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[脊柱裂的骨科治疗]

[Orthopedic management of spina bifida].

作者信息

Biedermann R

机构信息

Univ. Klinik für Orthopädie, Medizinische Universität Innsbruck, Anichstr. 35, 6020, Innsbruck, Österreich,

出版信息

Orthopade. 2014 Jul;43(7):603-10. doi: 10.1007/s00132-013-2215-9.

Abstract

BACKGROUND

Spina bifida is associated with congenital deformities, such as kyphosis, spinal malformations, teratological hip dislocations, clubfeet, vertical talus and also with acquired deformities due to muscle imbalance and impaired biomechanics. The degree of the acquired deformities and the mobility of the patient depend on the level of the spinal lesion.

DIAGNOSTICS

Neurological symptoms are mostly asymmetric and there is an inconsistent correlation between the anatomical level of the lesion and muscle function. Deficits of sensation are usually one to two levels lower than the motor level. An exact neurological diagnosis should not be made before the second or third year of life and an early prognosis about walking ability should be avoided. The level L3 and therefore function of the quadriceps is a functional milestone after which modified independent ambulation with the use of ankle foot orthoses (AFO) and crutches is possible.

THERAPY

The basic principle is to support verticalization and gait even when loss of ambulation is later expected. It is also important to support and maintain sitting ability for high lesions, if necessary with correction of the spinal deformity. Findings in gait analysis have shifted the focus of treatment from radiological criteria to functional improvement, thus maintenance of the flexibility of the hip is the main goal of hip surgery. Reduction of the hip often leads to stiffness and has a high redislocation rate. Clubfoot deformities should be treated early and foot arthrodesis and stiffness have to be avoided. Another focus is the prevention of joint contracture by early prophylactic treatment.

CONCLUSION

The purpose of management is to maximize the functional potential of the child. Subjective well-being, absence of pain, mobility and socialization are the main goals. This does not necessarily imply ambulation; nevertheless, verticalization and associated orthotic management is one major objective of the orthopedic management of spina bifida.

摘要

背景

脊柱裂与先天性畸形相关,如脊柱后凸、脊柱畸形、畸形性髋关节脱位、马蹄内翻足、垂直距骨,也与因肌肉失衡和生物力学受损导致的后天性畸形有关。后天性畸形的程度和患者的活动能力取决于脊柱病变的水平。

诊断

神经症状大多不对称,病变的解剖水平与肌肉功能之间的相关性不一致。感觉缺陷通常比运动水平低一到两个节段。在患儿出生后第二年或第三年之前不应进行精确的神经学诊断,且应避免对行走能力进行早期预后判断。L3水平以及股四头肌的功能是一个功能里程碑,在此之后使用踝足矫形器(AFO)和拐杖有可能实现改良的独立行走。

治疗

基本原则是即使预计后期会丧失行走能力,也要支持患儿直立和行走。对于高位病变,支持并维持坐位能力也很重要,必要时可矫正脊柱畸形。步态分析的结果已将治疗重点从放射学标准转向功能改善,因此维持髋关节的灵活性是髋关节手术的主要目标。髋关节复位往往会导致僵硬,且再脱位率很高。马蹄内翻足畸形应尽早治疗,必须避免足部关节融合和僵硬。另一个重点是通过早期预防性治疗预防关节挛缩。

结论

治疗的目的是使患儿的功能潜力最大化。主观幸福感、无疼痛、活动能力和社交能力是主要目标。这不一定意味着要行走;然而,直立和相关的矫形治疗是脊柱裂矫形治疗的一个主要目标。

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