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Infantile Idiopathic Scoliosis

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Infantile Idiopathic Scoliosis

A comprehensive guide to Infantile Idiopathic Scoliosis (Age 0-3), distinguishing resolving from progressive curves using the Mehta Angle and Rib Head Phases.

complete
Updated: 2026-01-02
High Yield Overview

Infantile Idiopathic Scoliosis

Age 0-3 Years

0 to 3 yearsAge
Male greater than Female (3Gender
Left Thoracic (Most common)Curve
80-90% spontaneousResolution

Mehta Classification

Resolving
PatternRVAD less than 20 degrees. Phase 1 ribs.
TreatmentObserve
Progressive
PatternRVAD greater than 20 degrees. Phase 2 ribs.
TreatmentCast (EDP)

Critical Must-Knows

  • Mehta Angle (RVAD): The only reliable predictor of progression.
  • Phase of Rib Head: Phase 1 (No overlap) vs Phase 2 (Overlap = Progressive).
  • MRI Mandatory: 20% incidence of neural axis abnormalities (Chiari/Syrinx).
  • Plagiocephaly: Strong association with Bat ear / Molded baby syndrome.
  • Hip Dysplasia: Associated in 2-10% (Screen hips!).

Examiner's Pearls

  • "
    Look for Plagiocephaly (flattening of skull)
  • "
    Check hips (DDH)
  • "
    Neurology: Abdominal reflexes essential
  • "
    Prone exam: Assess rotational prominence

Don't assume it's Idiopathic

Infantile Scoliosis is a diagnosis of exclusion.

  • You MUST rule out Congenital (Hemivertebra/Bar) and Neuromuscular causes first.
  • MRI is mandatory for every infant with a curve greater than 20 degrees or any progressive curve.
  • Neural axis abnormalities (Arnold-Chiari malformation, Syringomyelia) occur in up to 40% of patients with curves greater than 20 degrees.

Infantile vs Adolescent Idiopathic Scoliosis

FeatureInfantile (0-3)Adolescent (10+)
Male > FemaleFemale >>> Male
Left ThoracicRight Thoracic
Can Resolve (80%)Does not resolve (Progresses/Stable)
High (Alveoli hypoplasia)Low (Alveoli mature)
Mnemonic

Associations of Infantile Scoliosis

P
Plagiocephaly
Molded baby syndrome
H
Hip
DDH in up to 10%
M
Mental
Intellectual disability slightly higher
C
Cardiac
Congenital heart defects (rare)

Memory Hook:PHMC (Please Help My Child).

Mnemonic

Predictors of Progression

M
Mehta
RVAD greater than 20
O
Overlap
Rib head Phase 2
C
Cobb
Angle greater than 25-30

Memory Hook:MOC (Mock the progression).

Mnemonic

Treatment Hierarchy

O
Observe
Resolving type
C
Cast
Progressive type (Gold standard)
B
Brace
Maintenance / Older infants
S
Surgery
Growth rods (Last resort)

Memory Hook:OCBS (Observe, Cast, Brace, Surgery).

Overview/Epidemiology

Infantile Idiopathic Scoliosis typically presents in the first year of life (usually noticed by parents while bathing).

  • The "Molded Baby" Syndrome: Often associated with intrauterine packaging issues, leading to Plagiocephaly, Torticollis, DDH, and Metatarsus Adductus.
  • Epidemiology:
    • Rare in North America (0.5%).
    • Much more common in Europe/UK (historical association with prone sleeping position, though incidence dropped after "Back to Sleep").
    • Boys are more commonly affected than girls.
    • Left Thoracic curves are the canonical pattern. (A Right Thoracic curve in a male infant is highly suspicious for syrinx).

Pathophysiology and Mechanisms

Pediatric scoliosis PA radiographs with Cobb angle measurements
Click to expand
PA spine radiographs demonstrating left thoracic scoliotic curve with Cobb angle measurements: (a) Multiple angle measurements (25°, 37°, 17°) showing curve assessment, (b) 21° measurement. Illustrates radiographic technique for quantifying curve magnitude in infantile scoliosis. Left-sided thoracic curve is characteristic pattern in infantile idiopathic scoliosis.Credit: Open-i / NIH via Open-i (NIH) (Open Access (CC BY))
Pediatric scoliosis plain radiograph and 3D reconstruction
Click to expand
Multi-modality imaging of severe pediatric scoliosis: (a) Full-length PA and lateral radiographs showing scoliotic curve, (b) 3D surface reconstruction demonstrating severe three-dimensional spinal deformity. Shows relationship between spine and pelvis, illustrating comprehensive assessment approach for complex curves.Credit: Amzallag-Bellenger E et al. via Insights Imaging via Open-i (NIH) (Open Access (CC BY))

The Mehta Angle (RVAD) Described by Min Mehta in 1972.

  • Concept: Since ribs attach to vertebrae, as the vertebra rotates, the rib on the convex side is pushed posteriorly (hump) and the rib on the concave side is pushed anteriorly.
  • Measurement: Line along the vertebral endplate relative to a line along the rib head/neck.
  • Difference: Convex angle minus Concave angle.
  • Rule of 20:
    • RVAD less than 20 degrees = Resolving.
    • RVAD greater than 20 degrees = Progressive.

Rib-Head Phases

  • Phase 1: No overlap of rib head on vertebral body apical corner.
  • Phase 2: Rib head overlaps the vertebral body. (Indicates severe rotation and pending progression).

Classification Systems

Mehta / James Classification

Based on prognosis: 1. Resolving (Benign)

  • RVAD less than 20.
  • Curve usually less than 30.
  • Phase 1 Ribs.

2. Progressive (Malignant)

  • RVAD greater than 20.
  • Curve often greater than 30.
  • Phase 2 Ribs.

Double Structural Curves

  • Occasionally infants present with Double Major curves.
  • These have a worse prognosis and almost always progress.
  • High association with intraspinal pathology.

Clinical Assessment

History:

  • Age: Onset? (Must be less than 3).
  • Development: Is the child hitting milestones?
  • Pain: Pain is rare and suspicious.

Physical Exam:

  1. Head: Check for Plagiocephaly.
  2. Neck: Torticollis (sternocleidomastoid tight?).
  3. Spine: Left sided prominence? Flexibility?
  4. Hips: Ortolani/Barlow.
  5. Neurology: Tone, reflexes (Abdominal!), clonus.

Investigations

X-rays:

  • PA and Lateral whole spine.
  • Supine vs Standing: Infants are usually imaged supine or sitting.
  • Measurement: Cobb angle + RVAD (Mehta).

MRI:

  • Mandatory.
  • Sedation usually required (General Anaesthesia) for high quality feed-and-wrap MRI is difficult in older infants.
  • Must see the entire neuraxis from craniocervical junction to sacrum.

Management Algorithm

1. Observation

  • Indication: RVAD less than 20 degrees, Cobb less than 30.
  • Protocol: X-ray every 4-6 months. Watch for Mehta angle crossing the threshold.

2. Serial Casting (EDP - Early Derotation Plastering)

  • Indication: RVAD greater than 20 degrees, Cobb greater than 30, or Documented Progression.
  • Timing: Best results if started before age 2 (ideally 12-18 months).
  • Protocol: Cast changes every 8-12 weeks under GA.
  • Outcome: Potential for CURE (Complete resolution) if curve is flexible and treatment is early.

3. Growing Rods

  • Indication: Failure of casting. Curve too large/stiff for casting.
  • Type: Magnet rods (MCGR) preferred.

4. VEPTR

  • Indication: Associated rib fusions or severe thoracic insufficiency.

Surgical Techniques

Mehta Casting Technique

  1. Anaesthesia: General Anaesthesia with intubation.
  2. Position: Cotrel traction frame (Risser table).
  3. Traction: Longitudinal traction applied.
  4. Derotation: The surgeon applies a distinct "posterolateral to anteromedial" force on the rib hump. The goal is to untwist the spine.
  5. Molding: Plaster (POP) is molded meticulously over the ribs and iliac crests (for gripping).
  6. Windows: Large anterior "mushroom" window to allow belly expansion. Posterior window for spinal cord monitoring if needed (rarely done for casting).

Duration: Worn for 2-3 months. Repeat X-ray in cast to confirm correction.

Weaning Protocol

  • Once the curve is less than 10 degrees and RVAD is less than 0 (concave > convex angle), casting can be stopped.
  • Transition to TLSO Brace full time, then weaning to night time.
  • Close surveillance until skeletal maturity.

Deep Dive: Casting Pearls

1. The Mushroom Window Infants breathe primarily with their diaphragm / abdomen. A tight abdominal cast will cause respiratory distress. The anterior window must be large and "mushroom shaped" - wide at the bottom over the belly, narrower at the top over the sternum.

2. Over-the-shoulder?

  • Under arm: For low thoracic / lumbar curves.
  • Over shoulder: Required for upper thoracic curves (Apex T6 or higher) to control the upper lever arm.

3. Skin Care The most common complication is skin breakdown (iliac crests, scapula). Meticulous padding and molding are essential. Educate parents on keeping the cast dry.

4. The Risser Table The casting frame (Risser table) is critical. It allows the patient to be suspended by the head (halter) and pelvis, allowing the surgeon 360-degree access to the torso for molding. The longitudinal traction itself provides significant correction before any rotation force is applied.

Complications

Cast-Related Complications

ComplicationRatePrevention/Management
Skin UlcerationCommonPadding, molding, windowing.
Respiratory DistressRareEnsure large abdominal window.
Chest Wall DeformityRareAvoid excessive rib compression.
PsychosocialCommonBurden of cast changes under GA.
Failure/ProgressionVariableTransition to growing rods.

Skin Breakdown Prevention

Skin complications are the most common issue with serial casting. Key prevention strategies include:

  • Meticulous padding of bony prominences (iliac crests, scapulae, clavicles, spinous processes)
  • Appropriate window cutting for pressure relief while maintaining correction
  • Parent education on skin inspection, cast hygiene, and early signs of problems
  • Regular cast changes (typically every 2-3 months) to assess skin integrity

Respiratory Monitoring

Infants rely predominantly on diaphragmatic breathing. A restrictive cast can cause respiratory compromise:

  • Warning signs: Increased respiratory rate, accessory muscle use, poor feeding, irritability
  • Prevention: Large mushroom-shaped abdominal window, careful molding to avoid chest restriction
  • Management: Immediate cast removal if respiratory distress suspected

Progressive Curves Despite Treatment

Some curves continue to progress despite optimal casting. Risk factors for casting failure include:

  • Initial RVAD greater than 40 degrees
  • Phase 2 rib head at presentation
  • Late presentation (after age 2 years)
  • Underlying syndromic or neuromuscular cause

For refractory cases, transition to growing rod constructs may be necessary to control the curve while preserving thoracic growth.

Postoperative Care

Cast Care Instructions

  • Hygiene: Casting requires keeping the cast dry (sponge baths only). Use "Moleskin" or "Petal" tape around edges to prevent skin irritation.
  • Reflux: Gastric reflux can be worsened by the abdominal pressure. Recommend smaller, more frequent feeds.
  • Development: Casting generally does NOT delay walking, but may make infants "top heavy" initially.

Follow-Up Protocol

Regular monitoring is essential during serial casting treatment:

  • In-cast X-ray: Obtained 1-2 weeks after each cast application to confirm correction
  • Clinical review: Every 2-3 months with cast change under general anaesthesia
  • Curve measurements: Track RVAD and Cobb angle progression
  • Growth monitoring: Weight, length, and thoracic development

Family Education and Support

Infantile scoliosis treatment places significant burden on families. Key support measures include:

  • Clear explanation of the treatment rationale and expected duration
  • Written instructions for cast care and warning signs
  • Access to multidisciplinary team (physiotherapy, occupational therapy, social work)
  • Parent support groups and online resources
  • Psychological support for managing repeated general anaesthetics

Transition from Cast to Brace

Once the curve has been corrected to less than 10 degrees with RVAD less than 0:

  • Transition to a custom TLSO brace
  • Initial full-time wear (23 hours per day)
  • Gradual weaning based on maintenance of correction
  • Continue monitoring until skeletal maturity

Outcomes/Prognosis

Resolving Curves (80-90%)

The majority of infantile scoliosis cases resolve spontaneously without intervention:

  • Spontaneous resolution: Typically occurs within the first 2-3 years of life
  • No treatment required: Observation with periodic radiographs only
  • Excellent long-term prognosis: No residual deformity or functional limitation
  • Normal growth: Thoracic development and lung function unaffected

Progressive Curves - Treated Early

For progressive curves identified early and treated with serial casting:

  • Cure rate (curve less than 10 degrees): 70-80% with optimal casting technique
  • Conversion to non-progressive: Many curves can be stabilized for brace management
  • Normal thoracic development: Early treatment preserves lung growth
  • Avoidance of surgery: Many children avoid the need for growing rods or fusion

Progressive Curves - Delayed Treatment or Refractory

Untreated progressive infantile scoliosis leads to severe deformity:

  • Curve progression: Relentless progression to greater than 100 degrees without treatment
  • Thoracic Insufficiency Syndrome (TIS): Restricted lung development and respiratory compromise
  • Cor pulmonale: Right heart failure from chronic hypoxia
  • Reduced life expectancy: Significant impact on survival if severe deformity develops

Long-Term Follow-Up Considerations

All patients with infantile scoliosis require monitoring until skeletal maturity:

  • Growth spurts: Risk of curve progression during adolescent growth
  • Residual deformity: May require bracing or surgical intervention
  • Pulmonary function: Serial monitoring for thoracic insufficiency
  • Transition to adult care: Appropriate handover for ongoing surveillance

Evidence Base

Level III
📚 Sanders et al
Key Findings:
  • Results of casting in infantile scoliosis
  • Average age 18 months
  • Cure rate (curve less than 10 deg) was high in flexible curves started early
  • Key predictor: RVAD correction
Clinical Implication: Start casting early!
Source: Spine 2009

level IV
📚 Mehta
Key Findings:
  • Long term follow up of EDP (Casting)
  • Significant reduction in need for surgery
  • Confirmed the RVAD rule of 20
Clinical Implication: The classic paper supporting casting.
Source: JBJS Br 2005

Level III
📚 Fletcher et al
Key Findings:
  • Casting usually delays surgery rather than curing it in older children
  • If started after age 2, cure is less likely
  • Still valuable to delay rods until age 6-8
Clinical Implication: Window of opportunity is 6-24 months.
Source: Spine 2012

Level IV
📚 Koop
Key Findings:
  • Natural history of infantile scoliosis
  • Many resolve spontaneously
  • Observation is safe if RVAD less than 20
Clinical Implication: Don't cast everyone. Measure RVAD.
Source: JBJS Br 1988

Level IV
📚 Dobbs et al
Key Findings:
  • Neural axis abnormalities in infantile scoliosis
  • Prevalence 22%
  • Only 1 in 5 had neurological findings on exam
Clinical Implication: MRI is mandatory regardless of exam.
Source: J Pediatr Orthop 2000

Classic
📚 Riseborough and Wynne-Davies
Key Findings:
  • Comparison of Infantile vs Adolescent Scoliosis
  • Infantile curves are more rigid
  • Higher association with Plagiocephaly and Hip Dysplasia
  • Pulmonary compromise is the main differentiator
Clinical Implication: Infantile Scoliosis is a systemic disease.
Source: JBJS Br 1975

Viva Scenarios

Practice these scenarios to excel in your viva examination

VIVA SCENARIOStandard

The Resolving Curve

EXAMINER

"12-month-old male. Left thoracic curve 20 degrees. RVAD 12 degrees."

EXCEPTIONAL ANSWER

This fits the profile of a **Resolving** Infantile Idiopathic Scoliosis. The RVAD is less than 20 degrees. The risk of progression is low. I would perform a full exam (hips, neurology) and order an MRI (mandatory). Assuming MRI is normal, I would **Observe** with serial X-rays every 4-6 months to ensure the curve and RVAD are decreasing. No bracing/casting needed yet.

KEY POINTS TO SCORE
RVAD less than 20 = Benign
MRI mandatory
Observation strategy
COMMON TRAPS
✗Bracing immediately
✗Discharging without follow-up
LIKELY FOLLOW-UPS
"What if the RVAD increases to 25 degrees at next visit?"
VIVA SCENARIOStandard

The Progressive Curve

EXAMINER

"18-month-old female. Right thoracic curve 45 degrees. RVAD 35 degrees."

EXCEPTIONAL ANSWER

This is a **High Risk** case. Female gender + Right curve is atypical for Infantile (suggests juvenile/AIS pattern or pathology). RVAD is much greater than 20 degrees, indicating malignancy. MRI is critical (high syrinx risk). Assuming MRI clears, treatment is **Serial Mehta Casting** under GA urgently. The goal is to maximize correction while flexible. Bracing is insufficient.

KEY POINTS TO SCORE
Red flags (Female/Right)
High RVAD
Casting indication
COMMON TRAPS
✗Missing the atypical pattern
✗Suggesting fusion
LIKELY FOLLOW-UPS
"How often do you change the cast?"
VIVA SCENARIOStandard

Casting Complication

EXAMINER

"Child in Mehta cast presents with vomiting and dehydration."

EXCEPTIONAL ANSWER

This could be **Cast Syndrome** (SMA syndrome - Superior Mesenteric Artery compression) although rare in infants, or simply reflux exacerbated by abdominal pressure. It could also be intercurrent gastroenteritis. I would assess hydration and abdominal exam. If distended or obstructive symptoms, the cast must be **removed** or bi-valved / windowed urgently to relieve pressure. X-ray abdomen. Paediatric review.

KEY POINTS TO SCORE
Abdominal compression
Cast removal threshold
Reflux vs Obstruction
COMMON TRAPS
✗Treating with anti-emetics only
✗Ignoring the cast as a cause
LIKELY FOLLOW-UPS
"What is the window for optimal casting results?"

MCQ Practice Points

Diagnosis MCQ

Q: Which factor most strongly predicts resolution of infantile scoliosis? A: RVAD less than 20 degrees.

Anatomy MCQ

Q: During Mehta casting, where is the corrective force applied? A: Posterolateral force on the convex rib hump, combined with traction.

Association MCQ

Q: What is the most common associated musculoskeletal condition? A: Plagiocephaly (and Torticollis). Hip dysplasia is also common (intrauterine molding).

Imaging MCQ

Q: An infant has a 25 degree Left thoracic curve. Neural axis abnormalities are found in what percentage of cases? A: Approx 20-25%. (Up to 40% if curve greater than 20 deg).

Technique MCQ

Q: Why is an anterior window needed in Mehta casts? A: Infants are diaphragmatic/abdominal breathers. Constricting the abdomen causes respiratory failure.

Australian Context

  • Referral: Early referral to a Spine centre is critical. "Wait and see" by GPs can miss the window for cure.
  • Casting: Available in major children's hospitals (SCH, RCH, QCH, WCH, PCH).
  • Support: "Scoliosis Australia" provides support for parents managing casts (hygiene/clothing).
  • Clinics: Most tertiary paediatric hospitals run dedicated "Scoliosis Clinics" with multidisciplinary teams (Surgeons, Orthotists, Physiotherapists).
  • Transition: Adolescents with infantile scoliosis often require transition to adult spine units (e.g., Royal North Shore, Royal Adelaide) if they have ongoing issues into adulthood.

INFANTILE SCOLIOSIS

High-Yield Exam Summary

BASICS

  • •Age 0-3
  • •Male > Female
  • •Left > Right
  • •80% Resolve

MEHTA RULES

  • •RVAD less than 20 (Good)
  • •RVAD greater than 20 (Bad)
  • •Phase 1 (Gap)
  • •Phase 2 (Overlap)

WORKUP

  • •MRI Mandatory (Syrinx)
  • •Hips (DDH)
  • •Head (Plagiocephaly)
  • •Renal US (in congenital)

TREATMENT

  • •Observe (Resolving)
  • •Cast (Progressive)
  • •Rod (Salvage)
  • •Fuse (Last resort)

Deep Dive: How to Measure RVAD

  1. Identify the Apical Vertebra: The most rotated/deviated vertebra.
  2. Draw the Endplate Line: A line along the perpendicular of the vertebral body endplate.
  3. Draw the Rib Line: A line bisecting the head and neck of the corresponding rib.
  4. Measure the Angle: The angle between these two lines on the Convex side and Concave side.
  5. Calculate: Difference = Convex Angle minus Concave Angle.
    • Example: Convex 35 deg - Concave 10 deg = RVAD 25 deg. (Progressive).

Self-Assessment Quiz

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