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Microsurgical efficacy in 326 children with tethered cord syndrome: a retrospective analysis

机译:326例脊髓栓系综合征儿童的显微手术疗效:回顾性分析

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Tethered cord syndrome is a progressive disease with a typically insidious onset in infants and children, and which can lead to persistent progress of neurological deficits and a high rate of disability without timely intervention. The purpose of this study was to investigate the curative effect of microsurgery in children with different types of tethered cord syndrome. In this study, we analyzed 326 patients with tethered cord syndrome, aged from 2 months to 14 years old, who were followed for 3–36 months after microscopic surgery. Based on clinical manifestations and imaging findings, these patients were classified into five types: tight filum terminale (53 cases), lipomyelomeningocele (55 cases), lipomatous malformation (124 cases), postoperative adhesions (56 cases), and split cord malformation (38 cases). All patients underwent microsurgery. Curative effects were measured before and 3 months after surgery by Spina Bifida Neurological Scale based on sensory and motor functions, reflexes, and bladder and bowel function. The results showed that Spina Bifida Neurological Scale scores improved in all five types after surgery. Overall effective rates in these patients were 75%. Effective rates were 91% in tight filum terminale, 84% in lipomyelomeningocele, 65% in lipomatous malformation, 75% in postoperative adhesion, and 79% in split cord malformation. Binary logistic regression analysis revealed that types of tethered cord syndrome (lipoma-type or not) and symptom duration before surgery were independent influencing factors of surgical outcome. These results show that therapeutic effect is markedly different in patients with different types of tethered cord syndrome. Suitable clinical classification for tethered cord syndrome will be helpful in predicting prognosis and guiding treatment. This trial has been registered in the Chinese Clinical Trial Registry (registration number: ChiCTR1800016464).
机译:系绳脊髓综合征是一种进行性疾病,通常在婴儿和儿童中起隐匿性发作,如果不及时干预,可能会导致神经功能缺损的持续发展和高残疾率。这项研究的目的是研究显微手术对不同类型的脊髓栓系综合征儿童的疗效。在这项研究中,我们分析了326例年龄在2个月至14岁之间的系绳综合征患者,在显微手术后对其进行了3–36个月的随访。根据临床表现和影像学检查结果,将这些患者分为五种类型:紧致终末期(53例),脂膜膜脑膜膨出(55例),脂质体畸形(124例),术后粘连(56例)和脊髓分离畸形(38例)情况)。所有患者均接受了显微手术。脊柱裂双歧神经量表根据感觉和运动功能,反射,膀胱和肠功能,在手术前和术后3个月测量疗效。结果显示,在所有五种类型的手术后,脊柱裂生物神经量表评分均得到改善。这些患者的总有效率为75%。有效的比率是:在紧致的终末期为91%,在脂膜膜脑膜膨出中为84%,在脂瘤性畸形中为65%,在术后粘连中为75%,在分离脊髓畸形中为79%。二元逻辑回归分析显示,系绳综合征的类型(是否为脂肪瘤)和术前症状持续时间是影响手术结局的独立因素。这些结果表明,在患有不同类型的系绳综合征的患者中,治疗效果明显不同。脊髓栓系综合征的适当临床分类将有助于预测预后和指导治疗。该试验已在中国临床试验注册中心注册(注册号:ChiCTR1800016464)。

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