脑瘫:一种独特的图解体验。

Aamir Jalal Al-Mosawi
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引用次数: 4

摘要

背景:脑瘫是一种异质性疾病,与非进行性病变相关,可导致永久性运动障碍和活动受限,通常与大运动发育迟缓有关。在中度至重度脑瘫病例中,行走等运动发育里程碑可能永远无法实现。认知障碍和语言迟缓也很常见。本文的目的是描述我们对脑瘫的图解经验,重点是多因素治疗。患者和方法:本文选取17例脑瘫患者,其中2例女性患者早期治疗过程被既往文献收录,15例新病例(男11例,女4例)在2019年5月- 11月的7个月内观察到。他们的年龄从10个月到9岁不等。10例患者有明显的痉挛,限制了他们的活动。所有患者均有发育迟缓,包括言语迟缓。9名患者在没有支撑的情况下无法坐下,包括1名有明显肌张力障碍的患者和1名在没有支撑的情况下可以站立和行走但无法坐下的患者。只有两名病人能够独立行走,但速度缓慢且困难。2例患者有出生窒息史,1例患者有遗传病史,其2个兄弟均有感染。患者根据我们发表的个体化治疗方案进行治疗,提供各种干预措施的组合,包括营养支持、肌肉松弛剂、口服吡啶醇、肌内吡拉西坦、胞胆碱(口服和注射)、肌内脑溶素和肌内癸酸诺龙。这些治疗的目的包括克服痉挛,修复大脑和改善其功能,最终改善活动能力和促进发育。结果:所有患者的运动发育均有改善,未发生任何副作用。然而,不可能记录所有患者的治疗和随访细节,但可以提供7例患者的改善说明。结论:脑瘫是一种异质性疾病,短期内很难出现一种能全面改善其表现的单一治疗药物。因此,建议采用循证多因子疗法。适当的肌肉放松对于防止挛缩并发症是至关重要的,这些并发症可能会导致进行性残疾。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cerebral Palsy: A Unique Illustrated Experience.
Abstract Background: Cerebral palsy is a heterogeneous condition associated with a non-progressive lesion causing permanent disorder of movement with limited mobility and is generally associated with gross motor developmental delay. In moderate to severe cases of cerebral palsy, motor developmental milestones such as walking may never be achieved. Impaired cognition and delayed speech are also commonly seen. The aim of this paper is describing our illustrated experience with cerebral palsy with emphasis on treatment with multi-factorial therapies. Patients and methods: Seventeen patients with cerebral palsy are described in this paper including two female patients whose early treatment courses were included in previous publications and 15 new cases (11 males and 4 females) observed during seven months period (May-November, 2019). Their ages ranged from 10 months to 9 years. Ten patients had significant spasticity limiting their movements. All patients had developmental delay including delayed speech. Nine patients were unable to sit without support, including a patient with significant dystonia and a patient who could stand and walk with support but was unable to sit without support. Only two patients were able to walk alone, but slowly and with difficulty. Two patients had history of birth asphyxia and one patient had a genetic condition with 2 of his brothers being affected. The patients were treated based on our published experiences with individualized treatment plans providing a combination of various interventions including nutritional support, muscle relaxants, oral pyritinol, intramuscular piracetam, citicoline (oral and injectable), intramuscular cerebrolysin and intramuscular nandrolone decanoate. The aims of these therapies include overcoming spasticity, repairing the brain and improving its function and ultimately improving mobility and advancing development. Results: All patients experienced improvement in motor development without the occurrence of any side effect. However, it was not possible to document the details of treatments and follow-up for all patients, but it was possible to provide an illustrated demonstration of improvement in seven patients. Conclusion: Cerebral palsy is a heterogeneous condition and the emergence of a single therapeutic agent that offers a comprehensive effect to improve its manifestations is very unlikely is the near future. Therefore, the use of evidence-based multi-factorial therapies is advisable. Adequate muscle relaxation is vital to prevent the complications of contractures which appear to cause a progressive disability.
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