Method of Selecting Surgical Treatment for Children with Congenital Deformity of the Spine and Thorax

S. Vissarionov, M. S. Asadulaev, A. S. Shabunin, Kristina N. Rodionova, E. A. Orlova, Yury A. Novosad, Polina A. Pershina, Timofey S. Rybinskikh
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Abstract

Introduction. Spinal anomalies are considered to be the most severe pathology of the axial skeleton. Intrauterine formation of deformity with its subsequent progression during growth is the reason for the need for surgical intervention. The prevalence of patients with congenital scoliosis in the total structure of spinal deformities is up to 2%. In terms of the malignancy of the course of the disease, children with unsegmented rod and rib synostosis represent one of the most unfavorable groups of patients. Aim. To perform a comparative analysis of the results of surgical treatment of children with congenital scoliosis with unilateral lateral vertebral segmentation disorder and rib synostosis using different techniques. Methods. The work is a monocenter cohort study of “case-control” type (III level of evidence). The design of the work is a monocenter cohort retro and prospective study. The results of surgical treatment of patients between 2010 and 2020 were analyzed. The study included 45 patients aged 3 to 7 years with the diagnosis of congenital scoliosis with unilateral lateral segmentation disorder of vertebral bodies and rib synostosis. The patients were divided into 2 groups depending on the surgical treatment method applied. In the first group (n = 24), patients underwent thoracoplasty with implantation of an individual rib/rib/vertebral distractor; in the second group (n = 21), patients underwent spinal surgery in the scope of vertebrotomy at the apex of the curvature and correction of the deformity with a multifocal spinal system. The data of medical records, as well as MSCT, radiographs, and pulse oscillometry were included in the analysis of the results. Results. Me (median) of scoliosis before treatment in group 1 patients 58.5, IQR = 19.75; after treatment — Me = 40.0, IQR = 20.0. Me of kyphosis before surgery 22, IQR = 4.5; after surgery Me = 26.0, IQR = 4.0. In the second group, Me of scoliosis before treatment 58.0, IQR = 3.0; after treatment, Me = 20.0, IQR = 6.0. Me of kyphosis before surgery 22, IQR = 2.0; after surgery Me 28.0, IQR = 4.0. When comparing MSCT data, group 1 patients showed an increase in lung tissue volume by 21% of the initial lung volume, in group 2 the increase amounted to 27%. The analysis of external respiratory function indices demonstrates improvement of reactive component indices by 21.1%, frequency dependence of resistive component by 46.4%, resistive component by 50% in group 1 patients, in group 2 there is an improvement of reactive component indices by 21.1%, resistive component by 50.9% and frequency dependence of reactive component by 46.7%. Conclusion. Corrective intervention on the spine at an early age makes it possible to achieve effective correction of the deformity; similar changes are observed both in lung volume and functional state of the respiratory system due to the mediated correction of the thorax shape.
先天性脊柱和胸部畸形儿童手术治疗的选择方法
简介脊柱畸形被认为是轴向骨骼最严重的病变。宫内形成的畸形及其随后在成长过程中的发展是需要手术干预的原因。在整个脊柱畸形结构中,先天性脊柱侧弯症患者的发病率高达 2%。就病程的恶性程度而言,患有无节杆和肋骨突的儿童是最不利的患者群体之一。研究目的比较分析使用不同技术对患有先天性脊柱侧弯伴单侧侧椎分节紊乱和肋骨突的儿童进行手术治疗的结果。方法。该研究是一项 "病例对照 "类型的单中心队列研究(证据等级为 III 级)。研究设计为单中心队列复古和前瞻性研究。研究分析了 2010 年至 2020 年间患者的手术治疗结果。研究对象包括45名年龄在3至7岁之间、诊断为先天性脊柱侧弯伴单侧椎体侧向分节紊乱和肋骨突节的患者。根据手术治疗方法的不同,患者被分为两组。第一组(24 人)的患者接受了胸廓成形术,并植入了单个肋骨/肋骨/椎体牵引器;第二组(21 人)的患者接受了脊柱手术,在弯曲顶点进行椎体切除术,并用多焦点脊柱系统矫正畸形。结果分析包括病历数据、MSCT、X光片和脉搏震荡仪。结果第1组患者治疗前脊柱侧弯的Me(中位数)为58.5,IQR=19.75;治疗后--Me=40.0,IQR=20.0。手术前脊柱侧弯的中位数为 22,IQR = 4.5;手术后中位数为 26.0,IQR = 4.0。在第二组中,治疗前脊柱侧凸的 Me 为 58.0,IQR = 3.0;治疗后 Me = 20.0,IQR = 6.0。手术前脊柱后凸 Me = 22,IQR = 2.0;手术后 Me = 28.0,IQR = 4.0。对比 MSCT 数据,第 1 组患者的肺组织容积增加了 21%,第 2 组增加了 27%。外部呼吸功能指数分析表明,第一组患者的反应性成分指数提高了 21.1%,阻力性成分的频率依赖性提高了 46.4%,阻力性成分提高了 50%;第二组患者的反应性成分指数提高了 21.1%,阻力性成分提高了 50.9%,反应性成分的频率依赖性提高了 46.7%。结论在早期对脊柱进行矫正干预可有效矫正畸形;由于对胸廓形状进行了介导矫正,肺活量和呼吸系统的功能状态也发生了类似的变化。
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