Pre-operative clinical deterioration and long-term surgical outcomes in 41 patients with split cord malformation type 1.

IF 1.3 4区 医学 Q4 CLINICAL NEUROLOGY Child's Nervous System Pub Date : 2024-10-03 DOI:10.1007/s00381-024-06626-y
Rajasekhar Narayanan, Vedantam Rajshekhar
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Abstract

Purpose: 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.

Methods: 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.

Results: 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.

Conclusions: 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.

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41 名脊髓分裂畸形 1 型患者术前临床恶化情况和长期手术效果。
目的:记录一组脊髓分裂畸形1型(SCM 1)患者的术前临床恶化率以及这些患者的早期和长期手术效果:回顾性研究了2008年1月至2023年6月期间由同一外科医生(VR)手术治疗的41名脊髓分裂畸形1型患者的术前临床恶化史以及早期和长期手术效果:患者发病时的平均年龄为 79.3 个月,男女比例为 1:1.93。12例(29%)患者有先天性缺陷,4例(10%)患者无神经功能缺陷。26名(63%)患者有脊柱后凸,25名(61%)患者有运动功能障碍。33名患者(81%)(8/12(67%)有先天性缺陷)在手术前临床症状恶化。到两岁时,56%的患者临床症状恶化。手术后,18 名(55%)症状进行性加重的患者在长期随访中(平均 63.4 个月)一种或多种症状有所改善。手术结果没有预测因素:结论:由于半数以上的SCM 1患者在2岁前出现先天性肢体缺损或肢体缺损,因此应尽快为这些儿童实施手术。在术后的长期随访中,预计半数以上的患者病情会有所改善。
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来源期刊
Child's Nervous System
Child's Nervous System 医学-临床神经学
CiteScore
3.00
自引率
7.10%
发文量
322
审稿时长
3 months
期刊介绍: The journal has been expanded to encompass all aspects of pediatric neurosciences concerning the developmental and acquired abnormalities of the nervous system and its coverings, functional disorders, epilepsy, spasticity, basic and clinical neuro-oncology, rehabilitation and trauma. Global pediatric neurosurgery is an additional field of interest that will be considered for publication in the journal.
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