlap present with high risk of curve progression
MRI is needed for evaluation of neural axis abnormalities.
15.
16. Juvenile Scoliosis
Most common in females
Right thoracic curve most common
High risk of progression, 95 percent in one study
Least likely resoonds to bracing
MRI needed for evaluation
Rate of spinal cord deformity is 25 percent
17. Adolescent Scoliosis
Most common scoliosis in children
Female predominant
Right sided thoracic curve
Not associated with pain
19. History
Age of patient
Duration
Antenatal history
Birth history
Vaccination history
Complete neurological history
Family history
20. Examination
Skin Inspection i. e tuft of hairs, local defect, curvature ,
symmetry of shoulder and iliac crest, foot shape
Height measurement
Assessmentvof pubertal development
Neurlogical examination
Gait
21. Assessment of Scoliosis
Four parameters are evaluated
Curvature
Rotation
Flexibility
Skeletal maturuty
23. Plumb line
On posterior aspect, a line drawn from
occiput and should allign with gluteal
cleft.
24.
25.
26.
27.
28.
29.
30.
31. Imaging
Standing full length PA radiograph, lateral radiograph, right
and left bending films, push prone radiograph
Stagnara view:eliminate rotational component of cuve
Radiographic, parameters to assess maturity, hand and
wrist(tanner white house) , development of iliac crest
apophysis(Risers sign), triradiate cartilage
CT scan
PFTs
Echo
MRI
46. Infantile Scoliosis
Resolving curves:
Observation e serial physical examination and
radiographic monitoring
Sleeping in prone position is recommended
Progressive Curves:
Treated e serial casting followed by orthotic treatment
47. Treatment Options
Serial casting plus bracing plus later fusion
pre-oprative traction plus later fusion
Growing rod or vertical expandable prosthesis titanium rib
(VEPTR)
Best results obtained with in casting started before 20 months
and 60 degreee curve.
Cast cahnges after every 2-4 months
48.
49.
50.
51. Juvenile idiopathic Scoliosis
Orthotic treatment is indicated if curves is witn in 25 to 30
degree.
Surgical treatment is considered when curve magnitude
exceeds 50 degree.
52.
53.
54. Adolescent idiopathic scoliosis
Depends on likelihood of cuve progression
Obesrvation:skeletal immature patients with curve less than 20-25 degree
Skeletally mature patuents with curve less than 45 degree
Bracing:slow curve progression in skeletal immature patients(Risser 0-2)bracing doesn’t
reverse the curve.
Indication:
Curve of more than 25 degree or progression of 20 degree with documentation
progression
Types:
Milwaukee brace
Throcolumbosacral brace
Brace should wear 18 hours per day in risser 0
It is dose dependant effective when wear more than 12 hours in a day