Infantile Idiopathic Scoliosis
Age 0-3 Years
Mehta Classification
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
| Feature | Infantile (0-3) | Adolescent (10+) |
|---|---|---|
| Male > Female | Female >>> Male | |
| Left Thoracic | Right Thoracic | |
| Can Resolve (80%) | Does not resolve (Progresses/Stable) | |
| High (Alveoli hypoplasia) | Low (Alveoli mature) |
Associations of Infantile Scoliosis
Memory Hook:PHMC (Please Help My Child).
Predictors of Progression
Memory Hook:MOC (Mock the progression).
Treatment Hierarchy
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


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.
Clinical Assessment
History:
- Age: Onset? (Must be less than 3).
- Development: Is the child hitting milestones?
- Pain: Pain is rare and suspicious.
Physical Exam:
- Head: Check for Plagiocephaly.
- Neck: Torticollis (sternocleidomastoid tight?).
- Spine: Left sided prominence? Flexibility?
- Hips: Ortolani/Barlow.
- 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.
Surgical Techniques
Mehta Casting Technique
- Anaesthesia: General Anaesthesia with intubation.
- Position: Cotrel traction frame (Risser table).
- Traction: Longitudinal traction applied.
- Derotation: The surgeon applies a distinct "posterolateral to anteromedial" force on the rib hump. The goal is to untwist the spine.
- Molding: Plaster (POP) is molded meticulously over the ribs and iliac crests (for gripping).
- 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.
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
| Complication | Rate | Prevention/Management |
|---|---|---|
| Skin Ulceration | Common | Padding, molding, windowing. |
| Respiratory Distress | Rare | Ensure large abdominal window. |
| Chest Wall Deformity | Rare | Avoid excessive rib compression. |
| Psychosocial | Common | Burden of cast changes under GA. |
| Failure/Progression | Variable | Transition 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
- 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
- Long term follow up of EDP (Casting)
- Significant reduction in need for surgery
- Confirmed the RVAD rule of 20
- 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
- Natural history of infantile scoliosis
- Many resolve spontaneously
- Observation is safe if RVAD less than 20
- Neural axis abnormalities in infantile scoliosis
- Prevalence 22%
- Only 1 in 5 had neurological findings on exam
- Comparison of Infantile vs Adolescent Scoliosis
- Infantile curves are more rigid
- Higher association with Plagiocephaly and Hip Dysplasia
- Pulmonary compromise is the main differentiator
Viva Scenarios
Practice these scenarios to excel in your viva examination
The Resolving Curve
"12-month-old male. Left thoracic curve 20 degrees. RVAD 12 degrees."
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.
The Progressive Curve
"18-month-old female. Right thoracic curve 45 degrees. RVAD 35 degrees."
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.
Casting Complication
"Child in Mehta cast presents with vomiting and dehydration."
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.
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
- Identify the Apical Vertebra: The most rotated/deviated vertebra.
- Draw the Endplate Line: A line along the perpendicular of the vertebral body endplate.
- Draw the Rib Line: A line bisecting the head and neck of the corresponding rib.
- Measure the Angle: The angle between these two lines on the Convex side and Concave side.
- Calculate: Difference = Convex Angle minus Concave Angle.
- Example: Convex 35 deg - Concave 10 deg = RVAD 25 deg. (Progressive).