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脑性瘫痪中的肌肉骨骼病理学:一种分类系统及可靠性研究

Musculoskeletal Pathology in Cerebral Palsy: A Classification System and Reliability Study.

作者信息

Graham H Kerr, Thomason Pam, Willoughby Kate, Hastings-Ison Tandy, Stralen Renee Van, Dala-Ali Benan, Wong Peter, Rutz Erich

机构信息

Department of Paediatrics, University of Melbourne, Parkville, VIC 3052, Australia.

Hugh Williamson Gait Laboratory, Royal Children's Hospital, Parkville, VIC 3052, Australia.

出版信息

Children (Basel). 2021 Mar 23;8(3):252. doi: 10.3390/children8030252.

Abstract

This article presents a classification of lower limb musculoskeletal pathology (MSP) for ambulant children with cerebral palsy (CP) to identify key features from infancy to adulthood. The classification aims to improve communication, and to guide referral for interventions, which if timed appropriately, may optimise long-term musculoskeletal health and function. Consensus was achieved by discussion between staff in a Motion Analysis Laboratory (MAL). A four-stage classification system was developed: Stage 1: Hypertonia: Abnormal postures are dynamic. Stage 2: Contracture: Fixed shortening of one or more muscle-tendon units. Stage 3: Bone and joint deformity: Torsional deformities and/or joint instability (e.g., hip displacement or pes valgus), usually accompanied by contractures. Stage 4: Decompensation: Severe pathology where restoration of optimal joint and muscle-tendon function is not possible. Reliability of the classification was tested using the presentation of 16 clinical cases to a group of experienced observers, on two occasions, two weeks apart. Reliability was found to be very good to excellent, with mean Fleiss' kappa ranging from 0.72 to 0.84. Four-stages are proposed to classify lower limb MSP in children with CP. The classification was reliable in a group of clinicians who work together. We emphasise the features of decompensated MSP in the lower limb, which may not always benefit from reconstructive surgery and which can be avoided by timely intervention.

摘要

本文提出了一种针对患有脑瘫(CP)的能行走儿童的下肢肌肉骨骼病理学(MSP)分类方法,以识别从婴儿期到成年期的关键特征。该分类旨在改善沟通,并指导干预措施的转诊,如果时机恰当,这可能会优化长期的肌肉骨骼健康和功能。通过运动分析实验室(MAL)的工作人员之间的讨论达成了共识。开发了一个四阶段分类系统:第1阶段:张力亢进:异常姿势是动态的。第2阶段:挛缩:一个或多个肌腱单位的固定缩短。第3阶段:骨与关节畸形:扭转畸形和/或关节不稳定(例如,髋关节脱位或扁平足),通常伴有挛缩。第4阶段:失代偿:严重的病理学情况,无法恢复最佳的关节和肌腱功能。通过向一组经验丰富的观察者展示16个临床病例来测试该分类的可靠性,分两次进行,间隔两周。结果发现可靠性非常好至优秀,平均Fleiss' kappa范围为0.72至0.84。提出了四个阶段来对患有CP的儿童的下肢MSP进行分类。该分类在一组共同工作的临床医生中是可靠的。我们强调下肢失代偿性MSP的特征,其可能并不总是能从重建手术中获益,并且可以通过及时干预来避免。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/968f/8004848/0988b5836d75/children-08-00252-g001.jpg

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