Tikoo Agnivesh, Kothari Manish K, Shah Kunal, Nene Abhay
(FNB Spine Surgery) Wockhardt Hospitals, 1877, Dr. Anand Rao Nair Road, Mumbai Central (E), Mumbai- 400 011, India.
(MS Ortho) Wockhardt Hospitals, 1877, Dr. Anand Rao Nair Road, Mumbai Central (E), Mumbai- 400 011, India.
Open Orthop J. 2017 Apr 28;11:337-345. doi: 10.2174/1874325001711010337. eCollection 2017.
Congenital scoliosis is one of the 'difficult to treat' scenarios which a spine surgeon has to face. Multiple factors including the age of child at presentation, no definite pattern of deformity and associated anomalies hinder the execution of the ideal treatment plan. All patients of congenital scoliosis need to be investigated in detail. X rays and MRI of spine is usually ordered first. Screening investigations to rule out VACTERL (Visceral, Anorectal, Cardiac, Tracheo-esophageal fistula, Renal and Lung) abnormalities are required. They are cardiac echocardiography and ultrasonography of abdomen and pelvis. CT scan is required to understand the complex deformity and is helpful in surgical planning.
A comprehensive medical literature review was done to understand the current surgical and non surgical treatment options available. An attempt was made to specifically study limitations and advantages of each procedure.
The treatment of congenital scoliosis differs with respect to the age of presentation. In adults with curves more than 50 degrees or spinal imbalance the preferred treatment is osteotomy and correction. In children the goals are different and treatment strategy has to be varied according to the age of patient. A single or two level hemivertebra can easily be treated with hemivertebra excision and short segment fusion. However, more than 3 levels or multiple fused ribs and chest wall abnormalities require a guided growth procedure to prevent thoracic insufficiency syndrome. The goal of management in childhood is to allow guided spine growth till the child reaches 10 - 12 years of age, when a definitive fusion can be done. The current research needs to be directed more at the prevention and understanding the etiology of the disease. Till that time, diagnosing the disease early and treating it before the sequels set in, is of paramount importance.
The primary aim of treatment of congenital scoliosis is to allow the expansion of chest and abdominal cavity, while keeping the deformity under control. Various methods can be categorized into definitive (hemivertebrectomy) or preventive (guided growth). Casting, Growth rods, Convex Epiphysiodesis are all guided growth measures. The guided growth procedure either 'corrects the deformity' or will have to be converted to a final fusion surgery once the child completes the spinal growth which is preferably done around 10 - 12 years of age. Future directions should aim at genetic counselling and early detection.
先天性脊柱侧弯是脊柱外科医生必须面对的“难治”情况之一。多种因素,包括患儿就诊时的年龄、畸形无明确模式以及相关异常,阻碍了理想治疗方案的实施。所有先天性脊柱侧弯患者都需要进行详细检查。通常首先会安排脊柱的X线和磁共振成像(MRI)检查。需要进行筛查以排除VACTERL(内脏、肛门直肠、心脏、气管食管瘘、肾脏和肺部)异常,即心脏超声心动图以及腹部和盆腔超声检查。需要进行CT扫描以了解复杂畸形情况,这有助于手术规划。
进行了全面的医学文献综述,以了解当前可用的手术和非手术治疗选择。试图具体研究每种手术的局限性和优势。
先天性脊柱侧弯的治疗因就诊年龄而异。对于侧弯超过50度或存在脊柱失衡的成年人,首选治疗方法是截骨矫正。对于儿童,目标不同,治疗策略必须根据患者年龄而有所不同。单个或两个节段的半椎体可通过半椎体切除和短节段融合轻松治疗。然而,超过3个节段或多个融合肋骨及胸壁异常则需要采用引导生长手术以预防胸廓发育不全综合征。儿童期治疗的目标是允许脊柱引导生长,直至儿童达到10至12岁,此时可进行确定性融合手术。当前的研究需要更多地针对疾病的预防和病因理解。在此之前,早期诊断疾病并在后遗症出现之前进行治疗至关重要。
先天性脊柱侧弯治疗的主要目标是在控制畸形的同时,允许胸腔和腹腔扩张。各种方法可分为确定性(半椎体切除术)或预防性(引导生长)。石膏固定、生长棒、凸侧骨骺阻滞术均为引导生长措施。引导生长手术要么“矫正畸形”,要么在儿童完成脊柱生长(最好在10至12岁左右)后必须转换为最终融合手术。未来的方向应旨在进行遗传咨询和早期检测。