Adolescent idiopathic scoliosis (AIS) is the most common form of pediatric scoliosis. It occurs in individuals between the ages of 10 to 18. By definition, idiopathic scoliosis implies that the etiology is unknown or not related to a specific syndromic, congenital, or neuromuscular condition. Treatment options include conservative management, bracing, or operative intervention.
Idiopathic scoliosis is a diagnosis of exclusion of other forms of scoliosis. As of today, there is no identifiable cause for idiopathic scoliosis. Theories include hormonal causes, asymmetric growth, muscle imbalance, and genetic factors. Nearly 30% of patients with AIS have a family member with scoliosis.
The prevalence is about 1% to 3% for AIS. There is a preference for females and a right-sided curvature. To be considered for the classification of scoliosis the curve must be at least 10 degrees in the coronal plane. The prevalence is approximately 0.1% for curves measuring more than 40 degrees (those which tend to be those requiring operative intervention).
A thorough history and physical is warranted. Particular attention should be paid to the developmental history to rule out any other etiologies of scoliosis. Attention must also be placed on questions focused on skeletal maturity including the age of menarche and determination of Risser classification. In a gross generalization, most adolescent patients presenting with idiopathic scoliosis will not have dramatic back pain from the curvature. Many tend to be very active including athletes, cheerleaders, and otherwise very healthy children.
The physical exam must include a neurologic assessment as well as evaluation of the curve’s shape, form, and flexibility. Patient privacy and sensitivity in this age demographic are important to consider while ensuring proper evaluation of the spinal curve. Photographic documentation with the patient standing upright as well as bending over is vital to track progression as well as the operative outcome. Spinal curvature is not isolated to a spinal deformity. Rib prominence, waistline, and shoulder height should also be documented.
Evaluation is generally a screening evaluation either through a school entity, sports coach, or pediatrician. The proper formal evaluation includes x-ray imaging. Patients need a standing coronal x-ray, sagittal x-ray, left and right bending x-rays. Risser classification can generally be calculated from the iliac crest on the coronal x-ray platform. Consensus holds that a CT scan and MRI imaging for typical AIS patients is not warranted. However, certain intraoperative imaging guidance techniques do require either preoperative or intraoperative CT imaging. This is surgeon and technology specific. Patients who are pre-operative candidates undergo a standard laboratory workup including CBC, BMP, INR/PTT, urinalysis, and a urine pregnancy test for all females.
Historically speaking, those with curves less than 10 degrees do not meet the specification for diagnosis of AIS. Furthermore, the US Preventative Services Task Force has recently questioned whether school screenings positively impact the patient-centered-health outcomes.
Generally speaking, those with curves of 10 to 25 degrees are monitored for surveillance with serial x-rays. This is usually at 3, 6 or 12-month intervals.
Those with curves greater than 25 degrees but less than 40 to 45 degrees are candidates for bracing. The Bracing in Adolescent Idiopathic Scoliosis Trial (BrAIST) was an NIH funded randomized control trial that illustrated the effectiveness of bracing in the adolescent population.
Those with curves over 40 to 45 degrees who are skeletally immature are operative candidates. The mainstay of operative treatment is surgical fusion. Historically this could be anterior or posterior fusion or a combined anterior-posterior approach. Currently, the leading technique is posterior fusion with pedicle screws and bilateral rod placement. Selection of operative levels is a complex decision algorithm taking into account coronal deformity location, regional kyphosis, shoulder height, L4 tilt, and lumbar alignment. Furthermore, a ratio comparison between the main thoracic curve Cobb angle and the thoracolumbar curve Cobb angle as well as the apical vertical translation and apical vertebral rotation must be considered for advanced operative planning.
New non-fusion techniques such as tethering procedures are gaining traction as well.
These are gross generalizations, and actual patient care operative decisions must account for patient-specific factors, skeletal maturity, deformity progression, patient’s socioeconomic factors, and surgeon experience.
It is essential to rule out scoliosis from other causes such as neurologic conditions, neuromuscular conditions, congenital, or syndromic issues.
The Lenke Classification scheme best categorizes staging. The purpose of this classification scheme is to create a uniform approach to naming and described curves. The overall intent at an advanced level is also to give some preference toward the operative treatment protocol.
The Lenke Classification takes into account the coronal curve (1-6), the sagittal deformity (-, N, or +), and the lumbar spine modifier (A, B, C). This creates a descriptor such as 3C+ or 1B-. Formal education of the Lenke classification and memorization of the criteria is beyond the scope of this text. However, it is the preferred method for spinal deformity surgeons to communicate about AIS.
Patients with adolescent idiopathic scoliosis that go untreated into adulthood can have a rate of progression that is approximately 0.5 to 1 degree per year once the patient has reached a 50-degree coronal angle. Furthermore, in gross generalization, curves in adulthood tend to be much stiffer and more rigid than in the adolescent cohort requiring more aggressive and invasive surgical techniques.
Complications from untreated scoliosis include deformity progression. This can generate back pain, lumbar radiculopathy, cosmetic problems, and even cardiac and pulmonary restriction. Untreated patients with a curve of more than 80 degrees in the coronal plane can have increased shortness of breath.
Surgical complications are generally lower than in adult spinal deformity surgery but present. One national data series estimated the post-surgical neurologic injury at 0.9%, respiratory complications at 2.8%, cardiac complications at 0.8%, infection at 0.5%, and 2.7% for gastrointestinal complications.
Surgeon expertise and volume of surgery are also important factors regarding outcome and cost of surgery.
Most patients undergoing adolescent idiopathic scoliosis surgery are expected to return to home following their operative intervention. Length of stay can vary based on surgical procedure, surgeon preference, institutional algorithms, and other medical or socioeconomic sequel. Bracing is generally not needed as a post-operative therapy.
Challenges do present in the management of bracing with this population. Furthermore, a study has illustrated improved outcomes with increased compliance to bracing protocols. Adherence requires significant involvement from both the patient and the patient’s support structure. Furthermore, significant education of the parents is required regarding operative risk, operative planning, and purpose of the operative intervention.
The management of scoliosis is by a multidisciplinary team that includes a physical therapist, orthopedic surgeon, pulmonologist, rheumatologist and a neurologist. The vast majority of patients do not require surgery and can be managed with non-surgical therapies. Surgery is recommended for symptomatic patients with severe deformity-but the patient needs to be educated about the complications of scoliosis which are not trivial. Surgery can improve function and aesthetics but a significant number of patients do remain with residual pain or other neurological deficit that can reduce the quality of life.
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