Division of Spinal Surgery, Ilizarov Center, Kurgan, Russia.
Childs Nerv Syst. 2022 Jan;38(1):163-172. doi: 10.1007/s00381-021-05382-7. Epub 2021 Oct 9.
Case series, literature review, and technical note.
To compare two different approaches to treat the spinal deformity with split cord malformation type I (SCM I). To present a new method of one-stage surgical treatment of congenital spinal deformity with wide bony septum (SCM I).
Analysis of the literature on the different types of combined surgical treatment of spinal deformities with SCM I was performed. We have provided our own data on 27 patients treated for congenital spinal deformity and SCM I, one of which underwent Schwab IV type osteotomy at the apex of the deformity through the bony septum and pedicles. Inclusion criteria were presence of spinal deformity in combination with SCM 1, performed surgery to correct spinal deformity, and follow-up period of at least 2 years.
The result of the literature review was controversial and requires additional research. The average age of patients was 8.8 ± 6.6 years old. One-stage treatment of SCM I and spinal deformity was performed in 10 patients (group I) and two-stage in 14 patients (group II). Three patients with severe myelodysplasia, SCM I, and congenital kyphoscoliosis underwent correction of spinal deformity without SCM I removing (group III). The group I had the longest surgery duration (mean 289 ± 75 min) and largest blood loss (mean 560 ± 386 ml), a high percentage of deformity correction (mean 69.6%), and the highest rate of complications (60%). The most optimal was the two-stage treatment with the mean surgery duration 191 ± 137 min, mean blood loss 339 ± 436 ml, mean correction rate 63%, and frequency of complications 21%. The average follow-up time was 6.0 ± 2.6 years.
One stage surgery associated with a large surgical invasion and a large number of complications. It can be used in some cases, for example when the wide bony septum (SCM I) is localized at the apex of the congenital scoliosis or kyphosis. In all other cases, it is worth adhering to a two-stage treatment. Many new works demonstrate the relative safety and effectiveness of deformity correction without removing the SCM. In our opinion, indications for treatment of spinal deformity without SCM I removing can be the need to perform a shortening ostetomy outside the SCM zone. The remaining cases require a thorough assessment and a balanced decision.
病例系列、文献回顾和技术说明。
比较治疗脊髓纵裂合并脊髓分裂症 I 型(SCM I)脊柱畸形的两种不同方法。介绍一种治疗先天性脊柱畸形合并宽骨性隔(SCM I)的一期手术新方法。
分析了不同类型的脊髓纵裂合并 SCM I 的联合手术治疗的文献。我们提供了 27 例先天性脊柱畸形伴 SCM I 患者的自身数据,其中 1 例通过骨性隔和椎弓根在畸形的顶点行 Schwab IV 型截骨术。纳入标准为存在合并 SCM 1 的脊柱畸形,行手术矫正脊柱畸形,随访时间至少 2 年。
文献回顾的结果存在争议,需要进一步研究。患者平均年龄为 8.8±6.6 岁。10 例患者(I 组)行 SCM I 和脊柱畸形一期治疗,14 例患者(II 组)行二期治疗。3 例严重脊髓发育不良、SCM I 和先天性脊柱后凸患者未行 SCM I 切除行脊柱畸形矫正(III 组)。I 组手术时间最长(平均 289±75min),出血量最大(平均 560±386ml),畸形矫正率最高(平均 69.6%),并发症发生率最高(60%)。二期治疗最理想,手术时间平均 191±137min,出血量平均 339±436ml,矫正率平均 63%,并发症发生率 21%。平均随访时间为 6.0±2.6 年。
一期手术与较大的手术侵袭和较多的并发症相关。它可以用于某些情况,例如宽骨性隔(SCM I)局限于先天性脊柱侧凸或后凸的顶点时。在所有其他情况下,值得坚持进行两期治疗。许多新的研究工作表明,不切除 SCM 进行畸形矫正具有相对的安全性和有效性。在我们看来,不切除 SCM I 治疗脊柱畸形的适应证为需要在 SCM 区域外进行缩短截骨术。其余病例需要进行全面评估和平衡决策。