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Pediatric Scoliosis — Magnetic Growing Rods (MAGEC System)

Revolutionary growth-friendly surgical technique for early-onset scoliosis (EOS, presenting <10 years) using MAGEC (MAGnetic Expansion Control) system with magnetically distractable rods that allow non-invasive lengthening every 3–6 months in clinic via external remote controller, eliminating the need for repeated surgical lengthenings (every 6 months under general anesthesia) required by traditional growing rods, dramatically reducing patient morbidity, infection rate, surgical scarring, and emotional burden while permitting continued spinal and chest growth essential for pulmonary development; treatment for severe progressive EOS with curves >40-50 degrees not amenable to bracing.

Written by: Saygı Hospital Health Guide Editorial Board
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This content is for general information; please consult your physician for diagnosis and treatment.

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What is Pediatric Scoliosis — Magnetic Growing Rods (MAGEC System)?

Magnetic growing rods (MAGEC — MAGnetic Expansion Control system, NuVasive Specialized Orthopedics) represent paradigm-shifting innovation in surgical management of early-onset scoliosis (EOS), defined as scoliosis presenting before age 10 years (or before puberty per some definitions). EOS represents diagnostic and therapeutic challenge — curves often progressive and respond poorly to bracing alone, while definitive fusion in skeletally immature patient causes thoracic stunting and pulmonary compromise.

Early-onset scoliosis epidemiology and natural history: affects 0.1-3 percent of children depending on subtype; categories include idiopathic infantile scoliosis (<3 years), juvenile idiopathic (3-10 years), congenital (vertebral malformations), neuromuscular (cerebral palsy, spina bifida, muscular dystrophy, spinal muscular atrophy), syndromic (Marfan, Ehlers-Danlos, neurofibromatosis), thoracogenic (after thoracic surgery in infancy). Natural history: lung development critically depends on chest growth — alveolar number triples by age 8 years and chest cage size doubles; severe scoliosis or thoracic insufficiency syndrome (TIS) impairs lung development, causing irreversible pulmonary insufficiency; progressive curves >50-60 degrees in EOS associated with chronic respiratory failure, cor pulmonale, and shortened life expectancy. Treatment goals: control curve progression while preserving spinal and chest growth essential for pulmonary development; ultimately definitive fusion at skeletal maturity (typically Risser 4-5 or after age 10-12) with rod removal.

Treatment options for EOS by severity and patient factors: (1) Observation for mild curves (<25 degrees) with regular monitoring every 4-6 months; (2) Casting (Mehta casting) for infantile idiopathic scoliosis with promising results in some patients; (3) Bracing for moderate curves (25-40 degrees) — TLSO bracing, Milwaukee brace, full-time wear; (4) Growing rod systems for progressive moderate-severe curves not controlled by bracing in skeletally immature patients with adequate growth potential and spine length: traditional growing rods (TGR — open surgical lengthening), magnetic growing rods (MAGEC — non-invasive magnetic lengthening), MCGR variants; (5) Vertical Expandable Prosthetic Titanium Rib (VEPTR) — rib-to-rib or rib-to-pelvis distraction for thoracic insufficiency syndrome with congenital rib anomalies; (6) Final fusion at skeletal maturity following growth-friendly treatment; (7) Definitive fusion in older children (usually >10 years) with progression amenable to fusion.

MAGEC (MAGnetic Expansion Control) system specifics: FDA approved 2014, CE marked in Europe; consists of titanium rods with internal magnetic actuator (small motor with magnet), External Remote Controller (ERC — handheld device with strong magnetic field generator), and accessory components; rod available in different lengths (70-120 mm actuator stroke); single or dual rod construct possible; magnetically actuated lengthening (1-3 mm per session) by aligning ERC over actuator location and engaging mechanism externally; lengthening painless and quick (10-15 minutes per session); typically performed every 3-6 months in outpatient clinic; total lengthening potential per rod 48 mm before reaching maximum stroke. Compared with traditional growing rods: TGR requires repeat open surgical lengthening every 6 months under general anesthesia (7-15 procedures per patient over years), with cumulative complications including infection (10-20 percent), implant failure, anesthesia exposure, psychological trauma; MAGEC eliminates repeated surgeries while maintaining all growth-friendly benefits — major advantage in patient quality of life, family burden, healthcare costs, and complication profile.

Symptoms

Visible spinal curvature in young child (uneven shoulders, prominent rib hump on forward bending — Adams test)
Truncal asymmetry, uneven waist, leaning to one side
Progressive curve documented on serial radiographs (Cobb angle increasing)
Curve progression despite bracing in young patient
Pulmonary symptoms with severe curves (decreased exercise tolerance, dyspnea)
Failure to thrive in severe EOS with thoracic insufficiency
Underlying syndrome features (Marfan, NF1, congenital heart disease, hemivertebrae, etc.)
Family history of EOS or scoliosis
Neuromuscular disease symptoms (weakness, abnormal gait, spasticity)
Café-au-lait macules (NF1 — neurofibromatosis-associated scoliosis)
Skin dimples, hair patches, sinuses over spine (occult spinal dysraphism)
Chest wall deformity with rib anomalies (congenital cases)

Risk Factors

Onset before age 10 years (EOS by definition)
Congenital vertebral anomalies (hemivertebrae, fused vertebrae)
Neuromuscular disease (cerebral palsy, spina bifida, SMA, muscular dystrophy, Friedreich ataxia)
Syndromic associations (Marfan, Ehlers-Danlos, neurofibromatosis 1, Prader-Willi)
Family history of scoliosis (idiopathic forms)
Female sex (slight predominance in juvenile idiopathic)
Chest wall surgery in infancy (thoracogenic scoliosis)
Severe curves >40-50 degrees at presentation
Rapid curve progression (>10 degrees per year)
Skeletally immature with significant remaining growth potential (Risser 0-1, Sanders <5)
Failure of bracing trial
Thoracic insufficiency syndrome features (chest cage compression, lung volume loss)

When to See a Doctor?

If you experience any of the following symptoms, seek medical attention promptly:

  • Visible spinal asymmetry or curve in young child — pediatric spine specialist evaluation
  • Documented scoliosis progression on serial radiographs
  • Failed bracing for moderate curve in young child
  • Severe curve >40-50 degrees at presentation requiring surgical planning
  • Underlying syndrome with new spinal deformity
  • Pulmonary symptoms with severe spinal deformity (thoracic insufficiency syndrome)
  • Recommendation for growing rod surgery (MAGEC, TGR, VEPTR) for second opinion
  • MAGEC patient with new pain, neurologic deficit, or rod failure suspicion
  • Need for elective MAGEC lengthening (every 3-6 months in clinic)
  • Wound concerns or signs of infection at rod site
  • Pre-operative or post-operative surgical planning consultation
  • Final fusion timing assessment as patient approaches skeletal maturity

Treatment Methods

01
Diagnostic workup: comprehensive history (symptom onset, progression rate, family history, syndrome features, comorbidities, neurodevelopmental status), thorough physical examination (Adams forward-bend test, scoliometer measurement of trunk rotation angle, leg length discrepancy, neurologic examination including reflexes, strength, gait, signs of underlying neuromuscular disease), full-length standing posteroanterior and lateral spinal radiographs (measure Cobb angle of major curves, identify levels involved, vertebral anomalies, spinal balance — sagittal and coronal); MRI for atypical presentations including unusual curve patterns, painful scoliosis, neurologic findings, syndromic features (rule out spinal dysraphism, Chiari malformation, syrinx, intraspinal pathology); CT for congenital vertebral anomalies; pulmonary function tests in severe cases (vital capacity, oxygenation); echocardiogram for syndromic cases (heart anomalies in Marfan, CHARGE)
02
Multidisciplinary evaluation: pediatric orthopedic surgeon (spinal subspecialist), pediatric pulmonologist, geneticist for syndromic cases, rehabilitation specialist, social worker for family support and resources, anesthesiologist for surgical planning, child life specialist; family meeting to discuss treatment options, goals, expectations, and informed consent
03
Conservative management: serial monitoring with X-ray every 4-6 months for mild progressing curves; bracing for moderate curves (25-40 degrees) in skeletally immature patients (TLSO brace, Milwaukee brace, full-time wear 23 hours daily; effective in 70-80 percent of compliant patients with appropriate curves); Mehta casting series for infantile idiopathic scoliosis (early aggressive casting may achieve curve resolution in some); physical therapy for general fitness, posture, breathing; activity restrictions generally not required for young patients except contact sports during MAGEC implant period
04
Indications for growing rod surgery (MAGEC, TGR, VEPTR): severe progressive EOS curves >40-50 degrees not controlled by bracing, rapidly progressive curves, thoracic insufficiency syndrome, neuromuscular scoliosis with severe curves, syndromic scoliosis with severe progression, failure of conservative management, age typically 4-10 years (though expanded boundaries with experience), adequate spinal length for fixation, family acceptance and understanding
05
MAGEC surgical technique: standard posterior approach with subperiosteal exposure of spine over fixation levels (typically T2-L4 or shorter constructs depending on curve); proximal foundation with claw construct (sub-laminar wires, hooks) or pedicle screws at upper thoracic levels (T2-T4); distal foundation with pedicle screws at lower thoracic or lumbar level (T11-L4); MAGEC rod connection (single or dual rods, dual generally preferred for stability); careful rod positioning to allow magnetic actuator activation by external controller; intraoperative neuromonitoring (somatosensory evoked potentials SSEP, motor evoked potentials MEP); blood loss management (cell saver, antifibrinolytic agents); surgical drains; meticulous closure
06
Non-invasive distraction (lengthening): performed every 3-6 months in outpatient clinic; External Remote Controller (ERC) device positioned over rod actuator location (use ultrasound to localize); device activated to engage internal magnetic mechanism, distracting rod by 1-3 mm per session (target 1.5 mm per month — limited by tissue stretching); painless and well-tolerated by children; quick (10-15 minutes per session per rod); post-procedure radiograph or ultrasound to confirm distraction; serial monitoring of curve correction, growth, complications
07
Long-term management plan: continue MAGEC distractions every 3-6 months; monitor for complications including infection, implant failure, rod breakage, foundation failure (proximal hook or screw loosening), wound problems, metallosis (titanium wear debris from internal mechanism), neurologic complications (rare); periodic radiographs to assess curve correction, growth, implant integrity; pulmonary function follow-up in severe cases
08
Definitive fusion: planned at skeletal maturity (typically Risser 4-5 or post-puberty growth completion, approximately age 12-15) with removal of MAGEC rods and definitive posterior spinal fusion using pedicle screw construct; sometimes anterior approach combined; aim is final correction and permanent stabilization; ongoing follow-up after fusion
09
Complications and concerns: implant infection (5-15 percent — usually requires implant revision and antibiotics), rod breakage and need for revision (cumulative risk 20-30 percent over years), proximal foundation failure with hook pull-out or screw loosening, wound complications, metallosis (titanium wear debris reported with concerning long-term findings — under active surveillance and study; some MAGEC system batches recalled in Europe in 2020 for wear debris concerns, later reintroduced with modifications), MRI compatibility limitations (specific protocols required, limits routine MRI use), psychological adjustment to chronic surgical implant, family stress and resource burden, high device cost, anesthesia exposure during initial surgery and revisions
10
Long-term outcomes: significant reduction in number of surgical procedures compared to traditional growing rods (eliminate repeat lengthening procedures), improved quality of life metrics, equivalent curve correction outcomes, generally similar implant survival, but ongoing surveillance for metallosis and long-term implant performance; functional and pulmonary outcomes after definitive fusion generally good; multidisciplinary follow-up essential throughout childhood and into adolescence; consider patient and family education, support resources, transition to adult care for ongoing follow-up if needed; major advance in pediatric spinal deformity treatment

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Health Disclaimer: The information on this page is prepared for general informational purposes only. It does not replace medical diagnosis and treatment. Please consult your physician for your complaints. Saygı Hospital does not accept responsibility for actions taken based on the information on this page.