Cobb angle measures curve magnitude; progression risk relates to age, Risser stage, menarchal status, and curve size. Bracing indicated for skeletally immature curves 25–40° with documented progression; surgery typically considered for >45–50°. Pre‑op planning includes flexibility (bending) films, sagittal alignment, and neurologic monitoring readiness. Posterior spinal fusion with segmental pedicle screws is standard; anterior approaches reserved for specific curves. Pulmonary considerations critical for large thoracic curves (>70–80°).
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Scoliosis is a three-dimensional spinal deformity defined by a lateral curvature of the spine of 10° or greater (Cobb angle) in the coronal plane, almost invariably accompanied by rotation of the vertebral bodies (the rotational component causes the rib hump seen on Adam`s forward bend test) and an alteration of the normal sagittal profile. It is not simply a lateral bend — the rotational component is fundamental to its pathoanatomy and must be addressed in surgical planning. Understanding the various aetiological classifications, the measurement tools, the natural history by curve type and patient characteristics, and the evidence-based indications for surgical intervention is essential.
| Type | Aetiology | Key Features | Most Common / Notes |
|---|---|---|---|
| Adolescent idiopathic scoliosis (AIS) | Unknown — likely multifactorial (genetic + biomechanical); positive family history in 30% | Onset 10–18 years; female predominance (larger curves — F:M ratio for curves requiring treatment is 10:1); right thoracic curve is the most common (70%); by definition, a diagnosis of exclusion — must exclude neuromuscular, congenital, and syndromic causes | MOST COMMON scoliosis type (~80% of all scoliosis); a single left thoracic or unusual curve pattern should prompt MRI to exclude an underlying cause (syrinx, tethered cord) |
| Congenital scoliosis | Failure of formation (hemivertebra) or failure of segmentation (unilateral unsegmented bar) during embryogenesis; may be combined | Present from birth; associated anomalies in 60% — cardiac (VACTERL — Vertebral, Anorectal, Cardiac, Tracheo-Esophageal, Renal, Limb defects); renal anomalies in 20–33%; Klippel-Feil syndrome; occult spinal cord anomalies in 20% | A unilateral unsegmented bar (failure of segmentation) opposite a contralateral hemivertebra = worst prognosis (certain progression); all congenital scoliosis requires full imaging workup (renal USS, cardiac ECHO, full spine MRI) |
| Neuromuscular scoliosis | Upper motor neuron (cerebral palsy, spinal cord injury) or lower motor neuron (spina bifida, spinal muscular atrophy, Duchenne muscular dystrophy, Charcot-Marie-Tooth); spinal cord tumours | Long C-shaped curves extending into the pelvis (pelvic obliquity); rapidly progressive; may affect respiratory function; pelvis often involved (Cobb from T1 to pelvis); Duchenne MD — 90% develop progressive scoliosis; treatment often includes pelvic fixation | Surgical thresholds often lower than AIS (operate earlier due to rapid progression and respiratory compromise risk); outcomes depend on underlying condition and non-ambulatory status |
| Degenerative (de novo) adult scoliosis | Asymmetric disc degeneration, facet joint OA, and vertebral body remodelling in adulthood; not present in childhood | Adults >50 years; pain-dominant presentation (unlike AIS which is predominantly cosmetic in mild-moderate cases); associated with spinal stenosis and neurogenic claudication; lumbar or thoracolumbar location | Increasingly common with ageing population; treatment goals in adults are pain relief and neurological decompression, not curve correction per se |
| Syndromic scoliosis | Marfan syndrome, Neurofibromatosis type 1, Ehlers-Danlos syndrome, osteogenesis imperfecta | Each syndrome has characteristic curve patterns and treatment challenges; Marfan scoliosis — long sweeping curves, ligamentous laxity, dural ectasia, high risk of pseudarthrosis after fusion; NF1 — short angular `dystrophic` curves that progress even after bracing, require early surgery | Syndromic scoliosis should be managed at specialist centres; associated systemic features complicate management |
| Factor | Higher Progression Risk | Lower Progression Risk |
|---|---|---|
| Skeletal maturity | Risser 0–1 (immature); pre-menarche; Sanders Stage 2; high growth remaining | Risser 4–5 (mature); post-menarche; minimal growth remaining |
| Sex | Female — 10× more likely to progress to surgery than males with the same curve | Male — lower progression risk |
| Curve magnitude | Cobb >25° at presentation in a skeletally immature patient — high progression risk; curves >45° in the skeletally mature will continue to progress at approximately 1°/year in adulthood | <25° in skeletally mature patient — generally stable |
| Curve type / location | Double curve patterns; thoracic curves; longer structural curves | Lumbar curves; single minor thoracic curves |
| Rotation | High apical vertebral rotation (Nash-Moe Grade II–III) at presentation | Minimal rotation |
| Cobb Angle (AIS) | Skeletal Maturity | Treatment | Evidence / Notes |
|---|---|---|---|
| <25° | Any | Observation — clinical and radiological review every 4–6 months during growth; reassure patient and family; physiotherapy (Schroth method — scoliosis-specific exercise) may be offered; no active treatment indicated for small curves | Schroth physiotherapy — evidence for modest curve improvement and stabilisation; not proven to prevent surgery but may improve quality of life and delay progression |
| 25°–45° | Skeletally immature (Risser 0–2) | Bracing — the BRAIST trial (Weinstein et al., NEJM 2013): the first high-quality RCT demonstrating that bracing significantly reduces the risk of curve progression to surgical threshold (>50°) vs observation alone; success rate (treatment success defined as Cobb <50° at skeletal maturity) ~72% brace vs 48% observation; brace must be worn ≥18 hours/day for maximum effectiveness (dose-response relationship); the Boston TLSO (thoracolumbar sacral orthosis) is the most widely used design; full-time wear during the growth spurt is critical | BRAIST trial landmark evidence; dose-response confirmed (more hours wearing = better outcome); brace stopped when Risser 5 or no further progression; night-time-only bracing (Providence nocturnal brace) — evidence supports for curves <35° and correction >50% in brace |
| >45–50° (skeletally immature) or >40–45° (skeletally mature and progressing) | Any | Surgical — posterior spinal fusion with pedicle screw instrumentation and deformity correction; the gold standard surgical treatment; fusion across the structural curves only (compensatory curves not fused — they correct spontaneously); selective thoracic fusion or selective lumbar fusion depending on the Lenke curve type | Surgery achieves approximately 60–70% curve correction; prevents further progression; improves cosmesis; long-term outcomes excellent for AIS; blood loss can be significant — cell salvage, antifibrinolytics (tranexamic acid), and controlled hypotension reduce transfusion requirements; intraoperative neurophysiological monitoring (IONM — MEPs + SSEPs) is mandatory to detect spinal cord injury early during correction |
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