新生儿臂丛神经损伤后手功能的恢复。

IF 0.5 Q4 SURGERY
Bharath K Kadadi, Madhusudhan N C
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引用次数: 0

摘要

新生儿臂丛神经麻痹(BBPP)可导致严重的上肢功能损害,特别是影响手部功能。尽管在原发性神经重建方面取得了进展,但许多患者需要二次手术来优化手部使用。本研究评估了旨在恢复BBPP手部功能的手术策略,强调了干预的时机、神经转移的选择和重建技术。全面回顾直接根转移、二次肌腱转移,并分析感觉再教育和长期功能结果。早期神经重建,特别是神经转移到下干或内侧束,在运动终板存活的关键时期进行,显示出良好的功能恢复。继发肌腱和游离肌肉转移被证明对持续性缺陷患者有益,特别是对增强抓握、捏握和固有手功能。感觉恢复仍然是整体手效用的关键决定因素,有针对性的神经转移改善保护感觉。优化BBPP的手功能需要针对每个患者的残余缺陷采用多模式方法。早期神经外科手术为有意义的恢复提供了最大的潜力,而二次手术在改善结果中起着至关重要的作用。了解运动和感觉恢复之间的相互作用是实现最佳功能恢复的必要条件。证据等级:V级(治疗性)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Restoration of Hand Function in Birth Brachial Plexus Injury.

Birth brachial plexus palsy (BBPP) can lead to significant functional impairment of the upper limb, particularly affecting hand function. Despite advancements in primary nerve reconstruction, many patients require secondary procedures to optimise hand use. This study evaluates surgical strategies aimed at restoring hand function in BBPP, emphasising the timing of intervention, nerve transfer options and reconstructive techniques. A comprehensive review of direct root transfers, secondary tendon transfers, along with an analysis of sensory re-education and long-term functional outcomes. Early nerve reconstruction, particularly nerve transfers to the lower trunk or medial cord, demonstrated superior functional recovery when performed within the critical period of motor endplate viability. Secondary tendon and free muscle transfers proved beneficial in patients with persistent deficits, particularly for enhancing grasp, pinch and intrinsic hand function. Sensory recovery remained a key determinant of overall hand utility, with targeted nerve transfers improving protective sensation. Optimising hand function in BBPP requires a multimodal approach tailored to each patient's residual deficits. Early nerve surgery provides the best potential for meaningful recovery, while secondary procedures play a crucial role in refining outcomes. Understanding the interplay between motor and sensory recovery is essential for achieving the best functional restoration. Level of Evidence: Level V (Therapeutic).

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CiteScore
0.90
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