Department of Neurological Sciences, Christian Medical College, Vellore, Tamil Nadu, India.
Childs Nerv Syst. 2024 Dec;40(12):4065-4073. doi: 10.1007/s00381-024-06626-y. Epub 2024 Oct 3.
To document the pre-operative rate of clinical deterioration in a cohort of patients with split cord malformation type 1 (SCM 1) and the early- and long-term surgical outcome in these patients.
Data from 41 patients with SCM 1 operated upon by the same surgeon (VR) between January 2008 to June 2023 were retrospectively reviewed with respect to history of clinical deterioration prior to surgery and early and long-term surgical outcomes.
The mean age of the patients at presentation was 79.3 months and the male to female ratio was 1:1.93. Twelve (29%) patients had congenital deficits whereas 4 (10%) patients had no neurological deficits. Twenty-six (63%) patients had kyphoscoliosis and 25 (61%) patients had motor dysfunction. Thirty-three (81%) patients (8/12 (67%) with congenital deficits) had clinical deterioration prior to surgery. By the age of 2 years, 56% of patients had clinical deterioration. After surgery, 18 (55%) patients with progressive symptoms had improvement in one or more of their symptoms on long-term follow-up (mean, 63.4 months). There were no predictors of surgical outcome.
Since over half of our patients with SCM 1 developed progression of congenital deficits or developed deficits by the age of 2 years, surgery should be performed as soon as possible in these children. On long-term follow-up after surgery, improvement can be expected in over half the patients.
记录 1 型脊髓分裂畸形(SCM 1)患者队列术前临床恶化的发生率,并评估这些患者的早期和长期手术结果。
回顾性分析了 2008 年 1 月至 2023 年 6 月间由同一位外科医生(VR)治疗的 41 例 SCM 1 患者的术前临床恶化史以及早期和长期手术结果。
患者就诊时的平均年龄为 79.3 个月,男女比例为 1:1.93。12 例(29%)患者存在先天性缺陷,4 例(10%)患者无神经功能障碍。26 例(63%)患者存在脊柱后凸侧凸,25 例(61%)患者存在运动功能障碍。33 例(81%)患者(12 例中有先天性缺陷的患者中 8 例,占 67%)术前出现临床恶化。到 2 岁时,56%的患者出现临床恶化。术后,18 例(55%)出现进行性症状的患者在长期随访中(平均 63.4 个月)其一个或多个症状得到改善。手术结果无预测因素。
由于我们超过一半的 SCM 1 患者出现先天性缺陷的进展或在 2 岁前出现缺陷,因此应尽快为这些儿童进行手术。术后长期随访中,超过一半的患者可获得改善。